Designing Semipermeable Hydrogel Shells with Controlled Thickness through Internal Osmosis in Triple-Emulsion Droplets

Hydrogel shells that compartmentalize the water core from the aqueous surrounding provide molecular selectivity on size and charge in transmembrane transport. It is highly demanding to produce thin hydrogel shells to minimize diffusion length and maximize core volume. Here, internal osmosis in water-in-oil-in-water-in-oil (W/O/W/O) triple-emulsion droplets is used to produce thin hydrogel shells enclosing a large water core. The triple-emulsion droplets are prepared to have an ultrathin middle oil layer using a capillary microfluidic device. The innermost water droplet has a higher osmolarity than the outer water layer containing photopolymerizable hydrogel precursors, which pumps water from the outer layer to the core through the ultrathin oil layer by the osmosis. Therefore, the outer layer gets thinner and hydrogel precursors are enriched while the size of the triple-emulsion droplets remains unchanged. Through photopolymerization of precursors and phase transfer from oil to water, hydrogel shells enclosing water core are produced in the water environment; the oil layer is ruptured for molecular exchange through the shells. The thickness and composition of the hydrogel shells are precisely controllable by the osmotic conditions. The shells show a high permeation rate due to the thinness as well as controlled cut-off threshold of permeation for neutral and charged molecules.     

Effect of cellulose acetate/cellulose triacetate ratio on reverse osmosis blend membrane performance

Surface functionalization and modification including the grafting process are effective approaches to improve and enhance the reverse osmosis (RO) membrane performance. This work is aimed to synthesize grafted/crosslinked cellulose acetate (CA)/cellulose triacetate (CTA) blend RO membranes using N-isopropylacrylamide (N-IPAAm) as a monomer and N,N-methylene bisacrylamide (MBAAm) as a crosslinker. The morphology of these membranes was analyzed by scanning electron microscopy and their surface roughness was characterized by atomic force microscopy. The performance of these membranes was evaluated through measuring two major parameters of salt rejection and water flux using RO unit at variable operating pressures. It was noted that the surface average roughness obviously decreased from 148 nm for the pure CA/CTA blend membrane with 2.5% CTA to 110 nm and 87 nm for the grafted N-IPAAm and grafted/crosslinked N-IPAAM/MBAAm/CA/CTA-RO membranes, respectively. Moreover, the contact angle decreased from 51.98° to 47.6° and 43.8° after the grafting and crosslinking process. The salt rejection of the grafted CA/CTA-RO membrane by 0.1% N-IPAAm produced the highest value of 98.12% and the water flux was 3.29 L/m²h at 10 bar.     

炼油达标污水回用处理试验研究

采用曝气生物滤池、多介质过滤、超滤、反渗透工艺,对炼油达标外排污水进行回用处理中试试验。结果表明,曝气生物滤池对油、COD和浊度去除效果良好,超滤、反渗透膜化学清洗周期达到 2个月以上,脱盐率稳定在98％以上,产水品质达到回用要求。     

Oxidative degradation of polyamide reverse osmosis membranes: Studies of molecular model compounds and selected membranes

Selected aromatic amides were used to model the chemical reactivity of aromatic polyamides found in thin‐film composite reverse osmosis (RO) membranes. Chlorination and possible amide bond cleavage of aromatic amides upon exposure to aqueous chlorine, which can lead to membrane failure, were investigated. Correlations are made of the available chlorine concentration, pH, and exposure time with chemical changes in the model compounds. From the observed reactivity trends, insights are obtained into the mechanism of RO membrane performance loss upon chlorine exposure. Two chemical pathways for degradation are shown, one at constant pH and another that is pH‐history dependent. An alternative strategy is presented for the design of chlorine‐resistant RO membranes, and an initial performance study of RO membranes incorporating this strategy is reported. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1173–1184, 2003     

QS-R02反渗透阻垢分散剂工业应用试验

介绍QS-R02新型反渗透阻垢分散剂在齐鲁股份有限公司橡胶厂反渗透系统的工业试验情况,同QS-R01反渗透阻垢分散剂进行了对比。工业应用试验结果表明:新型QS-R02反渗透阻垢分散剂的碳酸钙临界饱和指数LSI达到2.5,阻垢分散效果明显优于QS-R01,能够实现橡胶厂反渗透系统运行过程不加酸的目的。同时,QS-R02药剂磷含量低,浓水总磷含量达到国家污水综合排放二级标准要求,无环境污染,具有良好的经济效益和社会效益。     

反渗透膜仓用韧性环氧树脂基体研究

工业上广泛使用反渗透膜仓制备高纯水,为了用玻璃钢替代不锈钢,研究了一种适合湿法缠绕的反渗透膜仓用韧性环氧基体。在配方中采用液体酸酐固化剂甲基四氢邻苯二甲酸酐和高效活性增韧剂,对树脂基体和复合材料力学性能及耐水性能的研究表明该树脂基体具有许多优良性能,如拉伸强度≥86.2MPa,断裂延伸率≥5.2%,弯曲强度≥139MPa,制得膜仓爆破时纤维强度转化率高达88.7%,耐疲劳达10万次而无损伤。此外,配方体系室温下粘度为0.35～0.4Pa·s,适用期≥8h,室温下在水中浸泡180d后吸水率低于0.5%,同不锈钢相比成本降低1/2。实验结果表明,该韧性环氧基体完全适用于反渗透膜仓使用。     

PAA-PSF交联复合膜的制备及对低浓度有机醇水溶液反渗透分离性能研究

进行了ＰＡＡ（ＰｏｌｙａｃｒｙｌｉｃＡｃｉｄ）－ＰＳＦ（Ｐｏｌｙｓｕｌｆｏｎｅ）交联复合膜的制备，研究了交联剂、添加剂对膜性能的影响，并通过扫描电镜观察了膜的断面结构．研究了ＰＡＡ－ＰＳＦ交联复合膜对低浓度有机醇类水溶液反渗透分离性能．发现对于１０００×１０－６乙醇水溶液截留率达到６６．２％，透过流束可达０．９×１０－６（ｍ３·ｍ－２·ｓ－１）．随醇的分子量的增加，截留率不断上升，对戊醇的截留率达９４．３％，而透过流束则保持相对稳定．对不同结构醇类的分离性能研究表明，截留率存在有：ｔｅｒｔ－＞ｓｅｃ－＞ｉｓｏ－＞ｎ－的规律．     

从制药废水中回收金霉素的研究

本文介绍用微孔管表面预涂助滤剂、反渗透浓缩技术从抗生素厂废水中回收金霉素的研究，取得了较好的效果。从而为抗生素厂金霉素废水提供一种新的治理途径。     

超滤-反渗透集成工艺处理玉米酒糟废水

研究了玉米酒精生产过程中产生的玉米酒糟废水的膜分离过程,开发了处理玉米酒糟废水的超滤-反渗透集成工艺。超滤选用截留相对分子质量为6 000的GR81PP膜平板分离器,入口压力控制为0.6 MPa,操作温度为50℃;反渗透选用标准脱盐率为90%的ESNAI-4040卷式膜分离器,入口压力控制为2.2 MPa,操作温度为40℃。反渗透透过液中蛋白质的平均截留率为94.70%,甘油的平均截留率为65.15%,COD值降到1 000 mg/L左右,可作为工艺回用水,而且反渗透浓缩液中可回收甘油等有用物质,超滤浓缩液可浓缩成饲料,节能效果显著。     

工业污水深度处理回用技术研究

通过对石化企业工业污水进行曝气生物滤池、连续微滤、反渗透等深度处理,使出水满足工业化用水的水质要求,从而得以回用。