JPS5836268A - Oil agent for treating synthetic fiber - Google Patents

Oil agent for treating synthetic fiber

Info

Publication number
JPS5836268A
JPS5836268A JP13159881A JP13159881A JPS5836268A JP S5836268 A JPS5836268 A JP S5836268A JP 13159881 A JP13159881 A JP 13159881A JP 13159881 A JP13159881 A JP 13159881A JP S5836268 A JPS5836268 A JP S5836268A
Authority
JP
Japan
Prior art keywords
acid
yarn
oil agent
oil
lid
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
JP13159881A
Other languages
Japanese (ja)
Other versions
JPS6253630B2 (en
Inventor
正夫 内田
克巳 吉田
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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP13159881A priority Critical patent/JPS5836268A/en
Publication of JPS5836268A publication Critical patent/JPS5836268A/en
Publication of JPS6253630B2 publication Critical patent/JPS6253630B2/ja
Granted legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は合成繊維の挑理剤に関するものである。さらに
詳しくは合成繊維の製造工程並びに加工工1におい(繊
輪糸条に高度な平滑性と静電気防止性能を付与する新規
な繊維処理用油剤に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a challenge agent for synthetic fibers. More specifically, it relates to a novel fiber processing oil agent that imparts high smoothness and antistatic performance to fiber yarns in the manufacturing process and processing process 1 of synthetic fibers.

従来より会!j1.練雑1%にフィラメントの製造加工
に当っては生麿性向上のためのスピードアップが図られ
ているが、糸条速度のスピードアップとともに糸条と各
種接触体(例えばガイド。
More than ever! j1. At 1% kneading, efforts are being made to speed up the filament manufacturing process to improve the maturation properties, but as well as speeding up the yarn speed, the yarn and various contact objects (for example, guides) have to be increased.

−一ツー、ヒーターなど)との接圧の増大、熱4611
11度のアップ等など、製糸条件もきびしい方向に向っ
ている。これに伴い、糸条と各種接触体間の摩擦も極め
て増大する結果、繊維糸条の損傷による毛羽や断糸の発
生及び接触体の摩MKよる後触体寿命減少、及び摩擦静
電気発生の増大による各種の障害(p−ラ捲付、断糸及
び品質の低下)が著しく、生産効串1品質低下りるいは
後触体寿命減少にともな59換周期の短縮什等によるコ
ストアップが大きくなる傾向にある。
-Increase in contact pressure with (one-two, heater, etc.), heat 4611
The spinning conditions are also becoming stricter, such as an 11-degree increase. Along with this, the friction between the yarn and various contact bodies increases significantly, resulting in the occurrence of fuzz and yarn breakage due to damage to the fiber yarn, reduction in the life of the contact body due to friction MK of the contact body, and increase in the generation of frictional static electricity. Various problems (p-ra winding, yarn breakage, and quality deterioration) are significant, and production efficiency and quality are reduced, and the life of the trailing body is shortened, resulting in a significant increase in costs due to shortening of the exchange cycle, etc. There is a tendency to

例えば仮撚捲縮加工糸の製造において◆言、従来のスピ
ンドル方式に代って摩擦仮撚加工法が採用されるに至り
fL撚加工速度が飛躍的にスピードアップがされてきた
。そして摩擦仮撚加工方式でさえ諸機械設備の遊歩から
さらにスピードアップされ最近では400〜600 v
/分更にはxOO(1+n/分を越えるはどの高速加工
が行なわれるようになっていzl。それと同時にヒータ
一温度も従来の160〜190℃とい5範囲から200
−230℃ないし250℃に上昇されてきた。しかも、
^連化、i%温化の過酷な条件下では、繊維糸条と糸導
や張力を制御規制するガイド類やコンベン七−ター、p
−ツー及び熱処理ヒーター等との摩擦が増大する結果。
For example, in the production of false-twisted crimped yarn, the frictional false-twisting method has been adopted in place of the conventional spindle method, and the speed of fL twisting has been dramatically increased. Even the frictional false twisting method has been further speeded up due to the advances in various machinery and equipment, and is now 400 to 600 V.
/min and even xOO(1+n/min), which high-speed machining is performed.At the same time, the heater temperature has also increased from the conventional range of 160 to 190℃ to 200℃
It has been raised to -230°C to 250°C. Moreover,
Under the harsh conditions of continuous heating and i% warming, guides, convenors, etc. that control and regulate fiber threads, thread guidance and tension,
- As a result of increased friction with tools, heat treatment heaters, etc.

繊維糸条が損傷し毛羽や断糸を誘発し、―シ(生産効率
が低下することになる。又他の例として織物や編物の製
造においても高速化が進んでおり、筬や編針などと糸条
の摩擦増大によって糸条の損傷そしてさらには筬−針な
どの摩耗が非常に多くなり、*に@化チタンやカーボン
ブラック等の硬質の無機物を比較的多量に名有する糸条
を用いる場合には特にこの軸向は顧!忙なる。
The fiber threads are damaged, leading to fuzz and yarn breakage, resulting in a decrease in production efficiency.As another example, the production speed of woven and knitted products is increasing, and the production of reeds, knitting needles, etc. The increased friction of the threads causes damage to the threads and even more wear and tear on the reeds and needles. This axis is particularly busy.

一方こうした高速化では摩擦が増大することによってl
111IA糸粂と各種接触間で摩擦静電気の発生も著し
く増大する結果、フィラメントの延伸および加エエ騙な
とにおいて糸掛時や走行時Kp−ツ一部分に単糸が咎付
いたり、場合によっては断糸したりして作業性がきわめ
て低下する。このような現象は1%に熱処理を受けた場
合KIIIKおこる。即ち静電気の発生は一般に低一時
になると急激に増大するため、仮撚加工時のように高温
で熱セクトを受けた糸は絶乾状態に近く静電気が非常に
発生しやすい状況にある。
On the other hand, at such high speeds, friction increases and l
As a result of the significant increase in the generation of frictional static electricity between various contacts with the 111IA yarn pike, the single yarn may become stuck in a part of the Kp-ts during threading or running during filament drawing and processing, and in some cases may break. This will cause threads to form, which will greatly reduce work efficiency. This phenomenon occurs when 1% is subjected to heat treatment. That is, since the generation of static electricity generally increases rapidly when the temperature is low, yarns that have undergone heat section at high temperatures, such as during false twisting, are in a nearly bone-dry state and are in a situation where static electricity is very likely to be generated.

一方、低張力下で糸がj!口するよ5な工程では糸が接
触部からはずれたりして糸質そのものに塵が生じ品質の
低下を招くこともしばしばある本発明の目的は上述の好
ましくない演象俸すなわち繊維糸条の製造、加工条件の
^連化、高温化に伴なって糸条と各種接触体間との摩擦
が増大する結果、糸条の損傷、!!触体の摩耗が誘起す
る生産効率の低下9品質の低下などに基(コストアップ
の招来を防止し、高速化、All化を中心とする革新技
術を成功させるため糸条に対し′C更に高度な平滑性反
び静電気防止性能を付与し得る繊維処理用油剤を提供す
ることにある。
On the other hand, under low tension, the thread is j! In the process described above, the yarn often comes off from the contact area and dust is generated on the yarn itself, resulting in a decrease in quality.The purpose of the present invention is to eliminate the above-mentioned undesirable effects, that is, the production of fiber yarn. As the processing conditions become more continuous and the temperature increases, the friction between the yarn and various contact bodies increases, resulting in damage to the yarn. ! Decrease in production efficiency caused by abrasion of the contact body (9) Based on the reduction in quality (9) In order to prevent the increase in costs and to succeed in innovative technology centered on high speed and aluminum alloy, The object of the present invention is to provide an oil agent for treating fibers that can impart smoothness and anti-static properties against warpage.

本発明者等は上記の目的を達成せんとして種々検討した
結果、従来、一般に繊維糸条に対して処理されている油
剤は平滑剤、帯電肋止剤。
The inventors of the present invention have conducted various studies to achieve the above object, and have found that the lubricants that have conventionally been used to generally treat fiber yarns include smoothing agents and antistatic agents.

乳化剤等で構成されて(・るが、本発明者らはこうした
既存のII&m用油剤によっては、畠速化さらには高温
化にともなう各種の障害を克服することは非常K11i
Lいことを知り、更に高度な平滑性、静電気防止性能を
得るべく種々検討した結果、特定の化合物を含む油剤に
よって前記目的を達成できることを見出し、本発明に到
達したものである。
However, the present inventors believe that it is extremely difficult to overcome the various obstacles associated with increased feed speed and higher temperatures using existing II&M lubricants.
As a result of various studies in order to obtain even higher level of smoothness and antistatic performance, the inventors discovered that the above object could be achieved by using an oil agent containing a specific compound, and thus arrived at the present invention.

即ち本発明は、・ 1ないし2個の水酸基を有する多価カルボンII(At
に炭lA数が8以上の鮨肪族7シルハ2イド(mlを反
応させて得られる化合!15 (CIのアルカリ金属、
7ンモニワ^又は有機7ミンの塩(2)を含有すること
を特徴とする合成繊維処理用油剤である。
That is, the present invention provides polyvalent carbon II (At
A compound obtained by reacting sushi aliphatic 7-silhydride (ml) with a carbon lA number of 8 or more!15 (alkali metal of CI,
This is an oil agent for treating synthetic fibers characterized by containing a salt (2) of heptamine or organic heptamine.

更に本発明について詳しく述べると、本発明の要旨は油
剤に高度な平滑性及び静電気防止性能を与るべく油剤中
に前記中+Ti、分を含有せしめることKある。
To describe the present invention in more detail, the gist of the present invention is to include the above-mentioned Ti content in the oil agent in order to give the oil agent a high degree of smoothness and antistatic performance.

以下ム〜Dの各成分について挙げる。Each of the components M to D will be listed below.

(4)の化合物; モノオキシジカルボン酸としてリンゴ酷。(4) Compound; Apples are harsh as monooxydicarboxylic acids.

モノオキシトリカルボン酸としてクエン骸。Citric skeleton as monooxytricarboxylic acid.

ジオキシジカルボン酸とし?il!1石酷なと挙げられ
るがこれに一定されるものではない。
Dioxydicarboxylic acid? Il! It is said to be one of the worst, but it is not fixed.

俤)の化合物; 鮨訪族7シルハライドとしては炭素数8以上からなる通
常の^級鮨肪酸の餘りρす゛ド化合物が用いられる。例
えばラウリン酸りpリド、パルミチン酸りρリド、ミリ
スチン酷りpリド、ステアリン酷りpリド、オレイン酸
りρリドなどが用いられる。
The compound of 俤): As the Sushiwa group 7 syl halide, a normal compound containing a higher grade Sushi fatty acid having 8 or more carbon atoms is used. For example, lauric acid p-lide, palmitic acid p-lide, myristic acid p-lide, stearic acid p-lide, oleic acid p-lide, etc. are used.

(CIの化合物; ((転)及び(Blの化合物を説塩酸反応の下に、容易
に合成できる。
Compounds of (CI); ((conversion)) and (Bl) can be easily synthesized under a hydrochloric acid reaction.

(至)の化合物; +CIで得られた合成物を水酸化リチ9ム、Iy性ソー
ダ、lff性カリなどのアルカリ水酸化物あるい番言7
ンモニ7またはモノエタノールアミン、ジェタノールア
ミン、トリエタノール7iンなどのフルカノールアミン
塩さらにはトリメチルアミン、トリエチルアミン、トリ
ブチルアミン、ラワリルアミン等のフルキル7ミンを用
いて中和させて製造することができる。もちろん、これ
らの塩類は単独乃至混合物の形であってもよ(、その中
和度も完全。
Compound (to); The compound obtained by +CI is combined with an alkali hydroxide such as lithium hydroxide, Iy-based soda, lff-based potash, etc.
It can be produced by neutralizing it with a flukanolamine salt such as ummoni-7 or monoethanolamine, jetanolamine, triethanolamine, etc., or a flukyl-7mine such as trimethylamine, triethylamine, tributylamine, and lavalylamine. Of course, these salts may be used alone or in the form of a mixture (the degree of neutralization is also complete).

部分いずれでも良い。Any part is fine.

次に本発明で好適な−1化合物(ロ)としては、例えば
次のものが挙げられる。
Next, examples of the -1 compound (b) suitable for the present invention include the following.

リンゴ酸とツクリン酷りρリドか・ら得られる反応物の
カリク^塩 リンゴ酸とパルミチン酸りρリドから得られる反応物の
ナトリワム塩 クエン酸とラウリン酸りpリドから慢られる反応物のカ
リクム塩 クエン酸とステアリン酷りpリドから得られる反応物の
カリクム塩 酒石酸とツクリン酷りpリドから得られる反応物のナト
リワム堪 酒石酸とステアリン鹸クロリドから得られる反応物のカ
リクム塩。
Calicum, a reaction product obtained from malic acid and tuclinic acid, Natriwam salt, a reaction product obtained from malic acid and palmitic acid, Calicum, a reaction product obtained from citric acid and lauric acid, prid. A potassium salt of a reaction product obtained from salt citric acid and stearic acid chloride A potassium salt of a reaction product obtained from tartaric acid and a reaction product obtained from salt citric acid and stearic acid chloride.

本発明は上記の如き化合物を従来の各種の繊維用油MK
加えることによって平滑性、静電気防止性能を有する新
規な油剤を提供せんとするものである0例えば潤滑剤と
して鉱物油、動植物油、各種合成エステル潤滑剤、ポリ
フルキレン/lコール系潤滑剤1合成シリコン鯛滑剤及
びそれらの乳化剤からなる油剤系に過室添加することに
よって達成される。その添加ilLは2%(重量)以上
が有効であり、%Ks〜20ヂ(重量)が好ましい。
The present invention uses the above-mentioned compounds in various conventional textile oil MKs.
The purpose is to provide a new oil having smoothness and antistatic performance by adding lubricants such as mineral oil, animal and vegetable oil, various synthetic ester lubricants, polyfulkylene/l coal-based lubricant, and synthetic silicone. This is achieved by addition of lubricants and their emulsifiers into an oil system. It is effective to add IL of 2% (weight) or more, and preferably %Ks to 20゜ (weight).

本発明の油剤を使用するに当っての付着方式としては水
系エマルジ厘ン、ストレート方式いずれでも良く、その
付着量Mはその目的に応じて紡糸、j11N伸などの製
糸段階又は各種の加工工Ii#階などいずれの工程にお
いて行なうこともできる。即ち紡糸油剤として使用した
場合、紡糸、砥伸工程における毛羽、断糸が減少し、さ
らに整径工程、撚糸工程、!3!編繊工程、仮撚加工工
程においても静電気障害およびガイドローラーN對の摩
擦体の摩耗な肪止゛する上で修めて有効である。なお油
剤の付着量は上記のよりな工11によって異なるが、例
えば仮撚加工用の一合へ2〜201L量ダ(対厭維)の
範囲内で選定するのが過当である。このような本発明の
油剤はいずれの合成繊維にも有効であるが、4IKポリ
エステル、ボリア!ド等のマルチフィラメントヤーンに
対し′C%にすぐれた効果を発揮する。
When using the oil agent of the present invention, either an aqueous emulsion method or a straight method may be used as the adhesion method, and the amount M of the adhesion may be determined depending on the purpose at the spinning stage, such as spinning or J11N drawing, or at various processing steps. This can be done at any step such as the # floor. In other words, when used as a spinning oil, fuzz and yarn breakage are reduced in the spinning and abrasive drawing processes, and furthermore, in the diameter adjustment process, yarn twisting process, etc. 3! It is also effective in the knitting process and the false twisting process to prevent static electricity damage and wear of the friction bodies of the guide rollers. Although the amount of oil applied differs depending on the above-mentioned twisting process 11, it is reasonable to select it within the range of 2 to 201 L (per fiber) for a false twisting process, for example. The oil agent of the present invention is effective for any synthetic fibers, including 4IK polyester, Boria! It exhibits an excellent effect on 'C% for multifilament yarns such as C.

以下実施例に2いて述べるが、実施例中の摩擦帯電圧、
対摩耗性1作業性、加工“性は次の方法で評価した。
As will be described in Example 2 below, the frictional charging voltage in the example,
Wear resistance 1 Workability and machinability were evaluated by the following method.

(1)  摩擦帯電圧(ト) 試料糸を20℃相対湿度61sチの雰囲気下でμメータ
ー(エイコー―j器製)Kて張カー寛(2051)のも
とK】00111/分の糸速でヒータープレート温度2
10℃(ヒーター長@@偏)上を走行させ、その後金属
摩擦体(表m1l1度ls・℃のホットピン)K接触(
II触角900)させ摩擦体から5側後の位置でフィラ
メント糸の摩擦帯電圧な集電式電位欄定■(春日電機I
I)を使用して測定した。
(1) Frictional charging voltage (g) The sample yarn was measured at 20°C under an atmosphere of relative humidity 61 seconds using a μ meter (manufactured by Eiko-J) and at a yarn speed of 00111/min under Kerahiro Zhang (2051). and heater plate temperature 2
Run it over 10℃ (heater length @@biased), and then touch the metal friction body (hot pin at 1 degree ls・℃) K contact (
(Kasuga Denki I
I).

(!l  It摩耗性 試料糸を20℃相対湿度65%の雰囲気ト初張力31#
、*触角17G’ のもと10011/分の糸速で編針
と接触走行させ、2時間11に編針表面を顕微鏡観察し
た。判定は摩耗痕の有無により耐摩耗性の良否を判定し
た。
(!l) The abrasive sample yarn was placed in an atmosphere of 20°C and 65% relative humidity with an initial tension of 31#.
, *The yarn was run in contact with a knitting needle at a yarn speed of 10011/min under an antenna angle of 17 G', and the surface of the knitting needle was observed under a microscope at 2 hours 11. The wear resistance was judged based on the presence or absence of wear marks.

(3)  加工安定性 加工中における毛羽の発生の大小ならびに断糸串、捲縮
性などから○が良好、Δやや劣る、×劣るの6段階で示
した。
(3) Processing stability Based on the degree of occurrence of fuzz during processing, yarn breakage skewer, crimp property, etc., the results were given in 6 grades: ○ is good, Δ is slightly poor, and × is poor.

実施例 ポリエチレンテレフタレートを3300 tm/分の紡
糸速度で熔融紡糸するに際し、紡糸糸条に、次表に記載
したような処理組成物を水系エマルシヨンでエマルジョ
ン盛度1o%(重量)として純分付着量がαSS<重量
)になるように付着させた。得られた115デニール/
s6フイラメントの未延伸糸を延伸倍率L5、延伸速度
900w/分、ヒータープレー)200℃で延伸し、得
られた7sデニール/36フイラメントの砥伸糸を20
℃相対潴度6s−の11囲気下で一畳夜放置したものを
試料とし糸走行時の摩擦帯電圧、金属摩擦体の摩耗性を
絆価した。
Example When polyethylene terephthalate was melt-spun at a spinning speed of 3300 tm/min, a treatment composition as shown in the following table was applied to the spun yarn using an aqueous emulsion with an emulsion content of 10% (by weight) in pure amount. It was attached so that αSS<weight). Obtained 115 denier/
The undrawn yarn of s6 filament was stretched at a stretching ratio of L5, a stretching speed of 900 w/min, and 200°C (heater play), and the resulting abrasive yarn of 7 s denier/36 filament was stretched at 200°C.
Samples were left for one night in an atmosphere of 11 s at a relative humidity of 6 s-, and the frictional charge voltage during thread running and the abrasion resistance of the metal friction body were evaluated.

−4,11Sfニール/36フイラメントの未延伸糸を
IIL%45■の円板をそなえた七うlツク調の外接式
摩擦仮撚装置を用いて延伸倍率Ll、ヒータ一温度z 
z ot’、摩擦円板回転数628 (1v、p、@、
加工速度toes1分で延伸しながら仮撚加工をおこな
った。その結果も次表に併(て示した。尚、表中のD−
1へD−3は夫々以下のものである。
- 4,11Sf Neil/36 filament undrawn yarn was drawn using a 7-luck type external friction false twisting device equipped with a disk of IIL% 45■ at a drawing ratio of Ll and a heater temperature of Z.
z ot', friction disk rotation speed 628 (1v, p, @,
False twisting was performed while stretching at a processing speed of 1 minute. The results are also shown in the table below.
1 to D-3 are as follows, respectively.

D −1ビスツク−イルオキシコハク際のジカリワム塩 D −1パルミトイルオキシコハク酸のジナトリウム塩 D−1ラフ−イルオキシクエン酸のジカリウ^塩 !!21の結果をみてもわかるように1本発明の化合物
(D成分)を油剤中に配合することにより糸条にすぐれ
た性能を付与できることがわかる。
D-1 Dicaliwum salt of bisstuc-yloxysuccinic acid D-1 Disodium salt of palmitoyloxysuccinic acid D-1 Dicaliwum salt of rough-yloxycitric acid! ! As can be seen from the results of No. 21, it can be seen that by incorporating the compound of the present invention (component D) into the oil agent, excellent performance can be imparted to the yarn.

Claims (3)

【特許請求の範囲】[Claims] (1)1ないし2個の水酸基を有する多価カルボン酸に
嶽素数が8以上の高級鮨訪族7シルハライドを反応させ
′C得られる化合物のアルカリ金属、アンモニラ^又は
有機アミンの塩を含有することを%黴とする合成轍雑処
N用油剤。
(1) Contains an alkali metal, ammonia^ or organic amine salt of the compound obtained by reacting a polyhydric carboxylic acid having 1 or 2 hydroxyl groups with a high grade 7-sil halide having a base number of 8 or more. Synthetic rut and miscellaneous oil agent that contains % mold.
(2)  多価カルボン酸がリンゴ酸、li石酸及びク
エン酸より成る群から選ばれたものである特許請求の範
囲鶴1項記載の合成−帷処理用油剤。
(2) The oil agent for synthetic fabric treatment according to claim 1, wherein the polyhydric carboxylic acid is selected from the group consisting of malic acid, litoric acid, and citric acid.
(3)  ^級詣訪族7シルノ・ライドがラフリン酸り
ρリド、パルミチン瞥りpリド、ミリスチン酸りρリド
ステアリン餘クーリド及びオレイン際クーリドより成る
群から選ばれたものである轡許lI末のIlI!@第】
項記載の合成繊維地履用油剤。
(3) ^Class Pilgrimage 7 Silno Ride is selected from the group consisting of Laughlin acid ρ lid, palmitic acid ρ lid, myristic acid ρ lid, stearic curid, and oleic chloride. The last IlI! @No.]
Oil for synthetic fibers as described in Section 1.
JP13159881A 1981-08-24 1981-08-24 Oil agent for treating synthetic fiber Granted JPS5836268A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13159881A JPS5836268A (en) 1981-08-24 1981-08-24 Oil agent for treating synthetic fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13159881A JPS5836268A (en) 1981-08-24 1981-08-24 Oil agent for treating synthetic fiber

Publications (2)

Publication Number Publication Date
JPS5836268A true JPS5836268A (en) 1983-03-03
JPS6253630B2 JPS6253630B2 (en) 1987-11-11

Family

ID=15061800

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13159881A Granted JPS5836268A (en) 1981-08-24 1981-08-24 Oil agent for treating synthetic fiber

Country Status (1)

Country Link
JP (1) JPS5836268A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60167973A (en) * 1984-02-10 1985-08-31 帝人株式会社 Oil agent for treating synthetic fiber
US5473103A (en) * 1993-12-16 1995-12-05 Yissum Research Development Co. Of The Hebrew University Of Jerusalem Biopolymers derived from hydrolyzable diacid fats
WO1996022270A1 (en) * 1995-01-18 1996-07-25 Yissum Research Development Co. Of The Hebrew University Of Jerusalem Biopolymers derived from hydrolyzable diacid fats

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4834557A (en) * 1971-09-04 1973-05-19

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4834557A (en) * 1971-09-04 1973-05-19

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60167973A (en) * 1984-02-10 1985-08-31 帝人株式会社 Oil agent for treating synthetic fiber
JPH0129906B2 (en) * 1984-02-10 1989-06-14 Teijin Ltd
US5473103A (en) * 1993-12-16 1995-12-05 Yissum Research Development Co. Of The Hebrew University Of Jerusalem Biopolymers derived from hydrolyzable diacid fats
WO1996022270A1 (en) * 1995-01-18 1996-07-25 Yissum Research Development Co. Of The Hebrew University Of Jerusalem Biopolymers derived from hydrolyzable diacid fats

Also Published As

Publication number Publication date
JPS6253630B2 (en) 1987-11-11

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