GB587378A - Improvements in or relating to the manufacture of ethylene - Google Patents
Improvements in or relating to the manufacture of ethyleneInfo
- Publication number
- GB587378A GB587378A GB2417244A GB2417244A GB587378A GB 587378 A GB587378 A GB 587378A GB 2417244 A GB2417244 A GB 2417244A GB 2417244 A GB2417244 A GB 2417244A GB 587378 A GB587378 A GB 587378A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dehydration
- polymerization
- atmospheres
- pressure
- catalyst
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
- C07C1/24—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms by elimination of water
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
- C07C11/04—Ethylene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/02—Boron or aluminium; Oxides or hydroxides thereof
- C07C2521/04—Alumina
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/14—Phosphorus; Compounds thereof
- C07C2527/16—Phosphorus; Compounds thereof containing oxygen
- C07C2527/167—Phosphates or other compounds comprising the anion (PnO3n+1)(n+2)-
- C07C2527/173—Phosphoric acid or other acids with the formula Hn+2PnO3n+1
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Ethylene is produced directly under pressure by subjecting ethanol to contact with a dehydration catalyst at a pressure between 350 and 1500 atmospheres and at high temperature preferably 300-600 DEG C., and if desired cooling and/or scrubbing the ethylene obtained. The ethylene produced is contacted with an ethylene polymerization catalyst while still at an elevated temperature and pressure to produce polymerization products. Dehydration catalysts include acid catalysts such as phosphoric acid which may be suspended on an inert porous material such as coke or pumice, cadmium phosphate, and inorganic catalysts such as alumina and activated clays. Polymerization catalysts include oxygen, peroxides such as hydrogen peroxide, alkyl and acyl peroxides and alkyl hydroperoxides; per acids and their salts such as persuccinic acid, alkali persulphates, percarbonates and perborates, amine oxide, hydrazine, oximes; and organo-metallic compounds such as lithium butyl. For oxygen catalyst the polymerization temperature is greater than 100 DEG C., and the pressure exceeds 500 atmospheres. For catalysts such as per compounds, the temperature is preferably 60 DEG to 150 DEG C. and the pressure 70 to 1000 atmospheres. It is advantageous to use the same pressure for dehydration and polymerization. Some cooling of the dehydration products is generally necessary and the crude ethylene should be separated from the dehydration catalyst. Liquid polymerization products are obtained when temperatures of 300-400 DEG C. and pressures of 50-100 atmospheres are employed. Interpolymers with compounds having carbon-carbon double bonds may also be obtained by adding such compounds after dehydration. Dehydration is preferably conducted in a hot reaction zone such as a tubular reaction vessel and the dehydration products are then passed continuously through a cooler and then into a second reaction zone for polymerization. In examples: (1) dehydration is effected at 310 DEG C. and 1500 atmospheres pressure with orthophosphoric acid as catalyst; (2) using the same catalyst dehydration is carried out at 300 DEG C. and 300 atmospheres. The temperature is lowered to 120 DEG C. and polymerization is effected in the presence of benzoyl peroxide. Specifications 317,500, [Class 2 (iii)], 471,590, 497,643, 578,584 and 8070/40 (as open to inspection under Sect. 91) are referred to. In the first Provisional Specification, the dehydration catalysts also include concentrated sulphuric acid and caustic soda and the dehydration pressure is above 50 atmospheres. The second Provisional Specification states that dehydration and polymerization may be carried out simultaneously.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL63902D NL63902C (en) | 1944-12-04 | ||
GB2417244A GB587378A (en) | 1944-12-04 | 1944-12-04 | Improvements in or relating to the manufacture of ethylene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2417244A GB587378A (en) | 1944-12-04 | 1944-12-04 | Improvements in or relating to the manufacture of ethylene |
Publications (1)
Publication Number | Publication Date |
---|---|
GB587378A true GB587378A (en) | 1947-04-23 |
Family
ID=10207541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2417244A Expired GB587378A (en) | 1944-12-04 | 1944-12-04 | Improvements in or relating to the manufacture of ethylene |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB587378A (en) |
NL (1) | NL63902C (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2978396A (en) * | 1956-12-18 | 1961-04-04 | Exxon Research Engineering Co | Radiation induced ethylene polymerization |
US4232179A (en) * | 1977-08-09 | 1980-11-04 | Petroleo Brasileiro S.A.-Petrobras | Process for preparing ethene |
WO2000001335A1 (en) * | 1998-07-02 | 2000-01-13 | Sca Hygiene Products Ab | Use of a polyethene material produced from renewable raw material as component of an absorbent article, and the absorbent article |
EP2188051A1 (en) * | 2007-08-13 | 2010-05-26 | Agency for Science, Technology and Research | Modified catalyst composition for conversion of alcohol to alkene |
DE102012200996A1 (en) | 2012-01-24 | 2013-07-25 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Process for the preparation of ethylene and other olefins from aqueous solutions of the corresponding alcohols |
EP2367777B1 (en) * | 2008-12-11 | 2019-04-03 | Total Research & Technology Feluy | Process to make alpha olefins from ethanol |
-
0
- NL NL63902D patent/NL63902C/xx active
-
1944
- 1944-12-04 GB GB2417244A patent/GB587378A/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2978396A (en) * | 1956-12-18 | 1961-04-04 | Exxon Research Engineering Co | Radiation induced ethylene polymerization |
US4232179A (en) * | 1977-08-09 | 1980-11-04 | Petroleo Brasileiro S.A.-Petrobras | Process for preparing ethene |
WO2000001335A1 (en) * | 1998-07-02 | 2000-01-13 | Sca Hygiene Products Ab | Use of a polyethene material produced from renewable raw material as component of an absorbent article, and the absorbent article |
EP2188051A1 (en) * | 2007-08-13 | 2010-05-26 | Agency for Science, Technology and Research | Modified catalyst composition for conversion of alcohol to alkene |
EP2188051A4 (en) * | 2007-08-13 | 2011-11-02 | Agency Science Tech & Res | Modified catalyst composition for conversion of alcohol to alkene |
EP2367777B1 (en) * | 2008-12-11 | 2019-04-03 | Total Research & Technology Feluy | Process to make alpha olefins from ethanol |
DE102012200996A1 (en) | 2012-01-24 | 2013-07-25 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Process for the preparation of ethylene and other olefins from aqueous solutions of the corresponding alcohols |
WO2013110723A1 (en) | 2012-01-24 | 2013-08-01 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Process for preparing ethylene and other olefins from aqueous solutions of the corresponding alcohols |
US9714200B2 (en) | 2012-01-24 | 2017-07-25 | Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung E.V. | Process for preparing ethylene and other olefins from aqueous solutions of the corresponding alcohols |
DE102012200996B4 (en) * | 2012-01-24 | 2017-09-07 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Process for the preparation of ethylene and other olefins from aqueous solutions of the corresponding alcohols |
Also Published As
Publication number | Publication date |
---|---|
NL63902C (en) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB641250A (en) | Process for the manufacture of di-isopropyl-benzene hydro-peroxides and products resulting therefrom | |
GB587378A (en) | Improvements in or relating to the manufacture of ethylene | |
GB623669A (en) | Manufacture of glycol esters of terephthalic acid | |
GB991818A (en) | Improvements in or relating to the preparation of sultones | |
US1586803A (en) | Process of polymerizing vinyl esters | |
GB627293A (en) | Improvements in and relating to the hydrogenation of furfural | |
US2728756A (en) | Di-tert-butyl peroxydicarbonate for ethylene polymerization | |
GB654035A (en) | Manufacture of beta-isopropylnaphthalene hydroperoxide and beta-naphthol | |
US2365264A (en) | Production of oxygen-containing | |
US2189655A (en) | Conversion of hydrocarbons | |
GB638754A (en) | Improvements in and relating to the synthesis of primary alcohols | |
GB873614A (en) | Improvements in or relating to the production of substituted cyclohexanone peroxides | |
GB566344A (en) | Polymerization of allyl type primary alcohols and products obtainable thereby | |
MX7150E (en) | PROCEDURE FOR OBTAINING DIESTERS OF SULFO-SUCCINIC ACID | |
US2420749A (en) | Treatment of monocyclic olefinic hydrocarbons | |
US2447414A (en) | Oxidation of isopropylbiphenyl | |
GB942367A (en) | Continuous production of carboxylic acids from olefines, carbon monoxide and water | |
US2375024A (en) | Isomerization of poly-olefinic hydrocarbons | |
SU490796A1 (en) | Method for producing alkylcyclohexane hydroperoxides | |
US1510425A (en) | Process for the production of ethylesters of halogen sulphonic acids | |
GB908497A (en) | Process for the preparation of ª-,ª--dialkylbranched carboxylic acids | |
SU283221A1 (en) | Method for producing unsaturated organic peroxides | |
GB616829A (en) | Improvements in and relating to the production of alkyl phenols | |
JPS6434929A (en) | Method for dehydrating reaction of ethanol | |
GB368935A (en) | Improvements in the manufacture and production of aliphatic alcohols |