JP2003514751A5 - - Google Patents
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- JP2003514751A5 JP2003514751A5 JP2001539268A JP2001539268A JP2003514751A5 JP 2003514751 A5 JP2003514751 A5 JP 2003514751A5 JP 2001539268 A JP2001539268 A JP 2001539268A JP 2001539268 A JP2001539268 A JP 2001539268A JP 2003514751 A5 JP2003514751 A5 JP 2003514751A5
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- 238000000034 method Methods 0.000 description 36
- 239000000126 substance Substances 0.000 description 26
- 239000000463 material Substances 0.000 description 21
- 239000010936 titanium Substances 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- 229910052719 titanium Inorganic materials 0.000 description 16
- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 229910052726 zirconium Inorganic materials 0.000 description 12
- 239000010457 zeolite Substances 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 10
- 229910052732 germanium Inorganic materials 0.000 description 9
- 239000002243 precursor Substances 0.000 description 9
- 229910052718 tin Inorganic materials 0.000 description 9
- 239000003153 chemical reaction reagent Substances 0.000 description 8
- 125000000524 functional group Chemical group 0.000 description 8
- JMXKSZRRTHPKDL-UHFFFAOYSA-N titanium ethoxide Chemical compound [Ti+4].CC[O-].CC[O-].CC[O-].CC[O-] JMXKSZRRTHPKDL-UHFFFAOYSA-N 0.000 description 8
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 6
- 229910021536 Zeolite Inorganic materials 0.000 description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 6
- -1 hexamesyleneimine Chemical compound 0.000 description 6
- 150000002432 hydroperoxides Chemical class 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 5
- 150000002894 organic compounds Chemical class 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 125000003396 thiol group Chemical group [H]S* 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 229910052796 boron Inorganic materials 0.000 description 4
- 229910052733 gallium Inorganic materials 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 150000001282 organosilanes Chemical class 0.000 description 4
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 4
- 125000001174 sulfone group Chemical group 0.000 description 4
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 150000004703 alkoxides Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000003100 immobilizing effect Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- RXYPXQSKLGGKOL-UHFFFAOYSA-N 1,4-dimethylpiperazine Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 2
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000005700 Putrescine Substances 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- 229910007926 ZrCl Inorganic materials 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 150000001343 alkyl silanes Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 2
- BYLOHCRAPOSXLY-UHFFFAOYSA-N dichloro(diethyl)silane Chemical compound CC[Si](Cl)(Cl)CC BYLOHCRAPOSXLY-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229910001657 ferrierite group Inorganic materials 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000004820 halides Chemical group 0.000 description 2
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 229910001867 inorganic solvent Inorganic materials 0.000 description 2
- 239000003049 inorganic solvent Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012229 microporous material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 125000002524 organometallic group Chemical group 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 238000002211 ultraviolet spectrum Methods 0.000 description 2
- 238000001429 visible spectrum Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 description 2
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 2
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 1
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- NILZGRNPRBIQOG-UHFFFAOYSA-N 3-iodopropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCI NILZGRNPRBIQOG-UHFFFAOYSA-N 0.000 description 1
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical class OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- PDSNLYSELAIEBU-UHFFFAOYSA-N Longifolene Chemical compound C1CCC(C)(C)C2C3CCC2C1(C)C3=C PDSNLYSELAIEBU-UHFFFAOYSA-N 0.000 description 1
- ZPUKHRHPJKNORC-UHFFFAOYSA-N Longifolene Natural products CC1(C)CCCC2(C)C3CCC1(C3)C2=C ZPUKHRHPJKNORC-UHFFFAOYSA-N 0.000 description 1
- 229910008051 Si-OH Inorganic materials 0.000 description 1
- 229910006358 Si—OH Inorganic materials 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000004808 allyl alcohols Chemical class 0.000 description 1
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
- NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 229940117948 caryophyllene Drugs 0.000 description 1
- NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- MKNXBRLZBFVUPV-UHFFFAOYSA-L cyclopenta-1,3-diene;dichlorotitanium Chemical compound Cl[Ti]Cl.C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 MKNXBRLZBFVUPV-UHFFFAOYSA-L 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000006735 epoxidation reaction Methods 0.000 description 1
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Chemical class 0.000 description 1
- 229930195729 fatty acid Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 229960002050 hydrofluoric acid Drugs 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- NBTOZLQBSIZIKS-UHFFFAOYSA-N methoxide Chemical compound [O-]C NBTOZLQBSIZIKS-UHFFFAOYSA-N 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- IKNCGYCHMGNBCP-UHFFFAOYSA-N propan-1-olate Chemical compound CCC[O-] IKNCGYCHMGNBCP-UHFFFAOYSA-N 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical group CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- FEFXFMQVSDTSPA-UHFFFAOYSA-N trichloro(methyl)germane Chemical compound C[Ge](Cl)(Cl)Cl FEFXFMQVSDTSPA-UHFFFAOYSA-N 0.000 description 1
- YFRLQYJXUZRYDN-UHFFFAOYSA-K trichloro(methyl)stannane Chemical compound C[Sn](Cl)(Cl)Cl YFRLQYJXUZRYDN-UHFFFAOYSA-K 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP9902655 | 1999-11-24 | ||
| ES009902655A ES2178910B1 (es) | 1999-11-24 | 1999-11-24 | Materiales microporosos de alta superficie activos en reacciones de oxidacion. tiq-6 y metiq-6. |
| PCT/ES2000/000456 WO2001037629A2 (es) | 1999-11-24 | 2000-11-24 | Materiales microporosos de alta superficie activos en reacciones de oxidación. tiq-6 y metiq-6 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003514751A JP2003514751A (ja) | 2003-04-22 |
| JP2003514751A5 true JP2003514751A5 (enExample) | 2007-11-22 |
Family
ID=8310795
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001539268A Pending JP2003514751A (ja) | 1999-11-24 | 2000-11-24 | 酸化反応に活性を有する高表面積微多孔質物質（ｔｉｑ−６およびｍｅｔｉｑ−６） |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6843978B2 (enExample) |
| EP (1) | EP1243333B1 (enExample) |
| JP (1) | JP2003514751A (enExample) |
| CN (1) | CN1191884C (enExample) |
| AT (1) | ATE286432T1 (enExample) |
| AU (1) | AU782301B2 (enExample) |
| DE (1) | DE60017286T2 (enExample) |
| DK (1) | DK1243333T3 (enExample) |
| EA (1) | EA004784B1 (enExample) |
| ES (2) | ES2178910B1 (enExample) |
| IN (1) | IN2002KO00840A (enExample) |
| NZ (1) | NZ519657A (enExample) |
| WO (1) | WO2001037629A2 (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2179753B1 (es) | 2000-10-11 | 2005-02-16 | Universidad Politecnica De Valencia | Proceso y catalizadores para la eliminacion de compuestos de azufre de la fraccion gasolina. |
| ES2183710B1 (es) * | 2001-04-12 | 2004-01-16 | Univ Valencia Politecnica | Proceso y catalizadores para la eliminacion de compuestos de azufre de la fraccion diesel. |
| WO2005012458A1 (en) * | 2003-08-01 | 2005-02-10 | Bp Corporation North America Inc. | Preparation of components for refinery blending of transportation fuels |
| US7491316B2 (en) * | 2004-07-29 | 2009-02-17 | Bp Corporation North America Inc. | Preparation of components for refinery blending of transportation fuels |
| ES2281299B1 (es) * | 2006-03-15 | 2008-12-16 | Universidad Politecnica De Valencia | Un procecimiento para la sintesis de esteres. |
| GB0702327D0 (en) * | 2007-02-07 | 2007-03-21 | Leuven K U Res & Dev | Zeolite materials and synthesis method thereof |
| CN101602012B (zh) * | 2008-06-12 | 2012-04-18 | 中国石油化工股份有限公司 | 含有芳烃磺酸基团的介孔材料及其制备方法和应用 |
| TWI399242B (zh) * | 2009-12-11 | 2013-06-21 | China Petrochemical Dev Corp Taipei Taiwan | Method for preparing large-diameter titanium-silicon molecular sieve and method for producing cyclohexanone oxime using the molecular sieve |
| US9522390B2 (en) * | 2010-12-10 | 2016-12-20 | The Regents Of The University Of California | Oxide materials and synthesis by fluoride/chloride anion promoted exfoliation |
| CN103402991A (zh) * | 2011-01-27 | 2013-11-20 | 索尔维公司 | 用于制造1,2-环氧-3-氯丙烷的方法 |
| CN102442683A (zh) * | 2011-09-27 | 2012-05-09 | 华东理工大学 | 一种制备多级孔道含钛沸石的溶剂挥发法 |
| KR101394133B1 (ko) * | 2012-08-22 | 2014-05-15 | 주식회사 이엔에프테크놀로지 | 몰리브덴 합금막 및 인듐 산화막 식각액 조성물 |
| WO2014191475A1 (en) * | 2013-05-29 | 2014-12-04 | Basf Se | Process for the oxidation of sulfoxides |
| FR3007405B1 (fr) * | 2013-06-21 | 2016-07-29 | Centre Nat De La Rech Scient (C N R S ) | Procede de preparation d'une composition comprenant des particules silico/germano-metalliques fonctionnalisees et composition obtenue |
| CN111278552A (zh) * | 2017-10-30 | 2020-06-12 | 巴斯夫欧洲公司 | 由层状硅酸盐前体制备包封过渡金属纳米粒子的沸石的方法 |
| CN108947939B (zh) * | 2018-08-16 | 2022-03-11 | 福州大学 | 一种异松油烯4,8-环氧化物的合成方法 |
| CN111924852B (zh) * | 2019-04-26 | 2023-11-03 | 中国石油大学(华东) | 一种钛硅分子筛的制备方法 |
| CN110902691B (zh) * | 2019-11-25 | 2021-07-20 | 北京化工大学 | 一种y型分子筛疏水改性的方法 |
| CN111167471B (zh) * | 2020-01-17 | 2020-10-02 | 浙江新和成股份有限公司 | 一种金属氧化物涂覆的陶瓷波纹板催化剂、制备及其在制备柠檬醛关键中间体中的应用 |
| TW202346272A (zh) * | 2022-04-25 | 2023-12-01 | 日商住友化學股份有限公司 | 含鈦氧化矽之製造方法、環氧化物之製造方法、及含鈦氧化矽 |
| CN118620617B (zh) * | 2024-08-09 | 2025-03-04 | 电子科技大学长三角研究院(湖州) | 一种晶态GaTiS-AEP有机开放骨架绿色光致发光源及其制备方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3923843A (en) | 1972-03-13 | 1975-12-02 | Shell Oil Co | Epoxidation process with improved heterogeneous catalyst |
| US4016245A (en) * | 1973-09-04 | 1977-04-05 | Mobil Oil Corporation | Crystalline zeolite and method of preparing same |
| US3966883A (en) * | 1974-10-16 | 1976-06-29 | W. R. Grace & Co. | Synthetic ferrierite synthesis |
| DK84884A (da) * | 1983-03-07 | 1984-09-08 | Res Ass Petroleum Alternat Dev | Krystallinsk aluminiumsilicat og fremgangsmaade til fremstilling deraf |
| GB8818452D0 (en) * | 1988-08-03 | 1988-09-07 | British Petroleum Co Plc | Process for preparation of crystalline(metallo)silicates & germanates |
| US5374747A (en) | 1993-12-23 | 1994-12-20 | Arco Chemical Technology, L.P. | Epoxidation process and catalyst therefore |
| ES2124154B1 (es) * | 1995-11-08 | 1999-12-01 | Univ Politecnica De Valencia C | Metodo de preparaciion y propiedades cataliticas de un solido microporoso con alta superficie externa. |
| ES2137885B1 (es) * | 1997-12-19 | 2000-08-16 | Univ Valencia Politecnica | Zeolita itq-5. |
| DK1102630T3 (da) * | 1998-08-04 | 2003-02-17 | Bp Oil Int | Delamineret mikroporøst faststof |
| ES2156514B1 (es) * | 1998-12-04 | 2002-02-16 | Univ Valencia Politecnica | Materiales microporosos de alta superficie activos en reacciones de oxidacion. |
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1999
- 1999-11-24 ES ES009902655A patent/ES2178910B1/es not_active Expired - Fee Related
-
2000
- 2000-11-24 EA EA200200583A patent/EA004784B1/ru not_active IP Right Cessation
- 2000-11-24 DE DE60017286T patent/DE60017286T2/de not_active Expired - Lifetime
- 2000-11-24 AT AT00979683T patent/ATE286432T1/de not_active IP Right Cessation
- 2000-11-24 DK DK00979683T patent/DK1243333T3/da active
- 2000-11-24 AU AU17085/01A patent/AU782301B2/en not_active Ceased
- 2000-11-24 JP JP2001539268A patent/JP2003514751A/ja active Pending
- 2000-11-24 EP EP00979683A patent/EP1243333B1/en not_active Expired - Lifetime
- 2000-11-24 CN CNB008186006A patent/CN1191884C/zh not_active Expired - Fee Related
- 2000-11-24 WO PCT/ES2000/000456 patent/WO2001037629A2/es not_active Ceased
- 2000-11-24 ES ES00979683T patent/ES2236000T3/es not_active Expired - Lifetime
- 2000-11-24 NZ NZ51965700A patent/NZ519657A/en unknown
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2002
- 2002-05-24 US US10/155,564 patent/US6843978B2/en not_active Expired - Fee Related
- 2002-06-24 IN IN840KO2002 patent/IN2002KO00840A/en unknown
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