SE500299C2 - En vattenhaltig, alkalisk metallbearbetningsvätska innehållande en primär amin - Google Patents

En vattenhaltig, alkalisk metallbearbetningsvätska innehållande en primär amin

Info

Publication number: SE500299C2
Authority: SE; Sweden
Prior art keywords: synthetic; semi; primary amine; corrosion; carbon atoms
Prior art date: 1992-11-25

Application number

SE9203539A

Other languages

English (en)

Swedish (sv)

Other versions

SE9203539D0 (sv

SE9203539L (sv

Inventor

Rolf Skoeld

Patrick J Ruane

Original Assignee

Berol Nobel Ab

Castrol Ltd

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.)

1992-11-25

Filing date

1992-11-25

Publication date

1994-05-30

1992-11-25 Application filed by Berol Nobel Ab, Castrol Ltd filed Critical Berol Nobel Ab

1992-11-25 Priority to SE9203539A priority Critical patent/SE500299C2/sv

1992-11-25 Publication of SE9203539D0 publication Critical patent/SE9203539D0/xx

1993-11-11 Priority to PCT/SE1993/000958 priority patent/WO1994012028A1/en

1993-11-11 Priority to JP6513032A priority patent/JPH08503726A/ja

1993-11-11 Priority to DK94901103T priority patent/DK0670675T3/da

1993-11-11 Priority to ES94901103T priority patent/ES2132370T3/es

1993-11-11 Priority to AU55805/94A priority patent/AU5580594A/en

1993-11-11 Priority to DE69324155T priority patent/DE69324155T2/de

1993-11-11 Priority to AT94901103T priority patent/ATE177901T1/de

1993-11-11 Priority to EP94901103A priority patent/EP0670675B1/en

1994-05-26 Publication of SE9203539L publication Critical patent/SE9203539L/

1994-05-30 Publication of SE500299C2 publication Critical patent/SE500299C2/sv

Links

238000005555 metalworking Methods 0.000 title claims abstract description 22
125000002924 primary amino group Chemical class [H]N([H])* 0.000 title claims 4
239000012530 fluid Substances 0.000 title abstract description 13
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
150000003839 salts Chemical class 0.000 claims abstract description 15
125000002015 acyclic group Chemical group 0.000 claims abstract description 4
239000007788 liquid Substances 0.000 claims description 18
125000000217 alkyl group Chemical group 0.000 claims description 8
239000000839 emulsion Substances 0.000 claims description 5
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
150000003141 primary amines Chemical class 0.000 abstract description 17
XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 abstract description 6
239000004599 antimicrobial Substances 0.000 abstract description 3
238000005260 corrosion Methods 0.000 description 27
230000007797 corrosion Effects 0.000 description 25
238000012360 testing method Methods 0.000 description 19
239000000203 mixture Substances 0.000 description 17
150000001412 amines Chemical class 0.000 description 16
-1 3-aminopropyl alkyl ethers Chemical class 0.000 description 13
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
238000009472 formulation Methods 0.000 description 12
239000003112 inhibitor Substances 0.000 description 10
150000002430 hydrocarbons Chemical group 0.000 description 9
239000002054 inoculum Substances 0.000 description 8
239000000314 lubricant Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 6
150000001298 alcohols Chemical class 0.000 description 6
230000001580 bacterial effect Effects 0.000 description 6
241000233866 Fungi Species 0.000 description 5
229910052500 inorganic mineral Inorganic materials 0.000 description 5
239000011707 mineral Substances 0.000 description 5
XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 4
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239000002028 Biomass Substances 0.000 description 4
239000003945 anionic surfactant Substances 0.000 description 4
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239000002736 nonionic surfactant Substances 0.000 description 4
239000003921 oil Substances 0.000 description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
239000000126 substance Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
239000005662 Paraffin oil Substances 0.000 description 3
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150000001408 amides Chemical class 0.000 description 3
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150000001991 dicarboxylic acids Chemical class 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
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230000002401 inhibitory effect Effects 0.000 description 3
239000002609 medium Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
150000002763 monocarboxylic acids Chemical class 0.000 description 3
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
239000005642 Oleic acid Substances 0.000 description 2
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000003973 alkyl amines Chemical class 0.000 description 2
CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
239000004327 boric acid Substances 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
239000002173 cutting fluid Substances 0.000 description 2
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
239000012895 dilution Substances 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000008103 glucose Substances 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
238000011081 inoculation Methods 0.000 description 2
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
229920013639 polyalphaolefin Polymers 0.000 description 2
230000009467 reduction Effects 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000000344 soap Substances 0.000 description 2
150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
230000004083 survival effect Effects 0.000 description 2
239000000725 suspension Substances 0.000 description 2
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
208000035143 Bacterial infection Diseases 0.000 description 1
240000002791 Brassica napus Species 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
241000282465 Canis Species 0.000 description 1
229910001018 Cast iron Inorganic materials 0.000 description 1
241000135254 Cephalosporium sp. Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
206010017533 Fungal infection Diseases 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
208000031888 Mycoses Diseases 0.000 description 1
OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
241000589517 Pseudomonas aeruginosa Species 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
AMZKGJLFYCZDMJ-WRBBJXAJSA-N [2,2-dimethyl-3-[(z)-octadec-9-enoyl]oxypropyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCC\C=C/CCCCCCCC AMZKGJLFYCZDMJ-WRBBJXAJSA-N 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
239000008272 agar Substances 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
JMJRNNLOJLYQLM-UHFFFAOYSA-N azane;propan-1-ol Chemical compound N.CCCO JMJRNNLOJLYQLM-UHFFFAOYSA-N 0.000 description 1
208000022362 bacterial infectious disease Diseases 0.000 description 1
239000002585 base Substances 0.000 description 1
239000007853 buffer solution Substances 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
235000013351 cheese Nutrition 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
229960005091 chloramphenicol Drugs 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000002826 coolant Substances 0.000 description 1
150000004696 coordination complex Chemical class 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
238000010908 decantation Methods 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
244000144992 flock Species 0.000 description 1
238000005187 foaming Methods 0.000 description 1
238000004362 fungal culture Methods 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
150000002443 hydroxylamines Chemical class 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
230000003993 interaction Effects 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
230000007774 longterm Effects 0.000 description 1
238000003754 machining Methods 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
239000004530 micro-emulsion Substances 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
239000003002 pH adjusting agent Substances 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000002304 perfume Substances 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000001603 reducing effect Effects 0.000 description 1
239000003507 refrigerant Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
239000008137 solubility enhancer Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
238000010998 test method Methods 0.000 description 1
150000004867 thiadiazoles Chemical class 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
LBSIDDOMEWFXBT-UHFFFAOYSA-N tridecan-3-ol Chemical compound CCCCCCCCCCC(O)CC LBSIDDOMEWFXBT-UHFFFAOYSA-N 0.000 description 1
HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
229940038773 trisodium citrate Drugs 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/08—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic with only one hydroxy group and one amino group bound to the carbon skeleton
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/08—Amines; Quaternary ammonium compounds containing oxygen or sulfur
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Lubricants (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SE9203539A 1992-11-25 1992-11-25 En vattenhaltig, alkalisk metallbearbetningsvätska innehållande en primär amin SE500299C2 (sv)

Priority Applications (9)

Application Number	Priority Date	Filing Date	Title
SE9203539A SE500299C2 (sv)	1992-11-25	1992-11-25	En vattenhaltig, alkalisk metallbearbetningsvätska innehållande en primär amin
EP94901103A EP0670675B1 (en)	1992-11-25	1993-11-11	An aqueous alkaline metal working fluid containing a primary amine
ES94901103T ES2132370T3 (es)	1992-11-25	1993-11-11	Fluido acuoso alcalino para la mecanizacion de metales conteniendo una amina primaria.
JP6513032A JPH08503726A (ja)	1992-11-25	1993-11-11	第一級アミンを含む水溶性のアルカリ金属加工流体
DK94901103T DK0670675T3 (da)	1992-11-25	1993-11-11	Vandig alkalisk metalbearbejdningsvæske, der indeholder en primær amin
PCT/SE1993/000958 WO1994012028A1 (en)	1992-11-25	1993-11-11	An aqueous alkaline metal working fluid containing a primary amine
AU55805/94A AU5580594A (en)	1992-11-25	1993-11-11	An aqueous alkaline metal working fluid containing a primary amine
DE69324155T DE69324155T2 (de)	1992-11-25	1993-11-11	Wässrige alkalimetall-bearbeitungsflüssigkeit, die ein primäres amin enthält
AT94901103T ATE177901T1 (de)	1992-11-25	1993-11-11	Wässrige alkalimetall-bearbeitungsflüssigkeit, die ein primäres amin enthält

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE9203539A SE500299C2 (sv)	1992-11-25	1992-11-25	En vattenhaltig, alkalisk metallbearbetningsvätska innehållande en primär amin

Publications (3)

Publication Number	Publication Date
SE9203539D0 SE9203539D0 (sv)	1992-11-25
SE9203539L SE9203539L (sv)	1994-05-26
SE500299C2 true SE500299C2 (sv)	1994-05-30

Family

ID=20387926

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE9203539A SE500299C2 (sv)	1992-11-25	1992-11-25	En vattenhaltig, alkalisk metallbearbetningsvätska innehållande en primär amin

Country Status (9)

Country	Link
EP (1)	EP0670675B1 (da)
JP (1)	JPH08503726A (da)
AT (1)	ATE177901T1 (da)
AU (1)	AU5580594A (da)
DE (1)	DE69324155T2 (da)
DK (1)	DK0670675T3 (da)
ES (1)	ES2132370T3 (da)
SE (1)	SE500299C2 (da)
WO (1)	WO1994012028A1 (da)

Families Citing this family (12)

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Publication number	Priority date	Publication date	Assignee	Title
US5723418A (en) *	1996-05-31	1998-03-03	Ecolab Inc.	Alkyl ether amine conveyor lubricants containing corrosion inhibitors
US5932526A (en) *	1997-06-20	1999-08-03	Ecolab, Inc.	Alkaline ether amine conveyor lubricant
US7741257B2 (en)	2005-03-15	2010-06-22	Ecolab Inc.	Dry lubricant for conveying containers
US7745381B2 (en)	2005-03-15	2010-06-29	Ecolab Inc.	Lubricant for conveying containers
CN101631457B (zh)	2007-01-12	2013-09-25	安格斯化学公司	用于水基体系的氨基醇和杀生物剂组合物
BRPI0908613A8 (pt)	2008-05-15	2017-10-31	Angus Chemical	Mistura, mistura de combustível e método para prover resistência microbiana a um combustível biodiesel
EP3135109B1 (en)	2008-05-15	2020-02-12	ANGUS Chemical Company	Aminoalcohol and biocide compositions for aqueous based systems
US9359579B2 (en)	2010-09-24	2016-06-07	Ecolab Usa Inc.	Conveyor lubricants including emulsions and methods employing them
EP4410935B1 (en)	2013-03-11	2026-01-21	Ecolab USA Inc.	Lubrication of transfer plates using oil in water emulsions
CN112616848A (zh)	2013-11-19	2021-04-09	奥麒化工股份有限公司	增强了的防腐剂
CA3009323C (en)	2015-12-23	2023-01-24	Henkel Ag & Co. Kgaa	Metal working fluid
CN117730135A (zh) *	2021-08-24	2024-03-19	陶氏环球技术有限责任公司	水基半合成金属加工流体组合物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4196217A (en) *	1976-02-17	1980-04-01	Laboratoires Pharmascience	Hydroxylated amines with bacteriostatic activity
GB8327911D0 (en) *	1983-10-19	1983-11-23	Ciba Geigy Ag	Salts as corrosion inhibitors
US4749503A (en) *	1986-03-07	1988-06-07	Chemical Exchange Industries, Inc.	Method and composition to control microbial growth in metalworking fluids
SE460671B (sv) *	1988-03-30	1989-11-06	Berol Kemi Ab	Vattenbaserad metallbearbetningsvaetska innehaallande en alkanolaminfoerening som antimikrobiellt medel och ett saett att bearbeta metaller under anvaendning av samma alkanolaminfoerening
FR2667761B1 (fr) *	1990-10-11	1993-01-08	Produits Ind Cie Fse	Composition desinfectante pour l'industrie agro-alimentaire et la medecine veterinaire.

1992
- 1992-11-25 SE SE9203539A patent/SE500299C2/sv unknown
1993
- 1993-11-11 JP JP6513032A patent/JPH08503726A/ja active Pending
- 1993-11-11 ES ES94901103T patent/ES2132370T3/es not_active Expired - Lifetime
- 1993-11-11 AT AT94901103T patent/ATE177901T1/de not_active IP Right Cessation
- 1993-11-11 DE DE69324155T patent/DE69324155T2/de not_active Expired - Fee Related
- 1993-11-11 WO PCT/SE1993/000958 patent/WO1994012028A1/en not_active Ceased
- 1993-11-11 DK DK94901103T patent/DK0670675T3/da active
- 1993-11-11 AU AU55805/94A patent/AU5580594A/en not_active Abandoned
- 1993-11-11 EP EP94901103A patent/EP0670675B1/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
AU5580594A (en)	1994-06-22
JPH08503726A (ja)	1996-04-23
WO1994012028A1 (en)	1994-06-09
SE9203539D0 (sv)	1992-11-25
EP0670675A1 (en)	1995-09-13
ATE177901T1 (de)	1999-04-15
DK0670675T3 (da)	1999-10-11
ES2132370T3 (es)	1999-08-16
EP0670675B1 (en)	1999-03-24
DE69324155T2 (de)	1999-11-18
SE9203539L (sv)	1994-05-26
DE69324155D1 (de)	1999-04-29

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