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公开(公告)号:US20180333702A1
公开(公告)日:2018-11-22
申请号:US15540425
申请日:2016-11-30
Applicant: LG CHEM, LTD.
Inventor: Myung Ji SUH , Yoon Jae MIN , Dong Hyun KO , Kyong Yong CHA , Se Won BAEK , Jun Kyu HAN
IPC: B01J23/889 , B01J23/80 , B01J23/78 , B01J21/16 , B01J35/00 , B01J35/10 , B01J37/00 , B01J37/03 , B01J37/08 , C07C5/48
CPC classification number: B01J23/8892 , B01J21/12 , B01J21/16 , B01J23/005 , B01J23/78 , B01J23/80 , B01J35/0006 , B01J35/006 , B01J35/04 , B01J35/108 , B01J37/0018 , B01J37/0036 , B01J37/033 , B01J37/035 , B01J37/038 , B01J37/08 , B01J2523/00 , C07C5/48 , C07C2521/12 , C07C2523/78 , C07C2523/80 , C07C2523/889 , B01J2523/27 , B01J2523/31 , B01J2523/842
Abstract: The present invention relates to a catalyst for oxidative dehydrogenation and a method of preparing the same. More particularly, the present invention provides a catalyst for oxidative dehydrogenation having a porous structure which may easily control heat generation due to high-temperature and high-pressure reaction conditions and side reaction due to the porous structure and thus exhibits superior product selectivity, and a method of preparing the catalyst.
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122.
公开(公告)号:US20180326400A1
公开(公告)日:2018-11-15
申请号:US15776837
申请日:2016-11-11
Applicant: Evonik Roehm GmbH
Inventor: Alexander LYGIN , Steffen KRILL , Matthias GROEMPING , Andreas TEPPERIS
IPC: B01J21/04 , B01J21/08 , B01J23/89 , B01J23/52 , B01J35/00 , B01J35/02 , B01J35/10 , B01J37/02 , B01J37/06 , B01J37/08 , B01J37/14
CPC classification number: B01J21/04 , B01J21/08 , B01J21/10 , B01J23/52 , B01J23/8906 , B01J23/8913 , B01J35/006 , B01J35/0066 , B01J35/008 , B01J35/023 , B01J35/1019 , B01J35/1057 , B01J35/1061 , B01J37/0201 , B01J37/0205 , B01J37/0207 , B01J37/0211 , B01J37/024 , B01J37/06 , B01J37/08 , B01J37/12 , B01J37/14 , B01J2231/49 , B01J2523/19 , B01J2523/27 , B01J2523/842 , B01J2523/845 , C07C67/39 , C07C67/42 , C07C69/54
Abstract: The present invention relates to novel catalysts for oxidative esterification, by means of which, for example, (meth)acrolein can be converted to methyl (meth)acrylate. The catalysts of the invention are especially notable for high mechanical and chemical stability even over very long periods. This especially relates to an improvement in the catalyst service life, activity and selectivity over prior art catalysts which lose activity and/or selectivity relatively quickly in continuous operation in media having even a small water content.
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公开(公告)号:US20180305473A1
公开(公告)日:2018-10-25
申请号:US15495116
申请日:2017-04-24
Applicant: Chevron Phillips Chemical Company LP
Inventor: Eric D. SCHWERDTFEGER , Max P. MCDANIEL , Ted H. CYMBALUK , Jeremy M. PRAETORIUS , Kathy S. CLEAR , Alan L. SOLENBERGER
IPC: C08F10/02
CPC classification number: C08F10/02 , B01J23/26 , B01J35/023 , B01J35/1019 , B01J35/1023 , B01J35/1038 , B01J35/1042 , B01J35/1047 , B01J37/0203 , B01J37/0205 , B01J37/08 , B01J37/086 , B01J37/14 , B01J2523/00 , C08F2/34 , C08F4/025 , C08F4/24 , C08F4/76 , C08F4/78 , C08F110/02 , B01J2523/41 , B01J2523/47 , B01J2523/67
Abstract: A method comprising calcining a catalyst precursor comprising chromium and a silica support material at a temperature in the range of from about 95° C. to about 400° C. in a bed fluidized by a gas flowing at a volumetric flow rate of from about 2.5 to about 30 times the settled volume of the bed per minute to form a calcined catalyst precursor. A method comprising calcining a catalyst precursor comprising chromium and silica at a temperature in the range of from about 95° C. to about 400° C. with a gas flowing through the bed at a gas hourly space velocity of from about 15 to about 200 per hour. A method comprising calcining a catalyst precursor comprising chromium and silica at a temperature in the range of from about 95° C. to about 400° C. with a gas flowing through the bed at a weight hourly space velocity of from about 1.9 to about 240 per hour.
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124.
公开(公告)号:US20180290131A1
公开(公告)日:2018-10-11
申请号:US15570661
申请日:2016-03-11
Applicant: IFP Energies nouvelles
Inventor: Pierre-Louis CARRETTE
CPC classification number: B01J31/0209 , B01J21/04 , B01J23/85 , B01J23/882 , B01J27/19 , B01J31/04 , B01J35/1019 , B01J35/1042 , B01J35/1061 , B01J37/0009 , B01J37/0201 , B01J37/0203 , B01J37/0205 , B01J37/0236 , B01J37/024 , B01J37/08 , B01J37/20 , B01J37/28 , B01J2523/00 , C10G45/08 , C10G47/20 , B01J2523/31 , B01J2523/51 , B01J2523/68 , B01J2523/845
Abstract: The invention relates to a catalyst comprising a support based on alumina or silica or silica-alumina, at least one element of group VIII, at least one element of group VIB and at least one additive selected from γ-valerolactone, 4-hydroxyvaleric acid, 2-pentenoic acid, 3-pentenoic acid or 4-pentenoic acid. The invention also relates to the process for the preparation of said catalyst and the use thereof in a hydrotreatment and/or hydrocracking process.
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公开(公告)号:US20180280955A1
公开(公告)日:2018-10-04
申请号:US15996460
申请日:2018-06-02
Inventor: Sulaiman AL-KHATTAF , Palani Arudra , Amr Abdalla
CPC classification number: B01J35/0086 , B01J21/08 , B01J29/40 , B01J37/0221 , B01J37/0244 , B01J37/08 , C07C4/06 , C07C2521/08 , C07C2529/40 , C07C11/04 , C07C11/06
Abstract: A method of producing propylene and ethylene from a butene-containing hydrocarbon stream by cracking olefin compounds in the butene-containing hydrocarbon stream in the presence of a core-shell ZSM catalyst, wherein the core-shell ZSM catalyst comprises a ZSM-5 core and a silica shell disposed thereon. Various embodiments of the method of producing propylene and ethylene, and the method of making the core-shell ZSM catalyst are also provided.
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公开(公告)号:US20180273454A1
公开(公告)日:2018-09-27
申请号:US15761385
申请日:2016-09-13
Applicant: SABIC GLOBAL TECHNOLOGIES B.V.
Inventor: Khalid A. ALMUSAITEER , Ahmed AL-HADHRAMI , Abdulaziz KHAN , Abdulaziz AL-AMER
CPC classification number: C07C29/154 , B01J23/002 , B01J23/83 , B01J35/006 , B01J37/0036 , B01J37/031 , B01J37/036 , B01J37/04 , B01J37/08 , B01J37/086 , B01J37/18 , B01J2523/00 , Y02P20/52 , B01J2523/17 , B01J2523/27 , B01J2523/3706 , B01J2523/3712 , B01J2523/48 , B01J2523/36 , B01J2523/25 , B01J2523/14 , B01J2523/3756 , B01J2523/24 , C07C31/04
Abstract: Mixed metal oxide catalysts capable of catalyzing hydrogenation of carbon dioxide to methanol reaction are disclosed, as well as a method for producing methanol from carbon dioxide and hydrogen. The mixed metal oxide catalysts include copper (Cu), and M1 and M2 oxides. M1 can be zinc (Zn), zirconium (Zr), or cerium (Ce), or any combination thereof, and M2 can be yttrium (Y), barium (Ba), rubidium (Rb), terbium (Tb), strontium (Sr), or molybdenum (Mo), or any combination thereof, with the proviso that M2 is not Y when the mixed metal oxide catalyst is [Cu/Zn/M2]0n or [Cu/Zr/M]0n, where n is determined by the oxidation states of the other elements.
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公开(公告)号:US20180272281A1
公开(公告)日:2018-09-27
申请号:US15907638
申请日:2018-02-28
Applicant: NGK INSULATORS, LTD.
Inventor: Tetsuya MAKINO , Shogo HIROSE
IPC: B01D53/94 , B01J23/22 , B01J29/072 , B01J35/04 , B01J35/10 , B01J37/02 , B01J37/08 , B01J35/02 , F01N3/20 , F01N3/10 , F01N3/022 , F01N13/00 , F01N3/28
CPC classification number: B01D53/9477 , B01D53/9418 , B01D53/944 , B01D2255/20723 , B01D2255/50 , B01D2255/904 , B01D2255/9202 , B01D2255/9205 , B01J23/22 , B01J29/072 , B01J35/023 , B01J35/04 , B01J35/10 , B01J37/0225 , B01J37/08 , F01N3/0222 , F01N3/103 , F01N3/2066 , F01N3/2803 , F01N3/2828 , F01N13/009 , F01N13/0093 , F01N13/0097 , F01N2330/30 , F01N2330/48 , F01N2370/04 , F01N2610/02 , Y02T10/24
Abstract: An exhaust gas purifying device includes a first SCR catalyst converter, an oxidation catalyst converter, a filter section, and a second SCR catalyst converter arranged in series to a flow direction of an exhaust gas. The first SCR catalyst converter includes a pillar-shaped honeycomb structure a cell density of which is from 31 to 78 cells/cm2, a porosity of the partition walls of which is from 50 to 65%, and in which a first SCR catalyst is loaded onto the surfaces of the partition walls and inner portions of pores formed in the partition walls, and an amount of the first SCR catalyst to be loaded onto the surfaces of the partition walls and the inner portions of the pores is from 200 to 500 g/L and an amount of the first SCR catalyst to be loaded onto the inner portions of the pores is from 5 to 80 g/L.
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128.
公开(公告)号:US20180264447A1
公开(公告)日:2018-09-20
申请号:US15882718
申请日:2018-01-29
Applicant: China University of Petroleum-Beijing
Inventor: Yu FAN , Shanlei HAN , Chenglong WEN , Shihua WANG
IPC: B01J29/85 , C01B39/54 , B01J23/42 , B01J23/883 , B01J37/04 , B01J37/00 , B01J37/08 , B01J37/02 , C07C5/13
CPC classification number: B01J29/85 , B01J23/42 , B01J23/883 , B01J37/0018 , B01J37/0201 , B01J37/0236 , B01J37/04 , B01J37/08 , B01J2203/068 , C01B39/54 , C07C5/13 , C07C2523/42 , C07C2529/85 , Y02P20/544 , C07C9/16
Abstract: A SAPO-11 molecular sieve, preparation method thereof and use thereof in the isomerization of hydrocarbons is disclosed. The preparation method includes dissolving an aluminum source in ethylene glycol, and stirring to give a solution A; adding a structure-directing agent and a phosphorus source to the solution A, and stirring to give a solution B; adding a silicon source to the solution B, and stirring to give a solution C; transferring the solution C to a supercritical CO2 reactor, and introducing CO2 into the reactor to increase the pressure in the reactor; heating the supercritical CO2 reactor to the reaction temperature for crystallization; and after crystallization, lowering the temperature of the supercritical CO2 reactor, removing the solution from the reactor, separating the product, drying and calcining to obtain the SAPO-11 molecular sieve. A hydrocarbon isomerization catalyst can be obtained by molding the molecular sieve, loading a metal component, drying and calcining.
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129.
公开(公告)号:US10076746B2
公开(公告)日:2018-09-18
申请号:US15103583
申请日:2014-12-08
Applicant: IFP Energies nouvelles
Inventor: Magalie Roy-Auberger , Ali Jahel
IPC: B01J27/19 , B01J37/20 , B01J23/882 , B01J31/02 , B01J31/04 , B01J37/02 , C10G45/08 , B01J37/28 , B01J35/10 , B01J37/08 , C10G45/50 , B01J23/883
CPC classification number: B01J27/19 , B01J23/882 , B01J23/883 , B01J31/0202 , B01J31/0237 , B01J31/0271 , B01J31/04 , B01J35/1019 , B01J37/0203 , B01J37/0207 , B01J37/0236 , B01J37/08 , B01J37/20 , B01J37/28 , C10G45/08 , C10G45/50 , C10G2300/703
Abstract: The invention concerns a process for the preparation of a catalyst starting from a pre-catalyst comprising at least one catalytic metal and a support, said pre-catalyst having undergone a heat treatment at at least 60° C. without calcining, in which process said pre-catalyst is impregnated with a basic solution having a pH of more than 7.5 and containing at least one molecule in the zwitterionic form, and the impregnated pre-catalyst is dried at a temperature of at most 240° C. without subsequent calcining.The molecule in the zeolite form is selected from the group formed by amino-alcohol acids containing secondary or tertiary amine groups and containing at least one carboxylic acid function (and preferably only one) and at least one alcohol function. It is bicine or tricine, for example.The invention also concerns the catalyst prepared using this process, and its use in hydrotreatment and/or hydroconversion.
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公开(公告)号:US10071366B2
公开(公告)日:2018-09-11
申请号:US15258090
申请日:2016-09-07
Applicant: Johnson Matthey PLC
Inventor: Sebastian John Kipling Forrest , Jonathan Geoffrey Oliver , Samuel Arthur French , Mikael Per Uno Carlsson
IPC: B01J23/58 , B01J23/78 , B01J21/00 , B01J21/02 , B01J23/00 , B01J23/755 , B01J35/00 , B01J37/02 , B01J37/18 , C01B3/40 , C01B3/58 , B01J21/04 , B01J35/02 , B01J35/10 , B01J37/04 , B01J37/08
CPC classification number: B01J23/78 , B01J21/005 , B01J21/02 , B01J21/04 , B01J23/005 , B01J23/755 , B01J35/008 , B01J35/02 , B01J35/023 , B01J35/1009 , B01J35/1014 , B01J35/1038 , B01J37/0203 , B01J37/0205 , B01J37/04 , B01J37/08 , B01J37/18 , C01B3/40 , C01B3/586 , C01B2203/0233 , C01B2203/0238 , C01B2203/0445 , C01B2203/047 , C01B2203/1058 , C01B2203/1082 , Y02P20/52
Abstract: A method is described for preparing a catalyst including the steps of: (i) impregnating a calcined support comprising a metal aluminate with a solution of nickel acetate at a temperature ≥40° C. and drying the impregnated support, (ii) calcining the dried impregnated support, to form nickel oxide on the surface of the support and (iii) optionally repeating steps (i) and (ii) on the nickel oxide coated support. The method provides an eggshell catalyst in which the metal oxide is concentrated in an outer layer on the support.
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