纳米二氧化钛薄膜光催化剂的合成及特性

研究采用溶胶-凝胶技术以载玻片为基质制备了纳米TiO2薄膜,向溶胶中添加乙酰丙酮后改善了溶胶的稳定性及薄膜的牢固性。用扫描探针显微镜(DFM)、X射线衍射(XRD)、红外光谱(IR)及X射线光电子能谱(XPS)对薄膜进行了表征。结果表明:扫描探针显微镜(DFM)观察到薄膜中颗粒的粒径为20~40nm,X射线衍射(XRD)表明TiO2为锐钛型,用红外光谱(IR)表征了溶胶及粉末样品的物性并探讨了反应的机理,X射线光电子能谱(XPS)结果显示薄膜中除含有Ti、O元素外,还有少量从玻璃表面扩散至薄膜中的Na和Si元素。TiO2薄膜对光降解甲基橙水溶液具有很好的光催化性,通过掺SnO2、酸处理途径明显提高了其性能。     

TS系列水处理药剂在炼油企业的应用

介绍了TS系列水处理药剂在炼油企业循环水系统长期泄漏条件下的应用情况。实际监测结果表明,杀菌灭藻剂TS-781。缓蚀阻垢剂TS-50911在该条件下具有良好的清洗剥离和缓蚀作用,使企业取得了良好的经济效益。     

一体化锅炉水处理剂的制备及性能研究

利用自制SW-56共聚物，复配有机磷酸盐和焦亚硫酸钠除氧剂及消泡剂，成功制备XF-4一体化锅炉水处理剂。对XF-4锅炉水处理剂的阻垢、缓蚀进行了试验研究，表明其具有优良的阻垢能力，可以明显抑制热水锅炉积垢现象；加入改性除氧剂能降低锅炉水中溶解氧的含量，使腐蚀控制较理想；配方中的消泡剂组分可防止锅炉水表面起泡，抑制高悬浮物下的携带作用。     

高浓度成衣水洗染色废水的处理

采用混凝沉淀-水解-接触氧化-气浮-沉淀工艺处理高浓度成衣水洗染色废水,设计规模为6000m^3／d。处理后,CODcr、BOD5、SS和色度的去除率分别达到92．6％、94．2％、90．4％、94．6％,总排放口水质：pH=7．07,CODcr=93mg／L,BOD5=22．8mg／L,SS=50mg／L,色度为16倍。     

新型反应器-USSB处理生活污水的研究

对上流式分段污泥床(UpflowStagedSludgeBed)反应器在中温(35±2℃)下厌氧处理生活污水进行了试验研究。反应器内污泥经过40d的培养驯化后,用于处理生活污水。重点探讨了不同停留时间(HRT)对COD和SS去除率等的影响,并考察了反应器各段间微生物相的变化情况。结果表明,当水力停留时间为4.7h时,其出水pH=6.5,COD和SS的去除率分别在52%和70%以上,有较好的运行效果。     

好氧颗粒污泥同步除磷脱氮研究的新进展

结合近年来国内外除磷脱氮的最新研究成果,对好氧颗粒污泥除磷脱氮的机理及工艺进行了探讨和研究。研究表明通过适当的SBR定向培养,可以在颗粒污泥中培养出不同的微生物菌群(硝化菌、反硝化菌、聚磷菌、反硝化聚磷菌等),使其能够实现同步除磷脱氮,从而为污水生物除磷脱氮工艺研究提供了一个新思路。     

Modeling of the drying process in paper plants

In this study a model for the drying process in paper production plants was developed based on the mass and heat balances around drying cycles. Relationships for the heat transfer coefficients between the web and the air as well as between the drying cylinder and the web were extracted from the closed-loop plant operation data. It was found that the heat transfer coefficients could be represented effectively in terms of moisture content, basis weight and reel velocity. The effectiveness of the proposed model was illustrated through numerical simulations. From the comparison with the operation data, the proposed model represents the paper plant being considered with sufficient accuracy.     

Effect of degree of polymerization on gelation and flow processability of poly(vinyl chloride)

The effect of degree of polymerization (DP) on the gelation and flow processability of poly(vinyl chloride) (PVC) was studied. Sheets with adjusted degree of gelation were prepared by rolling rigid pipe formulation suspension PVC compounds with DPs of 800, 1050 and 1300 by changing the milling temperature. Their degrees of gelation were measured with DSC and their capillary flow properties were measured with a capillary rheometer at 150, 170 and 190°C and the effect of DP on the relation between gelation and flow processabilities was studied. Because of the higher shearing heat during milling, the sample with the higher DP had a higher history temperature and thus tended to show a higher degree of gelation. The viscosity increased as the gelation increased. The dependency of viscosity on DP was higher at higher milling and extrusion temperatures and thus at a higher degree of gelation and a lower shear rate. This was assumed to be attributed to the more prominent uniform molecular flow as against the particle flow. The die swell increased with increasing the milling and extrusion temperatures and hence with increasing the gelation. A sample with a lower DP tended to show a larger die swell and this tendency was even more pronounced at the higher extrusion temperature. The melt fracture easily occurred when a sample with advanced gelation was extruded at low temperature. Whereas at low milling temperatures a sample with the lower DP showed a lower critical shear rate at onset of melt fracture, and thus easily generating melt fracture, at high milling temperatures it showed a higher critical shear rate and hence scarcely generated melt fracture. These experimental results were explained by the fact and concept that a sample with a lower DP shows a higher increase in the gelation during extrusion and/or the slighter feature of particle flow as against the uniform molecular flow at the same gelation level. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1915–1938, 2004     

Study on processing of ultrahigh molecular weight polyethylene/polypropylene blends

The processing of ultrahigh molecular weight polyethylene (UHMWPE) by the addition of polypropylene (PP) and high‐density polyethylene (HDPE) was investigated. The results show that the addition of PP improves the processability of UHMWPE more effectively than does the addition of HDPE. UHMWPE/PP blends can be effectively processed with a twin‐roller and general single‐screw extruder. In the extrusion of UHMWPE/PP blends, PP is enriched at the surface of the blend adjacent to the barrel wall, thus increasing the frictional force on the wall; the conveyance of the solid down to the channel can then be carried out. The melt pool against the active flight flank exerts a considerable pressure on the UHMWPE powder in the passive flight flank, which overcomes the hard compaction of UHMWPE. The PP penetrates into the gaps between the particles, acting as a heat‐transfer agent and adhesive, thus enhancing the heat‐transfer ability in the material. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 977–985, 2004     

Structural changes and mechanical performance of recycled poly(vinyl chloride) bottles exposed to ultraviolet light at 313 nm

The structural changes and mechanical performance of virgin poly(vinyl chloride) (PVC) bottle (VB) compounds blended with postconsumer PVC bottles collected from a specified factory (RB‐F) and houses (RB‐H), were examined before and after UV irradiation at 313‐nm UV wavelength for different periods of time up to 28 days. The results indicated that, when exposed to UV light, the RB‐F/VB blends containing greater conjugated double bonds with higher yellowness index appeared to exhibit better mechanical performance than that of the RB‐H/VB blends. It was found that the amount of conjugated double bonds was not a linear function of the discoloration level of PVC compounds. Tensile strength of the VB compounds was not affected when incorporated with RB‐F recyclate, but progressively decreased with increasing RB‐H recyclate. An optimum concentration for RB recyclates to be added into the virgin compound was recommended for obtaining a maximum impact strength. Both tensile and impact strengths decreased with increasing UV exposure time, a severe degradation being obvious after a UV exposure time of 21 days. Hardness was not affected significantly by the addition of PVC recyclate, but increased with increasing UV exposure time. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 84–94, 2004