Abstract: Oligomeric polyesters and polyamides containing dipiperidyl triazine moieties are effective light stabilizers for synthetic polymers and particularly polyolefins.

Abstract: Tetramethylpiperidyl terminated triazine oligomeric esters and amides having a plurality of tetramethyl piperidyl moieties are useful as polymer additives to impart resistance to degradation when exposed to actinic radiation.

Abstract: Triazine-based compounds having a multiplicity of 2,2,6,6-tetraalkyl piperidine moieties are light and thermal stabilizers for organic polymers.

Abstract: Melamine-based compounds having a multiplicity of 2,2,6,6-tetraalkyl piperidine moieties are light stabilizers for organic polymers.

Abstract: Acetal esters and amides possessing the polyalkyl piperidin-4-yl moiety are useful light stabilizers with synthetic polymer resins such as polyolefins and, in particular, polypropylene.

Abstract: Monomeric and oligomeric derivatives of the dialkyl esters of polyalkyl 1,5-dioxa-9-azaspiro-[5.5]undecane-3,3-diacetic acid are useful light stabilizers for synthetic polymer resins such as polyolefins, and in particular, polypropylene.

Abstract: A method of preparing certain 2-halo-5-methylpyridines, useful as herbicide intermediates, is presented starting from acyclic pentenes. The pentene is difunctionalized, e.g., by making the epoxide, and is then reacted with a nitrogen source to close the ring. The nitrogen-containing 6-membered heterocycle may then be aromatized readily to produce the 2-halo-5-methylpyridine desired. Also part of the invention are novel acyclic and cyclic intermediates used in the process.

Abstract: Malonate-based spiroacetals of polyalkylpiperidin-4-ones are useful light stabilizers for synthetic polymer resins such as polyolefins, and in particular, polypropylene.

Abstract: A method of preparing certain 2-halo-5-methylpyridines, useful as herbicide intermediates, is presented starting from acyclic pentenes. The pentene is difunctionalized, e.g., by making the epoxide, and is then reacted with a nitrogen source to close the ring. The nitrogen-containing 6-membered heterocycle may then be aromatized readily to produce the 2-halo-5-methylpyridine desired. Also part of the invention are novel acyclic and cyclic intermediates used in the process.

Abstract: Malonate-derived acetal esters and amides possessing the polyalkyl piperidin-4-yl moiety are useful light stabilizers with synthetic polymer resins such as polyolefins and, in particular, polypropylene.

Abstract: Monomeric and oligomeric derivatives of the diethyl ester of polyalkyl 1,4-dioxa-8-azaspiro-[4.5]-decane-2,3-dicarboxylic acid are useful light stabilizers for synthetic polymer resins such as polyolefins, and in particular, polypropylene.

Abstract: Oligomeric derivatives of the dialkyl esters of polyalkyl 1,5-dioxa-9-azaspiro-[5.5]undecane-3,3-dicarboxylic acid are useful light stabilizers for synthetic polymer resins such as polyolefins, and in particular, polypropylene.

Abstract: Tartrate-derived acetal esters and amides possessing the polyalkyl piperidin-4-yl moiety are useful light stabilizers with synthetic polymer resins such as polyolefins and, in particular, polypropylene.

Abstract: The present invention is used to separate gas from liquid while being placed downhole in a hydrocarbon producing well. It essentially comprises a means to divert hydrocarbon production fluid from within a tubing string into the annulus of the well. This diversion turbulently mixes the fluid and releases free gas from the liquid. Thereafter, the liquid migrates downward while the free gas migrates upward to a gas collection apparatus. The liquid is reuptaken at an intake spot below the point at which it was diverted. It travels upward through a concentric chamber and subsequently reenters the tubing string at a point above that which it was diverted.

Abstract: A method of preparing certain 2-halo-5-methylpyridines, useful as herbicide intermediates, is presented starting from acyclic pentenes. The pentene is difunctionalized, e.g., by making the epoxide, and is then reacted with a nitrogen source to close the ring. The nitrogen-containing 6-membered heterocycle may then be aromatized readily to produce the 2-halo-5-methylpyridine desired. Also part of the invention are novel acyclic and cyclic intermediates used in the process.

Abstract: A method of preparing certain 2-halo-5-methylpyridines, useful as herbicide intermediates, is presented starting from acyclic pentenes. The pentene is difunctionalized, e.g., by making the epoxide, and is then reacted with a nitrogen source to close the ring. The nitrogen-containing 6-membered heterocycle may then be aromatized readily to produce the 2-halo-5-methyl-pyridine desired. Also part of the invention are novel acyclic and cyclic intermediates used in the process.