US2108455A - Process for rendering a textile material resistant to moisture - Google Patents
Process for rendering a textile material resistant to moisture Download PDFInfo
- Publication number
- US2108455A US2108455A US71851634A US2108455A US 2108455 A US2108455 A US 2108455A US 71851634 A US71851634 A US 71851634A US 2108455 A US2108455 A US 2108455A
- Authority
- US
- United States
- Prior art keywords
- ester
- moisture
- cellulose
- rendering
- salt
- 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
- 239000000463 material Substances 0.000 title description 23
- 238000000034 method Methods 0.000 title description 13
- 239000004753 textile Substances 0.000 title description 11
- 238000009877 rendering Methods 0.000 title description 8
- 229920002678 cellulose Polymers 0.000 description 25
- 239000004744 fabric Substances 0.000 description 17
- 150000003839 salts Chemical class 0.000 description 15
- 150000002148 esters Chemical class 0.000 description 14
- 239000000243 solution Substances 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 239000004014 plasticizer Substances 0.000 description 7
- 230000001172 regenerating effect Effects 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 238000009736 wetting Methods 0.000 description 6
- 229920000623 Cellulose acetate phthalate Polymers 0.000 description 5
- 229940081734 cellulose acetate phthalate Drugs 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 4
- -1 dicarboxylic acid ester Chemical class 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
- 241000208140 Acer Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- GAMPNQJDUFQVQO-UHFFFAOYSA-N acetic acid;phthalic acid Chemical compound CC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O GAMPNQJDUFQVQO-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- XSDQTOBWRPYKKA-UHFFFAOYSA-N amiloride Chemical compound NC(=N)NC(=O)C1=NC(Cl)=C(N)N=C1N XSDQTOBWRPYKKA-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 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
- D06M15/01—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
- D06M15/03—Polysaccharides or derivatives thereof
- D06M15/05—Cellulose or derivatives thereof
- D06M15/07—Cellulose esters
-
- 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
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2213—Coating or impregnation is specified as weather proof, water vapor resistant, or moisture resistant
Definitions
- Qne object of our invention is to provide a process for preparing a fabric impregnated with a cellulose ester and resistant to moisture in which the use-of a solution of a cellulose ester in a volatile organic solvent is unnecessary.
- Another object of our invention is to provide a process of impregnating textile materials with a cellulose ester in which the danger of explosions or fires from solvent vapors is eliminated. Other objects will appear herein.
- the salt may even be decomposed at room temperature, however a period of or 6 hours or even more is necessary to remove substantially all of the basic constituent.
- the ester will soften so that temperatures above 160 C. will not usually be employed unless that softening is unobjectionable. For instance if the process is carried out in such a manner that the ester will not adhere to the rolls or otherparts of the apparatus if it is subjected to a softening temperature, ob-' viously such a temperature may be employed.
- a plasticizer may also be incorporated'in the cellulose ester by dissolving it in either the impregnating bath containing the salt of the cellulose ester or the acid bath for the precipitation of the ester or by spraying the plastieizer on the cloth as it passes thru the dryer or just prior to passing it thru calenderlng rolls.
- a water soluble plasticizer such as diethylene glycol, triethylene, glycol or diethyiene glycol diacetate rather than modifying the bath to render it soluble of the plasticizer which it is desired to employ.
- a salt of a mono ester of phthalic acid can also be employed as plasticizer.
- Thissalt is Water soluble and can be incorporated in the water solution of the salt of the dicarboxylic acid ester of cellulose. During the-subsequent acid treatment the water insoluble mono-ester is regenerated. if the plasticizer is to be incorporated in the ester by spraying it upon the cloth any of the ordinary liquid plasticizers such as dimethyl phthalate, diethyl phthalate etc. may be employed.
- Example I 15 lbs. of the sodium salt of cellulose acetate phthalate is dissolved in 10 gallons of water and 4 yards of a loosely woven unsized cotton cloth is steeped therein until completely wet with the solution. The cloth is then allowed to drain and v maple. 5'lbs. of the ammonium salt of cellulose acetate phthalate is dissolved in 2 gallons of water and lib. of diethylene glycol is added to plasticize the ester formed. 2 yards of unsized cloth is soaked therein until the entire cloth has been wet by the solution after which the cloth is drained and dried. The cloth is then passed thru calendering rolls at a temperature of about 105 C. which treatment liberates the ammonia and regenerates the cellulose acetate phthalate.
- the preparation of the water soluble salts of the dicarboxylic acid esters of cellulose is disclosed and claimed in Malm and Waring applications Serial Nos. 38G,252 filed July 22, 1929, 627,149 filed July 30, 1932 and in Fordyce Patent No. 1,969,741.
- the sodium salt of cellulose acetate phthalate may be prepared by dissolving the acetate phthalate in ethylene glycol monomethyl ether and adding thereto a solution of sodium hydroride in a mixture of equal volumes of water and ethylene glycol monomethyl ether until the point of neutrality is reached.
- the ammonium salt may be prepared by dissolving the cellulose acetate phthalate in anhydrous acetone and then introducing a current of dry ammonia gas therein.
- the pyridine salt is formed by esterifying a cellulosic material with a dicarboxylic acid anhydride in the presence of pyridine.
- the cloth treated in accordance with the present invention exhibits the characteristic of resistance to the passage of moisture so that in addition to the ordinary uses to which it might be put it is also eminently suitable for making sugar sacks or in fact containers for any material which is afiected either by the loss or the addition of moisture.
- the aqueous solution of the salt may be applied to the textile material by steeping, by a coating blade or by any of the well known means of treating fabrics.
- a coating blade for continuous operation it is desirable to provide rolls for continuously passing the cloth thru the respective baths and leading it thru the drying and calendering means.
- aqueous solution of a mineral acid such as sulfuric, hydrochloric or phosphoric or of some strong organic acid such as formic might be employed in this connection.
- the liquid be a solvent for the acid employed and substantially a non-solvent of the cellulose ester resulting from the acid treatment.
- a process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a wate soluble salt of a cellulose ester containing a d carboxylic acid radical and then regenerating the cellulose ester.
- a process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a water-soluble salt of a cellulose ester containing a dicarboxylic acid radical and then regenerating the cellulose ester by means of a dilute acid having an ionization constant greater than that or the second hydrogen of the dicarboxylic acid corresponding to the radical present in the ester.
- a process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of an ammonium salt of a cellulose ester containing a dicarboxylic acid radical and then regenerating the cellulose ester by subjecting the material to a non-scorching temperature of at least 105 C.
- a process for rendering a mxtile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a water-soluble salt of a cellulose ester containing phthalyi groups and then regenerating the cellulose ester by means of acetic acid.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Description
Patented Feb. 15, 1938' UNITED STATES PROCESS FOR RENDERING A TEXTILE MA- TERIAL RESISTANT T MOISTURE Herbert G. Stone; Kingsport, Tenn, and Carl J. Malm, Rochester, N. Y., assignors, by mesne assignments, to Eastman Kodak Company, Jersey City, N. J., a corporation of New Jersey No Drawing. Application March 31, 1934,
I Serial No. 718,516
6 Claims. (on. 91-68) with a cellulose ester to dissolve the ester in a volatile organic solvent which solution is then employed to apply the ester to the fabric. This process of treating fabrics has numerous disadvantagessome of which are: expense of making up dopes or solutions of cellulom esters in volatile organic solvents, the danger of inflammability in dissolving the ester and in drying the cloth which has been treated with the solution, the necessity of recovering the solvent vapors to assure economy of operation and the care necessary to avoid stiffness or hardness in the fabric which has been treated.
Qne object of our invention is to provide a process for preparing a fabric impregnated with a cellulose ester and resistant to moisture in which the use-of a solution of a cellulose ester in a volatile organic solvent is unnecessary. Another object of our inventionis to provide a process of impregnating textile materials with a cellulose ester in which the danger of explosions or fires from solvent vapors is eliminated. Other objects will appear herein.
We have found that a textile material such as a fabric may beimpregnated. with a cellulose ester by treating that material with an aqueous solution of a water-soluble salt of a dicarboxylic acid ester of cellulose and then regenerating the ester "therefrom by treating the material with a solution of an acid (either organic or mineral) which has an ionization constant greater than that of the second hydrogen of the dicarboxylic acid corresponding to the dicarboxylic radical which is joined to the cellulose; or in the case where the ammonium salt (or an amine salt which may be decomposed by heat) is employed in the treat-.
The temperatures which are preferableemployed. The salt may even be decomposed at room temperature, however a period of or 6 hours or even more is necessary to remove substantially all of the basic constituent. At temperatures above 160 C. the ester will soften so that temperatures above 160 C. will not usually be employed unless that softening is unobjectionable. For instance if the process is carried out in such a manner that the ester will not adhere to the rolls or otherparts of the apparatus if it is subjected to a softening temperature, ob-' viously such a temperature may be employed.
If desired a plasticizer may also be incorporated'in the cellulose ester by dissolving it in either the impregnating bath containing the salt of the cellulose ester or the acid bath for the precipitation of the ester or by spraying the plastieizer on the cloth as it passes thru the dryer or just prior to passing it thru calenderlng rolls. in the case where the plasticizer is added to the bath it is preferable to employ a water soluble plasticizer such as diethylene glycol, triethylene, glycol or diethyiene glycol diacetate rather than modifying the bath to render it soluble of the plasticizer which it is desired to employ. A salt of a mono ester of phthalic acid can also be employed as plasticizer. Thissaltis Water soluble and can be incorporated in the water solution of the salt of the dicarboxylic acid ester of cellulose. During the-subsequent acid treatment the water insoluble mono-ester is regenerated. if the plasticizer is to be incorporated in the ester by spraying it upon the cloth any of the ordinary liquid plasticizers such as dimethyl phthalate, diethyl phthalate etc. may be employed.
' The following examples are illustrative of the carrying out of the present invention:
Example I 15 lbs. of the sodium salt of cellulose acetate phthalate is dissolved in 10 gallons of water and 4 yards of a loosely woven unsized cotton cloth is steeped therein until completely wet with the solution. The cloth is then allowed to drain and v maple. 5'lbs. of the ammonium salt of cellulose acetate phthalate is dissolved in 2 gallons of water and lib. of diethylene glycol is added to plasticize the ester formed. 2 yards of unsized cloth is soaked therein until the entire cloth has been wet by the solution after which the cloth is drained and dried. The cloth is then passed thru calendering rolls at a temperature of about 105 C. which treatment liberates the ammonia and regenerates the cellulose acetate phthalate. The preparation of the water soluble salts of the dicarboxylic acid esters of cellulose is disclosed and claimed in Malm and Waring applications Serial Nos. 38G,252 filed July 22, 1929, 627,149 filed July 30, 1932 and in Fordyce Patent No. 1,969,741. For instance the sodium salt of cellulose acetate phthalate may be prepared by dissolving the acetate phthalate in ethylene glycol monomethyl ether and adding thereto a solution of sodium hydroride in a mixture of equal volumes of water and ethylene glycol monomethyl ether until the point of neutrality is reached. The ammonium salt may be prepared by dissolving the cellulose acetate phthalate in anhydrous acetone and then introducing a current of dry ammonia gas therein. The pyridine salt is formed by esterifying a cellulosic material with a dicarboxylic acid anhydride in the presence of pyridine.
As was pointed out before the cloth treated in accordance with the present invention exhibits the characteristic of resistance to the passage of moisture so that in addition to the ordinary uses to which it might be put it is also eminently suitable for making sugar sacks or in fact containers for any material which is afiected either by the loss or the addition of moisture. I
Various water-soluble salts of the dicarboxyiic acid esters of cellulose are suitable for use in a process embodying the present invention some of which are:
In carrying out the present process the aqueous solution of the salt may be applied to the textile material by steeping, by a coating blade or by any of the well known means of treating fabrics. For continuous operation it is desirable to provide rolls for continuously passing the cloth thru the respective baths and leading it thru the drying and calendering means.
Instead of using acetic acid in aqueous solution for removing the basic constituent of the salt,
other acids or other solutions might be employed. For instance an aqueous solution of a mineral acid such as sulfuric, hydrochloric or phosphoric or of some strong organic acid such as formic might be employed in this connection.
Other solvents such as alcohol (ethyl or methyl) or ethyl ether might be employed as the diluent of the acid in this neutralization step,
. the only criterion being that the liquid be a solvent for the acid employed and substantially a non-solvent of the cellulose ester resulting from the acid treatment.
It is also to be understood that other solvents than water which are similar in character such as an alcohol (ethyl or methyl) might be employed as the solvent for the water-soluble salt, which solution is employed to impregnate the textile material.
We claim as our invention:
1. A process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a wate soluble salt of a cellulose ester containing a d carboxylic acid radical and then regenerating the cellulose ester.
2. A process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a water-soluble salt of a cellulose ester containing a dicarboxylic acid radical and then regenerating the cellulose ester by means of a dilute acid having an ionization constant greater than that or the second hydrogen of the dicarboxylic acid corresponding to the radical present in the ester.
3. A process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of an ammonium salt of a cellulose ester containing a dicarboxylic acid radical and then regenerating the cellulose ester by subjecting the material to a non-scorching temperature of at least 105 C.
4. .A process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a water-soluble salt of a cellulose. ester containing phthalyl groups and then regenerating the cellulose ester.
5. A process for rendering a mxtile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a water-soluble salt of a cellulose ester containing phthalyi groups and then regenerating the cellulose ester by means of acetic acid.
6. A process for rendering a textile material resistant to moisture which comprises thoroughly wetting the material with a substantially neutral aqueous solution of a water-soluble salt of a cellulose ester containing a dicarboxylic acid radical containing a water-soluble plasticizing material and then regenerating the cellulose ester.
HERBERT G. STONE. CARL J. MALM.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71851634 US2108455A (en) | 1934-03-31 | 1934-03-31 | Process for rendering a textile material resistant to moisture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71851634 US2108455A (en) | 1934-03-31 | 1934-03-31 | Process for rendering a textile material resistant to moisture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2108455A true US2108455A (en) | 1938-02-15 |
Family
ID=24886360
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US71851634 Expired - Lifetime US2108455A (en) | 1934-03-31 | 1934-03-31 | Process for rendering a textile material resistant to moisture |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2108455A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2422573A (en) * | 1937-09-07 | 1947-06-17 | Lilicnfeld Patents Inc | Xanthated cellulose derivative and process of coating with same |
-
1934
- 1934-03-31 US US71851634 patent/US2108455A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2422573A (en) * | 1937-09-07 | 1947-06-17 | Lilicnfeld Patents Inc | Xanthated cellulose derivative and process of coating with same |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2759787A (en) | Cellulose citrates and their preparation | |
| US2107852A (en) | Sizing fabric | |
| US2108455A (en) | Process for rendering a textile material resistant to moisture | |
| US2036424A (en) | Impregnation of cotton materials | |
| US2147640A (en) | Production of artificial materials | |
| US1546211A (en) | Manufacture of products containing cellulose | |
| US2095334A (en) | Manufacture of cellulose esters | |
| US2170024A (en) | Cellulose esters and method | |
| US2071333A (en) | Manufacture of organic esters of cellulose | |
| US2039290A (en) | Production of highly acetylated cellulose acetates | |
| US2261237A (en) | Manufacture of cellulose derivatives | |
| US2805171A (en) | High acetyl cellulose acetate molding compositions and the manufacture of molded pieces therefrom | |
| US2000603A (en) | Treatment of cellulosic material prior to esterification | |
| US1948517A (en) | Treatment of derivatives of cellulose | |
| US920828A (en) | Process of making a cellulose material. | |
| US2103018A (en) | Process for enhancing the stability to water of effects produced mechanically on textiles containing cellulose | |
| US2417535A (en) | Production of textile materials which are sensitive towards water | |
| US2360239A (en) | Process for stabilizing cellulose esters | |
| US2552190A (en) | Method for activating cellulose to prepare it for esterification | |
| US1999406A (en) | Method of preparing stable cellulose acetate | |
| US1236578A (en) | Acetyl cellulose and a process of making the same. | |
| US2084833A (en) | Process for the manufacture of highly acetylated cellulose acetates | |
| US2078418A (en) | Cellulose film and foil and method of making the same | |
| US2110642A (en) | Manufacture of cellulose esters | |
| US2006661A (en) | Process of treating regenerated cellulose articles |