SI9620009A - Method of producing anhydrous ethylene chlorohydrin of high purity - Google Patents
Method of producing anhydrous ethylene chlorohydrin of high purity Download PDFInfo
- Publication number
- SI9620009A SI9620009A SI9620009A SI9620009A SI9620009A SI 9620009 A SI9620009 A SI 9620009A SI 9620009 A SI9620009 A SI 9620009A SI 9620009 A SI9620009 A SI 9620009A SI 9620009 A SI9620009 A SI 9620009A
- Authority
- SI
- Slovenia
- Prior art keywords
- reactor
- stage
- hydrogen chloride
- ethylene
- ech
- Prior art date
Links
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 title claims abstract description 55
- 238000000034 method Methods 0.000 title claims description 30
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 44
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 42
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims abstract description 42
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims abstract description 42
- 238000006243 chemical reaction Methods 0.000 claims abstract description 26
- 239000006096 absorbing agent Substances 0.000 claims abstract description 8
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 5
- 238000004519 manufacturing process Methods 0.000 claims description 14
- 239000002912 waste gas Substances 0.000 claims description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 4
- 230000004060 metabolic process Effects 0.000 claims description 4
- -1 polytetrafluoroethylene Polymers 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 3
- 238000006386 neutralization reaction Methods 0.000 claims description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims 1
- 239000002250 absorbent Substances 0.000 claims 1
- 230000002745 absorbent Effects 0.000 claims 1
- 238000003860 storage Methods 0.000 abstract description 4
- 239000007789 gas Substances 0.000 abstract description 3
- 238000005201 scrubbing Methods 0.000 abstract 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000000376 reactant Substances 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- HUTXVUPGARJNHM-UHFFFAOYSA-N 1-(2-chloroethoxy)ethanol Chemical compound CC(O)OCCCl HUTXVUPGARJNHM-UHFFFAOYSA-N 0.000 description 2
- LECMBPWEOVZHKN-UHFFFAOYSA-N 2-(2-chloroethoxy)ethanol Chemical compound OCCOCCCl LECMBPWEOVZHKN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000007033 dehydrochlorination reaction Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VZIQXGLTRZLBEX-UHFFFAOYSA-N 2-chloro-1-propanol Chemical compound CC(Cl)CO VZIQXGLTRZLBEX-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000007038 hydrochlorination reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001577 simple distillation Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 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
- C07C29/64—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by simultaneous introduction of -OH groups and halogens
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SK419-95A SK282309B6 (sk) | 1995-03-31 | 1995-03-31 | Spôsob výroby bezvodého etylénchlórhydrínu vysokej čistoty |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI9620009A true SI9620009A (en) | 1997-08-31 |
Family
ID=20433528
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI9620009A SI9620009A (en) | 1995-03-31 | 1996-03-28 | Method of producing anhydrous ethylene chlorohydrin of high purity |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPH10501820A (cs) |
| CZ (1) | CZ288187B6 (cs) |
| HU (1) | HU218823B (cs) |
| PL (1) | PL185059B1 (cs) |
| SI (1) | SI9620009A (cs) |
| SK (1) | SK282309B6 (cs) |
| WO (1) | WO1996030324A1 (cs) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2277082C1 (ru) * | 2004-09-27 | 2006-05-27 | Открытое акционерное общество "Сибур-Нефтехим" | Способ вакуумной ректификации этиленхлоргидрина |
| FR2935968B1 (fr) * | 2008-09-12 | 2010-09-10 | Solvay | Procede pour la purification de chlorure d'hydrogene |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE968902C (de) * | 1952-07-26 | 1958-04-10 | Basf Ag | Verfahren zur Herstellung von Alkylenchlorhydrinen |
| SU130502A1 (ru) * | 1959-11-11 | 1959-11-30 | А.Я. Берштейн | Способ получени безводного этиленхлоргидрина |
| RO60731A2 (cs) * | 1971-01-05 | 1976-07-15 | ||
| DD137096A1 (de) * | 1978-06-13 | 1979-08-15 | Klaus Gaertner | Verfahren zur kontinuierlichen herstellung von wasser-und chlorwasserstofffreiem aethylenchlorhydrin |
| DD298237A5 (de) * | 1989-02-03 | 1992-02-13 | Buna Ag,De | Verfahren zur herstellung von reinem ethylenchlorhydrin aus ethylenoxid und chlorwasserstoff |
-
1995
- 1995-03-31 SK SK419-95A patent/SK282309B6/sk unknown
-
1996
- 1996-03-28 WO PCT/SK1996/000004 patent/WO1996030324A1/en not_active Ceased
- 1996-03-28 HU HU9603307A patent/HU218823B/hu not_active IP Right Cessation
- 1996-03-28 SI SI9620009A patent/SI9620009A/sl not_active IP Right Cessation
- 1996-03-28 PL PL96317398A patent/PL185059B1/pl not_active IP Right Cessation
- 1996-03-28 CZ CZ19963636A patent/CZ288187B6/cs not_active IP Right Cessation
- 1996-03-28 JP JP8529286A patent/JPH10501820A/ja not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CZ363696A3 (en) | 1997-06-11 |
| HUP9603307A3 (en) | 1998-04-28 |
| WO1996030324A1 (en) | 1996-10-03 |
| SK282309B6 (sk) | 2002-01-07 |
| JPH10501820A (ja) | 1998-02-17 |
| PL317398A1 (en) | 1997-04-14 |
| PL185059B1 (pl) | 2003-02-28 |
| CZ288187B6 (en) | 2001-05-16 |
| HU218823B (hu) | 2000-12-28 |
| SK41995A3 (en) | 1997-06-04 |
| HUP9603307A2 (en) | 1997-05-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP3024779B1 (en) | Synthesis of hydrogen bis(fluorosulfonyl)imide | |
| KR102659513B1 (ko) | 수소 비스(플루오로설포닐)이미드의 제조 방법 | |
| KR100365081B1 (ko) | 포스겐의제조방법 | |
| CN114011101B (zh) | 环状碳酸亚烷基酯的工业制造方法 | |
| CN112723313A (zh) | 一种制备三氟化氯的方法 | |
| KR20080085717A (ko) | 고순도 실리콘의 제조 방법 | |
| US3839475A (en) | Process for the production of ethylene dichloride | |
| CN108409526B (zh) | 一种一氯甲烷节能生产系统及方法 | |
| KR101392944B1 (ko) | 사염화실란으로부터 삼염화실란을 제조하는 방법 및 이에 사용되는 트리클 베드 반응기 | |
| JP4134761B2 (ja) | 亜硝酸アルキルの製法 | |
| SI9620009A (en) | Method of producing anhydrous ethylene chlorohydrin of high purity | |
| JP3650581B2 (ja) | アンモニア製造のための方法及びコンバータ | |
| CN102101650B (zh) | 一种采用微反应器进行氯化氢氧化制备氯气的方法 | |
| JP2003183191A (ja) | 塩化メチルの製造方法 | |
| US3059035A (en) | Continuous process for producing methyl chloroform | |
| CN115924864B (zh) | 一种丁酮连氮水解制备水合肼的方法 | |
| CN113511954B (zh) | 一种1,2,3-三氯丙烷的连续流制备方法 | |
| CN113549027B (zh) | 2-氯-5-氯甲基噻唑连续化生产工艺 | |
| RU2041194C1 (ru) | Способ получения октафторпропана и реактор для его осуществления | |
| CN108484524A (zh) | 一种氯甲基硫氮茂的合成方法 | |
| US9617155B2 (en) | Production of trisilylamine from monochlorosilane and ammonia by use of inert solvent | |
| EP4045458B1 (en) | Process for preparation of chlorine from hydrogen chloride | |
| EP0057629B1 (en) | Vapor state process for the preparation of diesters of oxalic acid | |
| KR100734383B1 (ko) | 삼플루오르화질소의 제조 방법 | |
| KR0134544B1 (ko) | 디플루오로메탄의 제조방법 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| IF | Valid on the event date | ||
| KO00 | Lapse of patent |
Effective date: 20060206 |