A review of the enhancement of bio-hydrogen generation by chemicals addition

Bio-hydrogen production (BHP) produced from renewable bio-resources is an attractive route for green energy production, due to its compelling advantages of relative high efficiency, cost-effectiveness, and lower ecological impact. This study reviewed different BHP pathways, and the most important enzymes involved in these pathways, to identify technological gaps and effective approaches for process intensification in industrial applications. Among the various approaches reviewed in this study, a particular focus was set on the latest methods of chemicals/metal addition for improving hydrogen generation during dark fermentation (DF) processes; the up-to-date findings of different chemicals/metal addition methods have been quantitatively evaluated and thoroughly compared in this paper. A new efficiency evaluation criterion is also proposed, allowing different BHP processes to be compared with greater simplicity and validity

「医療的ケア」基本研修修了者の就職後の動向に関する調査 : アンケートから見えてくるもの

Two lab-scale wetland systems were studied for the removal of dissolved Cu, Mn, Fe, Pb and Zn. Vegetated with Typha domingensis, each system consisted of two units, a vertical and a horizontal flow wetland column, which were filled with either crushed sea shell grits or composted green waste as main media. A synthetic acidic wastewater was prepared by dissolving H2SO4, Pb(CH3COO)2, MnCl2, FeSO4, CuSO4 and ZnSO4 in a distilled water. As it passed through each column, metal concentrations, pH and conductivity were monitored. The pH value of the wastewater increased in the shell grit columns, where dissolved metals were almost completely (>99%) removed. In the wetland columns filled with the green waste, the average percentage removals were 90, 77, 27, 98 and 75% for Cu, Mn, Fe, Pb and Zn, respectively. Scanning electron microscopy and energy-dispersive spectroscopy (SEM-EDS) analysis showed that the surface characteristics of the shell grits remained largely unchanged before and after being used in the columns; but the mass compositions of carbon increased, whereas calcium and oxygen decreased. Infrared spectroscopy (IR) and X-ray diffraction (XRD) were used to further analyse the chemical compositions and functional groups of the surfaces of the shell grits

Binding mechanism of arsenate on rutile (110) and (001) planes studied using grazing-incidence EXAFS measurement and DFT calculation

Characterization of contaminant molecules on different exposed crystal planes is required to conclusively describe its behavior on mineral surfaces. Here, the structural properties and relative stability of arsenate adsorbed on rutile TiO2 (110) and (001) surfaces were investigated using grazing-incidence extended X-ray absorption fine structure (GI-EXAFS) spectra and periodic density functional theory (DFT) calculation. The combined results indicated that arsenate mainly formed inner-sphere bidentate binuclear (BB) and monodentate mononuclear (MM) complexes on both surfaces, but the orientational polar angles of arsenate on the (110) surface were commonly smaller than that on the (001) surface for the two adsorption modes. The DFT calculation showed that the (110) plane had a higher affinity toward arsenate than the (001) plane, suggesting that, for a given adsorption mode (i.e., MM or BB structure), a small polar angle was more favorable for arsenate stabilized on the rutile surfaces

Structure and stability of arsenate adsorbed on α-Al2O3 single-crystal surfaces investigated using grazing-incidence EXAFS measurement and DFT calculation

Direct characterization of contaminants on single-crystal planes is required because the specific adsorption characteristics on different exposed crystal planes constitute their actual behavior at water–mineral interfaces in aquifers. Here, the structure and stability of arsenate on α-Al2O3 (0001) and (View the MathML source112¯0) surfaces were characterized by using a combination of grazing-incidence extended X-ray absorption fine structure (GI-EXAFS) spectra and periodic density functional theory (DFT) calculation. The combined results indicated that arsenate was mainly adsorbed as inner-sphere monodentate and bidentate complexes on both surfaces, but the orientational polar angles on the (0001) surface were commonly 10–20° greater than that on the (View the MathML source112¯0) surface. The DFT calculation showed that the large polar angle was more favorable for arsenate stabilized on the alumina surfaces. Based on the spectroscopic and computational data, the dominant bonding modes of arsenate on the two crystal planes of α-Al2O3 were identified as bidentate binuclear structures, and the (0001) surface displayed a stronger affinity toward arsenate

Molecular dynamics simulations of structural transformation of perfluorooctane sulfonate (PFOS) at water/rutile interfaces

Concentration and salinity conditions are the dominant environmental factors affecting the behavior of perfluorinated compounds (PFCs) on the surfaces of a variety of solid matrices (suspended particles, sediments, and natural minerals). However, the mechanism has not yet been examined at molecular scales. Here, the structural transformation of perfluorooctane sulfonate (PFOS) at water/rutile interfaces induced by changes of the concentration level of PFOS and salt condition was investigated using molecular dynamics (MD) simulations. At low and intermediate concentrations all PFOS molecules directly interacted with the rutile (110) surface mainly by the sulfonate headgroups through electrostatic attraction, yielding a typical monolayer structure. As the concentration of PFOS increased, the molecules aggregated in a complex multi-layered structure, where an irregular assembling configuration was adsorbed on the monolayer structure by the van der Waals interactions between the perfluoroalkyl chains. When adding CaCl2 to the system, the multi-layered structure changed to a monolayer again, indicating that the addition of CaCl2 enhanced the critical concentration value to yield PFOS multilayer assemblies. The divalent Ca2+ substituted for monovalent K+ as the bridging counterion in PFOS adsorption. MD simulation may trigger wide applications in study of perfluorinated compounds (PFCs) from atomic/molecular scale

A Novel Small Molecule Inhibitor of Hepatitis C Virus Entry

Small molecule inhibitors of hepatitis C virus (HCV) are being developed to complement or replace treatments with pegylated interferons and ribavirin, which have poor response rates and significant side effects. Resistance to these inhibitors emerges rapidly in the clinic, suggesting that successful therapy will involve combination therapy with multiple inhibitors of different targets. The entry process of HCV into hepatocytes represents another series of potential targets for therapeutic intervention, involving viral structural proteins that have not been extensively explored due to experimental limitations. To discover HCV entry inhibitors, we utilized HCV pseudoparticles (HCVpp) incorporating E1-E2 envelope proteins from a genotype 1b clinical isolate. Screening of a small molecule library identified a potent HCV-specific triazine inhibitor, EI-1. A series of HCVpp with E1-E2 sequences from various HCV isolates was used to show activity against all genotype 1a and 1b HCVpp tested, with median EC50 values of 0.134 and 0.027 µM, respectively. Time-of-addition experiments demonstrated a block in HCVpp entry, downstream of initial attachment to the cell surface, and prior to or concomitant with bafilomycin inhibition of endosomal acidification. EI-1 was equally active against cell-culture adapted HCV (HCVcc), blocking both cell-free entry and cell-to-cell transmission of virus. HCVcc with high-level resistance to EI-1 was selected by sequential passage in the presence of inhibitor, and resistance was shown to be conferred by changes to residue 719 in the carboxy-terminal transmembrane anchor region of E2, implicating this envelope protein in EI-1 susceptibility. Combinations of EI-1 with interferon, or inhibitors of NS3 or NS5A, resulted in additive to synergistic activity. These results suggest that inhibitors of HCV entry could be added to replication inhibitors and interferons already in development

Role of Carbonaceous Aerosols in Catalyzing Sulfate Formation

The persistent and fast formation of sulfate is a primary factor driving the explosive growth of fine particles and exacerbating China’s severe haze development. However, the underlying mechanism for the persistent production of sulfate remains highly uncertain. Here, we demonstrate that soot is not only a major component of the particulate matter but also a natural carbocatalyst to activate molecular O₂ and catalyze the oxidation of SO₂ to sulfate under ambient conditions. Moreover, high relative humidity, typically occurring in severe haze events, can greatly accelerate the catalytic cycle by reducing the reaction barriers, leading to faster sulfate production. The formation pathway of sulfate catalyzed by carbonaceous soot aerosols uses the ubiquitous O₂ as the ultimate oxidant and can proceed at night when photochemistry is reduced. The high relative humidity during haze episodes can further promote the soot-catalyzed sulfate-producing process. Therefore, this study reveals a missing and widespread source for the persistent sulfate haze formation in the open atmosphere, particularly under highly polluted conditions characterized by high concentrations of both SO₂ and particulate carbon, and is helpful to the development of more efficient policies to mitigate and control haze pollution