基于SOF-FTIR方法走航观测南京市重点区域特征挥发性有机物

介绍了污染源挥发性有机物(VOCs)排放的常用监测方法,以及基于红外掩日通量-傅里叶变换红外光谱(SOF-FTIR)的走航观测系统结构与测试原理。以2014年南京青奥会期间对一些重点区域VOCs的走航观测为例,提出了借鉴前期现状调查结果,结合手工采样分析,确定特征目标组分的监测方案。观测结果表明,该方法在柱浓度监测和排放总量核算方面具有一定优势,不足之处在于受日照条件、走航速度和路况、地面风速限制,测量时需避开不利因素影响。     

在线分析宁波市北仑区VOCs组成、趋势及来源

利用VOCs在线监测技术,对2010年宁波市北仑区空气内的VOCs的浓度、组成、变化规律及来源进行分析研究。结果表明,在北仑区域内的16种VOCs中,苯、甲苯、二甲苯、乙苯和己烷的比例占到了总数的82．9％,且该5种有机物浓度存在较为典型的季节性变化规律和日变化规律;采用CMD模型法对VOCs的来源进行解析后发现,北仑区域内的VOCs主要来源于汽车尾气、汽油蒸气和石油液化气,而且汽车尾气的贡献值要比一些大城市低得多,且夏季和冬季的成分源贡献率存在明显差异。     

CuO（-CeO2）/SBA-15对萘氧化的催化活性及CO2选择性研究

通过浸渍法制备CuO/SBA-15和CuO-CeO2/SBA-15两种介孔材料催化剂,采用BET、XRD、TPR和XPS等对催化剂进行表征,重点考察催化剂对萘氧化反应的催化活性及对产物CO2的选择性。BET、XRD和XPS等实验结果表明CuO高度分散于介孔分子筛SBA-15中,CeO2可促进CuO在载体上的分散,同时能降低催化剂的TPR还原温度。活性测试结果表明CuO/SBA-15对萘氧化反应的催化活性较高,但是催化氧化的CO2选择性较低,温度在380℃时CO2的生成率仅为60%左右;CeO2的添加不仅提高了CO2的生成率,15%CuO-15%CeO2/SBA-15在325℃使CO2生成率达到99%,而且CeO2增强了催化剂的稳定性。     

活性炭吸附和脱附-等离子体氧化净化有机废气的研究

根据滑动弧放电等离子体适于降解高浓度有机物废气的特性,结合活性炭吸附法,提出了吸附器的吸附浓缩和热脱附-等离子体氧化净化有机废气的方法。在活性炭吸附过程中,最初2 h内甲苯净化率达到100%,随着时间的增加净化率下降;在热脱附滑动弧放电等离子体净化过程中,甲苯降解效率最高为97.3%。将滑动弧放电等离子体反应器出口气相产物收集进行FT-IR检测,发现放电后有CO2、CO、H2O和NO2产生,并分析了甲苯的降解机理。     

生物基质活性炭对挥发性有机物的吸附

以咖啡渣和柚子皮生物基质为原料用磷酸活化法制成活性炭,探讨了制备条件对活性炭制备的影响,并研究了其对正丁烷的吸附行为。磷酸活化过程中磷酸的用量为生物基质质量的1.5倍为宜,咖啡渣采用超声干燥法,柚子皮采用水热法制备。制备的活性炭对正丁烷均有较好的吸附能力,以柚子皮为原料、磷酸用量为原料质量两倍活化制成的活性炭吸附性能最佳,最大吸附量约为商用活性炭的2倍。吸附剂均能较好地与兰格缪尔曲线相拟合,计算了不同正丁烷覆盖度下的等量吸附热,其变化规律与吸附曲线变化规律相一致。     

Effect of ozone injection on the long-term performance and microbial community structure of a VOCs biofilter

For biofilters treating waste gases containing volatile organic compounds(VOCs), biomass accumulation is a common problem which will induce bed clogging and significant decrease in VOCs removal efficiency during long-term operation. In this study, ozone injection was developed as a biomass control strategy, and its effects on the biofilter performance and the microbial community structure were investigated in long-term operation. Two biofilters,identified as BF1 and BF2, were operated continuously for 160 days treating gaseous toluene under the same conditions, except that 200 mg/m3 ozone was continuously injected into BF1 during days 45–160. During the operation period, ozone injection did not change the toluene removal efficiency, while the pressure drop of BF1 with ozone injection was significantly lowered compared with BF2. The wet biomass accumulation rate of BF1 was 11 g/m~3/hr, which was only46% of that in BF2. According to the carbon balance result, ozone injection also increased the toluene mineralization rate from 83% to 91%, which could be an important reason for the low biomass accumulation. The PMA-q PCR result indicated that ozone injection increased the microbial viability of the biofilm. The high-throughput sequencing result also revealed that the dominant phyla and genera were not changed significantly by ozone injection, but some ozonetolerant genera such as Rhodanobacter, Dokdonella and Rhodococcus were enhanced by ozone exposure. All the results verified that ozone injection is capable of sustaining the long-term performance of biofilters by lowering the biomass accumulation, increasing the microbial viability and changing the microbial community structure.     

泄漏检测与维修技术在芳烃抽提装置的应用研究

采用泄漏检测与维修（ LDAR）技术进行了全面检测和统计分析，分析泄漏的原因并通过维修减少泄漏。结果表明：芳烃抽提装置容易泄漏的元件主要为连接件和阀门，主要分布在泵区；SV≥5000μmol／mol的泄漏密封点占总密封点数的0.57％，对总泄漏量的贡献达到了82％，是造成泄漏排放的主要部分。设备管阀件泄漏造成的加工损失率为0.0009％，泄漏点停工维修修复率为83％，停工维修后整体泄漏率为0.03％；VOCs减排率为71％。     

Cu–Mn–Ce ternary mixed-oxide catalysts for catalytic combustion of toluene

Cu–Mn, Cu–Mn–Ce, and Cu–Ce mixed-oxide catalysts were prepared by a citric acid sol–gel method and then characterized by XRD, BET, H₂-TPR and XPS analyses. Their catalytic properties were investigated in the toluene combustion reaction. Results showed that the Cu–Mn–Ce ternary mixed-oxide catalyst with 1:2:4 mole ratios had the highest catalytic activity, and 99% toluene conversion was achieved at temperatures below 220°C. In the Cu–Mn–Ce catalyst, a portion of Cu and Mn species entered into the CeO₂ fluorite lattice, which led to the formation of a ceria-based solid solution. Excess Cu and Mn oxides existed on the surface of the ceria-based solid solution. The coexistence of Cu–Mn mixed oxides and the ceria-based solid solution resulted in a better synergetic interaction than the Cu–Mn and Cu–Ce catalysts, which promoted catalyst reducibility, increased oxygen mobility, and enhanced the formation of abundant active oxygen species.     

Remarkable promotion effect of trace sulfation on OMS-2 nanorod catalysts for the catalytic combustion of ethanol

OMS-2 nanorod catalysts were synthesized by a hydrothermal redox reaction method using MnSO₄ (OMS-2-SO₄) and Mn(CH₃COO)₂ (OMS-2-AC) as precursors. SO₄^2 −-doped OMS-2-AC catalysts with different SO₄^2 − concentrations were prepared next by adding (NH₄)₂SO₄ solution into OMS-2-AC samples to investigate the effect of the anion SO₄^2 − on the OMS-2-AC catalyst. All catalysts were then tested for the catalytic oxidation of ethanol. The OMS-2-SO₄ catalyst synthesized demonstrated much better activity than OMS-2-AC. The SO₄^2 − doping greatly influenced the activity of the OMS-2-AC catalyst, with a dramatic promotion of activity for suitable concentration of SO₄^2 − (SO₄/catalyst = 0.5% W/W). The samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectroscopy (ICP-OES), NH₃-TPD and H₂-TPR techniques. The results showed that the presence of a suitable amount of SO₄^2 − species in the OMS-2-AC catalyst could decrease the Mn–O bond strength and also enhance the lattice oxygen and acid site concentrations, which then effectively promoted the catalytic activity of OMS-2-AC toward ethanol oxidation. Thus it was confirmed that the better catalytic performance of OMS-2-SO₄ compared to OMS-2-AC is due to the presence of some residual SO₄^2 − species in OMS-2-SO₄ samples.