低浓度二氧化碳检测管的研制

应用活性氧铝—百里香酚酞吸附ＣＯ２线性比长法研制出低浓度ＣＯ２检测管。测定范围０．０５～０．９０％;灵敏度为０．０５％;检测管变色长度与ＣＯ２浓度的相关系数γ＝０．９９８１,精密度与准确度符合国家标准８３ＧＢ７２２０～７２８０。其可靠性与经典的何氏气体分析器比较,结果基本一致。低浓度的ＳＯ２、Ｈ２Ｓ和ＮＨ３对测定无明显干扰,现场监测应用效果可靠,值得推广应用。     

多功能户外运动防护靴设计与开发

户外环境穿用的鞋靴应该具有防护性和功能性,在减少脚部受伤几率的前提下,协助穿用者完成各种行动。新研制出的一款鞋靴非常适合户外环境穿用,其主要具备以下特点：1、穿脱快速、便捷;2、耐穿性优异;3、防水性、阻燃性、防滑性等功能优异,能提高户外活动效率。     

铂载钴钼二元硫化物对H_2S电催化活性研究

为考察溶胶凝胶法制备的Co-Mo二元硫化物对H_2S气体的电催化活性,通过循环伏安法和Tafel曲线分析对铂载不同Co、Mo掺杂比的电催化剂进行表征.结果表明,不同阳极电催化剂交换电流密度J_0由大到小依次为,铂载n(Co):n(Mo)=2:3、铂载n(Co):n(Mo)=2:1、铂载n(Co):n(Mo)=1:1和铂,即铂载n(Co):n(Mo)=2:3阳极电催化剂具有较好的活性,这与循环伏安曲线测试结果一致.电解质溶液pH值为6～7时,随着温度的升高铂载n(co):n(Mo)=2:3阳极电催化剂活性呈现上升的趋势.优化后的Co、Mo掺杂原子比约为0.66,此类电催化剂在操作温度80℃下,交换电流密度为1.318mA/cm~2,表观活化焙值为616.6 kJ/mol .研究表明,铂载钴钼二元硫化物适合作为低温H_2S燃料电池阳极电催化剂,其中Co、Mo掺杂比对电催化活性影响较大.     

Soil erosion hazard evaluation—An integrated use of remote sensing,GIS and statistical approaches with biophysical parameters towards management strategies

Soil erosion hazard maps can be an essential tool in erosion prone areas as they explain and display the distribution of hazards and areas likely to be affected to different magnitudes. Therefore, it is very useful to planners and policy makers initiating remedial measures and for prioritizing areas. In this study, a numerical model was developed for soil erosion hazard assessment, in which Z-score analysis was combined with a geographical information system (GIS) to compute a synthetic soil erosion hazard index (SEHI). For this model, nine factors which have notable impact on soil erosion were selected. To generate the selected factors remote sensing, analytical hierarchy process (AHP) and GIS techniques along with spatial models were applied. To standardize all of the factors and establish the factor weights, the AHP method was adopted. For Z-score analysis with selected standardized factors, the Integrated Land and Water Information System (ILWIS) software was used and nine individual layers with Z-scores were prepared. Afterwards, the layers were integrated with their factor weights by means of a weighted linear combination to derive a SEHI value for each pixel. To classify the discrete SEHI map to represent a meaningful regionalization of soil erosion hazard, the equal distance cluster principle was used and graded into four levels of hazard; very high, high, moderate and low. The results depicted that in general, a moderate hazardous condition of soil erosion was found in the study area and the proposed approach was also able to identify the areas under high and very high hazards that require urgent intervention on a priority basis. Based on this study, comprehensive erosion hazard management strategies were anticipated for the efficient management of present and future erosion disaster in the area.     

磁性纳米Fe3O4@C对SBR脱氮除磷性能及其微生物种群组成的影响

为探究磁性纳米Fe₃O₄@C对序批式活性污泥反应器(SBR)污水处理系统脱氮除磷性能的影响,建立了2个相同的SBR(编号分别为0号和1号),其中,0号反应器未投加任何磁性材料(对照组),1号反应器中投加0.5 g·L^-1的Fe₃O₄@C(实验组),并采用高通量测序和实时定量PCR(qPCR)技术对2个反应器内生物种群结构及关键脱氮除磷功能菌群进行分析.结果表明:(1)Fe₃O₄@C对SBR除污性能有显著影响,其中,1号反应器化学需氧量(COD)的去除性能得到增强,24 d后去除率稳定在90%左右;0号和1号反应器总氮(TN)平均去除率分别为35.83%和52.18%;从第43 d起,1号反应器除磷性能明显高于0号反应器,运行70 d后,0号和1号反应器对总磷(TP)的平均去除率分别为47.52%和56.33%.(2)添加Fe₃O₄@C材料后,反应器内变形菌门(Proteobacteria)的...     

基于高通量测序的工业园区地下水和土壤细菌群落结构比较研究

为探究工业园区地下水和土壤细菌群落结构、多样性变化特征,采用高通量测序技术对地下水和土壤细菌16S r RNA基因高变区域进行序列测定。通过对Alpha多样性、物种组成、丰度和群落结构的分析,比较地下水和土壤细菌群落结构的异同。Alpha多样性的比较结果表明,土壤细菌群落多样性和丰富度明显高于地下水,地下水细菌群落多样性指数反映出地下水已受到周边污染源的影响。物种注释结果表明,地下水样品共检出48个细菌门,土壤样品共检出50个细菌门。变形菌门(Proteobacteria)、拟杆菌门(Bacteroidetes)和厚壁菌门(Firmicutes)是地下水细菌群落的优势类群,共占93.54%,且该工业园区地下水细菌群落呈现出典型的淡水种群特征;土壤中优势细菌门为Proteobacteria、放线菌门(Actinobacteria)、酸杆菌门(Acidobacteria)、Firmicutes和芽单胞菌门(Gemmatimonadetes),共占85.21%。由于地下水和土壤两者的生态系统和理化环境的差异,致使Actinobacteria、Acidobacteria、绿弯菌门(Chloroflexi)、硝化螺旋菌门(Nitrospirae)、α-变形菌纲(Alphaproteobacteria)、δ-变形菌纲(Deltaproteobacteria)和Gemmatimonadetes占比在地下水和土壤细菌群落间差异显著,同时使地下水和土壤细菌群落各含有一些特有的优势细菌属(地下水2个,土壤4个)。基于高通量测序技术对工业园区样品的测序结果可以为地下水和土壤环境的生态评价提供方法依据。     

用褐铁矿制备聚硅氯化硫酸铁的研究

通过正交实验研究了用盐酸、硫酸、褐铁矿和硅酸钠制备聚硅氯化硫酸铁（PSFCS）絮凝剂的工艺条件。实验结果表明,浸取时间为2.5～3 h,浸取温度为110℃,硫酸浓度为6 mol/L,盐酸浓度为3 mol/L,质量液固比为4∶1,铁的浸出率可达95.7%～96.3%。溶液中加入少量聚乙烯醇作稳定剂,亚硝酸钠作氧化催化剂。PSFCS的合成条件：Fe/Si摩尔比为2,硅酸活化pH值为2,硅酸活化时间是30～40 min,陈化时间是2～2.5 h。与聚合硫酸铁（PFS）和聚合氯化铝（PAC）比较了处理印染废水的效果,表明PSFCS具有良好的絮凝性能,COD和浊度的去除率分别可达81.4%和96.1%。     

北京南部城区PM2.5中碳质组分特征

为了解《大气污染防治行动计划》实施后北京市大气PM_2.5中碳质组分特征,于2017年12月至2018年12月在北京污染较重的南部城区进行了PM_2.5连续采样,对其中的有机碳(OC)和元素碳(EC)进行了全面研究.结果表明,北京大气PM_2.5、OC和EC浓度变化范围分别为4.2～366.3、 0.9～74.5和0.0～5.5μg·m^-3,平均浓度分别为(77.1±52.1)、(11.2±7.8)和(1.2±0.8)μg·m^-3,碳质组分(OC和EC)整体占PM_2.5的16.1%.OC质量浓度季节特征表现为:冬季[(13.8±8.7)μg·m^-3]>春季[(12.7±9.6)μg·m^-3]>秋季[(11.8±6.2)μg·m^-3]>夏季[(6.5±2.1)μg·m^-3],EC四季质量浓度水平均较低,范围为0.8～1.5μg·m^-3.二...     

Remediation of 2,4-dichlorophenol-contaminated groundwater using nano-sized CaO2 in a two-dimensional scale tank

• Nano CaO₂ is evaluated as a remediation agent for 2,4-DCP contaminated groundwater. • 2,4-DCP degradation mechanism by different Fe²⁺ concentration was proposed. • 2,4-DCP was not degraded in the system for solution pH>10. • The 2,4-DCP degradation area is inconsistent with the nano CaO₂ distribution area. This study evaluates the applicability of nano-sized calcium peroxide (CaO₂) as a source of H₂O₂ to remediate 2,4-dichlorophenol (2,4-DCP) contaminated groundwater via the advanced oxidation process (AOP). First, the effect and mechanism of 2,4-DCP degradation by CaO₂ at different Fe concentrations were studied (Fenton reaction). We found that at high Fe concentrations, 2,4-DCP almost completely degrades via primarily the oxidation of •OH within 5 h. At low Fe concentrations, the degradation rate of 2,4-DCP decreased rapidly. The main mechanism was the combined action of •OH and O₂^•−. Without Fe, the 2,4-DCP degradation reached 13.6% in 213 h, primarily via the heterogeneous reaction on the surface of CaO₂. Besides, 2,4-DCP degradation was significantly affected by solution pH. When the solution pH was>10, the degradation was almost completely inhibited. Thus, we adopted a two-dimensional water tank experiment to study the remediation efficiency CaO₂ on the water sample. We noticed that the degradation took place mainly in regions of pH<10 (i.e., CaO₂ distribution area), both upstream and downstream of the tank. After 28 days of treatment, the average 2,4-DCP degradation level was ≈36.5%. Given the inadequacy of the results, we recommend that groundwater remediation using nano CaO₂: (1) a buffer solution should be added to retard the rapid increase in pH, and (2) the nano CaO₂ should be injected copiously in batches to reduce CaO₂ deposition.     

Effects of water quality on the coagulation performances of humic acids irradiated with UV light

The presence of humic acid in drinking water treatment has received significant attention in recent years because of its adverse effects on the removal of many pollutants in coagulation. In this paper, the effects of water quality including pH, turbidity, alkalinity, and hardness on the removal of humic acid were investigated in a UV light hybridized coagulation process. Our results suggested that UV light radiation could effectively improve the removal rate of humic acid in coagulation under both neutral and basic conditions, and the variations of the selected water quality parameters had little adverse effect on the function of UV light. After UV light radiation, the removal rate of the nitro-humic acid (NHA) increased from 20% to 60% in coagulation, and increased further to 75% and 85% for the raw waters with 10.0 NTU kaolin and 100 mg·L^-1 hardness, respectively. In addition to NHA, the removal rates of the humic acid extracted from peat coal (PHA) and the humic acid provided by Japan metals and chemicals company (JHA) in coagulation were also improved, both in the range of 80%–90% after undergoing UV light radiation. By changing the radiation location from prior to coagulation to the flocculation process, similar experimental results were obtained. The formation of positive charged sites after UV light radiation was considered to be the primary factor that led to an enhanced removal of the humic acid in coagulation.