CA2018738A1 - Heavy duty washing process - Google Patents
Heavy duty washing processInfo
- Publication number
- CA2018738A1 CA2018738A1 CA002018738A CA2018738A CA2018738A1 CA 2018738 A1 CA2018738 A1 CA 2018738A1 CA 002018738 A CA002018738 A CA 002018738A CA 2018738 A CA2018738 A CA 2018738A CA 2018738 A1 CA2018738 A1 CA 2018738A1
- Authority
- CA
- Canada
- Prior art keywords
- weight
- detergent composition
- organic solvent
- fabric
- aqueous
- 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
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
- C11D3/16—Organic compounds
- C11D3/18—Hydrocarbons
-
- 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
-
- 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
- C11D3/43—Solvents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06F—LAUNDERING, DRYING, IRONING, PRESSING OR FOLDING TEXTILE ARTICLES
- D06F43/00—Dry-cleaning apparatus or methods using volatile solvents
- D06F43/08—Associated apparatus for handling and recovering the solvents
- D06F43/081—Reclaiming or recovering the solvent from a mixture of solvent and contaminants, e.g. by distilling
- D06F43/085—Filtering arrangements; Filter cleaning; Filter-aid powder dispensers
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
Abstract
ABSTRACT
A heavy duty process for laundering greasy stains from a fabric which comprises treating the fabric with an aqueous detergent composition comprising (a) 0.5 - 5 %
by weight of a nonionic surfactant and (b) 1 - 10 % by weight of an apolar solvent in a ratio from less than 1 : 1 to 1 : 10. Preferably, the hot wash liquor is treated in a filtering step using microfilters to separate the organic solvent phase from the aqueous phase, which is then recycled.
A heavy duty process for laundering greasy stains from a fabric which comprises treating the fabric with an aqueous detergent composition comprising (a) 0.5 - 5 %
by weight of a nonionic surfactant and (b) 1 - 10 % by weight of an apolar solvent in a ratio from less than 1 : 1 to 1 : 10. Preferably, the hot wash liquor is treated in a filtering step using microfilters to separate the organic solvent phase from the aqueous phase, which is then recycled.
Description
~J ~ 3 ~.i HEAVY DUTY WASHING PROCESS
The present invention relates to detergent compositions and their use in a washing process, more in particular, an industrial heavy duty washiny process for laundering greasy stains from a fabric.
It has always been difficult to obtain satisfactory results when washlng heavily soiled articles such as overalls 6tained with grease or motor oil. Good results can be obtained using chlorinated hydrocarbons as solvent in a dry-cleaning process, although there is a tendency ~or the workwear to show some greying and to have a harsh feel. However, the use of chlorinated hydrocarbons is becoming more and more restricted for environmental reasons.
Furthermore, it has been described in the British patent speci~ication 1,518,576 to remove oily stains from fabrics by means of a composition comprising a nonionic and an organic solvent in a weight ratio in the range of 1 : 1 to 100 : 1. In this process the soiled fabric is treated with an aqueous solution containing 0.01 to 2 %
by weight of said composition at a temperature above the phase coalescence temperature. A draw-back of this process is the large amount of organic waste containing waste water.
It is an object of the present invention to provide improvements on the wash process as described in the British patent 1,518,676.
We have now ~ound that one or more of these objects can be achi~ved by the process according to the present invention, which is characterized in that the soiled 5~ 8 :
The present invention relates to detergent compositions and their use in a washing process, more in particular, an industrial heavy duty washiny process for laundering greasy stains from a fabric.
It has always been difficult to obtain satisfactory results when washlng heavily soiled articles such as overalls 6tained with grease or motor oil. Good results can be obtained using chlorinated hydrocarbons as solvent in a dry-cleaning process, although there is a tendency ~or the workwear to show some greying and to have a harsh feel. However, the use of chlorinated hydrocarbons is becoming more and more restricted for environmental reasons.
Furthermore, it has been described in the British patent speci~ication 1,518,576 to remove oily stains from fabrics by means of a composition comprising a nonionic and an organic solvent in a weight ratio in the range of 1 : 1 to 100 : 1. In this process the soiled fabric is treated with an aqueous solution containing 0.01 to 2 %
by weight of said composition at a temperature above the phase coalescence temperature. A draw-back of this process is the large amount of organic waste containing waste water.
It is an object of the present invention to provide improvements on the wash process as described in the British patent 1,518,676.
We have now ~ound that one or more of these objects can be achi~ved by the process according to the present invention, which is characterized in that the soiled 5~ 8 :
2 C 7186 (R) ~abric is treated with an aqueous detergent composition comprising (a~ 0.5 to 5 % by weight of a nonionic surfactant, (b) 1 to 10 % by weight of an apolar organic solvent, whereby the ratio of (a) to (b) is from less than 1 : 1 to 1 : 10, preferably from l~ss than 1 : 1 to 1 : 5.
Suitable nonionic sur~actants which may be used include the reaction products of compoundra having a hydrophilic group and a reactive hydrogen atom, for example aliphatic alcohol6, acids, amides or alkyl phenols with alkylene ox~de~, especially ethylene oxide either alon~
or in combination with propylene oxide and/or butylene oxide. Specific nonionic detergent compounds are alkyl (C6~C22) phenols-ethylene oxide condensates, the condensation products of aliphatic (C8-Cl~) primary or secondary linear or branched alcohols with ethylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenedia~ine. So-called "capped" nonionics are also suitabl~ Other suitable nonionic surfactants include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
Pre~erably, the nonionic ~urfactant is an alkoxylated ~atty alcohol, wherein the alcohol is a primary or secondary branched or linear alkanol having 10 to 16 carbon atoms. Ths alkoxy moiety consists of 3 to 10 : ethoxy groups, propoxy groups and/or ~utoxy groups. Th~
hydrophilic lipophilic balance (HL~) of the nonionic surfactant, de~ined as one fifth of the weight : percentage o~ alkylene oxide in the nonionic, is chosen in the range of 10 to 14.
35 The apolar organic solvent may be an alkane, an alkanol, a low-E0 nonionic, etc., or a mixture thereof.
Suitable alkanols contain 6 to 18 carbon atoms. ~ low-E0 nonionic is ~or ~he purpo~e of thls invention defined as 2 ~ 3 ~
Suitable nonionic sur~actants which may be used include the reaction products of compoundra having a hydrophilic group and a reactive hydrogen atom, for example aliphatic alcohol6, acids, amides or alkyl phenols with alkylene ox~de~, especially ethylene oxide either alon~
or in combination with propylene oxide and/or butylene oxide. Specific nonionic detergent compounds are alkyl (C6~C22) phenols-ethylene oxide condensates, the condensation products of aliphatic (C8-Cl~) primary or secondary linear or branched alcohols with ethylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenedia~ine. So-called "capped" nonionics are also suitabl~ Other suitable nonionic surfactants include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
Pre~erably, the nonionic ~urfactant is an alkoxylated ~atty alcohol, wherein the alcohol is a primary or secondary branched or linear alkanol having 10 to 16 carbon atoms. Ths alkoxy moiety consists of 3 to 10 : ethoxy groups, propoxy groups and/or ~utoxy groups. Th~
hydrophilic lipophilic balance (HL~) of the nonionic surfactant, de~ined as one fifth of the weight : percentage o~ alkylene oxide in the nonionic, is chosen in the range of 10 to 14.
35 The apolar organic solvent may be an alkane, an alkanol, a low-E0 nonionic, etc., or a mixture thereof.
Suitable alkanols contain 6 to 18 carbon atoms. ~ low-E0 nonionic is ~or ~he purpo~e of thls invention defined as 2 ~ 3 ~
3 C 7186 (R) a ~atty alcohol, alkoxylated with less than 3 ethoxy groups. The apolar organic solvent is pre~erably an aliphatic linear alkane or a mixture of alkanes having 8 to 16 carbon atoms, preferably 11 to 13 carbon atoms. An attractive commercially available solvent is kerosine.
The detergent composition of the invention may comprise other ingredients which are usual for washing proce ses such as builders, alkaline agents to maintain a pH value in the range of 8 to 13, pre~erably of 10 to 12.
Bleaching agents, etc. may also be present.
The builder may be any material capable of redu~ing the level of free calcium ions in the wash liquor and will prefarably at the same time provide other beneficial properties such as the generation o~ an alkaline pH or the euspension of soil removed from the fabric. The builders may be inorganic such as tripolyphosphates or zeolites, organic non-poly~eric such as nitrilotriacetic acid, or organic polymeric such as copolymers o~ acrylic acid and maleic acid. Thé builder is preferably present in an amount of 0.25 to 2 % by weight of the composition.
In the process for laundering fabrics according to the present invention, the heavily soiled fabric is treated with the above mentioned detergent composition. The amount of detergent composition is relatively high, i.e.
in the order of 0.5 to 5 kg per kg soiled fabric.
Preferably, 1.5 to 2.5 kg per kg fabric is used. The process of the invention can be carried out in any suitable washing machine, such as a wash extractor or a tunnel washer.
The washing process may be preceded by a pre-rinse to re~ov~ loose dirt and soluble material. The actual wash process may comprise more than one wash cycle. It is preferably carried out at elevated temperatures. It was 2 ~ 3 8 4 C 7186 (R) found to be particularly effective to first raise the temperature to a~ove the so-called phase coalescence temperature, which is usually around 55 C, and then cycle around this temperature at least two times. After a sufficiently long period to complete the washing action of the detergent composition, usually in the order of 10 minutes, the wash liquor is pumped off.
A~ter one or more rinse cycles, the wash load i6 removed for further processing.
According to a further aspect of the present invention, the used wash liquor containing su~pended soil and emulgated grease and/or oil can be recycled instead of being pumped to the sewage system. The water of the pre-rinse and the first rinse cycle may be combined and treated in the sam~ way.
Although it is particularly useful to apply the recycling step to a wash process involving the aqueous detergent compositions according to the invention, the recycling step can al80 be used in combination with similar aqueou~ detergent compositions having a different nonionic to solvent ratio. For example, the aqueous detergent compositiQn may comprise Sa) 0.5 - 5 %
by weight of a nonionic surfactant and (b) 1 10 % by weight of an apolar organic solv~nt, whereby the ratio of (a) to (b) is 1 : 1 to 100 : 1.
It was found to be advantageous to dump the hot wash liquor ~rom the process into a storage tank from which it is gradually pumped to a filtration unit comprising one or more microfilters. In this unit the wash liquor is continuously filtered under a pressure of approximately 0.5 - 3 bar. The unit is preferably operated in a cross-flow mode to avoid clogging of the filter. The aqueous phase containing virtually all of the water soluble components is separated from the phase containing the organic solvent, the suspended ~3J S)~ 3 ~
C 7186 (R) solld and the emulgated oil and/or grease, and can be recycled. The phase containing the oil and most of the organic apolar solvent can now be distilled to recover the organic solvent, or Xur her treated to reduce the waste. Considerable savings in energy and chemicals can thus be achieved. The process i5 also advantageous from an environmental point of view because the amount of waste to be disposed off can be greatly reduced.
It is preferred to use hydrophilic microfilters in the present process. The aqueous phase passes through the filter and can be continuou~ly recycled to the wash process. The retantate contains increaslng amounts of oil and at a sufficiently high concentration the emulsion becomes unstable. Sometimes the emulsion will even break and a layer of oil will separate. After a certain amount of time, Por instance at the end of a working day, the filtration process can be stopped and the retentate can be removed for distillation, disposal or further treatment. Preferably, the retentate has first been concentrated to a water content of 50 to 70 by weight.
The microfilters to be used in the process of the invention can be made of any suitable material, provided that it is capable of withstanding elevated temperatures sf up to lO0 C and highly alkaline wash liquors, having pH values of up to 14. It should therPby also retain its hydrophilic properties. Wa found that microfilters having a pore size of 50 - lO00 nm, pre~erably approximately lO0 nm and made of a mixture of polyethersulphon and polyvinylpyrrolidon, are exceptionally suitable. The microfilters are preferably constructed of capillary tubes having an external diameter of 1 to 10 mm. Such ~ilters are co~mercially available, for instance from X-flow, Enschede, The Netherlands.
7 3 ~
6 C 7186 (R) The invention will now be further illustrated by means of the ~ollowing non-limiting axample.
EXAMPLE
The following heavy duty wash process was carried out.
400 kg overalls, heavily soiled ~ith motor oil and greasy stains were placed in a Milnor wash extractor.
The load was pre-rinsed to remove any sand and other loose dirt. The rinse water could be disposed off directly to the sewage system, as it was not noticeably polluted. Subsequently, the wash load was treated for 10 minutes at a temperature of 60 C with 1000 1 o~ an aqueous detergent composition containing 3 % by weight paraffin (ex Shell), 1.5 % by weight of a nonionic mixture consisting of Dobanol 25-3 and 25-9 in a ratio of 1 : 2.5 (ex Shell), 0.45 % by weight ~odium tripolyphosphate, 1.4 % by weight sodium metasilicate and 0.25 ~ by weight sodium hydroxide. The pH was adjusted to 11.8. After this first main wash, the hot wash liquor was pumped off to a thermally insulated waste water storage tanX having a capacity of 5.5 m3.
The wash process was then repeated using the same amount of detergent composition, whereby no paraffin was used and the amount of nonionic was raised to 3 ~ by weight.
Again, the hot wash liquor was transferred to the waste water storage tank. Thereafter, the was load as rinsed using 3.2 m3 water. The rin~ing was repeated -twice, whereby only the water ~rom the first rinse was pumped to the waste water storage tank. The amount of chemicals and solvant in the water of the second rinse was so low that it could be dumped to the sewage ~ystem. After drying, the wash load was inspected and it was found that and excellent cleaning result had been obtained, as substantially all greasy had been removed.
The combined waste water in the waste water storage tank was continuously pumped to a thermally insulated circulation tank having a capacity of approximately 5 m3. From this tank, the water was pumped under a ~J ~
7 C 7186 (R) pressure of 2 bar to a micro~iltration unit equipped with hydrophilic microfilters made of a mixture of polyethersulphon and polyvinylpyrrolidon, having a pore size of 100 nm. The filters were obtained from X-flow, Enschede, The Netherlands. The total ~urface area of the unit was 50 m2 and it had a maximum capacity o~ about 5000 l/hour. The filtration unit was operated in a cross-flow mode. The permeate contained water, nonionic and salts and was substantially free ~rom organic solvent. It was pumped to a permeate storage tank having a capacity of about 5 m3 from which it could be used again in ths wash process. It proved to be advantageous to supplement the permeate with some of the detergent composition after each cycle, to compensate for the detergent components consumed in the wash cycle in removing the soil. The retentate was then fed to a distillation unit and the freshly distilled solvent was also used again in the was process. Overnight the liquor in the circulation tank was concentrated to a water content of approximately 50 % by weight, whereby gel formation was observed. This concentrate was finally disposed off.
The detergent composition of the invention may comprise other ingredients which are usual for washing proce ses such as builders, alkaline agents to maintain a pH value in the range of 8 to 13, pre~erably of 10 to 12.
Bleaching agents, etc. may also be present.
The builder may be any material capable of redu~ing the level of free calcium ions in the wash liquor and will prefarably at the same time provide other beneficial properties such as the generation o~ an alkaline pH or the euspension of soil removed from the fabric. The builders may be inorganic such as tripolyphosphates or zeolites, organic non-poly~eric such as nitrilotriacetic acid, or organic polymeric such as copolymers o~ acrylic acid and maleic acid. Thé builder is preferably present in an amount of 0.25 to 2 % by weight of the composition.
In the process for laundering fabrics according to the present invention, the heavily soiled fabric is treated with the above mentioned detergent composition. The amount of detergent composition is relatively high, i.e.
in the order of 0.5 to 5 kg per kg soiled fabric.
Preferably, 1.5 to 2.5 kg per kg fabric is used. The process of the invention can be carried out in any suitable washing machine, such as a wash extractor or a tunnel washer.
The washing process may be preceded by a pre-rinse to re~ov~ loose dirt and soluble material. The actual wash process may comprise more than one wash cycle. It is preferably carried out at elevated temperatures. It was 2 ~ 3 8 4 C 7186 (R) found to be particularly effective to first raise the temperature to a~ove the so-called phase coalescence temperature, which is usually around 55 C, and then cycle around this temperature at least two times. After a sufficiently long period to complete the washing action of the detergent composition, usually in the order of 10 minutes, the wash liquor is pumped off.
A~ter one or more rinse cycles, the wash load i6 removed for further processing.
According to a further aspect of the present invention, the used wash liquor containing su~pended soil and emulgated grease and/or oil can be recycled instead of being pumped to the sewage system. The water of the pre-rinse and the first rinse cycle may be combined and treated in the sam~ way.
Although it is particularly useful to apply the recycling step to a wash process involving the aqueous detergent compositions according to the invention, the recycling step can al80 be used in combination with similar aqueou~ detergent compositions having a different nonionic to solvent ratio. For example, the aqueous detergent compositiQn may comprise Sa) 0.5 - 5 %
by weight of a nonionic surfactant and (b) 1 10 % by weight of an apolar organic solv~nt, whereby the ratio of (a) to (b) is 1 : 1 to 100 : 1.
It was found to be advantageous to dump the hot wash liquor ~rom the process into a storage tank from which it is gradually pumped to a filtration unit comprising one or more microfilters. In this unit the wash liquor is continuously filtered under a pressure of approximately 0.5 - 3 bar. The unit is preferably operated in a cross-flow mode to avoid clogging of the filter. The aqueous phase containing virtually all of the water soluble components is separated from the phase containing the organic solvent, the suspended ~3J S)~ 3 ~
C 7186 (R) solld and the emulgated oil and/or grease, and can be recycled. The phase containing the oil and most of the organic apolar solvent can now be distilled to recover the organic solvent, or Xur her treated to reduce the waste. Considerable savings in energy and chemicals can thus be achieved. The process i5 also advantageous from an environmental point of view because the amount of waste to be disposed off can be greatly reduced.
It is preferred to use hydrophilic microfilters in the present process. The aqueous phase passes through the filter and can be continuou~ly recycled to the wash process. The retantate contains increaslng amounts of oil and at a sufficiently high concentration the emulsion becomes unstable. Sometimes the emulsion will even break and a layer of oil will separate. After a certain amount of time, Por instance at the end of a working day, the filtration process can be stopped and the retentate can be removed for distillation, disposal or further treatment. Preferably, the retentate has first been concentrated to a water content of 50 to 70 by weight.
The microfilters to be used in the process of the invention can be made of any suitable material, provided that it is capable of withstanding elevated temperatures sf up to lO0 C and highly alkaline wash liquors, having pH values of up to 14. It should therPby also retain its hydrophilic properties. Wa found that microfilters having a pore size of 50 - lO00 nm, pre~erably approximately lO0 nm and made of a mixture of polyethersulphon and polyvinylpyrrolidon, are exceptionally suitable. The microfilters are preferably constructed of capillary tubes having an external diameter of 1 to 10 mm. Such ~ilters are co~mercially available, for instance from X-flow, Enschede, The Netherlands.
7 3 ~
6 C 7186 (R) The invention will now be further illustrated by means of the ~ollowing non-limiting axample.
EXAMPLE
The following heavy duty wash process was carried out.
400 kg overalls, heavily soiled ~ith motor oil and greasy stains were placed in a Milnor wash extractor.
The load was pre-rinsed to remove any sand and other loose dirt. The rinse water could be disposed off directly to the sewage system, as it was not noticeably polluted. Subsequently, the wash load was treated for 10 minutes at a temperature of 60 C with 1000 1 o~ an aqueous detergent composition containing 3 % by weight paraffin (ex Shell), 1.5 % by weight of a nonionic mixture consisting of Dobanol 25-3 and 25-9 in a ratio of 1 : 2.5 (ex Shell), 0.45 % by weight ~odium tripolyphosphate, 1.4 % by weight sodium metasilicate and 0.25 ~ by weight sodium hydroxide. The pH was adjusted to 11.8. After this first main wash, the hot wash liquor was pumped off to a thermally insulated waste water storage tanX having a capacity of 5.5 m3.
The wash process was then repeated using the same amount of detergent composition, whereby no paraffin was used and the amount of nonionic was raised to 3 ~ by weight.
Again, the hot wash liquor was transferred to the waste water storage tank. Thereafter, the was load as rinsed using 3.2 m3 water. The rin~ing was repeated -twice, whereby only the water ~rom the first rinse was pumped to the waste water storage tank. The amount of chemicals and solvant in the water of the second rinse was so low that it could be dumped to the sewage ~ystem. After drying, the wash load was inspected and it was found that and excellent cleaning result had been obtained, as substantially all greasy had been removed.
The combined waste water in the waste water storage tank was continuously pumped to a thermally insulated circulation tank having a capacity of approximately 5 m3. From this tank, the water was pumped under a ~J ~
7 C 7186 (R) pressure of 2 bar to a micro~iltration unit equipped with hydrophilic microfilters made of a mixture of polyethersulphon and polyvinylpyrrolidon, having a pore size of 100 nm. The filters were obtained from X-flow, Enschede, The Netherlands. The total ~urface area of the unit was 50 m2 and it had a maximum capacity o~ about 5000 l/hour. The filtration unit was operated in a cross-flow mode. The permeate contained water, nonionic and salts and was substantially free ~rom organic solvent. It was pumped to a permeate storage tank having a capacity of about 5 m3 from which it could be used again in ths wash process. It proved to be advantageous to supplement the permeate with some of the detergent composition after each cycle, to compensate for the detergent components consumed in the wash cycle in removing the soil. The retentate was then fed to a distillation unit and the freshly distilled solvent was also used again in the was process. Overnight the liquor in the circulation tank was concentrated to a water content of approximately 50 % by weight, whereby gel formation was observed. This concentrate was finally disposed off.
Claims (13)
1. Aqueous detergent composition comprising:
(a) 0.5 - 5 % by weight of a nonionic surfactant; and (b) 1 - 10 % by weight of an apolar organic solvent;
whereby the ratio of (a) to (b) is from less than 1 : 1 to 1: 10.
(a) 0.5 - 5 % by weight of a nonionic surfactant; and (b) 1 - 10 % by weight of an apolar organic solvent;
whereby the ratio of (a) to (b) is from less than 1 : 1 to 1: 10.
2. Detergent composition according to Claim 1, wherein the nonionic surfactant is an alkoxylated fatty alcohol.
3. Detergent composition according to Claim 1, wherein the organic solvent is an aliphatic hydrocarbon having 8-16 carbon atoms.
4. Detergent composition according to Claim 1, wherein the organic solvent is an aliphatic hydrocarbon having 11-13 carbon atoms.
5. Detergent composition according to Claim 1, further comprising 0.25 to 2 % by weight of a detergency builder.
6. Detergent composition according to Claim 1, having a pH in the range of 8 to 13, preferably from 10 to 12.
7. Process for laundering greasy stains from a fabric which comprises treating the fabric with an aqueous detergent composition comprising:
(a) 0.5 - 5 % by weight of a nonionic surfactant; and (b) 1 - 10 % by weight of an apolar organic solvent;
whereby the ratio of (a) to (b) is from less than 1 : 1 to 1 : 10.
(a) 0.5 - 5 % by weight of a nonionic surfactant; and (b) 1 - 10 % by weight of an apolar organic solvent;
whereby the ratio of (a) to (b) is from less than 1 : 1 to 1 : 10.
8. Process according to Claims 7, whereby the hot wash liquor is treated in a filtering step using microfilters to separate the organic solvent phase from the aqueous phase, which is then recycled.
9. Process for laundering greasy stains from a fabric which comprises treating the fabric with an aqueous detergent composition comprising:
(a) 0.5 - 5 % by weight of a nonionic surfactant; and (b) 1 - 10 % by weight of an apolar organic solvent;
whereby the ratio of (a) to (b) is 1 : 1 to 100 : 1, whereby the hot wash liquor is treated in a filtering step using microfilters to separate the organic solvent phase from the aqueous phase, which is then recycled.
(a) 0.5 - 5 % by weight of a nonionic surfactant; and (b) 1 - 10 % by weight of an apolar organic solvent;
whereby the ratio of (a) to (b) is 1 : 1 to 100 : 1, whereby the hot wash liquor is treated in a filtering step using microfilters to separate the organic solvent phase from the aqueous phase, which is then recycled.
10. Process according to any one of Claims 8 or 9, whereby the wash temperature is raised to above the phase coalescence temperature.
11. Process according to any one of Claims 8 or 9, whereby the filters are hydrophilic microfilters.
12. Process according to any one of Claims 8 or 9, whereby the filters are made of a mixture of polyethersulphon and polyvinylpyrrolidon, and have a pore size of 50 to 1000 nm, preferably of approximately 100 nm.
13. The aqueous detergent composition as claimed in claim 1 and substantially as described herein.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB898913881A GB8913881D0 (en) | 1989-06-16 | 1989-06-16 | Detergent compositions |
GB8913881.2 | 1989-06-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2018738A1 true CA2018738A1 (en) | 1990-12-16 |
Family
ID=10658557
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002018738A Abandoned CA2018738A1 (en) | 1989-06-16 | 1990-06-11 | Heavy duty washing process |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0402981A3 (en) |
AU (1) | AU627890B2 (en) |
CA (1) | CA2018738A1 (en) |
FI (1) | FI903011A0 (en) |
GB (1) | GB8913881D0 (en) |
NZ (1) | NZ234033A (en) |
ZA (1) | ZA904668B (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2672043B3 (en) * | 1991-01-24 | 1992-12-31 | Perrier Materiel | PROCESS FOR THE TREATMENT OF WASHING EFFLUENTS OF PRODUCTS, PARTICULARLY INDUSTRIAL FABRICS AND WASHING INSTALLATION USING THE SAME. |
JP2610552B2 (en) * | 1991-10-04 | 1997-05-14 | 花王株式会社 | Cleaning method |
US5314580A (en) * | 1992-07-08 | 1994-05-24 | Mauvin Material & Chemical Processing Limited | Process for the removal of ink, resin, and adhesive residues from paper, textile fabrics and solid surfaces |
AU675833B2 (en) * | 1994-03-23 | 1997-02-20 | Amway Corporation | Concentrated all-purpose light duty liquid cleaning composition and method of use |
US5531939A (en) * | 1994-03-23 | 1996-07-02 | Amway Corporation | Concentrated glass and window cleaning composition and method of use |
US5591236A (en) * | 1995-03-30 | 1997-01-07 | The Procter & Gamble Company | Polyacrylate emulsified water/solvent fabric cleaning compositions and methods of using same |
US6036727A (en) | 1995-06-05 | 2000-03-14 | Creative Products Resource, Inc. | Anhydrous dry-cleaning compositions containing polysulfonic acid, and dry-cleaning kits for delicate fabrics |
US6086634A (en) | 1995-06-05 | 2000-07-11 | Custom Cleaner, Inc. | Dry-cleaning compositions containing polysulfonic acid |
AU5950696A (en) | 1995-06-05 | 1996-12-24 | Creative Products Resource, Inc. | Dry-cleaning kit for in-dryer use |
US5658651A (en) | 1995-09-29 | 1997-08-19 | Creative Products Resource, Inc. | Fabric treatment and softener system for in-dryer use |
US6013185A (en) * | 1997-09-25 | 2000-01-11 | Rhodia Inc. | Recovery and reuse of nonionic surfactants from aqueous solutions |
WO2001094510A1 (en) * | 2000-06-06 | 2001-12-13 | Church & Dwight Company, Inc. | Recyclable cleaning compositions |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1518676A (en) * | 1975-10-30 | 1978-07-19 | Procter & Gamble Ltd | Detergent compositions |
ZA876158B (en) * | 1986-09-02 | 1989-04-26 | Colgate Palmolive Co | Laundry pre-spotter composition providing improved oily soil removal |
DE3707409A1 (en) * | 1987-03-07 | 1988-09-15 | Henkel Kgaa | METHOD FOR REMOVING TEXTILES |
US4857081A (en) * | 1987-10-15 | 1989-08-15 | Separation Dynamics, Inc. | Separation of water from hydrocarbons and halogenated hydrocarbons |
US4869842A (en) * | 1988-03-31 | 1989-09-26 | Colgate-Palmolive Co. | Liquid abrasive cleansing composition containing grease-removal solvent |
-
1989
- 1989-06-16 GB GB898913881A patent/GB8913881D0/en active Pending
-
1990
- 1990-06-05 EP EP19900201428 patent/EP0402981A3/en not_active Withdrawn
- 1990-06-11 CA CA002018738A patent/CA2018738A1/en not_active Abandoned
- 1990-06-12 NZ NZ234033A patent/NZ234033A/en unknown
- 1990-06-14 AU AU57093/90A patent/AU627890B2/en not_active Ceased
- 1990-06-15 FI FI903011A patent/FI903011A0/en not_active IP Right Cessation
- 1990-06-15 ZA ZA904668A patent/ZA904668B/en unknown
Also Published As
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AU627890B2 (en) | 1992-09-03 |
GB8913881D0 (en) | 1989-08-02 |
AU5709390A (en) | 1990-12-20 |
EP0402981A3 (en) | 1991-10-23 |
NZ234033A (en) | 1992-09-25 |
ZA904668B (en) | 1992-02-26 |
EP0402981A2 (en) | 1990-12-19 |
FI903011A0 (en) | 1990-06-15 |
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