ZA200105348B - Lavatory cleansing compositions. - Google Patents
Lavatory cleansing compositions. Download PDFInfo
- Publication number
- ZA200105348B ZA200105348B ZA200105348A ZA200105348A ZA200105348B ZA 200105348 B ZA200105348 B ZA 200105348B ZA 200105348 A ZA200105348 A ZA 200105348A ZA 200105348 A ZA200105348 A ZA 200105348A ZA 200105348 B ZA200105348 B ZA 200105348B
- Authority
- ZA
- South Africa
- Prior art keywords
- phase
- block according
- lavatory cleansing
- salt
- water
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title description 18
- 150000003839 salts Chemical class 0.000 claims description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 41
- 239000007844 bleaching agent Substances 0.000 claims description 22
- 239000002304 perfume Substances 0.000 claims description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 14
- 150000001450 anions Chemical class 0.000 claims description 13
- 239000004615 ingredient Substances 0.000 claims description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical group [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical group [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- MSFGZHUJTJBYFA-UHFFFAOYSA-M sodium dichloroisocyanurate Chemical group [Na+].ClN1C(=O)[N-]C(=O)N(Cl)C1=O MSFGZHUJTJBYFA-UHFFFAOYSA-M 0.000 claims description 2
- 238000004061 bleaching Methods 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 description 8
- -1 glycoluracils Chemical class 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 3
- 239000004150 EU approved colour Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- 239000004614 Process Aid Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000007973 cyanuric acids Chemical class 0.000 description 2
- WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 235000009088 Citrus pyriformis Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 241000009298 Trigla lyra Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229960001484 edetic acid Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 125000005543 phthalimide group Chemical class 0.000 description 1
- 229920000141 poly(maleic anhydride) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical class CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-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
- 229920001567 vinyl ester resin Polymers 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/1233—Carbonates, e.g. calcite or dolomite
-
- 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
- C11D17/0056—Lavatory cleansing blocks
-
- 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
- C11D3/046—Salts
-
- 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
- C11D3/395—Bleaching agents
- C11D3/3955—Organic bleaching agents
-
- 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
- C11D3/50—Perfumes
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)
- Cosmetics (AREA)
- Bidet-Like Cleaning Device And Other Flush Toilet Accessories (AREA)
Description
LAVATORY CLEANSING COMPOSITIONS
This invention is concerned with lavatory cleansing blocks which may be used to clean and/or perfume the flush water of a lavatory or urinal.
The use of toile: blocks to impart cleansing and/or other components to the flush water of a lavatory or urinal is well known. Such compositions may, for example, be immersed in the water of a lavatory or held under the rim of a toilet, in a suitable holder, for intermittent contact of the solid material with flush water. For convenience these two approaches will be referred to herein respectively as ‘cistern-blocks’ and ‘rim-blocks’
In recent years it has become commonplace for toilet blocks . ) to contain a halogen release agent or other bleaching agent.
From EP 0206725 it is clear that halogen release agents are, . by their nature, powerful chemically reactive species, : serving as halogenating or oxidising agents and it is consequently difficult to incorporate bleach-sensitive components such as perfumes and dyestuffs into blocks which contain bleaching agents.
Toilet blocks in which two incompatible components are separated by placing them in different phases of the toilet block are described in EP 0 101 402 (Henkel).
© WO 00/58434 PCT/EP00/01184
We have found that with dual phase tcilet one phase tends to dissolve faster than the other phase leading to a disparity in the dosing of the ingredients in the final flushes of the toilet.
We have determined that improved toilet blocks can be formulated in which the problem of uneven dissolution between the phases of a multiphase block can be mitigated.
Accordingly, the present invention provides a lavatory cleansing block comprising at least two phases one phase (phase 1) comprising a water insoluble salt as at least S50 wt% of the salt present within that phase and a second phase (phase 2) comprising a perfume and a water soluble salt such that the salts in both phases have the same anion.
The invention also relates to a process for producing the A toilet blocks, described in the above paragraph, the process - comprising the step of co-extruding the two phases to form a block. .
In order that the invention may be further understood the following description details preferred and optional features of the invention.
i - 3 =
Salts
The present invention preferably relates to a dual phase block.
Phase 1 of the block comprises a water insoluble salt as at least 50 wt% of the salt present, in the context of the present invention water insoluble salt refers to salts having a maximum solubility parameter of 0.05 gram per 100cc of water at 25°C.
The second phase (Phase 2) of the block comprises a perfume and a water soluble salt. The term water soluble salt refers to salts having a solubility parameter of at least 0.5 gram per 100cc of water at 0°C, more preferably greater than 1 gram per 100 cc of water. The salts in both phases should have the same anion.
Other salts with differing anions may also be present within each phase. However, it is highly preferable if phase 1 . - does not contain a water soluble salt having the same anion as the water insoluble salt.
The total level of water soluble salt having the same anion as the water insoluble salt within phase 2 is from 1 to 10 wt% of the total level of ingredients present in phase 2.
It is preferred if phase 2 further comprises a water insoluble salt having the same anion as the water soluble salt. More preferably the ratio of water soluble salt and the water insoluble salt both having the same anion within phase 2 of the toilet block is from 5:1 t 1:5. Most preferably the ratio of water soluble salt and the water insoluble salt both having the same anion within phase 2 of the toilet block is from 3:2 to 2:3.
A preferred water soluble salt for use with the present invention is sodium carbonate.
A preferred water insoluble salt for use with the present invention is calcium carbonate.
The total level of water insoluble salt in phase 1 is from 1 to 10 wt¥ of the total level of ingredients present in phase 1.
Blocks according to the present invention comprise 5 to 50 wt% to by weight of salt as a sum of the total ingredients of both phases inclusive of the anion present, more preferably 10-30 wt%.
Alcohol Ethoxylate :
The toilet blocks according to the invention may include an : alcohol ethoxylate. The alcohol ethoxylate preferably used in the present invention is ethoxylated with 8 or less moles . of alkylene oxide, more preferably the alcohol ethoxylate is ethoxylated with 5 or less moles of alkylene oxide.
Preferably the alcohol ethoxylate has a carbon chain length of C3 to C;,, more preferably from Cs to Cig
Preferably the alcohol ethoxylate is branched.
It is preferred if the alcohol ethoxylate has an H.L.B of 12 or less, more preferably an HLBR of 10 or less, most preferably of 8 cor less.
The alcohol ethoxylate should preferably have a cloud point cf less than 65 when measured in water at a 1% solution.
Preferably, the level of alcohol ethoxylate within the block is less than 5 wt% of the total weight of the block. More preferably the alcohol ethoxylate is in a separate phase to the perfume (that is phase 1). It is advantageous if the level of alcohol ethoxylate is from 0.5 to 6 wt % of the weight of the total composition (i.e. both phases), more preferably from 1.5 to 4 wt% of the weight of the total composition.
Bleaching Agents
Typically the blocks comprise up to 50% by weight of a at least sparingly water soluble bleaching agent. Typically levels of bleaching agents are 2-30% wt on product. For the purposes of the present specification the term bleaching agent is used to mean both a bleaching agent and a precursor . : which produces a bleaching agent unless the context demands otherwise.
Suitable bleaching agents active-halide and active-oxygen bleaching agents, particularly the so-called ‘halogen release agents’.
Chlorine bleaching agents are preferred. Suitable water- soluble, active chlorine, bleaching agents used in accordance with the invention include chlorinated cyanurates, phthalimides, p-toluene sulphonamides, azodicarbonamides, hydantoins, glycoluracils, amines and
WU 00/58434 PCT/EP00/01184 melamines. The alkali metal salts of cyanurates are preferred.
A particularly preferred bleaching agent is sodium dichlorocyanurate (NaDCCA). The bleaching agent is typically present in an amount of 10-30% and most preferably at around 25%. Oxidan DCN/WSG (TM) ex Sigma has been found to be a suitable bleaching agent.
In a particularly preferred embodiment of the invention the bleach resides in the same phase as the water insoluble salt (phase 1).
Anionic Surfactant
Preferably, the composition will also contain a surfactant component which is anionic in nature. This surfactant serves to provide a cleansing and foaming effect.
Suitable anionic surface active agents include alkali metal . or ammonium alkylaryl sulphonates (especially alkyl benzene : sulphonates), alkane sulphonates, alkyl sulphates and sarcosinates. .
We have determined that improved foaming properties are sometimes obtained by the use of a surfactant system which comprises primary alkyl sulphate (PAS) together with other anionic surfactants. Preferably the present invention provides a lavatory block comprising 1-15% wt (more preferably 1-5% wt) of a primary alkyl sulphate and 15-50%wt (more preferably 30-50%wt) of other anionic surfactants. We have determined that the use of this mixed surfactant system is advantageous in that it reduces the stickiness of the block during manufacture. The blocks with 1-5% PAS show improved wear characteristics.
Preferably the other anionic surfactants are sulphonates.
Suitable sulphonates include alkyl benzene sulphonate (ABS).
It is believed that the combination of relatively low levels of PAS together with higher levels of ABS promotes the foaming and the perfume delivery from the block.
The total amount of surfactant when present, may lie within wide limits. In practice, the surfactant will generally be for 10 to 70% by weight of the composition, but more preferable that surfactant comprises from 20 to 50% by weight thereof.
Process Aids
As will be described in further detail below extrusion is the preferred method of manufacture. Optionally, the blocks according to the invention further comprise a processing aid i - to assist in extrusion. Suitable processing aids include ) oils (including both mineral and silicone oils), esters {other than those derived from ethylenically unsaturated carboxyl group containing monomers), alcohol ethoxylates and polybutene.
Per fume
Preferably, the blocks comprise 2-15%wt of a hydrophobic oily liquid perfume. The blocks more preferably comprise, 2-10%, more preferably 3-6% wt of the perfume. Levels of around 4% wt perfume are particularly preferred. This oily perfume is typically of the kind described in the European patent application EP 167,210. It will be understood that the liquid oily perfume must be stable in the presence of the water-soluble, active chlorine, bleaching agent.
Suitable oily perfumes can be easily selected by testing them in combination with the water-soluble, active chlorine, bleaching agent.
In some instances, the toilet block may comprise two perfumes in this case it is preferable if the perfume present in each phase is at least 80 wt% of the total perfume present in that phase. More preferably different perfumes are present in phases.
Examples of suitable bleach-stable perfumes are Verdeo 898,
Bonanza 048 and Ponderosa 431 all ex IFF, and LB 132 ex
Quest. Particularly preferred perfumes are Icebreaker Super
Mod, Oxygen Supra Mod, Motebianco Supra and lemonfit Supra (all TM) ex Givaudan Roure.
Minors .
Minor components will generally be present but are optional.
These include colouring agents, and/or whiteners. These } materials should be chosen such that they are compatible with the bleaching agent and do not react therewith to a significant extent. Titanium dioxide is an acceptable whitener. Levels of colouring agents and/or whiteners as typically below 5% wt.
FPurther enhancement of the product may be obtained by the additional use of chelating agent, sequestrant or water- softening agent such as ethylene diamine tetra-acetic acid or a derivative thereof, nitrolotriacetic acid, phosphonates
. - 9g = of polyphosphates, metasilicates, boroheptonates, s.s- thylene-diamino disuccinate, dipicolinic acid, 2- phosphonobutane-1,2,4-tricarboxylic acid, or lower molecular weight polymeric materials capable of inhibiting crystal growth. Further reducing agents, such as alkali metal metabisulphates may be present to assist in the reduction of staining due to metals such as iron.
Typically, one phase of the blocks according to the present invention comprise 1-15% wt, more preferably 2-10% of a dyestuff on a carrier. It is preferable if the other phase of the block is totally coloured. In both cases it is preferable if the dye is water soluble.
Polymers
A water-insoluble, gelling polymers may be used in compositions of the invention, these are polycarboxylic acids derived from one or more ethylenically unsaturated carboxyl group-containing monomers, especially ethylenically . : unsaturated carboxylic acids such as acrylic acid or maleic acid.
Suitable polymers include polyacrylic acid, polymaleic anhydride and copolymers of either of the aforementioned with ethylene, styrene and methyl vinyl ester. If present it is preferred that the polymer is cross-linked. Polygel DB (TM) ex 3V Sigma, a cross-linked high molecular weight polyacrylate, has been found to be a suitable material at an inclusion level of around 2-3%wt.
. - 10 ~
Process
Compositions in accordance with the invention may be produced by a variety of routes. For example, they may be prepared by a so-called “hot-melt” process comprising melting the fusible constituents of each phase of the block followed by adding the other components, and subsequently casting the melt into moulds or are formed into the desired final shape by a compression technique, i.e., a technique involving the steps of forming a mixture of the ingredients of the compositions and then compressing that mixture into the desired shape. The two phases so formed are then compressed together.
An especially preferred process is an extrusion process in which mixtures of the components of each phase are co- extruded into a solid bar or rod which is subsequently cut into pieces of the desired size. )
It may be noted that when the compositions of the invention oo are used as free-standing lavatory cleansing blocks, these suitably have a weight from 30 to 150 gms. When extruding a } solid composition it is generally advantageous, as noted above, that some lubricant component or process aid be present to facilitate extrusion. The weight of each phase is preferably approximately the same as each other (approximately in this context meaning that the weight of each phase varies within 20% from each other, more preferably within 10%).
Compositions in accordance with the invention may also be formed into the final desired shape by a tabletting technique. 5S As used herein the term block is not intended to limit the shape of the eventual product. For cistern blocks the rod is cut into lengths which are short relative to their diameter.
The invention also provides a method of cleaning a lavatory or urinal using a block of a composition in accordance with the invention.
In order that the invention may well be understood, the following Examples are given by way of illustration only.
Examples of the invention are illustrated by a number, comparative Examples are illustrated by a letter.
Toilet blocks were formed by an extrusion process in which the mixture of the components of each phase were co-extruded as a plastified mass through an aperture to form a billet and said billet is cut into tablets of appropriate size.
The toilet blocks had the following formulation:
I E— ce —
I EE SS BE
EL A EE EY
Ea I NE J
Ee RC A EA cE | ares | wes | owes
EI ETE DT
ERE RE ETE EE
[Alcohol ethoxylate 2B0° | ~ - | - 73 [pipers | wesowe [Phase 2 ~~ | TT 1] I
EHR SC RCN RC
EE ETE TS
I BC I BL meso, se se se
INa.Cos | zz 2 IEE .
Fee | 5s | ss | 5s
ABS* Nansa HS 80/L ex Albright & Wilson
PAS?’ PAS-Empicol LZ-V ex Albright & Wilson
Coloured granules scdium carbonate ex Crosfield
Alcohol ethoxylate 2EO° Loradac 2-24 2EO ex DAC.
a 4 ) . —- 1 3 —-
The in-use lifetime of each block was measured by placing in a toilet, flushing 250 times and measuring the residual weight of the block. ~~ Example | Phase A of original Phase B % of block remaining original block remaining
IE
HE EL
I
IE eee er ——
It can thus be seen that the disparity between the two phases of the toilet block is less with the blocks of the invention.
Claims (12)
1. A lavatory cleansing block comprising at least two phases one phase (phase 1) comprising a water insoluble salt as at least 50 wt% of the salt present within that phase and a second phase (phase 2) comprising a perfume and a water soluble salt such that the salts in both phases have the same anion.
2. A lavatory cleansing block according to claim 1 in which phase 2 further comprises a water insoluble salt having the same anion as the water soluble salt.
3. A lavatory cleansing block according to claim 2 in which the ratio of water soluble salt and the water insoluble salt both having the same anion is from 5:1 to
1:5.
4. A lavatory cleansing block according any preceding claim in which phase 2 further comprises a bleaching ) material. :
5. A lavatory cleansing block according to claim 4 in which the bleaching agent is an halogen release agent.
6. A lavatory cleansing block according to claim 5 in which the bleaching agent is sodium dichlorocyanurate (NaDCCA) .
7. A lavatory cleansing block according to any preceding claim in which the water soluble salt is sodium carbonate.
8. A lavatory cleansing block according to any preceding claim in which the water insoluble salt is calcium carbonate.
3. A lavatory cleansing block according to any preceding claim in which the level of water soluble salt having the same anion as the water insoluble salt within phase 2 is from 1 to 10 wt% of the total level of ingredients present in phase 2.
10. A toilet block according to any preceding claim in which the total level of water insoluble salt in phase 1 is from 1 to 10 wt% of the total level of ingredients present in phase 1.
11. A lavatory cleansing block according to any preceding claim in which phase 1 further comprises an alcohol ethoxylate, ethoxylated with 8 or less moles of alkylene oxide.
i .
12. A process for producing a toilet block according to any ) preceding claim in which the process comprises the step of co-extruding the two phases to form the block.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99302453 | 1999-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200105348B true ZA200105348B (en) | 2002-06-28 |
Family
ID=8241298
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200105348A ZA200105348B (en) | 1999-03-29 | 2001-06-28 | Lavatory cleansing compositions. |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP1165740B1 (en) |
JP (1) | JP2002540288A (en) |
AR (1) | AR023177A1 (en) |
AT (1) | ATE265521T1 (en) |
AU (1) | AU748762B2 (en) |
BR (1) | BR0007502B1 (en) |
CA (1) | CA2361266C (en) |
DE (1) | DE60010245T2 (en) |
HU (1) | HUP0200401A3 (en) |
ID (1) | ID30170A (en) |
TR (1) | TR200102763T2 (en) |
WO (1) | WO2000058434A1 (en) |
ZA (1) | ZA200105348B (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE357502T1 (en) * | 2004-01-08 | 2007-04-15 | Unilever Nv | BAR TOILET CLEANING PRODUCTS |
US8984517B2 (en) | 2004-02-04 | 2015-03-17 | Intel Corporation | Sharing idled processor execution resources |
GB0428559D0 (en) | 2004-12-31 | 2005-02-09 | Jeyes Group Ltd | Lavatory cleansing block |
DE102008051173A1 (en) | 2008-10-14 | 2010-04-15 | Buck-Chemie Gmbh | Agent, useful e.g. as cold adhesive in sanitary applications, comprises fillers comprising a surfactant and a bonding agent comprising e.g. polyalkylene derivative, polyalkylene chains and polyglycerin polyether alkyl carbonic acid |
DE102008012092A1 (en) | 2008-02-29 | 2009-09-10 | Buck- Chemie Gmbh | Agent, useful e.g. as cold adhesive in sanitary applications, comprises fillers comprising a surfactant and a bonding agent comprising e.g. polyalkylene derivative, polyalkylene chains and polyglycerin polyether alkyl carbonic acid |
KR101622943B1 (en) | 2008-02-29 | 2016-05-23 | 벅-케미 게엠베하 | Adhesive agent for application on a sanitary object |
US8835371B2 (en) | 2008-02-29 | 2014-09-16 | Buck-Chemie Gmbh | Adhesive agent for application on a sanitary object |
US8444771B2 (en) | 2008-02-29 | 2013-05-21 | Buck-Chemie Gmbh | Method for cleaning and/or deodorizing toilet bowl or urinal using an adhesive agent |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4460490A (en) * | 1980-12-18 | 1984-07-17 | Jeyes Group Limited | Lavatory cleansing blocks |
DE3225292A1 (en) * | 1982-07-07 | 1984-01-12 | Henkel KGaA, 4000 Düsseldorf | CLEANING AND DISINFECTANT TABLET FOR THE WATER CASE OF RINSING TOILETS |
GB8417345D0 (en) * | 1984-07-06 | 1984-08-08 | Unilever Plc | Para-dichlorobenzene-free lavatory cleansing blocks |
GB8515181D0 (en) * | 1985-06-14 | 1985-07-17 | Jeyes Group Ltd | Lavatory cleansing compositions |
JPS6236500A (en) * | 1985-08-12 | 1987-02-17 | 花王株式会社 | Solid detergent |
US5759974A (en) * | 1994-11-07 | 1998-06-02 | Henkel Kommanditgesellschaft Auf Aktien | Block-form cleaners for flush toilets |
EP0906410B1 (en) * | 1996-06-12 | 2000-08-16 | Unilever Plc | Improvements relating to lavatory cleaning blocks |
GB2322632B (en) * | 1997-02-20 | 2001-02-21 | Reckitt & Colman Of India Ltd | A toilet block composition |
-
2000
- 2000-02-14 DE DE60010245T patent/DE60010245T2/en not_active Expired - Lifetime
- 2000-02-14 AU AU34223/00A patent/AU748762B2/en not_active Ceased
- 2000-02-14 EP EP00912460A patent/EP1165740B1/en not_active Expired - Lifetime
- 2000-02-14 WO PCT/EP2000/001184 patent/WO2000058434A1/en active IP Right Grant
- 2000-02-14 JP JP2000608715A patent/JP2002540288A/en active Pending
- 2000-02-14 TR TR2001/02763T patent/TR200102763T2/en unknown
- 2000-02-14 HU HU0200401A patent/HUP0200401A3/en unknown
- 2000-02-14 ID IDW00200102100Q patent/ID30170A/en unknown
- 2000-02-14 AT AT00912460T patent/ATE265521T1/en not_active IP Right Cessation
- 2000-02-14 CA CA002361266A patent/CA2361266C/en not_active Expired - Fee Related
- 2000-02-14 BR BRPI0007502-7A patent/BR0007502B1/en not_active IP Right Cessation
- 2000-03-27 AR ARP000101362A patent/AR023177A1/en active IP Right Grant
-
2001
- 2001-06-28 ZA ZA200105348A patent/ZA200105348B/en unknown
Also Published As
Publication number | Publication date |
---|---|
ATE265521T1 (en) | 2004-05-15 |
WO2000058434A1 (en) | 2000-10-05 |
BR0007502A (en) | 2001-10-02 |
CA2361266C (en) | 2009-10-06 |
ID30170A (en) | 2001-11-08 |
HUP0200401A2 (en) | 2002-07-29 |
DE60010245D1 (en) | 2004-06-03 |
EP1165740A1 (en) | 2002-01-02 |
AU3422300A (en) | 2000-10-16 |
CA2361266A1 (en) | 2000-10-05 |
AU748762B2 (en) | 2002-06-13 |
AR023177A1 (en) | 2002-09-04 |
JP2002540288A (en) | 2002-11-26 |
EP1165740B1 (en) | 2004-04-28 |
HUP0200401A3 (en) | 2004-03-01 |
DE60010245T2 (en) | 2005-04-14 |
BR0007502B1 (en) | 2009-01-13 |
TR200102763T2 (en) | 2002-04-22 |
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