7,582 research outputs found

    THE EFFECT OF GAS TEMPERATURE AND VELOCITY ON COAL DRYING IN FLUIDIZED BED DRYER

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    The objective of this research work is to develop fluidized bed coal dryer to overcome the disadvantages of low rank coal with high moisture such as low calorific values, costly transportation, high emissions of pollutants, and operational problem. In this paper, laboratory scale bubbling fluidized bed was used to dry high moisture, low-rank Indonesian coal to produce low moisture, high-rank coal. The effects of temperature, gas velocity and bed height to diameter ratio (L/D) on drying rate were studied to obtain information relating to optimum operating conditions. Coal characterizations (proximate analysis, ultimate analysis, Thermogravimetric Analysis (TGA), BET, Higher Heating Value (HHV), Lower Heating Value (LHV)) were performed to identify the effect of the change of moisture content. This investigation aims to study the drying process under moderated heating conditions. As a result of the experiments the conclusion is that the thermal fluidized bed process can be successfully applied to reducing moisture in Indonesian coal. Results also indicate that about 80~90% of total moisture could be reduced, including some of the inherent moisture, yielding high heating value product. The drying rate of coal in a fluidized bed is increased by increasing the temperature and velocity of the drying gas. However gas temperature had limitations causing from the spontaneous combustion and gas velocity has to be decided considering energy efficiency

    Improvement of retinoids production in recombinant E. coli using glyoxylic acid

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    Isoprenoids are the most chemically diverse compounds found in nature. They are present in all organisms and have essential roles in membrane structure, redox chemistry, reproductive cycles, growth regulation, signal transduction and defense mechanisms. In spite of their diversity of functions and structures, all isoprenoids are derived from the common building blocks of isopentenyl diphosphate (IPP) and its isomer dimethylallyl diphosphate (DMAPP). Optimization of IPP synthesis pathway is of benefit to mass production of various isoprenoids. There are two pathways of 2-C-Methyl-D-erythritol-4-phosphate (MEP) and mevalonate (MVA) for IPP synthesis. Prokaryotes including E. coli generally use MEP pathway whereas MVA pathway is used in eukaryotes. To improve isoprenoid production, it was performed the deletion of genes in E. coli, which are involved in both formation of fermentation by-products such as organic acids and alcohols, and consumption of precursors of MEP and MVA pathways, pyruvate and acetyl-CoA. As a result, we were able to develop a strain with improved fermentation productivity and carbon source utilization efficiency, the mutant strain was called AceCo. Higher lycopene production was achieved in the AceCo strain compared to the wild type MG1655 strain due to no formation of the inhibitory by-products. However, retinoids production of AceCo strain decreased to a half of that of MG1655 strain. Please click Additional Files below to see the full abstract

    A lab-on-a-disc platform enables serial monitoring of individual CTCs associated with tumor progression during EGFR-targeted therapy for patients with NSCLC

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    Rationale: Unlike traditional biopsy, liquid biopsy, which is a largely non-invasive diagnostic and monitoring tool, can be performed more frequently to better track tumors and mutations over time and to validate the efficiency of a cancer treatment. Circulating tumor cells (CTCs) are considered promising liquid biopsy biomarkers; however, their use in clinical settings is limited by high costs and a low throughput of standard platforms for CTC enumeration and analysis. In this study, we used a label-free, high-throughput method for CTC isolation directly from whole blood of patients using a standalone, clinical setting-friendly platform. Methods: A CTC-based liquid biopsy approach was used to examine the efficacy of therapy and emergent drug resistance via longitudinal monitoring of CTC counts, DNA mutations, and single-cell-level gene expression in a prospective cohort of 40 patients with epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer. Results: The change ratio of the CTC counts was associated with tumor response, detected by CT scan, while the baseline CTC counts did not show association with progression-free survival or overall survival. We achieved a 100% concordance rate for the detection of EGFR mutation, including emergence of T790M, between tumor tissue and CTCs. More importantly, our data revealed the importance of the analysis of the epithelial/mesenchymal signature of individual pretreatment CTCs to predict drug responsiveness in patients. Conclusion: The fluid-assisted separation technology disc platform enables serial monitoring of CTC counts, DNA mutations, as well as unbiased molecular characterization of individual CTCs associated with tumor progression during targeted therapy
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