US2067175A - Treatment and manufacture of textile materials - Google Patents
Treatment and manufacture of textile materials Download PDFInfo
- Publication number
- US2067175A US2067175A US628181A US62818132A US2067175A US 2067175 A US2067175 A US 2067175A US 628181 A US628181 A US 628181A US 62818132 A US62818132 A US 62818132A US 2067175 A US2067175 A US 2067175A
- Authority
- US
- United States
- Prior art keywords
- filaments
- hydroxy
- fibres
- cutting
- artificial
- 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
- 238000004519 manufacturing process Methods 0.000 title description 14
- 239000000463 material Substances 0.000 title description 7
- 239000004753 textile Substances 0.000 title description 3
- 239000007788 liquid Substances 0.000 description 22
- 238000005520 cutting process Methods 0.000 description 18
- -1 hydroxy alkylamines Chemical class 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 10
- 238000002791 soaking Methods 0.000 description 10
- 238000009987 spinning Methods 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 239000000344 soap Substances 0.000 description 5
- 229920002301 cellulose acetate Polymers 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000012237 artificial material Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- AOHAPDDBNAPPIN-UHFFFAOYSA-N myristicinic acid Natural products COC1=CC(C(O)=O)=CC2=C1OCO2 AOHAPDDBNAPPIN-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N n-hexadecanoic acid Natural products CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- AFSHUZFNMVJNKX-CLFAGFIQSA-N 1,2-dioleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCC\C=C/CCCCCCCC AFSHUZFNMVJNKX-CLFAGFIQSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- PHDVPEOLXYBNJY-KTKRTIGZSA-N 2-(2-hydroxyethoxy)ethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCOCCO PHDVPEOLXYBNJY-KTKRTIGZSA-N 0.000 description 1
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- MSILLSJAIFXEKY-UHFFFAOYSA-N n-ethyl-n-phenylhydroxylamine Chemical compound CCN(O)C1=CC=CC=C1 MSILLSJAIFXEKY-UHFFFAOYSA-N 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01G—PRELIMINARY TREATMENT OF FIBRES, e.g. FOR SPINNING
- D01G1/00—Severing continuous filaments or long fibres, e.g. stapling
-
- 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
- Y10T428/2904—Staple length fiber
- Y10T428/2907—Staple length fiber with coating or impregnation
Definitions
- filaments of artificial material such as cellulose acetate and other cellulose derivatives, celluluosic artificial silks, and to a less degree, natural silk are of a smooth nature, so that staple fibres of such materials are extremely liable to slip and are more difficult to spin into spun yarns than the relatively rough natural fibres such as cotton and wool. Further, spinning of such fibres, particularly in the case of fibres of cellulose acetate or other cellulose derivatives, is rendered difficult by reason of the tendency of the fibres to become electrified during the spinning operation. According to this invention these difiiculties are overcome in a simple manner by a treatment of the filaments during their manufacture into staple fibre.
- filaments of cellulose acetate or other artificial materials are out into staple lengths while wet following soaking in liquids consisting of or containing a substance selected from the class consisting of compounds having the formula Rl-X-RZ, Where R1 is a hydroxy-or basis amino radicle and R2 is a different radicle' that is a basic amino, acidylamino or acidyl hydroxy radicle and X is an aliphatic residue, and addition products of said compounds with acids.
- the compounds of this class therefore in all cases contain an aliphatic residue (X) and a salt-forming group (a hydroxy or basic amino radicle) and may also contain an acidylated salt-forming group (an acidylamino or acidyl hydroxy radicle).
- a salt-forming group a hydroxy or basic amino radicle
- an acidylated salt-forming group an acidylamino or acidyl hydroxy radicle.
- Such organic compounds which may be used in accordance with the present invention are the hydroxy alkylamines and/or their derivatives, such as salts, soaps, esters, acid amides, particularly of the higher fatty acids, w-amino-'alkylamides of the higher fatty acids, or dior poly-hydric alcohol derivatives in which some of the hydroxy groups of the alcohols are esterified by fatty acids, particularly the higher fatty acids.
- the filaments are preferably treated in thick bundles, so that the wetted filaments lie compactly, preferably parallel, or substantially so, it being found that such bundles of wet filaments are both easy to handle and that cutting is facilitated.
- the application of the hydroxy alkylamine or other'body is eifected in a convenient manner so as to leave a quantity of such material on the fibres being spun which overcomes any difllculty in the several spinning steps due to a tendency of electrification.
- the hydroxy alkylamines or other bodies may be employed as such, or, where convenient or desired, in the form of solutions or suspension in water or organic solvents in presence or absence of other materials.
- the bodies or any other liquid in which they are applied should not be capable of exerting any detrimental action on the material of the yarns.
- hydroxy alkylamines such as mono-, dior tri' ethanolamine, propanolamine, or dioxy-propylamine may be employed, it is, however, preferred that the hydroxy alkaylamines or other bodies employed have a relative high molecular weight.
- Substituted hydroxy alkylamines such for example as hydroXy-ethyl-aniline may also be used.
- the hydroxy alkylamines may be employed as such or in the form of their derivatives, such as salts, soaps, esters, and .acid amides and particularly their salts, soaps, esters, or acid amides of higher fatty acids such, for instance, as capric, lauric, myristic, oleic, and stearic acid.
- the salts or soaps may be the true salts or soaps i. e. containing the molecular equivalents of hydroxy alkylamine and acid or they may contain excess of the same or a different hydroxy alkylamine or of the same or a diiferent acid.
- partial esters of polyvalent alcohols which may be used according to the invention may be mentioned the higher fatty acid esters of glycols or glycerol, which esters contain free hydroxy groups, for example glycerol mono-oleate, glycerol di-oleate, ethylene glycol mono-oleate and diethylene glycol mono-oleate.
- esters of other saturated or unsaturated higher fatty acids containing more than 5, e. g. more than 10 carbon atoms, for example stearic, palmitic, or ricinoleic acid.
- the filament bundles are conveniently in ,the form of hanks and may be treated with the liquid while still on the swift, reel, or drum on which the hank is wound or after removal therefrom.
- a larger amount of liquid can be taken up, giving the mass a firmness and consistency which is advantageous in handling and cutting while offertioned as examples of solutions that may be ing no inconvenience because of excess liquid.
- the hanks prior to cutting may be placed while on the swift or other device on which they are wound, or after being removed therefrom, into a vessel containing the liquid to be applied.
- Solutions of ethanolamines in paraffin oils such for,instance as solutions of triethanolamine in parafiin oils with boiling points of about 110 and upwards, and containing from about 10 to 40% or more of triethanolamine, may be menemployed for the purposes of the invention.
- the hanks are cut into staple lengths as by means of a guillotine,
- Drying of the masses of cut fibres may be carried out-either by leaving the fibres on trays, conveyors or the like, or in bags or other containers exposed to the open air or by placing them in suitable chambers, and may be aided,
- the fibres are brought into a suitable condition for spinning, the hydroxy alkylamine or other body being left on the fibres to an amount dependent on the concentration of the applied liquid and the amount of liquid applied to the filaments.
- the drying operation referred to above may be preceded by a preliminary centrifuging operation, adapted to reduce the bulk of the liquid on the fibre from, say, which is a suitable proportion for the cutting operation, to, say, 30 to 40% of the weight of the fibre, the concentration of the hydroxy alkylamine or other body in the liquid applied being increased to correspond with the reduced bulk of liquid actually dried ofi the yarn.
- Roughening media such as silica, barytes, lithopone, and kieselguhr, -or the soluble salts described in U. S. application S. No. 585,381 filed 7th January, 1932, may be applied to the filaments or fibres conjointly with or separately from the hydroxy alkylamines or other bodies to increase the friction between the fibres and so aid the spinning operations.
- the filaments may be lubricated, e. g. with olive oil, prior to winding or cutting, or instead of or in addition to such lubricating, a lubricant may be added during the treatment with the hydroxy alkylamines or other bodies.
- liquids containing hydroxy alkylamines .or other bodies may be applied to hanks of filaments by dipping the hanks in solutions.
- Other methods may, however, be employed in which more accurate control of the amount of applied hydroxy alkylamine or other body may be eiiected.
- the hanks may be sprayed, or the bodies or liquids containing them may be applied to the filaments in winding operations, e. g. continuously with the production of filaments by the dry or evaporative method,- the hanks or the packages formed being left wet in readiness for the cutting operation.
- the fibres may be somewhat matted by the wet treatment, but this can be remedied by treatment of the fibres in an apparatus appropriate to their length. For example, in the case of fibres having, a length of say l -2 inches, passage of the dried fibres through an, opener, and subsequently through a scutcher, both of the type used in'the preliminary operations of cotton spinning, readily brings them into a suitable state for the carding operation forming the first of the spinning steps to which such fibres are subjected.
- the bodies applied to the fibres may be removed from'the yarns immediately after spinning, but in general it is suflicient to allow soaking continuous artificial filaments in a liquid containing a substance selected from the class consisting of compounds having the formula R1X-R2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic aminc and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
- a substance selected from the class consisting of compounds having the formula R1X-R2 where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic aminc and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
- Process for the production of staple lengths of artificial filaments comprising soaking continuous artificial filaments in a solution' of an ethanolamine in a 'parafiin oil, and then cutting the filaments into staple lengths while they are still wet.
- Process for the production of staple lengths of artificial filaments comprising soaking continuous artificial filaments in a liquid containing an w-amino-alkylamide of a higher fatty acid, and then cutting the filaments into staple lengths while they are still wet.
- Process for the production of staple lengths of artificial filaments comprising soaking continuous artificial'filaments in a liquid containing a substance selected from the class consistingpf compounds having the formula R1XR2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, forming the continuous filaments into bundles and then cutting the filaing of compounds having the formula Rl-X-Ri, 75
- R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
- Process for the production of staple lengths oi artificial filaments comprising soaking continuous artificialfilaments oi cellulose acetate in a liquid containing a substance selected from the class consisting of compounds having the formula RI-XR:, where R1 is a hydroxy group or basic amino radicle and R: is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition prodnets of said-compoimds with acids, and then cutting the filaments into staple lengths while they are stillwet.
- RI-XR a substance selected from the class consisting of compounds having the formula RI-XR:, where R1 is a hydroxy group or basic amino radicle and R: is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue
- Process for the production of artificial staple fibres which comprises soaking continuous artificial filaments in a liquid containing a hydroxy alkylamine and then cutting the filaments into staple lengths while they are still wet.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented Jan. 12, 1937 UNITED STATES TREATMENT AND MANUFACTURE OF TEXTILE MATERIALS William Alexander Dickie and William Ivan Taylor, Spondon, near Derby, England, assignors to Celanese Corporation of America, a corporation of Delaware No Drawing. Application August 10, 1932, Serial No. 628,181. In Great Britain August 26, 1931 10 Claims. (01. 18-54) This invention relates to the treatment and manufacture of textile materials and in particular to the manufacture of staple fibre from spun yarns.
It is well known that filaments of artificial material such as cellulose acetate and other cellulose derivatives, celluluosic artificial silks, and to a less degree, natural silk are of a smooth nature, so that staple fibres of such materials are extremely liable to slip and are more difficult to spin into spun yarns than the relatively rough natural fibres such as cotton and wool. Further, spinning of such fibres, particularly in the case of fibres of cellulose acetate or other cellulose derivatives, is rendered difficult by reason of the tendency of the fibres to become electrified during the spinning operation. According to this invention these difiiculties are overcome in a simple manner by a treatment of the filaments during their manufacture into staple fibre.
According to the invention filaments of cellulose acetate or other artificial materials are out into staple lengths while wet following soaking in liquids consisting of or containing a substance selected from the class consisting of compounds having the formula Rl-X-RZ, Where R1 is a hydroxy-or basis amino radicle and R2 is a different radicle' that is a basic amino, acidylamino or acidyl hydroxy radicle and X is an aliphatic residue, and addition products of said compounds with acids. The compounds of this class therefore in all cases contain an aliphatic residue (X) and a salt-forming group (a hydroxy or basic amino radicle) and may also contain an acidylated salt-forming group (an acidylamino or acidyl hydroxy radicle). Such organic compounds which may be used in accordance with the present invention are the hydroxy alkylamines and/or their derivatives, such as salts, soaps, esters, acid amides, particularly of the higher fatty acids, w-amino-'alkylamides of the higher fatty acids, or dior poly-hydric alcohol derivatives in which some of the hydroxy groups of the alcohols are esterified by fatty acids, particularly the higher fatty acids. Mixtures of two or more of such bodies may also be used. The filaments are preferably treated in thick bundles, so that the wetted filaments lie compactly, preferably parallel, or substantially so, it being found that such bundles of wet filaments are both easy to handle and that cutting is facilitated. At the same time, the application of the hydroxy alkylamine or other'body is eifected in a convenient manner so as to leave a quantity of such material on the fibres being spun which overcomes any difllculty in the several spinning steps due to a tendency of electrification.
The hydroxy alkylamines or other bodies may be employed as such, or, where convenient or desired, in the form of solutions or suspension in water or organic solvents in presence or absence of other materials. In fact, it is preferable to apply the bodies in solvents which can be wholly or partially removed from the fibres after cutting to leave the fibres with the required quantity of the applied body and at the degree of dryness necessary for the subsequent spinning operation. The bodies or any other liquid in which they are applied should not be capable of exerting any detrimental action on the material of the yarns.
Though any of the simple hydroxy alkylamines such, for example, as mono-, dior tri' ethanolamine, propanolamine, or dioxy-propylamine may be employed, it is, however, preferred that the hydroxy alkaylamines or other bodies employed have a relative high molecular weight. Substituted hydroxy alkylamines such for example as hydroXy-ethyl-aniline may also be used. The hydroxy alkylamines may be employed as such or in the form of their derivatives, such as salts, soaps, esters, and .acid amides and particularly their salts, soaps, esters, or acid amides of higher fatty acids such, for instance, as capric, lauric, myristic, oleic, and stearic acid. The salts or soaps may be the true salts or soaps i. e. containing the molecular equivalents of hydroxy alkylamine and acid or they may contain excess of the same or a different hydroxy alkylamine or of the same or a diiferent acid.
As examples of partial esters of polyvalent alcohols which may be used according to the invention may be mentioned the higher fatty acid esters of glycols or glycerol, which esters contain free hydroxy groups, for example glycerol mono-oleate, glycerol di-oleate, ethylene glycol mono-oleate and diethylene glycol mono-oleate. Instead of the oleai-es there may be used corresponding esters of other saturated or unsaturated higher fatty acids containing more than 5, e. g. more than 10 carbon atoms, for example stearic, palmitic, or ricinoleic acid.
The filament bundles are conveniently in ,the form of hanks and may be treated with the liquid while still on the swift, reel, or drum on which the hank is wound or after removal therefrom. By arranging the filaments compactly, a larger amount of liquid can be taken up, giving the mass a firmness and consistency which is advantageous in handling and cutting while offertioned as examples of solutions that may be ing no inconvenience because of excess liquid. Thus the hanks prior to cutting may be placed while on the swift or other device on which they are wound, or after being removed therefrom, into a vessel containing the liquid to be applied. Solutions of ethanolamines in paraffin oils, such for,instance as solutions of triethanolamine in parafiin oils with boiling points of about 110 and upwards, and containing from about 10 to 40% or more of triethanolamine, may be menemployed for the purposes of the invention.
'After being allowed to drainuntil they contain the desired amount of liquid, the hanks are cut into staple lengths as by means of a guillotine,
cutting machine.
Drying of the masses of cut fibres may be carried out-either by leaving the fibres on trays, conveyors or the like, or in bags or other containers exposed to the open air or by placing them in suitable chambers, and may be aided,
if desired-by such means as air currents, vacuum, or heat, or combinations thereof for the removal of less volatile constituents of the applied liquid. In this way the fibres are brought into a suitable condition for spinning, the hydroxy alkylamine or other body being left on the fibres to an amount dependent on the concentration of the applied liquid and the amount of liquid applied to the filaments. The drying operation referred to above may be preceded by a preliminary centrifuging operation, adapted to reduce the bulk of the liquid on the fibre from, say, which is a suitable proportion for the cutting operation, to, say, 30 to 40% of the weight of the fibre, the concentration of the hydroxy alkylamine or other body in the liquid applied being increased to correspond with the reduced bulk of liquid actually dried ofi the yarn.
Roughening media such as silica, barytes, lithopone, and kieselguhr, -or the soluble salts described in U. S. application S. No. 585,381 filed 7th January, 1932, may be applied to the filaments or fibres conjointly with or separately from the hydroxy alkylamines or other bodies to increase the friction between the fibres and so aid the spinning operations. The filaments may be lubricated, e. g. with olive oil, prior to winding or cutting, or instead of or in addition to such lubricating, a lubricant may be added during the treatment with the hydroxy alkylamines or other bodies.
As stated above, liquids containing hydroxy alkylamines .or other bodies may be applied to hanks of filaments by dipping the hanks in solutions. Other methods may, however, be employed in which more accurate control of the amount of applied hydroxy alkylamine or other body may be eiiected. For example, the hanks may be sprayed, or the bodies or liquids containing them may be applied to the filaments in winding operations, e. g. continuously with the production of filaments by the dry or evaporative method,- the hanks or the packages formed being left wet in readiness for the cutting operation.
The fibres may be somewhat matted by the wet treatment, but this can be remedied by treatment of the fibres in an apparatus appropriate to their length. For example, in the case of fibres having, a length of say l -2 inches, passage of the dried fibres through an, opener, and subsequently through a scutcher, both of the type used in'the preliminary operations of cotton spinning, readily brings them into a suitable state for the carding operation forming the first of the spinning steps to which such fibres are subjected. v 1
If desired the bodies applied to the fibres may be removed from'the yarns immediately after spinning, but in general it is suflicient to allow soaking continuous artificial filaments in a liquid containing a substance selected from the class consisting of compounds having the formula R1X-R2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic aminc and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
2. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a liquid containing an ethanolamine, and then cutting the filaments into staple lengths while they are still wet.
3. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a solution' of an ethanolamine in a 'parafiin oil, and then cutting the filaments into staple lengths while they are still wet.
4. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a solution of triethanolamine in a parafiin oil, and then cutting the filaments into staple lengths while they are still wet. 1
5. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a liquid containing an w-amino-alkylamide of a higher fatty acid, and then cutting the filaments into staple lengths while they are still wet.
6. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial'filaments in a liquid containing a substance selected from the class consistingpf compounds having the formula R1XR2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, forming the continuous filaments into bundles and then cutting the filaing of compounds having the formula Rl-X-Ri, 75
where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
8. Process for the production of staple lengths oi artificial filaments, said process comprising soaking continuous artificialfilaments oi cellulose acetate in a liquid containing a substance selected from the class consisting of compounds having the formula RI-XR:, where R1 is a hydroxy group or basic amino radicle and R: is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition prodnets of said-compoimds with acids, and then cutting the filaments into staple lengths while they are stillwet.
9. Process for the production of artificial staple fibres, which comprises soaking continuous artificial filaments in a liquid containing a hydroxy alkylamine and then cutting the filaments into staple lengths while they are still wet.
1 10. Process for the production of artificial staple fibres, which comprises soaking continuous artificial filaments in a liquid containing a partial acidyl derivative oi a hydroxy alkylaminc, and then cutting the filaments into staple lengths while they are still wet.
WILLIAM Amman mcxm. WILLIAM IVAN rams.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2067175X | 1931-08-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2067175A true US2067175A (en) | 1937-01-12 |
Family
ID=10897548
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US628181A Expired - Lifetime US2067175A (en) | 1931-08-26 | 1932-08-10 | Treatment and manufacture of textile materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2067175A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2493031A (en) * | 1946-03-29 | 1950-01-03 | Reid John David | Prevention of degradation of textile fibers by acids |
| US2628937A (en) * | 1949-01-18 | 1953-02-17 | Courtaulds Ltd | Antistatic textile treating composition of triethanolamine-aliphatic carboxylic acidsalts |
| US2713547A (en) * | 1952-08-08 | 1955-07-19 | Edward R Frederick | Simulated down filler and method of making the same |
| US2948103A (en) * | 1960-08-09 | Process for the manufacture of | ||
| US3203821A (en) * | 1961-05-25 | 1965-08-31 | Plate Gmbh Dr | Flocks for the production of velvet-like or plush-like materials and process for theproduction of such materials by electrostatic means |
-
1932
- 1932-08-10 US US628181A patent/US2067175A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2948103A (en) * | 1960-08-09 | Process for the manufacture of | ||
| US2493031A (en) * | 1946-03-29 | 1950-01-03 | Reid John David | Prevention of degradation of textile fibers by acids |
| US2628937A (en) * | 1949-01-18 | 1953-02-17 | Courtaulds Ltd | Antistatic textile treating composition of triethanolamine-aliphatic carboxylic acidsalts |
| US2713547A (en) * | 1952-08-08 | 1955-07-19 | Edward R Frederick | Simulated down filler and method of making the same |
| US3203821A (en) * | 1961-05-25 | 1965-08-31 | Plate Gmbh Dr | Flocks for the production of velvet-like or plush-like materials and process for theproduction of such materials by electrostatic means |
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