US2610983A - Prevention of pinking in rubber articles containing di-beta-naphthyl-para-phenylene diamine antioxidant - Google Patents
Prevention of pinking in rubber articles containing di-beta-naphthyl-para-phenylene diamine antioxidant Download PDFInfo
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- US2610983A US2610983A US107640A US10764049A US2610983A US 2610983 A US2610983 A US 2610983A US 107640 A US107640 A US 107640A US 10764049 A US10764049 A US 10764049A US 2610983 A US2610983 A US 2610983A
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- pinking
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/925—Natural rubber compositions having nonreactive materials, i.e. NRM, other than: carbon, silicon dioxide, glass titanium dioxide, water, hydrocarbon or halohydrocarbon
Definitions
- This invention relates to the compounding of rubber in such manner that development of the pink discoloration which results from the presence in the rubber of symmetrical di-betanaphthyl-para-phenylene diamine as an antioxidant is prevented.
- Symmetrical di-beta-naphthylpara-phenylene diamine is one ofthe best all-around antioxidants for vulcanized rubber thus far developed. However, it exhibits the objectionable characteristic that it turns pink when it is subjected to certain conditions, particularly when subjected to light and oxidizing conditions. Under ordinary storage conditions pinking does not occur. However, pinking appears to be catalyzed by light, and certain oxidizing media such as nitric oxide fumes and ozone; and where these conditions prevail, pinking often becomes very rapid. Pinking occurs also during bleaching operations, such as with chlorine and hydrogen peroxide, especially the former. This pink discoloration changes the color or shade desired for'the article and is highly objectionable.
- Theproblem of pinking - is especially serious in the case of articles or materials made from or containing elastic yarn comprising a core of vulcanized rubber containing the above anti-oxidant and a wound covering of textile yarn.
- This problem is particularly serious where white or lightcolored textile yarns are used as'the'covering for the elastic core or in association with the elastic yarn to make'the fabric of which the article or material is formed or woven.
- Thepink discoloration-which occurs asa result ofthe above'antioxidant in the vulcanized rubber core of the elastic yarn usually shows through the associated white or light-colored textile yarns and fibers, often in an irregular or non-uniform manner, and this is highly objectionable.
- Elastic yarn of the type just'referred' to is described in detail in the Adams on Pate nt 1,822,847.
- This elastic yarn typically has a core of elastic vulcanized rubber under tension with a covering of a plurality'Iof helical, preferably both right and left, windings which hold 2,5-di-tertiary butyl hydroquinone.
- This compound has the structural formula t-butyl t-butyl oil
- 2,5di-tertiary butyl hydroquinone by itself is a poor rubber antioxidant, it operates in some manner not understood at present to greatly suppress the normal tendency of symmetrical di-beta-naphthyl paraphenylene diamine to cause a pink discoloration.
- the basic formulation was:
- Ew pl There was included in the above formulation on'epart ofsymmetrical di-beta-naphthyl-paraphenylene diamine.
- The'resulting thread upon subjection to an accelerated pinking test (inthe Weatherometer but withthe samples facing away from the carbon arc) began to pink after 15minutes and after one hour was a very pronounced red.
- the unaged material had a tensile strength of 6000 p. s. i. and an elongation of 715%.
- Example 2 Emample 3 With the basic formulation there was included one part of symmetrical di-beta-naphthyl-paraphenylene diamine and two parts of 2,5-ditertiary butyl hydroquinone.
- the aging properties of the vulcanizate were equal to those of the vulcanizate of Example 1. a The material was subjected to accelerated pinking exactly as in Example 1. Pinking did not begin until 100 minutes had elapsed.
- Example 3 clearly indicates that the employment of two parts of 2,5-di-tertiary butyl hydroquinone is highly effective in inhibiting pinking when one part of the anti-oxidant in question is employed.
- the inhibiting of pinking effected by use of two parts of 2,5-di-tertiary butyl hydroquinone in accordance with this example is sufiicient to eliminate pinking under ordinary conditions.
- Example 4 Example 3 is duplicated exactly except that four parts of 2,5-di-tertiary butyl hydroquinone are employed. When the resulting material was subjected to the standard pinking test as before, it did not begin to pink until 220 minutes had elapsed.
- the amount of symmetrical di-beta-naphthylparaphenylene diamine employed may vary widely. However, it will usually range from 0.25 to 2.0% by Weight based on the rubber. In any event, the amount should be sufiicient to be effective as an anti-oxidant for the vulcanizate.
- the amount of 2,5-di-tertiary butyl hydroquinone may vary widely.
- the inhibiting effect is roughly proportional to the amount employed.
- the amount used will depend upon the extent of inhibition desired'and upon the conditions to which the vulcanizate is subjected.
- the amount of 2,5-ditertiary butyl hydroquinone will range from 0.25 to 5% by weight based on the rubber. I prefer to employ 2% by weight of the inhibitor based on the rubber as giving practically complete protection against pinking under field conditions.
- the pinking inhibitor of the present invention confers the additional benefit that it markedly decreases discoloration of the vulcanizate upon exposure to light. Such discoloration is to be distinguished from pinking.
- symmetrical di-beta-naphthyl-paraphenylene diamine turns gray upon exposure to light.
- a vulcanizate of the regular production type made with one part of this anti-oxidant per 100 parts of rubber turns dark gray in 00101 upon direct exposure for two hours to the carbon arc of the Weatherometer.
- the product of Example 3 which contains two parts of the inhibitor turns only a medium gray upon the same exposure while the product of Example 4 turns only a very light gray upon the same exposure.
- the use of the inhibitor of my invention is without any disadvantages. It does not adversely affect the properties of the vulcanizate in any respect. Its advantages are great.
- the principal advantage is that it prevents the pinking due to the anti-oxidant. As just mentioned it has the additional advantage of greatly reducing light discoloration.
- My invention can be applied to any rubber stock in which symmetrical di-beta-naphthyl-paraphenylene diamine is used as an anti-oxidant, includin stocks wherein the rubber is natural rubber, or synthetic rubber such as rubbery copolymers of butadiene and styrene, neoprene, etc.
- the invention is generally applied to natural rubber stocks.
- a sulfur-vulcanized rubber article containing from 0.25 to 2.0% by weight based on the rubber of symmetrical di-beta-naphthyl-paraphenylene diamine incorporated before vulcanization and effective to protect the vulcanized rubber against oxidation, the formulation of said vulcanized rubber article being such that in the absence of the hereinafter specified 2,5-di-tertiary butyl hydroquinone it would exhibit an objectionable tendency to develop a visible'pink discoloration by reason of the presence of said diamine, said vulcanized rubber article being protected against said tendency to develop said visible pink discoloration by the presence therein of from 0.25 to 5.0% by weight based on the rubber of 2,5-ditertiary butyl hydroquinone incorporated before vulcanization.
- Elastic yarn having a core of sulfur-vulcanized rubber under tension and having a wound covering of textile yarn, said vulcanized rubber containing a small amount of symmetrical clibeta-naphthyl-para-phenylene diamine incorporated before vulcanization and eiiective to protect the vulcanized rubber against oxidation, the formulation of said vulcanized rubber being such that in the absence of the hereinafter specified 2,5-di-tertiary butyl hydroquinone it would exhibit an objectionable tendency to develop a visible pink discoloration by reason of the presence of said diamine, said vulcanized rubber being protected against said tendency to develop said visible pink discoloration by the presence therein of a small amount of 2,5-di-tertiary butyl hydroquinone incorporated before vulcanization.
- a vulcanizable composition containing rubber, sulfur as a vulcanizing agent therefor, and a small amount of symmetrical di-beta-naphthylpara-phenylene diamine effective to protect the rubber after vulcanization against oxidation, the formulation of said composition being such that in the absence of the hereinafter specified 2,5-ditertiary butyl hydroquinone the vulcanizate of said composition would exhibit an objectionable tendency to develop a visible pink discoloration by reason of the presence of said diamine, said composition being protected against said tendency to develop said visible pink discoloration by the presence therein of a small amount of 2,5-ditertiary butyl hydroquinone.
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Description
patented Sept. 16, 195 2 PREVENTION or" PINKING IN RUBBER AR ICL S ON A NING DI- BETA NAPHF' THYL-PARA-PHENYLENE DIAMINE I TIOXIDANT- 1 'David G.S lovin, Providence, RI. assignpr td United States} Rubber Company, New York,
N. Y., a corporation of New Jersey NoDrawing. Application July 29, 1949,
Serial No. 107,640
This invention relates to the compounding of rubber in such manner that development of the pink discoloration which results from the presence in the rubber of symmetrical di-betanaphthyl-para-phenylene diamine as an antioxidant is prevented.
Symmetrical di-beta-naphthylpara-phenylene diamine is one ofthe best all-around antioxidants for vulcanized rubber thus far developed. However, it exhibits the objectionable characteristic that it turns pink when it is subjected to certain conditions, particularly when subjected to light and oxidizing conditions. Under ordinary storage conditions pinking does not occur. However, pinking appears to be catalyzed by light, and certain oxidizing media such as nitric oxide fumes and ozone; and where these conditions prevail, pinking often becomes very rapid. Pinking occurs also during bleaching operations, such as with chlorine and hydrogen peroxide, especially the former. This pink discoloration changes the color or shade desired for'the article and is highly objectionable.
The problem of pinking as a result of the use of this anti-oxidant in rubber compositions and articles containing the same is particularly serious in the case of light-colored vulcanized rubber compounds, such as those which are creamcolored, blue, yellow, so-called natural, white, etc. The reason is that the development of the pink by decomposition or other change of the anti oxidant changes the shade from that which is desired.
Theproblem of pinking -is especially serious in the case of articles or materials made from or containing elastic yarn comprising a core of vulcanized rubber containing the above anti-oxidant and a wound covering of textile yarn. This problem is particularly serious where white or lightcolored textile yarns are used as'the'covering for the elastic core or in association with the elastic yarn to make'the fabric of which the article or material is formed or woven. Thepink discoloration-which occurs asa result ofthe above'antioxidant in the vulcanized rubber core of the elastic yarn usually shows through the associated white or light-colored textile yarns and fibers, often in an irregular or non-uniform manner, and this is highly objectionable.
Elastic yarn of the type just'referred' to is described in detail in the Adams on Pate nt 1,822,847. This elastic yarn typically has a core of elastic vulcanized rubber under tension with a covering of a plurality'Iof helical, preferably both right and left, windings which hold 2,5-di-tertiary butyl hydroquinone.
(SClaims. (crest-sit) the core elongated, the yarn having a predetermined capacity to stretch.
I have now made the surprising discovery that the development of pink discoloration in vulcanized rubber articles containing symmetrical di-beta-napthyl-para-phenylene diamine as an anti-oxidant can be prevented by incorporating in the rubber composition, prior to vulcanization,
This compound has the structural formula t-butyl t-butyl oil Although I have found that 2,5di-tertiary butyl hydroquinone by itself is a poor rubber antioxidant, it operates in some manner not understood at present to greatly suppress the normal tendency of symmetrical di-beta-naphthyl paraphenylene diamine to cause a pink discoloration. This is illustrated by the following examples. In all of the examples, the same basic formulation was used, the only difference being the addition of symmetrical di-beta-naphthyl-para-phenylene diamine alone in Example 1, theuse of 2,5 di-tertiary butyl hydroquinone in Example 2 and the use of the two compounds in combination in Examples ,3 and 4.
The basic formulation was:
Parts by weight Rubber solids (from natural rubber latex) 3 Accelerator 1 Titanium oxide '5 Zinc oxide 3 In each example the foregoing compounding in gredients, together with the anti-oxidant or pink ing' inhibitor, or both, were commingled with natural rubber latex, the resulting mixture was then coagulated as a thread in the conventional way and theresulting thread was cured in conventional manner.
. Ew pl There was included in the above formulation on'epart ofsymmetrical di-beta-naphthyl-paraphenylene diamine. The'resulting thread upon subjection to an accelerated pinking test (inthe Weatherometer but withthe samples facing away from the carbon arc) began to pink after 15minutes and after one hour was a very pronounced red. The unaged material had a tensile strength of 6000 p. s. i. and an elongation of 715%. After aging 400 hours in the Bierer-Davis oxygen bomb it showed a tensile strength of 3550 p. s. i. and an elongation of 600%.
Example 2 Emample 3 With the basic formulation there was included one part of symmetrical di-beta-naphthyl-paraphenylene diamine and two parts of 2,5-ditertiary butyl hydroquinone. The aging properties of the vulcanizate were equal to those of the vulcanizate of Example 1. a The material was subjected to accelerated pinking exactly as in Example 1. Pinking did not begin until 100 minutes had elapsed.
Example 3 clearly indicates that the employment of two parts of 2,5-di-tertiary butyl hydroquinone is highly effective in inhibiting pinking when one part of the anti-oxidant in question is employed. The inhibiting of pinking effected by use of two parts of 2,5-di-tertiary butyl hydroquinone in accordance with this example is sufiicient to eliminate pinking under ordinary conditions.
Example 4 Example 3 is duplicated exactly except that four parts of 2,5-di-tertiary butyl hydroquinone are employed. When the resulting material was subjected to the standard pinking test as before, it did not begin to pink until 220 minutes had elapsed.
The inhibition of pinking effected by the use of four parts of inhibitor in accordance with Example 4 is sufficient to eliminate pinking even under the most severe conditions encountered in practice.
The amount of symmetrical di-beta-naphthylparaphenylene diamine employed may vary widely. However, it will usually range from 0.25 to 2.0% by Weight based on the rubber. In any event, the amount should be sufiicient to be effective as an anti-oxidant for the vulcanizate.
The amount of 2,5-di-tertiary butyl hydroquinone may vary widely. The inhibiting effect is roughly proportional to the amount employed. The amount used will depend upon the extent of inhibition desired'and upon the conditions to which the vulcanizate is subjected.
Generally speaking the amount of 2,5-ditertiary butyl hydroquinone will range from 0.25 to 5% by weight based on the rubber. I prefer to employ 2% by weight of the inhibitor based on the rubber as giving practically complete protection against pinking under field conditions.
The pinking inhibitor of the present invention confers the additional benefit that it markedly decreases discoloration of the vulcanizate upon exposure to light. Such discoloration is to be distinguished from pinking. As is well known, symmetrical di-beta-naphthyl-paraphenylene diamine turns gray upon exposure to light. For example, a vulcanizate of the regular production type made with one part of this anti-oxidant per 100 parts of rubber turns dark gray in 00101 upon direct exposure for two hours to the carbon arc of the Weatherometer. In contrast, the product of Example 3 which contains two parts of the inhibitor turns only a medium gray upon the same exposure while the product of Example 4 turns only a very light gray upon the same exposure.
The use of the inhibitor of my invention is without any disadvantages. It does not adversely affect the properties of the vulcanizate in any respect. Its advantages are great. The principal advantage, of course, is that it prevents the pinking due to the anti-oxidant. As just mentioned it has the additional advantage of greatly reducing light discoloration.
My invention can be applied to any rubber stock in which symmetrical di-beta-naphthyl-paraphenylene diamine is used as an anti-oxidant, includin stocks wherein the rubber is natural rubber, or synthetic rubber such as rubbery copolymers of butadiene and styrene, neoprene, etc. The invention is generally applied to natural rubber stocks.
Having thus described my invention, what I claim and desire to protect by Letters Patent is:
1. A sulfur-vulcanized rubber article containing a small amount of symmetrical di-beta-naphthyl-para-phenylene diamine incorporated before vulcanization and effective to protect the vulcanized rubber against oxidation, the formulation of said vulcanized rubber article being such that in the absence of the hereinafter specified 2,5-ditertiary butyl hydroquinone it would exhibit an objectionable tendency to develop a visible pink discoloration by reason of the presence of said diamine, said vulcanized rubber article being protected against said tendency to develop said visible pink discoloration by the presence therein of a small amount of 2,5-di-tertiary butyl hydroquinone incorporated before vulcanization.
2. A sulfur-vulcanized rubber article containing from 0.25 to 2.0% by weight based on the rubber of symmetrical di-beta-naphthyl-paraphenylene diamine incorporated before vulcanization and effective to protect the vulcanized rubber against oxidation, the formulation of said vulcanized rubber article being such that in the absence of the hereinafter specified 2,5-di-tertiary butyl hydroquinone it would exhibit an objectionable tendency to develop a visible'pink discoloration by reason of the presence of said diamine, said vulcanized rubber article being protected against said tendency to develop said visible pink discoloration by the presence therein of from 0.25 to 5.0% by weight based on the rubber of 2,5-ditertiary butyl hydroquinone incorporated before vulcanization.
3. A sulfur-vulcanized rubber article containing approximately 1% by weight based on the rubber of symmetrical di-beta-naththyl-paraphenylene diamine incorporated before vulcanization and effective to protect the vulcanized rubber against oxidation, the formulation of said vulcanized rubber article being such that in the absence of the hereinafter specified 2,5-di-tertiary butyl hydroquinone it would exhibit an objectionable tendency to develop a visible pink discoloration by reason of the presence of said diamine, said vulcanized rubber article being protected against said tendency to develop said visible pink discoloration by the presence therein of approximately 2% by weight based on the rubber of 2,5- di-tertiary butyl hydroquinone incorporated before vulcanization.
4. Elastic yarn having a core of sulfur-vulcanized rubber under tension and having a wound covering of textile yarn, said vulcanized rubber containing a small amount of symmetrical clibeta-naphthyl-para-phenylene diamine incorporated before vulcanization and eiiective to protect the vulcanized rubber against oxidation, the formulation of said vulcanized rubber being such that in the absence of the hereinafter specified 2,5-di-tertiary butyl hydroquinone it would exhibit an objectionable tendency to develop a visible pink discoloration by reason of the presence of said diamine, said vulcanized rubber being protected against said tendency to develop said visible pink discoloration by the presence therein of a small amount of 2,5-di-tertiary butyl hydroquinone incorporated before vulcanization.
5. A vulcanizable composition containing rubber, sulfur as a vulcanizing agent therefor, and a small amount of symmetrical di-beta-naphthylpara-phenylene diamine effective to protect the rubber after vulcanization against oxidation, the formulation of said composition being such that in the absence of the hereinafter specified 2,5-ditertiary butyl hydroquinone the vulcanizate of said composition would exhibit an objectionable tendency to develop a visible pink discoloration by reason of the presence of said diamine, said composition being protected against said tendency to develop said visible pink discoloration by the presence therein of a small amount of 2,5-ditertiary butyl hydroquinone.
6. In the manufacture of a sulfur-vulcanized REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,026,442 Somerville Dec. 31, 1935 2,335,089 Sibley Nov. 23, 1943 2,356,929 Hart Aug. 29, 1944 2,370,987 Neal et a1. Mar. 6, 1945 OTHER REFERENCES Institute Rubber Industry Trans, volume 5 of 1930, pp. 317 to 327 incl.
Chemical and Engineering News, vol. 23, No. 18, September 25, 1945, page 1681.
Claims (1)
1. A SULFUR-VULCANIZED RUBBER ARTICLE CONTAINING A SMALL AMOUNT OF SYMMETRICAL DI-BETA-NAPHTHYL-PARA-PHENYLENE DIAMINE INCORPORATED BEFORE VULCANIZATION AND EFFECTIVE TO PROTECT THE VULCANIZED RUBBER AGAINST OXIDATION, THE FORMULATION OF SAID VULCANIZED RUBBER ARTICLE BEING SUCH THAT IN THE ABSENCE OF THE HEREINAFTER SPECIFIED 2,5-DITERTIARY BUTYL HYDROQUINONE IT WOULD EXHIBIT AN OBJECTIONABLE TENDENCY TO DEVELOP A VISIBLE PINK DISCOLORATION BY REASON OF THE PRESENCE OF SAID DIAMINE, SAID VULCANIZED RUBBER ARTICLE BEING PROTECTED AGAINST SAID TENDENCY TO DEVELOP SAID VISIBLE PINK DISCOLORATION BY THE PRESENCE THEREIN OF A SMALL AMOUNT OF 2,5-DI-TERTIARY BUTYL HYDROQUINONE INCORPORATED BEFORE VULCANIZATION.
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US107640A US2610983A (en) | 1949-07-29 | 1949-07-29 | Prevention of pinking in rubber articles containing di-beta-naphthyl-para-phenylene diamine antioxidant |
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US107640A US2610983A (en) | 1949-07-29 | 1949-07-29 | Prevention of pinking in rubber articles containing di-beta-naphthyl-para-phenylene diamine antioxidant |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1041684B (en) * | 1954-06-04 | 1958-10-23 | Ici Ltd | Process for improving the properties of natural and synthetic rubber |
DE1083046B (en) * | 1954-05-18 | 1960-06-09 | Us Rubber Co | Method for protecting a molding compound |
US3043672A (en) * | 1956-08-22 | 1962-07-10 | Ethyl Corp | Substituted catechol antioxidants |
WO2020084359A1 (en) | 2018-10-25 | 2020-04-30 | Candiani S.P.A. | A method for making an elasticised yarn and fabric manufactured from said yarn |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2026442A (en) * | 1934-12-05 | 1935-12-31 | Albert A Somerville | Rubber compounding |
US2335089A (en) * | 1940-11-27 | 1943-11-23 | Monsanto Chemicals | Method of preserving rubber |
US2356929A (en) * | 1941-11-07 | 1944-08-29 | Us Rubber Co | Anti-flex-cracking agents |
US2370987A (en) * | 1943-06-23 | 1945-03-06 | Du Pont | Preserving rubber |
-
1949
- 1949-07-29 US US107640A patent/US2610983A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2026442A (en) * | 1934-12-05 | 1935-12-31 | Albert A Somerville | Rubber compounding |
US2335089A (en) * | 1940-11-27 | 1943-11-23 | Monsanto Chemicals | Method of preserving rubber |
US2356929A (en) * | 1941-11-07 | 1944-08-29 | Us Rubber Co | Anti-flex-cracking agents |
US2370987A (en) * | 1943-06-23 | 1945-03-06 | Du Pont | Preserving rubber |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1083046B (en) * | 1954-05-18 | 1960-06-09 | Us Rubber Co | Method for protecting a molding compound |
DE1041684B (en) * | 1954-06-04 | 1958-10-23 | Ici Ltd | Process for improving the properties of natural and synthetic rubber |
US3043672A (en) * | 1956-08-22 | 1962-07-10 | Ethyl Corp | Substituted catechol antioxidants |
WO2020084359A1 (en) | 2018-10-25 | 2020-04-30 | Candiani S.P.A. | A method for making an elasticised yarn and fabric manufactured from said yarn |
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