深水型水库藻类功能组时空演替及生境变化的影响

藻类功能分组是近年来生态学藻类研究的重要理论和方法.为了探明西安某深水型水源水库藻类功能组时空演替及生境变化的影响,于2011年8月起开展实验研究.研究采用现场在线监测和实验室分析相结合的方法.结果表明,水库藻类可分为10个功能组类别:B、D、P、X1、X3、F、G、J、LM、MP.其中,功能组B、P、F、X1、MP、D、J在水库中较为常见,X3、G、LM出现几率较低,功能组B、D、P、X1、X3的藻类数量占优.通过分析环境因子的变化对功能组时空演替的影响,发现水温为最主要的影响因子.水库藻类生长策略为:春季R/CR策略藻种→春末夏初CR/C策略藻种→夏末秋初C/CR/R/CS/S策略藻种→秋末及冬季CR/R策略藻种.此研究可为深水型水库安全取水提供理论支持.     

基于废陶瓷的多孔陶瓷研制及其对Ni2+的吸附性能

通过SEM、XRD、FT-IR表征及多孔陶瓷对废水中镍的去除能力,确定多孔陶瓷的制备条件:原料中田菁粉掺杂质量分数为4%,焙烧温度为800℃.SEM和孔结构表征说明,焙烧使多孔陶瓷形貌、结构发生变化;随着焙烧温度的升高,多孔陶瓷的比表面积和孔容呈现降低的趋势,而孔径呈现增大的趋势;EDS分析能表明,原废瓷粉和多孔陶瓷的主要元素组成均为Si、Al、O.SEM、XRD和FT-IR分析表明,多孔陶瓷吸附前后结构稳定.吸附Ni2+的系列实验表明,多孔陶瓷用量为10 g·L-1,吸附时间为60 min,进水pH值为6.32,进水Ni2+浓度在100 mg.L-1以内.在此条件下废水的Ni2+去除率可达89.7%,多孔陶瓷对废水中镍有较好的去除效果.以制备的多孔陶瓷处理含镍废水,考察多孔陶瓷对废水中Ni2+的吸附动力学和吸附等温线,结果表明,多孔陶瓷对Ni2+的吸附过程符合准二阶动力学模型(R2=0.999 9),Qe为9.09 mg·g-1;吸附过程可用Freundlich方程和Langmuir方程来描述,温度由20℃升高至40℃,最大吸附量Qm由14.49 mg·g-1上升至15.38 mg·g-1.     

陶粒CANON反应器的接种启动与运行

通过CANON接种污泥,以人工配制无机高氨氮废水为对象,研究以陶粒为填料的CANON反应器启动与运行情况,结果表明:①陶粒可以作为CANON反应器合适填料,温度通过水浴控制在30℃±1℃,HRT为9 h、pH控制在7.00~8.08之间,经过60 d成功启动了CANON反应器,TN的去除负荷达到0.79 kg·(m3·d)-1;②在温度30℃时,陶粒CANON反应器中临界DO范围在1.12~1.69 mg·L-1之间,CANON反应器中短程硝化和厌氧氨氧化性能可维持稳定,高于此范围时,会出现CANON反应器中短程硝化不稳定现象;③在温度25℃,控制DO在1.01~1.54 mg·L-1之间时,尽管NO-3-N变化值与TN变化值的比值(δNO-3-N/δTN)略微偏离理论值0.127,为0.150~0.204,但CANON反应器脱氮性能趋于稳定,TN去除率最高为75.56%,TN的去除负荷最高达到0.97 kg·(m3·d)-1,这意味着CANON工艺的适宜温度范围至少可以降低至25℃.     

混凝-超滤处理径流雨水效果——以华南地区为例

采用超滤膜(UF)为核心,以混凝作为预处理措施,对混凝-超滤工艺处理径流雨水的特性和膜通量变化与污染现象进行了研究,并对聚合硫酸铁(PFS)单独混凝、UF、PFS-UF组合工艺进行了对比;在优化混凝基础上,考察了混凝-UF对常规水质指标及总磷、生物可同化有机碳(AOC)、可生物降解溶解性有机碳(BDOC)等生物稳定性指标的去除效果.结果表明,混凝可有效去除TOC、UV254和总磷,混凝剂投加量与污染物去除近似呈线性关系.各混凝剂除浊效能均良好.综合考虑混凝处理效率与经济性,实验采用混凝方案为10 mg·L-1的PFS.PFS、UF、PFS-UF工艺除浊率均在95%以上,PFS和UF对TOC和UV254的去除较为接近,采用PFS-UF可提高去除率13%—15%;PFS-UF处理后雨水的AOC、BDOC分别降低至61.8μg·L-1、0.19 mg·L-1,残余总磷可降至3.8μg·L-1,雨水生物稳定性明显提高.PFS、UF和PFS-UF对颗粒物的去除率分别达80.5%、99.6%和99.9%.膜通量的变化和SEM图分析表明,混凝在一定程度上减轻了UF膜污染;形成的凝胶层具有一定整体强度,水力清洗时易于清除,膜通量恢复较好;但同时凝胶层的产生也增大了透膜阻力,PFS-UF工艺的周期内膜通量衰减有增加的趋势.     

土壤颗粒对纳米TiO_2悬浮稳定性作用机制的实验研究

在不含表面活性剂和含有表面活性剂两种条件下,研究了土壤颗粒对纳米TiO2(nTiO2)悬浮稳定性的影响.结果表明,土壤颗粒降低了nTiO2在水相中的悬浮稳定性.当体系中不含表面活性剂时,nTiO2在土壤大颗粒上的沉积是导致nTiO2脱稳沉淀的主要原因.在含有表面活性剂的溶液中,土壤颗粒降低nTiO2悬浮稳定性的作用变得更加明显了.一方面,表面活性剂加速了土壤颗粒本身的沉降从而增强了nTiO2在其中的沉降,另一方面,表面活性剂在土壤上的强烈吸附促进了表面活性剂-nTiO2在土壤上的沉积.扫描电镜显示,nTiO2不仅吸附在土壤大颗粒上,还会吸附在土壤小颗粒表面.3种表面活性剂中,十六烷基三甲基溴化铵(CTAB)悬浮的nTiO2与土壤颗粒共沉淀现象最明显.除了土壤对CTAB的吸附作用之外,XDLVO/DLVO能量计算显示CTAB体系中土壤颗粒与nTiO2之间存在显著第二极小值,表明nTiO2能够在第二极小值位置与土壤颗粒结合,从而与土壤颗粒一起快速沉淀.     

Application of a hydroxylamine nitrate stability model to plutonium purification process equipment

A mathematical model that predicts hydroxylamine nitrate (HAN) (NH₂OH·HNO₃) stability is applied to aqueous solutions containing HAN, nitric acid and plutonium that are used in plutonium purification processes. The model estimates the stability of these solutions with respect to the rapid, hazardous, autocatalytic reaction of HAN with nitric acid that generates heat and gas. It also accounts for reaction kinetics, temperature changes, gas generation rates, solution volumes and flow rates, and distribution of plutonium and nitric acid between aqueous and organic phases. The model is applied to three typical process vessels used in solvent extraction purification of plutonium – a countercurrent aqueous/organic plutonium stripping column, an oxidation column used for HAN and hydrazine destruction, and a plutonium rework tank. Both normal and off-normal process scenarios are modeled. Two of the off-normal scenarios lead to the rapid autocatalytic reaction of HAN with nitric acid where heat and gas are generated and that could lead to damage of the process equipment and/or release of hazardous plutonium solution from the vessel. In these two cases, stationary aqueous solutions containing HAN, Pu(III), and nitric acid were allowed to slowly react until conditions for the autocatalytic reaction were reached.     

Effect of urea on detonation characteristics and thermal stability of ammonium nitrate

A study has examined the effect of urea on the thermal stability and detonation characteristics of ammonium nitrate (AN). The thermal decomposition temperature and surface morphology of samples were investigated by differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). For further research on the thermal sensitivity and shock sensitivity of the samples, the Koenen test and UN gap test were conducted. The results indicate that urea can substantially increase the thermal stability of AN (the greatest exothermic peak is increased by more than 100 °C) and reduce the thermal sensitivity of AN. However, AN-50wt. % urea mixtures can still produce a steady detonation in the UN gap test. Urea cannot reduce the ability to propagate a detonation. Possible explanations for these results are discussed.     

内排压脚与边坡稳定性的关系

为了研究边坡角及边坡形状与边坡稳定性的关系,采用有限元软件ANSYS模拟了不同边坡角对应的稳定系数,以及不同平盘宽度和压脚高度所形成的等储备强度边坡的稳定系数。模拟中假设材料符合相关联的理想弹塑性本构关系,强度准则符合Drucker-Prager准则,用计算收敛性作为边坡稳定性的准则,用强度折减法得出边坡的稳定系数。为了形成等储备强度边坡,由下到上分步骤进行压脚。先在平面边坡最下台阶压脚,这样提高了边坡稳定系数,在边坡进入临界状态时,最下两台阶的塑性状态相同,则压脚停止;再在最下两台阶同时压脚,在边坡进入临界状态时,最下3个台阶的塑性状态相同,则压脚停止;以此类推,在最下边n个台阶同时压脚,在边坡进入临界状态时,压到与第n+1个台阶的塑性状态相同为止。结果表明,边坡总是从坡脚开始形成塑性区,在重力加载过程中,塑性区以弧形条带向坡顶扩展,形成滑带。最有效的内排压脚是从最下台阶开始形成等储备强度边坡的压脚。     

围岩稳定性评价的改进物元可拓模型与应用

为弥补现有地下工程围岩稳定性评价方法的不足,建立了改进的物元可拓模型。通过构造一种新的关联函数,解决了因传统的物元可拓模型的关联函数是一个分段函数而存在的不便于计算的缺陷,以及评价指标间的互不相容性问题,拓宽了物元可拓法的应用范围。将改进的物元可拓模型应用于某地下工程围岩的稳定性评价,结果表明,样本1、2、5属于Ⅱ级(较稳定),样本3、4属于Ⅰ级(稳定)。通过将其评价结果与传统可拓法及模糊数学综合评判结果进行比较分析,证明该评价方法的正确性。研究表明,改进的物元可拓模型的评价结果与实际工程地质情况更为吻合,准确度更高,能够反映各因素对围岩稳定性的影响,其合理性和可行性得到了验证。     

Thermal decomposition mechanism of 65% lysine sulfate powder and its thermal stability based on thermal analysis

Lysine is widely used in the fields of food, medicine and feed, which generally appears in the form of lysine sulfate or lysine hydrochloride dust because of the high instability of the free L-lysine. The L-lysine Sulfate is in high risk of decomposition, spontaneous ignition and even the dust explosion, because the control temperature in its production process is high up to 90 °C. Thus, the thermal behaviors and its thermal stability of 65% lysine sulfate are experimentally explored in Air and Nitrogen using the simultaneous TG-DSC measurements. Results show: (1) the decomposition of 65% lysine sulfate can be divided into three stages both in the atmospheres of air and nitrogen, and most of the weight loss occurred in the first two stages, which are related with the decarboxylation and deamination process. (2) The effects of atmosphere on the decomposition of 65% lysine sulfate mainly occur at the third stage. In this stage, the weight loss in nitrogen is only 14.2%, which is much lower than that in air (34.3%), which is related to the oxidative degradation at high temperature. Besides, the active energy is slightly increased in nitrogen compared to that in air. (3) The initial temperatures of the decomposition of the 65% lysine sulfate are 145 °C and 155 °C, for the air and nitrogen atmosphere, respectively, which are much lower than that (260 °C) of the pure lysine.