Chemistry in Carbon Black Dispersion

1955 ◽  
Vol 28 (1) ◽  
pp. 202-212
Author(s):  
Bernard C. Barton ◽  
Hugh M. Smallwood ◽  
George H. Ganzhorn

Abstract The properties of carbon black and their effect on the physical properties of rubber vulcanizates have been extensively reported. The importance of particle size, reticulate structure, and surface characteristics are generally accepted. The beneficial effects of carbon black are believed to be due in large part to strong adsorption of rubber molecules on the carbon black surface. Many investigators have described the physical nature of this adsorption and have related it to the surface properties of the carbon black. Chemical bonding has also been suggested as being an important factor in the surface interaction between carbon black and rubber. The contribution of chemical bonding to the dispersion of carbon black and its effect on the physical properties of vulcanizates is the subject of the present paper. Gerke, Ganzhorn, Howland, and Smallwood and Bradley found almost twenty years ago that, when rubber-carbon black mixtures were heated at temperatures of 275–400° F, vulcanizates prepared from the mixtures had lower electrical conductivity, lower hysteresis, lower durometer hardness, higher modulus at large deformations, and greater resistance to abrasion than did vulcanizates of the corresponding unheated mixtures. These changes were ascribed to changes in the dispersion of the carbon black. Experimental data will be presented in this paper which suggest that these changes in carbon black dispersion are the result of chemical reactions between carbon black and rubber.

1997 ◽  
Vol 70 (1) ◽  
pp. 15-24 ◽  
Author(s):  
H. Takino ◽  
S. Iwama ◽  
Y. Yamada ◽  
S. Kohjiya

Abstract Rubber and carbon black compounds show complex behaviors in their mixing process due to their complicated microcomposite structure. Therefore, establishing a clear relationship between the mixing state of the rubber compound and the physical properties of its cured rubber has still remained to be solved in spite of formidable efforts by many rubber technologists. This paper investigated the influence of a processing additive on the carbon black incorporation and its dispersion behavior by inspecting Banbury power curves. From this investigation, we considered that good wettability toward the carbon black surface was necessary for processing additives in order to improve carbon black dispersion. The function of the processing additive was thought to enhance the surface lubrication of carbon black for disagglomeration in the early steps of mixing. The dry grip properties of a tire was estimated from the temperature dependence of dynamic viscoelastic properties of rubber compounds, with improved carbon black dispersion due to the processing additive; and it was confirmed by an actual tire running evaluation. Consequently, we found that tread compounds with improved carbon black dispersion had a remarkable effect on tire dry-grip properties at high temperatures.


1957 ◽  
Vol 30 (1) ◽  
pp. 122-140 ◽  
Author(s):  
D. C. Edwards ◽  
E. B. Storey

Abstract 1. Heat enhancement effects with HAF black-GMF systems do not appear to involve a chemical bonding of the polymer to the carbon surface. The principal reasons for this view are : (a) Very similar physical properties are obtained, in the case of 50-part carbon black masterbatches, whether or not the black is present during the heat treatment. (b) When the carbon black content is increased, it is necessary to increase the quantity of GMF in order to produce a given degree of gelation. 2. With GMF, very satisfactory properties are obtained by heat-treating a highly loaded mixture and diluting this masterbatch with fresh polymer. Such a process is less sensitive to the time and temperature conditions of the heat treatment operation. 3. The application of such a procedure to Butyl-HAF black mixtures results in modulus and hysteresis properties approaching those of a conventionally mixed cold-rubber tread.


1968 ◽  
Vol 41 (2) ◽  
pp. 382-399 ◽  
Author(s):  
Marvin L. Deviney ◽  
Lawrence E. Whittington

Abstract Radiotracer techniques have been applied to the study of interactions of carbon black surface functional groups with two chosen organic systems. The basic reaction mechanisms demonstrated in this study may have implications in elastomer reinforcement. Direct radiochemical evidence supports the conclusions of Hallum and Drushel (based on less direct polarographic data) that surface quinonic groups exhibit hydrogen abstraction activity toward tertiary hydrogens in paraffinic hydrocarbons. Studies on the system carbon black and styrene using tritium radiotracer have provided direct evidence that phenolic hydrogens participate in the polymerization acceleration and graft polymer formation reaction and are transferred to the growing polystyrene chains as postulated by Donnet. Several methods have been developed for specifically labelling certain oxygenated functional groups on the carbon surface with tritium and for tritium labelling carbon black in aromatic hydrogen positions. The techniques developed in this work and the basic reaction mechanisms derived will permit this investigation to be extended into a radiochemical study of carbon black surface interactions with elastomer related systems of interest to the rubber industry.


1964 ◽  
Vol 37 (5) ◽  
pp. 1245-1298 ◽  
Author(s):  
F. A. Heckman

Abstract Although the microstructure of carbon black has been under investigation for more than fifty years, there are still many aspects which are controversial and some which are virtually unexplored. The inherently low degree of crystallinity and the finely-divided state of carbon blacks have greatly hindered efforts to understand them. The purpose of this article is to cite the principal contributors to our understanding of carbon black microstructure, to discuss the significance of their contribution, to present a clear picture of the present state of our knowledge, and to note areas where controversy exists and where our knowledge is incomplete. The scope of this article is necessarily limited to a reasonably complete treatment of the several aspects of carbon black microstructure; that is, the arrangement of carbon atoms to form graphite layer planes, the arrangement of layer planes to form crystallites, and the arrangement of crystallites to form the more familiar carbon black “particles” or aggregates. Particular attention is paid to more recent articles and those which have shaped our thinking on carbon black microstructure. This article also includes a fairly complete review of various studies on the changes in microstructure which are brought about by heat treatment or oxidation. In general, the rather large number of studies reporting on the microstructure of other forms of carbon have not been reviewed (except for the work of Franklin whose contribution to our understanding of carbon-black microstructure is so immense that it must be included). Although gross, morphological features such as particle size, primary aggregate size and shape are studied briefly in order to relate them to microstructure, no effort was made to review comprehensively the body of literature pertinent to this subject. Also porosity and surface characteristics per se (as measured by gas adsorption techniques) are not treated in detail here. Rather than review a dreary list of papers which have only the slightest bearing on carbon black, the author has taken the liberty of dividing the articles reviewed into two categories. The first category, which is reviewed in some detail, includes those publications in which an important contribution was made to the understanding of carbon-black microstructure. The second category includes all those articles which are discussed only briefly or not at all because the authors have reported superficial or routine studies or they (probably unknown to them) have essentially duplicated the work of an earlier worker, or have reported uncorrected results which are thus so inaccurate as to be without real value to this article; or because they comprise work which is only peripherally related to carbon black microstructure. Also, references taken from other papers, but not reviewed here, are included in the latter category. Articles by Warren, Hofmann and Wilm, Steward and Cook and Walker contain bibliographies which will be helpful to those interested in the earlier work or in the microstructure of carbons other than carbon black. For the reader whose time is limited, an adequate picture of current understanding of carbon black microstructure can be gained by reading Sections II, IV, and V which are relatively short. Finally, a word about the spirit in which the review was written. At the request of the late Dr. Craig, a critical review was prepared in which every effort was made to point out shortcomings as well as classic contributions contained in the pertinent literature. Where the experts have disagreed, the reviewer, often with skill unequal to the task, has attempted to decide which one was the more correct in the light of current knowledge. It is with deep humility and great respect for those who have gone before that this review is submitted.


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