The effects of four conditioning approaches Acid, Acid-zero-valent iron (ZVI)/peroxydisulfate (PMS), Fe(II)/PMS and ZVI/PMS, on wastewater activated sludge (WAS) dewatering and organics distribution in supernatant and extracellular polymeric substances (EPS) layers were investigated. The highest reduction in bound water and the most WAS destruction was achieved by Acid-ZVI/PMS, and the optimum conditions were pH 3, ZVI dosage 0.15 g/g dry solid (DS), oxone dosage 0.07 g/g DS and reaction time 10.6 min with the reductions in capillary suction time (CST) and water content (Wc) as 19.67% and 8.49%, respectively. Four conditioning approaches could result in TOC increase in EPS layers and supernatant, and protein (PN) content in tightly bound EPS (TB-EPS). After conditioning, organics in EPS layers could migrate to supernatant. Polysaccharide (PS) was easier to migrate to supernatant than PN. In addition, Acid, Acid-ZVI/PMS or Fe(II)/PMS conditioning promoted the release of some polysaccharides containing ring vibrations v PO, v C-O-C, v C-O-P functional groups from TB-EPS. ESR spectra proved that both radicals of SO4-· and ·OH contributed to dewatering and organics transformation and migration. CST value of WAS positively correlated with the ratios of PN/PS in LB-EPS and total EPS, while it negatively correlated with TOC, PN content and PS content in TB-EPS, as well as PS content in supernatant and LB-EPS. BWC negatively correlated to zeta potential and TOC value, PN content, and HA content in supernatant. V.Ion-exchange polymer and modified carbonization bacterial cellulose (CBC) electrodes were fabricated using varying amounts of cation-exchange polymers (glutaric acid (GA) and sulfosuccinic acid (SSA)) and assembled within an asymmetric capacitive deionization unit (p-CDI).  https://www.selleckchem.com/  The performance of selective NO2- electro-adsorption was studied. The AC/CBC-SSA group showed a better salt adsorption capacity (14.56 mg/g) and nitrite removal efficiency (71.01%) than the AC/CBC-GA (10.72 mg/g, 47.83%) and AC/AC (4.81 mg/g, 12.74%) groups. It was confirmed that the CBC-SSA/GA electrodes enhanced nitrite selectivity and increased the adsorption capacity, and the total amounts of adsorbed anions increased when the applied voltage was increased from 0.8 to 1.2 V, while the molar fraction of nitrate decreased. The competitive and preferential adsorption of anions was further investigated using different binary solutions of anions and occurred in the following sequence NO2- >SO42- >NO3- >F-≈ Cl-. Furthermore, the p-CDI units were applied to remove nitrite in real wastewater samples, and the results showed that they had excellent reusability and application for use in dyeing wastewater treatment. V.Landfill biogas is a potential alternative for fossil fuel, but the containing impurities, volatile methyl siloxanes (simplified as siloxanes), often cause serious problems in gas turbines when applied to generate electricity. In this research, a collecting and analyzing method based on solvent adsorption and purge and trap-gas chromatography-mass spectrometry was established to determine the siloxanes in biogas from a landfill in Jinan, China, and adjacent ambient samples, such as soil, air, and leachate of the landfill. The results showed that, octamethylcyclotetrasiloxane (D4) and decamethylcyclopentasiloxane (D5) accounted for 63% of total siloxanes; and without considering D4 and D5, the order of detected siloxanes in concentration was found relating to Gibbs free energies of molecules, namely that higher abundant siloxane (except for D4 and D5) usually had lower Gibbs free energy. Additionally, the mass ratio between D4 and octamethyltrisiloxane (L3) in the biogas varied with different garbage age in landfills, possibly revealing the breaking-down of larger siloxane molecules with time. The samples, which were collected from environmental samples adjacent to the landfill, such as soil, water, and air, presented much higher siloxane level than urban or rural area away from landfills. The current H2S scrubber of the landfill biogas could decrease the total siloxanes from 10.7 to 5.75 mg/m3 due to Fe2O3 and a refrigerant drier in a purification system and cyclic siloxanes were more easily removed than linear ones. V.In the study, the catalyst precursors of Ce-modified γ-MnO2 were washed with deionized water until the pH value of the supernatant was 1, 2, 4 and 7, and the obtained catalysts were named accordingly. Under space velocity of 300,000 hr-1, the ozone conversion over the pH = 7 catalyst under dry conditions and relative humidity of 65% over a period of 6 hr was 100% and 96%, respectively. However, the ozone decomposition activity of the pH = 2 and 4 catalysts distinctly decreased under relative humidity of 65% compared to that under dry conditions. Detailed physical and chemical characterization demonstrated that the residual sulfate ions on the pH = 2 and 4 catalysts decreased their hydrophobicity and then restrained humid ozone decomposition activity. The pH = 2 and 4 catalysts had inferior resistance to high space velocity under dry conditions, because the residual sulfate ion on their surface reduced their adsorption capacity for ozone molecules and increased their apparent activation energies, which was proved by temperature programmed desorption of O2 and kinetic experiments. Long-term activity testing, X-ray photoelectron spectroscopy and density functional theory calculations revealed that there were two kinds of oxygen vacancies on the manganese dioxide catalysts, one of which more easily adsorbed oxygen species and then became deactivated. This study revealed the detrimental effect of surface acid ions on the activity of catalysts under humid and dry atmospheres, and provided guidance for the development of highly efficient catalysts for ozone decomposition. V.Much attention has been paid to the pollutant dimethylarsenic acid (DMA), because of its high toxicity even at very low doses. Although TiO2 photocatalytic oxidation (PCO) is one of the few effective methods for treating DMA-containing water, the efficient decomposition of DMA and simultaneous removal of toxic arsenic species remains a significant but challenging task. Here, defective mesoporous TiO2 with mixed-phase structure was synthesized and used as both photocatalyst and adsorbent for DMA removal. Due to the reduced band-gap and enhanced separation of photogenerated charge carriers, the oxygen-deficient TiO2 nanostructures exhibited 4.2 times higher PCO efficiency than commercial TiO2 (P25). More importantly, the high surface area of the mesoporous TiO2 provided sufficient active sites for in-situ adsorption and reaction, resulting in the efficient removal of as-formed As(V). Combining the experimental and characterization results, the different roles of reactive species during PCO reactions were clarified.