BE487527A - - Google Patents
Info
- Publication number
- BE487527A BE487527A BE487527DA BE487527A BE 487527 A BE487527 A BE 487527A BE 487527D A BE487527D A BE 487527DA BE 487527 A BE487527 A BE 487527A
- Authority
- BE
- Belgium
- Prior art keywords
- emi
- rubber
- sulfur dioxide
- processes
- catalyst
- Prior art date
Links
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims description 14
- 229920001971 elastomer Polymers 0.000 claims description 12
- 239000005060 rubber Substances 0.000 claims description 12
- 229920000126 latex Polymers 0.000 claims description 6
- 239000004816 latex Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 239000000047 product Substances 0.000 claims description 3
- 230000001476 alcoholic effect Effects 0.000 claims 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N 4-methylpenta-1,3-diene Chemical compound CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- -1 dioxane Chemical compound 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/24—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of aliphatic compounds with more than one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Description
'Perfectionnements aux procédés de fabrication de fils, etc.., constitués par le produit de réaction de caoutchouc et d'anhydrid sulfureux'
La présente invention est relative à un procédé de
<EMI ID=1.1>
par le produit de réaction de caoutchouc et d'anhydride sulfureux.
On connaît déjà la fabrication de fils, filaments, rubans,
films et analogues en caoutchouc et qui sont soumis ensuite à l'act
de S02 en présence d'un catalyseur. toutefois, dans ce cas, on util
une solution de caoutchouc comme matière initiale.
<EMI ID=2.1>
et le danger résultant de leur uaage. De plus, le traitement auquel le caoutchouc doit être soumis avant que la solution soit préparée, rend l'usage des solutions de caoutchouc onéreux.
<EMI ID=3.1>
solution à l'ctat partiellement rompu, ce qui a une influence préjudiciable sur la soliaité du produit obtenu à partir de la
solution.
Le procédé, appliqué quand on part de caoutchouc en solution, ne peut être utilisé quand on se sert de latex comme matière initiale. Quand on mélange le catalyseur nécessaire, si on le désire en solutior. au latex, quand on transforme ce latex, par extrusion dans un bain
<EMI ID=4.1>
ne se produit pratiquement aucune réaction entre le caoutchouc et le S02 perdant la période de contact qui convient industriellement.
Selon l'invention, on obtient un fil, un ruban, un film ou article similaire en coagulant d'abord le latex de la manière connue, par exemple par extrusion, dans un bain acide. Cet objet en caoutchou
<EMI ID=5.1>
d'abord pendant peu de temps dans une solution du catalyseur désiré et ensuite dans un bain contenant de l'annyaride sulfureux. Un a
<EMI ID=6.1>
d'être miscibles à l'eau. Comme exemples de solvants convenables, on peut citer le methanol, l'éthanol, des éthers, tels que le dioxane, et des cétones, tels que l'acétone.
<EMI ID=7.1> <EMI ID=8.1>
La matière initiale peut être du latex de caoutchouc naturel ou d'un caoutchouc synthétique capable de former un profit
<EMI ID=9.1>
de fournir des fils ou produits analogues par le proche selon l'invention, on peut citer, :. titre d'exemple, le polybutadiène, le
<EMI ID=10.1>
et les copolymères du butadiène, de l'isoprène, du methylpentadiène ou le dimetnyl butadiène avec des composes de vinyle.
Bien que l'on ait seulement considéré la fabrication d'un fil, dans les 'exemples ci-dessous, le procédé selon l'invention peu être applique, sans modification, a la fabrication de bandes, ruban
<EMI ID=11.1>
seulement à la filière ou tuyère, par laquelle on expulse le latex
<EMI ID=12.1>
moulant un coagulum sous forme d'une bande, d'un ruban, d'un film c
<EMI ID=13.1>
Exemple I. On forme, par extrusion dans un bain d'acide
<EMI ID=14.1>
<EMI ID=15.1> temps a lieu une extension du fil au cours de cette réaction. On obtient un fil ayant une teneur en soufre de 11,1 %.
<EMI ID=16.1>
'Improvements in manufacturing processes for yarns, etc., consisting of the reaction product of rubber and sulfur dioxide'
The present invention relates to a process for
<EMI ID = 1.1>
by the reaction product of rubber and sulfur dioxide.
We already know the manufacture of threads, filaments, ribbons,
rubber films and the like and which are subsequently subjected to the
of SO2 in the presence of a catalyst. however, in this case, we use
a rubber solution as the starting material.
<EMI ID = 2.1>
and the danger resulting from their use. In addition, the treatment to which the rubber must be subjected before the solution is prepared makes the use of rubber solutions expensive.
<EMI ID = 3.1>
solution in the partially broken state, which has a detrimental influence on the solidity of the product obtained from the
solution.
The process, applied when starting with rubber in solution, cannot be used when using latex as the starting material. When mixing the necessary catalyst, if desired as a solution. latex, when this latex is transformed, by extrusion in a bath
<EMI ID = 4.1>
Virtually no reaction occurs between the rubber and SO2 losing the period of contact which is suitable for industrial purposes.
According to the invention, a thread, tape, film or the like is obtained by first coagulating the latex in known manner, for example by extrusion, in an acid bath. This rubber object
<EMI ID = 5.1>
first for a short time in a solution of the desired catalyst and then in a bath containing annyaride sulfur. A
<EMI ID = 6.1>
to be miscible with water. As examples of suitable solvents, there may be mentioned methanol, ethanol, ethers, such as dioxane, and ketones, such as acetone.
<EMI ID = 7.1> <EMI ID = 8.1>
The starting material can be natural rubber latex or a synthetic rubber capable of forming a profit.
<EMI ID = 9.1>
to provide son or similar products by the relative according to the invention, mention may be made of :. for example, polybutadiene,
<EMI ID = 10.1>
and copolymers of butadiene, isoprene, methylpentadiene or dimetnyl butadiene with vinyl compounds.
Although we have only considered the manufacture of a thread, in the 'examples below, the method according to the invention can be applied, without modification, to the manufacture of bands, tape.
<EMI ID = 11.1>
only to the die or nozzle, through which the latex is expelled
<EMI ID = 12.1>
molding a coagulum in the form of a strip, tape, film c
<EMI ID = 13.1>
Example I. By extrusion in an acid bath is formed
<EMI ID = 14.1>
<EMI ID = 15.1> wire extension takes place during this reaction. A wire is obtained having a sulfur content of 11.1%.
<EMI ID = 16.1>
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL981164X | 1948-03-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE487527A true BE487527A (en) |
Family
ID=19866493
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE487527D BE487527A (en) | 1948-03-04 |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE487527A (en) |
| FR (1) | FR981164A (en) |
| NL (1) | NL66287C (en) |
-
0
- NL NL66287D patent/NL66287C/xx active
- BE BE487527D patent/BE487527A/fr unknown
-
1949
- 1949-02-22 FR FR981164D patent/FR981164A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL66287C (en) | |
| FR981164A (en) | 1951-05-23 |
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