改性生物炭负载纳米零价铁活化过硫酸盐降解活性蓝19的机理及老化研究

采用磷酸改性的黍糠基生物炭作为纳米零价铁(Nanoscale zero-valent iron,nZVI)载体,成功制备出一种高效非均相活化材料一磷酸改性生物炭负载纳米零价铁(nZVI@PBC),用来活化过硫酸盐(Persulfate,PS)降解印染废水中的典型染料—活性蓝(Reactive Blue 19,RB19)...     

基于BP神经网络的矿车运行时矿井摩擦阻力的预测*

为了快速有效地确定矿车等运输设备在巷道内运行时矿井摩擦阻力的变化情况,克服模拟软件计算量和现场实测工作量大的问题,以巷道风流速度、矿车运行速度、阻塞比、矿车长度4个矿车运行时巷道摩擦阻力的影响因素作为切入点,采用动网格技术模拟得到矿车在巷道内运行时有关矿井摩擦阻力的数据,以此为样本构建基于BP神经网络的矿井摩擦阻力预测模型,运用MATLAB软件进行网络训练,并将BP神经网络预测值与FLUENT模拟值进行对比。研究结果表明:BP神经网络结构比较简单,能以较快速度收敛,预测值与模拟值最大误差在7%以内,该神经网络模型用于求解矿车等运输设备在巷道内运行时摩擦阻力的变化情况是可行的。     

含磷酸盐对聚乙烯粉尘爆燃的抑制影响实验研究

为了揭示含磷酸盐(KH₂PO₄,NH₄H₂PO₄,Ca(H₂PO₄)₂)对聚乙烯粉尘爆炸的抑制作用,通过哈特曼管实验装置和20 L球形爆炸罐,研究含磷酸盐对聚乙烯粉尘爆炸火焰和压力传播特性的抑制效果。采用高速摄影方法记录含磷酸盐对聚乙烯粉尘爆炸火焰传播的影响;采用20 L球形爆炸罐,收集压力传感器数据,分析含磷酸盐对聚乙烯粉尘爆炸压力的影响;采用同步热分析仪研究聚乙烯粉尘和含磷酸盐的热解行为。研究结果表明：含磷酸盐对聚乙烯粉尘爆炸火焰传播特性参数和爆炸压力特性参数均有显著的影响,通过对比得到NH₄H₂PO₄抑制效果相对最好。研究结果可为含磷酸盐在抑爆剂工程应用提供理论基础。     

Inhibition effects of aluminum dust explosions by various kinds of ammonium polyphosphate

In this work, vinyltriethoxysilane (A151) and 3-aminopropyltriethoxysilane (KH550) were used to modify ammonium polyphosphate (APP), showing that the dispersibility of APP could be improved remarkably by A151 and KH550. The maximum explosion pressure of aluminum dust explosion decreased with the addition of APP, A151-APP (APP-A) and KH550-APP (APP-B), with the exception of the case where the inerting ratio (α) of APP-A was less than 0.4. After the addition of APP-B, there was little difference in flame propagation behavior and explosion pressure compared with that of adding APP, indicating that APP-B could retain the inhibition performance of APP compared with APP-A. When the inerting ratios of APP, APP-A and APP-B were 1.2, 1.4 and 1.4, respectively, the aluminum dust explosion could be completely inhibited. The explosion residues of aluminum dust/APP mainly consisted of Al₂O₃, P-containing and N-containing compounds. It could be analyzed that APP exerted the inhibition effect through both chemical and physical effects.     

Experimental and theoretical research on the inhibition performance of ethanol gasoline/air explosion by C6F12O

The safety issue of ethanol gasoline and the methods to control or weaken its explosion have attracted attention. To clarify the effect of C₆F₁₂O (perfluoro(2-methyl-3-pentanone)) on the explosion of ethanol gasoline-air mixtures and intrinsic mechanism, the explosion overpressure and flame propagation behavior under different equivalence ratios (φ = 0.6–0.8) and C₆F₁₂O concentrations (χ_inh = 0–4.0%) were experimentally obtained. The detailed inhibitor reaction process was also obtained by CHEMKIN based on a new assembly kinetic mechanism. The results show that the effects of C₆F₁₂O on the explosion characteristics of ethanol gasoline varied with χ_inh and φ. For rich flames, C₆F₁₂O is more effective than and heptafluoropropane (C₃HF₇) and nitrogen (N₂) in suppressing explosions; for lean and equivalence ratio flames, the addition of C₆F₁₂O may result in more severe explosions. The decrease in chemical reactivity is mainly because the mole fractions of OH and H radicals and the proportion of paths H radicals involved decrease after adding C₆F₁₂O, and R1500: CF₃COF + H = CF₃CO + HF, R965: CF₂:O + H = CF:O + HF, R863: CF₃ + H = CF₂ + HF are main suppressing reactions.     

Experimental investigation of the performance of modified expanded graphite powder doped with zinc borate in extinguishing sodium fires

Sodium is the main cooling medium in the circuit of fourth-generation nuclear reactors, and its leakage constitutes a severe fire hazard because of its high chemical activity. In this study, expandable graphite (EG), which is a traditional sodium fire-extinguishing agent, was modified with zinc borate (ZB) as an intercalator, and the modified EG_ZB was characterized. Moreover, the effectiveness of the modified EG_ZB in extinguishing sodium fires was tested using a self-developed fire-extinguishing experimental device. This study's results indicated that EG, EG_ZB had a smaller particle size, higher thermal stability, higher fire-extinguishing speed, and lower powder mass consumption than EG. During the fire-extinguishing process, ZnO decomposed by ZB captured free radicals and inhibited the combustion reaction. Furthermore, B₂O₃ was adsorbed on the surface of the EG layer, which strengthened covering and asphyxiation. The findings of this study provide crucial information for effectively controlling fires caused by active metals and metallo-organic compounds.     

O3-BAC深度处理工艺中细菌群落时空分布及动态变化规律

为弄清饮用水O₃-BAC深度处理工艺过程中细菌群落的时空分布和动态变化规律,本研究以我国南方某O₃-BAC深度处理工艺水厂为研究对象,采用NovaSeq6000高通量测序技术对夏季和冬季各工艺单元出水及滤砂和活性炭生物膜等细菌群落进行解析.结果表明,出厂水pH、浊度、COD_Mn、菌落总数等指标均满足《生活饮用水卫生标准》(GB5749-2006)的要求.夏季细菌群落多样性明显高于冬季,活性炭生物膜的细菌群落多样性高于滤砂生物膜;混凝沉淀、臭氧化和消毒是影响细菌群落多样性的主要工艺单元.水样和生物膜样品绝对优势菌门均为变形菌门(Proteobacteria),且主要菌门组成大体相同,但细菌群落门水平相对丰度存在一定的时空差异,属水平上差异则更为明显.此外,检测到的条件致病菌属主要包括芽孢杆菌属(Bacillus)、不动杆菌属(Acinetobacter)、假单胞菌属(Pseudomonas)和分支杆菌属(Mycobacterium),且其所占核心微生物OTUs数目不受季节性影响.水温和生物可降解溶解性有机碳(BDOC)是显...     

Ag3PO4/g-C3N4复合光催化剂的制备及其可见光催化性能

采用简单的原位沉淀法合成了可见光驱动型光催化剂Ag₃PO₄/g-C₃N₄.利用X-射线衍射（XRD）、傅里叶红外光谱（FT-IR）、扫描电子显微镜（SEM）、X-射线能谱（XPS）以及紫外可见漫反射光谱（UV-Vis DRS）等表征手段对合成的样品进行了表征.与单一的Ag₃PO₄和g-C₃N₄相比,Ag₃PO₄/g-C₃N₄复合材料对左氧氟沙星表现出了更高的催化效率.根据能带分析和自由基捕获试验,提出了Ag₃PO₄/g-C₃N₄复合材料Z型异质结构的作用机制.     

气溶胶辐射效应对气象和环境影响的观测与模拟研究

选取2015年和2019年不同代表年份,结合外场观测和数值模拟,分析了天津地区不同季节不同天气(晴天、多云、霾)下,气溶胶辐射效应对整层大气透过率和地表入射太阳辐射的影响,以及这种影响在不同年份的差异.借助WRF-Chem模式模拟分析了重污染期间气溶胶辐射效应对垂直方向上气象要素廓线、边界层结构以及PM_2.5浓度的反馈机制.结果表明:霾污染可导致大气透过率明显下降,春、秋、冬不同季节,霾污染导致中午大气透过率分别下降0.09,0.11和0.09.全年平均霾污染可导致大气透过率降低约15.5%.云量的增多也可导致大气透过率明显下降,多云天气下大气透过率相比晴天减小约22.4%.霾和云对大气透过率的影响还与太阳高度角有关,当太阳高度角>60°时,霾污染导致大气透过率下降8.6%.随污染等级提高,气溶胶对太阳辐射的衰减作用也越强,天津地区空气质量分别为Ⅰ～Ⅰ级时,中午地表入射短波辐射呈稳定下降趋势,依次为484,446,439,342,328和253W/m².重污染期间,气溶胶辐射效应导致大气低层(250m以下)降温(0.8℃)增湿(3.8%...     

Layered sphere-shaped TiO2 capped with gold nanoparticles on structural defects and their catalysis of formaldehyde oxidation

We describe here a one-step method for the synthesis of Au/TiO₂ nanosphere materials, which were formed by layered deposition of multiple anatase TiO₂ nanosheets. The Au nanoparticles were stabilized by structural defects in each TiO₂ nanosheet, including crystal steps and edges, thereby fixing the Au–TiO₂ perimeter interface. Reactant transfer occurred along the gaps between these TiO₂ nanosheet layers and in contact with catalytically active sites at the Au–TiO₂ interface. The doped Au induced the formation of oxygen vacancies in the Au–TiO₂ interface. Such vacancies are essential for generating active oxygen species (*O⁻) on the TiO₂ surface and Ti^3 + ions in bulk TiO₂. These ions can then form Ti^3 +–O⁻–Ti^4 + species, which are known to enhance the catalytic activity of formaldehyde (HCHO) oxidation. These studies on structural and oxygen vacancy defects in Au/TiO₂ samples provide a theoretical foundation for the catalytic mechanism of HCHO oxidation on oxide-supported Au materials.