Abstract: The present invention relates to a thermoformable sheet, for example, an acrylic sheet, comprising particles proximate to the top surface, wherein the textured sheet, when thermoformed, provides a low-gloss, textured surface that is less sensitive to marring, blemishes (including blemishes resulting from the mold), household wear and tear, and visibly reduces the appearance of oil deposits on its surface.

Abstract: Acrylic compositions which can be processed into thermoformable acrylic sheet material with variegated non-homogeneous granite appearance are disclosed. The acrylic compositions comprise a matrix of polymethyl methacrylate having dispersed within it particles of a thermoplastic such as polymethyl methacrylate and one or more comonomers wherein the thermoplastic is in the shape of thin wafers 0.05 to 9.53 mm thick, 0.18 to 12.8 wide and 0.18 to 7.62 mm long.

Abstract: Novel compositions of homopolymers and copolymers containing an olefinic polymerizable end group wherein the monomeric units comprise methacrylate, acrylate, acrylic acid, styrene, vinyl esters, acrylonitrile, methacrylonitrile, vinyl halides, vinylidene halides, substituted butadienes, ethylene-sulfonic acid derivatives, acrylamide derivatives, methacrylamide derivatives, and other monomers, and mixtures thereof are disclosed.

Abstract: Free radical polymerization processes employing cobalt(II) chelates of vicinal iminohydroxyimino- and dihydroxyiminoalkanes, N,N'-bis(salicylidene)ethylenediamines and porphyrins as catalytic chain transfer agents, in admixture with certain Lewis bases, for controlling the molecular weight of the homopolymers and copolymers produced.

Abstract: Process for functionalizing saturated hydrocarbons comprising:(a) reacting said saturated hydrocarbons of the formula:R.sub.1 Hwherein H represents a hydrogen atom; and R.sub.1 represents a saturated hydrocarbon radical, with a metal complex of the formula:CpRh[P(R.sub.2).sub.3 ]H.sub.2whereinCp represents a cyclopentadienyl or alkylcyclopentadienyl radical;Rh represents a rhodium atom;P represents a phosphorus atom;R.sub.2 represents a hydrocarbon radical;H represents a hydrogen atom,in the presence of ultraviolet radiation to form a hydridoalkyl complex of the formula:CpRh[P(R.sub.2).sub.3 ](R.sub.1)H(b) reacting said hydridoalkyl complex with an organic halogenating agent such as a tetrahalomethane or a haloform of the formulas:CX'X''X'''X'''' or CHX'X''X'''wherein X', X'', X'", X"" represent halogens selected from bromine, iodine or chlorine atom, at a temperature in the range of about -60.degree. to -17.degree. C. to form the corresponding haloalkyl complex of step (a) having the formula:CpRhPMe.sub.

Abstract: A process for controlling the molecular weight of polymer and copolymer in radical initiated polymerization with a bimetallic catalytic chain transfer agent is disclosed.

Abstract: A process for preparing low molecular weight methacrylate polymer and copolymer with a pentacyanocobaltate(II) catalytic chain transfer agent is disclosed.

Abstract: Free radical polymerization processes employing cobalt(II) chelates of vicinal iminohydroxyimino compounds, dihydroxyimino compounds, diazadihydroxyiminodialkyldecadienes and diazadihydroxyiminodialkylundecadienes as catalytic chain transfer agents for controlling the molecular weight of the homopolymers and copolymers produced.

Abstract: Free radical polymerization processes employing cobalt(II) chelates of vicinal iminohydroxyimino compounds, diazadihydroxyiminodialkyldecadienes and -undecadienes, tetraazatetraalkylcyclotetradecatetraenes and -dodecatetraenes, N,N'-bis(salicylidene)ethylenediamines and dialkyldiazadioxodialkyldodecadienes and -tridecadienes as catalytic chain transfer agents for controlling the molecular weight of the homopolymers and copolymers produced.

Abstract: Process for functionalizing saturated hydrocarbons selectively in the terminal position comprising:(a) reacting said saturated hydrocarbons of the formula:RHwhere:H represents a hydrogen atom, andR represents a saturated hydrocarbon radical,with a metal complex of the formula:CpRhPMe.sub.3 H.sub.2where:Cp represents a pentamethylated cyclopentadienyl radical,Rh represents a rhodium atom,P represents a phosphorous atom,Me represents a methyl group,H represents a hydrogen atom,in the presence of ultraviolet radiation at a temperature maintained at about -60.degree. to -17.degree. C. to form a hydridoalkyl complex of the formula:CpRhPMe.sub.3 RH(b) reacting said hydridoalkyl complex with a haloform of the formula:CHX.sub.3where:X represents a bromine, iodine or chlorine atom,at a temperature in the range of about -60.degree. to -17.degree. C. to form the corresponding haloalkyl complex of step (a) having the formula:CpRhPMe.sub.3 RX; and,(c) reacting said haloalkyl complex formed in (b) with halogen (X.sub.