JPH0411785Y2 - - Google Patents
Info
- Publication number
- JPH0411785Y2 JPH0411785Y2 JP7641486U JP7641486U JPH0411785Y2 JP H0411785 Y2 JPH0411785 Y2 JP H0411785Y2 JP 7641486 U JP7641486 U JP 7641486U JP 7641486 U JP7641486 U JP 7641486U JP H0411785 Y2 JPH0411785 Y2 JP H0411785Y2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- fabric
- fragrance
- aromatic
- resin film
- 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
- 229920005989 resin Polymers 0.000 claims description 41
- 239000011347 resin Substances 0.000 claims description 41
- 239000004744 fabric Substances 0.000 claims description 36
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 238000013268 sustained release Methods 0.000 claims description 12
- 239000012730 sustained-release form Substances 0.000 claims description 12
- 230000035699 permeability Effects 0.000 claims description 6
- 229920000178 Acrylic resin Polymers 0.000 claims description 4
- 239000004925 Acrylic resin Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229920002681 hypalon Polymers 0.000 claims description 2
- 229920001195 polyisoprene Polymers 0.000 claims description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 2
- 239000011342 resin composition Substances 0.000 claims 1
- 239000003205 fragrance Substances 0.000 description 33
- 239000000126 substance Substances 0.000 description 23
- 238000000034 method Methods 0.000 description 10
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 230000002688 persistence Effects 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 239000004677 Nylon Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 235000019645 odor Nutrition 0.000 description 4
- 239000002304 perfume Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000005923 long-lasting effect Effects 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 2
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- -1 terpene compounds Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 208000035985 Body Odor Diseases 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 244000068485 Convallaria majalis Species 0.000 description 1
- 235000009046 Convallaria majalis Nutrition 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
- 244000215562 Heliotropium arborescens Species 0.000 description 1
- 241001632576 Hyacinthus Species 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 206010040904 Skin odour abnormal Diseases 0.000 description 1
- 244000290333 Vanilla fragrans Species 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 238000007500 overflow downdraw method Methods 0.000 description 1
- 229940100595 phenylacetaldehyde Drugs 0.000 description 1
- 229940081310 piperonal Drugs 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000009637 wintergreen oil Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Description
(産業上の利用分野)
本考案は、香りの持続性に優れた徐放性芳香布
帛に関するものである。
(従来技術)
布帛に香りをつける習慣は、古くから行われて
おり、その作用は、芳香性物質である香水やオー
デコロン等を衣服又は体に付与することにより体
内から発生する体臭を芳香物質の香りと置き換え
ることで不快な匂いを取り除くことである。
従来、布帛に香りを付与するには、芳香性物質
をアルコール等の揮発性溶剤に溶解したものをス
プレー等により直接布帛に付与させるか、あるい
は、芳香性物質を皮膜形成用樹脂に添加した後、
布帛に塗布し、樹脂皮膜内部に芳香性物質を含有
した樹脂皮膜を布帛上に形成させるかのいずれか
の方法により行われていた。
(考案が解決しようとする問題点)
スプレー等の噴露方式によれば、簡単に芳香性
を付与出来るが、元来、芳香性物質そのものが気
化し易い物質であるため持続性に乏しいものしか
得られない。一方、樹脂への添加方式によれば、
樹脂皮膜が無孔の場合、芳香性物質の空気中への
揮散が小さいため、香りの効果の点で、不充分で
ある。また、樹脂皮膜が多孔質膜の場合、芳香性
物質の揮散が大きくなり、逆に持続性に乏しいも
のとなる。さらに、最近これらの点を改善する目
的で芳香性物質の多孔質マイクロカプセル化によ
り、徐放性を与える試みも見られるが、香りの持
続性とコスト及び歩留りの点で満足すべきものが
得られていないのが現状である。
本考案は、上記の問題点を解決するものであつ
て、その目的は、香りの持続性があり、しかも洗
濯耐久性に優れている徐放性芳香布帛を提供する
ことにある。
(問題点を解決するための手段)
本考案者らは、このような問題点を解決するた
めに、鋭意研究の結果、香りの持続性に優れた徐
放性布帛を得るためには、樹脂膜の平均厚みと樹
脂皮膜自身の気体の透過性とを検討することによ
り本考案に到達したものである。
すなわち、本考案は、徐放性芳香布帛におい
て、布帛の表面を芳香剤を含有した中程度の気体
透過係数を有する樹脂皮膜で被覆したことを特徴
とする徐放性芳香布帛を要旨とするものである。
以下、本考案を詳細に説明する。
図面は、本考案になる徐放性布帛の概略図を示
したものである。1は、布帛、2は、樹脂皮膜に
含有する芳香性物質、3は、樹脂皮膜である。
布帛1は、芳香性物質を含有した樹脂皮膜層を
布帛上に形成出来るものであれば繊維として木
綿、麻、絹、羊毛等の天然繊維、ビスコース、ア
セテート等の化学繊維、ナイロン、ポリエステル
等の合成繊維のうちいずれの繊維を用いたもので
もよい。また、布帛としては、織物や編物あるい
は不織布のいずれもが使用出来る。さらに、上記
布帛について他繊維の混紡や混繊、交織あるいは
交編等のいずれもが使用出来る。
次に、樹脂皮膜中に含有される芳香性物質2
は、おもに香料からなる揮発性物質であり、香料
とは常温において揮発性を有し、その“香り”に
より香粧品、し好品などの賦香料に使用しうる有
機性物質をいう。香料には、天然香料と合成香料
とがあり、天然香料は天然物から香成分のみを採
取したものである。一方、合成香料は、テルペン
化合物並びにその誘導体からなるもので、本考案
で使用される化合物として次に示す2種類のもの
が製造されている。その一つは、天然香料の成分
と全く同一の化学構造を有する化合物、例えばバ
ニリン(バニラ実の主成分)、サリチル酸メチル
(ウインターグリーン油の主成分)、β−フエニル
エチルアルコール(バラ油の主成分)等であり、
もう一つは、天然物と類似の芳香を有する化合物
例えば、オキシシトロネラール(スズランのにお
い)、フエニルアセトアルデヒド(ヒヤシンスの
におい)、ピペロナール(ヘリオトロープのにお
い)等が上げられる。なお、本考案では天然香料
及び合成香料あるいは天然香料と合成香料との混
合物のいずれもが使用出来る。
次に、上記香料を適宜選択した後、樹脂溶液を
調整する時に樹脂とともに添加する。添加する量
については芳香効果を得るために樹脂固形分中に
0.1−2重量%(以下重量%を単に%と略称す
る。)含有させることが望ましい。なお、樹脂溶
液の調整の場合においては、作業性及び芳香性物
質の揮散の点から開放系での調合作業を避け、密
閉系で行うべきである。
布帛上に芳香性物質を含有した樹脂皮膜を形成
させるには、パデイング法、スプレー法、コーテ
イング法、ラミネート法のいずれもが使用出来る
が、布帛上に均一な厚みを有する皮膜を形成する
にはコーテイング法やラミネート法が好ましい。
コーテイング機械としてフローテイングナイフコ
ーター、グラビアロール、コンマロールコーター
等が使用出来る。また、ラミネート法では先ず離
型紙上に樹脂皮膜を形成させた後、接着剤法、転
写法、熱融着法のいずれかの方法で樹脂皮膜と布
帛とを接合させる。
本考案における中程度の気体透過係数を有する
樹脂とは、ガスバリヤー性能の高いポリビニルア
ルコール、ポリ塩化ビニリデン、ナイロン樹脂等
のクラスと逆に気体透過性の高いシリコンエラス
トマーやアミノ酸・ウレタンブロツクコポリマー
のクラスとの中間にランクされるものである。具
体的には繊維製品用途への展開を考え、アクリル
樹脂、ウレタン樹脂、クロルスルホン化ポリエチ
レン樹脂、ポリイソプレン樹脂が好ましく用いら
れる。上記樹脂が本考案で好ましく用いられる理
由は、樹脂皮膜中に含有した芳香性物質が空気中
に徐々に揮散する機能を有していることと、これ
らの樹脂が繊維との接着性及び機械的強度や風合
いの点で優れているからである。
次に、樹脂皮膜の平均厚みが少なくとも5μm以
上、好ましくは10−40μmが望ましい。5μmより
薄い場合、風合い面では柔軟なものが得られる
が、香りの持続性が乏しくなり易く、一方、
40μmを超えると香りの面で効果が少なくなり易
く、また風合い面でも硬くなることがある。
なお、布帛からの芳香性物質の揮散速度を上げ
たい場合、香料の添加量を増すか、樹脂皮膜の厚
みを薄くすればよい。
(実施例)
以下、本考案の具体的説明を実施例により行
う。
実施例 1
ナイロンマルチフイラメント(セミダル)420
デニール/48フイラメント糸条を経糸及び緯糸に
用い、鞄材用織物をウオータージエツトルームに
て製織した。{織物組織;平組織、生機密度;(経
糸)51本/2.54cm、(緯糸)32本/2.54cm、}引き
続き、オープンソーパーにて精錬、ジツガーにて
酸性染料を使用し、青色に染色を行い(98℃×60
分)、その後テンターにて150℃×1分の条件でヒ
ートセツトした。次いで、フツ素系撥水材(商品
名アサヒガードAG−710、旭硝子k.k.製品)5%
水溶液中に浸漬し、絞り率60%で均一に絞り、
100℃×5分で乾燥の後150℃×1分の条件にて熱
処理をした。
次に、鏡面仕上げ鋳鉄製ロールとコツトンボウ
ルからなるカレンダー加工機を使用し、温度160
℃、圧力30Kg/cm2、布速20m/minの条件で目つ
ぶし加工を行つた。
上記織物のカレンダー加工面にフローテイング
ナイフコーターを使用し、塗布厚50μmにて処方
1に示すアクリル樹脂(樹脂固形分濃度25%)を
塗布した後100℃で乾燥し、次いで150℃×1分の
条件にて熱処理を行い、芳香性物質を含有した布
帛を得た。
(処方1)
アクリル樹脂 100部
(商品名;クリスコートP−1330大日本インキ
化学k.k.製品)
香料 2部
(β−フエニルエチルアルコール 純分20%)
(商品名;ローズ R−5392高砂香料k.k.製
品)
トルエン 20部
次に、本考案と比較する目的で比較例1,2を
作成した。
比較例 1,2
実施例1にて使用したナイロン織物を用意し、
コーテイング樹脂処方(処方2,3)を除き、他
は実施例1と全く同一条件にて加工を行つた。
(処方2)
ブチラール樹脂 30部
(重合度 600 ブチラール化度60モル%)
香料
(β−フエニルエチルアルコール 純分20%)
2部
(商品名;ローズ R−5392高砂香料k.k.製
品)
エタノール/トルエン 88部
VOL 比 1/1
(処方3)
シリコン樹脂
(メチルハイドロジエンポリシロキサン/ジメ
チルポリシロキサン混合物) 100部
(商品名;ポロンコート 固形分15%信越化学
k.k.製品)
キヤタリスト
PC(有機金属塩) 1部
PC(反応用助触媒) 1部
香料(β−フエニルエチルアルコール 純分20
%) 2部
(商品名;ローズ R−5392高砂香料k.k.製
品)
得られたコーテイング織物について芳香性能を
調べ、その結果を第1表に示す。なお、芳香性能
については、パネラー10人がそれぞれ20℃×65%
RH、風速0.6m/sec気積18m3の室内にて各試作
サンフル(サイズ;50cm×50cm)から50cm離れた
距離において“香り”の有無を調べた。
(Industrial Application Field) The present invention relates to a sustained-release aromatic fabric with excellent fragrance persistence. (Prior art) The custom of adding fragrance to fabrics has been practiced for a long time, and its effect is to apply aromatic substances such as perfume or cologne to clothing or the body to remove body odor generated from within the body. The purpose is to remove unpleasant odors by replacing them with scents. Traditionally, in order to impart fragrance to fabric, an aromatic substance dissolved in a volatile solvent such as alcohol is applied directly to the fabric by spraying, or the aromatic substance is added to a film-forming resin and then added. ,
This has been done by applying it to a fabric and forming a resin film containing an aromatic substance inside the resin film on the fabric. (Problem that the invention aims to solve) Although it is possible to easily impart aromatic properties using a spray method, it is difficult to maintain the fragrance because the aromatic substance itself is easily vaporized. I can't get it. On the other hand, according to the addition method to the resin,
If the resin film is non-porous, the volatilization of the aromatic substance into the air is small, so the aroma effect is insufficient. Furthermore, when the resin film is a porous film, the aromatic substance volatilizes to a large extent, resulting in poor sustainability. Furthermore, in order to improve these points, there have recently been attempts to provide sustained release by porous microencapsulation of aromatic substances, but these efforts have not been satisfactory in terms of fragrance sustainability, cost, and yield. The current situation is that this is not the case. The present invention is intended to solve the above-mentioned problems, and its purpose is to provide a sustained-release fragrance fabric that has a long-lasting fragrance and is excellent in washing durability. (Means for Solving the Problems) In order to solve these problems, the present inventors conducted intensive research and found that in order to obtain a sustained-release fabric with excellent fragrance persistence, resin The present invention was arrived at by examining the average thickness of the film and the gas permeability of the resin film itself. That is, the gist of the present invention is a sustained-release aromatic fabric characterized in that the surface of the fabric is coated with a resin film containing an aromatic agent and having a medium gas permeability coefficient. It is. The present invention will be explained in detail below. The drawing shows a schematic diagram of the sustained-release fabric according to the present invention. 1 is a fabric, 2 is an aromatic substance contained in the resin film, and 3 is a resin film. The fabric 1 may be any fiber that can form a resin film layer containing an aromatic substance on the fabric, such as natural fibers such as cotton, hemp, silk, and wool, chemical fibers such as viscose and acetate, nylon, and polyester. Any synthetic fiber may be used. Further, as the fabric, any of woven fabrics, knitted fabrics, and non-woven fabrics can be used. Further, the above-mentioned fabric may be blended with other fibers, mixed fibers, mixed weaving, mixed knitting, or the like. Next, the aromatic substance 2 contained in the resin film
is a volatile substance consisting mainly of perfume, and perfume is an organic substance that is volatile at room temperature and can be used as a flavoring agent for cosmetics, cosmetics, etc. due to its "scent". There are two types of fragrances: natural fragrances and synthetic fragrances, and natural fragrances are those obtained by collecting only fragrance ingredients from natural products. On the other hand, synthetic fragrances are made of terpene compounds and derivatives thereof, and the following two types of compounds have been produced as compounds used in the present invention. One of them is compounds that have the exact same chemical structure as natural fragrance ingredients, such as vanillin (the main component of vanilla fruit), methyl salicylate (the main component of wintergreen oil), and β-phenylethyl alcohol (the main component of rose oil). main components), etc.
The other is a compound having a scent similar to a natural product, such as oxycitronellal (lily of the valley odor), phenylacetaldehyde (hyacinth odor), piperonal (heliotrope odor), and the like. In the present invention, both natural fragrances and synthetic fragrances or mixtures of natural fragrances and synthetic fragrances can be used. Next, after appropriately selecting the above perfume, it is added together with the resin when preparing the resin solution. Regarding the amount added, it is necessary to add it to the resin solid content in order to obtain the aromatic effect.
It is desirable to contain 0.1-2% by weight (hereinafter, % by weight is simply abbreviated as %). In addition, in the case of preparing the resin solution, preparation work in an open system should be avoided from the viewpoint of workability and volatilization of aromatic substances, and should be carried out in a closed system. To form a resin film containing an aromatic substance on a fabric, any of the padding method, spray method, coating method, and lamination method can be used, but in order to form a film with a uniform thickness on the fabric, A coating method or a lamination method is preferred.
Floating knife coaters, gravure rolls, comma roll coaters, etc. can be used as coating machines. In the lamination method, a resin film is first formed on a release paper, and then the resin film and the fabric are bonded to each other by an adhesive method, a transfer method, or a heat fusion method. In the present invention, resins with a medium gas permeability coefficient refer to classes such as polyvinyl alcohol, polyvinylidene chloride, and nylon resins, which have high gas barrier properties, and classes such as silicone elastomers and amino acid/urethane block copolymers, which have high gas permeability. It is ranked in between. Specifically, considering the use in textile products, acrylic resin, urethane resin, chlorosulfonated polyethylene resin, and polyisoprene resin are preferably used. The reason why the above resins are preferably used in the present invention is that the aromatic substances contained in the resin film have the function of gradually volatilizing into the air, and that these resins have good adhesion to fibers and mechanical properties. This is because it is superior in terms of strength and texture. Next, it is desirable that the average thickness of the resin film is at least 5 μm or more, preferably 10-40 μm. If it is thinner than 5μm, a soft texture can be obtained, but the persistence of the fragrance tends to be poor, and on the other hand,
If the thickness exceeds 40 μm, the fragrance tends to be less effective, and the texture may become hard. Note that if it is desired to increase the volatilization rate of the aromatic substance from the fabric, the amount of fragrance added may be increased or the thickness of the resin film may be reduced. (Example) Hereinafter, the present invention will be specifically explained using examples. Example 1 Nylon multifilament (semidull) 420
A fabric for bag material was woven in a water jet loom using denier/48 filament yarn for the warp and weft. {Woven structure: flat structure, fabric density: (warp) 51 threads/2.54cm, (weft) 32 threads/2.54cm,} Continuously refined with an open soaper and dyed blue using acid dye in a jitzger. Conducted (98℃×60
minutes), and then heat set in a tenter at 150°C for 1 minute. Next, 5% fluorine-based water repellent material (product name Asahi Guard AG-710, Asahi Glass KK product)
Immerse it in an aqueous solution and squeeze it uniformly at a squeezing rate of 60%.
After drying at 100°C for 5 minutes, heat treatment was performed at 150°C for 1 minute. Next, a calendar processing machine consisting of a mirror-finish cast iron roll and a cotton bowl is used to heat the product to a temperature of 160.
The blinding process was carried out under the conditions of ℃, pressure of 30 kg/cm 2 , and cloth speed of 20 m/min. Using a floating knife coater, the acrylic resin shown in Formulation 1 (resin solids concentration 25%) was applied to the calendered surface of the fabric at a coating thickness of 50 μm, and then dried at 100°C, and then dried at 150°C for 1 minute. Heat treatment was performed under the following conditions to obtain a fabric containing an aromatic substance. (Formulation 1) Acrylic resin 100 parts (Product name: Criscoat P-1330 Dainippon Ink Chemical KK product) Fragrance 2 parts (β-phenylethyl alcohol pure content 20%) (Product name: Rose R-5392 Takasago Perfume KK product) Product) Toluene 20 parts Next, Comparative Examples 1 and 2 were prepared for the purpose of comparison with the present invention. Comparative Examples 1 and 2 The nylon fabric used in Example 1 was prepared,
Processing was carried out under exactly the same conditions as in Example 1, except for the coating resin formulations (Formulations 2 and 3). (Formulation 2) Butyral resin 30 parts (polymerization degree 600 butyralization degree 60 mol%) Fragrance (β-phenylethyl alcohol pure content 20%)
2 parts (Product name: Rose R-5392 Takasago Fragrance KK product) Ethanol/Toluene 88 parts VOL ratio 1/1 (Formulation 3) Silicone resin (Methylhydrodiene polysiloxane/dimethyl polysiloxane mixture) 100 parts (Product name: Poron Coat Solid content 15% Shin-Etsu Chemical
kk product) Catalyst PC (organic metal salt) 1 part PC (cocatalyst for reaction) 1 part fragrance (β-phenylethyl alcohol, purity 20
%) 2 parts (trade name: Rose R-5392 Takasago Fragrance KK product) The aroma performance of the obtained coated fabric was examined and the results are shown in Table 1. Regarding the aroma performance, 10 panelists each tested 20℃ x 65%.
The presence or absence of a "scent" was examined at a distance of 50 cm from each prototype Sunful (size: 50 cm x 50 cm) in a room with RH, wind speed of 0.6 m/sec, and air volume of 18 m 3 .
【表】
第1表より明らかなように、樹脂の種類により
芳香性能は、異なつており、本考案においては、
芳香効果及び芳香持続性の両方とも満足の出来る
ものであつた。すなわち、洗濯における耐久性に
ついては、JIS L−0217(103)法にて処理した10
回洗濯後においても十分に“香り”が認められ
た。また、芳香持続性においても徐放効果により
加工後6カ月経過しても“香り”が認められ、十
分に芳香持続性を有していた。
一方、ブチラール樹脂の場合、PVA樹脂と同
様、気体のバリヤー性があるため、芳香効果は認
められなかつた。また、シリコン樹脂の場合、コ
ラーゲン物質と同様、気体の透過性が高過ぎ、加
工直後では、“香り”が認められたが、香りの持
続性及び洗濯耐久性に乏しいものであつた。
(考案の効果)
本考案による徐放性布帛は、香りの持続性があ
り、しかも洗濯耐久性に優れたものであるため、
鞄や靴等の雑貨、壁材やカーテン等のインテリア
関係あるいはおむつカバーやベツトカバー等の衛
生関係等広範囲に利用出来るものである。[Table] As is clear from Table 1, the aroma performance differs depending on the type of resin, and in this invention,
Both the fragrance effect and fragrance persistence were satisfactory. In other words, regarding durability in washing, 10
Even after washing twice, the "fragrance" was sufficiently observed. In addition, due to the sustained release effect, "fragrance" was observed even after 6 months of processing, indicating that the fragrance had sufficient persistence. On the other hand, in the case of butyral resin, similar to PVA resin, it has gas barrier properties, so no aromatic effect was observed. In addition, in the case of silicone resin, the gas permeability is too high, as is the case with collagen materials, and although a "scent" was observed immediately after processing, the persistence of the scent and washing durability were poor. (Effects of the invention) The sustained-release fabric according to the invention has a long-lasting fragrance and has excellent washing durability.
It can be used in a wide range of applications, including miscellaneous goods such as bags and shoes, interior items such as wall materials and curtains, and sanitary items such as diaper covers and bed covers.
第1図は本考案の徐放性芳香布帛を概略的に例
示した断面図である。
1……布帛、2……芳香性物質、3……樹脂皮
膜。
FIG. 1 is a cross-sectional view schematically illustrating the sustained-release aromatic fabric of the present invention. 1...Fabric, 2...Aromatic substance, 3...Resin film.
Claims (1)
剤を含有した中程度の気体透過係数を有する樹
脂皮膜で被覆したことを特徴とする徐放性芳香
布帛。 (2) 樹脂皮膜を形成する樹脂組成物がアクリル樹
脂、ウレタン樹脂、クロルスルホン化ポリエチ
レン樹脂、ポリイソプレン樹脂及びそれらの混
合樹脂よりなる群から選ばれた樹脂である実用
新案登録請求の範囲第1項記載の徐放性芳香布
帛。 (3) 布帛表面に被覆した樹脂皮膜の平均厚みが少
なくとも5μm以上である実用新案登録請求の範
囲第1項又は第2項記載の徐放性芳香布帛。[Claims for Utility Model Registration] (1) A sustained-release aromatic fabric characterized in that the surface of the fabric is coated with a resin film containing an aromatic agent and having a medium gas permeability coefficient. . (2) Utility model registration claim No. 1 in which the resin composition forming the resin film is a resin selected from the group consisting of acrylic resin, urethane resin, chlorosulfonated polyethylene resin, polyisoprene resin, and mixed resins thereof. The sustained-release aromatic fabric described in Section 1. (3) The sustained-release aromatic fabric according to claim 1 or 2, wherein the average thickness of the resin film coated on the fabric surface is at least 5 μm or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7641486U JPH0411785Y2 (en) | 1986-05-21 | 1986-05-21 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7641486U JPH0411785Y2 (en) | 1986-05-21 | 1986-05-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62187729U JPS62187729U (en) | 1987-11-30 |
| JPH0411785Y2 true JPH0411785Y2 (en) | 1992-03-24 |
Family
ID=30923467
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7641486U Expired JPH0411785Y2 (en) | 1986-05-21 | 1986-05-21 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0411785Y2 (en) |
-
1986
- 1986-05-21 JP JP7641486U patent/JPH0411785Y2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62187729U (en) | 1987-11-30 |
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