ZA200503619B - - Google Patents
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- Publication number
- ZA200503619B ZA200503619B ZA200503619A ZA200503619A ZA200503619B ZA 200503619 B ZA200503619 B ZA 200503619B ZA 200503619 A ZA200503619 A ZA 200503619A ZA 200503619 A ZA200503619 A ZA 200503619A ZA 200503619 B ZA200503619 B ZA 200503619B
- Authority
- ZA
- South Africa
- Prior art keywords
- catalyst
- support
- organic
- metal
- catalytically active
- Prior art date
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- 229910052751 metal Inorganic materials 0.000 claims description 249
- 239000002184 metal Substances 0.000 claims description 249
- 239000003054 catalyst Substances 0.000 claims description 235
- 238000000034 method Methods 0.000 claims description 188
- 230000008569 process Effects 0.000 claims description 135
- -1 1-hydroxy-n-propyl Chemical group 0.000 claims description 121
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 94
- 239000000463 material Substances 0.000 claims description 85
- 229910052739 hydrogen Inorganic materials 0.000 claims description 79
- 239000001257 hydrogen Substances 0.000 claims description 78
- 239000006185 dispersion Substances 0.000 claims description 75
- 238000011282 treatment Methods 0.000 claims description 74
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 73
- 238000000354 decomposition reaction Methods 0.000 claims description 73
- 150000002739 metals Chemical class 0.000 claims description 71
- 150000002894 organic compounds Chemical class 0.000 claims description 68
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 54
- 150000001875 compounds Chemical class 0.000 claims description 53
- 239000000203 mixture Substances 0.000 claims description 51
- 230000015572 biosynthetic process Effects 0.000 claims description 47
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 41
- 239000012018 catalyst precursor Substances 0.000 claims description 40
- 238000004519 manufacturing process Methods 0.000 claims description 40
- 229910052702 rhenium Inorganic materials 0.000 claims description 40
- 230000009467 reduction Effects 0.000 claims description 38
- 238000001354 calcination Methods 0.000 claims description 37
- 239000000377 silicon dioxide Substances 0.000 claims description 36
- 239000002243 precursor Substances 0.000 claims description 35
- 150000003839 salts Chemical class 0.000 claims description 35
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 30
- 238000006243 chemical reaction Methods 0.000 claims description 30
- 230000036961 partial effect Effects 0.000 claims description 29
- 230000003197 catalytic effect Effects 0.000 claims description 28
- 229910052707 ruthenium Inorganic materials 0.000 claims description 28
- 229960004418 trolamine Drugs 0.000 claims description 28
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 27
- 229910052717 sulfur Inorganic materials 0.000 claims description 27
- 239000011593 sulfur Substances 0.000 claims description 27
- 238000003786 synthesis reaction Methods 0.000 claims description 26
- 230000004580 weight loss Effects 0.000 claims description 23
- 238000000197 pyrolysis Methods 0.000 claims description 22
- 229910052759 nickel Inorganic materials 0.000 claims description 18
- 239000003638 chemical reducing agent Substances 0.000 claims description 17
- 238000001035 drying Methods 0.000 claims description 17
- 229910017052 cobalt Inorganic materials 0.000 claims description 16
- 239000010941 cobalt Substances 0.000 claims description 16
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 16
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 15
- 235000001014 amino acid Nutrition 0.000 claims description 15
- 239000012298 atmosphere Substances 0.000 claims description 15
- 239000007789 gas Substances 0.000 claims description 15
- 150000001413 amino acids Chemical class 0.000 claims description 14
- 150000001412 amines Chemical class 0.000 claims description 13
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 12
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 12
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 11
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 10
- 150000002430 hydrocarbons Chemical class 0.000 claims description 9
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 8
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 claims description 7
- 239000003463 adsorbent Substances 0.000 claims description 7
- 239000012972 dimethylethanolamine Substances 0.000 claims description 7
- 238000011065 in-situ storage Methods 0.000 claims description 7
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 6
- 239000010949 copper Substances 0.000 claims description 6
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 230000008929 regeneration Effects 0.000 claims description 6
- 238000011069 regeneration method Methods 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 5
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- 239000013335 mesoporous material Substances 0.000 claims description 5
- 229910052763 palladium Inorganic materials 0.000 claims description 5
- 229910052697 platinum Inorganic materials 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 229930064664 L-arginine Natural products 0.000 claims description 4
- 235000014852 L-arginine Nutrition 0.000 claims description 4
- 238000010521 absorption reaction Methods 0.000 claims description 4
- 150000004696 coordination complex Chemical class 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- 229940087646 methanolamine Drugs 0.000 claims description 4
- 125000001477 organic nitrogen group Chemical group 0.000 claims description 4
- 230000000717 retained effect Effects 0.000 claims description 4
- 229910052703 rhodium Inorganic materials 0.000 claims description 4
- 239000010948 rhodium Substances 0.000 claims description 4
- 229910052726 zirconium Inorganic materials 0.000 claims description 4
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 229960002887 deanol Drugs 0.000 claims description 3
- 229910052735 hafnium Inorganic materials 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- BFIAIMMAHAIVFT-UHFFFAOYSA-N 1-[bis(2-hydroxybutyl)amino]butan-2-ol Chemical compound CCC(O)CN(CC(O)CC)CC(O)CC BFIAIMMAHAIVFT-UHFFFAOYSA-N 0.000 claims description 2
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 claims description 2
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 claims description 2
- ITBPIKUGMIZTJR-UHFFFAOYSA-N [bis(hydroxymethyl)amino]methanol Chemical compound OCN(CO)CO ITBPIKUGMIZTJR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052733 gallium Inorganic materials 0.000 claims description 2
- 229910052737 gold Inorganic materials 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- 229910052738 indium Inorganic materials 0.000 claims description 2
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- 229910052746 lanthanum Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 claims description 2
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 claims description 2
- 150000002830 nitrogen compounds Chemical class 0.000 claims description 2
- 229910052762 osmium Inorganic materials 0.000 claims description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052706 scandium Inorganic materials 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 229910052715 tantalum Inorganic materials 0.000 claims description 2
- 229910052713 technetium Inorganic materials 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 2
- NCXUNZWLEYGQAH-UHFFFAOYSA-N 1-(dimethylamino)propan-2-ol Chemical compound CC(O)CN(C)C NCXUNZWLEYGQAH-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- ZYWUVGFIXPNBDL-UHFFFAOYSA-N n,n-diisopropylaminoethanol Chemical compound CC(C)N(C(C)C)CCO ZYWUVGFIXPNBDL-UHFFFAOYSA-N 0.000 claims 1
- 239000000243 solution Substances 0.000 description 67
- 239000000523 sample Substances 0.000 description 65
- 238000002360 preparation method Methods 0.000 description 38
- 239000002245 particle Substances 0.000 description 35
- 238000005470 impregnation Methods 0.000 description 28
- 230000002829 reductive effect Effects 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- 238000005259 measurement Methods 0.000 description 21
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 21
- 239000000047 product Substances 0.000 description 17
- 239000002808 molecular sieve Substances 0.000 description 15
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 15
- 238000001179 sorption measurement Methods 0.000 description 14
- 229940024606 amino acid Drugs 0.000 description 13
- 230000006378 damage Effects 0.000 description 12
- 238000000151 deposition Methods 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 238000004458 analytical method Methods 0.000 description 10
- 230000008021 deposition Effects 0.000 description 10
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 125000003118 aryl group Chemical group 0.000 description 9
- 239000002923 metal particle Substances 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 8
- 238000009826 distribution Methods 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- 239000011148 porous material Substances 0.000 description 8
- 229910044991 metal oxide Inorganic materials 0.000 description 7
- 150000004706 metal oxides Chemical class 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 238000001757 thermogravimetry curve Methods 0.000 description 7
- 238000003917 TEM image Methods 0.000 description 6
- 241001122767 Theaceae Species 0.000 description 6
- QGUAJWGNOXCYJF-UHFFFAOYSA-N cobalt dinitrate hexahydrate Chemical compound O.O.O.O.O.O.[Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O QGUAJWGNOXCYJF-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 6
- 230000003068 static effect Effects 0.000 description 6
- QSHYGLAZPRJAEZ-UHFFFAOYSA-N 4-(chloromethyl)-2-(2-methylphenyl)-1,3-thiazole Chemical compound CC1=CC=CC=C1C1=NC(CCl)=CS1 QSHYGLAZPRJAEZ-UHFFFAOYSA-N 0.000 description 5
- 238000007792 addition Methods 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt dinitrate Chemical compound [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 5
- 229910001981 cobalt nitrate Inorganic materials 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 5
- AOPCKOPZYFFEDA-UHFFFAOYSA-N nickel(2+);dinitrate;hexahydrate Chemical compound O.O.O.O.O.O.[Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O AOPCKOPZYFFEDA-UHFFFAOYSA-N 0.000 description 5
- YLPJWCDYYXQCIP-UHFFFAOYSA-N nitroso nitrate;ruthenium Chemical compound [Ru].[O-][N+](=O)ON=O YLPJWCDYYXQCIP-UHFFFAOYSA-N 0.000 description 5
- 241000894007 species Species 0.000 description 5
- 229910001220 stainless steel Inorganic materials 0.000 description 5
- 239000010935 stainless steel Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000004408 titanium dioxide Substances 0.000 description 5
- 239000010457 zeolite Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 238000004566 IR spectroscopy Methods 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 4
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 238000005984 hydrogenation reaction Methods 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- 238000002329 infrared spectrum Methods 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(ii) nitrate Chemical compound [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 description 4
- PNPIRSNMYIHTPS-UHFFFAOYSA-N nitroso nitrate Chemical class [O-][N+](=O)ON=O PNPIRSNMYIHTPS-UHFFFAOYSA-N 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 238000002411 thermogravimetry Methods 0.000 description 4
- 238000004448 titration Methods 0.000 description 4
- PVXVWWANJIWJOO-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)-N-ethylpropan-2-amine Chemical compound CCNC(C)CC1=CC=C2OCOC2=C1 PVXVWWANJIWJOO-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000004475 Arginine Substances 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229910001369 Brass Inorganic materials 0.000 description 3
- QMMZSJPSPRTHGB-UHFFFAOYSA-N MDEA Natural products CC(C)CCCCC=CCC=CC(O)=O QMMZSJPSPRTHGB-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- 125000003158 alcohol group Chemical group 0.000 description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 3
- 239000010951 brass Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 150000002823 nitrates Chemical class 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 229910000510 noble metal Inorganic materials 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000003870 refractory metal Substances 0.000 description 3
- 239000012266 salt solution Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 150000003624 transition metals Chemical class 0.000 description 3
- JQCSUVJDBHJKNG-UHFFFAOYSA-N 1-methoxy-ethyl Chemical group C[CH]OC JQCSUVJDBHJKNG-UHFFFAOYSA-N 0.000 description 2
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 description 2
- CKUAXEQHGKSLHN-UHFFFAOYSA-N [C].[N] Chemical compound [C].[N] CKUAXEQHGKSLHN-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 description 2
- 229910000323 aluminium silicate Inorganic materials 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 2
- 235000009697 arginine Nutrition 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 229910000428 cobalt oxide Inorganic materials 0.000 description 2
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 2
- 125000006202 diisopropylaminoethyl group Chemical group [H]C([H])([H])C([H])(N(C([H])([H])C([H])([H])*)C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
- C10G2/32—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
- C10G2/33—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts characterised by the catalyst used
- C10G2/331—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts characterised by the catalyst used containing group VIII-metals
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- B01J20/08—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04 comprising aluminium oxide or hydroxide; comprising bauxite
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- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
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- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
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- C07C7/12—Purification; Separation; Use of additives by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers
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- C—CHEMISTRY; METALLURGY
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- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G25/00—Refining of hydrocarbon oils in the absence of hydrogen, with solid sorbents
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/04—Metals, or metals deposited on a carrier
Landscapes
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- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Water Supply & Treatment (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
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| GBGB0227081.7A GB0227081D0 (en) | 2002-11-20 | 2002-11-20 | Methods for preparing catalysts |
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| GB0107908D0 (en) | 2001-03-29 | 2001-05-23 | Bp Oil Int | Decolourisation method |
| GB0227086D0 (en) * | 2002-11-20 | 2002-12-24 | Exxonmobil Res & Eng Co | Hydrogenation processes |
| JP4604051B2 (ja) * | 2004-02-17 | 2010-12-22 | エクソンモービル リサーチ アンド エンジニアリング カンパニー | 金属装填触媒を用いた立体障害の大きなアミノ−エーテルアルコール類の触媒的調製 |
| EP1718597B1 (en) | 2004-02-17 | 2016-09-07 | ExxonMobil Research and Engineering Company | Improved synthesis of severely sterically hindered amino-ether alcohols and diaminopolyalkenyl ethers using a high activity powder catalyst |
| US20050195966A1 (en) * | 2004-03-03 | 2005-09-08 | Sigma Dynamics, Inc. | Method and apparatus for optimizing the results produced by a prediction model |
| JP5031185B2 (ja) * | 2004-08-31 | 2012-09-19 | 日揮触媒化成株式会社 | 燃料処理剤の製造方法 |
| US20060223704A1 (en) * | 2005-03-30 | 2006-10-05 | Tiejun Zhang | Activated carbon for fuel purification |
| US7745373B2 (en) * | 2005-04-08 | 2010-06-29 | Exxonmobil Research And Engineering Company | Single step decomposition and activation of noble metal complexes on catalytic supports |
| JP4827432B2 (ja) * | 2005-04-20 | 2011-11-30 | 新日本製鐵株式会社 | Ｆ−ｔ合成反応用触媒 |
| US7718564B2 (en) | 2005-06-24 | 2010-05-18 | Exxonmobil Research And Engineering Company | Partially decomposed catalyst and hydrocarbon oxidation processes using the same |
| WO2007071701A1 (en) * | 2005-12-22 | 2007-06-28 | Shell Internationale Research Maatschappij B.V. | Zirconium stabilised fischer tropsch catalyst and catalyst support |
| US7674369B2 (en) * | 2006-12-29 | 2010-03-09 | Chevron U.S.A. Inc. | Process for recovering ultrafine solids from a hydrocarbon liquid |
| EP2128312A4 (en) * | 2007-03-19 | 2016-09-21 | Ube Industries | SILICA-BASED OXYGEN FIBER, COMPOSITE CATALYST FIBER AND METHOD OF MANUFACTURING THEREOF |
| US7813523B1 (en) * | 2007-04-03 | 2010-10-12 | Nanostellar, Inc. | Dispersion and metal particle size characterization of nanocatalysts |
| US7817819B1 (en) * | 2007-04-03 | 2010-10-19 | Nanostellar, Inc. | Characterization of metal particle distributions in a supported catalyst |
| US7833316B2 (en) * | 2007-05-01 | 2010-11-16 | Auburn University | Doped supported zinc oxide sorbents for regenerable desulfurization applications |
| WO2008137463A2 (en) | 2007-05-01 | 2008-11-13 | Auburn University | Doped supported zinc oxide sorbents for desulfurization applications |
| EP2153157A4 (en) | 2007-05-11 | 2014-02-26 | Sdcmaterials Inc | WATER COOLING SYSTEM AND HEAT TRANSFER SYSTEM |
| US8158545B2 (en) | 2007-06-18 | 2012-04-17 | Battelle Memorial Institute | Methods, systems, and devices for deep desulfurization of fuel gases |
| CA2698875A1 (en) * | 2007-09-10 | 2009-03-19 | Shell Internationale Research Maatschappij B.V. | Process for producing purified synthesis gas from synthesis gas comprising trace amounts of sulphur contaminants with a metal-organic framework |
| US8481449B1 (en) | 2007-10-15 | 2013-07-09 | SDCmaterials, Inc. | Method and system for forming plug and play oxide catalysts |
| CN102015588B (zh) * | 2008-04-25 | 2013-09-25 | 埃克森美孚化学专利公司 | 生产苯酚和/或环己酮的方法 |
| US20100022388A1 (en) * | 2008-07-25 | 2010-01-28 | Soled Stuart L | Preparation of high activity cobalt catalysts, the catalysts and their use |
| US8148292B2 (en) * | 2008-07-25 | 2012-04-03 | Exxonmobil Research And Engineering Company | Preparation of high activity cobalt catalysts, the catalysts and their use |
| JP5411664B2 (ja) * | 2008-11-18 | 2014-02-12 | 大阪瓦斯株式会社 | 高カロリーガス製造用触媒およびその製造方法および高カロリーガス製造用触媒を用いた高カロリーガス製造方法 |
| US8105969B2 (en) * | 2008-12-29 | 2012-01-31 | Fina Technology Inc. | Catalyst with an ion-modified binder |
| KR101841689B1 (ko) * | 2009-10-30 | 2018-03-29 | 삼성전자주식회사 | 메조 기공성 복합 촉매 및 그의 제조방법 |
| US9126191B2 (en) | 2009-12-15 | 2015-09-08 | SDCmaterials, Inc. | Advanced catalysts for automotive applications |
| US9149797B2 (en) | 2009-12-15 | 2015-10-06 | SDCmaterials, Inc. | Catalyst production method and system |
| US8557727B2 (en) | 2009-12-15 | 2013-10-15 | SDCmaterials, Inc. | Method of forming a catalyst with inhibited mobility of nano-active material |
| US8470112B1 (en) | 2009-12-15 | 2013-06-25 | SDCmaterials, Inc. | Workflow for novel composite materials |
| US20110143930A1 (en) * | 2009-12-15 | 2011-06-16 | SDCmaterials, Inc. | Tunable size of nano-active material on nano-support |
| US8545652B1 (en) | 2009-12-15 | 2013-10-01 | SDCmaterials, Inc. | Impact resistant material |
| US8803025B2 (en) * | 2009-12-15 | 2014-08-12 | SDCmaterials, Inc. | Non-plugging D.C. plasma gun |
| US9090475B1 (en) | 2009-12-15 | 2015-07-28 | SDCmaterials, Inc. | In situ oxide removal, dispersal and drying for silicon SiO2 |
| US8652992B2 (en) | 2009-12-15 | 2014-02-18 | SDCmaterials, Inc. | Pinning and affixing nano-active material |
| WO2011072992A1 (en) | 2009-12-15 | 2011-06-23 | Exxonmobil Chemical Patents Inc. | Temperature control of an oligomerisation process and reactor |
| US20110152546A1 (en) * | 2009-12-17 | 2011-06-23 | Sumitomo Chemical Company, Limited | Process for producing olefin oxide |
| US8476187B2 (en) * | 2010-01-06 | 2013-07-02 | General Electric Company | Process for preparing catalyst powder |
| CN102711985B (zh) | 2010-02-05 | 2016-02-03 | 埃克森美孚化学专利公司 | 脱氢方法 |
| WO2011096991A1 (en) | 2010-02-05 | 2011-08-11 | Exxonmobil Chemical Patents Inc. | Dehydrogenation process |
| CN102741201A (zh) | 2010-02-05 | 2012-10-17 | 埃克森美孚化学专利公司 | 脱氢方法 |
| WO2011096996A1 (en) | 2010-02-05 | 2011-08-11 | Exxonmobil Chemical Patents Inc. | Iridium-containing catalysts, their production and use |
| JP5676120B2 (ja) * | 2010-02-26 | 2015-02-25 | Ｊｘ日鉱日石エネルギー株式会社 | 活性化フィッシャー・トロプシュ合成触媒の製造方法及び炭化水素の製造方法 |
| KR101172159B1 (ko) | 2010-06-01 | 2012-08-07 | 순천향대학교 산학협력단 | 열분해를 이용한 아민 공급 장치 및 방법 |
| CN102294260B (zh) * | 2010-06-24 | 2013-12-18 | 中国石油化工股份有限公司 | 由合成气制低碳含氧化合物的方法 |
| CN102294259A (zh) * | 2010-06-24 | 2011-12-28 | 中国石油化工股份有限公司 | 由合成气制低碳含氧化合物的催化剂及其制备方法 |
| US9486786B2 (en) * | 2010-07-02 | 2016-11-08 | Savannah River Nuclear Solutions, Llc | Highly dispersed metal catalyst |
| US9376637B2 (en) * | 2010-08-13 | 2016-06-28 | Shell Oil Company | Method of making a hydroprocessing catalyst with a single step metal and chelant incorporation, the catalyst, and the use of the catalyst |
| CN102452036B (zh) * | 2010-10-29 | 2016-08-24 | 安集微电子（上海）有限公司 | 一种钨化学机械抛光方法 |
| US8445550B2 (en) * | 2010-11-23 | 2013-05-21 | Chevron U.S.A. Inc. | Ruthenium hybrid fischer-tropsch catalyst, and methods for preparation and use thereof |
| US8669202B2 (en) | 2011-02-23 | 2014-03-11 | SDCmaterials, Inc. | Wet chemical and plasma methods of forming stable PtPd catalysts |
| JP2014522382A (ja) | 2011-03-28 | 2014-09-04 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 脱水素化法 |
| AU2012299065B2 (en) | 2011-08-19 | 2015-06-04 | SDCmaterials, Inc. | Coated substrates for use in catalysis and catalytic converters and methods of coating substrates with washcoat compositions |
| CN102989511B (zh) * | 2011-09-08 | 2015-04-29 | 中国石油化工股份有限公司 | 一种费托合成催化剂及其制备和应用 |
| CN102989458B (zh) * | 2011-09-08 | 2015-03-18 | 中国石油化工股份有限公司 | 一种费托合成催化剂的制备方法以及由该方法制备的催化剂 |
| US9764283B2 (en) | 2012-07-17 | 2017-09-19 | Siemens Aktiengesellschaft | Scrubbing solution for absorption of carbon dioxide and method for accelerating the absorption by germanium dioxide |
| US9156025B2 (en) | 2012-11-21 | 2015-10-13 | SDCmaterials, Inc. | Three-way catalytic converter using nanoparticles |
| US9511352B2 (en) | 2012-11-21 | 2016-12-06 | SDCmaterials, Inc. | Three-way catalytic converter using nanoparticles |
| CN105531027B (zh) * | 2013-07-24 | 2017-11-07 | 国际壳牌研究有限公司 | 制备含氯催化剂的方法、所制备的催化剂及其用途 |
| WO2015010941A1 (en) * | 2013-07-24 | 2015-01-29 | Shell Internationale Research Maatschappij B.V. | Process for preparing a chlorine comprising catalyst, the prepared catalyst, and its use |
| US9586179B2 (en) | 2013-07-25 | 2017-03-07 | SDCmaterials, Inc. | Washcoats and coated substrates for catalytic converters and methods of making and using same |
| US9861960B2 (en) | 2013-10-18 | 2018-01-09 | Exxonmobil Chemical Patents Inc. | Hydrogenation catalyst, its method of preparation and use |
| US10130938B2 (en) | 2013-10-18 | 2018-11-20 | Exxonmobil Chemical Patents Inc. | Hydrogenation catalyst, its method of preparation and use |
| WO2015057312A1 (en) | 2013-10-18 | 2015-04-23 | Exxonmobil Chemical Patents Inc. | A hydrogenation catalyst, its method of preparation and use |
| CA2926135A1 (en) | 2013-10-22 | 2015-04-30 | SDCmaterials, Inc. | Compositions of lean nox trap |
| US9427732B2 (en) | 2013-10-22 | 2016-08-30 | SDCmaterials, Inc. | Catalyst design for heavy-duty diesel combustion engines |
| CN104667989B (zh) * | 2013-11-29 | 2017-04-12 | 中国石油化工股份有限公司 | 湿式氧化催化剂载体的制备方法 |
| CN104667991B (zh) * | 2013-11-29 | 2017-04-12 | 中国石油化工股份有限公司 | 催化湿式氧化催化剂载体的制法 |
| WO2015143225A1 (en) | 2014-03-21 | 2015-09-24 | SDCmaterials, Inc. | Compositions for passive nox adsorption (pna) systems |
| CN105318711B (zh) * | 2014-07-22 | 2017-11-03 | 中国石油化工股份有限公司 | 一种固相粉体混合焙烧设备及催化剂制备方法 |
| KR20170074848A (ko) | 2014-10-29 | 2017-06-30 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 벤젠폴리카복실산 및 이의 유도체의 수소화를 위한 개선된 방법 |
| WO2016136969A1 (ja) * | 2015-02-27 | 2016-09-01 | 国立大学法人九州大学 | 後周期遷移金属微粒子担持体の製造方法 |
| CN104862083A (zh) * | 2015-04-08 | 2015-08-26 | 南昌大学 | 一种降低氢化油脂反式脂肪酸含量的方法 |
| CN105498759B (zh) * | 2015-12-01 | 2018-03-16 | 中国科学院大连化学物理研究所 | 一种乙炔环三聚制备苯高性能催化剂及其制备方法和应用 |
| EP3510012A1 (en) | 2016-09-09 | 2019-07-17 | ExxonMobil Chemical Patents Inc. | Processes for the hydrogenation of phthalate esters |
| CN107224962A (zh) * | 2017-06-29 | 2017-10-03 | 安徽天顺环保设备股份有限公司 | 一种乙醇胺负载改性的氧化镁基烟气干法脱硫吸附剂及制备方法 |
| CN107899579A (zh) * | 2017-11-23 | 2018-04-13 | 西北大学 | 一种高活性费‑托合成钴基催化剂的制备方法 |
| CN107930630A (zh) * | 2017-11-23 | 2018-04-20 | 西北大学 | 一种高活性高稳定性费‑托合成钴基催化剂的制备方法 |
| US10543480B2 (en) * | 2018-04-16 | 2020-01-28 | Chevron Phillips Chemical Company Lp | Methods of preparing a catalyst utilizing hydrated reagents |
| US10722874B2 (en) | 2018-04-16 | 2020-07-28 | Chevron Phillips Chemical Company Lp | Methods of preparing a catalyst utilizing hydrated reagents |
| CN110496614A (zh) * | 2018-05-16 | 2019-11-26 | 中国科学院大连化学物理研究所 | 金属催化剂、其制备方法及在水相催化糠醛加氢制备糠醇中的应用 |
| US11110438B2 (en) | 2018-07-31 | 2021-09-07 | Board Of Regents, The University Of Texas System | Methods for preparation and use of liquid synthesis catalysts |
| CN110416555A (zh) * | 2019-06-28 | 2019-11-05 | 北京航天石化技术装备工程有限公司 | 一种Pt-Ni合金催化剂及其制备方法与应用 |
| KR102248115B1 (ko) | 2019-07-01 | 2021-05-03 | 한국화학연구원 | 피셔―트롭쉬 합성반응용 촉매 및 그 제조방법 |
| KR20210009160A (ko) * | 2019-07-16 | 2021-01-26 | 삼성전자주식회사 | 전이금속 칼코겐 화합물 박막의 형성방법 |
| KR102284848B1 (ko) | 2019-10-11 | 2021-08-02 | 한국화학연구원 | 피셔-트롭시 합성촉매의 제조방법 및 피셔-트롭시 합성촉매를 이용한 액체연료의 제조방법 |
| CN112916007A (zh) * | 2019-12-05 | 2021-06-08 | 中国科学院大连化学物理研究所 | 一种费托合成催化剂的制备方法 |
| US11715834B2 (en) | 2019-12-27 | 2023-08-01 | Toyota Motor Engineering And Manufacturing North America, Inc. | Fuel cell cathode catalyst |
| GB202014184D0 (en) * | 2020-09-09 | 2020-10-21 | Johnson Matthey Plc | Modifed catalyst supports and catalysts supported thereon |
| CN114425337B (zh) * | 2020-10-10 | 2024-01-30 | 中国石油化工股份有限公司 | 一种甲醇胺化催化剂及其应用 |
| CN112121848B (zh) * | 2020-10-30 | 2022-08-05 | 万华化学集团股份有限公司 | 改性多级孔分子筛催化剂及其制备方法、3-甲基-2-丁烯-1-醇的生产方法 |
| CN113663707A (zh) * | 2021-08-13 | 2021-11-19 | 中山大学 | 一种宏量制备多种甲醛分解催化剂的方法 |
| CN115337933B (zh) * | 2022-07-11 | 2024-03-22 | 华东理工大学 | 一种高效光催化还原co2的锡掺杂带有氧空位的四氧化三钴材料的制备方法及其应用 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL68368C (enExample) * | 1949-03-31 | |||
| US2889287A (en) * | 1954-10-04 | 1959-06-02 | California Research Corp | Catalyst and method of catalyst preparation |
| FR2080099A5 (enExample) * | 1970-02-23 | 1971-11-12 | Inst Francais Du Petrole | |
| US3953368A (en) * | 1971-11-01 | 1976-04-27 | Exxon Research And Engineering Co. | Polymetallic cluster compositions useful as hydrocarbon conversion catalysts |
| US4073750A (en) * | 1976-05-20 | 1978-02-14 | Exxon Research & Engineering Co. | Method for preparing a highly dispersed supported nickel catalyst |
| FR2505205B1 (fr) * | 1981-05-05 | 1986-05-23 | Inst Francais Du Petrole | Nouveaux catalyseurs de metaux nobles du groupe viii supportes a haute dispersion et grande activite leur fabrication et leur utilisation notamment dans les reactions d'hydrogenation |
| US4634515A (en) * | 1985-10-25 | 1987-01-06 | Exxon Research And Engineering Company | Nickel adsorbent for sulfur removal from hydrocarbon feeds |
| US5332705A (en) * | 1992-06-19 | 1994-07-26 | Exxon Chemical Patents Inc. | Regeneration of acetylene converter catalysts by hydrogen stripping |
| JP2771749B2 (ja) * | 1992-12-17 | 1998-07-02 | 出光興産株式会社 | 水素化触媒製造用含浸液及び水素化触媒の製造方法 |
| US5344553A (en) * | 1993-02-22 | 1994-09-06 | Mobil Oil Corporation | Upgrading of a hydrocarbon feedstock utilizing a graded, mesoporous catalyst system |
| US5863856A (en) * | 1997-04-22 | 1999-01-26 | Exxon Research And Engineering Company | Preparation of high activity catalysts the catalysts and their use |
| US6118037A (en) * | 1997-04-22 | 2000-09-12 | Snamprogetti S.P.A. | Process for the removal of contaminant compounds containing one or more heteroatoms of sulfur, nitrogen and/or oxygen from hydrocarbon streams |
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| CN1717278A (zh) | 2006-01-04 |
| JP4504815B2 (ja) | 2010-07-14 |
| KR20050083911A (ko) | 2005-08-26 |
| WO2004045767A2 (en) | 2004-06-03 |
| EP1569751B1 (en) | 2015-10-07 |
| US20060166809A1 (en) | 2006-07-27 |
| CN1717278B (zh) | 2011-07-13 |
| AU2003292042A1 (en) | 2004-06-15 |
| US7585808B2 (en) | 2009-09-08 |
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