US3298956A - Lime soap dispersants - Google Patents
Lime soap dispersants Download PDFInfo
- Publication number
- US3298956A US3298956A US500170A US50017065A US3298956A US 3298956 A US3298956 A US 3298956A US 500170 A US500170 A US 500170A US 50017065 A US50017065 A US 50017065A US 3298956 A US3298956 A US 3298956A
- Authority
- US
- United States
- Prior art keywords
- soap
- lime
- lime soap
- dispersant
- groups
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000344 soap Substances 0.000 title claims description 176
- 235000008733 Citrus aurantifolia Nutrition 0.000 title description 73
- 235000011941 Tilia x europaea Nutrition 0.000 title description 73
- 239000004571 lime Substances 0.000 title description 73
- 239000002270 dispersing agent Substances 0.000 title description 65
- 239000000203 mixture Substances 0.000 claims description 51
- 150000001875 compounds Chemical class 0.000 claims description 24
- -1 amine ions Chemical class 0.000 description 49
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 39
- 229910052739 hydrogen Inorganic materials 0.000 description 30
- 239000001257 hydrogen Substances 0.000 description 27
- 239000002253 acid Substances 0.000 description 24
- 150000007513 acids Chemical class 0.000 description 18
- 229910052783 alkali metal Inorganic materials 0.000 description 17
- 150000004985 diamines Chemical class 0.000 description 15
- 238000000034 method Methods 0.000 description 15
- 150000002431 hydrogen Chemical class 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 13
- 229920001281 polyalkylene Polymers 0.000 description 12
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 150000001768 cations Chemical group 0.000 description 10
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 10
- 229910001413 alkali metal ion Inorganic materials 0.000 description 9
- 239000003568 Sodium, potassium and calcium salts of fatty acids Substances 0.000 description 7
- 125000002947 alkylene group Chemical group 0.000 description 7
- 159000000000 sodium salts Chemical class 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000002156 mixing Methods 0.000 description 5
- 235000013875 sodium salts of fatty acid Nutrition 0.000 description 5
- 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 4
- 150000001340 alkali metals Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003240 coconut oil Substances 0.000 description 4
- 235000019864 coconut oil Nutrition 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- SKVFQANNTIZUQZ-UHFFFAOYSA-N n-[2-[bis[hydroxy(methoxy)phosphoryl]amino]ethyl]-n-[hydroxy(methoxy)phosphoryl]-methoxyphosphonamidic acid Chemical compound COP(O)(=O)N(P(O)(=O)OC)CCN(P(O)(=O)OC)P(O)(=O)OC SKVFQANNTIZUQZ-UHFFFAOYSA-N 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000008233 hard water Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- QIISAGSPBUUPEL-UHFFFAOYSA-N n-[3-[bis[hydroxy(methoxy)phosphoryl]amino]propyl]-n-[hydroxy(methoxy)phosphoryl]-methoxyphosphonamidic acid Chemical compound COP(O)(=O)N(P(O)(=O)OC)CCCN(P(O)(=O)OC)P(O)(=O)OC QIISAGSPBUUPEL-UHFFFAOYSA-N 0.000 description 2
- SPDJZXXKQOBLBT-UHFFFAOYSA-N n-[6-[bis[hydroxy(methoxy)phosphoryl]amino]hexyl]-n-[hydroxy(methoxy)phosphoryl]-methoxyphosphonamidic acid Chemical compound COP(O)(=O)N(P(O)(=O)OC)CCCCCCN(P(O)(=O)OC)P(O)(=O)OC SPDJZXXKQOBLBT-UHFFFAOYSA-N 0.000 description 2
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 235000013966 potassium salts of fatty acid Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 239000000271 synthetic detergent Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical group COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 101150065749 Churc1 gene Proteins 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
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 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
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical group C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- PWSKHLMYTZNYKO-UHFFFAOYSA-N heptane-1,7-diamine Chemical compound NCCCCCCCN PWSKHLMYTZNYKO-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical group [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- CSDLJVNYTSFFMX-UHFFFAOYSA-N n-[1-[bis[hydroxy(methoxy)phosphoryl]amino]propan-2-yl]-n-[hydroxy(methoxy)phosphoryl]-methoxyphosphonamidic acid Chemical compound COP(O)(=O)N(P(O)(=O)OC)CC(C)N(P(O)(=O)OC)P(O)(=O)OC CSDLJVNYTSFFMX-UHFFFAOYSA-N 0.000 description 1
- DTFVZBDOFYGMCY-UHFFFAOYSA-N n-[10-[bis[hydroxy(methoxy)phosphoryl]amino]decyl]-n-[hydroxy(methoxy)phosphoryl]-methoxyphosphonamidic acid Chemical compound COP(O)(=O)N(P(O)(=O)OC)CCCCCCCCCCN(P(O)(=O)OC)P(O)(=O)OC DTFVZBDOFYGMCY-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000006324 propenyl amino group Chemical group 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/34—Organic compounds, e.g. vitamins containing phosphorus
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/36—Organic compounds containing phosphorus
- C11D3/364—Organic compounds containing phosphorus containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/30—Organic compounds, e.g. vitamins containing nitrogen
Definitions
- This invention relates to lime soap dispersants and more particularly to the use of organo-amino polymethyl phosphonic acids and/ or the salts thereof as lime soap dispersants in soap formulations, to the compositions resulting therefrom, and to the use of such compositions in aqueous systems.
- lime soap i.e., the water insoluble scum or curd of wash water when soap is used for laundering, personal washing and bathing is, of course, familiar.
- the lime soap which results from the reaction of soap with so called hardness i-ons such as, calcium, magnesium and iron is particularly objectionable because of its ability to stick to surfaces such as bathtubs, Washing tubs, clothes and the like with which it comes into contact, and its ability to resist removal therefrom.
- lime soap dispersants In general, the most widely accepted method for reducing and minimizing the objectionable effects of the lime soap involves the use of lime soap dispersants. These agents are believed to disperse the lime soap and keep the lime soap dispersed by a peptizing action in the aqueous system in order to reduce or minimize the build up of lime soap thereby reducing the objectionable tendencies to stick to the surfaces with which they come into contact.
- the more Widely used lime soap dispersants are synthetic surface active agents although only a very few of these synthetic surface active agents have the necessary qualifications to be useful as lime soap dispersants. As can be appreciated, therefore, there is a constant demand for better and more economical lime soap dispersants.
- Another object of this invention is to provide a soap composition having incorporated therein a lime soap dispersant.
- a still further object of this invention is to provide an improved soap composition having incorporated therein a lime soap dispersant, said soap composition exhibiting improved properties in aqueous systems.
- X is a cation selected from the class consisting of hydrogen, alkali metal ion, ammonium ion, and amine ions
- Y and Y are members selected from the class con sisting of hydrogen and lower alkyl groups (1-4 carbon atoms);
- R is a member selected from the class consisting of hydrogen, aliphatic groups containing from 1 to 30 carbon atoms, and
- R is a member selected from the class consisting of hydrogen, aliphatic groups containing from 1 to 30 carbon atoms,
- n is an integer from 1 to 30;
- organoaamino polymethylphosphonic acids or the salts thereof generically described all of the foregoing.
- the groups may be branched or straight chained and wherein R and R represent aliphatic groups, the groups may be branched or straight chained as Well as being saturated or unsaturated although it is preferred that if the groups are unsaturated they be ethylenically unsaturated.
- the foregoing mentioned groups may contain substituent groups, such as, hydroXyl, halides, i.e., fluoride, chloride, bromide, and iodide, alkoxy groups, sulfonyl groups, carboxyl groups, amide groups and amino groups.
- the lime soap dispersant of the instant invention need contain only two phosphonic acid groups, in most cases the more such groupings the compound contains the better lime soap dispersant it appears to be and, therefore, it is preferred that the lime soap dispersant of the instant invention contain at least 3 phosphonic acid groups and especially preferred are those containing 4 or more phosphonic acid groups.
- the organo-amino polymethylphosphonic acids or the salts thereof may be prepared by various means.
- the method comprises as a first step the preparation of the corresponding esters by reacting under reactive conditions a primary amine or secondary amine, a compound containing a carbonyl group such as an aldehyde or ketone, and a dialkylphosphite.
- the free organo-amino polymethylphosphonic acids may be prepared by hydrolysis of the esters.
- R R Y and Y represent the same groups as in the foregoing general Formula I and R represents an alkyl group.
- Another method for preparing organo-amino polymethylphosphonic acids or the salts thereof comprises preparing the free acid directly by reacting under reactive conditions a primary or secondary amine, a compound containing a carbonyl group such as an aldehyde or ketone, and orthophosphorous acid. This process is set-forth in co-pending application Serial No. 217,276.
- R R Y and Y represent the same groups as in the foregoing general Formula I.
- a still further method for preparing organo-amino polymethylphosphonic acids or the salts thereof comprises preparing the free acid by the substitution reaction between a halomethylphosphonic acid and an alkylene amine (preferably a di or poly alkylene amine).
- n is an integer between 1 and 30 and X is a halogen (preferably chlorine or bromine).
- the salts of the organo-amino polymethylphosphonic acids can be prepared by the neutralization of the acids with a stoichiometric amount of a base that contains essentially the desired cation.
- Bases such as those containing an alkali metal, ammonium and amines are especially suited.
- a sodium salt one of organo-amino polyrnethylphosphonic acids can be neutralized with a stoichiometric amount of a base containing the sodium cation, such as NaOH, Na CO and the like.
- any water soluble salt such as the ammonium salt and the amine salts, which exhibit the characteristics of the alkali metal salt may be used to practice the invention.
- amine salts prepared from low molecular weight amines i.e., having a molecular weight below about 300, and more particularly the alkyl amines, alkylene amines and alkanol amines containing not more than 2 amine groups, such as, ethyl amine, diethyl amine, propyl amine, propylene diamine, hexyl amine, Z-ethyl hexyl amine, N-butyl ethanolamine, triethanol amine and the like, are the preferred amine salts.
- soap means an alkali metal, ammonium, or amine salt of a fatty acid or mixtures of 55 fatty acids which are capable of being used as washing and cleansing agents in aqueous mediums, and any of the Water soluble soaps formulated for industrial, household or toilet use may be employed.
- the character of the soap constituent may vary widely in its composition depending on, inter alia, whether the final soap composition is to be in powder, spray-dried, flake, bar, paste, liquid or other form.
- Water soluble soaps such as the sodium soaps and other suitable alkali metal, ammonium, or amine soaps derived from such fats and oils as tallow, coconut oil, cottonseed oil, soy bean oil, corn oil, olive oil, palm oil, peanut oil, palm kernal oil, lard, greases, fish oils and the like as well as their hydrogenated derivatives, and mixtures thereof, properly blended to yield the desired soap quality may be used in the soap composition of the present invention.
- Illustrative examples of such soaps include a soap containing about 15 to 20% of sodium salts of fatty acids derived from coconut oil and 80 to 85% of sodium salts of fatty acids derived from tallow, a soap containing about 100% of sodium salts of fatty acids derived from tallow, a soap containing about 20% of potassium salts of fatty acids derived from coconut oil and about of potassium salts of fatty acids derived from soy bean oil and the like.
- the amount of the lime soap dispersant necessary to be used with the soap may vary, depending upon, inter alia, the end use, type of soap employed, pH conditions and the like. In general, any amount and especially amounts above about 1 weight percent based on the weight of soap in the compositions exhibit lime soap dispersant properties, however, it is preferred that amounts of lime soap dispersants on a weight ratio to soap of from about 5:95 and 70:30 percent be utilized.
- organo-amino polymethylphosphonic acids may be used by adjusting the pH, if required, of the soap compositions or the resulting aqueous solution to the desired alkaline pH condition.
- the pH of the soap composition or the aqueous medium be such as to result in an aqueous washing solution having at least a pH of 7 or above and at least a pH of 9 or above is especially preferred such as a pH of from about 9 to about 11, when the soap composition is used in amounts to give effective cleansing action.
- the resulting soap composition that is, the soap and the lime soap dispersant composition, of the present invention is generally effective when used in aqueous systems in conventional amounts such as is normally used with soap compositions and which is generally above about .01% concentration.
- the lime soap dispersant can be used with any form of the soap, i.e., bar soap, soap flakes, soap powder and the like and can be blended with the soap prior to the time the final soap composition is formed or can be added to the aqueous medium in which the soap composition is intended to be used prior to or after the soap composition has been added.
- the blending operation with soap can be carried out, if desired, in conventional soap equipment such as a crutcher, or in practically any mixing vessel that can be used to formulate soap (i.e., in which molten soap can be handled), such as a conventional amalgamator, a conventional refiner, or even a conventional soap mill.
- the soap composition After the soap composition is formed it can generally be handled via conventional techniques and equipment in a manner similar to that in which lain or conventional soap is handled: for example, through the usual plodding, sizing, cooling, stamping and packaging operations.
- the lime soap dispersant is intended to be used with the soap at the time of application as a cleansing agent.
- the soap compositions in which the lime soap dispersant may be incorporated may contain, if desired, other materials, usually in amounts below about 50% by weight of soap, which are commonly used with soaps, such as, synthetic detergents of the anionic and nonionic class, polyphosphate builders, antiredepositon agents (e.g. carboxy methyl cellulose), brightening agents (e.g. fluorescent dyes), bleaching agents and the like as long as the usual considerations of compatability are applied.
- synthetic detergents of the anionic and nonionic surface active compound type these may be any of the conventional detergents which are suitable as cleansing agents.
- Anionic surface active compounds can be broadly described as compounds which contain hydrophilic and hydrophobic .groups in their molecular structure and which ionize in an aqueous medium to give anions containing the hydrophobic group.
- These compounds are usually the alkali metal salts of oragnic sulfonates or sulfates, particularly the sodium salts, such as alkyl, aryl, sulfonates (e.g. sodium dodecylbenzene sulfonate), sulfates of straight chain primary alcohols (e.g. sodium lauryl sulfate) and the like.
- Nonionic surface active compounds can be broadly described as compounds which do not ionize but acquire hydrophilic characteristics from an oxygenated side chain, usually polyorryethylene, While the hydrophobic part of the molecule may come from fatty acids, phenols, alcohols, amides or amines.
- the polyethylene oxide condensates of alkyl phenols e.g., condensation product formed from 1 .mole nonyl phenol and moles ethylene oxide
- the condensation products of aliphatic alcohols and ethylene oxide e.g., condensation product formed from 1 mole tridecanol and 12 moles ethylene oxide
- alkyl phenols e.g., condensation product formed from 1 .mole nonyl phenol and moles ethylene oxide
- condensation products of aliphatic alcohols and ethylene oxide e.g., condensation product formed from 1 mole tridecanol and 12 moles ethylene oxide
- polyalkylene diamine polymethylphosphonic acids or the water soluble salts thereof are particularly effective as lime soap dispersants and are, therefore, the preferred lime soap dispersants of the organo-amino polymethylphosphonic acids or the salts thereof.
- These polyalkylene diamine polymethylphosphonic acids or the salts thereof have the following formula:
- n is an integer from 2 to inclusive;
- R R R and R are selected from the class consisting of H and with not more than two of the groups being H and wherein X is a cation selected from the class consisting of hydrogen, alkali metal ions, ammonium ion and amine ions.
- polyalkylene diamine polymethylphosphonic compounds containing four phosphonic groups that is, a pair of two phosphonic groups separated by a nitrogen-polyalkylene-nitrogen chain containing not more than 14 carbon atoms.
- Such polyalkylene diamine tetra(rnethylphosphonic) compounds include ethylene diamine tetra(methylphosphonic acid), trimethylene diamine tetra(methylphosphonic acid), hexamethylene diamine tetra(methylphosphonic acid), octamethylene diamine tetra(methylphosphonic acid), decamethylene diamine tetra(methylphosphonic acid), dodecamethylene diamine tetra(methyl-phosphonic acid), and tetradecamethylene diamine tetra-(methylphosphonic acid).
- Table 1 illustrates some of the benefits that can result from utilizing the preferred polyalkylene diamine polymethylphosphonic acids or the salts thereof as lime soap dispersants.
- the test which is used herein i.e., the measurement of the relative stickiness of lime soap scum or curds, has been found to correlate remarkably Well with the effectiveness of the lime soap dispersant in actual use. Effective lime soap dispersants decrease or minimize the stickiness of the lime soap curds.
- the test which is conducted at a temperature between 30 and 35 C., 250 parts per million hard water (calculated as CaCO having a CazMg ratio of 2:1 is utilized. Five mls.
- soap and lime soap dispersant blend a 1 weight percent soap solution (or soap and lime soap dispersant blend) are shaken vigorously in a 50 ml. test tube. Then the resulting foam is immediately stirred slowly into 500 mls. of hard water in a 600 ml. beaker. After all of the foam is quenched and the solution has stood undisturbed for 2 hours, the amount and particle size of scum, or suspended lime soap curd, are observed and rated in comparison with soap alone and standard soap and lime soap dispersant composition. Soap gives a rating of 10, while the standard soap and lime soap dispersant composition is rated 3 in a test such as that just described.
- the soap is comprised of about 15% of sodium salts of fatty acids derived from coconut oil (primarily ltttll'ic acid) and 85% of sodium salts of fatty acids derived from tallow (approximritfily 40% stearic acid, 30% oleic acid and 30% palmitic ac
- the preferred compounds of the instant invention function as lime soap dispersants as well as or better than conventional lime soap dispersants when compared with the standard soap and lime soap dispersant composition and by comparison with the soap control they markedly affect the lime soap formation in aqueous systems.
- n is an integer from 1 to 30;
- Z is a member selected from the class consisting of hydrogen and and Z is a member selected from the class consisting of hydrogen,
- m is an integer from 1 to 30; with at least one of the groups represented by R and R containing at least one group.
- a process for utilizing an organo-amino polymethylphosphonic compound as a lime soap dispersant comprises adding soap and said lime soap dispersant simultaneously or in any order to water and dissolving said addition mixture in said water, said organoamino polymethylphosphonic compound having the formula R YO N( l Br Y wherein X is a cation selected from the class consisting of hydrogen, alkali metal ion, ammonium ion, and lower molecular weight alkyl, alkylene and alkanol amine ions; Y and Y are members selected from the class consisting of hydrogen and lower alkyl groups containing from 1 to 4 carbon atoms; R is a member selected from the class consisting of hydrogen aliphatic groups containing from 1 to 30 carbon atoms, and
- R is a member selected from the class consisting of hydrogen, aliphatic groups containing from 1 to 30 carbon atoms,
- n is an integer from 1 to 30;
- m is an integer from 1 to 30; with at least one of the groups represented by R and R containing at least one group and said lime soap dispersant being added in amounts of at least 1% by Weight based on the weight of said soap.
- a process of making a soap composition having low scumming characteristics which comprises blending into a molten soap at least 1 weight percent based on the 10 weight of said soap of a compound capable of being represented by the formula wherein X is a cation selected from the class consisting of hydrogen, alkali metal ion, ammonium ion, and lower molecular weight ,alkyl, alkylene and alkanol amine ions; Y and Y are members selected from the class consisting of hydrogen and lower alkyl groups containing from 1 to 4 carbon atoms; R is a member selected from the class consisting of hydrogen aliphatic groups containing from 1 to 30 carbon atoms, and
- R is a member selected from the class consisting of hydrogen, aliphatic groups containing from 1 to 30 carbon atoms wherein n is an integer from 1 to 30;
- Z is a member selected from the class consisting of hydrogen and and Z is a member selected from the class consisting of hydrogen,
- m is an integer from 1 to 30; with at least one of the group represented by R and R containing at least one OOX with not more than two of the groups being H and wherein X is a cation selected from the class consisting of hydrogen, alkali metal ions, ammonium ion and lower molecular weight alkyl, alkylene and alkanol amine ions. 5.
- a process of making a soap composition having low scumming characteristics which comprises blending into molten soap in amounts of from about 5% to about 70% by weignt based on said soap of a compound capable of being represented by the formula 1 1 wherein n is an integer from 2 to 20 inclusive; R R R and R are selected from the class consisting of H and OOX with not more than two of the groups being H and wherein X is a cation selected from the class consisting of hydrogen, alkali metal ions, ammonium ion and lower molecular weight alkyl, alkylene and alkanol amine ions. 6.
- a soap composition consisting essentially of soap and a lime soap dispersant in a weight ratio of said soap to said lime soap dispersant of from about 95:5 to 30:70, said lime soap dispersant being an alkali metal salt of polyalkylene diamine polymethylphosphonic acid, said salt having the formula N H2)n N R, R wherein n is an integer from 2 to 20 inclusive; R R R and R are selected from the class consisting of H and OOX with not more than two of the groups being H and wherein X is an alkali metal cation.
- a soap composition coonsist essentially of, in addition to soap, a lime soap dispersant in a weight ratio of said soap to said lime soap dispersant of from about 95 to 35 :70, said lime soap dispersant being a polyalkylenediamine tetra(methylphosphonic) compound having the formula wherein n is an integer from 2 to 14 inclusive and X is a cation selected from the class consisting of hydrogen, alkali metal ions, ammonium ion, and lower molecular weight alkyl, alkylene and alkanol amine ions.
- a soap composition consisting essentially of, in addition to soap, a lime soap dispersant in a weight ratio of said soap to said lime soap dispersant of from about 95:5 to 30:70, said lime soap dispersant being an alkali metal salt of a polyalkylene diamine tetra(methylphosphonic acid) having the formula HO 0 0 OH i 11.0 ol-ni 110 011 no 0 0 on i HzC CHzi wherein n is an integer from 2 to 14 inclusive.
- a soap composition consisting essentially of, in addition to soap, a lime soap dispersant in a weight ratio of said soap to said lime soap dispersant of from about 95:5 to 30:70, said iime soap dispersant being an alkali metal salt of ethylene diamine tetra(methylphosphonic acid).
- a soap composition consisting essentially of, in addition of soap, a lime soap dispersant in a weight ratio of said soap to said lime dispersant of from about :5 to 30:70, said lime soap dispersant being an alkali metal salt of hex-amethylene diamine tetra(met-hylphosphonic acid).
- a process for utilizing a polyalkylene diamine tetra(methylphosphonic) compound as a lime soap dispersant comprises adding soap and said lime soap dispersant simultaneously or in any order to water and dissolving said addition mixture in said water, said polyalkylene diamine tetra(methylphosphonic) compound having the formula X0 0 0 OX ii H2O CHZIIL/ X0 ⁇ OX X0 0 0 0X ii' HzC CH2ii X0 OX wherein n is an integer from 2 to 14 inclusive and X is a cation selected from the class consisting of hydrogen, alkali metal ions, ammonium ion, and lower molecular weight alkyl, alkyene and alkanol amine ions, said lime soap dispersant being added in amounts
- said lime soap dispersant is a sodium salt of said polylalkylene diamine tetra(methylphosphonic acid).
- a process of making a soap composition having low scurnming characteristics which comprises blending into molten soap in amounts of from about 5 to 70% by weight based on said soap of a polyalkylene diamine tetra(methylphosphonic) compound capable of being represented by the formula wherein n is an integer from 2 to 14 inclusive and X is a cation selected from the class consisting of hydrogen, alkali metal ions, ammonium ions, and lower molecular weight alkyl, alkylene and alkanol amine ions.
- said lime soap dispersant is a sodium salt of said polyalkylene diamine tetra- (methylphosphonic acid).
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Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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DENDAT1250042D DE1250042B (da) | 1965-10-21 | ||
US500170A US3298956A (en) | 1965-10-21 | 1965-10-21 | Lime soap dispersants |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US500170A US3298956A (en) | 1965-10-21 | 1965-10-21 | Lime soap dispersants |
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US3298956A true US3298956A (en) | 1967-01-17 |
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US500170A Expired - Lifetime US3298956A (en) | 1965-10-21 | 1965-10-21 | Lime soap dispersants |
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Cited By (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3475293A (en) * | 1964-09-22 | 1969-10-28 | Monsanto Co | Electrodeposition of metals |
US3483178A (en) * | 1968-04-18 | 1969-12-09 | Monsanto Co | Esters,salts,and acids of organo-phosphono-amine oxides |
US3678164A (en) * | 1969-02-12 | 1972-07-18 | Procter & Gamble | Compositions for inhibiting anomalous deposition and mobilization of calcium phosphate in animal tissue |
US3714067A (en) * | 1971-07-07 | 1973-01-30 | Monsanto Co | Methods of inhibiting corrosion with condensed polyalkylenepolyamine phosphonates |
US3723347A (en) * | 1972-05-17 | 1973-03-27 | Monsanto Co | Corrosion inhibition compositions containing substituted diamine phosphonates and processes for using the same |
USB336566I5 (da) * | 1973-02-28 | 1975-01-28 | ||
US3974209A (en) * | 1971-08-04 | 1976-08-10 | Monsanto Company | Substituted tertiary amines and processes for preparing the same |
US3976589A (en) * | 1971-08-04 | 1976-08-24 | Monsanto Company | Methods of scale inhibition |
US4033896A (en) * | 1976-06-18 | 1977-07-05 | Monsanto Company | Method of corrosion inhibition and compositions therefor |
US4065491A (en) * | 1974-06-27 | 1977-12-27 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt. | Process for the preparation of N-phosphonomethyl-glycine |
US4080375A (en) * | 1971-02-05 | 1978-03-21 | Petrolite Corporation | Methylene phosphonates of amino-terminated oxyalkylates and uses therefor |
US4084950A (en) * | 1972-03-24 | 1978-04-18 | Petrolite Corporation | Use of polyquaternary ammonium methylene phosphonates as microbiocides |
US4143128A (en) * | 1976-02-25 | 1979-03-06 | Colgate Palmolive Company | Oral compositions for calculus retardation |
US4144324A (en) * | 1976-10-08 | 1979-03-13 | Colgate Palmolive Company | Oral compositions for calculus retardation |
US4177258A (en) * | 1978-10-13 | 1979-12-04 | Colgate Palmolive Company | Dentifrice for dental remineralization |
US4183915A (en) * | 1978-10-13 | 1980-01-15 | Colgate-Palmolive Company | Stable solution for dental remineralization |
US4184912A (en) * | 1976-08-09 | 1980-01-22 | Nalco Chemical Company | Pitch control method |
US4187245A (en) * | 1975-06-02 | 1980-02-05 | Petrolite Corporation | Hydroxypropylene-amino-phosphonic-sulfonic acids |
US4229294A (en) * | 1979-05-24 | 1980-10-21 | Petrolite Corporation | Hydroxypropylene-amino-phosphonic-sulfonic acids for inhibiting scale formation |
US4297299A (en) * | 1980-01-10 | 1981-10-27 | National Starch And Chemical Corporation | Novel N-(alkyl)-N-(2-haloethyl)-aminomethylphosphonic acids, a method for the preparation thereof and their use in the preparation of starch ether derivatives |
US4450116A (en) * | 1981-07-21 | 1984-05-22 | Hoechst Aktiengesellschaft | 3-Oxypropyleneimino-bis-(methylene phosphonic acids) and their salts, process for their manufacture and their use |
US4548757A (en) * | 1984-03-02 | 1985-10-22 | The Procter & Gamble Company | Aqueous aminomethylenephosphonic acid solutions containing organic carboxylate stabilizing agent |
US4950474A (en) * | 1988-08-01 | 1990-08-21 | Texaco Inc. | Combination corrosion and scale inhibiting system containing phosphonate/amine reaction product |
US5068042A (en) * | 1990-07-26 | 1991-11-26 | Mobil Oil Corporation | Dissolution of sulfate scales |
US5864003A (en) * | 1996-07-23 | 1999-01-26 | Georgia-Pacific Resins, Inc. | Thermosetting phenolic resin composition |
US5962603A (en) * | 1996-07-23 | 1999-10-05 | Georgia-Pacific Resins, Inc. | Intumescent composition and method |
US6264839B1 (en) * | 1989-08-07 | 2001-07-24 | Basf Aktiengesellschaft | Phosphonomethylated polyvinylamines and preparation and use thereof |
US6274541B1 (en) | 1994-02-23 | 2001-08-14 | Ecolab Inc. | Alkaline cleaners based on alcohol ethoxy carboxylates |
US20030139315A1 (en) * | 1994-02-23 | 2003-07-24 | Man Victor Fuk-Pong | Alkaline cleaners based on alcohol ethoxy carboxylates |
US20060020102A1 (en) * | 2004-07-26 | 2006-01-26 | Georgia-Pacific Resins, Inc. | Phenolic resin compositions containing etherified hardeners |
US20060191851A1 (en) * | 2005-02-25 | 2006-08-31 | Mizuno William G | Method for treating feedwater, feedwater treatment composition, and apparatus for treating feedwater |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2240957A (en) * | 1935-10-30 | 1941-05-06 | Gen Aniline & Film Corp | Process for avoiding and rendering harmless the precipitates of water insoluble metal salts |
-
0
- DE DENDAT1250042D patent/DE1250042B/de active Pending
-
1965
- 1965-10-21 US US500170A patent/US3298956A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2240957A (en) * | 1935-10-30 | 1941-05-06 | Gen Aniline & Film Corp | Process for avoiding and rendering harmless the precipitates of water insoluble metal salts |
Cited By (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3475293A (en) * | 1964-09-22 | 1969-10-28 | Monsanto Co | Electrodeposition of metals |
US3483178A (en) * | 1968-04-18 | 1969-12-09 | Monsanto Co | Esters,salts,and acids of organo-phosphono-amine oxides |
US3678164A (en) * | 1969-02-12 | 1972-07-18 | Procter & Gamble | Compositions for inhibiting anomalous deposition and mobilization of calcium phosphate in animal tissue |
US4080375A (en) * | 1971-02-05 | 1978-03-21 | Petrolite Corporation | Methylene phosphonates of amino-terminated oxyalkylates and uses therefor |
US3714067A (en) * | 1971-07-07 | 1973-01-30 | Monsanto Co | Methods of inhibiting corrosion with condensed polyalkylenepolyamine phosphonates |
US3974209A (en) * | 1971-08-04 | 1976-08-10 | Monsanto Company | Substituted tertiary amines and processes for preparing the same |
US3976589A (en) * | 1971-08-04 | 1976-08-24 | Monsanto Company | Methods of scale inhibition |
US4084950A (en) * | 1972-03-24 | 1978-04-18 | Petrolite Corporation | Use of polyquaternary ammonium methylene phosphonates as microbiocides |
US3723347A (en) * | 1972-05-17 | 1973-03-27 | Monsanto Co | Corrosion inhibition compositions containing substituted diamine phosphonates and processes for using the same |
USB336566I5 (da) * | 1973-02-28 | 1975-01-28 | ||
US4065491A (en) * | 1974-06-27 | 1977-12-27 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt. | Process for the preparation of N-phosphonomethyl-glycine |
US4187245A (en) * | 1975-06-02 | 1980-02-05 | Petrolite Corporation | Hydroxypropylene-amino-phosphonic-sulfonic acids |
US4143128A (en) * | 1976-02-25 | 1979-03-06 | Colgate Palmolive Company | Oral compositions for calculus retardation |
US4033896A (en) * | 1976-06-18 | 1977-07-05 | Monsanto Company | Method of corrosion inhibition and compositions therefor |
US4184912A (en) * | 1976-08-09 | 1980-01-22 | Nalco Chemical Company | Pitch control method |
US4144324A (en) * | 1976-10-08 | 1979-03-13 | Colgate Palmolive Company | Oral compositions for calculus retardation |
US4177258A (en) * | 1978-10-13 | 1979-12-04 | Colgate Palmolive Company | Dentifrice for dental remineralization |
US4183915A (en) * | 1978-10-13 | 1980-01-15 | Colgate-Palmolive Company | Stable solution for dental remineralization |
US4229294A (en) * | 1979-05-24 | 1980-10-21 | Petrolite Corporation | Hydroxypropylene-amino-phosphonic-sulfonic acids for inhibiting scale formation |
US4297299A (en) * | 1980-01-10 | 1981-10-27 | National Starch And Chemical Corporation | Novel N-(alkyl)-N-(2-haloethyl)-aminomethylphosphonic acids, a method for the preparation thereof and their use in the preparation of starch ether derivatives |
US4450116A (en) * | 1981-07-21 | 1984-05-22 | Hoechst Aktiengesellschaft | 3-Oxypropyleneimino-bis-(methylene phosphonic acids) and their salts, process for their manufacture and their use |
US4548757A (en) * | 1984-03-02 | 1985-10-22 | The Procter & Gamble Company | Aqueous aminomethylenephosphonic acid solutions containing organic carboxylate stabilizing agent |
US4950474A (en) * | 1988-08-01 | 1990-08-21 | Texaco Inc. | Combination corrosion and scale inhibiting system containing phosphonate/amine reaction product |
US6264839B1 (en) * | 1989-08-07 | 2001-07-24 | Basf Aktiengesellschaft | Phosphonomethylated polyvinylamines and preparation and use thereof |
US5068042A (en) * | 1990-07-26 | 1991-11-26 | Mobil Oil Corporation | Dissolution of sulfate scales |
US6274541B1 (en) | 1994-02-23 | 2001-08-14 | Ecolab Inc. | Alkaline cleaners based on alcohol ethoxy carboxylates |
US6479453B2 (en) | 1994-02-23 | 2002-11-12 | Ecolab Inc. | Alkaline cleaners based on alcohol ethoxy carboxylates |
US20030139315A1 (en) * | 1994-02-23 | 2003-07-24 | Man Victor Fuk-Pong | Alkaline cleaners based on alcohol ethoxy carboxylates |
US7037884B2 (en) | 1994-02-23 | 2006-05-02 | Ecolab Inc. | Alkaline cleaners based on alcohol ethoxy carboxylates |
US5962603A (en) * | 1996-07-23 | 1999-10-05 | Georgia-Pacific Resins, Inc. | Intumescent composition and method |
US5864003A (en) * | 1996-07-23 | 1999-01-26 | Georgia-Pacific Resins, Inc. | Thermosetting phenolic resin composition |
US20060020102A1 (en) * | 2004-07-26 | 2006-01-26 | Georgia-Pacific Resins, Inc. | Phenolic resin compositions containing etherified hardeners |
US7087703B2 (en) | 2004-07-26 | 2006-08-08 | Georgia-Pacific Resins, Inc. | Phenolic resin compositions containing etherified hardeners |
US20060191851A1 (en) * | 2005-02-25 | 2006-08-31 | Mizuno William G | Method for treating feedwater, feedwater treatment composition, and apparatus for treating feedwater |
US20080223791A1 (en) * | 2005-02-25 | 2008-09-18 | Ecolab Inc. | Method for treating feedwater |
US7537705B2 (en) | 2005-02-25 | 2009-05-26 | Ecolab Inc. | Method for treating feedwater |
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