浓度效应对卡马西平在生物炭上的吸附动力学影响

为了解人工合成药物在生物炭上的吸附动力学特征及其浓度效应的影响,选择卡马西平(CBZ)为目标污染物。探讨不同初始质量浓度(2、4、25、50 mg·L~(-1))在不同裂解温度(200、300、500℃)下制备的生物炭上的吸附动力学特征。结果表明,双室一级动力学模型可以精确地描述CBZ在生物炭上的吸附动力学特征。CBZ的快室吸附对总体吸附的贡献随初始浓度的增大而减小,而慢室吸附贡献则增大。π-π作用可能对CBZ的吸附贡献较大。孔隙填充可以描述慢室吸附过程,可能是吸附速率的控制环节。     

重金属Cd、Pb对褐菖鲉肝脏组织中HSPs基因表达的影响

为了解重金属污染对海洋鱼类热休克蛋白(HSPs)基因表达的影响,将褐菖鲉(Sebastiscus marmoratus)分别暴露于1.6、8、40、200、500μg·L~(-1)Cd、Pb溶液中,用环介导等温扩增技术(loop-mediated isothermal amplification,LAM P)定量检测褐菖鲉肝脏HSP60、HSP70、HSP90、HSC70 mRNA表达量。结果表明:Pb仅在40μg·L-1时显著抑制HSP60、HSP90、HSC70 mRNA表达量,8μg·L~(-1)时即可显著抑制HSP70 m RNA表达量,并在40μg·L~(-1)时达到最小值;Cd对HSP60、HSP90、HSC70的诱导不明显,但能显著诱导HSP70,并在500μg·L~(-1)时达到最大值。相比之下,褐菖鲉肝HSP70基因对重金属Cd、Pb污染较为敏感,有潜力成为监测海洋重金属污染的预警分子。     

Fe-Mn-sepiolite as an effective heterogeneous Fenton-like catalyst for the decolorization of reactive brilliant blue

A study of the decolorization of reactive brilliant blue in an aqueous solution using Fe-Mn-sepiolite as a heterogeneous Fenton-like catalyst has been performed. The Fourier transform infrared (FTIR) spectra of the catalyst showed bending vibrations of the Fe-O. The X-ray diffraction (XRD) patterns of the catalyst showed characteristic diffraction peaks of α-Fe₂O₃, γ-Fe₂O₃ and MnO. A four factor central composite design (CCD) coupled with response surface methodology (RSM) was applied to evaluate and optimize the important variables (catalyst addition, hydrogen peroxide dosage, initial pH value and initial dye concentration). When the reaction conditions were catalyst dosage= 0.4 g, [H₂O₂]= 0.3 mL, pH= 2.5, [reactive brilliant blue]_o = 50 mg·L⁻¹, and volume of solution= 500 mL at room temperature, the decolorization efficiency of reactive brilliant blue was 91.98% within 60 min. Moreover, the Fe-Mn-sepiolite catalyst had good stability for the degradation of reactive brilliant blue even after six cycles. Leaching of iron ions (<0.4 mg·L⁻¹) was observed. The decoloring process was reactive brilliant blue specific via a redox reaction. The benzene ring and naphthalene ring were first oxidized to open ring; these were then oxidized to the alcohol and carboxylic acid. The reactive brilliant blue was decomposed mainly by the attack of ·OH radicals including surface-bound ·OH radicals generated on the catalyst surface.     

Improved blending strategy for membrane modification by virtue of surface segregation using surface-tailored amphiphilic nanoparticles

Membrane modification is one of the most feasible and effective solutions to membrane fouling problem which tenaciously hampers the further augmentation of membrane separation technology. Blending modification with nanoparticles (NPs), owing to the convenience of being incorporated in established membrane production lines, possesses an advantageous viability in practical applications. However, the existing blending strategy suffers from a low utilization efficiency due to NP encasement by membrane matrix. The current study proposed an improved blending modification approach with amphiphilic NPs (aNPs), which were prepared through silanization using 3-(Trimethoxysilyl)propyl methacrylate (TMSPMA) as coupling agents and ZnO or SiO₂ as pristine NPs (pNPs), respectively. The Fourier transform infrared and X-ray photoelectron spectroscopy analyses revealed the presence of appropriate organic components in both the ZnO and SiO₂ aNPs, which verified the success of the silanization process. As compared with the pristine and conventional pNP-blended membranes, both the ZnO aNP-blended and SiO₂ aNP-blended membranes with proper silanization (100% and 200%w/w) achieved a significantly increased blending efficiency with more NPs scattering on the internal and external membrane surfaces under scanning electron microscope observation. This improvement contributed to the increase of membrane hydrophilicity. Nevertheless, an extra dosage of the TMSPMA led to an encasement of NPs, thereby adversely affecting the properties of the resultant membranes. On the basis of all the tests, 100% (w/w) was selected as the optimum TMSPMA dosage for blending modification for both the ZnO and SiO₂ types.

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Wastewater-nitrogen removal using polylactic acid/starch as carbon source: Optimization of operating parameters using response surface methodology

The use of PLA/starch blends for nitrogen removal was achieved. The influence of different operating parameters on responses was verified using RSM. The conditions for desired responses were successfully optimized simultaneously. Blends material may have a promising application prospect in the future. Nitrogen removal from ammonium-containing wastewater was conducted using polylactic acid (PLA)/starch blends as carbon source and carrier for functional bacteria. The exclusive and interactive influences of operating parameters (i.e., temperature, pH, stirring rate, and PLA-to-starch ratio (PLA proportion)) on nitrification (Y₁), denitrification (Y₂), and COD release rates (Y₃) were investigated through response surface methodology. Experimental results indicated that nitrogen removal could be successfully achieved in the PLA/starch blends through simultaneous nitrification and denitrification. The carbon release rate of the blends was controllable. The sensitivity of Y₁, Y₂, and Y₃ to different operating parameters also differed. The sequence for each response was as follows: for Y₁, pH>stirring rate>PLA proportion>temperature; for Y₂, pH>PLA proportion>temperature>stirring rate; and for Y₃, stirring rate>pH>PLA proportion>temperature. In this study, the following optimum conditions were observed: temperature, 32.0°C; pH 7.7; stirring rate, 200.0 r·min^-1; and PLA proportion, 0.4. Under these conditions, Y₁, Y₂, and Y₃ were 134.0 μg-N·g-blend^-1·h^-1, 160.9 μg-N·g-blend^-1·h^-1, and 7.6 × 10³ μg-O·g-blend^-1·h^-1, respectively. These results suggested that the PLA/starch blends may be an ideal packing material for nitrogen removal.     

Simulation of long-term nutrient removal in a full-scale closed-loop bioreactor for sewage treatment: an example of Bayesian inference

In this study, the performance of nitrogen and phosphorus removal in a full-scale closed-loop bioreactor (oxidation ditch) system was simulated using the ASM2d model. Routine data describing the process for two years were compiled for calibration and validation. To overcome the identifiability problem, the classic Bayesian inference approach was utilized for parameter estimation. The calibrated model could describe the long-term trend of nutrient removal and short-term variations of the process performance, showing that the Bayesian method was a reliable and useful tool for the parameter estimation of the activated sludge models. The anoxic phosphate uptake by polyphosphate accumulating organisms (PAO) contributed 71.2% of the total Poly-P storage, which reveals the dominance of denitrifying phosphorus removal process under the oxygen limiting conditions. It was found that 58.7% of the anoxic Poly-P storage and denitrification by PAO in the reactor was achieved in the aerated compartment, implying that the PAO’s anoxic activity was significantly stimulated by the low dissolved oxygen (DO) level in this compartment due to the oxygen gradient caused by brush aerator.     

三种微生物对铀的吸附行为研究

开展了酵母菌(真菌)、枯草芽孢杆菌(细菌)、小球藻(藻类)对水体中铀(Ⅵ)的吸附性能及机理研究.结果表明:3种微生物对铀都具有较好的吸附效果.酵母菌,小球藻,枯草芽孢杆菌对铀的最佳吸附率分别为97.19%、97.13%、98.03%;且最大吸附量分别达到341.2、356.5、512.5mgU/g(DW).3种微生物对铀的吸附过程和机理有所不同,酵母菌和小球藻符合Langmuir模型,枯草芽孢杆菌更适合Freundlich模型,吸附至12h,酵母菌表面逐渐出现铀和磷的片状结晶及含铀沉积物堆积,小球藻和枯草芽孢杆菌与铀(50mgU/L)作用后细胞出现明显变形,菌体表面未出现铀的结晶物.     

一种PM_(2.5)辅助监测系统的设计与实现

为解决目前国内外PM2.5监测仪器价格昂贵,运行成本高,单点负责区域大,监测点少的问题,提出以国家监测网络为基础,以低成本、高精度为特点的PM2.5辅助监测方法。系统采用DSM501A作为PM2.5浓度采集传感器,完成粒子数量浓度到质量浓度的转换,通过在一定区域内布置监测终端,并借助于GPRS网络和参数曲面构建方法,建立了一定区域内PM2.5质量浓度网络图,填补了国家监测点间的监测盲区,并利用高斯消元法建立了从历史数据到未来浓度的预测算法。实验结果表明:实测数据与国家监测点数据基本一致,具有广阔的应用前景。     

电视、中波发射塔对电磁辐射环境的影响

通过对包头市城区历年的电磁环境监测,以及电视和中波发射塔周围电磁辐射情况,了解其环境质量状况和主要污染源。历年环境监测综合场强为0.30~0.47 V/m,年平均值为0.41 V/m。而广播和电视发射塔因距离而异,它们综合场强均值分别为1.26~3.43 V/m、1.44~5.34 V/m。虽然这些监测值都在标准限值之内,但可以看出广播和电视发射塔对电磁辐射综合场强的影响极大。     

BS EN ISO 20345：2011《个体防护装备安全鞋》标准的解析和建议

本文通过对最新的BS EN ISO 20345：2011《个体防护装备安全鞋》标准的列表介绍和概括性分析,找出了新标准检测项目仍存在的遗留问题和未考虑到的缺陷以及需要界定的术语,并提出了今后标准的再修订意见。此再修订意见的给出,为推动今后与安全鞋标准BS EN ISO 20345：2011属于同一体系的我国GB 21148-2007《个体防护装备安全鞋》标准修订提供参考意见。