Abstract: The present invention provides a method for preparing 1,5-pentanediol via hydrogenolysis of tetrahydrofurfuryl alcohol. The catalyst used in the method is prepared by supporting a noble metal and a promoter on an organic polymer supporter or an inorganic hybrid material supporter, wherein the supporter is functionalized by a nitrogen-containing ligand. When the catalyst is used in the hydrogenolysis of tetrahydrofurfuryl alcohol to prepare 1,5-pentanediol, a good reaction activity and a high selectivity can be achieved. The promoter and the nitrogen-containing ligand in the supporter are bound to the catalyst through coordination, thereby the loss of the promoter is significantly decreased, and the catalyst has a particularly high stability. The lifetime investigation of the catalyst, which has been reused many times or used continuously for a long term, suggests that the catalyst has no obvious change in performance, thus reducing the overall process production cost.

Abstract: The present invention provides an epoxy resin material, a preparation method therefor and an application thereof. The present method for preparing an epoxy resin material comprises: heating a mixture of an epoxy resin main agent and a curing agent that are placed at room temperature to 40-85° C. for reaction and curing. The curing agent contains an adduct of an olefinic nitrile compound and an amine compound. The present method for preparing an epoxy resin material has the characteristics of low mixing viscosity, long operation time, and low amount of heat released during preparation.

Abstract: An organic-base functionalized silicalite-1 molecular sieve-encapsulated metal nanoparticles catalyst and a preparation method therefor, as well as a method for preparing 1,2-pentanediol from biomass-derived furfuryl alcohol by hydrogenolysis using said catalyst. When the catalyst is used in a reaction preparing 1,2-pentanediol from furfuryl alcohol by hydrogenolysis, the catalyst has high hydrogenolysis activity under relatively mild reaction conditions, significantly increasing the conversion rate of furfuryl alcohol and 1,2-pentanediol selectivity in the reaction, while also not generating obvious byproducts furfuryl alcohol polymers; the catalyst has good stability and long life, and may be recovered for reuse after the reaction is complete by means of a simple filtration, greatly reducing reaction costs and separation difficulty.

Abstract: Disclosed is an imine-type quaternary ammonium salt catalyst, wherein the catalyst has a general structure formula shown by formula I below; in the formula, R1 and R2, respectively, are independently selected from a C1-C20 linear alkyl or a branched C3-C20 alkyl, and a C1-C20 hydroxylalkyl, a C3-C8 cycloalkyl, and arylated alkyl; R3 is a linear or branched alkyl, cycloalkyl or aryl; and R4 is hydrogen, aryl, a linear C1-C15 alkyl or branched C3-C15 alkyl. Also disclosed are a method for preparing the catalyst and a polyisocyanate composition prepared therefrom. The catalyst, by introducing an imine structure, on the basis of ensuring high catalytic activity thereof, is allowed to have properties of high temperature decomposition and inactivation, and when applied to the synthesis of polyisocyanate, can effectively prevent the risk of explosive polymerization caused by an uncontrolled reaction.

Abstract: The present invention relates to a catalyst for aminating a polyether polyol and preparation method thereof and a method of preparing a polyetheramine using the catalyst. The catalyst has active components and a carrier. The active components are Ni, Cu, and Pd. The method of preparing the catalyst comprises the following steps: using a metal solution or a metal melt impregnated carrier, obtaining a catalyst precursor; and drying and calcinating the obtained catalyst precursor, so as to obtain a catalyst. By introducing the active component Pd in the catalyst, the present invention clearly improves selectivity of an amination catalyst with respect to a preaminated product, and increases raw material conversion rate.

Abstract: Provided are an emulsifiable isocyanate composition and a preparation method therefor. The emulsifiable isocyanate composition comprises the following components: (a) a polymethylene polyphenyl polyisocyanate, (b) an emulsifier, (c) an adduct derived from a diisocyanate, and optionally (d) a terpene monomer. The emulsifiable isocyanate composition is used in artificial board adhesives, and has a smaller mold cumulative effect, an improved demoulding performance and an extended pot life.

Abstract: Disclosed is a preparation method of a catalyst for liquid phase hydrogenation of acetophenone in preparation of ?-phenylethanol, including: adding water, a small alcohol, a Gemini surfactant and an organic pore-forming agent to a reactor, followed by adding a silica sol and stirring well to prepare an aqueous dispersion of silica sol; preparing an alkaline precipitant and a mixed solution containing salts of a copper containing compound, a zinc containing compound, a rare-earth metal containing compound and an alkaline-earth metal containing compound, adding the alkaline precipitant and the mixed solution together to the aqueous dispersion of silica sol, followed by precipitation, ageing, filtration, washing, drying, calcination and molding to obtain the catalyst.

Abstract: Disclosed is a light colored modified isocyanate mixture and a preparation method thereof. The method comprises the following steps: a) reacting isocyanate groups of a raw material isocyanate under the action of a phospholenecatalyst, and finally obtaining a modified isocyanate reaction solution containing carbodiimide and/or uretonimine derivatives; and b) adding a compounded terminator of a halosilane organic and a sulfonic anhydride to the reaction solution obtained in step a so as to terminate the reaction of carbodiimidization. The modified isocyanate prepared by the method has the characteristics of a liquid state at room temperature, being stable in storage at room temperature and high temperature, and low color number.

Abstract: A preparation method for a propylene epoxidation catalyst: pre-hydrolyzing a silicon source, adding a titanium source and reacting to form a sol, atomizing the sol and then spraying it into liquid ammonia for molding, implementing pore broadening, and performing drying, calcination, and silanization treatment to obtain a Ti—SiO2 composite oxide catalyst. The present catalyst can be used in the chemical process of preparing propylene oxide by epoxidation of propylene, the average propylene oxide selectivity being up to 97.5%, having prospects for industrial application.

Abstract: A method for treating reverse osmosis concentrated water, comprises adding precipitant and oxidant to reverse osmosis concentrated water for treatment, filtering to obtain clear liquid, and adding catalyst for water treatment to clear liquid for catalytic oxidation to obtain a first-stage treated water. Optionally, the liquid may be subjected after catalytic oxidation to an adsorption treatment; performing reverse osmosis treatment on first-stage treated water to obtain second-stage reverse osmosis product water and second-stage reverse osmosis concentrated water; and adding oxidant to second-stage reverse osmosis concentrated water for oxidation treatment to obtain directly discharged effluent water. The obtaining of effluent water may further comprise subjecting liquid after oxidation treatment to adsorption treatment. The above method can recycle 75-85 wt % of water, and operates easily.

Abstract: Disclosed a no-added formaldehyde composite wood product binder, a no-added formaldehyde composite wood product manufactured by same, and a preparation method for the composite wood product. The no-added formaldehyde composite wood product binder comprises an agent A and an agent B. The agent A is an isocyanate-based binder, and the agent B is an aqueous dispersion of polyester based aliphatic polyurethane and/or a modified polyester-based aliphatic polyurethane. The no-added formaldehyde composite wood product is formed under hot-pressing after a wooden and/or straw material is mixed with the no-added formaldehyde composite wood product binder. The composite wood product manufactured by the no-added formaldehyde composite wood product binder has excellent water-proof and mechanical properties and a good saw cutting performance, and the amount of isocyanate used is also reduced, thereby reducing costs.

Abstract: A heater for heating and vaporizing droplets in gas stream, comprising a heater housing and a heater body located inside the heater housing, wherein the heater housing is provided with an airflow inlet and an airflow outlet, the airflow enters into the heater housing via the airflow inlet, flows through the heater body, and then is discharged via the airflow outlet; the heater body comprises a stereoscopic network structure formed by interweaving one or more electrical heating wires. The use of the heater and a method for preparing isocyanate using the heater. The heater has a simple structure, a low pressure loss, uniform heating and a high heat utilization ratio during preparing isocyanate.

Abstract: An isocyanate polymerization catalyst, a preparation method thereof and a method for preparing polyisocyanates comprising isocyanurate groups by using the same. The catalyst is a carboxylic acid salt containing a di-quaternary ammonium ion. The structure of the catalyst contains hydroxyl-containing aromatic heterocyclic residues. The catalyst is highly active. Only a small quantity of the catalyst is required for the polymerization of isocyanates. The prepared polyisocyanates have color values lower than 25 Hazen, monomer contents of less than 0.5% by weight, high contents of isocyanurates and low viscosities.

Abstract: The present invention relates to a catalyst for producing chlorine by oxidation of hydrogen chloride and a method for preparing the same. The catalyst comprises a support and active ingredients that comprise 1-20 wt % of copper, 0.01-5 wt % of boron, 0.1-10 wt % of alkali metal element(s), 0.1-15 wt % of one or more rare earth elements, and 0-10 wt % of one or more elements selected from magnesium, calcium, barium, manganese, iron, nickel, cobalt, zinc, ruthenium or titanium based on the total weight of the catalyst. The catalyst is prepared by a two-step impregnation method. Comparing with the available catalysts of the same type, the catalyst according to the present invention has greatly improved conversion and stability.

Abstract: A catalyst for preparing chlorine gas by hydrogen chloride oxidation, comprising the following components calculated according to mass content based on the total weight of the catalyst: 0.5-20 wt % copper; 2-10 wt % manganese; 0.05-2 wt % boron; 0.01-3 wt % chromium; 0.1-10 wt % rare earth metal; 0.1-10 wt % potassium; and 3-15 wt % titanium; also comprising 0.02-1.1 wt % phosphorus; and 0.03-1.9 wt % iron; the carrier content is 55-90 wt %. In the case of a fluidized bed reactor, the present catalyst can achieve a one-way hydrogen chloride conversion rate of 80-85%. Almost all of the 0-1000 mg/kg of chlorinated benzene contained in hydrogen chloride gas can be converted into CO2 and H2O without generating polychlorinated benzene.

Abstract: The present invention relates to a composite catalyst, preparation process thereof, and process for catalyzing the trimerization of butadiene using the composite catalyst. The composite catalyst comprises: (A) a titanium compound catalyst active component, (B) an organometallic compound co-catalyst component, (C) a sulfoxide compound catalyst-modifying component, (D) a monoester compound catalyst-modifying component, and (E) a solvent component. The composite catalyst has advantages of excellent selectivity, high catalytic activity, easy preparation and so on.

Abstract: A supported catalyst used for synthesizing a polyether amine, and a manufacturing method of the catalyst. The catalyst comprises: a porous oxide as a support; Ni, Cu, Pd, and Rh as active components; and one or more of any of Zr, Cr, Mo, Fe, Zn, Sn, Bi, Ce, La, Hf, Sr, Sb, Mg, Be, Re, Ta, Ti, Sc, Ge and related metals as an auxiliary agent. The catalyst can be used in an amination reaction for a large molecular weight polyether polyol, and is particularly active and selective for an amination reaction of a low molecular weight polyether polyol. The catalyst has a simple and economic manufacturing technique and good potential for future applications.

Abstract: A method for treating reverse osmosis concentrated water, comprises adding a precipitant and oxidant to reverse osmosis concentrated water for treatment, filtering to obtain clear liquid, and adding catalyst for water treatment to clear liquid for catalytic oxidation to obtain a first-stage treated water. Optionally, the liquid may be subjected after catalytic oxidation to an adsorption treatment; performing reverse osmosis treatment on first-stage treated water to obtain second-stage reverse osmosis product water and second-stage reverse osmosis concentrated water; and adding oxidant to second-stage reverse osmosis concentrated water for oxidation treatment to obtain directly discharged effluent water. The obtaining of effluent water may further comprise subjecting liquid after oxidation treatment to adsorption treatment. The above method can recycle 75-85 wt % of water, and operates easily.

Abstract: A catalyst for catalytic oxidation treatment of organic wastewater, comprising aluminum oxide, and nickel, ferrum, manganese, and cerium supported on the aluminum oxide in oxide form. Based on the weight of aluminum oxide, the contents of the following components in the catalyst are: nickel: 5.0-20 wt %; ferrum: 0.5-5.5 wt %; manganese: 0.5-3.5 wt %; and cerium: 1.5-3.0 wt %. The present invention has a good effect in catalytic oxidation for degrading COD organic pollutants in wastewater and has high reactivity.

Abstract: The present invention relates to a method for preparing catalyst used for preparing chlorine by oxidizing hydrogen chloride. The method is mixing a slurry mainly containing boron and chromium with a slurry mainly containing copper, boron, alkali-metal elements, rare-earth elements, aluminum sol, silica sol, carrier and optionally other metal elements, the mixing temperature being not more than 100° C., and the residence time being not more than 120 minutes, the mixed slurry is successively treated with spray drying, high temperature calcination, so that the catalyst is obtained. The present invention also relates to the catalyst prepared through the method, use of the catalyst used in the process of preparing chlorine by oxidizing hydrogen chloride and a method for preparing chlorine by using the catalyst. The catalyst is used for preparing chlorine by oxidizing hydrogen chloride with oxygen or air in fluidized bed reactor.