NO782640L - Aminoalkylenfosfonsyre-derivater med avsetnings- og korrosjonshemmende virkning - Google Patents
Aminoalkylenfosfonsyre-derivater med avsetnings- og korrosjonshemmende virkningInfo
- Publication number
- NO782640L NO782640L NO782640A NO782640A NO782640L NO 782640 L NO782640 L NO 782640L NO 782640 A NO782640 A NO 782640A NO 782640 A NO782640 A NO 782640A NO 782640 L NO782640 L NO 782640L
- Authority
- NO
- Norway
- Prior art keywords
- dioxide
- thiophenamine
- phosphonomethyl
- compound according
- identified
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims description 17
- 230000000694 effects Effects 0.000 title description 9
- 238000000151 deposition Methods 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 39
- -1 alkali metal salts Chemical class 0.000 claims description 33
- 230000007797 corrosion Effects 0.000 claims description 19
- 238000005260 corrosion Methods 0.000 claims description 19
- 238000000576 coating method Methods 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 229910052783 alkali metal Inorganic materials 0.000 claims description 12
- 239000010802 sludge Substances 0.000 claims description 12
- 239000000498 cooling water Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- BQIVITALMXDPBY-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-(phosphonomethyl)amino]methylphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)C1CCS(=O)(=O)C1 BQIVITALMXDPBY-UHFFFAOYSA-N 0.000 claims description 10
- 150000007513 acids Chemical class 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 150000001340 alkali metals Chemical group 0.000 claims description 6
- 238000012546 transfer Methods 0.000 claims description 6
- 239000000853 adhesive Substances 0.000 claims description 5
- 230000001070 adhesive effect Effects 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 230000008021 deposition Effects 0.000 claims description 5
- 239000003112 inhibitor Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 claims description 4
- 229920000388 Polyphosphate Polymers 0.000 claims description 4
- 230000002401 inhibitory effect Effects 0.000 claims description 4
- 239000001205 polyphosphate Substances 0.000 claims description 4
- 235000011176 polyphosphates Nutrition 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- VCZBGNAGOYJIHO-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-(2-hydroxyethyl)amino]methylphosphonic acid Chemical compound OCCN(CP(O)(O)=O)C1CCS(=O)(=O)C1 VCZBGNAGOYJIHO-UHFFFAOYSA-N 0.000 claims description 3
- 235000021317 phosphate Nutrition 0.000 claims description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 claims description 2
- 229920001732 Lignosulfonate Polymers 0.000 claims description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- UQAICKBXFRTBDL-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-methylamino]methylphosphonic acid Chemical compound OP(=O)(O)CN(C)C1CCS(=O)(=O)C1 UQAICKBXFRTBDL-UHFFFAOYSA-N 0.000 claims description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 2
- 239000012964 benzotriazole Substances 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
- 150000001845 chromium compounds Chemical class 0.000 claims description 2
- 150000002460 imidazoles Chemical class 0.000 claims description 2
- 229920005610 lignin Polymers 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 150000002826 nitrites Chemical class 0.000 claims description 2
- 229920000620 organic polymer Polymers 0.000 claims description 2
- 150000002916 oxazoles Chemical class 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- 239000001648 tannin Substances 0.000 claims description 2
- 229920001864 tannin Polymers 0.000 claims description 2
- 235000018553 tannin Nutrition 0.000 claims description 2
- ZLOBIZSLPMOPDW-UHFFFAOYSA-N thiophene 1,1-dioxide Chemical compound O=S1(=O)[C]=CC=C1 ZLOBIZSLPMOPDW-UHFFFAOYSA-N 0.000 claims description 2
- 150000003751 zinc Chemical class 0.000 claims description 2
- VGQDGZPHGWGHDA-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-(2-hydroxypropyl)amino]methylphosphonic acid Chemical compound CC(O)CN(CP(O)(O)=O)C1CCS(=O)(=O)C1 VGQDGZPHGWGHDA-UHFFFAOYSA-N 0.000 claims 1
- IWYQUPPVBVJTGA-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-(2-methylpropyl)amino]methylphosphonic acid Chemical compound CC(C)CN(CP(O)(O)=O)C1CCS(=O)(=O)C1 IWYQUPPVBVJTGA-UHFFFAOYSA-N 0.000 claims 1
- WXNLUTMRLHEQKO-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-ethylamino]methylphosphonic acid Chemical compound OP(=O)(O)CN(CC)C1CCS(=O)(=O)C1 WXNLUTMRLHEQKO-UHFFFAOYSA-N 0.000 claims 1
- JPCSUWWPEKJRSB-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-propan-2-ylamino]methylphosphonic acid Chemical compound OP(=O)(O)CN(C(C)C)C1CCS(=O)(=O)C1 JPCSUWWPEKJRSB-UHFFFAOYSA-N 0.000 claims 1
- NBALGHXSIVVWHG-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)-propylamino]methylphosphonic acid Chemical compound CCCN(CP(O)(O)=O)C1CCS(=O)(=O)C1 NBALGHXSIVVWHG-UHFFFAOYSA-N 0.000 claims 1
- JCOXGTJTEFDVME-UHFFFAOYSA-N [(3-chloro-2-hydroxypropyl)-(1,1-dioxothiolan-3-yl)amino]methylphosphonic acid Chemical compound ClCC(O)CN(CP(O)(O)=O)C1CCS(=O)(=O)C1 JCOXGTJTEFDVME-UHFFFAOYSA-N 0.000 claims 1
- MJZBIYUVAGANTI-UHFFFAOYSA-N [[4-[bis(phosphonomethyl)amino]-1,1-dioxothiolan-3-yl]-(phosphonomethyl)amino]methylphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)C1CS(=O)(=O)CC1N(CP(O)(O)=O)CP(O)(O)=O MJZBIYUVAGANTI-UHFFFAOYSA-N 0.000 claims 1
- SNHXJSQKCPWEGB-UHFFFAOYSA-N [butan-2-yl-(1,1-dioxothiolan-3-yl)amino]methylphosphonic acid Chemical compound CCC(C)N(CP(O)(O)=O)C1CCS(=O)(=O)C1 SNHXJSQKCPWEGB-UHFFFAOYSA-N 0.000 claims 1
- CEUIJOQHEVTVRS-UHFFFAOYSA-N [butyl-(1,1-dioxothiolan-3-yl)amino]methylphosphonic acid Chemical compound CCCCN(CP(O)(O)=O)C1CCS(=O)(=O)C1 CEUIJOQHEVTVRS-UHFFFAOYSA-N 0.000 claims 1
- HNLCQMZDWNGSKQ-UHFFFAOYSA-N [tert-butyl-(1,1-dioxothiolan-3-yl)amino]methylphosphonic acid Chemical compound OP(=O)(O)CN(C(C)(C)C)C1CCS(=O)(=O)C1 HNLCQMZDWNGSKQ-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 33
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 20
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 19
- 239000000243 solution Substances 0.000 description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
- 239000000203 mixture Substances 0.000 description 15
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 14
- 235000011007 phosphoric acid Nutrition 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 10
- 229910000019 calcium carbonate Inorganic materials 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 229920002125 Sokalan® Polymers 0.000 description 8
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 8
- 229930040373 Paraformaldehyde Natural products 0.000 description 7
- 235000011132 calcium sulphate Nutrition 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 229920002866 paraformaldehyde Polymers 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000001175 calcium sulphate Substances 0.000 description 5
- IIIGXUANQZOIHI-UHFFFAOYSA-N 1,1-dioxothiolan-2-amine Chemical class NC1CCCS1(=O)=O IIIGXUANQZOIHI-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- MBDNRNMVTZADMQ-UHFFFAOYSA-N sulfolene Chemical compound O=S1(=O)CC=CC1 MBDNRNMVTZADMQ-UHFFFAOYSA-N 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 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 4
- OVKIDXBGVUQFFC-UHFFFAOYSA-N 1,1-dioxothiolan-3-amine Chemical compound NC1CCS(=O)(=O)C1 OVKIDXBGVUQFFC-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 239000000908 ammonium hydroxide Substances 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 125000002843 carboxylic acid group Chemical group 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000002198 insoluble material Substances 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000003009 phosphonic acids Chemical class 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- VCMVJUKSMDLDPE-UHFFFAOYSA-N (1,1-dioxothiolan-3-yl)-methylazanium;chloride Chemical compound [Cl-].C[NH2+]C1CCS(=O)(=O)C1 VCMVJUKSMDLDPE-UHFFFAOYSA-N 0.000 description 2
- MGZQMSFXPSKBDY-UHFFFAOYSA-N (1,1-dioxothiolan-3-yl)azanium;chloride Chemical compound Cl.NC1CCS(=O)(=O)C1 MGZQMSFXPSKBDY-UHFFFAOYSA-N 0.000 description 2
- UYORTFNECMHCAN-UHFFFAOYSA-N 1,1-dioxothiolane-3,4-diamine;dihydrochloride Chemical compound Cl.Cl.NC1CS(=O)(=O)CC1N UYORTFNECMHCAN-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- JJAQVUUCQRGKIM-UHFFFAOYSA-N [(1,1-dioxothiolan-3-yl)amino]azanium;chloride Chemical compound [Cl-].[NH3+]NC1CCS(=O)(=O)C1 JJAQVUUCQRGKIM-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 150000008064 anhydrides Chemical group 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000002455 scale inhibitor Substances 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- 150000003752 zinc compounds Chemical class 0.000 description 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
- KWEAOWRIBUGWDC-UHFFFAOYSA-N 1,1-dioxo-n-propan-2-ylthiolan-3-amine Chemical compound CC(C)NC1CCS(=O)(=O)C1 KWEAOWRIBUGWDC-UHFFFAOYSA-N 0.000 description 1
- POJSXHDVRJSEOP-UHFFFAOYSA-N 1,1-dioxo-n-propylthiolan-3-amine Chemical compound CCCNC1CCS(=O)(=O)C1 POJSXHDVRJSEOP-UHFFFAOYSA-N 0.000 description 1
- SHSRKYMXSFBHOU-UHFFFAOYSA-N 1,1-dioxothiolane-3,4-diamine Chemical compound NC1CS(=O)(=O)CC1N SHSRKYMXSFBHOU-UHFFFAOYSA-N 0.000 description 1
- NJLAVYYOBGCWOU-UHFFFAOYSA-N 1-[(1,1-dioxothiolan-3-yl)amino]propan-2-ol Chemical compound CC(O)CNC1CCS(=O)(=O)C1 NJLAVYYOBGCWOU-UHFFFAOYSA-N 0.000 description 1
- HAAGBMKNDSCMBY-UHFFFAOYSA-N 1-chloro-3-[(1,1-dioxothiolan-3-yl)amino]propan-2-ol Chemical compound ClCC(O)CNC1CCS(=O)(=O)C1 HAAGBMKNDSCMBY-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- DVLLSFLKNWESFH-UHFFFAOYSA-N 2-[(1,1-dioxothiolan-3-yl)amino]ethanol;hydrochloride Chemical compound Cl.OCCNC1CCS(=O)(=O)C1 DVLLSFLKNWESFH-UHFFFAOYSA-N 0.000 description 1
- CGWKQCYAMPDEGC-UHFFFAOYSA-N 3,4-dibromothiolane 1,1-dioxide Chemical compound BrC1CS(=O)(=O)CC1Br CGWKQCYAMPDEGC-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 239000004117 Lignosulphonate Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- QKZQLFJIVPUZMY-UHFFFAOYSA-N N,N'-bis(thiolan-3-yl)methanediamine Chemical compound C1CSCC1NCNC1CCSC1 QKZQLFJIVPUZMY-UHFFFAOYSA-N 0.000 description 1
- 239000007832 Na2SO4 Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 description 1
- 229910001626 barium chloride Inorganic materials 0.000 description 1
- 229910001422 barium ion Inorganic materials 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical group [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 description 1
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 235000011148 calcium chloride Nutrition 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- MSNWSDPPULHLDL-UHFFFAOYSA-K ferric hydroxide Chemical compound [OH-].[OH-].[OH-].[Fe+3] MSNWSDPPULHLDL-UHFFFAOYSA-K 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- FVIZARNDLVOMSU-UHFFFAOYSA-N ginsenoside K Natural products C1CC(C2(CCC3C(C)(C)C(O)CCC3(C)C2CC2O)C)(C)C2C1C(C)(CCC=C(C)C)OC1OC(CO)C(O)C(O)C1O FVIZARNDLVOMSU-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- QODRMDYLPGFPRH-UHFFFAOYSA-N n-(2-methylpropyl)-1,1-dioxothiolan-3-amine Chemical compound CC(C)CNC1CCS(=O)(=O)C1 QODRMDYLPGFPRH-UHFFFAOYSA-N 0.000 description 1
- IYMHRCANDIVXEC-UHFFFAOYSA-N n-butan-2-yl-1,1-dioxothiolan-3-amine Chemical compound CCC(C)NC1CCS(=O)(=O)C1 IYMHRCANDIVXEC-UHFFFAOYSA-N 0.000 description 1
- DROVFJSAGGLUJN-UHFFFAOYSA-N n-butyl-1,1-dioxothiolan-3-amine Chemical compound CCCCNC1CCS(=O)(=O)C1 DROVFJSAGGLUJN-UHFFFAOYSA-N 0.000 description 1
- BNVNYCSJNTUPFM-UHFFFAOYSA-N n-ethyl-1,1-dioxothiolan-3-amine Chemical compound CCNC1CCS(=O)(=O)C1 BNVNYCSJNTUPFM-UHFFFAOYSA-N 0.000 description 1
- MGNJNMNVFHVRHJ-UHFFFAOYSA-N n-methyl-1,1-dioxothiolan-3-amine Chemical compound CNC1CCS(=O)(=O)C1 MGNJNMNVFHVRHJ-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
- C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
- C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
- C02F5/14—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing phosphorus
-
- 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
- C23F11/167—Phosphorus-containing compounds
- C23F11/1676—Phosphonic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Metallurgy (AREA)
- General Chemical & Material Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/914,250 US4181806A (en) | 1978-06-09 | 1978-06-09 | Aminoalkylenephosphonic acids and salts thereof and their use in aqueous systems |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO782640L true NO782640L (no) | 1979-12-11 |
Family
ID=25434083
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO782640A NO782640L (no) | 1978-06-09 | 1978-08-02 | Aminoalkylenfosfonsyre-derivater med avsetnings- og korrosjonshemmende virkning |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4181806A (pt) |
| JP (1) | JPS54163567A (pt) |
| AR (1) | AR219118A1 (pt) |
| AT (1) | AT360444B (pt) |
| AU (1) | AU509872B2 (pt) |
| BE (1) | BE869794A (pt) |
| BR (1) | BR7805732A (pt) |
| DE (1) | DE2836306A1 (pt) |
| DK (1) | DK331078A (pt) |
| ES (1) | ES472712A1 (pt) |
| FI (1) | FI782476A (pt) |
| FR (1) | FR2428037A1 (pt) |
| GB (1) | GB2022588A (pt) |
| GR (1) | GR63760B (pt) |
| IE (1) | IE790171L (pt) |
| IT (1) | IT1109209B (pt) |
| NL (1) | NL7808787A (pt) |
| NO (1) | NO782640L (pt) |
| NZ (1) | NZ188000A (pt) |
| PT (1) | PT68388A (pt) |
| SE (1) | SE7808309L (pt) |
| ZA (1) | ZA784373B (pt) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5002697A (en) * | 1988-03-15 | 1991-03-26 | Nalco Chemical Company | Molybdate-containing corrosion inhibitors |
| US4933472A (en) * | 1988-04-08 | 1990-06-12 | Yamanouchi Pharmaceutical Co., Ltd. | Substituted aminomethylenebis(phosphonic acid) derivatives |
| US5068059A (en) * | 1990-01-16 | 1991-11-26 | Drew Chemical Corporation | Corrosion inhibitor |
| CN107381840B (zh) * | 2017-09-06 | 2020-10-16 | 钟司雨 | 一种环保型阻垢缓蚀剂及其制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3546216A (en) * | 1967-03-21 | 1970-12-08 | Phillips Petroleum Co | Schiff bases of amino-substituted tetrahydrothiophene 1,1-dioxides |
| US3705005A (en) * | 1971-06-21 | 1972-12-05 | Betz Laboratories | Aminoalkylene phosphonate derivatives as corrosion inhibitors in aqueous systems |
| US4120686A (en) * | 1975-06-28 | 1978-10-17 | Bayer Aktiengesellschaft | Composition for combating slimes |
| US4101441A (en) * | 1975-12-29 | 1978-07-18 | Chemed Corporation | Composition and method of inhibiting corrosion |
-
1978
- 1978-06-09 US US05/914,250 patent/US4181806A/en not_active Expired - Lifetime
- 1978-07-25 AU AU38323/78A patent/AU509872B2/en not_active Expired
- 1978-07-25 DK DK331078A patent/DK331078A/da not_active Application Discontinuation
- 1978-07-25 AR AR273058A patent/AR219118A1/es active
- 1978-07-27 NZ NZ188000A patent/NZ188000A/xx unknown
- 1978-08-01 SE SE7808309A patent/SE7808309L/ not_active Application Discontinuation
- 1978-08-02 ZA ZA00784373A patent/ZA784373B/xx unknown
- 1978-08-02 NO NO782640A patent/NO782640L/no unknown
- 1978-08-03 AT AT563478A patent/AT360444B/de not_active IP Right Cessation
- 1978-08-04 PT PT68388A patent/PT68388A/pt unknown
- 1978-08-14 FI FI782476A patent/FI782476A/fi unknown
- 1978-08-17 BE BE189923A patent/BE869794A/xx unknown
- 1978-08-18 DE DE19782836306 patent/DE2836306A1/de not_active Withdrawn
- 1978-08-21 ES ES472712A patent/ES472712A1/es not_active Expired
- 1978-08-24 FR FR7824560A patent/FR2428037A1/fr active Pending
- 1978-08-25 NL NL7808787A patent/NL7808787A/xx not_active Application Discontinuation
- 1978-08-31 BR BR7805732A patent/BR7805732A/pt unknown
- 1978-09-18 GR GR57258A patent/GR63760B/el unknown
- 1978-09-25 JP JP11783278A patent/JPS54163567A/ja active Pending
- 1978-10-12 IT IT51476/78A patent/IT1109209B/it active
-
1979
- 1979-01-12 GB GB7901177A patent/GB2022588A/en not_active Withdrawn
- 1979-01-30 IE IE790171A patent/IE790171L/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES472712A1 (es) | 1979-02-16 |
| PT68388A (en) | 1978-09-01 |
| NL7808787A (nl) | 1979-12-11 |
| IE790171L (en) | 1979-12-09 |
| AR219118A1 (es) | 1980-07-31 |
| GR63760B (en) | 1979-12-07 |
| GB2022588A (en) | 1979-12-19 |
| AU3832378A (en) | 1980-01-31 |
| IT7851476A0 (it) | 1978-10-12 |
| AT360444B (de) | 1980-01-12 |
| SE7808309L (sv) | 1979-12-10 |
| JPS54163567A (en) | 1979-12-26 |
| DE2836306A1 (de) | 1979-12-20 |
| BR7805732A (pt) | 1979-12-18 |
| US4181806A (en) | 1980-01-01 |
| AU509872B2 (en) | 1980-05-29 |
| FI782476A (fi) | 1979-12-10 |
| DK331078A (da) | 1979-12-13 |
| IT1109209B (it) | 1985-12-16 |
| BE869794A (fr) | 1978-12-18 |
| FR2428037A1 (fr) | 1980-01-04 |
| NZ188000A (en) | 1980-05-08 |
| ATA563478A (de) | 1980-05-15 |
| ZA784373B (en) | 1979-07-25 |
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