纳米二氧化锰的制备及其对亚甲基蓝的吸附研究

利用微乳液还原法,用甲苯还原KMnO4制得纳米MnO2。借助傅立叶红外光谱(FTIR)、扫描电镜(SEM)等手段对其结构性质进行了表征。通过吸附试验研究了溶液pH、煅烧温度、染料初始质量浓度对纳米MnO2吸附亚甲基蓝效果的影响。结果表明,所得纳米MnO2为球型颗粒,其粒径范围为50～80 nm,比表面积大,表面存在大量活性-OH基团,对亚甲基蓝有较强的吸附作用及较强的催化氧化降解能力;在酸性环境下,纳米MnO2对亚甲基蓝的去除能力随pH增大、煅烧温度的升高而呈现减弱趋势。pH=3时,未经煅烧的纳米MnO2对亚甲基蓝去除率高达98.4%,符合Langmuir模型。     

泡沫镍负载二氧化钛光电协同催化氧化砷

通过化学复合镀的方法制备成催化材料,TiO2粉末与镍磷合金共沉积在泡沫镍表面上,并通过光、电催化的方法将3价砷(As(III))氧化为5价砷(As(V))进行吸附试验。结果表明,As(III)吸附在7 h后达到平衡,As(V)吸附在5 h后达到平衡;As(III)和As(V)的吸附动力学与拟2级动力学特征相一致。在光催化、电催化和光电催化3种氧化As(III)的方法中,光电催化的效果最好;当As(III)的初始质量浓度为1 mg/L时,使用光电催化方法的除砷率能达到80.76%。     

西北地区人工湿地处理效果影响因素试验研究

针对北方地区冬季气候寒冷的特点,在对基质材料、填料深度、填料结构、布集水系统和水位调整、导淤方式进行优化创新的基础上,建造了垂直潜流人工湿地中试模型;并采取了预处理与人工湿地组合工艺调节各季节运行效果;经过两年多的连续运行试验,研究了模型湿地运行的工艺条件(深度、水力负荷、污染负荷)。为寒冷地区人工湿地的设计、运行管理提供了可供参考的经验和数据。     

软粘土的次固结变形特性

在笔者所改装的应力式三轴压缩仪和一维压缩仪上,用杜湖、杭州和萧山三种粘土做了一定数量的固结试验。基于这些试验资料的分析,提出了一种新的主、次固结变形划分法,同时还探讨了固结应力和应力比对次固结系数的影响、固结后期的孔隙水压力、高载增量比对次固结变形比例的影响。根据室内外试验资料,分析了主固结阶段的粘滞蠕变效应。结果表明,主固结阶段的粘滞变形很不显著,可忽略不计。     

给矿粒度对棒磨产品粒度分布和能耗的影响

使用装有扭矩测试系统的半工业规模棒磨机,研究了磨机给矿粒度和分批作业磨矿机时间对棒磨产品粒度分布及能量消耗的影响;讨论了棒磨机中的粒度选择性磨矿现象.     

紫穗槐碱法纸浆的漂白性能研究

紫穗槐烧碱—蒽醌浆的实验室漂白的研究表明,其白度可达到生产一般书写纸和有光纸的要求。采用常规次氯酸盐单段或次氯酸盐两段漂白,白度能达到66—70°。研究中发现,碱法紫穗槐浆的硬度对漂白的影响最大,当硬度为高锰酸钾值14～16时,其漂率相当于麦草浆的漂率。研究中还发现,选用HA—P(次氯酸盐/酸处理—过氧化氢)法漂白时,也能获得较好的白度。     

单片机在H^＋—ISFET PH计中的应用

本文是单片机氢离子敏场效应管pH计的研制总结。文中论述了把单片机应用于氢离子敏场效应管pH计中的数学模型和实现方法,以及软件、硬件的组成方式等。     

Isothermal crystallization kinetics and subsequent melting behavior of β‐nucleated isotactic polypropylene/graphene oxide composites with different ordered structure

The effects of ordered structure on isothermal crystallization kinetics and subsequent melting behavior of β‐nucleated isotactic polypropylene/graphene oxide (iPP/GO) composites were studied using differential scanning calorimetry. The ordered structure status was controlled by tuning the fusion temperature (T_f). The results showed that depending on the variation of crystallization rate, the whole T_f range could be divided into three regions: Region I (T_f > 179 °C), Region II (170 °C ≤ T_f ≤ 179 °C) and Region III (T_f < 170 °C). As T_f decreased from Region I to Region III, the crystallization rate would increase substantially at two transition points, due to the variation of the ordered structure status. Calculation of Avrami exponent n indicated that the ordered structure induced the formation of two‐dimensional growing crystallites rather than three‐dimensional growing crystallites. Moreover, in the case of isothermal crystallization, the ordered structure effect (OSE) can also greatly increase the relative content of β‐phase (β_c). In Region II, OSE took place, resulting in evident increase of β_c, achieving 92.4% at maximum. The variation of the isothermal crystallization temperature (T_iso) had little influence on the T_f range (Region II) of the OSE. The higher T_f in Region II was more favorable for the formation of higher β_c. The ordered structure was favorable for the improvement of the nucleating efficiency of β‐nucleating agent (β‐NE), and was more effective for the improvement of lower β‐NE. © 2018 Society of Chemical Industry     

The effect of BaTiO3 addition on the dielectric constant of Si3N4 ceramics

Si₃N₄ ceramics with different BaTiO₃ contents have been fabricated by pressureless sintering in a N₂ atmosphere at 1680°C for 2 h. Al₂O₃ and Nd₂O₃ were used as sintering additives to promote the densification of Si₃N₄ ceramics. The effect of BaTiO₃ addition on the densification, mechanical properties, phase compositions, microstructure, and dielectric properties of Si₃N₄ ceramics was investigated. The relative density and flexural strength of Si₃N₄ ceramics increased with the addition of BaTiO₃ up to 15 wt% and then decreased, while the dielectric constant increased continuously as the BaTiO₃ contents increased. The dielectric constant of Si₃N₄ ceramics can be tailored in the range from 8.42 to 12.96 by the addition of 5 wt%‐20 wt% BaTiO₃. Meanwhile, these Si₃N₄ ceramics all had flexural strength higher than 500 MPa.     

Assessment of conversion efficiency of Cr4+ ions by aliovalent cation additives in Cr:YAG ceramic for edge cladding

0.25at.% Cr:YAG ceramics were successfully fabricated as the edge cladding of Yb:YAG transparent ceramic slabs through vacuum sintering of co‐precipitated powders, using oxide additives to introduce different cations. The effects of various cation additives (Si⁴⁺, Ca²⁺, and Si⁴⁺ + Ca²⁺) on the conversion efficiency of Cr⁴⁺ ions and optical characteristics of the Cr:YAG edge cladding were investigated. Measurements of the absorption spectra of the Cr:YAG ceramics without any additives revealed 2 absorption bands centered at 430 nm and 600 nm, which imparted the sample with a green color. The introduction of only Si⁴⁺‐bearing additive did not promote the transition of Cr ions from the 3+ to 4+ state. Theoretical analysis and experimentation revealed that the addition of CaO not only enhanced the microstructure and improved the transmittance of the Cr:YAG ceramic, but also introduced vacancies that assisted in the formation of Cr⁴⁺ ions. It was determined that CaO has the same effect on the conversion efficiency of Cr⁴⁺ ions whether it is added as a single additive or in combination with SiO₂. The underlying mechanisms by which these aliovalent cation additives influence the formation of Cr⁴⁺ ions and affect optical properties are discussed in detail. High quality composite ceramics with Yb:YAG transparent ceramic slabs and dark brown‐colored Cr⁴⁺: YAG ceramic edge cladding were achieved through the addition of 0.05 wt.% CaO to the edge cladding, with no interfacial effects between the 2 regions being observed.