US2302779A - Process of matting textile materials - Google Patents
Process of matting textile materials Download PDFInfo
- Publication number
- US2302779A US2302779A US296525A US29652539A US2302779A US 2302779 A US2302779 A US 2302779A US 296525 A US296525 A US 296525A US 29652539 A US29652539 A US 29652539A US 2302779 A US2302779 A US 2302779A
- Authority
- US
- United States
- Prior art keywords
- matting
- bath
- urea
- liquor
- grams
- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
Definitions
- the present invention relates to the performance of the process in a continuously operating or standing bath, that is'to say, that the bath is used repeatedly and the fresh reagents are olurea during 3 hours of matting operation and at a temperature of C. It is generally advantageous to operate the temperature below 40 C. advantageously at room temperature, that is to sayat Ill- C. However matting proceeds best at about 20 C. and requires a somewhat longer period at a higher or lower temperature v than this. a
Description
Patented Nov. 24, 1942 MATERIALS Albert Landolt, Riehen, and Hans Benz, Basel, Switzerland, assignors to the firm oi Society oi Chemical Industry in Basie, Basel, Switzerland No Drawing. Application September 25, 1939, Se-
rial No. 296,525. In Switzerland September 30,
1 Claim.
In the specifications of U. S. Patent No. 2,145,- 011 and of application Serial'No. 271,392, filed May 2, 1939, there is described a process of thatting textile materials, especially those consisting of regenerated cellulose or cellulose esters or ethers by treating the material ina matting bath containing urea and formaldehyde or a sol uble urea-formaldehyde compound, for instance mono or dimethylolurea. I
The process of the said specifications consists in adding to the matting bath a condensing agent (acid) and by suitable choice of temperature, concentration and liquor. ratio, bringing about a precipitation of the condensation product produced by the action of the condensing agent in a pigment-like form on the fibre.
The present invention relates to the performance of the process in a continuously operating or standing bath, that is'to say, that the bath is used repeatedly and the fresh reagents are olurea during 3 hours of matting operation and at a temperature of C. It is generally advantageous to operate the temperature below 40 C. advantageously at room temperature, that is to sayat Ill- C. However matting proceeds best at about 20 C. and requires a somewhat longer period at a higher or lower temperature v than this. a
If for any reason the matting process is to be interrupted, the matting bath is brought to added to keep up'the concentration. The urea and formaldehyde or the water-soluble condensation product from urea and formaldehydeis added to the bath with the addition of so much acid that the bath has a feeble but pronounced reaction to Congo. Under such conditions there is immediately formed in the bath a water-soluthe essential factor to be considered is the hydrogen ion concentration. The latter may vary according to the concentration of the soluble urea compound, namely the higher the concentration neutrality by an addition of alkali. When the matting is to be restarted the bath receives the necessary proportion of acid before the operation begins.
The invention is applicable to both the dyed and undyed materials. The dyeing may follow the matt ng operation. For producing a given matting efl'ect the duration of the matting process. must be adjusted in accordance with the various factors indicated above. 'Thus the user is able of the urea-formaldehyde compound, the lower permit. An' advantage of the invention however is that a long liquor ratio is commercially possible. Thus for instance the operation-may be performed with a liquor ratio of 1:10, but it is of value as stated that the operation can be conducted at liquor ratios of at least 1:15 for exby increasing or diminishing the concentrationof the matting agent or the acid or by lengthening or shortening the bath to accelerate or retard the matting operation.
The following examples illustrate the inven-- tion:
' Example 1 4 kilos of dimethylolurea are dissolved in litres of water at 70 C. The liquor is then cooled to 20 C. and made up to 200 litres by addition of water at the sanie temperature. 10 kilos of viscose artificial .silk in hank form are reeled in this bath for 15 minutes and there are then added 3.2 litres'of hydrochloric acid of 36 per cent strength. The artificial silk which has been thus treated for 2 hours has agood matting for 2 hours.
fast to washing.
There is then added to the bath 1 kilo of dis solved dimethylolurea, 10 kilos' of viscose artificial silk areentered and the reeling is repeated The material then shows a strong matting fast to washing. For further batches of artificial silk to be matted the same addition of dimethylolurea is made and if necessary further acid is added. a
have a strong matting effect.
Example 2 1 kilo of viscose artificial silk is reeled during 1 hour at 20 C. in 80 litres of liquor containing 0.32 kilo of urea, 0.48 litre of a formaldehyde solution containing 360 grams of formaldehyde per litre and 1.28 litres of hydrochloric acid of 36 per cent strength. The artificial silk thus treated is strongly matted. For further matting in the same bath the liquor receives 0.1 kilo of urea and 0.16 litre of formaldehyde solution, whereupon it is ready for similarly matting a further l-kilo of the viscose artificial silk.
Example 3 10 kilos of viscose artificial silk tricot are matted at 20 C. in 100 litres of liquor containing per litre 10 grams of monomethylolurea and 10 cc. of hydrochloric acid of 36 per cent strength After reeling for 1 hour the goods are rinsed and dried, whereupon the artificial silk is found to For the next batch of tricot there is added to the liquor per litre 6 grams of monomethylolurea and 2 cc. of hydro chloric acid of 36 per cent strength. If instead of 10 grams of monomethylolurea per litre only grams are used, the matting effect is weaker.
Example 4 kilos of viscose artificial silk crepe are reeled at 20 C. in 400 litres of liquor containing per litre 3.5 grams of monomethylolurea and 20cc. of hydrochloric acid of 36 per cent strength. After matting has continued for 1 hour the goods are rinsed, neutralized and dried, whereupon they-are found to have a matting of medium strength. Before starting to mat the next batch of viscose artificial silk crepe there are added to the bath per litre 1.5 grams of monomethylolurea and 1 cc. of hydrochloric acid of 36 per cent strength and the operation is renewed in the manner described above. If instead of 3.5 grams of monomethylolurea per litre there are used 5 grams of monomethylolurea a stronger matting effect is obtained.
What we claim is:
In the process of matting textiles which comprises handling the textiles in a bath containing a member of the group consisting of (a) urea and formaldehyde and (b) a water-soluble ureaformaldehyde compound under conditions whereby a water-insoluble urea-formaldehyde condensation is formed and is adsorbed by the textiles to be matted, the steps of repeatedly adding fresh reagents to the treating bath as the old reagents are consumed in order to maintain the proper concentration thereof, and repeatedly subjecting fresh textiles to matting in the replenished treating bath, the said bath having a liquor ratio of at least 1: 15 and a hydrogen ion concentration corresponding to that of a solution of at least 2 cc. per liter of hydrochloric acid of 36 per cent strength.
ALBERT LANDOLT.
HANS BENZ.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH537467X | 1938-09-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2302779A true US2302779A (en) | 1942-11-24 |
Family
ID=4518854
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US296525A Expired - Lifetime US2302779A (en) | 1938-09-30 | 1939-09-25 | Process of matting textile materials |
Country Status (5)
Country | Link |
---|---|
US (1) | US2302779A (en) |
BE (1) | BE436481A (en) |
DE (1) | DE742993C (en) |
FR (1) | FR860388A (en) |
GB (1) | GB537467A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2416988A (en) * | 1935-09-12 | 1947-03-04 | Tootal Broadhurst Lee Co Ltd | Delustring and weighting textile materials |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE915329C (en) * | 1950-10-12 | 1957-07-11 | Bayer Ag | Process for the production of pigment prints or pads |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL49150C (en) * | 1935-09-12 | 1940-09-16 | ||
NL53846C (en) * | 1936-08-07 | |||
CH202522A (en) * | 1936-12-16 | 1939-01-31 | Chem Ind Basel | Process for the production of matting baths. |
-
0
- BE BE436481D patent/BE436481A/xx unknown
-
1938
- 1938-10-05 DE DEG98760D patent/DE742993C/en not_active Expired
-
1939
- 1939-09-25 US US296525A patent/US2302779A/en not_active Expired - Lifetime
- 1939-09-26 FR FR860388D patent/FR860388A/en not_active Expired
- 1939-09-26 GB GB26668/39A patent/GB537467A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2416988A (en) * | 1935-09-12 | 1947-03-04 | Tootal Broadhurst Lee Co Ltd | Delustring and weighting textile materials |
Also Published As
Publication number | Publication date |
---|---|
BE436481A (en) | |
GB537467A (en) | 1941-06-24 |
FR860388A (en) | 1941-01-13 |
DE742993C (en) | 1943-12-30 |
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