US2535919A - Manufacture of sheets of webs of fibrous textile materials - Google Patents
Manufacture of sheets of webs of fibrous textile materials Download PDFInfo
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- US2535919A US2535919A US54728A US5472848A US2535919A US 2535919 A US2535919 A US 2535919A US 54728 A US54728 A US 54728A US 5472848 A US5472848 A US 5472848A US 2535919 A US2535919 A US 2535919A
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- cellulose
- fibers
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- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000004753 textile Substances 0.000 title description 7
- 239000000463 material Substances 0.000 title description 6
- 239000000835 fiber Substances 0.000 claims description 36
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 27
- 229920002678 cellulose Polymers 0.000 claims description 26
- 239000001913 cellulose Substances 0.000 claims description 26
- 239000000853 adhesive Substances 0.000 claims description 14
- 230000001070 adhesive effect Effects 0.000 claims description 12
- 230000000397 acetylating effect Effects 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 229920002284 Cellulose triacetate Polymers 0.000 claims description 6
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 claims description 6
- 239000004745 nonwoven fabric Substances 0.000 claims description 4
- 238000009877 rendering Methods 0.000 claims description 4
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 24
- 235000010980 cellulose Nutrition 0.000 description 24
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 11
- 229960000583 acetic acid Drugs 0.000 description 10
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- 240000008564 Boehmeria nivea Species 0.000 description 8
- 230000021736 acetylation Effects 0.000 description 8
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- 238000005886 esterification reaction Methods 0.000 description 6
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
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- 238000002441 X-ray diffraction Methods 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 238000009960 carding Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
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- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
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- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
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- 235000009120 camo Nutrition 0.000 description 1
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- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229940106135 cellulose Drugs 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/54—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
- D04H1/552—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving by applying solvents or auxiliary agents
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/425—Cellulose series
- D04H1/4258—Regenerated cellulose series
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/188—Monocarboxylic acids; Anhydrides, halides or salts thereof
Definitions
- FIG.2 MANUFACTURE OF SHEETS 0R WEBS 0F FIBROUS TEXTILE MATERIALS Filed Oct. 15. 1948 30 J 3- C U20 0 I23456789l0lll2l3l4 nucmouns) FIG.2.
- This invention relates to the manufacture of sheets or webs of fibrous textile materias, such as for example felts, fieeces, and non-woven fabrics for' use as towels or other cleaning tissues, hereinafter referred to generally as "sheets.
- non-adhesive fibres and potentially-adhesive fibres that is fibres which can be rendered adhesive by suitable treatment such as by heating, pressing or treating with a solvent, and to treat the blend subsequently in order to render adhesive the potentially-adhesive fibres and to bind the fibres together.
- suitable treatment such as by heating, pressing or treating with a solvent
- sheets or other shaped bodies of fibrous materials and felt substitutes are made by carding natural or artificial fibres in admixture with threads of a thermoplastic artificial material and subjecting the card fieece or web to pressure, if desired with the application of heat.
- the object of the present invention is to improve the manufacture of sheets of fibrous textile materials by the use of particular potentiallyadhesive fibres.
- a process for the manufacture of sheets of fibrous textile materia s comprises forming a layer of fibres at least part of which are incompletelyesterified cellulose fibres which have been prepared by esterifying cellulose fibres with an organic acid whilst maintaining their fibrous structure, and rendering the incompletely-esterified fibres adhesive so that the fibres in the layer are bonded together.
- the fibres are preferably incompletely-acetylated and they may be rendered adhesive by heating, preferab y with the simultaneous or subsequent application of pressure, or by treatment with a solvent or plasticiser; methylene chloride is suitable for example as a solvent for cellulose acetate.
- FIG. 1 is a graph showing one example of the course of fibrous acetylation using ramie fibres.
- Cellulose fibres are known to include at least two types of cellulose namely an amorphous cellulose and a highly crystalline cellulose.
- the amorphous cellulose A forms a continuous matrix or network. which surrounds and merges into the highly crystalline cellulose B; in the drawing a line separation of thetwo varieties of cellulose A and B is shown for clarity but actually the two varieties are separated by zones of graded intercrystalline cellulose.
- the esterifying solution first penetrates the amorphous cellulose A and effects its esterification to the triester stage so that after a time (usually about l-3 hours) the matrix of amorphous cellulose is converted into cellulose triester.
- the highly crystalline cellulose B is substantially unchanged and X-ray analysis shows that substantially no crystalline cellulose triester has been formed.
- the amorphous triester formed swells and so opens up the structure of the fibre with the result that the esterifying solution now penetrates through the outer layers of highly crystalline cellulose B and as it penetrates, a highly-crystalline cellu lose triester is formed and this triester can be detected by X-ray analysis.
- the fibre will contain a number of highly crystalline cellulose nuclei surrounded by cellulose triester.
- Figure 2 is a graph showing the rate of fibrous acetylation of ramie fibres.
- the acetylation was effected as follows, parts and percentages being by weight:
- the cellulose of the fibre is in a hydrated form, a similar two-phase product is obtained but in this casethe triester has a different crystal lattice from that obtained on esterification oi. native cellulose, and the unreacted phase is hydrated cellulose.
- the present invention takes advantage of the presence 01- the triester present in the fibre by causing it to act as the adhesive material for bonding the fibres together.
- the incompletely-esterified cellulose fibres may be prepared from natural cellulose such as cotton and the bast fibres such as hemp, ramie, jute and flax, or from regenerated cellulose such as viscose rayon fibres in either continuous or discontinuous lengths.
- the degree of esterification of cellulose fibres may be varied over a wide range and we have obtained good results by using a cellulose acetylated to give only an 8 per cent acetyl value, this value being defined herein as the percentage of acetic acid present based on the final weight of the fibre.
- the layer of fibres may be built up from the incompletely-esterified cellulose fibres alone or from mixtures of these fibres and other natural or synthetic fibres such as cotton, wool, casein fibres, viscose rayon and cellulose acetate rayon.
- particularly good bond may be obtained by using incompletely-acetylated cellulose fibres as the potentially adhesive fibre in the fibre layer.
- the layer of fibres may be prepared by carding the fibres from a carded web or several carded webs may be overlaid and laminated together.
- Continuous filaments may .also be formed into several laps of single filament thickness and the layers assembled on top of each other with the filaments in adjacent laps crossing at approximately 90.
- the layer may also be formed from a slurry of fibres in a manner similar to the process used in the paper industry.
- the fibrous sheet made according to the invention may be treated if desired with a saponii'ying agent in order to remove some or all of the ester groupings, the physical form of the sheet remaining unchanged.
- Example 1 Ramie fibres were mixed with half their weight of glacial acetic acid and allowed to stand for 16 hours at ordinary temperature to 20 centigrade). The fibres were then immersed for 1 hour at centigrade in an acetylating bath contain ing 700 parts of sulphur-free toluene, 650 parts of acetic anhydride and 2 parts of sulphuric acid per 100 parts or ramie fibre. The ramie fibres on removal from the bath were washed with alcohol and water and were dried at centigrade. The acetyl value of the fibres was approximately 8.5.
- the incompletely-acetylated fibres were formed into three laps consisting of substantially parallel fibres, and the laps were placed on top of each other with the threads in adjacent layers at right angles.
- the assembly was then treated by spraying with methylene chloride to render the fibres adhesive; when the methylene chloride had evaporated, the fibres had united to form a nonwoven fabric sheet. A more compact fabric sheet was obtained by lightly pressing the assembly at room temperatures.
- Example 2 parts or viscose staple fibre (3 denier, 2% inches staple length) were pretreated at 25 centigrade for 24 hours with 75 parts of glacial acetic acid containing 1 per cent by volume of concentrated sulphuric acid (QB-per cent w./w.).
- the pretreated fibres were then immersed for 3 hours at 45 centigrade in an acetylating bath containing 750 parts of sulphur-free toluene and 375 parts of acetic anhydride (substantially per cent).
- the fibres were then removed from the bath, washed in alcohol and water till free from acid and were dried at 60 centigrade.
- the acetyl value or the fibres was 30 per cent.
- the incompletely acetylated fibre was then carded to form a web which was sprayed with methylene chloride, pressed lightly to compact the web and then allowed to stand till the methylene chloride had evaporated.
- the product was a non-woven tissue particularly suitable for wiping and cleansing purposes. A sample oi the tissue was immersed in water for one month; it was found on drying the tissue that the fabric had maintained its strength and form.
- Example 3 1 part of cotton linters was pretreated with part of glacial acetic acid at 25 centigrade for 18 hours. The pretreated linters were then immersed at 45 centigrade for 1% hours in an acetylating bath containing 10 parts of sulphurfree toluene, 5 parts of acetic anhydride and 0.002 part of sulphuric acid (98 per cent w./w.). The linters were then washed first with alcohol. then with water and were finally dried at 60 centigrade. The acetyl content 01' the fibres was 15 per cent.
- the incompletely acetylated fibres were carded and treated with methylene chloride as described in Example 2 to form a non-woven tissue.
- a similar type of product may be obtained by forming the web from a mixture of equal parts of the incompletely acetylated fibre and untreated viscose staple fibre.
- Example 4 1 part of ramie fibre was pretreated with It; part of glacial acetic acid .at 25 centlgrade for 8 hours. The pretreated fibre was then immersed at 45 centigrade for 1% hours in an acetylating form a web which was treated as described in Example 2 to form a non woven tissue.
- Example 5 1 part of viscose staple fibre (3 denier, 2 inches staple length) was pretreated at 25 centigrade for 18 hours with /3 part of glacial acetic acid. The pretreated fibres were then immersed at 45 centigrade for 24 hours in a bath containing parts of carbon tetrachloride, 5 parts of acetic anhydride and 0.002 part of sulphuric acid (98 per cent w./w.). The fibres were then washed with hot water and carbon tetrachloride was removed by steam distillation. The product was then dried. Its acetyl content was 12 per cent.
- the fibres were formed into a web and treated with methylene chloride as described in Example 2 to provide a non-woven tissue.
- Example 6 The fibers were formed into a web and treated with methylene chloride as described in Example 2 to provide a non-woven tissue.
- a process for the manufacture of non-woven fabrics which comprises the steps of acetylating unspun cellulose fibers while maintaining their fiber structure until the acetyl content of the fibers is from about 8 to about 40 per cent, calculated as the percentage of acetic acid on the finalweight of the fibers, forming a fibrous web of unspun fibers at least the major proportion of which consists of the unspun, incompletelyacetylated cellulose fibers so obtained, and rendering adhesive the cellulose triacetate phase of the unspunincompletely-acetylated cellulose fibers whereby the fibers in the web are bonded together at their pointsof contact to form a unified fibrous structure.
- a process for the manufacture of non-woven bonded fabrics which comprises the steps of acetylating unspun cellulose fibers while maintaining their fiber structure until the acetyl content of the fibers is from about 8 to about 40 per cent,
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Nonwoven Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Dec. 26, 1950 F. HAPPEY ETAL 2,535,919
MANUFACTURE OF SHEETS 0R WEBS 0F FIBROUS TEXTILE MATERIALS Filed Oct. 15. 1948 30 J 3- C U20 0 I23456789l0lll2l3l4 nucmouns) FIG.2.
/nven/0r$ FrankHappey John Herberf Grimes By Ihe/r afforneys Patented Dec. 26, 1950 MANUFACTURE OF SHEETS OR WEBS F FIBROUS TEXTILE MATERIALS Frank Happey, Coventry, and John Herbert Grimes, Cheylesmore, Coventry, England, assignors to Courtaulds Limited, London, England, a British company Application October 15, 1948, Serial No. 54,728 In Great Britain November I, 1947 2 Claims.
This invention relates to the manufacture of sheets or webs of fibrous textile materias, such as for example felts, fieeces, and non-woven fabrics for' use as towels or other cleaning tissues, hereinafter referred to generally as "sheets.
In the manufacture of fibrous textile materials in the form of felts, sheets and the like, it is known to blend non-adhesive fibres and potentially-adhesive fibres, that is fibres which can be rendered adhesive by suitable treatment such as by heating, pressing or treating with a solvent, and to treat the blend subsequently in order to render adhesive the potentially-adhesive fibres and to bind the fibres together. For example, in void British application No. 10,246/1938 as laid open to public inspection, sheets or other shaped bodies of fibrous materials and felt substitutes are made by carding natural or artificial fibres in admixture with threads of a thermoplastic artificial material and subjecting the card fieece or web to pressure, if desired with the application of heat.
The object of the present invention is to improve the manufacture of sheets of fibrous textile materials by the use of particular potentiallyadhesive fibres.
In accordance with the present invention, a process for the manufacture of sheets of fibrous textile materia s comprises forming a layer of fibres at least part of which are incompletelyesterified cellulose fibres which have been prepared by esterifying cellulose fibres with an organic acid whilst maintaining their fibrous structure, and rendering the incompletely-esterified fibres adhesive so that the fibres in the layer are bonded together. The fibres are preferably incompletely-acetylated and they may be rendered adhesive by heating, preferab y with the simultaneous or subsequent application of pressure, or by treatment with a solvent or plasticiser; methylene chloride is suitable for example as a solvent for cellulose acetate.
It is already known, see for example United States specification No. 1,861,320 that cellulose in fibrous form may be esterfied whilst maintaining its fibrous structure by immersing the Figure 2 is a graph showing one example of the course of fibrous acetylation using ramie fibres.
Cellulose fibres are known to include at least two types of cellulose namely an amorphous cellulose and a highly crystalline cellulose. As shown in Figure 1, the amorphous cellulose A forms a continuous matrix or network. which surrounds and merges into the highly crystalline cellulose B; in the drawing a line separation of thetwo varieties of cellulose A and B is shown for clarity but actually the two varieties are separated by zones of graded intercrystalline cellulose. When the fibre is esterifled by the fibrous esterification process, the esterifying solution first penetrates the amorphous cellulose A and effects its esterification to the triester stage so that after a time (usually about l-3 hours) the matrix of amorphous cellulose is converted into cellulose triester. At this stage 01' the esterification process, the highly crystalline cellulose B is substantially unchanged and X-ray analysis shows that substantially no crystalline cellulose triester has been formed. The amorphous triester formed swells and so opens up the structure of the fibre with the result that the esterifying solution now penetrates through the outer layers of highly crystalline cellulose B and as it penetrates, a highly-crystalline cellu lose triester is formed and this triester can be detected by X-ray analysis. Until the esterification is complete therefore, the fibre will contain a number of highly crystalline cellulose nuclei surrounded by cellulose triester.
Figure 2 is a graph showing the rate of fibrous acetylation of ramie fibres. The acetylation was effected as follows, parts and percentages being by weight:
25 parts of ramie fibres, containing 3 per cent of water were pretreated for 24 hours with 12 parts of glacial acetic acid and the pretreated fibres were then immersed in an acetylation solution consisting of a mixture of 520 parts of toluene, 330 parts of acetic anhydride (97 per cent pure) and 1.8 parts of concentrated sulphuric acid. The mixture was maintained at 45 centigrade in a thermostat. Samples of the fibre were withdrawn at intervals and the: acetyl contents calculated as acetic acid, .were determined and X-ray analyses of the fibres were carried out. Up to and at point C on the graph (corresponding to a 29 per cent acetyl content after 1 hour's acetylation), the acetylation was rapid and no crystalline cellulose triacetate was detected by x-ray analysis. The graph from the ori in to point therefore corresponds to the acetylation of the amorphous cellulose. Beyond the point C. x-ray analysis showed the presence oi increasing quantities of highly crystalline cellulose triacetate, thus indicating that acetylation of the highly crystalline cellulose was being efiected.
I! the cellulose of the fibre is in a hydrated form, a similar two-phase product is obtained but in this casethe triester has a different crystal lattice from that obtained on esterification oi. native cellulose, and the unreacted phase is hydrated cellulose.
The present invention takes advantage of the presence 01- the triester present in the fibre by causing it to act as the adhesive material for bonding the fibres together.
The incompletely-esterified cellulose fibres may be prepared from natural cellulose such as cotton and the bast fibres such as hemp, ramie, jute and flax, or from regenerated cellulose such as viscose rayon fibres in either continuous or discontinuous lengths.
The degree of esterification of cellulose fibres may be varied over a wide range and we have obtained good results by using a cellulose acetylated to give only an 8 per cent acetyl value, this value being defined herein as the percentage of acetic acid present based on the final weight of the fibre. In general for making non-woven tissues suitable for cleansing purposes, it is preferred. to use incompletely-acetylated cellulose fibres containing from about 8 to about 40 per cent acetyl content. Should the incompletelyacetyla'ted cellulose fibres be used in admixture with non-adhesive fibres, it is in general desirable to use fibres having a higher acetyl value than that of fibres used without such admixtures.
The layer of fibres may be built up from the incompletely-esterified cellulose fibres alone or from mixtures of these fibres and other natural or synthetic fibres such as cotton, wool, casein fibres, viscose rayon and cellulose acetate rayon.
When using fibres of cellulose acetate rayon, a
particularly good bond may be obtained by using incompletely-acetylated cellulose fibres as the potentially adhesive fibre in the fibre layer.
The layer of fibres may be prepared by carding the fibres from a carded web or several carded webs may be overlaid and laminated together. Continuous filaments may .also be formed into several laps of single filament thickness and the layers assembled on top of each other with the filaments in adjacent laps crossing at approximately 90. The layer may also be formed from a slurry of fibres in a manner similar to the process used in the paper industry.
The fibrous sheet made according to the invention may be treated if desired with a saponii'ying agent in order to remove some or all of the ester groupings, the physical form of the sheet remaining unchanged.
The present invention is illustrated by the following examples, parts and percentages being by weight unless otherwise stated:
Example 1 Ramie fibres were mixed with half their weight of glacial acetic acid and allowed to stand for 16 hours at ordinary temperature to 20 centigrade). The fibres were then immersed for 1 hour at centigrade in an acetylating bath contain ing 700 parts of sulphur-free toluene, 650 parts of acetic anhydride and 2 parts of sulphuric acid per 100 parts or ramie fibre. The ramie fibres on removal from the bath were washed with alcohol and water and were dried at centigrade. The acetyl value of the fibres was approximately 8.5.
The incompletely-acetylated fibres were formed into three laps consisting of substantially parallel fibres, and the laps were placed on top of each other with the threads in adjacent layers at right angles. The assembly was then treated by spraying with methylene chloride to render the fibres adhesive; when the methylene chloride had evaporated, the fibres had united to form a nonwoven fabric sheet. A more compact fabric sheet was obtained by lightly pressing the assembly at room temperatures.
Example 2 parts or viscose staple fibre (3 denier, 2% inches staple length) were pretreated at 25 centigrade for 24 hours with 75 parts of glacial acetic acid containing 1 per cent by volume of concentrated sulphuric acid (QB-per cent w./w.). The pretreated fibres were then immersed for 3 hours at 45 centigrade in an acetylating bath containing 750 parts of sulphur-free toluene and 375 parts of acetic anhydride (substantially per cent). The fibres were then removed from the bath, washed in alcohol and water till free from acid and were dried at 60 centigrade. The acetyl value or the fibres was 30 per cent.
The incompletely acetylated fibre was then carded to form a web which was sprayed with methylene chloride, pressed lightly to compact the web and then allowed to stand till the methylene chloride had evaporated. The product was a non-woven tissue particularly suitable for wiping and cleansing purposes. A sample oi the tissue was immersed in water for one month; it was found on drying the tissue that the fabric had maintained its strength and form.
Example 3 1 part of cotton linters was pretreated with part of glacial acetic acid at 25 centigrade for 18 hours. The pretreated linters were then immersed at 45 centigrade for 1% hours in an acetylating bath containing 10 parts of sulphurfree toluene, 5 parts of acetic anhydride and 0.002 part of sulphuric acid (98 per cent w./w.). The linters were then washed first with alcohol. then with water and were finally dried at 60 centigrade. The acetyl content 01' the fibres was 15 per cent.
The incompletely acetylated fibres were carded and treated with methylene chloride as described in Example 2 to form a non-woven tissue.
A similar type of product may be obtained by forming the web from a mixture of equal parts of the incompletely acetylated fibre and untreated viscose staple fibre.
Example 4 1 part of ramie fibre was pretreated with It; part of glacial acetic acid .at 25 centlgrade for 8 hours. The pretreated fibre was then immersed at 45 centigrade for 1% hours in an acetylating form a web which was treated as described in Example 2 to form a non woven tissue.
Example 5 1 part of viscose staple fibre (3 denier, 2 inches staple length) was pretreated at 25 centigrade for 18 hours with /3 part of glacial acetic acid. The pretreated fibres were then immersed at 45 centigrade for 24 hours in a bath containing parts of carbon tetrachloride, 5 parts of acetic anhydride and 0.002 part of sulphuric acid (98 per cent w./w.). The fibres were then washed with hot water and carbon tetrachloride was removed by steam distillation. The product was then dried. Its acetyl content was 12 per cent.
The fibres were formed into a web and treated with methylene chloride as described in Example 2 to provide a non-woven tissue.
Example 6 The fibers were formed into a web and treated with methylene chloride as described in Example 2 to provide a non-woven tissue.
What we claim is:
1. A process for the manufacture of non-woven fabrics which comprises the steps of acetylating unspun cellulose fibers while maintaining their fiber structure until the acetyl content of the fibers is from about 8 to about 40 per cent, calculated as the percentage of acetic acid on the finalweight of the fibers, forming a fibrous web of unspun fibers at least the major proportion of which consists of the unspun, incompletelyacetylated cellulose fibers so obtained, and rendering adhesive the cellulose triacetate phase of the unspunincompletely-acetylated cellulose fibers whereby the fibers in the web are bonded together at their pointsof contact to form a unified fibrous structure.
2. A process for the manufacture of non-woven bonded fabrics which comprises the steps of acetylating unspun cellulose fibers while maintaining their fiber structure until the acetyl content of the fibers is from about 8 to about 40 per cent,
calculated as the percentage of acetic acid on the final weight of the fibers, forming a fibrous web of unspun fibers at least the major proportion of which consists of the unspun, incompletelyacetylated cellulose fibers so obtained, and rendering adhesive the cellulose triacetate phase of the unspun incompletely-acetylated cellulose fibers by treatment with a solvent for the cellulose triacetate followed by removal of the solvent; whereby the fibers in the web are bonded together at their points of contact to form a unified fibrous construction.
FRANK HAPPEY. JOHN HERBERT GRIIHES.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS med Oct. 23, 1945 Certificate of Correction Patent No. 2,535,919 December 26, 1950 FRANK HAPPEY ET AL.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows:
and that the said Letters Patent should be read as corrected above, so that the same may conform to the record of the case in the Patent Olfice. Signed and sealed this 13th day of February, A. D. 1951.
[SEAL] THOMAS F. MURPHY,
Assistant Commissioner 0f Patents.
Claims (1)
1. A PROCESS FOR THE MANUFACTURE OF NON-WOVEN FABRICS WHICH COMPRISES THE STEPS OF ACETYLATING UNSPUN CEULLULOSE FIBERS WHILE MAINTAINING THEIR FIBER STRUCTURE UNTIL THE ACETYL CONTENT OF THE FIBERS IS FROM ABOUT 8 TO ABOUT 40 PER CENT, CALCULATED AS THE PERCENTAGE OF ACETIC ACID ON THE FINAL WEIGHT OF THE FIBERS, FORMING A FIBROUS WEB OF UNSPUN FIBERS AT LEAST THE MAJOR PROPORTION OF WHICH CONSISTS OF THE UNSPUN, INCOMPLETELYACETYLATED CELLULOSE FIBERS SO OBTAINED, AND RENDERING ADHESIVE THE CELLULOSE TRIACETATE PHASE OF THE UNSPUN INCOMPLETELY-ACETYLATED CELLULOSE FIBERS WHEREBY THE FIBERS IN THE WEB ARE BONDED TOGETHER AT THEIR POINTS OF CONTACT TO FORM A UNIFIED FIBROUS STRUCTURE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB29702/47A GB638591A (en) | 1947-11-07 | 1947-11-07 | Improvements in and relating to the manufacture of sheets or webs of fibrous textilematerials |
Publications (1)
Publication Number | Publication Date |
---|---|
US2535919A true US2535919A (en) | 1950-12-26 |
Family
ID=10295754
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US54728A Expired - Lifetime US2535919A (en) | 1947-11-07 | 1948-10-15 | Manufacture of sheets of webs of fibrous textile materials |
Country Status (2)
Country | Link |
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US (1) | US2535919A (en) |
GB (1) | GB638591A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2772944A (en) * | 1953-03-27 | 1956-12-04 | American Viscose Corp | Process for the acetylation of regenerated cellulose fibers and product resulting therefrom |
WO2012007397A1 (en) | 2010-07-13 | 2012-01-19 | Centre National De La Recherche Scientifique (Cnrs) | Novel cellulose composite materials |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2252999A (en) * | 1937-05-24 | 1941-08-19 | Sylvania Ind Corp | Article and process for the manufacture thereof |
US2387354A (en) * | 1937-02-05 | 1945-10-23 | Kendall & Co | Textile fabric |
-
1947
- 1947-11-07 GB GB29702/47A patent/GB638591A/en not_active Expired
-
1948
- 1948-10-15 US US54728A patent/US2535919A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2387354A (en) * | 1937-02-05 | 1945-10-23 | Kendall & Co | Textile fabric |
US2252999A (en) * | 1937-05-24 | 1941-08-19 | Sylvania Ind Corp | Article and process for the manufacture thereof |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2772944A (en) * | 1953-03-27 | 1956-12-04 | American Viscose Corp | Process for the acetylation of regenerated cellulose fibers and product resulting therefrom |
WO2012007397A1 (en) | 2010-07-13 | 2012-01-19 | Centre National De La Recherche Scientifique (Cnrs) | Novel cellulose composite materials |
FR2962735A1 (en) * | 2010-07-13 | 2012-01-20 | Centre Nat Rech Scient | NEW COMPOSITE MATERIALS BASED ON CELLULOSE |
CN103097447A (en) * | 2010-07-13 | 2013-05-08 | 国家科学研究中心 | Novel cellulose composite materials |
US9193851B2 (en) | 2010-07-13 | 2015-11-24 | Centre National De La Recherche Scientifique | Cellulose-based composite materials |
CN103097447B (en) * | 2010-07-13 | 2016-02-17 | 国家科学研究中心 | Based on cellulosic matrix material |
Also Published As
Publication number | Publication date |
---|---|
GB638591A (en) | 1950-06-14 |
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