HU177372B - Eljárás C2-6 -alkinek eltávolítására telített szénhidrogénekből, olefin- vagy dién-szénhidrogénekbői vagy ezeknek a szénhidrogéneknek az elegyeiből - Google Patents

Eljárás C2-6 -alkinek eltávolítására telített szénhidrogénekből, olefin- vagy dién-szénhidrogénekbői vagy ezeknek a szénhidrogéneknek az elegyeiből Download PDF

Info

Publication number: HU177372B
Authority: HU; Hungary
Prior art keywords: saturated; mixture; hydrocarbons; alkyne; propylene
Prior art date: 1974-05-21

Application number

Other languages

English (en)

Hungarian (hu)

Inventor

Carlo Rescalli

Antonio Pacifico

Original Assignee

Snam Progetti

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.)

1974-05-21

Filing date

1975-05-20

Publication date

1981-09-28

1975-05-20 Application filed by Snam Progetti filed Critical Snam Progetti

1981-09-28 Publication of HU177372B publication Critical patent/HU177372B/hu

Links

238000000034 method Methods 0.000 title claims description 16
239000000203 mixture Substances 0.000 title claims description 15
229920006395 saturated elastomer Polymers 0.000 title claims description 5
125000004432 carbon atom Chemical group C* 0.000 title claims 2
150000001337 aliphatic alkines Chemical class 0.000 title description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 19
229930195733 hydrocarbon Natural products 0.000 claims description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 14
150000002430 hydrocarbons Chemical class 0.000 claims description 12
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 10
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 10
150000001345 alkine derivatives Chemical class 0.000 claims description 7
-1 diene hydrocarbons Chemical class 0.000 claims description 7
WFYPICNXBKQZGB-UHFFFAOYSA-N butenyne Chemical group C=CC#C WFYPICNXBKQZGB-UHFFFAOYSA-N 0.000 claims description 5
239000003456 ion exchange resin Substances 0.000 claims description 5
229920003303 ion-exchange polymer Polymers 0.000 claims description 5
MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 claims description 5
229930195734 saturated hydrocarbon Natural products 0.000 claims description 5
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 claims description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
239000005977 Ethylene Substances 0.000 claims description 4
230000002378 acidificating effect Effects 0.000 claims description 4
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
150000001993 dienes Chemical class 0.000 claims description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
238000004821 distillation Methods 0.000 claims description 2
150000001336 alkenes Chemical class 0.000 claims 4
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
239000011347 resin Substances 0.000 description 10
229920005989 resin Polymers 0.000 description 10
239000007788 liquid Substances 0.000 description 7
150000002170 ethers Chemical class 0.000 description 4
239000004215 Carbon black (E152) Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
XNMQEEKYCVKGBD-UHFFFAOYSA-N 2-butyne Chemical compound CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 2
KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical compound CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 2
ORMNPSYMZOGSSV-UHFFFAOYSA-N dinitrooxymercury Chemical compound [Hg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ORMNPSYMZOGSSV-UHFFFAOYSA-N 0.000 description 2
238000006266 etherification reaction Methods 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
239000012071 phase Substances 0.000 description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N 4-penten-2-one Chemical compound CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
238000005341 cation exchange Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000007599 discharging Methods 0.000 description 1
238000000895 extractive distillation Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
BRMYZIKAHFEUFJ-UHFFFAOYSA-L mercury diacetate Chemical compound CC(=O)O[Hg]OC(C)=O BRMYZIKAHFEUFJ-UHFFFAOYSA-L 0.000 description 1
BQPIGGFYSBELGY-UHFFFAOYSA-N mercury(2+) Chemical group [Hg+2] BQPIGGFYSBELGY-UHFFFAOYSA-N 0.000 description 1
KVICROHOONHSRH-UHFFFAOYSA-N mercury(2+);dinitrate;hydrate Chemical compound O.[Hg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KVICROHOONHSRH-UHFFFAOYSA-N 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000006886 vinylation reaction Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

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

HUSA002794 1974-05-21 1975-05-20 Eljárás C2-6 -alkinek eltávolítására telített szénhidrogénekből, olefin- vagy dién-szénhidrogénekbői vagy ezeknek a szénhidrogéneknek az elegyeiből HU177372B (hu)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT2301174A IT1012688B (it)	1974-05-21	1974-05-21	Metodo per la eliminazione di come posti acstilenici da idrocarburi saturi olefinici e dienici o loro miscele

Publications (1)

Publication Number	Publication Date
HU177372B true HU177372B (hu)	1981-09-28

Family

ID=11202849

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HUSA002794 HU177372B (hu)	1974-05-21	1975-05-20	Eljárás C2-6 -alkinek eltávolítására telített szénhidrogénekből, olefin- vagy dién-szénhidrogénekbői vagy ezeknek a szénhidrogéneknek az elegyeiből

Country Status (5)

Country	Link
CS (1)	CS194226B2 (cs)
HU (1)	HU177372B (cs)
IT (1)	IT1012688B (cs)
MW (1)	MW2975A1 (cs)
ZA (1)	ZA752913B (cs)

1974
- 1974-05-21 IT IT2301174A patent/IT1012688B/it active
1975
- 1975-05-06 ZA ZA00752913A patent/ZA752913B/xx unknown
- 1975-05-12 MW MW2975A patent/MW2975A1/xx unknown
- 1975-05-20 HU HUSA002794 patent/HU177372B/hu unknown
- 1975-05-20 CS CS351675A patent/CS194226B2/cs unknown

Also Published As

Publication number	Publication date
CS194226B2 (en)	1979-11-30
IT1012688B (it)	1977-03-10
ZA752913B (en)	1976-04-28
MW2975A1 (en)	1976-05-12

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