Abstract: In the process of removing heavy metals from aqueous solutions (groundwater) by precipitation of a salt thereof, an oxidizing agent is optionally used to increase the valence of said metal, and a precipitation-enhancing agent is added to maximize particle size of the precipitate and to facilitate its separation from said solution.

Abstract: A process of coating a substrate such as aluminum by the steps of (a) applying thereon a powder coating composition prepared by (i) blending a mix containing a poly(vinylidene fluoride) resin, a thermoplastic resin, a pigment, and a vinylidene fluoride/tetrafluoroethylene/hexafluoropropylene terpolymer, (ii) pelletizing the blend from (i), and (iii) cryogenically grinding the pellets from (ii); (b) heating the powder coating composition above its melt temperature; and (c) cooling the coated substrate.

Abstract: Improved stabilizer compositions are provided which impart significant long-term stabilization to halogen containing polymers such as polyvinyl chloride. The improved stabilizer compositions incorporate an alkali-metal hydrogen phosphate compound, such as anhydrous disodium hydrogen phosphate, of a predetermined surface area. The novel inorganic phosphate enables a reduction in the amount of organmetallic stabilizer, if desired, while still yielding long-term stability in the resultant polymer, or the ability to raise process temperature and reduce cycle times of molding operations.

Abstract: A process is disclosed for the removal of dissolved heavy metals from aqueous solution contaminated therewith wherein at least one of said heavy metals is reacted with a water-soluble inorganic sulfide or hydrosulfide at a defined elevated temperature and a controlled pH of between about 2 to about 3.5 to thereby precipitate heavy metal sulfide, and thereafter separating the precipitate from the filtrate.

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: The present invention relates to electroactive compounds capable of undergoing a change in light absorption and refraction due to an applied electric field and a permanent change in refraction due to exposure to predetermined bands of optical radiation. The present invention also relates to electroactive compositions containing such electroactive compounds, electrooptical components comprised of such electroactive compositions and electrooptical devices comprised of such electrooptical components, as well as novel processes of making the same.

Abstract: Fire resistant hydraulic fluid compositions comprising (a) one or more esters of polyhaloaromatic acids per se or in combination with (b) one or more hydraulic fluids independently selected from mineral oil, poly-.alpha.-olefins, alkylated aromatics, cycloaliphatics, esters of dibasic acids, polyol esters, polyglycols, silicones, silicate esters, phosphate esters, and halogenated compositions other than (a); a method for imparting fire resistant properties to known hydraulic fluids by adding one or more esters of polyhaloaromatic acids alone or combined; and the use of the inventive compositions as fire resistant hydraulic fluids. The fire resistant compositions may, optionally, contain one or more shear-stable polymers which have been found to increase the fire resistance of the hydraulic fluid composition.

Abstract: The present invention relates to a partial ester derived from the reaction product of an oxirane containing acid or derivative thereof, and a reactive hydroxyl compound selected from the group consisting of diols, triols, di-diols and 1,4-dihydroxy butane and a halogen containing polymer compositon thereof. The oxirane compound can be derived from the group consisting of epoxidized vegetable oil, epoxidized fish oil, an aliphatic or arylaliphatic containing craboxyl compound having an oxirane group in the aliphatic chain.

Abstract: An improvement in dough compositions comprising the replacement of bromate improvers in conventional doughs with compositions comprising ascorbic acid, azodicarbonamide, and mixtures thereof in combination with peroxy compounds such as benzoyl peroxide and hydrogen peroxide in the presence or absence of fungal enzymes such as fungal alpha amylase and processes for their use are disclosed.

Abstract: Hydrazide functionalized benzotrialzole 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 the general formulas: ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.9, X, Y, all substituents thereof, and n are set forth in the Summary of the Invention.

Abstract: Novel functionalized peroxides which may be used as crosslinking, grafting and curing agents, initiators for polymerization reactions and as monomers for condensation polymerizations to form peroxy-containing polymers, which in turn can be used to prepare block and graft copolymers, have the following Formula I: ##STR1## R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, X, Y.sup.1, Y.sup.2, Y.sup.3, Z.sup.1, Z.sup.2, x, y and z are as defined in the Summary of the Invention. The compounds of Formula I may be prepared by reacting hydroxy-containing tertiary hydroperoxides with diacid halides, phosgene, dichloroformates, diisocyanates, anhydrides and lactones to form the functionalized peroxides. These reaction products may be further reacted, if desired, with dialcohols, diamines, aminoalcohols, epoxides, epoxy alcohols, epoxy amines, diacid halides, dichloroformates and diisocyanates to form additional functionalized peroxides.

Abstract: A process is disclosed for the preparation of pure ammonium thioglycolate from thioglycolic acid contaminated with the isopropyl ester of thioglycolic acid wherein the contaminated acid is reacted with aqueous ammonia or ammonium hydroxide at a pH of at least 6.5 to about 9.0 at elevated temperature.

Abstract: OO-t-alkyl O-polycaprolactone monoperoxy carbonate compounds comprising polycaprolactones end capped with OO-t-alkyl peroxy carbonate groups which compounds are useful in the preparation of polycaprolactone block and graft copolymers are disclosed. Also disclosed are processes for the preparation and use of the above compounds including use of the above compounds as compatibilizing agents for otherwise immiscible polymers, as well as intermediates useful in the preparative processes.

Abstract: A process for removing sulfur from an organic sulfide containing three or more chemically bound sulfur atoms is disclosed wherein said sulfide is contacted with a defined catalyst at elevated temperature to increase the disproportionation rate and the corresponding sulfide of lower sulfur rank is continuously removed from the reaction zone.

Abstract: An aqueous solvent composition for pre-etching plastic materials prior to plating with metal consists essentially of an aqueous solution containing a component selected from diethylene glycol monobutyl ether acetate, diethylene glycol monoethyl ether acetate, and mixtures thereof, and preferably containing a surfactant.

Abstract: Novel hydroxy peroxides of the Structure AHO--R.sub.11 --X--OO--R (A)[wherein R--, --R.sub.11 -- and --X-- are as defined in the Summary of the Invention Section], having 10 hour half-life temperatures of 85.degree.-100.degree. C., the processes for their preparation, and the use of these novel compositions in curing of unsaturated polyester resins and in initiating polymerization of ethylenically unsaturated monomers.

Abstract: N-(2,2,6,6-tetraalkyl-4-piperidinyl)amide-hydrazides of dicarboxylic acids contain a light stabilizing group, a heat stabilizing group, and a reactive hydrazide functionality in the same molecule. The reactive stabilizers are prepared by reacting 4-amino-2,2,6,6-tetraalkylpiperidines with diesters (or mono ester acid chlorides) of dicarboxylic acids or dialkyl itaconates followed by hydrazinolysis of the ester group of the intermediate mono esteramide. The compounds are useful for introducing permanent heat and light stability to coreactive polymers or copolymers. They are also useful in the stabilization of inert polymeric systems against the degradative effects of heat and light when merely mixed with, rather than reacted with, the polymers for which stabilization is sought.

Abstract: Functional chromium and chromium-alloy deposits are obtained from an electroplating solution having substantially the composition: 22 g/l Cr.sup.+3 ; 250 g/l KCl; 63 g/l H.sub.3 BO.sub.3 ; 30 g/l HCO.sub.2.sup.= ; 15 g/lKBr; and 120 ppm of a wetting agent. The plating solution provides improved efficiency, stress values and appearance over the prior art, and is tolerant of metallic iron and ionic iron and ammonium.

Abstract: The alkyl groups of dialkyl trisulfides are exchanged with the alkyl groups of mercaptans by reacting a tertiary dialkyl trisulfide with an alkyl mercaptan having a greater number of carbon atoms in its alkyl group than said trisulfide in the presence of an acidic or basic type catalyst for a time and a temperature sufficient to produce a dialkyl trisulfide having at least one transferred alkyl group from said mercaptan.

Abstract: The mixture consists of at least one organic peroxide, at least one hydroquinone derivative of the general formulae I and/or II and/or III ##STR1## wherein R and R.sup.1, which may be identical or different, stand for H or t-alkyl, and X stands, for example, for C.sub.1-18 -alkylene, and a crosslinkage promoter, and permits the crosslinkage of polymers and at the same time extends the scorch time, which must be understood as the processing time.