JPS6034594B2 - Water-soluble hot melt adhesive for temporarily fixing interlining - Google Patents
Water-soluble hot melt adhesive for temporarily fixing interliningInfo
- Publication number
- JPS6034594B2 JPS6034594B2 JP14423977A JP14423977A JPS6034594B2 JP S6034594 B2 JPS6034594 B2 JP S6034594B2 JP 14423977 A JP14423977 A JP 14423977A JP 14423977 A JP14423977 A JP 14423977A JP S6034594 B2 JPS6034594 B2 JP S6034594B2
- Authority
- JP
- Japan
- Prior art keywords
- interlining
- water
- melt adhesive
- hot melt
- degree
- 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.)
- Expired
Links
- 239000004831 Hot glue Substances 0.000 title claims description 11
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 13
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 13
- 238000006116 polymerization reaction Methods 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 238000007127 saponification reaction Methods 0.000 claims description 8
- 239000004744 fabric Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000853 adhesive Substances 0.000 description 11
- 230000001070 adhesive effect Effects 0.000 description 11
- 238000005406 washing Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 238000009958 sewing Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000012943 hotmelt Substances 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 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
- 239000003292 glue Substances 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009990 desizing Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 208000000260 Warts Diseases 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- -1 fatty acid salts Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 201000010153 skin papilloma Diseases 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Description
【発明の詳細な説明】
本発明は芯地仮止用水瀞性ホットメルト接着剤に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a water-repellent hot melt adhesive for temporarily fixing interlining.
近年衣料品の縫製に於いては接着剤が広く使用されてい
る。In recent years, adhesives have been widely used in sewing clothing.
例えばワイシャツの衿、袖口等を縫製する場合には、ま
ず芯地と表地とがずれない様に芯地に接着剤をほどこし
表地と仮接着したのち裁断し縫製される。従来用いられ
ている芯地仮止用接着剤としては熱熔融性の樹脂、例え
ばナイロン、ポリエチレン、エチレン−酢酸ビニル共重
合体などの疎水性樹脂の粉末状のものなどがあり、これ
らの樹脂は熱溶融性を利用し、ホットメルト型としては
有用であるが、疎水性であるため仮接着後の脱樹脂が出
来ず、衣料品の風合を著しく損なうという欠点を有して
いる。For example, when sewing the collar, cuffs, etc. of a dress shirt, the interlining is first coated with adhesive to prevent the interlining and outer material from slipping, and then temporarily bonded to the outer material, and then cut and sewn. Conventionally used adhesives for temporarily fixing interlining include hot-melt resins such as powdered hydrophobic resins such as nylon, polyethylene, and ethylene-vinyl acetate copolymer. Although it is useful as a hot melt type because of its thermal meltability, it has the disadvantage that it is hydrophobic and cannot be removed from the resin after temporary adhesion, which significantly impairs the feel of clothing.
また、デンプン、繊維素誘導体、アクリル酸譲導体等の
水熔‘性樹脂を芯地に塗布乾燥し、表地を重ね合せる際
に、水蒸気を吹付けるか「水を噴霧してその再編接着性
を利用して接着する方法もあるが、水を階霧する際に部
分的に芯地および表地へ樹脂が浸透して、しみが発生し
たり、風合を損なうなどの傾向があり、また熟練を要す
るなどの難点があり、更に芯地を該樹脂にて仮止用芯地
として加工する場合にも、塗布後乾燥する工程が必要と
なり、かかる工程がコストアップの原因ともなるのであ
る。In addition, water-meltable resins such as starch, cellulose derivatives, and acrylic acid derivatives are applied to the interlining and dried, and when the outer material is layered, water vapor is sprayed or water is sprayed to improve its re-adhesion. There is also a method of adhesion, but when spraying with water, the resin tends to partially penetrate into the interlining and outer material, causing stains and impairing the texture. Moreover, when processing the interlining material with the resin as a temporary interlining material, a drying process is required after application, and this process increases the cost.
更に、ポリビニルアルコールをアセトアセタール化した
ものや、ブチラール化したものなどがあり、再湿不用の
ホットメルト接着剤ではあるが、ホットメルト性を有し
、且つ本縫製後水洗除去出来るようなアセトアセタール
化度、ブチラール化度を有するものは、適度の粒子状に
粉末化が出来ず、粉末状としての使用には不適性であり
、水溶液として使用に供されるため芯地に塗布後の乾燥
が必要であることに加えて、ポリビニルアルコールを変
性するための変性剤、変性工程が必要となり、コスト的
に高価なものであるという欠点を有している。Furthermore, there are adhesives made from acetoacetal and butyral from polyvinyl alcohol, which are hot-melt adhesives that do not require rewetting, but acetoacetal has hot-melt properties and can be removed by washing with water after final sewing. Products with a high degree of oxidation or butyralization cannot be powdered into appropriate particles and are unsuitable for use in powder form.Since they are used as an aqueous solution, they do not need to be dried after being applied to the interlining. In addition to this, it also requires a denaturing agent and a denaturing step to denature polyvinyl alcohol, which has the disadvantage of being expensive.
本発明者らは、かかる従来の接着剤の欠点を解決し、し
かも安価で使用方法が簡便な芯地仮止用水溶性ホットメ
ルト接着剤に関して鋭意検討を重ねた。The present inventors have conducted intensive studies on a water-soluble hot melt adhesive for interlining temporary fixing that solves the drawbacks of such conventional adhesives, is inexpensive, and is easy to use.
その結果、平均重合度が200〜1000、ケン化度が
30〜75モル%であるカルボキシル基含有粉末状ポリ
ビニルアルコールであって、その粒度が10〜150メ
ッシュ、好ましくは60〜100メッシュのものが熱溶
融性であることによって、ホットメルト型として使用可
能であり、また水溶性であることによって本縫製後、水
洗によって除去可能であり衣料品の風合を損なうことが
全くなく、更に形状が粉末状であることによって、仮止
用芯地加工が簡便に行なうことが出来ることを見し、出
し本発明の完成にいたつたのである。As a result, a carboxyl group-containing powdered polyvinyl alcohol having an average degree of polymerization of 200 to 1000, a degree of saponification of 30 to 75 mol%, and a particle size of 10 to 150 mesh, preferably 60 to 100 mesh, was obtained. Because it is heat-meltable, it can be used as a hot melt type, and because it is water-soluble, it can be removed by washing with water after final sewing, so it does not affect the texture of the clothing at all, and the shape is similar to that of a powder. It was discovered that the interlining for temporary fixing could be easily processed due to the shape of the material, and the present invention was completed.
本発明の芯地仮止用水溶性ホットメルト接着剤は、13
0〜160℃という低温でのアイロンプレスによって溶
融接着が可能であるから、布地をいためることはなく、
また洗濯などによって容易に溶解除去出来るものである
から布地が硬くなることはなく、風合を損なう危険は皆
無である。The water-soluble hot melt adhesive for interlining temporary fixing of the present invention has 13
Melt bonding is possible by iron pressing at a low temperature of 0 to 160 degrees Celsius, so there is no damage to the fabric.
In addition, since it can be easily dissolved and removed by washing, the fabric will not become stiff and there is no risk of spoiling the texture.
従って婦人服薄物ジョーゼット等のワンピース類の衿芯
、袖口などの製品の風合を重視する用途には最適である
。さらに、本発明の接着剤は、粉末状であるから仮止用
芯地加工が容易であるという大きな特徴を有している。Therefore, it is ideal for applications where the texture of products is important, such as collars and cuffs of dresses such as thin georgette for women's clothing. Furthermore, since the adhesive of the present invention is in powder form, it has the great feature that it is easy to process the interlining for temporary fixing.
即ち芯地に連続的に散布機にて、該粉末状接着剤を散布
し130〜160qoの温度にて7〜1明度間加熱する
ことによって、樹脂は溶融し芯地に融着する。得られた
芯地は、目的に応じて裁断し、表地と重ねて熱プレスに
て仮接着がなされる、その際の初期接着力(セツテング
時間1硯妙、圧力0.3k9/塊)は200〜300タ
ノ(0寸)2 であり実用上充分である。以後本縫製し
、水洗にて除去され布地の風合を損なうことがなく製品
が得られる。本発明に用いられるカルボキシル基含有変
性ポリピニルアルコールは、平均重合度が200〜10
00ケン化度が30〜75モル%であることが必要であ
り、これらの範囲外では上記の如き効果は期待しえず、
なかんずく平均重合度が250〜600、ケン化度が4
0〜65モル%のものは一段と優れた効果を発揮しうる
ので、その使用が望ましい。That is, the powdered adhesive is continuously spread onto the interlining using a spreader and heated for 7 to 1 degree of brightness at a temperature of 130 to 160 qo, thereby melting the resin and fusing it to the interlining. The obtained interlining is cut according to the purpose, overlapped with the outer material, and temporarily bonded with a heat press.The initial adhesive strength (setting time: 1 inch, pressure: 0.3 k9/lump) is 200. ~300 tano (0 sun)2, which is sufficient for practical use. Thereafter, the final stitching is performed and the product is removed by washing with water to obtain a product without damaging the texture of the fabric. The carboxyl group-containing modified polypinyl alcohol used in the present invention has an average degree of polymerization of 200 to 10
It is necessary that the degree of saponification is 30 to 75 mol%; outside these ranges, the above effects cannot be expected.
Above all, the average degree of polymerization is 250 to 600, and the degree of saponification is 4.
It is desirable to use 0 to 65 mol% since it can exhibit even better effects.
カルボキシル基の導入量としては0.5〜10モル%の
範囲が望ましく、該基の存在が熱溶融性及び溶解除去性
を一段と向上させるのである。変性量がかかる範囲以上
になると、粉末状のものが得にくくなり、またコストア
ップともなるので、本発明には不適である。かかるカル
ポキシル基含有変性ポリピニルアルコールは酢酸ビニル
単量体と、(無水)マレィン酸、アクリル酸、メタアク
リル酸などのカルボキシル基含有単量体との共重合体の
ケン化物として得られるものである。本発明では上記粉
末状カルボキシル基含有変性ポリピニルアルコールは単
独使用のみならず、従来公知の水溶性ホットメルト接着
剤との併用も可能である。The amount of carboxyl group introduced is preferably in the range of 0.5 to 10 mol %, and the presence of this group further improves heat meltability and dissolution removability. If the amount of modification exceeds this range, it will be difficult to obtain a powder and the cost will increase, so it is not suitable for the present invention. Such carboxyl group-containing modified polypinyl alcohol is obtained as a saponified product of a copolymer of vinyl acetate monomer and a carboxyl group-containing monomer such as (anhydrous) maleic acid, acrylic acid, or methacrylic acid. be. In the present invention, the powdered carboxyl group-containing modified polypinyl alcohol can be used not only alone, but also in combination with a conventionally known water-soluble hot melt adhesive.
特に平均重合度200〜1000ケン化度30〜75モ
ル%の禾変性のポリビニルアルコールを併用する場合、
コスト面からより有用な使用方法となる。その際の使用
量は特に限定するものではないが、通常変性ポリビニル
アルコールに対して10〜100の重量%である。更に
熱溶融性及び溶解除去性を一層効果的ならしめるために
、可塑剤類を使用しても差支えない。In particular, when using together with a denatured polyvinyl alcohol having an average degree of polymerization of 200 to 1000 and a degree of saponification of 30 to 75 mol%,
This is a more useful usage method from a cost standpoint. The amount used in this case is not particularly limited, but is usually 10 to 100% by weight based on the modified polyvinyl alcohol. Furthermore, in order to make the heat meltability and dissolution removability more effective, plasticizers may be used.
可塑剤類としては、ソルピツト、マンニットなどの多価
アルコール類、グリセリン、ジグリセリン、エチレング
リコール、ポリエチレングリコール、プロピレングリコ
ール、メチルベンタントリオールなどのグリコール類、
ソルビタン脂肪族ェステル及びその酸化エチレン付加物
などの界面活性剤、酢酸ビニルオリゴマーなどがあげら
れる。添加量としては該ポリビニルアルコールに対して
1〜10の重量%の範囲が好ましい。本発明に用いられ
る粉末状カルボキシル基含有変性ポリビニルアルコール
の粒度は、10〜150メッシュのものが適しているが
、仮止芯地加工時に於ける散布機に対する適用性、芯地
に対するセッテング性及び溶融速度の点から、60〜1
00メッシュのものが好ましい。Examples of plasticizers include polyhydric alcohols such as solpit and mannitol, glycols such as glycerin, diglycerin, ethylene glycol, polyethylene glycol, propylene glycol, and methylbentantriol;
Examples include surfactants such as sorbitan aliphatic esters and their ethylene oxide adducts, and vinyl acetate oligomers. The amount added is preferably in the range of 1 to 10% by weight based on the polyvinyl alcohol. The particle size of the powdered carboxyl group-containing modified polyvinyl alcohol used in the present invention is suitably 10 to 150 mesh. In terms of speed, 60-1
00 mesh is preferred.
また仮止芯地加工された芯地は、巻取中に樹脂面でのブ
ロッキングが生ずることもありうるので、粉末にブロッ
キング防止剤として、ステアリン酸ソーダなどの高級脂
肪酸塩、コロィダルシリカなどの微粉末桂酸などを0.
01〜1%添加するのが好ましい。次に実施例によって
本発明を具体的に説明する。In addition, interlining processed with temporary interlining may cause blocking on the resin surface during winding. Therefore, anti-blocking agents such as higher fatty acid salts such as sodium stearate and fine powders such as colloidal silica are added to the powder. 0. citric acid etc.
It is preferable to add 0.01 to 1%. Next, the present invention will be specifically explained with reference to Examples.
実施例 1
綿の1掠奪単糸で50本/吋打込みの布地に重合度25
0ケン化度45モル%、変性度5モル%、粒度60〜1
00メッシュの粉末状マレイン酸変性ポリビニルアルコ
ールを10夕/あの割合で撒布し、160℃に設定した
熱風乾燥機中を35肌/分の速度で通過させて布地にホ
ットメルト接着剤を仮固着させ芯地を作成した。Example 1 Polymerization degree of 25 on a fabric with 50 threads/inch of single thread of cotton
0 saponification degree 45 mol%, modification degree 5 mol%, particle size 60-1
00 mesh powdered maleic acid-modified polyvinyl alcohol was spread at a rate of 10 min/min, and passed through a hot air dryer set at 160°C at a speed of 35 skin/min to temporarily fix the hot melt adhesive to the fabric. I created the interlining.
この芯地を婦人夏物ワンピース用服地のジョーゼット生
地の表、裏地の間にはさみ込み、業務用8ポンドアイロ
ンにて温度130〜150qoに設定し圧力0.3k9
/めで10秒間加熱圧着した。この接着芯地の剥離強度
は350夕/(吋)2であった。次にジョーゼットの表
、髪生地及び芯地の3枚重ね地をミシンで縫製し家庭用
洗濯機にて30qoの水で5分間渦流水洗して、これを
風乾した。Sandwich this interlining between the front and lining of the georgette fabric for women's summer dresses, and use a commercial 8-pound iron to set the temperature to 130 to 150 qo and press at 0.3 k9.
/ for 10 seconds. The peel strength of this adhesive interlining was 350 mm/(inch)2. Next, three layers of georgette outer fabric, hair fabric, and interlining were sewn using a sewing machine, washed in a household washing machine with 30 qo of water under a whirlpool for 5 minutes, and air-dried.
この縫製芯地の剥離強度は零であり、水洗で完全に糊抜
きされていた。またジョーゼット生地の風合はそのまま
保持されていた。・対照例 1
実施例1においてマレィソ酸変性ポリビニルアルコール
の代わりに重合度25以ケン化度45モル%、粒度60
〜100メッシュの未変性の粉末状ポリビニルアルコー
ルを用いた以外は同例に準じて芯地を作成し、加熱圧着
したところその剥離強度は300夕/(P寸)2であっ
た。The peel strength of this sewn interlining was zero, and the glue was completely removed by washing with water. Additionally, the texture of the georgette fabric was maintained.・Comparative example 1 In Example 1, instead of maleisic acid-modified polyvinyl alcohol, polymerization degree of 25 or higher, saponification degree of 45 mol%, particle size of 60
An interlining was prepared in accordance with the same procedure except that unmodified powdered polyvinyl alcohol of ~100 mesh was used, and when it was heat-pressed, its peel strength was 300 mm/(P dimension) 2.
また実施例1と同じ条件で糊抜きを行ったところ、糊抜
率は65%に過ぎなかった。Further, when desizing was performed under the same conditions as in Example 1, the desizing rate was only 65%.
このためジョーゼットの生地の風合も実施例1に比較し
て劣るものであった。対照例 2
テトロン/綿の混紡の1句蚤単糸で95本/吋打込みの
布地に重合度250、ケン化度45モル%、粒度60〜
100メッシュの粉末状ポリビニルアルコールを8夕/
めの割合で撒布し、16000に設定した熱風乾燥機中
を35の/分の速度で通過させて布地にホットメルト接
着剤を仮固着させ芯地を作成した。Therefore, the feel of the georgette fabric was also inferior to that of Example 1. Comparative Example 2 Tetoron/cotton blend fabric with 95 single threads per thread, polymerization degree 250, saponification degree 45 mol%, particle size 60~
8 evenings of 100 mesh powdered polyvinyl alcohol/
The hot-melt adhesive was spread on the fabric at a rate of 100 ml, and passed through a hot air dryer set at 16,000 ml at a speed of 35/min to temporarily fix the hot-melt adhesive to the fabric to create an interlining.
この芯地を婦人夏物ワンピース用服地のジョーゼット生
地の表、裏地の間にはさみ込み、家庭用2ポンドアイロ
ンにて温度130〜150つ0に設定し圧力0.3k9
/めで7秒間加熱圧着した。この接着芯地の剥離強度は
280夕/(吋)2であった。次にジョーゼットの表、
裏地及び芯地の3枚重ね地をミシンで縫製し、家庭用洗
濯機にて40午0の水で15分間渦流水洗し、これを2
回繰返した後風乾した。この縫製芯地の剥離強度は零で
あり、水洗で完全に糊抜きがされていた。またジョーゼ
ットの生地の風合はそのま)保持されていた。実施例
2綿の1掠奪単糸で50本/0寸打込みの布地に重合度
60リケン化度65モル%、変性度5モル%、粒度20
〜30メッシュの粉末状マレイン酸変性ポリビニルアル
コールを15夕/れの割合で撒布し、160℃に設定し
た熱風乾燥機中を20肌/分の速度で通過させて布地に
ホットメルト接着剤を仮固着させ芯地を作成した。This interlining material was sandwiched between the front and lining of the georgette fabric for women's summer dresses, and the temperature was set to 130-150 x 0 using a household 2-pound iron, and the pressure was 0.3 k9.
/ for 7 seconds. The peel strength of this adhesive interlining was 280 mm/(inch)2. Next is the Georgette table.
Sewn three layers of lining and interlining with a sewing machine, wash in a household washing machine with 40:00 water for 15 minutes, and then wash
After repeating the process several times, it was air-dried. The peel strength of this sewn interlining was zero, and the glue was completely removed by washing with water. Additionally, the texture of the georgette fabric was maintained. Example
Polymerization degree: 60, resaponization degree: 65 mol%, modification degree: 5 mol%, particle size: 20
~30 mesh powdered maleic acid-modified polyvinyl alcohol was spread at a rate of 15 coats/minute and passed through a hot air dryer set at 160°C at a rate of 20 coats/minute to temporarily apply the hot melt adhesive to the fabric. I fixed it and created an interlining.
この芯地を婦人用ブラウス用のブロード生地の表、裏地
の間にはさみ込み、業務用8ポンドアイロンにて温度1
30〜15び0に設定し圧力0.3kg/ので1鼠砂間
加熱圧着した。この接着芯地の剥離強度は350夕/(
吋)2であった。次にブロードの表、裏生地及び芯地の
3枚重ね地をミシンンで縫製し家庭用洗濯機にて4ぴ0
のの水で18分間渦流水洗し、これを2回線返した後風
乾した。この縫製芯地の剥離強度は零であり、水洗で完
全に糊抜きされていた。またブロード生地の風合はその
ま)保持されていた。対照例 3
実施例1と同様の生地に市販の重合度700、粒度60
〜100メッシュのエチレン一戦酸ビニル共重合樹脂(
エチレン/酢ビ=95/5)を実施例1と同様に処理し
、芯地を作成した。Sandwich this interlining between the front and lining of a women's broadcloth fabric and use an 8-pound commercial iron at 1 temperature.
The temperature was set at 30 to 150, and the pressure was 0.3 kg/h, and heat and pressure bonding was carried out between 1 piece of rat sand. The peel strength of this adhesive interlining is 350/(
吋) It was 2. Next, the front, lining, and interlining fabrics of the broadcloth are sewn together using a sewing machine, and then washed in a home washing machine for 4 plies.
The sample was washed with water under a vortex for 18 minutes, refluxed twice, and then air-dried. The peel strength of this sewn interlining was zero, and the glue was completely removed by washing with water. In addition, the texture of the broadcloth was maintained. Control example 3 A commercially available polymerization degree of 700 and particle size of 60 was added to the same fabric as in Example 1.
~100 mesh ethylene single-wart vinyl oxide copolymer resin (
Ethylene/vinyl acetate = 95/5) was treated in the same manner as in Example 1 to create an interlining.
Claims (1)
モル%、粒度10〜150メツシユの粉末状カルボキシ
ル基含有変性ポリビニルアルコールからなる芯地仮止用
水溶性ホツトメルト接着剤。1 Average degree of polymerization 200-1000, degree of saponification 30-75
A water-soluble hot-melt adhesive for temporarily fixing interlining, which is made of a powdered carboxyl group-containing modified polyvinyl alcohol having a mol% particle size of 10 to 150 mesh.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14423977A JPS6034594B2 (en) | 1977-11-30 | 1977-11-30 | Water-soluble hot melt adhesive for temporarily fixing interlining |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14423977A JPS6034594B2 (en) | 1977-11-30 | 1977-11-30 | Water-soluble hot melt adhesive for temporarily fixing interlining |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5476635A JPS5476635A (en) | 1979-06-19 |
| JPS6034594B2 true JPS6034594B2 (en) | 1985-08-09 |
Family
ID=15357475
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14423977A Expired JPS6034594B2 (en) | 1977-11-30 | 1977-11-30 | Water-soluble hot melt adhesive for temporarily fixing interlining |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6034594B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01277698A (en) * | 1988-04-30 | 1989-11-08 | Nippon Ferrofluidics Kk | Combined vacuum pump |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58208410A (en) * | 1982-05-25 | 1983-12-05 | 日本繊維化工株式会社 | Garment fabric |
| JPH0786159B2 (en) * | 1985-08-21 | 1995-09-20 | 日本合成化学工業株式会社 | Hot melt adhesive |
| JP7470493B2 (en) * | 2019-07-03 | 2024-04-18 | Juki株式会社 | How to join sheet materials |
-
1977
- 1977-11-30 JP JP14423977A patent/JPS6034594B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01277698A (en) * | 1988-04-30 | 1989-11-08 | Nippon Ferrofluidics Kk | Combined vacuum pump |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5476635A (en) | 1979-06-19 |
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