The Reinforcing Action and Other Properties of Titanium Fillers in Rubber Stocks

1933 ◽  
Vol 6 (1) ◽  
pp. 106-110
Author(s):  
W. H. Bodger ◽  
F. H. Cotton

Abstract (1) The reinforcing properties of a high-grade titanium white, containing 74 per cent barium sulfate in intimate combination with the oxide, are slightly better than those of “White Seal” zinc oxide in mixes vulcanized with diphenylguanidine. (2) Titanium dioxide is generally inferior to titanium white as a reinforcing agent, and at high loadings gave poor tensile properties, especially in compounds accelerated with mercaptobenzothiazole. (3) The titanium fillers are incapable of behaving as activators of organic accelerators, as zinc oxide does, and from 3 to 5 per cent of zinc oxide is required in the majority of titanium stocks containing organic accelerators. (4) The aging properties of compounds reinforced with titanium fillers are generally similar to those conferred by zinc oxide, but are inferior to the latter at low volume loadings. (5) Better pigmentary and water-resisting properties are conferred by titanium dioxide than by titanium white, and both these fillers are superior to zinc oxide in these respects.

1964 ◽  
Vol 47 (2) ◽  
pp. 391-394
Author(s):  
William B Link ◽  
Keith S Heine ◽  
J H Jones ◽  
Percy Wattlington

Abstract A method has been developed for determining 1 μg of mercury in 100 ml of aqueous acid solution with a precision of ± 0.25 μg. In the method, the mercury is adsorbed by anion resinloaded paper and determined by X-ray emission spectroscopy. The method gave 75—125% recoveries of 1 μg of mercury from acid solutions containing 10 g of sodium sulfate, sodium chloride, iron oxide, magnesium carbonate, and calcium carbonate, and satisfactory recoveries from the HCl extract of carbon, barium sulfate, chromic oxide, bentonite, kaolin, talc, titanium dioxide, and magnesium stearate. Substantial changes in flow rate or acid concentration seem to have little effect on mercury absorption from HC1 solution. Mercury in zinc oxide or bismuth oxychloride cannot be determined by this technique.


1966 ◽  
Vol 39 (4) ◽  
pp. 1347-1357 ◽  
Author(s):  
H. Baldyga ◽  
H. C. Jones

Abstract Oven aging properties at 350° F and 300° F of EPT polymers were substantially improved with additions of zinc oxide up to 10 and 20 phr. Zinc oxide enhanced the elongation retention after aging, and the improvement was significantly greater with French than with American Process zinc oxides. Finer particle size French Process zinc oxides imparted somewhat better aging properties than did the coarser zinc oxides of the same type. The aging advantage for high loadings of zinc oxide was notable both with whiting and clay-filled EPT compounds with low and normal amounts of sulfur. When the pigmentation of the EPT polymer was 50 phr of FEF black, the aging differences between the several American and French Process oxides at loadings of three to 20 phr were less prominent. Replacement of three per cent of EPT with an equal amount of several unsaturated elastomers increased the cure rate of the compound appreciably. Tear resistance was improved and compression set properties lowered. Improvement in heat resistance depends on the polymer added. Several anatase and rutile pigments were essentially equal in heat aging resistance at an equal volume loading in EPT. The reflectance of stocks with zinc oxide alone or in combination with titanium dioxide in an unfilled stock increased during the first three days of Atlas Weather-Ometer exposure. Beyond this point, there was a gradual degradation in reflectance with the loss in reflectance being somewhat greater with a zinc oxide-titanium dioxide blend than straight zinc oxide. These results reflect the observed differences in ultraviolet opacity between zinc oxide and titanium dioxide. In a comparison of anatase and rutile in a whiting loaded stock, anatase was poorer than rutile in reflectance through the initial exposure stages in the Atlas Weather-Ometer; however, after prolonged exposure, there was a reversal in reflectance, due to the chalk layer developed in the anatase sample. EPT stocks pigments with 79.5 phr of whiting with titanium dioxide between 18.5 and 25 phr, and activation amounts of zinc oxide showed no visible sunlight degradation after 70 weeks outdoors.


1943 ◽  
Vol 16 (2) ◽  
pp. 445-452
Author(s):  
E. B. Johnson ◽  
J. R. Scott

Abstract 1. It has been found possible, by the use of combinations of organic accelerators, to prepare accelerated rubbers which contain sufficient zinc oxide for activation but show no trace of pigmentation by the oxide, and are quite as transparent as a mixture containing only rubber and sulfur, and often lighter in color than the latter mixture. These accelerated rubbers have excellent tensile properties. The aging properties vary considerably according to the accelerators used, but in most cases are very good, even if the rubber is over-cured. It is, therefore, possible to make nonblooming rubbers without danger of bad aging. 2. Tests with other activators (zinc carbonate, zinc oleate, and zinc stearate plus magnesium carbonate) showed that these are less effective than zinc oxide, for the vulcanizates obtained had inferior mechanical properties and, in the case of zinc carbonate and oleate, showed a strong tendency to bloom. 3. A combination of accelerators which has been stated to work well without activator was shown to vulcanize very quickly, but to give poor mechanical properties, 4. The tendency of various accelerators to give rubbers, the surfaces of which are easily marked by scratching, presumably owing to efflorescence of accelerator, was noted. 5. The most promising of the mixtures tested for making transparent vulcanized rubbers was one accelerated with diphenylguanidine plus mercapto- benzothiazole, with zinc oxide as activator (mixture F). 6. A mixture is described (mixture K) which gives better aging when vulcanized beyond the optimum tensile properties than when vulcanized short of the optimum cure. 7. Rubbers can be toughened by the use of organic accelerators so as to possess greater resilience and lower permanent set than if toughened by the usual inorganic reinforcing agents. The aging tests described above were all made in the absence of light. For transparent rubber goods which are exposed to light during use, the addition of antioxidants and (or) softeners might be found necessary to give resistance to deterioration by light. In connection with fancy goods, the staining of paper in contact with the rubber may be of importance, and in such cases the choice of accelerators and antioxidants must be made with this in mind. The staining effects of numerous accelerators and antioxidants have already been described. In conclusion, it should be added that the experiments were directed in the first instance towards the production of brown transparent rubbers, for which reason smoked sheet was used. Where a light-colored vulcanizate is required, and especially when it is desired to obtain colored rubbers by adding organic dyes, the use of pale crepe is essential.


1950 ◽  
Vol 23 (2) ◽  
pp. 332-337
Author(s):  
A. Van Rossem

Abstract A description is given of a light phenomenon, first observed by W. C. Smith, when carrying out tear tests on some loaded vulcanized rubbers in a dark room. This phenomenon has been studied more systematically by high-speed extension tests. It appears that this light effect has nothing to do with the choice of accelerators, but with the compounding ingredients of loaded vulcanized rubbers. In general, those compounding ingredients which belong to the filler class, such as whiting, talc, and ground barium sulfate, show this light phenomenon very distinctly, while vulcanized rubbers with reinforcing compounding ingredients, such as zinc oxide, titanium dioxide, and carbon black, do not show any light effect when quickly extended. In accordance with this, Kalite and Calcene, which behave as reinforcing compounding ingredients, do not show any light phenomenon. It seems probable, that, on elongating the vulcanized rubbers containing fillers, the adhesion of rubber-filler particle is broken, and electrical charges appear on an extremely large surface, which lead to innumerable discharges into surrounding vacuoles, causing the general light phenomenon observed.


Alloy Digest ◽  
1954 ◽  
Vol 3 (2) ◽  

Abstract BELMALLOY is a high grade pearlitic malleable iron providing rigidity and shock resistance to high torque loads. This datasheet provides information on composition, physical properties, hardness, elasticity, tensile properties, and shear strength as well as fracture toughness. It also includes information on heat treating, machining, and joining. Filing Code: CI-6. Producer or source: Belle City Malleable Iron Company.


Alloy Digest ◽  
1975 ◽  
Vol 24 (4) ◽  

Abstract NJZ ALLOY No. 1 is produced from high-grade, high-purity zinc with additions of lead, cadmium and iron. It gives excellent deep-drawing performance because of a combination of low hardness and strength, high ductility and very little tendency to work harden. It can be formed readily by conventional processes including spinning and its applications include such items as deep-drawn cans and jewelry. This datasheet provides information on composition, physical properties, hardness, and tensile properties as well as creep and fatigue. It also includes information on corrosion resistance as well as casting, forming, heat treating, and machining. Filing Code: Zn-18. Producer or source: New Jersey Zinc Company.


Author(s):  
Jayaraman Kumaravel ◽  
Kandhasamy Lalitha ◽  
Murugan Arunthirumeni ◽  
Muthugounder Subramanian Shivakumar

Author(s):  
Xue Bian ◽  
Yuntao Yu ◽  
Nana Hao ◽  
Wenyuan Wu

Abstract Titanium dioxide supports, which were prepared by roasting metatitanic acid under different conditions, were used to prepare a series of Ce–W–Ti catalysts. The structure and denitration properties of the catalyst were studied. The results showed that TiO2 had different crystal types (mixed crystal phases with different proportions of anatase and rutile) under different roasting conditions, and the denitration efficiency of mixed crystal was better than that of pure phase TiO2. Ce–W/200 °C-1 hTiO2 catalyst exhibited a prominent NO conversion rate, and it can reach higher than 90% at a temperature range from 250 to 500°C. The large specific surface area, low content of rutile TiO2 in the support, high content of chemical adsorbed oxygen and high surface acidity were favorable to denitration performance of Ce–W–Ti catalyst.


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