US2478975A - Treatment of hosiery - Google Patents
Treatment of hosiery Download PDFInfo
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- US2478975A US2478975A US621379A US62137945A US2478975A US 2478975 A US2478975 A US 2478975A US 621379 A US621379 A US 621379A US 62137945 A US62137945 A US 62137945A US 2478975 A US2478975 A US 2478975A
- Authority
- US
- United States
- Prior art keywords
- hosiery
- filaments
- oil
- cellulose
- treatment
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 30
- 239000000463 material Substances 0.000 description 22
- 239000003921 oil Substances 0.000 description 20
- 235000019198 oils Nutrition 0.000 description 20
- 229920002678 cellulose Polymers 0.000 description 17
- 239000000243 solution Substances 0.000 description 14
- 239000004753 textile Substances 0.000 description 14
- 238000001035 drying Methods 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000001913 cellulose Substances 0.000 description 8
- 239000004744 fabric Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 229920002301 cellulose acetate Polymers 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
- 239000000944 linseed oil Substances 0.000 description 5
- 235000021388 linseed oil Nutrition 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 229920003086 cellulose ether Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229950011008 tetrachloroethylene Drugs 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- MQWCXKGKQLNYQG-UHFFFAOYSA-N 4-methylcyclohexan-1-ol Chemical compound CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
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
-
- 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
- D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
-
- 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
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
-
- 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
- D06M15/01—Treating 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
- D06M15/17—Natural resins, resinous alcohols, resinous acids, or derivatives thereof
-
- 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
Definitions
- Knitted hosiery of silk has long-been highly valued on account of its apparent transparency or .sheerness when on the wearer and the uniformity obtainable in respect of thisand other properties, for example lustre. It is very difficult if not impossible to secure these properties in the same degree in hosiery and other textile fabrics made from less expensive yarns of cotton or artificial filaments, for example those of regenerated cellulose.
- These artificial filaments include those obtained from viscose or from cuprammonium cellulose solutions and those obtained by saponifying cellulose ester filaments substantially completely.
- the textile material is first sub- J'ected to the clarifying treatment described in our co-pending U. S. application Serial No. 621,378, of even date.
- This treatment involves subjecting the materials to the combined action of water and hydrophobe liquid.
- the hydrophobe liquid includes aliphatic or aromatic hydrocarbons, for example, benzene, toluene, xylene, solvent naphtha or lightfractions of petroleum.
- the desired effects can be obtained with quite small proportions of the drying oil, for example from 10 to 35% e. g. about 20 or based on the weight of the material, can be used. Smaller or greater proportions can however be employed, for instance proportions as low as 10%.
- the propor- 5 tions employed can be such as merely to coat the yarn of which the fabric is made and should not be sufiicient to close the interstices of the fabric. To effect such closure a proportion of the order of 200% is usually necessary.
- drying oil it'is' convenient to apply the drying oil to the hosiery or other textile material as a solution in a volatile solvent therefor. vIn this way uniform distribution of the oil throughout the textile material can be readily secured. Thus a solution of a drying oil in benzene and of about 10% strength by volume can be employed. The oil may also be applied as an aqueous emulsion.
- the application of the oil can be combined with the clarifying treatment referred to above and described in our co-pending U. S. application S. No. 621,378, the oil being applied in solution in the hydrophobe liquid used, in conjunction With water, to treat the materials.
- Suitable solvents for the drying oil are aliphatic or aromatic hydrocarbons, for example the benzene mentioned above, toluene, xylene, solvent naphtha or light fractions of petroleum. Again halogenated hydrocarbons can be employed for example carbon tetrachloride or perchlorethylene. Solutions of drying oils in these solvents are suitable for application to the materials whether used as part of the clarifying treatment described in our above mentioned co-pending application or whether applied in a separate operation after the clarifying treatment.
- drying oils In place of drying oils other substances capable of yielding a water-insoluble film on the filaments of the textile material particularly such as are soluble in organic solvents and can be applied as solutions in .hydrophobe organic liquids.
- examples of suchother substances are natural resins and synthetic resins of the alkyd type whether oil-modified or not, resins of the polyvinyl acetal type, and those obtained by alkylati-ngurea formaldehyde condensation products or melamine formaldehyde condensation products. Againvarnishes of the resin/drying oil type can be em ployed. These can be diluted with volatile organic liquid and applied in the same manner as the simple solutions of drying oils referred to above.
- the new treatment is of especial value in the case of cellulose textiles whether of natural orregenerated cellulose.
- it can be applied to cotton materials or to materials of yarns of cellulose regenerated from viscose or cuprammonium solutions of cellulose or obtained by saponific'ation of cellulose ester yarns.
- It has been found of particular value in the case of textiles of filaments of high tenacity e. g. above 2 grams per denier, made by spinning viscose solutions or cuprammonium solutions of cellulose and stretching the filaments substantially when partially but not completely set or made by stretching cellulose acetate. or other cellulose ester filaments in a softened condition for example under the in-fl-uence of a hot aqueous medium, e. g.
- the treatment can be applied to fabrics consisting Wholly or in part of such stretched and saponified filaments.
- the process can, however, be applied to textile materials of filaments other than cellulose filaments e. g. to materials of natural silk or of cellulose acetate or other cellulose ester or ether-filaments, including cellulose ester or ether filaments which have been stretched substantially while in a softened condition: e. g. while under the influence of wet. steam or hot water, and cellulose ester or ether filaments produced by a wet spinning process.
- Example 1- Hosiery dyed in a medium, tan shade and knitted from 65 denier yarn obtained by stretch.- ing cellulose acetate yarn to. about 10. times its length in wet steam andthereafter. saponifying it substantially completely is wetted with a. mix..- ture of 100 parts by volume of acetone; with. 10 parts by volume of Water.
- the hosiery is. then drained and steepedinbenzene until the material appears clear therein. This may require a 'few r hours.
- the hosiery is then dried and oiled by immersion in a mixture; of 10 Volumes of boiled linseed oil and 100 volumes of benzene.
- Example 2 Dyed hosiery of the kind'referred t'o iii-Example 1. is subjected to the same clarifying treatment as that .described in that example and is then impregnated with a. solution containing; grams-0f the thermoplastic resin soldby-I; 'C; I: under the 4 trade name Bedafin 285 X per 100 cos. of benzene. After squeezing, the material is dried, the results being very similar to those obtained according to Example 1.
- Example 3 Dyed hosiery knitted from normal '75 denier filament cellulose acetate yarn (i. e. dry spun yarn which has not been subjected to substantial stretching after spinning) is immersed in a mixture of 10 volumes of boiled linseed oil and 100 volumes of benzene. It is then squeezed and dried as in Example 1. The sheerness is thereby increased, the colour rendered more intense, and the tendency to ladder reduced.
- Process of imparting sheerness and uniformity of appearance to hosiery of textile filaments made by stretching cellulose ester filaments while in a softened condition and saponifying them substantially completely which comprises Wetting the hosiery with an aqueous liquid and subjecting it while moist with water, to theaction of a hyd'rophobe organic liquid selected from the group consisting of benzene, toluene, xylene, solvent naphtha, light fractions of petroleum, carbon tetrachloride, perchloroethylene and methylcyclohexanol until it appears clear therein and then uniformly impregnating it with from 10% to of its weight of a drying oil and causing the latter to dry without closing the interstices in said hosiery.
- a hyd'rophobe organic liquid selected from the group consisting of benzene, toluene, xylene, solvent naphtha, light fractions of petroleum, carbon tetrachloride, perchlor
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented Aug. 16 1949 UNITED-STATE TREATMENT OF HOSIERY Albert Mellor, Ralph James Mann, Donald Finlayson, and Albert William Morledge-Hadfield, Spondon, near Derby, England, assignors to Celanese Corporation of America, a corporation of Delaware 7 No Drawing. Application October 9, 1945, Serial No. 621,379. In Great Britain October 30, 1944 This invention relates to textile materials and especially to light textile fabrics andparticularly light knitted fabrics of the kind of which hosiery is constituted.
Knitted hosiery of silk has long-been highly valued on account of its apparent transparency or .sheerness when on the wearer and the uniformity obtainable in respect of thisand other properties, for example lustre. It is very difficult if not impossible to secure these properties in the same degree in hosiery and other textile fabrics made from less expensive yarns of cotton or artificial filaments, for example those of regenerated cellulose. These artificial filaments include those obtained from viscose or from cuprammonium cellulose solutions and those obtained by saponifying cellulose ester filaments substantially completely.
We have now found that a great improvement in sheerness and uniformity of appearance of textile. materials and especially of light weight fabrics, for example knitted or woven fabrics having a weight of less than 2 ounces per sq. yard, can be secured by finishing them with a small proportion of a drying oil for example linseedoil or tung oil. After impregnation the material can be hung'in the air so as to dry the oil by oxidation.
Preferably, more particularly in thecase of cellulose materials, the textile material is first sub- J'ected to the clarifying treatment described in our co-pending U. S. application Serial No. 621,378, of even date. This treatment involves subjecting the materials to the combined action of water and hydrophobe liquid. By this preliminary treatment it is possible to enhance very considerably the desired effects. The hydrophobe liquid includes aliphatic or aromatic hydrocarbons, for example, benzene, toluene, xylene, solvent naphtha or lightfractions of petroleum.
5 Claims. (01. 1114-56) 2 while in a softened condition, for example While they are under the influence of steam or hot water, and thereafter saponifying them substantially completely. By applying the oiling treatment to such materials a very great improvement indeed can be secured as regards the sheerness and other properties. For examplewhere the hosiery has already been coloured as 'is'usually the case the limited application of drying oil'ree sults in a considerable apparent deepening, of colour so that to obtain a particular shade in the finished material a smaller proportion of dye can be employed than would otherwise be vnecessary. It is possible that the oiling treatment greatly reduces the surface reflection of light by the ma-.- terial. Further the oiled material shows less tendency to develop ladders than does the untreated material.
The desired effects can be obtained with quite small proportions of the drying oil, for example from 10 to 35% e. g. about 20 or based on the weight of the material, can be used. Smaller or greater proportions can however be employed, for instance proportions as low as 10%. The propor- 5 tions employed can be such as merely to coat the yarn of which the fabric is made and should not be sufiicient to close the interstices of the fabric. To effect such closure a proportion of the order of 200% is usually necessary.
It'is' convenient to apply the drying oil to the hosiery or other textile material as a solution in a volatile solvent therefor. vIn this way uniform distribution of the oil throughout the textile material can be readily secured. Thus a solution of a drying oil in benzene and of about 10% strength by volume can be employed. The oil may also be applied as an aqueous emulsion.
If desired the application of the oil can be combined with the clarifying treatment referred to above and described in our co-pending U. S. application S. No. 621,378, the oil being applied in solution in the hydrophobe liquid used, in conjunction With water, to treat the materials.
Suitable solvents for the drying oil are aliphatic or aromatic hydrocarbons, for example the benzene mentioned above, toluene, xylene, solvent naphtha or light fractions of petroleum. Again halogenated hydrocarbons can be employed for example carbon tetrachloride or perchlorethylene. Solutions of drying oils in these solvents are suitable for application to the materials whether used as part of the clarifying treatment described in our above mentioned co-pending application or whether applied in a separate operation after the clarifying treatment.
In place of drying oils other substances capable of yielding a water-insoluble film on the filaments of the textile material particularly such as are soluble in organic solvents and can be applied as solutions in .hydrophobe organic liquids. Examples of suchother substances are natural resins and synthetic resins of the alkyd type whether oil-modified or not, resins of the polyvinyl acetal type, and those obtained by alkylati-ngurea formaldehyde condensation products or melamine formaldehyde condensation products. Againvarnishes of the resin/drying oil type can be em ployed. These can be diluted with volatile organic liquid and applied in the same manner as the simple solutions of drying oils referred to above.
The new treatment is of especial value in the case of cellulose textiles whether of natural orregenerated cellulose. Thus it can be applied to cotton materials or to materials of yarns of cellulose regenerated from viscose or cuprammonium solutions of cellulose or obtained by saponific'ation of cellulose ester yarns. It has been found of particular value in the case of textiles of filaments of high tenacity e. g. above 2 grams per denier, made by spinning viscose solutions or cuprammonium solutions of cellulose and stretching the filaments substantially when partially but not completely set or made by stretching cellulose acetate. or other cellulose ester filaments in a softened condition for example under the in-fl-uence of a hot aqueous medium, e. g. wet steam or'hot water, and subsequently saponif-ying them substantially completely. The treatment can be applied to fabrics consisting Wholly or in part of such stretched and saponified filaments. The process can, however, be applied to textile materials of filaments other than cellulose filaments e. g. to materials of natural silk or of cellulose acetate or other cellulose ester or ether-filaments, including cellulose ester or ether filaments which have been stretched substantially while in a softened condition: e. g. while under the influence of wet. steam or hot water, and cellulose ester or ether filaments produced by a wet spinning process. e
Example 1- Hosiery dyed in a medium, tan shade and knitted from 65 denier yarn obtained by stretch.- ing cellulose acetate yarn to. about 10. times its length in wet steam andthereafter. saponifying it substantially completely is wetted with a. mix..- ture of 100 parts by volume of acetone; with. 10 parts by volume of Water. The hosiery is. then drained and steepedinbenzene until the material appears clear therein. This may require a 'few r hours. The hosiery is then dried and oiled by immersion in a mixture; of 10 Volumes of boiled linseed oil and 100 volumes of benzene. It is then squeezed so that it retains about 2 /2 times its weight of the oil solution and hung in a steam heated cupboard at 75-85 C. for about, 24 hours. The result is a considerable increase in the sheer;- ness of the hose and a great improvement asregards uniformity of appearance. Further the colour appears much deeperthan in the untreated hose. These properties are not materially affected by scouring for-15 minutes-in agram per litre soap solution at 65 0.
Example 2 Dyed hosiery of the kind'referred t'o iii-Example 1. is subjected to the same clarifying treatment as that .described in that example and is then impregnated with a. solution containing; grams-0f the thermoplastic resin soldby-I; 'C; I: under the 4 trade name Bedafin 285 X per 100 cos. of benzene. After squeezing, the material is dried, the results being very similar to those obtained according to Example 1.
Example 3 Dyed hosiery knitted from normal '75 denier filament cellulose acetate yarn (i. e. dry spun yarn which has not been subjected to substantial stretching after spinning) is immersed in a mixture of 10 volumes of boiled linseed oil and 100 volumes of benzene. It is then squeezed and dried as in Example 1. The sheerness is thereby increased, the colour rendered more intense, and the tendency to ladder reduced.
Having described our invention, What we desire to secure by Letters Patent is:
1. Process of imparting sheerness and uniformity of appearance to hosiery of textile filaments made by stretching cellulose ester filaments while in a softened condition and saponifying them substantially completely, which comprises Wetting the hosiery with an aqueous liquid and subjecting it while moist with water, to theaction of a hyd'rophobe organic liquid selected from the group consisting of benzene, toluene, xylene, solvent naphtha, light fractions of petroleum, carbon tetrachloride, perchloroethylene and methylcyclohexanol until it appears clear therein and then uniformly impregnating it with from 10% to of its weight of a drying oil and causing the latter to dry without closing the interstices in said hosiery.
2. Process of imparting sheerness and uniformity of appearance tohosiery of textile filaments made by stretching cellulose acetate filaments while in a softened condition andsap'onify ing them substantially completely, which comprises wetting the hosiery with anaqueous liquid and subjecting it while moist with water, to the action of a-hydrophob'e organic liquid selected from the group consisting ofbenzene, toluene, xylene; sol' vent naphtha, light fractions of petroleum, carbon tetrachloride, perchloroethy-lene and methyl cyclohexanol until it appears clear therein and then uniformly impregnating it with a solution of a drying oil in a volatile organic li'qui'd so-that the hosiery carries from 10% to 35% of its weight of 'dryi'ng'oil and causing the latter to-drywithout closing the interstices in said hosiery.
3; Process ofimparting sheerness and uniform ity of appearance to hosiery of textile filaments made by stretching cellulose acetate filaments while in a softened condition and saponifying them substantially completely, which comprises wetting the hosiery with an aqueous'liquid and subjecting itwhile' moist with water, to the action of benzene until it appears clear therein and then uniformly impregnating it with from 10% to 35% of itsweight of a drying oil and causingthe latter todry without closing the interstices in said hosiery-1 4". Process accordingto claim 1, wherein the hosiery is knitted from yarns of filaments made by stretching cellulose ester yarns under the influenceof a hot aqueous medium and thereafter saponifying them substantially completely.
5. Process for increasing the sheerness of hosiery knitted from yarns of filaments made by stretching cellulose ester yarns under the influence of a hot aqueous medium and thereafter saponifyin'g them substantially completely, which comprises damping: thev hosiery with water, steeping itin benzene" untili it appears clear therein,
. an'dthenlimpregnatingi it with a. benzene" solution 5 of boiled linseed oil and evaporating ofi the ben- 'zene so as to leave on the hosiery about 25 per cent of its Weight of the linseed oil without closing the interstices in said hosiery. ALBERT MELLOR. V RALPH JAMES MANN. DONALD FINLAYSON. ALBERT WILLIAM MORLEDGE-I-IADFIELD.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 7 138,302 Wagner Apr. 29, 1873 217,604 Francis July 15, 1879 682,367 Rosell Sept. 10, 1901 1,236,959 McIntosh Aug. 14, 1917 OTHER REFERENCES Randolph, Eliminating Bubbles in Fabric Impregnation C. & M. E. 35 306 (N0. 5).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2478975X | 1944-10-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2478975A true US2478975A (en) | 1949-08-16 |
Family
ID=10907965
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US621379A Expired - Lifetime US2478975A (en) | 1944-10-30 | 1945-10-09 | Treatment of hosiery |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2478975A (en) |
Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US138302A (en) * | 1873-04-29 | Improvement in paper | ||
| US217604A (en) * | 1879-07-15 | Improvement in water-proof fabrics | ||
| US682367A (en) * | 1900-03-24 | 1901-09-10 | Jeremiah A Scriven | Fabric. |
| US1236959A (en) * | 1917-07-05 | 1917-08-14 | Diamond State Fiber Company | Process of making fiber product. |
| US1277695A (en) * | 1917-07-20 | 1918-09-03 | Leander J Cavanaugh | Soilproof fabric and process of making the same. |
| GB359819A (en) * | 1930-01-15 | 1931-10-29 | Glanzstoff Ag | Improvements in or relating to the dressing of artificial-silk spinning cakes |
| DE620627C (en) * | 1931-03-11 | 1935-10-24 | Kalle & Co Akt Ges | Process for reducing the swellability of structures made from regenerated cellulose |
| US2036424A (en) * | 1933-04-18 | 1936-04-07 | Eastman Kodak Co | Impregnation of cotton materials |
| US2053766A (en) * | 1932-02-19 | 1936-09-08 | Dreyfus Henry | Production of filaments, yarns, fabrics, and like materials |
| US2075887A (en) * | 1932-12-08 | 1937-04-06 | Dreyfus Camille | Method of finishing knit fabrics |
| US2137404A (en) * | 1936-01-20 | 1938-11-22 | Wacker Chemie Gmbh | Drying process |
| US2177425A (en) * | 1937-06-16 | 1939-10-24 | Charles A Barker | Process for stopping runs in knitted wear |
| US2192919A (en) * | 1937-12-23 | 1940-03-12 | Paper Chemistry Inst | Proteinized hosiery |
| US2352747A (en) * | 1941-08-09 | 1944-07-04 | Celanese Corp | Coating process |
-
1945
- 1945-10-09 US US621379A patent/US2478975A/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US138302A (en) * | 1873-04-29 | Improvement in paper | ||
| US217604A (en) * | 1879-07-15 | Improvement in water-proof fabrics | ||
| US682367A (en) * | 1900-03-24 | 1901-09-10 | Jeremiah A Scriven | Fabric. |
| US1236959A (en) * | 1917-07-05 | 1917-08-14 | Diamond State Fiber Company | Process of making fiber product. |
| US1277695A (en) * | 1917-07-20 | 1918-09-03 | Leander J Cavanaugh | Soilproof fabric and process of making the same. |
| GB359819A (en) * | 1930-01-15 | 1931-10-29 | Glanzstoff Ag | Improvements in or relating to the dressing of artificial-silk spinning cakes |
| DE620627C (en) * | 1931-03-11 | 1935-10-24 | Kalle & Co Akt Ges | Process for reducing the swellability of structures made from regenerated cellulose |
| US2053766A (en) * | 1932-02-19 | 1936-09-08 | Dreyfus Henry | Production of filaments, yarns, fabrics, and like materials |
| US2075887A (en) * | 1932-12-08 | 1937-04-06 | Dreyfus Camille | Method of finishing knit fabrics |
| US2036424A (en) * | 1933-04-18 | 1936-04-07 | Eastman Kodak Co | Impregnation of cotton materials |
| US2137404A (en) * | 1936-01-20 | 1938-11-22 | Wacker Chemie Gmbh | Drying process |
| US2177425A (en) * | 1937-06-16 | 1939-10-24 | Charles A Barker | Process for stopping runs in knitted wear |
| US2192919A (en) * | 1937-12-23 | 1940-03-12 | Paper Chemistry Inst | Proteinized hosiery |
| US2352747A (en) * | 1941-08-09 | 1944-07-04 | Celanese Corp | Coating process |
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