DE2063986C3 - Alkylbenzol sulfomumsalze und deren Verwendung - Google Patents
Alkylbenzol sulfomumsalze und deren VerwendungInfo
- Publication number
- DE2063986C3 DE2063986C3 DE19702063986 DE2063986A DE2063986C3 DE 2063986 C3 DE2063986 C3 DE 2063986C3 DE 19702063986 DE19702063986 DE 19702063986 DE 2063986 A DE2063986 A DE 2063986A DE 2063986 C3 DE2063986 C3 DE 2063986C3
- Authority
- DE
- Germany
- Prior art keywords
- mol
- formula
- benzene
- hydroxyethyl
- salts
- 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
- 150000004996 alkyl benzenes Chemical class 0.000 title claims description 5
- 150000003839 salts Chemical class 0.000 title description 2
- -1 alkyl radical Chemical class 0.000 claims description 13
- 239000000523 sample Substances 0.000 claims description 13
- 239000003112 inhibitor Substances 0.000 claims description 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 238000005260 corrosion Methods 0.000 claims description 5
- 230000007797 corrosion Effects 0.000 claims description 5
- 239000011260 aqueous acid Substances 0.000 claims description 3
- 239000003345 natural gas Substances 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 150000001450 anions Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000003208 petroleum Substances 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 239000002253 acid Substances 0.000 description 9
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000005755 formation reaction Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 235000019738 Limestone Nutrition 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000006028 limestone Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical class OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 3
- 150000003568 thioethers Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- NYIQECIYDUSNRC-UHFFFAOYSA-N 1,2,3,5-tetrapropylbenzene Chemical compound CCCC1=CC(CCC)=C(CCC)C(CCC)=C1 NYIQECIYDUSNRC-UHFFFAOYSA-N 0.000 description 2
- OBQPKGCVMCIETH-UHFFFAOYSA-N 1-chloro-1-(1-chloroethoxy)ethane Chemical compound CC(Cl)OC(C)Cl OBQPKGCVMCIETH-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 101001121386 Homo sapiens Ovochymase-1 Proteins 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 102100026305 Ovochymase-1 Human genes 0.000 description 2
- 238000007265 chloromethylation reaction Methods 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 1
- HXNZYJWGJDFBHG-UHFFFAOYSA-N 1-(chloromethyl)-4-dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=C(CCl)C=C1 HXNZYJWGJDFBHG-UHFFFAOYSA-N 0.000 description 1
- FNPMWZUYKKDAMI-UHFFFAOYSA-N 1-chloroheptylbenzene Chemical compound CCCCCCC(Cl)C1=CC=CC=C1 FNPMWZUYKKDAMI-UHFFFAOYSA-N 0.000 description 1
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenylpropanol Natural products OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 1
- HALFEDSYDFTNIW-UHFFFAOYSA-N 4-tert-butyl-2-(chloromethyl)-1-methylbenzene Chemical compound CC1=CC=C(C(C)(C)C)C=C1CCl HALFEDSYDFTNIW-UHFFFAOYSA-N 0.000 description 1
- GOQSQIWQFWRJJL-UHFFFAOYSA-N CCCCCCCCCCCCC(CCC)(C1=CC=CC=C1)I Chemical compound CCCCCCCCCCCCC(CCC)(C1=CC=CC=C1)I GOQSQIWQFWRJJL-UHFFFAOYSA-N 0.000 description 1
- KLLAZLNVVUPERW-UHFFFAOYSA-M CCCCCCCCCCCCC(C[S+](CCC)CC1=CC=CC=C1)(O)O.[I-] Chemical compound CCCCCCCCCCCCC(C[S+](CCC)CC1=CC=CC=C1)(O)O.[I-] KLLAZLNVVUPERW-UHFFFAOYSA-M 0.000 description 1
- TZFZUKYGFYLZJT-UHFFFAOYSA-N CSCC(O)=C Chemical compound CSCC(O)=C TZFZUKYGFYLZJT-UHFFFAOYSA-N 0.000 description 1
- RZNUCYDMTAHQIH-UHFFFAOYSA-N ClCC(CC1=CC=CC=C1)CC(CCCCCCCC)CCl Chemical compound ClCC(CC1=CC=CC=C1)CC(CCCCCCCC)CCl RZNUCYDMTAHQIH-UHFFFAOYSA-N 0.000 description 1
- DNXHEGUUPJUMQT-CBZIJGRNSA-N Estrone Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 DNXHEGUUPJUMQT-CBZIJGRNSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 102100020846 Methylosome subunit pICln Human genes 0.000 description 1
- 101710201208 Methylosome subunit pICln Proteins 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- KIEKAILMEJNSKU-UHFFFAOYSA-N bis(sulfanyl) sulfate Chemical compound SOS(=O)(=O)OS KIEKAILMEJNSKU-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- ODLMAHJVESYWTB-UHFFFAOYSA-N ethylmethylbenzene Natural products CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- OCKPCBLVNKHBMX-UHFFFAOYSA-N n-butyl-benzene Natural products CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 1
- LIXVMPBOGDCSRM-UHFFFAOYSA-N nonylbenzene Chemical compound CCCCCCCCCC1=CC=CC=C1 LIXVMPBOGDCSRM-UHFFFAOYSA-N 0.000 description 1
- VXNSQGRKHCZUSU-UHFFFAOYSA-N octylbenzene Chemical compound [CH2]CCCCCCCC1=CC=CC=C1 VXNSQGRKHCZUSU-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- XDLNRRRJZOJTRW-UHFFFAOYSA-N thiohypochlorous acid Chemical compound ClS XDLNRRRJZOJTRW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/04—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in markedly acid liquids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/12—Sulfonium compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/72—Eroding chemicals, e.g. acids
- C09K8/74—Eroding chemicals, e.g. acids combined with additives added for specific purposes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19702063986 DE2063986C3 (de) | 1970-12-28 | 1970-12-28 | Alkylbenzol sulfomumsalze und deren Verwendung |
| DD15956671A DD103023A5 (cg-RX-API-DMAC7.html) | 1970-12-28 | 1971-12-14 | |
| GB6006671A GB1373510A (en) | 1970-12-28 | 1971-12-23 | Acid treatment of oil and gas wells |
| NL7117754A NL7117754A (cg-RX-API-DMAC7.html) | 1970-12-28 | 1971-12-23 | |
| IT3291371A IT944361B (it) | 1970-12-28 | 1971-12-24 | Sali di alchilbenzensolfonio e loro impiego nel trattamento aci do di sonde per petrolio e gas naturali |
| AR23981271A AR199273A1 (es) | 1970-12-28 | 1971-12-27 | Sales de alquilbenceno-sulfonico y composiciones que los contienen para el tratamiento de acidos de sondas depetroleo y gas natural |
| BR859371A BR7108593D0 (pt) | 1970-12-28 | 1971-12-27 | Sais de alquilbenzeno-sulfonico assim como sua utilizacao no tratamento acido de sondas de petroleo e de gas natura |
| BE777371A BE777371A (fr) | 1970-12-28 | 1971-12-28 | Sels d'alkyl-benzene-sulfonium et leurs applications |
| FR7147030A FR2120977A5 (cg-RX-API-DMAC7.html) | 1970-12-28 | 1971-12-28 | |
| SU1731619A SU426382A3 (ru) | 1970-12-28 | 1971-12-28 | Ингибитор коррозии |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19702063986 DE2063986C3 (de) | 1970-12-28 | 1970-12-28 | Alkylbenzol sulfomumsalze und deren Verwendung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2063986A1 DE2063986A1 (de) | 1972-07-06 |
| DE2063986B2 DE2063986B2 (de) | 1973-02-15 |
| DE2063986C3 true DE2063986C3 (de) | 1973-09-27 |
Family
ID=5792302
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19702063986 Expired DE2063986C3 (de) | 1970-12-28 | 1970-12-28 | Alkylbenzol sulfomumsalze und deren Verwendung |
Country Status (10)
| Country | Link |
|---|---|
| AR (1) | AR199273A1 (cg-RX-API-DMAC7.html) |
| BE (1) | BE777371A (cg-RX-API-DMAC7.html) |
| BR (1) | BR7108593D0 (cg-RX-API-DMAC7.html) |
| DD (1) | DD103023A5 (cg-RX-API-DMAC7.html) |
| DE (1) | DE2063986C3 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2120977A5 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1373510A (cg-RX-API-DMAC7.html) |
| IT (1) | IT944361B (cg-RX-API-DMAC7.html) |
| NL (1) | NL7117754A (cg-RX-API-DMAC7.html) |
| SU (1) | SU426382A3 (cg-RX-API-DMAC7.html) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2480620A1 (fr) * | 1980-04-18 | 1981-10-23 | Elf Aquitaine | Procede de preparation de microemulsions entre une phase acide et une phase hydrophobe |
| RU2726089C1 (ru) * | 2019-11-28 | 2020-07-09 | Публичное акционерное общество "Газпром" | Способ проведения обработки газовых скважин подземных хранилищ газа |
-
1970
- 1970-12-28 DE DE19702063986 patent/DE2063986C3/de not_active Expired
-
1971
- 1971-12-14 DD DD15956671A patent/DD103023A5/xx unknown
- 1971-12-23 GB GB6006671A patent/GB1373510A/en not_active Expired
- 1971-12-23 NL NL7117754A patent/NL7117754A/xx unknown
- 1971-12-24 IT IT3291371A patent/IT944361B/it active
- 1971-12-27 BR BR859371A patent/BR7108593D0/pt unknown
- 1971-12-27 AR AR23981271A patent/AR199273A1/es active
- 1971-12-28 FR FR7147030A patent/FR2120977A5/fr not_active Expired
- 1971-12-28 BE BE777371A patent/BE777371A/xx unknown
- 1971-12-28 SU SU1731619A patent/SU426382A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| BR7108593D0 (pt) | 1973-06-12 |
| DD103023A5 (cg-RX-API-DMAC7.html) | 1974-01-05 |
| GB1373510A (en) | 1974-11-13 |
| BE777371A (fr) | 1972-06-28 |
| AR199273A1 (es) | 1974-08-23 |
| DE2063986B2 (de) | 1973-02-15 |
| SU426382A3 (ru) | 1974-04-30 |
| IT944361B (it) | 1973-04-20 |
| NL7117754A (cg-RX-API-DMAC7.html) | 1972-06-30 |
| FR2120977A5 (cg-RX-API-DMAC7.html) | 1972-08-18 |
| DE2063986A1 (de) | 1972-07-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) |