Vulcanization of Latex. Differences in the Behavior of Fresh, Old, and Purified Latex

1943 ◽  
Vol 16 (2) ◽  
pp. 318-341
Author(s):  
J. W. Van Dalfsen

Abstract Patents granted to Schidrowitz show that when latex is vulcanized and then dried at room temperature, the product has the properties of vulcanized rubber. Films produced in this way show tensile strengths and elasticity which correspond to those of latex films vulcanized in the dry state. It is apparent, however, that when fresh latex is vulcanized under certain definite conditions, the product has fair tensile strength and elasticity only at a relative humidity of zero, but which under ordinary atmospheric conditions is brittle, seems to be overcured, and is practically without tensile strength. This tensile strength, however, is increased by additional dry vulcanization, so there can be no question of overcure. Just as soon as vulcanization has proceeded to a point where brittle films without tensile strength are obtained, the latex, when treated with acid, does not coagulate, but merely flocculates. Nor can such vulcanized fresh latex at this stage be made to coagulate coherently by other means. This form of latex is not sticky. The flocculate referred to can be obtained only by vulcanizing fresh latex in the presence of zinc oxide, and under conditions such that hydrolysis of the nonrubber substances is a minimum. It is, therefore, desirable to have recourse to ultra-accelerators and to be sure that the vulcanization temperature is not too high. By keeping fresh latex alkaline, or by purifying it, it will not flocculate. Latex that has been purified or aged may occasionally, under similar conditions, give a brittle and incoherent coagulum, whereas in other cases a normally coherent but somewhat brittle coagulum results. The nature of the coagulum is governed by the degree of purification and hydrolysis of the nonrubber substances; hence all transition stages between a flocculate and a completely coherent coagulum may occur. By adding serum from fresh latex to purified latex, the behavior of such purified latex changes in the sense that it behaves more like fresh latex. In studying experimentally the difference in behavior of fresh latex and purified latex, the first thing considered was the combination of sulfur. It was found that sulfur first dissolves in the serum, after which it dissolves in the rubber itself. Only then does vulcanization take place. This became evident from the definite acceleration of the combination of sulfur in the latex stage, when before vulcanization, latex was heated with sulfur alone. By this preparatory treatment too, dry vulcanization at room temperature was accelerated, but there was no noticeable effect on dry vulcanization at 80° and 110° C. At 30° C, about 1 per cent of the sulfur dissolved in the rubber particles, in the form of free sulfur. From this it was concluded that it is not possible to remove by mechanical means (as by clarification) excess free sulfur from vulcanized latex. No essential difference could be found between the combined sulfur of fresh latex and that of purified old latex.

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
W. H. Haniffah ◽  
S. M. Sapuan ◽  
K. Abdan ◽  
M. Khalid ◽  
M. Hasan ◽  
...  

This research studied the degradation of tensile properties of kenaf fibre reinforced polypropylene composites due to cyclic immersion into two different solutions, as well as comparison of the developed composites’ tensile properties under continuous and cyclic immersion. Composites with 40% and 60% fibre loadings were immersed in tap water and bleach for 4 cycles. Each cycle consisted of 3 days of immersion and 4 days of conditioning in room temperature (28°C and 55% humidity). The tensile strength and modulus of composites were affected by fibre composition, type of liquid of immersion, and number of cycles. The number of immersion cycles and conditioning caused degradation to tensile strength and modulus of kenaf fibre reinforced polypropylene composites. Continuous and cyclic immersion in bleach caused tensile strength of the composites to differ significantly whereas, for tensile modulus, the difference was insignificant in any immersion and fibre loadings. However, continuous immersion in the bleach reduced the tensile strength of composites more compared to cyclic immersion. These preliminary results suggest further evaluation of the suitability of kenaf fibre reinforced polypropylene composites for potential bathroom application where the composites will be exposed to water/liquid in cyclic manner due to discontinuous usage of bathroom.


1952 ◽  
Vol 25 (2) ◽  
pp. 209-229 ◽  
Author(s):  
Shu Kambara ◽  
Kumakazu Ohkita

Abstract In this study much information about the method of distinguishing the state in which sulfur is combined in simple organic compounds consisting of carbon, hydrogen, and sulfur was obtained, and a new theory of vulcanization was postulated as a result of its application to vulcanized rubber. When activated sulfur reacts with rubber, it first adds to the double bonds, forming thioketones, which in turn, as a characteristic of these radicals, combine with each other, with the formation of a thioether structure. This transformation of thioketone into thioether takes place, not only during vulcanization, but also gradually after vulcanization. Because of the presence of thioketone, treatment of vulcanized rubber with hydrazine, forms a new network, that is, a ketoazine cross-linkage. Combined sulfur of the thioketone type was determined by an oxidizing agent, and as the difference of this value and total combined sulfur a method of determining bridge type of combined sulfur has been proposed. By this method, it was found that, even in ebonite, about one-third of the combined sulfur is the thioketone type, and that the bridge type is only about two-thirds of the total. The thioketone type of combined sulfur in soft vulcanized rubber is transformed gradually into the thioether type of cross-linkage when allowed to stand at room temperature, and this transformation is accelerated when the temperature is raised. In the case of hard rubber, this phenomenon is also observable, but the rate of this transformation is much slower compared to the former. This tendency is the same in the case of ketoazine cross-linking when rubber vulcanizates are treated with hydrazine. From these facts, it seems that the distribution of the thioketone radicals is not uniform, and the magnitude of the probability for collision of these radicals to form cross-linkages has a great influence on the properties of rubber after vulcanization. That is, the property of the vulcanizate is greatly affected by the fact whether the thioketone radicals in the vulcanizates are comparatively uniformly distributed or whether they exist in sectional groups or in colonies. The authors are the first to advance this postulate concerning the chemical structure of vulcanized rubber and its transformation. We believe that when the study is extended, using this postulation, problems such as aging and the differences in the properties of vulcanized rubber accelerated with various accelerators will become clear. Moreover, we believe that it will be of interest to physicists studying rubber elasticity to suggest this idea of colony of cross-linkages. We are now carrying on researches on these problems, and we shall report on them later.


1935 ◽  
Vol 8 (4) ◽  
pp. 554-570 ◽  
Author(s):  
P. A. Gibbons

Abstract Hitherto two products of the reaction between sulfur and rubber have been studied and used commercially, soft rubber and ebonite. Few publications have appeared concerning the products obtained by vulcanization of proportions between 5 and 30 parts of sulfur with 100 parts of rubber. Before the introduction of organic accelerators of vulcanization the coefficient of vulcanization was considered a satisfactory criterion of the quality of soft vulcanized rubber. Mixes of rubber and sulfur vulcanized to a coefficient of more than 3.5 to 4 were usually considered overvulcanized in that experience showed that the optimum properties as regards tensile strength and elongation at rupture occurred at this degree of vulcanization. Semi-ebonites differ from soft rubber and ebonite in as much as they are extremely sensitive to small changes in the time of vulcanization. Their plasticity is such that the velocity of plastic flow just prior to break is relatively great, and thus they may experience a large elongation at constant load. Their plasticity decreases with further vulcanization, in fact, with advance in vulcanization they become almost rigid at room temperature. The decrease in plastic flow is accompanied by an increase in hardness and brittleness and the ultimate stage in the rubber-sulfur reaction, ebonite, is reached.


2013 ◽  
Vol 834-836 ◽  
pp. 175-179
Author(s):  
Kai Dian Wang ◽  
Mao Fang Huang ◽  
Chun Liang Yang ◽  
Zong Qiang Zeng ◽  
Zhi Xiong Liang ◽  
...  

The natural rubber samples produced by conventional tapping methods were used as a control, then analyzed the dry rubber property of natural rubber, the dynamic property and Physical & mechanical property of vulcanized rubber using Rubber processing analyzer and Thermogravimetric Analyze the difference between the properties of dry rubber and vulcanized rubber produced by Micro-cut Tapping with Gas-stimulation. The results indicated that the tensile strength, tear strength elastic modulus of dry rubber that produced by Micro-cut Tapping with Gas-stimulation are respectively 20%, 7% lower than the control. The protein content of dry rubber materials produced by Micro-cut Tapping with Gas-stimulation is 16.7% higher than control group.


1950 ◽  
Vol 23 (3) ◽  
pp. 581-586
Author(s):  
Chullchai Park ◽  
Usaburo Yoshida

Abstract The tensile strengths of crystallized crude rubber and vulcanized rubber are remarkably different from each other at room temperature, but are found to be almost the same at the temperature of liquid air. By assuming that the tensile strength of crystallized rubber at this low temperature is entirely due to its chain molecules, the forced needed to break a chain molecule of rubber at its weakest point is estimated.


1943 ◽  
Vol 16 (4) ◽  
pp. 924-925
Author(s):  
J. R. Scott

Abstract The work described below was carried out as a first step in determining whether an oxygen-bomb test at room temperature could be used as an accelerated aging test for unvulcanized rubber compositions, e.g., as used on surgical and adhesive plasters and for combining shoe fabrics, because a high-temperature test is unsatisfactory in such cases, owing to the melting of the compositions. The only infallible way of assessing the value of an accelerated test for such compositions is by comparison with natural aging, but as this is a very lengthy process and as the deterioration is difficult to measure quantitatively, it was decided to make preliminary tests on the effect of high oxygen concentration at room temperature by using vulcanized rubber. Although the results proved to be negative so far as the original purpose of the work was concerned, it is considered of interest to place them on record in view of the prominence given in some papers on aging to the relationship between oxygen concentration and rate of oxidation and deterioration of rubber. A mix composed of rubber 100, sulfur 3, zinc oxide 5, stearic acid 1, and diphenylguanidine 0.75, was vulcanized for 30 minutes at 153° C. Tensile tests, using standard ring-specimens and the Schopper machine, were made on unaged specimens and on specimens that had been aged (1) in an oxygen bomb at 300 lb. per sq. in. oxygen pressure and at room temperature (about 10° C), (2) in a Geer oven at 70° C. Four rings were used for each test, the tensile strength and breaking elongation figures quoted being the average for the two rings giving the highest tensile strength, and the figures for the elongations at constant loads the average of all four rings.


2017 ◽  
Vol 31 (10) ◽  
pp. 1341-1351 ◽  
Author(s):  
Yuheng Bao

By melt blending method, the Chinese medicine residue (CMR) and polylactide (PLA) were mixed together using dioctyl phthalate (DOP) as plasticizer. The extrusion and injection-molding processes were used to prepare all the specimens of CMR/PLA composites. Hydrothermal aging was implemented through immersing samples in distilled water at 60, 90°C, and room temperature in different aging cycles. The properties of the CMR/PLA composites were characterized by mechanical property testing and the analyses of thermogravimetric (TG), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The result showed that the temperature has a significant effect on the hydrothermal aging behavior of the composites. After 60°C hydrothermal aging of 8 days, the bending strength and the tensile strength have reduced to 7.04 and 4.32 MPa, respectively, while the bending strength and the tensile strength became to 1.32 and 2.48 MPa after 90°C hydrothermal aging of 15 h and then the mechanical properties completely lost after 20 h. When hydrothermal aged, the CMR/PLA composites continually undergo degradation, generating bare fibers and broken into small molecular chain structure from macromolecular. Through hydrolysis of ester group, fragmentation of macromolecule chain and the molecular weight decreased, and the interfacial adhesion between the CMR and the PLA is weakened.


1944 ◽  
Vol 17 (1) ◽  
pp. 221-226
Author(s):  
E. C. B. Bott ◽  
L. D. Gill

Abstract The deterioration of vulcanized rubber containing increasing percentages of copper and manganese compounds and the extent of the protection given to the stocks by a secondary naphthylamine have been investigated. Jones and Craig showed that the addition of copper stearate made no difference to the type of aging of stocks containing various percentages of antioxidant when measured by decrease in tensile strength, and the results of Taylor and Jones indicate that the decrease is proportional to the time of aging in the Geer oven. Preliminary work.—Experiments were made on the base mix to determine its suitability and its optimum cure. The optimum cures of the base mix plus copper or manganese compounds after storage for six weeks in the dark at normal room temperature and of the base mix plus sym. di-β-naphthyl-p-phenylenediamine also were obtained. The following compounds A, B, C and D were mixed on a laboratory mill having 12 × 6 in. rolls.


Author(s):  
T. Baird ◽  
J.R. Fryer ◽  
S.T. Galbraith

Introduction Previously we had suggested (l) that the striations observed in the pod shaped crystals of β FeOOH were an artefact of imaging in the electron microscope. Contrary to this adsorption measurements on bulk material had indicated the presence of some porosity and Gallagher (2) had proposed a model structure - based on the hollandite structure - showing the hollandite rods forming the sides of 30Å pores running the length of the crystal. Low resolution electron microscopy by Watson (3) on sectioned crystals embedded in methylmethacrylate had tended to support the existence of such pores.We have applied modern high resolution techniques to the bulk crystals and thin sections of them without confirming these earlier postulatesExperimental β FeOOH was prepared by room temperature hydrolysis of 0.01M solutions of FeCl3.6H2O, The precipitate was washed, dried in air, and embedded in Scandiplast resin. The sections were out on an LKB III Ultramicrotome to a thickness of about 500Å.


2019 ◽  
Vol 14 (1) ◽  
pp. 110
Author(s):  
Assiss. Prof. Dr. Sabiha Mahdi Mahdi ◽  
Dr. Firas Abd K. Abd K.

Aim: The aimed study was to evaluate the influence of silver nitrate on surfacehardness and tensile strength of acrylic resins.Materials and methods: A total of 60 specimens were made from heat polymerizingresins. Two mechanical tests were utilized (surface hardness and tensile strength)and 4 experimental groups according to the concentration of silver nitrate used.The specimens without the use of silver nitrate were considered as control. Fortensile strength, all specimens were subjected to force till fracture. For surfacehardness, the specimens were tested via a durometer hardness tester. Allspecimens data were analyzed via ANOVA and Tukey tests.Results: The addition of silver nitrate to acrylic resins reduced significantly thetensile strength. Statistically, highly significant differences were found among allgroups (P≤0.001). Also, the difference between control and experimental groupswas highly significant (P≤0.001). For surface hardness, the silver nitrate improvedthe surface hardness of acrylics. Highly significant differences were statisticallyobserved between control and 900 ppm group (P≤0.001); and among all groups(P≤0.001)with exception that no significant differences between control and150ppm; and between 150ppm and 900ppm groups(P>0.05).Conclusion: The addition of silver nitrate to acrylics reduced significantly the tensilestrength and improved slightly the surface hardness.


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