GB446757A - Process for the desulphurisation of viscose artificial silk - Google Patents
Process for the desulphurisation of viscose artificial silkInfo
- Publication number
- GB446757A GB446757A GB31737/34A GB3173734A GB446757A GB 446757 A GB446757 A GB 446757A GB 31737/34 A GB31737/34 A GB 31737/34A GB 3173734 A GB3173734 A GB 3173734A GB 446757 A GB446757 A GB 446757A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- acid
- fatty
- viscose
- acids
- 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
Links
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
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
- D01F11/02—Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
Abstract
In a process for desulphurizing viscose artificial silk, the silk is desulphurized by a physical method which consists in treating it with an aqueous solution of a washing or wetting agent belonging to one of the following groups: acid esters of fatty alcohols and polybasic acids, e.g. phthalic acid esters; higher fatty amines and their derivatives, e.g. stearylamine, stearylpyridinium chloride or oxethyloleylamine; fatty amides of aromatic amino-sulphonic acids, e.g. laurylnaphthionic acid; alkylated and oxyalkylated aromatic and hydroaromatic sulphonic acids, e.g. benzylnaphthalene sulphonic acids, diisopropyl benzene sulphonic acid or dodecylnaphthalene sulphonic acids, protalbinic acid or lysalbinic acid; sulphonated fatty acids, e.g. sulphonated palmitic acid; condensation products of fatty acid glycerides with naphthalene sulphonic acids; chlolic acid, glycollic acid and naphthenic acid, their salts or derivatives; mineral oil sulphonates, abietine sulphonates; semi-ether of glycol and polyglycol with fatty alcohol; amides, anilides, alkylanilides and naphthalides of oxy-fatty acids such as ricinoleic acid; fatty acid ethanolamides or ethanolamides glycolated with ethylene oxide; esters of glycerine and polyglycerine or of glycols and polyglycols; or lecithin. A concentration of 5--30 grams per litre and a temperature of 60--100 DEG C. is employed. The material may be in the form of a thread, a hank, spool or cake or small bands or foils may be desulphurized in this manner. Preferably a wetting agent is used which may be left in the fibre to serve as a softening or preparing agent. Oils or fats may be incorporated in the bath. Several sulphur removing agents may be employed together and with other substances such as hydrogen peroxide. Two baths may be employed one after the other. When treating viscose to which a substance which lowers the surface tension of aqueous solutions with respect to sulphur has been added, the temperature may be lowered to 20 DEG C. Such substances which may be added in proportions of 0,1--0,3 per cent are described in Specification 417,290. In examples, hanks of viscose artificial silk are treated for \ba1/2\be--2 hours at 70--90 DEG C., with a \ba1/2\be per cent solution of the sodium salt of mono-oleyl ester of phthalic acid at a pH value of 4,9--9,5 but preferably of 7, or in a two per cent solution of sodium diisopropyl-benzene-sulphonate at a pH value of 6,3--9; or undesulphurized silk is treated for 2 hours at 80 DEG C. with a 1 per cent solution of an oxyethylamide of a higher fatty acid. A 1,5 per cent solution of Laventin or an alkyl substituted naphthalene sulphonic acid containing terpene may be used. In other examples hanks of viscose silk are treated first with a 2 per cent solution of a polyglycol ether such as oleylpolyglycol ether, and then with a similar bath containing 0,03 per cent of hydrogen peroxide at 80 DEG C., or a viscose made from sulphite cellulose and containing 6,5 per cent cellulose, 6,5 per cent sodium hydroxide and either 0,25 per cent of bornyl xanthate, 0,3 per cent of turkey red oil or 0,2 per cent of sodium alkyl-naphthalene-sulphonate is spun in a bath containing 13 per cent sulphuric acid and 30 per cent sodium sulphate, washed, and treated with a 2 per cent solution of sodium diisopropyl-benzene sulphonate at 20 DEG C. for 1 hour.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE446757X | 1933-11-09 | ||
DE2128612X | 1934-10-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB446757A true GB446757A (en) | 1936-05-05 |
Family
ID=32043847
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31737/34A Expired GB446757A (en) | 1933-11-09 | 1934-11-05 | Process for the desulphurisation of viscose artificial silk |
Country Status (4)
Country | Link |
---|---|
US (2) | US2092203A (en) |
BE (1) | BE406095A (en) |
FR (1) | FR783563A (en) |
GB (1) | GB446757A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2418660A (en) * | 1943-04-24 | 1947-04-08 | Du Pont | Manufacture of regenerated cellulose structures |
US2585141A (en) * | 1945-09-05 | 1952-02-12 | Celanese Corp | Treatment of viscose products |
US2670266A (en) * | 1949-12-08 | 1954-02-23 | Du Pont | Textile bleach-finish process |
US2683072A (en) * | 1950-06-16 | 1954-07-06 | Du Pont | Removal of cs2 with oil from viscose yarn |
-
0
- BE BE406095D patent/BE406095A/xx unknown
-
1934
- 1934-11-05 GB GB31737/34A patent/GB446757A/en not_active Expired
- 1934-11-06 US US751784A patent/US2092203A/en not_active Expired - Lifetime
- 1934-11-07 FR FR783563D patent/FR783563A/en not_active Expired
-
1935
- 1935-10-10 US US44462A patent/US2128612A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US2128612A (en) | 1938-08-30 |
US2092203A (en) | 1937-09-07 |
FR783563A (en) | 1935-07-16 |
BE406095A (en) |
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