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Publication numberUS3193447 A
Publication typeGrant
Publication dateJul 6, 1965
Filing dateMar 8, 1962
Priority dateMar 15, 1961
Also published asDE1218871B
Publication numberUS 3193447 A, US 3193447A, US-A-3193447, US3193447 A, US3193447A
InventorsMarek Bruno Stefan Vladimir, Gneisz Josef
Original AssigneeSchweizerische Viscose
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Manufacture of paper-like materials comprising synthetic fibres
US 3193447 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 3,193,447 MANUFACTURE OF PAPER-LIKE MATERIALS COMPRISING SYNTHETIC FIBRES Bruno Stefan Viadimir March and Jasef Gneisz, Eminenbrucke, near Lucerne, Switzeriand, assignors to Societe de la Viscose Suisse, Emmenbrucke, near Lucerne, Switzerland, 2 Swiss body corporate No Drawing. Filed Mar. 8, 1962, Ser. No. 17 8,263 Claims priority, application Switzerland, Mar. 15, 1961, 3,133/61. 3 Qiaims. (Cl. 162-157) The present invention relates to the manufacture of paper-like materials comprising synthetic fibres.

The term paper-like materials as used herein denotes materials in sheet form such as can be manufactured by means known in the paper making art. In the manufacture of such materials the fibrous starting material must be homogeneously distributed in water. Where some or all of the fibres used are synthetic, then, since synthetic fibres are generally difiicult to wet, they may be given a coating of a dispersant in order to assist their distribution. A wide variety of compounds have been proposed as dispersants for synthetic fibres, for example cellulose ethers, partially hydrolysed polyvinyl acetate, polyethylene glycols, and also cationic and anionic compounds.

However, despite the use of dispersants a considerably difficulty involved in the manufacture of paper-like materials consisting of or containing synthetic fibres has been that in the preparation of the aqueous suspension synthetic fibres rapidly form coherent flocks; this has a disadvantageous effect on the formation of sheets. Furthermore, disturbing foaming may occur when unsuitable preparations are used.

An object of the present invention is to provide a dispersant for synthetic fibres which substantially reduces the difficulties heretofore involved in the preparation of aper-like materials comprising synthetic fibres.

A further object of the invention is to provide paperlike materials comprising synthetic fibres displaying a more even distribution of the fibres. Other objects will appear hereinafter.

It has now been found that improved dispersions of synthetic fibres having a reduced tendency to flocculate can be obtained by coating the fibres with a water-soluble N-ethoxylated polyamide. The present invention therefore provides a process for the production of paperlike material comprising synthetic fibres by forming the paper-like material from an aqueous suspension containing the synthetic fibres wherein the synthetic fibres have a coating of a Water-soluble N-ethoxylated polyamide.

The invention further comprises the paper-like materials so-produced which consist partially or wholly of synthetic fibres.

The degree of ethoxylation of the polyamide used as dispersant suitably corresponds to 8 to 12 mols of ethylene oxide per gram atom of nitrogen. Particularly suitable N-ethoxylated polyamides are N-ethoxylated polycaproamide and N-ethoxylated copolyamides obtainable from e-amino-caprolactam and hexamethylene diamine adipate, e.g., using 50 to 70%, especially 60%, of eamino-caprolactam and 50 to 30%, especially 40%, hexamethylene diamine adipate. These compounds dissolve in water readily, both insofar as the speed of solution and the maximum concentration of the solution are concerned.

To coat the synthetic fibres with the N-ethoxylated polyamide, they are preferably treated with an aqueous solution containing to grams of N-thoxylated polyamide per litre of water at a moderately raised temperature, e.g., to 50 C.

If it is not desired to use the resulting aqueous dispersion directly the fibres can then be removed from the dispersion and dried at room temperature or with the aid of heat, and later redispersed. I

The polymers from which the artificial fibres may be prepared include polyamides, for example polycaproamide, the polyamide of w-amino-undecanoic acid, polyhexamethylene adip-amide, polyhexamethylene sebacamide, and condensation products of dicarboxylic acids with aliphatic, alicyclic or aromatic diamines generally; polyurethanes; polyesters, e.g., polyethylene terephthalate and copolymers of terephthalic and isophthalic acids and ethylene glycol; polyvinyl acetate and c-opolymers of vinyl acetate, e.g., with vinyl chloride, vinylidene cyanide or acrylonitrile; polyacrylonitrile and copolymers of acrylonitrile, e.g., with vinyl chloride; and poly-tetrafiuoroethylene.

The synthetic fibres may be formed by melt, dry or wet spinning methods, as by extruding spinning compositions through spinnerets, or by precipitation from solutions.

The application of the N-ethoxylated polyamide to the synthetic fibres may be performed at any stage of their manufacture. The treatment of spun synthetic fibres with N-ethoxylated polyamides can be carried out during spinning, prior to the stretching operation, before or after cutting the filaments up into staple, or immediately prior to incorporation in the paper stock; If the synthetic fibres have previously been treated with other agents, it is in general possible to remove the latter (if desired) as by Washing with a warm dilute aqueous soda solution.

In the manufacture of the paper-like materials it is of particular importance to be able to vary the proportion of synthetic fibres in the mixture with other fibres (i.e., natural or modified natural fibres) within wide limits, because this makes it possible to manufacture papers having particular properties. This is readily achieved in the present invention. For example, synthetic fibres coated with N-ethoxylated polyamide as described above may be introduced into a suspension of cellulose fibres prepared in known manner, and from this mixture a sheet of adequate strength is produced in the wet state on a paper making machine. If in this method the cellulose component used is in the form ofso-called polynosic short staple fibres (see article in Reyon Zellwolle und andere Chemiefasern, 9, page 431 [1959]) or other viscose short staple fibres, it is possible to incorporate up to 70% by weight of polyamide or polyester fibres in the aqueous dispersion, from which a sheet having the corresponding content of synthetic fibres and having special properties can be made. With ground cellulose and rag cellulose, for example, paper-like materials containing up to by weight of synthetic fibres can be manufactured. A sheet produced in this manner is characterised by the even distribution of the fibres, as can be seen, for example, by looking through the finished paper. Papers made from fibre dispersions prepared with unsuitable dispersants display an uneven distribution of the fibres when inspected in transmitted light.

The invention is illustrated in the following examples, in which ratios and percentages given are by weight.

Example 1 The dispersing material used is an ethoxylated copolyamide from 60% of e-aminocaprolactam and 40% of hexamethylene diamine adipate containing 2.4% of nitrogen, which corresponds to a degree of ethoxylation of 10.5 mols of ethylene oxide per gram atom of nitrogen. The compound is soluble in water to an extent of 25 to 30%, and a 2% aqueous solution has at 20 C.

, being introduced into water.

It softens at135 C. and

Nylon short staple fibres 3 denier/ 6 mm. long were first V freed from dressing by being washed with water containing soda and then centrifuged. They were then treated with an aqueous solution of the dispersing material. From .part, ofthe dispersion so obtained the fibres were removed and then dried for 2 hours at 65 C. In both cases the fibres were very easily wetted by water, as revealed by the speed at which the fibres settled down on When the suspension was thoroughly stirred, very even suspensions substantially fast to flocculation were obtained.

These tests were repeated using polyester short staple fibres 1.5 denier/4 mm. long. Similar results were obtained.

Example 2 The dispersing material used was an N-ethoxylated polycaproamide which contained 2.68% of nitrogen, corresponding to a degree of ethoxylation of 9 mols of ethylene oxide per gram atom of nitrogen. A 2% aqueous solution of the product has a viscosity of 1.6 centipoises at C. The product melts at 151 C. After this N-ethoxylated polycaproamide has been absorbed on the fibres referred toin Example 1 in the manner described above, they are easy to moisten and are homogeneously distributed in water, that is to say their behaviour is identical with that of the fibres pretreated with the N- ethoxylated copolyamide described in Example '1.

Example 3 The fibres used in this example were-not melt spun through spinnerets but precipitated, being moist polyester fibrids '(product of E. I. du Pont de Nemours and Co.) Type 201, as described for instance in French specification No. 1,214,126, corresponding to 100 grams of' dry substance, are stirred for 40 minutes at C. in 10 times their own weight of a 2% solution of N-ethoxylated caproamide, as described in Example 2, then suctionfiltered and dried for 48 hours at room temperature over phosphorus pentoxide. In an identical manner 100 grams of dry substance of the above fibrids are treated'with water only and then dried.

After having been thoroughly dried for 48 hours and then moistened with water the fibrids treated with N- ethoxylated caproamide could be dispersed homogeneously within a short time. The fibrids treated with water only, on the other hand, are diflicult to moisten with water, and they require a much longer mechanical treatment in water to achieve their homogeneous distribution.

From the dispersions of each batch in water sheets weighing about 100 grams per square metre were made on a sheet making machine. The sheet made from the pretreated fibrids has a better water retention capacity than the sheet made from fibrids not pretreated with N- ethoxylated polyamide,

Example 4 wise, 0.48 kg. (40%) of viscose short'staple fibres 1.5

denier/4 mm. long are added, and the whole is stirred for 10 minutes. There are then further added 100 litres Of water and at the same time, while stirring vigorously,

0.36 kg. (30%) of polyamide fibres 3 denier/6 mm. long which have been treated with 10 grams per litre of the N-ethoxylated copolyamide described in Example 1 at a goods-to-liquor ratio of 1:20 for 30 minutes at 40 C., then centrifuged and finally dried at -105 C. From this stable suspension a sheet is made on aFourdrinier machine having a fourdrinier'wire 40 cm. wide. After drying, this sheet material can be impregnated with resins on a padder, then dried, pressed and calendered between metal rolls and paper rolls at ISO-180 C. The papers manufactured in this manner have excellent properties and in them the fibres are evenly distributed, as can be seen on inspection in transmitted light.

Example 5 660 grams of aspen sulphite cellulose and 180 grams of fibrillated rag cellulose are thoroughly beaten in litres of water in a stufi blending chest, and 360 grams of polyhexamethylene adipamide fibres (2 denier/4 mm. long) are stirred portionwise into the fibre suspension. Before being mixed with the cellulose pulp the polyamide fibres are treated for 30 minutes at 45 C. with a solution containing per litre 10 grams of an ethoxylated polycaproamide (degree of ethox-ylation: 9 moles of ethylene oxide per gram atom nitrogen), then centrifuged and dried in air. The mixture in the stock blending chest is made up to 200, litres, and the fibre suspension (stutt density of 0.2 to 0.3%) is processed on a Fourdrinier machine having a fourdrinier ,wire '40 cm. wide into a uniform, paper-like sheet. When viewed in transmitted light the paper has a much better appearance than similar paper made with polyamide fibres treated with conventional dispersants. On the Fourdrinier-machine no disturbing foaming is observed nor does sticking at the wet end or in the fourdrinier section occur.

We claim: I 1. In a process for the production of a paper-like material comprising synthetic fibers, in which process a uniform suspension of said fibers in water is formed into a sheet,,the improvement which comprises a step of coating said fibers with a solution consisting of water and N-ethoxylated polyamide, which N-ethoxylated .polyamide has a degree of ethoxylation corresponding to 8 to 12 mols of ethylene oxide per gram atom of nitrogen,

prior to the formation of said sheet. i

2. A process in accordance with claim 1 in which the fibers include fibers selected from the group consisting of natural polymeric fibers and modified natural polymeric fibers.

3. A process in accordance with claim 1 in which the N-ethoxylated polyamide is the N-ethoxylated copolyamide of e-aminocaprolactam and hexamethylene diamine adipate.

References Cited by the Examiner UNITED STATES PATENTS 2,467,186 4/49 Cairns 26029.2 2,810,645 10/57 Houghton 1624-157 2,844,491 7/58 Hubbard. 2,869,435 1/59 Sands 162l57 FOREIGN PATENTS 602,822 8/60 Canada. 847,617 9/60 Great Britain.

DONALL H. SYLVESTER, Primary Examiner. MORRIS O. WOLK, Examiner.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2467186 *Apr 20, 1945Apr 12, 1949Du PontAqueous dispersions of synthetic linear polyamide and process for obtaining same
US2810645 *Feb 9, 1950Oct 22, 1957American Viscose CorpMethod of making textile webs
US2844491 *Apr 29, 1955Jul 22, 1958Du PontPaper-like pellicle and method for producing same
US2869435 *Jan 3, 1956Jan 20, 1959Du PontProcess and product
CA602822A *Aug 2, 1960Portals LtdMethods of making webs of fibrous material
GB847617A * Title not available
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4392861 *Oct 14, 1980Jul 12, 1983Johnson & Johnson Baby Products CompanyTwo-ply fibrous facing material
Classifications
U.S. Classification162/157.3, 162/164.6, 162/146
Cooperative ClassificationD21H13/26, D21H5/1254, D21H17/55
European ClassificationD21H13/26, D21H17/55, D21H5/12M