Enhancing the production of light olefins and aromatics from catalytic fast pyrolysis of cellulose in a dual-catalyst fixed bed reactor.

In this study, the effects of a macroporous catalyst (CaO), mesoporous catalyst (MCM-41), and microporous catalysts (ZSM-5 and SAPO-34) on the production of light olefins and aromatics from cellulose catalytic fast pyrolysis were investigated in a dual-catalyst fixed bed reactor. Further the fractional catalytic pyrolysis of MCM-41 or CaO with ZSM-5 or SAPO-34 was explored. The results showed that ZSM-5 was the most efficient catalyst for the formation of light olefins and aromatics followed by MCM-41, CaO and SAPO-34, and no aromatics were found with SAPO-34 only. Moreover, 15% CaO combined 85% ZSM-5 produced the highest yield of light olefins (5.59%) and aromatic (13.42%). The addition of CaO and MCM-41 promoted the selectivity of C2H4 and decreased the production of naphthalene.

Tumor growth affects the metabonomic phenotypes of multiple mouse non-involved organs in an A549 lung cancer xenograft model.

The effects of tumorigenesis and tumor growth on the non-involved organs remain poorly understood although many research efforts have already been made for understanding the metabolic phenotypes of various tumors. To better the situation, we systematically analyzed the metabolic phenotypes of multiple non-involved mouse organ tissues (heart, liver, spleen, lung and kidney) in an A549 lung cancer xenograft model at two different tumor-growth stages using the NMR-based metabonomics approaches. We found that tumor growth caused significant metabonomic changes in multiple non-involved organ tissues involving numerous metabolic pathways, including glycolysis, TCA cycle and metabolisms of amino acids, fatty acids, choline and nucleic acids. Amongst these, the common effects are enhanced glycolysis and nucleoside/nucleotide metabolisms. These findings provided essential biochemistry information about the effects of tumor growth on the non-involved organs.