Abstract: Reaction of 1,3,5-tri-substituted-hexahydro-1,3,5-triazine is accelerated in H.sub.2 S scavenging by the addition of quaternary ammonium compound. The preferred hexahydro triazines are 1,3,5-tri-methyl-hexahydro-1,3,5-triazines and 1,3,5-tri-methoxypropyl-hexahydro-1,3,5-triazines. The blend of the hexahydro triazine and quaternary ammonium compounds can be used to treat sour gases and liquids (e.g. sour kerosene, crude oil, fuel oils, heating oils, distillate fuels, bunker fuel oil, and the like.

Abstract: Gaseous or liquid hydrocarbon is treated with a scavenging compound comprising an oil soluble 1,3,5-trihexahydro-1,3,5-tert.-butyltriazine. The compound is an effective nonregenerated scavenger for oil field produced fluids, particularly sour hydrocarbon liquids.

Abstract: Amines which are compounds of the formula I: ##STR1## where R is a C.sub.6-20 hydrocarbon;X is --NR.sub.1 -- or --O--;each R.sub.1 is independently H or --[(CH.sub.2).sub.1-4 ]COOH or a C.sub.6-20 hydrocarbon;n is 1, 2 or 3;and which contains at least one (CH.sub.2).sub.1-4 COOH group; or salt thereof are useful in inhibiting corrosion of metals in a marine or freshwater environment e.g. in oil- and gas-field applications since they show relatively low toxicity to marine organisms.

Abstract: A method of inhibiting corrosion of metal equipment in wells comprises contacting the metal surfaces with an inhibiting amount of a corrosion inhibitor which is the reaction product of a compound containing a carbonyl group (e.g. aldehydes), an amine, and a thiocyanate.

Abstract: The process of preparing thioethers by reacting aliphatic thioalcohols, e.g., mercaptans, including hydrogen sulfide with activated, alpha, beta unsaturated compounds ##STR1## capable of participating in the Michael Addition Rection* in which X is a suitable electron withdrawing group. The Addition, which is carried out in the presence of a catalytic base is greatly improved with respect to minimizing formation of side products by utilizing a specially selected catalyst comprising one or more cyclic tertiary nitrogen compounds having an excellent balance between reactivity and selectivity. The preparation of thioethers from acrylic acid derivatives especially esters (CH.sub.2 .dbd.CH--COOR', R'=C.sub.1 --C.sub.8) is preferred. The preparation of the dimethyl ester of 3,3'-thiodipropionic acid to result in dimethylthiodipropionate of relatively high purity is especially preferred.* See Vogel, PRACTICAL ORGANIC CHEMISTRY, p. 912-913, Third Enlarged Edition.