GB1122371A - Organotin compositions - Google Patents
Organotin compositionsInfo
- Publication number
- GB1122371A GB1122371A GB40441/65A GB4044165A GB1122371A GB 1122371 A GB1122371 A GB 1122371A GB 40441/65 A GB40441/65 A GB 40441/65A GB 4044165 A GB4044165 A GB 4044165A GB 1122371 A GB1122371 A GB 1122371A
- Authority
- GB
- United Kingdom
- Prior art keywords
- surfactant
- tin
- bond
- carbon
- alk
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title abstract 11
- 239000004094 surface-active agent Substances 0.000 abstract 17
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical group [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 8
- 230000002209 hydrophobic effect Effects 0.000 abstract 8
- 229910052718 tin Inorganic materials 0.000 abstract 8
- 150000001450 anions Chemical class 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000005702 oxyalkylene group Chemical group 0.000 abstract 4
- 150000003606 tin compounds Chemical class 0.000 abstract 4
- 230000000844 anti-bacterial effect Effects 0.000 abstract 3
- 230000000855 fungicidal effect Effects 0.000 abstract 3
- 239000003921 oil Substances 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- 229910001868 water Inorganic materials 0.000 abstract 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 abstract 2
- 230000002353 algacidal effect Effects 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- LINPIYWFGCPVIE-UHFFFAOYSA-N 2,4,6-trichlorophenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1Cl LINPIYWFGCPVIE-UHFFFAOYSA-N 0.000 abstract 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 abstract 1
- 239000004115 Sodium Silicate Substances 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 239000003899 bactericide agent Substances 0.000 abstract 1
- 239000012141 concentrate Substances 0.000 abstract 1
- 239000000498 cooling water Substances 0.000 abstract 1
- 239000010730 cutting oil Substances 0.000 abstract 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract 1
- 238000010410 dusting Methods 0.000 abstract 1
- 150000002731 mercury compounds Chemical class 0.000 abstract 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- -1 poly (ethyleneoxy) ethanol Chemical class 0.000 abstract 1
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 235000017550 sodium carbonate Nutrition 0.000 abstract 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 abstract 1
- 235000019795 sodium metasilicate Nutrition 0.000 abstract 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052911 sodium silicate Inorganic materials 0.000 abstract 1
- 229910052938 sodium sulfate Inorganic materials 0.000 abstract 1
- 235000011152 sodium sulphate Nutrition 0.000 abstract 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 abstract 1
- 229940001496 tribasic sodium phosphate Drugs 0.000 abstract 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 abstract 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
- C10M2227/083—Sn compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
Abstract
A bactericidal and fungicidal composition, suitable for addition to emulsifiable oil compositions and cleansing compositions comprises an organotin compound of the general formula YmSnX4- m; (Y2SnO)a; or (YSnO1. 5)a in which m is an integer from 1 to 3; a is at least 2; X is an inorganic or organic radical or anion attached to the tin atom by a bond other than a carbon-tin bond; and Y is an organic radical attached to the tin atom by a carbon-tin bond, and a surfactant having a critical balance of hydrophobic and hydrophilic groups therein such that the tin compound remains dissolved in the surfactant on standing and does not separate out, the surfactant having the general formula R-(Alk-O)zH in which R is a hydrophobic radical: Alk is an alkylene radical containing 2 to 4 carbon atoms, and z is the number of oxyalkylene units which impart a solubility of at least 3% to the surfactant. Emulsifiable oil compositions mentioned are cutting oils and oil concentrates which, when diluted with water, are used to prepare oily cloths for industrial dusting or wiping purposes. An example of a cleansing composition to which the organotin composition may be added is a household cleaner consisting of nonylphenoxypoly (ethyleneoxy) ethanol, tribasic sodium phosphate, tetrasodium pyrophosphate, sodium metasilicate, sodium carbonate, sodium sulphate and water.ALSO:A fungicidal and algicidal composition, suitable for inhibiting the formation of slime in cooling water systems and paper mills, comprises an organotin compound of the general formula YmSnX4- m; (Y2SnO)a; or (YSnO1.5)a in which m is an integer from 1 to 3; a is at least 2; X is an inorganic or organic radical or anion attached to the tin atom by a bond other than a carbon-tin bond; and Y is an organic radical attached to the tin atom by a carbon-tin bond, and a surfactant having a critical balance of hydrophobic and hydrophilic groups therein such that the tin compound remains dissolved in the surfactant on standing and does not separate out, the surfactant having the general formula R-(Alk-O)zH in which R is a hydrophobic radical; Alk is an alkylene radical containing 2 to 4 carbon atoms, and z is the number of oxyalkylene units which impart a solubility of at least 3% to the surfactant. Surfactants exemplified are nonyl phenol/ alkylene oxide/diethanolamine condensates. 2,4,6-Trichlorophenol may also be present.ALSO:A fungicidal and algicidal composition, suitable for inhibiting the formation of slime in paper mills, comprises an orgonotion compound of the general formula:- Ym Sn X4-m; (Y2 SnO)8; or (YSnO1,5)8 in which n is an integer from 1 to 3; a is at least 2; x is an inorganic or organic radical or anion attached to the tin atom by a bond or other than a carbon-tin bond; and Y is an organic radical attached to the tin atom by a carbon-tin bond and a surfactant having a critical balance of hydrophobic and hydrophilic groups therein such that the tin compound remains dissolved in the surfactant on standing and does not separate out, the surfactant having the general formula:- R-(Alk-0)zH in which R is a hydrophobic radical Alk is an alkylene radical containing 2 to 4 carbon atoms and z is the number of oxyalkylene units which impart a solubility of at least 3% to the surfactant. The composition may be added at the beater stage of operation or at other suitable points of application, such as to the white water.ALSO:A pesticidal and bactericidal composition comprises an organotin compound of the general formula: Ym SnX4-m; (Y2SnO)a; or (YSnO1,5)a in which m is an integer from 1 to 3; a is at least 2; X is an inorganic or organic radical or anion attached to the tin atom by a bond other than a carbon-tin bond; and Y is an organic radical attached to the tin atom by a carbon-tin bond, and a surfactant having a critical balance of hydrophobic and hydrophilic groups therein such that the tin compound remains dissolved in the surfactant on standing and does not separate out, the surfactant having the general formula: R - (Alk-O)z H in which R is a hydrophobic radical; Alk is an alkylene radical containing 2 to 4 carbon atoms, and z is the number of oxyalkylene units which impart a solubility of at least 3% to the surfactant. Organic mercury compounds and quaternary ammonium bactericides also may be present.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB40441/65A GB1122371A (en) | 1965-09-22 | 1965-09-22 | Organotin compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB40441/65A GB1122371A (en) | 1965-09-22 | 1965-09-22 | Organotin compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1122371A true GB1122371A (en) | 1968-08-07 |
Family
ID=10414918
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB40441/65A Expired GB1122371A (en) | 1965-09-22 | 1965-09-22 | Organotin compositions |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1122371A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4343815A (en) * | 1973-08-30 | 1982-08-10 | M&T Chemicals Inc. | Method for combating fungi and mites using certain triorganotin compounds |
| US4666956A (en) * | 1980-10-01 | 1987-05-19 | Dynamit Nobel Ag | Biocidal composition and its use in plastic molding compounds |
| WO1997001423A1 (en) * | 1995-06-26 | 1997-01-16 | Minnesota Mining And Manufacturing Company | Aqueous anti-microbial compositions containing organotin compounds |
-
1965
- 1965-09-22 GB GB40441/65A patent/GB1122371A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4343815A (en) * | 1973-08-30 | 1982-08-10 | M&T Chemicals Inc. | Method for combating fungi and mites using certain triorganotin compounds |
| US4666956A (en) * | 1980-10-01 | 1987-05-19 | Dynamit Nobel Ag | Biocidal composition and its use in plastic molding compounds |
| WO1997001423A1 (en) * | 1995-06-26 | 1997-01-16 | Minnesota Mining And Manufacturing Company | Aqueous anti-microbial compositions containing organotin compounds |
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