铁活化过二硫酸盐湿法氧化去除一甲胺恶臭气体

CH₃NH₂(一甲胺)作为一种重要的工业原料而被大量使用,其嗅阈值低,具有刺鼻的鱼臭味,是一种典型的恶臭气体. 选取PS(过二硫酸盐)作为氧化剂,采用湿法吸收氧化去除CH₃NH₂. 在探讨CH₃NH₂的吸收性能的基础上,比较了4种方式〔Fe2+活化PS、CA(柠檬酸)螯合Fe2+活化PS、Fe0活化PS、CA联合Fe0活化PS〕对CH₃NH₂湿法氧化去除效果的影响. 结果表明:CH₃NH₂ 气体在酸性条件下易溶于水;单独用Fe2+或Fe0活化PS处理CH₃NH₂时,Fe0活化后的去除效果明显优于Fe2+;然而,在联合使用螯合剂CA之后,Fe2+活化的去除效果反而优于Fe0. CA螯合Fe2+的CH₃NH₂去除率由单独Fe2+活化时的32%升至64%,Fe0活化与CA联合Fe0活化去除率均提升至40%. 究其原因,可能是由于不同活化方式下Fe2+释放速率不同所致,释放速率直接影响了Fe2+的存在时间,Fe2+活化PS速率对于氧化去除效果有影响,并最终影响CH₃NH₂的脱除.      

Fe(Ⅱ)、Fe(Ⅲ)和Fe(Ⅵ)活化过硫酸盐氧化降解水中的菲

分别采用Fe(Ⅱ)、Fe(Ⅲ)和Fe(Ⅵ)活化过硫酸盐(PS)氧化降解水中的菲,考察了反应pH、药剂投加量及氧化时间等因素的影响,并对比了不同价态铁活化PS对菲的氧化降解效果.在反应pH为8、n(菲):n(Fe):n(PS)为1:2:2的优化条件下,反应60 min后Fe(Ⅱ)-PS和Fe(Ⅲ)-PS体系对菲的去除率分...     

Mutagenicity of polyaromatic hydrocarbons by chemical models for cytochrome P450 in Ames assay

DNA damage is an important step in carcinogenesis. The Ames assay is a short-term screening of carcinogens that induce DNA damage. Most carcinogens require enzymatic activation through oxidation by cytochrome P450 (CYP450) in the presence of S9 mix. A combination of iron (Fe)(III) porphyrin and an oxidant is also able to oxidize compounds as an alternative metabolic pathway to CYP450. Previously it was reported that a chemical model containing a water-soluble 5,10,15,20-tetrakis(1-methylpyridinium4-yl)porphyrinatoiron(III) chloride (4-MPy) and tert-butyl hydroperoxide (t-BuOOH) activated aromatic amines and amides. In this study, a chemical model composed of an Fe porphyrin, water-insoluble 5,10,15,20-tetrakis(pentafluorophenyl)porphyrinatoiron(III) chloride (F₅P) or water-soluble 4-MPy was optimized with an oxidant – t-BuOOH, magnesium monoperoxyphthalate (MPPT), or iodosylbenzene (PhIO). Subsequently the mutagenicity of benzo[a]pyrene (B[a]P) and chrysene in Salmonella typhimurium TA strains was compared. B[a]P was activated by a combination of F₅P or 4-MPy plus MPPT or PhIO in S. typhimurium TA1538. The B[a]P-induced mutagenicity with F₅P plus oxidant was higher than 4-MPy plus oxidant. Mutagenicity of chrysene, a tetracyclic aromatic hydrocarbon, was not detected in the presence of F₅P/PhIO in S. typhimurium TA98, but was activated in the presence of F₅P/MPPT. The F₅P/MPPT activated other polyaromatic hydrocarbons (PAH) in the S. typhimurium TA98 assay including dibenz[a,c]anthracene, dibenz[a,h]anthracene, 3-methylcholanthrene, and benzo[a]anthracene. The results indicated that the F₅P/MPPT was the most efficient model for detecting PAH-induced mutagenicity in the Ames assay.     

低温驯化对自养脱氮颗粒污泥功能活性与菌群结构的影响分析

低温驯化是提高部分亚硝化-厌氧氨氧化（PN/A）组合工艺低温脱氮效能和运行稳定性的有效方法.为探究低温驯化对污泥特性的具体影响,本文从温度敏感性、颗粒外观形态、胞外聚合物（EPS）组成和微生物群落结构等方面,对中高温培养（30℃）和低温驯化（15℃）PN/A颗粒污泥之间的差异性进行了分析.反应热力学的研究结果表明,驯化污泥（G_L）在低温区（10~20℃）的脱氮性能较中高温培养污泥（G_H）有了显著提高,总无机氮去除的表观反应活化能（E_a）降低了28.4%.与G_H相比,G_L的平均粒径减小了25.8%,EPS含量增长了16.6%,颗粒的沉降性能明显下降.由高通量测序结果可知,G_L具有更高的菌群多样性,同时,污泥中好氧氨氧化菌（Nitrosomonas）与厌氧氨氧化菌（Candidatus_Kuenenia）的丰度比值（0.04）远小于G_H的0.34.这意味着颗粒污泥在低温环境中对慢速生长自养菌仍具有较强的截留能力.上述发现为解析PN/A污泥在低温条件下的自适应机制,推动组合工艺的工程化应用提供了重要参考.     

Investigation of the propensity of sulfide concentrates to spontaneous combustion in storage

Spontaneous combustion of sulfide concentrates can cause many serious problems during storage. In this study, two representative samples (sulfur-rich sulfide concentrate and iron-rich sulfide concentrate) were investigated for the self-heating behavior using the crossing-point temperature (CPT) method. The corresponding apparent activation energies were determined, 13.7366 kJ/mol for iron-rich sulfide concentrate and 21.3817 kJ/mol for sulfur-rich sulfide concentrate. Furthermore, the surface temperatures of sulfide concentrate stockpiles in different seasons were also measured by a thermal image apparatus. It was found the temperature for iron-rich sulfide concentrate stockpile was higher than that for rich-sulfur sulfide concentrate stockpile. These research results show iron-rich sulfide concentrate exhibits stronger propensity to spontaneous combustion than sulfur-rich sulfide concentrate. Particular attention should be paid to the fire hazard of iron-rich sulfide concentrate in daily safety check work. The combination of the CPT method with the infrared thermal image measurement provides a new approach for the risk assessment on the propensity of sulfide concentrates to spontaneous combustion during the production, storage and transportation. The useful data and experience achieved in this investigation can be also referenced in similar cases later.     

Efficient degradation of Rhodamine B by magnetically recoverable Fe3O4-modified ternary CoFeCu-layered double hydroxides via activating peroxymonosulfate

Environment-friendly nano-catalysts capable of activating peroxymonosulfate (PMS) have received increasing attention recently. Nevertheless, traditional nano-catalysts are generally well dispersed and difficult to be separated from reaction system, so it is particularly important to develop nano-catalysts with both good catalytic activity and excellent recycling efficiency. In this work, magnetically recoverable Fe₃O₄-modified ternary CoFeCu-layered double hydroxides (Fe₃O₄/CoFeCu-LDHs) was prepared by a simple co-precipitation method and initially applied to activate PMS for the degradation of Rhodamine B (RhB). X-ray diffraction (XRD), fourier transform infrared spectrometer (FT-IR), scanning electron microscope (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller method (BET), and vibrating sample magnetometer (VSM) were applied to characterize morphology, structure, specific surface area and magnetism. In addition, the effects of several key parameters were evaluated. The Fe₃O₄/CoFeCu-LDHs exhibited high catalytic activity, and RhB degradation efficiency could reach 100% within 20 min by adding 0.2 g/L of catalyst and 1 mmol/L of PMS into 50 mg/L of RhB solution under a wide pH condition (3.0-7.0). Notably, the Fe₃O₄/CoFeCu-LDHs showed good super-paramagnetism and excellent stability, which could be effectively and quickly recovered under magnetic condition, and the degradation efficiency after ten cycles could still maintain 98.95%. Both radicals quenching tests and electron spin resonance (ESR) identified both HO? and SO₄^?? were involved and SO₄^?? played a dominant role on the RhB degradation. Finally, the chemical states of the sample's surface elements were measured by X-ray photoelectron spectroscopy (XPS), and the possible activation mechanism in Fe₃O₄/CoFeCu-LDHs/PMS system was proposed according to comprehensive analysis.     

Cr/γ-Al_2O_3对乙酸乙酯的催化燃烧

使用浸渍法制备不同负载量的Cr/γ-Al_2O_3催化剂,研究乙酸乙酯的催化燃烧.BET,XRD结果表明,Cr在γ-Al_2O_3上负载存在分散阈值效应,负载量在阈值以下时呈单层分散形式,在超过阈值时Cr形成结晶,实验测得单层分散阈值与理论计算一致.Raman结果表明Cr在单层分散时为Cr~(6+),而在非单层分散时为Cr_2O_3.催化乙酸乙酯燃烧的活性研究显示,阈值效应对催化活性有显著影响:催化活性在单层分散阈值时最好,此时活化能最高,指前因子最大.     

Overestimate of remediation efficiency due to residual sodium persulfate in PAHs contaminated soil and a solution

Oxidation remediation is a commonly used technology for PAHs contaminated soil presently,but the overestimate of efficiency due to ongoing remediation by residual oxidants during extraction and testing has not been paid enough attention.In this study,persulfate was activated by Fe（Ⅱ） to inve stigate the effects of residual oxidants on PAHs removal during detection process and the elimination effects of adding Na₂ SO₃ and extending sampling time on residual oxidants.Results ...     

硬木地板材料和棉花秆的变氧浓度热解燃烧表观动力学的实验研究

本文采用TG-FTIR分析方法深入研究了火场中硬木地板材料和棉花秆变氧浓度燃烧过程,深入分析了氧浓度对纤维物质燃烧表观热失重影响;通过大量的动力学参数计算得出了可燃物的表观活化能与实际氧浓度成线性关系;分析了氧浓度对木材燃烧气体产物的影响,并探索了氧浓度影响热解和燃烧的机理。     

脱水污泥薄层干燥特性及动力学模型分析

采用薄层干燥方式进行脱水污泥热干燥的研究,考察了污泥的干燥特性,并引入薄层干燥模型进行数值分析.结果表明, Logarithmic模型比其他模型更适合薄层污泥干燥分析.应用Fick扩散模型,得到80~150℃条件下薄层污泥干燥的有效扩散系数的变化范围为8.486′10-10~4.386′10-9m2/s,并根据Arrhenius经验公式建立温度与扩散系数的关系,得到污泥干燥时水分扩散的活化能为29.56kJ/mol.