JPH03213575A - Treating lubricant for synthetic fiber intended for industrial material - Google Patents
Treating lubricant for synthetic fiber intended for industrial materialInfo
- Publication number
- JPH03213575A JPH03213575A JP858290A JP858290A JPH03213575A JP H03213575 A JPH03213575 A JP H03213575A JP 858290 A JP858290 A JP 858290A JP 858290 A JP858290 A JP 858290A JP H03213575 A JPH03213575 A JP H03213575A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- agent
- emulsifier
- particle size
- aqueous emulsion
- 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
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は産業資材用途に使用するポリエステル、ポリア
ミド等の合成繊維処理油剤に関するものでおる。さらに
詳しく粘着剤やゴムとの接着性に優れ、かつ耐熱性に優
れた、特に粘着テープ補強材、電線被覆材等の用途に使
用される合成繊維処理油剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an oil for treating synthetic fibers such as polyester and polyamide used for industrial material applications. More specifically, the present invention relates to a synthetic fiber treatment oil that has excellent adhesion to adhesives and rubber and excellent heat resistance, and is used particularly for applications such as adhesive tape reinforcing materials and electric wire covering materials.
[従来の技術]
合成繊維は寸法安定性、高強力、低収縮などの点で優れ
ているため、粘着テープ補強材、電線被覆材等の補強材
として使用されている。これらの用途では、粘着剤やゴ
ムと合成繊維との接着性、接着保持性、およびゴムの劣
化防止が重要な要求特性となる。また、これらの用途の
合成繊維の製造工程においては、一般に高温での熱処理
を行うため、繊維表面に付与する処理油剤も耐熱性の優
れていることが必要でおる。[Prior Art] Synthetic fibers are excellent in terms of dimensional stability, high strength, low shrinkage, etc., and are therefore used as reinforcing materials for adhesive tapes, wire covering materials, and the like. In these applications, the important properties required are adhesion between the adhesive or rubber and the synthetic fiber, adhesion retention, and prevention of rubber deterioration. Furthermore, in the manufacturing process of synthetic fibers for these uses, heat treatment at high temperatures is generally performed, so the treatment oil applied to the fiber surface must also have excellent heat resistance.
従来から粘着剤やゴムとの接着性に優れた合成繊維を得
る方法として、例えば特開昭53−2696号公報に記
載されるように粘着剤やゴムとの相互作用の少ない流動
パラフィンなどの鉱物油を主成分とする処理油剤が使用
されていたが、この方法では鉱物油の耐熱性が低く、発
煙発生が著しく、作業環境の悪化が実用上大きな障害と
なっていた。しかも、接着性自体の改善も満足できるも
のではなかった。接着性を向上させる油剤組成物の検討
も、例えば特開昭54−82497号公報で提案されて
いるように種々行なわれできたが、繊維の平滑性が損な
われたり、熱処理工程での発煙、タール等を発生し耐熱
性が充分でないなど、到底実用−ト満足できるものでは
なかった。Conventionally, as a method for obtaining synthetic fibers that have excellent adhesion with adhesives and rubber, minerals such as liquid paraffin that have little interaction with adhesives and rubber have been used, as described in JP-A No. 53-2696. Treated oil agents containing oil as a main component have been used, but with this method, the heat resistance of mineral oil is low, the generation of smoke is significant, and the deterioration of the working environment is a major impediment to practical use. Moreover, the improvement in adhesiveness itself was not satisfactory. Various studies have been conducted on oil compositions that improve adhesion, such as those proposed in JP-A No. 54-82497, but these have resulted in problems such as loss of fiber smoothness, smoke generation in the heat treatment process, etc. It was not completely satisfactory for practical use, as it generated tar and other substances and did not have sufficient heat resistance.
そこで本発明者らは、鋭意検討した結果、従来の処理油
剤組成物で20〜50重量%程度配合されている乳化剤
成分が粘着剤やゴムとの相互作用が極めて強く、繊維と
の接着性、粘着剤の粘着力、およびゴムの物性を損なう
主原因物質であることをつきとめ、本発明に至った。As a result of intensive studies, the present inventors found that the emulsifier component, which is blended in an amount of about 20 to 50% by weight in conventional treatment oil compositions, has extremely strong interaction with adhesives and rubber, and has a high adhesion with fibers. It was discovered that this is the main substance that impairs the adhesive strength of adhesives and the physical properties of rubber, leading to the present invention.
[発明が解決しようとする課題]
本発明の目的は、繊維の平滑性を損なうことなく、熱処
理時の発煙を防止したうえで、粘着剤やゴムとの接着性
が良好で、かつ粘着剤の粘着力を弱めたり、ゴム劣化の
ない産業資材用合成繊維処理油剤を提供するものである
。[Problems to be Solved by the Invention] The objects of the present invention are to prevent smoke generation during heat treatment without impairing the smoothness of the fibers, to have good adhesion to adhesives and rubber, and to provide adhesive-free adhesives. The purpose of the present invention is to provide a synthetic fiber treatment oil for industrial materials that does not weaken adhesive strength or cause rubber deterioration.
「課題を解決するための手段]
すなわち、本発明は平滑剤成分および添加剤成分に乳化
剤成分を配合するか、もしくは配合しない油剤組成物に
おいて
△9平滑剤成分の60重量%以上が全炭素数26以上の
脂肪族および/または芳香族カルボン酸エステルの1種
または2種以上で、
B、乳化剤成分の配合比が全油剤組成物中の0〜10重
量%であり、
かつ油剤粒子の平均粒径が1ミクロンゴス下の水系エマ
ルジョンであることを特徴とする産業資材用合成繊維処
理油剤の使用により目的を達成することができる。Means for Solving the Problems In other words, the present invention provides an oil composition in which an emulsifier component is blended into the smoothing agent component and the additive component, or in which 60% by weight or more of the △9 smoothing agent component has a total carbon number. one or more of 26 or more aliphatic and/or aromatic carboxylic acid esters, B, the blending ratio of the emulsifier component is 0 to 10% by weight in the total oil composition, and the average particle size of the oil particles The purpose can be achieved by using a synthetic fiber treatment oil for industrial materials, which is an aqueous emulsion with a diameter of 1 micron Goth or less.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
本発明の処理油剤の組成物である平滑剤成分としては、
従来公知の平滑剤のなかで全炭素数26以上の脂肪族お
よび/または芳香族カルボン酸エステルが必要であり、
全炭素数30以上とするのが好ましい。The smoothing agent component of the treated oil composition of the present invention includes:
Among the conventionally known smoothing agents, aliphatic and/or aromatic carboxylic acid esters having a total carbon number of 26 or more are required,
It is preferable that the total carbon number is 30 or more.
好適な例として、オレイルラウレート、オレイルオレー
1〜等の一価アルコールと一塩基性脂肪族カルボン酸の
エステル、ジオクチルセバケート、ジオレイルアジペー
ト、ジトリデシルヂオジプロピオネート等の一価アルコ
ールと多塩基性脂肪族カルボン酸、含イオウカルボン酸
のエステル、ジラウリルフタレート、lヘリオレイルト
リメリテート等の一価アルコールと芳香族カルボン酸の
エステル、エチレングリコールジオレート、トリメチロ
ールプロパントリカプリレート、グリセリントリオレー
ト、ビスフエノルジオレーI−等の多価アルコールと一
塩基性脂肪族カルボン酸のエステル、またこれらのエス
テルの誘導体としてラウリル(EO)nオクタノエート
等のアルキレンオキサイド付加エステル(但し、アルキ
レンオキサイド付加モル数として、化合物自体が水に可
溶または自己分散するほど大きいと平滑性が損なわれる
ので、5モル以下の付加が好ましい)などの単独、ある
いは混合使用を挙げることかできるが、特にこれらに限
定されるものではない。また、全炭素数26未満の脂肪
族および/または芳香族カルボン酸エステルや流動パラ
フィン、スピンドル油等の鉱物油についても単独使用の
場合には発煙、タールの発生等、耐熱性が損なわれるの
で好ましくないが、平滑剤成分のうち40重量%未満の
混合使用については、耐熱性を損なわない範囲で使用で
きる。Suitable examples include esters of monohydric alcohols such as oleyl laurate and oleyl ole-1 and monobasic aliphatic carboxylic acids, and monohydric alcohols and polyhydric alcohols such as dioctyl sebacate, dioleyl adipate, and ditridecyl diodipropionate. Basic aliphatic carboxylic acids, esters of sulfur-containing carboxylic acids, esters of monohydric alcohols and aromatic carboxylic acids such as dilauryl phthalate and l-helioyl trimellitate, ethylene glycol diolate, trimethylolpropane tricaprylate, glycerin Esters of polyhydric alcohols and monobasic aliphatic carboxylic acids such as triolate, bisphenol diole I-, and alkylene oxide-added esters such as lauryl (EO) n-octanoate as derivatives of these esters (however, alkylene oxide-added esters such as lauryl (EO) n-octanoate) If the number of moles is so large that the compound itself becomes soluble or self-dispersible in water, the smoothness will be impaired, so addition of 5 moles or less is preferable. It is not limited. Additionally, aliphatic and/or aromatic carboxylic acid esters having a total carbon number of less than 26, liquid paraffin, and mineral oils such as spindle oil are also preferable since heat resistance may be impaired due to the generation of smoke or tar when used alone. However, if less than 40% by weight of the smoothing agent component is mixed, it can be used within a range that does not impair heat resistance.
また本発明で処理油剤中の乳化剤成分としては、従来公
知のものが使用できるが、好適な例として、活性水素を
1以上有する化合物のアルキレンオキサイド付加物、即
ちラウリルアルコール、1−ステアリルアルコール、オ
レイルアルコール、オクチルフェノール、ノニルフェノ
ール等の一価ヒドロキシ化合物のアルキレンオキサイド
付加物、グリセリンのモノオレイン酸エステル、ソルビ
タンのモノラウリン酸エステル、トリメチロールプロパ
ンのジステアリン酸エステル等の多価アルコール部分エ
ステルおよびこれらのアルキレンオキサイド付加物、ヒ
マシ油のアルキレンオキサイド付加物、ラウリルアミン
、ステアリルアミン等のアルキルアミン類のアルキレン
オキサイド付加物、ミリスチン酸、ステアリン酸、オレ
イン酸等の高級脂肪酸のアルキレンオキサイド付加物、
およびこれらの脂肪酸から誘導されるアミドのアルキレ
ンオキサイド付加物などが挙げられるが、ここで付加す
るアルキレンオキナイドとしてはエチレンオキサイド、
プロピレンオキサイド等が単独あるいは混合使用される
。In addition, as the emulsifier component in the treated oil agent in the present invention, conventionally known emulsifier components can be used, but suitable examples include alkylene oxide adducts of compounds having one or more active hydrogens, such as lauryl alcohol, 1-stearyl alcohol, oleyl alcohol, etc. Alkylene oxide adducts of monohydric hydroxy compounds such as alcohol, octylphenol, and nonylphenol, polyhydric alcohol partial esters such as monooleic acid ester of glycerin, monolauric acid ester of sorbitan, distearic acid ester of trimethylolpropane, and alkylene oxide additions of these. products, alkylene oxide adducts of castor oil, alkylene oxide adducts of alkylamines such as laurylamine and stearylamine, alkylene oxide adducts of higher fatty acids such as myristic acid, stearic acid, and oleic acid,
and alkylene oxide adducts of amides derived from these fatty acids. Examples of alkylene oxide adducts include ethylene oxide,
Propylene oxide and the like are used alone or in combination.
このほかにポリエチレングリコールポリプロピレングリ
コールブロック共重合体や、さらにラウリン酸1〜リエ
タノールアミン、オレイン酸ジェタノールアミン、ロー
1〜油等のアニオン界面活性剤についても乳化力を有す
るものについては乳化剤として使用でき、本発明におい
ては乳化力をもつ成分はすべて乳化剤成分として分類さ
れる。In addition, polyethylene glycol polypropylene glycol block copolymers and anionic surfactants such as lauric acid 1-reethanolamine, oleic acid jetanolamine, and rho 1-oil can also be used as emulsifiers if they have emulsifying power. In the present invention, all components having emulsifying power are classified as emulsifier components.
しかしながら、上記の乳化剤は一般に粘着剤やゴムとの
相互作用が強く、本発明では乳化剤成分による接着剤や
ゴムと繊維との接着性低下、粘着剤の粘着力低下、さら
にはゴムの劣化等の障害を回避するため、乳化剤の配合
比は乳化剤が障害を引き起こさない範囲、すなわち、0
〜10重量%とする必要があり、0〜7重量%とするの
がより好ましい。However, the above-mentioned emulsifiers generally have a strong interaction with adhesives and rubber, and in the present invention, the emulsifier component reduces the adhesion between adhesives and rubber and fibers, decreases the adhesive strength of the adhesive, and further deteriorates the rubber. In order to avoid problems, the blending ratio of the emulsifier should be within a range where the emulsifier does not cause problems, that is, 0.
It is necessary to set it to 10 weight%, and it is more preferable to set it as 0 to 7 weight%.
さらに本発明の処理油剤では、必要に応じて添加剤、即
ちアルキルスルホネートのアルカリ金属塩、アルキルホ
スフェートのアルカリ金属塩、ポリアルギレングリコー
ルアルキルホスフ工−1〜のアルカリ金属塩、脂肪酸石
鹸、アルキルイミダシリン類等の帯電防止剤のほか、従
来公知の集束剤、防錆剤、防腐剤、抗酸化剤などを同時
に使用できる。これらの添加剤は処理油剤の要求特性に
応じて配合され、配合量も限定されないが、平滑性や耐
熱性が損われることがあるので、1〜6重量%が好まし
い。Furthermore, in the treated oil agent of the present invention, additives may be added as necessary, namely, alkali metal salts of alkyl sulfonates, alkali metal salts of alkyl phosphates, alkali metal salts of polyalgylene glycol alkyl phosphants-1, fatty acid soaps, alkyl immobilizers, etc. In addition to antistatic agents such as Dacilin, conventionally known sizing agents, rust preventives, preservatives, antioxidants, etc. can be used simultaneously. These additives are blended according to the required characteristics of the treated oil agent, and the blending amount is not limited, but since smoothness and heat resistance may be impaired, it is preferably 1 to 6% by weight.
本発明においては油剤粒子の平均粒子径を1ミクロン以
下とする必要があり、0.7ミクロン以下とするのが好
ましく、0.5ミクロン以下とすることがことがより好
ましい。平均粒子径が1ミクロンを越えると処理油剤の
乳化安定性が悪くなり、分離してしまうため、合成繊維
処理油剤として実用に供することはできないのである。In the present invention, the average particle diameter of the oil particles must be 1 micron or less, preferably 0.7 micron or less, and more preferably 0.5 micron or less. If the average particle size exceeds 1 micron, the emulsion stability of the treatment oil will deteriorate and it will separate, so it cannot be put to practical use as a synthetic fiber treatment oil.
本発明の処理油剤の製造方法は特願昭63173063
号で提案した方法が好ましく適用される。The method for producing the treated oil agent of the present invention is disclosed in Japanese Patent Application No. 63173063.
The method proposed in this issue is preferably applied.
すなわち、油剤組成中の乳化剤成分の配合比率を0〜1
0重量%、つまり従来の配合比よりも低くし、かつ乳化
安定性良好な水系エマルジョンを得るために、処理油剤
の高速液流微粒子化手段を適用する。従来のホモミキサ
ー、プロペラ等の攪拌装置による攪拌作用のみでは、乳
化剤配合比率が0〜10重量%にすると、乳化力不足の
ため水系エマルジョンが得られない。通常、エマルジョ
ン化した処理油剤は、実用上は5日以上、望ましくは1
週間以十安定な乳化状態を保つことが要求されている。That is, the blending ratio of the emulsifier component in the oil composition is 0 to 1.
In order to obtain an aqueous emulsion with a blending ratio of 0% by weight, that is, lower than the conventional blending ratio, and with good emulsion stability, a high-speed liquid flow atomization means for the treated oil agent is applied. If the mixing ratio of the emulsifier is 0 to 10% by weight, an aqueous emulsion cannot be obtained using only the stirring action of a conventional stirring device such as a homomixer or a propeller due to insufficient emulsifying power. Normally, the emulsified treated oil agent is practically used for 5 days or more, preferably 1 day.
It is required to maintain a stable emulsified state for more than 10 weeks.
乳化安定性不良の原因としては、水に溶けない物質が主
成分である油剤組成物を微粒子化させ、かつ水中に均一
に分散させるために必要な界面活性剤、すなわち乳化剤
成分の配合比が10重量%以下のため乳化力が不足して
いることと、従来使用されてきたホモミキサー等では機
械的せん断力により粒子をより細分化するまでの能力を
有していないのである。The cause of poor emulsion stability is that the blending ratio of the surfactant, that is, the emulsifier component, is 10%, which is necessary to make the oil composition whose main component is a water-insoluble substance into fine particles and uniformly disperse it in water. This is because the emulsifying power is insufficient because the amount is less than % by weight, and the homomixers and the like that have been used conventionally do not have the ability to further divide the particles by mechanical shearing force.
しかし、本発明においては乳化剤成分の配合比率が10
重量%以下でも、従来の乳化手段により一時的な乳化状
態にした後、さらに高速液流微粒子化手段により処理す
ると、処理油剤の油剤粒子の平均粒径を1ミクロン以下
とすることができ、20〜50重量%程度配合した従来
の処理油剤と比較しても乳化安定性の点でなんら遜色の
ない油剤が得られる。However, in the present invention, the blending ratio of the emulsifier component is 10
Even if it is less than 20% by weight, if it is made into a temporary emulsified state by conventional emulsification means and then further processed by high-speed liquid flow atomization means, the average particle size of the oil particles of the treated oil can be made 1 micron or less, and 20 An oil agent that is comparable in emulsion stability to conventional treated oil agents containing about 50% by weight can be obtained.
本発明において産業資材用途とは、特に粘着テープ用途
、電線被覆材用途等合成繊維と有機他素材、例えば粘着
剤、ゴム、]−ティング材等とを複合して使用する用途
をいう。In the present invention, industrial material uses refer to uses in which synthetic fibers are used in combination with organic and other materials, such as adhesives, rubber, coating materials, etc., particularly as adhesive tape uses and electric wire coating uses.
ここで、本発明で用いる高速液流微粒子化手段としては
処理液を高流速化とすることによる機械的せん断力によ
って油剤粒子を微粒子化す0
るのが好ましい。Here, as the high-speed liquid flow atomization means used in the present invention, it is preferable to atomize the oil particles by mechanical shearing force generated by increasing the flow rate of the processing liquid.
本発明の処理油剤を付与した合成繊維糸条は、粘着剤や
ゴムとの相互作用の強い乳化剤成分が従来の処理油剤と
比較して大幅に減少しているため、粘着剤やゴムとの接
着性か良好で、ゴム物性の低下、例えば電線被覆材に使
用したときの絶縁抵抗値の低下もない。また特定の平滑
剤成分を使用することにより、耐熱性も良好で、しかも
従来の処理油剤に比較して平滑剤成分の配合比率が上が
っているため、全炭素数26以上の脂肪族および/また
は芳香族カルボン酸エステルを使用しても平滑性が損な
われることはない。このため本発明の処理油剤を付与し
た合成繊維糸条は産業資材用途のうち、特に上記した粘
着テープ用途、電線被覆材用途に好適であり、さらに有
機細索(Aとの相互作用が小さいため、この他、例えば
タイヤコード用途、セールクロス用途等にも利用できる
。Synthetic fiber threads coated with the treated oil of the present invention have significantly less emulsifier components that interact strongly with adhesives and rubber compared to conventional treated oils. It has good properties, and there is no deterioration in the physical properties of the rubber, such as insulation resistance when used as a wire covering material. In addition, by using a specific smoothing agent component, heat resistance is also good, and since the blending ratio of the smoothing agent component is increased compared to conventional treated oil agents, aliphatic and/or Even if an aromatic carboxylic acid ester is used, smoothness is not impaired. For this reason, the synthetic fiber yarn to which the treated oil agent of the present invention has been applied is particularly suitable for the above-mentioned adhesive tape applications and electric wire coating applications among industrial material applications. In addition, it can also be used for tire cord applications, sail cloth applications, etc.
[実施例] 以下、実施例により本発明を具体的に説明す1す るが、本発明はこれらに限定される物ではない。[Example] Hereinafter, the present invention will be specifically explained with reference to Examples. However, the present invention is not limited thereto.
実施例1
表1のNo1〜3に示す油剤組成物の配合比からなる油
剤原液を水中に攪拌しながら添加して一次乳化液とした
後、高速液流微粒子化手段としてホモジナイザー(ゴー
リン社製15H−8TA型)で処理(処理液流速500
km/hr) L/て水系エマルジョンとした。Example 1 Oil stock solutions having the blending ratios of oil compositions shown in Nos. 1 to 3 in Table 1 were added to water with stirring to obtain a primary emulsion, and then a homogenizer (15H manufactured by Gorlin Co., Ltd.) was used as a high-speed liquid flow atomization means. -8TA type) (processing liquid flow rate 500
km/hr) L/h to make an aqueous emulsion.
2
得られた水系エマルジョン中の油剤粒子径、乳化安定性
の評価結果を表2実験No1〜3に示した。表中の水系
エマルジョン中の油剤粒子径は、遠心式自動粒度力イ5
測定装置((株)堀場製作所製CAPA−500)によ
り測定した。2 The evaluation results of the oil agent particle diameter and emulsion stability in the obtained aqueous emulsion are shown in Table 2 Experiment Nos. 1 to 3. The oil particle diameter in the aqueous emulsion in the table is based on the centrifugal automatic particle size
The measurement was performed using a measuring device (CAPA-500 manufactured by Horiba, Ltd.).
比較例として、表1のNo1〜牛に示す油剤組成物の配
合比からなる油剤原液をホモミキサーを用いて水系エマ
ルジョンとしたときの評価結果を表2実験No4〜7に
併せて示した。As a comparative example, the evaluation results were shown in Experiment Nos. 4 to 7 of Table 2 when oil solution stock solutions having the blending ratios of oil compositions shown in Table 1 No. 1 to Cattle were made into aqueous emulsions using a homomixer.
表1の油剤組成物No1〜3に示した乳化剤成分の配合
比が10重量%以下の油剤は乳化力不足のため、従来の
ホモミキサー等の攪拌装置による攪拌では、表2実験N
o4〜6に示すように、油剤粒子径が大きく、安定性良
好な水系エマル3
ジョンとすることはできず、数10分で完全に2層に分
離した。一方、表2実験Nol〜3の実施例は高速液流
微粒子化手段により処理しているため、格段に粒子径が
小さくなっており、比表面積が大きいことから乳化剤成
分の配合比が10重量%以下でも安定な乳化状態を保つ
ことが可能である。また、比較例として表2実験No7
には乳化剤成分配合比が20重量%の従来の油剤組成物
(表INa、4)をホモミキサーを用いて水系エマルジ
ョンとした例を加えたが、この場合にもまだ乳化力不十
分で、油剤粒子の平均粒径は1ミクロンを超えているた
め、1日経過後分離がみられた。Oils with a blending ratio of emulsifier components of 10% by weight or less as shown in Oil Compositions No. 1 to 3 in Table 1 lack emulsifying power, so when stirring with a conventional stirring device such as a homomixer, Table 2 Experiment N
As shown in Nos. 4 to 6, the particle size of the oil agent was large, and a water-based emulsion with good stability could not be obtained, and the emulsion completely separated into two layers within several tens of minutes. On the other hand, in the Examples of Experiments No. 3 to 3 in Table 2, the particle size was significantly reduced because the treatment was performed using a high-speed liquid flow atomization means, and the specific surface area was large, so the blending ratio of the emulsifier component was 10% by weight. It is possible to maintain a stable emulsified state even below. In addition, as a comparative example, Table 2 Experiment No. 7
An example was added in which a conventional oil composition (Table INa, 4) with a blending ratio of emulsifier components of 20% by weight was made into an aqueous emulsion using a homomixer, but the emulsifying power was still insufficient in this case, and the oil composition Since the average particle size of the particles exceeded 1 micron, separation was observed after one day.
実施例2
表3、実験No8〜12記載の油剤組成物の配合比から
なる油剤原液を70〜80’Cに加熱し、50°Cの温
水中に攪拌しながら添加して一次乳化液とした後、ホモ
ジナイザー(ゴーリン社製15H8TA型)で処理(処
理液流速500km/hr) L/て15重量%水系エ
マルジョンとした油剤を用意した。Example 2 An oil stock solution having the blending ratio of the oil compositions listed in Table 3, Experiment Nos. 8 to 12 was heated to 70 to 80'C and added to 50°C warm water with stirring to obtain a primary emulsion. Thereafter, the mixture was treated with a homogenizer (Model 15H8TA manufactured by Gorin Co., Ltd.) (processing liquid flow rate 500 km/hr) to prepare a 15% by weight aqueous emulsion.
4
用意された処理油剤をポリエステルフィルム上に一定量
、均一に塗布した後、市販の粘着テプを圧着したものを
試料とし、引っ張り強力を測定することにより油剤と粘
着テープとの接着性を測定評価した。4 After uniformly applying a certain amount of the prepared treated oil onto a polyester film, a commercially available adhesive tape was used as a sample and the tensile strength was measured to evaluate the adhesion between the oil and the adhesive tape. did.
また、ポリエチレンテレフタレートを1100m/分の
紡糸速度で溶融紡糸するに際し、紡糸糸条に表3に記載
した油剤組成物の配合比からなる処理油剤を純分イ」着
量が0.7重量%になるように付着させた。1qられた
未延伸糸を延伸倍率3.5侶、延伸速度300 m/分
、じ−タープレト温度220’Cで延伸し240デニー
ル/24フイラメントの延伸糸とした。こうして得た延
伸糸を用いて作成した編地に粘着テープをはり荷重10
Kgをかけて2日間放置したものを試料とし、粘着テー
プを剥離させるときの強力を測定することにより繊維糸
条と粘着テープとの接着性を評価した。In addition, when polyethylene terephthalate was melt-spun at a spinning speed of 1100 m/min, a treated oil having the blending ratio of the oil composition listed in Table 3 was applied to the spun yarn at a pure amount of 0.7% by weight. I attached it so that it would look like this. The 1q undrawn yarn was drawn at a draw ratio of 3.5 mm, a drawing speed of 300 m/min, and a tar plate temperature of 220'C to obtain a drawn yarn of 240 denier/24 filaments. Adhesive tape was applied to the knitted fabric made using the drawn yarn thus obtained, and a load of 10
The adhesion between the fiber thread and the adhesive tape was evaluated by measuring the strength when peeling the adhesive tape using a sample that was left for 2 days under a load of Kg.
比較例とし−で、表3実験No13〜16の従来の油剤
組成を持つ処理油剤についても、ホモミ5
キザーを用いて15重量%水系エマルジョンとした後、
上記と同一条件で延伸糸とし、同一条件で接着性を評価
した。As a comparative example, the treated oils having the conventional oil compositions of Experiment Nos. 13 to 16 in Table 3 were made into 15% by weight aqueous emulsions using a homomixer.
A drawn yarn was prepared under the same conditions as above, and adhesiveness was evaluated under the same conditions.
また、実験No8〜16に示した処理油剤を付与した糸
条の延伸工程での発煙状態についても併せて評価した。In addition, the state of smoke generation during the drawing process of the yarns to which the treatment oils shown in Experiment Nos. 8 to 16 were applied was also evaluated.
さらに、表3記載の油剤組成物につき上記の方法で得た
15重量%水系エマルジョンに市販のシリコンゴム被覆
電線を15 hr浸せきさせた後、JIS3005に基
づいて絶縁抵抗値を測定した。Furthermore, commercially available silicone rubber-coated electric wires were immersed for 15 hours in the 15% by weight aqueous emulsion obtained using the oil composition shown in Table 3 by the above method, and then the insulation resistance value was measured based on JIS3005.
以上の評価結果を表3に併せで示した。The above evaluation results are also shown in Table 3.
(以下余白〉
6
7
表3の実験No3〜12に示すように本発明の処理油剤
は、粘着剤との相互作用が大きく接着性低下素材である
乳化剤成分の配合比が10重量%以下と低いため、優れ
た接着性を有している。(The following is a blank space) 6 7 As shown in Experiment Nos. 3 to 12 in Table 3, the treated oil of the present invention has a low blending ratio of 10% by weight or less of the emulsifier component, which is a material that interacts strongly with the adhesive and deteriorates adhesion. Therefore, it has excellent adhesive properties.
処理油剤の耐熱性について、平滑剤成分として全炭素数
26未満のカルボン酸エステルを使用したものには発煙
の発生がみられた。Regarding the heat resistance of treated oils, smoke generation was observed in those using carboxylic acid esters having a total carbon number of less than 26 as a smoothing agent component.
また、本発明処理油剤で処理したシリコンゴム被覆電線
は、従来の処理油剤で処理した場合に比較して、格段に
高い絶縁抵抗値を示しており、本発明処理油剤がゴムと
の相互作用がなく、ゴム物性を損なうことがないことが
わかる。In addition, silicone rubber-coated electric wires treated with the treated oil of the present invention exhibited significantly higher insulation resistance values than those treated with conventional treated oil, indicating that the treated oil of the present invention does not interact with rubber. It can be seen that there is no damage to the physical properties of the rubber.
[発明の効果]
本発明は、粘着剤やゴムとの相互作用が極めて強く、粘
着剤やゴムとの接着性、粘着剤の粘着力、およびゴムの
物性を損なう主原因物質である従来の処理油剤組成物で
20〜50重量%程度配合されている乳化剤成分を減少
させ、繊維の平滑性を損なうことなく、熱処理時の発煙
を防8
止したうえで、粘着剤やゴムとの接着性が良好で、かつ
粘着剤の粘着力を弱めたり、ゴム劣化のない産業資材用
合成繊維処理油剤とすることができるのである。[Effects of the Invention] The present invention eliminates conventional treatments that have extremely strong interactions with adhesives and rubber and are the main cause of deteriorating the adhesion with adhesives and rubber, the adhesive strength of adhesives, and the physical properties of rubber. By reducing the emulsifier component, which is about 20 to 50% by weight in the oil composition, it prevents smoke generation during heat treatment without impairing the smoothness of the fibers, and improves the adhesion with adhesives and rubber. This makes it possible to create a synthetic fiber treatment oil for industrial materials that has good properties and does not weaken the adhesive force of the adhesive or cause rubber deterioration.
Claims (1)
、もしくは配合しない油剤組成物において A、平滑剤成分の60重量%以上が全炭素数26以上の
脂肪族および/または芳香族カルボン酸エステルの1種
または2種以上で、 B、乳化剤成分の配合比が全油剤組成物中の0〜10重
量%であり、 かつ油剤粒子の平均粒径が1ミクロン以下の水系エマル
ジョンであることを特徴とする産業資材用合成繊維処理
油剤。[Scope of Claims] In an oil composition in which an emulsifier component is blended into the smoothing agent component and the additive component or not, A, 60% by weight or more of the smoothing agent component is an aliphatic compound having a total carbon number of 26 or more and/or An aqueous emulsion containing one or more aromatic carboxylic acid esters, B, an emulsifier component in a blending ratio of 0 to 10% by weight based on the total oil composition, and an average particle size of oil particles of 1 micron or less. A synthetic fiber treatment oil for industrial materials, characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008582A JP2590575B2 (en) | 1990-01-17 | 1990-01-17 | Synthetic fiber treatment oil for industrial materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008582A JP2590575B2 (en) | 1990-01-17 | 1990-01-17 | Synthetic fiber treatment oil for industrial materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03213575A true JPH03213575A (en) | 1991-09-18 |
| JP2590575B2 JP2590575B2 (en) | 1997-03-12 |
Family
ID=11697004
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008582A Expired - Fee Related JP2590575B2 (en) | 1990-01-17 | 1990-01-17 | Synthetic fiber treatment oil for industrial materials |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2590575B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104594023A (en) * | 2015-01-26 | 2015-05-06 | 江苏文凤化纤集团有限公司 | Preparation method for chinlon spinning additive |
| US10601044B2 (en) | 2014-03-25 | 2020-03-24 | Hitachi Chemical Company, Ltd. | Negative electrode material for lithium-ion secondary battery, method for manufacturing negative electrode material for lithium-ion secondary battery, negative electrode material slurry for lithium-ion secondary battery, negative electrode for lithium-ion secondary battery, and lithium-ion secondary battery |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2819718B2 (en) | 1990-01-17 | 1998-11-05 | 東レ株式会社 | Synthetic fiber treatment oil for fluid injection processing |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5482497A (en) * | 1977-12-12 | 1979-06-30 | Asahi Chemical Ind | Oil composition for thermoplastic fiber |
-
1990
- 1990-01-17 JP JP2008582A patent/JP2590575B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5482497A (en) * | 1977-12-12 | 1979-06-30 | Asahi Chemical Ind | Oil composition for thermoplastic fiber |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10601044B2 (en) | 2014-03-25 | 2020-03-24 | Hitachi Chemical Company, Ltd. | Negative electrode material for lithium-ion secondary battery, method for manufacturing negative electrode material for lithium-ion secondary battery, negative electrode material slurry for lithium-ion secondary battery, negative electrode for lithium-ion secondary battery, and lithium-ion secondary battery |
| CN104594023A (en) * | 2015-01-26 | 2015-05-06 | 江苏文凤化纤集团有限公司 | Preparation method for chinlon spinning additive |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2590575B2 (en) | 1997-03-12 |
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