Relationship between groundwater cadmium and vicinity resident urine cadmium levels in the non-ferrous metal smelting area,China

● This study systematically examined the relationship between groundwater Cd and UCL. ● The study covered 211 UCL and sociological characteristic from nine groundwater samples. ● We found a significant positive correlation between groundwater Cd and UCL. ● Smoking status and education level also significantly affected UCL. Cadmium (Cd) has received widespread attention owing to its persistent toxicity and non-degradability. Cd in the human body is mainly absorbed from the external environment and is usually assessed using urinary Cd. Hunan Province is the heartland of the Chinese non-ferrous mining area, where several serious Cd pollution events have occurred, including high levels of Cd in the urine of residents. However, the environmental factors influencing high urinary Cd levels (UCLs) in nearby residents remain unclear. Therefore, 211 nearby residents’ UCLs and the corresponding sociological characteristics from nine groundwater samples in this area were analyzed using statistical analysis models. Groundwater Cd concentration ranged from 0.02 to 1.15 μg/L, aligning with class III of the national standard; the range of UCL of nearby residents was 0.37–36.60 μg/L, exceeding the national guideline of 0–2.5 μg/L. Groundwater Cd levels were positively correlated with the UCL (P < 0.001, correlation coefficient 95 % CI = 9.68, R² = 0.06). In addition, sociological characteristics, such as smoking status and education level, also affect UCL. All results indicate that local governments should strengthen the prevention and abatement of groundwater Cd pollution. This study is the first to systematically evaluate the relationship between groundwater Cd and UCL using internal and external environmental exposure data. These findings provide essential bases for relevant departments to reduce Cd exposure in regions where the heavy metal industry is globally prevalent.     

施肥对稻田甲烷排放的影响

采用自动连续测量系统，对不同施肥情况下稻田甲烷排放通量进行了监测。结果表明：施肥是影响稻田甲烷排放的重要因素。增施有机肥会导致甲烷排放量增加．应用化肥可降低甲烷排放，有机肥加倍处理，３２ｄ甲烷总排放量１６．４０ｇＣＨ＿４／ｍ￣２，是化肥加倍处理的１．５６倍；常规施肥处理介于两者之间。略高于常规加倍处理。肥料种类对甲烷排放量也有影响。全施有机肥高于有机肥加化肥（１：１）组，施沼渣肥组次之，全化肥组排放量最低，不到全有机肥处理排放量的１／５．有机肥又以施人畜粪的甲烷排放率最高，绿肥次之，沼渣肥和稻草的甲烷排放率最低。有机肥的多级利用是减少稻田甲烷排放的一条重要途径。     

山西省五台山区土壤氟元素的环境背景值及分布规律

对山西省五台山区垂直土壤主要土类的氟元素背景值进行了调查与分析，揭示了五台山区土壤氟元素区域背景的分布特征和变化趋势。结果表明：五台山区土壤氟背景值略高于我国平均水平，多数土壤Ｂ层含氟量最高。     

水稻施用耐氨固氮菌的效应研究

定位试验表明：施用耐氨固氮菌能促进水稻根系对氮素的吸收，显著增加水稻产量．耐氨固氮菌具有固氮能力，但按现行的施用量则固氮水平不足３０ｋｇ／ｈｍ２．在施氮水平较高的情况下。施用耐氨固氮菌能增加土壤有机质、全氮和碱解氮含量．     

分光光度法测定水稻土中有机酸的研究

本文以三种有机酸为代表,研究并建立了测定水稻土中有机酸的分光光度法。结果表明,三种有机酸的有色络合物具有相同的吸收光谱,且具有相同的最大吸收波长(λ_(mss)=500um)和相近的表观摩尔吸光系数。水分对酯化反应影响很大,含水量达4ml时,吸光值下降85％。酯化温度在10℃以上时,酯化率达最大值且保持稳定。在25℃时,显色反应20min趋干稳定,且在1h内吸光值下降不超过1.2％。土样中的有机酸采用NaCl溶液为提取剂,以3:1的液土比振荡提取30min,NaCl溶液浓度为1％就能达到良好的提取、过滤效果。提取液在烘干前需进行碱化,否则有机酸将损失30％以上。本法平均回收率为92.2％(n=5),标准差为0-0.0478cmol k8~(-1)(n=2-6),平均0.0142cmol kg~(-1)(n=26);变异系数为0—10％(n=2-6),平均4.87％(n=26);线性范围为0—0.0018mol L~(-1)。     

Odor Control for Land Application of Lime Stabilized Biosolids

Over three million dry metric tons of biosolids produced in the United States are land applied as Class B. Lime stabilization is employed for biosolids treatment at approximately 20% of the wastewater treatment plants because it is a simple and inexpensive process. During lime stabilization, the pH of sewage sludge is raised above 12 for pathogen inactivation and odor reduction. Lime dose and mixing have been found to greatly reduce odor generation from lime stabilized biosolids. A better quality biosolids product is less likely to create public opposition to land application programs. In this study, land application tests using Class B biosolids were conducted in order to determine whether better mixing can reduce odor generation during the land application of lime stabilized biosolids. The mixing quality of a treatment plant’s lime stabilized biosolids was improved by relocating the lime addition point, which prolonged the mixing time and produced a better mixed biosolids product. Based on field observations of land application, the poorly mixed biosolids were more odorous and offensive prior to incorporation. However, once incorporated into the soil, there was no appreciable odor difference between the biosolids. Another land application study was conducted to assess the odor of unincorporated Class A biosolids and compare it with incorporated Class A biosolids with the soil.     

含碳纳米TiO2光催化降解甲醇

采用管式光催化反应器,在石英玻璃管壁上涂镀含碳纳米TiO2薄膜,研究含碳纳米TiO2对甲醇气体的光催化降解性能。实验结果表明：随气体流量增加,甲醇降解率呈线性降低;在气体流量为200mL／min、相对湿度为40％、甲醇初始质量浓度为90～170mg／m^3的较佳条件下,甲醇降解率维持在80％以上,最高达85％;在甲醇初始质量浓度为150mg／m^3、气体流餐为200mL／min、相对湿度为40％的条件下,德国Degusa—P25光催化剂对甲醇的平均降解率为89％,含碳纳米TiO2对甲醇的平均降解率为82％,最人降解率为85％。     

高温烧结磷石膏钙渣制备轻质碳酸钙

以磷石膏钙渣为原料,通过高温煅烧,然后经消化、精制、碳化,制成轻质碳酸钙产品.研究结果表明:高温煅烧的最佳温度为 1 000 ℃,最佳煅烧时间为 1.0 h;沉淀反应的初始反应温度为 60 ℃,Ca(OH)2乳液质量浓度为 70 g/L,CO2流量为 1.8 L/h.制备的轻质碳酸钙产品各项指标均达到 HG/T2226...     

Methanolysis and Hydrolysis of Polycarbonate Under Moderate Conditions

Alkali-catalyzed methanolysis and hydrolysis of polycarbonate (PC) in a solvent in which PC can substantially dissolve such as N-methyl-2-pyrrolidone, 1,4-dioxane, tetrahydrofuran and so on were studied. Reaction conditions were optimized for the purpose of recycling PC in the form of bisphenol A and carbon carbonate. The results showed that both the methanolysis and hydrolysis of PC could take place under moderate conditions. Under the conditions of reaction temperature 40 °C, m(PC):m(MeOH) = 1:1, m(PC):m(NaOH) = 50:1, reaction time 35 min and using tetrahydrofuran as solvent, the methanolysis conversion of PC was almost 100% and the yield of bisphenol A was over 95%. Moreover, under the conditions of reaction temperature 100 °C, m(PC):m(H₂O) = 1:0.7, m(PC):m(NaOH) = 10:1, reaction time 8 h and using 1,4-dioxane as solvent, the hydrolysis conversion of PC was almost 100% and the yield of bisphenol A was over 94%.     

流动注射催化光度法测定环境水样中的痕量亚硝酸根

基于在pH为2.7的一氯乙酸缓冲溶液中亚硝酸根对溴酸钾氧化亮绿具有催化作用,建立了测定环境水样中痕量亚硝酸根的流动注射催化光度法。在室温下,当溴酸钾浓度为0.15mol/L、亮绿溶液浓度为1.12×10-3mol/L时,该方法的线性范围为0.04～0.36mg/L,检出限为7.44×10-4mg/L,测定频率为60次/h,相对标准偏差为1.1%(n=11)。