Abstract: A compatible blend of an engineering thermoplastic such as a polyamide and an olefin polymer material is prepared by (1) making an oxidized olefin polymer material containing carboxylic acid groups or derivatives thereof, (2) extruding a mixture of (a) the oxidized olefin polymer material from step (1), (b) an engineering thermoplastic, (c) optionally, an inorganic base, and (d) optionally, a non-oxidized olefin polymer material, and (3) recovering a blend of the engineering thermoplastic, the oxidized olefin polymer material or an ionomer thereof, which acts as a compatibilizer, and, optionally, the non-oxidized olefin polymer material.

Abstract: Irradiated, oxidized olefin polymer dispersing aids for use in the manufacture of additive concentrates and additive-containing olefin polymer compositions.

Abstract: Irradiated, oxidized olefin polymer coupling agents for use in the manufacture of non-halogenated flame retardant-containing and filler-containing olefin polymer compositions and coupling agent-containing olefin polymer concentrates.

Abstract: Irradiated, oxidized olefin polymer dispersing aids for use in the manufacture of additive concentrates and additive-containing olefin polymer compositions.

Abstract: Graft copolymers are prepared, in a non-oxidizing atmosphere, by (1) irradiating a particulate olefin polymer material with high energy ionizing radiation, (2) treating the irradiated olefin polymer material with at least one grafting monomer that is capable of forming side chains on the olefin polymer material, in the presence of at least one additive to control the molecular weight of the side chains of the polymerized grafting monomer selected from (a) at least one hydroxylamine derivative polymerization inhibitor, and (b) at least one thio-, nitro-, or halogen-substituted aliphatic or aromatic compound or an aliphatic or aromatic phosphine derivative, and (3) deactivating the residual free radicals in the resulting grafted olefin polymer material and removing any unreacted vinyl monomer from the material. Graft copolymers with low molecular weight side chains are produced that are easier to process and have improved internal and surface morphology.

Abstract: Graft copolymers with low molecular weight side chains are prepared by (1) irradiating a propylene polymer material in the absence of oxygen, (2) adding a controlled amount of oxygen to the irradiated polymer material so that the polymer is exposed to an amount of oxygen greater than 0.004% but less than 15% by volume at a temperature of 40° C. to 140° C., to produce an oxidized propylene polymer material containing greater than 1 mmol total peroxide per kilogram of propylene polymer material, (3) optionally, heating the oxidized propylene polymer material in a non-oxidizing atmosphere to a temperature of at least 80° C.

Abstract: A polymer blend having a high melt strength and a low Young's modulus after irradiation of the polymers contains (1) a propylene homopolymer or copolymer having an isotactic index of greater than 90 and (2) a propylene homopolymer or copolymer having a crystallinity of <24% made using a metallocene catalyst. The blend can be used for extrusion coating (including fabric coating), foam extrusion, blow molding, and thermoforming applications.

Abstract: A polymer blend having a high melt strength and a low Young's modulus after irradiation of the polymers contains (1) a propylene homopolymer or copolymer having an isotactic index of greater than 90 and (2) a propylene homopolymer or copolymer having a crystallinity of <24% made using a metallocene catalyst. The blend can be used for extrusion coating (including fabric coating), foam extrusion, blow molding, and thermoforming applications.

Abstract: Disclosed is a piperidinyl phosphite composition consisting of a piperidinyl phosphite compound and an additive having a melting point of greater than 155.degree. C. selected from the group consisting of (i) sorbitol compounds, (ii) phosphite compounds and (iii) sterically hindered phenolic compounds, and polyolefin compositions containing them.

Abstract: A processable thermoplastic conductive composite resin is formed by coating polypyrrole onto the surface of microbeads by in situ oxidative polymerization. The microbeads, generally having an average diameter from about 0.5 to about 500 microns, are coated with polypyrrole by combining pyrrole, oxidizing agent and the beads in a protic solvent such as water, methanol, ethanol, ethylene glycol and the like. The pyrrole polymerizes on the surface of the microbeads. The microbeads, which are thermoplastic, can then be processed and the conductivity of the processed polymer remains high, generally about 0.1 to about 10 S/cm. This is suitable for use as a conductive film. By incorporating a sulfonate counterion, the conductivity of the composite is significantly improved. Further, by incorporating a heat activated cross-linking agent such as a peroxide, the tensile strength of the processed polymer is significantly improved.

Abstract: Disclosed is a process for the preparation of hindered amine light stabilizers by reacting (a) an alkyl substituted-4-hydroxypiperidine with (b) a dicarboxylic acid ester, in the presence of a catalyst system comprising a basic inorganic compound and a polar aprotic organic compound.

Abstract: Disclosed is a process for the preparation of organic esters and amides by reacting (a) a 5 to 60 mole % excess of an ester of (substituted-4-hydroxyphenyl) alkanoic acid with (b) (i) a C.sub.4 -C.sub.20 aliphatic alcohol or thioether alcohol having one or more hydroxyl groups or (ii) an amine of the formula, (R"').sub.2 N(CH.sub.2).sub.n R"" wherein R"' is hydrogen, C.sub.1-7 alkyl, C.sub.5-12 cycloalkyl, or C.sub.6-12 aryl, provided that one R"' is hydrogen, and R"" is hydrogen or N(R"').sub.2 wherein R"' is a defined above, in the presence of a catalyst system comprising a basic inorganic compound and a polar aprotic organic compound. The process provides higher yields of the desired product, shorter reaction times, and reduces the production of undesirable side-products.

Abstract: A process for the preparation of fluoroformates of formula: ##STR1## in which R.sup.1 is a substituted or unsubstituted, saturated or unsaturated aliphatic, cycloaliphatic or polycyclic radical, or substituted or unsubstituted araliphatic radical or an aromatic radical, which consists of reacting a carbonate of formula: ##STR2## in which R.sup.1 has the same meaning as hereinabove and R.sup.2 is hydrogen, alkyl of 1-12 carbon atoms, cycloalkyl of 5-12 carbon atoms, saturated or unsaturated, unsubstituted or substituted by one or more halogen atoms or R.sup.2 is aryl, unsubstituted or substituted by one or more halogen atoms, with an alkali or alkaline earth fluoride, ammonium fluoride or a quaternary ammonium fluoride, of formula FNR.sup.3 R.sup.4 R.sup.5 R.sup.6, wherein R.sup.3, R.sup.4, R.sup.5, R.sup.6 are the same or different and are hydrogen, alkyl or aralkyl of 1-12 carbon atoms or a fluoride which is KHF.sub.2, NH.sub.4 HF.sub.2 or KSO.sub.2 F.