Classifications

• • 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
  • D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
  • D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
• • 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
  • D06M13/322—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
  • D06M13/35—Heterocyclic compounds
  • D06M13/355—Heterocyclic compounds having six-membered heterocyclic rings
  • D06M13/358—Triazines
• • 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
  • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
  • D06M2101/02—Natural fibres, other than mineral fibres
  • D06M2101/04—Vegetal fibres
  • D06M2101/06—Vegetal fibres cellulosic

Definitions

• the cellulose derivatives thus obtained can be further reacted if desired with a compound containing a replaceable hydrogen atom attached to nitrogen, oxygen or sulfur, such as a primary or secondary amine.
• the known finishing processes involving a reaction of alkali cellulose, acyl cellulose or alkyl cellulose with a substance containing at least one N C- halogen group and resulting in a substitution of cyanuric acid groups for the hydroxyl groups of the cellulose are carried out in order to render the cellulose inert to direct cellulose dyestuffs and to impart to it an afiinity for basic dyestuffs orupon further reaction with aminesacid dyestuffs.
• These processes necessitate a pretreatment of the cellulose with a strong alkali or an esterification or etherification of the cellulose prior to the reaction with the N C-- halogen compound.
• finishing processes Another condition for these finishing processes is the use of a large quantity of the modifying substance, e.g. cyanuric chloride, said quantity amounting to at least half of the quantity of the cellulose to be treated.
• the prior art finishing processes are conducted in an organic solvent and require a considerable amount of time, the duration of the reaction being in the order of several hours.
• the above finishing processes result in a considerable deterioration of the mechanical strength of the fibrous material treated, the loss in strength amounting frequently to as much as 12 to 26% of the original strength of the cellulose fibers subjected to the reaction-with the cyanuric halide.
• a further object of the present invention is to provide a process for preparing cellulose derivatives from' native and regenerated cellulose in the form of fibers, fabrics and the like which is not accompanied with a substantial loss in mechanical strength of the fibrous material.
• the present invention provides a process for finishing cellulosic materials which comprises treating the material for a short period of time with a dispersion of a compound containing at least one 3,124,414 Patented Mar. 10, 1964 within the range of about 7 to about 10; drying the material thus treated; and subjecting the material to a heat treatment at a temperature above 100 C.
• the process'of the present invention is applicable to filaments, fibers, threads and fabrics derived from native or regenerated cellulose.
• the fibrous material subjected to the process of this invention may be dry or wet.
• the known finishing processes serving to make the cellulose immune to direct dyestuffs use strong alkali, a long reaction time and generally high temperatures.
• the known finishing processes involving a treatment with a cyanuric halide are conducted under conditions which ensure a rapid replacement of the halogen atoms of the heterocyclic reagent, e.g. cyanuric chloride, so that reactive halogen'is left over only if an excess of the cyanuric halide is applied.
• the process of the present invention is distinguished by the application of a very small amount of the N C- halogen-containing finishing agent, which however is utilized to the maximum extent.
• the finishing agent e.g. cyanuric chloride
• the heating of the reaction product at a temperature above 100 C. results in cross-linking of the hydroxyl groups of the cellulose.
• a maximum of unsaponified, reactive halogen atoms is available since under the conditions of the first step only a small number of halogen atoms is split oif.
• the process of the present invention has the advantage that the fibrous material subjected thereto does not become brittle.
• the process of this invention also avoids the known difiiculties caused by an uneven distribution of the condensation resins, which are not directly absorbed from the bath.
• the reactive compound attached to the finishing agent may undergo a cross-linking reaction either with the cellulose or with itself.
• an aminecompound such as urea, melamine and aliphatic amine or the like
• hydrophobic groups into the cellulose molecule by reacting the cyanuric ring attached to the cellulose with a long-chain aliphatic amine, such as heptyl amine, oleyl amine, stearyl amine, etc.
• the amino compound is linked to the cellulose by means of a cyanuric halide whereupon the desired cross-linking reaction is brought about by an acid aldehyde condensation in the absence or in the presence of a suitable catalyst such as ammonium biphosphate.
• the nitrogen-containing bodies go on the cellulose like a direct dye-stuff while the pressing-off difficulties encountered in the impregnation with these substances are avoided. Finally, the cross-linking reaction prevents the fibrous material from becoming brittle.
• an amino compound such as urea, melamine, an aliphatic amine, and the like
• a cyanuric halide in an aqueous alkaline medium to thereby form a reaction product.
• the fibrous material to be finished is then placed in a bath containing this reaction product whereupon the fibrous material is dried and heated to a temperature above 100 C.
• previously prepared reaction products of a cyanuric halide with suitable compounds are attached to the cellulose by means of one or more free halogen atoms still contained therein.
• Representative examples of these compounds are cyanuric chloride, cyanuric bromide and other members of the triazine series having at least one reactive halogen atom.
• the finishing agent is applied in an aqueous dispersion and the fibrous material to be subjected to the treatment with the finishing agent may be dry or wet (as obtained from a spinning bath).
• the cross-linking reaction of the OH groups of the cellulose concentrates more and more on the periphery of the fiber.
• the temperature of the finishing bath it is therefore possible to produce either a fiber evenl-y cross-linked over its entire cross-section or a fiber crosslinked only in the outer layer.
• a buffer substance such as borax is added to the aqueous dispersion of the finishing agent in order -to prevent the pH of the bath from falling below 7 on account of the hydrohalic acid formed in the reaction.
• An alkaline buffer substance e.g. borax, is preferably present also during the final heat treatment carried out to promote the condensation reaction since otherwise the hydroxyl groups of the cellulose will not react satisfactorily. This applies to all finishing operations in accordance with the present invention except where the cyanuric halide-containing reaction product of the first step is further reacted prior to drying with such compounds as urea or an organic amine.
• the condition of having a buffer substance present during the heat treatment is met if the fibrous material treated with the aqueous dispersion containing the finishing agent and the buffer substance is not washed before drying.
• the fibrous material may be freed from excess finishing liquor by presiding or flinging if desired.
• the drying time may be shortened by pressing or flinging the treated material so as to :free it from excess liquor.
• the fibrous material is heated at -a temperature above C. It is preferred to conduct the heat treatment between about L100 and about C. but temperatures up to C. with correspondingly shorter heating periods may be used if desired.
• Example 1 1 kg. of staple rayon (Zellwolle) is treated at 20 C. for a period of 5 minutes with the 20-fold amount of a 2% aqueous bonax solution containing 60 g. of cyanuric chloride dispersed therein. It is also possible to recycle the borax solution and to contact it with the corresponding amount of cyanuric chloride separated therefrom by means of a filter.
• the cyanuric chloride is absorbed completely by the cellulose fibers from the bath having a pH of about 8 during the indicated period.
• the fibrous material is then taken out of the bath and liquor adhering to its surface is removed by pressing or flinging. Thereupon the material is dried as usual without washing and heated at about 120 C. for about 30 minutes.
• the fibers thus finished are insoluble in cellulose solvents, nearly incapable of swelling and have the following characteristics.
• Example l In order to provide spun rayon fibers with an external layer insoluble in cellulose solvents, the procedure of Example l is repeated except that the temperature of the bath is kept between 40 and 50 C.
• Example 3 A staple rayon fabric is finished by the procedure described in Example 1. As a result, the fabric becomes insoluble in cellulose solvents. The swelling value of the fabric falls from 90% to'7'8% while its resistance to scouring rises from 285 to 940. The tensile strength and the elongation values of the threads remain practically unchanged. 1
• Example 4 1 kg. of freshly spun desulfurized staple rayon (still moi-st) is treated at 2.0 C. for a period of 5 minutes with the 20-fold quantity of .a 2% aqueous solution of borax containing 60 g. of cyanuric chloride dispersed therein. The fibrous material is removed from the bath and freed from excess liquor by pressing or flinging. Then the material is dried without being washed and heated at 120 for about 30 minutes.
• the treatment with cyanuric chloride can be followed immediately by an impregnation in a brightening bath containing 2% borax, a fatty alcohol sulfate or the like. After the impregnation, the material is dried and heated at an elevated temperature.
• the following table shows the decrease in swelling and the improvement of the resistance to scouring obtained as a result of this treatment.
• Example 5 1 kg. of spin bath-moist staple rayon is treated in a suspension of 50 g. of'cyanuric chloride in a 2% solution of borax at 20 7 C. for a period of 5 minutes. After the absorption of the'cyanuric chloride, the material is rinsed for 5 minutes at 20 C.,Wlth a 5% solution of urea I buffered with borax to .a pH of 8.0. After pressing or flinging off this solution, the material is impregnated with a 2.5% solution of formaldehyde containing 0.2% of ammonium biphosphate as a catalyst. Upon removal of excess solution the material is dried as usual and heated at about 120 C for about 30 minutes.
• the fibers thus finished have a swelling value of 50.2% and a scouring number of 1839 as compared with a swelling value of 105%, and a scouring number of 210 of the untreated, dried fiber.
• Example 6 Following the procedure described in Example 1, fibrous material derived from cellulose is reacted with 60 g. of cyanuric chloride per 1 kg. of cellulose in a boraxalkaline solution. After the absorption of the cyanuric chloride 30 g. of oleyl amine dissolved in acetone are added to the bath. The fibrous material is then freed from excess liquor dried and heated at 120 C. for 30 minutes. The fibrous material thus obtained is waterrepellent.
• Example 7 5 g. of urea are dissolved in 20 l. of a 2% borax solution. Then 60 g. of cyanuric chloride dissolved in acetone are added to the borax solution at 20 C. while sitrring. After completion of the reaction (about 5 minutes), 1 kg. of viscose fiber from sulfite cellulose obtained from beech wood are placed in the bath and the latter is heated to 50 C. in order to add the urea-cyanuric chloride reaction product on to the cellulose. The final condensation occurs after drying the fibrous material by heating at 120 C. During the condensation reaction borax residue adhering to the material bind the hydrochloric acid liberated.
• the fibers thus finished have a swelling value of 84% and resistance to scouring of 21,400 while the correspond- 6 ing values of the untreated fibers are 102% and 4,350, respectively.
• Process for treating a fibrous material derived from cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a short period of time with a small proportion of an aqueous dispersion of a cyanuric halide, said dispersion having a pH within the range of between about 7 to 10; drying the thustreated material; and subjecting the material to a heat treatment at a temperature between above C. and 160 C., whereby a material of substantially decreased swelling characteristics, substantially insoluble in solvents for cellulose, and of high resistance to scouring is obtained.
• Process for treating a fibrous material derived from cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a period of between about 1 and 30 minutes at a temperature of between about 15 C. and 60 C. with an aqueous dispersion of a cyanuric halide, said dispersion having a pH within the range of between about 7 to 10 and containing between about 10 and 100 grams of said cyanuric halide for each kilogram of said material being treated; drying the thus-treated material; and subjecting the material to a heat treatment at a temperature between above 100 C.
• a material of substantially decreased swelling characteristics, substantially insoluble in cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a period of between about 1 and 30 minutes at a temperature of be- ,tween about 15 C. and 60 C.
• aqueous dispersion of a cyanuric halide selected from the group consisting of cyanuric chloride and cyanuric bromide said dispersion having a pH within the range of between about 7 to 10 and containing between about 10 and 100 grams of said cyanuric halide for each kilogram of said material being treated; drying the thus-treated material; and subjecting the material to a heat treatment at a temperature between above 100 C. and 160 C. whereby a material of substantially decreased swelling characteristics, substantially insoluble in solvents for cellulose, and of high resistance to scouring is obtained.
• Process for treating a fibrous material derived from cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a period of about 5 minutes at a temperature of between about 15 C. and 60 C. with an aqueous dispersion of a cyanuric halide, said dispersion having a pH of about 8 and containing between about 30 and 60 grams of said cyanuric halide for each kilogram of said material being treated; drying the thus-treated material without washing; and subjecting the material to a heat treatment at a temperature between about and C., whereby a material of substantially decreased swelling characteristics, substantially insoluble in solvents for cellulose, and of high resistance to scouring is obtained.
• Process for treating a fibrous material derived from cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a period of between about 1 and 30 minutes at a temperature of between about 15 C. and 60 C. with an aqueous dispersion of a cyanuric halide in a dilute aqeuous borax solution, said dispersion being maintained at a pH of about 8; drying the thus-treated material; and subjecting the material to a'heat treatment at a temperature between above 100 C. and 160 C., whereby a material of substantially decreased swelling characteristics, substantially insoluble in solvents for cellulose, and of high resistance to scouring is obtained.
• Process for treating staple rayon substantially without prior alkali treatment, esterification and etherification of the same comprising the steps of treating said staple rayon for a period of about five minutes at a temperature of between about 40 C. and 50 C. with a dispersion of a cyanuric halide in a dilute aqueous borax solution, the pH of said dispersion being maintained at about eight and said dispersion containing between about 30 grams and 60 grams of cyanuric halide for each kilogram of said staple rayon; drying the thus-treated staple rayon without washing; and subjecting the staple rayon to a heat treatment at a temperature of between about 110 C. and 120 C. for a period of about 30 minutes.
• Process for treating a fibrous material derived from cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a period of between about 1 and 30 minutes at a temperature of between about 15 and 60 C.
• aqueous dispersion of a cyanuric halide said dispersion having a pH within the range of between about 7 to 10 and containing between about 10 and 100 grams of said cyanuric halide for each kilognam of said material being treated; contacting the material with an organic amino compound selected from the group consisting of urea, melamine and aliphatic amines; drying the thus-treated material; and subjecting the material to a heat treatment at, a temperature between above 100 C. and 160 C., whereby a material (If substantially decreased swelling characteristics, substantially insoluble in solvents for cellulose, and of high resistance to scouring is obtained.
• Process for treating a fibrous material derived from cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a period of between about 1 and 30 minutes at a temperature of between about C. and 60 C.
• aqueous dispersion of a cyanuric halide said dispersion having a pH within the range of between about 7 to 10 and containing between about 10 and 100 grams of said cyanuric halide for each kilogram of said material being treated; contacting the material with an organic amino compound selected from the group consisting of urea, melamine and aliphatic amines; treating the material with an aldehyde; drying the thus-treated materials; and subjecting the material to a heat treatment at a temperature between above 100 C. and 160 C., whereby a material of substantially decreased swelling characteristics, substantially insoluble in solvents for cellulose, and of high resistance to scouring is obtained.
• Process for treating a fibrous material derived from cellulose comprising the steps of treating said fibrous material substantially without prior alkali treatment, esterification and etherification of the same for a period of between about 1 and 30 minutes at a temperature of between about 15 C. and C.
• aqueous dispersion of a cyanuric halide said dispersion having a pH within the range of between about 7 to 10 and containing between about 10 and grams of said cyanuric halide for each kilogram of said material being treated; contacting the material with an organic amino compound selected from the group consisting of urea, melamine and aliphatic amines; treating the material with an aldehyde selected from the group consisting of formaldehyde and glyoxal in the presence of ammonium biphosphate; drying the thus-treated material; and subjecting the material to a heat treatment at a temperature between above 100 C. and C., whereby a material of substantially decreased swelling characteristics, substantially insoluble in solvents for cellulose, and of high resistance to scouring is obtained.
• a process for treating a fibrous material derived from cellulose the steps of treating the material substantially without prior alkali treatment, esterification and etherification of the same with a dispersion of a product obtained by reacting in an aqueous alkaline medium a cyanuric halide with an organic amino compound selected from the group consisting of urea, melamine and aliphatic amines; drying the thus-treated material; and subjecting the material to a heat treatment at a temperature higher than 100 C. and up to 160 C.

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• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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  • NL NL245557D patent/NL245557A/xx unknown
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• 1959
  • 1959-02-11 DE DEP22207A patent/DE1141973B/de active Pending
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