Inhibition of steam gasification of char by volatiles in a fluidized bed under continuous feeding of a brown coal

Steam gasification of a Victorian brown coal was performed in an atmospheric bubbling fluidized-bed reactor with continuous feeding of the coal. The gasification converted no more than 28, 51 and 71% of the nascent char (on a carbon basis) at 1120, 1173 and 1223 K, respectively. The char recovered from the fluidized bed was, nonetheless, gasified toward complete conversion when exposed to steam in another reactor, in which volatiles from the pyrolysis were absent while interaction between the char and products from the gasification was minimized. Atmosphere created in the fluidized bed thus prevented the char gasification from taking place beyond upper-limit conversion. In the absence of volatiles, nascent char underwent gasification catalyzed by inherent metallic species and non-catalytic gasification in parallel. The non-catalytic gasification was greatly decelerated by the presence of H₂ in the gas phase due to its dissociative chemisorption onto free carbon sites forming H-laden carbon. H₂ was, however, not a so strong inhibitor as to terminate the gasification. It was rather suggested that much more H-laden carbon was formed through dissociative chemisorption of volatiles and/or chemisorption of hydrogen radical from thermal cracking of volatiles in the gas-phase, which resulted in prevention of the non-catalytic gasification. It seemed that the char was converted in the fluidized-bed mainly by the catalytic gasification, while the conversion was limited due to deactivation of metallic species within the char matrix and their release from the char.     

Selective expression of the scaffold protein JSAP1 in spermatogonia and spermatocytes

Scaffold proteins of mitogen-activated protein kinase (MAPK) intracellular signal transduction pathways mediate the efficient and specific activation of the relevant MAPK signaling modules. Previously, our group and others have identified c-Jun NH2-terminal kinase (JNK)/stress-activated protein kinase-associated protein 1 (JSAP1, also known as JNK-interacting protein 3) as a scaffold protein for JNK MAPK pathways. Although JSAP1 is expressed in the testis in adults, its expression during development has not been investigated. In addition, it is unknown which types of cells in the testis express the scaffold protein. Here, we examined the expression of JSAP1 in the testis of mice aged 14 days, 20 days, 6 weeks, and 12 weeks by immunohistochemistry and Western blotting. The specificity of the anti-JSAP1 antibody was evaluated from its reactivity to exogenously expressed JSAP1 and a structurally related protein, and by antigen-absorption experiments. The immunohistochemical analyses with the specific antibody showed that the JSAP1 protein was selectively expressed in the spermatogonia and spermatocytes, but not in other cell types, including spermatids and somatic cells, during development. However, not all spermatogonia and spermatocytes were immunopositive either, especially in the 12-week-old mouse testis. Furthermore, we found by Western blotting that the expression levels of JSAP1 protein vary during development; there is high expression until 6 weeks after birth, which approximately corresponds to the end of the first wave of spermatogenesis. Collectively, these results suggest that JSAP1 function may be important in spermatogenic cells during early postnatal development.