Systems for producing performic acid and methods for producing performic acid. The systems may include two or more reactor units, two or more servient programmable logic controllers, a control panel, and a master programmable logic controller. The system may modify the production of performic acid in at least one of the two or more reactor units upon and/or after the occurrence of a disruptive event in order to maintain a desired level of performic acid production and/or a desired level of disinfection.

The oxidative coupling of methane (OCM) and the oxidative dehydrogenation (ODH) of ethane and higher hydrocarbons is described using SO.sub.3 and sulfate, sulfite, bisulfite and metabifulfite salts as oxygen transfer agents in the presence of one or more elements selected from Groups 3 to 14 of the periodic table, optionally further in the presence of alkali or alkaline salts and/or sulfur-containing compounds.

The oxidative coupling of methane (OCM) and the oxidative dehydrogenation (ODH) of ethane and higher hydrocarbons is described using SO.sub.3 and sulfate, sulfite, bisulfite and metabifulfite salts as oxygen transfer agents in the presence of one or more elements selected from Groups 3 to 14 of the periodic table, optionally further in the presence of alkali or alkaline salts and/or sulfur-containing compounds.

An ionic liquid as a solvent in the hydration reaction of α-pinene to α-terpineol. The ionic liquid is obtained from the reaction of an amine and an inorganic acid. The use of the ionic liquid as solvent favors the selectivity towards the formation of α-terpineol and once the reaction product has been brought to room temperature, the organic phase can be physically separated from the inorganic one by decantation. The inorganic phase contains the ionic liquid, water and reaction catalyst and can be directly reused for a new reaction batch.

Zn.sub.xZr.sub.yO.sub.z mixed oxide catalysts having improved stability for the conversion of ethanol to isobutene are described, together with methods for making such catalysts.

Zn.sub.xZr.sub.yO.sub.z mixed oxide catalysts having improved stability for the conversion of ethanol to isobutene are described, together with methods for making such catalysts.

Provided is a method of efficiently preparing alkyl lactate from by-products which are generated during a process of converting lactic acid into lactide, or from poly(lactic acid) (PLA).

Provided is a method of efficiently preparing alkyl lactate from by-products which are generated during a process of converting lactic acid into lactide, or from poly(lactic acid) (PLA).

A method for dehydrocoupling silanes and amines. The method comprises contacting: (a) an aliphatic amine; (b) a silane; and (c) a catalyst which is ZnX.sub.2, wherein X is alkyl, chloride, bromide, iodide, trifluoromethanesulfonate, bis(trifluoromethane)sulfonamide, tosylate, methanesulfonate or O.sub.3S(CF.sub.2).sub.xCF.sub.3 wherein x is an integer from 1 to 10.

The present invention relates to a monolith catalyst for carbon-dioxide/methane reforming and a method of manufacturing the same, and more particularly to a novel monolith catalyst for a reforming reaction having improved thermal durability, configured such that a sintering inhibiting layer is formed by coating the surface of a monolith support with at least one element selected from the group consisting of Group 2, 3, 6, 13, 15 and 16 elements among elements in Period 3 or higher and an active catalyst layer is formed on the sintering inhibiting layer, thereby preventing carbon deposition and catalyst deactivation due to deterioration even upon reaction at high temperatures.