JPH01280071A - Modification of polyester fiber - Google Patents
Modification of polyester fiberInfo
- Publication number
- JPH01280071A JPH01280071A JP10276888A JP10276888A JPH01280071A JP H01280071 A JPH01280071 A JP H01280071A JP 10276888 A JP10276888 A JP 10276888A JP 10276888 A JP10276888 A JP 10276888A JP H01280071 A JPH01280071 A JP H01280071A
- Authority
- JP
- Japan
- Prior art keywords
- polyester fiber
- polyester
- graft
- fiber
- polyester fibers
- 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
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明はグラフト重合によるポリエステル繊維の改質方
法に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for modifying polyester fibers by graft polymerization.
〈従来の技術〉
従来、ポリエステル繊維の化学的改質として、グラフト
重合が種々試みられている。<Prior Art> Various attempts have been made to graft polymerization as a chemical modification of polyester fibers.
従来の方法によると、主にビニル系モノマーにラジカル
開始剤を応用したり、高エネルギー照射を行なってグラ
フト重合する方法が殆んどである。Most conventional methods involve applying a radical initiator to vinyl monomers or performing graft polymerization by high-energy irradiation.
しかしなが ら、通常のポリエステル繊維を使用した場
合、モノマーの利用率、すなわちグラフト効率が低く、
そのため加エコストアツブ、ホモポリマーに起因した排
水処理の問題などの欠点を有している。However, when ordinary polyester fibers are used, the utilization rate of monomers, that is, the grafting efficiency, is low;
Therefore, it has drawbacks such as problems in wastewater treatment due to additives and homopolymers.
〈発明が解決しようとする問題点〉
本発明者らは、上記従来技術の問題点を解消すべく研究
を重ねた結果、紡糸速度7000m/分以上で紡糸した
ポリエステル繊維を使用することにより、通常のポリエ
ステル繊維よりもグラフト効率が良くなることを見い出
し、本発明に至った。<Problems to be Solved by the Invention> As a result of repeated research to solve the above-mentioned problems of the prior art, the present inventors have found that by using polyester fibers spun at a spinning speed of 7000 m/min or higher, It has been discovered that the grafting efficiency is better than that of polyester fibers, leading to the present invention.
く問題点を解決するための手段〉
すなわち、本発明は紡糸速度7000m/分以上で紡糸
したポリエステル繊維に、ビニルモノマーをグラフト重
合することを特徴とするポリエステル繊維の改質方法で
ある。Means for Solving the Problems> That is, the present invention is a method for modifying polyester fibers, which is characterized by graft polymerizing a vinyl monomer to polyester fibers spun at a spinning speed of 7000 m/min or more.
本発明でいうポリエステル繊維は、公知の重合法で得ら
れ、実質的にポリエチレンテレフタレートからなってい
る。例えば、その製造方法は、特開昭57−12161
3号公報に記載されており、その物性値は同公報にある
ように、初期モジュラスが50g/d以上の実質的にポ
リエチレンテレフタレートからなる繊維であって、測定
周波数110H,に於ける力学的堝失正接(tan δ
)のピーク温度が110℃以下であり、かつピーク値(
(tanδ)IIlax、)が0.135以下である繊
維が開示されている。繊維形態については、フィラメン
ト、ステープル、トウ、スライバー系、編地、織物等、
いずれの形態でも良いが好ましくは加工操作の面からは
布帛類が良い。The polyester fiber referred to in the present invention is obtained by a known polymerization method and consists essentially of polyethylene terephthalate. For example, the manufacturing method is disclosed in Japanese Patent Application Laid-Open No. 57-12161.
3, and its physical properties are as stated in the same publication.It is a fiber consisting essentially of polyethylene terephthalate with an initial modulus of 50 g/d or more, and its physical properties are as follows: Loss tangent (tan δ
) has a peak temperature of 110°C or less, and the peak value (
Disclosed are fibers in which (tan δ) II lax, ) is 0.135 or less. Regarding the fiber form, filament, staple, tow, sliver type, knitted fabric, woven fabric, etc.
Any form may be used, but from the viewpoint of processing operations, fabrics are preferred.
本発明でいうグラフト重合法は、ポリエチレンテレフタ
レートを製造せしめる重合性同様に公知の技術を応用し
たものである。すなわち、開始剤としては、過酸化ベン
ゾイル及びその誘導体、アゾビスイソブチロニトリル及
びその誘導体、あるいは光エネルギーのようなもので良
く、開始剤との組合せ叉は必要に応じて、モノクロルベ
ンゼン、ベンジルアルコール、テトラクロルエタン、ニ
トロベンゼンの様な潤滑剤を使用できるが、上記のもの
に特に限定されない。The graft polymerization method referred to in the present invention is an application of a known technique similar to the polymerization method for producing polyethylene terephthalate. That is, the initiator may be benzoyl peroxide and its derivatives, azobisisobutyronitrile and its derivatives, or light energy, and monochlorobenzene, benzyl Lubricants such as, but not limited to, alcohol, tetrachloroethane, and nitrobenzene can be used.
さらにグラフト重合工程についても公知の方法を応用し
たちのでるが、浸漬加熱法、パッド−キュア方式及び/
叉はパッド−スチーム方式等、いずれの方法でも応用で
きる。Furthermore, for the graft polymerization process, well-known methods are applied, such as immersion heating method, pad-cure method and/or
Any method can be applied, such as a pad-steam method.
本発明でいうモノマーは、アクリル酸エステル、メタク
リル酸エステル、ビニルピリジン、酢酸ビニル、アクリ
ロニトリル等があり、特に親水性モノマーとしては、ア
クリル酸、メタクリル酸、ビニルスルホン酸、ビニルピ
ロリドン、アクリルアミド、メタクリルアミド等があり
、ビニル基含有であればこれらに限定されるものではな
い、好ましくは親水性ビニルモノマーが適する。特に好
ましくは、金属塩化可能な酸性基を有するビニルモノマ
ーが適し、例えばアクリル酸、メタクリル酸、ビニルス
ルホン酸類がその代表例である。Monomers referred to in the present invention include acrylic esters, methacrylic esters, vinyl pyridine, vinyl acetate, acrylonitrile, etc. Particularly hydrophilic monomers include acrylic acid, methacrylic acid, vinyl sulfonic acid, vinyl pyrrolidone, acrylamide, and methacrylamide. The monomer is not limited to these as long as it contains a vinyl group, and hydrophilic vinyl monomers are preferably used. Particularly preferred are vinyl monomers having acidic groups that can be converted into metal salts, representative examples of which are acrylic acid, methacrylic acid, and vinyl sulfonic acids.
〈実施例〉 以下に、実施例をあげて、本発明を説明する。<Example> The present invention will be explained below with reference to Examples.
実施例中に示す吸湿率、グラフト化率、グラフト効率は
次に示す方法によるものである。The moisture absorption rate, grafting rate, and grafting efficiency shown in the examples are based on the following methods.
吸湿率;
吸湿率(χ)=(試料の調湿重量−試料の絶乾重量)/
試料の絶乾重量、調湿条件20℃×65%RH中に2月
間放置。Moisture absorption rate; Moisture absorption rate (χ) = (humidified weight of sample - bone dry weight of sample) /
Absolute dry weight of sample, left for 2 months under humidity control conditions of 20°C x 65% RH.
グラフト化率;
グラフト化率(χ)=(グラフト化試料の絶乾重量−未
加工試料の絶乾重量)/未加工試料の絶乾重量
グラフト効率;
グラフト効率(χ)=(グラフト化試料の絶乾重量−未
加工試料の絶乾重量)/モノマー仕込み量絶乾重量は全
て50℃×24時間、真空乾燥して求める。Grafting rate; Grafting rate (χ) = (bone dry weight of grafted sample - bone dry weight of unprocessed sample) / bone dry weight of raw sample Grafting efficiency (χ) = (bone dry weight of grafted sample) Bone dry weight - Bone dry weight of unprocessed sample)/Amount of monomer charged All bone dry weights are determined by vacuum drying at 50° C. for 24 hours.
実施例
ベンゾイルパーオキサイド1重量部、モノクロルベンゼ
ン8重量1部、非イオン系界面活性剤(第1工業製薬製
ブライサーフA−2172)2重量部の混合物を1oo
o重量部の水に添加し、エマルジョンとし、これをグラ
フト重合浴とした。Example A mixture of 1 part by weight of benzoyl peroxide, 8 parts by weight of monochlorobenzene, and 2 parts by weight of a nonionic surfactant (Blysurf A-2172 manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
o parts by weight of water to form an emulsion, which was used as a graft polymerization bath.
処理布については、通常のポリエチレンテレフタレート
を紡速7000m/分及び比較として、2000m/分
で紡糸し、これを10編地とした。Regarding the treated fabric, ordinary polyethylene terephthalate was spun at a spinning speed of 7000 m/min and, for comparison, 2000 m/min, and 10 knitted fabrics were obtained.
この10編地を先述のグラフト重合浴に浴比1:150
で漫潰し、所定量のアクリル酸とメタクリル酸を同体積
の割合で添加し、ステンレス製密閉容器中で105℃で
60分間加熱処理した。処理後、布帛を取り出して、2
時間清水処理を行なった。導水処理後の布帛は必要に応
じて、0.5%Na、CO,水溶液中で80℃で30分
間処理した。These 10 knitted fabrics were added to the aforementioned graft polymerization bath at a bath ratio of 1:150.
The mixture was mashed with water, predetermined amounts of acrylic acid and methacrylic acid were added in the same volume ratio, and the mixture was heat-treated at 105° C. for 60 minutes in a stainless steel sealed container. After processing, remove the fabric and
A time clear water treatment was performed. The fabric after the water conduction treatment was treated, if necessary, in a 0.5% Na, CO, aqueous solution at 80° C. for 30 minutes.
その結果を第1表に導水処理後のグラフト効率、第2表
にN a z CO!処理後の吸湿率の紡速による比較
で示す。The results are shown in Table 1 and graft efficiency after water transfer treatment, and Table 2 shows N a z CO! A comparison of the moisture absorption rate after treatment according to the spinning speed is shown.
第1表
第2表
〈発明の効果〉
本発明の方法でポリエステル繊維を改質すると、グラフ
ト効率が向上するために、七ツマー使用量が軽減化され
、加工コストが低下する。さらに、ホモポリマー生成が
抑制されるために、排水処理工程での水質への影響が少
なくなる。また、酸性基を存する親水性ビニルモノマー
を使用し金属塩化した場合、通常のポリエステル繊維よ
りも、同じグラフト率でも吸湿性が高くなるため、より
低いグラフト率で吸湿性が達成される。このため、グラ
フト率軽減化による、物性低下、風合硬化、染色堅牢度
低下が抑制できる。Table 1 Table 2 <Effects of the Invention> When polyester fibers are modified by the method of the present invention, the grafting efficiency is improved, so the amount of hexamer used is reduced, and the processing cost is reduced. Furthermore, since homopolymer production is suppressed, the impact on water quality in the wastewater treatment process is reduced. Furthermore, when a hydrophilic vinyl monomer containing an acidic group is used and converted into a metal salt, the hygroscopicity is higher than that of ordinary polyester fibers even at the same grafting rate, so hygroscopicity can be achieved with a lower grafting rate. Therefore, deterioration of physical properties, hardening of hand, and deterioration of color fastness due to reduction in graft ratio can be suppressed.
特許出願人 旭化成工業株式会社Patent applicant: Asahi Kasei Industries, Ltd.
Claims (1)
維に、ビニルモノマーをグラフト重合することを特徴と
するポリエステル繊維の改質方法A method for modifying polyester fibers, which comprises graft polymerizing a vinyl monomer to polyester fibers spun at a spinning speed of 7,000 m/min or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10276888A JPH01280071A (en) | 1988-04-27 | 1988-04-27 | Modification of polyester fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10276888A JPH01280071A (en) | 1988-04-27 | 1988-04-27 | Modification of polyester fiber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01280071A true JPH01280071A (en) | 1989-11-10 |
Family
ID=14336352
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10276888A Pending JPH01280071A (en) | 1988-04-27 | 1988-04-27 | Modification of polyester fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01280071A (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5557071A (en) * | 1978-10-16 | 1980-04-26 | Toyo Boseki | Production of quality improved synthetic fabric |
| JPS57121613A (en) * | 1981-01-19 | 1982-07-29 | Asahi Chem Ind Co Ltd | Polyester fiber dyeable at normal pressure |
-
1988
- 1988-04-27 JP JP10276888A patent/JPH01280071A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5557071A (en) * | 1978-10-16 | 1980-04-26 | Toyo Boseki | Production of quality improved synthetic fabric |
| JPS57121613A (en) * | 1981-01-19 | 1982-07-29 | Asahi Chem Ind Co Ltd | Polyester fiber dyeable at normal pressure |
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