Abstract: Disclosed is a method of removing chlorine from a mixture of gases. The mixture of gases is contacted with dichlorotoluene, whereby chlorine in the mixture of gases is absorbed by the dichlorotoluene. The dichlorotoluene is separated from the mixture of gases and is heated to desorb the chlorine and separate it from the dichlorotoluene.

Abstract: A method of removing HMO.sub.2.sup.- anions from an aqueous silicate solution comprising contacting the solution with a cationic ion exchange resin, where M is manganese, zinc, copper, nickel, or a mixture thereof. The method is particularly applicable to solutions of sodium silicate or potassium silicate.

Abstract: Disclosed is method of sulfodechlorinating an aromatic compound. A composition is prepared of (1) an aromatic compound having the general formula ##STR1## Where R is CHO or COOH and n is 1 to 3, (2) an alkali metal or alkaline earth metal sulfite or bisulfite in an amount stoichiometric to about 20 mole % in excess of stoichiometric, (3) water in an amount sufficient to form a solution of the sulfite or bisulfite, and (4) sufficient base to raise the pH of the composition to about 10 to about 14. The composition is heated at about 150 to about 200.degree. C. No catalyst is present in the composition.

Abstract: Disclosed is a process for polymerizing vinyl chloride monomer in the presence of light. A mixture is formed of liquid vinyl chloride monomer, preferably about 10 to about 250 ppm of a metallocene catalyst, about 1 to about 2000 moles of an aluminum-containing cocatalyst per mole of catalyst, and up to about 500 moles of a Lewis base per mole of aluminum in the cocatalyst. Selected alkyl groups from the aluminum-containing cocatalyst can be placed on the ends of the poly (vinyl chloride) chains.

Abstract: Disclosed is a composition of (1) a substituted benzaldehyde having the general formula ##STR1## where X is a leaving group in the ortho or para position, (2) a mercaptide having the general formula MSR' in an amount about stoichiometric to about 20 mole % in excess of stoichiometric with the amount of said substituted benzaldehyde, where M is an alkali metal and R' is alkyl or haloalkyl from C.sub.1 to C.sub.8 or aryl, aralkyl, or alkyl from C.sub.6 to C.sub.12, (3) sufficient water to dissolve said mercaptide and MX, (4) about 0.1 to about 5 mole %, based on said substituted benzaldehyde, of a phase transfer catalyst, and (5) 0 to about 100 wt %, based on total composition weight, of a water-immiscible organic solvent. Heating the composition to a temperature between about room temperature and 100.degree. C. results in the formation of a substituted mercapto-benzaldehyde.

Abstract: Disclosed is a single phase mixture of about 1 to about 99 wt % of a compound having the general formula ##STR1## where "n" is 1 or 2 and about 0.1 to about 99 wt % of a liquid which can be a perfluoro aliphatic alkane from C.sub.5 to C.sub.8, a perfluoro cycloaliphatic alkane from C.sub.5 to C.sub.8, a perfluoro alkylcycloalkane having 5 to 8 carbon atoms in the ring and 1 or 2 branches of 1 to 3 carbon atoms each, a perfluoro-N-alkylmorpholine from C.sub.5 to C.sub.8, a perfluoro cycloether from C.sub.4 to C.sub.7, or a perfluoro polyether having an average molecular weight from about 400 to about 500.

Abstract: Disclosed is an improved process for reacting a halogenated ester with an alkali metal alkoxide to form an alkoxy ester and a salt. A solvent is added to the halogenated ester prior to the addition of the alkali metal alkoxide. This results in a substantial increase in the particle size of the salt which greatly facilitates its separation from the solution of the alkoxy ester product.

Abstract: Disclosed is a method of inhibiting the formation of scale on reactor surfaces in contact with a polymerizing vinyl monomer. The reactor surfaces are contacted with a composition that contains, as a scale reducing agent, an acidic hydrazone condensate or a salt thereof. The scale reducing agent can be added to the polymerizing monomer or it can be placed in a composition containing a surfactant and an inorganic binder and the composition can be applied to the reactor surfaces or added to the monomer.

Abstract: Disclosed is a method of making a substituted diphenyldisulfide from a substituted thiophenol. A two phase reaction mixture is prepared which comprises a substituted thiophenol having the general formula ##STR1## hydrogen peroxide, water, an organic solvent, a basic salt that will give a pH between about 7 and about 10, and an optional flocculating agent. In the formula, R is selected from the group consisting of halogen, alkyl from C.sub.1 to C.sub.6, alkoxy from C.sub.1 to C.sub.6, or nitro. After the exothermic reaction is complete, the reaction mixture is cooled to crystallize the substituted diphenyldisulfide product. The symmetrical product precipitates preferentially over the unsymmetrical product, thereby enhancing the purity of the product over the purity of the starting material. Optionally, the organic solvent and the aqueous phase are recycled.

Abstract: Disclosed is a piston having a cylindrical body made from a thermosetting molding compound. The body has a central well and a molded-on metal cap having sides that extend downward over the exterior of the body and into the well. There is insulation under and in contact with the metal cap.

Abstract: Disclosed is a valve assembly having a slidable valve stem that passes through a bushing enclosed in a bonnet. At least one circumferential stem seal seals the valve stem to the bushing. At least one passageway is provided through the bushing for injecting a fluid between the valve stem and the bushing to wash out deposits. A second optional passageway is also provided for injecting a lubricant around the valve stem.

Abstract: Disclosed is a method of preparing an aromatic compound having the general formula ##STR1## where R is CF.sub.3, OCF.sub.3, OC.sub.2 F.sub.5, CN, NCO, or COCl, m is 0, 1, or 2, n is 0, 1, or 2, q is 1 or 2, and q+m+n is an integer from 1 to 5. A vapor is prepared of a substrate having the general formula ##STR2## and a chlorinating agent. The mixture is reacted at a temperature above the boiling point of the substrate but below its decomposition temperature. The amount of chlorinating agent is about 0.5 to about 2 times the amount stoichiometrically required to replace the nitro groups on the substrate with chlorine. Unreacted substrate and partially reacted substrate are condensed from the product mixture and are recycled. The substrate is preferably in contact with the chlorinating agent before it is vaporized.

Abstract: Disclosed is a resol phenolic thermosetting resin made by preparing a composition of formaldehyde and a phenol in a molar ratio of about 1:1 to about 3:1, about 1 to about 20 wt %, based on the weight of said composition, of a phenol-formaldehyde polymerization catalyst, and about 0.5 to about 10 wt %, based on the weight of said phenol, of a polyvinyl alcoholic compound. The phenol can be benzophenol, an alkyl from C.sub.1 to C.sub.12 phenol, a bisphenol, or a mixture thereof. The bisphenol can be bisphenol A, bisphenol F, or bisphenol S. The polyvinyl alcoholic compound can be polyvinyl alcohol, polyvinyl acetate, an acetal derived from polyvinyl alcohol, or a mixture thereof. The composition is heated at about 50 to about 120.degree. C. to form the resin.

Abstract: Disclosed is a method of forming a pattern on a substrate. A first solution is formed of an organic solvent and monomers of diamine and dianhydride. The monomers are polymerized to form a polyamic acid soluble in the organic solvent. About 20 to about 95% of the amic acid groups in the polyamic acid are imidized to form a partially imidized polyamic acid. A more concentrated solution of the partially imidized polyamic acid is formed. This can be accomplished by precipitating the partially imidized polyamic acid from the first solution and dissolving it in a second organic solvent to form a second solution. The second solution is applied to the substrate and the solvent is evaporated to form a coating of the partially imidized polyamic acid on the substrate. A portion of the coating is removed to form a pattern on the substrate and the remaining partially imidized polyamic acid is fully imidized on the substrate.

Abstract: Disclosed is a method of reactivating a deactivated anode that has a coating of a noble metal or noble metal oxide on a substrate. A coating of a noble metal is deposited on the anode either electrolessly or electrolytically. The noble metal in the deposited coating can be platinum, palladium, iridium, rhodium, ruthenium, osmium, or a mixture thereof.

Abstract: Disclosed is a blend capable of forming a semi-interpenetrating network when cured of (A) a solution of about 30 to about 50 wt % solids in an organic solvent of a fully imidized polyimidesiloxane and (B) about 5 to about 30 pbw per 100 pbw of the polyimidesiloxane of an epoxy resin which comprises a cycloaliphatic epoxy and an epoxy curing agent. The polyimidesiloxane is the reaction product of an aromatic dianhydride and diamine. The diamine is about 5 to about 80 mole % non-siloxane containing aromatic diamine and the remainder a siloxane diamine, where the siloxane diamine is about 40 to about 80 wt % of the weight of the polyimidesiloxane. The blend is used to bond metal parts to ceramic packages.

Abstract: Disclosed is a process for reducing corrosion in a system in which aromatic hydrocarbons are separated from a mixture with aliphatic hydrocarbons. The aromatic hydrocarbons are extracted from the mixture using an extracting solvent. The aromatic hydrocarbons are stripped from the extracting solvent with steam and the steam is condensed to form water which is separated from the aromatic hydrocarbons. The separated water is passed through a basic anion exchange column and is then heated to produce the steam.

Abstract: Disclosed is a method of making a mercaptan by reacting an aliphatic alcohol with hydrogen sulfide in a continuous gaseous phase reaction. The reaction is performed in the presence of a catalyst which comprises a catalytically active carrier that contains base and/or acid active sites, an alkali metal or alkaline earth metal bicarbonate, carbonate, oxide, or hydroxide, and a transition metal acid or alkali metal or alkaline earth metal salt thereof. Selectivities of close to 100% are obtained.

Abstract: Disclosed is a method of making an o-arylbenzonitrile. A mixture is prepared of o-chlorobenzonitrile and about 1.0 to about 2.0 equivalents per equivalent of o-chlorobenzonitrile of a substituted phenylmagnesium halide in about 5 to about 30 mL per gram of o-chlorobenzonitrile of a solvent system of an ethereal solvent and N-methyl pyrrolidinone. The o-chlorobenzonitrile is reacted with the substituted phenylmagnesium halide at a temperature of about 10-.degree. to about 25.degree. C.

Abstract: Disclosed is a method of making an acid chloride having the general formula ##STR1## where each R contains no unsaturated groups and is preferably independently selected from aliphatic from C.sub.1 to C.sub.7 and aryl from C.sub.6 to C.sub.15. A solution is formed in an inert solvent of an aldehyde having the general formula ##STR2## and chlorine gas is sparged into said solution. The reaction between the aldehyde and the chlorine gas to produce the acid chloride is performed in the absence of a catalyst, an initiator, and ultraviolet light. A chlorinated acid chloride can be prepared from the acid chloride by reacting it with additional chlorine in the presence of a chlorine free radical generator.