Proposed is a recyclable epoxy compound containing an α,β-unsaturated ketone group and/or a hydroxy ketone group bonded through an aldol reaction between a ketone group and an aldehyde group containing a hydroxyl group among non-toxic natural materials, without using a bisphenol A type epoxy, a toxic material. In addition, proposed are a method of preparing the same compound, an epoxy composite material containing the same compound, and a method of degrading the same composite material.

A metal-organic framework (MOF) MIL-125 and a preparation method and a use thereof are provided. The MOF MIL-125 is a round cake-like crystal and has an external specific surface area (SSA) of 160 m.sup.2/g to 220 m.sup.2/g. The MOF MIL-125 provided in the present application has a large number of microporous structures, a large external SSA, and a high catalytic activity in oxidation.

An integrated process for making propylene oxide and propylene glycol involves reacting propene with an oxidant to provide propylene oxide, reacting a fraction of the propylene oxide with water to provide an aqueous glycol solution containing monopropylene glycol and dipropylene glycol, and separating monopropylene glycol and dipropylene glycol from the glycol solution by a multi-step distillation. The propylene oxide output can be increased without increasing capacity of the unit for reacting propene to propylene oxide, by reacting propene and hydrogen peroxide in the presence of a catalyst mixture, containing a phase transfer catalyst and a heteropolytungstate, in a liquid reaction mixture which contains an aqueous phase with a maximum apparent pH of 6 and an organic phase. The reaction mixture is separated into an organic phase, which is recycled to the reaction, and an aqueous phase containing monopropylene glycol and dipropylene glycol, which is passed to replace the glycol solution.

An integrated process for making propylene oxide and propylene glycol involves reacting propene with an oxidant to provide propylene oxide, reacting a fraction of the propylene oxide with water to provide an aqueous glycol solution containing monopropylene glycol and dipropylene glycol, and separating monopropylene glycol and dipropylene glycol from the glycol solution by a multi-step distillation. The propylene oxide output can be increased without increasing capacity of the unit for reacting propene to propylene oxide, by reacting propene and hydrogen peroxide in the presence of a catalyst mixture, containing a phase transfer catalyst and a heteropolytungstate, in a liquid reaction mixture which contains an aqueous phase with a maximum apparent pH of 6 and an organic phase. The reaction mixture is separated into an organic phase, which is recycled to the reaction, and an aqueous phase containing monopropylene glycol and dipropylene glycol, which is passed to replace the glycol solution.

An integrated process for making styrene and propene oxide which comprises the steps: a) dehydrogenating ethylbenzene in the presence of a dehydrogenation catalyst; b) separating styrene and hydrogen from the reaction mixture of step a); c) producing hydrogen peroxide from hydrogen separated in step b) and oxygen; d) reacting propene with the hydrogen peroxide obtained in step c) in the presence of an epoxidation catalyst to provide a reaction mixture comprising propene oxide; and e) separating propene oxide from the reaction mixture obtained in step d).

An integrated process for making styrene and propene oxide which comprises the steps: a) dehydrogenating ethylbenzene in the presence of a dehydrogenation catalyst; b) separating styrene and hydrogen from the reaction mixture of step a); c) producing hydrogen peroxide from hydrogen separated in step b) and oxygen; d) reacting propene with the hydrogen peroxide obtained in step c) in the presence of an epoxidation catalyst to provide a reaction mixture comprising propene oxide; and e) separating propene oxide from the reaction mixture obtained in step d).

A chemical molding comprising a zeolitic material which exhibits a type I nitrogen adsorption/desorption isotherm determined as described in Reference Example 1, and which has framework type MFI and a framework structure comprising Si, O, and Ti, the molding further comprising a binder for said zeolitic material, the binder comprising Si and O, wherein the molding exhibits a total pore volume of at least 0.4 mL/g and a crushing strength of at least 6 N.

A chemical molding comprising a zeolitic material which exhibits a type I nitrogen adsorption/desorption isotherm determined as described in Reference Example 1, and which has framework type MFI and a framework structure comprising Si, O, and Ti, the molding further comprising a binder for said zeolitic material, the binder comprising Si and O, wherein the molding exhibits a total pore volume of at least 0.4 mL/g and a crushing strength of at least 6 N.

The present invention relates to a method of preparing cyclododecanone. According to the present invention, a method of preparing cyclododecanone which allows implementation of a high conversion rate and minimization of production of unreacted materials and reaction by-products may be provided. In addition, the present invention implements a high conversion rate and a high selectivity even by a simplified process configuration, and thus may be usefully utilized in an economical method of preparing laurolactam, allowing commercially easy mass production.

The present invention provides: a method for producing an epoxyalkane capable of obtaining an epoxide in a high yield while attaining a high olefin conversion rate and a high selectivity for epoxides even when an olefin includes a long carbon chain, and a solid oxidation catalyst used in the method. The method for producing an epoxyalkane of the present invention comprises reacting an olefin with an oxidant in the presence of a solid oxidation catalyst, wherein the solid oxidation catalyst comprises a transition metal and a carrier that supports the transition metal, and the carrier is a metal oxide having a silyl group represented by the following general formula (1):

R.sup.1R.sup.2R.sup.3Si—  (1) wherein R.sup.1, R.sup.2, and R.sup.3 are each independently a single bond, a hydrocarbon group, a halogenated hydrocarbon group, an alkoxy group, or a halogen, and at least one of R.sup.1, R.sup.2, and R.sup.3 is a hydrocarbon group having 3 or more carbon atoms or a halogenated hydrocarbon group having 3 or more carbon atoms.