Report of the Raw Rubber Specifications Committee

1929 ◽  
Vol 2 (2) ◽  
pp. 335-339
Author(s):  
Ellwood B. Spear ◽  
C. R. Boggs ◽  
H. E. Simmons ◽  
H. L. Trumbull ◽  
N. A. Shepard

Abstract AS INTIMATED in a previous report of the Committee presented at the St. Louis meeting in April, 1928, a temporary procedure was adopted in order to ascertain whether or not the five laboratories represented on the Committee could obtain reasonably comparable stress-strain relationships using the same batch of rubber. A complete report is appended in which the procedure is outlined and the results of each laboratory are given in considerable detail. After careful deliberations the Committee has concluded that the testing of raw rubber is not in a very satisfactory state. It therefore makes the following recommendations: (1) The testing of raw rubber should be made the subject of thorough investigations. (2) The work should be undertaken by a Physical Testing Committee, preferably under the jurisdiction of the Rubber Division of the American Chemical Society.

1929 ◽  
Vol 2 (2) ◽  
pp. 318-322
Author(s):  
F. S. Conover

Abstract THE effect of relative humidity on rubber-testing has been the subject of much recent investigation. String-field and Conover and Depew have published papers on this subject. The last-named authors recommended that the rubber be stored in dry cabinets before milling, between milling and vulcanization, and between vulcanization and testing, at a temperature of 75° ±5° F. A short time later the Physical Testing Committee of the Rubber Division of the American Chemical Society recommended that all laboratory testing be carried out at 45 per cent relative humidity and 82° ±5°F. While both methods have undoubted merit, it was believed that for physical testing laboratories, particularly such as this one, zero humidity was both more conducive to reliable results and easier to maintain. Accordingly, equipment was installed for maintaining zero humidity and its performance has been consistently good. Since several of the larger rubber laboratories have shown interest in the equipment, it has been decided to present this description of the installation and its operation.


1928 ◽  
Vol 1 (4) ◽  
pp. 515-594
Author(s):  
J. E. Partenheimer ◽  
E. R. Bridgwater ◽  
D. F. Cranor ◽  
E. B. Curtis ◽  
J. W. Schade ◽  
...  

Abstract IN OCTOBER, 1926, R. P. Dinsmore, chairman of the Rubber Division of the AMERICAN CHEMICAL SOCIETY, appointed a Physical Testing Committee to investigate the effect of variables such as temperature and relative humidity upon the physical properties of rubber. This committee was continued by Harry L. Fisher, present chairman of the Rubber Division. The committee chose the problem of determining the importance of controlling atmospheric temperature and relative humidity while conditioning rubber test samples at various stages of preparation and testing. This report deals with the first study made—that of the effect of the above two variables on the stress-strain and tensile properties of rubber. In reading this report it should be kept in mind that the problem of this committee is to determine the effect of variables on the physical properties of rubber so that we may know the relative importance of controlling the factors involved. It was not intended to make this work include the relative value of specific tests for particular purposes or to become a research directed towards the development of new tests. It has been the intent to limit the work of the committee to the refinement of tests widely used and considered as routine and standard, and not to include development of new tests or work concerning broader lines of research. It is, however, hoped that in the future the work of this or another committee can be broadened to include fundamental research problems as well as specific work such as the present committee has undertaken. We believe that the work done demonstrates the desirability of carrying on cooperative investigations of this nature and hope that this committee is made a permanent institution of the Rubber Division with such changes in personnel as are necessary continually to broaden and improve the work. This report will raise many questions and point out several possible lines of research, but the committee has tried to stick to its job of determining the relative importance of controlling temperature and relative humidity in relation to stress-strain and tensile properties. The work has been carried out at the Bureau of Standards at Washington by F. E. Rupert as a research associate under the direction of the committee. The Bureau of Standards has contributed its facilities and to cover the expenditures of the committee for the first year each company represented by the members of the committee contributed $650. The Rubber Association of America is handling the finances of the committee for the present year, which amounts to $6000 and includes the appropriation of the Firestone Tire and Rubber Company. As the committee has needed special apparatus different companies have loaned machines, which have included a Scott tensile tester and U. S. abrasion machine from the Henry L. Scott Company, and a Grasselli abrader from the Grasselli Chemical Company.


1932 ◽  
Vol 5 (3) ◽  
pp. 351-355 ◽  
Author(s):  
M. Jones

Abstract The evaluation of rubber has centered largely around stress-strain phenomena, and the property of tensile strength is probably the one which has the most general application throughout the industry. Rubber exhibits stress-strain properties quite different from the majority of substances, and peculiar difficulties are introduced during the determination of tensile strength. Although tentative standards have recently been issued by the American Chemical Society, there is no evidence that these are being strictly adhered to, and there is still need for a more rigid standardization of tensile-testing methods. There are essentially two methods of tensile-testing: (1) Using dumb-bell test-pieces with a Bureau of Standards machine, or a Scott type of machine; and (2) Using ring test-pieces with a Schopper type of machine. It is generally supposed that higher tensile results are obtained by the former method. Recently, occasion has occurred to make a comparison between both types and to study the effect of certain factors upon each method.


1962 ◽  
Vol 35 (5) ◽  
pp. 27-40 ◽  
Author(s):  
Melvin Mooney

Abstract In accordance with custom, I have been asked, as a Goodyear Medalist, to address the Division of Rubber Chemistry of the American Chemical Society on the subject of my past work in the science and technology of elastomers. Hoping that I have correctly understood your desires, I shall now give you an informal, anecdotal story of some of this work. Going beyond this story of the past I shall also sketch, as I now see them, certain related unsolved problems, some of which have been rather neglected. While keeping in mind that detailed mathematics and theoretical argument would be inappropriate and even unwelcome on this occasion, I shall endeavor, with very little mathematics, to stimulate some of you to initiate programs of research on some of these problems, if you have not already done so. First let me tell you how, without realizing it, I became a rheologist. When I was employed by the United States Rubber Company in the fall of 1928, my first assignment was to study rubber plasticity, or the flow properties of crude rubbers and raw compounded stocks. When I was told of this problem in a conference with my group leader, Dr. Roscoe H. Gerke, there was a third person present, Dr. Ernest J. Joss, a physical chemist. Dr. Joss had only shortly before been given the same assignment; but with my appearance in the group, he was permitted to drop this work and give his full time to more congenial tasks. At the conference he turned over to me some talced strips of pale crepe which had been cut from a batch on a laboratory mill after various milling times. I knew nothing about rubber at that time; and if I had been asked to guess what these samples were, I could only have replied that they looked like fillets of sole sprinkled with flour and ready for the frying pan. The rheologieal testing devices for raw rubber that were available at that time were of two forms, the compression plastometer and the extrusion plastometer. I quickly decided that neither of these was suitable for the purpose, which, as I conceived it, was to measure the flow behavior of raw rubbers or stocks in their working condition as exhibited on a mill or calender or in a tuber.


1930 ◽  
Vol 3 (2) ◽  
pp. 179-184

Abstract THE accompanying report on the work of the Physical Testing Committee, Rubber Division, American Chemical Society, marks the conclusion of the research work on the standardization of physical tests of rubber, which have been conducted since early in 1927, at the rubber laboratory of the Bureau of Standards, Washington, D. C., under the sponsorship of the Rubber Manufacturers Association, the Rubber Division, A. C. S., and a number of rubber companies. The original committee was formed in October, 1926, by R. P. Dinsmore, chairman of the Rubber Division at that time. F. E. Rupert, research chemist at the Fisk Rubber Company, was chosen to conduct the research work. J. E. Partenheimer, also of Fisk, was chairman of the first committee, and was later succeeded by W. A. Gibbons, of United States Rubber Company, who in turn resigned last year and was succeeded by A. A. Somerville, of R. T. Vanderbilt Company, who has remained as chairman up to the present time. Two progress reports were made by the committee, one on the “Importance of Temperature and Humidity Control in Rubber Testing,” read at the April, 1927, Rubber Division meeting at Richmond, Va., and a later report on “The Effect of Humidity and Temperature on the Ability of Rubber Compounds to Resist Abrasion,” presented in September, 1927, at Detroit. This report was later amplified and released for publication in December, 1927.


1929 ◽  
Vol 2 (2) ◽  
pp. 197-208
Author(s):  
A. A. Somerville ◽  
J. M. Ball

Abstract CRUDE rubber is not of much use commercially or industrially until after it has been put through a chemical process discovered by Charles Goodyear: that of adding sulphur and heating. But sulphur is not the only material that can be used to change and improve the natural physical properties of raw rubber. There are other things than sulphur that are beneficial, one of which is Selenium. It is a pleasure to be permitted to talk here in Boston before a meeting of the Northeastern Section of the American Chemical Society and the Boston Rubber Group, devoted at this time particularly to the subject of rubber. It is a privilege to be permitted to talk on the subject of Selenium at this meeting because it is coming back very close to the home of Selenium so far as it is associated with the rubber industry.


1990 ◽  
Vol 63 (5) ◽  
pp. 81-95
Author(s):  
Benjamin Kastein

Abstract The Las Vegas meeting of the Rubber Division, ACS, provided attendees the opportunity to hear the interview of Mr. Arnold H. Smith, by Mr. Herbert A. Endres, recorded April 7, 1966. Mr. Smith, as Secretary-Treasurer of the Division from 1919 to 1928, and as Chairman in 1929, was the person most responsible for laying the foundation which supported the growth of the Division to its present status. The India Rubber Section was sanctioned by the American Chemical Society on December 30, 1909. The 28 chemists from the rubber industry who were the organizing members, had the objective of meeting together to solve mutual problems. The major problem for everyone in 1909 was the variable quality of the 36 varieties of wild rubber from the jungles of Central and South America and Africa. Para rubber from the Hevea Brasiliensis tree was considered to be the best type available, but there were at least 13 variations, identified by source of the Para rubber. Charles C. Goodrich, as first chairman of the India Rubber Section, moved immediately to resolve the problem and appointed a committee, chaired by Dr. Charles Knight of Buchtel College, to develop standard methods of testing and evaluation. The committee diligently addressed the subject and reported to the Section at each meeting for 10 years, but progress was slow. Members attending had been instructed by their superiors, “Listen—but don't talk!” Not a very satisfactory format for conducting a meeting. Several key individuals helping to organize the India Rubber Section were W. C. Geer, Chief Chemist at the B. F. Goodrich Co. and George Oenslager, of the Diamond Rubber Co. Geer invented the air oven used to accelerate heat aging of rubber samples, and Oenslager is famous for discovering the effect on vulcanization of organic accelerators in 1906 and for the use of carbon blacks in treads in 1911. Although the sharing of technical information was tantalizing slow during the early years, the American Chemical Society, at their meeting in Buffalo, April 7, 1919, approved the formation of the Division of Rubber Chemistry. John B. Tuttle, first chairman of the Division in 1919, with Arnold H. Smith as secretary-treasurer, determined to bring to the members technical information less restricted in content, and from their neutral position of employment at the National Bureau of Standards, thought results could be obtained.


2020 ◽  
Author(s):  
MAK Williams ◽  
V Cornuault ◽  
AH Irani ◽  
VV Symonds ◽  
J Malmström ◽  
...  

© 2020 American Chemical Society. Evidence is presented that the polysaccharide rhamnogalacturonan I (RGI) can be biosynthesized in remarkably organized branched configurations and surprisingly long versions and can self-assemble into a plethora of structures. AFM imaging has been applied to study the outer mucilage obtained from wild-type (WT) and mutant (bxl1-3 and cesa5-1) Arabidopsis thaliana seeds. For WT mucilage, ordered, multichain structures of the polysaccharide RGI were observed, with a helical twist visible in favorable circumstances. Molecular dynamics (MD) simulations demonstrated the stability of several possible multichain complexes and the possibility of twisted fibril formation. For bxl1-3 seeds, the imaged polymers clearly showed the presence of side chains. These were surprisingly regular and well organized with an average length of ∼100 nm and a spacing of ∼50 nm. The heights of the side chains imaged were suggestive of single polysaccharide chains, while the backbone was on average 4 times this height and showed regular height variations along its length consistent with models of multichain fibrils examined in MD. Finally, in mucilage extracts from cesa5-1 seeds, a minor population of chains in excess of 30 μm long was observed.


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