Research Institute of Petroleum Processing, Sinopec

China Petroleum & Chemical Corporation

Other

China Petroleum Chemical Corporation

Xuhong Mu

Xingtian Shu

Yibin Luo

Baoning Zong

Qiang Fu

Xiaoxin Zhang

Wenhua Xie

Jiushun Zhang

Bin Zhu

Qiang Liu

Min Lin

Chaogang Xie

Enze Min

Yongxiang Li

Chunfeng Shi

Jinyu Zheng

Chengxi Zhang

Hexin Hu

Yongrui Wang

Jincheng Zhu

Mingyi Sun

Zhiguo Wu

Ying Wang

Jun Long

Yong Xu

Hua Chen

Xieqing Wang

Xuan Wang

Minggang Li

Genquan Zhu

Yigong He

Zhiqiang Qiao

Langyou Wen

Zheng Man

Yingchun Ru

Yihua Yang

Shaobing Yu

Chenghan Yan

Xiangkun Meng

Hailong Lin

Minghui Dong

A solid acid catalyst has a macropore specific volume of about 0.30-0.50 ml/g, a ratio of macropore specific volume to specific length of catalyst particles of about 1.0-2.5 ml/(g·mm), and a ratio of specific surface area to length of catalyst particles of about 3.40-4.50 m/mm. The macropore refers to pores having a diameter of more than 50 nm. An alkylation catalyst is based on the solid acid catalyst and can be used in alkylation reactions. The solid acid catalyst and alkylation catalyst show an improved catalyst service life and/or trimethylpentane selectivity when used in the alkylation of isoparaffins with olefins.

Solid acid catalyst, preparation therefor and use thereof

An alkylation reaction apparatus has n reactors. In the n reactors, there are m reactors including the first reactor that have three reaction zones as defined below. According to the flow direction order of alkylation reaction streams, the three reaction zones are an x reaction zone, a y reaction zone and a z reaction zone respectively; based on the mixing intensity, the mixing intensity of the y reaction zone>the mixing intensity of the x reaction zone>the mixing intensity of the z reaction zone, wherein n≥1 and n≥m. An alkylation reaction system includes the aforementioned alkylation reaction apparatus, and a liquid acid catalyzed alkylation reaction process by using the aforementioned alkylation reaction apparatus or the aforementioned alkylation reaction system.

Alkylation reaction apparatus, reaction system, and liquid acid catalyzed alkylation reaction process

A NaY molecular sieve with an aluminum-rich surface is prepared using a process that includes the steps of: a. mixing a directing agent and a first silicon source to obtain a first mixture, wherein the directing agent has a molar composition of NaO:AlO:SiO:HO=(6-25):1:(6-25):(200-400); b. mixing the first mixture obtained in the step a with a second silicon source, an aluminum source and water to obtain a second mixture; c. carrying out hydrothermal crystallization on the second mixture obtained in the step b, and collecting a solid product. Calculated as SiO, the weight ratio of the first silicon source to the second silicon source is 1:(0.01-12). The NaY molecular sieve has larger aluminum distribution gradient from the surface to the center of the particle than the conventional molecular sieve.

NaY molecular sieve with an aluminum-rich surface and a process of preparing same

The present invention relates to a molecular sieve, particularly to an ultra-macroporous molecular sieve. The present invention also relates to a process for the preparation of the molecular sieve and to its application as an adsorbent, a catalyst, or the like. The molecular sieve has a unique X-ray diffraction pattern and a unique crystal particle morphology. The molecular sieve can be produced by using a compound represented by the following formula (I), 

Molecular sieve, its preparation and application thereof

A process for producing dimethyl sulfoxide, wherein said process comprises the following steps: (1) contacting hydrogen sulfide with methanol to produce a mixture containing dimethyl sulfide, and separating dimethyl sulfide from the mixture; and (2) in the presence or absence of a solvent, contacting dimethyl sulfide obtained in step (1) with at least one oxidant and a catalyst to produce a mixture containing dimethyl sulfoxide, said catalyst comprises at least one Ti&#x2014;Si molecular sieve.

Dimethylsulfoxide preparation method

The present invention provides a process for preparing methanol, dimethyl ether, and low carbon olefins from syngas, wherein the process comprises the step of contacting syngas with a catalyst under the conditions for converting the syngas into methanol, dimethyl ether, and low carbon olefins, characterized in that, the catalyst contains an amorphous alloy consisting of a first component Al and a second component, said second component being one or more elements or oxides thereof selected from Group IA, IIIA, IVA, VA, IB, IIB, IVB, VB, VIB, VIIB, VIII, and Lanthanide series of the Periodic Table of Elements, and said second component being different from the first component Al. According to the present process, the syngas can be converted into methanol, dimethyl ether, and low carbon olefins in a high CO conversion, a high selectivity of the target product, and high carbon availability.

Process for preparing methanol, dimethyl ether, and low carbon olefins from syngas

The present invention provides a process for preparing methanol, dimethyl ether, and low carbon olefins from syngas, wherein the process comprises the step of contacting syngas with a catalyst under the conditions for converting the syngas into methanol, dimethyl ether, and low carbon olefins, characterized in that, the catalyst contains an amorphous alloy consisting of components M and X wherein the component X represents an element B and/or P, the component M represents two or more elements selected from Group IIIA, IVA, VA, IB, IIB, IVB, VB, VIB, VIIB, VIII and Lanthanide series of the Periodic Table of Elements. According to the present process, the syngas can be converted into methanol, dimethyl ether, and low carbon olefins in a high CO conversion, a high selectivity of the target product, and high carbon availability.

A process for combining the catalytic conversion of organic oxygenates and the catalytic conversion of hydrocarbons: an organic oxygenate feedstock is contacted with a Y-zeolite containing catalyst to produce a reaction stream, and a coked catalyst and a product stream are obtained after separating the reaction stream; a hydrocarbon feedstock is contacted with a Y-zeolite containing catalyst to produce a reaction stream, a spent catalyst and a reaction oil vapor are obtained after separating the reaction stream, and the reaction oil vapor is further separated to give the products such as gas, gasoline and the like; a part or all of the coked catalyst and a part or all of the spent catalyst enter the regenerator for the coke-burning regeneration, and the regenerated catalyst is divided into two portions, wherein one portion returns to be contacted with the hydrocarbon feedstock, and the other portion, after cooling, returns to be contacted with the organic oxygenate feedstock. This process not only reasonably utilizes the excessive thermal energy of the hydrocarbon conversion, but also solves the problem of heat supply for the conversion of the organic oxygenate, thus ensuring the continuous catalytic conversion of the organic oxygenate.

Process for combining the catalytic conversion of organic oxygenates and the catalytic conversion of hydrocarbons

A noble metal-containing titanosilicate material, characterized in that said material is represented with the oxide form of xTiO.100SiO.yEO.zE, wherein x ranges from 0.001 to 50.0; (y+z) ranges from 0.0001 to 20.0 and y/z&#x3c;5; E represents one or more noble metals selected from the group consisting of Ru, Rh, Pd, Re, Os, Ir, Pt, Ag and Au; m is a number satisfying the oxidation state of E. The crystal grains of said material contain a hollow structure, or a sagging structure. In said material, the synergistic effect between the noble metal and the titanosilicate are enhanced. As compared with the prior art, the selectivity, catalytic activity and stability of the reaction product are obviously increased in the oxidation reaction, e.g. the reaction for preparing propylene oxide by epoxidation of propylene.

Noble metal-containing titanosilicate material and its preparation method

The present invention provides a composite solid acid catalyst consisting of from 50%-80% by weight of a porous inorganic support, from 15% to 48% by weight of a heteropoly compound loaded thereon, and from 2% to 6% by weight of an inorganic acid. The present invention further provides a process for preparing said composite solid acid catalyst and a process for conducting an alkylation reaction by using such catalyst. The composite solid acid catalyst of the present invention has the acid sites type of Br&#xf6;nsted acid and has an acid sites density of not less than 1.4&#xd7;10mol H/g. Moreover, said composite solid acid catalyst has the homogeneous acid strength distribution, and is a solid acid catalyst having excellent performances.

Composite solid acid catalyst, preparing process and application in the alkylation

A process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons: an ethanol feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, and a coked catalyst and an target product of ethylene are obtained after separating the reaction stream; a hydrocarbon feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, a spent catalyst and an oil vapor are obtained after separating the reaction stream, and the oil vapor is further separated to give the products such as gas, gasoline and the like; a part or all of the coked catalyst and a part or all of the spent catalyst enter the regenerator for the coke-burning regeneration, and the regenerated catalyst is divided into two portions, wherein one portion returns to be contacted with the hydrocarbon feedstock, and the other portion, after cooling, returns to be contacted with ethanol feedstock. This process not only reasonably utilizes the excessive thermal energy of the hydrocarbon conversion, but also solves the problem of heat supply for the conversion of ethanol, thus ensuring the continuous catalytic conversion of ethanol and generating enormous economic benefits. For the catalytic conversion of the ethanol, the content of ethylene is 95 vol % or more in the gas product; and the conversion of ethylene is not less than 99%. For the catalytic conversion of the hydrocarbons, the yield for the light olefins increases slightly by at least 2 mol %.

Process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons

This invention relates to a composition with desulfurization property, in which the desulfurization component is a kind of molecular sieves with incorporation of vanadium into the skeleton. The composition has high hydrothermal stability and the vanadium is hard to lose.

Composition for desulfurization

A process for adsorptive desulfurization of gasoline or diesel oil or aromatics lower than Ccontaining organic sulfide impurities, wherein these feedstocks contact an amorphous alloy adsorbent comprising nickel as a major active component in a fluidized bed reactor or a magnetic-stabilized fluidized bed reactor or a slurry bed reactor. There is only a single diffuse peak at 2&#x3b8;=45&#xb0; in the 2&#x3b8; range from 20&#xb0; to 80&#xb0; in the X-ray diffraction (XRD) pattern of the adsorbent. The adsorbent consists of 50-95 wt % of nickel, 1-30 wt % of aluminum, 0-35 wt % of iron, and 0-10 wt % of one or more metals selected from copper, zinc, molybdenum, chromium, and cobalt.

Process for adsorptive desulfurization of light oil distillates

An amorphous alloy catalyst for hydrogenation and its preparation method are disclosed herein. The catalyst essentially consists of nickel ranging between 60 and 98 wt %, iron ranging between 0 and 20 wt %, one doping metal element selected from the group consisting of chromium, cobalt, molybdenum, manganese and tungsten ranging between 0 and 20 wt %, and aluminum ranging between 0.5 and 30 wt % based on the weight of said catalyst, wherein the weight percentages of iron and the doping metal element component may not be zero at the same time; and just one broad diffusion peak appears at about 2 &thgr;&equals;45&plusmn;1&deg; on the XRD patterns of the catalyst within 2 &thgr; range from 20 to 80&deg;. The catalyst herein can be used in processes for hydrogenation of unsaturated compounds such as olefin, alkyne, aromatics, nitro, carbonyl groups, nitrile and soon, and for hydrorefining of caprolactam in particular.

Hydrogenation catalyst and its preparation

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Beijing, China

Xuhong Mu