JP3075374B2 - Processing of splittable composite fiber - Google Patents

Processing of splittable composite fiber

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Publication number
JP3075374B2
JP3075374B2 JP27542191A JP27542191A JP3075374B2 JP 3075374 B2 JP3075374 B2 JP 3075374B2 JP 27542191 A JP27542191 A JP 27542191A JP 27542191 A JP27542191 A JP 27542191A JP 3075374 B2 JP3075374 B2 JP 3075374B2
Authority
JP
Japan
Prior art keywords
processing
swelling
composite fiber
texture
split
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.)
Expired - Fee Related
Application number
JP27542191A
Other languages
Japanese (ja)
Other versions
JPH05117968A (en
Inventor
一幸 大家
義久 鈴木
淳一 生駒
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.)
Komatsu Seiren Co Ltd
Original Assignee
Komatsu Seiren 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 Komatsu Seiren Co Ltd filed Critical Komatsu Seiren Co Ltd
Priority to JP27542191A priority Critical patent/JP3075374B2/en
Publication of JPH05117968A publication Critical patent/JPH05117968A/en
Application granted granted Critical
Publication of JP3075374B2 publication Critical patent/JP3075374B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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、割繊性複合繊維の加工
法に関する。特に、本発明は、割繊性複合繊維を編織
後、膨潤加工により分割する方法に関するものである。
The present invention relates to a method for processing splittable conjugate fibers. In particular, the present invention relates to a method for dividing splittable conjugate fibers by swelling after weaving.

【0002】[0002]

【従来の技術】従来、割繊性複合繊維の分割方法とし
て、(1) あらかじめ分割した繊維を編織する方法、(2)
編織後、複合繊維の一成分を溶解する方法、(3) 編織
後、複合繊維に対し、膨潤作用のある薬品により膨潤さ
せて分割する方法、が知られている。
2. Description of the Related Art Conventionally, as a method of dividing splittable conjugate fibers, (1) a method of knitting and weaving previously divided fibers, (2)
There are known a method of dissolving one component of the composite fiber after weaving, and (3) a method of dividing the composite fiber after weaving by swelling with a swelling chemical.

【0003】これらの方法の中で、(3) 編織後、複合繊
維に対し、膨潤作用のある薬品により膨潤させて分割す
る方法については、ベンジルアルコールまたはフェニル
エチルアルコールの乳化分散液でポリアミド成分を膨潤
加工する方法(特公昭53−35633)や、安息香酸とアルコ
ールもしくは安息香酸とアルコールと安息香酸のアルカ
リ金属塩またはアルカリ土類金属からなる溶液によりポ
リアミド成分を膨潤し、分割する方法 (特公平2−2640
70) などが報告されている。
Among these methods, (3) a method of dividing a composite fiber after weaving by swelling the composite fiber with a chemical having a swelling effect is described below. The polyamide component is emulsified and dispersed in benzyl alcohol or phenylethyl alcohol. A method of swelling (Japanese Patent Publication No. 53-35633), a method of swelling and separating a polyamide component by a solution comprising benzoic acid and an alcohol or a benzoic acid and an alkali metal salt of an alcohol and a benzoic acid or an alkaline earth metal 2-2640
70) have been reported.

【0004】しかし、ベンジルアルコールを用いた場合
は、ベンジルアルコールが除去されにくいため、後工程
において染めムラが多発するという問題がある。また、
安息香酸を用いた場合には、水に対する溶解度が小さ
く、温度依存性が高いため、加工の間の温度低下により
安息香酸が析出し、これを再溶解する時に局部的に高濃
度となるため、繊維を腐食せしめ、一方安息香酸が析出
しない濃度では繊維が十分に分割されない。さらに、安
息香酸を用いた処理液に水酸化ナトリウムを添加する
と、安息香酸ナトリウムとなって可溶化し、膨潤がなく
なるという問題があり、同浴で水酸化ナトリウムが使用
できない。また、乳化系では、系の不安定さや不均一性
が目立ち、加工ムラになるという問題があり、さらに加
工機の腐食も多発していた。よって、従来の方法は、実
用上非常に問題が多く、改善が望まれている。
[0004] However, when benzyl alcohol is used, there is a problem that uneven dyeing frequently occurs in a subsequent step because benzyl alcohol is not easily removed. Also,
When benzoic acid is used, its solubility in water is small and its temperature dependency is high.Because benzoic acid precipitates due to a decrease in temperature during processing and becomes locally concentrated when it is redissolved, At concentrations that cause the fibers to corrode while benzoic acid does not precipitate, the fibers are not sufficiently split. Further, when sodium hydroxide is added to a treatment solution using benzoic acid, there is a problem that sodium benzoate is solubilized and loses swelling, and sodium hydroxide cannot be used in the same bath. In addition, in the emulsification system, instability and non-uniformity of the system are conspicuous, resulting in a problem of processing unevenness, and further, corrosion of the processing machine has frequently occurred. Therefore, the conventional method has many problems in practical use, and improvement is desired.

【0005】[0005]

【発明が解決しようとする課題】本発明は、上記の如き
従来技術の問題点を解決し、割繊性複合繊維を均一にか
つ安定して分割することができ、加工機の腐食を生じる
ことのない、割繊性複合繊維の分割方法を提供すること
を目的とする。
SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems of the prior art, and can uniformly and stably split splittable conjugate fibers, thereby causing corrosion of a processing machine. It is an object of the present invention to provide a splitting method of splittable conjugate fiber without any problem.

【0006】[0006]

【課題を解決するための手段】本発明は、上記課題を解
決するため、ポリアミドとポリエステルよりなる割繊性
複合繊維を膨潤加工により分割するに際し、膨潤剤とし
てエチレングリコールモノフェニルエーテルとアルカリ
剤および/もしくは無機塩を用いることを特徴とする複
合繊維の加工方法を提供する。
SUMMARY OF THE INVENTION In order to solve the above-mentioned problems, the present invention provides a method for splitting splittable composite fibers comprising polyamide and polyester by swelling, wherein ethylene glycol monophenyl ether is used as a swelling agent, an alkali agent and And / or a method for processing a conjugate fiber characterized by using an inorganic salt.

【0007】本発明において、割繊性複合繊維とは、単
一フィラメントの横断面において一方の成分が他方の成
分を完全に包含しない形状で、単一フィラメントの長手
方向に沿って接合されている形の繊維をいい、具体的に
はサイドバイサイド型複合繊維、サイドバイサイド繰り
返し型複合繊維、放射状に接合された複合繊維等であ
る。
In the present invention, splittable conjugate fiber is a shape in which one component does not completely include the other component in the cross section of the single filament and is joined along the longitudinal direction of the single filament. Shaped fiber, specifically, a side-by-side type composite fiber, a side-by-side repetition type composite fiber, a radially bonded composite fiber, and the like.

【0008】また、繊維を形成するポリマーとしては、
ポリアミドとポリエステルとが挙げられる。ポリアミド
としては、ナイロン6、ナイロン66、ナイロン11、
ナイロン12、ナイロン 610およびそれらを主成分とす
るコポリアミドが挙げられる。ポリエステルとしては、
ポリエチレンテレフタレート、ポリブチレンテレフタレ
ート、ポリエチレンオキシベンゾエート、ポリ1,4-ジメ
チルシクロヘキサンテレフタレート、ポリピバロラクト
ンおよびそれらを主成分とするコポリエステルが挙げら
れる。また、該複合繊維からなる布帛の形態としては、
織物、編み物、不織布等、いかなる形態であってもよ
く、何ら限定されるものではない。
Further, as the polymer forming the fiber,
Examples include polyamides and polyesters. As polyamide, nylon 6, nylon 66, nylon 11,
Nylon 12, Nylon 610 and copolyamides based on them. As polyester,
Examples include polyethylene terephthalate, polybutylene terephthalate, polyethylene oxybenzoate, poly 1,4-dimethylcyclohexane terephthalate, polypivalolactone, and copolyesters containing these as main components. In addition, as a form of the fabric composed of the composite fiber,
It may be in any form, such as a woven fabric, a knitted fabric, or a non-woven fabric, and is not limited at all.

【0009】本発明では、かかる布帛に対し、膨潤剤と
してエチレングリコールモノフェニルエーテルとアルカ
リ剤および/もしくは無機塩を用いて膨潤加工を行う。
エチレングリコールモノフェニルエーテルの量は2g/
l〜 500g/lであるのがよい。
In the present invention, such a fabric is subjected to swelling processing using ethylene glycol monophenyl ether as a swelling agent and an alkali agent and / or an inorganic salt.
The amount of ethylene glycol monophenyl ether is 2 g /
It is preferably 1 to 500 g / l.

【0010】さらに、割繊性複合繊維の分割の均一化お
よび安定化のために乳化系のエチレングリコールモノフ
ェニルエーテルを用いることもできる。この場合の乳化
剤としてはドデシルベンゼンスルホン酸ナトリウム、ポ
リオキシエチレンアルキルフェニルエーテル、ポリオキ
シエチレンソルビタンモノオレエート、オレイン酸トリ
エタノールアミン等が挙げられるが、エチレングリコー
ルモノフェニルエーテルを乳化可能なものであれば特に
限定するものではない。
Further, ethylene glycol monophenyl ether of an emulsifying type can be used for uniform and stable division of splittable conjugate fibers. Examples of the emulsifier in this case include sodium dodecylbenzenesulfonate, polyoxyethylene alkylphenyl ether, polyoxyethylene sorbitan monooleate, triethanolamine oleate, and the like, as long as it can emulsify ethylene glycol monophenyl ether. It is not particularly limited.

【0011】アルカリ剤としては、水酸化カリウム、水
酸化ナトリウム等が挙げられるが、特に限定されるもの
ではなく、5〜30g/l、好ましくは8〜15g/l
の量で用いられるのがよい。
Examples of the alkaline agent include potassium hydroxide and sodium hydroxide, but are not particularly limited, and are 5 to 30 g / l, preferably 8 to 15 g / l.
Should be used in an amount of

【0012】無機塩としては、芒硝、塩化ナトリウム等
が挙げられるが、無機塩類ならば特に限定されず、量と
しては20g/l〜 100g/lであるのがよい。
Examples of the inorganic salts include sodium sulfate and sodium chloride, but are not particularly limited as long as they are inorganic salts, and the amount is preferably 20 g / l to 100 g / l.

【0013】上記の膨潤剤を用いて膨潤加工を行うに際
しては、処理温度80℃〜 120℃、好ましくは 100℃〜
110℃、浴比1:5〜1:50で、20分間以上行うの
がよい。加工機としては密閉されているものであれば何
でもよく、ビーム染色機、液流染色機等が挙げられる。
次に、膨潤剤の除去のため洗浄を行う。洗浄時の条件に
ついては特に限定はないが、通常温度50℃〜80℃で
15分間洗浄をおこなうのがよく、ソーピング剤等の薬
剤は特に必要としないが、エチレンジアミンテトラアセ
ティックアシッド、ニトリロトリアセテート、ポリカル
ボン酸塩、ナフタリンスルホン酸ホルマリン縮合物のナ
トリウム塩等を添加してもよい。洗浄機としては、カウ
ンターフロータイプの洗浄機、例えばジェットソーパー
(小野森鉄工所(株)製)や液流染色機等を用いるのが
よい。
When swelling is carried out using the above-mentioned swelling agent, the treatment temperature is from 80 ° C to 120 ° C, preferably from 100 ° C to 100 ° C.
It is preferable to carry out at 110 ° C. and a bath ratio of 1: 5 to 1:50 for 20 minutes or more. Any processing machine may be used as long as it is hermetically sealed, and examples thereof include a beam dyeing machine and a liquid jet dyeing machine.
Next, washing is performed to remove the swelling agent. The conditions for washing are not particularly limited, but it is preferable to perform washing at a normal temperature of 50 ° C. to 80 ° C. for 15 minutes, and a chemical such as a soaping agent is not particularly required. A polycarboxylate, a sodium salt of a naphthalenesulfonic acid formalin condensate, or the like may be added. As the washing machine, it is preferable to use a counter flow type washing machine, for example, a jet soaper (manufactured by Onomori Iron Works, Ltd.), a jet dyeing machine or the like.

【0014】[0014]

【作用および効果】本発明によれば、ポリアミドとポリ
エステルよりなる割繊性複合繊維が均一にかつ安定して
分割され、加工機の腐食も発生しない。
According to the present invention, splittable conjugate fibers composed of polyamide and polyester are uniformly and stably split, and corrosion of the processing machine does not occur.

【0015】[0015]

【実施例】以下に、本発明の実施例を示し、さらに説明
する。
EXAMPLES Examples of the present invention will be shown below and further explained.

【0016】実施例1 グラセム糸(ナイロン6/ポリエステル、鐘紡株式会社
製)を用いた綾織物に対し、水中にエチレングリコール
モノフェニルエーテル(日本乳化剤株式会社製)50g
/lと水酸化ナトリウム10g/lを含む処理液を用
い、液流染色機で、浴比1:10、温度 110℃で20分
間処理し、80℃で20分間、ジェットソーパーで洗浄
した。得られた布帛の風合い、分割状態および染色状態
を表1に示す。
Example 1 50 g of ethylene glycol monophenyl ether (manufactured by Nippon Emulsifier Co., Ltd.) in water with respect to a twill fabric using glasem yarn (nylon 6 / polyester, manufactured by Kanebo Co., Ltd.)
Using a treatment solution containing 1 g / l and 10 g / l sodium hydroxide, the mixture was treated with a liquid jet dyeing machine at a bath ratio of 1:10 at a temperature of 110 ° C. for 20 minutes, and washed at 80 ° C. for 20 minutes with a jet soaper. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0017】比較例1 処理液にエチレングリコールモノフェニルエーテル50
g/lを用いた以外は実施例1と同一の条件で加工を行
った。得られた布帛の風合い、分割状態および染色状態
を表1に示す。
Comparative Example 1 Ethylene glycol monophenyl ether 50
Processing was performed under the same conditions as in Example 1 except that g / l was used. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0018】比較例2 処理液に水中でSF1024(アルキルフェニルEO付
加物、竹本油脂製)により乳化されたベンジルアルコー
ル50g/lおよび水酸化ナトリウム10g/lを用い
た以外は実施例1と同一の条件で加工を行った。得られ
た布帛の風合い、分割状態および染色状態を表1に示
す。
Comparative Example 2 Same as Example 1 except that 50 g / l of benzyl alcohol and 10 g / l of sodium hydroxide emulsified in water with SF1024 (alkylphenyl EO adduct, manufactured by Takemoto Yushi) were used as the treatment liquid. Processing was performed under the conditions. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0019】比較例3 処理液に安息香酸10g/lおよび水酸化ナトリウム1
0g/lを用いた以外は実施例1と同一の条件で加工を
行った。得られた布帛の風合い、分割状態および染色状
態を表1に示す。
Comparative Example 3 10 g / l of benzoic acid and sodium hydroxide 1
Processing was performed under the same conditions as in Example 1 except that 0 g / l was used. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0020】実施例2 処理液として水中にドデシルベンゼンスルホン酸10g
/lで乳化したエチレングリコールモノフェニルエーテ
ル(日本乳化剤株式会社製)50g/l、水酸化ナトリ
ウム10g/lおよび芒硝 100g/lを含む液を用いた
以外は実施例1と同一の条件で加工を行った。得られた
布帛の風合い、分割状態および染色状態を表1に示す。
Example 2 10 g of dodecylbenzenesulfonic acid in water as a treatment liquid
Processing was performed under the same conditions as in Example 1 except that a liquid containing 50 g / l of ethylene glycol monophenyl ether (manufactured by Nippon Emulsifier Co., Ltd.), 10 g / l of sodium hydroxide and 100 g / l of sodium sulfate was used. went. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0021】実施例3 ランプ糸(ナイロン6/ポリエステル、株式会社クラレ
製)を用いた朱子織物に対し、水中にエチレングリコー
ルモノフェニルエーテル(日本乳化剤株式会社製)30
g/lと芒硝 100g/lを含む処理液を用いた以外は実
施例1と同一の条件で加工を行った。得られた布帛の風
合い、分割状態および染色状態を表1に示す。
Example 3 For a satin fabric using a lamp yarn (nylon 6 / polyester, manufactured by Kuraray Co., Ltd.), ethylene glycol monophenyl ether (manufactured by Nippon Emulsifier Co., Ltd.) 30 in water was used.
Processing was performed under the same conditions as in Example 1 except that a processing solution containing g / l and 100 g / l of sodium sulfate was used. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0022】実施例4 ランプ糸(ナイロン6/ポリエステル、株式会社クラレ
製)を用いた朱子織物に対し、水中にエチレングリコー
ルモノフェニルエーテル(日本乳化剤株式会社製)10
g/lと芒硝50g/lを含む処理液を用いた以外は実
施例1と同一の条件で加工を行った。得られた布帛の風
合い、分割状態および染色状態を表1に示す。
Example 4 A satin fabric using a lamp thread (nylon 6 / polyester, manufactured by Kuraray Co., Ltd.) was treated with ethylene glycol monophenyl ether (manufactured by Nippon Emulsifier Co., Ltd.) 10 in water.
Processing was performed under the same conditions as in Example 1 except that a processing solution containing g / l and sodium sulfate 50 g / l was used. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0023】実施例5 ピセーム糸(ナイロン6/ポリエステル、株式会社東レ
製)を用いた綾織に対し、水中にエチレングリコールモ
ノフェニルエーテル(日本乳化剤株式会社製)100g/
l、水酸化ナトリウム20g/lおよび芒硝 100g/l
を含む処理液を用いた以外は実施例1と同一の加工条件
で加工を行った。得られた布帛の風合い、分割状態およ
び染色状態を表1に示す。
Example 5 A twill weave using a picame yarn (nylon 6 / polyester, manufactured by Toray Industries, Inc.) was 100 g of ethylene glycol monophenyl ether (manufactured by Nippon Emulsifier Co., Ltd.) in water.
l, sodium hydroxide 20 g / l and sodium sulfate 100 g / l
Processing was performed under the same processing conditions as in Example 1 except that a processing solution containing was used. Table 1 shows the texture, split state, and dyed state of the obtained fabric.

【0024】[0024]

【表1】 [Table 1]

【0025】なお、上記の評価は、次の基準により行っ
た。 風合い評価 ◎ 非常にふっくらと柔らかい風合
い ○ ふっくらと柔らかい風合い △ 硬めの風合い × 非常に硬い風合い 分割状態評価 A 完全に分割している B やや分割している C まったく分割していない 染色状態 ○ 均染している △ イラツキがみられる × 染めムラがみられる
The above evaluation was performed according to the following criteria. Texture evaluation ◎ Very soft and soft texture ○ Fluffy and soft texture △ Hard texture × Very hard texture Split condition evaluation A Completely split B Somewhat split C Not split Dyeing state ○ Level dyeing △ Irritability is observed × Dye unevenness is observed

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭60−75665(JP,A) 特開 昭62−289611(JP,A) 特開 昭50−4320(JP,A) (58)調査した分野(Int.Cl.7,DB名) D06M 13/165 ────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-60-75665 (JP, A) JP-A-62-289611 (JP, A) JP-A-50-4320 (JP, A) (58) Field (Int. Cl. 7 , DB name) D06M 13/165

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ポリアミドとポリエステルよりなる割繊
性複合繊維を膨潤加工により分割するに際し、膨潤剤と
してエチレングリコールモノフェニルエーテルとアルカ
リ剤および/もしくは無機塩を用いることを特徴とする
複合繊維の加工方法。
1. A processing of a conjugate fiber comprising splitting a splittable conjugate fiber comprising a polyamide and a polyester by swelling, wherein ethylene glycol monophenyl ether and an alkali agent and / or an inorganic salt are used as a swelling agent. Method.
JP27542191A 1991-10-23 1991-10-23 Processing of splittable composite fiber Expired - Fee Related JP3075374B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27542191A JP3075374B2 (en) 1991-10-23 1991-10-23 Processing of splittable composite fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27542191A JP3075374B2 (en) 1991-10-23 1991-10-23 Processing of splittable composite fiber

Publications (2)

Publication Number Publication Date
JPH05117968A JPH05117968A (en) 1993-05-14
JP3075374B2 true JP3075374B2 (en) 2000-08-14

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014227622A (en) * 2013-05-22 2014-12-08 東レ株式会社 Method for manufacturing polyester yarn containing fabric, and fabric wiper

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