scholarly journals Revaporization Behavior of Cesium and Iodine Compounds from Their Deposits in the Steam–Boron Atmosphere

ACS Omega ◽  
2021 ◽  
Author(s):  
Muhammad Rizaal ◽  
Shuhei Miwa ◽  
Eriko Suzuki ◽  
Junpei Imoto ◽  
Masahiko Osaka ◽  
...  
Keyword(s):  
Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1897
Author(s):  
Hideyasu China ◽  
Nami Kageyama ◽  
Hotaka Yatabe ◽  
Naoko Takenaga ◽  
Toshifumi Dohi

We report a convenient and practical method for the preparation of nonexplosive cyclic hypervalent iodine(III) oxidants as efficient organocatalysts and reagents for various reactions using Oxone® in aqueous solution under mild conditions at room temperature. The thus obtained 2-iodosobenzoic acids (IBAs) could be used as precursors of other cyclic organoiodine(III) derivatives by the solvolytic derivatization of the hydroxy group under mild conditions of 80 °C or lower temperature. These sequential procedures are highly reliable to selectively afford cyclic hypervalent iodine compounds in excellent yields without contamination by hazardous pentavalent iodine(III) compound.


2005 ◽  
Vol 2 (4) ◽  
pp. 282 ◽  
Author(s):  
Carl J. Palmer ◽  
Thorsten L. Anders ◽  
Lucy J. Carpenter ◽  
Frithjof C. Küpper ◽  
Gordon B. McFiggans

Environmental Context.Various organic iodine compounds (including CH3I, CH2ClI, CH2BrI, CH2I2) are present throughout the marine boundary layer as a result of their production from seaweeds, phytoplankton, and photolysis reactions occurring in seawater. In air, these compounds rapidly photolyse to give atomic I which subsequently reacts with ozone to form iodine oxide, potentially leading to perturbations of the tropospheric oxidative capacity and nucleation of atmospheric particles. Recent research has identified molecular iodine as an additional source of iodine atoms to coastal areas. Here we study the relative roles and controls of gaseous organic and molecular iodine release from the seaweed Laminaria digitata. Abstract.Changes in the halocarbon, I2 and particle production of the brown algal kelp Laminaria digitata as a response to different chemical stresses have been investigated. Oxidative stress (caused by either exogenous hydrogen peroxide, gaseous ozone or a solution of oligoguluronates, known elicitors of oxidative stress) caused increased halocarbon and I2 production by the seaweed. The maximum I2 release was observed under exposure to O3 (at several hundred parts per billion by volume (ppbv)), whereas oligoguluronates elicited the highest release of iodine-containing halocarbons including CH2I2. Significantly greater production of I2, compared to CH2I2, was observed at atmospheric levels of ozone. Particle production was observed only when the Laminaria samples were exposed to ozone (up to 16 000 cm−3 s−1 per gram fresh weight (FW) of seaweed with a ~2 min residence time and with a total I atom flux of 1.6 × 108 cm−3 s−1 g−1 FW from photolysis of I2); passing O3-free air over the unstressed seaweed followed by secondary mixing with ozone did not result in any measurable particle formation. Our limited data indicate that ozone elicits abiotic production of I2 from Laminaria and that there is a direct relationship between the amount of I2 released and the number of particles formed. The results support the recent hypothesis that molecular iodine rather than volatile organic iodine (e.g. CH2I2) release from exposed seaweeds is the major source of coastal new particle production.


1959 ◽  
Vol 46 (20) ◽  
pp. 584-584 ◽  
Author(s):  
Z. Böszörményi ◽  
Edith Cseh ◽  
L. Gáspár

It has been found that the hexaearbonyls of group VI metals in the presence of some organic halogen compounds are active initiators of vinyl polymerization. Molybdenum hexacarbonyl is the most active, and halogen compounds containing —CC1 3 , —CBr 3 are generally more effective than those with fewer halogen atoms joined to a single carbon. Fluorine and iodine compounds are inactive. A study has been made of the initiation of the polymerization of methyl methacrylate by the Cr(CO) 6 + CCl 4 system. The polymerization is markedly retarded by carbon monoxide. It is shown that the reaction proceeds through free-radical intermediates, and a kinetic mechanism for initiation is derived (equation (4)) leading to the expression (5) for the rate of chain starting. This quantity may be calculated from (5) with the aid of the numerical values in table 3. Kinetic observations are in satisfactory agreement with this mechanism. The nature of the participating reactions is discussed.


1983 ◽  
Vol 21 (3) ◽  
pp. 289-293 ◽  
Author(s):  
A. Habersbergerová ◽  
B. Bartoníček

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