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61.
阿替洛尔在硝酸根溶液中的光降解研究 总被引:1,自引:0,他引:1
以氙灯为模拟太阳光光源,研究了β阻滞剂阿替洛尔(ATL)在硝酸根溶液中的光解,探讨了硝酸根离子浓度、溶液pH值、碳酸氢根离子浓度和腐殖质浓度对ATL光解的影响.结果表明,ATL在不同浓度硝酸根溶液中的光解反应符合准一级动力学规律,增大硝酸根离子浓度促进了ATL的光降解率,当硝酸根离子浓度由0增至5 mmol.L-1时其速率常数由0.002 26min-1增至0.009 4 min-1;酸性或碱性溶液有利于ATL在硝酸根溶液中的光解,碳酸氢根离子浓度对光解无明显影响,而加入Suwannee富里酸(SRFA)对光解产生抑制作用.采用异丙醇作为羟基自由基分子探针检测到.OH存在于ATL光解过程中.采用SPE-LC-MS方法鉴定了ATL在硝酸根溶液中的主要光解产物,并提出了可能的光解途径. 相似文献
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63.
若尔盖高原湿地藻类多样性研究 总被引:1,自引:1,他引:0
分别于夏、冬两季采集若尔盖高原湿地水样,利用传统培养及显微镜检的方法和现代分子生物学方法对其藻类多样性进行了研究.结果表明,夏季水样至少培养出4种绿藻,分别为普通小球藻(Chlorella vulgaris Beij.)、浮球藻(Planktosphaeriagelatinosa G.M.Smith)、繁茂栅列藻(Scenedesmus abundans Kirchner)和柱状栅列藻(Scenedesmus bijuga Turp.),均属于绿球藻(Chlorococcales),其中普通小球藻为优势藻种,并被分离纯化.显微镜检结果表明冬季水样中主要的藻类种群为硅藻,此结果符合在低温季节天然水体中常以硅藻为主的常理.蓝藻16S rRNA基因克隆文库中的主要类群为硅藻(Bacillaripiophyta,35.3%),其次为蓝藻,包括色球藻(Chroococcales,5.9%)、念珠藻(Nostocales,11.8%)、颤藻(Oscillatoriales,11.8%)和一些未知种属的蓝藻类群(Unclassified Cyanobacteria,35.3%),还发现一些与低温环境微生物相关的类群,如颤藻目细纤菌属(Leptolyngbya). 相似文献
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65.
Yanhui Li Bing Xi Quansheng Zhao Fuqiang Liu Pan Zhang Qiuju Du Dechang Wang Da Li Zonghua Wang Yanzhi Xia 《环境科学学报(英文版)》2011,23(3):404-411
Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal
adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized
kaolin (kaolin/CA), was prepared using a sol-gel method. The e ects of contact time, pH, adsorbent dose, and temperature on Cu2+
adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum
Cu2+ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction
was a spontaneous and endothermic process. 相似文献
66.
Removal of polycyclic aromatic hydrocarbons (PAHs), e.g., naphthalene, acenaphthene, phenanthrene and pyrene, from aqueous solution by raw and modified plant residues was investigated to develop low cost biosorbents for organic pollutant abatement. Bamboo wood, pine wood, pine needles and pine bark were selected as plant residues, and acid hydrolysis was used as an easily modification method. The raw and modified biosorbents were characterized by elemental analysis, Fourier transform infrared spectroscopy and scanning electron microscopy. The sorption isotherms of PAHs to raw biosorbents were apparently linear, and were dominated by a partitioning process. In comparison, the isotherms of the hydrolyzed biosorbents displayed nonlinearity, which was controlled by partitioning and the specific interaction mechanism. The sorpfion kinetic curves of PAHs to the raw and modified plant residues fit well with the pseudo second-order kinetics model. The sorption rates were faster for the raw biosorbents than the corresponding hydrolyzed biosorbents, which was attributed to the latter having more condensed domains (i.e., exposed aromatic core). By the consumption of the amorphous cellulose component under acid hydrolysis, the sorption capability of the hydrolyzed biosorbents was notably enhanced, i.e., 6-18 fold for phenanthrene, 6-8 fold for naphthalene and pyrene and 5-8 fold for acenaphthene. The sorpfion coefficients (Kd) were negatively correlated with the polarity index [(O+N)/C], and positively correlated with the aromaticity of the biosorbents. For a given biosorbent, a positive linear correlation between logKoc and logKow for different PAHs was observed. Interestingly, the linear plots of logKoc-logKow were parallel for different biosorbents. These observations suggest that the raw and modified plant residues have great potential as biosorbents to remove PAHs from wastewater. 相似文献
67.
Arsenic in the environment is attracting increasing attention due to its chronic health effects. Although arsenite(As(III)) is generally more mobile and more toxic than arsenate(As(V)), reducing As(V) to As(III) may still be a means for decontamination, because As(III) can be removed from solution by precipitation with sulfide or by adsorption or complexation with other metal sulfides. The performance of As(V) bio-reduction under autohydrogenotrophic conditions was investigated with batch experiments. The results showed that As(V) reduction was a biochemical process while both acclimated sludge and hydrogen were essential. Most of the reduced arsenic remained in a soluble form, although 20% was removed with no addition of sulfate, while 82% was removed when sulfate was reduced to sulfide. The results demonstrated that the reduced arsenic was re-sequestered in the precipitates, probably as arsenic sulfides. Kinetic analysis showed that pseudo first-order kinetics described the bio-reduction process better than pseudo second-order. In particular, the influences of pH and temperature on As(V) reduction by acclimated sludge under autohydrogenotrophic conditions and total soluble As removal were examined. The reduction process was highly sensitive to both pH and temperature, with the optimum ranges of pH 6.5–7.0 and 30–40°C respectively. Furthermore, Arrhenius modeling results for the temperature effect indicated that the As(V) reduction trend was systematic. Total soluble As removal was consistent with the trend of As(V) reduction. 相似文献
68.
重金属抗性解磷细菌的磷溶解特性研究 总被引:2,自引:1,他引:1
从湖南省湘西州花垣县的铅锌矿表层土壤中,筛选出两株具有重金属抗性和解磷特性的细菌T PSB1和T PSB2.通过16S rRNA基因序列比对,分别鉴定为嗜麦芽寡养单胞菌(Stenotrophomonas maltophilia)和唐菖蒲伯克霍尔德菌(Burkholderia gladioli).T PSB1和T PSB2在含有难溶性无机磷液体培养基中,其上清液的可溶性磷含量最高分别达到了402.9 mg·L-1和589.9 mg·L-1;在难溶性有机磷固体和液体培养基中,固体平板上均出现解磷圈,而液体培养基上清液中,可溶性磷含量也分别达到了2.97 mg·L-1和4.69 mg·L-1.另外,两株细菌对重金属Zn2+的抗性最高,在其浓度为2000 mg·L-1固体和液体培养基条件下均可以生长,磷溶解浓度分别为114.8 mg·L-1和125.1 mg·L-1.而在含铬和铅的浓度为1 000 mg·L-1的液体培养基中,两株细菌同样表现出重金属抗性.在Pb2+浓度为1000 mg·L-1的液体培养基中,磷溶解浓度分别达到了57.9 mg·L-1和71.7 mg·L-1;而在Cr2+浓度为1000 mg·L-1的培养基中磷溶解浓度分别为60.1 mg·L-1和98.4 mg·L-1. 相似文献
69.
金山湖闸坝型水体表层沉积物重金属分布特征及生态风险评价 总被引:7,自引:3,他引:4
采集金山湖闸坝型水体表层沉积物,经HNO3-HF-HClO4消解后,通过电感耦合等离子质谱法(ICP)测定沉积物As、Cu、Pb、Cd、Zn、Cr等6种重金属含量,通过富集系数、地累积指数法、潜在生态风险评价以及溯源分析等对沉积物重金属的分布特征进行综合评价.结果表明:1金山湖表层沉积物As、Pb、Cu、Zn、Cr、Cd的平均值分别为23.22、26.20、24.42、143.12、245.30、0.67 mg·kg-1,其中,Pb、Cu含量低于土壤环境质量标准一、二级标准,Zn、Cr含量介于土壤环境质量标准一级标准与二级标准之间,As、Cd含量均超过土壤环境质量标准一、二级标准;从空间分布来看,Pb和Zn在北固山广场的1号样点形成最高值,As、Cu、Cr、Cd的含量分别在镇润洲码头附近的12号样点、运粮河河口区域的3号样点、湖中靠近征润州岛的14号样点、春江潮与解放路泵站之间往湖中心处的7号样点处出现最高值.2富集系数表现为As>Cr>Cd>Pb>Zn>Cu,表明金山湖表层沉积物中As的富集量最大,Cu最小.3根据地累积指数判断,金山湖未受Cu的污染,Pb、Zn、Cd则为轻度污染,As、Cr表现为偏中度污染;46种重金属的单项潜在生态危害系数表现顺序为Cd>As>Cr>Pb>Cu>Zn,其中,Cr、Pb、Cu、Zn均为轻微生态危害程度,As和Cd处于中等生态危害程度;从全湖分布看,北固湾广场附近(1号样点)、春江潮与解放路泵站之间靠近岸边区域(6号样)、春江潮与解放路泵站之间往湖中心处(7号样点)以及镇润洲码头附近(12号样点)样点的潜在生态危害为中等,其余采样点均为轻微潜在生态危害;5主成分分析结果表明,金山湖沉积物重金属的差异除了受到各样点沉积物环境背景值的影响外,还与各采样点周围人为活动、外源污水排放等有密切关系.6本次研究中发现闸坝对金山湖沉积物重金属分布的影响不明确,该部分内容尚需进行长时间尺度的研究. 相似文献
70.
相对海平面上升是一个缓慢、渐进过程,但长期的积累可以使得上升幅度相当可观,从而加剧风暴潮、海岸侵蚀、海水入侵和咸潮等灾害致灾程度。基于验潮位监测和卫星观测结果显示,全球海平面在20世纪中期平均上升1.5~2.0 mm/a,而近30年中国沿海海平面上升速率为2.6~2.7 mm/a,高于全球平均值。渤海湾天津地区由于地面沉降显著,而导致相对海平面大幅度上升。滨海地区地面沉降速率在未来50至100年内可能会稳定在1.0~2.0 cm/a范围,结合目前海平面上升速率2.7 mm/a,总的相对海平面上升速率处于12.7~22.7 mm/a范围。由此估计,到2050年,天津地区相对海平面将比2012年高出48.3~86.3 cm,而到2100年,将比2012年高出111.8~199.8 cm。 相似文献