Influence of Mg concentration on structural,morphological and optical properties of nanoceria

Nano crystalline pure and Mg doped ceriaparticles were synthesized by simple chemical co-precipitation method using cerium nitrate hexahydrate as a source material and magnesium nitrate as doping precursor at room temperature. The effect of doping were investigated by X-ray diffraction pattern(XRD), FT-Raman,fourier transform infrared spectroscopy(FTIR), Ultraviolet spectroscopy(UV), photoluminescence spectroscopy(PL), field emission scanning electron microscope(FESEM) and high resolution transmission electron microscopy with energy dispersive spectroscopy (HRTEM &EDS). The X-ray diffraction pattern and FT-Raman studies showed that the prepared samples were nano particulates with cubic fluorite structure. The XRD pattern analysis showed that the size of the particles ranged from 13 to 20?nm, however 4?wt% Mg doping results in reduction of particle size compared with other doping concentrations. The effects of Mg concentration on various structural parameters of the prepared samples were also determined. The slight blue shift observed upon doping in UV–Vis absorption region around 330–360nmrecorded for reduction in particle size. The FTIR unveils the presence of Metal oxygen bonds below 700?cm^?1in the prepared samples. All samples showed a broad emission band at 430?nm with linearly increasing intensity with respect to dopant concentrations. The Spherical morphology with weak agglomeration was identified through FESEM and HRTEM analysis. The elemental analysis of Ce, O and Mg were confirmed through EDS analysis.     

湿法炼锌赤铁矿法沉铁行为

湿法炼锌工艺过程中赤铁矿法沉铁技术是一种沉淀渣量小、分离效率高的锌、铁分离方法。针对湿法炼锌工艺过程中赤铁矿法沉铁技术开展了硫酸亚铁的氧化水解沉淀行为的研究，考察了时间、酸度、温度、硫酸盐浓度、晶种返回量等主要因素对赤铁矿法沉铁效果的影响、沉淀产物的析出特性和物相表征。     

Preparation of Aqueous Nanodispersions of Disperse Dye by High-Gravity Technology and Spray Drying

Disperse dyes are poorly water-soluble and difficult to stably disperse in an aqueous medium, which greatly limits their application in dyeing synthetic fibers. Micronization can solve this problem. Herein, a facile way to prepare stable aqueous nanodispersions of disperse dye (C.I. disperse yellow 54) is presented by combining high-gravity antisolvent precipitation in a rotating packed bed (RPB) with spray drying. The as-prepared product had an average particle size of 120 nm, which could be readily redispersed in water. Compared with raw dye, the wettability and dispersibility of disperse dye nanoparticles were remarkably improved. Furthermore, the dyeing properties of the nanodispersions were obviously better than those of the commercial dye, which was micronized by ball milling.     

化学沉淀-吸附法处理电镀废水的研究

采用化学沉淀-吸附法处理电镀废水。首先,采用沉淀剂MgSO4・7H2O和NazHPCX・12H2O对电镀废水进行化学沉淀处理。在优化条件下,氨氮的质量浓度由1600 mg/L降低至80 mg/L以下,磷的质量浓度为75.82 mg/Lo然后,采用吸附法对电镀废水做进一步处理。最终电镀废水中氨氮和磷的残余质量浓度均达到《电镀污染物排放标准》(GB 219002008)中规定的要求。     

钙化-酸浸提钒沉钒母液中锰的回收

对钙化?酸浸提钒沉钒母液中锰资源的回收，一方面可以提升提钒工艺的经济效益，另一方面可避免母液循环时锰浓度不断累积而影响氧化钒产品质量，从而有助于实现母液闭路循环而提升全流程的环境效益。本工作提出了采用草酸沉淀法高效回收沉钒母液中的Mn2+，考察溶液体系pH值、草酸加量系数、反应温度和时间对锰回收率及沉淀产物物相组成的影响，以及草酸沉淀分离锰后母液的循环次数对钒浸出过程的影响。结果表明，草酸沉淀法可高效分离沉钒母液中的Mn2+，在溶液体系pH=4.0、草酸加量系数为1.5、反应温度为50℃、反应时间为60 min的条件下，锰回收率达94.33%，所得产物为纯度大于98%的水合草酸锰，为片状晶体，并呈花簇状生长。将脱锰后的沉钒母液循环至酸浸段，对钒浸出率及浸出液中锰的浓度没有明显影响，表明该方法有助于实现钙化?酸浸提钒中废水的闭路循环。     

碳化钒析出对X80管线钢焊接热影响区韧性的影响

通过Gleeble-3500热模拟机对钒(V)含量分别为0.06%和0.02%的X80管线钢进行了峰值温度为1350℃和750℃的焊接热模拟试验,利用硬度计和光学显微镜(OM)分别分析了焊接热模拟试样硬度和试样中马氏体-奥氏体岛状组织(M-A)的数量、尺寸和形貌。利用透射电镜(TEM)对母材、粗晶区和部分相变区中粒子析出进行了表征。结果表明,与0.02%含V量X80管线钢相比,0.06%含V量的X80管线钢由于V含量较高,在受到多道次焊接热循环影响时,部分相变区有较大量碳化钒(VC)粒子析出,明显阻碍位错运动,使其强度明显提高的同时脆性增大、塑性变形难以进行,导致其焊接热影响区韧性下降。     

Precisely Controlled Microsphere Design via Visible‐Light Cross‐Linking of Functional Prepolymers

A new strategy for particle synthesis is enabled by utilizing modern synthetic, polymer, and photochemical techniques to facilitate the synthesis of highly narrow–disperse multifunctional microspheres from visible‐light induced crosslinking of prepolymers in both a single and dual polymer system. The approach requires no stabilizers, bases, or initiators, and proceeds at ambient temperature to yield microspheres with a tunable size range (0.25–5 µm) in less than 4 h, depending largely on solvent composition, but also polymer concentration (2–10 mg mL^?1), ratio, and irradiation intensity (3–20 W). Critically, the visible‐light induced dimerization reaction exploited herein enables simple functional particle syntheses via a single polymer system. Underpinned by an in‐depth kinetic analysis of the particle formation as well as a detailed small molecule study, the mechanism for particle formation is also elucidated. Importantly, inherent advantages of the system are exploited for surface functionalization of residual acrylate and hydroxyl groups (generating inherently fluorescent particles).