US2030739A - Process of producing silicon-rayon - Google Patents
Process of producing silicon-rayon Download PDFInfo
- Publication number
- US2030739A US2030739A US749488A US74948834A US2030739A US 2030739 A US2030739 A US 2030739A US 749488 A US749488 A US 749488A US 74948834 A US74948834 A US 74948834A US 2030739 A US2030739 A US 2030739A
- Authority
- US
- United States
- Prior art keywords
- silicon
- rayon
- solution
- aliphatic
- compounds
- 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
- 229920000297 Rayon Polymers 0.000 title description 17
- 239000002964 rayon Substances 0.000 title description 8
- 238000000034 method Methods 0.000 title description 7
- 238000009987 spinning Methods 0.000 description 14
- 229920002678 cellulose Polymers 0.000 description 10
- 239000001913 cellulose Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- -1 aliphatic silicon compounds Chemical class 0.000 description 8
- 150000003377 silicon compounds Chemical class 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- 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 3
- 239000000126 substance Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- GFDAFHTWDMJGEF-UHFFFAOYSA-N 2-chloroethyl(triethyl)silane Chemical compound CC[Si](CC)(CC)CCCl GFDAFHTWDMJGEF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- 229910003828 SiH3 Inorganic materials 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical class [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- UCKORWKZRPKRQE-UHFFFAOYSA-N bromo(triethyl)silane Chemical compound CC[Si](Br)(CC)CC UCKORWKZRPKRQE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- DCFKHNIGBAHNSS-UHFFFAOYSA-N chloro(triethyl)silane Chemical compound CC[Si](Cl)(CC)CC DCFKHNIGBAHNSS-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- KCWYOFZQRFCIIE-UHFFFAOYSA-N ethylsilane Chemical compound CC[SiH3] KCWYOFZQRFCIIE-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- KCIKCCHXZMLVDE-UHFFFAOYSA-N silanediol Chemical class O[SiH2]O KCIKCCHXZMLVDE-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- OLRJXMHANKMLTD-UHFFFAOYSA-N silyl Chemical compound [SiH3] OLRJXMHANKMLTD-UHFFFAOYSA-N 0.000 description 1
- VCZQFJFZMMALHB-UHFFFAOYSA-N tetraethylsilane Chemical compound CC[Si](CC)(CC)CC VCZQFJFZMMALHB-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- WVMSIBFANXCZKT-UHFFFAOYSA-N triethyl(hydroxy)silane Chemical compound CC[Si](O)(CC)CC WVMSIBFANXCZKT-UHFFFAOYSA-N 0.000 description 1
- ZHOVAWFVVBWEGQ-UHFFFAOYSA-N tripropylsilane Chemical compound CCC[SiH](CCC)CCC ZHOVAWFVVBWEGQ-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
- D01F2/08—Composition of the spinning solution or the bath
- D01F2/12—Addition of delustering agents to the spinning solution
Definitions
- the present invention relates to a process of luster cellulosic products obtained therefrom, preparing cellulosic spinning solutions from have the great disadvantage of being inflammawhich soft-lustre products, such as filaments, ble, while vegetable oils become rancid and form yarns, ribbons, films, etc., may be produced. skin-irritating acids.
- the primary object of my invention has to I have, unexpectedly, found that aliphatic silii wi t p a on of aliphatic silicon con compounds possess properties which render compounds into cellulosic spinning solutions, them especially suitable as delustering agents such as viscose and cuprammonium cellulose, for rayon products since they are very little inwhich will yield upon extrusion or molding softflammable and do not form irritating compounds. 1 lustre products of pleasing hand.
- Boiling or A fourth object of my invention has to do with 9 melting point the dispersion of silicon compounds in the aforementioned cellulosic solutions, these com- 1mm: centi- Methylqnonosflang W 2 0 31 which R represents an alkyl radical.
- a fifth object of this invention relates to the l fiiiifignm 2mm formation of novel, soft-lustre products per se lsoflmi'i-monosilane 275-279 Al hi 11 ml laralk l-sil as. containing aliphatic silicon compounds. so 2 er 0 y an
- Other objects of my invention will become apparent to those skilled in the art after a study Derivatives having the structure R'SzHZ'OH of the following specification. Boning f 5 In the early days of rayon manufacture, the melting point demand was entirely for yarns having the highest possibledegree of lustre.
- Hydroisobutyl-monosilane triiscamyl-monosilane, tetcarbons, emulsified with spinning solutions to deraisoamyl-monosilane, triethyl-ethoxy-monosilto the solution, may be varied at will.
- Example About 1 to 30% of an aliphatic silicon compound is dispersed in, and/or. emulsified with a cellulosic spinning solution, such as viscose and cuprammonium cellulose, the aforementioned percentage being based upon the cellulose content of the solution.
- a cellulosic spinning solution such as viscose and cuprammonium cellulose
- After uniformly distributing the delustering agent in the spinning solution it is extruded through suitable spinning nozzles into a conventional spinning bath.
- the solution may also be used for forming films or molding articles.
- Organic solvents, inorganic or organic pigments, etc. may be added to the spinning solutions besides silicon compounds.
- the amounts of aliphatic silicon compounds, added In this manner more" or less delustered rayon products may be obtained.
- aliphatic silicon compound is limited to such compounds which are substantially water-insoluble and resistant to attack by alkalis and acids of such concentrations conventionally used in the rayon art.
- a spinning solution for the manufacture of soft-lustre products comprising a solution of the group consisting of viscose and cuprammonium cellulose and a silicon compound having the structure R.SiHa, in which It represents an alkyl radical, said compound being liquid and stable in said spinning solution.
- a spinning solution for the manufacture 0! soft-lustre products comprising a solution of the group consisting of viscose and cuprammonilun cellulose together with a substance of the group consisting of aliphatic silicon compounds having the structure RBiH: in which R represents an alkyl radical, aliphatic silicon compounds having the structure R.SiH(OH)2 in which It represents an alkyl radical and aliphatic silicon compoimds' having the structure R.-.SiHz.OH in which R represents an alkyl radical, said substance being stable in said solution.
- a spinning solution for themanufacture of soft-lustre products comprising a solution of the group consisting of viscose and cuprammonium cellulose together with a silicon compound having the structure RBKOH): in which R represents an alkyl radical, said compound being stable in said solution.
- a spinning solution for the manufacture of soft-lustre products comprising a solution "of the group consisting of viscose and cuprammonium cellulose together with a silicon compound having the structure RBiHzDI-I in which R represents an alkyl radical, said compound being stable vin said solution,
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Artificial Filaments (AREA)
Description
Patented at. 11, 1936 v 2,030,739
UNITED STATES PATENT OFFICE r I PROCESS OF PRODUCING SILICON-RAYON Rudolph S. Blcy, Elizabethton, Tenn., asslgnor to North American Rayon Corporation, New York,
N. Y., a corporation of Delaware No Drawing. Application October 22, 1934,
Serial No. 749,488
8 Claims. (01. 106-40) The present invention relates to a process of luster cellulosic products obtained therefrom, preparing cellulosic spinning solutions from have the great disadvantage of being inflammawhich soft-lustre products, such as filaments, ble, while vegetable oils become rancid and form yarns, ribbons, films, etc., may be produced. skin-irritating acids.
The primary object of my invention has to I have, unexpectedly, found that aliphatic silii wi t p a on of aliphatic silicon con compounds possess properties which render compounds into cellulosic spinning solutions, them especially suitable as delustering agents such as viscose and cuprammonium cellulose, for rayon products since they are very little inwhich will yield upon extrusion or molding softflammable and do not form irritating compounds. 1 lustre products of pleasing hand. The following table depicts a number of aliphatic Another object of my invention relates to the silicon compoundswhich may be used to deluster admixture o Silicon D V 8 h u cellulosic products, although I wish to emphasizeture R.SlHa in which R represents an alkyl radithat my invention is not limited to these comcal, with viscose and cuprammonium cellulose. pounds since others may be used with equal A third object of my invention has to do with success. I the incorporation of silicon compounds into TABLE viscose and cuprammonium cellulose solutions, saidc ompou'nds having the structure R.SiH3.OH in which R. represents an alkyl radical.
I. Derivatives having the structure 12.8111:
Boiling or A fourth object of my invention has to do with 9 melting point the dispersion of silicon compounds in the aforementioned cellulosic solutions, these com- 1mm: centi- Methylqnonosflang W 2 0 31 which R represents an alkyl radical. E 322 23; ig}
A fifth object of this invention relates to the l fiiiifignm 2mm formation of novel, soft-lustre products per se lsoflmi'i-monosilane 275-279 Al hi 11 ml laralk l-sil as. containing aliphatic silicon compounds. so 2 er 0 y an Other objects of my invention will become apparent to those skilled in the art after a study Derivatives having the structure R'SzHZ'OH of the following specification. Boning f 5 In the early days of rayon manufacture, the melting point demand was entirely for yarns having the highest possibledegree of lustre. Later, when it was Duvet-1 cm!!- found that highly lustrous rayon too clearly indimnm mm m e 154 cated its origin-an artificial fibre-Pa demand f w i 1106-2118 55 arose tor artificial silk which more closely apgg g iffiiattt" 269470 proximated to natural silk. The earliest attempt Also higher molecular alkvlsilanolsto meet the demand of dull-lustre viscose yarn, for example, was a method of retaining sulphur III. Derivatives having the structure R.Si0.0H particles in the fibres by discontinuing the norto mal desulphurizing step during its manufacture. i Compound p Although this yarn showed decreased lustre, due to scattering of light by the sulphur particles, it smwmmtic acid Sand. was impermanent and exhibited an unattractive Siliconropionic acid Do. .bloom". This method has been improved by ai -gagg 8:
dispersing, instead of sulphur, fine inorganic or Also higher-molecularsilicon-iattyacid compounds. organic particles and globules in cellulosic spinhing 501111510118, for e P ments, hydrocar- In addition, I have found that other aliphatic bons, oils, etc, When inorganic compounds, such silicon compounds may be used for the purposes, as titanium dioxide, silica, etc., are dispersed in set forth above, such as tetraethyl-monosilane, cellulosic spinning solutions, they tend to cut the triethyl-chlorethyl-monosilane, triethyl-acetoxytread guides through which the yarns are led ethyl-monosilane, halogenated monosilanes, tetduring the extrusion process, and in addition they rapropyl-monosilane, tripropyl-monosilane, triweaken cellulosic yarns considerably. Hydroisobutyl-monosilane, triiscamyl-monosilane, tetcarbons, emulsified with spinning solutions to deraisoamyl-monosilane, triethyl-ethoxy-monosilto the solution, may be varied at will.
ans, triethyl-monosilanol, siliconheptyl carbonic acid, triethyl-silicon chloride, triethyl-silicon bromide, silicon heptyloxide, .tripropyl-monosilanol acetate, tripropyl-monosilyl bromide, bis- (tripropyl-monosilyl' ether) 'triisobutyl-monosilyl bromide, triisoamyl-monosilyl bromide, bis- (triamyl-monosilyl ether), monosilyl derivatives of an city-compound, derivatives of monosilandiols having the structure R.BiH( OH) methyl-orthosilicic acid-triethylester, ethylorthosillcic acid-trimethyiester, ethyl-orthosilicic acid-triethylester, orthosllico-butyric acid-triethylester, orthosilico-isocaproic acid-triethylester, etc.
Example About 1 to 30% of an aliphatic silicon compound is dispersed in, and/or. emulsified with a cellulosic spinning solution, such as viscose and cuprammonium cellulose, the aforementioned percentage being based upon the cellulose content of the solution. After uniformly distributing the delustering agent in the spinning solution, it is extruded through suitable spinning nozzles into a conventional spinning bath. The solution may also be used for forming films or molding articles. Organic solvents, inorganic or organic pigments, etc., may be added to the spinning solutions besides silicon compounds. The amounts of aliphatic silicon compounds, added In this manner more" or less delustered rayon products may be obtained.
' Modifications of my process will readily be recognized by those skilled in the art, and, I desire to include all those modifications falling within the scope of the appended claims. In these claims, the term aliphatic silicon compound is limited to such compounds which are substantially water-insoluble and resistant to attack by alkalis and acids of such concentrations conventionally used in the rayon art.
I claim: u 1 1. A spinning solution for the manufacture of soft-lustre products comprising a solution of the group consisting of viscose and cuprammonium cellulose and a silicon compound having the structure R.SiHa, in which It represents an alkyl radical, said compound being liquid and stable in said spinning solution.
, 2. As a new article of manufacture. r senerated cellulose containing a liquid finely dispersed silicon compound having the structure RBiHa, in which R represents an alkyl radical.
3..A spinning solution for the manufacture 0! soft-lustre products comprising a solution of the group consisting of viscose and cuprammonilun cellulose together with a substance of the group consisting of aliphatic silicon compounds having the structure RBiH: in which R represents an alkyl radical, aliphatic silicon compounds having the structure R.SiH(OH)2 in which It represents an alkyl radical and aliphatic silicon compoimds' having the structure R.-.SiHz.OH in which R represents an alkyl radical, said substance being stable in said solution.
4. A spinning solution for themanufacture of soft-lustre products comprising a solution of the group consisting of viscose and cuprammonium cellulose together with a silicon compound having the structure RBKOH): in which R represents an alkyl radical, said compound being stable in said solution.
5. A spinning solution for the manufacture of soft-lustre products comprising a solution "of the group consisting of viscose and cuprammonium cellulose together with a silicon compound having the structure RBiHzDI-I in which R represents an alkyl radical, said compound being stable vin said solution,
6. As a new article of manufacture, regenerated cellulose containing a finely dispersed substance of the group consisting of aliphatic silicon compounds having the structure R.SiI-Ia in which R.
represents an alkyl radical, aliphatic silicon com- I RUDOLPH B. BLEY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US749488A US2030739A (en) | 1934-10-22 | 1934-10-22 | Process of producing silicon-rayon |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US749488A US2030739A (en) | 1934-10-22 | 1934-10-22 | Process of producing silicon-rayon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2030739A true US2030739A (en) | 1936-02-11 |
Family
ID=25013948
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US749488A Expired - Lifetime US2030739A (en) | 1934-10-22 | 1934-10-22 | Process of producing silicon-rayon |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2030739A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2439689A (en) * | 1948-04-13 | Method of rendering glass | ||
| US2444555A (en) * | 1945-09-05 | 1948-07-06 | Corning Glass Works | Heat transfer media |
| US2510853A (en) * | 1946-06-06 | 1950-06-06 | Dow Chemical Co | Methyl octadecyl dichlorosilane |
| US2595465A (en) * | 1944-11-24 | 1952-05-06 | Minnesota Mining & Mfg | Structures involving particles or mineral granules treated with organic silicon compounds and method of making |
| US2698334A (en) * | 1945-03-27 | 1954-12-28 | Montclair Res Corp | Arylhalosilanes |
| US2751369A (en) * | 1945-03-30 | 1956-06-19 | Gen Tire & Rubber Co | Pigmented compositions and methods of making same |
| US2841566A (en) * | 1952-08-02 | 1958-07-01 | Gen Tire & Rubber Co | High polymers with chemically bonded reinforcing and method of making same |
-
1934
- 1934-10-22 US US749488A patent/US2030739A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2439689A (en) * | 1948-04-13 | Method of rendering glass | ||
| US2595465A (en) * | 1944-11-24 | 1952-05-06 | Minnesota Mining & Mfg | Structures involving particles or mineral granules treated with organic silicon compounds and method of making |
| US2698334A (en) * | 1945-03-27 | 1954-12-28 | Montclair Res Corp | Arylhalosilanes |
| US2751369A (en) * | 1945-03-30 | 1956-06-19 | Gen Tire & Rubber Co | Pigmented compositions and methods of making same |
| US2444555A (en) * | 1945-09-05 | 1948-07-06 | Corning Glass Works | Heat transfer media |
| US2510853A (en) * | 1946-06-06 | 1950-06-06 | Dow Chemical Co | Methyl octadecyl dichlorosilane |
| US2841566A (en) * | 1952-08-02 | 1958-07-01 | Gen Tire & Rubber Co | High polymers with chemically bonded reinforcing and method of making same |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2819173A (en) | Synthetic fibers and the like | |
| US2030739A (en) | Process of producing silicon-rayon | |
| US2030738A (en) | Cellulosic spinning solutions containing aliphatic silicon compounds | |
| US2072102A (en) | Spinning of artificial filaments | |
| US2030737A (en) | Cellulosic spinning solutions containing aromatic silicon derivatives | |
| US2030736A (en) | Process of producing disilanerayon | |
| GB508840A (en) | Process for the preparation of artificial silk, artificial spun fibres, horsehair, bands, films and the like from soya bean casein | |
| US2136463A (en) | Method of preparing tubular artificial textile threads | |
| US1987095A (en) | Spinning solutions for the manufacture of soft-luster rayon | |
| US2099441A (en) | Cellulosic product and method for preparing same | |
| US2136464A (en) | Method of preparing tubular artificial textile threads | |
| US2069805A (en) | Cellulosic structures and methods for producing same | |
| US2060787A (en) | Viscose and cuprammonium cellulose spinning solutions and products thereof | |
| US2324567A (en) | Manufacture of artificial filaments, threads, and the like | |
| US2069804A (en) | Cellulosic material and method for making same | |
| US2057141A (en) | Production of filaments, threads, bands, ribbons and the like, from cellulose derivatives | |
| US1931239A (en) | Process of producing artificial silk | |
| US2284839A (en) | Cellulose spinning solution and filament produced therefrom | |
| US2310221A (en) | Artificial filament and the like | |
| GB523864A (en) | Improvements in and relating to the manufacture and production of artificial threads and the like articles | |
| US2069800A (en) | Cellulosic structures | |
| US2432128A (en) | Method of improving the processing of refined chemical pulp into viscose | |
| US2063001A (en) | Cellulosic spinning solution | |
| US1922910A (en) | Manufacture of filaments, threads, etc. | |
| US2066340A (en) | Yarns and filaments and method of making the same |