US3038777A - Process for improving the properties of regenerated cellulose fibrous material - Google Patents

Process for improving the properties of regenerated cellulose fibrous material Download PDF

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US3038777A
US3038777A US819465A US81946559A US3038777A US 3038777 A US3038777 A US 3038777A US 819465 A US819465 A US 819465A US 81946559 A US81946559 A US 81946559A US 3038777 A US3038777 A US 3038777A
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fiber
cross
fibers
linking
cellulose
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George C Daul
Harold F Wise
Wharton John
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Courtaulds North America Inc
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Courtaulds North America Inc
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Priority to US819465A priority patent/US3038777A/en
Priority to GB20258/60A priority patent/GB950073A/en
Priority to FR829668A priority patent/FR1266007A/fr
Priority to CH667560A priority patent/CH393624A/de
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    • 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
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423—Amino-aldehyde resins
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/02—Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins
    • 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
    • D06M13/12—Aldehydes; Ketones
    • 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
    • D06M13/244—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 sulfur or phosphorus
    • D06M13/248—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 sulfur or phosphorus with compounds containing sulfur
    • D06M13/272—Unsaturated compounds containing sulfur atoms
    • D06M13/278—Vinylsulfonium compounds; Vinylsulfone or vinylsulfoxide compounds
    • 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
    • D06M13/322—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 nitrogen
    • D06M13/487—Aziridinylphosphines; Aziridinylphosphine-oxides or sulfides; Carbonylaziridinyl or carbonylbisaziridinyl compounds; Sulfonylaziridinyl or sulfonylbisaziridinyl compounds
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/02—Vinyl sulfones and precursors thereof

Definitions

  • the purpose of treating regenerated cellulose fibers with heat hardenable resinous materials is in general to improve the properties of the fiber, particularly by decreasing its water imbibition. This is accomplished by a cross-linking of the cellulose chains through the resin or resin derived groups.
  • these compounds are characterized in having two or more functional groups which are reactive with the hydroxyl groups of the cellulose and in remaining water-soluble when dried and heated to the temperatures required to eliect cross-linking of the cellulose.
  • the present invention therefore comprises a method for impregnating regenerated cellulose fibrous material with a permanently soluble cross-linking agent, which com- 3,038,777 Patented June 12, 1962 prises treating the fibrous material while it is still in the gel state and before it has ever been dried sulficiently to convert it from the gel state, with an aqueous liquid containing a permanently soluble material and then mechanically reducing the liquid content of the treated fiber to less than the normal water imbibition of the fiber in the gel state.
  • a permanently soluble cross-linking agent which com- 3,038,777 Patented June 12, 1962 prises treating the fibrous material while it is still in the gel state and before it has ever been dried sulficiently to convert it from the gel state
  • the impregnated fiber is normally dried and heated at a suitable temperature to elfect reaction of the cross-linking agent with the cellulose chains.
  • the term permanently soluble cross-linking agent means a compound which will react with the hydroxyl groups of the cellulose to link two cellulose chain together. It must therefore be polyfunctional, i.e. it must contain at least two functional groups or two labile atoms in the same functional group which will react with the cellulose hydroxy groups. It may be monomeric or polymeric, and it may or may not undergo polymerization under the conditions required for the crosslinking reaction, but if it is a polymer or if polymerization does occur concurrently with or prior to cross-linking, the resulting polymer, though it may be a solid, will normally be linear, rather than three dimensional, and remain water-soluble.
  • Crosslinking agents of the type described are well known in the industry. Many of them are presently used to make so-called wash and wear garments, and in other finishing processes. They include, for example, formaldehyde, dialdehydes such as glutaraldehyde and adipaldehyde; hydroxy aldehydes such as hydroxy adipaldehyde; mixed aldehydes such as acrolein; glycidyl aldehydes; polyacetals (including diacetals) of polyhydroxy compounds, for example, the products described in Patent No.
  • 2,786,081 which have been defined as polymeric acetal condensation products of at least one dialkylene glycol in which the alkylene radical has 2 to 4 carbon atoms in a straigth chain and at least one aliphatic monoaldehyde containing 1 to 8 carbon atoms, said condensation products containing, per molecule, at least two dioxyalkylene radicals derived from said dialkylene glycol and at least two alkylidene radicals derived from said aldehyde; divinyl sulfone; dihalohydrins, for example, dichlorohydrin; and diand tri-aziridinyl phosphine oxides and sulfides such as are described in Patent No. 2,859,134.
  • reactant type resins are heat hardenable resinous materials, but under the conditions required for cross-linking remain water soluble. They include, for example, modified urea resins, i.e. methylol compounds such as methylated methylol urea, methylated and unmethylated methylol ethylene ureas, such as dimethylol ethylene urea, and methylated and unmethylated methylol l,2-propylene ureas as well as dimethylol triazines, triazones and the like.
  • modified urea resins i.e. methylol compounds such as methylated methylol urea, methylated and unmethylated methylol ethylene ureas, such as dimethylol ethylene urea, and methylated and unmethylated methylol l,2-propylene ureas as well as dimethylol triazines, triazones and the like.
  • cross-linking agent may be used. It will be understood that the precise structure of the cross-linking agent is not a part of the present invention, so long as it remains soluble under the conditions required to elfect cross-linking of cellulose chains.
  • the regenerated cellulose fibrous material is treated with the cross-linking agent while the fiber is still in the initial gel or swollen state after its formation. It has been discovered that in this initial gel or swollen state, fibers have their highest degree of absorptive power, much higher than at any other time in their existence. Furthermore, it has been found that by reducing the liquid content of the fibers to below their normal water imbibition value in the gel state, there is in effect created a kind of negative pressure inside the fibers. If the fibers have been previously immersed in or contacted with a solution containing a cross-linking agent, they draw the liquid remaining on the fibers after squeezing, evenly into the interior of the fibers.
  • the absorptive power of regenerated cellulose fiber is measured by what is known in the industry as the water imbibition value which is defined as the percent by weight of water retained in saturated material after centrifuging a 0.5 gm. sample for five minutes at 1,000 G and is expressed as percent of the oven-dry weight of the fiber (see Journal of the Society of Dyers and Colorists, October 1948, page 331).
  • the water imbibition values for once dried normal textile rayon fibers are in the range of 90% to 115%.
  • fabrics made from such fibers are treated in the usual fashion with cross-linking agents for effects such as crease resistance and dimensional stability, even with the high mangle pressures used in conventional equipment, liquid retention of the padded fabric is in this approximate range.
  • the water imbibition values of never-dried normal textile rayon fibers are in the range of 120% to 150%. It has been found that by squeezing never-dried rayon fiber while still in the gel state it is possible to reduce the moisture content of this material much below the water imbibition range cited.
  • fibers having a gel Water imbibition value of 145% may be squeezed to contain as little as 60% moisture on the oven-dry weight of the fiber.
  • a cross-linking solution acts like a sponge which has newly been squeezed out and evenly draws in the excess liquid.
  • the invention is applicable to regenerated cellulose made by any of the conventional techniques, i.e. by the viscose, cuprammonium or nitrate processes. However, it is preferred to use regenerated cellulose which has been made by the viscose process.
  • the invention is applicable to all forms of fibrous regenerated cellulose, to both staple and continuous filament fibers. However, it is of particular importance in the treatment of staple fibers.
  • the cross-linking agent is preferably applied as an aqueous solution containing from about 0.5 to about 20% by weight of the cross-linking agent.
  • concentration of agent used will depend on the nature of the agent. In general it will vary inversely with the molecular Weight of the agent. Thus for a material such as formaldehyde a concentration of say 0.5 to will be sufiicient whereas for agents of higher molecular weight, such as dimethylol ethylene urea or glycol acetal, concentrations of say 3 to would normally be used.
  • concentrations of say 3 to would normally be used.
  • In order to insure penetration of the agent into the interior of the fiber its molecular weight should not normally be more than about 1000. Obviously there is no minimum molecular weight.
  • Formaldehyde with a molecular weight of The lower the water imbibition, the
  • the impregnating solution may contain various ingredients other than the cross-linking agent.
  • it may contain from 2 to 150% on the weight of the agent of a catalyst to aid in carrying out the cross-linking reaction.
  • the type of catalyst used will depend on the particular cross-linking agent.
  • the catalyst does not have to be put into the same bath as the cross-linking agent.
  • the cross-linking reaction with certain agents such as divinylsulfone and the chlorohydrins is catalysed by alkali.
  • the fiber may advantageously be first impregnated with the agent, then squeezed to below its water imbibition and then subjected to a second bath containing the alkali, followed by another squeeze to reduce the liquid content to below the water imbibition Value.
  • the alkali may be applied before the cross-linking agent.
  • the impregnating liquid may contain from 0.1% to 4% on the weight of the liquid of a finishing agent.
  • the finishing agent may be selected to add lubricity, cohesion, water repellancy, scroop or other desired properties to the fiber.
  • Materials well-known to the art such as polyglycol stearate, lauryl ketene dimer, silicone emulsions, stearamido methyl pyridinium chloride, octadecyl pyridinium sulfate and others may be used alone or in combination for this purpose.
  • the temperature of the impregnating solution is not a critical factor and will vary with the particular crosslinking agent being applied. Normally, it will be between about 15 C. and about 50 C., preferably between about 20 C. and about 40 C.
  • the manipulative steps which are used in carrying out the invention depend to a certain extent upon the form of the fibrous material which is being treated.
  • a different mechanical technique would be used in applying a cross-linking solution for a continuous filament than would be used in treating staple fiber.
  • Staple fiber is in general treated in the form of a mat or blanket in which the fiber is arranged more or less at random.
  • the thickness of the blanket is, in general, not a critical factor and the process may be employed with blankets of various thickness, although norm-ally the blanket thickness will be between about one-half inch and about two and onehalf inches.
  • the technique used in carrying out this invention is to pass the blanket between squeeze rollers to remove a large portion of the final wash water, then bring it into contact with the solution containing the cross-linking agent which is usually applied as a heavy spray onto the blanket.
  • the blanket When the blanket has been wet thoroughly with the cross-linking liquid, it is removed between another pair of rollers where it is squeezed to remove excess liquid. This process may be repeated several times to obtain uniform distribution and increase the total pickup of cross-linking agent. While there is no limit on the number of times the contacting step may be repeated, it has been found that four baths are usually sufficient.
  • the blanket, thoroughly wet with the cross-linking liquid then passes through squeeze rollers adjusted to remove enough liquid from the blanket so that the remaining liquid content is less than the normal water imbibition value of the fiber (in the gel state).
  • the liquid content is reduced to 10 to 65% below the gel water imbibition value which is equivalent to a liquid content of 60% to on the Weight of the oven-dry impregnated fiber.
  • the pressure required to accomplish this will vary with the past history of the fiber and with the thickness of the blanket, but will, in general, be between about 500 and about 3500 pounds per linear inch of nip.
  • a convenient way to determine the liquid content is to weigh the fiber immediately after squeezing and then dry it in the manner outlined below. During drying, water and a certain amount of other volatile material may be driven off. The dried fiber is weighed and the difierence in the two weights taken. The liquid content of the squeezed fiber, for purposes of the present invention, may then be calculated as Weight of squeezed fiber -weight of dried fiber Weight of dried, treated fiber After passing through the final squeeze rollers, the blanket may be opened by conventional methods, spread on a moving conveyor belt, dried and cured. The temperatures and conditions of drying and curing will depend on the particular agent being employed. However, in general the impregnated fiber will be dried between about 50 C. and about 100 C. for whatever time is required to bring the moisture content of the fiber into equilibrium with its environment. Normally this will be between about and about 45 minutes.
  • Curing i.e. the cross-linking reaction
  • Curing is usually conducted by heating the impregnated fiber at a temperature of between about 110 C. and about 160 C. for between about 3 and about 30 minutes. The precise time and temperature will vary with the particular cross-linking agent being used.
  • FIGURE is a schematic flow diagram illustrating treatment of viscose staple fiber in accordance with the invention.
  • a regenerated cellulose tow 10 is for-med in conventional fashion by extruding viscose from a spinnerette 11 into a coagulating bath 12.
  • the bath 12 may be of any conventional composition comprising, for example, between about 7% and about 12% H 80 between about 14% and about 25% Na SO from 0 to about 8% ZnSO and from 0 to about 10% MgSO
  • Other ingredients well-known to the art such, for example, as surface-active agents for preventing spinnerette incrus tation, may also be present.
  • the temperature of the bath will normally be from say 40 C. to 60 C.
  • the tow is withdrawn from the coagulating bath 12 and, in accordance with conventional practice, is cut up into staple fiber by a cutting device 13.
  • the staple falls on a continuous belt 14 and forms a mat or blanket 15 thereon. It may then be subjected to an aqueous spray 16 containing from 1% to 2% H 80 at a temperature of from 60 C. to 92 C. Following this, it may be given a neutral or slightly alkaline wash 17 (pH 7.5-9.5) at a temperature of say 75 C.-90 C.
  • the blanket may be treated with a desulfurization wash 18 containing from say 0.1% to 0.4% Nags at a temperature of between about 55 C. and about 70 C.
  • This wash may also contain up to about .4% of sodium carbonate or sodium hydroxide together with sequestering or wetting agents, if desired.
  • the desulfurization treatment is then normally followed with a sulfide wash 19 comprising neutral Water at 70 C.-90 C. to remove sulfide liquors.
  • a sour or acid wash 20 containing between about 0.2% and about 0.5 H 50 or HCl at a temperature of 20 C.- C. is then employed.
  • An additional water wash 21 at a temperature of say 60 C.-85 C. follows to remove acid.
  • the blanket 15 is then squeezed to remove excess water by passing it between squeeze rolls 2'2 and 23.
  • the squeezed gel fiber is now passed over another endless belt 24 where it is subjected to an aqueous liquid 25 containing between about 0.5% and about 20% by weight of a permanently fusible cross-linking agent, at a temperature of between about 20 C. and about 40 C.
  • the liquid may also contain a catalyst, the amount of catalyst being in general from about 2% to about 20% on the weight of the resinous material, the exact amount depending upon the concentration and kind of resin used.
  • the liquid may further comprise from say 0.1% to 4% of a finishing agent of any of the types customarily used in the art.
  • the blanket can be taken directly from treatment at 25, squeezed until its liquid content is below the gel water imbibition value and passed to a curing and drying stage.
  • the blanket having been treated at 25, is again subjected to a squeezing between rollers 26 and 27, then delivered to another endless belt 35 where it is contacted with additional cross-linking solution at 2.6, the solution at 28 being preferably the same as that at 25.
  • Further cross-linking treatments may be added, as desired, although these are not shown in the figure.
  • the blanket is passed through final squeeze rolls 29 and 30 Where it is squeezed with sufficient pressure to reduce the amount of liquid in the fibers to below the water imbibition value of the gel fiber.
  • the blanket leaves this set of squeeze rolls, substantially all of the liquid and the crosslinking agent dissolved therein is drawn into the fibers leaving only the larger molecular size finishing agents on the surfaces of the fibers.
  • the total liquid. in the treated fiber is now between about 60% and 120% on the weight of the oven-dry treated fiber.
  • the blanket is then delivered to a conventional opening device 31 where the blanket is pulled apart.
  • the resulting fibers are delivered to another endless belt 32 which carries them through to a drying oven 33 where they are dried at a temperature which is normally between about 50 C. and about C.
  • the dried fibers are then passed through a curing oven 34 where they are cured at a temperature of say to C.
  • the fibers obtained from the process have low water inhibition. They may be processed without difliculty on conventional cotton spinning machinery without the danger of excessive fly or breaking of the fibers.
  • the material has a good hand and is altogether satisfactory for all textile purposes. In particular it is evenly treated, so that the variation in water imbibition from fiber to fiber is very low, much lower than with fibers impregnated by other techniques. This permits even dyeing.
  • fiber made in accordance with the invention has higher break factor and higher elongation, wet and dry than when other impregnating processes are used.
  • Example I A blanket of 1% x 1 bright never-dried regenerated cellulose staple fiber still in the gel-state and having a water imbibition value of 127% was squeezed between pressure rolls to a liquid retention of 100% on the weight of the oven-dried cellulose.
  • the blanket was 2 /2" thick and the pressure of the rolls was 700 pounds per lineal inch of nip.
  • the squeezed blanket was then passed under a spray of an aqueous solution containing 12% of Kaurit G (an aqueous solution containing 50% of a glutaraldehyde-urea precondensate in which the mol ratio of glutaraldehyde to urea is about 2:1, sold by the Putnam Chemical Co.), 1.2% magnesium chloride hexahydrate catalyst and 0.4% of a polyglycol stearate softening agent.
  • the impregnation was carried out in two stages with an intermediate light squeeze and a final heavy squeeze between pressurized roll (750 pounds/lineal inch or 60 pound gauge pressure) to a final liquid retention of 80% on the oven-dry weight of the cellulose.
  • the fibrous blanket was then opened and dried at a temperature of 200 F. and cured at'a temperature of 310 F. for 7 minutes.
  • the water irnbibition values of four random samples of the product were 53, 52, 55, 51, respectively.
  • Single strand dry break factor 1 264 Single strand dry elongation percent 13.4 Single strand wet break factor 163 Single strand wet elongation -percent 16.6 Skein break factor 2187 Break factor is the cotton count of the yarn times the breaking load in ounces.
  • the yarn produced a strong fabric with uniform dyeing properties.
  • Single strand dry break factor 243 Single strand dry elongation percent 11.5 Single strand wet break factor 151 Single strand wet elongation "percent" 14.2 Skein break factor 2035
  • the fabric was also uneven, weak, and dyed non-uniformly.
  • Example II The procedure of Example I was followed to treat textile grade gel-state cellulose staple fiber with a solution containing 8% of 1,3-dimethylol, S-ethyl perhydrotriazone, 1.6% (Rohm and Haas) catalyst H-7 (buffered zinc nitrate solution) and 0.4% of a polyglycol stearate softener.
  • the final squeeze pressure was 750 pounds/lineal inch (60 pound gauge pressure).
  • the impregnated blanket was squeezed sufficiently to reduce the liquid content to 80% on the weight of the cellulose.
  • the treated fiber blanket was opened, dried and cured as before.
  • Random samples had water irnbibition values of 42, 44, 43, 42%, respectively, and the fiber dyed uniformly.
  • Single strand dry break factor 252 Single strand dry elongation percent 12.4 Single strand wet break factor 151 Single strand wet elongation percent 14.2 Skein break factor 2270 The procedure of the above experiment was repeated except that the final squeeze roll pressure was reduced to 10 pounds (gauge) or approximately 250 pounds/lineal inch to give a wet pickup of 135%.
  • Random samples of the fiber product had water imbibition values of 48, 36, 52, 39%, respectively, and dyed unevenly with direct or acid dyestuffs.
  • the fiber processed with some difficulty to 20/1 yarn had the following properties:
  • Single strand dry break factor 207 Single strand dry elongation percent 10.2
  • Single strand wet break factor 138 Single strand wet elongation percent 12.5 Skein break factor 1576 A weak fabric with uneven dyeing properties was produced from this yarn.
  • Example III The experiment in Example 11 was repeated using an impregnating liquid containing 6% by weight of the same cross-linking agent, with squeeze pressures adjusted to give wet pickup and 140% wet pickup using 700 pound and 200 pound/lineal inch pressure, respectively. The following results were obtained:
  • Example IV The procedure of Example I was followed to treat textile grade gel-state regenerated cellulose staple fiber (water irnbibition value of 128%) with a solution containing 8% of an N,N-dimethyl, tetramethylol triazine precondensate, 1.2% magnesium chloride hexahydrate and 0.4% of a polyglycol stearate softener. The final squeeze pressure was adjusted to give a liquid content in the blanket of 80% on the weight of the cellulose. The squeeze roll pressure was reduced for a second sample to give a liquid content of 130% on the weight of the cellulose.
  • Example V Heavy Light Squeeze Squeeze W'et pickup, percent 80 130 Fiber water irnbibition value r percent 47-51 40-49 Yarn single strand dry break factor 2G6 203 Yarn single strand dry elongation, percent. 13. 0 10.2 Yarn single strand wet break factor 177 Yarn single strand wet elongation, percent 14. 5 12. 5 Skein break factor". 2, 266 1, 495 Dyeing Even Uneven Example V The experiment in Example IV was repeated at reduced levels of triazine precondensate concentrations. Again, heavy and light squeeze pressures were used to make two samples. To insure that the same amount of cross-linking agent would be taken up with both light and heavy squeezes, the liquor used with the heavy squeeze contained 7% agent and that used with the light squeeze, 6% agent. The following results were obtained:
  • Example I The procedure of Example I was followed to treat textile grade, gel-state regenerated cellulose staple fiber (water irnbibition value 128%) with a solution containing 9% dimethylol ethylene urea, 1.35% magnesium chloride hexahydrate and 0.4% of a polyglycol stearate softener.
  • the final squeeze pressure was adjusted to give a liquid content in the blanket of 84% on the weight of the cellulose.
  • the squeeze roll pressure was reduced for a second sample to give a liquid content of 130% on the weight of cellulose.
  • Example VII The experiment in Example VI was repeated at reduced levels of dimethylol ethylene urea concentrations. Heavy and light squeeze pressures were used to make two samples. To assure equal quantities of cross-linking agent being retained by the fiber, a solution containing 8% of cross-linking agent was used with the heavy squeeze and a 7% solution was used with the light Example VIII The procedure in Example I was followed to treat textile grade, gel-state 3 denier crimped, regenerated cellulose staple fiber (water imbibition value 130%) with a solution containing 3.5% formaldehyde, 3.5% magnesium chloride hexahydrate and 0.5% of a polyglycol stearate softener. The final squeeze pressure was adjusted to give a liquid content of 75% on the weight of the cellulose. The impregnated blanket was passed through an opener. The opened fiber was laid down on a conveyor which passed through a drier set at 180 F. and then through a cure zone at 320 F.
  • the sample which had been squeezed below the gelstate water imbibition value had a water imbibition range after treatment of 34-37%, uniform dyeability and good processability.
  • the sample which had been squeezed to a liquid content which was higher than the gel-state water imbibition value had a water imbibition range after treatment of 32-50%, dyed non-uniformly and gave difficulties during processing because of brittle fibers and excessive fly.
  • the treatment of cellulose with formaldehyde and curing agents such as magnesium chloride is claimed in the copending application of Daul et al. Ser. No. 81,956, filed January 11, 1961.
  • Example IX The procedure in Example I was followed to treat textile grade, gel-state 1 /2 denier regenerated cellulose staple fiber (water imbibition value 127% with a solution containing 4% of an acetal of ethylene glycol (Quaker Chemical Company, Reactant 53), 2% magnesium chloride hexahydrate and 0.4% of a polyglycol stearate softener. Two samples were produced using squeeze pressures designed to give wet pickup in one and wet pickup in the other sample. The
  • a method for cross linking regenerated cellulose fiber which consists essentially of impregnating a mass of said fiber while said fiber is still in the gel state after spinning and before it has ever been dried sufficiently to convert it from the gel state, with a liquid consisting essentially of water, formaldehyde and a catalyst for the cross linking reaction, squeezing the impregnated mass of fiber until the liquid content is between about 60 and about 120%, based on the weight of oven dry impregnated fiber and less than the water imbibition of the fiber in the gel state, and drying and curing the impregnated material to cross link the cellulose.

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  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
US819465A 1959-06-10 1959-06-10 Process for improving the properties of regenerated cellulose fibrous material Expired - Lifetime US3038777A (en)

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Application Number Priority Date Filing Date Title
BE594748D BE594748A (zh) 1959-06-10
US819465A US3038777A (en) 1959-06-10 1959-06-10 Process for improving the properties of regenerated cellulose fibrous material
GB20258/60A GB950073A (en) 1959-06-10 1960-06-09 Process for improving the properties of regenerated cellulose fibrous material
FR829668A FR1266007A (fr) 1959-06-10 1960-06-10 Procédé de réticulation des fibres de cellulose régénérée et fibres obtenues
CH667560A CH393624A (de) 1959-06-10 1960-06-10 Verfahren zur Herstellung von fasrigem, vernetztem, regeneriertem Zellulosematerial

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US819465A US3038777A (en) 1959-06-10 1959-06-10 Process for improving the properties of regenerated cellulose fibrous material

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US3173752A (en) * 1961-10-05 1965-03-16 Courtaulds Ltd Method for impregnating regenerated cellulose filament tows and making staple fibers therefrom
US3285690A (en) * 1962-12-14 1966-11-15 Jr Albert S Cooper Method of improving the dimensional stability and elastic recovery of allcotton stretchable fabrics and products thereof
US3371983A (en) * 1961-09-05 1968-03-05 Burlington Industries Inc Prewetting cellulosic fabric before introduction to dehydrating solution of formaldehyde reactant in a continuous process
US3423167A (en) * 1964-12-15 1969-01-21 Fmc Corp Wet state cross-linking of carboxyalkyl cellulose ether modified regenerated cellulose fibers
US3507685A (en) * 1967-09-29 1970-04-21 Fmc Corp Method of preparing an anchor coated cellulosic base material
US3509249A (en) * 1966-05-11 1970-04-28 Fmc Corp Method of preparing shaped articles of cellulose graft copolymers
US3762188A (en) * 1972-04-05 1973-10-02 Pvo International Inc Apparatus for treating textile fibers in staple fiber form
US4472850A (en) * 1982-06-21 1984-09-25 Beu-Tex Corporation Method and apparatus for condensing and continuously treating staple length fibrous materials
US4539724A (en) * 1983-02-07 1985-09-10 Beu-Tex Corp. Method for continuously treating staple length textile fibrous materials
US6702862B1 (en) * 1998-01-27 2004-03-09 Shikokuizumisenni, Ltd Method and apparatus for stabilizing cloth, and method of manufacturing cloth
CN114009858A (zh) * 2021-12-03 2022-02-08 厦门悠派无纺布制品有限公司 一种具有高透气性能的一次性棉内裤及其制备方法

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US5882356A (en) * 1992-10-21 1999-03-16 Courtaulds Fibres (Holdings) Limited Fibre treatment
GB9304887D0 (en) 1993-03-10 1993-04-28 Courtaulds Plc Fibre treatment
US5662858A (en) * 1993-04-21 1997-09-02 Lenzing Aktiengesellschaft Process for the production of cellulose fibres having a reduced tendency to fibrillation
GB9407496D0 (en) * 1994-04-15 1994-06-08 Courtaulds Fibres Holdings Ltd Fibre treatment
GB9408742D0 (en) * 1994-05-03 1994-06-22 Courtaulds Fibres Holdings Ltd Fabric treatment
GB9410912D0 (en) 1994-06-01 1994-07-20 Courtaulds Plc Fibre treatment
US6514610B2 (en) * 1999-12-13 2003-02-04 Fuji Spinning Co., Ltd. Method for manufacturing improved regenerated cellulose fiber
CN106894104B (zh) * 2017-04-18 2018-12-25 广东洪兴实业有限公司 一种服装用的高强度耐磨铜氨纤维的制备方法

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US2436076A (en) * 1946-09-27 1948-02-17 Cluett Peabody & Co Inc Method of stabilizing against shrinkage textile materials of regenerated cellulose
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US2785947A (en) * 1954-01-08 1957-03-19 Quaker Chemical Products Corp Process for producing durable mechanical effects on cellulose fabrics by applying acetals and products resulting therefrom
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3371983A (en) * 1961-09-05 1968-03-05 Burlington Industries Inc Prewetting cellulosic fabric before introduction to dehydrating solution of formaldehyde reactant in a continuous process
US3173752A (en) * 1961-10-05 1965-03-16 Courtaulds Ltd Method for impregnating regenerated cellulose filament tows and making staple fibers therefrom
US3285690A (en) * 1962-12-14 1966-11-15 Jr Albert S Cooper Method of improving the dimensional stability and elastic recovery of allcotton stretchable fabrics and products thereof
US3423167A (en) * 1964-12-15 1969-01-21 Fmc Corp Wet state cross-linking of carboxyalkyl cellulose ether modified regenerated cellulose fibers
US3509249A (en) * 1966-05-11 1970-04-28 Fmc Corp Method of preparing shaped articles of cellulose graft copolymers
US3507685A (en) * 1967-09-29 1970-04-21 Fmc Corp Method of preparing an anchor coated cellulosic base material
US3762188A (en) * 1972-04-05 1973-10-02 Pvo International Inc Apparatus for treating textile fibers in staple fiber form
US4472850A (en) * 1982-06-21 1984-09-25 Beu-Tex Corporation Method and apparatus for condensing and continuously treating staple length fibrous materials
US4539724A (en) * 1983-02-07 1985-09-10 Beu-Tex Corp. Method for continuously treating staple length textile fibrous materials
US6702862B1 (en) * 1998-01-27 2004-03-09 Shikokuizumisenni, Ltd Method and apparatus for stabilizing cloth, and method of manufacturing cloth
CN114009858A (zh) * 2021-12-03 2022-02-08 厦门悠派无纺布制品有限公司 一种具有高透气性能的一次性棉内裤及其制备方法
CN114009858B (zh) * 2021-12-03 2024-05-14 厦门悠派无纺布制品有限公司 一种具有高透气性能的一次性棉内裤及其制备方法

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CH393624A (de) 1965-06-15
BE594748A (zh)

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