NO130154B - - Google Patents

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Info

Publication number: NO130154B
Authority: NO; Norway
Prior art keywords: gas; olefins; ethylene; concentration; hydration
Prior art date: 1969-12-01

Application number

NO704570A

Other languages

English (en)

Norwegian (no)

Inventor

W Ester

Original Assignee

Veba Chemie Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1969-12-01

Filing date

1970-11-27

Publication date

1974-07-15

1970-11-27 Application filed by Veba Chemie Ag filed Critical Veba Chemie Ag

1974-07-15 Publication of NO130154B publication Critical patent/NO130154B/no

Links

150000001336 alkenes Chemical class 0.000 claims description 31
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 21
239000005977 Ethylene Substances 0.000 claims description 21
230000036571 hydration Effects 0.000 claims description 19
238000006703 hydration reaction Methods 0.000 claims description 19
238000009835 boiling Methods 0.000 claims description 18
238000000034 method Methods 0.000 claims description 18
238000004821 distillation Methods 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 14
239000003921 oil Substances 0.000 claims description 12
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 12
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 12
229930195733 hydrocarbon Natural products 0.000 claims description 11
150000002430 hydrocarbons Chemical class 0.000 claims description 11
150000001298 alcohols Chemical class 0.000 claims description 10
239000012535 impurity Substances 0.000 claims description 9
238000009833 condensation Methods 0.000 claims description 6
230000005494 condensation Effects 0.000 claims description 6
230000003197 catalytic effect Effects 0.000 claims description 4
239000011541 reaction mixture Substances 0.000 claims description 3
239000007789 gas Substances 0.000 description 47
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 25
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 23
239000003054 catalyst Substances 0.000 description 17
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
238000000926 separation method Methods 0.000 description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
230000007423 decrease Effects 0.000 description 7
239000003344 environmental pollutant Substances 0.000 description 7
231100000719 pollutant Toxicity 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
238000005265 energy consumption Methods 0.000 description 6
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 5
239000007788 liquid Substances 0.000 description 5
229910000147 aluminium phosphate Inorganic materials 0.000 description 4
239000000047 product Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000001816 cooling Methods 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000003595 mist Substances 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000000126 substance Substances 0.000 description 3
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
238000002485 combustion reaction Methods 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
238000005470 impregnation Methods 0.000 description 2
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
238000013021 overheating Methods 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000000376 reactant Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
230000007306 turnover Effects 0.000 description 2
238000009834 vaporization Methods 0.000 description 2
230000008016 vaporization Effects 0.000 description 2
238000005406 washing Methods 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000003990 capacitor Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
238000005336 cracking Methods 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
239000000539 dimer Substances 0.000 description 1
238000007700 distillative separation Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
239000001282 iso-butane Substances 0.000 description 1
238000002386 leaching Methods 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000001294 propane Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000003507 refrigerant Substances 0.000 description 1
230000000630 rising effect Effects 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
239000013638 trimer Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/03—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
- C07C29/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

NO704570A 1969-12-01 1970-11-27 NO130154B (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE1960139A DE1960139B2 (de)	1969-12-01	1969-12-01	Verfahren zur Herstellung von Alkoholen durch Hydratisierung von Olefinen mit 2-3 C - Atomen

Publications (1)

Publication Number	Publication Date
NO130154B true NO130154B (fr)	1974-07-15

Family

ID=5752564

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO704570A NO130154B (fr)	1969-12-01	1970-11-27

Country Status (15)

Country	Link
JP (1)	JPS519728B1 (fr)
AT (1)	AT305225B (fr)
BE (1)	BE759556A (fr)
BR (1)	BR7024140D0 (fr)
CA (1)	CA927401A (fr)
CH (1)	CH545258A (fr)
DE (1)	DE1960139B2 (fr)
ES (1)	ES385953A1 (fr)
FI (1)	FI50619C (fr)
FR (1)	FR2072568A5 (fr)
GB (1)	GB1337570A (fr)
NL (1)	NL7017282A (fr)
NO (1)	NO130154B (fr)
SE (1)	SE393100B (fr)
ZA (1)	ZA708046B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3733368A (en) *	1971-07-02	1973-05-15	Shell Oil Co	Process for the separation of polymers from a recycle stream that contains ethylene
KR102673700B1 (ko) *	2021-05-31	2024-06-07	주식회사 엘지화학	이소프로필 알코올 제조방법

0
- BE BE759556D patent/BE759556A/fr not_active IP Right Cessation
1969
- 1969-12-01 DE DE1960139A patent/DE1960139B2/de not_active Ceased
1970
- 1970-11-25 BR BR224140/70A patent/BR7024140D0/pt unknown
- 1970-11-26 GB GB5629270A patent/GB1337570A/en not_active Expired
- 1970-11-26 SE SE7016059A patent/SE393100B/xx unknown
- 1970-11-26 NL NL7017282A patent/NL7017282A/xx unknown
- 1970-11-27 ES ES385953A patent/ES385953A1/es not_active Expired
- 1970-11-27 FI FI703202A patent/FI50619C/fi active
- 1970-11-27 ZA ZA708046A patent/ZA708046B/xx unknown
- 1970-11-27 JP JP45104146A patent/JPS519728B1/ja active Pending
- 1970-11-27 CH CH1759070A patent/CH545258A/de not_active IP Right Cessation
- 1970-11-27 FR FR7042823A patent/FR2072568A5/fr not_active Expired
- 1970-11-27 AT AT1069570A patent/AT305225B/de not_active IP Right Cessation
- 1970-11-27 NO NO704570A patent/NO130154B/no unknown
- 1970-11-30 CA CA099472A patent/CA927401A/en not_active Expired

Also Published As

Publication number	Publication date
DE1960139A1 (de)	1971-06-03
FI50619C (fi)	1976-05-10
ES385953A1 (es)	1973-05-01
BE759556A (fr)	1971-04-30
AT305225B (de)	1973-02-12
CH545258A (de)	1973-12-15
NL7017282A (fr)	1971-06-03
ZA708046B (en)	1971-09-29
JPS519728B1 (fr)	1976-03-30
FI50619B (fr)	1976-02-02
FR2072568A5 (fr)	1971-09-24
DE1960139B2 (de)	1978-10-05
CA927401A (en)	1973-05-29
BR7024140D0 (pt)	1973-01-16
GB1337570A (en)	1973-11-14
SE393100B (sv)	1977-05-02

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US4956513A (en)	1990-09-11	Recovery of BF3 from olefin oligomer process
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US3953533A (en)	1976-04-27	Process for the hydration of olefins to alcohols
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US2403977A (en)	1946-07-16	Dichlorides of the ethylene series
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