CN115335567A - Fiber product treating agent composition and fiber product treating method - Google Patents
Fiber product treating agent composition and fiber product treating method Download PDFInfo
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- CN115335567A CN115335567A CN202180024702.1A CN202180024702A CN115335567A CN 115335567 A CN115335567 A CN 115335567A CN 202180024702 A CN202180024702 A CN 202180024702A CN 115335567 A CN115335567 A CN 115335567A
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- fiber product
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- product treating
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- 230000003113 alkalizing effect Effects 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 1
- 239000004161 brilliant blue FCF Substances 0.000 description 1
- 235000012745 brilliant blue FCF Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 229940071118 cumenesulfonate Drugs 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- CZWHGIACASUWJC-UHFFFAOYSA-L disodium 5-acetamido-3-[(4-dodecylphenyl)diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].CCCCCCCCCCCCc1ccc(cc1)N=Nc1c(O)c2c(NC(C)=O)cc(cc2cc1S([O-])(=O)=O)S([O-])(=O)=O CZWHGIACASUWJC-UHFFFAOYSA-L 0.000 description 1
- FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 235000019233 fast yellow AB Nutrition 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 230000003165 hydrotropic effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- SXQCTESRRZBPHJ-UHFFFAOYSA-M lissamine rhodamine Chemical compound [Na+].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=C(S([O-])(=O)=O)C=C1S([O-])(=O)=O SXQCTESRRZBPHJ-UHFFFAOYSA-M 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920000333 poly(propyleneimine) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000656 polylysine Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000008237 rinsing water Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Inorganic materials O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229940043810 zinc pyrithione Drugs 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/61—Polyamines polyimines
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
A fiber product treating agent composition according to one embodiment of the present invention contains a component (a) which is at least 1 selected from an anionic surfactant and a nonionic surfactant, and a component (B) which is an alkylene oxide adduct of polyalkyleneimine; the content of the component (A) is more than 0 mass% and 10 mass% or less in the total mass of the fiber product treating agent composition; the content of the component (B) in the total mass of the fiber product treating agent composition is 0.5 to 10 mass%; the mass ratio of the component (B) to the component (A) is 0.1 or more.
Description
Technical Field
The present invention relates to a fiber product treating agent composition and a fiber product treating method.
This application claims priority to japanese patent application No. 2020-65856, filed in japan on day 1/4/2020, and the contents of which are incorporated herein by reference.
Background
With the recent increase in awareness of cleanliness, there is an increasing demand for such a living being who wants to remove malodor at a higher level.
Patent document 1 discloses a deodorant composition for fiber products, which contains at least 1 compound selected from an alkylene oxide adduct of polyalkyleneimine and an alkylene oxide adduct of polyalkyleneamine, and an aminocarboxylic acid type chelating agent.
Patent document 2 discloses a liquid detergent composition containing a nonionic surfactant, an anionic surfactant, a cationic surfactant, and an alkylene oxide adduct of polyalkyleneamine, wherein the mass ratio of the anionic surfactant/the nonionic surfactant is 0.15 to 1.
[ Prior art documents ]
[ patent document ]
[ patent document 1 ] Japanese patent application laid-open No. 2018-3196
[ patent document 2 ] Japanese patent application laid-open No. 2017-200972
Disclosure of Invention
[ problem to be solved by the invention ]
However, the deodorant effect of the deodorant composition for textile products of patent document 1 is insufficient. In addition, the deodorant composition for textile products of patent document 1 is filled in a spray container and sprayed on the textile products, and therefore, it is not easy to uniformly adhere the deodorant composition to the textile products. In addition, when a plurality of textile products are treated, it takes time and effort to spray one textile product.
The liquid detergent composition of patent document 2 is insufficient in deodorizing effect.
The invention aims to provide a fiber product treating agent composition capable of providing excellent deodorization effect to fiber products, and a fiber product treating method capable of providing excellent deodorization effect to fiber products through simple operation.
[ MEANS FOR SOLVING PROBLEMS ] A method for solving the problems
The present invention has the following aspects.
【1】 A fiber product treating agent composition comprising a component (A) which is at least 1 selected from an anionic surfactant and a nonionic surfactant, and a component (B) which is an alkylene oxide adduct of a polyalkyleneimine (polyalkyleneimine), wherein,
the content of the component (A) in the total mass of the fiber product treating agent composition is more than 0 mass% and 10 mass% or less,
the content of the component (B) in the total mass of the fiber product treating agent composition is 0.5 to 10% by mass,
the mass ratio of the component (B) to the component (A) is 0.1 or more.
【2】 The fiber product treatment composition according to [ 1 ], wherein the (a) component comprises the anionic surfactant.
【3】 The fiber product treating agent composition according to [ 1 ] or [ 2 ], wherein the component (B) is an ethylene oxide adduct of polyalkyleneimine.
【4】 A method for treating a textile, wherein the textile is immersed in a treatment solution obtained by diluting the textile treatment composition described in any one of [ 1 ] to [ 3 ] with water, dewatered, and dried without rinsing.
[ Effect of the invention ]
According to the present invention, it is possible to provide a fiber product treating agent composition capable of imparting an excellent deodorizing effect to a fiber product, and a fiber product treating method capable of imparting an excellent deodorizing effect to a fiber product by a simple operation.
Detailed Description
[ fiber product treating agent composition ]
The fiber product treatment agent composition of the present invention (hereinafter also referred to as "the present composition") contains the component (a) and the component (B).
The present compositions typically contain water.
The present composition may contain components other than the component (a), the component (B) and water (hereinafter, also referred to as "optional components") as necessary.
< ingredient (A) >
(A) The component (c) is at least 1 selected from an anionic surfactant (hereinafter also referred to as "component (A1)") and a nonionic surfactant (hereinafter also referred to as "component (A2)").
(A) The component (B) can impart permeability and detergency to a fiber product to the composition. The component (A) facilitates penetration of the component (B) described later into the fibers, and improves the deodorizing effect. Further, since the component (a) has detergency, even if the fiber product is merely immersed in the treatment liquid, the fiber product can be cleaned, and odor generation from the fiber product can be suppressed.
Examples of the component (A1) include sulfonic acid types such as linear alkylbenzene sulfonic acid or a salt thereof, α -olefin sulfonate (α -olefin sulfonate), internal olefin sulfonate (internal olefin sulfonate), and (alk) alkane sulfonate having an alkyl group; linear or branched alkyl sulfate ester salts, alkyl ether sulfate ester salts (hereinafter also referred to as "AES"), or (alk) alkenyl ether sulfate ester salts; a carboxylic acid type such as a higher fatty acid having 8 to 22 carbon atoms or a salt thereof, an alkyl ether carboxylate, a polyoxyalkylene ether carboxylate, an alkyl (or (alk) enyl) amide ether carboxylate, an acylamino carboxylate, etc.; phosphoric acid ester types such as alkyl phosphate ester salts, polyoxyalkylene alkyl phenyl phosphate ester salts, and glycerin fatty acid ester monophosphoric acid ester salts. Examples of the salt in these anionic surfactants include alkali metal salts such as sodium salt and potassium salt; alkaline earth metal salts such as magnesium salts, and alkanolamine salts such as monoethanolamine salt and diethanolamine salt. These anionic surfactants are readily available on the market.
Among the above, the linear alkyl benzene sulfonic acids or salts thereof are preferred to have a linear alkyl group having 8 to 16 carbon atoms, and particularly preferred to have a linear alkyl group having 10 to 14 carbon atoms.
The alpha-olefin sulfonate or internal olefin sulfonate is preferably one having 10 to 20 carbon atoms.
The (alk) alkanesulfonate having an alkyl group is preferably one in which the alkyl group has 10 to 20 carbon atoms, and more preferably one in which the alkyl group has 14 to 17 carbon atoms. Among them, it is particularly preferable that the alkyl group is a secondary alkyl group (i.e., secondary alkanesulfonate).
The alkyl sulfate salt is preferably one having an alkyl group with 10 to 20 carbon atoms.
The AES or (alk) alkenyl ether sulfate salt is preferably a salt of a (alk) alkenyl ether sulfate salt having a linear or branched alkyl group or (alk) alkenyl group having 8 to 20 carbon atoms to which ethylene oxide is added in an average amount of 1 to 10 moles, and more preferably a salt of a polyoxy (meth) ethylene (meth) oxy (meth) acrylic ether sulfate salt or a salt of a polyoxy (meth) ethylene (meth) oxy (meth) acrylic) (alk) alkenyl ether sulfate salt to which propylene oxide is added in an average amount of 0 to 6 moles.
When an adduct of both ethylene oxide and propylene oxide is added to AES or (alkenyl) ether sulfate, the method of adding ethylene oxide and propylene oxide is not particularly limited. The addition method may be, for example, random addition or block addition. Examples of the block addition method include a method in which ethylene oxide is added and then propylene oxide is added; a method in which propylene oxide is added and then ethylene oxide is added; a method in which ethylene oxide is added, propylene oxide is added, and ethylene oxide is further added.
The component (A1) is preferably AES or LAS, particularly preferably AES, from the viewpoint of relatively less adsorption to the fiber and excellent deodorizing effect. AES and other (A1) components may be used in combination.
The component (A1) preferably contains a higher fatty acid having 8 to 22 carbon atoms or a salt thereof in addition to AES and/or LAS. By containing a higher fatty acid having 8 to 22 carbon atoms or a salt thereof, foaming of the treatment liquid obtained by diluting the composition with water can be reduced, and the rinse property is excellent.
Examples of AES include a compound represented by the following formula (a 1) (hereinafter, also referred to as a "(a 1) component").
R 1 -O-[(EO) j /(PO) k ]-SO 3 - M + ···(a1)
In the formula (a 1), R 1 Is a linear or branched alkyl group having 8 to 20 carbon atoms, EO is an oxyethylene groupPO represents an oxypropylene group, j represents an average number of EO repeats and is a number of 0.5 or more, k represents an average number of PO repeats and is a number of 0 to 6, and M + Is a cation.
R 1 Preferably a linear or branched alkyl group having 10 to 20 carbon atoms, and more preferably a linear or branched alkyl group having 12 to 14 carbon atoms.
j is preferably 0.5 to 5, more preferably 0.5 to 4, still more preferably 0.5 to 3.5, and particularly preferably 1.5 to 2.5.
k is preferably 0 to 3, more preferably 0.
j + k is preferably 0.5 or more, and more preferably 0.5 to 5.
(a1) When the component (C) contains both EO and PO, EO and PO may be added in a block form or a random form. Examples of the method of adding EO and PO in a block form include a method of introducing ethylene oxide and then introducing propylene oxide, and a method of introducing propylene oxide and then introducing ethylene oxide. The distribution of the addition mole number of ethylene oxide and propylene oxide is not particularly limited.
As M + Alkali metal ions such as sodium ions and potassium ions; alkaline earth metal ions such as magnesium ions; alkanolamines such as monoethanolamine and diethanolamine, and the like.
(a1) The component (C) may be a commercially available component or may be produced by a known synthesis method. When the component (a 1) is produced by a known synthesis method, the component (a 1) can be produced by a method of reacting a polyoxyalkylene alkyl ether with sulfuric anhydride or chlorosulfonic acid. (a1) The components can be used alone in 1 kind, or can be used in combination in more than 2 kinds.
The component (A2) may be, for example, a polyoxyalkylene type nonionic surfactant.
Examples of the polyoxyalkylene nonionic surfactant include a compound represented by the following formula (a 2) (hereinafter, also referred to as a "component (a 2)").
R 2 -X-[(EO) s /(PO) t ]-R 3 ···(a2)
In the formula (a 2), R 2 Is a hydrocarbon group having 8 to 18 carbon atoms, X is O, COO or CONH, R 3 Is an alkyl group having 1 to 6 hydrogen atoms or carbon atomsA group or an (alkenyl) group having 2 to 6 carbon atoms, EO is an oxyethylene group, PO is an oxypropylene group, s represents an average number of repetition of EO and is a number of 6 to 20, and t represents an average number of repetition of PO and is a number of 0 to 6. EO and PO may be arranged mixedly.
Based on the angle of good detergency, R 2 The hydrocarbon group having 10 to 18 carbon atoms is preferred, and may be linear or branched. R 2 May have an unsaturated bond. As R 2 Examples thereof include those derived from a higher primary alcohol, a higher secondary alcohol, a higher fatty acid, a higher fatty amide, and the like.
As R 3 The alkyl group of (3) is preferably an alkyl group having 1 to 3 carbon atoms. As R 3 The (alkenyl) group of (2) is preferably an (alkenyl) group having 2 to 3 carbon atoms.
From the viewpoint of the deodorizing effect, X is preferably O or COO, more preferably COO.
When X is O, the component (a 2) is alkyl ether type nonionic surfactant. When X is O, R is selected from the group consisting of 2 Preferably a hydrocarbon group having 10 to 18 carbon atoms. R is 2 May have an unsaturated bond. In addition, R 3 Preferably a hydrogen atom.
When X is COO, the component (a 2) is a fatty acid ester type nonionic surfactant. When X is COO, R is selected from the group consisting of 2 Preferably a hydrocarbon group having 9 to 18 carbon atoms, and more preferably a hydrocarbon group having 11 to 18 carbon atoms. R 2 May have an unsaturated bond. R 3 Preferably an alkyl group having 1 to 3 carbon atoms, and more preferably a methyl group.
s is a number of 6 to 20, preferably a number of 10 to 20, more preferably a number of 10 to 18, and still more preferably a number of 14 to 18. When s is within the above range, the deodorizing effect is more excellent. Further, the HLB value does not become too high, and the detergency is easily improved.
t is a number of 0 to 6, preferably a number of 0 to 3, more preferably 0. When t is within the above range, the storage stability at high temperature tends to be good.
[ (EO) in the formula (a 2) s /(PO) t ]In (3), EO and PO may be arranged mixedly. When EO and PO are mixed, they may be in a random form or in a mixed formIs in a segment shape.
In the component (a 2), the distribution of the number of repeating EO s (i.e., the average molar number of addition of ethylene oxide) or the number of repeating PO t (i.e., the average molar number of addition of propylene oxide) is not particularly limited as long as the effects of the present invention are obtained. The distribution of s or t varies depending on the reaction method in producing the component (a 2). For example, when ethylene oxide or propylene oxide is added to a hydrocarbon-based raw material (higher primary or secondary alcohol, higher fatty acid, higher fatty amide, etc.) using a general alkali catalyst such as sodium hydroxide or potassium hydroxide, the distribution of the addition mole number of ethylene oxide or propylene oxide tends to be relatively broad. Further, al-added Al described in JP-B-6-15038 3+ 、Ga 3+ 、In 3+ 、Tl 3+ 、Co 3+ 、Sc 3+ 、La 3+ 、Mn 2+ When ethylene oxide or propylene oxide is added to the above-mentioned hydrocarbon-based raw material, the specific alkoxylation catalyst such as magnesium oxide of a metal ion tends to have a relatively narrow distribution.
(a2) The component (a) may be a commercially available product, or may be obtained by adding at least ethylene oxide of ethylene oxide and propylene oxide to a commercially available raw material (higher primary or secondary alcohol, higher fatty acid, higher fatty amide, etc.) by a known method.
Specific examples of the component (a 2) include those obtained by adding ethylene oxide in an amount of 12 molar equivalents or 15 molar equivalents to an alcohol such as Diadol (registered trademark) (trade name, C13, C represents the number of carbon atoms) manufactured by mitsubishi chemical corporation, neodol (registered trademark) (trade name, a mixture of C12 and C13) manufactured by Shell, safol (registered trademark) 23 (trade name, a mixture of C12 and C13) manufactured by Sasol corporation; ethylene oxide is added to a natural alcohol such as CO-1214 (trade name) or CO-1270 (trade name) manufactured by P & G company in an amount of 12 mol equivalents or 15 mol equivalents; ethylene oxide was added to a secondary alcohol having 12 to 14 carbon atoms in an amount of 15 molar equivalents (Softanol (registered trademark) 150 (trade name) manufactured by japan catalyst corporation); and (c) a method in which 15 molar equivalents of ethylene oxide (polyoxyethylene coconut fatty acid methyl ester (EO 15 mol)) is added to coconut fatty acid methyl ester (lauric acid/myristic acid = 8/2) using an alkoxylation catalyst.
(A) The components can be used alone in 1 kind, also can be combined with more than 2 kinds.
When 2 or more kinds are used in combination, only the component (A1) may be used, only the component (A2) may be used, or both the component (A1) and the component (A2) may be used.
The component (A) preferably contains the component (A1) from the viewpoint of improving detergency when used in combination with the component (B) due to the deodorizing effect. More than 2 kinds of the component (A1) may be used in combination.
Component (a) preferably contains component (A2) from the viewpoint of deodorizing effect and rinsing property (residual property in a textile). When the component (A2) is contained, it is suitable for a treatment without rinsing as described later. More than 2 kinds of the component (A2) may be used in combination.
< ingredient (B) >
(B) The component (A) is an alkylene oxide adduct of polyalkyleneimine.
The composition can impart a deodorant effect to a textile product by containing the component (B).
The polyalkyleneimine is represented by the following formula (b 1), for example.
NH 2 -R 5 -[N(A 1 )-R 5 ] n -NH 2 ···(b1)
In the formula (b 1), R 5 Each independently an alkylene group having 2 to 6 carbon atoms, A 1 Is a hydrogen atom or is based on a branched other polyamine chain, n is a number above 1. Wherein, A is 1 Not all are hydrogen atoms. That is, the polyalkyleneimine represented by the formula (b 1) has a branched polyamine chain in the structure.
As R 5 Examples thereof include a linear alkylene group having 2 to 6 carbon atoms and a branched alkylene group having 3 to 6 carbon atoms. As R 5 The alkylene group having 2 to 4 carbon atoms is preferable, and the alkylene group having 2 carbon atoms is more preferable.
For example, 1 or more kinds of alkyleneimines (alkylene imines) having 2 to 6 carbon atoms are polymerized by a conventional method to obtain a polyalkyleneimine. Examples of the alkyleneimine having 2 to 6 carbon atoms include ethyleneimine, propyleneimine, 1,2-buteneimine, 2,3-buteneimine, 1,1-dimethylethyleneimine.
The polyalkyleneimine is preferably polyethyleneimine (hereinafter also referred to as "PEI") or polypropyleneimine, and more preferably PEI. PEI is obtained by polymerizing ethyleneimine, and has a branched structure containing nitrogen atoms of primary amine, secondary amine, and tertiary amine in its structure.
The weight average molecular weight of the polyalkyleneimine is preferably 200 to 2000, more preferably 300 to 1500, further preferably 400 to 1000, and particularly preferably 500 to 800.
The polyalkyleneimine preferably has 5 to 30 active hydrogens in 1 molecule thereof, more preferably 7 to 25 active hydrogens, and further preferably 10 to 20 active hydrogens.
(B) The component (B) is obtained by adding an alkylene oxide to a polyalkyleneimine. Examples of the method include a method in which an alkylene oxide such as ethylene oxide is added to a polyalkyleneimine as a starting material in the presence of a basic catalyst such as sodium hydroxide, potassium hydroxide, or sodium methoxide at 100 to 180 ℃.
Examples of the alkylene oxide include alkylene oxides having 2 to 4 carbon atoms such as ethylene oxide, propylene oxide and butylene oxide, preferably ethylene oxide and propylene oxide, and more preferably ethylene oxide.
Examples of the component (B) include an ethylene oxide adduct of polyalkyleneimine, a propylene oxide adduct of polyalkyleneimine, and an ethylene oxide-propylene oxide adduct of polyalkyleneimine. The ethylene oxide-propylene oxide adduct of polyalkyleneimine is obtained by adding ethylene oxide and propylene oxide to polyalkyleneimine, and the addition order and addition form (block form, random form) of ethylene oxide and propylene oxide to polyalkyleneimine are arbitrary.
The component (B) is preferably an ethylene oxide adduct of polyalkyleneimine or an ethylene oxide-propylene oxide adduct of polyalkyleneimine, and more preferably an ethylene oxide adduct of polyalkyleneimine, from the viewpoint of a deodorizing effect.
The component (B) is preferably one obtained by adding 5 to 40 alkylene oxides on average, more preferably 8 to 30 alkylene oxides on average, still more preferably 10 to 30 alkylene oxides on average, and particularly preferably 10 to 20 alkylene oxides on average to 1 atom of active hydrogen of the raw material polyalkyleneimine. That is, the average amount of the alkylene oxide added is preferably 5 to 40 mol, more preferably 8 to 30 mol, even more preferably 10 to 30 mol, and particularly preferably 10 to 20 mol, based on 1 mol of active hydrogen contained in the raw material polyalkyleneimine.
Examples of the component (B) include compounds represented by the formula (B1-1).
In the formula (b 1-1), R 22 Each independently an alkylene group having 2 to 6 carbon atoms, and each m independently represents a number of 1 or more.
R 22 The alkylene group having 2 or 3 carbon atoms is preferable, and the alkylene group having 2 carbon atoms is more preferable.
m represents (R) 22 O) average number of repetitions. Each m is independently preferably a number of 5 to 40, more preferably a number of 8 to 30, further preferably a number of 10 to 30, and particularly preferably a number of 10 to 20.
(B) The weight average molecular weight of the component (B) is preferably 1000 to 80000, more preferably 2000 to 50000, still more preferably 5000 to 30000, particularly preferably 10000 to 20000.
The weight average molecular weight in the present specification is a value obtained by gel permeation chromatography using polyethylene glycol as a standard substance.
As the component (B), synthetic products may be used, or commercially available products may be used. Examples of the commercially available product include a product name "Sokalan (registered trademark) HP20" manufactured by BASF corporation.
< optional Components >
Examples of the optional component include a surfactant (optional surfactant) other than component (a), an antibacterial agent, a water-miscible organic solvent, an organic acid, a viscosity reducing agent (solubilizer), an alkalizing agent, a metal ion capturing agent, an antioxidant, a preservative, an enzyme (protease, lipase, cellulase, etc.), an enzyme stabilizer, a texture improving agent, an alkali builder (alkanolamine, etc.), a hydrotropic agent, a fluorescent brightener, an anti-migration agent, a redeposition inhibitor, a pearling agent, a soil releasing agent, an odorant, a colorant, an emulsifier, an extract of a natural product, a pH adjuster, and the like. These components can be used alone in 1 kind, also can be combined with more than 2 kinds.
Examples of the optional surfactant include a cationic surfactant, an amphoteric surfactant, and a semipolar surfactant.
Examples of the cationic surfactant include alkyltrimethylammonium salts, dialkyldimethylammonium salts, alkylbenzyldimethylammonium salts, and alkylpyridinium salts (alkyl pyridinium salts). Examples of the counter ion of these salts include a halogen ion and an alkylsulfate ion. Examples of the halogen ion include a fluorine ion, a chlorine ion, a bromine ion, and an iodine ion. The alkylsulfate ion is preferably an alkyl group having 1 to 3 carbon atoms, and examples thereof include methylsulfate ion and ethylsulfate ion.
Examples of the amphoteric surfactant include alkylcarboxylbetaines (alkylcarboxybetaines), alkylsulfobetaines (alkylsulfobetaines), alkylhydroxysultaines, alkylamidobetaines (alkylamidobetaines), imidazolinium betaines (imidazolinium betaines), and the like.
Examples of the semipolar surfactant include lauryl dimethyl amine oxide and laurylaminopropyldimethyl amine oxide (laurylaminopropylimine oxide) which are amine oxide type surfactants.
From the viewpoint of suppressing the proliferation of bacteria on the fiber product and suppressing the generation of unpleasant odor, an antibacterial agent may be used. The antimicrobial agent may be a degerming agent. Examples of the antibacterial agent include organic antibacterial agents such as biphenyl, alcohol, phenol, aldehyde, carboxylic acid, ester, ether, nitrile, peroxide, epoxy, halogen, pyridine, quinoline, triazine, isothiazolinone, imidazole, thiazole, aniline, biguanide, disulfide, thiocarbamate, saccharide, tropolone, and organometallic antibacterial agents; inorganic antibacterial agents such as metal oxides and silver. Specific examples thereof include triclosan, zinc bis (2-thio-1-pyridineoxide) (zinc pyrithione), polyhexamethylene biguanide hydrochloride, 8-hydroxyquinoline, and polylysine.
In the present invention, the water-miscible organic solvent means an organic solvent in which 50g or more is dissolved in 1L of ion-exchanged water at 25 ℃.
By mixing a water-miscible organic solvent, the stability and the preservative ability of the composition during storage at low temperatures can be improved.
Examples of the water-miscible organic solvent include alcohols such as ethanol, 1-propanol, 2-propanol and 1-butanol, glycols such as propylene glycol, butylene glycol and hexylene glycol, polyglycols such as dipropylene glycol, diethylene glycol monobutyl ether (butyl carbitol), diethylene glycol dimethyl ether, alkyl ethers such as 3-methoxy-3-methyl-1-butanol, and phenoxyethanol. Among them, ethanol, propylene glycol, diethylene glycol monobutyl ether (butyl carbitol), 3-methoxy-3-methyl-1-butanol, and phenoxyethanol are preferable from the viewpoints of availability, liquid stability of the composition, fluidity, and the like.
The stability of the present composition during storage at low temperatures can be improved by mixing a viscosity reducing agent (solubilizer).
Examples of the viscosity reducer include triethylene glycol, tetraethylene glycol, polyethylene glycol having an average molecular weight of about 200, polyethylene glycol having an average molecular weight of about 400, polyethylene glycol having an average molecular weight of about 1000, glycols such as dipropylene glycol, p-toluenesulfonic acid, cumene sulfonate (cumene sulfonate), benzoate, urea, and the like. Examples of the salt of cumene sulfonate and benzoate include sodium salt, potassium salt, and calcium salt.
Examples of the metal ion scavenger (chelating agent) include malonic acid, succinic acid, malic acid, diglycolic acid, tartaric acid, citric acid, and the like.
Examples of the antioxidant include butylated hydroxytoluene, distyrenated cresol, sodium sulfite, and sodium bisulfite.
Examples of the preservative include "Kathon CG" (trade name) manufactured by the Dow chemical company, "Acticide MBS" (trade name) manufactured by the Thor Japan company, and "NIPACIDE BIT 20" (trade name) manufactured by the Clariant company.
Examples of the soil release agent include water-soluble polymers having at least 1 unit selected from an alkylene terephthalate unit and an alkylene isophthalate unit and at least 1 unit selected from an oxyalkylene unit and a polyoxyalkylene unit, as described in PCT patent publication WO 2014/109380. Specific examples thereof include those commercially available under the trade name: texCare SRN-100 (manufactured by Clariant Japan, weight-average molecular weight: 2000 to 3000), trade name: texCare SRN-300 (manufactured by Clariant Japan, weight average molecular weight: 7000), trade name: reel-O-Tex Crystal (manufactured by Rodia corporation), trade name: and (3) a component sold by Rebel-O-Tex QCL (manufactured by Rodiya corporation).
Examples of the perfuming agent include perfume components described in Japanese patent application laid-open No. 2002-146399, and the like. The perfume component may be used alone in 1 kind, or may be used in combination in 2 or more kinds.
Examples of the coloring agent include general-purpose pigments and pigments such as acid Red 138, polar Red RLS, acid yellow 203, acid blue 9, blue No. 1, blue No. 205, green No. 3, red No. 106, yellow No. 203, and Turquoise P-GR (both trade names).
Examples of the pH adjuster include alkanolamines such as sulfuric acid, hydrochloric acid, phosphoric acid, sodium hydroxide, potassium hydroxide, monoethanolamine, diethanolamine, and triethanolamine, and ammonia. Among them, sulfuric acid, sodium hydroxide, potassium hydroxide, and alkanolamines are preferable, and sulfuric acid and sodium hydroxide are more preferable, from the viewpoint of improving the stability of the present composition over time of Yi Di. The pH adjuster may be used alone in 1 kind, or in combination with 2 or more kinds.
< contents of respective ingredients >
The content of the component (a) in the total mass of the present composition is more than 0 mass% and 10 mass% or less, preferably 0.1 to 10 mass%, more preferably 0.3 to 8 mass%, and still more preferably 0.5 to 5 mass%. When the content of the component (A) is not less than the lower limit, the composition is excellent in permeability into a textile product and is easy to obtain a deodorizing effect. When the content of component (A) is not more than the above upper limit, the adsorption amount of component (A) to the fiber product is small, component (B) as a deodorizing component is likely to remain in the fiber product, and the deodorizing effect is excellent when the fiber product is treated with the present composition.
The content of the component (B) in the total mass of the present composition is 0.5 to 10 mass%, preferably 0.8 to 8 mass%, more preferably 2 to 5 mass%. When the content of the component (B) is not less than the lower limit, the deodorizing effect is excellent. If the content of the component (B) is not more than the upper limit, the composition is less likely to turn yellow and has excellent appearance stability.
(B) The mass ratio of component/(A) (hereinafter also referred to as "B/A ratio") is 0.1 or more, preferably 0.3 or more, and particularly preferably 0.5 or more. If the B/A ratio is not less than the lower limit, the deodorizing effect is excellent.
The upper limit of the B/A ratio is, for example, 100, preferably 30, more preferably 10, and particularly preferably 1. If the B/A ratio is not more than the upper limit, the permeability of the component (B) into the laundry is excellent.
The B/a ratio may be 0.1 to 100, or 0.1 to 30, or 0.3 to 30, or 0.5 to 10, or 0.5 to 1.
The content of water is not particularly limited, but is preferably 70 to 99% by mass, more preferably 75 to 95% by mass, and still more preferably 80 to 90% by mass, based on the total mass of the present composition.
The content of the optional component is preferably 30% by mass or less, more preferably 10% by mass or less, based on the total mass of the present composition.
When the composition contains an antibacterial agent, the content of the antibacterial agent may be selected according to the type of the antibacterial agent. For example, in the case of an organic antibacterial agent such as a biphenyl-based antibacterial agent, the content thereof is preferably 0.01 to 1% by mass, more preferably 0.01 to 0.5% by mass, based on the total mass of the present composition.
When the present composition contains a water-miscible organic solvent, the content of the water-miscible organic solvent is preferably 0.1 to 10% by mass, more preferably 1 to 5% by mass, based on the total mass of the present composition.
When the present composition contains a viscosity reducing agent, the content of the viscosity reducing agent is preferably 0.01 to 10% by mass, more preferably 1 to 5% by mass, based on the total mass of the present composition.
When the present composition contains a metal ion scavenger, the content of the metal ion scavenger is preferably 0.1 to 10% by mass based on the total mass of the present composition.
When the present composition contains an antioxidant, the content of the antioxidant is preferably 0.01 to 2% by mass based on the total mass of the present composition.
When the present composition contains a preservative, the content of the preservative is preferably more than 0% by mass and 1% by mass or less based on the total mass of the present composition.
When the present composition contains an aromatizing agent, the content of the aroma is preferably 0.01 to 2% by mass based on the total mass of the present composition.
When the present composition contains a colorant, the content of the colorant is preferably 0.00005 to 0.005% by mass based on the total mass of the present composition.
<pH>
The pH of the present composition at 25 ℃ is preferably 5 to 9, more preferably 6 to 8. If the pH is within the preferred range, skin irritation can be reduced.
The pH can be measured by a pH meter (for example, "HM-30G" (product name) manufactured by Toyo DKK).
In a preferred embodiment, the composition comprises component (A), component (B), water, a viscosity-reducing agent and a water-miscible organic solvent, and has a pH of 5 to 9 at 25 ℃. In this embodiment, the preferable content of each component and the more preferable range of pH are as described above.
(method of treating textile product)
In the method for treating a textile product of the present invention, first, the textile product is immersed in the treatment liquid obtained by diluting the present composition with water, and then dehydrated.
Examples of the textile products include clothing, rags, sheets, curtains, pillow cases, and the like.
The material of the fiber product is not particularly limited, and examples thereof include natural fibers such as cotton, silk and wool, and chemical fibers such as polyester and polyamide.
The treatment liquid can be prepared by adding the present composition to water.
The amount of the present composition to be mixed with water is preferably 10 to 50mL per 30L of water, for example.
The proportion of the present composition to the total mass of the treatment liquid is preferably 0.01 to 0.3 mass%, more preferably 0.02 to 0.2 mass%.
If necessary, a known bleaching agent or softening agent may be added to the treatment liquid.
The content of the bleaching agent in the treatment liquid is not particularly limited. The bleaching agent is preferably added in an amount of, for example, 10 to 50mL per 30L of water. The proportion of the bleaching agent to the total mass of the treatment liquid is preferably 0.01 to 0.3 mass%, and more preferably 0.02 to 0.2 mass%. The content of the softening agent in the treatment liquid is not particularly limited. The ratio of the softening agent to the total mass of the treatment liquid is preferably 0.01 to 0.3 mass%, more preferably 0.02 to 0.3 mass%.
The fiber product can be treated with a known bleaching agent or softening agent before being treated with the treatment liquid (immersed and dehydrated in the treatment liquid). As a treatment method using a known bleaching agent or softening agent, there may be mentioned a method in which a bleaching agent or softening agent is dissolved in water in advance, a fiber product is immersed in the solution, and the fiber product taken out is washed in a washing machine or the like; a method of applying a bleaching agent or a softening agent to a textile, leaving the textile in place, and then washing the textile, and the like.
When the fiber product is immersed in the treatment liquid, the bath ratio of the mass of the treatment liquid to the mass of the fiber product (mass of the treatment liquid/mass of the fiber product) is preferably 5 to 50 times, and more preferably 15 to 25 times. If the bath ratio is within the above-mentioned preferable range, the deodorizing effect can be easily and stably imparted.
After the fiber product is impregnated in the treatment liquid, the treatment liquid may be left as it is or may be stirred. The composition can be used to replace detergent for washing fiber products in a washing machine. When the washing machine is used, the washing machine may be in a normal washing mode or in a mode in which the stirring force is weak, such as a soft washing mode. The present composition can be coated on a fibrous article and placed in place and then washed in a washing machine.
When the washing machine is used, dehydration can be continuously performed after washing.
The fiber product immersed in the treatment liquid may be dewatered and then rinsed with rinsing water, but from the viewpoint of the deodorizing effect, it is preferable to dry the fiber product without rinsing. When a washing machine is used, it is also preferable not to perform washing or rinsing after dehydration. By drying without rinsing, the component (B) is likely to remain in the textile product, and a more excellent deodorizing effect can be obtained.
The drying method may be a general drying method for a fiber product, and examples thereof include air drying, drying using a dryer (a clothes dryer, a bathroom dryer, etc.), and the like.
[ examples ] A method for producing a compound
The present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.
The materials used in the examples are as follows.
< materials used >
[ COMPONENT (A) ]
A-1: polyoxyethylene alkyl ether sulfate (polyoxyethylene alkyl ether sulfate salt, R in the formula (a 1)) 1 Is a linear alkyl group having 12 and 14 carbon atoms, j is 2, k is 0, M + A compound that is sodium ion. Kao Indonesia Chemicals, inc., trade name "EMAL 270").
A-2: a linear alkylbenzene sulfonate having an alkyl group having 10 to 14 carbon atoms (trade name "Lipon (registered trademark) LH-200" manufactured by lion Wang Zhushi).
A-3: polyoxyethylene alkyl (C12-C14) ether (average number of moles of ethylene oxide added)15 (15 molar equivalents of ethylene oxide added to natural alcohol). R in the formula (a 2) 2 Is a compound wherein at least 1 alkyl group selected from the group consisting of an alkyl group having 12 carbon atoms and an alkyl group having 14 carbon atoms, s is 15, t is 0, and X is O. Lion Wang Zhushi, trade name "LMAO").
A-4: polyoxyethylene fatty acid methyl ester (fatty acid having 12 to 14 carbon atoms and having an average number of moles of ethylene oxide added of 15) (in the formula (a 2), R 2 Is at least 1 alkyl selected from alkyl with 11 carbon atoms and alkyl with 13 carbon atoms, R 3 Is a compound in which s is 15, t is 0 and X is COO. Narrow ratio (narrow ratio) 30% by mass. Shi Wang Zhushi, trade name "MEE".
A-5: polyoxyethylene alkyl (12 to 14 carbon atoms) ether (average number of moles of ethylene oxide added 12) 'AE (12 EO)' (natural alcohol added with 12 molar equivalents of ethylene oxide in the formula (a 2), R 2 Is at least 1 alkyl selected from alkyl with 12 carbon atoms and alkyl with 14 carbon atoms, R 3 Is a hydrogen atom, X is O, s is 12, and t is 0.
[ COMPONENT (B) ]
B-1: an ethylene oxide adduct of polyethyleneimine (trade name "Sokaran HP20" manufactured by BASF corporation, the number of active hydrogens of polyethyleneimine in 1 molecule: 20, the average molar number of addition of ethylene oxide to 1 atom of active hydrogen: 20, and weight average molecular weight 14500).
[ Arbitrary ingredients ]
Antimicrobial agents: 5-chloro-2- (4-chlorophenoxy) phenol (common name: dichloro), manufactured by BASF corporation, under the trade name "Tinosan HP100".
Solvent 1: polyethylene glycol #1000 (trade name "PEG #1000-L60" manufactured by Mitsui chemical Co., ltd.).
Solvent 2: 3-methoxy-3-methyl-1-butanol (manufactured by Colorado corporation, trade name "Solfit").
Solvent 3: phenoxyethanol (manufactured by Sanyo chemical industries, ltd., trade name "Newpol EFP").
Na benzoate: sodium benzoate (manufactured by Toyao synthetic Co., ltd.).
Ethanol: ethanol (manufactured by JAPAN ALCOHOL sales co., ltd., trade name "specific 95 degree synthetic ethanol").
pH adjuster: sulfuric acid (available from Toyo chemical Co., ltd.), and sodium hydroxide (available from Toyo chemical Co., ltd.).
Perfuming agents: a perfume composition A described in tables 11 to 18 of JP-A-2002-146399.
[ WATER ] A pharmaceutical composition
Water: and (5) refining the water.
< examples 1 to 15 and comparative examples 1 to 3>
[ PREPARATION OF FIBER-PRODUCT TREATING AGENT COMPOSITION ]
Fiber product treating agent compositions of examples 1 to 15 and comparative examples 1 to 3 were prepared by adjusting the mixing amounts of the respective components as shown in tables 1 to 4 in the following manner.
The fiber product treating agent composition is obtained by mixing the component (A) and water uniformly, adding the component (B), stirring uniformly, adding an optional component, and stirring sufficiently.
In tables 1 to 4, the total amount of each component (mass%) is a ratio to the total mass of the fiber product treating agent composition, and indicates a value in terms of the pure component content unless otherwise specified. The "appropriate amount" means that the pH adjusting agent was mixed so that the pH of the fiber product treating agent composition at 25 ℃ became the values shown in tables 1 to 4. "balance" means that water is mixed so that the total mixing amount (mass%) of all the mixed components contained in the fiber product treating agent composition of each example is 100 mass%. That is, the amount of water is the remainder obtained by subtracting the total amount (in terms of purity) of the components to be mixed other than water from the total mass of the fiber product treating agent composition.
[ PREPARATION OF TEST CLOTH ]
Test cloths for odor evaluation were produced in the following order.
First, the test cloth was cleaned in the following procedure.
In a full-automatic electric washing machine (product name "JW-K33F" manufactured by hel corporation), about 30g of cotton knitted fabric (product name "CK43202" manufactured by riqing textile co., ltd., purchased from koku shop) and about 500g of cotton shirt (manufactured by b.v. d) were put, and the total mass of all the cloths to be washed was adjusted so as to be about 500g (bath ratio (washing water/total mass of cloths to be washed) in total).
Next, 10mL of a liquid detergent was added, and the washing operation of washing, rinsing, and dewatering was performed in this order according to the standard procedure. The washing time, rinsing, dewatering, and water volume (set to a low level, water volume of about 15L) were not adjusted at all, and were set using the standard program of the washing machine. This washing operation was repeated 5 times.
After the completion of the washing, the cotton knitted fabric taken out was dried in a constant temperature and humidity chamber having a humidity of 65% RH at 25 ℃. After drying, the test cloth was cut into a 5X 5cm square.
[ treatment based on fiber product treatment agent composition ]
The fiber product treatment agent composition was stirred at a ratio of 25mL to 30L of water for 30 seconds to prepare a treatment solution.
Next, a Terg-O-meter (manufactured by UNITED STATES TESTING) was prepared as a cleaning tester. The 5 test cloths and cotton shirts (manufactured by b.v.d) were put into a washing tester together with 900mL of the treatment liquid, and stirred at 120rpm and 15 ℃ for 10 minutes at a bath ratio of 20 times. Then, the test cloth and the cotton shirt were taken out, transferred to a dehydration tank of a two-tub washing machine (manufactured by TOSHIBA Co., ltd., product number: VH-30S (H)), dehydrated for 1 minute, and air-dried.
[ evaluation of deodorant Effect of body odor ]
On a test cloth treated with the fiber product treating agent composition, 200. Mu.L of a nonanoic acid solution diluted with 95 ℃ ethanol to 1000ppm was dropped as a body odor model. After 30 minutes, the odor intensity of the test cloths was evaluated organoleptically by a 6-person panel according to the 6-scale criteria described below. The lower the score of odor intensity, the weaker the odor, and the higher the odor-preventing effect (effect of suppressing body odor generation) indicating body odor.
Evaluation criteria for sensory evaluation "
And 5, dividing: the smell is strong.
And 4, dividing: the smell is strong.
And 3, dividing: can smell the smell easily.
And 2, dividing: weak odor if not present.
1 minute: the smell can be smelled only by exerting force.
0 minute: has no odor.
The average value of scores of odor intensity of 6 panelists was calculated (rounded to the second decimal place), and the odor-preventing effect was judged according to the following criteria. The evaluation was judged as good or good. The results are shown in tables 1 to 3.
Determination standard of deodorization effect "
Very good: the average odor intensity score was less than 2.5 points.
Good: the average value of the odor intensity score is more than 2.5 points and less than 3.0 points.
And (delta): the average value of the odor intensity score is 3.0 or more.
[ TABLE 1 ]
[ TABLE 2 ]
[ TABLE 3 ]
[ TABLE 4 ]
In examples 1 to 15, the excellent deodorizing effect can be imparted to the test cloth by a simple operation.
On the other hand, the deodorizing effect of comparative example 1 was poor. Since the component (a) is not contained, it is considered that the component (B) hardly permeates into the test cloth, and the component (B) hardly remains in the test cloth after the treatment.
In comparative example 2, since the component (B) was not contained, the deodorizing effect was poor.
The deodorizing effect of comparative example 3 was poor. It is considered that since the content of the component (a) is more than 10% by mass, the component (a) is selectively adsorbed on the test cloth, and the component (B) hardly remains on the test cloth after the treatment.
[ Industrial Applicability ]
According to the present invention, it is possible to provide a fiber product treating agent composition capable of imparting an excellent deodorizing effect to a fiber product, and a fiber product treating method capable of imparting an excellent deodorizing effect to a fiber product by a simple operation.
Claims (4)
1. A fiber product treating agent composition comprising a component (A) which is at least 1 selected from an anionic surfactant and a nonionic surfactant and a component (B) which is an alkylene oxide adduct of polyalkyleneimine,
the content of the component (A) in the total mass of the fiber product treating agent composition is more than 0 mass% and 10 mass% or less,
the content of the component (B) in the total mass of the fiber product treating agent composition is 0.5 to 10% by mass,
the mass ratio of the component (B) to the component (A) is 0.1 or more.
2. The fiber product treatment composition according to claim 1, wherein the (a) component comprises the anionic surfactant.
3. The fiber product treating agent composition according to claim 1 or 2, wherein the (B) component is an ethylene oxide adduct of polyalkyleneimine.
4. A method for treating a textile, characterized in that the textile is immersed in a treatment solution obtained by diluting the textile treatment agent composition according to any one of claims 1 to 3 with water, dewatered, and dried without rinsing.
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JP2018003196A (en) * | 2016-07-01 | 2018-01-11 | ライオン株式会社 | Deodorant composition for fiber product |
CN108699493A (en) * | 2016-02-16 | 2018-10-23 | 狮王株式会社 | Detergent composition |
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DE10124387A1 (en) * | 2001-05-18 | 2002-11-28 | Basf Ag | Hydrophobically modified polyethyleneimine and polyvinylamine as anticrease agents for treatment of cellulose containing textiles, useful as textile finishing agents in both solid and liquid formulations |
JP2003020571A (en) * | 2001-07-10 | 2003-01-24 | Nippon Shokubai Co Ltd | Fiber-finishing agent |
KR20140091015A (en) * | 2011-11-10 | 2014-07-18 | 닛폰 에쿠스란 고교 가부시키가이샤 | Moisture-absorbing deodorizing fibers, method for producing fibers, and fiber structure comprising fibers |
JP6832181B2 (en) * | 2016-02-16 | 2021-02-24 | ライオン株式会社 | Textile washing methods and textile processing kits |
JP2017200972A (en) | 2016-05-06 | 2017-11-09 | ライオン株式会社 | Liquid detergent composition |
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