Flocculation of Pigment in Carbon Black—Rubber Mixtures

1938 ◽  
Vol 11 (3) ◽  
pp. 575-584
Author(s):  
C. R. Park ◽  
Paul P. McClellan

Abstract NUMEROUS references occur in the literature as to the cause of so-called scorching or burning in rubber-pigment mixes containing no vulcanizing agent. It was suggested (6) that this stiffening effect may be caused by flocculation of the pigment particles. Green (8) demonstrated a relation between the stiffness and flocculating tendency of pigments in paint mixtures, and Depew and Ruby (4) and Green (7) suggested that the phenomenon of flocculation may have some relation to the properties of cured rubber mixes which contain pigments, especially carbon black pigments. Grenquist (9) reported that carbon black exists in a more or less flocculated condition in vulcanized rubber, and some evidence was presented by Park and Morris (11) that mill-scorched batches which exhibit abnormal stiffness possess a structure which suggests that the black has been flocculated. The increase in stiffness of unvulcanized rubber—carbon black mixes upon standing for periods of several days was mentioned by Stamberger (13). Busse and Davies (2) presented data showing the effect of heat upon the stiffness of such mixes and mentioned the possible relation between flocculation and increase in stiffness. In order to throw more light upon the behavior of carbon black in the stiffening of rubber, a series of experiments was planned following the general methods of Busse and Davies, which include heating the sample for various periods of time and attempting to follow the changes in gross physical properties and in the minute structure of the mix.

2005 ◽  
Vol 78 (2) ◽  
pp. 175-187 ◽  
Author(s):  
Takeshi Hotaka ◽  
Yasuhiro Ishikawa ◽  
Kunio Mori

Abstract Effect of several ingredients in the rubber on adhesion characteristics between brass-plated steel cord and rubber was thoroughly investigated. Amine component is generated by N,N'-dicyclohexylbenzothiazole-sulphenamide- (DCBS) accelerated sulfur vulcanization, and it is known to promote stress-induced corrosion crack in the brass layer at the brass plated steel cord. Hexamethoxymethylmelamine (HMMM), which is formulated for the condensation reaction of RF resin, has a function to trap amines, which was found to effectively improve the adhesive strength in water-aged degradation. It was clarified that the physical properties of the vulcanized rubber such as crosslink density and strain modulus are also improved by trapping the residual amine accompanying improved adhesive strength for the formulation with HMMM. Influence of carbon black on concentration of the residual amine and adhesive strength was also studied. Amount of the amine was inversely proportional to the carbon gel content, while adhesive strength linearly increased with the level of carbon gel. It was assumed that the carbon black dose enhances the adhesive strength due to a preferential entrapment of the amine at the stage of carbon gel formation.


1946 ◽  
Vol 19 (1) ◽  
pp. 125-150 ◽  
Author(s):  
J. R. Scott

Abstract 1. Shellac, even in quite large proportions, can readily be incorporated into raw rubber by the normal process of mixing on a roll mill. It does not assist the breakdown of the rubber during mastication, nor does it show the useful stiffening effect possessed, e.g., by benzidine and p-aminophenol. The effects of shellac on plasticity, indeed, are simply what would be expected of a solid that melts to a viscous liquid at about 80° C. The elastic recovery of masticated rubber after deformation is not increased by admixture of moderate proportions of shellac. Shellac greatly accentuates the calender grain produced by passing unvulcanized rubber between the rolls of a mill or calender. This grain, however, disappears during vulcanization. 2. Shellac does not increase the danger of scorching; indeed, there is evidence that it may exert a useful antiscorching effect, which merits further investigation. 3. Shellac tends to interfere with vulcanization, the attainment of optimum physical properties being retarded and the vulcanizate made weaker and softer. The extent of this interference depends greatly on the composition of the mix, particularly the accelerator. It is probably due largely, though not entirely, to the acidity of the shellac, since it can be reduced by adding a base, e.g., magnesium oxide, or by chemically modifying the shellac to reduce its acidity. Although the effect is always present, it is not serious in loaded mixes such as are used for most manufactured products, provided a suitable accelerator is chosen. Best results have been obtained with accelerators of the metallic dithiocarbamate class; mercaptobenzothiazole also is good, but diphenylguanidine and especially butyraldehydeaniline generally give poor results. Shellac can be used in conjunction with alkali-reclaimed rubber just as well as with new rubber. 4. In mixings containing large proportions of fillers or reinforcing agents, e.g., china clay and carbon black, addition of a relatively small proportion of shellac makes the vulcanizate much harder. As the unvulcanized stock is, if anything, softened by this addition, the use of shellac enables very hard vulcanizates to be produced without the processing difficulties that would arise from an attempt to obtain the hardness by using fillers alone. Tests with high carbon black stocks and with china clay flooring or tiling stocks have demonstrated the advantages of this procedure. In the former, abrasion resistance was somewhat impaired by using shellac, but there was evidence of an improvement in flex-cracking resistance, an effect that deserves further investigation. It is considered that the unexpectedly great hardening effect of shellac in mixes of this type should be more fully studied, in view of its potential utility. 5. Shellac is generally inert towards the aging of vulcanized rubber, and in no case has it been found detrimental. 6. The results obtained in this investigation do not support the claims that have been made to the effect that shellac improves the resistance of vulcanized rubber to swelling by gasoline, benzene, etc., and to absorption of water. 7. Dewaxed shellacs have given better results than TN shellac, as they produce less discoloration in mixes containing zinc oxide, and in some cases give better physical properties. Hard lac resin possesses the same advantages, particularly in the latter respect, but is difficult to disperse, as it does not readily melt. A sample of lac bleached by sodium hypochlorite interfered so seriously with vulcanization that it would probably be unsuitable for use in rubber. 8. Addition of TN shellac, sulfurized lac or hard lac resin to an unloaded (rubber-sulfur) ebonite has not been found to improve the mechanical or electrical properties; indeed, shellac would appear to be unsuitable when a low radio-frequency power loss is required. 9. Mixtures of rubber and shellac containing large proportions of the latter have thermoplastic properties which suggest their use, with or without the addition of fillers, vulcanizing agents, and accelerators of the hardening of shellac, as moulding materials, adhesives, impregnating agents, binders for fibrous materials, etc., and also, in view of the good electrical properties of rubber and shellac, as electrical insulants, particularly to replace gutta-percha. Promising results have been obtained with unvulcanized rubber-shellac mixtures as adhesives for making plywood. As the present research was concerned primarily with the use of shellac in vulcanized rubber products, these unvulcanized mixtures have not been extensively studied. They are considered to merit a more extended investigation, as they do not appear to have received any attention from scientific investigators hitherto.


2012 ◽  
Vol 501 ◽  
pp. 442-447
Author(s):  
Ping Fu ◽  
Feng Bao Bai ◽  
Chuan Sheng Wang ◽  
Shan Hu Li

In this paper adopting the orthogonal method, self-developed compound formulation had tested, and the relationship between the physical properties of vulcanized rubber and rectangular synchronous rotor mixer parameters had researched. The results showed that when the fill factor was 0.6, the rotor speed was 70r/min, cooling water temperature was 45 °C, pressure on the top bolt was 0.8Mpa, the physical properties of the vulcanized rubber was best.


1928 ◽  
Vol 1 (3) ◽  
pp. 485-497 ◽  
Author(s):  
C. R. Johnson

Abstract The rates of evolution of gas from carbon black with variation of time, temperature, and pressure have been determined. Complete analyses have been made of five types of carbon black, which involve an organic combustion of the original sample, an organic combustion of the sample after the gases have been removed, a determination of the loss in weight represented by the gases removed, analyses of the gases removed, and finally a complete accounting, or balance, of the carbon in the steps considered. In an attempt to supply some missing information not revealed by the foregoing, some special gas analyses under varying conditions were made. The relationship between the amount and composition of volatile matter evolved from carbon blacks and the properties imparted to vulcanized rubber when compounded with these blacks has been studied.


1928 ◽  
Vol 1 (3) ◽  
pp. 458-464
Author(s):  
D. J. Beaver ◽  
T. P. Keller

Abstract The data presented herein show that in general the presence of oxygen on carbon black retards the rate of vulcanization in direct proportion to the amount of oxygen present and also decreases the maximum physical properties obtainable with a given amount of accelerator. The aging data show that the presence of this oxygen on the black increases the rate of aging as the amount of oxygen increases, but not in direct proportion to the per cent of this oxygen present. It can be concluded, therefore, that compounds which contain a small amount of oxygen, such as thermatomic, G black, or acetylene black, will give better aging stocks than compounds containing higher amounts of oxygen such as lampblack and standard channel blacks. No correlation could be found between the acetone extract, iodine adsorption, or oil adsorption, and the effect of these blacks on the rate of cure or aging.


1941 ◽  
Vol 14 (4) ◽  
pp. 826-834
Author(s):  
B. S. Garvey ◽  
C. H. Alexander ◽  
F. E. Küng ◽  
D. E. Henderson

Abstract The vital role played by rubber in modern civilization is due in part to the physical properties displayed by soft vulcanized rubber in service and in part to the characteristics of unvulcanized milled rubber which make it amenable to manufacturing operations. Vulcanization of rubber is a change in condition usually induced by heating it with sulfur, and is best defined by contrasting the difference in physical properties: To illustrate, compare a mill-mixed composition before and after vulcanization. Before vulcanization it is easily pulled apart and, if considerably extended, shows little tendency to retract, although, under impact, the recovery or rebound is considerable. If heated it becomes even softer and more plastic, and can easily be formed into any desired shape. If cooled to 0° C or somewhat lower, it becomes stiff and boardy. It is readily soluble in hydrocarbon solvents. When two fresh surfaces are pressed together, they coalesce and become practically integral. This tack, as it is called, is valuable in manufacturing operations. After vulcanization, rubber is tough and strong and, after even a slow distortion, returns rapidly to its original shape. It has little tendency to flow and is devoid of tack. It swells but does not dissolve in hydrocarbon solvents. These characteristics change very little from −40° to well above 100° C.


1935 ◽  
Vol 8 (2) ◽  
pp. 174-176
Author(s):  
Yoshio Tanaka ◽  
Shū Kambara ◽  
Hironosuke Fujita

Abstract The experiments may be summarized as follows: 1. With an increase in the time of cure, the elongation and heating elongation diminish and the Joule effect increases. 2. An increase in the vulcanization coefficient is followed by a decrease in the elongation and heating elongation and an increase in the Joule effect. The increase in the Joule effect, however, has a limit. 3. An organic accelerator reduces the elongation and heating elongation and increases the Joule effect. 4. The greater the degree of mastication the greater the elongation and the heating elongation and the less the Joule effect. 5. By exposure to ultra-violet radiation, the elongation and heating elongation are increased and the Joule effect decreased. 6. A filler increases the heating elongation and decreases the elongation and the Joule effect. Thus samples with relatively high elongations at a definite tension have relatively high heating elongations and low Joule effects. Such specimens seem to have been affected by the disaggregation and depolymerization of the rubber molecules. The effects of the time of cure, mastication, and exposure to ultra-violet radiation prove this fact. Vulcanization increases the Joule effect, but on the other hand, it is accompanied by a disaggregation and depolymerization of the rubber molecules, so the increase in the Joule effect with the progress of vulcanization has a limit. On vulcanization with an accelerator, the combination of sulfur occurs so rapidly that the increase in the Joule effect is predominant. A filler, such as carbon black, behaves only as a diluent of Joule effect. These results lead to the conclusion that the more highly polymerized rubber molecules and their sulfur compounds seem to be the chief factor in the Joule effect of vulcanized rubber.


1934 ◽  
Vol 7 (4) ◽  
pp. 610-617 ◽  
Author(s):  
Takeo Fujiwara ◽  
Toramatsu Tanaka

Abstract The hardening of rubber at low temperatures is one of the well-known physical characteristics of rubber. The loss of elasticity of raw rubber by hardening at 0° to 10° C., its turning to the consistency of glass, and its fragility at −19° C. when cooled with liquid air, and its fibering when stretched to 60–70 per cent previous to breaking, give an experimental proof of the theory of the structure of rubber molecules. Vulcanization makes raw rubber physically less sensitive to heat and to low temperatures, and is of great significance, because it enables vulcanized rubber to be used around −30° C. without losing its elasticity. The effect of external heat on the physical properties, especially on the stress-strain relations, of vulcanized rubber has been discussed mainly for temperatures from −10° to +100° C., and only two papers deal with temperatures from −30° to −60° or −70° C. (cf. Le Blanc and Kröger, Kolloid Z., 37, 205 (1925); Tener, Kingsbury and Holt, Bureau of Standards Technologic Papers Vol. 22, No. 364). Of special importance are a means of recognizing changes m the physical properties (phenomenon of freezing-hard ness) of vulcanized rubber at −30° to −60° or −70° C., and the practical value of such information. Though there is a contradiction in the fundamental meaning of the “cold resistant theory” of rubber, investigations of the two phases of the subject may throw some light on practical problems and widen the scientific point of view.


2017 ◽  
Vol 737 ◽  
pp. 572-577
Author(s):  
Sompatsorn Wongwilatnurak ◽  
Surakit Tuampoemsab ◽  
Rapeephun Dangtungee

Geocell, a type of the geosynthetics, is normally used to improve natural geomaterial properties and performance because of confinement and confinement force. This work was an attempt to apply the solid natural rubber (NR) for producing the prototype of geocell with reinforcing the pavement structure of the road. There are three parts of all work in research, which consist of finding the optimal chemical formula, designing and producing the prototype and civil engineering testing of flexible pavement components. This research has emphasized and focused on finding the optimal chemical formula for the prototype production. The effect of silica-carbon black (CB) dual-phase filler on physical properties in terms of only static mechanical tests of the prototype was investigated. The total amount of hybrid reinforcing filler was fixed at 60 phr while the silica/CB ratios were 0/60, 10/50, 20/40, 30/30 and 40/20, respectively. Cure characteristic of the NR compound and physical properties in terms of static mechanical tests such as hardness, tensile and tear strengths of the NR vulcanizates were carried out. The results showed that time to 90% cross-linked (TC 90), hardness and tensile strength of the vulcanized rubber were increased with the increasing of silica content but not for its tear strength. Dispersion of the dual-phase filler in the prototype was reduced when the higher amount of silica in the dual-phase filler was employed as proved by images from the scanning electron microscope. There was only 60 phr CB that was selected as the optimal chemical formula for prototype production as the result of tensile and tear strength.


2015 ◽  
Vol 1107 ◽  
pp. 113-118
Author(s):  
Ahmad Kifli Che Aziz ◽  
Teku Zakwan Zaeimoedin ◽  
Mazlina Mustafa Kamal

The challenges of using Epoxidised Natural Rubber (ENR) in truck tyre tread are to achieve good cure reversion resistant and physical properties especially on abrasion resistance towards long vulcanization time. The objectives of the project are to study the effects of vulcanization additive on cure characteristics and physical properties of silica filled ENR compound. In this work, a variation of curing systems were employed and a standard carbon black filled Natural Rubber/Butadiene Rubber (NR/BR) compound as a comparison. Greater reversion resistance and physical properties were observed with inclusion of vulcanization additive in the silica compound as compared to compound containing any. The abrasion resistance on the hand improved in spite of long vulcanisation time which commonly practices in truck tyre manufacturing.Keywords: ENR, silica, vulcanization additive, cure reversion, abrasion resistance


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