超高强度钻杆低温断裂性能及裂纹扩展特征研究

超高强度钻杆在冬季低温环境下容易发生脆性断裂事故,为了从断裂力学角度揭示其冷脆现象的本质,采用ZBC2302-D型示波冲击试验机,获得了不同温度下超高强度钢在冲击断裂过程中的力-位移曲线,并对比分析了冲击功、起裂功和裂纹扩展功之间的变化关系。采用国家标准GB 4161—2007中的计算公式,计算了冲击试样的裂纹扩展量Δa和阻抗应力强度因子K_R;同时,引入K_R阻力曲线,得到超高强度钻杆在不同温度下的剩余强度图。结果表明,当冲击试样开始出现裂纹时,随温度降低,钻杆的初始起裂应力有所增加,出现硬化现象。当钻杆出现一定长度的裂纹时,随温度降低,阻抗应力强度因子越来越小,而且降低速度越来越快,剩余强度也表现出相同的变化趋势。随温度降低,材料抵抗裂纹扩展的能力逐渐下降,表明钻杆在低温下更容易断裂。     

Applicability of hybrid bionic optimization models with kernel-based extreme learning machine algorithm for predicting daily reference evapotranspiration: a case study in arid and semiarid regions,China

Environmental Science and Pollution Research - The accurate prediction of daily reference crop evapotranspiration (ETO) enables effective management decision-making for agricultural water...     

Study on phosphorus loadings in ten natural and agricultural watersheds in subtropical region of China

Water eutrophication in subtropical regions of southern China threatens watershed health and is of major concern. However, annual phosphorus (P) loading and its dominant causes are still unclear, especially at the watershed scale. In this study, we investigated dynamic P loadings and associated factors (e.g., land use, livestock production, and runoff depth) in ten watersheds that varied in area from 9 to 5,212 ha in a hilly area of Hunan Province, China. A flowmeter was installed at the outlet of each watershed, and total P (TP) and soluble P (SP) concentrations were monitored periodically from June 2010 to October 2012. The results showed that annual P loadings (APLs) in the ten watersheds ranged from 22.8 to 247.8 kg P/km² and that P loss primarily occurred from April to June of each year during the main rainfall season in the study area. In addition, the average eutrophication (>0.05 mg P/L) ratio for stream waters was 86.7 % during the study period, which was indicative of a potentially serious condition for the local water environments. Annual P loadings were linearly related to livestock density (LD; R?=?0.92, p?<?0.01), whereas the eutrophication ratio of stream water was significantly (p?<?0.05) correlated with LD (R?=?0.61), percentage cropland (R?=?0.71), and percentage forest cover (R?=??0.68). Thus, it is concluded that the control of livestock production has the greatest potential for reducing P loadings in watersheds in this subtropical area. This will be beneficial to the amelioration and protection of local environment.     

铜绿微囊藻吸附废水中镍离子的研究

生物吸附法治理重金属废水为目前的一个研究热点。本文以铜绿微囊藻为研究对象,考察铜绿微囊藻藻液和藻粉对重金属镍离子的吸附效果。原子吸收光谱结果表明:藻液和藻粉的去除率分别为23.6%和92%,藻粉相比于藻液有更好的处理效果。傅里叶红外光谱(FTIR)及扫描电镜(SEM)结果表明:吸附重金属后,两者的峰型大致一致,藻粉和藻液的空间结构均发生了明显的改变。上述研究结果证明铜绿微囊藻可以作为一种去除重金属的生物吸附剂,为后续藻类治理重金属污染奠定了理论基础。     

Groundwater geochemistry diagnostics during in situ ERH remediation

In situ remediation represents a series of challenges in interpreting the monitoring data on remedial progress. Among these challenges are problems in determining the progress of the remediation and the mechanisms responsible, so that the process can be optimized. The release of organic pollutants to groundwater systems and in situ remediation technologies alter the groundwater chemistry, but outside of natural attenuation studies using inorganic chemical analyses as indicators of intrinsic biodegradation, typically little attention has been paid to the changes in inorganic groundwater chemistry. Smith (2008) noted that during an electrical resistance heating remediation that took place at a confidential site in Chicago, a two‐orders‐of‐magnitude increase in chloride concentrations occurred during the remediation. This increase in chloride resulted in a corresponding increase in calcium as a result of what is known as the common ion effect. Carbon dioxide is the gas found in highest concentrations in natural groundwater (Stumm & Morgan, 1981), and its fugacity (partial pressure) corresponds directly with calcium concentrations. Carbon dioxide at supersaturation in groundwater is capable of dissolving organic compounds, such as trichloroethene, facilitating removal of nonaqueous‐phase liquids at temperatures below the boiling point of water. One means of diagnosing these reactions is through the use of compound‐specific isotopic analysis, which is capable of distinguishing between evaporation, biodegradation, and differences in sources. The appropriate diagnosis has the potential to optimize the benefits from these reactions, lower energy costs for removal of nonaqueous‐phase liquids, and direct treatment where it is needed most. © 2010 Wiley Periodicals, Inc.     

MicroRNA: a novel implication for damage and protection against ionizing radiation

Environmental Science and Pollution Research - Ionizing radiation (IR) is a form of high energy. It poses a serious threat to organisms, but radiotherapy is a key therapeutic strategy for various...     

Utilization of coal fly ash in China: a mini-review on challenges and future directions

Environmental Science and Pollution Research - The rapid economic development in China places a large demand for energy, and as a result, thermal power plants in China are producing an enormous...     

Migration and transformation of heavy metals in hyperaccumulators during the thermal treatment: a review

Environmental Science and Pollution Research - The pollution of heavy metals (HMs) in the soil has become one of the important factors affecting the national environment and human health....     

华北地区乡村站点(曲周)夏季PM2.5中二次无机组分的生成机制与来源解析

利用大气PM2.5水溶性组分及其气态前体物在线测量系统(GAC-IC)于2014年6月9日~7月11日对华北地区乡村站点曲周大气PM2.5中水溶性组分及其气态前体物进行了在线测量,分析了PM2.5中水溶性组分与气态前体物日变化规律及其相互作用,探讨了当地细颗粒物的气粒转化机制并分析了其来源.结果表明夏季曲周大气PM2.5中水溶性无机离子与相关气态前体物的浓度呈现明显的日变化规律.观测期间,PM2.5中SO2-4、NH+4和NO-3的平均浓度分别是26.28、18.08和16.36μg·m-3,是PM2.5中最主要的水溶性无机离子,约占PM2.5质量浓度的76.23%;气态前体物中,NH3浓度明显偏高、平均值为44.85μg·m-3,主要来源于当地的农业活动排放;硫氧化率(SOR)和氮氧化率(NOR)平均值分别是0.60和0.30,表现出明显的二次污染特征.经相关性分析发现:曲周大气PM2.5中NH+4与NO-3、SO2-4有良好的相关性,且表现为富氨状态,NH+4以(NH4)2SO4形式存在,NO-3的生成主要受HNO3的限制.对NH4NO3平衡进行研究发现:与夜间相反,白天曲周大气环境不利于NH4NO3生成和保持.结果也表明,二次转化是曲周夏季细颗粒物的主要来源,堆肥与农田释放的NH3是导致高浓度二次无机颗粒物(SNA)的重要因素.     

Metal distribution characteristic of MSWI bottom ash in view of metal recovery

Bottom ash is the major by-product of municipal solid waste incineration(MSWI), and is often reused as an engineering material, such as road-base aggregate. However, some metals(especially aluminum) in bottom ash can react with water and generate gas that could cause expansion and failure of products containing the ash; these metals must be removed before the ash is utilized. The size distribution and the chemical speciation of metals in the bottom ash from two Chinese MSWI plants were examined in this study, and the recovery potential of metals from the ash was evaluated. The metal concentrations in these bottom ashes were lower than that generated in other developed countries. Specifically, the contents of Al,Fe, Cu and Zn were 18.9–29.2, 25.5–32.3, 0.7–1.0 and 1.6–2.5 g/kg, respectively. Moreover,44.9–57.0 wt.% of Al and 55.6–75.4 wt.% of Fe were distributed in bottom ash particles smaller than 5 mm. Similarly, 46.6–79.7 wt.% of Cu and 42.9–74.2 wt.% of Zn were concentrated in particles smaller than 3 mm. The Fe in the bottom ash mainly existed as hematite, and its chemical speciation was considered to limit the recovery efficiency of magnetic separation.