ES239809A1 - A procedure for obtaining tri- and tetra-clorethylene (Machine-translation by Google Translate, not legally binding) - Google Patents

A procedure for obtaining tri- and tetra-clorethylene (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES239809A1
ES239809A1 ES0239809A ES239809A ES239809A1 ES 239809 A1 ES239809 A1 ES 239809A1 ES 0239809 A ES0239809 A ES 0239809A ES 239809 A ES239809 A ES 239809A ES 239809 A1 ES239809 A1 ES 239809A1
Authority
ES
Spain
Prior art keywords
translation
machine
legally binding
google translate
clorethylene
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
ES0239809A
Other languages
Spanish (es)
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.)
DAEELECTROCHIMIE D ELECTROMETA
Original Assignee
DAEELECTROCHIMIE D ELECTROMETA
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 DAEELECTROCHIMIE D ELECTROMETA filed Critical DAEELECTROCHIMIE D ELECTROMETA
Priority to ES0239809A priority Critical patent/ES239809A1/en
Publication of ES239809A1 publication Critical patent/ES239809A1/en
Expired legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Process for obtaining tri- and tetrachlorethylene in a single phase, by chlorination of 1,2-dichlorethylene, in relative molar proportions comprised between 0 and 80% of trichlorethylene, in the presence of catalysts, said method being characterized because it is passed through, preferably at high speed, through a fluidized solid catalytic mass maintained between 350º and 450º c, a mixture containing chlorine and dichlorethylene, in the proportions necessary to obtain in permanent regime the total chlorine fixation by formation of the desired relative amounts of tri- and tetrachlorethylene. (Machine-translation by Google Translate, not legally binding)
ES0239809A 1958-01-28 1958-01-28 A procedure for obtaining tri- and tetra-clorethylene (Machine-translation by Google Translate, not legally binding) Expired ES239809A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
ES0239809A ES239809A1 (en) 1958-01-28 1958-01-28 A procedure for obtaining tri- and tetra-clorethylene (Machine-translation by Google Translate, not legally binding)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES0239809A ES239809A1 (en) 1958-01-28 1958-01-28 A procedure for obtaining tri- and tetra-clorethylene (Machine-translation by Google Translate, not legally binding)

Publications (1)

Publication Number Publication Date
ES239809A1 true ES239809A1 (en) 1958-10-01

Family

ID=37841622

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0239809A Expired ES239809A1 (en) 1958-01-28 1958-01-28 A procedure for obtaining tri- and tetra-clorethylene (Machine-translation by Google Translate, not legally binding)

Country Status (1)

Country Link
ES (1) ES239809A1 (en)

Similar Documents

Publication Publication Date Title
FR1262906A (en) Preparation of inverted images by the electrophotographic process
OA03370A (en) Process for the preparation of 19-nor-4.9 (10) -steroids.
ES295136A1 (en) A procedure for preparing halogenated derivatives of aliphatic hydrocarbons (Machine-translation by Google Translate, not legally binding)
CH395062A (en) Process for preparing allyl chloride
ES295137A1 (en) Procedure for the preparation of halogenated derivatives of aliphatic hydrocarbons (Machine-translation by Google Translate, not legally binding)
ES290244A1 (en) A procedure to make foamed polyprolactama (Machine-translation by Google Translate, not legally binding)
FR1285236A (en) Process for the preparation of 1, 3-diaryl-5-amino-pyridazones- (6)
FR1245579A (en) Process for the preparation of alkaline adducts of certain aromatic hydrocarbons
GB1016383A (en) Improved process for the preparation of quaternary ammonium compounds
OA00958A (en) Process for the preparation of 1,4-benzodiapine derivatives.
FR1312859A (en) Process for preparing 1.2-dichloroethane by oxychlorination of ethylene
ES280868A1 (en) A continuous procedure for the preparation of organic compounds and/or chlorofluorates starting directly from methane (Machine-translation by Google Translate, not legally binding)
JPS5238489A (en) Xylene isomerization catalyst
FR1309871A (en) Process for preparing 1, 1-dichloroethane from vinyl chloride
ES294852A1 (en) Procedure and apparatus for the preparation of chlorine solvents (Machine-translation by Google Translate, not legally binding)
ES233923A1 (en) A procedure for obtaining halogenated hydrocarbons and mixtures thereof (Machine-translation by Google Translate, not legally binding)
ES295089A3 (en) A procedure for obtaining sulfa-alcoxypiridines (Machine-translation by Google Translate, not legally binding)
ES232444A1 (en) Procedure for the obtaining of cyclic dicarbonic acids and their salts (Machine-translation by Google Translate, not legally binding)
BE597958A (en) Process for preparing vinyl chloride starting from methane.
FR1272913A (en) Process for the preparation of 5-alkyl-2-p-halogenobenzenesulfonamido-1, 3, 4-thiadiazoles
BE603702A (en) Process for the preparation of 3-amino-1,2,3-benzotriazinones- (4)
ES239231A1 (en) A procedure for the isomerization of hydrocarbons (Machine-translation by Google Translate, not legally binding)
ES223024A1 (en) A procedure for the manufacture of poly-ethylene chlorification products (Machine-translation by Google Translate, not legally binding)
BE588830A (en) Process for the preparation of 2,3-dimercaptoquinoxaline derivatives.
FR1247414A (en) Improved process for the preparation of 18.20 alpha-oxidopregnans