混凝体系中铝盐水解行为及作用机制的研究与分析

采用Ferron逐时络合比色法对混凝体系中铝盐水解产物分布进行研究发现,铝盐在混凝体系发生水解反应获得的产物中Alb形态含量明显高于纯净水系,并且碱化度越低的铝盐,在适宜pH的混凝体系其水懈产物中Alb形态含量上升越快.而Alc形态含量变化不明显.提出混凝体系中铝盐水解反应的作用机制,指出HCO3-对H+浓度的良好控制是保证铝盐水解反应效率、获取高浓度Alb形态的关键.     

What determines selection and abandonment of a foraging patch by wild giant pandas (Ailuropoda melanoleuca) in winter?

Background, aim, and scope  Foraging patches can be described as a nested hierarchy of aggregated resources, implying that study of foraging by wild animals should be directed across different spatial scales. However, almost all previous research on habitat selection by the giant panda has concentrated upon one scale. In this research, we carried out a field study to understand foraging patch selection by giant pandas in winter at both microhabitat and feeding site scales and, for the first time, attempted to understand how long it would stay at the feeding sites before moving on. Materials and methods  The field survey was conducted from November 2002 to March 2003 at Fengtongzhai Nature Reserve (102°48′–103°00′ E, 30°19′–30°47′ N), Baoxing County of Sichuan Province, China, to collect data in both microhabitat and control plots. The microhabitat plots were located by fresh feces or foraging traces left by giant pandas, and the control plots were established to reflect the environment. Within each microhabitat plot, one 1 × 1 m² plot was centralized at the center of each feeding site, in which numbers of old bamboos and old shoots, including eaten and uneaten, were counted, respectively. Results  The results showed that winter microhabitats selected by this species were characteristic of gentle slopes and high old-shoot proportions and that the latter was even higher at feeding sites. Two selection processes, namely, from the environment to microhabitats and from the latter to feeding sites, were found during this species’ foraging patch utilization. Giant pandas preferred to eat old shoots to old bamboo at feeding sites in winter and did not leave unless old-shoot density fell to lower than the average in the environment. Discussion  Both microhabitats and feeding sites selected by giant pandas were characteristic of high old-shoot density, indicating that the preferred food item had a significant influence upon its foraging patch selection. The preference for gentle slopes by giant pandas was presumed to save energy in movement or reflect the need to sit and free its fore-limbs to grasp bamboo culms when feeding but also seemed to be correlated with an easier access to old shoots. The utilization of old shoots at feeding sites was assumed to help maximize energy or nutrient intake during their foraging. Conclusions  The difference between microhabitat plots and control plots and between microhabitats and feeding sites uncovered a continuous selection process from the environment via microhabitats to feeding sites. The utilization of old shoots at feeding sites was parallel to the marginal value theorem. The selection and abandonment of foraging patches by giant pandas was an optimal behavioral strategy adapted to their peculiar food with high cellulose and low protein. Recommendations and perspectives  Our results uncovered the importance of multiple scales in habitat selection research. To further understand the process of habitat selection, future research should pay more attention to resolve the question of how to locate foraging patches under dense bamboo forests by the giant panda, which was traditionally considered to have poor eyesight, although our research has answered what type of habitats the giant panda prefers and when to leave.     

纳米TiO2-Ag改性VACF处理氨气研究

利用浸渍法将纳米TiO2·Ag负载于粘胶基活性炭纤维上进行改性来处理低浓度氨气,扫描电镜观测和能量色散谱分析表明纳米TiO2和Ag均较成功地负载于VACF表面上,改性VACF对氨气脱除性能良好,最大脱除率为93.3%;当Ag*掺杂量为TiO2含量的0.5wt%时氨气脱除率达到最大值;存在最佳相对湿度为55%;在氨气浓度为13～65 mg/m3范围内,浓度越低,脱除效果越好;处理较高浓度氨气可通过增加改性VACF用量;随着反应连续进行,改性VACF稳定性受到影响,但仍具有脱除氨气能力.     

负载型混晶相TiO2光催化剂的低温制备及其光催化活性

以蒙皂石为载体,钛酸四丁酯为前驱物,在较低温度下由溶胶凝胶法制备得到负载型TiO₂光催化剂。研究了理论负载量、固定化温度、干燥、焙烧温度对TiO₂/蒙皂石复合光催化剂光催化性能的影响。采用XRD分析技术对复合材料进行了表征。结果表明,负载的TiO₂以锐钛矿-金红石的混晶相存在。当TiO₂理论负载量为15 mmol/g、溶胶反应温度为25℃、干燥温度为70℃时,TiO₂/蒙皂石复合光催化剂对偶氮染料光催化反应1 h降解率达93.40%。该制备技术的特点是在省去高温焙烧的条件下,制备出光催化活性高的负载型光催化剂。     

不同改性方式对竹炭净化气态氮氧化物效果的影响

为了研究不同表面改性方法对竹炭空气净化效果的影响,测定了化学药剂活化、超声处理、微波处理后的改性竹炭对低浓度氮氧化物的净化效果。结果表明:活化剂浸渍后的竹炭,对氮氧化物净化效率降低,净化速度减慢;微波功率越大、辐照时间越长,改性后竹炭对氮氧化物处理效率越大,但辐照时间达到一定程度后,竹炭对氮氧化物的处理效率增大变得缓慢;超声处理后的竹炭对NO的处理效率比改性前有明显提高。BET测试结果表明,竹炭产品用微波和超声处理后,平均孔径、微孔表面积和比表面积均比活化前增大;而经过活化剂浸渍后,微孔面积和比表面积都显著下降。因此建议采用微波及超声方式对竹炭进行活化。     

利用含油污泥生产油煤水浆的实验研究

利用降粘技术,将高粘度含油污泥降粘为流动性良好的浆体。实验表明:合适的降粘剂加入量为1.0%。利用降粘后的含油污泥制备出具有良好浆体特性的油煤水浆。当降粘后含油污泥加入量分别为油煤水浆总量的20%和30%时,制备的油煤水浆粘度均小于300mPa.s,浆体粘度随温度升高不断降低,具有良好的剪切变稀特性。制备的油煤水浆不需加入稳定剂,一个月内未发生硬沉淀或分层现象,具有较好的稳定性。     

废旧电路板上残留焊锡剥离液的研制

以硝酸-磺酸型退锡剂为基础配方,研制了一种脱除废旧电路板表面残留焊锡的剥离液.该剥离液以硝酸为氧化剂,氨基磺酸为稳定剂,苯并三氮唑为铜的缓蚀剂.实验结果表明:剥离液的最佳配比为硝酸浓度3 mol/L,氨基磺酸浓度0.4 mol/L,苯并三氮唑浓度0.08 mol/L;每升剥离液可处理3.5 kg废旧电路板,处理后电路板中的铅离子含量降至100 mg/kg以下.该剥离液处理后的电路板表面的铜箔保持完好,基本没有被剥离液浸蚀.     

两性高分子絮凝剂的制备及其应用研究

以天然植物粉Ｆ６９１为原料,通过羧甲基化、接枝共聚和曼尼期(Ｍａｎｎｉｃｈ)三步反应合成出两性天然高分子改性絮凝剂(ＣＧＡＡＣ),确定了其较佳的制备条件;ＣＧＡＡＣ对造纸抄纸白水和造纸混合污泥的絮凝脱水试验表明:１０ｍｇ·ｌ－１ＣＧＡＡＣ与４０ｍｇ·ｌ－１ＰＡＣ配合使用,ＣＯＤＣｒ去除率可达７２%,效果优于对比样ＰＨＰ;ＣＧＡＡＣ对造纸混合污泥的絮凝脱水性能优于对比样ＰＨＰ和ＰＡＭ－Ｃ．     

搅拌萃取-红外分光光度法测定污水中石油类

以四氯化碳为萃取溶剂,自动搅拌萃取污水样品中的总油,有机相经硅酸镁吸附脱除极性物质后,选择红外分光光度法测定其中的石油类,方法检出限为0.024 mg/L;对实际水样进行4个质量浓度水平的加标回收试验,回收率在88.0%~108%之间,6次测定的相对标准偏差为2.9%~6.1%,满足污水中石油类的测试要求。     

Occurrence of and risk posed by highly carcinogenic dibenzo[def,p]chrysene isomers in urban soil

Dibenzopyrene and its isomers are considered the most potent carcinogens of all polycyclic aromatic hydrocarbons tested to date. However, despite public concerns over their deleterious effects, they have not been extensively studied. The occurrence of four highly carcinogenic isomers of dibenzopyrene – dibenzo[def,p]chrysene, dibenzo[a,e]pyrene, dibenzo[a,i]pyrene, and dibenzo[a,h]pyrene in urban soil samples from Shanghai, China, have been determined in this study, as well as that of benzo[a]pyrene and coronene. A total of 14 peaks with ions at m/z 302 were detected by gas chromatography-mass spectrometry. Although the concentrations of benzo[a]pyrene and the sum of the 16 priority polycyclic aromatic hydrocarbons were greater than that of dibenzopyrene and its isomers, the carcinogenic potency of the latter was higher than that of benzo[a]pyrene. The results also indicate that the relative carcinogenic potency of the four dibenzopyrene isomers in the samples is higher than that of the 16 priority polycyclic aromatic hydrocarbons.