CA2036640A1 - Poly(oxydiphenylamines) - Google Patents

Abstract

Abstract of the Disclosure POLY(OXYDIPHENYLAMINES) The present invention relates to poly(oxydiphenylamines) of the formula:

(I) wherein n is an integer ranging from about 1 to 100.
The poly(oxydiphenylamines) are useful as a rubber additive and have shown improvement in the tear strength of the rubber as measured by increased peel adhesion.

Description

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POLY(OXYDIPHENYLA~INES) Background of the Invention The present invention relates to poly(oxydiphenylamines) which are useful as rubber additive.

Summary of the Invention The present invention relates to poly(oxydiphenylamines) of the formula:

~ 3 H ~ ~ H ~ (I) wherein n is an integer ranging from about 1 to 100.

Detailed Description of the referred Invention There is disclosed a poly(oxydiphenylamine) of the formula:

~ ~ H ~ O ~ ~ ~ (I) wherein n is an integer ranging from about 1 to 100.
Preferably, the poly(oxydiphenylamine) is of the formula:

2 ~ 3 ~ ~ H ~ ~ I ~ (II) n The term poly(oxydiphenylamine) is used herein to describe dimers (where n is 1), oligomers (where n is from about 2 to about 4) and polymers (where n is an integer of from 5 to 100).
The molecular weight of the poly(oxydiphenylamines) may range from about 370 to about 10,000. Preferably, the molecular weight will range from about 370 to about 1000. As can be appreciated after having read the present application, there may be dimers, oligomers and polymers in the crude reaction mixture which all will have different molecular weights within the above ranges.
There is also disclosed a rubber composition which comprises (1) a rubber selected from the group consisting of natural rubber, homopolymers of conjugated diolefins, copolymers of conjugated diolefins and ethylenically unsaturated monomers or mixtures thereof and a poly(oxydiphenylamine) of the formula:

~ ~ n (I) wherein n is an integer from about 1 to 100.
The poly(oxydiphenylamines) may be prepared by a number of methods. For example, the 2~3~

poly(oxydiphenylamines) may be prepared by the air oxidation of hydroxy diphenylamines. For example, the poly(oxydiphenylamines) may be prepared by reacting hydroxy diphenylamine with an oxygen containing gas such as air for a period of from about 1 day to about 30 days a~ a temperature ranging from about room temperature to about 200C. In the alternative, the poly(oxydiphenylamines) may be prepared by heating a hydroxy diphenylamine in the presence of a catalyst to speed up the reaction. Examples of catalysts that may be used include acid catalysts such as sulfuric acid, hydrochloric acid and toluenesulfonic acid. The amount the catalyst that will be used will vary depending on the particular catalyst that is selected. For example, when an acid catalyst is used from about 1 to about 20 percent by weight of the hydroxydiphenylamine is recommended.
The reaction may be conducted over wide temperatures. For example, the temperature may range from about room temperature to an elevated temperature depending on the particular type of reaction that is selected. In general, the reaction may be conducted at a temperature of between about room temperature to about 220C. The preferred temperature range is from about 100C to about 200C, while the most preferred temperature range is from about 140C to about 180~C.
If all reaction variables remain constant except the reaction temperature, it is believed that the reaction product will have varying reactivities in the rubber.
Examples of hydroxy diphenylamines which may be used include 4-hydroxydiphenylamine, 3-hydroxydiphenylamine and 2-hydroxydiphenylamine Preferably, the hydroxydiphenylamine is 4-hydroxydiphenylamine, and mixtures of the above.

2~36~3 An organic solvent may be used to dissolve the hydroxydiphenylamine. The solvent is preferably inert to the reaction. Illustrative of solvents suitable for use in the present invention include saturated and aromatic hydrocarbons, e.g., hexane, octane, dodecane, naphtha, decaline, tetrahydronaph~haleneS kerosene, mineral oil, cyclohexane, cycloheptane, alkylcycloalkane, benzene, toluene, xylene, alkyl-naphthalene and the like; ethers such as tetrahydrofuran, tetrahydropyran, diethylene ether, 1,2-dimethoxybenzene, 1,2-diethoxybenzene, the mono-and dialkyl ethers of ethylene glycol, propylene glycol, butylene glycol, diethylene glycol, dipropylene glycol, oxyethylene oxypropylene glycol, and the like;
fluorinated hydrocarbons that are inert under the reaction conditions such as perfluoroethane, monofluorobenzene and the like. Another class of solvents are sulfones such as dimethyl sulfone, diethyl sulfone, diphenol sulfone, sulfolane, and the like.
Mixtures of the aforementioned solvents may be employed so long as they are compatible with each other under the conditions of the reaction and will adequately dissolve the hydroxydiphenylamine and not interfere with the reaction.
The process for the preparation of the poly(oxydiphenylamines) may be carried out in a batch, semi-continuous or continuous manner. The reaction may be conducted in a single reaction zone or in a plurality of reaction zones, in series or in parallel, the reaction may be conducted intermittently or continuously in an elongated tubular zone or in a series of such zones. The material construction of the equipment should be such as to be inert during the reaction. The equipment should also be able to 2 ~

withstand the reaction temperatures and pressures. The reaction zone can be fitted with internal and/or external heat exchanges to control temperature fluctuations. Preferably, an agitation means is available to ensure uniform reaction. Mixing induced by vibration, shaker, stirrer, rotating, oscillation, etc. are all illustrative of the types of agitation means which are contemplated for use in preparing the composition of the present invention. Such agitation means are available and well known to those skilled in the art.
The reaction product will contain various poly(oxydiphenylamines) of various molecular weights.
For example, it is contemplated that with respect to the above formulae, various weight percentages of the reaction mixture may range from about lO~ to about 100%. Use of the various mixtures of poly(oxydiphenylamine) in rubber compounds is contemplated herein.
The poly(oxydiphenylamine) may be added to sulfur vulcanizable elastomers as an additive. The term "rubber" or "elastomer" as used herein embraces both natural and all its various raw and reclaimed forms as well as various synthetic rubbers. Representative synthetic elastomers are the homopolymerization products of butadiene and its homologues and derivatives, as for example, methylbutadiene, dimethylbutadiene, chloroprene (neoprene synthetic rubber) and pentadiene as well as copolymers such as ~0 those formed from butadiene or its homologues or derivatives with other unsaturated organic compounds.
Among the latter are acetylenes, e.g., vinyl acetylene;
olefins, for example, isobutylene, which copolymerizes with isoprene to form butyl rubber; vinyl compounds, 2~3~6~

for example, vinyl chloride, acrylic acid, acrylonitrile (which polymerizes with butadiene to form NBR), methacrylic acid and stvrene, the latter compound polymerizes with butadiene to form SBR, as well as vinyl esters and various unsaturated aldehydes, ketones and ethers, e.g., acrolein, methyl isopropenyl ketone and vinyl ethyl ether. Also included are the various synthetic rubbers prepared by the homopolymerization of isoprene and the copolymerization of isoprene with other diolefins and various unsaturated organic compounds. Additionally, included are the synthetic rubbers such as 1,4-cis polybutadiene and 1,4-cis polyisoprene and similar synthetic rubbers such as EPDM. The preferred rubbers for use with the poly(oxydiphenylamine) are SBR and polybutadiene or mixtures thereof.
The rubber vulcanizates containing the poly(oxydiphenylamine) may be used in the preparation of tires, motor mounts, rubber bushings, power belts, printing rolls, rubber shoe heels and soles, rubber floor tiles, caster wheels, elastomer seals and gaskets, conveyor belt covers, wringers, hard rubber battery cases, automobile floor mats, mud flaps for trucks, tires, ball mill liners and the like.
The poly(oxydiphenylamine) may be added to the w lcanizable elastomer in a variety of levels.
Generally speaking, the concentration of the polytoxydiphenylamine) ranges from about 0.1 parts per hundred rubber (phr) to 10 phr and is in intimate mixture with the elastomer. Preferably, the poly(oxydiphenylamine) is at a concentration ranging from about 0.5 phr to about 5 phr.
The poly(oxydiphenylamine) may be compounded in either the productive or nonproductive stock.

Preferably, the poly(oxydiphenylamine) is compounded in the nonproductive because uniform mixing is achieved.
Incorporation of the poly(oxydiphenylamine) into the sulfur vulcanizable rubber may be accomplished by conventional means of mixing such by the use of a Banbury o-; Brabender.
Cure properties were determined using the Monsanto Oscillating Disc Rheometer which was operated at a temperature of 150 and at a frequency of 100 CPM. A
description of Oscillating Disc Rheometers can be found in the Vanderbilt Handbook, edited by Robert O.
Babbitt, Norwalk, Connecticut, R. T. Vanderbilt Company, Inc., 1978 (pages 583-591). The use of this cure meter and standardized values read from the curve are specified in ASTM D-2084. A typical cure curve obtained on an oscillating disc rheometer is shown on page 588 of the 1978 edition of the Vanderbilt Rubber Handbook.
In such an oscillating disc rheometer, compounded rubber samples are subjected to an oscillating shearing action of constant amplitude. The torque of the oscillating disc embedded in the stock that is being tested is required to oscillate the rotor at the w lcanization temperature. The values obtained using this cure test are very significant since changes in the rubber or the compounded recipe are very readily detected. It is obvious that it is normally advantageous to have a very fast cure rate. Some of the following tables report cure properties that were determined from cure curves that were obtained for the various rubber formulations that were prepared. The properties include minutes to 90% of torque increase (t90 min.).

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Peel adhesion testing was done to determine the interfacial adhesion between various rubber formulations that were preparecl. The interfacial adhesion was determined by pulling one compound away from another at a right angle to the untorn test specimen with the two ends being pulled apart at 180 angle to each other using an Instron machine. The area of contact was determined from placement of a Mylar sheet between the compounds during cure. A window in the Mylar allowed the two materials to come into contact with each other during curing and subsequent testing.

Example 1 Preparation of Poly(oxy-4,4'-diphenylamine) Poly(oxy-4,4'-diphenylamine) was prepared by charging a one-liter 3-neck round bottom flask with 93 grams (0.5 mole) of 4-hydroxydiphenylamine, 11 grams of p-toluene sulfonic acid and 97 ml of m-xylene. The mixture was heated to 205C for 24 hours, wherein 6 ml of water were removed. HPLC analysis showed the formation of oligomers. The crude product was a black crystalline solid melting at 67C with an acid number of 46. The molecular weight range was from about 370 to several thousand.

Example 2 Four batches of poly(oxy-4,4'-diphenylamine) were prepared by this same procedure except different reaction temperatures were used. Each batch was prepared by charging a one-liter, 3-neck round bottom flask with 186 grams (1.0 mole) of 4-hydroxydiphenylamine, 22 grams of p-toluene sulfonic acid and 200 ml of m-xylene. The mixtures were heated 2~s~a _9_ to 160C (first batch), 180C (second batch~, 200C
(third batch), or 220C (fourth batch) for five hours.
HPLC analysis showed formation of dimers and oligomers.
The crude products were mostly dimers for the 160C
(first batch) and up to about 10,000 molecular ~eight polymers in the 220C (fourth batch). The second and third batches contained crude mixtures of poly(oxydiphenylamine) oligomers.

Example 3 Table I below shows the basic rubber compound that was used in this example. The rubber compound was prepared in a one stage Banbury mix. All parts and percentages are by weight unless otherwise noted.
15The control had no poly(oxy-4,4'-diphenylamine) whereas, sample 1 contained 2 phr of poly(oxy-4,4'diphenylamine). The poly(oxydiphenylamine) was prepared by the procedure of Example l. The physical data for each sample is shown in Table II.

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Table I

WeightBanbury Material PartsStage SBR 50.00 Polybutadiene 50.00 Carbon Black 64.50 Antiozonant/Antioxidant 1.75 Processing Materials34.90 10 Zinc Oxide 3.00 Poly(oxydiphenylamine) (1) 2.00 Sulfur/Accelerator 3.75 (1) Not used in control.
Table II

Control plus 2 phr Poly(oxy-4,4'-Controldiphenylamine t90 (min.) 29.3 25.6 Tensile Strength 11.2 13.6 % Elongation @ Break 385 460 Modulus 300% 9.0 8.8 Peel Adhesion 63.5 83.8 to Self 61.9 70.6 The addition of 2 phr of poly(oxy-4,4'-diphenylamine) results in a substantial increase in peel adhesion, tensile strength, percent elongation at break.

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Example 4 Table III below shows the basic rubber compound that was used in this example. The rubber compound was prepared in a two stage Banbury mix. All parts and percentages are by weight unless otherwise noted.
The two controls had no poly(oxy-4,4'-diphenylamine) wherein the sample was prepared in accordance with Example 2 (namely Sample 1) at 160C, Sample 2 at 180C, Sample 3 at 200C and Sample 4 at 220C. The physical data for the two controls and each sample are shown in Table IV.

Table III

Weight Banbury Parts Sta~e Natural Rubber 50 Filler 63.6 Processing Oil 19.5 Stearic Acid 2.0 Zinc Oxide 3.5 Antioxidant 2.95 Poly(oxy-4,4'-diphenylamine) Varied Sulfur, Accelerator 2.93 2 2~36~

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Claims (7)

1. A composition comprising a poly(oxydiphenylamine) of the formula:

(I) wherein n is an integer ranging from about 1 to 100.

2. The composition of claim 1 wherein the poly(oxydiphenylamine) is of the formula (II) wherein n is an integer ranging from about 1 to about 100.

3. The composition of claim 1 additionally comprising a sulfur vulcanized rubber.

4. The composition of claim 3 wherein the rubber is selected from the group consisting of natural rubber, polychloroprene, polybutadiene, polyisoprene, butyl rubber, EPDM, styrene/butadiene copolymers, terpolymers of acrylonitrile, butadiene and styrene and blends thereof.

5. The composition of claim 3 wherein the concentration of the poly(oxydiphenylamine) ranges from about 0.1 phr to about 50 phr.

6. A process for improving the tear properties of a sulfur vulcanized rubber comprising adding from about 0.2 to about 10 phr of a poly(oxydiphenylamine) of the formula:

(I) to a rubber selected from the group consisting of natural rubber, polychloroprene, polybutadiene, polyisoprene, butyl rubber, EPDM, styrene/butadiene copolymers, terpolymers of acrylonitrile, butadiene and styrene and blends thereof; wherein n is an integer of from 1 to 100.

7. The process of claim 6 wherein from about 0.5 to about 5 phr of a poly(oxydiphenylamine) is used.