CA2284005A1 - Detergent compositions - Google Patents
Detergent compositions Download PDFInfo
- Publication number
- CA2284005A1 CA2284005A1 CA002284005A CA2284005A CA2284005A1 CA 2284005 A1 CA2284005 A1 CA 2284005A1 CA 002284005 A CA002284005 A CA 002284005A CA 2284005 A CA2284005 A CA 2284005A CA 2284005 A1 CA2284005 A1 CA 2284005A1
- Authority
- CA
- Canada
- Prior art keywords
- detergent
- tablet
- weight
- tablet according
- 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.)
- Abandoned
Links
- 239000003599 detergent Substances 0.000 title claims abstract description 68
- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 239000004615 ingredient Substances 0.000 claims abstract description 14
- 239000007844 bleaching agent Substances 0.000 claims abstract description 11
- 229940045872 sodium percarbonate Drugs 0.000 claims abstract description 10
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 claims abstract description 9
- 239000012418 sodium perborate tetrahydrate Substances 0.000 claims abstract description 6
- 229910052816 inorganic phosphate Inorganic materials 0.000 claims abstract description 5
- IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000000129 anionic group Chemical group 0.000 claims description 8
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 8
- 238000005406 washing Methods 0.000 abstract description 8
- 239000004744 fabric Substances 0.000 abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- -1 alkylbenzene sulphonate Chemical class 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- 239000000344 soap Substances 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 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 5
- 239000011230 binding agent Substances 0.000 description 5
- 238000004090 dissolution Methods 0.000 description 5
- 150000002191 fatty alcohols Chemical class 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 229910021653 sulphate ion Inorganic materials 0.000 description 4
- 239000011800 void material Substances 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 239000012190 activator Substances 0.000 description 3
- 150000004996 alkyl benzenes Chemical class 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 238000005469 granulation Methods 0.000 description 3
- 230000003179 granulation Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 description 3
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 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
- 239000002585 base Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000005056 compaction Methods 0.000 description 2
- 238000000280 densification Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- 150000003333 secondary alcohols Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 150000004685 tetrahydrates Chemical class 0.000 description 2
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 2
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229920002535 Polyethylene Glycol 1500 Polymers 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 229940012017 ethylenediamine Drugs 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000001433 sodium tartrate Substances 0.000 description 1
- 229960002167 sodium tartrate Drugs 0.000 description 1
- 235000011004 sodium tartrates Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920005613 synthetic organic polymer Polymers 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- VUYXVWGKCKTUMF-UHFFFAOYSA-N tetratriacontaethylene glycol monomethyl ether Chemical compound COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO VUYXVWGKCKTUMF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- MPSJHIAGGNGGEZ-UHFFFAOYSA-K trisodium;2-(carboxylatomethoxy)butanedioate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)COC(C([O-])=O)CC([O-])=O MPSJHIAGGNGGEZ-UHFFFAOYSA-K 0.000 description 1
- 230000000007 visual effect Effects 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/0065—Solid detergents containing builders
- C11D17/0073—Tablets
- C11D17/0086—Laundry tablets
-
- 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3942—Inorganic per-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
- C11D1/22—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
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
A detergent tablet for fabric washing is compacted from a particulate composition containing 5 to 50 % detergent active, 2 to 60 % of water-soluble inorganic phosphate builder and other ingredients including 8 to 30 % of peroxygen bleach, wherein the tablet has a density of at least 1040 gm/litre and the bleach is sodium percarbonate, sodium perborate tetrahydrate or a mixture of them. This selection of peroxygen bleach leads to a better combination of strength before use with speed of disintegration at the time of use.
Description
DETERGENT COMPOSITIONS
This invention relates to the manufacture of detergent compositions in the form of tablets intended to be consumed when washing a single load of laundry.
When manufacturing a detergent composition for fabric washing there are a number of possible options. Such compositions have for many years been manufactured in particulate form, commonly referred to as powders.
Detergent compositions can also be manufactured as liquids.
Tablets, to which this invention relates, are yet another possibility.
When formulating a detergent composition there is scope to make both qualitative and quantitative choices concerning the ingredients. Anionic detergent actives are the most commonly used, usually together with nonionic detergent actives. Amongst the anionic detergent actives which are commercially available, linear alkylbenzene sulphonate and primary alkyl sulphate are commonly used. There has been a trend for particulate detergent compositions to be manufactured with a bulk density higher than 650 g/litre which is a departure from older practice when bulk densities were customarily lower.
This invention relates to the manufacture of detergent compositions in the form of tablets intended to be consumed when washing a single load of laundry.
When manufacturing a detergent composition for fabric washing there are a number of possible options. Such compositions have for many years been manufactured in particulate form, commonly referred to as powders.
Detergent compositions can also be manufactured as liquids.
Tablets, to which this invention relates, are yet another possibility.
When formulating a detergent composition there is scope to make both qualitative and quantitative choices concerning the ingredients. Anionic detergent actives are the most commonly used, usually together with nonionic detergent actives. Amongst the anionic detergent actives which are commercially available, linear alkylbenzene sulphonate and primary alkyl sulphate are commonly used. There has been a trend for particulate detergent compositions to be manufactured with a bulk density higher than 650 g/litre which is a departure from older practice when bulk densities were customarily lower.
Detergent compositions in tablet form have, potentially at least, several advantages over powder products. They do not require the user to measure out a volume of powder or liquid. Instead one or several tablets provide an appropriate quantity of composition for washing a single load in a washing machine or possibly by hand. They are thus easier for the consumer to handle and dispense.
Detergent compositions in tablet form are generally made by compressing or compacting a detergent powder which includes both detergent active and detergency builder. It is desirable that tablets have adequate strength when dry, yet disperse and dissolve quickly when added to wash water.
Detergent tablets for fabric washing typically contain at least 5% by weight of detergent active. This serves as a binder, but can also retard disintegration and dissolution of a tablet. (By contrast, tablets for use in automatic dishwashing machines typically contain 2o by weight or less of detergent active, customarily a low-foaming nonionic detergent, as in W096/23053 for instance). There have been a number of disclosures relating to the manufacture of detergent tablets for fabric washing which have both strength and rapidity of disintegration in water, for example EP-A-522766.
GB-A-1080066 teaches that tablets should have void space between particles in order to allow penetration of water into the tablet at the time of use. The teaching of this document is that the void volume should be from 35 to 600 of the total tablet volume. US-A-3081267 teaches that void space within a tablet and communicating with external air should be from 40 to 60% by volume of the tablet.
Both of these documents teach that after the tablets are made by compaction of the particulate detergent composition the tablets should be sprayed on their exterior with water, which is then allowed to dry. The effect of this is to cause partial hydration and dissolution at the exterior of the tablets thus cementing material together at the tablet exterior and enhancing tablet strength.
These documents date from 1963-1966. In more recent documents there has been disclosure of tablets of lower void volume and in Example 6 of EP 711828 tablets are disclosed which contain aluminosilicate as builder and have porosities corresponding to 30% or 20% of air in the tablet volume.
When making tablets from particulate detergent composition, it is desirable that the tablets should dissolve/disintegrate rapidly when added to water for use, yet have a good mechanical strength prior to use. These properties are antagonistic. As more pressure is used when a tablet is compacted, so the tablet density and strength m rise, but the speed of disintegration/dissolution goes down.
Detergent compositions in tablet form are generally made by compressing or compacting a detergent powder which includes both detergent active and detergency builder. It is desirable that tablets have adequate strength when dry, yet disperse and dissolve quickly when added to wash water.
Detergent tablets for fabric washing typically contain at least 5% by weight of detergent active. This serves as a binder, but can also retard disintegration and dissolution of a tablet. (By contrast, tablets for use in automatic dishwashing machines typically contain 2o by weight or less of detergent active, customarily a low-foaming nonionic detergent, as in W096/23053 for instance). There have been a number of disclosures relating to the manufacture of detergent tablets for fabric washing which have both strength and rapidity of disintegration in water, for example EP-A-522766.
GB-A-1080066 teaches that tablets should have void space between particles in order to allow penetration of water into the tablet at the time of use. The teaching of this document is that the void volume should be from 35 to 600 of the total tablet volume. US-A-3081267 teaches that void space within a tablet and communicating with external air should be from 40 to 60% by volume of the tablet.
Both of these documents teach that after the tablets are made by compaction of the particulate detergent composition the tablets should be sprayed on their exterior with water, which is then allowed to dry. The effect of this is to cause partial hydration and dissolution at the exterior of the tablets thus cementing material together at the tablet exterior and enhancing tablet strength.
These documents date from 1963-1966. In more recent documents there has been disclosure of tablets of lower void volume and in Example 6 of EP 711828 tablets are disclosed which contain aluminosilicate as builder and have porosities corresponding to 30% or 20% of air in the tablet volume.
When making tablets from particulate detergent composition, it is desirable that the tablets should dissolve/disintegrate rapidly when added to water for use, yet have a good mechanical strength prior to use. These properties are antagonistic. As more pressure is used when a tablet is compacted, so the tablet density and strength m rise, but the speed of disintegration/dissolution goes down.
This invention is concerned with tablets compacted from a detergent composition containing a substantial portion of water-soluble phosphate builder.
Unexpectedly, we have found that in such tablets, the combination of tablet strength and speed of disintegration is affected by the choice of material incorporated as peroxygen bleach. Sodium percarbonate and sodium perborate tetrahydrate both give properties which are better than those obtained with sodium perborate monohydrate.
Consequently, in a first aspect the present invention provides a detergent tablet compacted from a particulate composition containing:
from 2% preferably 5o up to 50% by weight of detergent active, from 20 to 60% by weight of water-soluble inorganic phosphate builder, and other ingredients, wherein the tablet has a density of at least 1040 gm/litre and contains from 8 to 30% by weight of peroxygen bleach which is sodium percarbonate or sodium perborate tetrahydrate or a mixture thereof.
Sodium percarbonate has been found to give even better strength than perborate tetrahydrate and is therefore preferred.
The amount of peroxygen bleach is preferably at least l00 by weight of the composition. The amount may be not more than 25% or even 20% by weight.
The peroxygen bleach is preferably distributed throughout 5 the tablet, although it may be present as a multiplicity of granules distributed throughout the tablet. Notably, sodium percarbonate may be utilised in the form of granules with a water-soluble coating of a protective material serving to keep moisture away from the percarbonate until the time of use.
Tablet density preferably lies in a range from 1040 or 1050gm/litre up to 1300gm/litre. The tablet density may well lie in a range up to 1250 or even 1200gm/litre.
Tablet density is inversely related to tablet porosity, which is conveniently expressed as the percentage of its volume which is air (i.e. empty space).
The air content of a tablet can be calculated from the volume and weight of the tablet, provided the true density of the solid content is known. The latter can be measured by compressing a sample of the material under vacuum with a very high applied force, then measuring the weight and volume of the resulting solid object.
The true density of a detergent composition is often about WO 98!42816 PCTlEP98/01769 1.6, in which case a tablet density range from 1040 to 1300g/litre is approximately 19 to 35o air by volume.
Ranges of 1040 to 1250 or 1200g/litre approximates to 22 or 25% to 35o air by volume. A preferred range of 1070 to S 1250g/litre approximates to 22 to 33o air by volume.
Preferably, part or all of the detergent active is anionic.
We have found that satisfactory strength and speed of disintegration can be obtained using a detergent active mixture in which anionic and nonionic detergent are in proportions from 1.5:1 to 4:1, better 1.8:1 to 3:1 or 4:1.
These proportions give good cleaning. Therefore, in a second aspect the invention provides a detergent tablet compacted from a particulate composition containing:
from 2% preferably at least 5% up to 50% by weight of detergent active, from 20 to 60o by weight of water-soluble inorganic phosphate builder, and other ingredients, wherein the tablet has a density of at least 1040gm/litre and the detergent active contains anionic and nonionic detergent in proportions of 1.5:1 to 4:1.
It is preferred that the nonionic detergent active is a mixture of an ethoxylated fatty alcohol with HLB value over 11.0 and an ethoxylated fatty alcohol with HLB value below 9.5 better below 9Ø
t ,. ~ ,.."
Unexpectedly, we have found that in such tablets, the combination of tablet strength and speed of disintegration is affected by the choice of material incorporated as peroxygen bleach. Sodium percarbonate and sodium perborate tetrahydrate both give properties which are better than those obtained with sodium perborate monohydrate.
Consequently, in a first aspect the present invention provides a detergent tablet compacted from a particulate composition containing:
from 2% preferably 5o up to 50% by weight of detergent active, from 20 to 60% by weight of water-soluble inorganic phosphate builder, and other ingredients, wherein the tablet has a density of at least 1040 gm/litre and contains from 8 to 30% by weight of peroxygen bleach which is sodium percarbonate or sodium perborate tetrahydrate or a mixture thereof.
Sodium percarbonate has been found to give even better strength than perborate tetrahydrate and is therefore preferred.
The amount of peroxygen bleach is preferably at least l00 by weight of the composition. The amount may be not more than 25% or even 20% by weight.
The peroxygen bleach is preferably distributed throughout 5 the tablet, although it may be present as a multiplicity of granules distributed throughout the tablet. Notably, sodium percarbonate may be utilised in the form of granules with a water-soluble coating of a protective material serving to keep moisture away from the percarbonate until the time of use.
Tablet density preferably lies in a range from 1040 or 1050gm/litre up to 1300gm/litre. The tablet density may well lie in a range up to 1250 or even 1200gm/litre.
Tablet density is inversely related to tablet porosity, which is conveniently expressed as the percentage of its volume which is air (i.e. empty space).
The air content of a tablet can be calculated from the volume and weight of the tablet, provided the true density of the solid content is known. The latter can be measured by compressing a sample of the material under vacuum with a very high applied force, then measuring the weight and volume of the resulting solid object.
The true density of a detergent composition is often about WO 98!42816 PCTlEP98/01769 1.6, in which case a tablet density range from 1040 to 1300g/litre is approximately 19 to 35o air by volume.
Ranges of 1040 to 1250 or 1200g/litre approximates to 22 or 25% to 35o air by volume. A preferred range of 1070 to S 1250g/litre approximates to 22 to 33o air by volume.
Preferably, part or all of the detergent active is anionic.
We have found that satisfactory strength and speed of disintegration can be obtained using a detergent active mixture in which anionic and nonionic detergent are in proportions from 1.5:1 to 4:1, better 1.8:1 to 3:1 or 4:1.
These proportions give good cleaning. Therefore, in a second aspect the invention provides a detergent tablet compacted from a particulate composition containing:
from 2% preferably at least 5% up to 50% by weight of detergent active, from 20 to 60o by weight of water-soluble inorganic phosphate builder, and other ingredients, wherein the tablet has a density of at least 1040gm/litre and the detergent active contains anionic and nonionic detergent in proportions of 1.5:1 to 4:1.
It is preferred that the nonionic detergent active is a mixture of an ethoxylated fatty alcohol with HLB value over 11.0 and an ethoxylated fatty alcohol with HLB value below 9.5 better below 9Ø
t ,. ~ ,.."
The particulate composition which is compacted may be a mixture of particles of individual ingredients, but usually will comprise particles which themselves contain a mixture of ingredients. Such particles containing a mixture of ingredients may be produced by a granulation process and may be used alone or together with particles or single ingredients.
The composition will contain detergent active and detergent builder. Other ingredients are optional, but usually there will be some other ingredients in addition to the detergent active and detergency builder.
The amount of detergent active in a tablet is suitably from 5 or 8wto up to 40 to 50wto. Detergent-active material present may be anionic (soap or non-soap?, cationic, zwitterionic, amphoteric, nonionic or any combination of these.
Anionic detergent-active compounds may be present in an amount of from 0.5 to 40 wto, preferably from 20, 40 or 50 up to 30 or 40 wt%.
Synthetic (i.e. non-soapy anionic surfactants are well known to those skilled in the art. Examples include alkylbenzene sulphonates, olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
The composition will contain detergent active and detergent builder. Other ingredients are optional, but usually there will be some other ingredients in addition to the detergent active and detergency builder.
The amount of detergent active in a tablet is suitably from 5 or 8wto up to 40 to 50wto. Detergent-active material present may be anionic (soap or non-soap?, cationic, zwitterionic, amphoteric, nonionic or any combination of these.
Anionic detergent-active compounds may be present in an amount of from 0.5 to 40 wto, preferably from 20, 40 or 50 up to 30 or 40 wt%.
Synthetic (i.e. non-soapy anionic surfactants are well known to those skilled in the art. Examples include alkylbenzene sulphonates, olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
Primary alkyl sulphate having the formula ROS03- M+
in which R is an alkyl or alkenyl chain of 8 to 18 carbon atoms especially 10 to 14 carbon atoms and M+ is a solubilising cation especially sodium, is commercially significant as an anionic detergent active. Linear alkyl benzene sulphonate of the formula R ~ - +
where R is linear alkyl of 8 to 15 carbon atoms and M+ is a solubilising cation, especially sodium, is also a l0 commercially significant anionic detergent active.
Frequently, such linear alkyl benzene sulphonate or primary alkyl sulphate of the formula above, or a mixture thereof will be the desired anionic detergent and may provide 75 to 100wto of any anionic non-soap detergent in the composition.
In some forms of this invention, the amount of non-soap anionic detergent lies in a range from 5 to 30 wt% of the composition, better 5 to 20 wto.
It may also be desirable to include one of more soaps of fatty acids. These are preferably sodium soaps derived . r..... , , ~ ,.. ...
in which R is an alkyl or alkenyl chain of 8 to 18 carbon atoms especially 10 to 14 carbon atoms and M+ is a solubilising cation especially sodium, is commercially significant as an anionic detergent active. Linear alkyl benzene sulphonate of the formula R ~ - +
where R is linear alkyl of 8 to 15 carbon atoms and M+ is a solubilising cation, especially sodium, is also a l0 commercially significant anionic detergent active.
Frequently, such linear alkyl benzene sulphonate or primary alkyl sulphate of the formula above, or a mixture thereof will be the desired anionic detergent and may provide 75 to 100wto of any anionic non-soap detergent in the composition.
In some forms of this invention, the amount of non-soap anionic detergent lies in a range from 5 to 30 wt% of the composition, better 5 to 20 wto.
It may also be desirable to include one of more soaps of fatty acids. These are preferably sodium soaps derived . r..... , , ~ ,.. ...
from naturally occurring fatty acids, for example, the fatty acids from coconut oil, beef tallow, sunflower or hardened rapeseed oil.
Suitable nonionic detergent compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
Specific nonionic detergent compounds are alkyl (Ce-2z~
phenol-ethylene oxide condensates, the condensation products of linear or branched aliphatic C8-2o primary or secondary alcohols with ethylene oxide, copolymers of ethylene oxide and propylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylene-diamine.
Especially preferred are the primary and secondary alcohol ethoxylates, especially the Clo-is Primary and secondary alcohals ethoxylated with an average of from 5 to 20 moles of ethylene oxide per mole of alcohol.
In certain forms of this invention the amount of nonionic detergent lies in a range from 1 to 200, better 2o up to 15% or 20o by weight of the composition.
WO 98/42816 PCT/EP98l01769 Preferred is to use from 5 to 20% of non-soap anionic detergent, especially linear alkyl benzene sulphonate or primary alkyl sulphate, together with 2 to 15% of nonionic detergent, especially ethoxylated fatty alcohol, where the 5 ratio of anionic to nonionic is in the range from 1.5:1 to 4:1.
Products of this invention also include phosphate detergency builder, which may be ari alkali metal orthophosphate, pyrophosphate or tripolyphosphate.
Suitable nonionic detergent compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
Specific nonionic detergent compounds are alkyl (Ce-2z~
phenol-ethylene oxide condensates, the condensation products of linear or branched aliphatic C8-2o primary or secondary alcohols with ethylene oxide, copolymers of ethylene oxide and propylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylene-diamine.
Especially preferred are the primary and secondary alcohol ethoxylates, especially the Clo-is Primary and secondary alcohals ethoxylated with an average of from 5 to 20 moles of ethylene oxide per mole of alcohol.
In certain forms of this invention the amount of nonionic detergent lies in a range from 1 to 200, better 2o up to 15% or 20o by weight of the composition.
WO 98/42816 PCT/EP98l01769 Preferred is to use from 5 to 20% of non-soap anionic detergent, especially linear alkyl benzene sulphonate or primary alkyl sulphate, together with 2 to 15% of nonionic detergent, especially ethoxylated fatty alcohol, where the 5 ratio of anionic to nonionic is in the range from 1.5:1 to 4:1.
Products of this invention also include phosphate detergency builder, which may be ari alkali metal orthophosphate, pyrophosphate or tripolyphosphate.
10 Preferred is sodium tripolyphosphate.
Examples of other water-soluble builders which may be present are carbonates, e.g. sodium carbonate; and organic builders containing up to six carbon atoms, e.g. sodium tartrate, sodium citrate, trisodium carboxymethyloxysuccinate.
The amount of phosphate or polyphosphate detergency builder is at least 20o by weight, often at least 26% or even-at least 33% by weight of the overall composition.
The total amount of detergency builder will generally lie in a range from 5 to 80wto of the composition. The amount may be at least 10 or l5wto and may lie in a range up to 50 or 60wto.
The sodium perborate tetrahydrate or sodium percarbonate is advantageously employed together with an activator. Bleach activators, also referred to as bleach precursors, have been widely disclosed in the art. Preferred examples include peracetic acid precursors, for example, tetraacetylethylene diamine (TAED), now in widespread commercial use in conjunction with sodium perborate; and perbenzoic acid precursors. Typically activator used as 1 to 10o by weight of a composition.
Other ingredients may also be present in the overall composition. These include sodium carboxymethyl cellulose, colouring materials, enzymes, fluorescent brighteners, germicides, perfumes and bleaches. Sodium alkaline silicate may be included, although the amount of this or at least the amount added as an aqueous liquid, is preferably restricted so as to keep to a particulate mixture prior to compaction.
The detergent composition may incorporate a binder which is water-soluble and serves as a disintegrant by disrupting the structure of the tablet when the tablet is immersed in water, as taught in our EP-A-522766.
Such a binder material should melt at a temperature of 35°C, better 40°C or above, which is above ambient temperatures in many temperate countries. For use in °
hotter countries it will be preferable that the melting temperature is somewhat above 40°C, so as to be above the ambient temperature.
For convenience the melting temperature of the binder material should be below 80°C.
Preferred binder materials are synthetic organic polymers of appropriate melting temperature, especially polyethylene glycol. Polyethylene glycol of average molecular weight 1500 (PEG 1500) melts at 45°C and has proved suitable.
Polyethylene glycols of molecular weight 4000 and 6000 melt at about 55°C and 62°C respectively.
Other possibilities are polyvinylpyrrolidone, and polyacrylates and water-soluble acrylate copolymers.
We have found it desirable that the particulate composition which is compacted should have a bulk density of at least 650 g/litre, preferably at least 700 g/litre, and advantageously at least 750 g/litre.
Granular detergent compositions of high bulk density can be prepared by granulation and densification in a high-speed mixer/granulator, as described and claimed in EP 340013A
(Unilever), EP 352135A (Unilever), and EP 425277A
(Unilever), or by the continuous granulation/densification processes described and claimed in EP 367339A (Unilever) and EP 390251A (Unilever).
Examples of other water-soluble builders which may be present are carbonates, e.g. sodium carbonate; and organic builders containing up to six carbon atoms, e.g. sodium tartrate, sodium citrate, trisodium carboxymethyloxysuccinate.
The amount of phosphate or polyphosphate detergency builder is at least 20o by weight, often at least 26% or even-at least 33% by weight of the overall composition.
The total amount of detergency builder will generally lie in a range from 5 to 80wto of the composition. The amount may be at least 10 or l5wto and may lie in a range up to 50 or 60wto.
The sodium perborate tetrahydrate or sodium percarbonate is advantageously employed together with an activator. Bleach activators, also referred to as bleach precursors, have been widely disclosed in the art. Preferred examples include peracetic acid precursors, for example, tetraacetylethylene diamine (TAED), now in widespread commercial use in conjunction with sodium perborate; and perbenzoic acid precursors. Typically activator used as 1 to 10o by weight of a composition.
Other ingredients may also be present in the overall composition. These include sodium carboxymethyl cellulose, colouring materials, enzymes, fluorescent brighteners, germicides, perfumes and bleaches. Sodium alkaline silicate may be included, although the amount of this or at least the amount added as an aqueous liquid, is preferably restricted so as to keep to a particulate mixture prior to compaction.
The detergent composition may incorporate a binder which is water-soluble and serves as a disintegrant by disrupting the structure of the tablet when the tablet is immersed in water, as taught in our EP-A-522766.
Such a binder material should melt at a temperature of 35°C, better 40°C or above, which is above ambient temperatures in many temperate countries. For use in °
hotter countries it will be preferable that the melting temperature is somewhat above 40°C, so as to be above the ambient temperature.
For convenience the melting temperature of the binder material should be below 80°C.
Preferred binder materials are synthetic organic polymers of appropriate melting temperature, especially polyethylene glycol. Polyethylene glycol of average molecular weight 1500 (PEG 1500) melts at 45°C and has proved suitable.
Polyethylene glycols of molecular weight 4000 and 6000 melt at about 55°C and 62°C respectively.
Other possibilities are polyvinylpyrrolidone, and polyacrylates and water-soluble acrylate copolymers.
We have found it desirable that the particulate composition which is compacted should have a bulk density of at least 650 g/litre, preferably at least 700 g/litre, and advantageously at least 750 g/litre.
Granular detergent compositions of high bulk density can be prepared by granulation and densification in a high-speed mixer/granulator, as described and claimed in EP 340013A
(Unilever), EP 352135A (Unilever), and EP 425277A
(Unilever), or by the continuous granulation/densification processes described and claimed in EP 367339A (Unilever) and EP 390251A (Unilever).
The invention can be put into effect using a conventional stamping press. A suitable press will generally have a pair of mould parts which move relatively towards and away from each other to compact particulate material between them. They may move within a surrounding sleeve or similar structure.
For any chosen composition, the density and strength of tablets varies with the pressure applied to compact the composition into tablets.
to The amount of pressure needed to obtain a density in the required range can be found by making tablets with varying amounts of applied force, and determining the density of the tablets obtained.
The tablets may be made without any spray on of water after stamping the tablets.
For any chosen composition, the density and strength of tablets varies with the pressure applied to compact the composition into tablets.
to The amount of pressure needed to obtain a density in the required range can be found by making tablets with varying amounts of applied force, and determining the density of the tablets obtained.
The tablets may be made without any spray on of water after stamping the tablets.
Example 1 Tablets for use in fabric washing were made, starting with a base powder of the following composition:
parts by weight S Sodium linear alkylbenzene sulphonate 9.62 C13-is fatty alcohol 7E0 1 . 07 X13-is fatty alcohol 3E0 3 . 21 Soap 0.27 Sodium tripolyphosphate, type lA 1 24.31 Sodium silicate 5.88 Sodium carboxymethyl cellulose 0.21 Acrylate/maleate copolymer 1.15 Salts, moisture and minor ingredients 8.9 54.60 1. This tripolyphosphate contained less than 30%
of the phase I form of anhydrous sodium tripolyphosphate.
Three powders were made by mixing this base powder with persalts, sodium tripolyphosphate specified to contain 700 phase I form and contain 3.5o water of hydration (Rhodia-Phos HPA 3.5 available from Rhone-Poulenc) and other detergent ingredients as tabulated below.
The compositions thus contained the following percentages by weight:
a by weight C
Base powder 54 . 54.60 54.60 HPA sodium tripolyphosphate 21 . 21.22 20.12 5 TAED granules 3 . 3.35 3.35 Sodium carbonate 3 . 4.95 --Sodium percarbonate 15.00 -_ Sodium perborate monohydrate -- 13.25 --Sodium perborate tetrahydrate ---- 19.30 10 Anti-foam granule 1 .16 1.16 1 Enzymes, phosphonate, perfume 1 .
. 1.47 1.47 The amounts of persalt were chosen to give the same amounts of available oxygen. The sodium percarbonate was in the form of granules with a water-soluble coating.
parts by weight S Sodium linear alkylbenzene sulphonate 9.62 C13-is fatty alcohol 7E0 1 . 07 X13-is fatty alcohol 3E0 3 . 21 Soap 0.27 Sodium tripolyphosphate, type lA 1 24.31 Sodium silicate 5.88 Sodium carboxymethyl cellulose 0.21 Acrylate/maleate copolymer 1.15 Salts, moisture and minor ingredients 8.9 54.60 1. This tripolyphosphate contained less than 30%
of the phase I form of anhydrous sodium tripolyphosphate.
Three powders were made by mixing this base powder with persalts, sodium tripolyphosphate specified to contain 700 phase I form and contain 3.5o water of hydration (Rhodia-Phos HPA 3.5 available from Rhone-Poulenc) and other detergent ingredients as tabulated below.
The compositions thus contained the following percentages by weight:
a by weight C
Base powder 54 . 54.60 54.60 HPA sodium tripolyphosphate 21 . 21.22 20.12 5 TAED granules 3 . 3.35 3.35 Sodium carbonate 3 . 4.95 --Sodium percarbonate 15.00 -_ Sodium perborate monohydrate -- 13.25 --Sodium perborate tetrahydrate ---- 19.30 10 Anti-foam granule 1 .16 1.16 1 Enzymes, phosphonate, perfume 1 .
. 1.47 1.47 The amounts of persalt were chosen to give the same amounts of available oxygen. The sodium percarbonate was in the form of granules with a water-soluble coating.
15 35g portions of each composition were made into cylindrical tablets of 44 mm diameter, using a Carver hand press. The force applied to make the tablets was the same (300kg) in each case.
The tablets were weighed and measured to determine their density which was found to be 1117gm/litre ~ 5% in each case.
The strength of the tablets was determined by the following test of their diametral fracture stress. The test procedure was carried out using a testing machine with flat faces which were urged together by a measured force, such as an Instron Universal Testing Machine.
The cylindrical tablet was placed between the platens of an Instron machine, so that the platens contact the curved surface of the cylinder at either end of a diameter through the tablet. The sample tablet was then compressed diametrically, by advancing the platens of the machine towards each other at a slow rate such as lcm/min until fracture of the tablet occurred, at which point the applied load required to cause fracture was recorded. The diametral fracture stress was then calculated from the following equation:
bo=
~t Dt where bo is the diametral fracture stress in Pascal (Pa), P
is the applied load in Newtons (N) to cause fracture, D is the tablet diameter in metres (M) and t is the tablet thickness, also in metres (M).
we have found it desirable in this invention that tablets should have a DFS of at least 6KPa, better at least BKPa.
DFS will usually not need to exceed 40KPa, and a range from 10 to 40KPa is particularly preferred. Values of DFS up to at least 60KPa may be used, however.
.,.w. ~......_ . , The break-up, dispersion and dissolution of tablets was measured by a test procedure in which a tablet is placed on a plastic sieve with 2mm mesh size which was immersed in 9 litres of demineralised water at ambient temperature of 22°C and rotated at 200 rpm. The water conductivity was monitored until it reached a constant value.
The time for break up and dispersion of the tablets was taken as the time (T9o) for change in the water conductivity to reach 900 of its final magnitude. This was alter, l0 confirmed by visual observation of the material remaining on the rotating sieve.
The results obtained were:
C
percarbonate perborate perborate mono- tetra-h drate h drate Tablet strength 32 20 27 (kPa) Tablet dissolution 3,5 5_2 3.8 T9o (min) This shows that tablets made with percarbonate and with perborate tetrahydrate had unexpectedly greater strength than tablets made with perborate monohydrate. They also ' 20 dissolved more quickly, in spite of their greater strength.
The tablets were weighed and measured to determine their density which was found to be 1117gm/litre ~ 5% in each case.
The strength of the tablets was determined by the following test of their diametral fracture stress. The test procedure was carried out using a testing machine with flat faces which were urged together by a measured force, such as an Instron Universal Testing Machine.
The cylindrical tablet was placed between the platens of an Instron machine, so that the platens contact the curved surface of the cylinder at either end of a diameter through the tablet. The sample tablet was then compressed diametrically, by advancing the platens of the machine towards each other at a slow rate such as lcm/min until fracture of the tablet occurred, at which point the applied load required to cause fracture was recorded. The diametral fracture stress was then calculated from the following equation:
bo=
~t Dt where bo is the diametral fracture stress in Pascal (Pa), P
is the applied load in Newtons (N) to cause fracture, D is the tablet diameter in metres (M) and t is the tablet thickness, also in metres (M).
we have found it desirable in this invention that tablets should have a DFS of at least 6KPa, better at least BKPa.
DFS will usually not need to exceed 40KPa, and a range from 10 to 40KPa is particularly preferred. Values of DFS up to at least 60KPa may be used, however.
.,.w. ~......_ . , The break-up, dispersion and dissolution of tablets was measured by a test procedure in which a tablet is placed on a plastic sieve with 2mm mesh size which was immersed in 9 litres of demineralised water at ambient temperature of 22°C and rotated at 200 rpm. The water conductivity was monitored until it reached a constant value.
The time for break up and dispersion of the tablets was taken as the time (T9o) for change in the water conductivity to reach 900 of its final magnitude. This was alter, l0 confirmed by visual observation of the material remaining on the rotating sieve.
The results obtained were:
C
percarbonate perborate perborate mono- tetra-h drate h drate Tablet strength 32 20 27 (kPa) Tablet dissolution 3,5 5_2 3.8 T9o (min) This shows that tablets made with percarbonate and with perborate tetrahydrate had unexpectedly greater strength than tablets made with perborate monohydrate. They also ' 20 dissolved more quickly, in spite of their greater strength.
Claims (12)
1. A porous detergent tablet compacted from a particulate composition wherein the composition and the tablet as compacted therefrom contain:
from 5 to 50% by weight of detergent active, from 20 to 60% by weight of water-soluble inorganic phosphate builder, and other ingredients, wherein the tablet has a density of at least 1040 gm/litre and contains from 8 to 30% by weight of peroxygen bleach which is sodium percarbonate or sodium perborate tetrahydrate or a mixture thereof.
from 5 to 50% by weight of detergent active, from 20 to 60% by weight of water-soluble inorganic phosphate builder, and other ingredients, wherein the tablet has a density of at least 1040 gm/litre and contains from 8 to 30% by weight of peroxygen bleach which is sodium percarbonate or sodium perborate tetrahydrate or a mixture thereof.
2. A tablet according to claim 1 wherein the peroxygen bleach is sodium percarbonate.
3. A tablet according to claim 1 or claim 2 containing from 30 to 60% by weight of sodium tripolyphosphate as the water-soluble inorganic phosphate builder.
4. A tablet according to any one of claims 1 to 3 which contains at least 4% by weight of anionic detergent and contains in total from 5 to 40% by weight of detergent active.
5. A tablet according to any one of claims 1 to 4 which contains from 5 to 30% by weight of anionic detergent.
6. A tablet according to claim 5, which contains from 2 to 20% by weight of nonionic detergent.
7. A tablet according to claim 4, claim 5, or claim 6 which contains from 5 to 30% by weight of anionic detergent and from 2 to 20% by weight of nonionic detergent.
8. A tablet according to any one of claims 1 to 7 wherein the detergent active contains anionic and nonionic detergent active in weight ratio of 1.5:1 to 4:1.
9. A tablet according to claim 6, claim 7, or claim 8 wherein the nonionic detergent is a mixture of a nonionic detergent with HLB value over 11.0 and a nonionic detergent with HLB value below 9.5, in a weight ratio lying in a range from 3:1 to 1:3.
10. A tablet according to any one of claims 1 to 9 having density in the range from 1075 to 1275 gm/litre.
11. A tablet according to any one of claims 1 to 10 having porosity in the range from 19 to 35% air by volume.
12. A tablet according to any one of claims 2 to 10 having porosity in the range from 22 to 33% air by volume.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9706083.4 | 1997-03-24 | ||
GBGB9706083.4A GB9706083D0 (en) | 1997-03-24 | 1997-03-24 | Detergent compositions |
PCT/EP1998/001769 WO1998042816A1 (en) | 1997-03-24 | 1998-03-18 | Detergent compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2284005A1 true CA2284005A1 (en) | 1998-10-01 |
Family
ID=10809776
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002284005A Abandoned CA2284005A1 (en) | 1997-03-24 | 1998-03-18 | Detergent compositions |
Country Status (15)
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EP (1) | EP0956332B2 (en) |
CN (1) | CN1255940A (en) |
AR (1) | AR011698A1 (en) |
AU (1) | AU7210698A (en) |
BR (1) | BR9808044A (en) |
CA (1) | CA2284005A1 (en) |
DE (1) | DE69803832T3 (en) |
ES (1) | ES2172134T5 (en) |
GB (2) | GB9706083D0 (en) |
HU (1) | HUP0001732A3 (en) |
IN (1) | IN190292B (en) |
PL (1) | PL335880A1 (en) |
TR (1) | TR199902316T2 (en) |
WO (1) | WO1998042816A1 (en) |
ZA (1) | ZA982343B (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
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GB9711829D0 (en) | 1997-06-06 | 1997-08-06 | Unilever Plc | Detergent compositions |
ZA984570B (en) | 1997-06-06 | 1999-11-29 | Unilever Plc | Cleaning compositions. |
DE69806406T3 (en) | 1997-10-22 | 2011-05-05 | Unilever N.V. | TABLETIC DETERGENT COMPOSITIONS |
GB9826097D0 (en) * | 1998-11-27 | 1999-01-20 | Unilever Plc | Detergent compositions |
DE19859807A1 (en) * | 1998-12-23 | 2000-06-29 | Henkel Kgaa | Phosphate compounds |
DE19910819A1 (en) * | 1999-03-11 | 2000-09-14 | Henkel Kgaa | Detergent tablets with surfactant-bleach-builder combination |
DE19932569A1 (en) * | 1999-07-13 | 2001-01-18 | Henkel Kgaa | Detergent tablets, in particular for machine dishwashing |
CN107488531A (en) * | 2017-08-29 | 2017-12-19 | 广州立白企业集团有限公司 | A kind of neutral Instant detergent bar composition and preparation method thereof |
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NL259594A (en) * | 1959-12-31 | |||
GB911204A (en) * | 1960-07-28 | 1962-11-21 | Unilever Ltd | Bleaching compositions |
BE632423A (en) † | 1962-05-17 | |||
CA795287A (en) * | 1965-03-09 | 1968-09-24 | P. Davis Robert | Detergent tablets |
US3557003A (en) * | 1967-06-21 | 1971-01-19 | Procter & Gamble | Detergent tablet |
JPS5070286A (en) * | 1973-10-25 | 1975-06-11 | ||
LU77094A1 (en) * | 1977-04-08 | 1978-11-03 | Interox Sa | |
GB8412537D0 (en) * | 1984-05-17 | 1984-06-20 | Unilever Plc | Detergent powder compositions |
AU647736B2 (en) * | 1989-04-24 | 1994-03-31 | Unilever Plc | Detergent compositions |
DE4010533A1 (en) † | 1990-04-02 | 1991-10-10 | Henkel Kgaa | Prodn. of high-density detergent granules |
GB9422925D0 (en) * | 1994-11-14 | 1995-01-04 | Unilever Plc | Detergent compositions |
DE19502774A1 (en) * | 1995-01-27 | 1996-08-01 | Henkel Kgaa | Process for the manufacture of break-resistant cleaning tablets |
-
1997
- 1997-03-24 GB GBGB9706083.4A patent/GB9706083D0/en active Pending
-
1998
- 1998-03-18 AU AU72106/98A patent/AU7210698A/en not_active Abandoned
- 1998-03-18 BR BR9808044-0A patent/BR9808044A/en not_active IP Right Cessation
- 1998-03-18 DE DE69803832T patent/DE69803832T3/en not_active Expired - Fee Related
- 1998-03-18 WO PCT/EP1998/001769 patent/WO1998042816A1/en not_active Application Discontinuation
- 1998-03-18 EP EP98919154A patent/EP0956332B2/en not_active Expired - Lifetime
- 1998-03-18 GB GB9913960A patent/GB2335435B/en not_active Expired - Fee Related
- 1998-03-18 PL PL98335880A patent/PL335880A1/en unknown
- 1998-03-18 TR TR1999/02316T patent/TR199902316T2/en unknown
- 1998-03-18 CA CA002284005A patent/CA2284005A1/en not_active Abandoned
- 1998-03-18 HU HU0001732A patent/HUP0001732A3/en unknown
- 1998-03-18 CN CN98805061A patent/CN1255940A/en active Pending
- 1998-03-18 ES ES98919154T patent/ES2172134T5/en not_active Expired - Lifetime
- 1998-03-19 ZA ZA9802343A patent/ZA982343B/en unknown
- 1998-03-23 IN IN163BO1998 patent/IN190292B/en unknown
- 1998-03-24 AR ARP980101326A patent/AR011698A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
DE69803832D1 (en) | 2002-03-21 |
HUP0001732A2 (en) | 2000-11-28 |
ES2172134T5 (en) | 2006-03-01 |
TR199902316T2 (en) | 1999-12-21 |
PL335880A1 (en) | 2000-05-22 |
AR011698A1 (en) | 2000-08-30 |
GB2335435A8 (en) | 1999-09-28 |
GB9706083D0 (en) | 1997-05-14 |
ES2172134T3 (en) | 2002-09-16 |
IN190292B (en) | 2003-07-12 |
GB2335435A (en) | 1999-09-22 |
AU7210698A (en) | 1998-10-20 |
EP0956332A1 (en) | 1999-11-17 |
DE69803832T2 (en) | 2002-09-26 |
GB9913960D0 (en) | 1999-08-18 |
CN1255940A (en) | 2000-06-07 |
HUP0001732A3 (en) | 2003-02-28 |
EP0956332B2 (en) | 2005-08-10 |
EP0956332B1 (en) | 2002-02-13 |
ZA982343B (en) | 1999-09-20 |
BR9808044A (en) | 2000-03-08 |
WO1998042816A1 (en) | 1998-10-01 |
DE69803832T3 (en) | 2006-04-13 |
GB2335435B (en) | 2000-11-08 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued |