Cyclized Rubber, Particularly Halide Transformations

1939 ◽  
Vol 12 (3) ◽  
pp. 556-567 ◽  
Author(s):  
H. P. Stevens ◽  
C. J. Miller

Abstract Boron trifluoride or materials which give rise thereto effect a “cyclization” of rubber in solution: that is, the product is less unsaturated than the original rubber. A particular degree of conversion has been shown to give a tough material, which produces strongly adherent films possessing a high degree of alkali-resistance. When used as a paint medium the material acts as an unsaponifiable “breather” and pigment protector, allowing (unlike “sealers”) the passage of aqueous solutions. For this reason it appears suitable for use on plaster and concrete. Analysis of the purified product indicates appreciable oxidation at some stage and it may be further oxidized by aging at raised temperature or by reagents such as hydrogen peroxide. The oxidation products are not identical. The conversion product yields also a hard vulcanized product resembling hard vulcanized rubber, but less thermoplastic and containing less sulfur than hard rubber produced under the same conditions. This work has been carried out on behalf of the Rubber Producers' Research Association, to whom the authors are indebted for permission to publish.

1956 ◽  
Vol 29 (1) ◽  
pp. 121-125 ◽  
Author(s):  
A. P. Sheinker ◽  
S. S. Medvedev

Abstract It has been established earlier that polymerization in aqueous solutions of emulsifiers takes place in the water or in the micellae of the emulsifier, depending on the solubility of the monomer and the initiator. The question of the topochemical properties of polymerization in emulsions has not yet been definitively explained. In a number of studies, the hypothesis was advanced that the process of emulsion polymerization takes place in the micellae of the emulsifier, according to the degree of conversion of the micellae into polymer-monomer particles, with the monomer dissolved in the polymer. In order to explain further the mechanism of emulsion polymerization, the kinetics of polymerization of isoprene in water, in solutions of emulsifier and N-cetylpyridinium bromide, and in emulsions in the presence of a water-soluble initiator (hydrogen peroxide) were studied. The dilatometric method was chosen for the kinetic measurements of solutions of emulsifier not saturated with isoprene, and for emulsions. Experiments with solutions of emulsifier saturated with monomer were made during continuous saturation of the emulsifierinitiator solution with isoprene in the gaseous phase. All the experiments were made at 50° C in the absence of oxygen.


1970 ◽  
Vol 48 (18) ◽  
pp. 2948-2948
Author(s):  
C. E. Burchill ◽  
I. S. Ginns

not available


1979 ◽  
Vol 18 (7) ◽  
pp. 1971-1973 ◽  
Author(s):  
Mark M. Morrison ◽  
Julian L Roberts ◽  
Donald T. Sawyer

1955 ◽  
Vol 3 (4) ◽  
pp. 379 ◽  
Author(s):  
W. V. Mayneord ◽  
W. Anderson ◽  
H. D. Evans ◽  
D. Rosen

2010 ◽  
Vol 184 (1-3) ◽  
pp. 308-312 ◽  
Author(s):  
Dongkyu Choi ◽  
O-Mi Lee ◽  
Seungho Yu ◽  
Seung-Woo Jeong

1992 ◽  
Author(s):  
Αναστασία Κοτρωναρου

The ultrasonic irradiation of para-nitrophenol, S(-II), and parathion is studied in aqueous solutions at 20 kHz and ~ 75 W-cnT2. Para-nitrophenol was degraded primarily by denitration and secondarily by ΌΗ radical attack to yield N 02, NO3, benzoquinone, hydroquinone, 4-nitrocatechol, formate and oxalate. These reaction products and the kinetic observations are consistent with a model involving high-temperature reactions of p-nitrophenol in the interfa.cia.1 region of cavitation bubbles. The average effective temperature of the interfacial region surrounding the cavitation bubbles was estimated to be T ~ 800 K. Ultrasonic irradiation of S(-II) is studied in aqueous solutions over the pH range 7 - 12. The reaction of HS“ with OH is the principal pathway for theoxidation of S(-II) at pH > 10; the oxidation products are SO2“, SO2", and S20 Upon prolonged sonication, SO2" is the only observed product. At pH < 8.5, thermal decomposition of H2S within or near collapsing cavitation bubbles becomes the important pathway and elemental sulfur is found as an additional product of the sonolysis of S(-II). The sonolytic oxidation of H2S at pH > 10 was successfully modeled with an aqueous-phase free-radical chemistry mechanism and assumingcontinuous and uniform ΌΗ input into solution from the imploding cavitation bubbles. Parathion degradation occurred primarily by enhanced hydrolysis and secondarily by direct ΌΗ radical attack.The effect of various physical and chemical parameters on sonolytic yields is examined. The observed effects are in qualitative agreement with the sonolysis mechanisms proposed for the chemicals of interest and the existing hydrodynamic theories of acoustic cavitation. The formation of iodine upon ultrasonic irradiation of potassium iodide solutions and the sonolysis of S(-II) are used as probes to compare the sonochemical efficiency of different experimental set-ups. This work elucidates the mechanisms of the ultrasonic decomposition of typical organic and inorganic pollutants. It is shown that ultrasound has the potential to become a viable alternative for the destruction of chemical contaminants in water and wastewater. The current limitation of sonolysis is its low energy utilization efficiency, but there is room for improvement by optimizing reactor design and physical/chemical operation conditions. This work offers some recommendations and insight in that respect.


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