US2238839A - Crease-resisting treatment of textile materials - Google Patents

Crease-resisting treatment of textile materials Download PDF

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Publication number
US2238839A
US2238839A US285625A US28562539A US2238839A US 2238839 A US2238839 A US 2238839A US 285625 A US285625 A US 285625A US 28562539 A US28562539 A US 28562539A US 2238839 A US2238839 A US 2238839A
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fabric
fibres
substances
reinforcement
crease
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Watkins William
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
    • D06M15/11Starch or derivatives thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating 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
    • D06M13/12Aldehydes; Ketones
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/15Proteins or derivatives thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins

Definitions

  • This invention relates to the finishing of textile fabrics for the purpose of imparting creaseresistant and crease-recovery properties thereto (as for example in the case of fabrics of cotton and artificial silks, which have little or none of such properties naturally), or for the purpose of improving the natural crease-resistant and crease-recovery properties thereof (as for example in the case of fabrics of silk and wool) without in either case depriving the materials of their natural suppleness or softness.
  • Fabrics are considered crease-resistant when they may be crushed or folded under pressure as by being crumbled in the hand, without having a permanent crease imparted to them, and are considered to have crease-recovery properties when, after being marked by crushing or crumpling, they recover from such marking;
  • the principal object of the present invention is to provide a process or processes of finishing textile fabrics, for the purpose set forth, which is or are entirely free from the drawbacks and limitations of the said previous proposals in that (a) much smaller quantities of reinforcing substances may be used (although the invention is in no way restricted to the use of small quantities) and the fine molecular division of the applied bodies is not a necessity, since it is immaterial whether the reinforcing substances are substantially within the fibres or merely coat them, or do both; (b) in which fillers or loadings may be used with the reinforcing substances, if
  • a furtherobject of the invention is to render the reinforcing substances, when of a hygroscopic nature, less or non-hygroscopic, and thus lessen or entirely obviate the tendency of the anti-crease finish to diminish during the passage of time, and also permit the use of a wider range of reinforcing substances.
  • the present invention is based upon the realisation that the essential requirement'in a creaseresistant or crease-recovery fabric is that the fibres should be individually reinforced to the correct degree, and that they should not adhere together, but should be as free from each other as in any ordinary untreated fabric, so that relative movement may take place between them when the fabrics are subjected to distortion, and so that the separated reinforced fibres may be free to accommodate themselves to new relative positions without losing their imparted springiness and permanent set. Given. such requirement, it appears to be a matter of little or no importance whether the reinforcing substances are impregnated within, or are substantially between the fibres or are in both such dispositions.
  • the present invention consists in applying to the fabrics in the form of a solution or dispersion reinforcement-forming substances of an aldehyde-hardenable nature selected from the group consisting of animal and vegetable filmforming substances and synthetic-resin-forming substances, in drying the fabrics after the application of such substances, in mechanically working the fabrics to unstick the constituent fibres from each other, and in heat treating the fabrics in the presence of an, aldehyde and an accelerator, the heat treatment being such as to harden the reinforcement-forming substance sufficiently to give the fabrics crease-resistant properties.
  • an aldehyde-hardenable nature selected from the group consisting of animal and vegetable filmforming substances and synthetic-resin-forming substances
  • the fabrics will be dried after the application of the reinforcement-forming substances, and before the mechanical treatment is carried'out on the fabric.
  • the mechanical treatment may be carried out during the drying and/or hardening treatments.
  • the mechanical treatment is done after the fabrics are dried and before the reinforcement-forming-substa1uces are hardened, and in such cases the fabrics require to be kept dry, in order to prevent the fibres re-- sticking together, as might be the case where the unhardened substances are soluble in water.
  • dry in this connection means normally dry, 1. e. the state of dryness which would subsist in a normal atmosphere.
  • reinforcement-forming sub- By the term reinforcement-forming sub- 'to impart to the fabrics a more vigorous individual fibres, and which can then be hardened by chemical treatment to a degree sufiicient a springiness or temper, the effect of which on the fabric be described as an anti-crease effect, according to the standards now adopted. Those dispersions or other forms of substance which on evaporation leave a granular or non-continuous deposit incapable of imparting the required springiness or temper, are not intended to be included in the term reinforcement-forming substances.
  • solutions or dispersions of the reinforcement-forming substances are frequently of a viscous consistency, more of a paste than a liquid,
  • aldehyde-hardenable reinforcement-forming-substance means a substance as defined in the last preceding paragraphs and which may be hardened by heat-treatment'in the presence of formaldehyde, paraform-aldehyde or an analogous or homologous aldehyde.
  • the reinforcement-forming substances will be of an adhesive or film-forming nature and may include such widely diverse substances as casein, albumen, starches, modified starches, dextrine,
  • animal glues and gelatines animal glues and gelatines, vegetable gelatines (such as those obtained from sea-weed), locustbean gum, gum arabic and like gums, algin, and metallic salts of alginic acid, and some of the synthetic resin-forming substances, all of which have the property of being hardened by heattreatment in the presence of an aldehyde, to form reinforcements to the extent required for an anti-crease effect.
  • Some'oi the reinforcementforming substances named are more efiective than others.
  • mechanical treatment is intended to include any mechanical or manual treatment which will separate (unstlck or prevent sticking together of) the individual fibres to which the reinforcement-forming sub stances have been applied, and does not include such processes as boiling or soaping off or other chemical treatment.
  • the fabrics will in .most cases require to be treated both in a warpwise and weftwise direction at least.
  • One method of mechanical treatment contemplated by this invention, and applicable to the treatment of fabrics according to all the following examples is the passing of the fabric under and over breaker bars and through a cold nip on a mangle several times, the treatment being carried out to a sufficient degree of intensity and a sufficient number of times to separate the individual fibres, A
  • .stentering process or the use of cxpanders may be included to give a weftwise treatment, especially if the fabrics havebeen dried narrow.
  • a manual treatment by crumpling and scrubbing together severely would have the desired result.
  • aration in that it is not to be a separation by complete removal of the fibres out of contact with each other, as bytearing apart, but is to be merely an avoidance of or elimination of adhesion together.
  • the basis of the invention is that the fibres, having had their springiness increased by the hardened'applied substances, are to be free to move relatively to each other; and a mechanical treatment during drying or hardening which would prevent sticking of the fibres together would serve the purpose also.
  • the primary object of the mechanical treatment is to unstick the fibres and thus make their relative movement possible.
  • the term hardening connotes a reaction which increases the hardness of the applied reinforcement-forming substances to such a degree that the treated fibres are rendered sufficiently springy to impart an anti-crease effect to the fabric. It has been found that the degree of hardening required is such that if applied to the reinforcement-forming substances alone, i. e., when not on or in textile fibres, it will make the resultant substance hard and brittle, i. e. glasslike. When the. reinforcement-forming substances are hardened to this extent, on or in the fibres of a fabric, the natural plasticity ofthe fibres modifies the brittleness of the reinforce- I ment, and the hardening process then results, in
  • the fibres have been separated, care will be taken to prevent any re-sticking of them by dissolving of the reinforcement-forming substances during the ageing period. Further, in some cases the hardening process will be carried out under pressure, if the required degree of hardness is not obtainable otherwise; This will be especially so with the natural substances such as casein, starch etc., where the anti-hygroscopic bodies referred to below are not added to the reinforcement.
  • the aldehyde which is to take part in the hardening process may be applied to the fabric,
  • the fabric may be passed through an aldehyde both first of all before having the reinforcement-forming substance applied to it, and in such event as well as when the reinforcement-forming substance and the aldehyde are applied simultaneously, the fabric may be allowed to steep in the bath for several hours, as this improves the result obtained.
  • aldehyde for example paraformaldehyde
  • Paraformaildehyde powder may be placed in the enclosed chamber in which the hardening is to be effected, the powder volatilising under the influence of heat and thereby obtaining contact with the treated fabrics;
  • the paraformaldehyde powder may be dusted on to the fabrics in known manner, say prior to their being placed in the pressure chamber, and the heat and pressure applied as in the previous case:
  • the paraformaldehyde may be dispersed in a viscous, inert, non-alkaline solution and padded on ma back-cloth, the back-cloth then being dried at a low temperature (say 40-50 C.) to prevent premature volatilisation and the treated fabric and back-cloth be rolled up together in batch form and placed in the heating chamber, the
  • the fabric After having been sprayed, the fabric is allowed to sand a little while to allow the solution to distribute itself evenly in the fabric, and the fabric is then placed in the heating chamber as usual: (e) Where the padding solution or paste containing the reinforcement-forming substances is sufilciently viscous to hold the paraformaldehyde in suspension, the paraformaldehyde may be dispersed in such padding solution or paste. In this case, the drying of the padded material will be carried out carefully so as not to vapourlse the paraiormaldehyde prematurely. In this method of application, no free alkali is allowed to be present as it would cause the paraformaldehyde to go into solution, with apparent alteration of its properties, since it wouldnot then do its hardening work so effectively.
  • Accelerators suitable for use in the hardening reaction are acid salts such as potassium tetroxalate, sodium bisulphate and alumina sulphate; acid-liberating salts such as ammonium salts of organic and of inorganic acids (e. g. ammoniuml oxalate, ammonium chloride and ammonium phosphate); and some weak acids, such as tartaric, acetic, and oxalic acid.
  • Other accelerators which may be employed are ammonium dihydrogen phosphate; and small amounts of urea mixed with ammonium chloride or with alumina sulphate or with formic acid.
  • the hardening treatment with paraformalldehyde or the like is carried out at an elevated temperature, either at atmospheric pressure, as for instance in an open oven, or at a superatmospheric pressure in a closed chamber. A mechanical pressure would not be used, as that would tend to stick the fibres together again.
  • synthetic resins are to be the reinforcing-substances the whole of the reaction between the resin-forming materials, may be completed in one stage.
  • the improved process presents at least three outstanding advantages over the prior proposals referred to above, in which the resins had to be substantially within and not between the fibres. Firstly, the quantity of resins necessary is much less than is required in the prior art; secondly, it is not necessary to condense the resins to an intermediate stage before their application to the textile materials; and thirdly, loading or filling materials may be added to the resins in quantities sufficient to give loaded or filled effects without detriment to the anti-crease result. Examples of loadings or fillers which may be added with the synthetic resins are French chalk, alumina salts, gum substances, starches,
  • the gum substances are especially beneficial as they overcome or counteract any harshness or dryness of feel which may otherwise be imparted to the fabric by the resins. It is a Wellknown fact that, weight for weight, a tube of material is, within certain limits. more resistant to bending than-is a rod. Since, by this invention, the reinforcing substances may be coated on the fibres in the form of a sheath or tube, as would be the case with such substances as starches, which do not readily penetrate the fibres.
  • the present invention gives a more eflicieiit and, in consequence, lose their reinforcing properties too rapidly, have their hygroscopy removed or counter-acted by the admixture with them or the formation among them of suitable nonhygroscopic bodies, such as those of the synthetic resins which do not interfere with the hardening process.
  • This step is not always required; for instance, when voiles or like fabrics dyed with aniline black are being treated, the very inert,
  • aniline pigment may itself be sufficient to counter-act the hygroscopic nature of the reinforcing substances.
  • those of the reinforcement-forming substances which are natural products, as distinct from the syntheticproducts will be hygroscopiceven after hardening and will therefore require to have the anti-hygroscopic substances added to them (unless these are already present in suflicient amounts in the fabrics) when more permanent results are. desired.
  • the condensation or polymerization of the synthetic resins (when used) to counteract hygroscopy may be effected by a process which will also harden the reinforcement-forming, substances, namely by heat-treatment with an aidehyde, the resin-forming bodies may be mixed with the reinforcement-forming substances, the
  • the reinforcing substance is other than casein
  • such substance is dissolved or dispersed in water to a concentration of say avoiding the presence of alkalies, and a quantity of an aldehydesubstance, such as formaldehyde, is added to the solution or dispersion.
  • the fabric is first impregnated with the solution or dis- 'persion and afterwardsnipped off on a "mangle solution or dispersion.
  • the fabric is next dried thoroughly, at about 110 C., and is then broken down, for example by being passed over and under knife-edged bars and through a cold nip on a mangle (Whilst still dry) to a degree.
  • casein When casein is to be employed as the reinforcing substance, variations in the above procedure are required.
  • the fabric is first impregnated with EXAMPLE1.Reinforcement formed from casein
  • the fabric is first impregnated with a 3% to 5% aqueous solution of casein, the casein having been brought into solution with the aid of ammonia, and is then dried and afterwards broken down to separate the fibres from each other.
  • the fabric is impregnated with the following:
  • Formalin (commercial 40%) cubic centimeters 30 The total being made to 100 ccs. with water.
  • the fabric was allowed to remain in this mixture for two hours, at the end of which time it was removed from the bath, nipped off in a mangle, and dried thoroughly at C., and then subjected to a second breaking down treatment to separate the fibres from each other again. After being conditioned to an 8% moisture content (or thereabouts) the fabric was heated for 30 minutes at a temperature of 130 C.
  • the heat-treatment may be carried out at atmospheric or superatmospheric pressure as desired.
  • the resin formed from the syrup acts as a protector for the casein, to present hygroscopy in the finished article, the quantity of resin used being much too little to be of itself a reinforcement for the fibres of the fabric.
  • Other protectors which maybe used with casein for a like purpose are, resorcin and lime, phthalic acid resins, and like substances which will harden to the required degree.
  • EXAMPLE 4 Reinforcement formed from albumen The fabric was impregnated in the following for two hours, and the process then continued as in Example 3.
  • EXAMPLE 7 --Reinfcrcement formed of resin The following mixture was padded on to the fabric and the fabric then dried at 110 C., and the process then continued as in Example 3.
  • Resin syrup commercial cubic centimeters' Formalin (40%) do 10 -Tartaric acid grarn 1 Bulked to 100.ccs. with water.
  • Formalin (40%) -cubic centimeters-.. 25 Water solution of a commercial resinsyrup containing 0.66 grm. urea and 0.66 grm. thio urea, already converted to an intermediate stage of concentration ccs- Bulked to ccs. with water.
  • gums or fillers can be used, and also where a waterproof effect is desired at the same time this can be obtained by the addition of acetate of alumina.
  • the processes constituting this invention may be applied to textile fabrics which have passed through the usual so-called finishing processes (dyeing, lustring, mercerlsing, etc.) or to unfinished or semi-finished materials, and in some cases may be incorporated with the usual finishlng processes.
  • the process of imparting crease-resistant properties to textile material which includes loading the fibres of the material with an encasing of aldehyde-hardenable organic reinforcement-forming substance, drying the, material after the application of the aldehyde-hardenable substance to form a coating around the constituent fibers, then subjecting the material while still dry to mechanical treatment without breaking the coating of the fibres to render the fibres in a state of non-adhesion to each other, incorporating an aldehyde capable of reacting with the aldehyde-hardenable reinforcement-forming substance to harden the same, and hardening the reinforcing substance by heat under superatmospheric pressure to a degree sufficient to give the material crease-resistant properties.
  • aldehyde-hardenable substance is a synthetic urea formaldehyde type resin-forming substance.
  • a process for imparting crease-resistant properties to textile fabric which includes applying to the fabric a liquid medium containing an. aldehyde-hardenable film-forming organic reinforcement substance, drying the fabric to deposit such substance as a coating around the constituent fibers, mechanically working the fabric to unstick the constituent fibers from each constituent fibers, mechanically working the fabric to unstick the constituent fibers from each other without breaking the reinforcement coating carried by the individualfibers, and heat treating the fabric under super-atmospheric pressure in contact with an aldehyde and an accelerator, the heat treatment being such as to harden the reinforcement-forming substances sufflciently to give the fabric crease-resistant properties.
  • the hardenable substance is an albuminous sub!- stance, and in which there is included with said albuminous substance, synthetic urea formaldehyde type resin forming materials and forming the resin during and by the heat treatment which forms the reinforcement.
  • a process for rendering textile fabric crease-resistant which includes first padding onto the fabric to an expression of from to a 5% dispersion in water of an albuminous substance, next in drying the fabric at about C. to form a coating around the constituent fibers, then in conditioning the fabric to about 8% moisture content, next in mechanically treating the fabric by passing it several times through a breaking machine and through a cold m'p on a. mangle to unstick the fibers, and finally in heat-treating the fabric in contact with an aldehyde at a temperature of about C., for 30 minutes.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
US285625A 1935-08-17 1939-07-20 Crease-resisting treatment of textile materials Expired - Lifetime US2238839A (en)

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GB23129/35A GB465875A (en) 1935-08-17 1935-08-17 Improvements in or relating to the finishing of textile fabrics

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US (1) US2238839A (de)
BE (1) BE420669A (de)
FR (1) FR829828A (de)
GB (2) GB465939A (de)
NL (1) NL54409C (de)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2417389A (en) * 1944-12-26 1947-03-11 Chemical Lab Inc Treatment of sericeous fibers
US2486399A (en) * 1947-10-28 1949-11-01 Dan River Mills Inc Polymeric polyhydric alcohol condensation products and treatment of cellulosic textiles therewith
US2512195A (en) * 1939-03-04 1950-06-20 Bener Christian Method of waterproofing cellulose textiles
US2661312A (en) * 1951-06-14 1953-12-01 Du Pont Textile finishing composition and method of treating textile materials therewith
US2899263A (en) * 1949-08-15 1959-08-11 Eneurea
US2978359A (en) * 1954-12-22 1961-04-04 Bohme Fettchemie Gmbh Preparation of hardenable water soluble condensation products and finishing of textile fabrics therewith
US3066996A (en) * 1955-09-06 1962-12-04 Ohio Commw Eng Co Process and composition for stabilizing and vat dyeing regenerated cellulose textiles employing formaldehyde and water-soluble dextran
US3265463A (en) * 1961-11-17 1966-08-09 Burlington Industries Inc Continuous method of imparting wet and dry crease resistance to cellulosic materials through reaction with formaldehyde
US3275402A (en) * 1958-12-24 1966-09-27 Courtaulds Ltd Formaldehyde modification of cellulose conducted in the presence of a stiffening agent and a lewis acid metallic salt
US3276885A (en) * 1962-04-05 1966-10-04 Nobel Bozel Permanent finishes for cellulosic articles
US3285775A (en) * 1965-06-14 1966-11-15 United Shoe Machinery Corp Penetration of collagen fibers through inclusion of protective colloid
US3351479A (en) * 1963-05-14 1967-11-07 Kelco Co Paper coating compositions and processes
CN112111976A (zh) * 2019-06-20 2020-12-22 浙江昶丰新材料有限公司 一种水性聚氨酯超细纤维合成革及其制备方法
CN117127403A (zh) * 2023-09-01 2023-11-28 佛山市智城汇纺织科技有限公司 一种抗皱针织面料的生产工艺

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021251917A1 (en) * 2020-06-12 2021-12-16 Ug Tekstil Tasarim Arge Uretim Ith. Ihr. Paz. San. Ve Tic. Ltd. Sti. Peice dyeing and drying technique of textile products by means of an ecological process in a single machine

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2512195A (en) * 1939-03-04 1950-06-20 Bener Christian Method of waterproofing cellulose textiles
US2417389A (en) * 1944-12-26 1947-03-11 Chemical Lab Inc Treatment of sericeous fibers
US2486399A (en) * 1947-10-28 1949-11-01 Dan River Mills Inc Polymeric polyhydric alcohol condensation products and treatment of cellulosic textiles therewith
US2899263A (en) * 1949-08-15 1959-08-11 Eneurea
US2661312A (en) * 1951-06-14 1953-12-01 Du Pont Textile finishing composition and method of treating textile materials therewith
US2978359A (en) * 1954-12-22 1961-04-04 Bohme Fettchemie Gmbh Preparation of hardenable water soluble condensation products and finishing of textile fabrics therewith
US3066996A (en) * 1955-09-06 1962-12-04 Ohio Commw Eng Co Process and composition for stabilizing and vat dyeing regenerated cellulose textiles employing formaldehyde and water-soluble dextran
US3275402A (en) * 1958-12-24 1966-09-27 Courtaulds Ltd Formaldehyde modification of cellulose conducted in the presence of a stiffening agent and a lewis acid metallic salt
US3265463A (en) * 1961-11-17 1966-08-09 Burlington Industries Inc Continuous method of imparting wet and dry crease resistance to cellulosic materials through reaction with formaldehyde
US3276885A (en) * 1962-04-05 1966-10-04 Nobel Bozel Permanent finishes for cellulosic articles
US3351479A (en) * 1963-05-14 1967-11-07 Kelco Co Paper coating compositions and processes
US3285775A (en) * 1965-06-14 1966-11-15 United Shoe Machinery Corp Penetration of collagen fibers through inclusion of protective colloid
CN112111976A (zh) * 2019-06-20 2020-12-22 浙江昶丰新材料有限公司 一种水性聚氨酯超细纤维合成革及其制备方法
CN112111976B (zh) * 2019-06-20 2024-02-06 浙江昶丰新材料有限公司 一种水性聚氨酯超细纤维合成革及其制备方法
CN117127403A (zh) * 2023-09-01 2023-11-28 佛山市智城汇纺织科技有限公司 一种抗皱针织面料的生产工艺
CN117127403B (zh) * 2023-09-01 2024-02-02 佛山市智城汇纺织科技有限公司 一种抗皱针织面料的生产工艺

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FR829828A (fr) 1938-07-06
GB465939A (en) 1937-05-18
BE420669A (de) 1937-04-30
NL54409C (de) 1943-05-15
GB465875A (en) 1937-05-18

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