Abstract: The shelf life of polyurethane polyol pre-blends containing halogenated olefins is extended by encapsulation of active components such as catalysts and/or surfactants. The active component is encapsulated in a crystallizable or thermoplastic polymer. The encapsulated particles have a size of 2,800 microns or less and the active components are not significantly leaked out, particularly in the presence of halogenated olefins.

Abstract: The invention also relates a process for the manufacture of trans 1-chloro3,3,3-trifluoropropene. The process comprises an isomerization step from cis 1233zd to trans 1233zd.

Abstract: The invention also relates a process for the manufacture of trans 1-chloro 3,3,3-trifluoropropene. The process comprises an isomerization step from cis 1233zd to trans 1233zd.

Abstract: A polyol pre-mix composition includes a blowing agent having a halogenated hydroolefin, a polyol, a surfactant, a catalyst composition, and a metal salt. The metal salt may be, for example, a carboxylate, acetylacetonate, alcoholate of a metal selected from the group consisting of Zn, Co, Ca, and Mg. The metal salt may be, for example, a carboxylate and/or alcoholate of a C1-C21 straight chain or branched aliphatic monocarboxylic acid or monoalcohol, such as magnesium formate, zinc octoate, calcium octoate, cobalt octoate, and magnesium octoate, and mixtures thereof. The metal acetylacetonate may be, for example, zinc acetylacetonate, cobalt acetylacetonate, magnesium acetylacetonate, or calcium acetylacetonate. A two-part system for producing a thermosetting foam blend includes (a) a polyisocyanate and, optionally, one or more isocyanate compatible raw materials; and (b) the polyol pre-mix composition.

Abstract: A stable polyol pre-mix composition comprises a blowing agent, a polyol, a surfactant, and a catalyst composition comprising an oxygen-containing amine catalyst. The oxygen-containing amine catalyst may be, an alkanol amine, an ether amine, or a morpholine group. containing compound such as, 2.(2.dimethylaminoethoxy)ethanol or N.N.N?.trimethylaminoethylethanolamine. A stabilized thermosetting foam blend comprises: (a) a polyisocyanate and, optionally, isocyanate compatible raw materials; and (b) a polyol pre. mix composition. A method for stabilizing thermosetting foam blends comprises combining: (a) a polyisocyanate and, optionally, isocyanate compatible raw materials; and (b) a polyol pre. mix composition. A polyurethane or polyisocyanurate foam having uniform cell structure with little or no foam collapse comprises a mixture of: (a) a polyisocyanate and, optionally, one or more isocyanate compatible raw materials; and (b) a polyol pre-mix composition.

Abstract: A method for using a fracture fluid in forming subterranean fractures includes delaying degradation of a polymer in a fracture fluid when the fracture fluid comprises a breaker by combining at least one radical scavenger with the fracture fluid. The mixture for use in a fracture fluid comprises a radical scavenger and a breaker. A method of fracturing a subterranean formation may include providing a fracture fluid comprising a proppant, a polymer, and a breaker and adding a radical scavenger to the fracture fluid. The fracture fluid is supplied to a desired location in the subterranean formation to form at least one fracture where the viscosity of the fracture fluid is maintained. The breaker is then allowed to degrade the polymer and reduce the viscosity of the fracture fluid at a specific time or temperature.

Abstract: Provided are dispersions which comprise more than about (40) percent by weight of an organic peroxide which is normally solid, an effective dispersing amount of a pharmaceutically acceptable dispersing agent and water. The water and about (40) percent or more peroxide forms a paste. Addition of the dispersing agent/surfactant to a non-flowing organic paste resulted in the formation of a shear thinning aqueous dispersion. The aqueous dispersions can also contain optional components such as thickening agents and anionic emulsifiers.

Abstract: The present invention is based upon the discovery that nontitanyl oxalates can enhance the catalytic functionality of titanyl oxalate catalysts. This invention provides a novel catalytic composition containing a titanyl oxalate catalyst and a metallic oxalate catalyst enhancer and optionally containing a metallic cocatalyst such as an antimony based catalyst. A synergistic relationship has been discovered between titanyl oxalate catalyst and the catalyst enhancer. A synergistic relationship has also been discovered between the titanyl oxalate catalyst, catalyst enhancer and a metallic cocatalyst such as antimony oxide or antimony triacetate.

Abstract: The present invention is based upon the discovery that nontitanyl oxalates can enhance the catalytic functionality of titanyl oxalate catalysts. This invention provides a novel catalytic composition containing a titanyl oxalate catalyst and a metallic oxalate catalyst enhancer and optionally containing a metallic cocatalyst such as an antimony based catalyst. A synergistic relationship has been discovered between titanyl oxalate catalyst and the catalyst enhancer. A synergistic relationship has also been discovered between the titanyl oxalate catalyst, catalyst enhancer and a metallic cocatalyst such as antimony oxide or antimony triacetate.

Abstract: The present invention is based upon the discovery that nontitanyl oxalates can enhance the catalytic functionality of titanyl oxalate catalysts. This invention provides a novel catalytic composition containing a titanyl oxalate catalyst and a metallic oxalate catalyst enhancer and optionally containing a metallic cocatalyst such as an antimony based catalyst. A synergistic relationship has been discovered between titanyl oxalate catalyst and the catalyst enhancer. A synergistic relationship has also been discovered between the titanyl oxalate catalyst, catalyst enhancer and a metallic cocatalyst such as antimony oxide or antimony triacetate.

Abstract: Dual cure organotin salts of strong organic acids, the use of such salts as catalysts and an improved process for producing the catalysts are provided. The catalysts are capable of effectively catalyzing esterification and transesterification reactions and urethane, silicone, melamine, ester and acrylic forming reactions and can simultaneously catalyze more than one reaction in a mixture of urethane, silicone, amino, ester and acrylic polymer forming reactants to produce a polymer mixture.

Abstract: The present invention comprises a polystannoxane catalyst, a curable composition containing the catalyst and a method of using the catalyst and curing the composition. The curable composition comprises:(i) a blocked isocyanate;(ii) a functional component containing reactive hydrogen;(iii) a polystannoxane catalyst for promoting the reaction of the blocked isocyanate with the functional component.A co-catalyst may also be employed based on Cu, Zn, Ni, Zr, Ce, Fe, Co, V, Sb and Bi and especially oxides, salts or chelates of said metals. The invention also relates to a method for curing a blocked isocyanate at a low reaction temperature which comprises combining the catalyst with the blocked isocyanate and functional component and heating to a temperature less than about 180.degree. C. to obtain a cured urethane.

Abstract: The invention relates to a surface treatment composition and a method of using the composition to provide the treated surface with a suitable surface conductivity for electrostatic painting of the surface. The surface treatment composition preferably comprises a mixture of: (a) a substituted or unsubstituted aromatic polycarboxylic acid, anhydride or salt thereof, and (b) a quaternary ammonium salt or (b') an ethoxylated tertiary fatty amine, in a compatible vehicle, said composition having a pH of below about 4.5, said polycarboxylic acid and said quaternary ammonium salt or ethoxylated fatty amine each being present in said composition in an amount effective to impart to said thermoplastic surface a resistivity value of between about 10.sup.8 ohms/cm.sup.2 and about 10.sup.12 ohms/cm.sup.2, or a 90% electrostatic charge decay time of less than five seconds, or both.