Photoelectrochemical degradation of Methylene Blue with -PbO2 electrodes driven by visible light irradiation

-PbO2 electrodes were prepared by electro-deposition and characterized by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and linear sweep voltammetry. We confirmed pure -PbO2 crystals were on the electrode and it had a high oxygen evolution potential. The photoactivity and photoelectrochemical (PEC) properties of the -PbO2 electrode were investigated under visible light irradiation ( > 420 nm) for the decolorization of Methylene Blue. Pseudo first-order kinetics parameter (Kapp) for dye decolorization using the -PbO2 electrode achieved 6.71×10?4 min?1 under visible light irradiation, which indicated its excellent visible light-induced photoactivity. The Kapp of the PEC process was as much as 1.41×10?3 min?1 and was 1.71 times that of visible light irradiation or electrolysis even in the presence of the -PbO2 electrode. A significant synergetic effect was observed in the PEC system. We also employed TiO2 modified -PbO2 electrodes in this test, which revealed that the TiO2 immobilized on the -PbO2 electrode inhibited the visible light-induced PEC efficiency despite the amount of TiO2 used for electrode preparation. The -PbO2 electrode was also superior to the dimensionally stable anode (Ti/Ru0:3Ti0:7O2) in visible light-induced photoactivity and PEC efficiency.     

Kappaphycus alvarezii waste biomass: A potential biosorbent for chromium ions removal

The Cr(III) sorption experiments onto Kappaphycus alvarezii waste biomass were conducted at different pH values (2–6) under the conditions of initial metal concentration of 10–50 mg/L and the chemical compositions of Cr-Cu and Cr-Cd. The Cr(III) sorption capacities were slightly dependent on pH, and the maximum sorption capacity was 0.86 mg/g at pH 3. The sorption capacities increased with increase in the initial metal concentration, whereas it was suppressed by the presence of Cu(II) and Cd(III) in the solution. The Cr(III) sorption equilibrium was evaluated using Langmuir, Freundlich and BET isotherms. The sorption mechanisms were characterised using scanning electron microscopy and Fourier transform infrared spectroscopy. The main mechanisms were ion exchange coupled with a complexation mechanism. Kappaphycus alvarezii waste biomass represents a potential for Cr(III) ion removal from aqueous solution.     

Rapid removal of bisphenol A on highly ordered mesoporous carbon

Bisphenol A (BPA) is of global concern due to its disruption of endocrine systems and ubiquity in the aquatic environment. It is important, therefore, that e orts are made to remove it from the aqueous phase. A novel adsorbent, mesoporous carbon CMK-3, prepared from hexagonal SBA-15 mesoporous silica was studied for BPA removal from aqueous phase, and compared with conventional powdered activated carbon (PAC). Characterization of CMK-3 by transmission electron microscopy (TEM), X-ray di raction, and nitrogen adsorption indicated that prepared CMK-3 had an ordered mesoporous structure with a high specific surface area of 920 m2/g and a pore-size of about 4.9 nm. The adsorption of BPA on CMK-3 followed a pseudo second-order kinetic model. The kinetic constant was 0.00049 g/(mg min), much higher than the adsorption of BPA on PAC. The adsorption isotherm fitted slightly better with the Freundlich model than the Langmuir model, and adsorption capacity decreased as temperature increased from 10 to 40°C. No significant influence of pH on adsorption was observed at pH 3 to 9; however, adsorption capacity decreased dramatically from pH 9 to 13.     

温度对发射药比热容影响规律研究

目的确定发射药比热容参数。方法选用发射药9/7单基药、SF-3和GATo推进剂为研究对象,利用热重分析仪研究发射药的热分解特性,确定实验温度区间。利用差示扫描量热仪采用动态温度调制法对温度区间内发射药比热容进行测量,对发射药比热容变化规律进行分析,并计算热力学函数。结果发射药的比热容随温度升高而逐渐变大。结论在进行发射药热模拟计算时,从安全角度出发,应该使用常温下发射药比热容。     

草鱼在2-硝基芴试验液中暴露后鳃组织结构变化的初步研究

用电镜观察的方法研究具有直接致突变性和致癌性的化合物－２硝基芴对草鱼鳃组织结构的影响,结果表明,２－硝基芴对鳃组织有明显的损伤,主要包括鳃小片的肿大和出现大量的泌氯细胞,并在作用１０ｄ时观察到上皮细胞死亡。     

土壤腐殖酸慢热解表征实验影响因素研究

以土壤提取的腐殖酸为研究对象,进行了差式量热扫描(DSC)和热重分析(TGA)的可重复性实验、样品质量对比实验和预处理对比实验。综合分析了影响慢热解特征温度参数的因素和效应,并根据作用原理将其总结为热滞后效应和反应平衡滞后效应。结果表明,高级热分析技术用于土壤慢热解表征可重复性良好,差式量热扫描与热重分析结果可比性强,然而热分析曲线和热特征参数对实验条件的响应灵敏,其中样品质量和升温速率的影响尤其显著。研究结果表明,慢热解技术用于土壤有机质分析具有良好的准确性和重现性,提出了保障土壤腐殖酸慢热解质量控制的最佳样品量[DSC为(10±0.1)mg]、最佳气体氛围(He)和最佳升温速率(10℃/min)、精确压实程度等实验条件。     

飞行时间二次离子质谱法在一次污染过程中PM2.5表面组分分析中的应用

团簇离子源的发明和使用,使飞行时间二次离子质谱（TOF-SIMS）法成为材料表面化学分析越来越重要的手段,TOF-SIMS法的主要测试功能包括表层质谱、化学成像及深度剖析3种。采用TOF-SIMS法对一次污染过程中的大气细颗粒物（PM_2.5）的表层进行检测,得到了PM_2.5表面成分的质谱及成像信息。结果表明：PM_2.5表层存在多种金属离子,通过扫描电子显微镜能谱仪的形貌与飞行时间二次离子质谱仪的成像亮度分析可知,K⁺、Na⁺、Mg²⁺响应强度相对较强,含量较高;通过原子吸收光谱仪进行金属离子定量可知,2018年11月4日和12月24日的K⁺、Na⁺、Mg²⁺的平均质量分别为1.809 5、0.443 8、1.526 2 mg;从形态分布上看,PM_2.5表面烟尘集合体含量较多,其次为燃煤飞灰、矿物颗粒和超细未知颗粒;PM_2.5表层的有机物离子C_xH_y片段也较多,经过m/z的测试数据进一步确定,表明颗粒物表层含有大量的脂肪烃和芳香烃;除此之外,还存在含N、O、S等的有机物和无机物。     

铜导线短路熔痕微观形貌特征分析与研究

采用模拟实验的方法制备了铜导线一次短路熔痕和二次短路熔痕,利用KYKY-2800B型扫描电子显微镜(SEM)对铜导线一次短路熔痕和二次短路熔痕的微观形貌进行了观察,并对内部气孔的数量、大小、分布等进行了统计分析,发现了一次短路气孔的数量、分布与二次短路之间的差别与长期采用的鉴定依据不同.     

大叶火焰草生物学特征的修订与补充

通过标本查阅、实地考察、扫描等方法和手段,对大叶火焰草的生物学特征进行了全面修订与补充。首次修正了该物种是2年生草本而非1年生草本植物,基生叶和茎生叶的形状和排列方式均不相同,并首次发现茎上可生腋芽,花药呈红色。同时,首次报道了大叶火焰草倒梯形状的心皮鳞片,扫描电镜下大叶火焰草的种子呈近矩圆球形,外壁被高脊状纵棱。     

固液共存氧化型聚硅酸铁(PSF-I)混凝剂的分析

对自制的聚硅酸铁(PSF)进行改性,加入高锰酸钾和稳定剂M,制备出固液共存氧化型聚硅酸铁(PSF-Ⅰ)混凝剂,用滤纸将PSF-Ⅰ过滤,并对PSF-Ⅰ、PSF-Ⅰ滤液及PSF进行紫外吸收(UVA)全波长扫描及前两者的混凝实验,然后将PSF-Ⅰ与PSF、聚合硫酸铁(PFS)进行混凝对比研究,最后对PSF-Ⅰ的混凝性能随储存时间的稳定性进行探讨。结果表明,高锰酸钾的加入改变了PSF的微观结构,使PSF的形态尺寸增大,导致PSF-I中Fe3+离子的UVA特征峰比PSF高,并且保存了独立的高锰酸钾特征吸收峰(530nm)。PSF-Ⅰ中的固相起到初级核子作用,有利于絮体成长。PSF-Ⅰ的最佳投药量为9mg?L^-1,而PSF-Ⅰ滤液 的最佳投药量为12 mg?L^-1。PSF-I是通过混凝吸附和催化氧化功能共同实现对有机物的去除,而PSF和PFS仅是通过常规的混凝吸附去除部分有机物,去除机理有本质的区别。