Abstract: Random, melt-processible copolyimides are disclosed herein. These copolyimides are semicrystalline and exhibit recoverable (semi)crystallinity from their melts. Associated processes, which entail either solution polymerization or melt polymerization, for producing and fabricating these copolyimides into useful articles having a predetermined shape are also disclosed.

Abstract: Random, melt-processible copolyimides are disclosed herein. These copolyimides are semicrystalline and exhibit recoverable (semi)crystallinity from their melts. Associated processes, which entail either solution polymerization or melt polymerization, for producing and fabricating these copolyimides into useful articles having a predetermined shape are also disclosed.

Abstract: Segmented, melt-processible, semicrystalline copolyimides are disclosed herein. These polymers are comprised of an amorphous or semicrystalline A segment (soft segment) and a semicrystalline B segment (hard segment), wherein the level of semicrystallinity in the A segment is less than that in the B segment. These copolyimides are semicrystalline and exhibit melting points in the range from about 330-395° C. In preferred embodiments, these copolyimides are end-capped and are crystallizable from their melts (i.e., they exhibit recoverable semicrystallinity). These copolyimides either inherently have suitably low melt visocosities to be melt-processible or can be made to have suitably low melt viscosities to be melt-processible by addition of certain additives. Tailoring of the melting points and glass transition temperatures of these copolyimides can be effected by changing their molecular architecture.

Abstract: Acid, electroplating baths having consistent leveler activity contain levelers which are quaternized near-monodisperse polymers of acrylic or methacrylic trialkyl amine esters. The polymers may contain hydroxyalkyl acrylate or methacrylate ester components, unquaternized acrylic or methacrylic amine component as well as other polymeric components.

Abstract: A stabilized spray displacement tin plating process of copper printed circuit innerlayers is disclosed for the manufacture of multilayer printed circuit boards. During prolonged use of spray tin plating, the plating solution becomes saturated with cupurous thiourea complex which precipitates interfering with spray nozzles and other mechanical components. The tin plating solution is stabilized by removing portions from the reservoir before saturation is reached, selectively precipitating the thiourea complex, and returning the remaining solution back to the reservoir. The precipitated cupurous thiourea complex is redissolved in acid and either disposed of by conventional waste treatment or the acid solution can be electrowinned to reclaim copper and oxidize thiourea to form a more acceptable acid solution for waste treatment.

Abstract: An environmentally innocuous effective replacement for thiourea is disclosed for use as a complexing agent in displacement plating processes in which the plating solution is applied to the substrate surface to be plated by immersion or by spraying, cascading, pouring and the like. The replacement complexing agent is an imidazole-2-thione compound having the formula: ##STR1## wherein A and B are the same or different --R--Y groups, wherein R is linear, branched or cyclic alkenyl group containing 1 to 12 carbon atoms and Y is a hydrogen, halogen, cyano, vinyl, phenyl, or ether moiety. Of this class of compounds, 1-methyl-3-propyl-imidazole-2-thione is preferred for immersion tin plating. This class of complexing agents is particularly useful in spray displacement tin plating for the manufacture of printed circuit boards wherein free tin metal is added to the plating solution.

Abstract: An apparatus for facilitating the movement of at least one container and preferably a plurality of containers is comprised of a base member having a plurality of gripping elements mounted thereon. Biasing means are provided for biasing the gripping elements to engage and hold the container or containers to be moved. Actuator means are provided for engaging and moving the gripping elements against the biased of the biasing means to disengage the gripping elements from the container or containers. The apparatus may also include alignment means mounted on the base member for aligning the container or containers with respect to the gripping elements.

Abstract: A titanium oxide/magnesium sulfate/magnesium oxide catalyst which is an ortho-selective methylation catalyst can be made to exhibit higher conversion and activity index for phenol methylation by the application of pressure. The pressure can be applied throughout the methylation period or can be applied for a short time at the beginning of the methylation period and then ceased, while higher activity continues. The pressure activation effects are assisted by the presence of phenol, methanol and/or water.

Abstract: A process for converting anisoles to ortho-methylated phenolic products in high selectivity is disclosed. The process comprises passing methoxybenzene, o-methylmethoxybenzene, 2,6-dimethylmethoxybenzene, or mixtures thereof, over gamma-alumina in the presence of an effective amount of water at a temperature in the range of about 225.degree. to about 295.degree. C.

Abstract: An improvement in the method of terminating the preparation of vinyl halide-containing polymers is disclosed. The improvement comprises injecting into the polymerization reactor at the desired level of conversion a free radical inhibitor obtained by the alkylation of p-methoxyphenol with nonene. The free radical inhibitor also functions as an antioxidant in the polymer product.

Abstract: A mixture of 2,4-/2,5-xylenol can be alkylated with a suitable alkylating agent over a strongly acidic divinylbenzene-styrene copolymer to afford a greater amount of 4-t-alkyl-2,5-xylenol than 6-t-alkyl-2,4-xylenol provided the alkylation is carried out at a suitably low temperature of 60.degree. C. or less.

Abstract: A mixture of 2,4-/2,5-xylenol can be alkylated with a suitable alkylating agent over a strongly acidic divinylbenzene-styrene copolymer to afford a greater amount of 4-t-alkyl-2,5-xylenol than 6-t-alkyl-2,4-xylenol provided the alkylation is carried out at a suitably low temperature of up to 60.degree. C.

Abstract: The relative amount of 2,5-xylenol in a 2,4-/2,5-xylenol mixture is significantly increased by passage of the xylenol mixture together with a suitable tertiary-alkylating agent through a reactor packed with a polymer-bound sulfonic acid catalyst at temperatures of 65.degree.-95.degree. C. and, preferably, 80.degree.-90.degree. C. The product stream from such a reactor under these conditions based on a 50:50 mixture of the two isomers contains a much greater amount of 6-t-alkyl-2,4-xylenol (t-alkylated 2,4-xylenol) than 4-t-alkyl-2,5-xylenol (t-alkylated 2,5-xylenol); consequently the resulting unalkylated 2,4-/2,5-xylenol mixture is greatly enriched in 2,5-xylenol. Recovery of the unalkylated mixture by fractionation thus affords a crude 2,5-xylenol which can be further purified to give pure 2,5-xylenol.

Abstract: A process for preparing 5-t-butyl alkylphenols from alkylphenols in high selectivity is disclosed, wherein the starting alkylphenol is a 3-alkylphenol or a 2,3-dialkylphenol and the alkyl group is a C.sub.1 -C.sub.6 primary alkyl. The process comprises reacting a 3-alkylphenol or a 2,3-dialkylphenol, wherein the alkyl group is a C.sub.1 -C.sub.6 primary alkyl, with isobutylene in the presence of a catalyst, which is a sulfonated polystyrene crosslinked with divinylbenzene, at a temperature of at least 100.degree. C.

Abstract: A process for preparing 6-t-butyl alkylphenols from alkylphenols in high selectivity is disclosed, wherein the starting alkylphenol is a 3-alkylphenol or a 2,3-dialkylphenol and the alkyl group is a C.sub.1 -C.sub.6 primary alkyl. The process comprises reacting a 3-alkylphenol or a 2,3-dialkylphenol, wherein the alkyl group is a C.sub.1 -C.sub.6 primary alkyl, with isobutylene in the presence of a catalyst, which is a sulfonated polystyrene crosslinked with a divinylbenzene, at a temperature of 50.degree. to 90.degree.C.

Abstract: A method is described for the selective dealkylation of 4-tertiary-alkyl-2,5-xylenol while it is admixed with 6-tertiary-alkyl-2,4-xylenol by contacting the mixture of alkylated xylenols with a polymer-bound sulfonic acid catalyst at temperatures of 60.degree. C. or less and pressures of from about 0.5 to 5 atmospheres. The method is useful in separating 2,4-/2,5-xylenol mixtures.

Abstract: Broadly, the present invention is directed to a process for preparing 1-methylnaphthalene and 2-methylnaphthalene wherein the process comprises reacting naphthalene and methanol in the vapor phase at elevated temperatures and optionally under pressure in the presence of an effective amount of activated alumina catalyst. In a preferred embodiment the invention is directed to a process for preparing 2-methylnaphthalene in high selectivity by reacting naphthalene and methanol in the vapor phase at elevated temperatures in the range of about 500.degree. to about 650.degree. C. in the presence of an effective amount of activated alumina catalyst.

Abstract: A method of preparing carbon-carbon coupled condensation products of alkylphenols is disclosed. Briefly, the method comprises oxidation of certain specific alkylphenols using palladium acetate as the catalyst in acetic acid or other suitable solvent.

Abstract: Trimethylhydroquinone (TMHQ) which is discolored in organic solution because of air oxidation can be made nearly colorless by addition of small amounts of alkali metal borohydride to the discolored solution. Products remaining in the TMHQ solution after discoloration removal can be extracted by water wash. This technique represents a very simple and efficient method for removing discoloration which has proved troublesome in the prior art.