lecture 27 more polymerswillson.cm.utexas.edu/teaching/chem328n/files/lecture 27-16.pdf ·...
TRANSCRIPT
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Chemistry 328N
Lecture 27 More Polymers
April 26, 2016
Step Chain
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Chemistry 328N
Midterm Exam III Where: WEL 1.316!!
When: Wed., May 4th , 7:00 – 9:00 PM
What: Covers lectures through 4/28
Review Session: Mon & Tues. 5-6 PM – Monday PAI -3.02, Tue. PAI – 2.48
Do: Study lecture notes, homework, reading assignments and practice hydrolysis and synthesis. Know signatures…
Please: Do a good job!
See web site for old exams
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Chemistry 328N
Flory’s Classification by Polymerization
Mechanisms
Chain-growth
Step-growth
Ring-openingO
OO
-
O
RO-
O
O
ROH+
CH2C
O
HO CH2 OH CH2C
O
O CH2 O HH
H2O
DimerTetramerOctamerHexamer
...
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Chemistry 328N
Chain-Growth Polymers
Chain-growth polymerization: a polymerization
that involves sequential addition reactions, either
to unsaturated monomers or to monomers
possessing other reactive functional groups
Reactive intermediates in chain-growth
polymerizations include radicals, carbanions,
carbocations, and organometallic complexes
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Chemistry 328N
Chain-Growth Polymers
We will concentrate on chain-growth
polymerizations of ethylene and substituted ethylenes
R
An alkeneR
n
n
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Chemistry 328N
Radical Chain Growth Polymerization
Among the initiators used for radical chain-growth
polymerization are diacyl peroxides, which
decompose as shown on mild heating
O
O
O
O
Dibenzoyl
peroxide
O
O
2 + 2 CO 2
A phenyl
radical
A benzoyloxy
radical
2
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Chemistry 328N
Radical Chain Growth Polymerization
Another common class of initiators are azo
compounds, which also decompose on mild
heating or with absorption of UV light
Azoisobutyronitrile (AIBN)
or hn N NN
C
N
C NNCN
+2
Alkyl radicals
•
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Chemistry 328N
Radical Chain Growth Polymerization
Chain initiation, chain propagation, and chain termination
steps for radical polymerization of a substituted ethylene
are shown for the monomer RCH=CH2
– chain initiation
+
In-In
In
or h 2 In
In
RR
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Chemistry 328N
Radical Chain Growth Polymerization
– chain propagation
In
RR
In
RR+
etc.
In
R
In
RRn
+R
R
n
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Chemistry 328N
Radical Chain Growth Polymerization
– Chain termination
In
RR
In
RR
In
R R
In
RR
In
RR
H
2
+
n n
nn
n
radical
coupling
dispropor-
tionation
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Chemistry 328N
Radical Chain-Growth
Chain-transfer reaction: the reactivity of an end
group is transferred from one chain to another, or
from one position on a chain to another position
on the same chain
– polyethylene formed by radical polymerization exhibits
a number of butyl branches on the polymer main chain
– these butyl branches are generated by a “back-biting”
chain transfer reaction in which a 1° radical end group
abstracts a hydrogen from the fourth carbon back
– polymerization then continues from the 2° radical
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Chemistry 328N
Radical Chain-Growth
A six-membered transition
state leading to
1,5-hydrogen abstraction
H H
n
nCH 2 =CH 2
••
Back biting
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Chemistry 328N
MALDI Mass Spectrum of Polystyrene
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Chemistry 328N
Molecular Weight All polymers are mixtures of individual polymer
molecules of variable MWs
– Number average Mn: count the number of chains of a particular MW, multiply each number by the MW, sum these values, and divide by the total number of polymer chains
– weight average Mw: record the weight of each chain of a particular length, sum these weights, and divide by the total weight of the sample
Ni
MiNiMn
NiMi
NiMi
Wi
WiMiMw
2
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Chemistry 328N
What the Weights Mean
Mn: This gives you the true average weight
Let's say you had the following polymer sample:
2 chains: 1,000,000 Dalton 2,000,000
5 chains: 700,000 Dalton 3,500,000
10 chains: 400,000 Dalton 4,000,000
4 chains: 100,000 Dalton 400,000
2 chains: 50,000 Dalton 100,000
10,000,000
10,000,000/23 = 435,000 Dalton
1 Dalton = 1 g/mole
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Chemistry 328N
Weight Average Molecular WeightMw: Since most of the polymer mass is in the heavier
fractions, this gives the average molecular weight of the
most abundant polymer fraction by mass.
2,000,000
10,000,000 0.20 1,000,000 200,000
3,500,000
10,000,000 0.35 700,000 245,000
4,000,000
10,000,000 0.40 400,000 160,000
400,000
10,000,000 0.04 100,000 4,000
100,000
10,000,000 0.01 50,000 500
Total 609,500
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Chemistry 328N
Distribution of Molecular Weights
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Chemistry 328N
Polymers: Molecular Weight
Ratio of Mw to Mn is known as the polydispersity index (PDI) Ð
– a measure of the breadth of the molecular weight
– Ð = 1 indicates Mw = Mn, i.e. all molecules have equal length (monodisperse)
– Ð = 1 is possible for natural proteins whereas synthetic polymers have 1.5 < PI < 5
– At best Ð < 1.1 can be attained with special techniques
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Chemistry 328N
Step Growth: The Carothers Legacy
Stuff is lost in this reaction
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Chemistry 328N
Let’s look at this closely….
Consider a flask of monomer….If there are No
molecules in the flask at time = 0 and N remaining at
time t then the DP at time t is the average degree of
polymerization… must just be N0/N!
The “Degree of Polymerization” , DP is the number of
monomer units in the average chain…it is the subscript
n in this notation:
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Chemistry 328N
Chain Growth Polymerization
DP = No/N = 12 / 7 = 1.7 (for 50%, b)
1 1 2 3 4 5 6 7
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Chemistry 328N
Step Growth Polymerization
DP = No/N = 12 / 9 = 1.3 (for 50%, b)
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Chemistry 328N
The chain growth vs. step growth
Step Chain
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Chemistry 328N
- Step-growth polymerization
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Chemistry 328N
- Chain-growth polymerization
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Chemistry 328N
The Carothers EquationHigh Molecular weights are hard to get this way
If there are No molecules at time = 0 and N remaining at time t
then the amount reacted is N0-N and we can define p as the
“conversion” or fraction reacted then as
P= (No – N ) / No or
N = No( 1 – P)
If DP is the average degree of polymerization… N0/N
….substituting gives
N/N = No/N( 1 – P) or
DP = 1 / (1 – P)
and for P = 0.98 (98% conversion), DP = only 50!
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Chemistry 328N
It all happens at the end!!!
DP = 1 / (1 – P)
The step growth system
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Chemistry 328N
More Historical Figures
Wilhelm Schlenk Michael Szwarc
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Chemistry 328N
Anionic polymerization
1914, Schlenk reacts Na with butadiene and styrene
1929, Ziegler proposes a mechanism
1952 Higginson, styrene, KNH2, kinetic study
1956 Szwarc, sodium naphthalene, Styrene,
living polymerization conception
60's, commercial products were available
90‘s, study on the living polymerization of polar
monomers
Some History
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Chemistry 328N
Alkenes with electron Withdrawing Groups
undergo anionic polymerization
CH2
CH
C N
CH2
CH
NO O
CH2
C
C O
CH3
O CH3
Acrylonitrile Nitroethene Methyl methacrylate
examples
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Chemistry 328N
Classical Monomers
CH2
CHCH
2C
CH3
styrene a-Me-styrene
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Chemistry 328N
Reactivity of monomers
Group A:
Group B:
Group C:
Group D:CH
2CH CH CH
2
CH2
C(CN)2 CH
2C
CN
COOC2H
5CH
2CH
NO2
> >
CH 2 CHCN CH 2 C
CN
CH 3 CH 2 CH C
O
CH 3> >
CH 2 CH
COOCH 3
CH 2 C CH 3
COOCH 3
>
CH2 CH CH2 C
CH3
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Chemistry 328N
Cyano Acrylate
CH2
C
CN
C
O
OC2H
5 OH2+ POLYMER
initiator
Jöns Jacob Berzelius
(1779-1848)
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Chemistry 328N
Initiators and initiation
(1) alkali metals ….one electron reductions
Lithium (Li) Sodium (Na) Potassium (K) as
mirrors or fine dispersions.
-Na CH
2CH
electron
transferCHCH
2Na++ .
e
-Na
-CH CH
2Na CHCH2
++dimerize
radical couple
Szwarc’s favorite
Radical anion
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Chemistry 328N
Break Seal Glassware
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Chemistry 328N
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Chemistry 328N
b
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Chemistry 328N
Anionic Polymerization Apparatus
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Chemistry 328N
Living test
Szwarc’s Experiment
Reddish Orange
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Chemistry 328N
The Living Polymerization
I
MDP
][
][
I
MDPt
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Chemistry 328N
Mn = 64.2 kDa
Mw = 65.7 kDa
PDI = 1.02
Mn = 54.2 kDa
Mw = 54.2 kDa
PDI = 1.00
Anionic Polymerization of diblock copolymer
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Chemistry 328N
Polymer Blends
Polymers do not generally form blends or “alloys”.
About 99% of binary blends are heterogeneous
except for small regions of the phase diagram
Ethylene and propylene are mutually soluble, but
polyethylene and polypropylene are not.
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Chemistry 328N
Block co-polymers
• Covalent linkage of two or more
polymers that are intrinsically
incompatible.
• Synthesis requires “special”
techniques.
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Volume Fraction A
A B
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SBS Thermoplastic Elastomer
45
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Orienting Block Copolymers
46
Wafer
Wafer
Wafer
Wafer||
CylindersLamellae
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Directed self-assembly
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8nm lines in block copolymers
48
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Chemistry 328N
Arthur K. Doolittle Award
The Arthur K. Doolittle Award, established by the UnionCarbide Corporation, is given to the authors of an outstandingpaper presented before the PMSE Division at each nationalmeeting of the ACS. A prize in the amount of $1,000.00 isfinanced with the gift of royalties from A. K. Doolittle's book,Technology of Solvents and Plasticizers. All papers areevaluated on the basis of content, with emphasis onoriginality and development of new concepts, and on thequality of presentation. Recipients are selected by ananonymous panel of judges appointed by the Chairman of theDoolittle Award Committee.