陶瓷膜处理含镍电镀废水

研究了平均孔径分别为0.8μm和0.5μm的陶瓷膜对含镍电镀废水在p H为9时的微滤过程,考察了操作时间、跨膜压差、错流速度、温度和浓缩因子对膜通量和镍截留率的影响,探究了陶瓷膜的清洗行为及该微滤过程的数学模型。结果表明:随操作时间延长,膜通量先迅速下降,然后基本不变;随跨膜压差增大或错流速度增大,膜通量上升至趋于稳定;温度升高使得膜通量增大。0.8μm膜适宜操作参数为跨膜压差0.12 MPa、错流速度3.0 m/s和温度30℃;0.5μm膜适宜操作参数为跨膜压差0.14 MPa、错流速度3.4 m/s和温度30℃。在浓缩过程中,膜通量快速下降至平缓阶段,再较快降低,镍截留率约为99%;采用质量浓度0.15%盐酸清洗,0.8μm污染陶瓷膜能使其通量恢复到新膜通量的98%,而0.5μm污染陶瓷膜能恢复到新膜通量的97.5%;该微滤过程符合修正后的完全堵塞数学模型。     

预涂动态膜在乳化油废水处理中的阻力分布及其抗污染特性

为讨论预涂动态膜的抗污染特性,测定了陶瓷膜、高岭土预涂动态膜和高岭土/MnO2复合预涂动态膜分别在乳化油废水处理中的阻力分布,并用SEM扫描电镜对污染预涂动态膜形貌进行了表征。结果表明,乳化油污染阻力明显高于基膜(或陶瓷膜)固有阻力及涂膜粒子形成的阻力,乳化油对预涂动态膜或陶瓷膜的污染是导致膜通量衰减的主要原因;高岭土和复合预涂动态膜所用基膜污染阻力低于陶瓷膜的内部污染阻力,其中复合预涂动态膜所用基膜的污染阻力最小;复合动态膜层比高岭土动态膜层的污染程度低;污染预涂动态膜表面呈现明显的凝胶态物质,其基膜外壁面未呈现凝胶态物质。处理乳化油废水中,动态膜层可有效保护基膜,表现出了较强的抗污染性能。     

SPEEK涂层纳滤膜处理草甘膦废水

以聚醚砜(PES)超滤膜为基膜,采用涂层法制备磺化聚醚醚酮(SPEEK)中空纤维复合纳滤膜,研究其对草甘膦的浓缩和去除。考察了该膜在浓缩草甘膦模拟废水中的操作条件,如跨膜压力、进料浓度、进料pH和离子强度等对通量和截留率的影响。结果表明,随跨膜压力的增加,草甘膦的截留率和水通量均增加,当跨膜压力由0.3 MPa增加到0.8 MPa时,水通量由34.0 L/(m2.h)增加至98.0 L/(m2·h),截留率高于98%;增加进料浓度和离子强度,截留率和通量均减小,当进料浓度由100 mg/L增至1 000 mg/L,水通量降低12.4%,截留率降低8.4%;而pH由3.0升至11.0时,截留率增加,但通量几乎不变。当把该膜材料用于浓缩含高浓度NaCl的草甘膦母液时,发现在0.5 MPa压力和pH=11.0下,复合纳滤膜对NaCl的截留率低于20%,对草甘膦的截留率可达90%。这说明该复合纳滤膜可以把草甘膦与NaCl有效分离开来,为草甘膦的回收利用提供了基础。     

颗粒物粒径和有机物分子量对超滤膜污染的影响

采用不同孔径和截留分子量的膜对原水进行预过滤,研究不同粒径的颗粒物和不同分子量的有机物对膜污染的影响。结果表明,随着预过滤膜孔径或截留分子量的减小,原水中浊度、CODMn、DOC和UV254的去除率逐渐提高,超滤膜运行的跨膜压力(TMP)比直接过滤原水时降低;经孔径为1.2μm和0.45μm的膜预过滤后,超滤膜运行的TMP仍上升较快,而经过截留分子量为100 kDa及以下膜预过滤后,膜污染比较缓慢。对膜阻力构成分析的结果表明,随着预过滤膜孔径或截留分子量的减小,超滤膜运行过程中的表面饼层阻力逐渐减小,堵孔阻力也有明显降低,但预膜滤不能有效降低膜的吸附阻力。超滤膜表面的扫描电镜观察结果表明,经过截留分子量在100 kDa及以下的膜预过滤后,超滤膜表面比较干净,此时的膜过滤阻力主要来源于吸附和堵孔阻力。     

微网材质对动态膜形成的影响

分别采用2种相同孔径不同材质的膜材料(39μm尼龙,39μm涤纶)进行死端过滤与错流过滤实验,以考察微网材质对动态膜(DM)形成的影响。死端过滤实验结果表明,尼龙和涤纶微网均可获得超过99.7%的悬浮物(SS)截留率,而涤纶微网比尼龙微网更容易形成致密的动态膜;错流过滤实验结果表明,尼龙和涤纶微网最终出水浊度均小于20NTU,同时发现,涤纶网在动态膜形成过程中,压力上升较慢,但动态膜更致密,因此,出水效果更好。     

超滤膜处理油田采出水用于回注的试验研究

试验采用截留分子量为100 ku的PVDF(聚偏氟乙烯)超滤膜组件对大庆油田采出水进行了处理,处理水用于油田回注以减少清水的消耗和降低环境污染,同时确定了最佳操作条件和膜清洗方法并考察了超滤出水水质的影响.结果表明最佳的操作条件为:跨膜压差0.30～0.35 MPa,膜面流速3.0～3.5 m/s,温度35～40 ℃.超滤出水中的悬浮物、含油量均低于1.00 mg/L,粒径中值和SRB不能检出,超滤出水水质完全满足油田回注水标准.     

粉煤灰基陶瓷微滤膜处理水中悬浮物的抗污染特性

粉煤灰基陶瓷微滤膜是一种新型的廉价无机膜,为研究其抗污染性能,研究了自制的管式膜在处理几种典型料液中的分离性能和渗透性能.考察了过滤不同料液过程中的阻力构成和膜的抗污染特性,并且和文献报道的同类过程中其他膜材料的性能进行了比较.实验进行了2～45 h无反冲、无清洗的连续运行.在过滤粉煤灰悬浮液、高龄土悬浮液和斜生栅藻悬浮液过程中,截留率可以达到100％,过滤阻力低于类似条件下的其他膜材料,在长时间运行后仍能保持较高的通量,表现出良好的抗污染性能.在过滤活性污泥时,截留率达到99.8％,单位压力下过滤通量达到1 170 L/(m·h·MPa).和其他膜材料相比,单位压力下的过滤通量表现出明显的优势.     

草甘膦模拟废水的纳滤分离过程研究

为研究草甘膦纳滤分离过程的影响因素及变化规律,选用GE Osmonic的DK膜对草甘膦模拟废水进行纳滤分离过程的研究。实验表明,20℃、浓度500 mg/L、pH=2.96的草甘膦模拟废水,其截留率随跨膜压力升高而略有升高,其渗透通量随跨膜压力的升高几乎线性增加;随操作温度升高渗透通量增加,但截留率下降;渗透通量和截留率均随料液初始浓度的增加而降低;在pH值为3~5的范围内,草甘膦的截留率随pH值升高而下降,在膜的等电点附近达到最低,该pH值范围内渗透通量在膜的等电点附近较高;在pH值为5~11的范围内,草甘膦的截留率随pH值升高而升高,在该pH值范围内渗透通量随pH值升高而降低;由于屏蔽效应,草甘膦的截留率随NaCl浓度的升高而降低。     

无纺布动态膜生物反应器处理碱减量印染废水

应用无纺布动态膜生物反应器（DMBR）处理碱减量印染废水,对该反应器处理碱减量印染废水过程中的实验结果表明,动态膜形成过程、影响因素和系统的运行效果进行了研究。通过测定临界通量得到反应器稳定运行的亚临界条件。实验结果表明,反应器运行70 min后,形成了稳定的动态膜。动态膜的形成速度与曝气量有关,当曝气量过大时,使得膜面错流速度过大,从而影响动态膜的形成。孔径对动态膜形成的初期影响较大,小孔径膜基材比大孔径膜基材更容易形成动态膜,而当动态膜稳定形成后,小孔径膜基材形成的动态膜性能略好,对污染物的去除效果更好。实验条件下,动态膜生物反应器对COD、UV254、色度和浊度的去除率分别为74%~85%、74%~79%、79%~86%和96.8%~98.6%,出水水质达到《纺织染整工业水污染物排放标准》（GB4287-2012）排放要求。     

应用POMS复合膜分离去除废气中挥发性有机污染物

依靠POMS平板单层膜或POMS卷式膜上选择性分离层的选择性溶解和渗透作用,常温负压分离回收废气中乙酸乙酯等挥发性有机污染物(VOC)组分.结果表明,膜两侧操作压差和原料气流量对乙酸乙酯分离效率影响较大;当原料气处理量为1.770 0～2.810 0 m3/(m2·h)、膜两侧操作压差为0.08 MPa,POMS卷式膜乙酸乙酯渗透速率可达7.86 × 10-7 mol/(s·m2·Pa);乙酸乙酯为1 500～4 500 mg/m3时,其去除率可达80%.测得几种VOC组分在POMS复合膜中的溶解吸附量都比较可观,由此预测该膜处理废气中VOC可取得很好的净化效果.甲苯在POMS复合膜中的溶解吸附量低于乙酸乙酯,其实验测得渗透速率也小于乙酸乙酯.甲苯去除率也能达到80%.     

超细TiO2粒子的超滤分离及回用特性

针对TiO2超细粒子的超滤分离特性进行了试验研究,探讨了操作压力、膜面流速、TiO2投量、pH、电解质等参数条件对膜通量的影响规律及作用机理,证实了浓差极化及滤饼层阻力是影响通量变化的主导因素,在此基础上确定了适宜的超滤工艺条件及膜清洗方式.以甲基橙为降解基质分别测试了经混凝与超滤分离后的TiO2光催化活性,结果表明,超滤不仅可实现TiO2粒子与水的彻底分离,且分离后TiO2催化活性与初次使用相当.研究表明超滤用于悬浮光催化体系的固液分离及催化剂再用是可行的.     

TiO2/Ti转盘液膜反应器光电催化处理罗丹明B

采用溶胶-凝胶法制备了TiO2/Ti电极,X射线衍射(XRD)分析表明,TiO2主要为锐钛矿,晶粒尺寸约为46 nm.以TiO2/Ti电极作阳极,Cu电极作阴极,组装成转盘液膜反应器,考察了其光电催化处理染料罗丹明B(RhB)的影响因素(转盘转速、偏压、溶液初始pH、RhB初始浓度和电解质浓度).得到最佳处理条件为:转盘转速90 r/min,偏压0.4V,溶液初始pH2.5,电解质(硫酸钠)质量浓度0.5 g/L.在最佳处理条件下,处理20 mg/L RhB染料废水90 min的脱色率和总有机碳(TOC)去除率分别达到97.2％和72.7％.结果表明,由于同时强化了激发光源的利用率和溶液的传质效率,TiO2/Ti转盘液膜反应器可高效光电催化处理染料废水.     

Investigation on the effect of sintering temperature on kaolin hollow fibre membrane for dye filtration

Despite its extraordinary price, ceramic membrane can still be able to surpass polymeric membrane in the applications that require high temperature and pressure conditions, as well as harsh chemical environment. In order to alleviate the high cost of ceramic material that still becomes one of the major factors that contributes to the high production cost of ceramic membrane, various attempts have been made to use low cost ceramic materials as alternatives to well-known expensive ceramic materials such as alumina, silica, and zirconia in the fabrication of ceramic membrane. Thus, local Malaysian kaolin has been chosen as the ceramic material in this study for the preparation of kaolin hollow fibre membrane since it is inexpensive and naturally abundant in Malaysia. Due to the fact that the sintering process plays a prominent role in obtaining the desired morphology, properties, and performances of prepared ceramic membrane, the aim of this work was to study the effect of different sintering temperatures applied (ranging from 1200 to 1500 °C) in the preparation of kaolin hollow fibre membrane via dry/wet phase inversion-based spinning technique and sintering process. The morphology and properties of membrane were then characterised by SEM, AFM, FTIR, XRD, and three-point bending test, while the performances of membrane were investigated by conducting water permeation and Reactive Black 5 (RB5) dye rejection tests. From the experimental results obtained, the sintering temperature of 1400 °C could be selected as the optimum sintering temperature in preparing the kaolin hollow fibre membrane with the dense sponge-like structure of separation layer that resulted in the good mechanical strength of 70 MPa with the appreciable water permeation of 75 L/h m² bar and RB5 rejection of 68%.     

制革废水中丙烯酸类鞣剂的膜分离特征

针对3种丙烯酸类鞣剂超滤(UF)、反渗透(RO)分离参数进行了实验研究,探索其在废水深度处理中膜去除的可行性,研究结果表明,3种鞣剂在分离参数:浓度为200 mg/L,超滤的操作压力(P UF)为0.11 MPa,反渗透的操作压力(P RO)为0.4 MPa的条件下UF-RO分离,效果最好。其次,丙烯酸类鞣剂对膜通量影响较大,导致产生的清液较少,所以用UF、RO处理含有这类物质的制革废水时,应尽可能对废水进行预处理。最后,丙烯酸类鞣剂分子中含有极性较强的基团时,粒径分离效果不同。     

Parameters governing permeate flux in an anaerobic membrane bioreactor treating low-strength municipal wastewaters: a literature review.

The objective of this review was to conduct a comprehensive literature survey to identify the parameters that govern the permeate flux in an anaerobic membrane bioreactor (AnMBR) treating municipal wastewater. Based on the survey, research to date indicates that the optimal membrane system for an AnMBR consists of an organic, hydrophilic, and negatively charged membrane with a pore size of approximately 0.1 microm. The use of both external and submerged membrane configurations shows promise. The operating parameters that affect permeate flux in an external membrane system are transmembrane pressure (TMP) and cross-flow velocity. The operating parameters that affect permeate flux in a submerged membrane system are TMP, sparging intensity, and duration of the relaxation period. Both cross-flow velocity and sparging intensity impart a significant amount of shear force on the biomass in an AnMBR. High shear forces can reduce the microbial activity in an AnMBR. In addition, high shear forces can reduce the size of the biosolids in the mixed liquor and increase the release of soluble microbial products. In this respect, external and submerged membrane systems are expected to perform differently because the magnitude of the shear forces to which the biomass is exposed in an external membrane system is significantly greater than that in a submerged system. The size of the biosolid particles and concentration of soluble microbial products in the mixed liquor affect permeate flux. Higher concentrations of soluble microbial products may be present in the mixed liquor when an AnMBR is operated at relatively low operating temperatures. Aerobic polishing following anaerobic treatment can potentially significantly reduce the concentration of some components of the soluble microbial products in the mixed liquor. It is not possible to remove the foulant layer on an organic membrane with caustic cleaning alone. Acidic cleaning or acidic cleaning followed by caustic cleaning is required to remove the foulant layer. This suggests that both biological/organic and inorganic material contribute to membrane fouling.     

Effect of alum addition on the performance of submerged membranes for wastewater treatment.

The effect of aluminum sulfate (alum) addition on membrane performance was investigated, with a particular focus on membrane fouling. During initial operation, alum was added and the performance monitored. After terminating alum addition, the transmembrane pressure (TMP), which is indicative of membrane resistance to flow or fouling, increased. Accompanying the increase in TMP was an increase in the organic nonsettleable fraction (colloidal + dissolved) content of the mixed liquor and deterioration of permeate quality and floc strength. Permeate polysaccharide concentrations increased significantly, suggesting a preferential binding of solution polysaccharides by alum. Upon reinitiating alum addition, the TMP only partially recovered, indicating some irreversible fouling, while mixed liquor nonsettleable organic material, permeate quality, and floc strength returned to initial levels. These results suggest that direct alum addition to membrane bioreactors can improve membrane performance by reducing the organic fouling material and improving floc structure and strength. It appears that bulk liquid polysaccharides may contribute to irreversible membrane fouling, and this fraction can be efficiently controlled through the alum addition.     

Fouling mitigation and cleanability of TiO<Subscript>2</Subscript> photocatalyst-modified PVDF membranes during ultrafiltration of model oily wastewater with different salt contents

In the present study, TiO₂-coated ultrafiltration membranes were prepared and used for oily water filtration (droplet size <?2 μm). The aim of this work was to investigate the effect of different salt contents on fouling and filtration properties of neat and TiO₂-coated membranes during oil-in-water emulsion filtration. The effect of the TiO₂ coating on the flux, surface free energy, and retention values was measured and compared with the neat membrane values. The cleanability of the fouled TiO₂-coated membranes by UV irradiation was also investigated by measuring flux recovery and contact angles, and the chemical changes during cleaning were characterized by ATR-IR. It was found that increasing the salt content of the model wastewaters, oil-in-water emulsions, increased the zeta potential and the size of the droplets. The presence of the TiO₂ coating decreases the membrane fouling during oily emulsion filtration compared to the neat membrane, due to the hydrophilicity of the coating regardless of the salt content of the emulsions. The neat and coated membrane oil retention was similar, 96?±?2%. The coated membrane can be effectively cleaned with UV irradiation without additional chemicals and a significant flux recovery can be achieved. Monitoring of the cleaning process by following the membrane surface wettability and ATR-IR measurements showed that the recovery of flux does not mean the total elimination of the oil layer from the membrane surface.     

好氧膜-生物反应器中微滤膜选择的实验研究

用扫描电镜表面观察和全自动压汞仪测定了2种亲水化改性PVDF微滤膜的平均孔径、孔隙率等基本性能参数。对2种膜的纯水通量,及其平板膜组件在好氧膜生物反应器内污染过程进行分析。结果显示,2种膜污染过程均呈现先缓慢后快速的"二阶段"趋势,第二阶段是膜污染的主导阶段。尽管平均孔径小、孔隙率高的膜本身阻力大、纯水通量低,但其污染速率较低,物理及化学清洗恢复率较高。膜孔径及孔隙率指标是影响其在MBR中运行的污染速率的主要因素,平均孔径小、孔隙率高的膜抗污染能力强。     

Capture of CO2 on γ-Al2O3 materials prepared by solution-combustion and ball-milling processes

A series of porous γ-Al₂O₃ materials was prepared by solution-combustion and ball-milling processes. The as-prepared powders were physicochemically characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), and N₂ physisorption measurements and their performances in CO₂ adsorption at different pressures (0.5 to 1.5 MPa) and temperatures (40 to 60ºC) were investigated. It was found that γ-Al₂O₃ synthesized by the solution-combustion process and ball milled at 10 hr exhibited the best CO₂ adsorption performance at 60ºC and 1.5 MPa, achieving a maximum of 1.94 mmol/g compared to the four studied materials, as a result of their interesting microstructure and surface properties (i.e., nanocrystallinity, specific surface area, narrow pore size distribution, and large total pore volume). Our study shows that the γ-Al₂O₃ prepared by solution combustion followed by ball milling presents a fairly good potential adsorbent for efficient CO₂ capture.

Implications: In this work, γ-Al₂O₃ materials were successfully obtained by solution combustion and modified via ball milling. These improved materials were systematically investigated as solid adsorbents of accessible surface areas, large pore volumes, and narrow pore size distribution for the CO₂ capture. These studied solid adsorbents can provide an additional contribution and effort to develop an efficient CO₂ capture method as means of alleviating the serious global warning problem.