Adsorption behaviors of activated carbons for the exhaust from spray painting booths in vehicle surface coating

Adsorption performance of activated carbon adsorbers in the downstream duct of vehicle spray painting booths has been studied to understand whether fine paint particles in the off-gas would deteriorate the adsorption capacity of volatile organic compounds (VOCs) on activated carbons. Three forms of activated carbons were selected and their properties were determined using nitrogen adsorption analysis, the measurement of pH value and total ash content, energy dispersion spectrometer, field-emission scanning electron microscopy, and thermogravimetric analysis. Results show that the adsorption capacity of activated carbon strongly depends upon its available specific surface area. When the total uptake on activated carbon approaches saturation, the vapors adsorbed would commence to get displaced by the paint particles gradually as time elapses and finally the uptake of vapors and paint particles reach equilibrium. Microporous carbons, in particular, were much more susceptible to paint particles. A Langmuir-type model for the uptake on activated carbons was suggested, which successfully described the adsorption behaviors of the off-gas released from vehicle spray painting booth.     

Scanning electron microscopy study of the gills,scales and erythrocytes of Anabas testudineus upon exposure to chlorpyrifos

The present study was undertaken to assess the toxicity of sublethal concentrations (125, 250, and 375 µg L^?1) of chlorpyrifos on Anabas testudineus for 21 days. The morphological changes on the gills, scales, and erythrocytes of A. testudineus were observed using scanning electron microscopy. Gill alterations included highly active mucous cells, epithelial hyperplasia, and fusion of secondary lamellae. The scales showed damaged lepidonts. Oozed out cytoplasmic content and lobopodial projections were observed in the erythrocytes after exposure to chlorpyrifos.     

Performance of activated carbon coated graphite bipolar electrodes on capacitive deionization method for salinity reduction

• Graphite bipolar electrodes act as an appropriate bed for the CDI process. • Activated carbon Coating improves the application of the electrodes. • CDI is an environmentally friendly method to apply for brackish water. • Initial concentration is the most important parameter in the CDI method. • CDI process in a batch-mode setup needs more development. This research investigates a capacitive deionization method for salinity reduction in a batch reactor as a new approach for desalination. Reductions of cost and energy compared with conventional desalination methods are the significant advantages of this approach. In this research, experiments were performed with a pair of graphite bipolar electrodes that were coated with a one-gram activated carbon solution. After completing preliminary tests, the impacts of four parameters on electrical conductivity reduction, including (1) the initial concentration of feed solution, (2) the duration of the tests, (3) the applied voltage, and (4) the pH of the solution, were examined. The results show that the maximum efficiency of electrical conductivity reduction in this laboratory-scale reactor is about 55%. Furthermore, the effects of the initial concentration of feed solution are more significant than the other parameters. Thus, using the capacitive deionization method for water desalination with low and moderate salt concentrations (i.e., brackish water) is proposed as an affordable method. Compared with conventional desalination methods, capacitive deionization is not only more efficient but also potentially more environmentally friendly.     

Utilization of nano/micro-size iron recovered from the fine fraction of automobile shredder residue for phenol degradation in water

Phenol removal by n/m Fe in the presence of H₂O₂ was highly effective. Increasing the amounts of n/m Fe and H₂O₂?increased the phenol removal rate. Phenol removal was decreased with an increase in the concentration of phenol. The natural pH (6.9) of the solution was highly effective for phenol removal. The pseudo-first-order kinetics was best fitted for the degradation of phenol. The study investigates the magnetic separation of Fe from automobile shredder residue (ASR) (<0.25 mm) and its application for phenol degradation in water. The magnetically separated Fe was subjected to an ultrasonically assisted acid treatment, and the degradation of phenol in an aqueous solution using nano/micro-size Fe (n/m Fe) was investigated in an effort to evaluate the possibility of utilizing n/m Fe to remove phenol from wastewater. The prepared n/m Fe was analyzed by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The effects of the dosages of n/mFe, pH, concentration of phenol and amount of H₂O₂ on phenol removal were evaluated. The results confirm that the phenol degradation rate was improved with an increase in the dosages of n/mFe and H₂O₂; however, the rate is reduced when the phenol concentration is higher. The degradation of phenol by n/mFe followed the pseudo-first-order kinetics. The value of the reaction rate constant (k) was increased as the amounts of n/m Fe and H₂O₂ increased. Conversely, the value of k was reduced when the concentration of phenol was increased. The probable mechanism behind the degradation of phenol by n/m Fe is the oxidation of phenol through hydroxyl radicals which are produced during the reaction between H₂O₂ and n/m Fe.     

Comparison between linear and non-linear forms of pseudo-first-order and pseudo-second-order adsorption kinetic models for the removal of methylene blue by activated carbon

The best-fit equations of linear and non-linear forms of the two widely used kinetic models, namely pseudo-first-order and pseudo-second-order equations, were compared in this study. The experimental kinetics of methylene blue adsorption on activated carbon was used for this research. Both the correlation coefficient (R ²) and the normalized standard deviation Δq(%) were employed as error analysis methods to determine the best-fitting equations. The results show that the non-linear forms of pseudo-first-order and pseudo-second-order models were more suitable than the linear forms for fitting the experimental data. The experimental kinetics may have been distorted by linearization of the linear kinetic equations, and thus, the non-linear forms of kinetic equations should be primarily used to obtain the adsorption parameters. In addition, the Δq(%) method for error analysis may be better to determine the best-fitting model in this case.     

Development of pretreatment protocol for DNA extraction from biofilm attached to biologic activated carbon (BAC) granules

The biologic activated carbon (BAC) process is widely used in drinking water treatments. A comprehensive molecular analysis of the microbial community structure provides very helpful data to improve the reactor performance. However, the bottleneck of deoxyribonucleic acid (DNA) extraction from BAC attached biofilm has to be solved since the conventional procedure was unsuccessful due to firm biomass attachment and adsorption capacity of the BAC granules. In this study, five pretreatments were compared, and adding skim milk followed by ultrasonic vibration was proven to be the optimal choice. This protocol was further tested using the vertical BAC samples from the full-scale biofilter of Pinghu Water Plant. The results showed the DNA yielded a range of 40 μg·g^-1 BAC (dry weight) to over 100 μg·g^-1 BAC (dry weight), which were consistent with the biomass distribution. All results suggested that the final protocol could produce qualified genomic DNA as a template from the BAC filter for downstream molecular biology researches.     

推荐管理措施情景下黄淮海地区旱地土壤固碳潜力模拟研究——以河南省获嘉县为例

农田土壤固碳不仅可以减缓气候变化,而且能够提高土壤质量。推荐管理措施,如少、免耕和秸秆还田等,具有促进农田土壤有机碳（SOC）增加的巨大潜力。旱地占中国农田面积的70%以上,在固定大气CO2方面可以发挥重要作用。本研究基于黄淮海地区的一个旱地土壤肥力长期监测点数据并运用Century模型模拟了监测期间（1998～2007）土壤有机碳动态变化。在此基础上,设计了1种基础管理措施情景和4种推荐管理措施情景并模拟了它们未来20年的固碳潜力。模拟结果表明,监测期间监测点土壤有机碳密度增加2.72 Mg.hm-2,年均增加0.27 Mg.hm-2。土壤有机碳的增加主要是因为氮肥施用量的增加。模型验证结果表明,Century模型很好地模拟了监测点土壤有机碳的动态变化。各推荐管理措施均具有较大的固碳潜力,其中50%秸秆还田是比少、免耕更有效的固碳措施,而少耕＋50%秸秆还田的固碳潜力最大。因此,在黄淮海地区旱地推广实施推荐管理措施是促进农田土壤固碳的有效策略,有助于减缓大气CO2浓度升高和保障国家粮食安全。     

Acidogenic sludge fermentation to recover soluble organics as the carbon source for denitrification in wastewater treatment: Comparison of sludge types

For biological nitrogen (N) removal from wastewater, a sufficient organic carbon source is requested for denitrification. However, the organic carbon/nitrogen ratio in municipal wastewater is becoming lower in recent years, which increases the demand for the addition of external organic carbon, e.g. methanol, in wastewater treatment. The volatile fatty acids (VFAs) produced by acidogenic fermentation of sewage sludge can be an attractive alternative for methanol. Chemically enhanced primary sedimentation (CEPS) is an effective process that applies chemical coagulants to enhance the removal of organic pollutants and phosphorus from wastewater by sedimentation. In terms of the chemical and biological characteristics, the CEPS sludge is considerably different from the conventional primary and secondary sludge. In the present study, FeCl₃ and PACl (polyaluminum chloride) were used as the coagulants for CEPS treatment of raw sewage. The derived CEPS sludge (Fe-sludge and Al-sludge) was then processed with mesophilic acidogenic fermentation to hydrolyse the solid organics and produce VFAs for organic carbon recovery, and the sludge acidogenesis efficiency was compared with that of the conventional primary sludge and secondary sludge. The results showed that the Fe-sludge exhibited the highest hydrolysis and acidogenesis efficiency, while the Al-sludge and secondary sludge had lower hydrolysis efficiency than that of primary sludge. Utilizing the Fe-sludge fermentation liquid as the carbon source for denitrification, more than 99% of nitrate removal was achieved in the main-stream wastewater treatment without any external carbon addition, instead of 35% obtained from the conventional process of primary sedimentation followed by the oxic/anoxic (O/A) treatment.

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