US2297731A - Processes for rendering textiles water repellent - Google Patents
Processes for rendering textiles water repellent Download PDFInfo
- Publication number
- US2297731A US2297731A US289395A US28939539A US2297731A US 2297731 A US2297731 A US 2297731A US 289395 A US289395 A US 289395A US 28939539 A US28939539 A US 28939539A US 2297731 A US2297731 A US 2297731A
- Authority
- US
- United States
- Prior art keywords
- processes
- water
- carbamic acid
- water repellent
- acid chloride
- 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
- 239000004753 textile Substances 0.000 title description 15
- 238000000034 method Methods 0.000 title description 13
- 239000005871 repellent Substances 0.000 title description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 5
- 230000002940 repellent Effects 0.000 title description 4
- 238000009877 rendering Methods 0.000 title description 3
- 239000000463 material Substances 0.000 description 33
- -1 acyl carbamic acid chlorides Chemical class 0.000 description 13
- 239000000243 solution Substances 0.000 description 10
- 229920002678 cellulose Polymers 0.000 description 8
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 8
- 239000001913 cellulose Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000009987 spinning Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 238000005108 dry cleaning Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 229920002955 Art silk Polymers 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- 240000000491 Corchorus aestuans Species 0.000 description 2
- 235000011777 Corchorus aestuans Nutrition 0.000 description 2
- 235000010862 Corchorus capsularis Nutrition 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 229940081735 acetylcellulose Drugs 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000282461 Canis lupus Species 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000003313 weakening effect Effects 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/425—Carbamic or thiocarbamic acids or derivatives thereof, e.g. urethanes
Definitions
- Patented Oct. 6, 1942 PROCESSES FOR RENDERING TEXTILES WATER REPELLENT Ernst Waltmann andEdgar Wolf, Krefeld, Germany, assignors to Heberlein Patent Corporation, New York, N. Y., a corporation of New York No Drawing. Application August 10, 1939, Serial No. 289,395. In Germany February 19, 1936 4 Claims.
- This invention relates to processes for producing water repellent fibrous materials and products therefrom.
- R is intended to designate an alkyl, cycloalkyl or aralkyl radical conit is believed.
- a chemical reaction with the textile material occurs, as we are not sure that such is the case.
- the result of this action is to produce a surface structure which is water-repellent.
- Materials falling under the formula mentioned above are distinguished by extremely high rapidity of action towards textile materials, particularly towards cellulose and cellulose derivatives. It
- aqueous solution by soaking, spraying orthe like.
- the filaments so formed are, when dry, subject-.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented Oct. 6, 1942 PROCESSES FOR RENDERING TEXTILES WATER REPELLENT Ernst Waltmann andEdgar Wolf, Krefeld, Germany, assignors to Heberlein Patent Corporation, New York, N. Y., a corporation of New York No Drawing. Application August 10, 1939, Serial No. 289,395. In Germany February 19, 1936 4 Claims.
This invention relates to processes for producing water repellent fibrous materials and products therefrom.
This application is a continuation-in-partof our copending application Serial No. 126,521 filed February 18, 1937, now Patent No. 2,173,029.
.We have found that acyl carbamic acid chlorides may be employed for the production of water repellent fibrous materials.
The principal object of the present invention is to provide a simple process to increase waterrepellence in materials such as cotton, jute, linen, hemp and various artificial silks and wool, presenting advantages ove the known fatty acid chloride and fatty acid anhydride processes.
We have found in accordance" with ourinvention that acyl carbamic acid chloride deriva tives having the general formula R.CONH.COCl
can be employed with great success for rendering textiles water-repellent. In the formula just mentioned and in the appended claims in which said formula is employed, R is intended to designate an alkyl, cycloalkyl or aralkyl radical conit is believed. However, we do not Wish to state w unequivocally that a chemical reaction with the textile material occurs, as we are not sure that such is the case. The result of this action is to produce a surface structure which is water-repellent.
Materials falling under the formula mentioned above are distinguished by extremely high rapidity of action towards textile materials, particularly towards cellulose and cellulose derivatives. It
is necessary only to bring the textile material incontact with the acyl carbamic acid chloride as by passing the textile material briefly through a solution of the substance in benzine or a suitable solvent and immediately thereafter subjecting it for several minutes to an elevated temperature, usually 60 C. or above.
Impregnation of the textile materials with the halides herein mentioned may be carried out in any desired manner with or without the use of organic solvents by means of emulsiflcation in an embodiments of the invention for producing waclaims.
aqueous solution by soaking, spraying orthe like.
To avoid any weakening of the fibres by the hydrogen halide split off from the carbamic acid chloride during the drying process the textile materials are advantageously treated before im pregnation takes place with slight aqueous solutions of sodium hydroxide, sodium carbonate or sodium acetate.
Also organic bases such as pyridine may be added to the solutions of acyl carbamic acid chlorides in organic solvents.
It is also possible to add the acyl carbamic acid chlorides mentioned herein to the spinning solution of viscose or to the spinning solution of cellulose esters or ethers in order thus to combine the process of producing water-repellence with the spinning process.
Also one may treat the fibers of cellulose or cellulose derivatives immediately after the spinning process with the chlorides herein mentioned to obtain water-repellence. The addition of catalytic agents, such as for the purpose of securing the desired effect, may be made but such addition is not necessary. The water-repellent effect secured by these treatments'resists domestic washing. After thorough rinsing out with soap employed in such washing and'drying the textile material again manifests water-repellent properties. It is also resistant to dry cleaning.
The following examples represent preferred ter-repellence in accordance with the manner in which I now prefer to practice it. It is to be understood that these examples are illustrative and the invention is not to be considered as limited thereto except as indicated in the appended Examples 1. A poplin from mercerized cotton is passed through a 1% solution of stearic acid-butyl-carbamic acid chloride in benzol for 4 seconds at a temperature of 25 C. The solution also contains 10 grams of pyridine per liter. After evaporating of the benzol the material is heated for minutes to 60 C. F.). The effect is proof to washing with soap, as Well as to the solvents customary in dry cleaning.
2. A cotton tent? cloth is passed through an aqueous solution of IO-grams per liter of sodium acetate, dried, and then passed through a 1% in carbon tetrachloride for 4 seconds at a temperature'of 25 C. After evaporating of the solvent the material is heated 60 minutes to 70 C. (158 F.). The resulting effect is similar to that of Example 1.
3. A clothing material of cuprammonium silk is passed through an aqueous solution of 5 grams per liter of sodium carbonate, dried and then passed through a 15% solution of montanic acid carbamic acid chloride in carbon tetrachloride for 3 seconds at a temperature of 25 C., and after evaporation of the solvent is heated for 30 minutes to 70 C. The material then becomes water-repellent. The effect is proof to washing with soap, as well as to the solvents customary in dry cleaning.
7 4. A wool muslin is passed through a 1% so lution of behenic acid ethyl carbamic acid chloride in carbon tetrachloride for 3 seconds at a temperature of 25 C. After evaporation of the solvent the materialis heated for 30 minutes to 75 C.
5. To 1000 parts of a viscose solution containing 7.7% cellulose there are added 20 parts of stearic acid carbamic acid chloride dissolved in 60 parts of carbon tetrachloride. The whole is homogeneously mixed and is spun in well known fashion. The precipitating bath which we prefer to employ contains ammonium sulfate.
6. To 100 parts of a 25% solution of cellulose acetate in a mixture of 950 parts of acetone and 50 parts of water, there is added 1000 parts of acetone containing 20 parts of stearic acid carbamic acid chloride. The resulting spinning solution is forced through a spinning nozzle into a current of warm air in the known manner.
The filaments so formed are, when dry, subject-.
ed to a dry heat for 10 minutes at 120 C. The resultant filaments have water-repellent properties which are resistant to washing and dry cleaning treatments.
The amount of the compound deposited in all of the above examples on the textile materials will naturally vary with the weight of the material and its receptivity. We have found that ordinarily an amount of the ester equal to about 0.5%-2% of the material is sufficient to give the effect.
The materials produced in accordance with the above examples show a high degree of waterrepellence. They show a lesser absorption of moisture as compared with the known processes for treatment with fatty acid chlorides and fatty acid anhydrides; They show also greatly improved durability toward dry-cleaning, soap washing, etc. as compared with these previous materials. The .feel and hang of the materials having water-repellence as produced above, has not been substantially altered.
The process of the invention, particularly as set forth in the specific embodiments above, may be carried out with simple apparatus at relatively small expense and in a relatively short time.
In the claims where the expression. textile material" is employed, it is intended to cover materials containing fibers, yarns, fabrics, or other forms of cotton, jute, linen, hemp or rayon including viscose, cuprammonium, or other precipitated cellulose or derivatives of cellulose such as acetyl cellulose, as well as wool in such various forms.
Whie the invention has been described in detail according to the preferred manner of carrying out the process, it will be obvious to those skilled in the art after understanding the invention, that changes and modifications may be made therein without departing from the spirit or scope of the invention, and it is intended in the appended claims to cover all such changes and modifications.
What is claimed as new and desired to be secured by Letters Patent, is:
1. A process for ennobling textile material which comprises impregnating the material with a carbamic acid chloride having the formula R.CONH.COC1, in which formula R is a higher molecular radical containing an alkyl radical of at least 10 carbon atoms and with the impregnated material substantially dry, heating it at an elevated temperature to increase the waterrepellency thereof.
2-. A process for ennobling textile material which comprises impregnating the material with an aliphatic acyl carbamic acid chloride which contains an alkyl radical of at least 10 carbon atoms in the presence of an alkaline substance to produce an'alterationof the surface and with the impregnated material substantially dry, heating it at an elevated temperature to increase the water-repellence of said material.
3. The process for ennobling artificial silk which comprises impregnating the artificial silk with montanic acid carbamic acid chloride and with the impregnated material substantially dry, heating it at an elevated temperature to increase the water-repellence thereof.
4. A process for ennobling textile material which comprises impregnating the material with an aliphatic acyl carbamic acid chloride which contains an alkyl radical of at least 10 carbon atoms and with the impregnated material substantially dry, heating it at a temperature of at least C. to increase the water-repellence of said material.
ERNST WALTMANN. EDGAR WOLF.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2297731X | 1936-02-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2297731A true US2297731A (en) | 1942-10-06 |
Family
ID=7994085
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US289395A Expired - Lifetime US2297731A (en) | 1936-02-19 | 1939-08-10 | Processes for rendering textiles water repellent |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2297731A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10378153B2 (en) * | 2015-06-29 | 2019-08-13 | Stora Enso Oyj | Method for hydrophobing a cellulose substrate |
-
1939
- 1939-08-10 US US289395A patent/US2297731A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10378153B2 (en) * | 2015-06-29 | 2019-08-13 | Stora Enso Oyj | Method for hydrophobing a cellulose substrate |
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