KR900009221B1 - Method of conditioning fabrics - Google Patents
Method of conditioning fabrics Download PDFInfo
- Publication number
- KR900009221B1 KR900009221B1 KR1019870007396A KR870007396A KR900009221B1 KR 900009221 B1 KR900009221 B1 KR 900009221B1 KR 1019870007396 A KR1019870007396 A KR 1019870007396A KR 870007396 A KR870007396 A KR 870007396A KR 900009221 B1 KR900009221 B1 KR 900009221B1
- Authority
- KR
- South Korea
- Prior art keywords
- fabric
- conditioning
- rinse
- conditioning agent
- water
- Prior art date
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- 239000004744 fabric Substances 0.000 title claims description 68
- 230000003750 conditioning effect Effects 0.000 title claims description 62
- 238000000034 method Methods 0.000 title claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 31
- 239000003795 chemical substances by application Substances 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 18
- 230000002401 inhibitory effect Effects 0.000 claims description 8
- 239000003792 electrolyte Substances 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 125000002015 acyclic group Chemical group 0.000 claims description 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 2
- 239000012188 paraffin wax Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 150000005846 sugar alcohols Polymers 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 238000005406 washing Methods 0.000 description 27
- 125000000217 alkyl group Chemical group 0.000 description 10
- 239000003760 tallow Substances 0.000 description 9
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000003112 inhibitor Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000002979 fabric softener Substances 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000002216 antistatic agent Substances 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 3
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- -1 alkyl imidazolinium salt Chemical class 0.000 description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229910001424 calcium ion Inorganic materials 0.000 description 2
- 239000004665 cationic fabric softener Substances 0.000 description 2
- PGZPBNJYTNQMAX-UHFFFAOYSA-N dimethylazanium;methyl sulfate Chemical compound C[NH2+]C.COS([O-])(=O)=O PGZPBNJYTNQMAX-UHFFFAOYSA-N 0.000 description 2
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- BIWFJGMQTHQTJE-UHFFFAOYSA-N 3-ethyl-4,5-dihydro-1h-imidazol-3-ium;chloride Chemical compound Cl.CCN1CCN=C1 BIWFJGMQTHQTJE-UHFFFAOYSA-N 0.000 description 1
- UFQDKRWQSFLPQY-UHFFFAOYSA-N 4,5-dihydro-1h-imidazol-3-ium;chloride Chemical compound Cl.C1CN=CN1 UFQDKRWQSFLPQY-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 229930003347 Atropine Natural products 0.000 description 1
- 0 CN(C1)C1(*)[N+] Chemical compound CN(C1)C1(*)[N+] 0.000 description 1
- 101100245381 Caenorhabditis elegans pbs-6 gene Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical group CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000006177 alkyl benzyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 description 1
- 229960000396 atropine Drugs 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000002752 cationic softener Substances 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- VKKVMDHHSINGTJ-UHFFFAOYSA-M di(docosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCCCC VKKVMDHHSINGTJ-UHFFFAOYSA-M 0.000 description 1
- OCTAKUVKMMLTHX-UHFFFAOYSA-M di(icosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCC OCTAKUVKMMLTHX-UHFFFAOYSA-M 0.000 description 1
- HPDYVEVTJANPRA-UHFFFAOYSA-M diethyl(dihexadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CCCCCCCCCCCCCCCC HPDYVEVTJANPRA-UHFFFAOYSA-M 0.000 description 1
- ZCPCLAPUXMZUCD-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC ZCPCLAPUXMZUCD-UHFFFAOYSA-M 0.000 description 1
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000011833 salt mixture Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000004753 textile Substances 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/046—Insoluble free body dispenser
-
- 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
-
- 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
- C11D17/0082—Coated tablets
-
- 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
- D06F39/00—Details of washing machines not specific to a single type of machines covered by groups D06F9/00 - D06F27/00
- D06F39/02—Devices for adding soap or other washing agents
-
- 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
- D06F39/00—Details of washing machines not specific to a single type of machines covered by groups D06F9/00 - D06F27/00
- D06F39/02—Devices for adding soap or other washing agents
- D06F39/024—Devices for adding soap or other washing agents mounted on the agitator or the rotating drum; Free body dispensers
-
- 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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/12—Soft surfaces, e.g. textile
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)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Detergent Compositions (AREA)
Abstract
내용 없음.No content.
Description
본 발명은 직물을 콘디셔닝하는 방법, 특히 세탁기에서의 직물 세탁과정중 세척단계에 수반되는 직물을 콘디셔닝하는 방법에 관한 것이다.The present invention relates to a method of conditioning a fabric, in particular a method of conditioning the fabric involved in the washing step of the fabric washing process in a washing machine.
통상적인 세제조성물로된 직물을 세탁하면 직물이 거칠어지는데 이것은 전통적으로 직물연화제로 직물을 처리함으로써 회복시킨다. 대다수의 직물연화제는 세제조성물과 양립할 수 없기 때문에 보통은 사후-세척단계에서 처리하는데 이 단계에서 직물연화제를 직물린스에 사용되는 린스워터에 첨가한다. 정전기 방지제 및 향료등의 기타 직물 콘디셔닝제도 흔히 첨가된다.Washing fabrics of conventional detergent compositions results in coarse fabrics, which is traditionally recovered by treating the fabrics with fabric softeners. Since most fabric softeners are incompatible with detergent compositions, they are usually treated in a post-washing step, in which the fabric softener is added to the rinse water used for rinsing the fabric. Other fabric conditioning agents, such as antistatic agents and perfumes, are often added.
유럽에서 보통 사용되는 형태의 세탁기, 즉 린스워터로 채워지고 교반되어 효율적으로 린스된 후 배수되는 통에서 직물이 린스되는 세탁기를 사용하는 경우에는 손에 의하든지 아니면 자동분산장치에 의하여 통속의 린스워터에 직물 콘디셔닝제를 첨가하는 것은 간단한 문제이다. 그러나 일부 세탁기는 직물이 흐르는 물에서 린스되도록 설계되어 있다. 이러한 세탁기에서 린스 초기에 통상적인 직물 콘디셔닝 조성물을 첨가하면 만족할만한 효과가 없으며 린스말기에 통상적인 직물 콘디셔닝 조성물을 첨가하는 것도 좋지 못하다. 예를들면 직물 콘디셔닝 조성물이 액체 또는 분말인 경우, 대부분의 조성물이 직물과 서로 접촉해서 직물을 콘디셔닝할 기회도 없이 흐르는 린스워터와 함께 세탁기로부터 배출되며 린스가 계속되는 동안에도 콘디셔닝제를 흡수한 직물로부터 콘디셔닝제가 다소 제거되는 현상이 나타난다.In the case of a washing machine of the type commonly used in Europe, that is, a washing machine filled with rinse water, efficiently rinsed and rinsed and then rinsed with a textile in a drain bucket, it is either by hand or by an automatic dispersing device. Adding fabric conditioning agents to is a simple matter. Some washing machines, however, are designed to rinse under running water. The addition of conventional fabric conditioning compositions at the beginning of the rinse in such a washing machine has no satisfactory effect and it is also not advisable to add conventional fabric conditioning compositions at the end of the rinse. For example, if the fabric conditioning composition is a liquid or powder, most of the composition is discharged from the washing machine with a flowing rinse water without the opportunity to contact the fabric and contact each other and absorb the conditioning agent while the rinse continues. A slight removal of the conditioning agent from one fabric occurs.
이러한 세탁기에서 직물을 콘디셔닝할 수 있으며 세탁기로부터의 조성물의 손실을 최소화할 수 있는 신규한 방법을 발명하게 되었다. 이 방법은 흐르는 린스의 말기부근에서 제품 품질을 첨가할 필요가 없는 특정물리적 형태의 콘디셔닝 물질에 의한 것이다.It has been invented a novel method which can condition the fabric in such a washing machine and minimize the loss of the composition from the washing machine. This method is due to the specific physical form of the conditioning material that does not need to add product quality near the end of the flowing rinse.
따라서 본 발명에 의하면, 다음의 단계들을 포함하는 직물 콘디셔닝법을 제공한다. 즉,Accordingly, according to the present invention, there is provided a fabric conditioning method comprising the following steps. In other words,
(i) 린스통내에 직물을 투입하는 단계.(i) introducing the fabric into the rinse bucket.
(ii) 최소한 한 디멘젼이 1.0㎝이상이고 콘디셔닝제를 함유하며, 콘디셔닝제가 물속으로 방출되는 것을 억제하는 수단을 가진 직물 콘디셔닝 아티클(article)의 존재하에서 직물을 접할수 있도록 통의 내부에서 외부로 린스워터를 계속적으로 공급하는 단계.(ii) at least one dimension of at least 1.0 cm and containing a conditioning agent, the interior and exterior of the keg being in contact with the fabric in the presence of a fabric conditioning article having a means of inhibiting the release of the conditioning agent into the water. Continuously supplying rinse water.
상기 방법으로는 린스워터가 계속해서 흐르는 경우에도 콘디셔닝 조성물이 통내에 남아 있는 것이 가능하며 린스과정중 직물을 효과적으로 콘디셔녕 할 수 있고 그럼으로써 통으로부터의 콘디셔닝제의 손실을 최소화할 수 있다.The method allows the conditioning composition to remain in the vat even if the rinse water continues to flow and effectively condition the fabric during the rinse process, thereby minimizing the loss of conditioning agent from the vat.
직물은 일반적으로 이미 세탁을 한 통에서 그대로 린스가 행해지거나 또는 특정의 린스목적을 위한 통에 옮겨진다. 이미 세탁을 한 통에서 린스를 하는 경우에는, 직물에 여전히 흡수되어 있거나 아니면 결합되어 있는 세제활성물질을 포함하는 세탁액이 최소한 약간은 남아 있을 것이며 이때 흐르는 물은 직물의 외부로 이러한 세탁액을 흘러넘쳐 버리게 하는 역할을 한다. 통속으로 공급되는 흐르는 린스워터는 실질적으로 어떠한 세제활성물질과도 반응하지 않는다.The fabric is generally rinsed as is in a previously washed tub or transferred to a vat for a particular rinse purpose. If you rinse in a bucket that has already been washed, there will be at least a small amount of washing liquid still containing or absorbing the detergent active material in the fabric and the running water will flow out of the washing liquid to the outside of the fabric. It serves to overflow. The flowing rinse water supplied to the keg does not react with virtually any detergent active material.
본 발명에 사용되는 직물은 어떠한 형태라도 된다. 그러나 면과 같은 천연섬유로된 직물은 콘디셔닝제가 직물연화제인 경우 특히 본 방법에 의해 효과적으로 처리되며 나일론과 같은 합성섬유로 된 직물은 콘디셔닝제가 정전기 방지제인 경우 본 방법으로 처리하면 효과적이다.The fabric used in the present invention may be in any form. However, fabrics made of natural fibers, such as cotton, are effectively treated by this method especially when the conditioning agent is a fabric softener, and fabrics made of synthetic fibers such as nylon are effective when treated by this method when the conditioning agent is an antistatic agent.
린스워터의 유속은 세탁기의 설계에 의해 결정되지만, 1시간당 5 내지 50회 통의 물을 완전히 갈아 채울 수 있을 정도, 즉 통의 용량이 약 35ℓ인 경우 1분당 3.5 내지 30ℓ채워지는 정도이어야 본 방법에 효과적이라는 것을 알게 되었다. 세탁수 온도로는 어느 온도는 되나, 0℃ 내지 30℃의 찬물이 적합하다. 사용되는 린스시간은 세탁기의 설계, 즉 세탁기의 린스 효율성 및 목적하는 린스정도에 의해 부분적으로 결정되지만, 20분이하, 바람직하게는 5분 내지 15분이 효율적이다.The flow rate of the rinse water is determined by the design of the washing machine, but it should be enough to completely change the water from 5 to 50 times per hour, that is, 3.5 to 30 liters per minute if the volume of the bucket is about 35 liters. I found it effective. The washing water temperature may be any temperature, but cold water of 0 ° C to 30 ° C is suitable. The rinse time used is determined in part by the design of the washing machine, ie the rinse efficiency of the washing machine and the desired degree of rinse, but less than 20 minutes, preferably 5 to 15 minutes is effective.
직물 콘디셔닝 아티클은 최소한 한 디멘젼이 1㎝이상이라는 전제하에 여러 형태를 취할 수 있다. 아티클이 이보다 작으면 흐르는 물과 함께 세탁기로부터 배출되어 버린다. 아티클은 콘디셔닝 조성물로 이루어져 있거나 또는 콘디셔닝 조성물을 내포한다. 분명히, 아티클이 조성물로 이루어져 있는 경우는 이 조성물이 1㎝ 이상의 필요로 하는 디멘젼을 가지지 못하기 때문에 액체 또는 미세한 분말의 형태일것이라는 가능성은 없다. 그러나 이 조성물이 직경 2 내지 10㎝의 디스크형 또는 구형 블럭(block)과 같은 필요로 하는 디멘젼을 가진 블럭 또는 타블렛(tablet) 형태인 것은 가능하다.Fabric conditioning articles can take many forms, provided that at least one dimension is greater than 1 cm. If the article is smaller than this, it will be discharged from the washing machine with running water. The article consists of or contains a conditioning composition. Clearly, if the article consists of a composition, it is unlikely that the composition will be in the form of a liquid or fine powder since it does not have the required dimensions of more than 1 cm. However, it is possible for the composition to be in the form of blocks or tablets with the required dimensions, such as disc shaped or spherical blocks having a diameter of 2 to 10 cm.
아티클이 조성물을 내포하는 경우 이 아티클은 최소한 한 디멘젼이 1㎝ 이상인 콘테이너의 형태를 취한다. 콘테이너는 콘디셔닝 조성물을 보유하는 형태로 제조되며 이 경우 상기 조성물은 액상 및 분말을 포함하여 적합한 물리적 형태이면 어느 형태든 된다. 이러한 적합한 콘테이너는 한변의 길이가 최소한 3㎝인 정사각형이고 물투과성 물질로 만들어진 주머니 형태이다.If the article contains a composition, the article takes the form of a container with at least one dimension of at least 1 cm. The container is prepared in a form having a conditioning composition, in which case the composition can be in any form as long as it is a suitable physical form, including liquid and powder. Such a suitable container is in the form of a bag of square and water-permeable material, with at least 3 cm on one side.
직물 콘더셔닝제라는 용어는 예를들면 연화, 정전기방지, 향, 드레이프, 구김방지, 다림질의 용이성, 또는 표백력 개선등의 잇점을 제공하는 모든 물질을 통틀어서 넓은 의미로 본 명세서에서 사용되지만, 직물연화제 또는 정전기방지제가 바람직하다. 본 발명은 직물 콘디셔닝제가 양이온 물질인 경우 특히 유용하다. 적합한 양이온 연화제로는 비 수용성 양이온 직물 연화제가 있다.The term fabric condensing agent is used herein in a broad sense throughout all materials, which provides benefits such as, for example, softening, antistatic, fragrance, drape, anti-wrinkling, ease of ironing, or improved bleaching. Softeners or antistatic agents are preferred. The present invention is particularly useful when the fabric conditioning agent is a cationic material. Suitable cationic softeners are water soluble cationic fabric softeners.
비-수용성 양이온 직물 연화제는 물에서의 용해도가 pH=2.5, 20℃에서 10g/ℓ이하인 직물에 작용하는 양이온 화합물이면 어떤것이든 된다.The non-water-soluble cationic fabric softener can be any cationic compound which acts on fabrics having a solubility in water of 10 g / l or less at pH = 2.5, 20 ° C.
특히 바람직한 물질은 -OH, -O-, -CONH, -COO- 등과 같은 작용기에 의해 임의로 치환되거나 반응될 수 있는, 2개의 알케닐사슬의 C12-C24알킬을 가진 4급 암모늄염이다.Particularly preferred materials are quaternary ammonium salts with C 12 -C 24 alkyl of two alkenylchains, which may be optionally substituted or reacted by functional groups such as —OH, —O—, —CONH, —COO— and the like.
실질적인 비-수용성 4급 암모늄 화합물로서 잘 알려진 종류는 다음의 일반식을 가진다.A class well known as a substantially non-aqueous quaternary ammonium compound has the following general formula.
상기식에서 R1및 R2는 단소원자 12 내지 24개의 하이드로카빌기를 나타내고, R3및 R4는 탄소원자 1 내지 4개의 하이드로카빌기를 나타내며 X-는 음이온으로서 할라이드, 메틸설페이트 및 에틸설페이트기로부터 선택되는 것이 바람직하다. 이러한 4급 연화물질의 대표적인 예로는 디탤로우 디메틸 암모늄 클로라이드, 디탤로우 디메필 암모늄 메틸설페이트, 디헥사데실 디메틸 암모늄 클로라이드, 디(수소화반응시킨 탤로우알킬) 디메틸 암모늄 클로라이드, 디옥타데실 디메딜 암모늄 클로라이드, 디에이코실 디메틸암모늄 클로라이드, 디도코실 디메틸 암모늄 클로라이드, 디(수소화반응시킨 탤로우) 디메틸 암모늄 메틸설페이트, 디헥사데실 디에틸 암모늄 클로라이드, 디(코코닛 알킬) 디메틸 암모늄 클로라이드 등이 있다. 디탤로우 디메틸암모늄 클로라이드, 디(수소화반응시킨 탤로우 알킬) 디메틸 암모늄 클로라이드, 디(코코닛 알킬) 디메틸암모늄 클로라이드 및 디(코코닛 알킬) 디메틸 암모늄 메토설페이트가 바람직하다.Wherein R 1 and R 2 represent 12 to 24 hydrocarbyl groups having a single atom, R 3 and R 4 represent hydrocarbyl groups having 1 to 4 carbon atoms, and X- represents a halide, methyl sulfate and ethyl sulfate group as an anion. It is preferably selected from. Representative examples of such quaternary softeners include ditallow dimethyl ammonium chloride, ditallow dimethyl ammonium methyl sulfate, dihexadecyl dimethyl ammonium chloride, di (hydrogenated tallowalkyl) dimethyl ammonium chloride, dioctadecyl dimedyl ammonium chloride , Diicosyl dimethylammonium chloride, didocosyl dimethyl ammonium chloride, di (hydrogenated tallow) dimethyl ammonium methyl sulfate, dihexadecyl diethyl ammonium chloride, di (coconet alkyl) dimethyl ammonium chloride, and the like. Ditallow dimethylammonium chloride, di (hydrogenated tallow alkyl) dimethyl ammonium chloride, di (coconet alkyl) dimethylammonium chloride and di (coconet alkyl) dimethyl ammonium methosulfate are preferred.
바람직한 비-수용성 양이온 물질의 다른 종류로는 다음 분자식의 알킬 이미다졸리늄염이 있다.Another class of preferred non-water soluble cationic materials is the alkyl imidazolinium salt of the following molecular formula.
상기식에서 R6는 1 내지 4 바람직하게는 1 또는 2개의 탄소원자를 가지는 알킬 또는 하이드록시알킬기이고, R7은 8 내지 25개의 탄소원자를 가지는 알킬 또는 알케닐기, R8은 탄소원자 8 내지 25의 알킬 또는 알케닐기, R9은 수소 또는 탄소원자 1 내지 4의 알킬기이며 A-는 음이온으로서 할라이드, 메토설페이트 또는 에토설페이트가 바람직하다. 바람직한 이미다졸리늄염으로는 1-메틸-1-(탤로우일아미도)에틸-2-탤로우일-4, 5-디하이드로이미다졸러늄 메트설페이트및1-메틸-1-(팔미토일아미도)에틸-2-옥타데실-4, 5-디하이드로이미다졸리늄 클로라이드가 있다. 기타 유용한 이미다졸리늄 물질은 2-헵타데실-1-메틸-1-(2 -스테아릴아미도)에 틸-이미다졸리늄 클로라이드 및 2-라우릴-1-하이드록시에틸-1-올레일- 이미다졸리늄 클로라이드이다. 또한 참고적으로 소개되는 미합중국 특허 제4 127 489호의 이미다졸리늄 직물 연화성분도 본 발명에 적합하다.Wherein R 6 is an alkyl or hydroxyalkyl group having 1 to 4 preferably 1 or 2 carbon atoms, R 7 is an alkyl or alkenyl group having 8 to 25 carbon atoms, and R 8 is an alkyl having 8 to 25 carbon atoms Or an alkenyl group, R 9 is hydrogen or an alkyl group of 1 to 4 carbon atoms and A- is preferably an halide, methosulfate or etosulphate as an anion. Preferred imidazolinium salts include 1-methyl-1- (tallowylamido) ethyl-2-tallowyl-4, 5-dihydroimidazolinium metsulfate and 1-methyl-1- (palmitoylamido Ethyl-2-octadecyl-4, 5-dihydroimidazolinium chloride. Other useful imidazolinium materials include 2-heptadecyl-1-methyl-1- (2-stearylamido) ethyl-imidazolinium chloride and 2-lauryl-1-hydroxyethyl-1-ole Mono-imidazolinium chloride. Also suitable for the present invention is the imidazolinium fabric softening component of US Pat. No. 4,127,489, which is incorporated by reference.
본 발명에 유용한 정전기 방지제는 분자식 [R9, R10, R11, R12, N]+Y-의 4급 암모늄염이다. 상기식에서 R9, R10, R11및 R12중의 최소한 하나(그러나 둘이하)는 C16-C22지방족기 또는 알킬사슬중에 10-16원자를 가진 알킬 페닐기 또는 알콜 벤질기로부터 선택되는 유기성기이며, 나머지 기 또는 기들은 1 내지 4개의 탄소원자를 가진 하이드로 카빌기, 또는 C2-C4하이드록시 알킬기로부터 선택되며 질소원자가 고리의 일부를 형성하는 환형구조이고, Y는 할라이드, 메틸설페이트 또는 에틸설페이트와 같은 음이온이다.Antistatic agents useful in the present invention is a molecular formula [R 9, R 10, R 11, R 12, N] + Y - is a quaternary ammonium salt. Wherein at least one (but not more than two) of R 9 , R 10 , R 11 and R 12 is an organic group selected from an alkyl phenyl group or an alcohol benzyl group having 10-16 atoms in a C 16 -C 22 aliphatic group or an alkyl chain; And the remaining groups or groups are selected from a hydrocarbyl group having 1 to 4 carbon atoms, or a C 2 -C 4 hydroxy alkyl group and a cyclic structure in which the nitrogen atom forms part of the ring, Y is halide, methylsulfate or ethyl It is an anion such as sulfate.
상기 정의와 관련해서, 유기성기 R9의 소수성부분(즉, C16-C22지방족기, C10-C16알킬페닐 또는 알킬벤질기)는 4급 질소에 직접붙거나 아니면 아미드, 에스테르, 알콕시, 에테르등의 기를 통해 간접적으로 붙게된다.In connection with the above definition, the hydrophobic portion of the organic group R 9 (ie, C 16 -C 22 aliphatic group, C 10 -C 16 alkylphenyl or alkylbenzyl group) is attached directly to a quaternary nitrogen or amide, ester, alkoxy Indirectly attached via groups such as ether.
직물 콘디셔닝 아티클은 콘디셔닝제를 셀화시키지 않으면서 콘디TU닝제가 물속으로 방출되는 깃을 억제하는 수단을 가지고 있다. 이 수단은 물리적 수단이거나 또는 화학적 수단이다. 콘디셔닝제의 방출을 억제하는 수단은 실질적으로 모든 콘디셔닝세가 린스진행중에 린스액속으로 방출되게 하며 콘디셔닝제의 30%, 특히 바람직하게는 50%가 린스과정의 후반중에 방출되도록 해야 한다.Fabric conditioning articles have a means of suppressing feathers that are released into the water without conditioning the conditioning agent. This means is either physical or chemical. The means of inhibiting the release of the conditioning agent should allow substantially all of the conditioning tax to be released into the rinse liquid during the rinse process and 30% of the conditioning agent, particularly preferably 50%, to be released later in the rinse process.
콘디셔닝제 방출을 충분히 억제하기에 적합한 한 방법은 파라핀 왁스, 환상 및 비환상 모노 및 폴리하이드릭 알콜, 치환된 및 치환되지 않은 지방족 카로복실산, 전술한 알콜과 산과의 에스테로, 전술한 어떠한 물질과 C1-C4알킬렌 옥사이드의 축합물 및 이들의 혼합물로부터 선택되는 물질은 콘디셔닝제와 혼합시키거나 또는 상기 물질들로 코팅시키거나 아니면 상기 물질들과 결합시키는 것이다.One method suitable for sufficiently inhibiting the release of the conditioning agent is paraffin wax, cyclic and acyclic mono and polyhydric alcohols, substituted and unsubstituted aliphatic carboxylic acids, esters of the aforementioned alcohols with acids, any of the foregoing The material selected from condensates of materials with C 1 -C 4 alkylene oxides and mixtures thereof is either mixed with the conditioning agent or coated with the materials or combined with the materials.
상기 물질중에 탤로우 알콜이 특히 바람직하다. 기타 적합한 1몰당 18 내지 25의 에톡실레이트기로 에톡실화된 탤로우 알콜과 거의 같은 녹는점을 가진 비이온물질이다.Among these materials tallow alcohols are particularly preferred. Other suitable nonionics have a melting point approximately equal to tallow alcohol ethoxylated with 18 to 25 ethoxylate groups per mole.
이러한 적합한 물질의 상세한 예는 이 물질이 분산억제제로서 언급되어 있는 미합중국 특허 제3936537호(바스커빌레)에서 찾을 수 있다.A detailed example of such a suitable material can be found in US Pat. No. 39,36537 (Baskerville), in which this material is referred to as a dispersion inhibitor.
조성물중 직물 콘디셔닝제 대 방출억제제의 비율은 목적하는 린스시간 및 린스온도와 같은 사용요인 및 제품의 의도에 좌우된다. 방출억제제의 선택도 또한 린스워터의 온도에 좌우된다.The ratio of fabric conditioning agent to release inhibitor in the composition depends on the intended use and the intended product such as the desired rinse time and rinse temperature. The choice of release inhibitor also depends on the temperature of the rinse water.
특히 직물 콘디셔닝 조성물이 고체형태인 경우, 방출억제제가 그 효력을 다한 후에 콘디셔녕제의 분산을 촉진하기 위해 전해질을 조성물에 함유시키는 것이 또한 유리하다. 이 전해질로는 염화나트륨과 같은 수용성 무기염이 바람직하다. 조성물중 전해질의 함량은 직물 콘디셔닝제 대 전해질의 비가 1 : 0.5 내지 1 : 10(중량)인 범위내에서 선택된다.In particular, when the fabric conditioning composition is in solid form, it is also advantageous to include an electrolyte in the composition to promote dispersion of the conditioning agent after the release inhibitor has reached its effect. As this electrolyte, a water-soluble inorganic salt such as sodium chloride is preferable. The content of the electrolyte in the composition is selected within the range of 1: 0.5 to 1:10 (weight) of fabric conditioning agent to electrolyte.
직물 콘디셔닝제가 계면활성제인 경우 린스과정에서 발생되는 포말을 억제하기 위해서 직물 콘디셔닝 조성물에 소포물질을 함유시키는 것이 또한 유리하다. 공지된 소포물질이면 어느 것이든 사용될 수 있으나 그함량은 소포제가 원하는 효과를 내기에 충분한 정도이어야 한다. 적합한 소포제는 우리의 유럽 특허 명세서 제 EP 94250-A호에 기술된 과립 소포제이다.If the fabric conditioning agent is a surfactant, it is also advantageous to include the antifoam material in the fabric conditioning composition in order to suppress the foam generated during the rinse process. Any known antifoam material may be used but its content should be sufficient to produce the desired effect. Suitable defoamers are granular defoamers described in our European patent specification EP 94250-A.
직물 콘디셔닝 아티클은 린스워터가 통내로 홀러들기 전에, 또는 린스워터와 동시에 또는 린스사이클중 한 경로에서 통내의 직물에 첨가할 수 있다.The fabric conditioning article may be added to the fabric in the bin before the rinse water is introduced into the bin, or simultaneously with the rinse water or in one of the rinse cycles.
[실시예 1-3]Example 1-3
61g/㎡의 멜트블로운(melt blown) 폴리프로필렌 라미네이트(킴벌리-클라크제품인 킴텍스 SMS)로 주머니를 제조하였다. 주머니 크기는 7㎝×7㎝었다. 이 주머니속에 거의 100%의 디스테아릴 디메틸 암모늄 클로라이드인 직물 연화제로서 시판중인 아로서프 TA 100(분말형태) 2g, 염(염화나트륨) 4g 및 이미 제조된 과립 소포제 1g을 넣었다. 주머니를 열밀봉하고 각 표면에 20×0.7㎜(직경)의 핀홀을 생기게 하였다. 방출억제수단으로서 1g의 탤로우 알콜 18EO(실시예 1) 또는 탤로우 알콜 25EO(실시예 2)로 주머니를 코팅하였다. 비교목적으로 코팅하지 않은 주머니(실시예 3)도 실험하였다.Pouches were made from a 61 g / m 2 melt blown polypropylene laminate (Kimtex SMS from Kimberly-Clark). The bag size was 7 cm x 7 cm. Into this bag was placed 2 g of commercially available atropes TA 100 (powder form), 4 g salt (sodium chloride) and 1 g granule defoamer prepared as a fabric softener which is almost 100% distearyl dimethyl ammonium chloride. The bag was heat sealed and a 20 x 0.7 mm (diameter) pinhole was created on each surface. The bag was coated with 1 g tallow alcohol 18 EO (Example 1) or tallow alcohol 25 EO (Example 2) as release control. A comparative uncoated bag (Example 3) was also tested.
[실시예 4-7]Example 4-7
블럭표면에 대해 1 또는 1/2톤(tonne) 압력의 유압식 램(ram)을 사용하여 30㎜ 다이에서 분발형태의 직물 콘디셔닝 조성물을 눌러펴서 블럭을 제조하였다. 각 블럭은 두께가 약 1㎝, 직경이 약 3㎝였다. 각 조성물은 2g의 아로서프 TA 100, 6 또는 11g의 염(각각 실시예 4 및 5) 및 1g의 미리 제조된 과립 소포제를 함유하였다. 방출억제수단으로서 0.3g의 탤로우 알콜 25EO로 블럭을 코팅하였다. 비교목적으로 블록을 코팅하지 않고 실시예 4 및 5의 방법을 반복하였다.(각각 실시예 6 및 7)Blocks were prepared by pressing a powdered fabric conditioning composition in a 30 mm die using a hydraulic ram of 1 or 1/2 ton pressure relative to the block surface. Each block was about 1 cm thick and about 3 cm in diameter. Each composition contained 2 g of atropine TA 100, 6 or 11 g of salts (Examples 4 and 5, respectively) and 1 g of a pre-made granular antifoam. The block was coated with 0.3 g tallow alcohol 25EO as a release inhibitor. For comparison purposes the methods of Examples 4 and 5 were repeated without coating the blocks (Examples 6 and 7, respectively).
실시예 1 내지 7에 서술된 제품들을 다음과 같이 실험하였다. 용량이 40ℓ인 2통식(twin-tub) 세탁기(내쇼날 NA-W 1018)를 사용하였다. 면/폴리에스터 혼방 시이팅 세탁물 1.3㎏을, 일본시장에서 구입가능한 세탁분말 "TOP"을 경도 6℉H(ℓ당 유리칼슘이온 6×10-4물)의 물에 녹인 1g/ℓ의 세탁액 35ℓ로 25에서 10분간 세탁하였다. 세탁후 세탁액을 세탁통으로부터 배수시키고. 직물을 꺼내어 탈수기에 넣은 다음 세탁액이 더이상 제거되지 않을때까지 회전시켰다. 그 다음 직물을 다시 세탁통으로 넣고, 실험하고자 하는 직물 콘디셔닝 아티클 존재하에 분당 10ℓ의 물을 공급하여 25℃에서 10분간 흐르는 상태로 린스하였다.The products described in Examples 1-7 were tested as follows. A 40-liter twin-tub washer (National NA-W 1018) was used. 1 g / l washing solution dissolved 1.3 kg of cotton / polyester blend seating laundry and washing powder “TOP” available in the Japanese market in water with a hardness of 6 ℉ H (6 × 10 -4 free calcium ions per liter) Wash at 35 L for 25 to 10 minutes. After washing the wash liquor was drained from the wash bin. The fabric was taken out and placed in the dehydrator and spun until the wash was no longer removed. The fabric was then placed back into the wash bin and rinsed with 10 liters of water per minute in the presence of the fabric conditioning article to be tested and flowing at 25 ° C. for 10 minutes.
린스워터를 배수시킨 후에, 직물을 꺼내서 회전 탈수시킨 다음 대기온도에서 줄에 널어 건조시켰다. 손의 감촉으로 직물의 연화도를 평가하여 연화도에 대한 등급을 정하였다. '8'은 풀먹이지 않은 면테리 타올의 거침을 나타내고 '5'는 5%의 아콰드 2C(디코코 디메틸 암모늄 클로라이드의 시판형)로 구성된 수성제품을 40g/ℓ의 농도로 사용하여 터고토미터 실험 실용 장치에서 세탁액 대 직물비 25 : 1의 양으로 풀먹이지 않은 면테리 타올을 5분간 린스한 후 펌블(tumble) 건조시킴으로써 얻어진 부드러움을 나타낸다.After draining the rinse water, the fabric was taken out, spin-dried and dried on a string at ambient temperature. The softness of the fabric was assessed by hand texture to grade the softness. '8' represents the roughness of untreated cotton terry towels, and '5' represents a turgotometer using an aqueous product composed of 5% AQUAD 2C (commercially available dicoco dimethyl ammonium chloride) at a concentration of 40 g / l. The softness obtained by rinsing the cotton terry towels, which were not fed with a washing solution to fabric ratio of 25: 1 in a laboratory apparatus, for 5 minutes and then tumble drying.
얻어진 결과는 다음과 같으며 등급수가 낮을수륵 연화도는 우수하다.The results obtained are as follows, and the softening degree is excellent.
*이 경우는 린스 초기에, 어떠한 방출억제수단도 사용하지 않고 2g의 아로서프 TA 100과 6g의 염혼합물을 분말로 첨가시킨 경우이다.In this case, 2 g of aroof TA 100 and 6 g of salt mixture were added to the powder at the beginning of the rinse without using any release inhibitor.
상기 결과는 본 제품을 사용하지 않는 것에 비해 또한 본 발명에 필수적인 방출억제수단없이 직물 콘디셔닝 제품을 사용하는 것에 비해 본 발명이 보다 유용하다는 것을 입증한다. 특히 상기 결과는 방출억제수단으로서 직물 콘디셔닝제를 코팅할 때의 잇점을 입증한다. 아르서프 TA 100대신 다음의 제품을 사용하는 경우 유사한 결과를 얻을 수 있다.The results demonstrate that the present invention is more useful than not using this product and also compared to using a fabric conditioning product without release control measures essential to the present invention. In particular, the results demonstrate the advantages of coating fabric conditioning agents as release inhibitors. Similar results can be obtained when using the following products instead of Arsuf TA 100:
a) 바리소프트 818(시어렉스 제품)-소량의 분산보조물을 함유한 수정된 디스테아릴 디메틸 암모늄 클로라이드.a) Barisoft 818 (Syrex) -modified distearyl dimethyl ammonium chloride containing small amounts of dispersion aids.
b) 아도겐 442-100P(레우오 제품)-디메틸 디경화 탤로우 암모늄 클로라이드를 기본물로 하는 양이온계직물 콘디셔닝제.b) Cationic fabric conditioning agent based on agenogen 442-100P (Leuo) -dimethyl dicured tallow ammonium chloride.
c) 쿼톤 442-SD(케노벨 제품)-디메틸 디경화 탤로우 암모늄 클로라이드를 기본물로 하는 분말 양이온계 콘디셔닝제.c) Powder cationic conditioning agent based on Qutone 442-SD (Kenobel) -dimethyl dicured tallow ammonium chloride.
[실시예 8-11]Example 8-11
네트×560(스미드 & 네퓨제품)으로 주머니를 제조하였다. 주머니 크기는 6㎝×6㎝였다. 알과드 2T(75%의 활성 페이스트로서 공급되는 디탤로우 디메틸 암모늄 클로라이드의 시판형) 52%와 이소프로필 미리스테이트 48%를 함유하는 비-수용성 직물 콘디셔닝 조성물 5g으로 주머니를 채운후 열밀봉하였다. 방출억제수단으로서 120g/㎡의 코팅수준의 폴리비닐 아세테이트 에멀죤으로 주머니를 코팅하였다.(실시예 8)The bag was produced with net x 560 (made by Smead & Nephew). Pouch size was 6 cm x 6 cm. The bag was filled with 5 g of a non-aqueous fabric conditioning composition containing 52% of Alward 2T (commercially available form of ditallow dimethyl ammonium chloride supplied as 75% active paste) and 48% isopropyl myristate, followed by heat sealing. The bag was coated with a polyvinyl acetate emulsion zone having a coating level of 120 g / m 2 as a release inhibiting means.
부직포물질인 PBS 6/85(캄브렐레 제품)으로 시이트를 제조하였다. 이 시이트는 상기의 비-수용성 조성물을 내포하였다.(실시예 9)The sheet was made from PBS 6/85 (Camberle), a nonwoven material. This sheet contained the above non-aqueous composition. (Example 9)
다음 방법으로 주머니형 및 시이트형 제품 실험하였다. 용량 40ℓ의 2통식 세탁기(내쇼날 NA-W1018)를 사용하였다. 면/폴리에스터 혼방 시이팅 세탁물 1.3㎏을, 일본시장에서 구입가능한 세탁분말 "TOP"을 경도 6℉hH(ℓ당 유리칼슘이온 6×10-4물)의 물에 녹인 1g/ℓ의 세탁액 35ℓ로 25℃에서 10분간 세탁하였다. 세탁후 세탁액을 세탁통으로부터 배수시키고 직물을 꺼내어 탈수기에 넣고 세탁액이 더이상 제거되지 않을때까지 회전시켰다. 그 다음 직물을 다시 세탁통에 넣고, 실험하고자 하는 직물 콘디셔닝 아티클콜 존재하에 분당 10ℓ의 물을 투입하여 10분간 흐르는 상태로 린스하였다. 린스워터의 온도는 10℃였다. 주머니형 제품을 사용한 경우 직물 콘디셔닝 조성물은 처음 3-4분 지연된 후 3-4분 동안에 흐르는 린스워터로 방출되었다. 시이트형 제품을 사용한 경우는 3-4분 동안에 흐르는 린스워터로 직물 콘디셔닝 조성물이 방출되었다. 이러한 형태의 제품에서는 직물 콘디셔너가 방출되기 이전에 초기지연이 없었다.Bag and sheet products were tested in the following manner. A 40 L two-wheel washing machine (National NA-W1018) was used. Cotton / polyester blends, Shi putting the laundry 1.3㎏, purchased from the Japanese market available washing powder "TOP" hardness 6 ℉ hH washing of 1g / ℓ dissolved in water (free calcium ion per ℓ 6 × 10 -4 water) solution Washed with 35 L at 25 ° C. for 10 minutes. After washing the wash liquor was drained from the wash bin and the fabric was taken out and placed in a dehydrator and spun until the wash liquor was no longer removed. The fabric was then placed back into the wash bin and rinsed with 10 liters of water per minute in the presence of the fabric conditioning article to be tested. The temperature of the rinse water was 10 ° C. The fabric conditioning composition was released into the flowing rinse water for 3-4 minutes after a delay of the first 3-4 minutes when using the bag-shaped product. The fabric conditioning composition was released with rinse water flowing for 3-4 minutes when the sheet type product was used. In this type of product, there was no initial delay before the fabric conditioner was released.
비교실험으로서(실시예 10) 시이트형 제품을 흐르는 린스워터에 5분간 첨가하였다. 또다른 비교실험으로서(실시예 11), 린스과정의 초기에 5g/ℓ의 농도의 비-수용성 액체 콘디셔닝 조성물을 투여하였다.As a comparative experiment (Example 10), the sheet-like product was added to a flowing rinse water for 5 minutes. As another comparative experiment (Example 11), a non-aqueous liquid conditioning composition at a concentration of 5 g / l was administered at the beginning of the rinse process.
직물을 10분간 흐르는 상태로 린스한 후 린스워터를 배수시키고, 직물을 꺼내서 회전 탈수시킨 다음에 대기온도에서 줄에 널어 건조시켰다. 그후에 상술한 방법에 의해 직물의 연화도를 측정하여 다음의 결과를 얻었다.After rinsing the fabric for 10 minutes, the rinse water was drained, the fabric was taken out, spin-dried, and hung on a string at ambient temperature to dry. Then, the softness of the fabric was measured by the method described above to obtain the following results.
Claims (6)
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GB868618428A GB8618428D0 (en) | 1986-07-29 | 1986-07-29 | Conditioning fabrics |
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JP (1) | JPS6342977A (en) |
KR (1) | KR900009221B1 (en) |
AU (1) | AU590435B2 (en) |
BR (1) | BR8703862A (en) |
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GB8721074D0 (en) * | 1987-09-08 | 1987-10-14 | Unilever Plc | Conditioning fabrics |
GB9011785D0 (en) * | 1990-05-25 | 1990-07-18 | Unilever Plc | Fabric treatment compositions |
EP1048714A1 (en) * | 1999-04-30 | 2000-11-02 | The Procter & Gamble Company | Method of dispensing a detergent composition |
EP1048712A1 (en) * | 1999-04-30 | 2000-11-02 | The Procter & Gamble Company | A process of treating fabrics with a laundry detergent additive tablet |
EP1048715A1 (en) * | 1999-04-30 | 2000-11-02 | The Procter & Gamble Company | Method of dispensing a detergent composition |
GB0119710D0 (en) * | 2001-08-13 | 2001-10-03 | Unilever Plc | Cleaning and rinsing of textile fabrics |
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US4259373A (en) * | 1976-07-12 | 1981-03-31 | The Procter & Gamble Company | Fabric treating articles and process |
US4082678A (en) * | 1976-11-10 | 1978-04-04 | The Procter & Gamble Company | Fabric conditioning articles and process |
US4203851A (en) * | 1978-06-16 | 1980-05-20 | Colgate-Palmolive Company | Fabric softening compositions and methods for manufacture thereof |
US4304562A (en) * | 1980-03-31 | 1981-12-08 | The Drackett Company | Fabric softener article for an automatic washer and method using same |
DE3211470A1 (en) * | 1982-03-29 | 1983-10-06 | Henkel Kgaa | AGENTS FOR CARE OF TEXTILES |
US4588080A (en) * | 1985-01-07 | 1986-05-13 | Ginn Martin E | Staged detergent/fabric treating preparation for use in washing machines |
GB8519363D0 (en) * | 1985-08-01 | 1985-09-04 | Procter & Gamble | Dispersible fabric softeners |
-
1986
- 1986-07-29 GB GB868618428A patent/GB8618428D0/en active Pending
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1987
- 1987-07-10 KR KR1019870007396A patent/KR900009221B1/en not_active IP Right Cessation
- 1987-07-24 JP JP62185322A patent/JPS6342977A/en active Granted
- 1987-07-24 AU AU76091/87A patent/AU590435B2/en not_active Ceased
- 1987-07-27 BR BR8703862A patent/BR8703862A/en unknown
- 1987-07-29 ZA ZA875589A patent/ZA875589B/en unknown
- 1987-07-29 EP EP87306709A patent/EP0255779A1/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
EP0255779A1 (en) | 1988-02-10 |
ZA875589B (en) | 1989-03-29 |
KR880001873A (en) | 1988-04-27 |
GB8618428D0 (en) | 1986-09-03 |
AU7609187A (en) | 1988-02-04 |
JPH0227471B2 (en) | 1990-06-18 |
JPS6342977A (en) | 1988-02-24 |
AU590435B2 (en) | 1989-11-02 |
BR8703862A (en) | 1988-03-29 |
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