US2151952A - Lubricating textile fibers and the like and product - Google Patents
Lubricating textile fibers and the like and product Download PDFInfo
- Publication number
- US2151952A US2151952A US223699A US22369938A US2151952A US 2151952 A US2151952 A US 2151952A US 223699 A US223699 A US 223699A US 22369938 A US22369938 A US 22369938A US 2151952 A US2151952 A US 2151952A
- Authority
- US
- United States
- Prior art keywords
- textile fibers
- ester
- fibers
- halogenated
- fatty acid
- 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
Links
- 239000000835 fiber Substances 0.000 title description 26
- 239000004753 textile Substances 0.000 title description 17
- 230000001050 lubricating effect Effects 0.000 title description 4
- 150000002148 esters Chemical class 0.000 description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- 235000014113 dietary fatty acids Nutrition 0.000 description 14
- 239000000194 fatty acid Substances 0.000 description 14
- 229930195729 fatty acid Natural products 0.000 description 14
- 238000000034 method Methods 0.000 description 12
- -1 so-called olein Chemical class 0.000 description 10
- 150000004665 fatty acids Chemical class 0.000 description 7
- 239000000314 lubricant Substances 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 238000005461 lubrication Methods 0.000 description 5
- 230000026030 halogenation Effects 0.000 description 4
- 238000005658 halogenation reaction Methods 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 4
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000010685 fatty oil Substances 0.000 description 2
- 230000002140 halogenating effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- GKGVPDQNHDBNDR-UHFFFAOYSA-N 2,2-dichlorooctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(Cl)(Cl)C(O)=O GKGVPDQNHDBNDR-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- ULRRMYHDWKTYFI-UHFFFAOYSA-N butyl 2,2-dichlorooctadecanoate Chemical compound ClC(C(=O)OCCCC)(CCCCCCCCCCCCCCCC)Cl ULRRMYHDWKTYFI-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 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
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31844—Of natural gum, rosin, natural oil or lac
Definitions
- This invention relates to novel, eflicient and economical procedure for the lubrication of textile fibers, such as'natural fibers, in connection with the manufacture of combed or worsted yarn, and of synthetic yarns, such as rayon, and the like, in preparation for twisting or throwing.
- This invention also contemplates the novel lubricated fibers or yarn produced in accordance with the procedure.
- pro- 85 cedure for the lubrication of textile fibers, synthetic yarns, and the like, and product thereof is provided which is at once highly efficient for treatment with the usual mechanical instrumentalities, highly economic in that a comparam tively small amount of the lubricant is required and the lubricant may be readily and economically washed out.
- halogenated esters of a saturated or an unsaturated fatty acid formed by the reaction of an alcohol with a saturated or an unsaturated fatty acid and halogenated either after formation of the ester, or through the halogenation of either the alcohol or of the fatty acid, may be used.
- the halogenated ester may be formed by reacting a monovalent or a polyvalent alcohol, such, for example, as ethyl, methyl, propyl, isopropyl, butyl, isobutyl, glycerol, sorbitol, mannitol, a glycol, as ethylene glycol, diethylene glycol, propylene glycol, and L the like, etc. with a saturated or an unsaturated fatty acid, such as stearic, lauric, myristic, the acids derived from cocoanut oil, palm oil, soya bean oil, linseed oil, and. the like, etc.
- a monovalent or a polyvalent alcohol such, for example, as ethyl, methyl, propyl, isopropyl, butyl, isobutyl, glycerol, sorbitol, mannitol, a glycol, as ethylene glycol, diethylene glycol, propylene glycol,
- the ester may be formed in any manner well known to those skilled in the art.
- the ester may be formed by' reacting the alcohol and the fatty acid insuitable proportion, depending upon whether it is desired that the ester be neutral or on the acid side.
- the esterification will be carried out in the presence of heat and of an esterification catalyst.
- the halogenation of the ester may be accomplished witli iise of a halogen, as, for example, chlorine, bromine, iodine, etc.
- the halogenation as has been indicated, may be accomplished in any usual manner well known to those skilled in the art and may be accomplished by halogenating the finished ester or by halogenating the alcohol or the fatty acid beforereaction for the formation of' the ester.
- the halogenation may be accomplished to an extent such as to produce mono-, dior higher halogenated esters.
- mono-, dior higher chlorinated esters will be preferred.
- a mono-, di-, or higher chlorinated monovalent alcohol ester will be used and as a specific examplebutyl dichlorstearate will be found to be highly efficient and economical for use.
- the halogenated esters will be applied to textile fibers or synthetic yarns in the usual manner for lubricating or greasing, the yarns will then be processed mechanically in the usual manner and then washed for the removal of the halogenated ester.
- the halogenated esters indicated as used in accordance with this invention will be found to possess all the properties required of a lubricant for the purpose indicated. They will be found to have a low viscosity, to be liquid at ordinary temperatures and to be readily picked up by the fibers or yarn and they will not stain or discolor the fibers or yarn.
- the halogenated esters will be found to be stable, not to oxidize or become rancid and to have practically no odor. They can be prepared completely neutral or with any desired amount of free acid, as may be desired or indicated.
- halogenated esters contemplated will be found to have a high oily character such that much smaller quantity is required for the lubrication of a. given amount of textile fiber or yarn than is required of the lubricating agents heretofore used and, indeed, it is surprising to note that due to the high oily character of the halogenated esters a much smaller quantity is required than in the case of the corresponding non-halo-
- the halogenated esters may be,-
- halogenated esters will be readily emulsified and hence may be very readily and economically scoured out after the processing of the fibers or yarn.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented Mar. 28, 1939 PATENT OFFICE LUBRICATING TEXTILE FIBERS AND THE LIKE AND PRODUCT Ludwig W. Wasum, Germantown, Pa., assignor to The Kessler Chemical Corporation, Philadelphia, Pa., a corporation of Maryland No Drawing. Application August 8, 1938, Serial No. 223,699
10 Claims.
This invention relates to novel, eflicient and economical procedure for the lubrication of textile fibers, such as'natural fibers, in connection with the manufacture of combed or worsted yarn, and of synthetic yarns, such as rayon, and the like, in preparation for twisting or throwing. This invention also contemplates the novel lubricated fibers or yarn produced in accordance with the procedure.
HI Heretofore, as is well known, it has been necessary, in the manufacture of combed or worsted yarn, and the like, and in the twisting or throwing of synthetic yarns, as rayon, and the like, to lubricate the fibers or yarn in order that the fibers or yarn may freely pass and be worked upon by the mechanical instrumentalities used.
, Heretofore textile fibers, synthetic yarns, and the like, have been lubricated variously with natural fatty acids, such as so-called olein, and
20 fatty oils and it has been suggested that certain monovalent alcohol esters of fatty acids be used.
The natural fatty acids and fatty oils as heretofore used have proved sufiicient for the purpose of lubrication, but have been variously open to very definite disadvantage in that their effect upon themechanical instrumentalities is generally deleterious." The monovalent esters of fatty acids have proved of certain advantage, but have 30 been found to be variously disadvantageous,
more particularly in that they are to a degree uneconomic in that substantial quantities must be used to obtain the necessary lubricating effect.
Now in accordance with this invention pro- 85 cedure for the lubrication of textile fibers, synthetic yarns, and the like, and product thereof is provided which is at once highly efficient for treatment with the usual mechanical instrumentalities, highly economic in that a comparam tively small amount of the lubricant is required and the lubricant may be readily and economically washed out.
In accordance with this invention lubrication of textile fibers, syntheiic yarns, and the like,
5 is accomplished by treating the fibers, yarn, and
the like, with a halogenated ester of a saturated or an unsaturated fatty acid.
Any of the halogenated esters of a saturated or an unsaturated fatty acid, formed by the reaction of an alcohol with a saturated or an unsaturated fatty acid and halogenated either after formation of the ester, or through the halogenation of either the alcohol or of the fatty acid, may be used.
Thus, by way of illustration the halogenated ester may be formed by reacting a monovalent or a polyvalent alcohol, such, for example, as ethyl, methyl, propyl, isopropyl, butyl, isobutyl, glycerol, sorbitol, mannitol, a glycol, as ethylene glycol, diethylene glycol, propylene glycol, and L the like, etc. with a saturated or an unsaturated fatty acid, such as stearic, lauric, myristic, the acids derived from cocoanut oil, palm oil, soya bean oil, linseed oil, and. the like, etc.
The ester may be formed in any manner well known to those skilled in the art. Thus, for example, the ester may be formed by' reacting the alcohol and the fatty acid insuitable proportion, depending upon whether it is desired that the ester be neutral or on the acid side. Desirably, the esterification will be carried out in the presence of heat and of an esterification catalyst.
The halogenation of the ester may be accomplished witli iise of a halogen, as, for example, chlorine, bromine, iodine, etc. The halogenation, as has been indicated, may be accomplished in any usual manner well known to those skilled in the art and may be accomplished by halogenating the finished ester or by halogenating the alcohol or the fatty acid beforereaction for the formation of' the ester. The halogenation may be accomplished to an extent such as to produce mono-, dior higher halogenated esters.
By way of more specifically illustrating this invention, the use of mono-, dior higher chlorinated esters will be preferred. Preferably, a mono-, di-, or higher chlorinated monovalent alcohol ester will be used and as a specific examplebutyl dichlorstearate will be found to be highly efficient and economical for use.
In the procedure in accordance with this invention, the halogenated esters will be applied to textile fibers or synthetic yarns in the usual manner for lubricating or greasing, the yarns will then be processed mechanically in the usual manner and then washed for the removal of the halogenated ester. The halogenated esters indicated as used in accordance with this invention will be found to possess all the properties required of a lubricant for the purpose indicated. They will be found to have a low viscosity, to be liquid at ordinary temperatures and to be readily picked up by the fibers or yarn and they will not stain or discolor the fibers or yarn. The halogenated esters will be found to be stable, not to oxidize or become rancid and to have practically no odor. They can be prepared completely neutral or with any desired amount of free acid, as may be desired or indicated.
The halogenated esters contemplated will be found to have a high oily character such that much smaller quantity is required for the lubrication of a. given amount of textile fiber or yarn than is required of the lubricating agents heretofore used and, indeed, it is surprising to note that due to the high oily character of the halogenated esters a much smaller quantity is required than in the case of the corresponding non-halo- The halogenated esters may be,-
genated esters. where desired or indicated, mixed with other lubricating agents thereby making it possible where other lubricating agents are used, to reduce the required amount of such lubricating agents.
The halogenated esters will be readily emulsified and hence may be very readily and economically scoured out after the processing of the fibers or yarn.
What I claim and desire to protect by Letters Patent is:
1. The process .of treating textile fibers, synthetic yarns, and the like, which includes applying thereto a halogenated fatty acid ester of an alcohol.
2. The process of treating textile fibers, synthetic yarns, and the like, which includes applying thereto a chlorinated fatty acid ester of an alcohoL' 3. The process of treating textile fibers, synthetic yarns, and the like, which includes applying thereto a halogenated fatty acid ester of a monovalent alcohol.
4. The process of treating textile fibers, synthetic yarns, and the like, which includes applying thereto a halogenated fatty acid ester of a polyvalent alcohol.
5. The process of treating textile fibers, synthetic yarns, and the like, which includes applying thereto a chlorinated fatty acid ester of a monovalent alcohol.
6. The process of treating textile fibers, synthetic yarns, and the like, which includes applyingthereto a chlorinated fatty acid ester of a polyvalent alcohol.
7. The process of treating textile fibers, synthetic yarns, and the like, which includes applying thereto a dihalogenated ester of a monovalent alcohol.
8. The process of treating textile fibers, synthetic yarns, and the like, which includes applying thereto a dihalogenated ester of a polyvalent alcohol.
9. The process of treating textile fibers, synthetic yarns, and the like, which includes applying thereto butyl dichlorstearate.
10. In combination, a yarn formed of fibrous material and a halogenated fatty acid ester of an alcohol coated on and intermingled with fibers of the yarn and in amount such as to lubricate the yarn to facilitate manipulation thereof by mechanical instrumentalities.
LUDWIG W. VVASUM.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US223699A US2151952A (en) | 1938-08-08 | 1938-08-08 | Lubricating textile fibers and the like and product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US223699A US2151952A (en) | 1938-08-08 | 1938-08-08 | Lubricating textile fibers and the like and product |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2151952A true US2151952A (en) | 1939-03-28 |
Family
ID=22837642
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US223699A Expired - Lifetime US2151952A (en) | 1938-08-08 | 1938-08-08 | Lubricating textile fibers and the like and product |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2151952A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419756A (en) * | 1943-11-06 | 1947-04-29 | Du Pont | Process of sizing packages of yarn |
| US2436980A (en) * | 1945-01-01 | 1948-03-02 | Ind Rayon Corp | Tire cord and method of manufacture |
| US2436979A (en) * | 1944-07-26 | 1948-03-02 | Ind Rayon Corp | Tire cord and method of manufacture |
| US4359859A (en) * | 1980-09-18 | 1982-11-23 | Maize-Tech, Inc. | Twine formed of corn husks and leaves |
| US5466406A (en) * | 1992-12-11 | 1995-11-14 | United States Surgical Corporation | Process of treating filaments |
-
1938
- 1938-08-08 US US223699A patent/US2151952A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419756A (en) * | 1943-11-06 | 1947-04-29 | Du Pont | Process of sizing packages of yarn |
| US2436979A (en) * | 1944-07-26 | 1948-03-02 | Ind Rayon Corp | Tire cord and method of manufacture |
| US2436980A (en) * | 1945-01-01 | 1948-03-02 | Ind Rayon Corp | Tire cord and method of manufacture |
| US4359859A (en) * | 1980-09-18 | 1982-11-23 | Maize-Tech, Inc. | Twine formed of corn husks and leaves |
| US5466406A (en) * | 1992-12-11 | 1995-11-14 | United States Surgical Corporation | Process of treating filaments |
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