Abstract: The corrosion of iron and steel surfaces by an aqueous alkanolamine conditioning solution used to remove CO.sub.2 from a gas stream is effectively inhibited by a combination of a vanadium containing ion and a di- or triamine. A surprising fact is that some of the amine co-inhibitors have been identified by others in the art as promoting ferrous metal corrosion.

Abstract: Alkyl substituted ethylene carbonates are converted to substituted ethylene oxides by heating the respective carbonates in the presence of a catalyst which is selected from the group of alkali metal halides consisting of lithium fluoride, sodium fluoride, potassium fluoride, sodium chloride and potassium chloride. The alkyl substituted ethylene carbonates have the general formula ##STR1## where R is alkyl, aryl, substituted alkyl, substituted aryl, alkaryl or aralkyl.

Abstract: The incorporation of a crosslinker comprising an ethylene oxide adduct of a Mannich condensate of nonyl phenol, diethanolamine and formaldehyde in molded polyurethane semiflexible foams is disclosed. Semiflexible polyurethane foams incorporating this crosslinker result in foams which offer many advantages including a significant improvement in moldability characteristics and materials utilization as well as other advantages. These improvements are demonstrable over similar formulations using other crosslinkers. The resulting foams find use in energy absorbing applications in the automotive industry and other industries.

Abstract: The corrosion of iron and steel surfaces by an aqueous alkanolamine conditioning solution used to remove CO.sub.2 from a gas stream is effectively inhibited by a combination of a vanadium containing ion and a soluble cobalt salt. This system allows the use of higher amine concentrations which in turn allows a higher carbon dioxide loading with low corrosion thereby improving the energy efficiency of the gas sweetening process.

Abstract: A process is disclosed for the production of high quality synthetic lubricants which comprises transforming ethylene into a mix of alpha olefins, separating from this mix of alpha olefins the alpha olefins in the range from about 14 to 20 carbon atoms, oligomerizing the alpha olefins in the range from about 14 to 20 atoms with a perfluorosulfonic acid resin catalyst and hydrogenating these oligomerized olefins. The olefins from the original mix of alpha olefins which are lighter and heavier than the 14 to 20 carbon atom alpha olefins processed above are combined and subjected to an isomerization/disproportionation process and the resulting olefins in the range of about 14 to 20 carbon atoms are oligomerized with perfluorosulfonic acid resin catalyst as above. Optionally, these olefins in the range of 14 to 20 carbon atoms may be combined with the olefins prepared directly from ethylene before oligomerization takes place. The resulting oligomers are hydrogenated.

Abstract: The invention is a method for making reaction injection molded polyurethane of improved paintability properties. The product comprises the reaction product of a high molecular weight polyhydric polyether, a low molecular weight active hydrogen containing compound of at least two functionality, a polyisocyanate and a catalyst combination comprising N,N-Dimethylethanolamine, dibutyltin dilaurate and an alkyltin mercaptide. This catalyst combination results in improved processing, a minimum of surface defects, excellent green strength and improved paintability using certain paints. Reaction injection molded elastomers are useful as molded articles of commerce including, but not limited to, vehicle body parts.

Abstract: The invention is a method for making reaction injection molded polyurethane of improved properties. The method comprises injecting into a mold cavity a high molecular weight polyhydric polyether, a low molecular weight active hydrogen containing compound of at least two functionality, a polyisocyanate and a catalyst comprising polymers substantially without active hydrogens containing tertiary amine moieties. This catalyst results in improved paintability when using high solids paint. Reaction injection molded elastomers are useful as molded articles of commerce including, but not limited to, vehicle body parts.

Abstract: A method of eliminating color-causing impurities in mixtures of t-butyl alkylphenols by treatment with N-(2-hydroxyethyl)oxazolidine at 90.degree. C. and at atmospheric pressure is described. These phenols are used as peroxide inhibitors in polyoxyalkylene glycols for polyurethane foams. Discoloration of the polyol occurs if the phenol mixture is not treated with N-(2-hydroxyethyl)oxazolidine. The t-butyl alkylphenol mixture is derived from an alkylphenol made over an acid catalyst.

Abstract: A primary amine may be reacted with formaldehyde and a 1,2-diol to produce N-substituted perhydrodioxazepines of the formula ##STR1## where R is alkyl, alkoxyalkyl, aminoalkyl or aryl alkyl and R' is hydrogen or lower alkyl. These compounds may be easily prepared and have a low odor which is essential in their utility as polyurethane catalysts. By varying the R group, the catalytic characteristics of the compounds may be altered as desired.

Abstract: A primary amine may be reacted with formaldehyde and a 1,2-diol to produce N-substituted perhydrodioxazepines of the formula: ##STR1## where R is alkyl, alkoxyalkyl, aminoalkyl or aryl alkyl and R' is hydrogen or lower alkyl. These compounds may be easily prepared and have a low odor which is essential in their utility as polyurethane catalysts. By varying the R group, the catalytic characteristics of the compounds may be altered as desired.

Abstract: The alkylene oxide adduct of bis(aminoethyl)ether may be reacted with formaldehyde in the presence of hydrogen and a hydrogenation-dehydration catalyst to produce new compounds of the formula ##STR1## where R is hydrogen or lower alkyl and R" is methyl or ##STR2## These compounds show unexpectedly high efficiency as polyurethane catalysts. Fewer equivalents of this amine are required to produce foams having the same reaction profile as foams made with prior art amine catalysts.

Abstract: A method of eliminating color-causing impurities in mixtures of t-butylalkyl phenols by treatment with trioxane at 100.degree. C. and 1 atmospheric pressure is described. These phenols are used as peroxide inhibitors in polyol formulations for polyurethane foams. Discoloration of the polyol occurs if the phenol mixture is not treated with trioxane. It is an essential part of the invention that the t-butyl alkylphenol mixture be derived from an alkylphenol made over an acid resin catalyst. Mixtures made by a BF.sub.3 process may not be decolorized by this method. Generally, the color decreases with increasing amounts of trioxane.

Abstract: The use of N-methoxypropylmorpholine, N-butylmorpholine and N,N'-dimethylpiperazine together as a catalyst system in an activator solution to give finer, more uniform cells to polyester-based polyurethane foams is described. While each of the amine catalysts has disadvantages when used alone in an activator solution, it was surprisingly discovered that together as a catalyst system none of the disadvantages were observed in the resulting polyurethane foam.

Abstract: A method of preparing polyether polyols in the 200-1000 molecular weight range by modifying a polyol initiator with an epoxy resin and one or more alkylene oxides is described. The modified polyols may be used in preparing rigid isocyanurate foams with improved compressability and flammability properties.

Abstract: A method for the production of ethylene glycol dialkyl ethers from dialkyl ethers and ethylene glycol monoalkyl ethers by means of passing these reactants over a heterogeneous anionic ion exchange resin catalyst is described. The reaction may be conducted at temperatures ranging from about 100.degree. to about 250.degree. C. and at pressures ranging from about 50 to about 500 psig. This method avoids some of the separation difficulties associated with preparing these compounds by prior wet chemistry methods.

Abstract: The modification of polyether polyols by their reaction with epoxy resin and alkylene oxides is described. The modified polyols of 2000 to 7000 molecular weight produce flexible polyurethane foams that have higher load bearing properties than foams made with nonmodified polyols. The ability of a modified polyol to make a higher load bearing foam is related to the position in the polyol chain the epoxy resin is added.

Abstract: The modification of rigid amino polyols by their reaction with epoxy resin and alkylene oxides is described. The modified polyols produce rigid polyurethane foams that have higher heat distortion temperatures and better low temperature properties than foams made with nonmodified polyols. The viscosities of the epoxy resin-modified amino polyols are not significantly different than those of the prior art amino polyols although they are of a higher functionality.

Abstract: Alkyl substituted ethylene carbonates are converted to substituted ethylene oxides by heating the respective carbonates in the presence of a catalyst comprising alkali metal halides or lanthanum iodide. The alkyl substituted ethylene carbonates have the general formula ##STR1## where R is alkyl, aryl, substituted alkyl, substituted aryl, alkaryl or aralkyl.