Methyl isocyanate methacrylate

Mercaptoacetic Add 2-Mercaptobenzoic Acid Methane Methanol Methionine Methotrexate Methylene Blue A-Methyl Glycine 5-Methylindole Methyl Isocyanate Methylmalonic Add Methyl Methacrylate Methylmethane Sulfonate Methyl Thiocyanate A-Methyl Thiourea Methyl Urea Naphthalene Nicotinic Acid Ornithine Orotic Acid Oxalic Acid Oxindole Palmitic Acid Paraldehyde Pentobarbital Phenol... 

Density used in volume calculations propylene oxide, 1.01 methyl isocyanate, 0.967 acetic anhydride, 1.049 acrylonitrile, 0.806 and methyl methacrylate, 0.. ... 

Mercury compounds Methanol Methoxychlor Methyl bromide Methyl chloride Methyl ethyl ketone Methyl hydrazine Methyl iodide Methyl isobutyl ketone Methyl isocyanate Methyl methacrylate Methyl f-butyl ether... 

M ethy Icy clo hexano 1 ds-2-Methylcyclohexanol trans-2-Methylcyclohexanol Methylcyclopentane 1 - M ethy Icy clo p ent ene 3-Methylcyclopentene Methyldichlorosilane Methylethyl ether Methylethyl ketone Methylethyl sulfide Methyl formate Methylisobutyl ether Methylisobutyl ketone Methyl Isocyanate Methylisopropyl ether Methylisopropyl ketone Methylisopropyl sulfide Methyl mercaptan Methyl methacrylate 2-Methyloctanoic acid 2- M ethy lp ent ane Methyl pentyl ether 2- M ethy lp ro p ane 2- M ethyl- 2- p rop ano 1 2-Methyl propene Methyl propionate Methylpropyl ether Methylpropyl sulfide Methylsilane... 

Hydroquinone Mercuric acetate Mercuric chloride Methacrolein diacetate Methacrylic anhydride Methacrylonitrile Methyl isocyanate Methyl vinyl ketone Nitrosodimethylamine Phenol... 

Additionally, reactions of isocyanate with amines provide another cross-linking approach to make nanogels. Cross-linked micelles with pH-responsive features were obtained by the addition of excess amounts of 1,8-diaminooctane to micellar aggregates consisting of poly (poly(ethylene glycol) methyl ether methacrylate)-b/oc -poly(methyl methacrylate-co-poly (3-isopropenyl-a,a-dimethylbenzyl isocyanate)) [PPEGMEMA-b-P(MMA-co-TMI)] (Figure 54.9). 

Many acrylic copolymers are currently used in the textile industry as binders for nonwoven fabrics. The purpose of these fibers is to stabilize the material. In many instances, these copolymers are used in conjunction with amino resins. Casanovas and Rovira have done a study of methyl methacrylate-ethyl acrylate-N-methylol-acrylamide by PY/GC-MS. Among the products identified were methane, ethylene, propene, isobutene, methanol, propionaldehyde, ethanol, ethyl acetate, methyl acrylate, methyl isobutyrate, ethyl acrylate, methyl methacrylate, n-propyl acrylate, and ethyl methacrylate. In this sample, clearly monomer reversion is the primary degradation process occurring however, several other degradation mechanisms are at work. When the sample contains an amino resin in the mixture, acrylonitrile is observed in the pyrogram. Another effect of the amino presence was a marked increase in the amount of methanol detected. Other products detected were meth-oxyhydrazine, methyl isocyanate, and methyl isocyanide. 

Methyl isocyanate Methyl methacrylate Methyl paraben Methylene blue Methylene chloride Naphthalene Nitric acid Nitrogen dioxide Oxalic acid Ozone... 

A number of methods such as ultrasonics (137), radiation (138), and chemical techniques (139—141), including the use of polymer radicals, polymer ions, and organometaUic initiators, have been used to prepare acrylonitrile block copolymers (142). Block comonomers include styrene, methyl acrylate, methyl methacrylate, vinyl chloride, vinyl acetate, 4-vinylpyridine, acryUc acid, and -butyl isocyanate. 

Type AD-G is used in an entirely different sort of formulation. The polymer is designed for graft polymerisation with methyl methacrylate. Typically, equal amounts of AD-G and methyl methacrylate are dissolved together in toluene, and the reaction driven to completion with a free-radical catalyst, such as bensoyl peroxide. The graft polymer is usually mixed with an isocyanate just prior to use. It is not normally compounded with resin. The resulting adhesive has very good adhesion to plasticised vinyl, EVA sponge, thermoplastic mbber, and other difficult to bond substrates, and is of particular importance to the shoe industry (42,43). 

Methanol Formaldehyde Ethylene Propylene oxide Phenol 1,4-Butanediol Tetrahydrofuran Ethylene glycol Adipic acid Isocyanates Styrene Methyl methacrylate Methyl formate Two-step, via CH4 steam reforming Three-step, via methanol Cracking of naphtha Co-product with t-butyl alcohol or styrene Co-product with acetone Reppe acetylene chemistry Multi-step Hydration of ethylene oxide Multi-step Phosgene chemistry Co-product with propylene oxide Two-step, via methacrolein Three-step, via methanol... 

Chemical methods used for the determination of hydroxyl groups or alcoholic constituents in polymers are based on acetylation [16-18], phthalation [18], and reaction with phenyl isocyanate [18,19] or, when two adjacent hydroxy groups are present in the polymers, by reaction with potassium periodate [9,17]. Alcoholic hydroxyl groups may be found in the following polymers (1) poly(ethylene terephthalate) (PET) [20], (2) poly(methyl acrylate), [21], (3) poly(methyl methacrylate) [21], and (4) polyhydric alcohols in hydrolysates of poly(ester) resins [22]. 

Southern pine with a dual treatment of chemical modification with butylene oxide or butyl isocyanate followed by lumen-fill treatment with methyl methacrylate, or southern pine impregnated with methyl methacrylate and polymerized in situ, resulted in modified woods that were resistant to accelerated weathering and to ultraviolet light alone. Physical, chemical, and microscopic changes occurring as a result of ultraviolet light irradiation are described. 

Process Economics Program Report SRI International. Menlo Park, CA, Isocyanates IE, Propylene Oxide 2E, Vinyl Chloride 5D, Terephthalic Acid and Dimethyl Terephthalate 9E, Phenol 22C, Xylene Separation 25C, BTX, Aromatics 30A, o-Xylene 34 A, m-Xylene 25 A, p-Xylene 93-3-4, Ethylbenzene/Styrene 33C, Phthalic Anhydride 34B, Glycerine and Intermediates 58, Aniline and Derivatives 76C, Bisphenol A and Phosgene 81, C1 Chlorinated Hydrocarbons 126, Chlorinated Solvent 48, Chlorofluorocarbon Alternatives 201, Reforming for BTX 129, Aromatics Processes 182 A, Propylene Oxide Derivatives 198, Acetaldehyde 24 A2, 91-1-3, Acetic Acid 37 B, Acetylene 16A, Adipic Acid 3 B, Ammonia 44 A, Caprolactam 7 C, Carbon Disulfide 171 A, Cumene 92-3-4, 22 B, 219, MDA 1 D, Ethanol 53 A, 85-2-4, Ethylene Dichloride/Vinyl Chloride 5 C, Formaldehyde 23 A, Hexamethylenediamine (HMDA) 31 B, Hydrogen Cyanide 76-3-4, Maleic Anhydride 46 C, Methane (Natural Gas) 191, Synthesis Gas 146, 148, 191 A, Methanol 148, 43 B, 93-2-2, Methyl Methacrylate 11 D, Nylon 6-41 B, Nylon 6,6-54 B, Ethylene/Propylene 29 A, Urea 56 A, Vinyl Acetate 15 A. 

In a more specific example, macromonomer composed of n-butyl methacrylate and methacrylic acid prepared by CCT was copolymerized with n-butyl acrylate containing a small portion of methyl methacrylate.341 Comparison to the equivalent copolymer made with a macromonomer prepared with a thiol chain-transfer agent demonstrated that the CCT macromonomer formed a copolymer while the thiol macromonomer did not. When these compositions were cured using trifunctional isocyanates, they were useful as both clear and pigmented automotive finishes. 

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