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UNCLASSIFIED AD NUMBER AD028666 NEW LIMITATION CHANGE TO Approved for public release, distribution unlimited FROM Distribution authorized to U.S. Gov't. agencies and their contractors; Administrative/Operational Use; 07 MAY 1952. Other requests shall be referred to US Army Springfield Armory, Springfield, MA. AUTHORITY USAWC ltr, 16 Sep 1969 THIS PAGE IS UNCLASSIFIED

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Page 1: UNCLASSIFIED AD NUMBER - DTICUNCLASSIFIED AD NUMBER AD028666 NEW LIMITATION CHANGE TO Approved for public release, distribution unlimited FROM Distribution authorized to U.S. Gov't

UNCLASSIFIED

AD NUMBER

AD028666

NEW LIMITATION CHANGE

TOApproved for public release, distributionunlimited

FROMDistribution authorized to U.S. Gov't.agencies and their contractors;Administrative/Operational Use; 07 MAY1952. Other requests shall be referred toUS Army Springfield Armory, Springfield,MA.

AUTHORITY

USAWC ltr, 16 Sep 1969

THIS PAGE IS UNCLASSIFIED

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armed Services Technical Information AgencyBecause of our limited supply, you are requested to return this copy WHEN IT HAS SERVEDYOUR PURPOSE so that it may be made available to other requesters. Your cooperationwill be appreciated.

NOTICE: WHEN GOVERNMENT OR OTHER DRAWINGS, SPECIFICATIONS OR OTHER DATAARE USED FOR ANY PURPOSE OTHER THAN IN CONNECTION WITH A DEFINITELY RELATEDGOVERNMENT PROCUREMENT OPERATION, THE U. S. GOVERNMENT THEREBY INCURSNO RESPONSIBILITY, NOR ANY OBLIGATION WHATSOEVER; AND THE FACT THAT THEGOVERNMENT MAY HAVE FORMULATED, FURNISHED, OR IN ANY WAY SUPPLIED THESAID DRAWINGS, SPECIFICATIONS, OR OTHER DATA IS NOT TO BE REGARDED BYIMPLICATION OR OTHERWISE AS IN ANY MANNER LICENSING THE HOLDER OR ANY OTHERPERSON OR CORPORATION, OR CONVEYING ANY RIGHTS OR PERMISSION TO MANUFACTURE,USE OR SELL ANY PATENTED INVENTION THAT'MAY IN ANY WAY BE RELATED THERETO.

Reproduced byDOCUMENT SERVICE CENTER

KNOTT BUILDING, DAYTON, 2, OHIO

UNLAS

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THE HENRY SOUTHER ENGINEERING CO

S~Report

4 to

Commanding OfficerSpringfield ArmorySpringfield, Mass.

on

Cr.

INVESTIGATION IP SALT SPRAY ?AeTHOD OFTESTI'IG CORRIOSION RESISTANCE(Contract 'A-19-058 ord. 652)

Report No. 3

Submitted by

The Henry Souther "-ngineering Co.Hartford, Conn.

May 7, 1952

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THE HENRY !TOUIH4FR ENGiNFERING COHAFIr*R0. CONN

00

"Objecti ve,IPhase III, which is covered in this report, was tocarry out the detailed risearch and test programdeveloped in Phase I, using equipment developed andstandardized in Phase Ii.

err" art ~r *igistnra ,.rin r'#rr--n ir an gw, talhtt ... i.1 ., t *il

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THE, HENRY SOUTHER LNGINEERING CO

HARIFORDl. (ONP0

summary

Twenty-foir 'eparate tests were carried out in acc•)rd-ance with data outlined In PMise I as follouW:

Test No. 1 was conducted to determine the rate of cor-roslon of steel panels in various locations In thesalt spray cabinet.

Test No. 2 was a repeat te!t on the corrodibility atvarious locations.

Test No. 3 was made to determine bth6 effect of nozzlepressure on tire rate of corrosion.

Test No, 4 was made to dot u rmne the rate of fog. col-lection at vari,-)us lo~adons in the salt spray cabinet.

Test No. 5 was made "at 9*P5, 21)' sodium chloride solution,using steel panels only, to determine trie effect of testlocation.

Test No. 6 was a 200-howr salt spray toaL run under thefollowing conditions: 20Q sodium chloride solution,pH 7.0, temperature 1000 F.

Test No. 7 was run under the following conditions:207 sodium cnloride solution, pH 7.0, temperatuxe .05F.

Test No. 8 was run under the following conditions:20ý sodi chloride solution, pH 7.0, ter:perature 70 0 F.

Test No. 9 was run under the following conditions:205 sodium chloride solution, pH 7.0, temperature 90*F.

Test No. 10 was run under the following conditions-l&- sodIi- chloride solution, pH 7.0, temperature 950 w.

Test No. 11 was run under the following conditions:5% sodium chloride solution, pH 7.0, temperature .5PF.

Test No. 12 was run under the following conditions:5;i sodium chloride solution, pH 7.0, temperature 70*?.

Test No. 13 was run under the following oonditions:206 sodium chloride solution, pH 6.', temperature 950P.

Test No. 14 was run under the following conditions:20,T sodium chloride solution, pH 8.0, temperature 950F.

-I-

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rHE HENRY SUOTHER ENGINEERING COHARTFOWfl. (CONN

Summary Cont'd

Test No. 15 was run wnder the followin- conditions:subst1tute ocean water, pH C3.9, temperature 950 F.

Test No. 16 was riun under the following conditions:•?ý?sodiu chloride solution containing 0.1+• sodiumiodide, QH 7.0, ternperltLire 9!i*P.

Test No. 17 was run under the following conditions:20.. sodim ohloride solution, pH 7.0, temperature 958F,with the particla size of the fo- reduced from 0.5 micron(used in all other tests) to 0.1 micron.

Test No. 18 was mm under the following conditions:distilled water, pil 7.0,, temperature 95°F.

Test No. 19 was a repeat test using 20% sodium chloridesolution,77H 7.0, teripeavture 9h 0 F.

Test No. 20 was made to determine the effect of corrodi-billoy' Ty-varying the anje of the specimens tected.

Teat N5o. 21 was made to tetcrmine the effect of loweringthe surf ;- tension of the 2G0 sodium chloride solutionby the addition of 0.1;:, kerosol OT when run at pH 7.0and 950F.

Test No. 22 was an outdoor exposure test conducted onLong Island Sound wIthin 150 feet of high water.

Test No. 23 was an outdoor exposure4 test conducted on theroof of tae laboratory building.

Test No. 24 was a humidity cabinet test, using a relativehumidity of 951 at 100"F.

Ai statistical study has- been made of the results obtainedand Is given in the kppendix of each test.

I:, -1-.tq, n U it h 04 r U.In *it h 4 I4tI l..

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TEST NO. 1

ObJect

The object of this test is to compare the corrosionrate of test specimens at the various locatlons within thesalt spray cabinet.

Tasts nave been conducted to determino if steelpanels will corrode at a more rapid rate due to their partic-ular location in the salt spray test cabinet. This is anecessary preliminary step before the rate of corrosion ofdifferent metals can be measured with sufficient accuracy.

Introduc tion

The purpose of this phase of the investigation wasto locate any hot-rpots" in the salt spray caoinet. "Hot-spots"in tnis case designate tnose areas where, due to their relativelocation in the cabinet with respect to the atomizer or forany other reason, panels of like material will corrode morerapidly than panels in another lozation.

Procedure

Thirty-six low-carbon, steel panels, measuring2" x 3" were abraded on both sides using 240 grit cloth andan oscillating electric sander. The panels were numbered con-secutively with stamped numerals and were cleaned In acetone,followed by AX-1 cleaner solution at lO6F and a hot waterrinse. The panels were then free from "water break." Afterdrying in a forced air oven at 110C, they were desiccatedover calcium chloride, cooled to room temperature and weighedto the nearest tenth of a milligram. Each panel was placedin an Individual paraffined wooden rack so slotted as toincline the panels at approximately 150 from the vertical.These holders and panels were arranged on a large wooden rackin the salt spray cabinet in nine rows of four each accordingto a previously determined random distrioution of 36. Allwood parts had been previously coated with paraffin.

The atomizing nozzle was directed away from thepanels and against the side wall of the box so that any sprayfalling on the panels nad been previously reflectod from thewall. This was done to provide a more even distribution offog in the cabinet. Distilled water was used to generate thefog, and the temperature of the box was maintained at QB*F.A, summary of the additional operating conditions is shown inAppendix A. After periods of 24 hours, corresponding to thelet, 2nd, 3rd, 4tn, 5th and 8th day, the panels were removed

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from the box and were scrubbed thoroughly under running waterwith a stiff nylon hand brush. The panels were then dried at1000C, desiccated and weighed as before. The individualweights and times of exrosure are also snown in Appendix A.The position of tre individual panels in the box ic shown inAppendix B. From the data compiled, the average weight loss,the standard deviation and the control limits were computed,and also appear in Appendix A.

A grouped frequency distribution chart, a controlline chart, a plot showing the amount of corrosion with re-spect to position in the box and a graph correlating tne per-centage of tne total amount corroded with the day, were alsoconstructed and are shown in Appendix C.

Discussion

The grouped frequency distribution chart in AppendixC indicates that the valu.es of the Individual weight lossesgroup themselves around the average in a normal ianr.ner andin accordance with the conventional "bell-shaped" distributioncurve .

The control chsrt method of analysis provides acriterion for detecting lack of statistical control of qualityand is used for determining when observed variations in qualityare greater than should be left to chance. The control limitsused are plus ana minup .hree times tae atendard deviation ansuggested bý the ASTM as a criterion for actfon to look forassignable curves of variation. This chart shows that theresults generally fall within the control limits and are fairlyevenly distributed between them. Since, however, certainvalues are outside the limits, it is indicated that there Isa variation in results that cannot be attributed solely tochance.

The plot depicting the amount of corrosion (weightloss) with respect to the position in the salt spray cabinetshows that there is a tendency toward a greater amount of cor-rosion in the side of the box nearer the exhaust and a smalleramount of corrosion nearer tne nozzle and along the front ofthe box. It is interesting to note that the two panels show-Ing the least amount of corrosion were tnose on the twocorners nearest the nozzle.

The graph correlating the percentage of the totalamount corroded with the day shows that the corrosion ratewas not constant but rose gradually to a maximum on the tnirdday and then decreased to a minimum on the eighth day.

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Conclusi ons

There is a definite gradation of the rate of corro-sion with the greatest amount of corroslcn occurring In thoseareas farthest removed from the nozzle and tWe plate glasswindow in the front of the caotnet.

Note: The A-1 cleaner mentioned above Is made in accordance%I W Springfield Armory Tentative Lanoratory SpecificationLS-b, dated March 23, 1950. The suggested composition oftnils alkali cleaner is as follows:

Sodium Carbonate, Soda Ash, Anhydrous 32.8%Fed. Spec. 0-S-571

TrIsodium Phosphate, Tech. 47.2*

Fed. Spec. 0-S-671

Non Ionic SurfAce Active Agent 5.2%

Anionic Surface Active Agent 14.8%

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APPENDIX A

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APPENDIX B

II

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ip.pEIDIX C

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TEST NO 2

Object

The object of this test is to compare the corrosionrate of test specimens at the various locations within thesalt spray cabinet.

Summary

Test No. 2 is a repeat oi :(un 41 and was for thepurpose of checking the results obtained in Run #1. Theoperating conditions and procedures followed were the same asthose of Run #1 w1th the following changes:

I. The panels were observed on the 1st, 2nd,3rd, 7th and 8th days.

2. The average air pressure was lower than InRun #1.

Discussion

The group frequency distribution for Test No. 2shows a much greater spread in the range of weight losses and,although the distribution is more irregular than in Run #1,the tendency toward an oven distribution around the averagevalue persists.

Due to the larger range of values, the standard

deviation and consequently the control limits are larger, andall of the values fall within these limits.

The plot depicting the amount of corrosion (weightloss) with respect to the position in the salt spray cabinetshows approxtmately the same-distribution pattern as was pre-

viously obtained.

The chart correlating the amount of corrosion withthe day shows a maximum weight loss on the second day as com-pared with a maximum on the third day, obtained in Run #1.

Conclusion

The results obtained in this test fall into thegeneral pattern of those obtained in Run #1. The same uneven-ness in the rate of corrosion exists and the greatest weightlosses occurred in the 4ame section of the box*

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APX-ENDIX

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TEST NO. 3

Object

The object of this test is to compare the corrosionrate of test specimens at the various locations within thesalt spray cabineto

Summary

Test No. 3 represents an effort to determine theeffect of a lower atomizing nozzle pressure on the rate ofcorrosion in the salt spray cabinet.

Introduction

The nozzle pressure directly controls the rate atwhich the solution is atomized and, therefore, should bg animportant determining factor on the ratie of corrosion. Lower-ing the pressure should make ;a change in the rate of corrosionaznd possibly in the pattern of the distribution of the rateof the corrosion within the box.

Procedure

The procedure was the same as previously obtainedexcept that the nozzle pressure was lowered to a value be-tween 4 and 6.5 psi. The panels were observed on the lt,4th, 5th, 6th, 7th and Pth days.

Discussion

The grouped frequency distribution for Run #3 showsa closer grouping of values than was obtained in Run #2 anddiffers from Runs #1 and #2 in that it shows a definite skew-ness that had not been ocserved before.

The control line chart shows a smaller overall varia-tion in values and an average that is lower than ttose pre-viously obtained.

The weight loss distribution presents an entirelydifferent pattern than those ootained in Runs #1 and #2. Theareas of maximum corrosion do not seem to group themselvesin any particular section of the box although the generalarea of the maximum corrosion rate is the middle third of thetest area. The maximum weight loss occurred on the firstday.

Concljsions

Lowering the air pressure has a definite effect onthe corrosion rate, and its correlation with the fog distri-bution pattern should be investigated.

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A P PE.iDix

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.. 4"

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JEST WO. 4

FOG DENSITY OBSDRVATIONS

Object

The object of tnis test is t6 determine the uni-formity of fog densities at the various locations within thesalt spray cabinet, the relationship between these fogdensities and the rates of corrosion of the specimens, andto attempt an improvement in fog distribution.

Summary

Tests have been conducted to determine the rateof fog collection at the various locations within the saltspray cabinet and compared with the corrosion rates of thesteel panels used in Tests Nos. 1, 2 and 3, and variationsmade in positions of the nozzle to attempt an improvement infog distrioution.

Introduction

The purpose of this phase of the investigation Isto determine the relationship of the fog densities at variouslocations within the salt spray cabinet to the weight lossesof the steel panels used in Tests Nos. 1, 2 and 5.

Procedure

Run 1 - Thirty-six, 600-millillter beakers, whichhad previou'sy been cleaned and dried, and weighed, wereplaced on a large wooden paraffined rack in the salt spraycabinet in the positions previously occupied by the steelspecimens. The atomising nozzle was directed away from thepanels and against an end wall of the box so that any sprayfalling into the beakers had been reflected from the wall.

This was to provide a more even distribution of the fog inthe cabinet and to duplicate the conditions of Test No. 1.Tap water was used to generate the fog, and the temperaturewas maintained at 950F. The air pressure was the same asthat in Test No. 1. At the end of 23.4 hours, the beakerswere removed from the cabinet, dried on the outside andweighed to the nearest tenth of a gram. From the data com-piled, the percentage* of fog collections were computed andappear in Appendix A, while plots of the densities appear inAppendix B.

Run 2 - A repeat run on the above was performed,and these results also appear in Appendixes A and B.

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Run 3 - In an attempt to provide a more even dis-tribution _oT7g, the beakers were placed in the cabinet asbefore and two nozzles, arranged at equal distances fromeither end of the cabinet, directed the sprays at the endwalls. The temperature was maintained at 950F, and thepressure the same as before. At the end of 23.4 hours, thebeakers were removed and weighed as before. From the datacompiled, the percentages of fog collections were computedand appear in Appendix A.

Run 4 - A repeat of Run 3 was performed, and theseresults als ppear in Appendixes A and B.

Run 5 - Again attempting to obtain a more evendistribution of fog, the rack in the salt spray cabinet wasraised 24 inches from the bottom of the cabinet and thebeakers placed as before. N single nozzle was plAced in thecenter pointing vertically downward, with the spray directedat a low cone-shaped glass piece 14 inches in diameter forthe purpose of directing the spray up and around the rackabove the nozzle. At the end of six hours, the beakers wereremoved and weighed as before. The results appear inAp:_endixes A and B.

Run 6 - For this tast, forty 600-milliliter beakerswere used. a wooden rack was removed from the cabinet andthe beakers were placed in two groups of twenty (four rows offive beakers) at either end of the box. The nozzle was setin the center of the box with the spray directed verticallydownward into a 14-inch circular section battery Jar. Atthe end of six hours, the beakers were removed and dried, andweighed, as before. The results of this run appear inAppendixes A and B.

Run 7 - This run was a repeat of Run 6, except thatthe cover was raised one inch. The results of this run ap-

,pear in Appendixes A and B.

Run 8 - This run was performed in the same manneras Run 1, except for 40 hours duration, with all the conditionssimilar with the exception of the air pressure which waslowered to 5 lbs. per square inch. The results of thisrun appear in Appendixes A and B.

Run 9 - This run was performed in a commercial saltspray cabinet manufactured by the Industrial Filter and PumpManufacturing Co. (Serial S-1540, Type CA l, 37-1/2 incheslong, 21j-1/2 inches wide and 48 Inches from the bottom of thebox to the apex). Thirty-five 600-milliliter beakers wereplaced on a wooden rack in the box at the level of the trough,

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and the box run for eight hours. The beakers were thenremoved from the box and weighed. The results appear inAppendixes A and B.

Run 10 - This was a repeat on Run 9, with theexception otTe number of beakers used which was forty.The run was for a period of 48 hours at which time thebeakers were removed and weo1ghed. The results appear inAppendixes A and B.

Discussion and Conclusions

Examination of the d8ta and charts coveringthese runs shows that only slight gains are made in the

uniformity of distribution )f fog by changinW nozzle posi-tions. The fog distribution is apparently closely tied upwLth the position of the riozzle in relation to the outletrather than the nozzle alone.

Good correlation of the test is apparent by thedistribution of fog nioted In Runs 1 and 2. Comparison ofthese results with the fo1 d1stribution at lower pressure,as shown in Run 8, shows that the rare of travel of thefop across the cabinet bears some relation with the fogdistributi on.

Comparison of the corrosion rates of Tests Nos.1, 2 and 3 with the fog densities of Runs 1, 2 and 8 showsthat the corrosion rate vqries inversely with the fogdensity. A more important relationship will be developedwhen these results are comoared with runs using salt spray.

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APPENDIX A

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I * 4, T

~u-br of e rI~*~a. hr.

I i•2.3 1.32 30.) 1.32 92.7

3 23 .3150 S3.*7

4 24.1 1.03 68.3

5 21 . . )/6 59.3

f 21.7 .990 60.2

7 30.3 1.32 9103

8 1C.6 .710 42.3

9 .%4 .700 41 0.5

10 10o3 .460 22.0Xl 1Q.3 .450 21.1

12 14., .62013 14.2 .*IO 34.1

14 1 .,,CB0 39,315 31o3 1 .37 97.6

16 20,1 .860 C4.

17 9.10 .3o0 1.3

13 19.46 .840 ;2.8

19 11.4 .490 24.4

20 11.2 .6ý0 37.4

22 1 ,•6 .430 21.*

23 U.1 1.42 I100

24 13.0 0,60 30.1

25 9o30 .420 18.7

26 24.6 1.23 84.627 fl. 10 ,3'/O 14*,!

28 19.9 .190 53.7

29 4.40 .190 0

30 15.9 .5,80 39.8

31 17.1 ,730 43.9

32 12.5 .'40 28.5

33 14.J .600 33o3

34 20.2 .860 .5.53

35 15.2 *570 30.9

36 11.5 .;10 26.0

CTNDITT3NS0-1 MET

Dolution Dist. Rate of Sett•ing 2 x 10

Compoeitton (m-.ec.) Av.

Dry Bulb 990 Air Prea.:re 15°ep( F.) ( v,,./in.)

Wet Bulb 990 Air e'emperauure 950

Temp.(0 F.) (OF.)

Relative l0o0 Rat.e of Flow .15

HumIdity ( )

-article Size .3 PI1 of Solution 6.0

(microns) and Fog

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DATrAW 1T~4 u,L-o1,er of Bealcer VIs. Collected

Mlu./ hr.1

21.9 1000 100.03 I.D ..780 36.14 1. 0900 87.85 21.6 .980 98.45 12.2 .550 4C.16 20.4 550 917 21.2 .930 91059 11.2 •510 40.69 16.6 .750 70.610 8.10 .30 2.3.211 8.90 .400 27.812 9.30 .420 30.013 7 .42 sol14

*70 .5;0 21,021, 8.0 .400 27.216 24.0 ,910 •,16 19,5 .•90 86.717 14.20 .390 23.913 1 8 .3 .3 30 2 919 13.G 490 65.420 .62.021 ,91 720 6-ý ,)22 10,3 ,330 ý9.323 1 0,8 C .4.40 37.824 13, , ý 850 61.725 13.3 .620 53,7258.50

,3•0 24.426 21.6 .24027 8.?0 )7*629 .400 2 ,2q 20.4 9 026.3

2 ,4.930 91.530

i )0 •180 030 1i.�J 1.10

76.832 1113 .560 46.3$3 11.1 .900 39.034 13.2 .600 51.2

35 8.70 * (00 63.436

V. .400 26.83 .0

.3 20 20.7

CO"•[Ti'rJ.•S OF ['.•v.cSolution i is t. HOCompolution

2 Rate of Settling 2 x 10-4

Dry !it 1b 990 MAi A5ep( F.)

Air Pressue( 1bs./n. )Net Bulb 920MP(O F.) Rat*eof ?I 15F(-. /-in.)

Relative 1O0•,gHumidity Air remperature 950(0 F.)

Particle 6tze g(aicrona) PH of Soouý'on 6.0( oand Pog

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DATA )N FE T 11 4, 1('N TT

iwumber of 'ealer mit. Collected %fls.ihr.

1 8.30 .3 4 62.7

2 7.Q0 .334 59.7

3 ./00 .030 2.40

4 5.30 .226 38.95 :; -,0 ,.248 42.3

6 1.20 .0151 6.35

7 6.10 .211" 45o23 ] ,60 .068 9.50

9 .400 .017 010 2.40 .102 13.9

11 1 .60 .068 9.50

12 1.'0 .056 7,10

13 3.20 .137 22.2

14 4.00 .171 33 .615 13.0 .556 100.016 .300 .034 3.20

17 1.20 .051 6.30

15 1.50 .056 7.1019 10 2J .051 6.3020 .)00 .033 4.00

21 4.40 .183 31e7

22 1.10 .047 5.60

23 9.60 .410 73.0

24 .jo00 .038 4.00

25 1.60 .068 90 d0

2.• 6 F.0 .235 40.527 1.10 .047 1.b0

23 3.10 .132 21.4.9U0 .034 3120

30 1.90 .064 1.7031 2.70 .115 15.332 .500 .021 1 qO0

33 .800 .034 3.20

34 4.40 .188 31.7

35 1,00 .043 4.,0

36 2.bo .111 1.45

C.)NtTrTOS OF T"2T

2 0-4Solution Dist*. 2 0 A Rate of tettling 2 x 10

Composirt n (1n*./see.)

Dry Bulb 99 Air roessVre 15

Tep.(O F.) (lbA./in. )

S990 Air remperature 950X et 3u~ b 99(o .rrnp.( F.)

Relative 100% Rabe of 'low .15Hmidit(rt, 3/,10.)

Particle S3iZ* .3 pH of Solution 6.0

(miorona) and Fog

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I1'A j 'vT 74' 4 LtU TV

,wnber of0 ie-r 's. Collected ihll./ hr.

1 I.SO 1.25 100.02 4.20 .700 53.53 2.30 .383 40.84 .40 .900 70.45 'p.20 .533 59.46 -.50 .383 26.77 1.20 .700 13 * 5

1 01SO0.2-0 15.4'.40 ,400 23,110 1060 ,207 16.9

1l '.20 .369 25.312 i.20 ,e88 25.313 1.43 .400 28.114 1 0:-0 #9F0 15,415 3.,;0 .583 43,816.0 .383 26.7

2.20 4363 28.3"2./0 .450 .2.513 1.90 .300 19.720 1.50 .2"ý0 15.421 "1110 o450 .12.322 ".40 .400 23.123 3.90 .630 49.224 3.30 .550 40.825 1.40 .233 14.026 '.40 .233 14.027 4100 .117 4,2029 3.10 .517 38.029 1.60 .267 16.9

30 1.40 .233 14.031 1.40 .233 14.032 .600 .100 2.8035 1.20 .200 I1.334 1.60 .267 16,b35 i.00 .333 220536 A400 4067 0

CJNi IT t JF r S.: T

Disat. 12 0 4'ate of Sottling 2 x 10-4COMPo61t ia,+n (mm'./,•.e .)Dry bulb

490Temp.( F.) (lr .rar)15

Wet Bulb 990 Air Tempora.ur* 95°Tmp.(O F.) (o .

Pelative 100% Rate f F•ow 15Humidity ( ft. 3Qn 01

PatrtJcle 6ize .3(microns) n of Solution 6*0and Fog

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J)ArA N) F 4, 4

Number of '.aker •1s. Coullcted a1I./ hr.

1 4.30 .716 9.312 4. :0 1113 11-.34 T71M5 3.'0 .617 06 1.10 .935 2 .07" 3.30 .T5 22.08

10 4.10 .684 6.2511 6.20 1.03 33.112 6.10 =1.02 3 *513 430 .968 32.814 6.00 1.00 36.015 030.10 1.00 36.016 6.00 1.14 43.4I:7.10 1019 !ý.113 •. .15 90.019 o 1.30 64.120

1.19 53.121 10. 10.68 100.022 .•0 1 .65 91.0

3.30 1.47 79.824 7.40 1.23 57.925 7.90 1.32 65.628 % ro 1.58 90.627 3.?0 0.45 78.128 9.00 1.0) 68.129 5.40 1.07 42.130 7.20 1.20 •4.831 4.30 1.18 71.932 ;.20 *.. 14 86.033 7.40 1.13 57.9'4 6.30 1.14 48.435 6.40 1.07 42.336 6.30 1.15 50.037 r.8 1.14 48.A38 .',00 1.15 50.039 C).:0 1.07 42.340 .30 .4`85 2*.0

COND If fj:s jF ry.;T

Solution Dist. it 0Compoaition 2Rate o f ttling 2 x 10

Dry Bulb 990Temp.(°F.) &ir Pressure 1b

Rot Sz1b 99,p. (p F.) A~r Temperature 950( .)

Relative Hu'nidi'ty I00•Rate of Flow

.15Particle Site ( et.3/,in.)(rtcrons) pH or lolution 6.0

and Fog

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:•ATA 'N T. T 't 4. UUU VI

11,ibrr of sIr'-sr M1,. Callected 'la./hr.

1 1.50 .300 e.50

2 2.30 .384 ?.15

15 1.10 .,So0.54 .100 .133 0

5 .100 .133 0.3 2 ý • 0 1 .434 11.7

"2.60 .434 11.73 1.60 .266 r.194 '.1 0 .300 6. 90

1.00 .'I, 1 .301.1 3.;0 .6 O 20.1

12 3.40 .iC 16.9I'l 2. q0 .41.7 1161

14 2.30 .394 9,741. S..130 .167 1.30

16 3.30 .S23 19.51 t .30 .716 22.7

15 q £.30 .384 3.4

19 .o0 .'83 V.5

20 9.10 .467 13.0

21 i".30 1.3s 45.7

22 ýw.20 1 .44 74.623 r.20 1.37 49.1

24 6.30 1.50 3i%72 4 n'30 ."67 24.7

26 ,.30 1.22 42.327 .00 1.34 46.028 3.00 1.34 46.823) 13

30 .20 1.20 41.5

32 6.10 '.14 33.0

33 7.00 1.17 40,.5

34 i1.3 i .38 1.3. S.' 1t.18 4003

36 13.2 2, 0 100.0

37 8.10 1.02 34.4

38 6.40 1,07 36.43:) 17.10 1 .02 34,4

49 4.90 .Ii8 26.6

""3lu Doi. 2') Rate of cettling 2 x J12

Go "pos I t' on 0(m./sec.)Dry 3ulb 99 Air Fresere 15Temp.(o F.)Wet B .lb 99 Air rempirature 950Temp.('F.) (0 F.)

Relative rtumidity 100. Rate, of Flow .15F-,rticie ý-Ize 13 (f't.•/Rib-.)

( icrons) [PH of Solution 6.0and For

S- ; , , •' - -.. .. .. . ... , - '"- ",-- - , ', , . , - , - , ,

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r A N, rT F, 4 h U11 VT

i •~Nmber of 8*&ý-*r ,l.C•ct ,!s/hr.

1 29.7 1.07 100.0S2 1/6 .134 52.4

3 10.5 .438 10.6

4 10.9 .454 12.9

S 14.6 .608 34.7

6 10.7 .446 11.878 T7.T9 .o30 .398 3. 3

10 12.5 .520 22.4

11 13.ý3 .575 30.0

12 11.2 .467 14.7

13 12.6 .0-25 23.0

14 12.6 .12 23.01• 23 0 .9P•0 1.

16 '9.4 .434 i0.011 I)09 .454 12.9

13 11 .3 .495 tees.

I' 9.10 .408 6.47

20 9. ,0 .404

21 22.1 .921 '.9

22 1.6 . 2 0

23 2U.9 .854 69.4

24 bi.2 .426 3.84

25 9.90 .415 7.0S26 1 .650 40.6

27 12,0 .500 19.4

23 1-to .621 35.7

29 ).:30 *3198 3.:30 9.30 .388 3.5331 13.0 .541 2 5.232 Bulb0 3967 r6033 4.140 .371 1.'•

34 14.7 .612 39.435 10.3 .429 9e4036 12.1 .1504 20.0

co-r+posi tion A(m ,ie.

Dry Bulb :99° Air Press re 115

T.,,'p.(° F.) ( Ut)a./ in. )

let Bulb +•9° iir ieoperature 950T "ý•p.(O F,.) (o F'.)

Relative Humndity I00/ Rate of Flow .15

Particle '.Aze 03 Os/A.pH of 'ýolution 6.0

and F,'or

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SA A ,; , 4, 7-:vl.r

Nuill e r of' qa1&kr !TIM. Co1i j Is! -1

1.40 .03

.00.025 (T*:3 1.20 .030 9.3c4 10.09031.9( .048.600 .020 3*13

7" .600 .015 08 !,30 ,032 10.91.70 .042 1 .9 .300 021 t. 210

140 .020 3.1310 l.Z10

33) 9.3812

1 .0,3 12.1S1 2.00 .050 21. q

1.50 21814 1 .20 " 14.1

.030 9.381f

12.0 .042 17.217

2.20 .0551l -. 0 .0-;2 23.4

19 1 .00 6Z2 .20 1.90

.041 20.221 2.90 .O/0 3W.422 2.90 6D 223 1,&0 04s024 2 ,3 0 ,0 59 i 3.e24 .40 or

.50 087426 2.30 0087 4;.4271.00

26.620 .005 31.529'.0.125

63.8.32.50

.J2 2J. 731

2.60 .08 31.23l 3.40 .097.

32 6.1i0 .013 3 .16 ( } ,33 2.02 .062.35 3.20

.080 40.636 i,40 1.35 75.036,'.0

.1t 10 l0.O

C )ýMIITTT 10010'I'•;

Soluti-n Composition Dt. •i20 Rate o'•' Ottin• 2 -104

Dry BulbTo',-p.(" F.) 990 Air krBsre

Not dulb

Air ?TparatureRelative Hunidtty

10" (0"

. Rato of Ilw 165i

pH of Solution 6.0and Fog

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FA PA )t F' 4~ T"

Nu-'rber of' "eavdr ~ 1cre.C' m1ls. 'hr.

1 1~.1 2.0 8.2 14.6 1., 72.0

3 14*0 1.8 72.0

4 12.6 1 . 5;.S

5 10.0 1.3 31,.2

6 1 .8 2.0' 81.0

7 12.7 1.6 5/93

8 11.9 1 5 52,2

9 10.7 1.3 4394

10 10.4 1.3 41,2

11 I1.1 2.3 97,812 i0,I 1 .35 39.0

13 9.7 1.2 36.0

14 80$3 1 29.4

15 9.1 1.1 31,6

16 18.4 2.3 100.011 40 1•, .1 31.6

18 8.6 1.1 27.9

19 1C.4 1.3 41.2

20 •-.0 1.1 30.9

21 1 .5 2.2 93.5

22 A3.0 1.0 23.5

23 6.7 . 90 14.0

24 •.? .7' 6.60

25 3..2 1.0 2-,0

26 16.7 2.1 87.5

27 7.3 .90 19.4

28 C.7 .80 A 1.0

29 4.,3 ."0 0

30 ý.3 .10O 3.7

31 1-3,2 1.9 7MS5

32 1.0 .90 18.2

33 .8 .10 8.1

34 6.2 80 10.in

35 .4 .70 4.4

CONIDTTTONS 0? 7•T

3lut•in conposi tin 20"• WOlI U1lae of SeAlinK 3 x 10

Re lk ive U-n~iiditY l0 Ctir Press r e 14

Splciic ~Gravity 1.10 (Ibs./tn.)

of olution0 o uAr femperature 95

(-'Icrons) pit of Solution 7.2

Ra;,•i3 o f ,'ow ,f g

(S --. )i • '• ..

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,. •-bmr ,1f 'i•eaer '• •. Colloeted i,/:,r.

1 A.0 .1.35 70°8

2 9. io .1 13 61123X) 73.1

4 :).30 .1'1 i.

6 .'0 .;A .2

't,• O .2,)3 i0.1

8 .21M l00.0

9 '. 0 .!ýJ 41Se

10 .40 .114 34.2

11 0.Q) .146 24,41 2 ,7 . 3 0 .1 153 3 1 . '!

13 '.70 181 41e5

14 3,10 .17,'1, 9.10 .115 -s.8

163 .20 . 1 ý2 '1 .0

17 , .0 ,125 0

18 6.10 .13'

19. r-. 0 .15 1/.

20 C." .0 . 22 1 F o •z O . ;222 /oJO '1 4 4r.3

23 .60 .'135 3),024 :'.20 C '.4l1 '9.0

2$ r. 0 .139 1 '.026 ;.30 .!31 .132

27 F. 0 .1,9 1'.0? '3 '. ,0 1. -' ý ) 4 .4

2d .10 .14q

30 i.iO .1S2

31 1.02 .169 51 2

32 9.10 .1l4 ',3

33 /.30 .1 2 11

34 F. 30 v141 19,4395t .162 43 .9

36 '.10 .1-18 26.9

,7 9.20 .1 1 •o6

33 9.20 .1 11 r,3.6

3t i.870 .I1I 6.9

110 -3.ý0 .119 83.5

T V; T

C)~li~v iunsildio SaI Rat Giof/sec.) g x10

Air Press&Ire 14

.,peoif'ic "ruvity 1 .1• Ai ( Prss/t, 9.14

of .')lu tion

Air Pe-periA. ire 95

(",icrons)

R! }I4 r of' .ol~it; ;n .RpAHe of ilow .46nf. ."!- PH of -!o& 7,.2

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APPENDIX B

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, i~T , 7 . 1

, **

* . **.1

* I

-i

.__• ..... . A I• l A

S S

: ./' : ** 2.

1 .... . ...

5'' -4--'

: 1..... ; "

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. .. . , :.R .. .. ... .

-.... ..... . .. .... .. .. .

-4-~~~7 ----T---- - ~ -

I .ril *

P7 A

S.... ... .. .4..[~ o

*. .i.... . ,..a

* . . . . 4,,,, ,

, q .I

NO

* V . I -

MA

-- H. .7• .. ,,•

77.

.P

i i

... 4.5 S;i •. . ..

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.. ... ..... ..i .i ... .. ... ...! "

7 .... ........... - - - -

• i... .. .. 1"' ... I. " . .

. * . ... .. .

I T 1

-- i ; :I i ...

,. • . '.

.- 4•- . .. 1-4- -- I , - •u;- "~ - ,- -

ii. L.i

S.... . . . *._r "- llz rf" iI", i - -i-

-. IC,

', ', ,,..I .i l .

- 4.....-..... -.. . .. . ... .- *-** . ...

, * ! ". .; .

S?.,

. .- ..... I L. ...

_ . .. .. 4L .. .. .2 .. . . .

• 7 .1

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i::_T.7Z1.77, 7V .....

... -.. - - T -

*1 L>7

I t I

j .?! . ,

• :, . .-' '

I -

- , .• .sa..

- I . .''

L: j; ,

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H .ft ..2 72 M..

. .. .. ....... .......

-, F4 ,2 rr,

112

,. a ... . .Ktr 1 .• ..

. ... .-. -. . .. . . 4 "'- L L. ; . .. * . . ' * . e

. . .9 .

. .. .- 4.--:..

.1 , , .. i

Ii : _.__. .. . -

-. V : ,1 . .

B -I

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OA

. .. . ..

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VI. r 7'- 1i AZV 42m~

svw"WMAA WM i- -K

.... . . .. .. ... . ...

.1-T -r-- -

--- ý MA

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ji t fwa TI

- - {....}..I..AL I -i-- -- *-

jrr

-w I- -o F- AM I

- - 7

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F4

-

-

7 J-- -r-r -I

2~I'll

vXZI~

-r-----------------------J,

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127 A7 ~ m 7-IjJ IO

--,

- - -

'Iiý

:7,1

Ii t " 1

tz zr --44-

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TES" NO. 5

7h o>tject 34f V-13 'zl of the I vesL;ý'tiqn Is todetermine the stiuinof wn,3-in of corrosion of steelp~anels In a salt fa.ý- atmos phere.

Summary

t Zst hais "oeer : at 95*F,, iSIn., a, 21); salt solu-tl),ta jýetcrrlne the axitojit if corr~sian if steel panels In

t2-,e diff~erent rarts 4ýý ttie t-st -4rcs of the salt spray caZinst.

Introdaction

In tne f~oregoinn tests, ar.1nvLes-t1,ation uas e--In-die ted- to correlate t'rie an-a-unt of ca-.voslan zfr a st-el pne..vlt~h tne fojz 1-orsity at pot sition~ In the estinet. Fog;

flsrtbiti npatterns irer- determ-1t-od auid wide varlitlans wereIL~erVedi. 7-h a-7o,.nt jfzrr.'sI~ varied, In general, * ythrsel;as th~e &-,cunt )f fog callected. All t!-e.7e runs were made -zsingwa7:er ai;A niot a salt sl--tior. *.A;;ce mos, -of tkie tests uslr1s9tL-1s cabinet irtý to ;:e !!a-de *71tv *89lt; z-AaLionxs, trie distribin-tinn flr corrosion In sucý-, ain at .zhr ..... ; &a ch~eck~ed i n-vaneis -if like -,st'risl L-fo-v c~vu 'jZ.-1o- can ze made. Inseqý:ent r~ans, panel~r~s -T -1lfferý.nt eoTPSIS

.Zanclaslons

Cn te basis 4f t !. e~,it Is evident that th~ecarr~sion rate ax-d distrib-at'l)n are mare even thwn trnoee Intile f'oregoing lests, ?isiný; distilled water. The elstributionzaf co-rroslan as rmessnre~j in tUie outlined manner appearl to be

scitn' -ciaative test can be =%de witth dissIriilar testPariels and that reasanaule cinclusionz can be drawn regardingcorrosion rates regardless of WS position l Ai the test panellIn the box.

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T:.ST NO. 6

Object

The object of this test Is to detormine the cor-rosive effects of a 20" sodium chloride solution, pH 7.0at 10°*F, ýn steel, brass, zinc, al=Irirn, cadmi im, nickelplate, and enameled and phosphated steel.

Summary

A tesL has'been conducted for a period of 200hours in the salt spray test cablnet to determine the effectof increasing the temperatuire 5,F abov,, the standard valueof 95OF. Operating conditions were: temperature 1000 F,207, salt solution at oH 7.0.

Introduc ti on

"The test shtall be conducted with a temperaturein the exposurn, zone maintained at 950 plus 2 or minus 3*F." -

Federal Specification QQ-V-151a. The aaintenaice of the properoperating temperature slould be an important factor in de-termining the corrosion rate of metals and protective coat-ings cecause of the increase Iti reaction rate of most chemicalchanges wi iu an Increase in temiperature. In t:,is and subse-quent tests, the temperature will be varied over the rangeof practically encountered temperatures, and its effect onthe corrosion rate detertined.

Procedure

The test was run for 200 hours, using a 20% sodiumchloride solution at pH 7.0. The cumulative weight losses,,panel ratings and operating conditions are tabulated inAppendix A and a plot of the cumulative weight losses forthe steel, brass, zinc and cadriim panels comprises AppendixB.

Discussion

The steel panels lost weight at a fairly consist 3ntrate, while the brass panels, after an initial loss in twocases, gainod weight steadily. The zinc panels, although moreirregular in their day to da; weights, showed a net loss inweight, whereas the cadmium panels attained a practicallysteady weight after tke first 24 hours of exposure . Theenameled panels and the sulfuric acid anodized panels showedlittle evidence of attack after the 200 hours. The chromicacid anodized aluminum panels showed definite evidence of

!ii__ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _

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corrosion after 176 hours exý,osure. The nickel platedsteel panels all failed after one hour exposure, threefailing after one-half hour. The phosphatod steel panelsshowed no evidence of rusting after one-half hour, butall failed before one hour in the test cabinet.

Conclusions

u a Thes, data collected dudang tits run will be

used as a measure of th, corrosion rate at lOQ@F, 20Osodium chloride, pH 7.0.

i'

___

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APPENTDIX A

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00

N0055S NtoO4' '5O "000 05000 0000 00

g- 4 8 02

,~.s4 ~ ~ Sss~' '~5~.0~.0 000s 0..-00

.~ 00 (0000 0000

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s0 ~ M10 0s 105*-S~ gins 0000 00

~~-p.55goo 00 000000 0

- 74* - - -I I p-s .

0#-0~ 0-~si 00 P10 -. 000 000 000

000

0000~ d00 0 0

OOW ' N OW -. N.P1- s.S-If.

0 84

qpeCC-*.4 --Q

--

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PkPPENDIX B

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*~. ..... -...

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k~ 1fJ W4LJ ZAA.ý.2-A m;

-L N

2 --

le

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CHth4ix ±-4

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-77

W N T . .....~....

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tt

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77~.j 7

~ .7

'-7 7. 774777T

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TEST NO. 7

Object

The object of th*is test and one of the primary

objects of this investigation is to determine the effectof various physical operating conditions on the corrosionrates of various materials in a salt spray cabinet.

Introluction

As a basis for comparison this test was run inaccordance with Specification ASTM B117-49T (similar to

QQ-M-I5la) for temperature, air pressure and solutioncomposition. From results obtained in t:.is test, comparisons

of corrosion resistance can be made when condiLions arevaried.

Conclusions

The test panels, in general, followed the expected

pattern of salt spray resistance. The length of time to

failure for the various materials will LO used as a basisfor comparison with those obtained in subsequent tests.

Procedure

Thirty-six panels, four each of nine different

materials, were used in tais test as summarized below. The

same number and types of panels will be used in the follow-

ing tests:

2 x 3" Steel panels FAE 10303 x 9" Brass panels 70% copper, 30o zinc

3 x 9" Zinc panels2 x 3" Cadmium panels3 x 10" Aluminum panels, chromic acid anodized

3 x 10" Aluminum panels. sulfuric acid anodized

2 x 3" Phosphated (manoanese) steel panels3 x 8" Nickel plated (.001") steel panels

4 x 10" Steel panels, phosphated and then coatedwith two coats of black enamel as de-scribed in Part 1 of this report.

The steel, brass and zinc panels were abraded with a 240-grit

Aloxite metal cloth, using an oscillating electric sander.

They were then cleaned with A-1 cleaner, water-rinsed, dried

at 1100 C, cooled and weighed to the nearest tenth of a

milligram.

Difficulty was encountered in attempting to

abrade the cadmium panels due to the -:oft nature of the

metal. These panels were dipped in a 2% hydrochloric acid

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solution at room temperature for five minutes and water-rinsed prior to weighing. The anodized aluminum, phosphated,nickel plated and enameled panels were placed in the saltspray box without any additional cleaning operation.

The steel, brass and zinc panels were removedfrom the box every 24 hours. They were scrubbed with astiff nylon bristle brush under runnift watcr until no morecorrosion product could be removed as indicated by visualinspection. They were then dried and weighed as before.

Previous experience has shown that the corrosionproducts of cadmium adhere tenaciously to the metal and arenot really soluble in water. As a result of tests conductedand elsewhere described in this report, the cadmium panelswere cleaned by immersion in a 2% sodium cyanide solutionfor five minutes at room temperature followed by a waterrinse.

A visual rating system was employed to evaluatethe anodized aluminum, nickel plated steel, phosphated andenameled panels as described in the ASTM article - "A VisualSystem for Ratin& Panels."

Observations were made on the phosphated steel

and nickel plated panels after 1/2, 1, 1-1/2 and 2 hours,

aand all panels were observed every 24 hours. The observa-tions and weight losses appear in Appendix A.

The box was operated at 95*F and a 20% salt solu-tion was used. The pH of the solution was adjusted to 7.0.The operating conditions and physical values mentioned arealso summarized in Appendix A.

The cumulative weight losses were calculated and

plots of these values versus the corresponding days are inAppendix B. The tests were limited to 200 hours durationsince the data required for evaluation were obtained wellwithin tnie time limit.

Dis oussion

The steel panels lost weight at a fairly oonstantrate. The values diverged in increasing amount with in-creasing time. Variations from a constant rate or corro-sion can possibly be ascribed to incomplete removal of

corrosion products on individual days.

C , , . . , II I • II

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The brass lanels all lost weight during thefirst 24 hours and then gained steadily, although not con-stantly for the remainder of the test. At 120 hours, allthe panels equalled or exceeded the original weight at thestart of the test. The changes in weight were only ap-proximately one-tenth those for the steel panels, althoughthe brass panels have 4-1/2 times the surface area of thesteel panels.

The zinc panels lost weight at % relativelysteady rate and were heavily streaked with white corrosionproducts, all of which could not be removed by scrubbing.

The enameled panels stood up well, as was to beexpected. Slight rust along the edges and a few rustspots were noted as shown in detail in Appendix A.

The phosphated steel panels all failed at theend of 2 hours - one failing at 1 hour and two at 1-1/2hours.

Conolusions

These test results are to be used as a standardfor comparison when deviations from standard practice aremade.

It

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_ýv!)IT,' N RAT111G PANELS*

Rating of 3" x 10" Chromic ½Aid and Sulfinric AcidAnodIzed Aluminnum Panels

Puumerical Corrosion Corrosi on CorrosionRating Dots Lo ts Areas

10 No corrosion No corrosion Nlo corrosion

9 10 5 2.5 small areas

7 20 10 5 small areas

5 40 20 10 small areas

3 F?0 40 20 small areas

1 160 80 40 small areas

0 Complete Corrosion

Rating of 4" x 10" Enameled Panels

10 No corrosion Yo corrosion Yro corrosion

9 15 6 3 sm'all rust areas

7 26 13 6 small rust areas

5 53 26 13 small rust areas

3 213 106 53 shiall rust areas

1 426 213 106 small rust areas

0 Complete Corrosion

Rating of 3" x 8" Nickel-Plated Steel Panels

1 rust spot in 24 square inches constitutes failure.

Rating of Phosphated Steel kanels

First sign of rust constitutes failure.

*Based on "A Visual Rating System for Rusted Steel Specimens" byHarry L. Faigen. Authorized reprint from the Copyrighted ASTMBulletin No. 154 October, 1948.

- --

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Object

The object of this investtgatlon is to developan effective mot, od for cleaning cadmiums tevt panels aftertheir exposure In the salt spray test cabinet.

Stummary

Tests havo been conducted to eiraluato the effec-tiveness of soaking the cadmium panels in a dilute cyanidesolution as a method for the removal of corrosion productsadhering to the surface of the panels.

Introduction

When cadmium panels wore exposed In the salt spraycabinet, there was an initial buildup of corros1lon productson the surface as indicated by a sharp gain in weight duringthe first 24 hours of exposure. After that, the weightsremained practically constant on successive days despitethorough scrubbing with a stiff nylon bristle brush underrunning water. This is probably due to the formation ofa film of cadmium oxide on the surfice which adheres tena-ciously enough so that it cannot be removed by scrubbing.A dilute solution of sodium cyanide was used to dissolve thecoating, and results -f qi investlg'it' -n of this method aresummarized below.

Pro cedure

Four cadmium :anels were cleaned in 5% hydro-chloric acid for 5 minutes, rinsed under running water,dried in a forced air oven at 110C, cooked, and weighedto the nearest tenth of a milligram. They were exposed tolaboratory air for 24 hours and then immersed in a 2%solution of sodium cyanide for 5 minutes, rinsed with runningwater and dried as before. This process of exposure andcyanide cleaning was repeated over a poriod of 12 days. Asummary of the individual day to day changes- in weight alongwith the average and standard deviation is attached.

Discussion

From the data in the summary, the weight losses

incurred appear to be insignificant especially when com-pared with the results obtained with cadmium panels andexposure to salt spray as shown ir. the salt spray tests,starting with Test No. 7.

Conclusion

The method of cleaning the cadmium panels asoutlined appears to be satisfactory and has been adoptedas a routine procedure.

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CADMIUM 4ETGHT LOSSES

Pariol No. 1 2 3 4

Day

1 .0009 .0012 .0008 .0005

2 .1005 .0004 .0007 .0005

3 .'005 no0,00 . )005 .0003

4 +.0003 .')07 . '•0 .0011

5 .106 .0001 .r-01 .0001

6 +.(I010 .0009 +.1008 +.0014

7 .)000 .)001 .0002 .0001

8 . .0001 .0-01 .0005

9 ."002 .0'0O .0001 . 007

10 .0 00 .0003 .1002 .0007

11 .0003 .0000 .0002 .0002

12 .1003 .10O .1000 •0 o04

Average .2)0167 .000317 .100175 .000308

Standard Deviation .000174 .000365 .000364 .000583

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APPENDIX A

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t ab

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1 9

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"-a 't "

t- ~ 0 00 '~8'8' p00048

IIN

8'~~ 8' 00

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000 0

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ol '-

eft~a

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APPENDIX B

iA

a

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TEST NO. 8

Object

The object of this test is to determine the cor-rosive effects of a 20" ' soditim chloride solution, pH 7.0at 70*F on the nine materials described in Test No. 7.

A test has been conducted for a period of 150hours in the salt spray test cabinet to determine the ef-fect of decreasing the tez:perature 25OF below the standardvalue of 950F. The concentration of the salt solution andits pH as well as the operating conditions of the box were-aintainod the same as in Test No. 7.

Introduction

70 0 F approxi-ates room temperoture and, therefore,the lowest conveniently obtained teiiperaturc for the opera-tion of a salt spray test cabinet. Corrosion rates at thistemperature obtained in t:•is test will be compared to thoseat elevated temperatures.

Procedu'e

A procedur similar to that described in TeE~t No. 7was followed. The test was li:nited to 150 hours, using a

20% sodium chloride solution at pH 7.0. The cumulative weightlossos, panel ratings and operating conditions are tabulatedin Appendix A, and a plot of the cumulative weight losses for

the steel, brass, zinc and cadmium panels comprises AppendixB.

Discussion

The steel panols lost weight consistently. It isinteresting to note that in Tests 6, 7 and 8, the order inwhich the pancals lost weight (2, 3, 4, 1) is the same.This is probably due to their position in the box. (Seeplot of positionE given in Appendix B of Test No. 1)

The brass panels lost weight during the first 24

hours and then sained qs has oeen previously experienced.

The zinc panels, however, showed a slight Increase in

weight compared with a marked decline experienced at the

higher temperature.

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The cadmium panels lomt consistently and theirweight losses were grouped closol: together.

The enamLeled panels s.,owed little evidence ofcorrosion at the end of the 150 hours.

The chromic acid anodized aluminum panels provedsuperior to those prepared by the sulfuric acid process,althoughi t e difference Yms not as great as had been ex-perienced at higher temperaturts.

Te nickel plated specimens all failed bufor'i 24hours exposure, and the phosphatnd steel panels failed be-fore 2 hours.

Conclusions

These data constitute a measure of the corrosionrate at 70F, 20% sodium chloride, 1,H 7.0. The results willbe used to determine the effect of concentration of saltsolution and temperature on the corrosion rate.

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A

APPENDIX A

dS

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m0a coo,-, ~ 00 0000 0 0 ý0

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040

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go *N000 .0 C, aN~ 00,

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APP1MNDX B

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r 1r

-~. ...........

(HiOUR

;11'7

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I . ........... .. . . . . . . . . 1 2 2J- (Ir

4.4

~~ARA L-*

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January 31, 1952

At the suggoesticrn of Arthur 'avarella ofSpringfield Armory, we are going to add oxidized steelpanels, prepared by PentratinS, to the series of speci-mens being tested in the salt spray cabinet. This isto be done because f the considerable use of oxidizedsteel for Ordnance.

Since the salt spray cabinet is being run on atotal of thirty-six panels, and because the box has al-ready been calibrated, using tnirty-six panels with arandom distribution which has not beeni changed, itseems desiraole to eliminate one set of specimens.As the tests on the baked enamel panels are not sig-nificant in a 200-hr. test period, further test workon enameled panels is to be eliminated.

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TEST NO. 9

Object

The object of this test is to determine the corrosive

effects of a 20% sodium chloride solutionr pH 7.0 at 90*F, onthe nine mnaterials described in Test No. 7.'

Summary

A test has been conducted for a period of 150 hoursin the salt spray test cabinet to determine the effect of de-

creasing the temperature 5*F below the standard value of 95FP.The concentration of the salt solution and its pH as well as

the operating conditions of thQ box were maintained the sameas in Test No. 7.

Introduction

This test, the fourth of the series, will be usedalong with the data from Tests Nos. 6, 7 and 8 to determinethe effect of temperature variation on the rate of corrosionin a salt spray cabinet.

Procedure

. procedure similar, to that outlined in Test No. 7

was followed and the test was run at 90OF with 20% sodium

chloride soldtion, pH 7.0, for 15n hours. The cumulativeweight losses, panel ratings and operating conditions aretabulated in Ap:)endix A and a plot of the cumulative weightlosses for the steel, brass,-zinc and cadmium panels compriseAppendix B.

Discussion

The steel panels lost weight at a fairly consistent

rate and the final order of their losses was the same as was

previously experienced (i.e. 2, 3, 4, 1).

The brass panels, after an initial loss, gained

weight but only two panels exceeded their original weight

in contrast to the more general case where all the final

weights exceed the original weights.

After some initial irregularities, the zinc panels lost

weight steadily.

The cadmium panels lost constantly, and their weight

losses were well grouped together.

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The pentrated steel panels all failed before1-1/? hours, two failing before 1 hour.

The sulphuric acid anodized al•unmnum panels allfailed oul'ore 22 hours, while the aluminum panels anodizedby the chromic acid process failed before 129 hours ex-posure.

The nickel panels all failed before I hour, twofailing before 1/2-hour.

The phosphated panels all failed before 2 hours

exn'osure in the salt spray cabinet.

Conclusions

The data obtained in tnus ran will be used in con-junction with those obtained on the three previous tests todetermine the effect of temperature on the corrosion rate inthe salt spray cabinet.

Sii l|

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&P1F'I,-D[X A

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II

i .1

y-L-44tr-- týtH~~S

--.

4D A w~ A 1, A

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TEST NO. 10

Object

The object of tiats test is to determine the corro-sive effects of a 10% sodium chloride solution, pH 7.0 at95'F on steel, brass, zinc, cadmium, pentrated steel, chromicand sulpharic acid anodized aluminum, nickel plated steeland phosphated steel panels.

Summary

A test hias ueen conducted for a period of 150 hoursin the salt spray test cabinet to determine the effect ofdecreqsing the concentration of salt in the salt spray solu-tion from 20% to 10%. The temperature and pH of the solutionwere maintained the same as in Test No. 7.

Introduction

In any chemical or electrochemical reaction, theconcentration of the reactants or electrolyte is of obviousimportance. The concentratlon of salt in the salt solutionused in this type of testing should, therefore, have aue direct effect on the rate of corrosion. In this test andin Test No. 11, the concentration of salt will be reducedand its effect on the corrosion rate observed.

Procedure

A procedure similar to that described in Test No. 7was followed. The test was run for 150 hours, using a 10%sodium chloride solution at pH 7.0. The cumulative weightlosses, panel ratings and operating conditions are tabulatedin Appendix A, and a plot of the cumulative weight lossesfor the steel, brass, zinc and cadmium pan'als comprisesAppendix b.

Discussion

The steel panels lost weight steadily and thebrass panels, after izitial losses, exceeded their originalweight in three out of four cases.

Mhe zinc and cadmium panels both lost weightin a manner similar to that previously experienced.

Three of the pentrated steel panels failed before1/2-hour ex.osure, the other failing before 1 hour.

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The aluminum panels anodized by the sul-huricacid process held up better than those prepared by thechromic acid process. The sulfuric acid anodized panelswere little affected at the end of 150 hours exposurewhile three of the chr,mlc acid aiodlzud panels failed be-fore 132 hours.

The nickel plated steel panels-a1l failed before

24 hours exposure and the phosphated steel panels all failedbefore 1 hour.

Conclusions

These data form a moasujro of tdle corrosion rate at

95 0 F, using a 10% sodium chloride solutiorn, pH 7.0. They

will be used in conjunction with Tests No. 7 and No. 11 to

determine the effect of salt 2oncentrat'on on uhe rate of cor-

rosion.

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APPENDIX A

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2. goof ~ o

A 30 .0... ..--

2 t-00(0000

-~ we..4

- S 00

S 0 50... C

14C5

au CS. P0 b5

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APPPENDIX B

.1;

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TEST NOo 11

Object

The object cf aJs test is to determine the corro-sIve effocts of a 5c/t, sodium chloride solutfon, PH 7.0 at 950F,on the nine materials listed in Test 'No. lo.

Summary

A test has been conducted for a period of 15() hoixrs_In the salt sprqy test cabiriet tQ deto.r:7ilne the effoct of de-creasing Ule concentration of salt In the solution from 210,7to 5%. -he temperature and pH were maintained the s&rie as InTest No.17.

Introduction

This test represents the lowest limit of salt con-

centration and will be used In conjunction with Tests Nr). 7and No. 10 to determine the effect of concentration of salt Inthe solution 3n the rato of corrosion In the salt spray test

cabinet.

Procedure

A procedure similar ti tnat described in Test No* 7

was followed. The test was run for lbO hours, using a 5?' sodlum

chloride solution at PH 7.n. The cumulative weight losses,

panel ratin,ýs and op,.,ratirV. conditions are tribulated In Ao-

pendix A and a plot of the cumulative weight losses for the

steel, brass, zinc and cadmium panels comprises Appendix B.

Discussion

The steel panels lost weight'at a fairly steady

rate with Panel No. I still showing the greaLest loss that

has been experienced on all previ,)us tests of this type.

The brass panels showed no Initial loss and gained

weight steadily, while the zinc and cadmium panels lost in

the previously experienced manner.

The pentrated steel panels all stiowed rust at the

end of 1/2-hour's exposure.

The aluminum panels anodized by the sulphurle acid

process showed a superiority over those prepared by the

chromic acid process. Three of the sulphuric acid anodized

panels showed no signs of corrosion after 150 hours exposure,

while all of the chromic acid 'anodized panels showed evidence

of attack after 110 hours.

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The nickol plated steel panuls all failed beforeA4 hours expostii, qnd the riiosphated Fteel panels all failedbefore 0 hours.

Conclusions

These data constitute a measurm of the corrosionrate at 95'F. 52• sodium criloride, -H 7.". Those r rults willbe used to determin•e the effect of c-nwentraton of salt int1he solution )n the rate of salt Frray c,)rroston.

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�r 1� F�IDIX A

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APPENDIX B

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T KST NO. 12

Object

The object of thIs t-st is to'determine the cor-r-osive effects of a 5e sýdlum chloride solution, pH 7.0 at700F on the va lous types of panels used in this series oftests.

Summary

A test has been eondji.ted in the salt spray testcabinet at 70*P, usine a 5% sodium chloride solution, pH7.0.

Introduction

The information collected in this test, the lastof n series, will be used together with the results fromTests 6 through 11 to determine the effect of concentrationof salt solution and temperature of operation on the cor-rosion rate. This test represents ihe lower limits oftemperature and *oncentration that will be. used for com-parison.

Procedure

A ")rocedure similar to that described in TestNo. 7 was followed. The test was rum for 150 hours, usinga 5% sodium chloride solution at pH 7.0. The temperature ofthe box was maintained at 700F. The cumulative weight losses,panel ratings and operating conditioneare tabulated inAppendix A and a plot of the cumulative weight losses forthe steel, brass, zinc and cadmium panels comprises AppendixB.

Discussion

The steel panels lost weight at a reasonably

steady rate and the order of their weight losses was thesame as has been previously experienced.

The brass panels showed no initial loss in weightand, with minor variations, gain weight consistently.

The zinc panels did not show their usual steadylosa in weight, but instead, after initial losses, tendedto approach a steady weirht value.

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The cadmium panels lost weight at a consistentrate, and the values were closely grouped as usual.

The pentrated panels all failed before 1 hour'sexposure, while both the sulfuric acid and ciromlc acidanodized aluminum panels showed very little evidence ofattack at the end of the test period of 150 hours.

The nickel plated steel panels all failed before24 hours, and the phosphated panels failed before 2 hours.

Conclusions

These data constitute a measure of the corrosionrate at 70F, using 5b salt, p 47.0. The information willbe used in comparisons with previous tests to determine theeffect of temperature and concentration on the corrosionrate.

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WMA~DX B

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TE6T NO. 13

Object

The object of tlis test is to determine the cor-rosive effects of a 20% sodium ciloride solution, oH 6.0at 95*F, on the various types of panels .Isd in the pre-vious tests.

Summary

A tett has been conducted In the salt spraycabinet at 95OF, using a 20% salt solution with a pH of 6.0as compared with 7.0 used heretofore.

Introduction

The pH and hence the acidity or alkalinity of thesalt spray solution should haVe a direct bearing on the rateof corrosion in the test cabinet. This test at pH 6.0, to-gether with the data to be obtained in Test No. 14 at pH 8.0,will be used in comearison with 'rest No. 7 to deturmine theeffect of pH on the corrosion rate.

Procedure

A procedure similar to that described in Test No. 7was followed. The test was run for 150 hours, using a 20%

sodium chloride solution at pH 6.0. The temperature of thebox was maintained at 95(F. The cumulative weight losses,panel ratings and a summary of the operating conditions aretabulated in Ap endix A, and a plot of the cumulative weightlosses for the steel, brass, zinc and cadmiut panels com-prises Appendix B.

Discussion

The steel panels lost at a reasonably consistentrate, while the brass panels showed wide variations and un-usually high gains in weihht.

The zinc panels lost at a fairly steady rate, the

weight losses being greater than those usually experienced.The cadmium panels lostE weight at an even rate in

a manner similar to that prfv~ousl; experienced.

The Dentrated panels all failed before one-halfhour's exposure.

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The chromic acid anodized aluminum panels provedsuperior to those prepared by the sulfuric acid process. Allthe sulfuric acld pari-l s towed signa of attack at 24 hours,while no appreciable slns of corrosion aop,•;red on thechr'omic acid panels until 8T hours.

The nit-kel plated steel panels all failed before2 hours, and the phospha-ed steel panrls all failed before

-1/2 hour .

.onclusions

The cWa cnlncted In t is run constitute ameasure of the corrosion ra-e at 950P with 20, salt solution,pH 6.0, and will be used to deternmine the effect of pHvariation on the rate )f corruslon in the salt spray cabinet.

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A~i-ENDT A

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.1

I

APSI4DIX B

I

3

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TEST NO. 14

Object

The object of' tA' t'ý;t !s to fetoeritne the cor-rosive effects of a P, sodiulmr cnloride sol ution, pli 8.0at 95 0 F, on the var-.-us t pi;s -f parnels used in previoustests.

Sum.mary

lk toit hqs boee c,)ndu1Ettd in the salt spraycabinet at 95'F, usinc 1 20> 'odiun chlor'de snlutlon ad-justed to p11 8.0.

Introduction

This test, the third of a series, will be usedti supply additional information as to the effect of achange in pH on the rate of corrosion.

Procedure

A procedure similar to that de:crlbed in TestNo. 7 was followed. The test was run for 150 hours, usinga 20% sodium chloride solution adjusted to oIi 8.0. Thetemperature of the box was maintained at 950 F. The cumu-lative weight losses, panel ratings and a summary of theoperating conditions are tabulated in Aptendix A, and aplot of the cumulative veieýht losses for the steel, brass,zinc and cadmium panels comprises kppendix B.

Discussion

The steel panels lost weight steadily and in aboutthe manner usually experienced. The brass panels, after aninitial loss, gained weight altho•ijh the time necessary toexceed their orit-inal weight varied widely.

The zinc panels showed high weight losses whencompared with the valiies unliqlly obtained. The cadmium panelslost weight, although the rate was not as constant as usual.

The pentrated steel panels all failed before 1/2hour. .ide variations were r'xp~renred in the time forfailure of the anodized alutninum pawels; two of týýose pre-pared by the sulfuric acid process failing before 24 hoursexposure. The chromic acid anodized aluminum panels failed'in between 66 to 110 hours exposuire.

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The nickel plated steel panels all failed before

2hours as did the phosphated steel panels.

Conc l•sions

The values collected in this test will be usedas a measure of the corrosion rate at 950F, using a 20%salt solution, pH P.0, and will be used in comparison withthe results from Tests No. 12 and No. 7 to determine theeffect of pH on the corrosion rate.

'p

S.. .. . / .... " ++ *

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IAi-Ft!,A.-rX A

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AiP,,NDIX B

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TEST NO. 15

Object

The object of this test is to determine the cor-rosive effects of a spray of substitute ocean water at 95OFon the various types of panels used in this series oftests.

Summary

A test has been conducted in the salt spraycabinet at 950F, using substitute ocean water at pH 8.2.

Introduction

One of the purposes of the salt sp ray test is tosimulate, under accelerated conditions, the effects ofnatural outdoor corrosion and, more particularly, the cor-rosive effects of a marine atmosphere. There have beenquestions raised as to whether the salt spray test measuresthe resistance to marine atmospheric corrosion. A sprayof sumstitute ocean water has been suggested as a bettersimulation of the actual c nditions of exoosure. Theresults of tris test and of Test No. 7 will be comparedand these in turn compared to results obtained from actualexposure tests made in a marine atmosphere.

Procedure

A procedure similar to that outlined in TestNo. 7 was followed. The substitute ocean water was pre-pared In accordance with direct'ons included in our firstreport. The heavy metals mentioned were added. The testwas run for 150 hours at 950F. The cumulative weightlosses, panel ratings and a summary of the operating condi-tions appear in Appendix A. A plot of the cumulativeweight losses for the steel, brass, zinc and cadmiumpanels comprises kppendlx E.

Discussion

The steel panels lost weight at a fairly con-sistent rate while the brass panels showed no initial loss,but gained weight steadily.

The zinc panels showed a very slight increasein weight as compared with the usual losses in weight.

The cadmium panels lost weight steadily, but thelosses were not as great as usual.

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The pentrated panels all failed before 1 hour'sexposure. Neither thie chromic acid nor the sulfuric acidanodized aluminum panels snowea any signs of failure atthe end of the test porlod of 150 hours.

Phe nickel plated steel panels all.failed before2 hour's expo!-ure, and tn:e phosphated sLeel p9nrels allfailed before 1 hour's exoourbe.

Conclusions

T he infrmaýAlon obtain-id fr,)m tLis tust will be

used as a measur- of the corrosive effects of a spray ofsubstitute ocean water. Theso rosulte will be compared withsalt spray and rmarine atmosphere corrosion rates.

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AFiýV1DTX A6

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A I)TV~X A.

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MN~ T A a

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TE2$T NOe 16

Object

The object of this test is to determine theeffect of the presence of iodide ions in approciablequantity in the salt solution used to generate the fogin salt spray testing.

Summary

4 test has been run at 95*F in the salt spraytest cabinet using a 20% sodium chloride solution, pH 7.0,with a 0.1% addition of Iodide ion in the form of sodiumiodide. Conditions of oporatlon and types of panels ex-posed were the same as previously described, the onlydifference being the addition of iodide ion.

Introduc tion

Specifications det-idling tho orocedure for salttpray testing roquire the use of iodide-free salt. Theeffect of another halogen ion besides cihlorine on the rateof corrosion should ther-efore be dettrmnined from thestandpoint of possible substitution of commercial gradesof plain or iodized salt. Results of tnis test will beused in comparison with those under the sane operatinCconditions, using C.F. 20% so !Ium chloride solution.

Procedure

A procedure similar to that outlined in Test ?'o.7 was followed. The test was run for a period of 150hours, using a solution composed of 20% sodium chlorideand 0.1% sodium iodide in distilled water, the pH beingadjusted to 7.0. A summary of the operating conditions,cumulative weight losses and panel ratings are shown inApoendix A, while a plot of the cumulative weight lossesof the steel, brass, zinc and cadmium panels comprisesAppendix B.

Discussion

The steel panels lost weight at a fairly steadyrate and no change was noted In the order of the rate ofcorrodibility with box position (i.e., 2, 3, 4, 1). Thebrass panels, after initial losses, gained weight in themanner usually experienced.

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VI

The zinc uariels and cadmium panels showed steadylosses of a magnitude greater than that generally experi-enced.

The pentrated steel panelv all failed before1/2 hour'l ex-o:-ure, while the aluminum panels, anodizedby ooth t:,e ch1rmic and sulphuric acid processes, showedvaried results with littlo possibility of comparlson.

The i:iclel platud steel all failed in between1-1/2 an! 2 hours exposure.

Three if the phosphated steel panels failed be-fore 1 hour's exposure, while the other failed before 2hours.

Conclusion

These data constitute a measure of the corrosionrate with a 0.",' addition of sodium iodide, and will beused in comparison Adth the results from Test No. 7 todetermine the effect of iodide ion on the rate of corrosion.

i f

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Ap1pENDIX A

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D

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T-'ST NO. 17

Object

The object (if t is ttost is to determine theeffect of reducing the size of the salt. spray fog particleson tne rate of corrosion in the salt spray test cabinet.

Summary

A test has been conducted at 95&F using a 20%salt solution, pH 7.0, and a modified atomizing nozzle soas to produce a fog of substantially reduced particle size.The same operating conditions and types of panels were usedqs have been employed in the previous tests, the onlyvariable from standard conditions being the particle size.

Introducti on

The particle size, although not directly specifiedin the description of standard salt spray test requirements,directly affects the wetness And density of the fog producedand, ther-fore, should have some bearing on the rate ofcorrosion. This test, made with a fog ctreduced particlesize, will be used in comparison with Test No. 7 which re-pr,:sents the samrn conditions with the exception of a largerparticle size.

Procedure

A procedure similar to that outlined in Test No. 7was followed. The change in particle size was broughtaboit by a slight increase in diameter of the hole feedingthe salt solution into the air Jeta. The test was conductedfor a poriod of 150 hours at 95 F, using a 20% sodiumchloride solution, pH 7.0. & summary of the operating con-ditions, cumulative weight losses and panel ratings com-prises Appendix A while a plot of the cumulative weightloeses for the steel, brass, zinc and cadmium panels isfound in Appendix B.

Disc'ission

The steel panils lost wei_.ht !n accordance withtheir usual pattern. The brass panels, after initiallosses, gained weight steadily and in ev•try case exceededtheir original weight before the end of the test.

The zinc panels lost weight from the beginningof the test, and the ca4mium panels showed very steadyand closely grouped weight losses.

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Three if the pontrated steel panels failed before1/2 hour, wVile the fourth failed before 1-1/2 hours.

Anocilzed -aluminum panels prep.i, ed by the chromicacild process s,,owed sup-riority over those prepared by thesulphuric acid roceso, tu!ree of these failing before 24hours expo: tire.

The nickel plated steel panels alr failed before24 hours exposure, and tue phovphated steel prinels allfailed before 1-1/2 hours exposure.

Conclusl ons

Tlesi data constitute a measure of the corrosionrate at stwadard conditions i,• th a reduced particle size,and will be used in comparison with Test bo. 7 to determinethe effect of particle size on the rate of corrosion.

fU

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kPPENDIX A

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AMC-

.. r~m c

I t 4 .. o.

p~t~a.. .¼.r Op~t ~ r

i~~'~4 0 .N..Frd5 P..9

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APPENDIX B

SI

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STEST NO. 18

ObJect

The object of tnls test is to determine the effectof a fog formed by spraying distilled watur on the ninetypes of material previ usly used in the £oregoing seriesof salt spray tests.

Summary

A test has been conducted at 950F in the saltspray test cabinet for a period of 150 hours using, as thetest solution, d~stilled water adjusted to pH 7.0.

Introduction

A spray of distilled water has been sugtrested asa possible substitute for salt spray in accelerated corro-sion testing. This test, using distilled water, will be usedas a measure of the effectiveness of this method and willalso be used in comparison with the results obtained fromsalt spray, humidity, and outdoor exposure tests.

Procedure

The salt spray test cabinet was thoroughly cleanedwith water to remove the salt adhering to the box, and wasrep'atedly rinsed wit•, city water until rinsings showed onlya very slight haze when tested with 0.14 N silver nitratesolution. The box was then operated with a dt&tilled waterspray for 24 hours and drained before the test panels wereput in. The test panels were prepared and evaluated in themanner described in Test No. 7. The test was run for aperiod of 150 hours, using distilled water with the pH ad-justed to 7.0. A summary of the operating conditions,cumulative weight losses and panel ratings Is shown inkpnendix A while a plot of the cumulative weight lossesfor the steel, brass, zinc and cadmium panels comprisesAppendix B.

Di scus sion

Lshe steel panels lost weight at every inspection,

but the rate of loss was not as steady as has been experi-enced with salt solution.

The brass panels snowed little or no initial loss,and their weight gains were extremely low and erratic.

t : _ ° . . . -. ...

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The zinc panels lost wei.,ht after 24 hours ex-posure, and the cadmium panels lost weight at a steadyrate and in a closely grouped pattern.

The rtontratei steel -nels all failed before2 hours exposure, wiIle neither the sulphuric nor thechromic acid aulodized aliimtnum panels showed any evidenceof attack after the l50-holir test period.

The nickel plated steel panels all failed before24 hours exposure and the Phosphated steel oanels allfailed before 2 hours ex. osure.

Conclusion

These data constitute a measure of the corrosiveeffects if a spray of distilled water and will be evaluatedby comparison with results obtained from salt spray,humidity and mutdoor city and marine exposure tests.

I.

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Xfr271: �

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A

B

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.... . ...

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7he c~i-1"i"m' panel> lost weight steadily.

Trhe nentm-tei1 steel. p~rtels all failed b~efore

r'%t chroniic ~icid -fvjd~zed aluminumw c~tnelszýr..ivd s-.iperior tz ~ose un pakred by theý acApjhuric, acid

The nickel plhtf-d stool panels all felled be-fore 24 hours ex~io& ure and te steel -ý?nels t~efor'e2 h~r's.

Coneluaions

"Niza data cmýst'tate a me~asure of the corrosi~nrate at. 95F usInZ a 20" solitw, chloride solution, AH7.D, and sill be uzed in cona,-Ivon with Test !No. - todet~er-lne the reproducluility of one particular salt spraytest.

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APPE~rIX A

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APYE1�IX B

U

C

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I.___- A

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TEST NO. 20

Object

The object of this test is to determine the effectof the angle of exposure in a salt spray test on the rateof corrosion.

A test has been run at 950F with 20% sodium chloridesolution, pH 7.0, and steel panels. The panels were held atevery 10 degrees of rotation through a full circle, only one

1 side being exposed to the salt spray. In addition, panelswere exposed at 150 from the vertical.

Introduction

What constitutes a significant surface in saltspray testing has been variously described and, in somecases, reference is made to a certain angle of exposure(e.g. 150 from vertical for phosphate finishes and 6 foranodized aluminum). This test, then, is an attempt tomeasure the dependency of the rate of corrosion on theangle of exposure and also the effect of the direction ofthe flow of fog on the rate of corrosion.

Procedure

Forty 2" x 3" low carbon steel panels wereabraded with a 240 grit Aloxite cloth, and one side of eachpanel covered with Scotch brand No. 33 electrical tape toprotect from corrosion. The panels were then cleaned inA-1 cleaner solution, water rinsed, dried and weighed tothe nearest tenth of a milligram. Twenty polystyrene holderswere made, each with two milled slots at the desired angleof exposure. Two panels were placed back to back with theunprotected sides out in each rack. A photograph of theassembled holders with and without the panels is shown inAppendix C.

Panel, were held in such a manner as to exposeone panel at every 100 of rotation through a full circle.Additional holders were used to expose panels at 15° fromthe vertical. Panels were so placed that the axis aroundwhich the panels were rotated was at right angles to thedirection of the principal flow of fog in the box. Thepanels were placed in the box so that no one holdershihlded another and each was exposed directly to the fog.A summary of the operating conditions appears in AppendixA.

p A

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The test was run for a period of 24 hours, afterwhich the panels were removed from the box, scrubbed with anylon bristle brush under running water, dried and reweighedto the nearest tenth of a milligram.

Weight losses were then computed and are shown inAppendix A. A plotaf these weight losses versus the angle ofexposure comprises Appendix B.

Discussion

Results show a clear dependency of rate of corro-@lon on the angle of exposure and on the position of thepanels with respect to the principal direction of flow offog. The angle of exposure is more critical and has apronounced effect on the rate of corrosion. Corrosion onthe underside was of a different character than that onthe upper side of the panel. Corrosion on the undersidewas characterized by a dark, finer-grained, adherentcover of rust that is not readily removed by scrubbing.Weight gains rather than losses were, therefore, ex erienced.Corrosion products on the upper surfaces were of a Coareer"

nature and lighter in color. They were easily removed byscrubbing, resulting in weight losses.

Corrosion increased to a maximum on the uppersurface at an angle of approximately 30* from the vertical.Corrosion on the underside showed a minimum at the hori-zontal.

The smaller nature of the fourth quadrant of thegraph as compared with the first is an indication of thedependency of the rate of corrosion on the position of thepanel in the box relative to the principal direction offlow of fog. Panels with their principal surface exposedto the horizontal as well as vertical impingement of saltfog particles are subject to greater corrosion than thosewhose principal surface is shielded from the horizontal

component.

Conolusion.

These data constitute a measure of the dependencyof the rate of corrosion on the angle of exposure and itsrelationship to the direction of the principal flow of fogin the test cabinet. They show the importance of properconsideration of the angle of exposure in salt spray testing.

__ _ __ _ _ __ _ _ __ _ _;- .

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hPPENDIX A

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_ _ _ 0TEST NUM1BER I CORROSION RATES AT 95 F., EV. q'DTU1J CH{L)RTDR, pH 7.0

VAPTABLE - Angle of Exposure L-NGTH OF TEST - 24 hoursS~~:tATERTAL - ,t. eol

ANGpj, X TUMSURE 'TGHT LOSS -grams

00 -. 0171100 -. 039820P -. 0387s00 -. 0448

40 -. 0443sop -.0488600 -. 047570° -. 0513750 -. 0462

80P -.0357900 .0084

100° .0136lOd° .02051100 .)1641200 .01071300 .0184

j 1400 .01341500 .01611600 .02381700 .00461800 .009

S190o .0182000 .01162100 .01522200 .02412300 .01672400 .01322500 .01612600 .014112700 .02362800 -. 0261/2850 -. 02672900 -. 0301300° -. 03013100 -. 03613200 -. 0371330 -. 04,17

S3400 -. 03463500 -. 0289

COTDITIE8 OF TFST

Solutia Composition 20S IaCi pH of SolutionDry 3ulb Teip.(° F.) 95 pH of Fog 7.0•Vet Bulb Temp.(° F.) 950 Rate of 'ogRelative Humidity 100% Colleotion&1u.Ar.) 1.0

Particle Size .5 Impurities in SaltR oronf) 4 x 10 SolutionRate of Settling 01. Assay(Mu1./bec.) 2. br and IAir PressVre 11.5 3. Aeavy Metal a(lbe./in. ) 3peoifio 'iravl t --Room Temp.(0 F.) 950 or saluttin 1.150Rate of Flow .46 Volme of S31ution(ft. 3hin.) in Reasrvolr 5 &&l,

___,___,____.____________- . j

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.P; " 1X B

I

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LP07 I

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kPPENDIX C

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1

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Tr.ST NO. 21

Ob ect

The object of this test is to determine the ef-fect of a substantial reduction of the surface tension ofthe test solution on the rate (f corrosion in the saltspray method of accelerated corrosion testing.

Summarl

A test has been conducted at 95*F, using a 20%sodium chloride solution, pH 7.0, for a period of 150 ,oursin the salt spray test cabinet. The surface tension of thesolution used to generate the fog was reduced to approxi-mately half its usual value by the addition of an organicwetting agent.

Introduction

The surface tension of a liquid is a measure ofits cohesive nature. Liquids with high surface tensionstend to form droplets on a surface rather than an evenlydistributed film as liquids of lower surface tension would.The surface tension of the salt spray test solution, there-fore, is of primary importance in determining the "wettabilitiof the solution and should directly affect the rate of cor-rosion. The results of this test will be compared with thoseof Tests No. 7 and No. 19 to determine the effect of surfacetension on the rare of corrosion.

Procedure

A procedure similar to that outlined in Test No. 7was followed. The test was run for a period of 150 hours at95oF, using a 20', sodium ciloride solution, pH 7.0. The sur-face tension was lowered from a normal value of 64 dyne. per

Scentimeter to 37 dynes per centimeter by the addition of awater solution of Aerosol OT wetting agent (manufactured byS American Cyanamid Corp.) Surface tensions were measuredwith a stalagmometer at 25 0 C. A summary of the operatingconditions, cumulative weight losses and panel ratings appearsin Appendix A while a plot of the cumulative weight lossesfor the steel, brass, zinc and cadmium panels comprisesAppendix B.

Discusaion

The steel panels lost weight at a reasonablysteady rate and the weight losses showed their usual dependencyon a position in the box.

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The brass panels, after initial losses, gainedweight mteadily as has been previously experienced.

The zinc panels showed unusually high weightlosses, while the cadmium panels lost weight at a steadyrate in a closely grouped pattern.

The pentrated steel pasnels all failed before1 hour's exposure, three falling before 1/2 hour.

The aluminum panels anodized by the chromic acidprocess showed a definite superiority over tCose preparedby the sulphuric acid process. The sulphuric acid panelsall failed before 24 hours, while at the end of 66 hours,none of the chromic acid panels stiowed ri,-ns of attack.

The nickel plated steel panels all failed before5 hours, one panel failing at the end bf 1-1/2 hours.The phosphated steel panels all failed before 1-1/2 hoursexposure.

Conclusions

These data constitute a measure of the corrosionrate, using a test solution of lowered surface tension andwill be compared with the r:sults from Tests No. 7 and No.19 to evaluate its effect on the various types of panelsused in this series of tests.

I~I.

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All : A

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A &PPEIIDIX B

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TEST NO. 22

Object

The object of this tost is to determine thecorrosive effects of a marine atmosphere on the varioustypes of test panels used in the salt spray. investiga-tion.

Summary

An )utdoor test has been conducted at Westbrook,Connecticut on the steel, brass, zinc, cadmium, pentrated,steel, anodized aluminum, nickel plated steel and phosphatedsteel panels used in the foregoing series of salt spraytests. This test in a marine atmosphere will be used incomparison with exposure tests made in an industrial at-mosphere as well as salt)spray and humidity tests.

Introduction

A frequent and possibly well grounded criticismof the salt spray test is that it does not duplicate actualconditions of exposure in service. Furthermore, it has beenstated that comparisons between salt spray rrsults andmarine exposure tests show less correlation than with re-sults of exposure tests made in non-marine atmospheres.The type of corrosion is said to be different in each caseas evidenced by a different character of products obtainedin the corrosion of nickel plated steel panels. This test,therefore, is an attempt to measure the possible agree-ments and disagreements between salt spray and marine ex-posure tests.

Procedure

A full set of thirty-six panels, four each of thenine different types, were cleaned and prepared according

4 to methods described in Test No. 7. A special rack wasconstructed so as to Incline the panels at an angle of 300from the vertical. The panels were supported on both topand bottom by slotted racks which were securely fastenedto prevent removal by sudden gusts of wind. The wholeassembly was secured to the roof by sandbags. The panelswere so situated that their major surface was parallel tothe shore and exposed in a general southerly direction.This test was conducted at Westbrook, Connecticut and thepanels were approximately 150 feet from high water.

A sumuary of observations and times of exposureare shown in Ap,'endix A.

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The steel, brass, zinc and cadmium panels werecleanod according to the usual meithods after 1,032 hoursexposure and reweighed. The weight losses computed alsoappear in Appendix A.

Discussion

The observations made at the vorious timesthroughout the test are self-explanatory$ It is Interest-ing to note, however, the somewhat apparent superiorityof the anodized aluminum panels over those prepared by thesulphuric acid process.

The total weight losses after 1,032 hours ex-posure for the cadmium panels are of the same order asthose obtained in the first 24 hours of salt spray exposure.This would indicate the inertness and tenaciousness of theprotective oxide film that forms.

The verj sllght weight changes of the brasspanels also srLow the protective nature of the initialcorrosion products.

Conclusions

These data are a measure of the corrosive ef-foots of a marine atmosphere, and will be used in comparisonwith outdoor exposure tests in an industrial atmosphereand salt spray tests to determine any possible correlationbetween the three.

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I

APPENDIX A

C,

-- - A N-.

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-t"f t. A

'4 O T' I

t. t~) 1 5

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TEST NO. 23

Object

The object of this test is to determine the cor-rosive effect of an industrial atmosphem on the varioustypes of panels used in tnis series of tests and to corre-late, if possible, the results obtained with those fromsalt spray, humidity and marine exposure ýests.

_1ummary

A test has been conducted for a period of 1,190hours on the roof of the Henry Soutber Engineering Co., onthe steel, brass, sine, cadmium,,enameled steel, anodizedaluminum, nickel plated steel and phosphated stool panelsused in tnis series of tests. Periodic observations weremade and weight losses for the steel, brass, zinc andcadmium panels computed.

Introduction

Outdoor exposure tests have ahown wide variancewhen compared with th.' results of salt spray tests onsimilar materials. For the purpose of comparison with re-sults of other types of corrosion tests, this test is anattempt to measure the corrosive effects of an industrialatmospherp.

Procedure

The thirty-six panels used in the foregoingseries of tests were prepared and cleaned according tomethods outlined in Test No. 7. They were placed in aspecially constructed rack and securely held at both topand bottom by adjustable nails. The panels were inclinedat an angle of 3 0e from the vertical and the principalsurface of the panel was directed toward the south. Thewhole assembly was held on the roof by sand bags. Thetest rack was located about 50 feet from an exhaust hoodwhich discharges a variety of fumes, many of an acidicnature. The test was run for a p nrod of 1,190 hours.Observations made during this time appear in Appendix Aas well as the weight losses of the steel, brass, zincand cadmium panels, determined at the end of the test.

Discussion

The periodic observations of the panels a& self-explanatory. The same standards of failure were used asin the salt spray tests.

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The chromio acid anodized aluminum panels showeda definite superiority over those prepared by the sulphuricacid process.

The greater weight losses experienced for thesteel, brass, zinc and cadmium panels when compared withthe results obtained from the marine exposure test could bedue to the corrosive nature of the fumes from the adjacentexhaust fan.

Conclusions

The results obtained in this test will be used asa measure of the corrosiveness of an industrial atmospherefor the purpose of comparison with results obtained fromother types of corrosion tests herein described.

-A

N-i

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APPENDIX A

2,

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-- e go-.nu - gs

nmr3 1 F e

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TEST NO. 24

Object

The object of this test is to determine theeffects of humidity cabinet exposure on the steel, brass,zinc, cadmium, pentrated steel, anodized aluminum,nickel plated steel and phosphated steel panels used inthe foregoing series of salt spray and outdoor exposuretests.

Summary

(ij A test has been conducted in the humiditycabinet for a period of 976 hours at 100*F and a relativehumidity of 95%. Weight losses were measured and panelsrated according to tho same system as used in the saltspray tests.

Introduction

Humidity cabinet exposure tests would be apossible substitution for salt spray as a method ofaccelerated corrosion testing. The effect of a humidatmosphere on the various types of panels used in thisseries of tests should be determined in order that possiblecomparisons might be made between this method and saltspray and outdoor exposure testa.

Procedure

The thirty-six panels used in this s'ries oftests were prepared according to methods outlined inTest No. 7. Details of construction of the humiditycabinet appear in Phase II of this rJport. A specialwood rack was constructed to support the individual panelholders. The panels were placed in the box in a randomdistribution as shown in Appendix A. The temperature wasmaintained at IO1F and the relative humidity adjusted toa minimum value of 95%. The test was conducted for aperiod of 976 hours during which time daily observationswere made and weight losses determined. A summary ofthese observations and weight losses for the steel, brass,zinc and cadmium appears in Appendix B, while a plot ofthese weight losses comprises Appendix C.

Discussion

The steel panels lost weight in a rather ir-regular pattern although the overall picture is one ofa steady weight loss. Corrosion products obtained wereof the same character as those in outdoor exposure tests

Ai .' . N.'4 ,•. , ,

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or those experienced on the underside of panels in saltspray teats| that is, the products were dark, fine-grainedand difficult to remove by scrubbing.

The brass panels gained weight in a highly ir-regular day to day variation. The general tendency wasan approach to a constant value in excess of the originalweight.

The zinc panels gained weight steadily and in afairly closely grouped pattern. The tendency again was to

C approach a steady value that is in excess of the originalweight.

The cadmium panels showed the largest weightlosses which was probably due to the fact that this was theonly series of panels in which complete removal of thecorrosion products could be accomplished (i.e. cyanidecleaning).

The pentrated steel panels all failed before24 hours Vxposure.

The sulphuric acid anodized aluminum panelsproved superior to those prepared by the chromic aaidprocess. The sulphuric acid panels snowed no signs offailure at the end of the test (976 hours), while three ofthe chromic acid anodized panels failed after 576 hoursexposure.

The nickel plated steel panels all failed before72 hours exposure as did the phosphated steel panels.

Conclusions

These data constitute a measure of the corrosiveeffects of a humid atmosphere on the test panels underobservation and will be used in comparison with the re-sults from salt spray and outdoor exposure tests toevaluate the effectiveness of humidity cabinet exposureas a method of accelerated corrosion testing.

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£

APPENDIX A

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APi7r!MX B

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APPEIMIX C

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