JP2003113581A - Elastic fiber-treating agent and elastic fiber - Google Patents

Elastic fiber-treating agent and elastic fiber

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Publication number
JP2003113581A
JP2003113581A JP2001345417A JP2001345417A JP2003113581A JP 2003113581 A JP2003113581 A JP 2003113581A JP 2001345417 A JP2001345417 A JP 2001345417A JP 2001345417 A JP2001345417 A JP 2001345417A JP 2003113581 A JP2003113581 A JP 2003113581A
Authority
JP
Japan
Prior art keywords
elastic fiber
oil
treating agent
weight
silicone
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
Application number
JP2001345417A
Other languages
Japanese (ja)
Other versions
JP3888669B2 (en
Inventor
Masayuki Hiramatsu
雅之 平松
Satoru Kodama
悟 兒玉
Michihiro Shibano
道宏 柴野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Matsumoto Yushi Seiyaku Co Ltd
Original Assignee
Matsumoto Yushi Seiyaku Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Matsumoto Yushi Seiyaku Co Ltd filed Critical Matsumoto Yushi Seiyaku Co Ltd
Priority to JP2001345417A priority Critical patent/JP3888669B2/en
Publication of JP2003113581A publication Critical patent/JP2003113581A/en
Application granted granted Critical
Publication of JP3888669B2 publication Critical patent/JP3888669B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To provide a treating agent excellent in smooth property and antistatic property as an elastic fiber-treating agent by using a specific silicone resin. SOLUTION: This elastic fiber-treating agent is obtained by blending 0.1-15 wt.% silicone resin having R1 R2 SiO or R3 SiO3/2 of which R1 , R2 , R3 are each a 2-10C hydrocarbon group or phenyl group, and of which base component is selected from a silicone oil, a mineral oil and an ester oil, and using at least >=5 wt.% mineral oil or ester oil. The elastic fiber is provided by imparting 0.1-15 wt.% treating agent on it.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は制電性および平滑性に優
れる弾性繊維用処理剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a treatment agent for elastic fibers which is excellent in antistatic property and smoothness.

【0002】[0002]

【従来の技術】特公昭42−8438号公報には、アミ
ルシロキサンレジンとジメチルシリコーンを配合した弾
性繊維用処理剤が記載されている。特開平57−617
76号公報にはシリコーンレジンとジメチルシロキサン
よりなる糸仕上用組成物が記載されている。特開平9−
188974号公報にはMQ比が0.4〜1.5のシリ
コーンレジンを用いた弾性繊維用油剤が記載されてい
る。
2. Description of the Related Art JP-B-42-8438 describes a treatment agent for elastic fibers containing an amylsiloxane resin and dimethyl silicone. Japanese Patent Laid-Open No. 57-617
Japanese Patent Publication No. 76 describes a yarn finishing composition comprising a silicone resin and dimethylsiloxane. JP-A-9-
No. 188974 discloses an oil agent for elastic fibers using a silicone resin having an MQ ratio of 0.4 to 1.5.

【0003】[0003]

【発明が解決しようとする課題】弾性繊維用処理剤はシ
リコーン油、鉱物油およびエステル油などの疎水性のベ
ース成分を用いているために制電性を付与するために、
極性の強い成分を溶解させることが出来ず、変性率の少
ない変性シリコーンを用いて若干の制電性を付与してい
るに過ぎない。また、平滑性については、向上させる成
分がほとんど見出されていないのが現状である。
Since the treatment agent for elastic fibers uses a hydrophobic base component such as silicone oil, mineral oil and ester oil, it is necessary to impart antistatic property to the treatment agent.
A component having strong polarity cannot be dissolved, and only a slight antistatic property is imparted by using a modified silicone having a small modification rate. In addition, as for the smoothness, at present, almost no component for improving the smoothness is found.

【0004】[0004]

【課題を解決するための手段】本発明の処理剤は、ベー
ス成分が、シリコーン油、鉱物油、エステル油より選ば
れ、少なくとも鉱物油またはエステル油を5重量%以上
使用し、R,R,Rが炭素数2〜10の炭化水素
基またはフェニル基であるRSiOまたはR
iO3/2を基本単位とするシリコーンレジンを0.1
〜15重量%配合した弾性繊維用処理剤である。また、
本発明は上記処理剤が0.1〜15重量%付与されてい
ることを特徴とする弾性繊維である。
Treatment agent of the present invention SUMMARY OF THE INVENTION, the base component is a silicone oil, mineral oil, selected from ester oils, using at least a mineral oil or ester oil 5 wt% or more, R 1, R R 1 R 2 SiO or R 3 S in which 2 , R 3 is a hydrocarbon group having 2 to 10 carbon atoms or a phenyl group
0.1% silicone resin based on iO 3/2
It is a treating agent for elastic fibers which is blended up to 15% by weight. Also,
The present invention is an elastic fiber to which the above-mentioned treating agent is added in an amount of 0.1 to 15% by weight.

【0005】本発明の処理剤は30℃における粘度が通
常3〜30mm/sである3mm/s未満では、処
理剤の揮発が問題となり、30mm/sを超えると平
滑性に劣る。
[0005] In treating agent less than 3 mm 2 / s viscosity is usually 3 to 30 mm 2 / s at 30 ° C. of the present invention, the volatile treatment agent is a problem, inferior in smoothness exceeds 30 mm 2 / s.

【0006】本発明は、ベース成分が、シリコーン油、
鉱物油、エステル油より選ばれ、少なくとも鉱物油また
はエステル油を5重量%以上使用する必要がある。シリ
コーン油をベース成分として、100%用いると本発明
に配合するシリコーンレジンの制電性が発揮されない。
好ましくは、鉱物油またはエステル油を30重量%以上
より好ましくは50重量%以上使用すると制電性・平滑
性の向上効果が大きい。本発明ではR,R,R
炭素数2〜10の炭化水素基またはフェニル基であるR
SiOまたはRSiO3/2を基本単位とする
シリコーンレジンを用いる。Rとしては、プロピル、ブ
チル、イソペンチル、ヘキシル、ペンチル、オクチル、
ベンジル、フェニルなどが用いられる。該シリコーンレ
ジンにはRSiO1/2,SiOの基本単位を必要
に応じて共重合しても良い
In the present invention, the base component is silicone oil,
It is selected from mineral oil and ester oil, and it is necessary to use at least 5% by weight or more of mineral oil or ester oil. If 100% of silicone oil is used as a base component, the antistatic property of the silicone resin blended in the present invention will not be exhibited.
Preferably, when mineral oil or ester oil is used in an amount of 30% by weight or more, more preferably 50% by weight or more, the effect of improving antistatic property / smoothness is great. In the present invention, R 1 , R 2 , and R 3 are hydrocarbon groups having 2 to 10 carbon atoms or phenyl groups.
A silicone resin having 1 R 2 SiO or R 3 SiO 3/2 as a basic unit is used. R is propyl, butyl, isopentyl, hexyl, pentyl, octyl,
Benzyl, phenyl, etc. are used. The silicone resin may be copolymerized with a basic unit of R 3 SiO 1/2 , SiO 2 if necessary.

【0007】本発明の処理剤には、平滑性及び制電性の
効果を高めるために高級脂肪酸の金属石鹸が0.01〜
5重量部添加されていても良い。高級脂肪酸の金属石鹸
としては、従来弾性繊維に用いられている公知のものを
用いることができ、ステアリン酸Ca、ステアリン酸亜
鉛、ステアリン酸Mg、ステアリン酸Al、ステアリン
酸Ba等が好ましい。また、本発明の処理剤には従来公
知の変性シリコーン(アルキル変性シリコーン、エステ
ル変性シリコーン、ポリエーテル変性シリコーン、アミ
ノ変性シリコーン、カルビノール変性シリコーン、カル
ボキシ変性シリコーン、メルカプト変性シリコーン、リ
ン酸変性シリコーン、エポキシ変性シリコーン、MQシ
リコーンレジン、MQTシリコーンレジン、Tシリコー
ンレジン等)やつなぎ剤、制電剤、酸化防止剤、紫外線
吸収剤等、通常弾性繊維の処理剤に用いられる成分を配
合することができる。
The treating agent of the present invention contains a metal soap of higher fatty acid of 0.01 to 0.01 in order to enhance the smoothness and antistatic effect.
5 parts by weight may be added. As the metal soap of higher fatty acid, known soaps used for conventional elastic fibers can be used, and Ca stearate, zinc stearate, Mg stearate, Al stearate, Ba stearate and the like are preferable. Further, the treatment agent of the present invention includes conventionally known modified silicone (alkyl modified silicone, ester modified silicone, polyether modified silicone, amino modified silicone, carbinol modified silicone, carboxy modified silicone, mercapto modified silicone, phosphoric acid modified silicone, Epoxy-modified silicone, MQ silicone resin, MQT silicone resin, T silicone resin, etc.), binders, antistatic agents, antioxidants, UV absorbers, and other components that are commonly used in elastic fiber treatment agents can be added. .

【0008】本発明の処理剤は、通常、弾性繊維に対し
て0.1〜15重量%付与される。
The treating agent of the present invention is usually applied in an amount of 0.1 to 15% by weight based on the elastic fiber.

【0009】[0009]

【実施例】以下実施例により本発明を具体的に説明す
る。なお具体例における、各油剤特性の評価は次の方法
に従って行った。
The present invention will be described in detail with reference to the following examples. In addition, in each of the specific examples, the evaluation of each oil agent property was performed according to the following methods.

【0010】解舒速度比:図1において、解舒速度比測
定機の解舒側に処理剤を付与した繊維のチーズ(1)を
セットし、巻き取り側紙管(2)をセットする。巻き取
り速度を一定速度にセットした後、ローラー(3)及び
(4)を同時に起動させる。この状態では糸(5)に張
力はほとんどかからないため、糸はチーズ上で膠着して
離れないため解舒点(6)は図1に示す状態にある。解
舒速度を変えることによって、チーズからの糸(5)の
解舒点(6)が変わるので、この点がチーズとローラー
との接点(7)と一致するように解舒速度を設定する。
解舒速度比は式1によって求める。この値が小さいほ
ど、解舒性が良いことを示す。 解舒速度比(%)=(巻取速度比−解舒速度)/解舒速度X100 (式1) 編成張力:図2において、チーズ(8)から縦取りした
弾性糸(9)をコンペンセーター(10)を経てローラ
ー(11)、編み針(12)を介して、Uゲージ(1
3)に付したローラー(14)を経て速度計(15)、
巻き取りローラー(16)に連結する。速度計(15)
での走行速度が定速(例えば、10m/分、100m/
分)になるように巻き取りローラーの回転速度を調整し
て、巻き取りローラーに巻き取り、そのときの編成張力
をUゲージ(13)で測定し、繊維/編み針間の摩擦
(g)を計測する。走行糸条より1cmのところで春日
式電位差測定装置(17)で発生静電気を測定する。 ローラー静電気:解舒速度比測定機の解舒側にチーズを
セットし、50m/分の周速で回転させ、チーズ上2c
mのところにおいて、春日式電位差測定装置で、回転を
始めて1時間後の発生静電気を測定する
Unwinding speed ratio: In FIG. 1, a fiber cheese (1) to which a treating agent is applied is set on the unwinding side of the unwinding speed ratio measuring machine, and a paper tube (2) on the winding side is set. After setting the winding speed to a constant speed, the rollers (3) and (4) are simultaneously activated. In this state, the yarn (5) has almost no tension, and the yarn sticks on the cheese and does not separate, so the unwinding point (6) is in the state shown in FIG. By changing the unwinding speed, the unwinding point (6) of the thread (5) from the cheese changes, so the unwinding speed is set so that this point coincides with the contact point (7) between the cheese and the roller.
The unwinding speed ratio is calculated by Equation 1. The smaller this value is, the better the unwinding property is. Unwinding speed ratio (%) = (Winding speed ratio-Unwinding speed) / Unwinding speed X100 (Formula 1) Knitting tension: In Fig. 2, the elastic yarn (9) vertically taken from the cheese (8) is used as a compensator. U gauge (1) through roller (11) and knitting needle (12) through (10).
3) via the roller (14) attached to the speedometer (15),
Connect to take-up roller (16). Speedometer (15)
Driving speed is constant (eg 10m / min, 100m /
Adjust the rotation speed of the take-up roller so that it will be equal to 1 minute), take up the take-up roller, measure the knitting tension at that time with a U gauge (13), and measure the friction (g) between the fiber and the knitting needle. To do. The static electricity generated is measured with a Kasuga type potentiometer (17) at a distance of 1 cm from the running yarn. Roller static electricity: Set cheese on the unwinding side of the unwinding speed ratio measuring machine, rotate it at a peripheral speed of 50 m / min, and put it on the cheese 2c
At m, measure the static electricity generated one hour after starting rotation with the Kasuga type potentiometer

【0011】実施例1〜8 紡糸原液の調整:数平均分子量2000のポリテトラメ
チレンエーテルグリコールと4,4‘−ジフェニルメタ
ンジイソシアネートをモル比率1:2で反応させ、次い
で1,2−ジアミノプロパンのジメチルホルムアミド溶
液を用いて鎖延長し、ポリマー濃度27%のジメチルホ
ルムアミド溶液を得た。30℃での濃度は1500mP
aSであった。ポリウレタン紡糸原液を190℃のN
気流中に吐出して乾式紡糸した。紡糸中走行糸に表1に
記載の処理剤(表中の配合量は重量部)をオイリングロ
ーラーにより繊維に対して6重量%付与した後、毎分5
00mの速度でボビンに巻き取り77dtexモノフィ
ラメントチーズ(巻き量400g)を得た。得られたチ
ーズを35℃、50%RHの雰囲気中に48時間放置し
て評価に供した。
Examples 1 to 8 Preparation of spinning dope: Polytetramethylene ether glycol having a number average molecular weight of 2000 and 4,4'-diphenylmethane diisocyanate were reacted at a molar ratio of 1: 2, and then 1,2-diaminopropane dimethyl was reacted. Chain extension was performed using a formamide solution to obtain a dimethylformamide solution having a polymer concentration of 27%. The concentration at 30 ℃ is 1500mP
was aS. Polyurethane spinning solution is N 2 at 190 ℃
It was discharged into an air stream and dried. After the treatment agent shown in Table 1 (the compounding amount in the table is a weight part) was applied to the running yarn during spinning in an amount of 6% by weight with respect to the fiber with an oiling roller, 5 minutes per minute
It was wound around a bobbin at a speed of 00 m to obtain 77 dtex monofilament cheese (roll amount 400 g). The obtained cheese was left for 48 hours in an atmosphere of 35 ° C. and 50% RH for evaluation.

【0012】[0012]

【表1】 [Table 1]

【0013】実施例9〜13及び比較例1〜4 紡糸原液の調整 数平均分子量2000のポリテトラメチレングリコール
100重量部と4,4‘−ジフェニルメタンジイソシア
ネート25重量部を70℃で反応させ、N,N’−ジメ
チルアセトアミド250重量部を加え冷却しながら反応
混合物を溶解させた。1,2−ジアミノプロパン5重量
部をN,N’−ジメチルアセトアミド184重量部に溶
解させたものを添加し、ジメチルシリコーン10000
mm/sを0.2重量%添加した。この様にして得ら
れたポリウレタン紡糸原液を4つの細孔を有する紡糸口
金より180℃のN気流中に吐出して乾式紡糸した。
紡糸中走行糸に表4に記載の処理剤をオイリングローラ
ーにより繊維に対して6重量%付与した後、毎分500
mの速度でボビンに巻き取り、44dtexマルチフィ
ラメントのチーズ(巻き量400g)を得た。得られた
チーズを35℃、50%RHの雰囲気中に48時間放置
して評価に供した。
Examples 9 to 13 and Comparative Examples 1 to 4 Preparation of spinning dope 100 parts by weight of polytetramethylene glycol having a number average molecular weight of 2000 and 25 parts by weight of 4,4'-diphenylmethane diisocyanate were reacted at 70 ° C. to give N, 250 parts by weight of N'-dimethylacetamide was added and the reaction mixture was dissolved while cooling. A solution prepared by dissolving 5 parts by weight of 1,2-diaminopropane in 184 parts by weight of N, N'-dimethylacetamide was added, and dimethyl silicone 10000 was added.
0.2 wt% of mm 2 / s was added. The polyurethane spinning dope thus obtained was discharged from a spinneret having four pores into a N 2 stream at 180 ° C. for dry spinning.
After the treatment agent shown in Table 4 was applied to the running yarn during spinning by an oiling roller in an amount of 6% by weight based on the fiber, the amount was 500 per minute.
It was wound on a bobbin at a speed of m to obtain 44 dtex multifilament cheese (roll amount 400 g). The obtained cheese was left for 48 hours in an atmosphere of 35 ° C. and 50% RH for evaluation.

【0014】[0014]

【表2】 [Table 2]

【0015】[0015]

【発明の効果】本発明の処理剤を用いることにより安定
した解舒性及び制電性を弾性繊維に与えることができ
る。
EFFECTS OF THE INVENTION By using the treating agent of the present invention, it is possible to impart stable unwinding property and antistatic property to the elastic fiber.

【図面の簡単な説明】[Brief description of drawings]

【図1】解舒速度比の測定方法を説明する模式図。FIG. 1 is a schematic diagram illustrating a method for measuring an unwinding speed ratio.

【図2】編成張力の測定方法を説明する模式図。FIG. 2 is a schematic diagram illustrating a method for measuring knitting tension.

【符号の説明】[Explanation of symbols]

1 チーズ 2 巻き取り用紙管 3 ローラー 4 ローラー 5 走行糸条 6 解舒点 7 チーズとローラーの接点 8 チーズ 9 走行糸条 10 コンペンセーター 11 ローラー 12 編み針 13 Uゲージ 14 ローラー 15 速度計 16 巻き取りローラー 17 春日式電位差測定装置 1 cheese 2 Winding paper tube 3 rollers 4 rollers 5 Running yarn 6 Unwinding point 7 Cheese and roller contact 8 cheese 9 Running yarn 10 compensator 11 roller 12 knitting needles 13 U gauge 14 roller 15 Speedometer 16 Take-up roller 17 Kasuga type potentiometer

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】ベース成分が、シリコーン油、鉱物油、エ
ステル油より選ばれ、少なくとも鉱物油またはエステル
油を5重量%以上使用し、R,R,Rが炭素数2
〜10の炭化水素基またはフェニル基であるR
iOまたはRSiO3/2を基本単位とするシリコー
ンレジンを0.1〜15重量%配合した弾性繊維用処理
剤。
1. A base component is selected from silicone oil, mineral oil and ester oil, at least 5% by weight of mineral oil or ester oil is used, and R 1 , R 2 and R 3 have 2 carbon atoms.
R 1 R 2 S which is a hydrocarbon group of 10 to 10 or a phenyl group
A treatment agent for elastic fibers, containing 0.1 to 15% by weight of a silicone resin having iO or R 3 SiO 3/2 as a basic unit.
【請求項2】ベース成分として、鉱物油またはエステル
油を30重量%以上使用する請求項1に記載の弾性繊維
用処理剤。
2. The treatment agent for elastic fibers according to claim 1, wherein 30% by weight or more of mineral oil or ester oil is used as a base component.
【請求項3】請求項1に記載の処理剤が0.1〜15重
量%付与されていることを特徴とする弾性繊維。
3. An elastic fiber containing 0.1 to 15% by weight of the treating agent according to claim 1.
JP2001345417A 2001-10-05 2001-10-05 Elastic fiber treatment agent and elastic fiber Expired - Lifetime JP3888669B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001345417A JP3888669B2 (en) 2001-10-05 2001-10-05 Elastic fiber treatment agent and elastic fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001345417A JP3888669B2 (en) 2001-10-05 2001-10-05 Elastic fiber treatment agent and elastic fiber

Publications (2)

Publication Number Publication Date
JP2003113581A true JP2003113581A (en) 2003-04-18
JP3888669B2 JP3888669B2 (en) 2007-03-07

Family

ID=19158755

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3888669B2 (en)

Also Published As

Publication number Publication date
JP3888669B2 (en) 2007-03-07

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