A quantitative study of carbon monoxide and carbon dioxide evolution during thermal degradation of flame retarded epoxy resins

2007 ◽  
Vol 92 (5) ◽  
pp. 765-776 ◽  
Author(s):  
Bhaskar Biswas ◽  
Baljinder K. Kandola ◽  
A. Richard Horrocks ◽  
Dennis Price
2011 ◽  
Vol 67 (5) ◽  
pp. 859-873 ◽  
Author(s):  
Xin Wang ◽  
Yuan Hu ◽  
Lei Song ◽  
Weiyi Xing ◽  
Hongdian Lu

1978 ◽  
Vol 56 (15) ◽  
pp. 1965-1969 ◽  
Author(s):  
William R. Cullen ◽  
Brian R. James ◽  
Giorgio Stukul

The reactions of the title complexes Rh4Cl4(CO)4(O2)2P2 (where P is a tertiary phosphine type ligand, in particular diphenylisobutylphosphinite) with both dihydrogen and carbon monoxide were studied in solution in the absence and presence of excess P. The reaction stoichiometries, particularly a measured carbon dioxide evolution, confirm the formulation of the reactant tetranuclear complexes. The complexes are effective for catalytic hydrogenation and hydroformylation of olefinic substrates, and the nature of the active catalysts is considered.


2018 ◽  
Vol 216 ◽  
pp. 03001 ◽  
Author(s):  
Evgeny Ivanayskiy ◽  
Aleksei Ishkov ◽  
Aleksandr Ivanayskiy ◽  
Iakov Ochakovskii

The paper studies the influence of shielding gas on the composition and the structure of weld joint metal of 30MnB5 steel applied in essential parts of automobiles and tractors. The welding was performed in inert, oxidizing and reducing atmospheres. It was established that TIG welding with argon used as shielding gas did not provide the required mechanical properties when using conventional welding materials. Carbon dioxide during MAG welding caused partial burning of alloying elements. Carbon monoxide used as shielding gas was proved to form reducing atmosphere enabling to obtain chemical composition close to the base metal composition. Metallographic examinations were carried out. The obtained results provided full-strength weld, as well as the required reliability and durability of welded components and joints.


Author(s):  
Douglas P Harrison ◽  
Zhiyong Peng

Hydrogen is an increasingly important chemical raw material and a probable future primary energy carrier. In many current and anticipated applications the carbon monoxide impurity level must be reduced to low-ppmv levels to avoid poisoning catalysts in downstream processes. Methanation is currently used to remove carbon monoxide in petroleum refining operations while preferential oxidation (PROX) is being developed for carbon monoxide control in fuel cells. Both approaches add an additional step to the multi-step hydrogen production process, and both inevitably result in hydrogen loss. The sorption enhanced process for hydrogen production, in which steam-methane reforming, water-gas shift, and carbon dioxide removal reactions occur simultaneously in the presence of a nickel-based reforming catalyst and a calcium-based carbon dioxide sorbent, is capable of producing high purity hydrogen containing minimal carbon monoxide in a single processing step. The process also has the potential for producing pure CO2 that is suitable for subsequent use or sequestration during the sorbent regeneration step. The current research on sorption-enhanced production of low-carbon monoxide hydrogen is an extension of previous research in this laboratory that proved the feasibility of producing 95+% hydrogen (dry basis), but without concern for the carbon monoxide concentration. This paper describes sorption-enhanced reaction conditions – temperature, feed gas composition, and volumetric feed rate – required to produce 95+% hydrogen containing low carbon monoxide concentrations suitable for direct use in, for example, a proton exchange membrane fuel cell.


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