JPH0641870A - Textile structure with ph buffering nature - Google Patents
Textile structure with ph buffering natureInfo
- Publication number
- JPH0641870A JPH0641870A JP22513192A JP22513192A JPH0641870A JP H0641870 A JPH0641870 A JP H0641870A JP 22513192 A JP22513192 A JP 22513192A JP 22513192 A JP22513192 A JP 22513192A JP H0641870 A JPH0641870 A JP H0641870A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- fabric
- value
- buffering
- mol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 230000003139 buffering effect Effects 0.000 title claims abstract description 35
- 239000004753 textile Substances 0.000 title abstract 5
- 239000002253 acid Substances 0.000 claims abstract description 16
- 229920001577 copolymer Polymers 0.000 claims abstract description 14
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 6
- 239000000835 fiber Substances 0.000 claims description 23
- 229920000642 polymer Polymers 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 12
- 230000001747 exhibiting effect Effects 0.000 claims description 2
- 239000004744 fabric Substances 0.000 abstract description 48
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 20
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract description 15
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 abstract description 9
- 159000000000 sodium salts Chemical class 0.000 abstract description 7
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 abstract description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract description 3
- 229920002994 synthetic fiber Polymers 0.000 abstract description 3
- 239000012209 synthetic fiber Substances 0.000 abstract description 3
- 239000004745 nonwoven fabric Substances 0.000 abstract description 2
- 230000002378 acidificating effect Effects 0.000 abstract 3
- 239000000463 material Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 description 21
- 239000007788 liquid Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 12
- 229920000728 polyester Polymers 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000012986 chain transfer agent Substances 0.000 description 11
- 238000000576 coating method Methods 0.000 description 11
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 238000012545 processing Methods 0.000 description 9
- 238000005406 washing Methods 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000002759 woven fabric Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000004925 Acrylic resin Substances 0.000 description 6
- 229920000178 Acrylic resin Polymers 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 239000012153 distilled water Substances 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000003916 acid precipitation Methods 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000006174 pH buffer Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000003672 processing method Methods 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- -1 wool and silk Polymers 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004373 Pullulan Substances 0.000 description 1
- 229920001218 Pullulan Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- 229910026551 ZrC Inorganic materials 0.000 description 1
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 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
- 159000000007 calcium salts Chemical class 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 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
- 238000004898 kneading Methods 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- ZIWDVJPPVMGJGR-UHFFFAOYSA-N n-ethyl-2-methylprop-2-enamide Chemical compound CCNC(=O)C(C)=C ZIWDVJPPVMGJGR-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000006179 pH buffering agent Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明はpH緩衝性を有する繊維
構造物に関する。TECHNICAL FIELD The present invention relates to a fiber structure having a pH buffering property.
【0002】[0002]
【従来の技術】合成繊維或は天然繊維の加工において強
酸或は強塩基で処理した場合、処理後弱酸或は弱塩基で
中和処理を実施するが、このような処理では繊維にpH
緩衝性を持たせることはできない。その他、通常用いら
れる帯電防止加工、樹脂加工等の加工でもpH緩衝性、
特に耐洗濯性のあるpH緩衝性を持たせることは困難で
ある。2. Description of the Related Art When synthetic fibers or natural fibers are treated with a strong acid or a strong base, neutralization is carried out with a weak acid or a weak base after the treatment.
It cannot be buffered. In addition, pH buffering is possible even in the commonly used antistatic processing, resin processing, etc.
In particular, it is difficult to provide a pH buffering property with washing resistance.
【0003】[0003]
【発明が解決しようとする問題点】本発明の目的とする
ところは繊維にpH緩衝作用を有する化合物を付着させ
ることにより、欧米で深刻化し日本でも影響が心配され
ている酸性雨に対し中和能を有する繊維構造物を提供す
ることにある。DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention An object of the present invention is to neutralize acid rain, which has become serious in Europe and the United States and may be affected in Japan, by attaching a compound having a pH buffering action to fibers. It is to provide a fiber structure having a function.
【0004】[0004]
【問題点を解決するための手段】本発明は、繊維構造物
の少なくとも繊維の表面上に酸として作用する物質とそ
の塩類が付着され、湿潤時にpH5〜7を示すことを特
徴とするpH緩衝性繊維構造物に関するものである。さ
らに、本発明は、酸として作用する物質とその塩類から
なる化合物がカルボキシル基及び塩形に中和されたカル
ボキシル基を含む重量平均分子量1,000〜1,00
0,000の重合体及び共重合体であるpH緩衝性繊維
構造物をその要旨とする。DISCLOSURE OF THE INVENTION The present invention provides a pH buffer characterized in that a substance acting as an acid and salts thereof are deposited on at least the surface of fibers of a fiber structure and exhibit a pH of 5 to 7 when wet. The present invention relates to a natural fiber structure. Furthermore, the present invention provides a compound comprising a substance acting as an acid and salts thereof, having a carboxyl group and a carboxyl group neutralized into a salt form, and having a weight average molecular weight of 1,000 to 1,000.
The gist is a pH buffering fibrous structure which is a polymer and a copolymer of 10,000.
【0005】本発明において繊維構造物とは、特に限定
されるものでなく、綿,羊毛,絹等の天然繊維、ポリエ
ステル,ナイロン,アクリル,アセテート等の化合繊の
すべてを含む織物、編物又は不織布等のすべてが含まれ
る。In the present invention, the fiber structure is not particularly limited, and includes woven fabrics, knitted fabrics or non-woven fabrics including all natural fibers such as cotton, wool and silk, and synthetic fibers such as polyester, nylon, acryl and acetate. Etc. are all included.
【0006】本発明においては、繊維構造物の少なくと
も繊維の表面上に酸として作用する物質とその塩類から
なる化合物が付着されていることが必要である。本発明
において酸として作用する物質とは水溶液中で水素イオ
ンを生じ、塩基を中和して塩を生ずるような物質で、例
えば、硫酸,塩酸,リン酸,酢酸,ギ酸,シュウ酸,酒
石酸,乳酸,クエン酸,マロン酸,コハク酸,アジピン
酸,アクリル酸,メタアクリル酸,オレイン酸,リノー
ル酸,安息香酸等があげられる。本発明において塩類と
はナトリウム塩,カリウム塩,カルシウム塩,バリウム
塩,リチウム塩等があげられる。In the present invention, it is necessary that a compound consisting of a substance acting as an acid and salts thereof is attached to at least the surface of the fiber of the fiber structure. In the present invention, the substance acting as an acid is a substance which produces hydrogen ions in an aqueous solution and neutralizes a base to produce a salt, such as sulfuric acid, hydrochloric acid, phosphoric acid, acetic acid, formic acid, oxalic acid, tartaric acid, Examples include lactic acid, citric acid, malonic acid, succinic acid, adipic acid, acrylic acid, methacrylic acid, oleic acid, linoleic acid and benzoic acid. In the present invention, the salts include sodium salt, potassium salt, calcium salt, barium salt, lithium salt and the like.
【0007】酸として作用する物質は弱酸特にカルボキ
シル基を含む化合物が好ましく用いられる。該化合物は
疎水性モノマー残基を含む不飽和カルボン酸の重合体、
共重合体、不飽和カルボン酸とエチレン性不飽和単量体
との共重合体、又は、これらの混合物である。重合度の
制御は公知の連鎖移動剤の添加量の変化で行う。上記重
合体、共重合体の分子量は1,000〜1,000,0
00、好ましくは10,000〜500,000であ
る。分子量はゲルパーミエーションクロマトグラフィに
より分子量既知の水溶性ポリマー、プルランを標準物質
として検量線を作成、これを利用して重量平均分子量を
求めた。不飽和カルボン酸とエチレン性不飽和単量体と
の共重合体は1〜10モル%のエチレン性不飽和単量体
を含有するものが好ましい。As the substance acting as an acid, a weak acid, particularly a compound containing a carboxyl group is preferably used. The compound is a polymer of unsaturated carboxylic acid containing a hydrophobic monomer residue,
It is a copolymer, a copolymer of an unsaturated carboxylic acid and an ethylenically unsaturated monomer, or a mixture thereof. The degree of polymerization is controlled by changing the addition amount of a known chain transfer agent. The molecular weight of the above polymers and copolymers is 1,000 to 1,000,0.
00, preferably 10,000 to 500,000. Regarding the molecular weight, a calibration curve was prepared by gel permeation chromatography using pullulan, which is a water-soluble polymer of known molecular weight, as a standard substance, and the weight average molecular weight was determined using this. The copolymer of unsaturated carboxylic acid and ethylenically unsaturated monomer preferably contains 1 to 10 mol% of ethylenically unsaturated monomer.
【0008】不飽和カルボン酸としては、例えばアクリ
ル酸,メタクリル酸,クロトン酸,オレイン酸,ケイ皮
酸,マレイン酸,フマル酸,シトラコン酸,メサコン酸
等を挙げることができる。エチレン性不飽和単量体とし
ては例えば2−ヒドロキシエチルアクリレート,2−ヒ
ドロキシエチルメタクリレート,ヒドロキシプロピルア
クリレート,アクリルアミド,N−メチルアクリルアミ
ド,N,N−ジメチルアクリルアミド,N−メチロール
アクリルアミド,N,N−ジヒドロキシエチルメタアク
リルアミド等を挙げることができる。好ましい重合体
は、アクリル酸と2−ヒドロキシエチルアクリレートの
共重合体,アクリル酸とN−メチロールアクリルアミド
の共重合体,アクリル酸と2−ヒドロキシエチルメタク
リレートとアクリルアミドとの共重合体等が挙げられ
る。該重合体は水酸化ナトリウム,水酸化カリウム等の
塩基によって所定のpH値まで中和された塩を形成す
る。Examples of unsaturated carboxylic acids include acrylic acid, methacrylic acid, crotonic acid, oleic acid, cinnamic acid, maleic acid, fumaric acid, citraconic acid and mesaconic acid. Examples of the ethylenically unsaturated monomer include 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, hydroxypropyl acrylate, acrylamide, N-methyl acrylamide, N, N-dimethyl acrylamide, N-methylol acrylamide, N, N-dihydroxy. Examples thereof include ethyl methacrylamide. Preferred polymers include copolymers of acrylic acid and 2-hydroxyethyl acrylate, copolymers of acrylic acid and N-methylol acrylamide, and copolymers of acrylic acid, 2-hydroxyethyl methacrylate and acrylamide. The polymer forms a salt neutralized to a predetermined pH value with a base such as sodium hydroxide or potassium hydroxide.
【0009】エチレン性不飽和単量体の含有効果はpH
緩衝性の洗濯耐久性の向上に役立つ。更にpH緩衝性の
洗濯耐久性を向上させるためには上記、重合体及び共重
合体に水溶性エポキシ化合物の添加が好ましい。The effect of containing the ethylenically unsaturated monomer is pH.
Helps to improve the durability of the buffered laundry. Further, in order to improve the washing durability of pH buffering property, it is preferable to add a water-soluble epoxy compound to the above-mentioned polymers and copolymers.
【0010】本発明の加工方法は特に限定されるもので
はなく、コーティング法,パットードライ法,パットー
スチーム法,スプレー法,浸漬法等、繊維構造物の少な
くとも繊維の表面に薄膜を形成できる方法であればよ
い。例えば樹脂加工法として通常行われているパットー
ドライ法において本発明の化合物を所定量含浸後搾液
し、100〜130℃で乾燥、150〜180℃で熱処
理することで耐久性にすぐれた付着が可能である。The processing method of the present invention is not particularly limited, and may be a method capable of forming a thin film on at least the surface of the fiber of the fiber structure, such as a coating method, a Patto dry method, a put steam method, a spray method and a dipping method. I wish I had it. For example, in the Patto dry method, which is usually used as a resin processing method, a compound having a predetermined amount of the compound of the present invention is impregnated, squeezed, dried at 100 to 130 ° C., and heat treated at 150 to 180 ° C. to achieve excellent adhesion. Is.
【0011】前述の加工方法において、コーティング方
法が特に好ましく、本発明で用いるコーティング樹脂と
して、アクリル樹脂,ウレタン樹脂,シリコン樹脂等を
挙げることができる。pH緩衝性は、多孔性樹脂におい
て効果が大きく、例えばウレタン系多孔性樹脂をあげる
ことができる。また、二酸化ケイ素,二酸化チタン,ア
ルミナ,ジルコニア,マグネシア,窒化チタン,炭化ジ
ルコニウム,酸化ジルコニウム等の多孔性粒子を樹脂に
練り込むことによりpH緩衝性効果を上げることができ
る。前記樹脂液のコーティング方法としては、乾式コー
ティング,湿式コーティングの何れでもよく、フローテ
ィングナイフコーター,ナイフオーバーロールコータ
ー,リバースロールコーター,ロールドクターコータ
ー,グラビアロールコーター,キスロールコーター等の
塗布方式が利用できる。又、コーティング皮膜を公知の
方法で多孔性のものとしてもよい。本発明では、コーテ
ィング加工のほかに、撥水,柔軟などの諸処理を施して
もよいことは勿論である。但し、撥水加工はコーティン
グ加工前あるいはコーティング加工後のどちらでも行え
るが、コーティング加工前に行う場合には、接着強度に
十分な注意を払う必要がある。Of the above-mentioned processing methods, the coating method is particularly preferable, and as the coating resin used in the present invention, acrylic resin, urethane resin, silicone resin and the like can be mentioned. The pH buffering effect is highly effective for porous resins, and examples thereof include urethane-based porous resins. Further, the pH buffering effect can be improved by kneading porous particles such as silicon dioxide, titanium dioxide, alumina, zirconia, magnesia, titanium nitride, zirconium carbide and zirconium oxide into the resin. The coating method of the resin liquid may be dry coating or wet coating, and a coating method such as a floating knife coater, a knife over roll coater, a reverse roll coater, a roll doctor coater, a gravure roll coater, and a kiss roll coater can be used. . Further, the coating film may be made porous by a known method. In the present invention, it goes without saying that various treatments such as water repellency and softness may be applied in addition to the coating process. However, the water-repellent treatment can be performed either before or after coating, but if it is performed before coating, it is necessary to pay sufficient attention to the adhesive strength.
【0012】本発明の適用において、繊維上への化合物
の付着量のコントロールは、水溶液中の化合物の濃度で
行うことができる。繊維上への化合物の付着量は固形分
換算で0.05〜5重量%が好ましい。付着量が0.0
5重量%以下では目的とするpH緩衝作用効果が得られ
にくく、好ましくない。一方5重量%を越えると処理布
の形態によっては風合が粗硬になるばかりか、他の加工
処理を行うのに妨げとなる傾向がでる。In the application of the present invention, the amount of the compound attached on the fiber can be controlled by the concentration of the compound in the aqueous solution. The amount of the compound deposited on the fiber is preferably 0.05 to 5% by weight in terms of solid content. Adhesion amount is 0.0
When it is 5% by weight or less, the desired pH buffering effect is difficult to obtain, which is not preferable. On the other hand, if it exceeds 5% by weight, not only does the texture become rough and hard depending on the form of the treated cloth, but it also tends to hinder other processing treatments.
【0013】[0013]
【実施例】以下、実施例を示して本発明を更に詳細に説
明する。実施例中のpH測定方法及び加工布帛の洗濯試
験は次の通りである。 (1)溶液のpH値測定は堀場製作所社製F−12pH
メーターで測定EXAMPLES The present invention will be described in more detail below with reference to examples. The pH measuring method and the washing test of the processed fabric in the examples are as follows. (1) The pH value of the solution is F-12pH manufactured by Horiba Ltd.
Measured with a meter
【0014】(2)布帛のpH緩衝性を評価するpH値
測定法Aは堀場製作所社製TwinB−112pHメー
ターの電極部に一定量の液体で湿潤させた布帛を接触さ
せて測定した。布帛の重量は0.02gとし、0.1ml
の液体で湿潤させpH値測定に供した。布帛を湿潤させ
る液は蒸留水及び酸又はアルカリで調製した溶液を用い
た。布帛のpH値を例えばpH3の液で湿潤したとき測
定した値が、蒸留水で湿潤したとき測定した値に近い程
pH緩衝性があると判断する。(2) The pH value measuring method A for evaluating the pH buffering property of the cloth was measured by bringing a cloth moistened with a certain amount of liquid into contact with the electrode part of Twin B-112 pH meter manufactured by Horiba Ltd. Fabric weight is 0.02g, 0.1ml
The sample was moistened with the above liquid and subjected to pH value measurement. As a liquid for wetting the cloth, a solution prepared with distilled water and an acid or an alkali was used. It is judged that the closer the pH value of the cloth when wet with a liquid having a pH of 3 is closer to the value measured when wet with distilled water, the more the pH buffering property is.
【0015】(3)布帛のpH緩衝性を評価するpH値
測定法Bは径約9cmのヌッチェの漏斗に2gの布帛を
のせ、布帛の上から蒸留水及び酸又はアルカリで調製し
た溶液50mlを注ぎ、布帛を濾過した濾液のpH値を測
定した。濾液のpH値が例えばpH4の溶液を注いだと
き測定した値が蒸留水を注いだときの値に近い程pH緩
衝性があると判断する。(3) The pH value measuring method B for evaluating the pH buffering property of cloth is 2 g of cloth placed on a funnel of Nutsche having a diameter of about 9 cm, and 50 ml of a solution prepared with distilled water and an acid or alkali is put on the cloth. The pH value of the filtrate after pouring and filtering the cloth was measured. The pH value of the filtrate is judged to be more pH buffering as the value measured when pouring a solution having a pH of 4 is closer to the value when pouring distilled water.
【0016】(4)洗濯試験 JIS L−0217
103法(4) Washing test JIS L-0217
103 method
【0017】(5)付着量(5) Adhesion amount
【数1】 [Equation 1]
【0018】実施例中「部」とは「重量部」を表し、透
湿度,耐水圧は、JIS−L−1099,JIS−L−
1092(A法)により測定した。In the examples, "part" means "part by weight", and the water vapor transmission rate and water pressure resistance are JIS-L-1099 and JIS-L-.
It was measured by 1092 (method A).
【0019】実施例1 ポリエステル織物に、アクリル酸(90モル%),ブタ
ジエン(10モル%)及び連鎖移動剤の組成でナトリウ
ム塩に中和された重量平均分子量85,000の重合体
と、アクリル酸(95モル%),2−ヒドロキシエチル
メタクリレート(5モル%)及び連鎖移動剤の組成で重
量平均分子量160,000の重合体を6:2の割合で
混合し、1.2重量%(対繊維)付与した。付与方法は
重合体の水溶液を調製した加工液に織物を浸漬し、マン
グルでしぼり、次いでピンテンター型の熱風乾燥機で乾
燥及び熱処理を行った。比較例1としてポリエステル織
物に吉村油化学社製PMX−56(帯電防止剤)の1.
5%水溶液を加工液として実施例1の付与方法と同じ方
法で加工した。加工布帛のpH値測定結果を表1に示
す。Example 1 A polyester woven fabric was polymerized with acrylic acid (90 mol%), butadiene (10 mol%) and a chain transfer agent, a polymer having a weight average molecular weight of 85,000 neutralized to a sodium salt, and an acrylic resin. A polymer having a composition of acid (95 mol%), 2-hydroxyethyl methacrylate (5 mol%) and a chain transfer agent and having a weight average molecular weight of 160,000 was mixed at a ratio of 6: 2 to obtain 1.2 wt% (vs. Fiber) added. As the application method, the woven fabric was dipped in a working liquid prepared by preparing an aqueous solution of a polymer, squeezed with a mangle, and then dried and heat-treated with a pintenter type hot air dryer. As Comparative Example 1, a polyester woven fabric containing 1. PMX-56 (antistatic agent) manufactured by Yoshimura Oil Chemical Co., Ltd. was used.
A 5% aqueous solution was used as a processing liquid and processed by the same method as the applying method of Example 1. The results of measuring the pH value of the processed fabric are shown in Table 1.
【0020】[0020]
【表1】 [Table 1]
【0021】表1の結果より本発明の加工布帛はpH3
の液に対して緩衝作用を示している。これに対し比較例
1の加工布帛は緩衝作用を示していない。このことは本
発明の加工布帛の緩衝作用の大きさ即ち緩衝容量が大き
いことを示している。From the results shown in Table 1, the processed fabric of the present invention has a pH of 3.
It shows a buffering effect on the liquid of. On the other hand, the processed fabric of Comparative Example 1 does not exhibit a cushioning effect. This indicates that the processed fabric of the present invention has a large buffering effect, that is, a large buffering capacity.
【0022】実施例2 ポリエステル織物に、アクリル酸(95モル%),ブタ
ジエン(10モル%)及び連鎖移動剤の組成でナトリウ
ム塩に中和された重量平均分子量85,000の重合体
と、アクリル酸(95モル%),2−ヒドロキシエチル
メタクリレート(2.5モル%),N−メチロールアク
リルアミド(2.5モル%)及び連鎖移動剤の組成で重
量平均分子量100,000の重合体を6:3の割合で
混合し、1.5重量%(対繊維)付与した。付与方法は
実施例1と同じ方法で行った。比較例2としてポリエス
テル織物に一方社油脂社製ELETAT AK−10
(帯電防止剤)の2%水溶液を加工液として実施例1の
付与方法と同じ方法で加工した。加工布帛のpH値測定
結果を表2に示す。Example 2 A polyester fabric was polymerized with a polymer having a weight average molecular weight of 85,000 neutralized to a sodium salt with a composition of acrylic acid (95 mol%), butadiene (10 mol%) and a chain transfer agent, and acrylic. An acid (95 mol%), 2-hydroxyethyl methacrylate (2.5 mol%), N-methylol acrylamide (2.5 mol%) and a chain transfer agent were used to prepare a polymer having a weight average molecular weight of 100,000 6: 6. The mixture was mixed in a ratio of 3 and added to 1.5% by weight (to the fiber). The application method was the same as in Example 1. As Comparative Example 2, a polyester woven fabric was manufactured by ELETAT AK-10 manufactured by Yushisha Co., Ltd.
A 2% aqueous solution of (antistatic agent) was used as a processing liquid and processed in the same manner as the applying method of Example 1. Table 2 shows the results of measuring the pH value of the processed fabric.
【0023】[0023]
【表2】 [Table 2]
【0024】表2の結果より比較例2の加工布帛はpH
3の液に対し緩衝作用を示していない。本発明の加工布
帛はpH3の液に対して緩衝作用を示している。From the results shown in Table 2, the processed fabric of Comparative Example 2 had a pH value of
It does not have a buffering effect on the solution of No. 3. The processed fabric of the present invention exhibits a buffering action for a liquid of pH 3.
【0025】実施例3 ポリエステル織物にアクリル酸(80モル%),マレイ
ン酸(10モル%),イソアミレン(10モル%)及び
連鎖移動剤の組成でカリウム塩に中和された重量平均分
子量50,000の重合体6重量%とアクリル酸(95
モル%)と2−ヒドロキシエチルメタアクリレート(5
モル%)及び連鎖移動剤の組成で重量平均分子量35
0,000の重合体2重量%及び、エチレングリコール
ジグリシジルエーテル3重量%の混合物の水溶液を加工
液として実施例1の付与方法と同じ方法で付与した。付
与後更に50℃の温湯で10分間湯洗を行った。比較例
3としてポリエステル織物に大日本インキ社製ベッカミ
ンAPM0.3重量%,キャタリスト376 0.3重
量%を加工液として実施例1と同じ方法で付与した。加
工布帛のpH値測定結果を表3に示す。Example 3 A polyester woven fabric was prepared by adding acrylic acid (80 mol%), maleic acid (10 mol%), isoamylene (10 mol%) and a chain transfer agent to the potassium salt to neutralize the weight average molecular weight of 50, 6% by weight of polymer and acrylic acid (95
Mol%) and 2-hydroxyethyl methacrylate (5
Mol%) and the composition of the chain transfer agent, the weight average molecular weight of 35
An aqueous solution of a mixture of 2% by weight of a polymer of 50,000 and 3% by weight of ethylene glycol diglycidyl ether was applied as a working fluid in the same manner as in Example 1. After application, it was washed with hot water at 50 ° C. for 10 minutes. As Comparative Example 3, 0.3% by weight of Beckamine APM manufactured by Dainippon Ink and 0.3% by weight of Catalyst 376 were applied as processing liquids to a polyester fabric in the same manner as in Example 1. Table 3 shows the results of measuring the pH value of the processed fabric.
【0026】[0026]
【表3】 [Table 3]
【0027】表3の結果より比較例3では緩衝作用が得
られないが実施例3では緩衝作用が得られている。実施
例3では、水溶性エポキシ化合物の添加によって洗濯耐
久性が更に向上している。From the results shown in Table 3, the buffering effect is not obtained in Comparative Example 3, but the buffering effect is obtained in Example 3. In Example 3, the washing durability was further improved by adding the water-soluble epoxy compound.
【0028】実施例4 経,緯40番綿糸よりなる平織を実施例1に示されてい
る加工液を用いて実施例1と同じ付与方法で加工を行っ
た。比較例4として上記綿織物に、第一工業製薬社製ス
ーパーフレックスE2000 3重量%を加工液として
実施例1と同じ方法で付与した。加工布帛のpH値測定
結果を表4に示す。Example 4 A plain weave composed of warp and weft 40 cotton yarn was processed by the same application method as in Example 1 using the processing liquid shown in Example 1. As Comparative Example 4, 3% by weight of Superflex E2000 manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd. was applied as a processing liquid to the above cotton fabric in the same manner as in Example 1. Table 4 shows the results of measuring the pH value of the processed fabric.
【0029】[0029]
【表4】 表4の結果より綿織物に対しても本発明はpH緩衝性を
付与することができる。[Table 4] From the results shown in Table 4, the present invention can impart pH buffering property to cotton fabrics.
【0030】実施例5 ポリエステル織物にpH5〜7の範囲を示すpH緩衝物
質を付与した。付与方法はpH緩衝物質の水溶液を加工
液とし織物を浸漬し、マングルで絞り、次いでピンテン
ター型の熱風乾燥機で乾燥及び熱処理を行った。加工布
帛はpH緩衝性を評価するためpH値測定法Aによっ
て、湿潤時のpH値を測定した。結果を表5に示す。Example 5 A polyester fabric was provided with a pH buffering substance exhibiting a pH range of 5-7. As the application method, an aqueous solution of a pH buffer substance was used as a processing liquid, the fabric was dipped, squeezed with a mangle, and then dried and heat-treated with a pintenter type hot air dryer. In order to evaluate the pH buffering property of the processed fabric, the wet pH value was measured by the pH value measuring method A. The results are shown in Table 5.
【0031】[0031]
【表5】 [Table 5]
【0032】表5の結果より、pH緩衝物質を選択して
付与することにより、蒸留水での湿潤時にpH5〜7を
示し、更にpH3液で湿潤時のpH値も緩衝効果のある
値を示し、pH緩衝性のある加工布帛が得られる。但
し、洗濯耐久性は得られていない。From the results shown in Table 5, by selecting and adding a pH buffer substance, a pH of 5 to 7 is exhibited when moistened with distilled water, and a pH value when moistened with a pH 3 liquid also exhibits a buffering effect. A processed fabric having a pH buffering property can be obtained. However, washing durability is not obtained.
【0033】実施例6 実施例1及び比較例1で得た加工布帛の評価をpH値測
定法Bによって測定した。結果を表6に示す。Example 6 The evaluation of the processed fabrics obtained in Example 1 and Comparative Example 1 was measured by pH value measuring method B. The results are shown in Table 6.
【表6】 表6の結果より、本発明に加工布帛を濾過した濾液のp
H値より、本発明の加工布帛のpH緩衝性が認められ
る。[Table 6] From the results of Table 6, p of the filtrate obtained by filtering the processed fabric according to the present invention
From the H value, the pH buffering property of the processed fabric of the present invention is recognized.
【0034】実施例7 実施例3及び比較例3で得た加工布帛をpH値測定法A
によって測定した。結果を表7に示す。表7中のpH8
及びpH10は炭酸ナトリウムによって調製した。Example 7 The processed fabrics obtained in Example 3 and Comparative Example 3 were subjected to pH value measuring method A.
Measured by The results are shown in Table 7. PH 8 in Table 7
And pH 10 was prepared with sodium carbonate.
【表7】 表7の結果、本発明品は、アルカリに対して、洗濯耐久
性のあるpH緩衝性が認められる。[Table 7] As a result of Table 7, the product of the present invention has a pH buffering property which is durable against washing with respect to alkali.
【0035】実施例8 60d/48fのポリエステルフィラメント糸を用いた
平織物(経密度98本/inch,緯密度94本/in
ch)に、染色とフッ素系撥水剤による撥水処理を施し
て布帛を得た。そして、アクリル系樹脂(帝国化学社製
テイサンレジンSG−51(固形分17%))100
部にアクリル酸(90モル%),ブタジエン(10モル
%)及び連鎖移動剤の組成でナトリウム塩に中和された
重量平均分子量85,000の重合体(固形分30%)
12部にアクリル酸(95モル%),2−ヒドロキシエ
チルメタクリレート(5モル%)及び連鎖移動剤の組成
で重量平均分子量160,000の重合体(固形分30
%)4部を調合し、フローティングナイフコーターを用
いて塗布した。直ちに120℃の温度にて乾燥を行い、
そして熱処理(170℃)を行った。並びに比較例8と
してポリエステル織物にアクリル系樹脂のみを実施例8
と同様にフローティングナイフコーターにより加工し
た。加工布帛の物性結果を表8に示す。ここでW=5と
は、洗濯5回行ったものの結果を示す。Example 8 Plain woven fabric using polyester filament yarn of 60d / 48f (warp density 98 yarns / inch, weft density 94 yarns / in)
ch) was subjected to dyeing and water repellent treatment with a fluorine-based water repellent to obtain a cloth. And acrylic resin (Teisan Resin SG-51 (solid content 17%) manufactured by Teikoku Chemical Co., Ltd.) 100
Polymer having a weight average molecular weight of 85,000 neutralized to a sodium salt with a composition of acrylic acid (90 mol%), butadiene (10 mol%) and a chain transfer agent in a part (solid content 30%)
12 parts of acrylic acid (95 mol%), 2-hydroxyethyl methacrylate (5 mol%) and a chain transfer agent having a weight average molecular weight of 160,000 (solid content 30)
%) 4 parts were prepared and applied using a floating knife coater. Immediately dry at a temperature of 120 ℃,
Then, heat treatment (170 ° C.) was performed. In addition, as Comparative Example 8, only the acrylic resin was added to the polyester fabric Example 8
It processed with the floating knife coater like. Table 8 shows the physical properties of the processed fabric. Here, W = 5 indicates the result of washing 5 times.
【0036】[0036]
【表8】 表8の結果より、本発明の加工布帛を濾過した濾液のp
H値より、本発明の加工布帛のpH緩衝性が認められ
る。[Table 8] From the results of Table 8, p of the filtrate obtained by filtering the processed fabric of the present invention
From the H value, the pH buffering property of the processed fabric of the present invention is recognized.
【0037】実施例9 多孔性ウレタン系樹脂(大日精化工業社製 ハイムレン
X−3040(固形分30%))100部に、アクリル
酸(90モル%),ブタジエン(10モル%)及び連鎖
移動剤の組成でナトリウム塩に中和された重量平均分子
量85,000の重合体(固形分30%)12部とアク
リル酸(95モル%),2−ヒドロキシエチルメタクリ
レート(5モル%)及び連鎖移動剤の組成で重量平均分
子量160,000の重合体(固形分30%)4部を水
34部とメチルエチルケトン5部の溶剤にて混合させた
ものを徐々に滴下させて調合した。そして、実施例8で
用いた生地に、ナイフオーバーロールコーターを用いて
塗布し、直ちに80℃の温度にて乾燥を行い、そして熱
処理(170℃)を行った。並びに比較例9としてポリ
エステル織物にウレタン系樹脂のみを実施例9と同様に
ナイフオーバーロールコーターにより加工した。加工布
帛の物性結果を表9に示す。Example 9 100 parts of a porous urethane resin (Heimren X-3040 (solid content: 30%, manufactured by Dainichiseika Co., Ltd.)) was added with acrylic acid (90 mol%), butadiene (10 mol%) and chain transfer. 12 parts of a polymer (solid content 30%) having a weight average molecular weight of 85,000 neutralized with sodium salt in the composition of the agent, acrylic acid (95 mol%), 2-hydroxyethyl methacrylate (5 mol%) and chain transfer 4 parts of a polymer having a weight-average molecular weight of 160,000 (solid content: 30%) was mixed with 34 parts of water and 5 parts of methyl ethyl ketone as a solvent, and the mixture was gradually added dropwise to prepare. Then, the dough used in Example 8 was applied using a knife over roll coater, immediately dried at a temperature of 80 ° C., and heat-treated (170 ° C.). In addition, as Comparative Example 9, polyester fabric was processed with only a urethane resin by a knife over roll coater as in Example 9. Table 9 shows the results of physical properties of the processed fabric.
【0038】[0038]
【表9】 表9の結果より、本発明の加工布帛を濾過した濾液のp
H値より、本発明の加工布帛のpH緩衝性が認められ
る。[Table 9] From the results in Table 9, p of the filtrate obtained by filtering the processed fabric of the present invention
From the H value, the pH buffering property of the processed fabric of the present invention is recognized.
【0039】実施例10 実施例8で用いた生地に、アクリル系樹脂(帝国化学社
製 テイサンレジンSG−51(固形分17%))10
0部に、二酸化ケイ素多孔性粒子(平均粒子径2.7
μ)40部とイソプロピルアルコール60部を混合し、
多孔質シリカ液を調整したものを13部を加え、そして
アクリル酸(90モル%),ブタジエン(10モル%)
及び連鎖移動剤の組成でナトリウム塩に中和された重量
平均分子量85,000の重合体(固形分30%)12
部及びアクリル酸(95モル%),2−ヒドロキシエチ
ルメタクリレート(5モル%)及び連鎖移動剤の組成で
重量平均分子量160,000の重合体(固形分30
%)4部を調合し、フローティングナイフコーターを用
いて塗布し、直ちに120℃の温度にて乾燥を行い、そ
して熱処理(170℃)を行った。並びに比較例10と
して、ポリエステル織物にアクリル系樹脂及び多孔質シ
リカ液を調整した物のみを実施例10と同様にフローテ
ィングナイフコーターにより加工した。加工布帛の物性
結果を表10に示す。Example 10 An acrylic resin (Teisan Resin SG-51 manufactured by Teikoku Kagaku Co., Ltd. (solid content: 17%)) 10 was added to the cloth used in Example 8.
In 0 part, silicon dioxide porous particles (average particle size 2.7
μ) 40 parts and isopropyl alcohol 60 parts are mixed,
13 parts of a prepared porous silica liquid was added, and acrylic acid (90 mol%), butadiene (10 mol%)
And a polymer having a weight average molecular weight of 85,000 (solid content: 30%) neutralized to a sodium salt with the composition of a chain transfer agent 12
Part and acrylic acid (95 mol%), 2-hydroxyethyl methacrylate (5 mol%) and chain transfer agent, and a polymer having a weight average molecular weight of 160,000 (solid content 30
%) 4 parts were prepared, coated using a floating knife coater, immediately dried at a temperature of 120 ° C. and heat treated (170 ° C.). Further, as Comparative Example 10, only a polyester woven fabric prepared by adjusting an acrylic resin and a porous silica liquid was processed by a floating knife coater in the same manner as in Example 10. Table 10 shows the physical properties of the processed fabric.
【0040】[0040]
【表10】 表10の結果より、本発明の加工布帛を濾過した濾液の
pH値より、本発明の加工布帛のpH緩衝性が認められ
る。[Table 10] From the results of Table 10, the pH buffering property of the processed cloth of the present invention is recognized from the pH value of the filtrate obtained by filtering the processed cloth of the present invention.
【0041】[0041]
【発明の効果】本発明によれば、pH緩衝作用を有する
酸として作用する物質とその塩類を繊維に付着させるこ
とにより、繊維に付着した酸性雨等を中和し、繊維構造
物を通過して肌に接触した酸性雨等のpH値を皮膚表面
の平均的pH値といわれているpH5〜7に近付ける効
果がある。さらに本発明は、アルカリに対しても、洗濯
耐久性のあるpH緩衝性が認められる。According to the present invention, a substance acting as an acid having a pH buffering action and salts thereof are attached to the fiber to neutralize acid rain and the like attached to the fiber and pass through the fiber structure. It has the effect of bringing the pH value of acid rain or the like that comes into contact with the skin close to pH 5 to 7, which is said to be the average pH value on the skin surface. Further, in the present invention, a pH buffering property with washing durability is recognized even with respect to alkali.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 田中 豊宏 滋賀県長浜市鐘紡町1番11号 (72)発明者 柴岡 浩 滋賀県彦根市松原町1849−94 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Toyohiro Tanaka 1-11 Kanebocho, Nagahama-shi, Shiga (72) Inventor Hiroshi Shibaoka 1849-94 Matsubara-cho, Hikone-shi, Shiga
Claims (2)
酸として作用する物質とその塩類が付着され、湿潤時に
pH5〜7を示すことを特徴とするpH緩衝性繊維構造
物。1. A pH buffering fiber structure, wherein a substance acting as an acid and salts thereof are deposited on at least the surface of the fiber of the fiber structure and exhibiting a pH of 5 to 7 when wet.
る化合物がカルボキシル基及び塩形に中和されたカルボ
キシル基を含む重量平均分子量1,000〜1,00
0,000の重合体及び共重合体である請求項1記載の
pH緩衝性繊維構造物。2. A weight average molecular weight of 1,000 to 1.00 in which a compound consisting of a substance acting as an acid and salts thereof contains a carboxyl group and a carboxyl group neutralized into a salt form.
The pH buffering fibrous structure of claim 1 which is 20,000 polymers and copolymers.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22513192A JPH0641870A (en) | 1992-01-29 | 1992-07-31 | Textile structure with ph buffering nature |
| JP4315790A JP2623493B2 (en) | 1992-01-29 | 1992-10-30 | pH buffering fiber structure and method for producing the same |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4042892 | 1992-01-29 | ||
| JP22513192A JPH0641870A (en) | 1992-01-29 | 1992-07-31 | Textile structure with ph buffering nature |
| JP4-40428 | 1992-07-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0641870A true JPH0641870A (en) | 1994-02-15 |
Family
ID=26379895
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22513192A Pending JPH0641870A (en) | 1992-01-29 | 1992-07-31 | Textile structure with ph buffering nature |
| JP4315790A Expired - Fee Related JP2623493B2 (en) | 1992-01-29 | 1992-10-30 | pH buffering fiber structure and method for producing the same |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4315790A Expired - Fee Related JP2623493B2 (en) | 1992-01-29 | 1992-10-30 | pH buffering fiber structure and method for producing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (2) | JPH0641870A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6565981B1 (en) | 1999-03-30 | 2003-05-20 | Stockhausen Gmbh & Co. Kg | Polymers that are cross-linkable to form superabsorbent polymers |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4214967B2 (en) | 2004-02-06 | 2009-01-28 | マックス株式会社 | Part fixing tool and temporary holding mechanism for nailing machine of this part fixing tool |
| JP5183980B2 (en) * | 2007-06-15 | 2013-04-17 | 小松精練株式会社 | Waterproof fabric and method for producing the same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1594596A (en) * | 1977-02-04 | 1981-07-30 | Prod Sandoz Sa | Textile teatment process and composition for use therein |
-
1992
- 1992-07-31 JP JP22513192A patent/JPH0641870A/en active Pending
- 1992-10-30 JP JP4315790A patent/JP2623493B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6565981B1 (en) | 1999-03-30 | 2003-05-20 | Stockhausen Gmbh & Co. Kg | Polymers that are cross-linkable to form superabsorbent polymers |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0641871A (en) | 1994-02-15 |
| JP2623493B2 (en) | 1997-06-25 |
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