GB885871A - Process for the manufacture of carbonyl sulfide - Google Patents

Process for the manufacture of carbonyl sulfide

Info

Publication number
GB885871A
GB885871A GB25686/60A GB2568660A GB885871A GB 885871 A GB885871 A GB 885871A GB 25686/60 A GB25686/60 A GB 25686/60A GB 2568660 A GB2568660 A GB 2568660A GB 885871 A GB885871 A GB 885871A
Authority
GB
United Kingdom
Prior art keywords
alo2
sio2
cos
condensed
flows
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
GB25686/60A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Oil Corp
Original Assignee
Socony Mobil Oil Co Inc
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.)
Filing date
Publication date
Application filed by Socony Mobil Oil Co Inc filed Critical Socony Mobil Oil Co Inc
Publication of GB885871A publication Critical patent/GB885871A/en
Expired legal-status Critical Current

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  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

Carbonyl sulphide, COS, is prepared by reacting CO and S vapour in molar ratio 0,5-2:1 at 500-900 DEG F. in the presence of a dehydrated crystalline alumino-silicate catalyst having rigid three-dimensional networks made up of unit cells characterized by absence of change in unit cell dimensions upon dehydration and rehydration, and a sorption capacity at 760 mm. and 25 DEG C. of at least 4% of n-butane. Pressure may be atmospheric-50 psig. and space velocities 5-25,000 v/v/hr. Catalysts may be zeolitic molecular sieves, e.g. Na12(AlO2)12(SiO2)12, 27 H2O, Na86[(AlO2)86(SiO2)106 267H2O, or the corresponding Ca salts. CO enters externally heated jacket 11 at 12 and flows through molten S and aperture 13 to cylindrical reactor 10. Further CO may be added at 15 and the mixture flows through catalyst on sintered disc 14. The <PICT:0885871/III/1> resulting mixture flows through S condenser 18 maintained at 120 DEG C. by steam in jacket 19, and condensed S is separated in 22. Remaining gas is condensed in trap 25 at -78 DEG C. and COS is distilled from column 27 at 28.
GB25686/60A 1959-07-22 1960-07-22 Process for the manufacture of carbonyl sulfide Expired GB885871A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US885871XA 1959-07-22 1959-07-22

Publications (1)

Publication Number Publication Date
GB885871A true GB885871A (en) 1961-12-28

Family

ID=22212237

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25686/60A Expired GB885871A (en) 1959-07-22 1960-07-22 Process for the manufacture of carbonyl sulfide

Country Status (1)

Country Link
GB (1) GB885871A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522793A (en) * 1983-06-28 1985-06-11 Phillips Petroleum Company Removing H2 S from natural gas using two-stage molecular sieves
CN113336227A (en) * 2021-05-31 2021-09-03 成都市科隆化学品有限公司 Benzene-free carbon disulfide and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522793A (en) * 1983-06-28 1985-06-11 Phillips Petroleum Company Removing H2 S from natural gas using two-stage molecular sieves
CN113336227A (en) * 2021-05-31 2021-09-03 成都市科隆化学品有限公司 Benzene-free carbon disulfide and preparation method thereof

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