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A novel sintered metal fiber microfiltration of bio-ethanol fermentation broth
Qian Kang,Jan Baeyens,Tianwei Tan,Raf Dewil 한국화학공학회 2015 Korean Journal of Chemical Engineering Vol.32 No.8
In bio-ethanol fermentation, the broth consists of mainly water and ethanol, together with particulate residues of unreacted feedstock and additives (mostly yeast). Prior to further processing (distillation), and to avoid fouling of heat exchangers and distillation columns, the solids residues of the broth need to be removed to as low a concentration as possible. The current mechanical separation (belt filter or centrifuge) can only remove +10 μm particles representing about 90% of the total solids content. The remaining 10% is usually recovered in the bottom stream of the first distillation column, and forms the stillage that is further treated. To avoid fouling and even eliminate the first distillation column where the ethanol fraction is only increased from 12% (feed) to 16% (top), a better particulate removal is required. Novel sintered metal fiber (SFM) fleeces are highly efficient for microfiltration, and the removal of suspended solids largely exceeds 99%. The paper (i) positions microfiltration in the overall bio ethanol process; (ii) describes the novel sintered metal fiber microfiltration application; (iii) experimentally determines the major operating characteristics of SFM and (iv) predicts the up-scaled operation by using a simplified filtration model. At an ambient feed temperature, the flux of permeate exceeds 5m3/m2h for a TMP of 1.5 bar and a yeast concentration of 15 g/l, as commonly encountered in the fermenter broth.
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Ke Tao,Ming Li,Xuefeng Gu,Ming Wang,Tianwei Qian,Lijun Hu,Jiang Li 대한약리학회 2022 The Korean Journal of Physiology & Pharmacology Vol.26 No.5
Abdominal aortic aneurysm (AAA) is a life-threatening disorder worldwide. Fibroblast growth factor 21 (FGF21) was shown to display a high level in the plasma of patients with AAA; however, its detailed functions underlying AAA pathogenesis are unclear. An in vitro AAA model was established in human aortic vascular smooth muscle cells (HASMCs) by angiotensin II (Ang-II) stimulation. Cell counting kit-8, wound healing, and Transwell assays were utilized for measuring cell proliferation and migration. RT-qPCR was used for detecting mRNA expression of FGF21 and activating transcription factor 4 (ATF4). Western blotting was utilized for assessing protein levels of FGF21, ATF4, and markers for the contractile phenotype of HASMCs. ChIP and luciferase reporter assays were implemented for identifying the binding relation between AFT4 and FGF21 promoters. FGF21 and ATF4 were both upregulated in Ang-II-treated HASMCs. Knocking down FGF21 attenuated Ang-IIinduced proliferation, migration, and phenotype switch of HASMCs. ATF4 activated FGF21 transcription by binding to its promoter. FGF21 overexpression reversed AFT4 silencing-mediated inhibition of cell proliferation, migration, and phenotype switch. ATF4 transcriptionally upregulates FGF21 to promote the proliferation, migration, and phenotype switch of Ang-II-treated HASMCs.
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