CH626267A5 - - Google Patents
Download PDFInfo
- Publication number
- CH626267A5 CH626267A5 CH872976A CH872976A CH626267A5 CH 626267 A5 CH626267 A5 CH 626267A5 CH 872976 A CH872976 A CH 872976A CH 872976 A CH872976 A CH 872976A CH 626267 A5 CH626267 A5 CH 626267A5
- Authority
- CH
- Switzerland
- Prior art keywords
- process according
- acetylene
- gem
- saturated
- rectification
- Prior art date
Links
- 229920005989 resin Polymers 0.000 claims description 24
- 239000011347 resin Substances 0.000 claims description 24
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims description 13
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 13
- 150000002430 hydrocarbons Chemical class 0.000 claims description 13
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 12
- 150000002500 ions Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 239000007789 gas Substances 0.000 claims description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- 229920001567 vinyl ester resin Polymers 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 claims description 6
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 6
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- -1 polyphenylene, divinyl benzene Polymers 0.000 claims description 5
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 5
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims description 4
- WFYPICNXBKQZGB-UHFFFAOYSA-N butenyne Chemical group C=CC#C WFYPICNXBKQZGB-UHFFFAOYSA-N 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 claims description 3
- 239000004925 Acrylic resin Substances 0.000 claims description 2
- 229920000178 Acrylic resin Polymers 0.000 claims description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- 239000004793 Polystyrene Substances 0.000 claims description 2
- 238000007259 addition reaction Methods 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 150000005690 diesters Chemical class 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- MJBPUQUGJNAPAZ-AWEZNQCLSA-N butin Chemical compound C1([C@@H]2CC(=O)C3=CC=C(C=C3O2)O)=CC=C(O)C(O)=C1 MJBPUQUGJNAPAZ-AWEZNQCLSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 230000008030 elimination Effects 0.000 description 6
- 238000003379 elimination reaction Methods 0.000 description 6
- 229960000583 acetic acid Drugs 0.000 description 5
- MJBPUQUGJNAPAZ-UHFFFAOYSA-N Butine Natural products O1C2=CC(O)=CC=C2C(=O)CC1C1=CC=C(O)C(O)=C1 MJBPUQUGJNAPAZ-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000010517 secondary reaction Methods 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- WRYNUJYAXVDTCB-UHFFFAOYSA-M acetyloxymercury Chemical compound CC(=O)O[Hg] WRYNUJYAXVDTCB-UHFFFAOYSA-M 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
- C07C7/17—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound with acids or sulfur oxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/04—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/52—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C07C67/54—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/56—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/40—Ethylene production
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Water Supply & Treatment (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT25171/75A IT1039740B (it) | 1975-07-08 | 1975-07-08 | Procedimento per l addizione di acidi organici a composti acetile nici contenuti in correnet i idrocar buriche inorganiche do organiche |
Publications (1)
Publication Number | Publication Date |
---|---|
CH626267A5 true CH626267A5 (no) | 1981-11-13 |
Family
ID=11215901
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH872976A CH626267A5 (no) | 1975-07-08 | 1976-07-07 |
Country Status (34)
Country | Link |
---|---|
US (1) | US4066713A (no) |
JP (1) | JPS602287B2 (no) |
AR (1) | AR221029A1 (no) |
AT (1) | AT345263B (no) |
AU (1) | AU500172B2 (no) |
BE (1) | BE843917A (no) |
BR (1) | BR7605717A (no) |
CA (1) | CA1086330A (no) |
CH (1) | CH626267A5 (no) |
CS (1) | CS194770B2 (no) |
DD (2) | DD130572A5 (no) |
DE (1) | DE2630783C3 (no) |
DK (1) | DK303876A (no) |
EG (1) | EG12199A (no) |
ES (1) | ES449922A1 (no) |
FR (1) | FR2317256A1 (no) |
GB (1) | GB1499646A (no) |
HU (1) | HU178719B (no) |
IE (1) | IE43389B1 (no) |
IN (1) | IN144603B (no) |
IT (1) | IT1039740B (no) |
LU (1) | LU75312A1 (no) |
MX (1) | MX144146A (no) |
NL (1) | NL7607525A (no) |
NO (1) | NO145572C (no) |
PH (1) | PH13775A (no) |
PL (1) | PL108187B1 (no) |
PT (1) | PT65331B (no) |
RO (1) | RO74131A (no) |
SE (1) | SE425385B (no) |
SU (1) | SU751320A3 (no) |
TR (1) | TR18997A (no) |
YU (1) | YU164576A (no) |
ZA (1) | ZA763798B (no) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3127751A1 (de) * | 1981-07-14 | 1983-02-03 | EC Erdölchemie GmbH, 5000 Köln | Verfahren zur hydrierung von kohlenwasserstoffen |
GB9314514D0 (en) * | 1993-07-13 | 1993-08-25 | Ici Plc | Hydrocarbon processing |
US5952523A (en) * | 1997-07-24 | 1999-09-14 | Praxair Technology, Inc. | Method for producing vinyl acetate |
DE10113381A1 (de) * | 2001-02-13 | 2002-08-14 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von hochreinem Diisobuten |
US8742194B2 (en) * | 2012-05-21 | 2014-06-03 | CM Global Systems, LLC | Hydrocarbon-containing mixture and method and system for making the same |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL291243A (no) * | 1962-04-25 | 1900-01-01 | ||
US3287402A (en) * | 1964-05-25 | 1966-11-22 | Mobil Oil Corp | Synthesis of vinyl esters in the presence of a crystalline aluminosilicate catalyst |
-
1975
- 1975-07-08 IT IT25171/75A patent/IT1039740B/it active
-
1976
- 1976-06-25 NO NO762205A patent/NO145572C/no unknown
- 1976-06-25 ZA ZA763798A patent/ZA763798B/xx unknown
- 1976-06-30 AU AU15437/76A patent/AU500172B2/en not_active Expired
- 1976-07-05 YU YU01645/76A patent/YU164576A/xx unknown
- 1976-07-05 DK DK303876A patent/DK303876A/da not_active Application Discontinuation
- 1976-07-06 US US05/703,121 patent/US4066713A/en not_active Expired - Lifetime
- 1976-07-06 GB GB28110/76A patent/GB1499646A/en not_active Expired
- 1976-07-06 ES ES449922A patent/ES449922A1/es not_active Expired
- 1976-07-06 DD DD7600200188A patent/DD130572A5/xx unknown
- 1976-07-06 DD DD193730A patent/DD127302A5/xx unknown
- 1976-07-06 IN IN1196/CAL/1976A patent/IN144603B/en unknown
- 1976-07-06 EG EG407/76A patent/EG12199A/xx active
- 1976-07-06 TR TR18997A patent/TR18997A/xx unknown
- 1976-07-06 LU LU75312A patent/LU75312A1/xx unknown
- 1976-07-06 CS CS764466A patent/CS194770B2/cs unknown
- 1976-07-07 CA CA256,496A patent/CA1086330A/en not_active Expired
- 1976-07-07 FR FR7620820A patent/FR2317256A1/fr active Granted
- 1976-07-07 AT AT498776A patent/AT345263B/de not_active IP Right Cessation
- 1976-07-07 PT PT65331A patent/PT65331B/pt unknown
- 1976-07-07 CH CH872976A patent/CH626267A5/it not_active IP Right Cessation
- 1976-07-07 RO RO7686861A patent/RO74131A/ro unknown
- 1976-07-07 NL NL7607525A patent/NL7607525A/xx not_active Application Discontinuation
- 1976-07-07 IE IE1502/76A patent/IE43389B1/en unknown
- 1976-07-07 HU HU76SA2940A patent/HU178719B/hu unknown
- 1976-07-08 AR AR263905A patent/AR221029A1/es active
- 1976-07-08 DE DE2630783A patent/DE2630783C3/de not_active Expired
- 1976-07-08 PH PH18661A patent/PH13775A/en unknown
- 1976-07-08 PL PL1976191023A patent/PL108187B1/pl unknown
- 1976-07-08 SU SU762379564A patent/SU751320A3/ru active
- 1976-07-08 MX MX165433A patent/MX144146A/es unknown
- 1976-07-08 JP JP51080431A patent/JPS602287B2/ja not_active Expired
- 1976-07-08 BE BE168744A patent/BE843917A/xx not_active IP Right Cessation
- 1976-07-08 BR BR7605717A patent/BR7605717A/pt unknown
- 1976-07-08 SE SE7607853A patent/SE425385B/xx unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1017970A (en) | Process for preparing olefinic hydrocarbons | |
US3401112A (en) | Separation of hydrocarbons by cuprous salts | |
CH626267A5 (no) | ||
KR0173121B1 (ko) | 알킬 메타크릴레이트의 제조 방법 | |
US3020293A (en) | Process for the manufacture of olefin oxidation products from olefin-mercury complexes | |
CH626266A5 (en) | Process for the addition of alcohols or glycol to acetylenic compounds contained in hydrocarbon streams for removing alkyne impurities from the latter | |
CH624084A5 (en) | Process for the preparation of carbonyl products from hydrocarbon streams coming from steam cracker plants | |
JPS60331B2 (ja) | シクロヘキサノンの製造方法 | |
GB1489036A (en) | Process for the continuous preparation of percarboxylic acids in organic solution | |
KR800000899B1 (ko) | 무기 또는 유기 탄화수소류내에 함유된 아세티렌 화합물에 유기산을 첨가하는 방법 | |
US2014850A (en) | Manufacture of carboxylic acid esters from olefines | |
CN210544208U (zh) | 一种尾气处理装置 | |
US3085112A (en) | Preparation of hydrocarbon boron compounds | |
CH618955A5 (en) | Process for the decomposition of tert.-alkyl ethers | |
DK173114B1 (da) | Fremgangsmåde til genvinding af brugt sulfonsyrekatalysator samt anvendelse af fremgangsmåden | |
US4162268A (en) | Process for preparing diacetylbenzene | |
Whitlock Jr | A Convenient Preparation of Benzo [k] fluoranthene | |
FR2329622B1 (no) | ||
Hotta et al. | The Autoxidation of Ethylbenzene in the Presence of the Aqueous Phase | |
Ichikawa et al. | The Kinetics of the Reactions of β-Acetoxyethylmercuric, β-Acetoxypropylmercuric and β-Acetoxy-β-phenylethylmercuric Acetate with Aromatic Substances | |
JPS5522630A (en) | Preparation of alpha-phenylethylamine | |
SU1664783A1 (ru) | Способ удалени примеси ионов железа из концентрированной уксусной кислоты | |
JPS6055513B2 (ja) | 無水マレイン酸の製造方法 | |
ITMI991613A1 (it) | Procedimento per la separazione di olefine leggere da paraffine | |
RU96118976A (ru) | Способ алкилирования изопарафинов c4 - c5 олефинами c3 - c5 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PL | Patent ceased | ||
PL | Patent ceased |