US2846402A - Alkyl sulfate detergent compositions - Google Patents
Alkyl sulfate detergent compositions Download PDFInfo
- Publication number
- US2846402A US2846402A US2846402DA US2846402A US 2846402 A US2846402 A US 2846402A US 2846402D A US2846402D A US 2846402DA US 2846402 A US2846402 A US 2846402A
- Authority
- US
- United States
- Prior art keywords
- foam
- detergent
- alkyl
- sulfate
- sodium
- 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
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- 239000003599 detergent Substances 0.000 title claims description 156
- 239000000203 mixture Substances 0.000 title claims description 112
- 150000008051 alkyl sulfates Chemical class 0.000 title description 66
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 50
- 239000000194 fatty acid Substances 0.000 claims description 50
- 150000004665 fatty acids Chemical class 0.000 claims description 46
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 24
- 239000003760 tallow Substances 0.000 claims description 24
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 claims description 20
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 16
- 229940077388 benzenesulfonate Drugs 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 4
- 239000006260 foam Substances 0.000 description 128
- 239000000654 additive Substances 0.000 description 52
- -1 saturated aliphatic alcohols Chemical class 0.000 description 44
- 230000002688 persistence Effects 0.000 description 34
- 230000000996 additive Effects 0.000 description 30
- 239000011780 sodium chloride Substances 0.000 description 30
- 235000002639 sodium chloride Nutrition 0.000 description 30
- 238000005406 washing Methods 0.000 description 30
- 150000003839 salts Chemical class 0.000 description 26
- 239000000243 solution Substances 0.000 description 24
- 239000011734 sodium Substances 0.000 description 22
- 229910052708 sodium Inorganic materials 0.000 description 22
- IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 20
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 20
- 125000000217 alkyl group Chemical group 0.000 description 18
- 239000002002 slurry Substances 0.000 description 18
- 125000004432 carbon atoms Chemical group C* 0.000 description 16
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 16
- 239000002689 soil Substances 0.000 description 16
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical group S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 16
- KWKXNDCHNDYVRT-UHFFFAOYSA-N Dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 12
- 230000002085 persistent Effects 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000003792 electrolyte Substances 0.000 description 10
- 159000000000 sodium salts Chemical class 0.000 description 10
- VQOIVBPFDDLTSX-UHFFFAOYSA-M sodium;3-dodecylbenzenesulfonate Chemical class [Na+].CCCCCCCCCCCCC1=CC=CC(S([O-])(=O)=O)=C1 VQOIVBPFDDLTSX-UHFFFAOYSA-M 0.000 description 10
- GHNRTXCRBJQVGN-UHFFFAOYSA-N 4-dodecan-6-ylbenzenesulfonic acid Chemical compound CCCCCCC(CCCCC)C1=CC=C(S(O)(=O)=O)C=C1 GHNRTXCRBJQVGN-UHFFFAOYSA-N 0.000 description 8
- POULHZVOKOAJMA-UHFFFAOYSA-N Lauric acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 8
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 238000007792 addition Methods 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 238000005755 formation reaction Methods 0.000 description 8
- 239000008233 hard water Substances 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- 238000004900 laundering Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 230000001264 neutralization Effects 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 235000003441 saturated fatty acids Nutrition 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 6
- 230000002411 adverse Effects 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000003240 coconut oil Substances 0.000 description 6
- 235000019864 coconut oil Nutrition 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 230000003472 neutralizing Effects 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- 238000001694 spray drying Methods 0.000 description 6
- 230000003068 static Effects 0.000 description 6
- 238000006277 sulfonation reaction Methods 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 4
- LQZZUXJYWNFBMV-UHFFFAOYSA-N Dodecanol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
- 239000005639 Lauric acid Substances 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N Oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 235000021314 Palmitic acid Nutrition 0.000 description 4
- 239000004115 Sodium Silicate Substances 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N Sodium silicate Chemical class [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 4
- FQENQNTWSFEDLI-UHFFFAOYSA-J Tetrasodium pyrophosphate Chemical class [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 4
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 4
- 150000001805 chlorine compounds Chemical class 0.000 description 4
- 230000000875 corresponding Effects 0.000 description 4
- 238000002036 drum drying Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000002708 enhancing Effects 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 150000007522 mineralic acids Chemical class 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 150000004028 organic sulfates Chemical class 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 239000008117 stearic acid Substances 0.000 description 4
- 239000012085 test solution Substances 0.000 description 4
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 206010010071 Coma Diseases 0.000 description 2
- 230000035693 Fab Effects 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- 210000003491 Skin Anatomy 0.000 description 2
- 241000618809 Vitales Species 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 description 2
- 230000002152 alkylating Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 238000010936 aqueous wash Methods 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 2
- 229910001424 calcium ion Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 230000005591 charge neutralization Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000008504 concentrate Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000012343 cottonseed oil Nutrition 0.000 description 2
- 239000002385 cottonseed oil Substances 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000004851 dishwashing Methods 0.000 description 2
- 239000003974 emollient agent Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 230000002209 hydrophobic Effects 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 235000014666 liquid concentrate Nutrition 0.000 description 2
- 238000011068 load Methods 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 229910001425 magnesium ion Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 230000003287 optical Effects 0.000 description 2
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 230000001737 promoting Effects 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical class [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000001187 sodium carbonate Substances 0.000 description 2
- 235000011182 sodium carbonates Nutrition 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- 235000019830 sodium polyphosphate Nutrition 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 235000019351 sodium silicates Nutrition 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 239000008234 soft water Substances 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000001180 sulfating Effects 0.000 description 2
- 238000005670 sulfation reaction Methods 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000271 synthetic detergent Substances 0.000 description 2
- 238000009827 uniform distribution Methods 0.000 description 2
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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/37—Mixtures of compounds all of which are anionic
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0094—High foaming compositions
Definitions
- the present invention relates to anionic synthetic detergent compositions. More particularly, it applies to detergent compositions, which contain an alkyl sulfate as their active organic detergent ingredient and which are capable of producing dense, stable and persistent foams when dissolved in water to form conventional household or commercial laundering solutions.
- the detergent products be capable of producing substantial lather or foam when used in dilute aqueous solutions, and that this foam be persistent (maintain its volume) throughout the washing process.
- a number of otherwise efficient synthetic anionic detergents when employed to form dilute aqueous solutions for washing purpose in the house and in commercial laundries, produce an unstable foam having a lacy texture, as contrasted to the small-sized bubbles and dense cream-like consistency of conventional soapsuds.
- the foam of these detergents lacks the desired persistence, and rapidly collapses and disappears before the completion of the washing operation.
- alkylolamides of lauric acid e. g., lauric isopropanolamide and lauric ethanolamide
- alkyl sulfates derived from coconut oil C -C fatty acids upon being added to alkyl sulfates derived from coconut oil C -C fatty acids, improve the foam persistence of corresponding aqueous wash solutions; however, the foam heights and the static foam stability achieved by the use of these additives, are definitely inadequate.
- Salts of alkyl sulfuric acids suitable for the preparation of the detergent compositions of my invention include water-soluble salts of straight-chain alkyl sulfuric acids, ,H-hydroxyalkyl sulfuric acids and 'y-hydroxyalkyl sulfuric acids which contain from 8 to 18 carbon atoms in the hydrophobic alkyl group and in which the hydrophilic group occupies the terminal position on the carbon chain.
- These salts include among their number sodium, potassium, magnesium, ammonium, alkyl ammonium and alkylol ammonium salts.
- sodium salts of C -C straight-chain alkyl sulfuric acids sodium C -C n-aliphatic alcohol sulfates
- C -C alkyl sulfates may be prepared by any known suitable method, e. g., by any of the methods of sulfation of aliphatic alcohols described at pages 53 to 58 of the book Surface-Active Agents, by A. M. Schwartz and I. W. Perry (I'nterscience Publishers, 1949, New York), followed by neutralization of the resulting C C alkyl sulfuric acids to the corresponding water-soluble salts.
- the fatty acid alkylolamide additive responsible for the improvement of foam properties may be prepared by any of the known methods of the art, e. g., by reacting. an ester of a suitable O -C saturated fatty acid with a C -C alkylolamine; or by reacting the fatty acid directly with the alkylolamine and heating the resulting amine salt; or by reacting a fatty acid chloride with an excess of alkylolamine; or yet by reacting the fatty acid chloride with a stoichiometrical amount of the alkylolamine, but in the presence of a suitable base such as sodium hydroxide or pyridine to neutralize the hydrogen chloride being formed.
- stearic as well as hydrogenated tallow fatty acids and their esters and chlorides, may be thus employed.
- the foam of the wash solutions of the aforementioned detergent composition attains adequate heights, has good stability and quality and is persistent, even though the wash solutions are made up with hard water (300 p. p. m. Ca-Mghardness).
- C -C alkyl sulfate and C -C monoalkyl benzene sulfonate designate in accordance with the established usage of the detergent art, water-soluble salts of C C alkyl sulfuric acids and C9-C18 monoalkyl benzene sulfonic acids, respectively, Because of their lesser cost and availability, sodium salts of the aforementioned organic sulfuric and sulfonic acids are usually employed, although water-soluble salts other than those of sodium may be employed whenever required by the particular washing or cleaning application.
- the water-soluble salts of monoalkyl benzene sulfonic acids employed in the preparation of the detergent compositions of my invention, are those containing from 9 to 18 carbon atoms, and preferably from 12 to 15 carbon atoms, in the alkyl chain.
- These salts are prepared by any of the several methods disclosed in the art, e. g., by starting with the condensation of propylene polymers and benzene as shown in U. S. Patent No. 2,477,383, issued to A. H. Lewis, or with the chlorination of a kerosene fraction boiling from 205 to 245 (3., followed by the reaction of the resulting keryl chloride with benzene as shown in the U. S. patent issued to Kyrides.
- the resulting alkyl benzene stock produced by either technique is then sulfonated, and the sulfonic acid in the sulfonation reaction mixture is separated from the unreacted sulfuric acid and neutralized. Thereupon, the neutralized slurry may be reduced to the particle form by conventional drying techniques (spray-drying or drum-drying).
- This foam retains its stability for relatively long periods of time, both under static conditions and under conditions of agitation in the presence of soil in the washing machine throughout the length of the washing cycle, i. e., as long as 20 minutes and frequently longer. Furthermore, the detergency of the wash solutions containing these improved detergent compositions is not adversely affected by the presence of the foam-improving alkylolamide additive.
- alkyl aryl sulfonates and alkyl sulfates are generally improved by the addition of water-soluble inorganic electrolyte salts or builders.
- detergency builders added to detergent compositions exert a number of beneficial effects on the properties and actions of the detergent composition. For instance, they neutralize the acid soil, deflocculate (suspend) the soil and prevent its redeposition, sequester magnesium and calcium ions from hard water, aid micelle formation, etc.
- sulfates and chlorides as detergent (detergency) builders in the aforedescribed mixtures of alkyl sulfates and alkyl benzene sulfonates, in amounts ranging fiom 60 to 90% by weight of the total solids in a particular detergent composition, does in no way interfere with the improvement in foam characteristics thereof, brought about by the introduction of a C -C alkylolamide of a Gig-C13 saturated fatty acid in accordance with my invention.
- inorganic sodium salt builders are usually employed, particularly in view of the general preference due to economic reasons for sodium salts of alkyl sulfuric and alkyl benzene sulfonic acids as active components of detergent formulations.
- These inorganic sodium salt detergent builders for alkyl sulfates and alkyl benzene sulfonates include sodium sulfate, sodium carbonates, sodium silicates, sodium polyphosphates, sodium pyrophosphates, borax, sodium chloride, etc.
- the additives other than the detergent builders coma prise various compatible anti-caking compounds, optical bleaches, perfume, coloring agents (if required) and skin emollients such as various N-alkyl glycines and diglycines.
- Sodium carboxymethyl cellulose and sodium celluronates may be also employed and act not only as extenders,
- the detergent compositions of my invention are to contain only the C -C alkyl sulfates as the detergent ingredient or the alkyl sulfates are to be used with an admixture of (l -C monoalkyl benzene sulfonates, it is preferred to prepare these compositions by blending (mixing) the active ingredients with the alkylolamide foam-improving additive, detergent builders and other additives in the solution or slurry stage, and then to dry the resulting mixture.
- alkyl sulfate detergent ingredient When aliphatic alcohols derived from hydrogenated tallow c c fatty acids are available for the production of the alkyl sulfate detergent ingredient of mixed alkyl sulfate-alkyl benzene sulfonate detergent compositions of my invention, it is preferred to sulfonate a suitable alkyl benzene stock with an excess of concentrated (98100 sulfuric acid, or
- the quantity of the sulfonating agent'required for the preparation of a particular mixture of alkyl benzene sulfonic and alkyl sulfuric acid is governed by the desired weight ratio of detergent alkyl sulfate to alkyl benzene sulfonate in the ultimate neutral ized product.
- the mixture of alkyl benzene sulfonic and alkyl sulfuric acids is neutralized with aqueous NaOH, Na CO or other suitable neutralizing agent.
- the resulting neutralized slurry is then blended with the alkylolamide foam-improving additive, detergent builders and other additives, and the blend is dried to the desired solid-particle form and size.
- the alkylolamide foam-improving additive such as palmitic ethanolamide into the aqueous slurry of neutralized alkyl sulfuric and alkyl benzene sulfonic acids
- the introduction of the alkylolamide additive is effected simultaneously with the blending of the detergent builders and other additives with the neutralized slurry of alkyl sulfates and alkyl benzene sulfonates. After spray-drying or drum-drying of the slurry, the product contains all ingredients uniformly distributed within each solid particle.
- the slurry may be processed into a paste, or, yet, it may be diluted to form a salable liquid concentrate.
- the weight ratio of the alkyl sulfate component to the monoalkyl benzene sulfonate component ranged from 1:1 to 1:6, the foam-improving alkylolarnide additive was present in amounts from 1 to 3 parts by weight in each 22 parts of the organic active component.
- the sodium alkyl sulfate component for these tests was prepared by neutralizing sulfated fatty alcohols derived from hydrogenated tallow fatty acids by conventional reduction procedures.
- the alkyl chains in these organic sulfates contain from 14 to 18 carbon atoms, the major proportion (65-70%) being C alkyl sulfates.
- the sodium monoalkyl benzene sulfonate component for the tests was prepared by alkylating benzene with a mixture of pentamers and tetramers of propylene, sulfonating the resulting C -C monoalkyl benzene product and neutralizing in accordance with the aforementioned disclosure of U. S. Patent 2,477,383.
- Various alkylolamides of fatty acids were employed in combination with the detergent organic sulfates and sulfonates in order to observe the effects of these additives on foam properties.
- Detergent builders were present in the following amounts: 30 parts by weight of sodium tripolyphosphate; 20 parts by weight of tetrasodium pyrophosphate; parts by weight of liquid sodium silicate (known as N grade in the trade and characterized by a soda to silica ratio of 123.2); the remainder of the builder portion of the composition being tested was essentially sodium sulfate.
- the solid particle-form detergent formulations were dissolved in soft water (50 p. p. m. of Ca-Mg hardness) at 120 F. to make up 500 ml. of 0.15% solution in a 2-liter beaker.
- the test solutions were agitated with the aid of a propeller-type stirrer for 1 minute and then allowed to stand for 1 minute, whereupon foam heights in millimeters were measured. minutes after the agitation was terminated, the foam heights were measured again and the stability and quality of the foam were ascertained.
- Foam stability was rated by observing the rate of foam decay under mechanical stress, as by blowing on a small volume of foam gently with air. In the case of unstable foam this procedure resulted in a rapid collapse of foam'bubbles.
- Foam of Good quality have uniformly small-sized bubbles and a high bulk viscosity. They are white and opaque. Poor quality is manifested by uniformly large-sized foam bubbles, a low bulk viscosity, and a tendency towards laciness. These foams are more transparent and gray in color. Ratings of Fair were assigned to foams of intermediate stability and quality.
- the foam persistence was given a rating of 1.
- the foam persistence was assigned a rating of 2.
- the suds disappeared in a period of time from 10 to 20 minutes its persistence was assigned a rating of 3.
- a rating of 4 was assigned to the foam persistence.
- the height of the suds above the surface of the liquid was from 1 to 3 inches, a rating of 5 was assigned to the foam persistence.
- a rating of 6 was given to the persistence of the suds which stayed at a height of 3 to 6 inches after 20 minutes of operation. Finally, a maximum rating of 7 was assigned to the persistence of studs which remained higher than 6 inches above the surface of the liquid after 20 minutes of operation.
- alkylolamide additives and examples are only illustrative of the invention, and of any invention, as exemplified by palmitic ethanolamide that any modification thereof consistent with its spirit and resides in the low volatility and a very low odor as comscope areto be included in the terms of the following pared with lauryl alcohol and other similar foam-improvclaims. ing additives. Detergency of the wash solutions conta-in- I claim: I ing the improved detergent compositions of my inven- 1.
- a detergent composition consisting essentially, by tion, particularly the removal of soil from cotton fabrics weight, of a normal aliphatic alcohol sulfate detergent soiled with an oily vsoil, favorably compares with the derived from hydrogenated tallow fatty acids predominatdetergency of good-quality domestic laundry fatty acid 40 ing in C n-alkyl sulfate, about 1 to 6 parts per part of soaps.
- sulfate detergent of C C monoalkyl benzene sulfonate 'In another series of test runs, sodium alkyl sulfate obdetergent, and, as a foam-improving agent, about 3 to tained by sulfating aliphatic alcohols derived from hydro- 75%, based on the sulfate detergent, of a C C; monogenated cocoanu-t oil fatty acids was employed as the alkylolamide of a c -c saturated fatty acid. essential active organic constituent of the detergent for- 2.
- the foam performance (foam quality, stability 3.
- a detergent composition according to claim 1 in and persistence) and the detergency observed in these which the C n-alkyl sulfate is present in an amount series of test runs were substantially the same as those from about to 7 observed in test runs Nos. 1, 2 and 3.of the foregoing 4.
- a built detergent composition consisting essentially table.
- stabilizers e. g., lauric isopropanolamide or lauric ethanol- 55 amide, may be employed, if desired, in the detergent References Clted the file of thls P119311t compositions prepared in accordance with my invention.
- UNITED STATES PATENTS Their presence enhances the soil tolerance without inter- 2,342,562 Tucker Fab.
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- Chemical & Material Sciences (AREA)
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Description
United States Patent C ALKYL SULFATE DETERGENT COMPOSITIONS Henry Y. Lew, San Francisco, Calif., assignor to California Research Corporation, San Francisco, Calif., a corporation of Delaware No Drawing. Application December 28, 1953 Serial No.- 400,765
4 Claims. (Cl. 252-152) The present invention relates to anionic synthetic detergent compositions. More particularly, it applies to detergent compositions, which contain an alkyl sulfate as their active organic detergent ingredient and which are capable of producing dense, stable and persistent foams when dissolved in water to form conventional household or commercial laundering solutions.
Small scale users of synthetic anionic detergents prefer that the detergent products be capable of producing substantial lather or foam when used in dilute aqueous solutions, and that this foam be persistent (maintain its volume) throughout the washing process.
A number of otherwise efficient synthetic anionic detergents, and, in particular, those of the alkyl sulfate and alkylbenzene sulfonate type, when employed to form dilute aqueous solutions for washing purpose in the house and in commercial laundries, produce an unstable foam having a lacy texture, as contrasted to the small-sized bubbles and dense cream-like consistency of conventional soapsuds. Moreover, in the presence of soil and under conditions of agitation in a washing machine, the foam of these detergents lacks the desired persistence, and rapidly collapses and disappears before the completion of the washing operation.
The various additives suggested in the art for the purpose of improving the foam characteristics of the aforementioned alkyl sulfate detergents, for instance, C C saturated aliphatic alcohols, are often found to be incapable of insuring formation of persistent foam without impairing at the same time the detergency of the composition, or without adversely affecting some other properties thereof. Thus, while the addition of lauryl alcohol improves the sudsing preformance, a fatty odor is imparted by the presence of this alcohol to the finished dried detergent particles and, furthermore, a considerable proportion of the alcohol additive is lost in spray-drying 'of the neutralized slurries of alkyl sulfates to the desired particle-form. Likewise, it is known that certain alkylolamides of lauric acid, e. g., lauric isopropanolamide and lauric ethanolamide, upon being added to alkyl sulfates derived from coconut oil C -C fatty acids, improve the foam persistence of corresponding aqueous wash solutions; however, the foam heights and the static foam stability achieved by the use of these additives, are definitely inadequate.
I have found that by adding to an alkyl sulfate containing from '8 to 18 carbon atoms in the alkyl chain from 3 to 75% by weight thereof of a monoalkylolamide of a saturated fatty acid, in which the alkylol portion contains 2 to 3 carbon atoms and the fatty acid portion contains 16 to 18 carbon atoms, a detergent com-' position having improved foam characteristics is obtained. Such a detergent composition, when employed to make up dilute aqueous solutions or baths for washing purposes, produces foams of excellent quality, adequate volume and good static stability. The foam of these compositions possesses a remarkable degree of persistence under agitation in the presence of soil in the wash solutions.
tub or bowl of a washing machine. For all practical purposes an addition of from 20 to 30% of the aforementioned fatty acid monoalkylolamides, based on the weight of alkyl sulfate, secures the desirable foam properties atconventional concentrations of the detergent composition, namely, from 0.1 to 0.4%, in the aqueous Any of the C C alkylolamides of the C C saturated fatty acids can be employed to obtain the desired improvement of foam, properties, for instance, C -C monoalkylolamides of palmitic acid and C -C monoalkylolamides of mixtures of G -C fatty acids known in the market under the name of pressed stearic acid and containing 67% by weight of palmitic, 29% by weight of stearic and 4% by weight of oleic acid. Palrnitic ethanolamide is found to be particularly effective as an additive for the improvement of foam characteristics.
Salts of alkyl sulfuric acids suitable for the preparation of the detergent compositions of my invention include water-soluble salts of straight-chain alkyl sulfuric acids, ,H-hydroxyalkyl sulfuric acids and 'y-hydroxyalkyl sulfuric acids which contain from 8 to 18 carbon atoms in the hydrophobic alkyl group and in which the hydrophilic group occupies the terminal position on the carbon chain. These salts include among their number sodium, potassium, magnesium, ammonium, alkyl ammonium and alkylol ammonium salts. As a practical matter, however, sodium salts of C -C straight-chain alkyl sulfuric acids (sodium C -C n-aliphatic alcohol sulfates) are usually employed. These C -C alkyl sulfates may be prepared by any known suitable method, e. g., by any of the methods of sulfation of aliphatic alcohols described at pages 53 to 58 of the book Surface-Active Agents, by A. M. Schwartz and I. W. Perry (I'nterscience Publishers, 1949, New York), followed by neutralization of the resulting C C alkyl sulfuric acids to the corresponding water-soluble salts.
The fatty acid alkylolamide additive responsible for the improvement of foam properties may be prepared by any of the known methods of the art, e. g., by reacting. an ester of a suitable O -C saturated fatty acid with a C -C alkylolamine; or by reacting the fatty acid directly with the alkylolamine and heating the resulting amine salt; or by reacting a fatty acid chloride with an excess of alkylolamine; or yet by reacting the fatty acid chloride with a stoichiometrical amount of the alkylolamine, but in the presence of a suitable base such as sodium hydroxide or pyridine to neutralize the hydrogen chloride being formed. Pure fatty acids, such as palimitic, or,
stearic, as well as hydrogenated tallow fatty acids and their esters and chlorides, may be thus employed. The C -C alkylolamides of palmitic acid, and particularly palmitic ethanolamide, represent the most effective additives for the improvement of foam characteristics in accordance with my invention.
It is noted, however, that the addition of a C -C alkylolamide of a O -C saturated fatty acid, such as palmitic ethanolamide, to the compositions having as their active detergent component a C -C alkyl sulfate which may have been derived from hydrogenated fatty acids of tallow, cottonseed oil, soybean oil, and other. similar organic fatty materials, fails to secure an adequate foam height and foam volume, and, consequently, does not result in the formation of a persistent foam under conditions of agitation.
I found that by replacing up to by weight of the active alkyl sulfate in a detergent composition containing a C -C alkylolamide of a C -C saturated fatty acid in accordance with my invention with detergent 0 -0 monoalkyl benzene sulfonates, good foam stability, qnality and persistence are obtained not only where the alkyl sulfate component is derived from the lower molecular weight C -C hydrogenated coconut oil fatty acids, but also where the alkyl sulfate component is derived from the higher molecular weight hydrogenated tallow fatty acids, or the like. Notwithstanding the presence of up to 85% by weight of C -C alkyl benzene sulfonate, the foam of the wash solutions of the aforementioned detergent composition attains adequate heights, has good stability and quality and is persistent, even though the wash solutions are made up with hard water (300 p. p. m. Ca-Mghardness).
' Considering the fluctuating prices of the coconut oil, which tend to increase excessively the cost of alkyl sulfate detergents derived therefrom, the discovery that C -C alkyl sulfates derived from tallow, a much cheaper and readily available raw material, may be employed in combination with the inexpensive Cg-C1 alkyl benzene sulfonates to satisfy the washing needs of the housewife and of the commercial laundry operator constitutes an important-advance in the detergent art.
The terms C -C alkyl sulfate and C -C monoalkyl benzene sulfonate, as employed in this specification to describe detergent compositions containing a mixed active organic component, designate in accordance with the established usage of the detergent art, water-soluble salts of C C alkyl sulfuric acids and C9-C18 monoalkyl benzene sulfonic acids, respectively, Because of their lesser cost and availability, sodium salts of the aforementioned organic sulfuric and sulfonic acids are usually employed, although water-soluble salts other than those of sodium may be employed whenever required by the particular washing or cleaning application.
The water-soluble salts of monoalkyl benzene sulfonic acids, employed in the preparation of the detergent compositions of my invention, are those containing from 9 to 18 carbon atoms, and preferably from 12 to 15 carbon atoms, in the alkyl chain. These salts are prepared by any of the several methods disclosed in the art, e. g., by starting with the condensation of propylene polymers and benzene as shown in U. S. Patent No. 2,477,383, issued to A. H. Lewis, or with the chlorination of a kerosene fraction boiling from 205 to 245 (3., followed by the reaction of the resulting keryl chloride with benzene as shown in the U. S. patent issued to Kyrides. The resulting alkyl benzene stock produced by either technique is then sulfonated, and the sulfonic acid in the sulfonation reaction mixture is separated from the unreacted sulfuric acid and neutralized. Thereupon, the neutralized slurry may be reduced to the particle form by conventional drying techniques (spray-drying or drum-drying). When aqueous solutions of detergent compositions containing detergent -0 alkyl sulfates or a mixture of detergent C -C alkyl sulfates and C C monoalkyl benzene sulfonates in weight ratios ranging from 1:1 to 1:6, and, furthermore, containing from about 3 to about 75% by weight of an alkylolamide of a C -C fatty acid, in which the alkylol portion contains from 2 to 3 carbon atoms (based on the weight of the C -C alkyl sulfate), are employed to wash fabrics in dilute concentrations in water (from 0.1 to 0.4%), in accordance with the conventional laundering practice, they produce a rich cream-like foam of densely agglomerated small bubbles. This foam retains its stability for relatively long periods of time, both under static conditions and under conditions of agitation in the presence of soil in the washing machine throughout the length of the washing cycle, i. e., as long as 20 minutes and frequently longer. Furthermore, the detergency of the wash solutions containing these improved detergent compositions is not adversely affected by the presence of the foam-improving alkylolamide additive.
It is well known that the detergent action of alkyl aryl sulfonates and alkyl sulfates is generally improved by the addition of water-soluble inorganic electrolyte salts or builders. These detergency builders added to detergent compositions exert a number of beneficial effects on the properties and actions of the detergent composition. For instance, they neutralize the acid soil, deflocculate (suspend) the soil and prevent its redeposition, sequester magnesium and calcium ions from hard water, aid micelle formation, etc. Whatever be the particular effect of a specific detergent builder on the properties of alkyl benzene sulfonates and alkyl sulfates i-n detergent compositions, all builders contribute to enhance the over-all washing efliciency of detergent compositions.
I have found that the presence of water-soluble, alkaline, electrolyte salts of weak inorganic acids, e. g., carbonates, silicates, phosphates and borates, and of watersoluble, neutral, electrolyte salts of strong inorganic acids, e. g., sulfates and chlorides, as detergent (detergency) builders in the aforedescribed mixtures of alkyl sulfates and alkyl benzene sulfonates, in amounts ranging fiom 60 to 90% by weight of the total solids in a particular detergent composition, does in no way interfere with the improvement in foam characteristics thereof, brought about by the introduction of a C -C alkylolamide of a Gig-C13 saturated fatty acid in accordance with my invention. Although any of the water-soluble alkaline and neutral inorganic electrolyte salt builders may be used in the detergent formulations prepared in accordance with the present invention, inorganic sodium salt builders are usually employed, particularly in view of the general preference due to economic reasons for sodium salts of alkyl sulfuric and alkyl benzene sulfonic acids as active components of detergent formulations. These inorganic sodium salt detergent builders for alkyl sulfates and alkyl benzene sulfonates include sodium sulfate, sodium carbonates, sodium silicates, sodium polyphosphates, sodium pyrophosphates, borax, sodium chloride, etc.
The additives other than the detergent builders coma prise various compatible anti-caking compounds, optical bleaches, perfume, coloring agents (if required) and skin emollients such as various N-alkyl glycines and diglycines. Sodium carboxymethyl cellulose and sodium celluronates may be also employed and act not only as extenders,
but also exert a marked action in preventing redeposition of the soil. These various additives are employed in amounts readily determinable by those skilled in the art to suit the requirements of each particular application without interference with the improvement of foam characteristics, brought about by the introduction of the alkylolamide additive. Usually they constitute not more than 5% of the total weight of solids in the final detergent formulation.
Whether the detergent compositions of my invention are to contain only the C -C alkyl sulfates as the detergent ingredient or the alkyl sulfates are to be used with an admixture of (l -C monoalkyl benzene sulfonates, it is preferred to prepare these compositions by blending (mixing) the active ingredients with the alkylolamide foam-improving additive, detergent builders and other additives in the solution or slurry stage, and then to dry the resulting mixture. When aliphatic alcohols derived from hydrogenated tallow c c fatty acids are available for the production of the alkyl sulfate detergent ingredient of mixed alkyl sulfate-alkyl benzene sulfonate detergent compositions of my invention, it is preferred to sulfonate a suitable alkyl benzene stock with an excess of concentrated (98100 sulfuric acid, or
Y 22% oleum, and then to add molten or flaked aliphatic alcohols derived from C C tallow fatty acids into the 'sulfonation reaction mixture to produce the desired alkyl sulfuric acid. Details of sulfonation of alkyl benzene stocks are described in the bulletin entitled Alkane- Product and Processingv Information, published by Oronite Chemical Company of San Francisco, California, in 1950. In all events, the quantity of the sulfonating agent'required for the preparation of a particular mixture of alkyl benzene sulfonic and alkyl sulfuric acid is governed by the desired weight ratio of detergent alkyl sulfate to alkyl benzene sulfonate in the ultimate neutral ized product. The mixture of alkyl benzene sulfonic and alkyl sulfuric acids is neutralized with aqueous NaOH, Na CO or other suitable neutralizing agent. The resulting neutralized slurry is then blended with the alkylolamide foam-improving additive, detergent builders and other additives, and the blend is dried to the desired solid-particle form and size.
In introducing the alkylolamide foam-improving additive such as palmitic ethanolamide into the aqueous slurry of neutralized alkyl sulfuric and alkyl benzene sulfonic acids, it may be necessary to dissolve the alkylolamide in some ethanol or isopropanol to insure a uniform distribution of the additive within the slurry. The introduction of the alkylolamide additive is effected simultaneously with the blending of the detergent builders and other additives with the neutralized slurry of alkyl sulfates and alkyl benzene sulfonates. After spray-drying or drum-drying of the slurry, the product contains all ingredients uniformly distributed within each solid particle.
If desired, instead of drying the slurry to the dry particle-form, it may be processed into a paste, or, yet, it may be diluted to form a salable liquid concentrate.
A number of foam-evaluation bench tests were carried out in the laboratory, employing dilute aqueous solutions of dried particulate detergent formulations prepared in accordance with the invention in concentrations ranging from 0.1 to 0.4%. In a particular representative test series, each 100 parts by weight of the built detergent formulation employed for making up test solutions contained in its active organic portion a total of from 20 to 22 parts by Weight of a composition consisting of detergent sodium alkyl sulfate and sodium monoalkyl benzene sulfonate, including the alkylolamide foam-improving additive. The weight ratio of the alkyl sulfate component to the monoalkyl benzene sulfonate component ranged from 1:1 to 1:6, the foam-improving alkylolarnide additive was present in amounts from 1 to 3 parts by weight in each 22 parts of the organic active component. The sodium alkyl sulfate component for these tests was prepared by neutralizing sulfated fatty alcohols derived from hydrogenated tallow fatty acids by conventional reduction procedures. The alkyl chains in these organic sulfates contain from 14 to 18 carbon atoms, the major proportion (65-70%) being C alkyl sulfates.
The sodium monoalkyl benzene sulfonate component for the tests was prepared by alkylating benzene with a mixture of pentamers and tetramers of propylene, sulfonating the resulting C -C monoalkyl benzene product and neutralizing in accordance with the aforementioned disclosure of U. S. Patent 2,477,383. Various alkylolamides of fatty acids were employed in combination with the detergent organic sulfates and sulfonates in order to observe the effects of these additives on foam properties.
Detergent builders were present in the following amounts: 30 parts by weight of sodium tripolyphosphate; 20 parts by weight of tetrasodium pyrophosphate; parts by weight of liquid sodium silicate (known as N grade in the trade and characterized by a soda to silica ratio of 123.2); the remainder of the builder portion of the composition being tested was essentially sodium sulfate.
The solid particle-form detergent formulations were dissolved in soft water (50 p. p. m. of Ca-Mg hardness) at 120 F. to make up 500 ml. of 0.15% solution in a 2-liter beaker. The test solutions were agitated with the aid of a propeller-type stirrer for 1 minute and then allowed to stand for 1 minute, whereupon foam heights in millimeters were measured. minutes after the agitation was terminated, the foam heights were measured again and the stability and quality of the foam were ascertained. Foam stability was rated by observing the rate of foam decay under mechanical stress, as by blowing on a small volume of foam gently with air. In the case of unstable foam this procedure resulted in a rapid collapse of foam'bubbles. Quality of the foam,fi. e, the size of its bubbles, and the feel or the body thereof, was also observed and rated. Foam of Good quality have uniformly small-sized bubbles and a high bulk viscosity. They are white and opaque. Poor quality is manifested by uniformly large-sized foam bubbles, a low bulk viscosity, and a tendency towards laciness. These foams are more transparent and gray in color. Ratings of Fair were assigned to foams of intermediate stability and quality.
A parallel series of Washing machine test runs, using the same dilute aqueous solutions of detergent formulations as employed in the bench tests, was carried out to ascertain persistence of the foam under the conditions of operation, prevailing in the commonly used non-automatic agitator-type domestic washing machines. After adding to the bowl of the machine a quantity of the wash solution, normally required for the operation, a load of soiled cotton towels was placed in the bowl of the machine. The contents were agitated in each test run under substantially identical conditions of operation and temperature, approximating the conditions and temperature of the regular laundering practice. The foam was observed at regular intervals and its persistence was rated as follows:
When the sud-s disappeared in less than 5 minutes after starting the operation of the washing machine, the foam persistence was given a rating of 1. When the suds disappeared in an interval of time equal from 5 to 10 minutes, the foam persistence was assigned a rating of 2. When the suds disappeared in a period of time from 10 to 20 minutes, its persistence was assigned a rating of 3. Whenever the suds lasted 20 minutes under the conditions of agitation, but the height of the suds on the surface of the liquid in the bowl of the machine was lower than 1 inch, a rating of 4 was assigned to the foam persistence. When, after 20 minutes of operation, the height of the suds above the surface of the liquid was from 1 to 3 inches, a rating of 5 was assigned to the foam persistence. A rating of 6 was given to the persistence of the suds which stayed at a height of 3 to 6 inches after 20 minutes of operation. Finally, a maximum rating of 7 was assigned to the persistence of studs which remained higher than 6 inches above the surface of the liquid after 20 minutes of operation.
Thetable presented hereinafter, contains results of the aforedescribed series of test runs, illustrating the advantages attained by the employment of the improved detergent formulations of the present invention.
The results shown in the table clearly point out that foam persistence is improved by the presence of a C -C alkylolamide of a C C saturated fatty acid. The foam of solutions, formed with hard water (300 p. p. m., Ca-Mg hardness) and containing a detergent composition, the organic active component whereof consisted of a mixture of an alkyl sulfate detergent derived from hydrogenated tallow fatty acid and a monoalkyl benzene sulfonate detergent is more persistent in the presence of the alkylolamide additive (runs #1, 2 and 7) than the foams of similar hard water solutions containing either the alkyl sulfate alone (run #18) or the alkyl benzene sulfonate alone (run #5), both notoriously deficient (runs #19 and 20) as regards foam persistence. The results of the bench tests show that the C C alkylolamides of C -C saturated fatty acids, and, in particular, palmitic ethanolamide, improve foam heights, foam stability and foam quality, whereas alkylolamides of lower molecular weight fatty acids, e. g., of lauric acid, are incapable of Y promoting the formation of stable, good-quality foam.
7 whidhresembles that of the foams ofthe better fatty acid soaps. They-are light in color, made up of small-sized bubbles agglomerated to a cream-likeconsistency and impart to thehands the same creamy,-dense-bodied feeling -8 are normally present in sulfated alcohol compositions, does' not adversely affect the performance improvement achieved by the alkylola mides employedsin the detergent compositions of my invention. I
It is to be understood that the aforegiven description as the conventional soap suds familiar to housewives. o
* Bench Tests Parts by Foam Persistence in whet Parts by Washing Machine Run hydrowt. of Parts by Foam Height Tests genated alkyl Additive Wt.'of inmin. tallow benzene additive Foam Foam alkyl sulfonate Stability Quality sulfate After After 1 Soft Hard 1 min. 15 min. Water Water 10 10 Palmitio ethanolamide 2 84 70 1o 10 -..-.do 1 s 67 1'0- 10 a so 74 5. 15 2 87 77 o 20 2 7s 50 10 10 Palmitie n-propanolamide-.- 2 82' 65. 10 10 Hydrogenated tallow fatty.-- 2 68 58 acid ethanolamide. -10 to d 1 72 62 15 2 78 e5 '0 17 2 s5 12 1O Stearic dlethanolamide 2 60 15 5 15 Stearie isopropanolamide.-.. 1 83 68 10 10 Laurie ethanolamide..- 2 83 41 10 10 Laurie n-propauolamid 2 81 33 10 1O Lauricisopropanolamide. 2 82 43 10 10 Laurie diethanolamide. 2 70 24 10 10 None 0 as 17 20 0 Palmitle ethanolamide 2 60 48 20 0 None 0 28 8 d 0 20 ..do 0 85 75 do.- Poor.... 1 10 10 Ethanolamide of pressed 1 '2 85 64 Good... Good... 7
stearic acid."
An important advantage of the alkylolamide additives and examples are only illustrative of the invention, and of any invention, as exemplified by palmitic ethanolamide that any modification thereof consistent with its spirit and resides in the low volatility and a very low odor as comscope areto be included in the terms of the following pared with lauryl alcohol and other similar foam-improvclaims. ing additives. Detergency of the wash solutions conta-in- I claim: I ing the improved detergent compositions of my inven- 1. A detergent composition consisting essentially, by tion, particularly the removal of soil from cotton fabrics weight, of a normal aliphatic alcohol sulfate detergent soiled with an oily vsoil, favorably compares with the derived from hydrogenated tallow fatty acids predominatdetergency of good-quality domestic laundry fatty acid 40 ing in C n-alkyl sulfate, about 1 to 6 parts per part of soaps. sulfate detergent of C C monoalkyl benzene sulfonate 'In another series of test runs, sodium alkyl sulfate obdetergent, and, as a foam-improving agent, about 3 to tained by sulfating aliphatic alcohols derived from hydro- 75%, based on the sulfate detergent, of a C C; monogenated cocoanu-t oil fatty acids was employed as the alkylolamide of a c -c saturated fatty acid. essential active organic constituent of the detergent for- 2. A detergent composition according to claim '1 mulations containing the C -C alkylolamides of wherein the sulfate and sulfonate detergents are sodium C -C saturated fatty acids in accordance with the insulfate and sodium sulfonate detergents. vention. The foam performance (foam quality, stability 3. A detergent composition according to claim 1 in and persistence) and the detergency observed in these which the C n-alkyl sulfate is present in an amount series of test runs were substantially the same as those from about to 7 observed in test runs Nos. 1, 2 and 3.of the foregoing 4. A built detergent composition consisting essentially table. of 10 to 40%, by weight, of the detergent composition It may be mentioned, in addition, that alkyl'olamides defined in claim 1 and 60 to of essentially watercommonly employed in the art as foam promoters and soluble inorganic electrolyte salt builders. stabilizers, e. g., lauric isopropanolamide or lauric ethanol- 55 amide, may be employed, if desired, in the detergent References Clted the file of thls P119311t compositions prepared in accordance with my invention. UNITED STATES PATENTS Their presence enhances the soil tolerance without inter- 2,342,562 Tucker Fab. 22, 1944 fering in any way With the beneficial efffiCts 0f the C -C 2 333 737 i h d A 2 1945 .alkylolarnides of C C saturated fatty acids on foam 60 2 477 3 3 Lewis July 2 1.949 characteristics of the dishwashing and laundering so-lu- 2,519,052 i k 1 15, 0 tions prepared by using these concentrates. Also, the 2,733,214 vitale Jan, 31, 1956 presence of small amounts of unsulfated alcohols, which 2,757,143 Katzman July 31, 1956
Claims (1)
1. A DETERGENT COMPOSITION CONSISTING ESSENTIALLY, BY WEIGHT, OF A NORMAL ALIPHATIC ALCOHOL SULFATE DETERGENT DERIVED FROM HYDROGENATED TALLOW FATTY ACIDS PREDOMINATING IN C18 N-ALKYL SULFATE, ABOUT 1 TO 6 PARTS PER PART OF SULFATE DETERGENT OF C12-C15 MONOALKYL BENZENE SULFONATE DETERGENT, AND, AS A FOAM-IMPROVING AGENT, ABOUT 3 TO 75%, BASED ON THE SULFATE DETERGENT, OF A C2-C3 MONOALKYLOLAMIDE OF A C15-C18 SATURATED FATTY ACID.
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US2846402A true US2846402A (en) | 1958-08-05 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US2846402D Expired - Lifetime US2846402A (en) | Alkyl sulfate detergent compositions |
Country Status (1)
Country | Link |
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US (1) | US2846402A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3332876A (en) * | 1964-10-15 | 1967-07-25 | Procter & Gamble | Detergent composition |
US3609089A (en) * | 1967-08-22 | 1971-09-28 | Grace W R & Co | Process for cleaning road vehicles and composition |
US4253993A (en) * | 1978-05-29 | 1981-03-03 | The Procter & Gamble Company | Shampoo in flake form |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2342562A (en) * | 1941-12-12 | 1944-02-22 | Procter & Gamble | Process of producing improved wetting, sudsing, and detergent agents |
US2383737A (en) * | 1942-02-18 | 1945-08-28 | Procter & Gamble | Detergent composition |
US2477383A (en) * | 1946-12-26 | 1949-07-26 | California Research Corp | Sulfonated detergent and its method of preparation |
US2519062A (en) * | 1946-04-18 | 1950-08-15 | Nopeo Chemical Company | Lotion shampoo |
US2733214A (en) * | 1956-01-31 | Synthetic detergent compositions | ||
US2757143A (en) * | 1956-07-31 | Detergent composition |
-
0
- US US2846402D patent/US2846402A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2733214A (en) * | 1956-01-31 | Synthetic detergent compositions | ||
US2757143A (en) * | 1956-07-31 | Detergent composition | ||
US2342562A (en) * | 1941-12-12 | 1944-02-22 | Procter & Gamble | Process of producing improved wetting, sudsing, and detergent agents |
US2383737A (en) * | 1942-02-18 | 1945-08-28 | Procter & Gamble | Detergent composition |
US2519062A (en) * | 1946-04-18 | 1950-08-15 | Nopeo Chemical Company | Lotion shampoo |
US2477383A (en) * | 1946-12-26 | 1949-07-26 | California Research Corp | Sulfonated detergent and its method of preparation |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3332876A (en) * | 1964-10-15 | 1967-07-25 | Procter & Gamble | Detergent composition |
US3609089A (en) * | 1967-08-22 | 1971-09-28 | Grace W R & Co | Process for cleaning road vehicles and composition |
US4253993A (en) * | 1978-05-29 | 1981-03-03 | The Procter & Gamble Company | Shampoo in flake form |
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