Studies in the Vulcanization of Rubber. IV—A Theory of Vulcanization of Rubber

1930 ◽  
Vol 3 (4) ◽  
pp. 659-667
Author(s):  
G. R. Boggs ◽  
J. T. Blake

Abstract A new theory has been advanced which, it is believed, explains completely the various phenomena connected with the vulcanization of rubber. It is entirely a chemical theory based on the existence of two separate and distinct rubber compounds, soft vulcanized rubber and ebonite. The theory explains satisfactorily the aging of rubber, the variation in combined sulfur at optimum cure caused by acceleration, the kinetics of vulcanization, the characteristics of various vulcanizing agents, the thermochemistry of vulcanization, the electrical properties of rubber, the reclaiming of rubber, and the Joule effect. A brief review and discussion of the phenomena and past theories of vulcanization have also been given.

2018 ◽  
Vol 91 (4) ◽  
pp. 701-718 ◽  
Author(s):  
Vincenzina Barbera ◽  
Sara Musto ◽  
Giuseppe Infortuna ◽  
Valeria Cipolletti ◽  
Attilio Citterio ◽  
...  

ABSTRACT 2-amino-1,3-propandiol (serinol) was used as the starting building block of synthetic pathways that led to the preparation of innovative chemicals suitable as ingredients for rubber compounds. Serinol based reactions were performed in the frame of a sustainable process, in the absence of any solvent and catalyst, with aldehydes and ketones, such as acetone, cinnamaldehyde and camphor. The synthesis of either imines or oxazolidines was obtained with high selectivity. Serinol, imine and oxazolidine derivatives of serinol were used as accelerator for the vulcanization of diene rubbers. They were proved to be efficient secondary accelerators in silica based compounds based on poly(styrene-co-butadiene) in place of diphenyl guanidine. The kinetics of vulcanization was investigated for natural rubber based compounds in the absence of any filler. With respect to serinol, the imine derivatives were able to enhance the induction time of vulcanization and to afford a similar vulcanization rate.


Author(s):  
O. A. Dulina ◽  
A. D. Tarasenko ◽  
A. M. Bukanov ◽  
A. A. Ilyin

The properties of butadiene-nitrile rubbers obtained by various methods of synthesis and isolation from latex and rubbers based on them were studied in the article. The surface free energy of samples was determined using the Owens, Wendt, Rabel and Kaelble method. It was shown that the surface energy of elastomeric materials is affected 1) by non-rubber components, the content and nature of which are determined by the method of obtaining and isolating rubber from latex and 2) by the number of nitrile groups in the rubber macromolecule. The kinetics of vulcanization of rubber compounds based on the investigated rubbers has been studied. It was shown that rubber compounds based on rubbers containing a residual emulsifier are vulcanized longer. Elastic-strength properties were studied, and it was concluded that rubbers based on butadienenitrile rubbers synthesized by various methods with the same content of bound nitrilacrylic acid have different physico-mechanical properties and cannot be used interchangeably without changing the formulation and technological parameters of their processing.


1976 ◽  
Vol 49 (4) ◽  
pp. 937-959 ◽  
Author(s):  
S. Cesca ◽  
M. Bruzzone ◽  
A. Priola ◽  
G. Ferraris ◽  
P. Giusti

Abstract New catalyst systems based on alkylaluminum derivatives and halogen or interhalogen compounds were found highly efficient in the synthesis of high-molecular-weight IIR at temperatures above − 50°C. The reaction mechanism was studied in detail for the system Et2AlCl + Cl2. The reactions occurring between chlorine, isobutene, Et2AlCl, and the solvent (CH3Cl) were elucidated and studied under various experimental conditions (e.g. presence or absence of light, simultaneous presence of the copolymerization system components, temperature, type of halogen, use of model compound of isobutene). It was concluded that halogenium ions, i.e. Cl+, Br+, or I+, are the initiating species. Kinetic and conductometric investigations showed that scarcely dissociated ion pairs, e.g. Cl+[Et2AlCl2]−, were formed in the absence of monomer; but in the presence of isobutene, a noticeable increase of the electrical conductivity and rapid polymerization occurred. The maximum polymerization rate was first order with respect to the concentrations of monomer, Cl2, and Et2AlCl. In the homopolymerization of isobutene, transfer to monomer and termination reactions were negligible. The MW of IIR was found to be mainly dependent on the concentrations of the catalyst components, on isoprene concentration, and on temperature. The reactivity ratio of isobutene with isoprene was found to be r1=2.5±0.5 at −35°C, while the activation energies relative to MW were −5.8 ± 0.4, kcal/mol for polyisobutene, and −5.7 ± 0.7 and − 4.3 ± 0.5 kcal/mol for IIR containing, respectively, 1.3 and 1.9 mol% of isoprene. The evaluation of some physicochemical and technological properties of typical IIR produced with the system Et2AlCl + Cl2, indicated that isoprene is randomly distributed along the chains and that the MWD is monomodal, while the glass transition temperature, tensile properties, mechanical-dynamic spectra, and kinetics of vulcanization are very similar to those of commercial IIR. Very preliminary data, referring to several classes of new catalyst systems yielding IIR having good properties, were also obtained. The syncatalyst systems here described can work in a homogeneous phase consisting of an aliphatic hydrocarbon besides methyl chloride, still giving IIR with high MW. Therefore, a completely homogeneous process can be envisioned for the synthesis of IIR at −50°C thus avoiding a great part of the fouling problems of the slurry process. The economic advantage of using “high” temperatures of polymerization is briefly discussed in terms of energy savings.


1960 ◽  
Vol 33 (2) ◽  
pp. 335-341
Author(s):  
Walter Scheele ◽  
Karl-Heinz Hillmer

Abstract As a complement to earlier investigations, and in order to examine more closely the connection between the chemical kinetics and the changes with vulcanization time of the physical properties in the case of vulcanization reactions, we used thiuram vulcanizations as an example, and concerned ourselves with the dependence of stress values (moduli) at different degrees of elongation and different vulcanization temperatures. We found: 1. Stress values attain a limiting value, dependent on the degree of elongation, but independent of the vulcanization temperature at constant elongation. 2. The rise in stress values with the vulcanization time is characterized by an initial delay, which, however, is practically nonexistent at higher temperatures. 3. The kinetics of the increase in stress values with vulcanization time are both qualitatively and quantitatively in accord with the dependence of the reciprocal equilibrium swelling on the vulcanization time; both processes, after a retardation, go according to the first order law and at the same rate. 4. From the temperature dependence of the rate constants of reciprocal equilibrium swelling, as well as of the increase in stress, an activation energy of 22 kcal/mole can be calculated, in good agreement with the activation energy of dithiocarbamate formation in thiuram vulcanizations.


1931 ◽  
Vol 4 (3) ◽  
pp. 426-436
Author(s):  
K. J. Soule

Abstract Further work is very desirable on the effect of different accelerators, antioxidants, and fluxes. It is possible that their study will throw more light on the mechanism of the swelling phenomena, and also help to explain the anomalous behavior of some of the fillers tested. It would also seem to be worth while to study the action of a few selected stocks in water, at several temperatures between room temperature and 100° C., to determine if the water absorption and swelling merely increase with rising temperatures, or whether there might be an actual change in behavior at different temperatures.


1941 ◽  
Vol 14 (2) ◽  
pp. 347-355 ◽  
Author(s):  
Norman Bekkedahl ◽  
Lawrence A. Wood

Abstract The formation of crystals at room temperature by stretching rubber, vulcanized or unvulcanized, has been the subject of considerable study. The crystallization of unstretched rubber at low temperatures is also well known, but with a single exception to be discussed later, the effect has commonly been considered to be limited to the unvulcanized material. In the present investigation, however, the crystallization of unstretched specimens of vulcanized rubber of low sulfur content has been accomplished. In commercial vulcanized rubber products, crystallization has not hitherto been recognized as a factor of practical importance. It is probably significant in cold climates, where some rubber products slowly undergo a great increase in rigidity and permanent set. Automobile traffic counters, for example, have been rendered inoperative by the hardening of the rubber tubing used with them. Laboratory tubing and other products made of a number of different commercial rubber compounds have become rigid after storage for some weeks in a refrigerator at about 0° C. Previous work on unvulcanized rubber showed that it can be crystallized at temperatures between + 10° and −40° C, the crystals melting in a range from about 6° to 16° C. Crystallization and fusion are accompanied by changes in volume, heat capacity, light absorption, birefringence, x-ray diffraction, and mechanical properties such as hardness. x-Ray diffraction and birefringence, of course, give the most direct evidence of crystalline structure, but in the present work change of volume, measured in a mercury-filled dilatometer, was chosen as the criterion of crystallization or fusion. Quantitative results are more easily obtained in this manner, and the experimental observations are simple. Furthermore, the method is well adapted to continuous observations over long periods of time, such as were found necessary in the present work.


1983 ◽  
Vol 24 ◽  
Author(s):  
S. E. Dorris ◽  
D. S. Erickson ◽  
T. O. Mason

ABSTRACTThe point defect reaction which governs the magnetic and electrical properties of transition metal oxide spinels is the distribution of cations between tetrahedral and octahedral sublattices. Two types of redistribution occur -- ionic and electronic. The thermodynamics and kinetics of these processes can be studied via the electrical properties, thermoelectric coefficient and conductivity.


1974 ◽  
Vol 16 (1) ◽  
pp. 256-264 ◽  
Author(s):  
A.A. Dontsov ◽  
A.A. Kanauzova ◽  
G.M. Sas'kova ◽  
B.A. Dogadkin

1987 ◽  
Vol 60 (1) ◽  
pp. 140-158 ◽  
Author(s):  
Dancheng Kong ◽  
James L. White ◽  
Frederick C. Weissert ◽  
Nobuyuki Nakajima

Abstract A fundamental study on curing of rubber compounds in molds is presented. We have measured the thermal conductivity of a range of rubber compounds determining the influence of carbon black, other fillers, and oil. The heats of reaction associated with the curing kinetics of model compounds were measured. A mathematical model is proposed to predict the temperature profiles for curing a reactive slab. This involves inclusion of an energy generation rate, which depends on time and temperature. This is expressed through a Damkohler number. Solutions of the heat conduction equation are interpreted in terms of the Fourier number and the Damkohler number. Calculations are carried out using experimentally determined thermal conductivities and curing kinetics. Thick parts are shown to heat up more slowly (associated with the Fourier number) and to show greater overshoots of cure temperature (associated with the Damkohler number).


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