SA112330866B1 - طريقة لمعالجة غاز مهدور - Google Patents
طريقة لمعالجة غاز مهدور Download PDFInfo
- Publication number
- SA112330866B1 SA112330866B1 SA112330866A SA112330866A SA112330866B1 SA 112330866 B1 SA112330866 B1 SA 112330866B1 SA 112330866 A SA112330866 A SA 112330866A SA 112330866 A SA112330866 A SA 112330866A SA 112330866 B1 SA112330866 B1 SA 112330866B1
- Authority
- SA
- Saudi Arabia
- Prior art keywords
- propane
- propylene
- catalyst
- acrylic acid
- oxygen
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 43
- 239000002912 waste gas Substances 0.000 title description 7
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims abstract description 76
- 239000001294 propane Substances 0.000 claims abstract description 39
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 35
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 32
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 44
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 44
- 239000003054 catalyst Substances 0.000 claims description 41
- 238000006243 chemical reaction Methods 0.000 claims description 38
- 239000007789 gas Substances 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 15
- 239000001301 oxygen Substances 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims description 12
- 239000006227 byproduct Substances 0.000 claims description 7
- 239000012071 phase Substances 0.000 claims description 7
- 239000012467 final product Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 4
- 229910003455 mixed metal oxide Inorganic materials 0.000 claims description 4
- ATRMIFNAYHCLJR-UHFFFAOYSA-N [O].CCC Chemical compound [O].CCC ATRMIFNAYHCLJR-UHFFFAOYSA-N 0.000 claims description 2
- 230000004224 protection Effects 0.000 claims 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 239000013067 intermediate product Substances 0.000 claims 2
- 241000196324 Embryophyta Species 0.000 claims 1
- QRSFFHRCBYCWBS-UHFFFAOYSA-N [O].[O] Chemical compound [O].[O] QRSFFHRCBYCWBS-UHFFFAOYSA-N 0.000 claims 1
- 239000007792 gaseous phase Substances 0.000 claims 1
- 239000002699 waste material Substances 0.000 abstract description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 15
- 238000007254 oxidation reaction Methods 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 13
- 230000003647 oxidation Effects 0.000 description 11
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 150000002430 hydrocarbons Chemical class 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 238000010960 commercial process Methods 0.000 description 5
- 239000007800 oxidant agent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000004231 fluid catalytic cracking Methods 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229910000323 aluminium silicate Inorganic materials 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- 229920001600 hydrophobic polymer Polymers 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012263 liquid product Substances 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 description 1
- 235000017399 Caesalpinia tinctoria Nutrition 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 101100181494 Cricetulus griseus LDLR gene Proteins 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 241000388430 Tara Species 0.000 description 1
- 241001197925 Theila Species 0.000 description 1
- DHIXVMCNTGJBQF-UHFFFAOYSA-N [He].[Ar].[Ar] Chemical compound [He].[Ar].[Ar] DHIXVMCNTGJBQF-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000010961 commercial manufacture process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 235000012489 doughnuts Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
- 230000000476 thermogenic effect Effects 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
- C07C51/252—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
- C07C45/35—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Processing Of Solid Wastes (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161548372P | 2011-10-18 | 2011-10-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SA112330866B1 true SA112330866B1 (ar) | 2015-07-07 |
Family
ID=46982923
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SA112330866A SA112330866B1 (ar) | 2011-10-18 | 2012-09-24 | طريقة لمعالجة غاز مهدور |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9120735B2 (enExample) |
| EP (1) | EP2768794B1 (enExample) |
| CN (1) | CN103889942B (enExample) |
| BR (1) | BR112014008712A2 (enExample) |
| IN (1) | IN2014CN02757A (enExample) |
| SA (1) | SA112330866B1 (enExample) |
| SG (1) | SG11201401606WA (enExample) |
| TW (1) | TW201332959A (enExample) |
| WO (1) | WO2013058888A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112014008712A2 (pt) | 2011-10-18 | 2017-04-25 | Rohm & Haas | processo |
| EP3341350B1 (en) * | 2015-08-24 | 2019-09-25 | Rohm and Haas Company | Method of determining the inertness of materials for use in monomer production |
| EP3341351B1 (en) * | 2015-08-24 | 2019-10-02 | Rohm and Haas Company | Method of determining the inertness of materials for use in monomer production |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0731077B1 (de) | 1995-03-10 | 1999-10-13 | Basf Aktiengesellschaft | Verfahren zur Herstellung von Acrolein, Acrylsäure oder deren Gemisch aus Propan |
| EP1090684A1 (en) | 1999-10-01 | 2001-04-11 | Rohm And Haas Company | A catalyst useful for the gas phase oxidation of alkanes, alkenes or alcohols to unsaturated aldehydes or carboxylic acids |
| US6407031B1 (en) | 2000-09-28 | 2002-06-18 | Rohm And Haas Company | Promoted multi-metal oxide catalyst |
| US6461996B2 (en) | 2000-09-28 | 2002-10-08 | Rohm And Haas Company | Halogen promoted multi-metal oxide catalyst |
| US6589907B2 (en) | 2000-09-28 | 2003-07-08 | Rohm And Haas Company | Zn and/or Ga promoted multi-metal oxide catalyst |
| US6403525B1 (en) | 2000-09-28 | 2002-06-11 | Rohm And Haas Company | Promoted multi-metal oxide catalyst |
| US6407280B1 (en) | 2000-09-28 | 2002-06-18 | Rohm And Haas Company | Promoted multi-metal oxide catalyst |
| US6383978B1 (en) | 2001-04-25 | 2002-05-07 | Rohm And Haas Company | Promoted multi-metal oxide catalyst |
| DE10148566A1 (de) | 2001-10-01 | 2003-04-10 | Basf Ag | Verfahren zur Herstellung von Acrylsäure durch heterogen katalysierte Gasphasenoxidation |
| US20050137422A1 (en) * | 2003-12-19 | 2005-06-23 | Saudi Basic Industries Corporation | Process for producing an unsaturated carboxylic acid from an alkane |
| US8193387B2 (en) * | 2003-12-19 | 2012-06-05 | Saudi Basic Industries Corporation | Process for producing an unsaturated carboxylic acid from an alkane |
| US7553986B2 (en) * | 2003-12-23 | 2009-06-30 | Rohm And Haas Company | Process for the selective (amm)oxidation of lower molecular weight alkanes and alkenes |
| BRPI0500615B1 (pt) | 2004-03-10 | 2015-07-14 | Rohm And Haas Company | Catalisador modificado, e, sistema de catalisador modificado |
| CN100544821C (zh) * | 2004-12-23 | 2009-09-30 | 中国科学院大连化学物理研究所 | 一种用于丙烷选择氧化制丙烯酸反应的钼钒碲铌催化剂及其制备方法 |
| DE102005062026A1 (de) | 2005-12-22 | 2007-06-28 | Basf Ag | Verfahren der heterogen katalysierten partiellen Gasphasenoxidation von Propylen zu Acrylsäure |
| DE102006024901A1 (de) * | 2006-05-24 | 2007-11-29 | Basf Ag | Verfahren zur Herstellung von Acrolein, oder Acrylsäure oder deren Gemisch aus Propan |
| BR112014008712A2 (pt) | 2011-10-18 | 2017-04-25 | Rohm & Haas | processo |
-
2012
- 2012-09-10 BR BR112014008712A patent/BR112014008712A2/pt not_active Application Discontinuation
- 2012-09-10 IN IN2757CHN2014 patent/IN2014CN02757A/en unknown
- 2012-09-10 US US14/351,404 patent/US9120735B2/en not_active Expired - Fee Related
- 2012-09-10 CN CN201280051022.XA patent/CN103889942B/zh not_active Expired - Fee Related
- 2012-09-10 SG SG11201401606WA patent/SG11201401606WA/en unknown
- 2012-09-10 WO PCT/US2012/054414 patent/WO2013058888A1/en not_active Ceased
- 2012-09-10 EP EP12769529.4A patent/EP2768794B1/en not_active Not-in-force
- 2012-09-24 SA SA112330866A patent/SA112330866B1/ar unknown
- 2012-10-17 TW TW101138161A patent/TW201332959A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SG11201401606WA (en) | 2014-05-29 |
| TW201332959A (zh) | 2013-08-16 |
| US9120735B2 (en) | 2015-09-01 |
| CN103889942B (zh) | 2016-05-11 |
| IN2014CN02757A (enExample) | 2015-07-03 |
| EP2768794A1 (en) | 2014-08-27 |
| CN103889942A (zh) | 2014-06-25 |
| BR112014008712A2 (pt) | 2017-04-25 |
| EP2768794B1 (en) | 2017-08-23 |
| US20140243554A1 (en) | 2014-08-28 |
| WO2013058888A1 (en) | 2013-04-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7062686B2 (ja) | 精製された形態でメタンスルホン酸を回収するための方法及びシステム | |
| BRPI0721008A2 (pt) | Método para preparar ácido acrílico a partir de glicerol | |
| BRPI0807736A2 (pt) | Processo para síntese de acrilonitrila a partir de glicerol | |
| KR101388541B1 (ko) | 비닐 아세테이트의 제조 방법 | |
| SA516370808B1 (ar) | طريقة لانتاج ميثاكرولين وتكييفه/تصريفه من أجل الأسترة التأكسدية المباشرة | |
| JP2014205670A (ja) | グリセリンから生物起源のポリマーグレートのアクリル酸を製造する方法 | |
| TW201235340A (en) | Processes for the production of ethylene glycol | |
| UA122561C2 (uk) | Спосіб одержання диметилового ефіру з газоподібних сумішей монооксиду вуглецю, водню і метилацетату | |
| SA112330866B1 (ar) | طريقة لمعالجة غاز مهدور | |
| WO2007135102A3 (de) | Herstellung von phthalsäureanhydrid durch gasphasenoxidation von o-xylol in einem haupt- und nachreaktor | |
| KR102771123B1 (ko) | 알칸설폰산의 제조방법 | |
| US20120203029A1 (en) | Production of acetates from acetic acid and alcohols | |
| TWI577657B (zh) | 酸溶液之純化方法 | |
| EP3956302B1 (en) | Process for the production of anhydrous methanesulfonic acid from methane and so3 | |
| JP3220234B2 (ja) | オゾンによる無水酢酸または無水酢酸および酢酸の混合物の精製法 | |
| US12071400B2 (en) | Process of selective oxidation of glycerol | |
| WO2017085604A2 (en) | Process for oxidative dehydrogenation of ethane to ethylene using a mixture of oxygen and co2 | |
| KR20250056242A (ko) | 액체 탄화수소 생성물을 형성하는 방법 | |
| US20220267179A1 (en) | Elimination of formaldehyde in wastewater through oxidation treatment | |
| US5175362A (en) | Recovery of acetyl values from ethylidene diacetate | |
| CN111848386B (zh) | 用于处理可变乙酰流的系统和方法 | |
| US20130296602A1 (en) | Conversion of Methyl-2-Acetoxy Propionate to Methyl Acrylate and Acrylic Acid | |
| TWI422565B (zh) | 自粗製甲醇之二甲醚的製造 | |
| JP5098266B2 (ja) | フェノールの製造方法 | |
| WO2022168695A1 (ja) | プロピレンの製造方法 |