膜生物反应器处理甲苯废气的挂膜实验

采用假单胞菌在硅橡胶复合膜生物反应器上进行甲苯废气降解的挂膜启动实验,研究膜生物反应器挂膜启动特性,对挂膜启动过程中循环液吸光度、压力损失、甲苯降解效率和生物膜干重的变化进行考察,并观察挂膜稳定后的生物膜形态.结果表明:挂膜过程主要由生物膜成膜期(0~5 d)、生长期(6~10 d)、稳定期(11~14 d)3个阶段组成.循环液吸光度、反应器内液相压力损失、甲苯降解效率和生物膜干重等参数在成膜期都快速增加;进入膜生长期,循环液吸光度略微下降,而生物膜干重、压力损失和甲苯降解效率都继续增大;在稳定期各参数均趋于相对稳定,稳定后循环液吸光度维持在0.75左右,液相压力损失达到了180 Pa,甲苯降解效率维持在78%以上,生物膜干重为2.25 mg/cm2.试验表明,对循环液吸光度、液相压力损失、甲苯降解效率和生物膜干重等参数的综合分析,可作为膜生物反应器挂膜启动进程的判据.图9参15     

Fertilizer drawn forward osmosis as an alternative to 2nd pass seawater reverse osmosis: Estimation of boron removal and energy consumption

• The boron concentration in diluted DS can satisfy the irrigation water standard. • The boron concentration in diluted DS equaled that in two-pass RO permeate. • FDFO process SEC was slightly lower than the 2nd pass RO SEC. • FDFO has potential as an alternative to 2nd pass RO for irrigation water production. Agriculture is the largest consumer of freshwater. Desalinated seawater is an important alternative water source for sustainable irrigation. However, some issues of the current desalination technology hinder its use for agriculture irrigation, including low boron removal and high energy consumption. This study systematically explored the feasibility of employing fertilizer drawn forward osmosis (FDFO) as an alternative to 2nd pass reverse osmosis (RO) by considering the boron removal performance and specific energy consumption (SEC). Different operating conditions were investigated, such as the boron and NaCl concentrations in feed solution (FS), draw solution (DS) concentration, pH, the volume ratio of FS to DS, membrane orientation, flow rate, and operating temperature. The results indicated that a low boron concentration in FS and high pH DS (pH= 11.0) decreased the boron solute flux, and led to low final boron concentration in the DS. The other operating conditions had negligible influence on the final DS boron concentration. Also, a lower flow rate and higher specific water flux with certain permeate water volumes were conducive to reducing the SEC of the FDFO process. Overall, our study paves a new way of using FDFO in irrigation, which avoids the phytotoxicity and human health risk of boron. The results show the potential of FDFO as an alternative to 2nd pass RO for irrigation water production.     

Removal of boron by electrocoagulation

Boron compounds are used in many manufacturing products and may be introduced into the environment in the form of hazardous materials. Here the feasibility of removal of boron from aqueous solutions by electrocoagulation was investigated. The process was examined under various factors in order to assess optimal operating conditions. The results showed that electrocoagulation for boron removal depends on current density, initial concentration and time. Under a current density of 30 mA/cm² the percentage of boron removal from aqueous solutions is in the range of 92–96%.     

Polymeric microspheres with <Emphasis Type="Italic">N</Emphasis>-methyl-<Emphasis Type="SmallCaps">d</Emphasis>-glucamine ligands for boron removal from water solution by adsorption–membrane filtration process

Polymeric microspheres with N-methyl-d-glucamine (NMDG) ligands have been tested in the adsorption–membrane filtration process for boron removal from aqueous solutions. The chelating resins were synthesized by reacting NMDG with the vinylbenzyl chloride–styrene–1,4-divinylbenzene (VBC/S/DVB) copolymer at the reflux temperature and in the microwave reactor. VBC/S/DVB spheres with a gel structure that contained 6 wt% DVB were obtained by membrane emulsification followed by suspension polymerization. By selecting the optimal emulsification and polymerization parameters, it was possible to obtain 25-μm-diameter particles with a narrow size distribution. Resins obtained by microwave modification showed the higher boron adsorption capacity.     

Experimental and computational assessment of 1,4-Dioxane degradation in a photo-Fenton reactive ceramic membrane filtration process

• 1,4-Dioxane was degraded via the photo-Fenton reactive membrane filtration. • Degradation efficiency and AQY were both enhanced in photocatalytic membrane. • There is a tradeoff between photocatalytic degradation and membrane permeation flux. • Degradation pathways of 1,4-Dioxane is revealed by DFT analysis. The present study evaluated a photo-Fenton reactive membrane that achieved enhanced 1,4-Dioxane removal performance. As a common organic solvent and stabilizer, 1,4-Dioxane is widely used in a variety of industrial products and poses negative environmental and health impacts. The membrane was prepared by covalently coating photocatalyst of goethite (α-FeOOH) on a ceramic porous membrane as we reported previously. The effects of UV irradiation, H₂O₂ and catalyst on the removal efficiency of 1,4-Dioxane in batch reactors were first evaluated for optimized reaction conditions, followed by a systematical investigation of 1,4-Dioxane removal in the photo-Fenton membrane filtration mode. Under optimized conditions, the 1,4-Dioxane removal rate reached up to 16% with combination of 2 mmol/L H₂O₂ and UV₃₆₅ irradiation (2000 µW/cm²) when the feed water was filtered by the photo-Fenton reactive membrane at a hydraulic retention time of 6 min. The removal efficiency and apparent quantum yield (AQY) were both enhanced in the filtration compared to the batch mode of the same photo-Fenton reaction. Moreover, the proposed degradation pathways were analyzed by density functional theory (DFT) calculations, which provided a new insight into the degradation mechanisms of 1,4-Dioxane in photo-Fenton reactions on the functionalized ceramic membrane.     

Characterization of boron tolerant bacteria isolated from a fly ash dumping site for bacterial boron remediation

Boron is an essential micronutrient for plants, but can above certain concentrations be toxic to living organisms. A major environmental concern is the removal of boron from contaminated water and fly ash. For this purpose, the samples were collected from a fly ash dumping site, Nagasaki prefecture, Japan. The chemical characteristics and heavy metal concentration of the samples were performed by X-ray fluorescent analysis and leaching test. For bacterial analysis, samples were collected in sterile plastic sheets and isolation was carried out by serial dilution method. The boron tolerant isolates that showed values of maximum inhibitory concentration toward boron ranging from 100 to 260 mM level were screened. Based on 16S rRNA sequencing and phylogenetic analysis, the isolates were most closely related to the genera Bacillus, Lysinibacillus, Microbacterium and Ralstonia. The boron tolerance of these strains was also associated with resistant to several heavy metals, such as As (III), Cr (VI), Cd, Cu, Pb, Ni, Se (III) and Zn. Indeed, these strains were arsenic oxidizing bacteria confirmed by silver nitrate test. These strains exhibited their salt resistances ranging from 4 to 15 % were determined in Trypticase soy agar medium. The boron tolerant strains were capable of removing 0.1–2.0 and 2.7–3.7 mg l^?1 boron from the medium and fly ash at 168 h. Thus, we have successfully identified the boron tolerant and removal bacteria from a fly ash dumping site for boron remediation.     

Effect of iron addition on the performance of anoxic-oxic membrane process and biological phosphorus removal北大核心CSCD

In order to solve the problem of poor treatment of phosphorus in membrane bioreactor (MBR) with long sludge retention time (SRT), a ferric salt was added to enhance phosphorus removal; FeCl36H2O (Fe/P = 2.0) was added to the reactor. The removal efficiency of nitrogen, organic matters, and phosphorus in the MBR was investigated systematically. Moreover, this study focused on the membrane performance, the change of active sludge flora, and the effect of adding a ferric salt on membrane fouling before and after the addition. It was seen that adding the ferric salt could not affect the removal of COD and NH4 +-N and the removal rate of COD and NH4 +-N reached over 90%. However, the average removal rate of phosphorus was 52%, while the removal rate increased by nearly 40% after adding the ferric salt. The effects of adding ferric salts on the dominant bacteria and biological phosphorus removal of activated sludge were further studied. The results showed that the addition of ferric salt (Fe/P = 2.0) decreased the diversity of active sludge flora and relative abundance of some phosphorusaccumulating organisms and had a negative effect on biological phosphorus removal. The analysis of transmembrane pressure difference (TMP) recording revealed that the concentration of iron salts did not exacerbate membrane fouling. The results showed that the concentration of iron salts entering the membrane bioreactor would reduce the relative abundance and phosphorus removal efficiency of the activated sludge in the system to a certain extent, but it had no obvious effect on membrane fouling. It allowed the effluent to attain acceptable standards, especially with respect to phosphorus removal efficiency. © 2018 Science Press. All rights reserved.     

乳状液膜法分离提取醋酸的模拟试验

研究了LMS－2－煤油－NaOH液膜体系处理醛酸水溶液的最佳操作条件，讨论了表面活性剂浓度、搅拌速度、试剂比、油内比及乳水比对提取率的影响，得出了制乳的最佳稳定条件，提取率可达96％以上。     

Electro-conductive crosslinked polyaniline/carbon nanotube nanofiltration membrane for electro-enhanced removal of bisphenol A

● A crosslinked polyaniline/carbon nanotube NF membrane was fabricated. ● Electro-assistance enhanced the removal rate of the NF membrane for bisphenol A. ● Intermittent voltage-assistance can achieve nearly 100% removal of bisphenol A. ● Membrane adsorption–electro-oxidation process is feasible for micropollutant removal. Nanofiltration (NF) has attracted increasing attention for wastewater treatment and potable water purification. However, the high-efficiency removal of micropollutants by NF membranes is a critical challenge. Owing to the adsorption and subsequent diffusion, some weakly charged or uncharged micropollutants, such as bisphenol A (BPA), can pass through NF membranes, resulting in low removal rates. Herein, an effective strategy is proposed to enhance the BPA removal efficiency of a crosslinked polyaniline/carbon nanotube NF membrane by coupling the membrane with electro-assistance. The membrane exhibited a 31.9% removal rate for 5 mg/L BPA with a permeance of 6.8 L/(m²·h·bar), while the removal rate was significantly improved to 98.1% after applying a voltage of 2.0 V to the membrane. Furthermore, when BPA coexisted with humic acid, the membrane maintained 94% removal of total organic carbon and nearly 100% removal of BPA at 2.0 V over the entire filtration period. Compared to continuous voltage applied to the membrane, an intermittent voltage (2.0 V for 0.5 h with an interval of 3.5 h) could achieve comparable BPA removal efficiency, because of the combined effect of membrane adsorption and subsequent electrochemical oxidation. Density functional theory calculations and BPA oxidation process analyses suggested that BPA was adsorbed by two main interactions: π–π and hydrogen-bond interactions. The adsorbed BPA was further electro-degraded into small organic acids or mineralized to CO₂ and H₂O. This work demonstrates that NF membranes coupled with electro-assistance are feasible for improving the removal of weakly charged or uncharged micropollutants.     

Health Impact Evaluation of Boron in Drinking Water: A Geographical Risk Assessment in Northern France

Objective: To evaluate health impact of boron in drinking water. Methods: A regional scale geographical study in Northern France was conducted. Assessment of boron blood levels in a group of 180 healthy individuals and correlation with boron content in drinking water were followed by an assessment of health indicators such as birth rates, mortality rates, and sex ratios in zones of different boron content in drinking water. Results: After necessary adjustments, men living in municipalities with more than 0.30 mg/L of boron in drinking water had elevated but not significant boron blood levels compared with those living in municipalities with boron water levels of less than 0.30 mg/L (159.1 versus 123.0 ng/g; p > 0.05). The standardized birth ratio adjusted for the reference geographic zone and calendar time period was 1.07 and 1.28 in the low and high (>0.3 mg/L) boron content municipalities, respectively. The birth rate in municipalities with high boron content in drinking water was higher than that of the reference geographic zone and of the French general population (p < 10^-4). The standardized mortality ratio adjusted for the reference geographic zone and calendar time period was 0.94 and 0.92 in the low and high boron content municipalities, respectively. The mortality rate in municipalities with high boron content in drinking water was less than that of the reference geographic zone and of the French general population (p < 10^-3). No statistical difference was noted in the male–female sex ratios between the different municipality zones (p = 0.45). Conclusions: The results of this study do not support the idea of a deleterious effect of boron on human health, at the boron water level contents found in this specific region. In fact, there is a tendency toward a beneficial effect with low-dose environmental exposure (less than 1 mg/L of boron) in drinking water.     

A Biosurfactant-Enhanced Soil Flushing for the Removal of Phenanthrene and Diesel in Sand

In order to examine the potential of biosurfactants in soil remediation, and to investigate the effects of several operating conditions, such as flow rate, biosurfactant concentration and surfactant type, biosurfactant-enhanced soil flushing was conducted. In the biosurfactant-enhanced soil flushing process, the removal efficiency increased as the flow rate decreased. Rhamnolipid showed no effect on the removal efficiency of phenanthrene and diesel from sand in the concentration range 0.3-0.5%. However, rhamnolipid showed higher efficiencies for the removal of phenanthrene and diesel from sand than Tween 80. Based on total recovery, following an equivalent pore volume flush, it was more difficult to remove diesel than phenanthrene. In order to obtain the specific removal efficiency, more pore volumes of surfactant solution may be required in field applications. Under optimum conditions, the biosurfactant removed as much as 70% of the phenanthrene and 60% of the diesel in the sand. These results indicate that the use of biosurfactants in the flushing process is favorable, not only with respect to the environment, but also on removal efficiencies.     

鼠李糖脂对沉积物中Cd和Pb的去除作用

用铜绿假单胞菌(Pseudomonas aeruginosa)产生的鼠李糖脂生物表面活性剂对沉积物中重金属的去除作用进行了研究．研究表明,鼠李糖脂对沉积物中的Cd和Pb有明显的去除作用,在鼠李糖脂溶液的pH值为10．0的条件下对重金属的去除效率最好,而且当鼠李糖脂在沉积物上的吸附达到饱和时去除效率达到最大．通过连续萃取对提取前和提取后沉积物样品中重金属的形态进行分析,发现可交换态和有机结合态的重金属较容易去除．通过4次连续的提取,使cd和Pb的去除效率分别达到80．1％和36．5％．     

Transport of antibiotic resistance plasmids in porous media and the influence of surfactants

Transport of engineered antibiotic resistance plasmids in porous media has been reported to potentially cause significant spreading of antibiotic resistance in the environment. In this work, transport of an indigenous resistance plasmid pK5 in porous media was investigated through packed column experiments. At identical ionic strengths in CaCl₂ solutions, the breakthroughs of pK5 from soil columns were very close to those from quartz sand columns, indicating that transport of pK5 in quartz sand and soil was similar. A similarity in transport behavior was also found between pK5 and an engineered plasmid pBR322 that has approximately the same number of base pairs as pK5. The influence of surfactants, a major group of constituents in soil solutions, was examined using an engineered plasmid pcDNA3.1(+)/myc-His A. The impact of an anionic surfactant, sodium dodecyl sulfate (SDS), was negligible at concentrations up to 200 mg·L^–1. Cetyltrimethyl ammonium bromide (CTAB), a cationic surfactant, was found to significantly enhance plasmid adsorption at high concentrations. However, at environmentally relevant concentrations (<1 mg·L^–1), the effect of this surfactant was also minimal. The negligible impact of surfactants and the similarity between the transport of engineered and indigenous plasmids indicate that under environmentally relevant conditions, indigenous plasmids in soil also have the potential to transport over long distances and lead to the spreading of antibiotic resistance.

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Alkyl polyglucosides as cell surface modification factors: influence of the alkyl chain length

The use of surfactants in a bioremediation process is aimed at increasing the efficiency of the removal of hydrophobic contaminants from the environment. The subjects of the study were three alkyl polyglucosides (APGs) of different alkyl chain length: Glucopon 215 CS UP, Glucopon 600 CS UP, and Glucopon 650 EC. The impact of these surfactants on the surface properties of the test strain Pseudomonas fluorescens ATCC 14700, as well as on the biodegradation of diesel was tested. It was observed, that the length of alkyl chain has an influence on the cell surface properties. The modification of the cell surface hydrophobicity and the electrokinetic potential on the bacteria cells is dependent on the structure of Glucopon molecules. The elongation of alkyl chains in surfactant molecule caused an increase of the hydrophobic properties and a reduction of the electrokinetic potential on the bacteria cells. Moreover, the use of APGs below critical micelle concentration caused an increase of diesel oil biodegradation, especially in the case of Glucopons with longer alkyl chain (Glucopon 600 CS UP and 650 EC). The better diesel oil removal by tested strain after surfactant addition was correlated with the hydrophobic properties of bacteria strain.     

High boron removal by functionalized magnesium ferrite nanopowders

Hydroxyl-enriched materials are promising boron adsorbents. However, the use of these materials is hampered by issues of separation, recovery, and selectivity, notably due to the presence of interfering ions. Therefore, we synthesized here a cheap magnetic nanopowder, which was further functionalized with polyvinyl alcohol and glycidol to produce boron-selective adsorbents. We studied their selectivity and removal efficiency using batch and fixed-bed systems. Sorption was studied at both concentrated and trace amounts of boron. Results show that nanopowders have 5.3–6.5 nm pore sizes and 145–203 m²/g surface areas, using Brunauer–Emmett–Teller analysis. Polyvinyl alcohol-functionalized particles removed 93 % of boron at 5 mg/L at pH 7 in 30 min, whereas only 68 % of boron was removed by glycidol-functionalized particles. However, at higher boron concentration, of 50 mg/L, glycidol-functionalized particles showed higher adsorption affinity of 68.9 mg/g. We conclude that internal hydroxyl groups of polyvinyl alcohol-functionalized particles are less accessible at higher boron concentration. This is the first report on magnesium ferrites for boron recovery. The spent adsorbents were separated easily from the aqueous media by an external magnet and repeatedly used. Overall, our findings demonstrated that the hydroxyl-enriched magnetic nanopowders are a better alternative to the existing boron adsorbents regarding magnetic separation, reusability, and selectivity.     

植物对硼素不足的反应及其成因探讨

硼是植物生长过程中必不可少的微量元素之一,缺硼将严重影响植物的正常生长与发育。文章综述了植物对硼素不足的反应,包括细胞壁和生物膜的结构与功能变化、糖类运输、酶活性的改变以及植物根、茎、叶和生殖生长的变化等,探讨了植物缺硼的可能原因,并提出了防止植物缺硼的对策。     

Electrocatalytic reduction of nitrate using Pd-Cu modified carbon nanotube membranes

● Pd-Cu modified CNT membranes were prepared successfully by electrodeposition method. ● The deposition voltage and deposition time were optimized for Pd-Cu co-deposition. ● NO₃⁻-N was removed efficiently from water by Pd-Cu modified CNT membranes. ● The presence of dissolved oxygen did not affect the nitrate reduction performance. ● Mass transfer rate was promoted significantly with the increase in membrane flux. Excessive nitrate in water is harmful to the ecological environment and human health. Electrocatalytic reduction is a promising technology for nitrate removal. Herein, a Pd-Cu modified carbon nanotube membrane was fabricated with an electrodeposition method and used to reduce nitrate in a flow-through electrochemical reactor. The optimal potential and duration for codeposition of Pd and Cu were −0.7 V and 5 min, respectively, according to linear scan voltammetry results. The membrane obtained with a Pd:Cu ratio of 1:1 exhibited a relatively high nitrate removal efficiency and N₂ selectivity. Nitrate was almost completely reduced (~99 %) by the membrane at potentials lower than −1.2 V. However, −0.8 V was the optimal potential for nitrate reduction in terms of both nitrate removal efficiency and product selectivity. The nitrate removal efficiency was 56.2 %, and the N₂ selectivity was 23.8 % for the Pd:Cu=1:1 membrane operated at −0.8 V. Nitrate removal was enhanced under acidic conditions, while N₂ selectivity was decreased. The concentrations of Cl⁻ ions and dissolved oxygen showed little effect on nitrate reduction. The mass transfer rate constant was greatly improved by 6.6 times from 1.14 × 10⁻³ m/h at a membrane flux of 1 L/(m²·h) to 8.71 × 10⁻³ m/h at a membrane flux of 15 L/(m²·h), which resulted in a significant increase in the nitrate removal rate from 13.6 to 133.5 mg/(m²·h). These findings show that the Pd-Cu modified CNT membrane is an efficient material for nitrate reduction.     

Removal of malachite green from water samples by cloud point extraction using Triton X-100 as non-ionic surfactant

A surfactant mediated cloud point extraction (CPE) procedure has been developed to remove color from wastewater containing malachite green using Triton X-100 as non-ionic surfactant. The effects of the concentration of the surfactant, temperature and salt concentration on the different concentrations of dye have been studied and optimum conditions were obtained for the removal of malachite green. The concentration of malachite green in the dilute phase was measured using UV–Vis spectrophotometer. It was found that the separation of phases was complete and the recovery of malachite green was very effective in the presence of NaCl as an electrolyte. The results showed that up to 500 ppm of malachite green can quantitatively be removed (>95%) by CPE procedure in a single extraction using optimum conditions.     

有机酸与表面活性剂联合作用对土壤重金属的浸提效果研究

重金属污染土壤的原位淋洗修复既要实现对重金属的高效去除,还要尽量减少对土壤性质的破坏,这一点在农业污染土壤修复中尤为重要。以张士污灌区农田土壤为研究对象,利用振荡浸提技术筛选有机酸和表面活性剂组合,并确定了两者联合淋洗修复污染土壤的最佳配比。结果表明：有机酸（酒石酸、乙酸、柠檬酸和苹果酸）中的酒石酸浓度为0.5 mol.L-1和表面活性剂（SDBS、鼠李糖和皂素）中的皂素质量分数为0.7%时对土壤Cd、Pb、Zn的浸提效果较好;在酒石酸与皂素体积配比为1∶1时,对重金属Cd、Pb、Zn浸提效果最好,浸提率分别为87.62%、36.30%、20.67%;单一有机酸、表面活性剂或者有机酸与表面活性剂的混合溶液,对土壤重金属的浸提效果均为Cd〉Pb〉Zn。虽然有机酸与表面活性剂联合浸提效果略低于酒石酸浸提,但其弱酸性对土壤性质影响较小,在原位淋洗修复工程中有较好的应用前景。     

液膜法处理硫普罗宁废水的研究

采用W／O型乳状液膜法提取水溶液中的硫普罗宁，考察了载体、温度、硫普罗宁浓度以及油内比、试剂比、乳水比对提取率的影响，并得出了液膜法提取硫普罗宁的最佳乳液配方：油内比＝1：1，乳水比＝1：2，试剂比＝6－8，载体浓度＝5％，温度20℃，转速＝240－250r.min^-1，其提取率高达90％。