JPS6317978A - Hot-melt adhesive - Google Patents
Hot-melt adhesiveInfo
- Publication number
- JPS6317978A JPS6317978A JP16079086A JP16079086A JPS6317978A JP S6317978 A JPS6317978 A JP S6317978A JP 16079086 A JP16079086 A JP 16079086A JP 16079086 A JP16079086 A JP 16079086A JP S6317978 A JPS6317978 A JP S6317978A
- Authority
- JP
- Japan
- Prior art keywords
- interlining
- polymerization
- adhesive
- resin
- copolymer
- 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.)
- Granted
Links
- 239000004831 Hot glue Substances 0.000 title claims description 9
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 27
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 8
- 229920001577 copolymer Polymers 0.000 claims abstract description 8
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000853 adhesive Substances 0.000 abstract description 23
- 230000001070 adhesive effect Effects 0.000 abstract description 23
- 239000004744 fabric Substances 0.000 abstract description 14
- 238000009958 sewing Methods 0.000 abstract description 5
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 abstract description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 abstract description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract description 2
- 210000003739 neck Anatomy 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 26
- 239000011347 resin Substances 0.000 description 26
- 238000005406 washing Methods 0.000 description 14
- 239000000463 material Substances 0.000 description 13
- 230000000903 blocking effect Effects 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 9
- 239000002245 particle Substances 0.000 description 8
- 239000003513 alkali Substances 0.000 description 7
- 239000003599 detergent Substances 0.000 description 7
- 230000004927 fusion Effects 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 238000007127 saponification reaction Methods 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000005038 ethylene vinyl acetate Substances 0.000 description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000010953 base metal Substances 0.000 description 3
- 238000005108 dry cleaning Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-N sodium;hydron;carbonate Chemical compound [Na+].OC(O)=O UIIMBOGNXHQVGW-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 238000004804 winding Methods 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
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920001756 Polyvinyl chloride acetate Polymers 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
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- UCTLHLZWKJIXJI-LXIBVNSESA-N [(3s,8r,9s,10r,13s,14s)-17-chloro-16-formyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1h-cyclopenta[a]phenanthren-3-yl] acetate Chemical compound C([C@@H]12)C[C@]3(C)C(Cl)=C(C=O)C[C@H]3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)C)C1 UCTLHLZWKJIXJI-LXIBVNSESA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000001771 impaired effect Effects 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 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
- 238000012546 transfer Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacturing Of Multi-Layer Textile Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
衣料品、例えばブラウス、ワイシャツの衿、袖口等は、
ずれないよう罠表地と接着剤を付与した芯地をアイロン
等で加熱プレスにより接着してから裁断、縫製されてい
る。本発明は、その際に用いるホットメルト接着剤に関
するものである。[Detailed description of the invention] [Industrial application field] Clothing, such as blouses, shirt collars, cuffs, etc.
The trap outer material and the adhesive-applied interlining are bonded together using a hot press using an iron, etc. to prevent them from slipping, and then cut and sewn. The present invention relates to a hot melt adhesive used in that case.
従来より用いられている芯地用ホットメルト接着剤はナ
イロン、ポリエステル、ポリエチレン、ポリ塩化ビニル
、エチレン−酢酸ビニル共重合体(以下EVAという)
、変性EVAであるが、水中洗剤に不溶であり、ドライ
クリーニング溶剤に対する耐溶剤性があるために、縫製
後に水洗、洗剤洗濯、ドライクリーニング等の処置を行
ってもほとんど脱樹脂出来ず、衣料品の風合いを著しく
損うばかりでなく、耐ドライクリーニング性の悪い樹脂
の場合には、中途半端な脱樹脂によりしみ出しが発生す
る危険性がある。Conventionally used hot melt adhesives for interlining include nylon, polyester, polyethylene, polyvinyl chloride, and ethylene-vinyl acetate copolymer (hereinafter referred to as EVA).
Although modified EVA is insoluble in underwater detergents and has solvent resistance to dry cleaning solvents, it is difficult to remove the resin even after washing with water, detergent washing, dry cleaning, etc. after sewing, and it is difficult to remove the resin from clothing. In addition to significantly impairing the feel of the product, in the case of resins with poor dry cleaning resistance, there is a risk that oozing may occur due to half-hearted removal of the resin.
またデンプン、CMC等の水浴性樹脂を芯地に塗布乾燥
し、表地と接着する際、水や水蒸気等で再湿化して接着
する方法がある。この場合樹脂が表地や芯地に浸透して
、じみが発生したり、風合いを損う傾向が大きく、塗布
後も乾燥工程が必要となり、コストアップの原因となっ
ている。There is also a method of applying a water-bathable resin such as starch or CMC to an interlining, drying it, and then rewetting it with water or steam when adhering it to the outer material. In this case, there is a strong tendency for the resin to penetrate into the outer material and interlining, causing bleeding and impairing the texture, and a drying process is required even after application, leading to increased costs.
更に、特開昭60−17178号公報には平均重合度5
0〜200、ケン化度50〜70モルチの部分ケン化ポ
リビニルアルコールや特公昭60−54594号公報に
は平均重合度200〜1000、ケン化度30〜75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が芯地仮止用ホットメ
ルト接着剤として示されている。これらは芯地にホット
メルトし、表地と重ね合わせ、プレス、裁断し、縫製後
水洗にて脱樹脂を行い、布地の風合いを損わない製品を
得ることを目的とするものであるが、この場合、樹脂が
水可溶性であるがために、芯地に融着した樹脂が大気中
等の水分を吸収し、芯地巻き取りの際、芯地同士がブロ
ッキングするケースが多い。Furthermore, in JP-A-60-17178, the average degree of polymerization is 5.
Partially saponified polyvinyl alcohol with a saponification degree of 0 to 200 and a saponification degree of 50 to 70 mol%, and powder with an average polymerization degree of 200 to 1000, a saponification degree of 30 to 75 mol%, and a particle size of 10 to 150 mesh is disclosed in Japanese Patent Publication No. 60-54594. Modified polyvinyl alcohol containing carboxyl groups has been shown as a hot melt adhesive for interlining temporary fixing. The purpose of these products is to hot-melt the interlining material, overlap it with the outer material, press it, cut it, remove the resin by washing with water after sewing, and obtain a product that does not impair the texture of the fabric. In this case, since the resin is water-soluble, the resin fused to the interlining absorbs moisture from the atmosphere, and the interlining often blocks each other when the interlining is wound up.
ブロッキング防止のため、炭酸カルシウム等のブロッキ
ング防止剤を0.o1〜2チ添加しているが夏期等の高
温、多湿時には防止することが出来ない。このためポリ
エチレンシート等を芯地の間にはさみブロッキングを防
止する対策が取られているが、生産性や経済性が悪くな
り、又樹脂そのものの管理や樹脂融着芯地の管理に充分
注意を払う必要があるといった欠点を有している。To prevent blocking, add 0.0% anti-blocking agent such as calcium carbonate. Although 1 to 2 chlorides are added, it cannot be prevented during high temperature and high humidity such as in summer. For this reason, measures have been taken to prevent blocking by sandwiching polyethylene sheets between interlinings, but this results in poor productivity and economic efficiency.In addition, sufficient care must be taken in managing the resin itself and the resin-fused interlining. The disadvantage is that you have to pay for it.
〔発明が解決しようとする問題点〕
この発明は以下に示した従来技術の問題点を解決しよう
としたものである。[Problems to be Solved by the Invention] This invention attempts to solve the following problems of the prior art.
1、 縫製後に洗濯等の処理を行っても脱樹脂出来ない
ため、樹脂の硬さにより、布地の風合いを損なう。1. Since the resin cannot be removed even after washing or other treatments after sewing, the hardness of the resin impairs the texture of the fabric.
2、耐タライクリーニング性の悪い樹脂におけるしみ出
し発生の問題
3、水可溶型接着剤に見られる樹脂融着芯地巻き取りの
際、吸湿等によるブロッキングの問題〔問題点を解決す
るための手段〕
本発明は、酢酸♂ニル98−85
レン性不飽和カルボン酸2〜15モル%、平均重合度2
00〜1500の共重合体からなる芯地用アルカリ可溶
性ホットメルト接着剤である。2. The problem of seepage caused by resins with poor cleaning resistance. 3. The problem of blocking due to moisture absorption when winding up the resin fusion interlining that occurs with water-soluble adhesives. Means] The present invention uses ♂yl acetate 98-85 lenically unsaturated carboxylic acid 2 to 15 mol%, average degree of polymerization 2
This is an alkali-soluble hot melt adhesive for interlining made of a copolymer of 00 to 1500.
酢酸ビニルの一部は、本発明の要旨を損わなり範囲内で
他のビニル単量体(例えば酢酸ビニル以外のビニルエス
テル、メタアクリル酸エステル、アクリル酸エステル等
)に置換しても良い。エチレン性不飽和カルボン酸とし
てはアクリル酸、メタクリル酸、クロトン酸、無水マレ
イン酸、マレイン酸モノエステル、イタコン酸等が好ま
しい。A portion of vinyl acetate may be replaced with other vinyl monomers (for example, vinyl esters other than vinyl acetate, methacrylic esters, acrylic esters, etc.) within the scope of the invention. As the ethylenically unsaturated carboxylic acid, acrylic acid, methacrylic acid, crotonic acid, maleic anhydride, maleic acid monoester, itaconic acid, etc. are preferable.
熱プレスにより溶融接着が出来る。そのため熱により布
地をいためることはない。Melt bonding can be done by heat pressing. Therefore, the fabric will not be damaged by heat.
又、本接着剤は水に不溶であるが、炭酸ソーダ、カセイ
ソーダ、アンモニア水等のアルカリ剤の存在下で、水可
溶となるもので、アルカリ剤の存在しない条件下ではナ
イロン、EVA等の疎水性樹脂と同様に脱樹脂しない特
徴を有している。又、家庭用洗剤で代表される弱アルカ
リ性洗剤でも容易に本接着剤を脱樹脂出来る。そのため
、水溶性樹脂接着剤に見られる樹脂の表地や芯地への浸
透によるじみの発生、EVA,ナイロンに見られる洗濯
等の処置を施しても脱樹脂出来ないことによる布地の風
合いを損うという危険性は全くない。又、水不溶性であ
るため、水溶性樹脂に見られる接着剤を融着した芯地が
大気中の水分を吸収し、芯地巻き取りの際、芯地同士が
ブロッキングする危険性も全くない。Although this adhesive is insoluble in water, it becomes water-soluble in the presence of alkaline agents such as soda carbonate, caustic soda, and aqueous ammonia. Like hydrophobic resins, it has the characteristic of not removing the resin. In addition, the resin of this adhesive can be easily removed using a weakly alkaline detergent such as household detergents. As a result, bleed occurs when the resin penetrates into the outer material and interlining, which occurs with water-soluble resin adhesives, and the feel of the fabric deteriorates due to the inability to remove the resin even after washing, which occurs with EVA and nylon. There is no danger of that happening at all. Furthermore, since it is water-insoluble, the interlining to which the adhesive found in water-soluble resins is fused absorbs moisture in the atmosphere, and there is no risk of the interlinings blocking each other when the interlining is wound up.
本発明のアルカリ可溶性ホットメルト接着剤のエチレン
性不飽和カルボン酸の共重合割合は2〜15−1=ルチ
好ましくは6〜10モルチである。エチレン性不飽和カ
ルボン酸の2モルチ未満ではアルカリ可溶性が低下し、
一方、15モルチを越えると本質的には可能であるが重
合性が悪く、重合時間が長くなり、経済的デメリットが
生ずる。又、共重合体の皮膜が硬くなり、芯地の風合い
を損う欠点を有する。重合度は200〜150oの範囲
で性能上問題はないが好ましくは200〜1200であ
る。重合度200未満では重合時にブロッキングしやす
く、目的とする粒状ポリマーが得られにくい。又、重合
度1500を越えると溶融温度が高くなり、接着剤の芯
地融着ならびに接着に高温を必要とし、作業性並びに布
地をいためる危険性が生ずる。加えて、アルカリ溶解性
も悪くなる。The copolymerization ratio of the ethylenically unsaturated carboxylic acid in the alkali-soluble hot melt adhesive of the present invention is 2 to 15-1 moles, preferably 6 to 10 moles. If the ethylenically unsaturated carboxylic acid is less than 2 molar, the alkali solubility decreases,
On the other hand, if it exceeds 15 molt, although it is essentially possible, the polymerizability will be poor and the polymerization time will be long, resulting in economic disadvantages. Another disadvantage is that the copolymer film becomes hard, impairing the feel of the interlining. The degree of polymerization is within the range of 200 to 150° without causing any performance problems, but is preferably 200 to 1,200. If the degree of polymerization is less than 200, blocking occurs easily during polymerization, making it difficult to obtain the desired granular polymer. Moreover, if the degree of polymerization exceeds 1500, the melting temperature becomes high, and high temperatures are required for interlining fusing and adhesion of the adhesive, resulting in a risk of damaging workability and fabric. In addition, alkali solubility also deteriorates.
その為、四塩化炭素、アセトアルデヒr等重合度調節剤
を重合系に一部加え、重合度を低下させる事が望ましい
。更に、粒度は60メツシュ篩下品が好ましく、30メ
ツシュ篩上品は溶融性及びアルカリ溶解性に劣る。Therefore, it is desirable to partially add a degree of polymerization regulator such as carbon tetrachloride or acetaldehyde to the polymerization system to lower the degree of polymerization. Furthermore, the particle size is preferably one that passes through a 60-mesh sieve, and one that passes through a 30-mesh sieve has poor meltability and alkali solubility.
以下本発明を製造例、実施例により具体的に説明する。 The present invention will be specifically explained below with reference to production examples and examples.
製造例1
分散剤として部分ケン化ポリビニルアルコール(商品名
デンカポパールB −17) 0.3部を溶存させた水
200部に酢酸ビニル95部、クロトン酸5部及び重合
度調節剤として四塩化炭素0.20部、重合触媒として
アゾビスイソブチロニトリル2部を混合した溶液を重合
器に仕込み、重合温度60〜66℃に保ち重合をすすめ
た。重合開始後5時間で重合を停止し、減圧下で未反応
モノマーを除去、濾過乾燥後、白色パール状の共重合体
を得た。得られた共重合体の物性値を第1表に示す。Production Example 1 95 parts of vinyl acetate, 5 parts of crotonic acid, and 0 carbon tetrachloride as a degree of polymerization regulator were added to 200 parts of water in which 0.3 parts of partially saponified polyvinyl alcohol (trade name Denka Popal B-17) was dissolved as a dispersant. A solution containing 20 parts of azobisisobutyronitrile and 2 parts of azobisisobutyronitrile as a polymerization catalyst was charged into a polymerization vessel, and the polymerization temperature was maintained at 60 to 66°C to proceed with polymerization. Polymerization was stopped 5 hours after the start of polymerization, unreacted monomers were removed under reduced pressure, and a white pearl-like copolymer was obtained after filtration and drying. Table 1 shows the physical properties of the obtained copolymer.
熱融着性、アルカリ溶解性共に良好で、アルカリ可溶型
ホットメルト接着剤として、使用出来る。It has good heat fusion properties and alkali solubility, and can be used as an alkali soluble hot melt adhesive.
製造例2〜9
製造例1と同様に酢酸ビニルの量、エチレン性不飽和カ
ルボン酸の種類及び量を変えたもの、あるいは連鎖移動
剤の種類及び量を変えたもので重合し、得られた共重合
体の物性値を第1表に示す。Production Examples 2 to 9 Polymerization was performed in the same manner as in Production Example 1, with different amounts of vinyl acetate, types and amounts of ethylenically unsaturated carboxylic acids, or types and amounts of chain transfer agents. Table 1 shows the physical properties of the copolymer.
製造例2〜5は製造例1と同様良好で、アルカリ可溶型
ホットメルト接着剤として使用出来る。Production Examples 2 to 5 are as good as Production Example 1 and can be used as alkali-soluble hot melt adhesives.
製造例6.7はカルボン酸量が本発明範囲を逸脱した例
でありそれぞれアルカリ溶解性不良、及び重合中のブロ
ッキングにより粉末状のものが得られない為、使用出来
ない。Production Examples 6 and 7 are examples in which the amount of carboxylic acid is outside the range of the present invention, and cannot be used because a powder cannot be obtained due to poor alkali solubility and blocking during polymerization.
製造例8.9は重合度が本発明の範囲を逸脱した例であ
り、それぞれ、重合中のブロッキングにより粉粒状のも
のが得られない。さらに熱融着性不良により使用出来な
い。Production Examples 8 and 9 are examples in which the degree of polymerization is outside the range of the present invention, and powder-like products cannot be obtained due to blocking during polymerization. Furthermore, it cannot be used due to poor heat fusion properties.
第1表に示す物性評価は下記の方法により行った。The physical properties shown in Table 1 were evaluated by the following method.
く熱融着性〉
生成した重合体の32〜100メツシユ間の粒子を用い
て1010X12の布地(テトロン/コツトン一般デo
++ p目付1509/m” )上に159/m”の
散布量で均一に散布し、乾燥機内で180℃の温度で6
D秒間加熱融着させる。15分間自然冷却した後、融着
面を刷毛で軽く10往復掃く。そして、融着した重合体
の量を測定する。熱融着率は以下の式により求める。Heat fusion property> Using particles between 32 and 100 meshes of the produced polymer, fabric of 1010 x 12 (Tetron/Cotton general deo
++ Spray it evenly at a rate of 159/m" on the surface (1509/m") and dry it in a dryer at a temperature of 180°C.
Heat and fuse for D seconds. After cooling naturally for 15 minutes, lightly sweep the fused surface with a brush 10 times. Then, the amount of fused polymer is measured. The thermal fusion rate is determined by the following formula.
熱融着性の評価
O:熱融着率 90%以上
△: 1 50係以上
X:#50チ未満
〈アルカリ溶解性〉
300−三角フラスコに生成した重合体の62〜100
メツシユ間の粒子を19入れ、純水神99g入れる。次
に炭酸ソーダを0.15 、y加え、振とう機忙て20
0ストロ一ク/分、10cIIL/ストロークの速さで
、20°Cの条件下60分間振と5、溶解させる。下記
評価方法によりアルカリ溶解性を判定する。Evaluation of heat fusion property O: Heat fusion rate 90% or more △: 1 50 coefficient or more
Add 19 particles between mesh and 99g of pure water. Next, add 0.15 y of soda carbonate and shake the shaker for 20 y.
Dissolve by shaking for 60 minutes at 20°C at a speed of 0 strokes/min and 10 cIIL/stroke. Alkali solubility is determined by the following evaluation method.
O:重合体粒子が完全に溶解している。O: Polymer particles are completely dissolved.
Δ: が一部溶解せずに残っている。Δ: Part of remains undissolved.
×: が全く溶解していない。×: Not dissolved at all.
実施例1
市販のTシャツ芯地(テトロン/コツトン −般プロー
?)に製造例1の生成重合体32〜100メツシュ品を
1597m”の割合で均一に散布し、180℃に設定し
た乾燥機内で60秒間熱融着させて接着芯地を作成した
。Example 1 A 32 to 100 mesh product of the polymer produced in Production Example 1 was uniformly sprinkled on a commercially available T-shirt interlining material (Tetron/Cotton - General Pro?) at a rate of 1597 m'' and dried in a dryer set at 180°C. An adhesive interlining was created by heat-sealing for 60 seconds.
表地との接着力、洗濯層の接着力、布地の風合い、しみ
出し、芯地間ブロック性に対する性能評価を第2表に示
す。Table 2 shows the performance evaluation of the adhesive strength with the outer material, the adhesive strength of the wash layer, the texture of the fabric, the seepage, and the blockiness between interlinings.
実施例2〜5
製造例2〜5の生成重合体を実施例1と同様に接着芯地
を作成した。性能評価を第2表に示す。Examples 2 to 5 Adhesive interlinings were prepared from the polymers produced in Production Examples 2 to 5 in the same manner as in Example 1. Performance evaluation is shown in Table 2.
比較例1
製造例6の生成重合体を実施例1と同様に接着芯地金作
成した。性能評価を第2表に示す。Comparative Example 1 An adhesive interlining base metal was prepared from the polymer produced in Production Example 6 in the same manner as in Example 1. Performance evaluation is shown in Table 2.
比較例2
市販の重合度700、粒度60〜100メツシユのEV
A (エチレン/酢tin’ニル−9515) 全実施
例1と同様に接着芯地金作成した。性能評価を第2表に
示す。Comparative Example 2 Commercially available EV with polymerization degree of 700 and particle size of 60 to 100 mesh
A (ethylene/acetate tin'nyl-9515) An adhesive interlining base metal was prepared in the same manner as in Example 1. Performance evaluation is shown in Table 2.
比較例6
重合度150、ケン化度40モル%、粒度60〜100
メツシユの粉末状ポリビニルアルコールを実施例1と同
様に接着芯地を作成した。性能評価を第2表に示す。Comparative Example 6 Polymerization degree 150, saponification degree 40 mol%, particle size 60-100
An adhesive interlining was prepared using mesh powder polyvinyl alcohol in the same manner as in Example 1. Performance evaluation is shown in Table 2.
比較例4
重合度300、ケン化度40モル%、酸変性量5モル%
、粒度30〜80メツシユのマレイン酸変性ポリビニル
アルコールを実施例1と同様に接着芯地金作成した。性
能評価を第2表に示す。Comparative Example 4 Polymerization degree 300, saponification degree 40 mol%, acid modification amount 5 mol%
An adhesive interlining base metal was prepared in the same manner as in Example 1 using maleic acid-modified polyvinyl alcohol having a particle size of 30 to 80 mesh. Performance evaluation is shown in Table 2.
第2表に示す性能評価は下記の方法により行った。The performance evaluation shown in Table 2 was performed by the following method.
く接着力〉(表地との接着性)
接着芯地に芯地と同じYシャツ布地をのせ、温度140
℃に設定したアイロンで、0.3kg/cm”の荷重を
かげ10秒間加熱プレスした。この試験片を25關幅に
切断し、剥離強度を測定、接着力とした。Adhesive strength〉(Adhesiveness with outer material) Place the same Y-shirt fabric as the interlining on the adhesive interlining, and heat it at a temperature of 140℃.
The test pieces were heated and pressed for 10 seconds under a load of 0.3 kg/cm'' using an iron set at 0.degree.
く洗濯層の接着力〉
接着力の項で作成した試験片を10X12CIlに切断
し、69/lの家庭用アルカリ洗剤(商品名ニュービー
ズ)溶液80酢酸tjを入れた比色管の中に浸漬させた
。そして4cIIL/ストロークで1往復する振とう機
に比色管をセットし、300ストロ一ク/分の速さで1
5分間洗洗濯層水で良く洗浄して洗剤分を落とし、60
℃で20分間乾燥した。この試験片を251iI幅に切
断し、剥離強度を測定、洗濯層の接着力とした。Adhesive strength of washing layer> The test piece prepared in the adhesive strength section was cut into 10 x 12 CIl and immersed in a colorimetric tube containing 69/l household alkaline detergent (trade name Newbeads) solution 80 acetic acid tj. I let it happen. Then, set the colorimetric tube on a shaker that makes one reciprocation at 4 cIIL/stroke, and
Wash thoroughly with washing water for 5 minutes to remove detergent, and
It was dried at ℃ for 20 minutes. This test piece was cut into a width of 251iI, and the peel strength was measured, which was taken as the adhesive strength of the washing layer.
く布地の風合い〉
洗濯層の接着力の項で作成した、洗濯、乾燥層の試験片
を手触りにより布地の風合いを評価した。Texture of the fabric> The texture of the fabric was evaluated by touching the test pieces of the washing and drying layers prepared in the section of the adhesive strength of the washing layer.
判定基準は以下の通り。The judgment criteria are as follows.
O:表地の風合いを維持している
Δ: が損なわhうやや硬くなっている
。O: The texture of the outer material is maintained.Δ: The texture of the outer material is impaired and it becomes slightly hard.
X: が損なわれ、硬くなっている。X: is damaged and hardened.
くしみ出し〉
洗濯層の接着力の項で作成した、洗濯、乾燥層の試験片
を再度温度140℃に設定したアイロンで0.5 ’1
ean”の荷重をかけ10秒間加熱プレスした。この試
験片の表地に接着剤樹脂がしみ出しているかを肉眼によ
り判定した。判定基準は以下の通り。Combing out> The test piece of the washing and drying layer prepared in the section on the adhesion of the washing layer was 0.5'1 with an iron set at a temperature of 140℃ again.
The test piece was heated and pressed for 10 seconds under a load of 1000 yen.The test piece was visually judged to see if the adhesive resin had oozed out from the outer surface of the test piece.The criteria for judgment were as follows.
○:しみ出し全くなし
Δ:若干しみ出し有り
×ニジみ出し多い
く芯地間ブロッキング性〉
接着芯地に、芯地と同一の布地をのせて、湿度90%、
温度30℃、荷重1 klin”の条件下で24時間放
置してブロッキングテストを実施した。判定は、放置層
の試験片の剥離強度により行い、芯地間ブロッキング性
の評価とした。○: No oozing Δ: Slight oozing x Lots of oozing (blocking property between interlining) Place the same fabric as the interlining on the adhesive interlining, and place at 90% humidity.
A blocking test was carried out by leaving it for 24 hours under conditions of a temperature of 30° C. and a load of 1 klin''. Judgment was made based on the peel strength of the test piece of the left layer, and the interlining blocking property was evaluated.
1、 縫製後、アルカリ剤あるいは弱アルカリ性洗剤で
洗濯することにより、脱樹脂が出来るため、表地の風合
いを保持出来る。1. After sewing, the resin can be removed by washing with an alkaline agent or weakly alkaline detergent, so the texture of the outer material can be maintained.
2、 アルカリ剤洗濯により、完全に脱樹脂出来るため
、表地への樹脂のしみ出しの危険性が全くない。2. Since the resin can be completely removed by washing with an alkaline agent, there is no risk of resin seeping into the outer material.
6、水可溶型樹脂忙見られる融着芯地巻き取りの際、吸
湿等による芯地間のブロッキングは本発明の樹脂が水不
溶性であるため、全く問題ない。6. When winding up the fused interlining, which is often the case with water-soluble resins, there is no problem with blocking between the interlinings due to moisture absorption, etc., because the resin of the present invention is water-insoluble.
Claims (1)
ン酸2〜15モル%、平均重合度200〜1500の共
重合体からなる芯地用アルカリ可溶性ホットメルト接着
剤。An alkali-soluble hot melt adhesive for interlining comprising a copolymer of 98 to 85 mol% of vinyl acetate, 2 to 15 mol% of ethylenically unsaturated carboxylic acid, and an average degree of polymerization of 200 to 1,500.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61160790A JP2610831B2 (en) | 1986-07-10 | 1986-07-10 | Hot melt adhesive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61160790A JP2610831B2 (en) | 1986-07-10 | 1986-07-10 | Hot melt adhesive |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6317978A true JPS6317978A (en) | 1988-01-25 |
JP2610831B2 JP2610831B2 (en) | 1997-05-14 |
Family
ID=15722508
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61160790A Expired - Lifetime JP2610831B2 (en) | 1986-07-10 | 1986-07-10 | Hot melt adhesive |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2610831B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6931877B2 (en) | 2002-05-22 | 2005-08-23 | Sanden Corp. | Refrigerating open showcase |
JP2009161602A (en) * | 2007-12-28 | 2009-07-23 | Denki Kagaku Kogyo Kk | Polyvinyl acetal composition containing modified polyvinyl acetate, polyvinyl acetal sheet comprised of the polyvinyl acetal composition, and interlayer film for laminated glass comprising the polyvinyl acetal composition |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS516260A (en) * | 1974-07-05 | 1976-01-19 | Kyowa Gas Chem Ind Co Ltd |
-
1986
- 1986-07-10 JP JP61160790A patent/JP2610831B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS516260A (en) * | 1974-07-05 | 1976-01-19 | Kyowa Gas Chem Ind Co Ltd |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6931877B2 (en) | 2002-05-22 | 2005-08-23 | Sanden Corp. | Refrigerating open showcase |
JP2009161602A (en) * | 2007-12-28 | 2009-07-23 | Denki Kagaku Kogyo Kk | Polyvinyl acetal composition containing modified polyvinyl acetate, polyvinyl acetal sheet comprised of the polyvinyl acetal composition, and interlayer film for laminated glass comprising the polyvinyl acetal composition |
Also Published As
Publication number | Publication date |
---|---|
JP2610831B2 (en) | 1997-05-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2735585B2 (en) | Binder for planar textiles, comprising aqueous dispersion of (meth) acrylate copolymer and process for producing the same | |
EP0474415B1 (en) | Method of treating a porous substrate | |
US3961125A (en) | Temporary interlining coated with foamed adhesive | |
JPH09291482A (en) | Latex | |
JP2005089655A (en) | Polyvinyl alcohol resin and film | |
JP3251695B2 (en) | Double-layer fusible interlining and method for producing the same | |
JPS6317978A (en) | Hot-melt adhesive | |
JP5225693B2 (en) | Fibrous flat product with quality-improved coating, its manufacture and its use | |
WO2001004230A1 (en) | Process for producing adhesive for fusion bonding, adhesive for fusion bonding obtained by the process, and adhesive fabric containing the adhesive for fusion bonding | |
JP2797936B2 (en) | Hot melt adhesive | |
JPS6020502B2 (en) | Liquid laundry glue composition | |
JPS6034594B2 (en) | Water-soluble hot melt adhesive for temporarily fixing interlining | |
JPS6395281A (en) | Water-soluble hot melt adhesive for temporary bonding of padding cloth | |
JP2000504360A (en) | Poly (vinyl alcohol) copolymer ionomers, their preparation and use in textile glues | |
JP2523951Y2 (en) | Detergent pack bag | |
JPS5966474A (en) | Water-soluble and heat-weldable adhesive for temporary bonding of interlining cloth | |
CN106634721B (en) | Acrylic ester aquosity hot melt latex solution of adhesion lining cloth and preparation method thereof | |
JPS5953784A (en) | Heat adhesive false adhered core cloth | |
JPS58141275A (en) | Film for temporary bonding of interlining cloth | |
JPH02294334A (en) | Aqueous plastic dispersion | |
JP3720420B2 (en) | Laundry paste for textile products | |
JPH0786159B2 (en) | Hot melt adhesive | |
JPH07286154A (en) | Alkali-soluble hot-melt adhesive | |
JPH093781A (en) | Bonding cloth | |
JPS599276A (en) | Adhesive fabric |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |