Previous Page TABLE 1. cont'd Polymer I of
Polymer II of
Method
Monoalkyl itaconate
Single T g ; FTIR
Vinyl acetate-co-vinyl alcohol
Single Tg; FTIR
Vinyl butyral
SALS
2-Vinylpyridine
Aramide
Single Tg\ FTIR
4-Vinylpyridine
Methylocellulose Sulfone, carboxylated
Single 7 g ; NMR Single Tg; transparency
p-Phenylene terephthalamide 2,6-Xylenyl methacrylate
Transparency; microscopy Single Tg
2,3-Xylenyl methacrylate
Comments
Refs.
I was 2- or 4-vinylpyridine; II had an 939,1014, alkyl group or methyl or ethyl 1212 (4 miscible systems); formed complexes I was 2- or 4-vinylpyridine (2 miscible 934,935,991 systems); II had 29-88 mol% vinyl alcohol I was 2- or 4-vinylpyridine (2 miscible 1003 systems) II was made from hexamethylene767 diamine and a mixture of terephthaloyl and isophthaloy] dichlorides 559 II had degree of carboxylation 256 0.43-1.93 ~ 329 1158
TABLE 2, POLYMER PAIRS CONTAINING ONE MONOMER IN COMMON, MISCIBLE IN THE AMORPHOUS STATE AT ROOM TEMPERATURE
Polymer I of
Polymer II of
Method
Acrylic acid-co-styrene
Methyl methacrylate-co-styrene
Single Tg
Acrylonitrile-co-butadiene
Acrylonitrile-co-butadiene Acrylonitrile-co-styrene Acrylonitrile-co-vinylidene chloride
Single T 8 ; clear films; electron microscopy Single ^ g Single T g
Acrylonitrile-co-styrene
Single T%
Maleic anhydride-co-styrene
Single Tg
Acrylonitrile-co-Af-phenylitaconimide
Single Tg
Itaconic anhydride-co-methyl methacrylate Methyl methacrylate-coN-phenylitaconimide Methyl methacrylate
Single Tg
Styrene-co-maleic anhydride~co-acrylonitrile
Acrylonitrile-co-methyl methacrylate
Acrylonitrile-co-methyl methacrylate-coa-methylstyrene Acrylonitrile-co-methyl methacrylate-co-styrene Acrylonitrile-co-a-methylstyrene
Acrylonitrile-co-a-methylstyreneco-styrene Acrylonitrile-co-styrene
Comments
-
Refs.
Miscibility depended on compositions 72 of I and II Difference in composition between 19,47,101,106, I and II < 2 2 % acrylonitnle 149,390,452 162 I had 23.6-49.6 vol% AN; II had 19 966 wt.% AN Miscibility depended on compositions 965 of I and II Miscibility depended on compositions 965 of I and II 168 Miscibility depended on compositions of I and II -
920
Single TB
I had 20/20/60 = aerylonitrile/methyl methacrylate/a-methylstyrene
633
Acrylonitrile-co-styrene
Light scattering
-
358
Methyl methacrylate Acrylonitrile-co-methyl methacrylate Acrylonitrile-co-styrene
Light scattering Single Tg Single Tg
-
358
Acrylonitrile-co-a-methyl styrene-co-styrene Acrylic acid-co-styrene Acrylonitrile-co-benzyl methacrylate Acrylonitrile-co-fumaronitrileco-styrene Acrylonitrile-co-methyl methacrylate Acrylonitrile-co-Af-phenylitaconimide Acrylonitrile-co-styrene
Clear films
p-(2-Hydroxy-hexafluoroisopropyl)styrene-co-styrene Maleic anhydride-co-styrene
Single Tz
Single Tg Single Tg Single Tg Single T% Single Tg Single Tg; no visible phase separation Single Tg; clear film Single Tg
168
152
I had 32.3 wt.% acrylonitrile; II had 27 wt.% acrylonitrile Difference in composition between I and II < 12% acrylonitrile I had 32-40 wt.% AN; II had 11-17 wt.% fumaronitrile Difference in composition between I and II 20% I had 25% styrene; II had M w < 917; 138,139 < 50% II; two loss peaks when 75% II Difference in composition between I 453 and II 25% butyl aery late; immiscible when composition difference 50% butyl acrylate I had 6 or 48 mol% electron donating 723 carbozoyl groups; II had 10 or 63 mol% electron withdrawing dinitrobenzoyl groups Difference in composition between I 453 and II 25% ethyl acrylate; immiscible when composition difference 50% ethyl acrylate I had 75% ethyl acrylate; immiscible 453 when I had < 50% ethyl acrylate Difference in composition between I 447,448 and II < 10% methyl methacrylate II had > 90 wt.% K-butyl methacrylate 238 76
n-Butyl methacrylate-co-styrene Caprolactam-co-caprolactone Caprolactam-co-caprolactone-coIaurolactam 2,6-Dimethyl-l,4-phenylene ether, sulfonylated
;?-Butyl methacrylate-co-styrene Styrene Caprolactone-co-laurolactam Caprolactam-co-laurolactam
Single Single Single Single
2,6-Dimethyl-l,4-phenylene ether, sulfonylated
Single Tg
Dimethylsiloxane, functionalized
Dimethylsiloxane, functionalized
Single T1
3-Bromo-2,6-dimethyl1,4-phenylene ether 3-Bromo-2,6-dimethyl1,4-phenylene ether-co2,6-dimethyl-1,4-phenylene ether p-Bromostyrene-co-styrene Butadiene
Butadiene-c0-styrene
Single Tg Single Tg Single Tg; microscopy
Refs.
films
films
Single T g ; clear films Single T g ; microscopy Single Tg
Clear
II had > 48 mol% 3-bromo2,6-dimethyl-l,4-phenylene oxide
I had 9 mol% carbazoyl groups; II had 9 mol% dinitrobenzoyl groups films
T g ; microscopy T g ; clear films Tg Tg
Difference in composition between I and II < 20-30% butyl methacrylate, depending on compositions of I and II I had > 90 wt.% styrene I and II had various compositions I and II had various compositions Difference in degree of sulfonylation between I and II in the range of 20-26 wt.% I had 4-15 mol% electron-donating carbazoyl or /V-methylaniline groups; II had 4-15 mol% electron-accepting
164 25,26 402
402
723
76,447
76 239 1126 992 410
723
References page VI-461
TABLE 2. cont'd Polymer I of
Polymer II of
Method
Comments
Refs.
Vinyl chloride Ethylene naphthalene2,6-dicarboxylate-co4-hydroxybenzoate Ethyl methacrylate-co-methyl Ethyl methacrylate-co-methyl methacrylate methacrylate o-Fluorostyrene-co-p-fluorostyrene o-Fluorostyrene-co-p-fluorostyrene
Single Tg NMR
dinitrobenzoyl groups; donor/ acceptor = 1 /1 I was Hydrin 100; II was Hydrin 200 I and II had 25, 50 or 75% ethyl acrylate I had 75 wt.% ethyl methacrylate; immiscible when I had < 50 wt.% ethyl methacrylate Difference in composition between I and II < 20-27% ethyl acrylate depending on compositions of I and II Difference in composition between I and II < 1.2-13.3 wt.% Cl depending on compositions of I and II SemicrystalUne when I had 25 wt.% Cl; I had 25 or 48 wt.% Cl I had 35.4-52.6 wt.% Cl; II had 50-60 wt.% ethylene 1:11 = 50:50 I and II had 7-100 wt.% vinyl acetate I had 21 mol% vinyl acetate; II had 21 mol% vinyl alcohol Difference in vinyl chloride or ethylene content of I and II < 15 mol% I had > 80 mol% vinyl chloride II had 20 mol% 4-hydroxybenzoate
Single Tg
-
Single Tg
o-Fluorostyrene-co-styrene
o-Fluorostyrene-co-styrene
Single Tg
Styrene
Single Tg
p-Fluorostyrene-co-styrene
Styrene
Single Tg
Hydrocarbon polymer, chlorinated
Hydrocarbon polymer, chlorinated
Clear
p-Hydroxybenzoic acid-co6-hydroxy-2-naphthoic acidco-terephthalic acid-cohydroquinone Hydroxybutyrate
p-Hydroxy ben zoic acid-co6-hydroxy-2-naphthoic acid
Single T g ; X-ray diffraction
I and II had 10 and 23 mol% 1144 p-fluorostyrene, respectively I had 18 or 49% o-fluorostyrene; II had 716,1144 40 or 77% o-fluorostyrene I had 18, 40 or 49% o-fluorostyrene 716,1144 and II had Mn = 15 kg/mol I had 18% o-fluorostyrene and II had Mn = 110 kg/mol I had 8 or 16 mol% p-fluorostyrene; II 1144 had Mn = 4 0 or 326 kg/mol One series derived from reduction of 75 polyvinyl chloride and one series derived from chlorination of polyethylene X-ray diffraction showed no significant 92 transesterification occurred in the mixture
Isoprene
Hydroxybutyrate Hydroxybutyrate-co-hydroxyvalerate Isoprene-styrene block copolymer
Microscopy; SAXS Microscopy; melting behavior Electron microscopy
Maleic anhydride-co-styrene
Acrylonitrile-co-styrene
Single T g , transparency, microscopy
Maleic anhydride-co-styrene
Single Tg
Methyl methacrylate-co-styrene
Single Tg
Styrene-co-2-vinylpyridine
Single Tg\ FTIR
Epichlorohydrin Ethyl acrylate-co-ethyl methacrylate
Epichlorohydrin-co-ethylene glycol Ethyl acrylate-co-ethyl methacrylate
Single Tg Clear
films
Ethyl methacrylate
Clear
films
Ethyl acrylate-co-methyl methacrylate
Ethyl acrylate-co-methyl methacrylate Clear
films
Ethylene, chlorinated
Ethylene, chlorinated
Single Tg; clear
Ethylene-co-methyl acrylate Ethylene-co-vinyl acetate
Single Tg; phase contrast microscopy Single 7V, microscopy
Ethylene, low density Ethylene-co-vinyl acetate Ethylene-co-vinyl alcohol
Single Tg Single 7 g ; microscopy Single Tg\ FTlR
Vinyl acetate-co-vinyl chloride Ethylene-co-vinyl chloride
Single Tg Single Tg
Ethylene-co-vinyl acetate
Ethylene-co-vinyl chloride
Ethylene naphthalene2,6-dicarboxylate
Maleimide-co-styrene
films
films
373 453 453
447
97,98, 636,817 396 849 1172 925 960 745,746 70,71 70 1027
98
I was isotactic; II was atactic 903 II had 3.8-22.3 mol% hydroxyvalerate 1142,1143 I had Mn = 6.5-53.9 kg/mol; II was diblock, 378 triblock or four-arm star copolymer having total Mn = 26-622 kg/mol I had 15.3 wt.% maleic anhydride; II 436,555 had 15.0, 19.5 or 25.0 wt.% acrylonitrile Miscibility occurred when difference in 1159 MA contents between I and II was