A novel co-catalyzed system between persulfate and chlorite by sonolysis for removing triphenylmethane derivative

Triphenylmethane (tpm) derivatives (e.g. tpm_CV) have threatened the safety of the aquatic environment due to the potential toxicity and carcinogenicity. In this study, the novel ultrasonic/persulfate/chlorite (US/S₂O₈²⁻/ClO₂⁻) oxidation process was developed for the effective removal of tpm_CV in wastewater. The apparent non-integer kinetics (n around 1.20) of tpm_CV degradation under different factors (R²_Adj > 0.990) were investigated, respectively. Inhibiting effects of anions were greater than those of cations (except Fe(II/III)). The adding of micromolecule organic acids could regulate degradation towards positive direction. The double response surface methodology (RSM) was designed to optimize tpm_CV removal process, and the acoustic-piezoelectric interaction was simulated to determine the propagation process of acoustic wave in the reactor. The possible degradation pathway was explored to mainly include carbonylation, carboxylation, and demethylation. The estimated effective-mean temperature at the bubble-water interface was calculated from 721 to 566 K after introducing the ClO₂⁻, however, the adsorption or partitioning capacity of tpm_CV in the reactive zone was widened from 0.0218 to 0.0982. The proposed co-catalysis of US/S₂O₈²⁻/ClO₂⁻ was based on the determined active species mainly including ClO₂, SO₄⋅⁻, and ⋅OH. Compared with other US-based processes, the operating cost (3.97 $/m³) of US/S₂O₈²⁻/ClO₂⁻ with the EE/O value (16.8 kWh/m³) was relatively reduced.     

超声提取-电感耦合等离子体质谱法分析土壤中重金属化学形态

采用超声提取处理土壤样品,用ICP-MS分析样品中Cu、Zn、Pb、Cd、Ni、Cr等6种重金属元素形态,通过试验分析超声提取时土壤样品粒径、超声提取时间对提取效率的影响。方法在0.500μg/L~100μg/L之间线性良好,检出限为0.007μg/L~0.8μg/L,实际样品测定结果的RSD为4.7%~22.7%。土壤中重金属4种形态之和的总量与全量的相对偏差为11.0%~36.4%。将该方法与连续振荡法的试验结果比对,表明两方法对土壤样品的提取效率无显著性差异。     

超声提取-气相色谱质谱法测定大气PM2.5中正构烷烃

建立了超声提取-气相色谱质谱法测定大气PM2.5中32种正构烷烃方法,经离子温度优化、前处理比较、空白滤膜考察等获得了最佳的实验条件。研究发现,高、中、低3种浓度标准曲线的相关系数均在0.995以上,3种浓度的空白样品加标回收率分别为72.2%~117.8%、73.5%~104.4%、73.8%~109.5%,精密度均小于10%,实际样品加标回收率为75.7%~108.9%。当采样体积为24 m3时,各目标化合物的方法检出限为0.046~2.6 ng/m~3;经正构烷烃浓度范围为0.17~64.3 ng/m~3的1月及浓度范围为0.53~7.67 ng/m~3的6月的实际样品验证,该方法的检出限和测量范围也可较好的满足实际样品的测定。     

高级氧化技术在造纸废水处理中的研究进展

高级氧化技术是近几年很受关注的废水处理新技术，用其处理造纸废水的研究也在广泛展开。从这种技术的机理、研究现状及存在问题出发，阐述了这些新方法在造纸废水处理中的实验研究及应用的可能性。     

超声波强化污水生物处理的可行性探讨

通过对超声波空化处理难降解有机废水机理和超声波辐射促进微生物活性作用机制的分析研究，提出将超声波应用于强化污水生物处理的可行性。同时设计了利用超声波空化反应单元作为污水生物处理的前处理工艺，提高污水的可生化性，和在生物处理反应器中直接进行超声波辐射提高生物处理能力的工艺。分析了超声波强化污水生物处理的影响因素，并对未来的研究方向进行了展望。     

Disintegration of municipal waste activated sludge by simultaneous combination of acid and ultrasonic pretreatment

The individual and simultaneous effects of acid and ultrasonic pretreatment on the disintegration of municipal waste activated sludge (WAS) were investigated based on chemical properties of WAS. In the combination of acid and ultrasonic pretreatment methods (ultrasonic-acid pretreatment), lowering pH accelerated and enhanced the disintegration of waste biological sludge. Therefore, the same disintegration efficiency (obtained by ultrasonic pretreatment alone) was achieved by the combined pretreatment in shorter sonication times. Optimum pretreatment conditions were ultrasonic power density of 1.0 W/mL and pretreatment time of 10 min for ultrasonic pretreatment alone, and ultrasonic power density of 1.0 W/mL, pretreatment time of 10 min and initial sludge pH of 2.0 for the combined pretreatment. Sludge disintegration degrees were about 30% and 40% under these optimized conditions, respectively. Optimum sludge concentration was found to be 1.0% total solid (TS) content for the combined pretreatment. As a result, ultrasonic-acid pretreatment has been determined as a new and effective combined sludge pretreatment method to improve the sludge disintegration.     

基于风险的工业管道在线检测技术研究

化工装置工业管道面临焊接和腐蚀两大问题,装置的长期运行与管道定期检验的矛盾日益突出.通过对数字射线、脉冲涡流、超声导波三种管道在线检测技术的对比分析,结合基于风险的检验(RBI)理念,探索出一套适用于工业管道在线检验的技术,对节约企业成本、保障管道安全具有重要意义.     

Sonolytic reactions of phenanthrene in organic extraction solutions

Ultrasonic extraction is a common method used to extract semi-volatile and nonvolatile organic compounds such as polycyclic aromatic hydrocarbons (PAHs) from solid matrices. However, ultrasonic energy has been suspected to lead to undesired reactions of the solute and thus affect qualitative and quantitative results. In this paper, sonolytic reactions of phenanthrene in common organic extraction solutions were examined using a 20 kHz ultrasonic probe under conditions commonly used for ultrasonic extraction. Extraction parameters including phenanthrene concentration, solvent type, pulse length, and sonication time were investigated. Hexane:acetone (1:1 V/V) resulted in less phenanthrene degradation than dichloromethane (DCM):acetone (1:1 V/V). Initial solute concentration, length of sonication time, and solvent type affected the degradation of phenanthrene. Reaction byproducts including methylphenanthrene and methylnaphthalene detected after sonication indicate that phenanthrene reacts by both direct pyrolysis and reaction with methyl or ethyl radicals formed from solvent pyrolysis.     

超声波萃取/气相色谱法测定土壤中的多氯联苯

采用超声波萃取法提取土壤中的多氯联苯系列7种混合物Arochlor1016、Arochlor1221、Arocldor1232、Arochlor1242、Arochlor1248、Arochlor1254、Arochlor1260,萃取溶液经弗罗里硅土柱净化,用气相色谱GC/ECD进行测定,方法检出限0.01mg/kg,加标回收率在62.3%～106%之间,RSD 5.4%～11.1%.     

Rapid detection of multiple class pharmaceuticals in both municipal wastewater and sludge with ultra high performance liquid chromatography tandem mass spectrometry

This work described the development, optimization and validation of an analytical method for rapid detection of multiple-class pharmaceuticals in both municipal wastewater and sludge samples based on ultrasonic solvent extraction, solid-phase extraction, and ultra high performance liquid chromatography-tandem mass spectrometry quantification. The results indicated that the developed method could effectively extract all the target pharmaceuticals （25） in a single process and analyze them within 24 min. The recoveries of the target pharmaceuticals were in the range of 69%-131% for wastewater and 54%-130% for sludge at different spiked concentration levels. The method quantification limits in wastewater and sludge ranged from 0.02 to 0.73 ng/L and from 0.02 to 1.00μg/kg, respectively. Subsequently, this method was validated and applied for residual pharma- ceutical analysis in a wastewater treatment plant located in Beijing, China. All the target pharmaceuticals were detected in the influent samples with concentrations varying from 0.09 ng/L （tiamulin） to 15.24 μg/L （caffeine）; meanwhile, up to 23 pharmaceuticals were detected in sludge samples with concentrations varying from 60 ng/kg （sulfamethizole） to 8.55 mg/kg （ofloxacin）. The developed method demonstrated its selectivity, sensitivity, and reliability for detecting multiple-class pharmaceuticals in complex matrices such as municipal wastewater and sludge.