Abstract:
A polymeric peroxide comprising a divalent recurring unit having the formula: wherein the recurring unit of Formula I has a 10 hour half-life temperature of at least 80 °C and optionally a divalent recurring unit having the formula: wherein R 1 , R 2 , R 3 , R 5 , X, X 1 , Y, Z, y and z are as defined in the Detailed Description of the Preferred Embodiments and the polymeric peroxide has a molecular weight of 1,000 to 200,000. The polymeric peroxides are derived from hydroxy-hydroperoxides or dihydroxy dialkyl peroxides. These polymeric peroxides can be used for preparing block copolymers and compatibilizing polymer blends and alloys.
Abstract:
1,1-Difluoroethane is converted to vinylidene fluoride by contact with a Cr₂O₃/Al₂O₃ catalyst, in the presence of a co-reactant gas, at a reaction temperature of from about 300°C to about 700°C. The co-reactant gas advantageously comprises air, oxygen, carbon dioxide, or mixtures thereof.
Abstract translation:在共反应物气体存在下,在约300℃至约700℃的反应温度下,通过与Cr 2 O 3 / Al 2 O 3催化剂接触将1,1-二氟乙烷转化为偏氟乙烯。共反应气体 有利地包括空气,氧气,二氧化碳或其混合物。
Abstract:
Flame retardancy of polyphenylene ether resins is increased by blending with the resin a flame retarding amount of a halogenated polyester which is the reaction product of a halogenated phthalic acid or phthalic anhydride with an epoxide or hydroxy compound containing at least two hydroxyl groups. The polyphenylene ether resin may include homopolymers or copolymers of polyphenylene ethers or blends of polyphenylene ethers with vinyl aromatic resins such as styrene polymers and copolymers. The flame retarding polyesters are also effective as processing aids in improving the flowability and moldatility of the polyphenylene ether resins during melt processing.
Abstract:
A positive displacement piston pump (110) includes a cylinder (112) having a working end (114), an inlet port (118), an outlet port (120) and a working chamber bounded by the outlet port and the working end; a piston (128) rotatably and reciprocably movable in the cylinder between a retracted position and an extended position, the piston including a free end having a recessed section alternately in fluid communication with the inlet port and the outlet port; a drive motor rotatably and reciprocably driving the piston in the cylinder; a yoke (154) and ball and socket joint (158) pivotally connecting the piston to the drive motor; a base (136) having an upper surface (136a) with an elongated slot (172) below the pivot point of the piston and an arcuate slot (174) adjacent the opposite end of the cylinder; and first and second pivot pins (188, 190) secured to a swivel plate (182) which is, in turn, secured to the cylinder through a vertical column (180), whereby the recessed section is positioned entirely in the working chamber when the piston is at the end of its pressure stroke, regardless of the angle between the piston and the drive motor.
Abstract:
Hydrazide functionalized benzotriazole and oxanilide ultraviolet absorbers (formulas I and II) useful for stabilizing coreactive or inert polymeric compositions and novel intermediates (formula III used to make certain types of compounds of formula I) are disclosed and have general formulas (I) or (II) or (III), wherein R?1, R2, R3, R4, R5, R6, R7, R8, R9¿, X, Y, all substituents thereof, and n are set forth in the summary of the invention.
Abstract:
A process for converting carbon disulfide (CS₂) to hydrogen sulfide (H₂S) in mixtures of H₂S and CS₂ is provided. The H₂S/CS₂ mixture is combined with water to form a hydrolysis feed mixture. The hydrolysis feed mixture is passed through a hydrolysis reactor containing e.g., an alumina-based catalyst, wherein a substantial portion of the CS₂ is converted to additional H₂S. A vapor product comprising H₂S, CO₂, unreacted H₂O, unconverted CS₂ and sulfur is formed by the hydrolysis reaction. The vapor product is cooled to form a H₂S/CO₂ vapor phase and a sour water condensate phase. The H₂S/CO₂ vapor phase is separated from the sour water condensate phase and subsequently recovered. The sour water condensate phase, which contains small amounts of solid sulfur particles, is optionally then combined with additional CS₂ and decanted to form a sulfur-free sour water layer and a CS₂ layer containing dissolved sulfur. The sour water layer is recycled and combined with the original H₂S/CS₂ mixture. The CS₂ layer is recycled to a sulfur removal device to remove the sulfur dissolved in the CS₂.
Abstract translation:提供了一种用于二硫化碳(CS 2)转化为在H 2 S的混合物和CS2硫化氢(H2S)的过程。 的H 2 S / CS2混合物与水混合,以形成水解混合物进料。 水解进料混合物通过水解反应器含有E. G.基于氧化铝的催化剂的,通过,worin的CS2的相当一部分被转化成额外的H 2 S. 蒸气产品,包括H 2 S,CO 2,未反应的H 2 O,未转化的CS2和硫通过水解反应而形成。 蒸汽产物被冷却以形成H 2 S / CO 2蒸汽相和酸性水冷凝物相。 的H 2 S / CO 2蒸气相从酸性水冷凝物相分离,并随后回收。 酸性水冷凝物相,其中含有固体硫颗粒的少量,任选然后用另外的CS2合并,并倾析以形成无硫酸性水层和层CS2含溶解的硫。 酸性水层再循环并与原来的H 2 S / CS2混合物合并。 所述CS2层再循环到硫去除装置来去除CS2溶解的硫。
Abstract:
A lubricant additive that includes antimony thioantimonate and antimony trioxide in a specified ratio for enhancing the extreme pressure, antiwear, and antiabrasive properties of conventional lubricants as well as for use in lubrication of a wide variety of lubricated contact surfaces.
Abstract:
N-(2,2,6,6-tetraalkyl-4-piperidinyl)amic acid hydrazides contain a light stabilizing group, a heat stabilizing group and an amic acid hydrazide functionality in the same molecule. The amic acid hydrazide functionality in the compounds enhances the photooxidative stabilizing properties of the hindered amine groups and contributes thermal and oxidative stabilizing and metal complexing properties to the compounds. The novel compounds are excellent light stabilizers for polyolefins, have low volatility and are not readily lost from polymeric systems via volatilization, migration or extraction.
Abstract:
N,N'-hydrocarbylenebis[N-(2,2,6,6-tetraalkyl-4-piperidinyl)amic acid hydrazides] and their derivatives are useful for stabilizing polymeric systems which are subject to degradation and/or discoloration upon exposure to heat and/or light. The novel compounds contain at least two hindered amine light stabilizing groups and two hydrazide or hydrazide derivative thermal oxidative stabilizing groups. The novel compounds are excellent light stabilizers for polyolefins, have low volatility and are not readily lost from polymeric systems via volatilization, migration or extraction.