The role of light wavelengths in regulating algal-bacterial granules formation, protein and lipid accumulation, and microbial functions.

High value-added products recovery from algal-bacterial granular sludge (ABGS) has received great attention recently. This study aimed to explore the role of different light wavelengths in regulating granule formation, protein and lipid production, and microbial functions. Bacterial granular sludge (BGS, R0) was most conducive to forming ABGS under blue (R2) light with the highest chlorophyll a (10.2 mg/g-VSS) and diameter (1800 µm), followed by red (R1) and white (R3) lights. R0-R3 acquired high protein contents (>164.8 mg/g-VSS) with essential amino acids above 44.4%, all of which were suitable for recycling, but R2 was the best. Also, blue light significantly increased total lipid production, while red light promoted the accumulation of some unsaturated fatty acids (C18:2 and C18:3). Some unique algae and dominant bacteria (e.g., Stigeoclonium, Chlamydomonas, and Flavobacteria) enrichment and some key functions (e.g., amino acid, fatty acid, and lipid biosynthesis) up-regulation in R2 might help to improve proteins and lipids quality. Combined, this study provides valuable guidance for protein and lipid recovery from ABGS.

Influence of dissolved organic matter on methylmercury transformation during aerobic composting of municipal sewage sludge under different C/N ratios.

Current knowledge about the transformation of total mercury and methylmercury (MeHg) in aerobic composting process is limited. In this study, the composition and transformation of mercury and dissovled organic matter (DOM) in aerobic composting process of municipal sewage sludge were were comprehensively characterized, and the differences among the three C/N ratio (20, 26 and 30) were investigated. The main form of mercury in C/N 20 and 26 was organo-chelated Hg (F3, 46%-60%); while the main form of mercury in C/N 30 was mercuric sulfide (F5, 64%-70%). The main component of DOM in C/N 20 and 26 were tyrosine-like substance (C1, 53%-76%) while the main fractions in C/N 30 were tyrosine-like substance (C1, 28%-37%) and fulvic-like substance (C2, 17%-39%). The mercury and DOM varied significantly during the 9 days composting process. Compared to C/N 20 and 26, C/N 30 produced the less MeHg after aerobic composting process, with values of 658% (C/N 20), 1400% (C/N 26) and 139% (C/N 30) of the initial, respectively. Meanwhile, C/N 30 produced the best compost showed greater degree of DOM molecular condensation and humification. Hg fraction had been altered by DOM, as indicated by a significant correlation between mercury species and DOM components. Notably, C/N 30 should be used as an appropriate C/N ratio to control the methylation processes of mercury and degration of DOM.

[Speciation and Ecological Risk Assessment of Heavy Metal(loid)s in the Municipal Sewage Sludge of China].

To reveal the speciation and pollution status of heavy metal(loid) s (HMs) in the dewatered sewage sludge(SS) of municipal wastewater treatment plants(MWTPs) in China, SS samples were collected from 40 MWTPs located in different regions of China. The total concentrations and geochemical fractions of As, Cd, Cr, Cu, Ni, Pb, and Zn in the SS samples were analyzed. The ecological risks induced by HMs in the SS were assessed based on the toxicity characteristic leaching procedure(TCLP), risk assessment code(RAC), and potential ecological risk index(RI). The median values of HMs in SS followed the order Zn > Cu > Cr > Pb > Ni > As > Cd. The general attainment rates of HMs in SS were satisfactory(>90%). As showed a generally even distribution among all the fractions; Cd and Zn mainly existed in the reducible fraction; Cr mainly occurred in the residual fraction, followed by oxidizable and reducible fractions; Cu mainly occurred in the oxidizable fraction; Ni occurred mainly as exchangeable forms; and Pb mainly occurred in the reducible and residual fractions, with its exchangeable form being the lowest fraction. According to the RAC method, the environmental risks induced by HMs in the SS followed the order Ni > As > Zn > Cd > Cu > Cr > Pb. The ecological risk of Ni was high; Zn, As, and Cd had a medium level of risk; Cr and Cu had a low level of risk; and the risk of Pb was negligible. According to the RI method, Cd and Cu showed the highest potential ecological risk, indicating that these are the primary HM pollutants in the SS. However, if the agricultural application of SS is carried out in accordance with the national standards, the overall level of risk from soil HM pollution is considered relatively low.

Heavy metal(loid)s in sewage sludge in China: concentrations and spatial-temporal variations.

Sewage sludge (SS) production in China has increased rapidly, accompanying the fast expansion of its sewage treatment capacity. Heavy metals (HMs) in SS have been a great concern, hampering the utilization and disposal of SS. In this study, heavy metal (HM) contents in SS from throughout China were determined. The median values of HMs in SS decreased in the order Zn > Cu > Cr > Pb > Ni > As > Hg > Cd. The general attainment rates of HMs in SS are satisfying (> 90%). Combining the present data with those obtained from references, spatial distributions and temporal trends of HMs in SS were analyzed. Depending on the specific HM element, the spatial variation trend might be decreasing trends from south to north and from east to west of China. The element-specific hot spots of SS with relatively high HM contents were identified. Analysis of the historical data in different time intervals reviewed obvious decreasing trends in HM contents of SS in China, indicating the well implementation of more and more stringent environmental regulations.

Leaching behavior and transformation of total mercury and methylmercury from raw and lime-conditioned sewage sludge under simulated rain.

Mercury (Hg) that leaches from municipal sewage sludge (MSS) landfill under natural rain is of increasing concern. The column leaching experiments were conducted to investigate the leaching characteristics of total mercury (THg) and methylmercury (MeHg) as well as pH, total organic carbon (TOC), and total suspended solids (TSS) in the raw sludge (RS) and lime-conditioned sludge (LCS) under simulated rain with different acidities (pH 6.5 and 2.9). Results showed the release of MeHg in the leachates presented different patterns from THg. And the final amounts of MeHg in the MSS columns were 1.49 (RS at pH = 6.5), 1.88 (RS at 2.9), 1.97 (LCS at pH = 6.5), and 2.06 times (LCS at pH = 2.9) higher than the initial amounts, suggesting methylation of inorganic Hg (IHg) occurred in the leaching process. The leaching efficiencies of THg and MeHg in RS was lower than that in LCS, indicating lime was more favorable for the release of THg and MeHg. And lower values of pH of the simulated rain promoted the release of THg and MeHg from RS while the opposite was true for LCS. This study provides a better understanding of the release and biogeochemical transformations of Hg in MSS.

Piezoelectric Performance of a Symmetrical Ring-Shaped Piezoelectric Energy Harvester Using PZT-5H under a Temperature Gradient.

With the rapid development of microelectronics technology, low-power electronic sensors have been widely applied in many fields, such as Internet of Things, aerospace, and so on. In this paper, a symmetrical ring-shaped piezoelectric energy harvester (SR-PEH) is designed to provide energy for the sensor to detect the ambient temperature. The finite element method is used by utilizing software COMSOL 5.4, and the electromechanical coupling model of the piezoelectric cantilever is established. The output performance equations are proposed; the microelectromechanical system (MEMS) integration process of the SR-PEH, circuit, and sensor is stated; and the changing trend of the output power density is explained from an energy perspective. In the logarithmic coordinate system, the results indicate that the output voltage and output power are approximately linear with the temperature when the resistance is constant. In addition, the growth rate of the output voltage and output power decreases with an increase of resistance under the condition of constant temperature. In addition, with an increase of temperature, the growth rate of the output power is faster than that of the output voltage. Furthermore, resistance has a more dramatic effect on the output voltage, whereas temperature has a more significant effect on the output power. More importantly, the comparison with the conventional cantilever-shaped piezoelectric energy harvester (CC-PEH) shows that the SR-PEH can improve the output performance and broaden the frequency band.

Structure, adsorption and magnetic properties of chiral metal-organic frameworks bearing linear trinuclear secondary building blocks.

The reactions of new chiral organic ligands trimesoyltri(L-alanine) (L-TMTAH(3)) or trimesoyltri(D-alanine) (D-TMTAH(3)) with transition metal salts in the presence of an ancillary ligand of 4,4'-bipyridine gave two pairs of three dimensional frameworks [Co(3)(L-TMTA)(2)(4,4'-bpy)(4)]·28H(2)O (1), [Co(3)(D-TMTA)(2)(4,4'-bpy)(4)]·28H(2)O (2) [Ni(3)(L-TMTA)(2)(4,4'-bpy)(4)]·2C(2)H(5)OH·14H(2)O (3) and [Ni(3)(D-TMTA)(2)(4,4'-bpy)(4)]·2C(2)H(5)OH·14H(2)O (4). These compounds were characterized by elemental analysis, IR, and X-ray powder diffraction analysis and the structures of 1-3 were determined from X-ray single crystal diffraction analysis. Complexes 1-4 feature linear trinuclear secondary building blocks [M(3)(COO)(4)](2+) formed via the connection of three metal ions by four carboxylato groups from four TMTA(3-) ligands. Every adjacent two linear trinuclear secondary building blocks are linked by one and three 4,4'-bipyridine molecules along the a and c axis, respectively, to form two-dimensional sheets, which are further connected by TMTA(3-) ligands to construct a porous three dimensional framework with one-dimensional channels. Compound 3 was taken as an example to investigate the adsorption properties of compounds 1-4. It revealed a saturated hydrogen uptake of 216.6 cm(3) g(-1) (2.0 wt%) at 11.1 atm measured at 77 K, a maximum CO(2) uptake of 119.4 cm(3) g(-1) (23.5 wt%) at 19.5 atm measured at 298 K and a saturated CH(4) uptake of 77.8 cm(3) g(-1) (5.6 wt%) at 27.1 atm measured at 298 K. The magnetic studies of complexes 1 and 3 indicate the presence of antiferromagnetic interactions between the metal ions in the two compounds.