JPH0538728A - Production of solidified material of silk - Google Patents

Production of solidified material of silk

Info

Publication number
JPH0538728A
JPH0538728A JP19453791A JP19453791A JPH0538728A JP H0538728 A JPH0538728 A JP H0538728A JP 19453791 A JP19453791 A JP 19453791A JP 19453791 A JP19453791 A JP 19453791A JP H0538728 A JPH0538728 A JP H0538728A
Authority
JP
Japan
Prior art keywords
silk
powder
vinyl
based monomer
silk powder
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
JP19453791A
Other languages
Japanese (ja)
Other versions
JP3105582B2 (en
Inventor
Daijiro Akiyama
山 大二郎 秋
Masahiko Murayama
山 雅 彦 村
Kiyoshi Hirabayashi
林 潔 平
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.)
Nippon Valqua Industries Ltd
Nihon Valqua Kogyo KK
Original Assignee
Nippon Valqua Industries Ltd
Nihon Valqua Kogyo KK
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 Nippon Valqua Industries Ltd, Nihon Valqua Kogyo KK filed Critical Nippon Valqua Industries Ltd
Priority to JP19453791A priority Critical patent/JP3105582B2/en
Publication of JPH0538728A publication Critical patent/JPH0538728A/en
Application granted granted Critical
Publication of JP3105582B2 publication Critical patent/JP3105582B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the solidified material of silk which holds the intrinsic properties of silk by mixing a vinyl-based monomer with silk powder at a specified rate and using this mixture, heating and compressing the same in a mold, for example, at the specified temperature and pressure. CONSTITUTION:A vinyl-based monomer is mixed with silk powder and this mixed powder is pressurized and heated. For example, the mixed powder is pressurized and molded at ordinary temperature at >=100kg/cm<2> and thereafter the molded form is heated at <=200 deg.C in an electric furnace or the like. The blending amount of both the vinyl-based monomer and silk powder is not especially limited. The vinyl-based monomer is preferably used at amount of 5-100 pts.wt. for 100 pts.wt. silk powder. When the blending amount of the vinyl-based monomer exceeds 100 pts.wt., the silky touch of the obtained moldings is decreased. There is a tendency so that water absorption property and moisture release properties of silk are deteriorated. Further there is the tendency so that workability is deteriorated in the amount less than 5 pts.wt. In this method, the solidified material of silk is obtained which is excellent in water resistance, workability and mechanical strength or the like and also holds the intrinsic properties of silk.

Description

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

【0001】[0001]

【発明の技術分野】本発明は、絹の固形化物の製造方法
に関し、さらに詳しくは強度、耐水性、感触、外観など
に優れ、象牙代替品、判子など各種の用途に用い得るよ
うな絹の固形化物の製造方法に関する。
TECHNICAL FIELD The present invention relates to a method for producing a solidified silk product, and more particularly, to a silk product excellent in strength, water resistance, feel and appearance, which can be used in various applications such as ivory substitutes and discs. The present invention relates to a method for producing a solidified product.

【0002】[0002]

【発明の技術的背景】絹は、例えば衣料用素材として広
く用いられてきている。絹は、衣料用として用いられる
場合には、繭から生糸に製糸して利用されるが、例え
ば、繊維度が著しく異なる糸、製糸工程で生じる屑糸、
傷繭などは、絹糸として利用されることなく、廃棄処分
される。
BACKGROUND OF THE INVENTION Silk has been widely used as a material for clothing, for example. When silk is used for clothing, it is used by spinning it from cocoons into raw silk.
Wounds and cocoons are discarded without being used as silk threads.

【0003】しかしながら、このように傷繭などを廃棄
してしまうことは省資源の観点からは好ましくない。ま
た、絹は、衣料用分野以外に、多方面にわたる新規用途
の開発、研究が進められている。たとえば、絹フィブロ
インフィルム、絹フィブロインのゲル化物及びその食
品、手術用の縫合糸、生体酵素の固定化材料等のバイオ
材料等々に応用されることが期待されている。
However, discarding such cocoons as described above is not preferable from the viewpoint of resource saving. Further, in addition to the field of clothing, silk is being developed and researched in various new applications. For example, it is expected to be applied to silk fibroin film, silk fibroin gel and its foods, surgical sutures, biomaterials such as bioenzyme immobilization materials and the like.

【0004】ところで、各種機能材料として用いられる
軽量な固形物としては、プラスチックが代表的である。
しかしながら、プラスチックは、廃棄処分にした場合
に、酸化などによって分解することなく長期間にわたり
そのまま存在し、ゴミ処理上社会問題となっている。
By the way, as a light-weight solid material used as various functional materials, plastic is typical.
However, when disposed of, plastic remains as it is for a long period of time without being decomposed due to oxidation or the like, which is a social problem in waste disposal.

【0005】そこで、本願出願人は、上記問題点を解決
するべく鋭意検討した結果、絹の粉末を金型内にて20
0℃以下の温度及び100kg/cm2以上の圧力で加
熱圧縮すると、廃棄しても公害源とならず、機械的性質
などに優れた絹の固形化物が得られることなどを見い出
して、既に提案している(特願平2ー7925号参
照)。 しかしながら、耐水性、加工性(切削加工
性)、感触、外観などの点については、さらなる改良が
望まれている。
Therefore, the applicant of the present invention has made earnest studies to solve the above-mentioned problems, and as a result, silk powder has been applied in a mold.
It has already been proposed by discovering that when heated and compressed at a temperature of 0 ° C or lower and a pressure of 100 kg / cm 2 or higher, it does not become a pollution source even if it is discarded, and a solid silk product excellent in mechanical properties is obtained. (See Japanese Patent Application No. 2-7925). However, further improvements in water resistance, workability (cutting workability), feel, appearance, etc. are desired.

【0006】[0006]

【発明の目的】本発明は、このような実情に鑑みてなさ
れたものであって、耐水性、加工性(切削加工性)、機
械的強度などに優れ、しかも絹の有する特有な性質
(例:保湿性、感触、外観など)が保持された絹の固形
化物を容易に得ることができるような、絹の固形化物の
製造方法を提供することを目的としている。
SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances and is excellent in water resistance, workability (machining workability), mechanical strength and the like, and has unique properties of silk (examples). It is an object of the present invention to provide a method for producing a solidified silk product, which enables easy production of a solidified silk product having retained moisturizing properties, touch, appearance, and the like.

【0007】また、本発明は、繭の有効利用を図り、各
種機能材料としても用いることが可能であり、しかも廃
棄処分とした場合に早期に腐敗・分解し、ゴミ処理上の
不都合もないような絹の固形化物を提供することを目的
とする。
Further, the present invention enables effective use of cocoons and can be used as various functional materials. Moreover, when discarded, they are decomposed and decomposed at an early stage, and there is no inconvenience in waste disposal. An object of the present invention is to provide a solid silk product.

【0008】[0008]

【発明の概要】本発明に係る絹の固形化物の製造方法
は、絹粉末とビニル系モノマーとを、好ましくは絹粉末
と、該絹粉末100重量部に対して5〜100重量部の
量のビニル系モノマーとを、例えば金型内にて、200
℃以下の温度及び100kg/cm2以上の圧力で加熱
圧縮することを特徴としている。
SUMMARY OF THE INVENTION The method for producing a solidified silk product according to the present invention comprises a silk powder, a vinyl monomer, preferably silk powder, and an amount of 5 to 100 parts by weight per 100 parts by weight of the silk powder. For example, if a vinyl-based monomer is used in a mold, 200
It is characterized in that it is heated and compressed at a temperature of not more than 0 ° C. and a pressure of not less than 100 kg / cm 2 .

【0009】このような本発明に係る絹の固形化物の製
造方法によれば、耐水性、加工性(切削加工性)、機械
的強度などに優れ、しかも絹の有する特有な性質(例:
吸水性、放湿性、感触、外観)などを保持した絹の固形
化物を容易に得ることができる。
According to such a method for producing a solidified silk product according to the present invention, water resistance, processability (machining property), mechanical strength, etc. are excellent, and the peculiar properties of silk (eg:
It is possible to easily obtain a solidified silk product that retains water absorbency, moisture release, touch, and appearance).

【0010】このようにして得られた絹の固形化物は、
たとえば人工骨、人工皮膚、コンタクトレンズなどの生
体適合材、または模造象牙、模造鼈甲、日用雑貨(判
子、ボタン等)などとして利用される。
The silk solid product thus obtained is
For example, it is used as artificial bones, artificial skin, biocompatible materials such as contact lenses, or imitation ivory, imitation tortoise, daily miscellaneous goods (decisors, buttons, etc.).

【0011】しかも、このような絹の固形化物は、廃棄
処分に付された場合に、容易に分解されることから、ゴ
ミ処理上の不都合も解消できる。
Moreover, since such a solidified product of silk is easily decomposed when it is disposed of, it is possible to eliminate the inconvenience in waste disposal.

【0012】[0012]

【発明の具体的説明】以下、本発明に係る絹の固形化物
の製造方法について具体的に説明する。本発明により得
られる絹の固形化物は、以下に述べるような製造方法で
製造される。絹粉末 本発明では、絹の固形化物を製造する際には絹粉末が用
いられるが、この絹粉末の平均粒径は、0.3〜300
μm、好ましくは50〜200μmである。
DETAILED DESCRIPTION OF THE INVENTION The method for producing a solidified silk product according to the present invention will be specifically described below. The solidified silk product obtained by the present invention is produced by the following production method. Silk Powder In the present invention, silk powder is used when producing a solidified product of silk, and the average particle size of this silk powder is 0.3 to 300.
μm, preferably 50 to 200 μm.

【0013】このような絹粉末は、例えば以下のように
して調製することができる。まずはじめに、繭または絹
を塩化カルシウムの水溶液に入れて絹溶液とし、これを
沸騰水中で処理し、透析膜を通して絹の濃縮を行う(絹
溶液のゲル化)。
Such silk powder can be prepared, for example, as follows. First, cocoon or silk is placed in an aqueous solution of calcium chloride to form a silk solution, which is treated in boiling water and silk is concentrated through a dialysis membrane (gelation of silk solution).

【0014】次いで、これを冷凍し、再度常温に戻し、
次いで水を分離除去して得られた絹を凍結乾燥して絹粉
末を得る。また、その他の絹粉末の調製方法としては、
従来公知の種々の方法が採用され得るが、たとえば、繭
または絹を炭酸カルシウムの水溶液に入れ、攪拌後、析
出した凝固物を水に懸濁させ、塩酸を加えて二酸化炭素
を発生させ、その後絹の粉末を得る方法もある(特開昭
61-276825 号公報)。さらに、酸アルカリなどに一定時
間繭または絹を浸漬し、それらを機械的に、粉末化する
方法である。
Then, this is frozen and returned to room temperature again,
Then, the silk obtained by separating and removing water is lyophilized to obtain silk powder. Further, as another method for preparing silk powder,
Although various conventionally known methods can be adopted, for example, cocoon or silk is placed in an aqueous solution of calcium carbonate, and after stirring, the precipitated coagulated product is suspended in water, hydrochloric acid is added to generate carbon dioxide, and then, There is also a method to obtain silk powder
61-276825). Further, it is a method of immersing cocoons or silk for a certain period of time in an acid-alkali or the like and mechanically powdering them.

【0015】本発明においては、このようにして得られ
た絹粉末と後述するビニル系モノマーとを、後述するよ
うに加熱圧縮するに先立ち、絹粉末に次のような前処理
を施してもよい。
In the present invention, the silk powder thus obtained and the vinyl-based monomer described below may be subjected to the following pretreatment before being heated and compressed as described below. ..

【0016】第1の前処理手段としては、ホルマール化
処理がある。絹の粉末にホルマール化処理すると、乾強
度及び湿潤強度の増大、耐アルカリ製の向上、耐膨潤性
並びに耐摩耗性の改善を図ることができる。
As the first pretreatment means, there is formalization treatment. When the silk powder is formalized, it is possible to increase dry strength and wet strength, improve alkali resistance, and improve swelling resistance and abrasion resistance.

【0017】絹のホルマール化処理は、たとえば次のよ
うにして行う。すなわち、ヘキサメチレンテトラミン水
溶液に酢酸を加え、その溶液に絹粉末を所定割合で浸漬
し、その溶液を所定温度に加熱する。加熱を終えたとこ
ろで、その溶液を吸引濾過し、処理粉末を取り出して、
所定温度でキュアリングを行う。そして、それを硫酸ナ
トリウム溶液などで洗浄し、さらに十分水洗して、脱
水、乾燥し、ホルマール化処理された絹粉末を得る。
The silk formalization is performed, for example, as follows. That is, acetic acid is added to an aqueous solution of hexamethylenetetramine, silk powder is dipped in the solution at a predetermined ratio, and the solution is heated to a predetermined temperature. When heating is completed, the solution is suction filtered, the treated powder is taken out,
Curing is performed at a predetermined temperature. Then, it is washed with a sodium sulfate solution or the like, further washed sufficiently with water, dehydrated and dried to obtain a formalized silk powder.

【0018】第2の前処理手段としては、ウレタン化処
理がある。絹の粉末にウレタン化処理すると、機械的性
質を向上させることができる。絹のウレタン化処理は、
絹にイソシアネート類を反応させることにより行い、具
体的には、たとえば以下のようにして行う。
As the second pretreatment means, there is urethane treatment. When the silk powder is urethanized, the mechanical properties can be improved. Urethane treatment of silk is
It is performed by reacting silk with isocyanates, and specifically, for example, as follows.

【0019】すなわち、たとえば熱反応型水溶液性ウレ
タン樹脂を濃度に応じて水と混合し攪拌する。次に、こ
の溶液に絹粉末を浸漬し、同時にウレタン化触媒を加
え、所定時間後に濾過、水洗、乾燥を順次行い、ウレタ
ン化処理された絹の粉末を得る。
That is, for example, a heat-reactive aqueous urethane resin is mixed with water according to the concentration and stirred. Next, silk powder is dipped in this solution, and a urethanization catalyst is added at the same time, and after a predetermined period of time, filtration, washing with water and drying are sequentially performed to obtain a urethanized silk powder.

【0020】なお、絹の前処理手段としては、前述した
例に限定されるものではなく、種々の手段を採用するこ
とができる。ビニル系モノマー 本発明では、上記の絹粉末とともに、ビニル系モノマー
が用いられる。
The silk pretreatment means is not limited to the above-mentioned examples, and various means can be adopted. Vinyl Monomer In the present invention, a vinyl monomer is used together with the above silk powder.

【0021】ビニル系モノマーとしては、グリシジルメ
タアクリレート(GMA)、メチルメタアクリレーレー
ト(MMA)、ポリエチレングリコールメタクリレート
(PEGDMA)、ヒドロキシメチルメタクリレート
(HEMA)、スチレン、塩化ビニル、アクリル酸、な
どが挙げられ、中でもGMA、MMAが好ましく用いら
れる。
Examples of vinyl monomers include glycidyl methacrylate (GMA), methyl metaacrylate (MMA), polyethylene glycol methacrylate (PEGDMA), hydroxymethyl methacrylate (HEMA), styrene, vinyl chloride and acrylic acid. Among them, GMA and MMA are preferably used.

【0022】本発明においては、このような絹粉末とビ
ニル系モノマーとの配合量は、特に限定されないが、好
ましくは、絹粉末100重量部に対してビニル系モノマ
ーは、5〜100重量部、さらに好ましくは10〜60
重量部の量で用いられる。
In the present invention, the blending amount of such a silk powder and a vinyl-based monomer is not particularly limited, but preferably, the vinyl-based monomer is 5 to 100 parts by weight, relative to 100 parts by weight of the silk powder. More preferably 10 to 60
Used in parts by weight.

【0023】ビニル系モノマーの配合量が100重量部
を超えると、得られる成形品の絹的感触が薄れ、絹の吸
水性、放湿性が低下してしまう傾向があり、また5重量
部未満の量では、加工性が低下する傾向がある。
When the amount of the vinyl-based monomer is more than 100 parts by weight, the silky feel of the resulting molded article tends to be weakened, and the water absorbency and moisture release of the silk tend to be lowered. The amount tends to reduce the workability.

【0024】なお、絹の固形化物を製造する際には、上
記絹粉末およびビニル系モノマー以外に、充填剤、重合
開始剤、重合促進剤、乳化剤、PH調整剤、などを用い
てもよい。
When producing a solidified silk product, a filler, a polymerization initiator, a polymerization accelerator, an emulsifier, a pH adjusting agent, etc. may be used in addition to the silk powder and the vinyl monomer.

【0025】充填剤としては、タンパク質、キトサン、
コラーゲンなどが挙げられる。本発明では、上記絹粉末
と上記ビニル系モノマーとを加熱・加圧するが、このよ
うな加熱加圧処理に先立ち、下記のように絹粉末とビニ
ル系モノマーとを混合して用いてもよく、あるいは、絹
粉末に該ビニル系モノマーをグラフト重合して、絹粉末
のグラフト処理物として用いてもよい。
As the filler, protein, chitosan,
Examples include collagen. In the present invention, the silk powder and the vinyl-based monomer are heated and pressed, but prior to such heating and pressure treatment, the silk powder and the vinyl-based monomer may be mixed and used as described below, Alternatively, the vinyl monomer may be graft-polymerized on silk powder and used as a graft-treated product of silk powder.

【0026】絹粉末とビニル系モノマーとを混合するに
は、公知の方法を採用することができ、例えば、絹粉末
にミキサーなどを用いてビニル系モノマーを分散させる
などの方法を採用することができる。
To mix the silk powder and the vinyl-based monomer, a known method can be adopted. For example, a method of dispersing the vinyl-based monomer in the silk powder by using a mixer or the like can be adopted. it can.

【0027】また、絹粉末にビニル系モノマーをグラフ
ト重合するには、例えば、絹粉末およびビニル系モノマ
ーとともに、必要により、重合開始剤あるいは重合促進
剤、PH調整剤、乳化剤等を水に分散・混合したのち加
熱し、絹粉末に該ビニル系モノマーをグラフト重合し
て、絹粉末のグラフト処理物を得る。
In order to graft-polymerize the vinyl-based monomer on the silk powder, for example, a polymerization initiator or a polymerization accelerator, a pH adjusting agent, an emulsifier, etc. may be dispersed in water together with the silk powder and the vinyl-based monomer. After mixing and heating, the vinyl monomer is graft-polymerized on the silk powder to obtain a silk powder graft-treated product.

【0028】次いで、得られた絹粉末のグラフト処理物
を水洗、乾燥する。なお、重合開始剤あるいは重合促進
剤としては、過硫酸アンモニウム、過硫酸カリウム、過
酸化水素ベンゾル、第2セリウム塩アゾビスイソブチロ
ニトリルなどが挙げられ、PH調整剤としては、酢酸、
氷酢酸、蟻酸、硫酸などが挙げられ、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、ラウリル硫酸
ナトリウム、ラウリルエーテルなどが挙げられる。
Next, the obtained silk powder graft-treated product is washed with water and dried. Examples of the polymerization initiator or the polymerization accelerator include ammonium persulfate, potassium persulfate, benzol hydrogen peroxide, cerium (II) azobisisobutyronitrile, and the like.
Glacial acetic acid, formic acid, sulfuric acid, etc. can be mentioned, and as an emulsifier,
Examples thereof include sodium dodecylbenzene sulfonate, sodium lauryl sulfate, and lauryl ether.

【0029】また、絹粉末にビニル系モノマーをグラフ
ト重合するには、絹粉末を、上述したビニル系モノマー
が溶解されている有機溶媒に分散混合して、絹粉末表面
にグラフト重合による結合を形成し、絹粉末のグラフト
処理物を得ることもできる。
In order to graft-polymerize the vinyl-based monomer on the silk powder, the silk-based powder is dispersed and mixed in the organic solvent in which the vinyl-based monomer is dissolved to form a bond by graft polymerization on the surface of the silk powder. Alternatively, a silk powder graft-treated product can be obtained.

【0030】本発明においては、上記のように必要によ
り、予め、絹粉末とビニル系モノマーとを混合してなる
混合粉末、または、絹粉末にビニル系モノマーをグラフ
ト重合してなる絹のグラフト処理粉末を加圧・加熱する
が、このような加圧・加熱処理は、例えば常温にて、1
00kg/cm2以上の圧力、好ましくは500〜2
0,000kg/cm2程度の圧力で、通常5分間以
上、好ましくは10〜120分間程度加圧・成形したの
ち、次いで電気炉等で200℃以下の温度、好ましくは
100〜150℃程度の温度で、10〜120分間程度
加熱してもよい。
In the present invention, if necessary, as described above, a mixed powder prepared by mixing silk powder and a vinyl monomer in advance, or a silk graft treatment obtained by graft-polymerizing a vinyl monomer on silk powder. The powder is pressed and heated. Such pressurization and heat treatment is performed at room temperature, for example,
Pressure of 00 kg / cm 2 or more, preferably 500 to 2
After pressurizing and molding at a pressure of about 50,000 kg / cm 2 for usually 5 minutes or more, preferably for 10 to 120 minutes, then in an electric furnace or the like, a temperature of 200 ° C. or lower, preferably a temperature of 100 to 150 ° C. Then, it may be heated for about 10 to 120 minutes.

【0031】あるいは、絹粉末とビニル系モノマーとを
混合してなる混合粉末、または絹のグラフト処理粉末
を、例えば金型に充填し、上記と同様の加圧・加熱条件
下に10〜120分間程度加圧・加熱し、成形してもよ
い。
Alternatively, a mixed powder obtained by mixing silk powder and a vinyl-based monomer or a silk-grafted powder is filled in, for example, a mold, and the same pressurization and heating conditions as described above are applied for 10 to 120 minutes. It may be pressed and heated to some extent and molded.

【0032】加熱の最適温度は、圧力によっても相違
し、一概に決定され得ないが、一般に、このように20
0℃以下の温度で加熱すると、絹の炭化が生じることが
少ない。また、100kg/cm2以上の圧力で加圧す
ると、プレス圧の上昇に応じて、得られる固形物の引張
強度が増大する傾向がある。
The optimum temperature for heating depends on the pressure and cannot be unconditionally determined.
Carbonization of silk is less likely to occur when heated at a temperature of 0 ° C. or lower. Further, when pressure is applied at a pressure of 100 kg / cm 2 or more, the tensile strength of the obtained solid tends to increase as the pressing pressure increases.

【0033】なお、本発明においては上記のように、絹
粉末とビニル系モノマーとの混合物を加圧した後に加熱
するなど、加熱と加圧とを別々に行ってもよく、また、
加熱と加圧とを同時に行ってもよい。
In the present invention, as described above, heating and pressurizing may be performed separately, such as heating after pressurizing the mixture of silk powder and vinyl-based monomer.
Heating and pressurizing may be performed simultaneously.

【0034】このようにして得られた絹の固形化物は、
X線解析により観察すると、β-シート構造をとってい
ることが確認される。絹の粉末に圧力と熱とを加えるこ
とにより、絹の分子構造がαーヘリックス構造からβ-シ
ート構造に転移したと考えられる。
The silk solid thus obtained is
Observation by X-ray analysis confirms that it has a β-sheet structure. It is considered that the molecular structure of silk was transferred from the α-helix structure to the β-sheet structure by applying pressure and heat to the silk powder.

【0035】また、本発明により得られる絹の固形化物
は耐水性、加工性に優れ、引張強度が約190kg/c
2以上であり、硬度が85(JISショアD硬度)以
上であり、伸びが0.5〜0.9%程度である。なお、
比重の減少に従い、強度が向上する傾向がある。
The silk solid product obtained by the present invention has excellent water resistance and workability, and has a tensile strength of about 190 kg / c.
m 2 or more, the hardness is 85 (JIS Shore D hardness) or more, and the elongation is about 0.5 to 0.9%. In addition,
The strength tends to increase as the specific gravity decreases.

【0036】しかも、このような絹の固形化物は、絹繊
維の持つ諸特性(吸湿性、放湿性、電気絶縁性、紫外線
防止作用など)を有効に保持している。
Moreover, such a solidified product of silk effectively retains the various properties of the silk fiber (hygroscopicity, moisture release, electrical insulation, UV protection, etc.).

【0037】[0037]

【発明の効果】以上説明してきたように、本発明に係る
絹の固形化物の製造方法によれば、所定の機械的強度を
有し、しかも絹の有する特殊な性質を保持した絹の固形
化物を容易に得ることができる。このようにして得られ
た絹の固形化物は、その性質を利用して、たとえば生体
適合材、または模造象牙、模造鼈甲などとして利用する
ことが期待される。しかも、このような絹の固形化物
は、廃棄処分に付された場合に、容易に腐敗するためゴ
ミ処理上の不都合もない。
As described above, according to the method for producing a solidified silk product according to the present invention, the solidified silk product has a predetermined mechanical strength and retains the special properties of silk. Can be easily obtained. The solidified silk thus obtained is expected to be utilized as a biocompatible material, imitation ivory, imitation tortoise shell or the like by utilizing its properties. Moreover, such a solidified product of silk is easily decomposed when it is disposed of, so that there is no inconvenience in waste disposal.

【0038】[0038]

【実施例】以下、本発明をさらに詳細な実施例に基づき
説明するが、本発明はかかる実施例になんら制約される
ものではない。
EXAMPLES The present invention will be described below based on more detailed examples, but the present invention is not limited to these examples.

【0039】[0039]

【実施例1】絹粉末400g、グリシジルメタアクリレ
ート(GMA)400g、過硫酸アンモニウム20g
を、pH3.0、浴比1:30の水浴中で、重合温度6
0℃、重合時間60分の条件下に反応させた後、マルセ
ル石鹸5g/リットル、浴比1:30、60℃で30分
ソーピングを行い水洗後乾燥し粉砕した。
Example 1 400 g of silk powder, 400 g of glycidyl methacrylate (GMA), 20 g of ammonium persulfate
At a polymerization temperature of 6 in a water bath having a pH of 3.0 and a bath ratio of 1:30.
After reacting at 0 ° C. for 60 minutes of polymerization time, Marcel soap 5 g / liter, bath ratio 1:30, soaping at 60 ° C. for 30 minutes, washing with water, drying and pulverization.

【0040】上記グリシジルメタアクリレートで処理さ
れた絹粉末を金型に充填し、120℃の温度、700k
g/cm2の圧力で10分間の加熱加圧成形を行い角柱
体(15mm×15mm×60mm)を得た。
The silk powder treated with the above glycidyl methacrylate was filled in a mold and the temperature was 120 ° C. and 700 k.
Heat and pressure molding was performed at a pressure of g / cm 2 for 10 minutes to obtain a prism (15 mm × 15 mm × 60 mm).

【0041】得られた角柱体について、下記の試験方法
に従って、比重、強度(kg/cm 2)、ショアD硬
度、伸度(%)を測定し、また耐水性、加工性を評価し
た。結果を第1表に示す。
The following test method was applied to the obtained prismatic body.
Specific gravity, strength (kg / cm 2), Shore D hard
Degree and elongation (%) are measured, and water resistance and workability are evaluated.
It was The results are shown in Table 1.

【0042】[試験方法] 比重:JIS K 0061に準拠。 強度(kgf/cm2):短冊(5mm×20mm)をT
ENSILON UTM -III型(東洋測機(株)製)万能引張試験
機にて測定。 ショアD硬度:スプリング硬度計にて測定。 伸度(%):短冊(5mm×20mm)を万能引張試験
機にて測定。 耐水性:得られた角柱体を常温下に24時間放置した
後、水中に24時間浸漬し、形状を観測した。耐水性
は、良好(○)、やや悪い(△)、悪い(×)の三段階
にて評価した。 加工性:回転切削加工(537r.p.m)して、加工
性を判断した。加工性は、良好(○)、やや悪い
(△)、不可(×)の三段階にて評価した。
[Test Method] Specific Gravity: According to JIS K 0061. Strength (kgf / cm 2 ): T for a strip (5 mm x 20 mm)
ENSILON UTM-III type (manufactured by Toyo Sokki Co., Ltd.) Universal tensile tester. Shore D hardness: Measured with a spring hardness meter. Elongation (%): A strip (5 mm x 20 mm) is measured with a universal tensile tester. Water resistance: After the obtained prismatic body was left at room temperature for 24 hours, it was immersed in water for 24 hours and the shape was observed. The water resistance was evaluated in three grades of good (◯), slightly bad (Δ) and bad (x). Workability: The workability was judged by performing rotary cutting (537 rpm). The workability was evaluated in three grades of good (◯), slightly bad (Δ) and poor (x).

【0043】[0043]

【実施例2】実施例1において、シルクとビニル系モノ
マーとの配合比(シルク:ビニル系モノマー)を10
0:20とした以外は、実施例1と同様とした。結果を
第1表に示す。
Example 2 In Example 1, the blending ratio of silk and vinyl monomer (silk: vinyl monomer) was 10
Same as Example 1 except 0:20. The results are shown in Table 1.

【0044】[0044]

【実施例3】実施例1において、シルクとビニル系モノ
マーとの配合比(シルク:ビニル系モノマー)を10
0:10とした以外は、実施例1と同様とした。結果を
第1表に示す。
[Example 3] In Example 1, the blending ratio of silk and vinyl monomer (silk: vinyl monomer) was 10
Same as Example 1 except that it was 0:10. The results are shown in Table 1.

【0045】[0045]

【実施例4】実施例1において、絹粉末400g、メチ
ルメタアクリレーレート(MMA)320g、過硫酸カ
リウム10g、ラウリル硫酸ナトリウム60gを用い、
pH3.0、浴比1:30の水浴中で、重合温度90
℃、重合時間60分の条件下に反応させた後、実施例1
と同様の条件下にソーピング(後処理)を行い、水洗後
乾燥し粉砕した。
[Example 4] In Example 1, 400 g of silk powder, 320 g of methyl meta acrylate (MMA), 10 g of potassium persulfate, and 60 g of sodium lauryl sulfate were used.
Polymerization temperature 90 in a water bath with pH 3.0 and bath ratio 1:30
After the reaction was carried out under the conditions of a temperature of 60 ° C. and a polymerization time of 60 minutes, Example 1
Soaping (post-treatment) was performed under the same conditions as above, followed by washing with water, drying and pulverization.

【0046】次いで、得られた粉砕物を実施例1と同様
に加熱加圧成形して角柱体を得、実施例1と同様の試験
を行った。結果を第1表に示す。
Then, the obtained pulverized product was heated and pressed in the same manner as in Example 1 to obtain a prism, and the same test as in Example 1 was conducted. The results are shown in Table 1.

【0047】[0047]

【実施例5】実施例1において、グリシジルメタアクリ
レート(GMA)400gに代えて、スチレンモノマー
320gを用いた以外は実施例1と同様とした。
Example 5 Example 1 was repeated except that 320 g of styrene monomer was used instead of 400 g of glycidyl methacrylate (GMA).

【0048】結果を第1表に示す。The results are shown in Table 1.

【0049】[0049]

【実施例6】実施例1において、絹粉末400g、ヒド
ロキシメチルメタクリレート(HEMA)320g、過
硫酸カリウム20g、ドデシルベンゼンスルホン酸ナト
リウム6gを用い、pH3.0、浴比1:15の水浴中
で、重合温度80℃、重合時間45分の条件下に反応さ
せた後、実施例1と同様の条件下にソーピング(後処
理)を行い、水洗後乾燥し粉砕した。
Example 6 In Example 1, 400 g of silk powder, 320 g of hydroxymethylmethacrylate (HEMA), 20 g of potassium persulfate, and 6 g of sodium dodecylbenzenesulfonate were used in a water bath having a pH of 3.0 and a bath ratio of 1:15. After reacting under the conditions of a polymerization temperature of 80 ° C. and a polymerization time of 45 minutes, soaping (post-treatment) was performed under the same conditions as in Example 1, washing with water, drying and pulverization.

【0050】次いで、得られた粉砕物を実施例1と同様
に加熱加圧成形して角柱体を得、実施例1と同様の試験
を行った。結果を第1表に示す。
Then, the obtained pulverized product was heated and pressed in the same manner as in Example 1 to obtain a prism, and the same test as in Example 1 was conducted. The results are shown in Table 1.

【0051】[0051]

【比較例1】実施例1において、絹粉末のみを直接金型
に充填し、実施例1と同様な条件下に加熱加圧成形を行
い角柱体を得た。
[Comparative Example 1] In Example 1, only the silk powder was directly filled in the mold, and heat and pressure molding was performed under the same conditions as in Example 1 to obtain a prism.

【0052】得られた角柱体について、実施例1と同様
の試験を行った。結果を第1表に示す。
The same tests as in Example 1 were conducted on the obtained prismatic body. The results are shown in Table 1.

【0053】[0053]

【表1】 [Table 1]

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08L 89:00 6770−4J 101:00 7167−4J ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location C08L 89:00 6770-4J 101: 00 7167-4J

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 絹粉末とビニル系モノマーとを100k
g/cm2以上の圧力で圧縮し、かつ、200℃以下の
温度で加熱することを特徴とする絹の固形化物の製造方
法。
1. 100 k of silk powder and vinyl-based monomer
A method for producing a solidified silk product, which comprises compressing at a pressure of g / cm 2 or more and heating at a temperature of 200 ° C. or less.
【請求項2】前記絹粉末とビニル系モノマーとを、絹粉
末100重量部に対してビニル系モノマー5〜100重
量部の量で用いることを特徴とする請求項1記載の、絹
の固形化物の製造方法。
2. The solidified silk product according to claim 1, wherein the silk powder and the vinyl monomer are used in an amount of 5 to 100 parts by weight of the vinyl monomer with respect to 100 parts by weight of the silk powder. Manufacturing method.
JP19453791A 1991-08-02 1991-08-02 Method for producing solidified silk Expired - Fee Related JP3105582B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19453791A JP3105582B2 (en) 1991-08-02 1991-08-02 Method for producing solidified silk

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19453791A JP3105582B2 (en) 1991-08-02 1991-08-02 Method for producing solidified silk

Publications (2)

Publication Number Publication Date
JPH0538728A true JPH0538728A (en) 1993-02-19
JP3105582B2 JP3105582B2 (en) 2000-11-06

Family

ID=16326186

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19453791A Expired - Fee Related JP3105582B2 (en) 1991-08-02 1991-08-02 Method for producing solidified silk

Country Status (1)

Country Link
JP (1) JP3105582B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014012101A1 (en) * 2012-07-13 2014-01-16 Trustees Of Tufts College Silk powder compaction for production of constructs with high mechanical strength and stiffness

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW202144386A (en) * 2020-02-12 2021-12-01 美商保爾特紡織品公司 Recombinant silk solids and films

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014012101A1 (en) * 2012-07-13 2014-01-16 Trustees Of Tufts College Silk powder compaction for production of constructs with high mechanical strength and stiffness
US10034945B2 (en) 2012-07-13 2018-07-31 Trustees Of Tufts College Silk powder compaction for production of constructs with high mechanical strength and stiffness

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