JPH06158546A - Production of water absorbing cloth - Google Patents

Production of water absorbing cloth

Info

Publication number
JPH06158546A
JPH06158546A JP4326277A JP32627792A JPH06158546A JP H06158546 A JPH06158546 A JP H06158546A JP 4326277 A JP4326277 A JP 4326277A JP 32627792 A JP32627792 A JP 32627792A JP H06158546 A JPH06158546 A JP H06158546A
Authority
JP
Japan
Prior art keywords
water
short fibers
cloth
composite material
polyurethane elastomer
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.)
Pending
Application number
JP4326277A
Other languages
Japanese (ja)
Inventor
Hiroshi Okamura
浩 岡村
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.)
Showa Shell Sekiyu KK
Original Assignee
Showa Shell Sekiyu 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 Showa Shell Sekiyu KK filed Critical Showa Shell Sekiyu KK
Priority to JP4326277A priority Critical patent/JPH06158546A/en
Publication of JPH06158546A publication Critical patent/JPH06158546A/en
Pending legal-status Critical Current

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  • Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
  • Treatment Of Fiber Materials (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Woven Fabrics (AREA)

Abstract

PURPOSE:To raise the content of water absorbing collagen short fibers in a composite material at its maximum and to retain a composite material of a water absorbing collagen short fibers and urethane resin between napped fibers in water absorbing cloth wherein the composite material is formed on both sides of napped ground fabric. CONSTITUTION:A polyurethane elastomer is mixed with >=15% collagen short fibers modified with fish oil oxide and solid contents of the polyurethane elastomer and the collagen short fibers modified with fish oil oxide are made >=10% to give a processing solution, in which cotton fabric comprising both sides napped in >=7mm is immersed and the composite material is reacted and fixed in water.

Description

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

【0001】[0001]

【産業上の利用分野】この発明は、吸水性に優れた特性
を備える吸水性複合材を提供するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention provides a water-absorbing composite material having excellent water-absorbing properties.

【0002】[0002]

【従来の技術】従来、一般に使用されているセーム革は
吸水性は良好であるが、水切り性は綿布などに比較して
著しく劣っている。また、セーム革は魚油の酸化物で鞣
されているものであるが、皮組織中への魚油の浸透或は
油の酸化程度の調整が複雑である。吸水性及び吸油性に
優れた魚油酸化による改修コラーゲン繊維は知られてい
る。(岡村浩 白井邦郎:皮革化学Vol.23 15
〜19,1977)。
2. Description of the Related Art Conventionally used chamois leather has a good water absorption property, but its drainage property is significantly inferior to that of cotton cloth. Further, chamois leather is tanned with an oxide of fish oil, but it is complicated to infiltrate the fish oil into the skin tissue or adjust the degree of oxidation of the oil. Modified collagen fibers by oxidation of fish oil, which are excellent in water absorption and oil absorption, are known. (Hiroshi Okamura Kunio Shirai: Leather Chemistry Vol. 23 15
-19, 1977).

【0003】本発明者はこの吸水性に富む変性コラーゲ
ン短繊維を利用して吸水能の少い合成繊維製両面起毛織
布に吸水性を付与する目的で特願平2−53996を提
案した。この製法は、ポリウレタンエラストマに対し、
魚油酸化物で改修した変性コラーゲン短繊維を15%w
t以下として配合し、更に仕上げ工程で基布の両面にバ
フ処理を行なってスエード調の外観を形成させるもので
ある。この吸水性クロスの吸水度は、混用された変性コ
ラーゲン短繊維から計算した理論値より少ない上、吸水
速度は市販の吸水クロスより優れたものではなかった。
The present inventor has proposed Japanese Patent Application No. 2-53996 for the purpose of imparting water absorbency to a double-sided woven fabric made of synthetic fibers having a low water-absorbing ability by utilizing the modified collagen short fibers having a high water-absorbing ability. This manufacturing method, for polyurethane elastomers,
15% w of denatured collagen short fibers modified with fish oil oxide
It is compounded as t or less, and buffing is performed on both surfaces of the base fabric in the finishing step to form a suede-like appearance. The water absorption of this water absorbent cloth was less than the theoretical value calculated from the mixed modified collagen short fibers, and the water absorption rate was not superior to that of the commercially available water absorbent cloth.

【0004】[0004]

【解決しようとする問題点】この原因を検討したとこ
ろ、変性コラーゲン短繊維が基布の表面に積層されてポ
リウレタンエラストマと複合物質を形成し、クロス基布
付近には殆んど達せず、しかも表層の吸水性複合物質の
一部が含浸後の仕上げバフ処理によって除去されるた
め、製品における吸水性変性コラーゲン繊維含有量が著
しく少ないものとなることが確認された。本発明は、製
品クロスにおける変性コラーゲン短繊維含有量を2倍以
上高めることができるクロスの製造方法を提供するもの
である。
[Problems to be solved] When the cause of this problem was examined, denatured collagen short fibers were laminated on the surface of the base fabric to form a composite material with the polyurethane elastomer, and almost never reached near the cloth base fabric. It was confirmed that the content of the water-absorbed modified collagen fiber in the product was remarkably low, because a part of the water-absorbent composite material in the surface layer was removed by the finishing buffing after the impregnation. The present invention provides a method for producing a cloth capable of increasing the content of denatured collagen short fibers in the product cloth by a factor of 2 or more.

【0005】[0005]

【解決するための手段】本発明は、ポリウレタンエラス
トマのジメチルホルムアミド溶液に、魚油酸化物により
化学修飾を施した吸水性変性コラーゲン短繊維を前記ポ
リウレタンエラストマに対して15%wt以上配合する
と共に該溶液の固形分を10%以上になるように調整し
て加工液とし、該液中に両面を少なくても0.7mm起
毛した厚手平織木綿布を浸漬して水槽中で反応・固定さ
せた後、水洗し乾燥して製品とするものである。本発明
に使用する変性コラーゲン短繊維の製造において、床皮
を魚油の酸化油で改修する場合、まずコラーゲン繊維上
に油が被膜となって覆うような状態となり、魚油の酸化
が水分共存の状態で行われる。同時にその生成物である
高級アルデヒドが皮と反応して結合する。この場合にお
いて生皮の中心層まで油を浸透させなければならない。
本発明は、上記吸水性の変性コラーゲン繊維とポリウレ
タン樹脂よりなる複合物質の柔軟層を基布両面の起毛繊
維に保持させるものであるか起毛繊維長は長い程よく、
実験の結果から0.7mm以上の長起毛とする。更にポ
リウレタンエラストマに対する前記変性コラーゲン短繊
維の配合割合は、ポリウレタンエラストマ固形物に対し
約10〜25%wt、好ましくは15〜20%wtと
し、含浸液の固形物濃度は約10〜16%wtとする。
この条件は変性コラーゲン短繊維を吸水性複合材中に多
量混用するために必要である。また含浸後、仕上げバフ
処理を施さないことも必要である。
According to the present invention, a water-absorbing modified collagen short fiber chemically modified with fish oil oxide is blended in a dimethylformamide solution of polyurethane elastomer in an amount of 15% by weight or more with respect to the polyurethane elastomer, and the solution is added. After adjusting the solid content of the above to 10% or more to prepare a working liquid, a thick plain woven cotton cloth raised at least 0.7 mm on both sides is immersed in the working liquid and reacted and fixed in a water tank, It is washed with water and dried to obtain a product. In the production of the modified collagen short fibers used in the present invention, when the floor skin is repaired with an oxidized oil of fish oil, the collagen fiber is first covered with an oil film, and the oxidation of the fish oil is in the presence of water. Done in. At the same time, the product, a higher aldehyde, reacts with and binds to the skin. In this case the oil must penetrate into the central layer of the rawhide.
The present invention is to hold the flexible layer of the composite material consisting of the water-absorbent modified collagen fiber and the polyurethane resin on the napped fibers on both sides of the base fabric, or the napped fiber length is better,
From the results of the experiment, it is set to 0.7 mm or more. Further, the blending ratio of the modified collagen short fibers to the polyurethane elastomer is about 10 to 25% wt, preferably 15 to 20% wt with respect to the polyurethane elastomer solid matter, and the solid concentration of the impregnating liquid is about 10 to 16% wt. To do.
This condition is necessary in order to mix the modified collagen short fibers in the water-absorbent composite material in a large amount. It is also necessary not to apply a finishing buff treatment after impregnation.

【0006】[0006]

【実施例】【Example】

(A)変性コラーゲン繊維の調整 本発明に使用する変性コラーゲン繊維はポリウレタンエ
ラストマとの複合物質としての吸水性クロスを製造する
ことを目的としているため機械的強度を考慮する必要は
ない。従って、北米産塩蔵皮(ステアハイド,平均64
Lbs)より得られた頭部および隣接部位を使用し、短
時間の再石灰漬(2日間)および酸素処理を施した後、
再び再石灰漬を行なうことによりコラーゲン繊維の分離
と純化を十分行なう。 (1)コラーゲン繊維の分離と純化 床裸皮を2日間飽和石灰水中(2%石灰乳28℃)に浸
漬した後、30分間水洗を行なう。次いで水洗前の床皮
重量を基準として、3%塩化アンモンおよび200%温
水(35℃)と共にドラム中で30分間回転し、完全脱
灰した後に枯草菌プロテアーゼをカゼイン消化力として
皮質分1gに対し80Puを添加し4時間ドラム中で作
用させる。次いで再び2日間飽和石灰水中(2%石灰
乳、28℃)に浸漬し、コラーゲン繊維を分離および純
化させた後、塩化アンモニウムによる完全脱灰処理を行
った。 (2)ホリマリン処理 上記の床皮は、その重量の150%の水と5%の塩化ナ
トリウムと共に5分間ドラムを回転し、2%量のホルマ
リン溶液を10倍の水に希釈し、10分間隔で3回に分
け添加した。次いで6時間ドラムを回転し、炭酸ナトリ
ウムを適量加えPH8.5に溶液を調整した。更に2時
間回転してから約10時間ドラム中で浸漬後、10分間
流水で水洗した。 (3)解束処理 ホルマリン処理を終了した床皮は遠心脱水を行った後、
網ドラム中で回転しながら温風(38〜42℃)を通
じ、水分45%程度までに半乾燥した。この半乾燥物は
解束機を通過させ繊維の絡みを機械的に分離した。 (4)魚油酸化物による改修処理 解束処理終了後の重量を基準とし、200%の水、10
%の魚油酸化油および20%タラ油、0.5%の炭酸ナ
トリウムおよびこのタラ油重量に対して10%のオレイ
ン酸、1%のオレイン酸銅を混合し、ドラム(6r.
p.m.)中で6時間回転した。なお、タラ油はヨウ素
価:134.6,酸価:3.4,不けん化物:2.1で
あった。魚油酸化物は、魚油(タラ油)にその重量の8
%オレイン酸、0.5%のオレイン酸銅を加え湿潤な空
気を通し24時間60℃に保って酸化させ過酸化物価2
418meq/Kgを含むようになったものである。ド
ラム処理終了後、風乾により乾燥した。この乾燥重量を
基準として1000%の温水(40℃)、4%の炭酸ナ
トリウム、1%の非イオン活性剤と共に2時間ドラム中
で回転した後、30分間水洗し、引続き遠心脱水した。
脱水処理物は小型オプナーを改造した装置を使用し、叩
解と乾燥を同時に行い、含水量を30%〜40%に調製
した後、直ちに解繊維に通して変性コラーゲン繊維を得
た。 (B)クロスの製造 厚手平織木綿布(目付230g、巾95cm、厚さ0.
8mm)の生地の両面に0.5mm以上の起毛処理を施
した。ポリウレタンエラストマ(T.D.I.系)をジ
メチルフォルムアミドに溶解させ、上記の変性コラーゲ
ン短繊維をポリウレタンエラストマ重量に対し20%w
t量を除々に混入し撹拌した。この混合加工液を10〜
15%固形物溶液となるようジメチルフォルムアミドを
加えて調製した後、前記の基布に含浸させ、搾りロール
を通過させ、最終的に樹脂付着量を基布重量に対して4
0〜45%(重量)になるよう絞り程度で調製した。そ
の後、反応水槽に導入し、ウレタン・変性コラーゲン繊
維複合体を基布に固定した。引続き水槽中で水洗し、柔
軟剤を添加した後、温水で洗浄と共にミーリング処理を
施した。このようにして処理した加工布を乾燥し、バフ
処理を施すことなく吸水性クロスとする。この製品は仕
上げ巾93cm、目付330g、厚さ1.03mmであ
った。皮革(衣料革用JIS K 6554)による物
性測定値(40×20cm2 、10試料、横軸方向)は 引張強さ:0.72±0.06kgf/mm2 切断時の伸び:54.6±4.2% 引裂強さ:3.74±0.27kgf/mm 剛軟度:201.5±8.4mgfであった。
(A) Preparation of Modified Collagen Fiber The modified collagen fiber used in the present invention is intended to produce a water-absorbent cloth as a composite material with a polyurethane elastomer, and therefore mechanical strength need not be considered. Therefore, North American salted hide (stairhide, average 64
Lbs) using the head and adjacent parts obtained from Lbs, after a short time of recalcification (2 days) and oxygen treatment,
By re-calcining again, the collagen fibers are sufficiently separated and purified. (1) Separation and Purification of Collagen Fibers Naked skins are immersed in saturated lime water (2% lime milk 28 ° C.) for 2 days, and then washed with water for 30 minutes. Next, based on the weight of the bark before washing with water, the mixture was rotated in a drum for 30 minutes with 3% ammonium chloride and 200% warm water (35 ° C), and after complete decalcification, Bacillus subtilis protease was used as a casein digestive power for 1 g of cortical matter Add 80 Pu and allow to work in drum for 4 hours. Then, it was immersed again in saturated lime water (2% lime milk, 28 ° C.) for 2 days to separate and purify the collagen fibers, and then a complete decalcification treatment with ammonium chloride was performed. (2) Forimarin treatment For the above-mentioned floor skin, the drum was rotated for 5 minutes with 150% of its weight of water and 5% of sodium chloride, a 2% amount of formalin solution was diluted with 10 times water, and 10 minutes interval Was added in three times. Then, the drum was rotated for 6 hours, and an appropriate amount of sodium carbonate was added to adjust the solution to pH 8.5. It was further rotated for 2 hours, immersed in a drum for about 10 hours, and then washed with running water for 10 minutes. (3) Debunching treatment After removing the formalin-treated floor skin by centrifugal dehydration,
While rotating in a mesh drum, warm air (38 to 42 ° C.) was passed through to semi-dry the water to about 45%. This semi-dried product was passed through a debunker to mechanically separate the fiber entanglement. (4) Remediation treatment with fish oil oxide Based on the weight after completion of the debinding treatment, 200% water, 10
% Oxidized fish oil and 20% cod oil, 0.5% sodium carbonate and 10% oleic acid, 1% copper oleate based on the weight of the cod oil, mixed in a drum (6r.
p. m. ) Rotated for 6 hours. The cod oil had an iodine value: 134.6, an acid value: 3.4, and an unsaponifiable matter: 2.1. Fish oil oxide is 8 parts by weight of fish oil (cod oil).
% Oleic acid and 0.5% copper oleate are added, and moist air is passed for 24 hours at 60 ° C. for oxidation to oxidize the peroxide value to 2
It contains 418 meq / Kg. After the completion of the drum treatment, it was dried by air drying. Based on this dry weight, 1000% warm water (40 ° C.), 4% sodium carbonate, 1% nonionic activator were rotated in a drum for 2 hours, followed by washing with water for 30 minutes and subsequent centrifugal dehydration.
The dehydrated product was prepared by using a device modified from a small-sized opener, and performing beating and drying at the same time to adjust the water content to 30% to 40%, and then immediately passing through defiberized fiber to obtain denatured collagen fiber. (B) Manufacture of cloth Thick plain-woven cotton cloth (weight of 230 g, width of 95 cm, thickness of 0.
Both sides of the fabric (8 mm) were subjected to a raising treatment of 0.5 mm or more. Polyurethane elastomer (TDI type) is dissolved in dimethylformamide, and the above-mentioned modified collagen short fiber is 20% w based on the weight of polyurethane elastomer.
The amount of t was gradually mixed and stirred. 10 ~ this mixed processing fluid
Dimethylformamide was added to the solution to prepare a 15% solids solution, which was then impregnated into the above base cloth and passed through a squeeze roll, and finally the resin adhesion amount was set to 4 with respect to the base cloth weight.
It was prepared by squeezing so as to be 0 to 45% (weight). Then, it was introduced into a reaction water tank, and the urethane / denatured collagen fiber composite was fixed to the base cloth. Subsequently, it was washed with water in a water tank, and after adding a softening agent, it was washed with warm water and milled. The processed cloth thus treated is dried to obtain a water-absorbent cloth without being subjected to buffing. This product had a finished width of 93 cm, a basis weight of 330 g and a thickness of 1.03 mm. The physical properties measured by leather (JIS K 6554 for clothing leather) (40 × 20 cm 2 , 10 samples, horizontal axis direction) are tensile strength: 0.72 ± 0.06 kgf / mm 2 Elongation at break: 54.6 ± 4.2% Tear strength: 3.74 ± 0.27 kgf / mm Bending resistance: 201.5 ± 8.4 mgf.

【吸水量等の比較試験】本発明吸水性クロスと両面バフ
処理を行った吸水・保水性柔軟クロス(特願平2−53
996)を比較した結果は表のようであった。ただし、
両者とも木綿平織を基布とし、変性コラーゲン短繊維の
混用量を20%wtとした。
[Comparison Test of Water Absorption, etc.] The water absorbent cloth of the present invention and the water absorbent / water retentive flexible cloth subjected to double-sided buffing (Japanese Patent Application No. 2-53).
The results of comparing 996) are shown in the table. However,
Both of them were made of cotton plain weave, and the mixed amount of denatured collagen short fibers was 20% wt.

【0007】[0007]

【表1】 [Table 1]

【0008】吸水量の測定は、40×100mm2 の長
方形の試料片を蒸留水に30分間浸漬(20±2℃)し
浸漬前後の試験片の重量差を浸漬前の重量に対する%で
求め、これを吸水度(A)とした。浸漬後、遠心分離
(3000r.p.m)により脱水した後、重量を測定
し浸漬前の試料片の重量に対する%を計算し吸水度
(B)とした。吸水速度は、バイレックス法により測定
した。すなわち、20±2℃の蒸留水中に30×180
mm(垂直方向)の試料片を下端より15mm浸漬し1
0分間における水の上昇高さを測定した。測定は10回
行い、その平均値及び標準偏差を示した。更に夫々のク
ロスを3層に分割し、中央の層を除去、細断しピリジン
に浸漬し、変性コラーゲンおよび基布を分離して浄化
後、アセトンおよび蒸留水で洗浄した。濾紙と共にJI
S K 6550により皮質分を測定し、無水物に対す
る変性コラーゲン短繊維含有量を算出した。
The water absorption was measured by immersing a rectangular sample piece of 40 × 100 mm 2 in distilled water for 30 minutes (20 ± 2 ° C.), and determining the weight difference between the test piece before and after immersion in% of the weight before immersion. This was defined as the water absorption (A). After the immersion, it was dehydrated by centrifugation (3000 rpm), the weight was measured, and the% to the weight of the sample piece before immersion was calculated to be the water absorption (B). The water absorption rate was measured by the Bayrex method. That is, 30 × 180 in distilled water at 20 ± 2 ° C.
Immerse a 15 mm (vertical) sample piece from the bottom edge for 15 mm and
The rising height of water in 0 minutes was measured. The measurement was performed 10 times, and the average value and standard deviation were shown. Further, each cloth was divided into 3 layers, the central layer was removed, shredded and immersed in pyridine, the denatured collagen and the base cloth were separated and purified, and then washed with acetone and distilled water. JI with filter paper
The cortical content was measured by SK 6550, and the content of denatured collagen short fibers with respect to the anhydride was calculated.

【0009】[0009]

【効果】本発明による吸水性クロスは、バフ処理を施し
た従来の吸水性クロスに比較して、吸水度(A)につい
ては1.5倍、吸水速度については1.8倍も優れてい
る。これは表面層の変性コラーゲン短繊維含有量が2.
6倍も多く含有されているためと考えられ、新しい吸水
性複合クロスとして期待できるものである。
[Effect] The water-absorbent cloth of the present invention is superior in water absorbency (A) by 1.5 times and water-absorbing rate by 1.8 times in comparison with the conventional buff-treated water absorbent cloth. . This has a modified collagen short fiber content of 2.
It is considered that this is because it is contained 6 times as much, and it can be expected as a new water-absorbent composite cloth.

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 D06M 15/70 23/08 // D06C 11/00 A D06M 101:16 D06M 15/564 15/70 7199−3B 21/02 Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI Technical display location D06M 15/70 23/08 // D06C 11/00 A D06M 101: 16 D06M 15/564 15/70 7199-3B 21/02

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】ポリウレタンエラストマのジメチルホルム
アミド溶液に、魚油酸化物により化学修飾を施した吸水
性変性コラーゲン短繊維を前記ポリウレタンエラストマ
に対して15%wt以上配合すると共に該溶液の固形分
を10%以上になるように調整して加工液とし、該液中
に両面を少なくても0.7mm起毛した厚手平織木綿布
を浸漬して水槽中で反応・固定させた後、水洗し乾燥す
ることを特徴とする吸水性クロスの製造方法。
1. A solution of polyurethane elastomer in dimethylformamide is admixed with 15% by weight or more of water-absorbing modified collagen short fibers chemically modified with fish oil oxide with respect to the polyurethane elastomer, and the solid content of the solution is 10%. The processing liquid was adjusted as described above, and a thick plain woven cotton cloth raised at least 0.7 mm on both sides was dipped in the liquid to react and fix in a water tank, followed by washing with water and drying. A method for producing a water-absorbent cloth, which is characterized.
JP4326277A 1992-11-12 1992-11-12 Production of water absorbing cloth Pending JPH06158546A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4326277A JPH06158546A (en) 1992-11-12 1992-11-12 Production of water absorbing cloth

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4326277A JPH06158546A (en) 1992-11-12 1992-11-12 Production of water absorbing cloth

Publications (1)

Publication Number Publication Date
JPH06158546A true JPH06158546A (en) 1994-06-07

Family

ID=18185971

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4326277A Pending JPH06158546A (en) 1992-11-12 1992-11-12 Production of water absorbing cloth

Country Status (1)

Country Link
JP (1) JPH06158546A (en)

Cited By (5)

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CN103643369A (en) * 2013-11-20 2014-03-19 苏州工业园区友顺制衣厂 Manufacturing technology of ginkgo nut silk fabric
EP3205669A1 (en) * 2016-02-15 2017-08-16 Brendan Patrick Purcell Composite biofabricated material
EP3704202A4 (en) * 2019-01-17 2020-12-16 Modern Meadow, Inc. Layered collagen materials and methods of making the same
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US11913166B2 (en) 2015-09-21 2024-02-27 Modern Meadow, Inc. Fiber reinforced tissue composites

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103643369A (en) * 2013-11-20 2014-03-19 苏州工业园区友顺制衣厂 Manufacturing technology of ginkgo nut silk fabric
US11913166B2 (en) 2015-09-21 2024-02-27 Modern Meadow, Inc. Fiber reinforced tissue composites
EP3205669A1 (en) * 2016-02-15 2017-08-16 Brendan Patrick Purcell Composite biofabricated material
EP3205668A1 (en) * 2016-02-15 2017-08-16 Brendan Patrick Purcell Method for biofabricating composite material
US11001679B2 (en) 2016-02-15 2021-05-11 Modern Meadow, Inc. Biofabricated material containing collagen fibrils
US11286354B2 (en) 2016-02-15 2022-03-29 Modern Meadow, Inc. Method for making a biofabricated material containing collagen fibrils
US11525042B2 (en) 2016-02-15 2022-12-13 Modern Meadow, Inc. Composite biofabricated material
US11530304B2 (en) 2016-02-15 2022-12-20 Modern Meadow, Inc. Biofabricated material containing collagen fibrils
US11542374B2 (en) 2016-02-15 2023-01-03 Modern Meadow, Inc. Composite biofabricated material
US11214844B2 (en) 2017-11-13 2022-01-04 Modern Meadow, Inc. Biofabricated leather articles having zonal properties
EP3704202A4 (en) * 2019-01-17 2020-12-16 Modern Meadow, Inc. Layered collagen materials and methods of making the same
US11352497B2 (en) 2019-01-17 2022-06-07 Modern Meadow, Inc. Layered collagen materials and methods of making the same

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