CY1180A - Corrosion inhibited agricultural compositions - Google Patents
Corrosion inhibited agricultural compositions Download PDFInfo
- Publication number
- CY1180A CY1180A CY1180A CY118078A CY1180A CY 1180 A CY1180 A CY 1180A CY 1180 A CY1180 A CY 1180A CY 118078 A CY118078 A CY 118078A CY 1180 A CY1180 A CY 1180A
- Authority
- CY
- Cyprus
- Prior art keywords
- weight
- phosphonomethylglycine
- thiols
- parts
- thiol
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 92
- 238000005260 corrosion Methods 0.000 title claims description 43
- 230000007797 corrosion Effects 0.000 title claims description 43
- -1 alkane thiols Chemical class 0.000 claims description 89
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 54
- 239000004094 surface-active agent Substances 0.000 claims description 47
- 238000009472 formulation Methods 0.000 claims description 43
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 35
- 239000004202 carbamide Substances 0.000 claims description 35
- 238000002474 experimental method Methods 0.000 claims description 33
- 150000003573 thiols Chemical class 0.000 claims description 32
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 30
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 229910052751 metal Inorganic materials 0.000 claims description 25
- 239000002184 metal Substances 0.000 claims description 25
- 150000003839 salts Chemical class 0.000 claims description 25
- 239000002253 acid Substances 0.000 claims description 23
- 230000002363 herbicidal effect Effects 0.000 claims description 21
- 229910052783 alkali metal Inorganic materials 0.000 claims description 17
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 16
- 239000004480 active ingredient Substances 0.000 claims description 16
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 15
- 150000004662 dithiols Chemical class 0.000 claims description 15
- 230000005764 inhibitory process Effects 0.000 claims description 15
- 229910052725 zinc Inorganic materials 0.000 claims description 15
- 239000011701 zinc Substances 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical group [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims description 12
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 claims description 11
- 230000008635 plant growth Effects 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 235000006408 oxalic acid Nutrition 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 8
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 8
- 125000000129 anionic group Chemical group 0.000 claims description 8
- 239000004615 ingredient Substances 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 6
- 230000002401 inhibitory effect Effects 0.000 claims description 5
- 150000007522 mineralic acids Chemical class 0.000 claims description 5
- 239000004606 Fillers/Extenders Substances 0.000 claims description 4
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 4
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000002671 adjuvant Substances 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- ORTRWBYBJVGVQC-UHFFFAOYSA-N hexadecane-1-thiol Chemical compound CCCCCCCCCCCCCCCCS ORTRWBYBJVGVQC-UHFFFAOYSA-N 0.000 claims description 2
- IVTHSFJXIARUFL-UHFFFAOYSA-N triazanium;thiophosphate Chemical group [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=S IVTHSFJXIARUFL-UHFFFAOYSA-N 0.000 claims description 2
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 230000001105 regulatory effect Effects 0.000 claims 2
- LXUNZSDDXMPKLP-UHFFFAOYSA-N 2-Methylbenzenethiol Chemical compound CC1=CC=CC=C1S LXUNZSDDXMPKLP-UHFFFAOYSA-N 0.000 claims 1
- VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical compound NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 claims 1
- VZXOZSQDJJNBRC-UHFFFAOYSA-N 4-chlorobenzenethiol Chemical compound SC1=CC=C(Cl)C=C1 VZXOZSQDJJNBRC-UHFFFAOYSA-N 0.000 claims 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 claims 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims 1
- 229910000397 disodium phosphate Inorganic materials 0.000 claims 1
- 235000019800 disodium phosphate Nutrition 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- 235000019837 monoammonium phosphate Nutrition 0.000 claims 1
- 239000006012 monoammonium phosphate Substances 0.000 claims 1
- 231100000208 phytotoxic Toxicity 0.000 claims 1
- 230000000885 phytotoxic effect Effects 0.000 claims 1
- 239000001488 sodium phosphate Substances 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 description 22
- 229910000831 Steel Inorganic materials 0.000 description 12
- 239000010959 steel Substances 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 10
- 239000012141 concentrate Substances 0.000 description 10
- 235000008504 concentrate Nutrition 0.000 description 10
- NVUDVUDVVXAWGV-UHFFFAOYSA-N dodecane-1,12-dithiol Chemical compound SCCCCCCCCCCCCS NVUDVUDVVXAWGV-UHFFFAOYSA-N 0.000 description 9
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- XVIWVTWNQQUGQI-UHFFFAOYSA-L disodium;sulfanylidenemethanediolate Chemical compound [Na+].[Na+].[O-]C([O-])=S XVIWVTWNQQUGQI-UHFFFAOYSA-L 0.000 description 6
- AALQBIFJJJPDHJ-UHFFFAOYSA-K trisodium;thiophosphate;dodecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[Na+].[O-]P([O-])([O-])=S AALQBIFJJJPDHJ-UHFFFAOYSA-K 0.000 description 6
- 241000508725 Elymus repens Species 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000012669 liquid formulation Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- PMBXCGGQNSVESQ-UHFFFAOYSA-N 1-Hexanethiol Chemical compound CCCCCCS PMBXCGGQNSVESQ-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- 239000004471 Glycine Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- 239000003774 sulfhydryl reagent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000013011 aqueous formulation Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000008233 hard water Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- BDFAOUQQXJIZDG-UHFFFAOYSA-N 2-methylpropane-1-thiol Chemical compound CC(C)CS BDFAOUQQXJIZDG-UHFFFAOYSA-N 0.000 description 2
- NHWJLCJXIBETKO-UHFFFAOYSA-N 3-phenoxybenzene-1,2-disulfonic acid Chemical class OS(=O)(=O)C1=CC=CC(OC=2C=CC=CC=2)=C1S(O)(=O)=O NHWJLCJXIBETKO-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 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 2
- GIJGXNFNUUFEGH-UHFFFAOYSA-N Isopentyl mercaptan Chemical compound CC(C)CCS GIJGXNFNUUFEGH-UHFFFAOYSA-N 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- IASQPYXUGFCXJY-UHFFFAOYSA-L [K+].[K+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] Chemical compound [K+].[K+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] IASQPYXUGFCXJY-UHFFFAOYSA-L 0.000 description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- LOCHFZBWPCLPAN-UHFFFAOYSA-N butane-2-thiol Chemical compound CCC(C)S LOCHFZBWPCLPAN-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910001424 calcium ion Inorganic materials 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 2
- SIQGBUJXKSJZAV-UHFFFAOYSA-L disodium;2-(phosphonomethylamino)acetate Chemical compound [Na+].[Na+].OP(O)(=O)CNCC([O-])=O.OP(O)(=O)CNCC([O-])=O SIQGBUJXKSJZAV-UHFFFAOYSA-L 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 229910001425 magnesium ion Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- JWINRUZEIRYEJL-UHFFFAOYSA-N octadecan-1-amine 2-(phosphonomethylamino)acetic acid Chemical compound OC(=O)CNCP(O)(O)=O.CCCCCCCCCCCCCCCCCCN JWINRUZEIRYEJL-UHFFFAOYSA-N 0.000 description 2
- 150000007519 polyprotic acids Polymers 0.000 description 2
- SUVIGLJNEAMWEG-UHFFFAOYSA-N propane-1-thiol Chemical compound CCCS SUVIGLJNEAMWEG-UHFFFAOYSA-N 0.000 description 2
- KJRCEJOSASVSRA-UHFFFAOYSA-N propane-2-thiol Chemical compound CC(C)S KJRCEJOSASVSRA-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- YWICANUUQPYHOW-UHFFFAOYSA-M sodium;2-(phosphonomethylamino)acetate Chemical compound [Na+].OP(O)(=O)CNCC([O-])=O YWICANUUQPYHOW-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000006277 sulfonation reaction Methods 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- DHBXNPKRAUYBTH-UHFFFAOYSA-N 1,1-ethanedithiol Chemical compound CC(S)S DHBXNPKRAUYBTH-UHFFFAOYSA-N 0.000 description 1
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
- GSFSVEDCYBDIGW-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)-6-chlorophenol Chemical compound OC1=C(Cl)C=CC=C1C1=NC2=CC=CC=C2S1 GSFSVEDCYBDIGW-UHFFFAOYSA-N 0.000 description 1
- WSSAMLJXFBGUJI-UHFFFAOYSA-N 2-(phosphonomethylamino)acetic acid Chemical compound OC(=O)CNCP(O)(O)=O.OC(=O)CNCP(O)(O)=O WSSAMLJXFBGUJI-UHFFFAOYSA-N 0.000 description 1
- JHTKHBPGSTYSBH-UHFFFAOYSA-N 2-(phosphonomethylamino)acetic acid;propan-1-amine Chemical compound CCCN.CCCN.OC(=O)CNCP(O)(O)=O JHTKHBPGSTYSBH-UHFFFAOYSA-N 0.000 description 1
- DQNPFPHZAUMZHD-UHFFFAOYSA-N 2-aminoethanol;2-(phosphonomethylamino)acetic acid Chemical compound NCCO.OC(=O)CNCP(O)(O)=O DQNPFPHZAUMZHD-UHFFFAOYSA-N 0.000 description 1
- NFHONWFCTQWTOM-UHFFFAOYSA-N 2-chloroethanamine;2-(phosphonomethylamino)acetic acid Chemical compound NCCCl.OC(=O)CNCP(O)(O)=O NFHONWFCTQWTOM-UHFFFAOYSA-N 0.000 description 1
- ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical class COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 description 1
- JQVJHSLHRAOQTD-UHFFFAOYSA-N 2-phenoxyethanamine;2-(phosphonomethylamino)acetic acid Chemical compound NCCOC1=CC=CC=C1.OC(=O)CNCP(O)(O)=O JQVJHSLHRAOQTD-UHFFFAOYSA-N 0.000 description 1
- LTERAWRIKDPXBF-UHFFFAOYSA-N 3-(dodecanoylamino)propyl-trimethylazanium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCCCCCCCCCC(=O)NCCC[N+](C)(C)C LTERAWRIKDPXBF-UHFFFAOYSA-N 0.000 description 1
- FQHJBVUTSWQWSN-UHFFFAOYSA-N 4-methyl-1,3,2-dioxathietane 2,2-dioxide Chemical compound CC1OS(=O)(=O)O1 FQHJBVUTSWQWSN-UHFFFAOYSA-N 0.000 description 1
- WLHCBQAPPJAULW-UHFFFAOYSA-N 4-methylbenzenethiol Chemical compound CC1=CC=C(S)C=C1 WLHCBQAPPJAULW-UHFFFAOYSA-N 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 1
- 244000153158 Ammi visnaga Species 0.000 description 1
- 235000010585 Ammi visnaga Nutrition 0.000 description 1
- GTTOJXOMPHRXTF-UHFFFAOYSA-N C1COCCN1.OC(=O)CNCP(O)(O)=O Chemical compound C1COCCN1.OC(=O)CNCP(O)(O)=O GTTOJXOMPHRXTF-UHFFFAOYSA-N 0.000 description 1
- KQTHWILIRXZROE-UHFFFAOYSA-N CSC(OC)=S.[Na] Chemical compound CSC(OC)=S.[Na] KQTHWILIRXZROE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical class NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- PDYXIVPKOMYDOK-UHFFFAOYSA-N Glyphosate-monoammonium Chemical compound [NH4+].OC(=O)CNCP(O)([O-])=O PDYXIVPKOMYDOK-UHFFFAOYSA-N 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 description 1
- XIXFGHVXFFTSMA-UHFFFAOYSA-L N(CC(=O)[O-])CC(=O)[O-].[Na+].[Na+].[Na+] Chemical compound N(CC(=O)[O-])CC(=O)[O-].[Na+].[Na+].[Na+] XIXFGHVXFFTSMA-UHFFFAOYSA-L 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical class C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 240000002439 Sorghum halepense Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- KCNGRSQQOKXAKR-UHFFFAOYSA-N [(2-ethoxy-2-oxoethyl)amino]methylphosphonic acid Chemical compound CCOC(=O)CNCP(O)(O)=O KCNGRSQQOKXAKR-UHFFFAOYSA-N 0.000 description 1
- ZGGNVSKWCFLTQB-UHFFFAOYSA-N [(2-octoxy-2-oxoethyl)amino]methylphosphonic acid Chemical compound CCCCCCCCOC(=O)CNCP(O)(O)=O ZGGNVSKWCFLTQB-UHFFFAOYSA-N 0.000 description 1
- WTJXGSWRASYOOV-UHFFFAOYSA-K [K+].[K+].[K+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] Chemical compound [K+].[K+].[K+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] WTJXGSWRASYOOV-UHFFFAOYSA-K 0.000 description 1
- IZKSYXAOKNLDLT-UHFFFAOYSA-K [K+].[K+].[K+].[O-]P([O-])([O-])=S Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=S IZKSYXAOKNLDLT-UHFFFAOYSA-K 0.000 description 1
- BDIRUEMDTWYHDH-UHFFFAOYSA-L [Li+].[Li+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] Chemical compound [Li+].[Li+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] BDIRUEMDTWYHDH-UHFFFAOYSA-L 0.000 description 1
- LLPIQRJDHHFHTJ-UHFFFAOYSA-N [NH4+].[NH4+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] Chemical compound [NH4+].[NH4+].P(=O)(O)(O)CNCC(=O)[O-].P(=O)(O)(O)CNCC(=O)[O-] LLPIQRJDHHFHTJ-UHFFFAOYSA-N 0.000 description 1
- KUOXWPCYGDJLBQ-UHFFFAOYSA-N acetic acid methylphosphonic acid Chemical compound C(C)(=O)O.CP(O)(O)=O KUOXWPCYGDJLBQ-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- SMTOKHQOVJRXLK-UHFFFAOYSA-N butane-1,4-dithiol Chemical compound SCCCCS SMTOKHQOVJRXLK-UHFFFAOYSA-N 0.000 description 1
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 1
- 150000003940 butylamines Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical class NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 1
- VTXVGVNLYGSIAR-UHFFFAOYSA-N decane-1-thiol Chemical compound CCCCCCCCCCS VTXVGVNLYGSIAR-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- TVMUHOAONWHJBV-UHFFFAOYSA-M dehydroglycinate Chemical compound [O-]C(=O)C=N TVMUHOAONWHJBV-UHFFFAOYSA-M 0.000 description 1
- TVMUHOAONWHJBV-UHFFFAOYSA-N dehydroglycine Chemical compound OC(=O)C=N TVMUHOAONWHJBV-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- ISPMIQMKDKSQJY-UHFFFAOYSA-N di(propan-2-yl)azanium;2-(phosphonomethylamino)acetate Chemical compound CC(C)NC(C)C.OC(=O)CNCP(O)(O)=O ISPMIQMKDKSQJY-UHFFFAOYSA-N 0.000 description 1
- IKVVOMGOVBKDFG-UHFFFAOYSA-N diazanium;sulfanylidenemethanediolate Chemical compound [NH4+].[NH4+].[O-]C([O-])=S IKVVOMGOVBKDFG-UHFFFAOYSA-N 0.000 description 1
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical class CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical class CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- MZGNSEAPZQGJRB-UHFFFAOYSA-N dimethyldithiocarbamic acid Chemical compound CN(C)C(S)=S MZGNSEAPZQGJRB-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- XEQIERZCOHTONL-UHFFFAOYSA-L dipotassium;2-(carboxylatomethylamino)acetate Chemical compound [K+].[K+].[O-]C(=O)CNCC([O-])=O XEQIERZCOHTONL-UHFFFAOYSA-L 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- NHDJUIZMBBJKJT-UHFFFAOYSA-N ethanamine;2-(phosphonomethylamino)acetic acid Chemical compound CCN.CCN.OC(=O)CNCP(O)(O)=O NHDJUIZMBBJKJT-UHFFFAOYSA-N 0.000 description 1
- JOAUSGBGCLGDEE-UHFFFAOYSA-N ethane-1,2-diamine;2-(phosphonomethylamino)acetic acid Chemical compound NCCN.OC(=O)CNCP(O)(O)=O JOAUSGBGCLGDEE-UHFFFAOYSA-N 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical class CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- FCZFPMKLLXTSNP-UHFFFAOYSA-N ethyl 2-iminoacetate Chemical compound CCOC(=O)C=N FCZFPMKLLXTSNP-UHFFFAOYSA-N 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- ABNPJVOPTXYSQW-UHFFFAOYSA-N hexane-2-thiol Chemical compound CCCCC(C)S ABNPJVOPTXYSQW-UHFFFAOYSA-N 0.000 description 1
- VOIGMFQJDZTEKW-UHFFFAOYSA-N hexane-3-thiol Chemical compound CCCC(S)CC VOIGMFQJDZTEKW-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- NBBDVXGYHOWUHM-UHFFFAOYSA-N methanamine;2-(phosphonomethylamino)acetic acid Chemical compound NC.NC.OC(=O)CNCP(O)(O)=O NBBDVXGYHOWUHM-UHFFFAOYSA-N 0.000 description 1
- ONHFWHCMZAJCFB-UHFFFAOYSA-N myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 description 1
- ODJROLZGWWEEKS-UHFFFAOYSA-N n'-(2-aminoethyl)ethane-1,2-diamine;2-(phosphonomethylamino)acetic acid Chemical compound NCCNCCN.OC(=O)CNCP(O)(O)=O ODJROLZGWWEEKS-UHFFFAOYSA-N 0.000 description 1
- WGQXGEHRJAEFPO-UHFFFAOYSA-N n,n-diethylethanamine;2-(phosphonomethylamino)acetic acid Chemical compound CCN(CC)CC.OC(=O)CNCP(O)(O)=O WGQXGEHRJAEFPO-UHFFFAOYSA-N 0.000 description 1
- IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 1
- KXGGAOPWQWIKSW-UHFFFAOYSA-N n-methylmethanamine;2-(phosphonomethylamino)acetic acid Chemical compound CNC.CNC.OC(=O)CNCP(O)(O)=O KXGGAOPWQWIKSW-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- BZXFEMZFRLXGCY-UHFFFAOYSA-N octane-2-thiol Chemical compound CCCCCCC(C)S BZXFEMZFRLXGCY-UHFFFAOYSA-N 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- ZJLMKPKYJBQJNH-UHFFFAOYSA-N propane-1,3-dithiol Chemical compound SCCCS ZJLMKPKYJBQJNH-UHFFFAOYSA-N 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 description 1
- ONHIJCVRYPHITQ-UHFFFAOYSA-K trisodium;2-(phosphonomethylamino)acetate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CNCC([O-])=O.OP(O)(=O)CNCC([O-])=O.OP(O)(=O)CNCC([O-])=O ONHIJCVRYPHITQ-UHFFFAOYSA-K 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- 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
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/16—Sulfur-containing compounds
- C23F11/161—Mercaptans
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Metallurgy (AREA)
- Toxicology (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79708377A | 1977-05-16 | 1977-05-16 | |
| US05/862,691 US4159901A (en) | 1977-05-16 | 1977-12-27 | Corrosion inhibited agricultural compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1180A true CY1180A (en) | 1983-10-07 |
Family
ID=27121824
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY1180A CY1180A (en) | 1977-05-16 | 1978-05-12 | Corrosion inhibited agricultural compositions |
Country Status (33)
| Country | Link |
|---|---|
| JP (1) | JPS5417126A (de) |
| AR (1) | AR221337A1 (de) |
| AT (1) | AT362184B (de) |
| AU (1) | AU519686B2 (de) |
| BG (1) | BG29862A3 (de) |
| CA (1) | CA1095281A (de) |
| CS (1) | CS205121B2 (de) |
| CY (1) | CY1180A (de) |
| DD (1) | DD137050A5 (de) |
| DE (1) | DE2820903A1 (de) |
| DK (1) | DK210578A (de) |
| EG (1) | EG13404A (de) |
| ES (1) | ES469651A1 (de) |
| FI (1) | FI62458C (de) |
| FR (1) | FR2390901A1 (de) |
| GB (1) | GB1604526A (de) |
| GR (1) | GR68085B (de) |
| IE (1) | IE46894B1 (de) |
| IL (1) | IL54694A (de) |
| IT (1) | IT1094641B (de) |
| KE (1) | KE3266A (de) |
| LU (1) | LU79649A1 (de) |
| MY (1) | MY8400125A (de) |
| NL (1) | NL7805012A (de) |
| NO (1) | NO781691L (de) |
| NZ (1) | NZ187256A (de) |
| OA (1) | OA05961A (de) |
| PH (1) | PH15128A (de) |
| PL (1) | PL113460B1 (de) |
| PT (1) | PT68043B (de) |
| SE (1) | SE7805461L (de) |
| SG (1) | SG9483G (de) |
| TR (1) | TR20256A (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4608978A (en) * | 1983-09-26 | 1986-09-02 | Carol Block Limited | Method and apparatus for photoepiltion |
| KR860008713A (ko) * | 1985-05-29 | 1986-12-18 | 죤 알. 페넬 | 고체식물 훨성조성물 및 그 제조방법 |
| BR8605102A (pt) * | 1985-10-21 | 1987-07-21 | Stauffer Chemical Co | Composicao fitoativa liquida e composicao herbicida liquida |
| CA2031017A1 (en) * | 1989-12-01 | 1991-06-02 | Robert J. Goos | Ammonium thiosulfate as herbicide extender |
| KR102179943B1 (ko) | 2020-05-14 | 2020-11-18 | 이수인(주) | 세면기 수도꼭지에 부착되는 필터 토수구 |
-
1978
- 1978-05-10 IL IL54694A patent/IL54694A/xx unknown
- 1978-05-10 NL NL7805012A patent/NL7805012A/xx not_active Application Discontinuation
- 1978-05-10 EG EG302/78A patent/EG13404A/xx active
- 1978-05-10 ES ES469651A patent/ES469651A1/es not_active Expired
- 1978-05-12 FI FI781505A patent/FI62458C/fi not_active IP Right Cessation
- 1978-05-12 CS CS783059A patent/CS205121B2/cs unknown
- 1978-05-12 LU LU79649A patent/LU79649A1/xx unknown
- 1978-05-12 BG BG039748A patent/BG29862A3/xx unknown
- 1978-05-12 SE SE7805461A patent/SE7805461L/xx unknown
- 1978-05-12 GR GR56226A patent/GR68085B/el unknown
- 1978-05-12 AT AT346578A patent/AT362184B/de not_active IP Right Cessation
- 1978-05-12 OA OA56467A patent/OA05961A/xx unknown
- 1978-05-12 DK DK210578A patent/DK210578A/da unknown
- 1978-05-12 GB GB19157/78A patent/GB1604526A/en not_active Expired
- 1978-05-12 IT IT23368/78A patent/IT1094641B/it active
- 1978-05-12 DD DD78205356A patent/DD137050A5/de unknown
- 1978-05-12 AU AU36063/78A patent/AU519686B2/en not_active Expired
- 1978-05-12 IE IE969/78A patent/IE46894B1/en unknown
- 1978-05-12 FR FR7814306A patent/FR2390901A1/fr active Pending
- 1978-05-12 AR AR272152A patent/AR221337A1/es active
- 1978-05-12 NO NO78781691A patent/NO781691L/no unknown
- 1978-05-12 NZ NZ187256A patent/NZ187256A/xx unknown
- 1978-05-12 PH PH21132A patent/PH15128A/en unknown
- 1978-05-12 CY CY1180A patent/CY1180A/en unknown
- 1978-05-12 TR TR20256A patent/TR20256A/xx unknown
- 1978-05-12 DE DE19782820903 patent/DE2820903A1/de not_active Withdrawn
- 1978-05-12 JP JP5707078A patent/JPS5417126A/ja active Pending
- 1978-05-12 PL PL1978206727A patent/PL113460B1/pl unknown
- 1978-05-15 CA CA303,367A patent/CA1095281A/en not_active Expired
- 1978-05-15 PT PT68043A patent/PT68043B/pt unknown
-
1983
- 1983-03-03 SG SG94/83A patent/SG9483G/en unknown
- 1983-03-07 KE KE3266A patent/KE3266A/xx unknown
-
1984
- 1984-12-30 MY MY125/84A patent/MY8400125A/xx unknown
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