应用陆地卫星TM图象编制闽北土壤图(1:10万)的方法研究

以TM原图象合成的标准假彩色和似自然色图象作目视解译为主,根据土壤及其相关地物的野外光谱测定数据,分析其影象色调特征;用TM 7个波段原始黑白图象作对比解译,以预测不同地物的彩色合或效果并选择最佳合成方案;用TM6热红外图象作假彩色等密度分割处理,以提取随海而异的地面温度场和土壤类型垂直分带信息;用TM比值图象及其假彩色合成处理,以逐步增强并提取土壤信息;最后参照同比例尺地质图和地形图等相关资料,完成土壤图的编制。     

Effect of TiO2 surface properties on the SCR activity of NOx emission abatement catalyst

NOx emission abatement catalysts V2O5 supported on various TiO2 including anatase, rutile and mixture of both were investigated with various physico-chemical measurements such as BET, NH3-TPD, NARP, XRD and so on, and the effect of TiO2 surface properties on the SCR (selective catalytic reduction) activity of V20s/TiO2 catalysts was studied. It was found that the TiO2 surface properties had strong affect on the SCR activity of V2Os/TiO2 catalysts. The stronger acidic property resulted in the higher exposure of active sites as well as the higher SCR activity.     

Comparative study on pyrolysis of bamboo in microwave pyrolysis-reforming reaction by binary compound impregnation and chemical liquid deposition modified HZSM-5

The deactivation of catalyst is a significant reason for its limited application during the catalytic fast pyrolysis (CFP) process. To reduce the coke formation, binary compound impregnation (BCI) and chemical liquid deposition (CLD) were used to modify HZSM-5 catalysts. At the same time, the self-designed microwave reactor separated the pyrolysis of bamboo and catalytic upgrading of primary vapor, which made the catalytic effect more thorough. Experimental results indicated that CLD used TiO₂ deposition to cover external acid sites, while BCI by phosphorus-nickel could cover and partly destroy superficial acid sites through two different ways. Within the scope of the loaded amount studied, the yield of aromatic hydrocarbons in the oil phase increased at first and then decreased, while the coke formation reduced continuously. BTX (benzene, toluene and xylene), the most valuable product in bio-oil, drastically increased by 39.1% and 22.6% respectively over the CLD and BCI modified catalysts. Considering the catalytic performance as well as cost, CLD over HZSM-5 has more advantages in the CFP process to upgrade bio-oil.     

Surface characterization of metal oxides-supported activated carbon fiber catalysts for simultaneous catalytic hydrolysis of carbonyl sulfide and carbon disulfide

The sol–gel method was used to synthesize a series of metal oxides-supported activated carbon fiber (ACF) and the simultaneous catalytic hydrolysis activity of carbonyl sulfide (COS) and carbon disulfide (CS₂) at relatively low temperatures of 60°C was tested. The effects of preparation conditions on the catalyst properties were investigated, including the kinds and amount of metal oxides and calcination temperatures. The activity tests indicated that catalysts with 5 wt.% Ni after calcining at 400°C (Ni(5)/ACF(400)) had the best performance for the simultaneous catalytic hydrolysis of COS and CS₂. The surface and structure properties of prepared ACF were characterized by scanning electron microscope-energy disperse spectroscopy (SEM-EDS), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), carbon dioxide-temperature programmed desorption (CO₂-TPD) and diffuse reflectance Fourier transform infrared reflection (DRFTIR). And the metal cation defects were researched by electron paramagnetic resonance (EPR) method. The characterization results showed that the supporting of Ni on the ACF made the ACF catalyst show alkaline and increased the specific surface area and the number of micropores, then improved catalytic hydrolysis activity. The DRFTIR results revealed that -OH species could facilitate the hydrolysis of COS and CS₂; -COO and -C–O species could facilitate the oxidation of catalytic hydrolysate H₂S. And the EPR results showed that high calcination temperature conditions provide more active reaction center for the COS and CS₂ adsorption.     

瘤胃微生物强化醋糟厌氧消化及其机制

针对醋糟中木质纤维素利用效率低的问题,通过接种瘤胃微生物可强化木质纤维素水解.采用逐步提升体系有机负荷的方式,考察瘤胃微生物生物强化对醋糟厌氧消化性能的提升效果,并运用绝对定量实时聚合酶链锁反应（Q-PCR）技术探究其微生物学强化机制.结果表明:长期连续运行成功塑造了高效的木质纤维素瘤胃强化体系.该体系的最高有机负荷达8.90 g/（L·d）（以VS计）,是强化前的1.53倍,该有机负荷下半纤维素和纤维素降解率分别达73.9%和40.1%,单位质量底物沼气和甲烷产量相应地分别达到451和261 mL/g（以VS计）,半纤维素和纤维素较高的降解率是该体系维持高产气性能的主要原因.生物相机制研究表明,瘤胃微生物强化体系中与木质纤维素水解密切相关的GH5（糖苷水解酶家族5）水解菌逐步富集,其基因拷贝数从初始的964×1010 copies/g升至最高有机负荷下的6.83×1011 copies/g,这是底物在高有机负荷下仍能被高效生物转化的根本原因.研究显示,瘤胃微生物的介入可有效强化体系底物的降解能力,促进醋糟产甲烷性能的提升.      

高晶度Mn-Fe LDH催化剂活化过一硫酸盐降解偶氮染料RBK5

采用改进的共沉淀结合水热法制备高晶度锰铁层状双金属氢氧化物作为催化剂,用于高效活化过一硫酸盐(PMS)降解活性黑5(RBK5).通过X射线粉末衍射仪(XRD)、扫描电子显微镜(SEM)、X射线能谱分析(EDS)、傅里叶变换红外光谱仪(FTIR)以及X射线光电子能谱(XPS)对材料进行表征,证明成功合成了结晶度高、层状结构突出的Mn-Fe LDH.同时探究了锰铁量比,催化剂投加量,PMS浓度和初始pH值等因素对RBK5的吸附效果、催化降解及反应动力学的影响.结果表明,高晶度Mn-Fe LDH催化剂具有良好的吸附能力和高效的催化效率,在n(Mn)/n(Fe)比为1∶1,催化剂投加量为0.2 g·L~(-1),PMS浓度为1 mmol·L~(-1),初始pH为7时,RBK5(20 mg·L~(-1))在90 min内降解率可达86%,整个反应过程符合拟一级动力学(R~20.9).自由基猝灭实验表明,Mn-Fe LDH/PMS体系降解RBK5为SO~-_4·和·OH两种活性自由基共同作用的结果.反应前后催化剂的XPS分析表明Mn和Fe存在协同作用,Mn-Fe LDH的Mn(Ⅱ)和Fe(Ⅲ)与层间的CO~(2-)_3电荷平衡,使其层状结构稳定,从而促进了层状表面Mn和Fe的协同作用,提高了Mn-Fe LDH对PMS的活化效率.三维荧光光谱(3D-EEM)和UV-Vis扫描光谱分析初步探讨了RBK5的降解过程.     

NZVI/Na2S2O8/超声复合法降解污染土壤PCB-29

多氯联苯（polychlorinated biphenyls,PCBs）是一类具有高毒性、难降解的有机化合物,为了研发土壤中多氯联苯（PCBs）污染物高效处理技术,本研究采用PCBs中的2,4,5-三氯联苯（PCB-29）作为研究对象,以纳米零价铁（NZVI）活化Na₂S₂O₈,再辅以超声氧化对土壤中PCB-29进行降解试验,结果表明,NZVI/Na₂S₂O₈/超声复合法对污染土壤中PCB-29具有很好的去除效果,降解反应时间为1h时,去除率最高可达86.37%;NZVI/Na₂S₂O₈/超声复合法对PCB-29最佳降解条件为土壤初始pH值为5.0,Na₂S₂O₈浓度为12mmol/L,Na₂S₂O₈/NZVI物质的量比1：1.     

Fe-Ce/ZSM-5复合催化剂的制备及其催化性能

采用浸渍法制备了Fe-Ce/ZSM-5复合催化剂,并将其用于甲基橙的催化降解。利用单因素实验考察了溶液pH、初始甲基橙质量浓度、催化剂加入量、初始H_2O_2浓度及反应温度对准一级动力学方程反应动力学常数的影响,对催化剂的稳定性进行了测试,并探讨了甲基橙的催化降解机理。实验结果表明:在溶液pH 5.0、初始甲基橙质量浓度100 mg/L、催化剂加入量1.0 g/L、初始H_2O_2浓度20 mmol/L、反应温度20℃的优化条件下反应60min,反应动力学常数高达0.034 min~(-1),甲基橙降解率高达87%,铁离子流失量仅为0.019 mg/L;催化剂重复使用3次后,甲基橙降解率仍高于80%,保持了较高活性。     

北京地区不同时段平均PM2.5浓度与MODIS气溶胶光学厚度相关性分析

利用2014年北京市12个空气质量监测站的逐小时PM_(2.5)地面观测资料,以及Terra和Aqua卫星的MODIS气溶胶光学厚度(AOD)产品,在时间和空间数据匹配的基础上,研究了PM_(2.5)的5 h(10:00—14:00)和24 h(0:00—23:00)两种时段平均浓度及两颗卫星平均AOD的时空分布特征,并建立了AOD与不同时段平均PM_(2.5)浓度之间的回归模型.结果表明:PM_(2.5)的5 h平均浓度和24 h平均浓度值均在城区高、郊区低,最低值位于定陵站;匹配后逐时PM_(2.5)浓度的日变化呈"双峰型",最低值出现在下午,但北京西北部郊区的定陵和昌平镇站因局地山谷风环流和外部排放源的影响,其"双峰型"波动趋势较城区站偏弱,最低值出现在上午;AOD的空间分布特征与PM_(2.5)浓度分布一致,但在郊区由于污染水平分布不均,卫星采集的样本可能来自于周围的清洁大气,导致AOD的最小值在郊区站点明显低于城区站点;两颗卫星平均的AOD与5h PM_(2.5)平均浓度的决定系数高于AOD与24 h PM_(2.5)平均浓度的决定系数;AOD与PM_(2.5)的相关系数在城区高于郊区,郊区排放源分布不均和强的局地系统性环流是造成其相关系数低的重要原因.     

2014年泉州市区PM2.5浓度的时空变化特征分析研究

基于2014年泉州市区环境空气自动监测站的PM2.5、PM10等监测数据,讨论市区PM2.5的时空分布特征.结果表明,泉州市区PM2.5浓度存在较为明显的时空分布特征.(1)时间分布特征:PM2.5的年均值为34μg/m3,月均值最大值出现在1月,最小值出现在7月;PM2.5浓度冬季最高,夏季最低,春冬两季明显高于夏秋;PM2.5/PM10最高值出现在2月,最低值出现在7月;PM2.5/PM10冬季最高,夏季最低.(2)空间分布特征:3个监测点位中,PM2.5浓度涂山街最高,津头埔略低,万安最低;PM2.5/PM10万安最高,涂山街略低,津头埔最低.时间分布特征与气象条件有一定关系,而空间分布特征与建成区的建成时间先后、地理位置差异等有一定关系.