US2186889A - Process for improving textile materials - Google Patents
Process for improving textile materials Download PDFInfo
- Publication number
- US2186889A US2186889A US91802A US9180236A US2186889A US 2186889 A US2186889 A US 2186889A US 91802 A US91802 A US 91802A US 9180236 A US9180236 A US 9180236A US 2186889 A US2186889 A US 2186889A
- Authority
- US
- United States
- Prior art keywords
- textile materials
- materials
- ester
- chlorocarbonic
- water
- 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
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
- D06M13/10—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 oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
Definitions
- the present invention relates to a process for improving textile materials by treating. them with esters of chlorocarbonic acid.
- fibrous materials of a 5 great variety of kinds, particularly cellulosic materials can be improved and particularly an excellent water-repelling action can be imparted to them by treating them with esters of chlorocarbonic acid.
- esters of chlorocarbonic acid especially those derived from al- 10 cohols containing a greater number of say at least 4 carbon atoms are suitable for this purpose, for example the following compounds: chlorocarbonic esters of butyl, amyl, hexyl, cyclohexyl, or benzyl alcohol and the like, and more particularly the esters of high molecular aliphatic alcohols, for example those corresponding to the acids contained in natural oils, fats or waxes.
- esters of octyl, dodecyl, myristyl, cetyl, octodecyl or oleyl alcohol also of octodecandiol, l0 montanol (derived from montanic acids) or of alcohols obtainable by the oxidation of high molecular aliphatic hydrocarbons may be used.
- Substituents such as halogen atoms, hydroxy, ether, ester or nitro groups may also be present 85 in the molecule.
- the process may be employed for the improvement for example of cotton, artificial silks, linen,
- the process may be applied at any stage of the working up of-these materials.
- the said esters of chlorocarbonic acid are dissolved or dispersed in organic solvents such as carbon tetrachloride, benzine, benzene, tetrahydronaphthalene and the like, or in water and the textile material is handled in this solution or dispersion for some time.
- organic solvents such as carbon tetrachloride, benzine, benzene, tetrahydronaphthalene and the like
- agents capable of binding acids For example may be employed ammonia, bonate solution, amines, pyridine and the like.
- elevated temperatures for example-of from 50 to 100 C. 1he textile material treated is then squeezed and dried at normal or elevated temperature for example up to 100 C. In some 0 cases it is advantageous'to carry out the drying in vacuo. In this case organic solvents employed in this process may be recovered.-
- Water-repellent textile materials consisting of the reaction product of a textile material and a chlorocarbonic ester of an alcohol containing at least 4 carbon atoms.
- water-repellent textile materials consisting of the reaction product of a textile material and a chlorocarbonic ester of an aliphatic alcohol corresponding to the fatty acids contained in naturally occurring fatty substances.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented Jan. 9, 1940 UNITED STATES PROCESS FOR IMPROVING TEXTILE MATERIALS Heinrich Ulrich and Paul Koerding, Ludwigshafen-on-the-Rhine, Germany,
assignors to G. Farhenindustrie Aktiengesellschaft, Frankfort-on-the-Main, Germany No Drawing. Application July 21, 1936, Serial No. 91,802. In Germany 5 Claims.
The present invention relates to a process for improving textile materials by treating. them with esters of chlorocarbonic acid.
We have found that fibrous materials of a 5 great variety of kinds, particularly cellulosic materials, can be improved and particularly an excellent water-repelling action can be imparted to them by treating them with esters of chlorocarbonic acid. Especially those derived from al- 10 cohols containing a greater number of say at least 4 carbon atoms are suitable for this purpose, for example the following compounds: chlorocarbonic esters of butyl, amyl, hexyl, cyclohexyl, or benzyl alcohol and the like, and more particularly the esters of high molecular aliphatic alcohols, for example those corresponding to the acids contained in natural oils, fats or waxes. For example the esters of octyl, dodecyl, myristyl, cetyl, octodecyl or oleyl alcohol, also of octodecandiol, l0 montanol (derived from montanic acids) or of alcohols obtainable by the oxidation of high molecular aliphatic hydrocarbons may be used. Substituents such as halogen atoms, hydroxy, ether, ester or nitro groups may also be present 85 in the molecule.
The process may be employed for the improvement for example of cotton, artificial silks, linen,
wool and mixed fabrics. The process may be applied at any stage of the working up of-these materials.
For example the said esters of chlorocarbonic acid are dissolved or dispersed in organic solvents such as carbon tetrachloride, benzine, benzene, tetrahydronaphthalene and the like, or in water and the textile material is handled in this solution or dispersion for some time. In cases in which the fibrous material may be injured by the action of the hydrogen chloride which is formed by the reaction of the chlorocarbonic ester with the fibrous material it is advantageous to add agents capable of binding acids. For example may be employed ammonia, bonate solution, amines, pyridine and the like. Generally speaking it is advantageous to employ elevated temperatures, for example-of from 50 to 100 C. 1he textile material treated is then squeezed and dried at normal or elevated temperature for example up to 100 C. In some 0 cases it is advantageous'to carry out the drying in vacuo. In this case organic solvents employed in this process may be recovered.-
The textile materials treated a good water-repelling action whlchis not diminished by sodium car-V July 26, 1935 subsequent washing; very soft touch.
The following example will further illustrate the nature of this invention but the invention is not restricted to this example. The parts are by weight.
often the materials havea Ezrample Dyed cotton tweel is treated with a solution of 5 parts of chlorocarbonic octodecyl ester and 1 part of pyridine in 1000 parts of carbon tetrachloride and dried for an hour at 90 C. The material is rendered excellently impermeable to water by this treatment. The effect is not destroyed by subsequent washing.
What we claim is:--
1. The process for improving the water-repellency of textile materials which consists of treating said materials with a chlorocarbonic ester of an alcohol containing at least 4 carbon atoms and then drying the treated textile materials at a temperature suflicient to cause a reaction to occur between said textile materials and said ester.
2. The process for improving the water-repellency of textile materials which consists of treating said materials with a chlorocarbonic ester of an aliphatic alcohol corresponding to the fatty acids contained in naturally occurring fatty substances and then drying the treated textile materials at a temperature suflicient to cause a reaction to occur between said textile materials and said ester.
3. The process for improving the water-repellency of textile materials which consists of treating said materials with a chlorocarbonic ester of an aliphatic alcohol containing at least 4 carbon atoms in the presence of a diluent and a substance capable of binding any acid formed by the the textile materials and the 'chlorocarbonic ester at a temperature sufilcient to cause a reaction to occur between said textile materials and said ester.
4. Water-repellent textile materials consisting of the reaction product of a textile material and a chlorocarbonic ester of an alcohol containing at least 4 carbon atoms.
5. water-repellent textile materials consisting of the reaction product of a textile material and a chlorocarbonic ester of an aliphatic alcohol corresponding to the fatty acids contained in naturally occurring fatty substances.
' HEINRICH ULRICH.
PAUL KOERDING.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB22542/35A GB460602A (en) | 1935-08-09 | 1935-08-09 | A process for waterproofing fibrous materials |
Publications (1)
Publication Number | Publication Date |
---|---|
US2186889A true US2186889A (en) | 1940-01-09 |
Family
ID=10181089
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US91802A Expired - Lifetime US2186889A (en) | 1935-08-09 | 1936-07-21 | Process for improving textile materials |
Country Status (3)
Country | Link |
---|---|
US (1) | US2186889A (en) |
FR (1) | FR809404A (en) |
GB (1) | GB460602A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2523324A (en) * | 1947-04-23 | 1950-09-26 | United Shoe Machinery Corp | Tanning with esters of chloroformic acid in an nonaqueous medium |
US3079217A (en) * | 1961-04-11 | 1963-02-26 | Robert E Whitfield | Shrinkproofing wool with polycarbonates |
-
1935
- 1935-08-09 GB GB22542/35A patent/GB460602A/en not_active Expired
-
1936
- 1936-07-21 US US91802A patent/US2186889A/en not_active Expired - Lifetime
- 1936-07-24 FR FR809404D patent/FR809404A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2523324A (en) * | 1947-04-23 | 1950-09-26 | United Shoe Machinery Corp | Tanning with esters of chloroformic acid in an nonaqueous medium |
US3079217A (en) * | 1961-04-11 | 1963-02-26 | Robert E Whitfield | Shrinkproofing wool with polycarbonates |
Also Published As
Publication number | Publication date |
---|---|
GB460602A (en) | 1937-02-01 |
FR809404A (en) | 1937-03-03 |
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