Effects of typical additives on the thermal stability of ammonium peroxydisulfate

Ammonium peroxydisulfate (APS), one of the most widely used inorganic peroxides in the process industries, is a thermally unstable peroxide and potent oxidizer due to the presence of peroxy bond in the molecule and is incompatible with most substances. To investigate the effect of typical additives on the thermal decomposition of APS, in this paper, diamine phosphate (DAP), monoamine phosphate (MAP), and aluminum hydroxide (AH) were selected as additives; pure APS and samples with 10 wt% and 20 wt% of additives were first tested by differential scanning calorimetry (DSC). The experiments and analysis showed that the samples with 10 wt% of additive had better thermal stability than those with 20 wt% of additive. After screening, the three groups of 10 wt% AH, 10 wt% MAP, and 20 wt% MAP additive conditions could be considered to have a better thermal stability effect on the thermal decomposition of APS. Four groups of samples were, in turn, tested by Phi-Tec II. The adiabatic results showed two discontinuous exothermic processes; 10 wt% AH promoted the weak exothermic effect in the first stage. In contrast, the three groups of additives in the main exothermic stage showed different degrees of inhibition, and the inhibiting effect was ranked as 10 wt% AH, 10 wt% MAP, and 20 wt% MAP in order. Finally, the self-accelerated decomposition temperature (SADT) was calculated under the 25 kg standard package. The adiabatic results, including SADT, were combined to render feasible recommendations for the use of additives, which provides references for the packaging and transportation of additives and their applications.     

福建省生产废水和生活污水污染物排放的驱动力及其时空分异

采用对数平均迪氏指数方法,区分生产和生活两个体系,构建时空分解分析模型,追踪了福建省9个设区市2011—2019年水污染物排放变化的关键驱动力及其贡献的时空差异.结果显示：研究期内福建省工业废水污染物排放持续减少,并且各驱动力贡献的区域差距明显变小,趋于平衡;生活污水污染物排放量仍保持高位,各驱动力贡献的区域差距基本保持不变.其中,经济规模扩张是福建省水污染物排放的主导驱动力,主要源于福州、厦门、泉州经济赶超发展影响;城镇化发展对区域生活污水污染物排放的驱动影响表现为增排效应,以福州和厦门尤为显著;工业化发展对区域工业废水污染物排放的影响效应由正驱动逐渐转变为负驱动,这主要归功于三明和泉州产业结构调整优化的拉动 效应;技术效应一直是福建省水污染物排放控制的重要驱动力,但部分地区已逐渐步入生活污染物技术减排攻坚期.     

氧氟沙星敏化光解磺胺甲恶唑

抗生素是环境中广泛存在的一类新兴污染物,因其可诱导细菌抗药性及产生抗性基因而备受关注.本研究发现氟喹诺酮类抗生素具有的光化学活性,可能影响共存的磺胺类抗生素（SAs）的转化.系统考察了一种典型的氟喹诺酮类抗生素—氧氟沙星（OFLO）对磺胺甲恶唑（SMX）的光化学转化.结果表明,在365 nm紫外光照条件下,OFLO可以有效敏化光解SMX.激发三重态（³OFLO^*）是促进SMX光解的主要活性物质.密度泛函理论（DFT）计算结合高分辨率质谱（HRMS）分析表明,³OFLO^*将SMX分子中的氨基氮氧化成一个自由基阳离子（R-NH₂^?+）.该自由基阳离子可水解生成羟胺衍生物,并进一步氧化生成亚硝化和硝化产物.此外,它们也可以二聚生成偶氮产物.光反应过程中,敏化剂OFLO也发生了降解.但OFLO的光解产物均保留了核心喹诺酮结构,因此也保留了OFLO分子的光敏活性.该研究有助于进一步了解抗生素复合污染情况下的环境行为,具有重要的环境意义.     

长江三角洲创新发展空间溢出效应的测度与分解

一体化深化背景下,准确把握城市群创新互动关系,对于推动高质量发展具有重要现实意义。空间溢出是创新发展互动关系重要体现之一,基于城市尺度数据、空间计量方法,对长江三角洲创新发展空间溢出效应进行多角度研究。主要结论如下：（1）城市创新发展存在显著为正的空间溢出效应,创新人才、资金投入、经济发展、交通设施和对外开放等都是创新发展重要驱动因素,但不同因素空间溢出效应存在差异。（2）不同区域、不同时期对比发现,创新发展空间溢出效应存在显著差异,如区域对比核心区时间演变明显增强等。（3）空间溢出效应随距离增加呈现“倒U型”演变趋势,且这一效应在325 km处最大,而后空间溢出效应的缓慢波动下降与中心城市相对均衡分布有关。本文为识别城市创新发展互动关系提供了新视角,对推动城市群创新发展、一体化深化等具有现实指导意义。     

偶极子探头的低频特性分析

宽带电磁探头是电磁兼容测量中的一个重要器件。对宽带探头进行分析需要求解矩阵方程。对于目前所用的计算电磁学全波方法,当在低频计算的时候,会遇到阻抗矩阵奇异性的问题。针对低频阻抗矩阵奇异性问题,采用奇异值分解的方法求解矩量法方程。对比广义本征值方法,计算仿真分析表明,奇异值分解方法与广义本征值方法一样,可以有效地解决低频奇异性的问题。     

钼冶炼工艺的循环经济探讨

钼是重要的稀有金属之一,主要通过氧化分解辉钼矿来提取。我国普遍使用反射炉、回转窑等焙烧设备生产氧化钼,造成了严重的SO2污染和资源浪费问题。为改变辉钼矿焙烧分解工艺的污染状况,硝酸高压分解、碱性高压氧分解、次氯酸钠分解和电氧化分解等辉钼矿湿法工艺相继被开发出来。但是这工艺往往只关注在如何获取金属钼等资源,而忽视了辉钼矿中占40%的硫资源。从循环经济角度分析了不同辉钼矿分解工艺的物质流向,探讨符合清洁生产和循环经济精神的工艺革新方向,提出了纯氧氧化焙烧和浓硫酸氧化两种新工艺。     

Novel Co-Mg-Al-Ti-O catalyst derived from hydrotalcite-like compound for NO storage/decomposition

Catalysts of Co_1.5Mg_1.5/Al_0.9Ti_0.1O and Co_1.5Mg_1.5/AlO were successfully prepared by calcinations of corresponding hydrotalcite-like compounds at 800℃ for 4 hr. The derived oxides were of spinel phase and a small quantity of Ti substitution did not change the crystal purity. Their catalytic performance for the NO storage/decomposition was investigated. Ti incorporation enhanced the NO decomposition activity while has an opposite effect on the storage capacity of catalyst. In situ FT-IR spectra of the catalysts showed that the final adsorption species on the catalysts was coordinated nitrates/nitrites. In addition, NO storage/decomposition mechanism has been discussed on the basis of these observations.     

闽江口秋茄红树林凋落物产量及分解动态

于2017年以闽江口粗芦岛秋茄(Kandelia obovata)红树林为研究对象,分别采用凋落物收集框和分解袋法,研究秋茄凋落物产量及其碳(C)、氮(N)、磷(P)含量月动态及凋落叶分解过程中C、N、P含量与水解酶活性.结果表明:①秋茄凋落物年产量为618.79 g·m~(-2)·a~(-1),其中,叶占61.2%,果、枝和花分别占23.7%、10.5%和4.6%.②凋落叶总氮(TN)含量8月显著高于其他月份(p0.05),而TP含量在1—3月显著高于其他月份;C/N在8月显著低于其他月份(p0.05),而C/P及N/P在9月显著升高(p0.05).③在凋落叶分解过程中,C、N、P含量及其化学计量比随时间存在明显差异(p0.01),并且地上组TC、TN、C/N和C/P明显不同于地下组(p0.05).④在分解过程中,4种水解酶随时间存在明显差异(p0.01).⑤凋落叶酸性磷酸酶活性与土壤温度、电导率和凋落叶TP含量存在显著相关关系(p0.01).这些结果说明,秋茄凋落物产量及元素含量随季节变化存在明显差异;沉积作用对凋落叶分解过程中元素含量有显著影响,水解酶活性主要受凋落叶元素含量和土壤环境因子的控制.     

基于数据分解的AQI的CEEMD-Elman神经网络预测研究

针对Elman神经网络在预测空气质量指数（AQI）时易受到数据非平稳性的影响导致预测趋势良好但准确度较低的问题,提出以互补集合经验模态分解（Complementary Ensemble Empirical Mode Decomposition,CEEMD）为基础的CEEMD-Elman模型.应用CEEMD对AQI序列分解成不同时间尺度上的本征模态函数分量和剩余分量,进而首次将对非平稳的AQI序列的预测研究转化为对多个平稳的本征模态函数分量的研究.分别与Elman单一模型、EMD-Elman模型、BP单一模型及CEEMD-BP模型进行实验对比.结果表明：应用该方法建立的模型的均方误差、平均绝对误差和平均绝对百分比误差分别为4.80、0.71、1.84%,均小于其他模型结果;对应空气质量等级预报正确天数的频率为94.12%.该模型能有效的降低非平稳性对实验预测结果的影响,实现对空气质量等级的准确预报;该研究为进一步预测AQI的走向提供了有效依据,也为政府决策和管理部门制定空气污染控制提供了更充分的参考.     

Facile synthesis of Ag-modified manganese oxide for effective catalytic ozone decomposition

O₃ decomposition catalysts with excellent performance still need to be developed. In this study, Ag-modified manganese oxides (AgMnO_x) were synthesized by a simple co-precipitation method. The effect of calcination temperature on the activity of MnO_x and AgMnO_x catalysts was investigated. The effect of the amount of Ag addition on the activity and structure of the catalysts was further studied by activity testing and characterization by a variety of techniques. The activity of 8%AgMnO_x for ozone decomposition was significantly enhanced due to the formation of the Ag_1.8Mn₈O₁₆ structure, indicating that this phase has excellent performance for ozone decomposition. The weight content of Ag_1.8Mn₈O₁₆ in the 8%AgMnO_x catalyst was only about 33.76%, which further indicates the excellent performance of the Ag_1.8Mn₈O₁₆ phase for ozone decomposition. The H₂ temperature programmed reduction (H₂-TPR) results indicated that the reducibility of the catalysts increased due to the formation of the Ag_1.8Mn₈O₁₆ structure. This study provides guidance for a follow-up study on Ag-modified manganese oxide catalysts for ozone decomposition.