钢铁企业多源废水处理与再生回用集成技术

为解决长期困扰企业的水资源紧缺和水质差的问题,设计建设了多源废水处理与再生回用工程.该工程以钢铁废水、生活污水、工业废水、雨水等非常规水源为处理对象,处理出水分质回用于厂区生产工艺用水和循环冷却水系统补充水,使企业年节水量迭1 095万t,年COD、BOD、NH3-N以及TP等污染物减排量分别达1 300t、170t、500t及16t.     

污水处理厂出水的聚硅硫酸铝铁混凝除磷研究

研究新型混凝剂聚硅硫酸铝铁(PSFA)对城市污水处理厂出水中磷的混凝去除效果,考察了混凝剂投加量、原水pH、与聚丙烯酰胺(PAM)复配等因素对混凝除磷效果的影响,同时进行了聚合氯化铝(PAC)、聚合硫酸铁(PFS)和Al2(SO4)3混凝除磷效果的比较试验。结果表明,PSFA可有效降低城市污水处理厂出水TP含量,当投加量为36mg·L-1时,可以使出水TP的质量浓度从1.51mg·L-1下降到0.32mg·L-1,出水达到上海市地方标准DB31/199-2009规定的TP排放一级标准;PSFA混凝除磷适宜pH为6～10;PAM可以有效提高PSFA混凝除浊和除磷效果,减少混凝剂投加量;PSFA比PAC、PFS、Al2(SO4)3具有更好的混凝除磷效果,具有很好的应用前景。     

焦化废水MBR深度处理试验研究

采用多孔聚合物载体内循环一体式膜生物反应器对二级生化处理后的焦化废水进行深度处理试验,以达到目的.结果表明,采用间歇进水、间歇曝气出水的运行方式,当进水COD在120～320 mg·L-1,在人工配水中添加焦化废水比例为50.0％时,平均COD去除率可达75.0％,出水COD最低为46.9 mg·L-1,当完全使用焦化废水时,出水COD升高到132.8 mg·L-1,继续采用Fenton氧化处理后出水COD低于75 mg·L-1;反应器对于人工配水的TN去除率达79.1％,但对于焦化废水的TN去除效果较差;载体的加入对反应器的稳定运行和减少膜污染具有重要作用.一体式膜生物反应器可用于新建或改造已建二级生化处理的焦化废水系统.     

壳聚糖絮凝剂在水处理中的应用研究进展

介绍了壳聚糖及其衍生物作为水处理絮凝剂的优势,探讨了其絮凝机理,并总结了壳聚糖及其衍生物作为絮凝剂在饮用水、城市污水、工业废水以及污泥处理中的应用研究现状.在此基础上,为壳聚糖及其衍生物作为絮凝剂的进一步研究提出了意见和建议.     

金属离子印迹改性壳聚糖对水中Ni2+的去除研究

利用金属Ni2+印迹法,通过交联和胺化反应自制Ni2+印迹改性壳聚糖吸附剂小球(P-C-CTS(Ni)),通过比较中间产品的含水率、吸附容量及FT-IR谱,分析壳聚糖在改性过程中的反应机理,验证吸附剂P-C-CTS( Ni)合成路线的正确性,并证明交联前对壳聚糖分子中的活性氨基进行保护的必要性.低浓度Ni2+(CNi=0.852 mmol·L-1)条件,考察不同酸度下吸附容量的变化和酸度对水中低浓度Ni2+去除率的影响规律.结果表明,酸度对P-C-CTS(Ni)去除重金属Ni2+效率的影响显著,酸度对Ni2+去除率的影响规律与对吸附容量的影响基本一致,并对吸附机理进行深入分析.P-C-CTS(Ni)在经过“吸附-脱附-再生”8次循环,颜色与外观等基本不变,重复使用性能稳定.     

Preparation of raspberry‐like poly(methyl methacrylate) particles by seeded dispersion polymerization

The facile preparation of nonspherical raspberry‐like poly(methyl methacrylate) (PMMA) particles by seeded dispersion polymerization of methyl methacrylate (MMA) on micron‐sized PMMA seed particles was described. Various polymerization parameters influencing the particle morphology, as well as the polymerization kinetic and morphological stability, were investigated in detail. It was found that the following polymerization conditions were necessary to prepare this kind of nonspherical particles: a relatively low temperature, an appropriate ratio of seed/MMA, an initiator with a relatively low decomposition rate, and a relatively low initiator concentration. These particles showed very good morphological stability at room temperature, but they changed to the spherical ones when heat treated at 60°C in methanol solution of MMA. The experimental results suggest that the prepared PMMA particles were kinetically favored and the localized polymerization of the MMA monomer on PMMA seed particle surface was responsible for the formation of the raspberry‐like particles. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

High transmittance and environment‐friendly flame‐resistant optical resins based on poly(methyl methacrylate) and cyclotriphosphazene derivatives

Highly transparent optical resins based on poly(methyl methacrylate) (PMMA) and two cyclotriphosphazene derivatives which acting as halogen‐free flame retardants were prepared. The refractive indices, visible light transmittance, water absorption, flame‐resistant characteristic, and the mechanical properties of the resins were studied. Comparing with pure PMMA, the as‐prepared resins with the two additives exhibited higher refractive index (n_d), longer UV cutoff wavelength and better surface hardness. The water absorption of the resins was decrease with increasing of the additives. The visible light transmittance of all the samples adding Additive A was higher than 90%. When the weight ratio of additive/MMA was 20/100, the limiting oxygen index (LOI) of the samples were 26 (with Additive A) and 22 (with Additive B), respectively. The surface hardness was increased from HB to 2H with increasing the content of the additives, and the impact and the tensile strength changed little for the formulas of the additives lower than 30% by weight. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

The failure behavior of a polyurethane composite coating in 3.5% NaCl solution under ultraviolet irradiation

The failure process of inorganic zinc‐rich/micaceous iron oxide epoxy/aliphatic polyurethane composite coating in 3.5% NaCl solution under ultraviolet irradiation (UV) was studied with electrochemical impedance spectroscopy (EIS) and Fourier transform infrared (FTIR) spectroscopy. UV irradiation significantly accelerated failure process of the composite coating in NaCl solution. The effect of UV on failure process of the coating system in 3.5% NaCl solution may be divided into two stages: in the early stage, the thermal effect generated by the ultraviolet irradiation is the main reason leading to the increase in coating porosity, but this effect is not serious and the coating remains high impedance and good protection ability. In the latter stage, the fracture of polymer chains in the top coating by UV irradiation is the main factor resulting in quick decrease of coating performance. C N and C O bonds in polyurethane coating are broken by UV irradiation, leading to quick increase of the coating porosity and decrease of the coating resistance. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Surface,tribological, and mechanical characterization of synthetic skins for tribological applications in cosmetic science

Synthetic skin as an ideal human‐tissue substitute is needed for the research and assessment of hair‐ and skin‐care products. In this study, a systematic study was carried out of the surface, tribological, and mechanical properties of two synthetic skins and rat skin with and without skin‐cream treatment with scanning electron microscopy, atomic force microscopy, and a nanoindenter. The film thickness, adhesive force, coefficient of friction, surface roughness, and contact angle of the two synthetic skins and rat skin were comparable. The hardness of one synthetic skin was more similar to rat skin. After treatment with skin cream, the trends of the properties of the two synthetic skins and rat skin were similar. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

The formation of β‐polypropylene crystals in a compatibilized blend of isotactic polypropylene and polyamide‐6

Compatibilized polypropylene (PP)/polyamide (PA6) blends with and without β nucleating agent (β‐NA) are prepared, and are designated as Blend‐0.3 and Blend‐0, respectively. The melting and crystallization characteristic of the blends crystallized under different cooling rates and different crystallization temperatures are studied. It is observed that high β‐PP content can be developed in Blend‐0.3 only at slow cooling rates (<5°C/min), whereas high α‐PP content is formed at fast cooling rates. Isothermal crystallization analysis of Blend‐0 indicates that PA6 is an effective NA for α‐PP in the lower temperature range, whereas the α‐nucleating effect disappears in the higher temperature range. Blend‐0.3 can, therefore, be viewed as a system containing both α‐ and β‐NAs, simultaneously. PA6 is competing with β‐NA in inducing PP crystallization. Under the normal injection of Blend‐0.3, the melt will be cooled through the higher temperature that favors the effectiveness of β‐NA rapidly because of the faster cooling rate. However, the α‐nucleation effect from PA6 predominate at the lower temperature. This explains the difficulty in obtaining high β‐PP content in Blend‐0.3 from injection molding. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers