JPH01282305A - Aromatic fiber and production thereof - Google Patents
Aromatic fiber and production thereofInfo
- Publication number
- JPH01282305A JPH01282305A JP11328588A JP11328588A JPH01282305A JP H01282305 A JPH01282305 A JP H01282305A JP 11328588 A JP11328588 A JP 11328588A JP 11328588 A JP11328588 A JP 11328588A JP H01282305 A JPH01282305 A JP H01282305A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- fragrance
- aromatic
- polymer
- microcapsules
- 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
- 239000000835 fiber Substances 0.000 title claims abstract description 38
- 125000003118 aryl group Chemical group 0.000 title claims abstract description 26
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000003094 microcapsule Substances 0.000 claims abstract description 28
- 238000009987 spinning Methods 0.000 claims abstract description 17
- 238000005406 washing Methods 0.000 claims abstract description 17
- 229920000728 polyester Polymers 0.000 claims abstract description 13
- 229920000642 polymer Polymers 0.000 claims abstract description 13
- 150000001875 compounds Chemical class 0.000 claims abstract description 11
- 238000002844 melting Methods 0.000 claims abstract description 8
- 230000008018 melting Effects 0.000 claims abstract description 8
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 8
- 239000000843 powder Substances 0.000 claims abstract description 7
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 6
- 239000012530 fluid Substances 0.000 claims abstract description 3
- 238000007599 discharging Methods 0.000 claims abstract 2
- 238000006116 polymerization reaction Methods 0.000 claims abstract 2
- 239000003205 fragrance Substances 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 12
- -1 polysiloxane Polymers 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 9
- 238000004898 kneading Methods 0.000 claims description 6
- 229930040373 Paraformaldehyde Natural products 0.000 claims description 3
- 229920006324 polyoxymethylene Polymers 0.000 claims description 3
- 239000004416 thermosoftening plastic Substances 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims 1
- 230000003068 static effect Effects 0.000 abstract description 9
- 239000002304 perfume Substances 0.000 abstract description 5
- 239000004014 plasticizer Substances 0.000 abstract description 2
- 239000011369 resultant mixture Substances 0.000 abstract 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 abstract 1
- 239000004205 dimethyl polysiloxane Substances 0.000 abstract 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 abstract 1
- 238000000034 method Methods 0.000 description 14
- 239000000306 component Substances 0.000 description 13
- 239000000796 flavoring agent Substances 0.000 description 7
- 239000002612 dispersion medium Substances 0.000 description 6
- 235000019634 flavors Nutrition 0.000 description 6
- 239000012209 synthetic fiber Substances 0.000 description 5
- 229920002994 synthetic fiber Polymers 0.000 description 5
- 238000000354 decomposition reaction Methods 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 229920005992 thermoplastic resin Polymers 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005177 Duracon® POM Polymers 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 description 1
- 241000156978 Erebia Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、香りを有する合成繊維の製造法に関するもの
であシ、さらに詳しくは、香りを有する物質を包含した
マイクロカプセルを熱可塑性樹脂中に分散混合せしめて
、長期間にわたシ一定の香りを有することのできる合成
繊維及びその製造法に関するものである。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for producing synthetic fibers having a fragrance.More specifically, the present invention relates to a method for producing synthetic fibers having a fragrance. The present invention relates to a synthetic fiber that can maintain a constant fragrance for a long period of time by being dispersed and mixed with the fibers, and a method for producing the same.
〈従来技術〉
従来、繊維及繊維製品に芳香性を付与させる手段として
香料を直接振シ掛ける方法が行なわれてきた。これは最
も簡単で有効な手段であるが、洗濯耐久性、長期持続性
がなく芳香耐久性を要求する用途には使えなかった。<Prior Art> Conventionally, a method of directly sprinkling fragrances on fibers and textile products has been used as a means of imparting aromatic properties to fibers and textile products. Although this is the simplest and most effective method, it lacks washing durability and long-term sustainability, and cannot be used in applications that require fragrance durability.
また、このほかの方法としてポリエステルやポリアミド
のような一般的な合成繊維に芳香性を持たせるため紡糸
時に練込、複合等の手法により、芳香成分を繊維中に含
有せしめる方法が特開昭48−93714号公報、特開
昭62−85010号公報等に記載されたが、ポリエス
テルやポリアミドは成形温度が非常に高いため、溶融ポ
リマー中に送られた香料が分解したり、反応したシ、又
ガスを発生したプすることにより紡糸性は非常に困難に
なることが予想される。In addition, in order to impart aromatic properties to common synthetic fibers such as polyester and polyamide, there is a method in which aromatic components are incorporated into the fibers by kneading, compounding, etc. during spinning. 93714, Japanese Patent Application Laid-open No. 62-85010, etc., the molding temperature of polyester and polyamide is very high, so the fragrance sent into the molten polymer may decompose, react or react. It is expected that spinnability will be extremely difficult due to the gas generated.
仮に紡糸が可能であったとしてもその糸に含有される芳
香成分は高沸点のものが多くなってしまう。芳香性とは
高沸点から低沸点のさまざまな香料成分がバランス良く
配合されることによって、始めて得られるものであるか
ら、その配合の・(ランスを無視し、単に香料が含有さ
れている状態を芳香性と称することは甚だ疑問である。Even if spinning were possible, many of the aromatic components contained in the yarn would have high boiling points. Aromatic properties are obtained through a well-balanced combination of various fragrance components with high to low boiling points, so it is important to ignore the balance of the combination and simply evaluate the state in which the fragrance is contained. Calling it aromatic is highly questionable.
また、紡糸時のこのような事態をあらかじめ考慮し、添
加しようとする香料を熱的に安定なもののみに限定して
用いる方法が考えられるが、このような方法によって得
られた繊維の匂い璃単一的であり、人間に対し゛芳香゛
という感じを与えるものではない。In addition, it is possible to consider this situation in advance during spinning and limit the flavoring agents to be added to only those that are thermally stable, but the odor of the fibers obtained by such a method It is monolithic and does not give a sense of fragrance to humans.
〈発明が解決しようとする課題〉
従って本発明は、香料成分がバランス良く配合されてい
る状態のまま芳香性物質が繊維中に含有されかつその芳
香性が長期間持続されうるような芳香性繊維及その製造
方法を提供せんとするものである。<Problems to be Solved by the Invention> Therefore, the present invention provides an aromatic fiber in which an aromatic substance is contained in the fiber with a well-balanced combination of fragrance components, and the aromatic property can be maintained for a long period of time. The present invention aims to provide a method for manufacturing the same.
〈課題を解決するための手段〉
本発明は調合香料などの芳香剤が元来持つ芳香性をでき
るだけ忠実に繊維形態で再現するために紡糸時に添加す
る芳香剤にかかる温度を低くすることと紡糸時の熱によ
る芳香剤の揮発性成分の揮発を抑えることをその手段と
した。<Means for Solving the Problems> The present invention aims to reduce the temperature applied to the fragrance added during spinning and to reduce the temperature applied to the fragrance added during spinning in order to reproduce the original aromatic properties of fragrances such as blended fragrances as faithfully as possible in the form of fibers. The method was to suppress the volatilization of the volatile components of the fragrance due to the heat of the air.
その結果、繊維の主成分となる熱可塑性樹脂として融点
176 ’Cのポリオキシメチレンを用い、さらに、芳
香剤をマイクロカプセルで包含した上でまず分散媒中に
分散してから、熱可塑性樹脂に分散させるという全く新
しい芳香性繊維及その製造法を発明するに至った。As a result, polyoxymethylene with a melting point of 176'C was used as the thermoplastic resin that is the main component of the fiber, and the aromatic agent was encapsulated in microcapsules and dispersed in a dispersion medium, and then added to the thermoplastic resin. This led to the invention of a completely new aromatic fiber that involves dispersion, and a method for producing the same.
ポリオキンメチレンは(1)式のような分子式で表わさ
れ、融点が低いこと、熱成形性に優れている−1−CH
20+rl(1)
+CHzO+−+CHzCHzテCH2O七伏CH2C
H2九(2)こと、樹脂が市販されていること、などの
状況から本発明に最も適切である。市販品にはポリオキ
/メチレン・コポリマーとしてさらに融点の低いタイプ
、−例えば(2)式で示されるような分子式をもつポリ
プラスチックス株式会社製のジュラコンのような融点1
65°Cのような樹脂があυ、本発明に用いる樹脂とし
てはさらに好都合である。Polyoxyquinmethylene is represented by the molecular formula (1), and has a low melting point and excellent thermoformability -1-CH
20+rl(1) +CHzO+-+CHzCHzteCH2O7bushCH2C
H29(2) is most suitable for the present invention because of the fact that the resin is commercially available. Commercially available polyoxy/methylene copolymers with even lower melting points, such as Duracon manufactured by Polyplastics Co., Ltd., which has a molecular formula as shown in formula (2), have a melting point of 1.
A resin having a temperature of 65° C. is more advantageous as a resin for use in the present invention.
本発明では香料をそのまま用いるのではなく、一端マイ
クロカプセル中に投入しそのマイクロカプセル微粉末を
繊維中に練込むという方法を採った。香料をマイクロカ
プセル化することによシ、(1)紡糸練込時、溶融ポリ
マーの熱が直接香料に伝わらないので熱による分解揮発
を抑えられる。(2)紡糸時熱による香料の揮発性成分
の揮発をマイクロカプセルが周υを覆うことによシ抑え
ることができる。(3)分解・揮発ガス等の発生が抑え
られるため紡糸性が良好である。(4)マイクロカプセ
ルの微孔よシ徐々に香シが放光れるので、長時間安定し
た芳香性を得ることができる。In the present invention, instead of using the fragrance as it is, a method is adopted in which the fragrance is first put into microcapsules and the fine powder of the microcapsules is kneaded into the fiber. By microcapsulating the fragrance, (1) the heat of the molten polymer is not directly transmitted to the fragrance during spinning and kneading, so decomposition and volatilization due to heat can be suppressed. (2) The volatilization of volatile components of the fragrance due to heat during spinning can be suppressed by covering the circumference υ with the microcapsules. (3) Since decomposition and generation of volatile gases are suppressed, spinnability is good. (4) Since the incense is gradually emitted through the pores of the microcapsules, stable aromatic properties can be obtained for a long period of time.
香料をマイクロカプセル化するKは様々な方法がある。There are various methods of microencapsulating fragrances.
本発明では、(1)ある程度の耐熱性があること、(2
)香料の徐放性があること、(3)粘稠液体に容易に分
散し、凝集しにくいこと等を考慮し、無水硅酸を壁成分
とする、核種と同重量の香料を包含した径0.1μの球
形マイクロカプセルを用いた。粒aがあtb大きくなる
と繊維化の際毛羽、断糸等の糸切れが多くなシ、好まし
くない。The present invention requires (1) a certain degree of heat resistance, (2)
) The fragrance has a sustained release property, and (3) it is easily dispersed in viscous liquid and is difficult to aggregate, and the diameter is such that the wall component is silicic anhydride and contains the same weight of the fragrance as the nuclide. Spherical microcapsules of 0.1μ were used. If grain a has a large atb, it is undesirable because there will be a lot of thread breakage such as fuzz and thread breakage during fiberization.
香料を包含したマイクロカプセル微粉体は、熱可塑性繊
維中に分散させるため、あらかじめ液状ポリエステル系
化合物か又は有機ポリシロキサン中に均一に分散してお
きある程度の流動性を保持させた状態で溶融した熱可塑
性樹脂流体中に添加し、スタティックミキサーで混練す
る。In order to disperse the microcapsule powder containing the fragrance into the thermoplastic fiber, it is dispersed uniformly in a liquid polyester compound or organic polysiloxane in advance, and heated to melt it while maintaining a certain degree of fluidity. Add to plastic resin fluid and knead with a static mixer.
ポリエステル化合物又は有機ボリア0キサンの粘度は2
5℃下で10ポイズ以上であることが望ましい。10ポ
イズ以下になってくると移行性が大きくなシ洗濯時に繊
維中よシ抜は出す危険性が大きくなる。また反対に極め
て高い粘度の場合。The viscosity of the polyester compound or organic borea xane is 2
It is desirable that the temperature is 10 poise or more at 5°C. When it becomes less than 10 poise, the transferability increases and there is a greater risk that the fiber will be removed during washing. On the other hand, if the viscosity is extremely high.
マイクロカプセル粉体を混合すると良好な流動性がなく
なることもあるので、粘度が高ければ良いというもので
はない。混合しようとするマイクロカプセルの量により
その流動性は大きく影響されるので混合後適切な流動性
を有するような粘度のものを選択すべきである。If microcapsule powder is mixed, good fluidity may be lost, so higher viscosity is not necessarily better. Since the fluidity of the microcapsules to be mixed is greatly affected by the amount of microcapsules to be mixed, a material with a viscosity that provides appropriate fluidity after mixing should be selected.
ポリエステル系化合物としては、例えばアデカアーガス
社製ADK CIZERシリーズ、あるいは大日本イン
キ化学社製POLYqIZERシリーズ等のポリエステ
ル可塑剤が好適なものとして挙げらルナのポリエステル
化合物のうち、酸成分として七バシン酸、アジピン酸、
フタル酸を主成分としグリコール成分を適宜選択したも
のを用いるのがコスト的にも物性的にも適当である。Suitable examples of polyester compounds include polyester plasticizers such as ADK CIZER series manufactured by Adeka Argus, or POLYqIZER series manufactured by Dainippon Ink Chemical Co., Ltd. Among Luna's polyester compounds, heptabasic acid, Adipic acid,
It is appropriate to use a material containing phthalic acid as the main component and an appropriately selected glycol component in terms of cost and physical properties.
有機ポリシロキサンとしてはジメテルポリシロキサン、
ジフェニルポリシロキサン、メテルフェニルポリシロキ
サンなどがあり、単独又は混合使用することができる。As organic polysiloxane, dimeter polysiloxane,
Examples include diphenylpolysiloxane and meterphenylpolysiloxane, which can be used alone or in combination.
本発明に用いる香料は特別なものではなく、各種調合香
料や食品用フレーバー等の液体香料である。The flavor used in the present invention is not special, and may be a liquid flavor such as various mixed flavors or food flavors.
繊維中への添加量としては香料とマイクロカプセルの壁
成分が重量比で50:50の香料含有マイクロカプセル
とポリエステル系化合物か又は有機ボリシロキプンとの
重量比が90:10〜20:80にある混合物を添加し
、繊維に対してマイクロカプセルが0.1〜10重量%
、香料が0.05〜5重量%、ポリエステル系化合物か
又は有機ボリンロキ丈ンとして0.1〜10重量%分散
していることが望ましい。The amount added to the fiber is a mixture in which the weight ratio of fragrance and microcapsule wall components is 50:50, and the weight ratio of fragrance-containing microcapsules and polyester compound or organic polysilocypone is 90:10 to 20:80. is added, and the microcapsules are 0.1 to 10% by weight based on the fiber.
It is preferable that 0.05 to 5% by weight of perfume and 0.1 to 10% by weight of a polyester compound or organic boroline compound are dispersed.
次に本発明の芳香繊維の製造方法について説明する。Next, the method for producing aromatic fibers of the present invention will be explained.
香料を含んだマイクロカプセルとポリエステル系化合物
か又は有機ポリシロキチンの混合物を所定量正確に計量
した後、紡糸直前に溶融状態の熱可塑性樹脂に添加し、
その後混練した後ノズル孔よシ吐出し繊維化する方法が
香料成分の揮発・分解・ポリマー粘度の低下等の問題を
発生させるため、望ましい。After accurately measuring a predetermined amount of a mixture of microcapsules containing a fragrance and a polyester compound or an organic polysilochitin, the mixture is added to a molten thermoplastic resin immediately before spinning,
A method in which the mixture is then kneaded and then discharged through a nozzle hole to form fibers is preferable because problems such as volatilization and decomposition of perfume components and a decrease in polymer viscosity occur.
スタティックミキサーを用いて混練する場合に大切なこ
とは、ある一定エレメント数以上のスタティックミキサ
ーを用いて混練する必要があることである。現在、実用
化されている静止型混合器は数種類あるが、例えばKe
nics社の180°左右にねじった羽根を90度ずら
して配列したnエレメント通過させると2n層分割する
タイプのスタティックミキサーを用いた場合は、エレメ
ント数が15以上のものを用いる必要がある。15エレ
メントよシ少なくなると添加物とポリマーとの均一混線
が十分でないため、紡糸時の断糸、毛羽捲付の発生が多
くなると同時に延時性も低下し、工程性上好ましくない
。工程性を向上させる点からも、エレメント数は15エ
レメント以上即ち2 層以上の分割は最低実施すること
が望ましく更には、エレメント数20以上、部ち220
層以上の分割が好ましい。What is important when kneading using a static mixer is that it is necessary to knead using a static mixer with a certain number of elements or more. Currently, there are several types of static mixers in practical use, such as the Ke
When using a static mixer made by NICS Corporation that divides the mixer into 2n layers by passing through n elements in which blades twisted 180° left and right are arranged at 90° shifts, it is necessary to use a mixer with 15 or more elements. If the number is less than 15 elements, uniform intermixing of the additive and the polymer is not sufficient, which increases the occurrence of yarn breakage and fluffing during spinning, and at the same time, the time extension property decreases, which is unfavorable in terms of process efficiency. From the point of view of improving process efficiency, it is desirable that the number of elements is 15 or more, that is, 2 or more layers.
Division into layers or more is preferred.
KeniCs社以外の静止型混合器を用いる場合も、2
15層以上の分割に相当するエレメント数に設定した混
合器を使用する必要があることは言うまでもない。東し
社製のHi−Mixer −? Charless &
Ross社製のロスISGミキサーなどは、nエレメ
ント通過する時の層分割数は4n層分割であるので、エ
レメント数は8工レメント以上、更に好ましくは10エ
レメント以上必要である。When using a static mixer other than KeniCs, 2.
Needless to say, it is necessary to use a mixer whose number of elements corresponds to division into 15 or more layers. Toshisha Hi-Mixer -? Charles &
In a Ross ISG mixer manufactured by Ross, etc., the number of layer divisions when passing through n elements is 4n layers, so the number of elements is 8 or more, preferably 10 or more.
本発明の製造工程の一例を第1図に示す。溶融押出機1
によシ押出された溶融ポリマー流は計量機2により所定
量計量される。一方、香料を含有したマイクロカプセル
とポリエステル系化合物か又は有機ポリシロキサンの混
合物は添加剤供給機4によりフィードされ、計量機3に
より所定量計量された後、計量機2により計量された溶
融ポリマーライン中へ添加される。その後所定エレメン
ト数を設置したスタティックミキサー中で該混合物とポ
リマーが混練され、紡糸口金バック6より吐出さhlR
m化される。スタチックミキサーはポリマー流うイン中
へ設置しても良いし、あるいは紡糸口金パック内に設置
しても良い。An example of the manufacturing process of the present invention is shown in FIG. Melt extruder 1
A predetermined amount of the extruded molten polymer stream is measured by a measuring device 2. On the other hand, a mixture of microcapsules containing a fragrance and a polyester compound or an organic polysiloxane is fed by an additive feeder 4, and a predetermined amount is weighed by a weighing machine 3. added to the inside. Thereafter, the mixture and the polymer are kneaded in a static mixer equipped with a predetermined number of elements, and are discharged from the spinneret bag 6.
It becomes m. The static mixer may be placed into the polymer flowing in or within the spinneret pack.
本発明の芳香繊維は香料をマイクロカプセルで包含し、
さらに、融点、熱成形温度の低い熱可塑性樹脂を用いる
ことによシ香料の繊維中への分散時、製糸時に香料の分
解・揮発等を極力抑え香料本来の芳香性を保持しかつ、
洗濯耐久性に優れた芳香性合成繊維を可能とした。The aromatic fiber of the present invention contains a fragrance in microcapsules,
Furthermore, by using a thermoplastic resin with a low melting point and thermoforming temperature, the decomposition and volatilization of the fragrance are minimized during dispersion into fibers and spinning, and the original aromatic properties of the fragrance are maintained.
Aromatic synthetic fibers with excellent washing durability have been made possible.
(実施例)
以下、実施例を挙げて本発明を具体的に説明する。実施
例中の洗濯条件は以下の試験方法によって行った。(Example) Hereinafter, the present invention will be specifically described with reference to Examples. The washing conditions in the examples were conducted according to the following test method.
く洗濯試験法〉
JIS LO217−103法に依って実施、液温4
0℃の水1tに22の割合で衣料用洗剤を添加溶解し洗
濯液とする。この洗濯液に浴比がl:30となるように
試料及び負荷布を投入して運転を開始する。5分間処理
した後運転を止め、試料及び負荷布を脱水機で脱水し、
次に洗濯液を常温の新しい水に替えて同一の浴比で2分
間すすぎ洗いを行い風乾させる。以上の操作を10回く
シ返し、1oHL後の測定サンプルとした。Washing test method> Conducted according to JIS LO217-103 method, liquid temperature 4
Laundry detergent is added and dissolved at a ratio of 22 parts to 1 ton of water at 0°C to obtain a washing liquid. The sample and load cloth are put into this washing liquid so that the bath ratio is 1:30, and operation is started. After processing for 5 minutes, stop the operation, dehydrate the sample and load cloth with a dehydrator,
Next, replace the washing liquid with fresh water at room temperature, rinse for 2 minutes at the same bath ratio, and air dry. The above operation was repeated 10 times to obtain a measurement sample after 1oHL.
〔実施例1〕
ポリプラスチックス株式会社製のアセタール・コポリ1
−′ジュラコン・タイプM−90−44”を40φ押出
機にて押出し、該ポリマーの溶融ポリマーラインにフモ
ンフレーバーを包含シタ粒径0、1μのマイクロカプセ
ルと25℃下で300ポイズの粘度を有するポリエステ
ル系可塑剤を重量比で40:60に混合し、ホーンミキ
サーを用いて十分攪拌後、脱泡のためそのまま12時間
放置した混合物をポリマー流に対し該混合物が4.8重
量%、つまり分散媒が2.9重f%、マイクロカプセル
が0.76ii%、フレーバーが1.14重量%になる
ように添加しその後KeliCB社製の40工レメント
スタテツクミギ丈−で混練し、丸孔ノズルよシ吐出し紡
糸した。[Example 1] Acetal Copoly 1 manufactured by Polyplastics Co., Ltd.
-'Duracon Type M-90-44'' was extruded using a 40φ extruder, and the molten polymer line contained fumone flavor and microcapsules with a particle size of 0.1μ and a viscosity of 300 poise at 25°C. The mixture was mixed at a weight ratio of 40:60, thoroughly stirred using a horn mixer, and left as it was for 12 hours for defoaming. The dispersion medium was added at 2.9% by weight, the microcapsules at 0.76%, and the flavor at 1.14% by weight, and then kneaded with a 40-piece element made by KeliCB. The material was discharged through a nozzle and spun.
該紡糸原糸をローラープレート方式で通常の条件で延時
し、75デニール36フイラメントのマルチフィラメン
トを得た。編地を作成し洗濯前と洗濯10回後の芳香性
を評価したところ洗濯前後ともフレーバー元来の芳香を
有することを確認した。The spun yarn was stretched under normal conditions using a roller plate method to obtain a multifilament of 75 denier and 36 filaments. A knitted fabric was prepared and its aromatic properties were evaluated before and after washing 10 times, and it was confirmed that the fabric had the original fragrance both before and after washing.
〔実施例2.3〕
実施例2ではフレグランス調香料を、実施例3ではヒノ
キ様香料を包含させたマイクロカプセルを調製し、分散
媒として25℃下で600ポイズの粘度を有する有機ポ
リシロキブンを用い、実施例1の方法に準じ芳香性線維
を得た。両側とも洗1前後すばらしい芳香性を示した。[Example 2.3] Microcapsules containing a fragrance perfume in Example 2 and a cypress-like fragrance in Example 3 were prepared, and an organic polysiloxane having a viscosity of 600 poise at 25°C was used as a dispersion medium. According to the method of Example 1, aromatic fibers were obtained. Both sides exhibited excellent aromatic properties before and after washing.
〔実施例4.5〕
実施例1と同様なマイクロカプセルを用い、フィクロカ
プセルと分散媒を重量比で実施例4では30 ニア0
、実施例5では25ニア5とし、実施例1と同様な方法
によシ芳香性繊維を得た。工程性、性能も十分満足でき
るものであった。[Example 4.5] Using the same microcapsules as in Example 1, the weight ratio of fibrocapsules and dispersion medium was 30 in Example 4, near 0.
In Example 5, the fiber was set to 25 near 5, and the aromatic fiber was obtained in the same manner as in Example 1. Processability and performance were also fully satisfactory.
〔実施例6〕
実施例4と同様な方法でマイクロカプセルを混練した溶
融ポリマーを芯成分とし、別のラインよ如押出した同様
なアセタール・コポリマーを鞘成分とし、芯/鞘=90
/10重″量比となるよう芯鞘複合紡糸を行った。該紡
糸原糸を通常の方法にょシ延沖し135デニール/36
フイラメントのマルチフィラメントを得た。芳香性、工
程性とも良好で耐洗濯性も十分であった。[Example 6] The core component was a molten polymer obtained by kneading microcapsules in the same manner as in Example 4, and the sheath component was a similar acetal copolymer extruded from a separate line, with a core/sheath ratio of 90.
Core-sheath composite spinning was carried out so that the weight ratio was 135 denier/36.
A multifilament of filament was obtained. Both the aroma and processability were good, and the washing resistance was also sufficient.
〔比較例1〕
実施例1と同様なマイクロカプセルを用いマイクロカプ
セルと分散媒が重量比で5=95である混合物を添加し
繊維化した。芳香性はあるものの、弱く匂いがハツキリ
としなかった。[Comparative Example 1] Using the same microcapsules as in Example 1, a mixture of microcapsules and dispersion medium in a weight ratio of 5=95 was added to form fibers. Although it was aromatic, it was weak and the smell was not very strong.
〔比較例2〕
分散媒としてプロピレンオキブイドとエチレンオキサイ
ドのランダム共重合体(POEO共重合体)で25℃で
の粘度が200ポイズの粘稠液体を用い、マイクロカプ
セルとの重量比が30ニア0になるように混合し実施例
4と同様な方法にょシ繊維化した。紡糸性・延呻性とも
良好で、洗濯前の芳香性も優れていたが、洗濯後、芳香
性の低下が著しく、耐洗濯性は認められなかった。[Comparative Example 2] As a dispersion medium, a viscous liquid made of a random copolymer of propylene oxide and ethylene oxide (POEO copolymer) with a viscosity of 200 poise at 25°C was used, and the weight ratio with the microcapsules was 30. The mixture was mixed so as to have a near-zero density, and the mixture was made into fibers in the same manner as in Example 4. Both spinnability and spreadability were good, and the fragrance before washing was also excellent, but after washing, the fragrance decreased significantly and washing resistance was not observed.
〔比較例3〕
実施例1と同様な練込剤を繊維全体に対し25重量%に
なるように添加、混練し、紡糸した。紡糸状況は、ノズ
ル面での糸の揺れが激しく、落ち着かなかった。また時
々ビスが発生し、断糸の原因となった。紡糸性不良の念
め捲取はほとんど不可能であった。[Comparative Example 3] The same kneading agent as in Example 1 was added in an amount of 25% by weight based on the entire fiber, kneaded, and spun. The spinning situation was unstable as the yarn was shaking violently on the nozzle surface. Also, screws sometimes occurred, causing thread breakage. It was almost impossible to wind up the yarn to avoid poor spinnability.
第1図は本発明の製造工程の一例を示す概略図である。 特許出願人 株式会社 り ラ し FIG. 1 is a schematic diagram showing an example of the manufacturing process of the present invention. Patent applicant RiRashi Co., Ltd.
Claims (3)
で10ポイズ以上の粘度を有する液状ポリエステル系化
合物か又は有機ポリシロキサンとの混合物が、融点10
0℃以上の熱可塑性繊維中に共に0.1〜10重量%分
散していることを特徴とする優れた洗濯耐久性を有する
芳香繊維。(1) Microcapsule powder containing fragrance and 25℃
A liquid polyester compound having a viscosity of 10 poise or more or a mixture with an organic polysiloxane has a melting point of 10 poise or more.
An aromatic fiber having excellent washing durability characterized by being dispersed in a thermoplastic fiber having a temperature of 0° C. or higher in an amount of 0.1 to 10% by weight.
主成分とするポリオレフィンである第一項記載繊維。(2) The fiber described in item 1, wherein the thermoplastic fiber is polyoxymethylene or a polyolefin having polyoxymethylene as a main component.
ステル系化合物か又は有機ポリシロキサンの混合物とを
、融点が100℃以上の繊維を構成する熱可塑性ポリマ
ーのポリマー重合完了後紡糸直前の間で該ポリマー溶融
流体中へ添加し、その後混練した後紡糸ノズルより吐出
し、繊維化することを特徴とする芳香性繊維の製造法。(3) Microcapsule powder containing a fragrance and a mixture of a polyester compound or an organic polysiloxane are mixed between after completion of polymerization and immediately before spinning of a thermoplastic polymer constituting the fiber with a melting point of 100°C or higher. 1. A method for producing aromatic fibers, which comprises adding them to a molten polymer fluid, then kneading them, and then discharging them from a spinning nozzle to form fibers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11328588A JPH01282305A (en) | 1988-05-09 | 1988-05-09 | Aromatic fiber and production thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11328588A JPH01282305A (en) | 1988-05-09 | 1988-05-09 | Aromatic fiber and production thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01282305A true JPH01282305A (en) | 1989-11-14 |
Family
ID=14608305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11328588A Pending JPH01282305A (en) | 1988-05-09 | 1988-05-09 | Aromatic fiber and production thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01282305A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1367152A1 (en) * | 2002-05-28 | 2003-12-03 | Atex S.r.l. | Method for producing a non-woven fabric made of synthetic fiber with fragrancing means |
JP2008163505A (en) * | 2006-12-27 | 2008-07-17 | Mitsubishi Gas Chem Co Inc | Oxymethylene conjugate fiber |
WO2009067840A1 (en) * | 2007-11-27 | 2009-06-04 | U-Bond Inc. | Imitating natural plant fiber, preparation method thereof and fabric made of it |
CN103445312A (en) * | 2013-09-13 | 2013-12-18 | 句容市后白镇迎瑞印花厂 | Production method for fragrant cashmere sweater |
CN109183184A (en) * | 2018-08-14 | 2019-01-11 | 北京麻世纪麻业科技发展有限公司 | A kind of preparation method and capsule fiber of capsule fiber |
-
1988
- 1988-05-09 JP JP11328588A patent/JPH01282305A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1367152A1 (en) * | 2002-05-28 | 2003-12-03 | Atex S.r.l. | Method for producing a non-woven fabric made of synthetic fiber with fragrancing means |
JP2008163505A (en) * | 2006-12-27 | 2008-07-17 | Mitsubishi Gas Chem Co Inc | Oxymethylene conjugate fiber |
WO2009067840A1 (en) * | 2007-11-27 | 2009-06-04 | U-Bond Inc. | Imitating natural plant fiber, preparation method thereof and fabric made of it |
EA017657B1 (en) * | 2007-11-27 | 2013-02-28 | Новеко Трейдинг 2008 Ллк | Imitating natural plant fiber, preparation method thereof and fabric made of it |
CN103445312A (en) * | 2013-09-13 | 2013-12-18 | 句容市后白镇迎瑞印花厂 | Production method for fragrant cashmere sweater |
CN109183184A (en) * | 2018-08-14 | 2019-01-11 | 北京麻世纪麻业科技发展有限公司 | A kind of preparation method and capsule fiber of capsule fiber |
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