ISOPHORONE DIISOCYANATE COPOLYMER

ABA ABS ABS-PC ABS-PVC ACM ACS AES AMMA AN APET APP ASA BR BS CA CAB CAP CN CP CPE CPET CPP CPVC CR CTA DAM DAP DMT ECTFE EEA EMA EMAA EMAC EMPP EnBA EP EPM ESI EVA(C) EVOH FEP HDI HDPE HIPS HMDI IPI LDPE LLDPE MBS Acrylonitrile-butadiene-acrylate Acrylonitrile-butadiene-styrene copolymer Acrylonitrile-butadiene-styrene-polycarbonate alloy Acrylonitrile-butadiene-styrene-poly(vinyl chloride) alloy Acrylic acid ester rubber Acrylonitrile-chlorinated pe-styrene Acrylonitrile-ethylene-propylene-styrene Acrylonitrile-methyl methacrylate Acrylonitrile Amorphous polyethylene terephthalate Atactic polypropylene Acrylic-styrene-acrylonitrile Butadiene rubber Butadiene styrene rubber Cellulose acetate Cellulose acetate-butyrate Cellulose acetate-propionate Cellulose nitrate Cellulose propionate Chlorinated polyethylene Crystalline polyethylene terephthalate Cast polypropylene Chlorinated polyvinyl chloride Chloroprene rubber Cellulose triacetate Diallyl maleate Diallyl phthalate Terephthalic acid, dimethyl ester Ethylene-chlorotrifluoroethylene copolymer Ethylene-ethyl acrylate Ethylene-methyl acrylate Ethylene methacrylic acid Ethylene-methyl acrylate copolymer Elastomer modified polypropylene Ethylene normal butyl acrylate Epoxy resin, also ethylene-propylene Ethylene-propylene rubber Ethylene-styrene copolymers Polyethylene-vinyl acetate Polyethylene-vinyl alcohol copolymers Fluorinated ethylene-propylene copolymers Hexamethylene diisocyanate High-density polyethylene High-impact polystyrene Diisocyanato dicyclohexylmethane Isophorone diisocyanate Low-density polyethylene Linear low-density polyethylene Methacrylate-butadiene-styrene... [Pg.958]

Fluorourethanes can also be applied using powder coating technology. Resins suitable for this should have Tg values between 35°C and 120°C (95°F and 248°F) to optimize flow out and cure at the annealing temperature. Blocked isocyanates, which form free isocyanates after being heated above certain temperatures, are frequently used [50]. Certain FEVE copolymers with hydroxyl and carboxyl functionalities combined with blocked isophorone diisocyanate are suitable for powder coating technology [51]. [Pg.159]

Typical gas-generating propellants are (1) AP-PB composite propellant composed of 50% AP and 50% HTPB that is cured with isophorone diisocyanate (IPDI), (2) NC-NG double-base propellant composed of 70% NC and 30% NG that is plasticized with diethyl phthalate (DEP), and (3) GAP propellant composed of GAP copolymer that is cured with 12.0% hexamethylene diisocyanate (HMDI) and cross-linked with 3.2 % trimethylolpropane (TM P). [Pg.227]

Isobutyl alcohol Isobutylene/isoprene copolymer Isobutylene/MA copolymer Isodecyl benzoate Isoheptane Isophorone Isophorone diisocyanate Isopropanolamine p-lsopropoxy diphenylamine Isopropyl acetate Isopropyl alcohol Itaconic acid Japan (Rhus succedanea) wax Kerosene Lauralkonium chloride... [Pg.4797]

Park et al. (1998b) have prepared compatibilized blends of PET with PE using PE grafted with 2-hydroxyethyl methacrylate-isophorone diisocyanate. See also Park et al. (2002), Bae et al. (2001), and Kim et al. (2000a, b). For PBT/ ethylene-octene copolymer blends compatibilized using masked isocyanate, see Yin et al. (2009a). [Pg.599]

The application of AFM and other techniques has been discussed in general terms by several workers [350-353]. Other complementary techniques covered in these papers include FT-IR spectroscopy, Raman spectroscopy, NMR spectroscopy, surface analysis by spectroscopy, GC-MS, scanning tunnelling microscopy, electron crystallography, X-ray studies using synchrotron radiation, neutron scattering techniques, mixed crystal infrared spectroscopy, SIMS, and XPS. Applications of atomic force spectroscopy to the characterisation of the following polymers have been reported polythiophene [354], nitrile rubbers [355], perfluoro copolymers of cyclic polyisocyanurates of hexamethylene diisocyanate and isophorone diisocyanate [356], perfluorosulfonate [357], vinyl polymers... [Pg.136]

Ferreira et al. [75] synthesized a HMA for medical use. Urethanes based on polycaprolactone diol (PCL) were synthesized by reaction of the molecule either with isophorone diisocyanate (IPD-isocyanate) or hexamethylene diisocyanate (HDI-isocyanate). Nies Berthold et al. [76] tried out an adhesive composition based on polymers or polymer blends consisting of caprolactone copolymers or caprolactone copolymers and polycaprolactone. The adhesive can be utilized as HMA for temporarily gluing together biological tissue and other materials in medicine. [Pg.231]

Other applications of AFM to the characterisation of polymers include polythiophene [9], nitrile rubbers [10], perfluoro copolymers of cyclic polyisocyanurates of hexamethylene diisocyanate and isophorone diisocyanate [11], perfluorosulfonate [12], vinyl polymers [13], polyhydroxybutyrate [14], polyacrylic acid nanogels [15], acrylic copolymers [16, 17], polyurethanes [18, 19], ethylene methacrylate copolymer [4, 20], polyamides [21], polyvinyl pyrrolidone [22], and polyethyl methacrylate dispersions [23], acryloyl chloride [13], aniline-4-sulfonic acid [24], ethylene propylene 5-ethylidene-2-norbornene terpolymer [25] and butylene adipate - butylene terephthalae [26]. [Pg.395]

The preparation of copolymers of aminopropyl endcapped dimethylsiloxane oligomers and isophorone diisocyanate with 1,4-benzenedimethanol as the chain extender outlined in Scheme 1 is similar to the method used by Pascault and co-workers to prepare alkoxy-silane terminated macromers.(27) This "hard segment first method allowed the separate isolation and characterization of the hard block. Thus, GPC analysis for the intermediate IPDI-BDM-IPDI-BDM-IPDI (desired 3 2" composition), also revealed peaks for IPDI-BDM-IPDI, and BDM-IPDI-BDM. The intensity ratio of the curves indicate that more than 85% of the molecules in the mixture were of the target "3 2" composition. [Pg.67]

Copolymers of maleic anhydride and (Cp3)2 CF0CH2CR==CH2 or CF3(CF2)6CH2=OC H2CR=CH2, R=H or CH3, treated with NaOH, H0(CH2CH20)3CH3 or C4H9NH2 FMC Fiuorinated diol-isophorone diisocyanate-... [Pg.622]

Hard Segment Characterization The preparation of copolymers of aminopropyl endcapped dimethylsiloxane oligomers and isophorone diisocyanate with 1,4-benzenedimethanol as the chain extender outlined in Scheme 1 is similar to the method used by Pascault and co-workers to prepare alkoxy-silane terminated... [Pg.67]

Chemistry Polyurethane is produced by the reaction of a polyol with an diisocyanate (or in some instances a polyisocyanate) in the presence of catalysts. The polyols of choice are poly(propylene glycol), block copolymers of ethylene oxide (10-15%) with propylene oxide, or the newer polymer polyols (based on polymers such as polystyrene or styrene-acrylonitrile copolymer). Polyester diols such as polycaprolactone diol can be used in place of the polyether polyol in this reaction. The isocyanate of choice is a mixture of the 2,4 and 2,6 isomers of tolylene di-isocyanate in the ratio of 80 20, generally referred to as 80 20TDI. Other isocyanates such as diphenylmethane di-isocyanate (MDI), hexamethylene di-isocyanate (HMDI), and isophorone di-isocyanate (IPDI) are also used. A tin-based or amine catalyst is used to promote the reaction. Given the wide choice of reactants available, the reaction can yield foams with a range of different mechanical and thermal characteristics. [Pg.115]