液相色谱法测定底泥中阿特拉津的不确定度评定

摘要：文章采用实验室内部的非标准方法《底泥中阿特拉津残留量的液相色谱测定方法》测定底泥中的阿特拉津残留量。通过对影响测定结果的不确定度分量的分析和量化,求出被测量的标准不确定度,给出各分量对测定结果不确定度的相对贡献,对测定结果进行了表述。对实际河道底泥样品中的阿特拉津残留量进行了测定,得到阿特拉津农药残留量的拓展不确定度为0．23ug/g,k=2。     

GM(1,1)灰色模型在真空预压沉降预测中的应用

土体固结度是真空预压法加固土体效果的一个重要评价指标,地基最大沉降量的计算是确定土体固结度的关键。本文结合工程实例,分析了GM(1,1)灰色模型在真空预压沉降预测中的可行性,根据部分实测数据计算了地基最大沉降量及土体固结度,并与常用的三点法和双曲线法计算结果进行对比,结果表明GM(1,1)灰色模型的预测结果更符合工程实际。该研究对真空预压施工具有一定的指导意义。     

基于水资源合理配置的河流“双总量”控制研究——以河北省唐山市为例

河道的最小控制流量和最大纳污控制量（简称“双总量”）是维系河流健康的决定性因子。论文初步建立了基于水资源合理配置的河流“双总量”控制研究技术框架,并对唐山市月尺度的“双总量”控制指标进行核算。通过水资源合理配置,除个别枯水年份和连续枯水年份外,唐山市河道的最小控制流量均可得到满足。在基准年、2010年和2020年3个规划水平年,唐山市规划河流COD的最大纳污控制量分别为16357．57、12659．19和11572．50t／a;NH3-N的最大纳污控制量分别为907．80、660．27和580．09t／a。在统一水资源配置平台上制定的“双总量”控制指标,从根本上保障了竞争用水条件下河流生态需水,客观确立了规划水平年河道纳污能力的年内分配,并整体上提高了河流的最大纳污能力。     

Residual dynamics of thiacloprid in medical herbs marjoram, thyme, and camomile and in soil

Thiacloprid is a new insecticide of the chloronicotinyl family. To assess its risk after application, residual characteristics of thiacloprid in marjoram, thyme, and camomile and in soil were studied under field conditions. The active ingredient was extracted from the plant material using a mixture of acetone-water. After filtration, the extract was concentrated to the aqueous phase, diluted with water, and portioned against ethyl acetate on a matrix solid phase dispersion column. Thiacloprid was extracted from soil using a mixture of methanol-water, filtered, and re.extracted （clean up） with dichloromethane. The residues were quantified using HPLC-MS-MS. The methods were validated by recovery experiments. Thiacloprid residues in marjoram, thyme, and camomile and in soil persisted beyond 10, 14, 14, and 21 d but no residues were detected after 14, 21, 21, and 28 d, respectively. The data obtained in this study indicated that the biexponential model is more suitable than the first-order function to describe the decline of thiacloprid in fresh marjoram, fresh thyme, and dried camomile flowers with half-life （t1/2） of 1.1, 0.7, and 1.2 d, respectively. However, both the first-order function and biexponential model were found to be applicable for dissipation of thiacloprid in soil with almost the same t1/2 values of 3.5 and 3.6 d. The results indicated that thiacloprid dissipates rapidly and does not accumulate in the tested herbs and in soil.     

广东省荔枝园土壤农药残留现状研究

荔枝收获完毕后在广东省荔枝主产区采集208个荔枝园土壤样本,检测了9种荔枝常用农药甲霜灵、代森锰锌、多菌灵、溴氰菊酯、氯氰菊酯、三氟氯氰菊酯、敌百虫、乐果和敌敌畏的残留含量.结果表明,农药检出率为氯氰菊酯(59.1%)多菌灵(51.0%)代森锰锌(11.1%)甲霜灵(6.7%)三氟氯氰菊酯(3.4%).乐果和敌敌畏仅在个别果园检出,溴氰菊酯和敌百虫均未检出.土壤同时检出不同种类农药果园的百分数为只检出1种农药(40.4%)同时检出2种(31.3%)未检出(18.8%)同时检出3种(8.2%)同时检出4种(1.4%).检出的7种农药中,代森锰锌残留平均含量最高达39.05μg·kg-1,氯氰菊酯次之为7.83μg·kg-1.其它5种农药平均含量为0.19～1.65μg·kg-1.整体上广东省荔枝园土壤农药残留状况较轻.     

五种重点关注的重金属废渣的处理方法与利用现状

近年来,随着我国经济的迅速发展,重金属废渣的总量逐步扩大,引发了很多社会、经济、环境问题,成为了企业和环保领域关注的热点问题,国家近期提出了五种需重点关注的重金属废渣。本文在对国内外资料的总结和回顾的基础上,着重论述了这五种重金属废渣的来源、产量,对于现在常用的各种处理方式进行对比分析,指出其优缺点;总结了一般重金属废渣的处理模式,提出了自己的看法;展望了重金属废渣处理技术的发展方向。     

戊唑醇残留分析方法实验室内质量控制研究

文章确立了小麦、香蕉中戊唑醇残留检测方法,小麦样品加水10 mL用丙酮为萃取溶剂,石油醚液液分配,中性氧化铝柱层析净化,用气相色谱(GC-NPD)检测。香蕉样品加水5 mL用丙酮为萃取溶剂,石油醚液液分配,浓缩后用气相色谱(GC-NPD)检测。分别设置不同时间批次,同一批次间的平行样及实验室内人员分析,分别从方法灵敏度、方法准确度、方法精密度及其质量控制图、标准工作液的稳定性来探讨该方法的可靠性,结果表明该方法可以作为香蕉和小麦种戊唑醇残留检测的标准分析方法。     

基于均匀分布的滑坡数值模拟参数取值概率研究--以甘肃黑方台黄土滑坡为例

针对数值模拟参数选取主观性强、量化难度大的问题,在高精度无人机地形数据的基础上,通过对11起滑坡案例进行了407组参数反演实验,对结果准确度定量评价后,得到基于Massflow数值软件关键参数λ0的分布范围,进而运用小样本极大似然估计理论,分析区间边界长度对反演精度的影响,最终提出基于均匀分布的参数取值概率模型,并选用案例验证该模型的准确性。结果表明:地形约束会导致反演过程中所需的内聚力减小,反演获得的11组最优λ0的极差和方差分别为0.29、0.01,在置信度为95%下,极大似然法得到区间边界估计长度仅为0.0998,表明参数λ收敛性较好;反演过程中质心滑动距离ψ准确度优于堆积面积重叠率η,在λ0±0.05的范围,参数估计区间内任意值对模拟误差影响较小,评价指标ψ、η与λ0对应案例的相对误差不超过15%;所选案例验证了在置信度为95%下,以反演得到的最优参数区间边界中点构建概率分布函数的可行性和准确性,研究方法可为单体滑坡数值模拟风险评价提供理论支撑。     

Removal of phosphate from wastewater using alkaline residue

Alkaline residue(AR) was found to be an efficient adsorbent for phosphate removal from wastewater. The kinetic and equilibrium of phosphate removal were investigated to evaluate the performance of modified alkaline residue. After treatment by NaOH(AR-NaOH), removal performance was significantly improved, while removal performance was almost completely lost after treatment by HCl(AR-HCl). The kinetics of the removal process by all adsorbents was well characterized by the pseudo second-order model. The Langmuir model exhibited the best correlation for AR-HCl, while AR was effectively described by Freundlich model. Both models were well fitted to AR-NaOH. The maximum adsorption capacities calculated from Langmuir equation were in following manner: AR-NaOH AR AR-HCl. Phosphate removal by alkaline residue was pH dependent process. Mechanisms for phosphate removal mainly involved adsorption and precipitation, varied with equilibrium pH of solution. For AR-HCl, the acid equilibrium pH( 6.0) was unfavorable for the formation of Ca-P precipitate, with adsorption as the key mechanism for phosphate removal. In contrast, for AR and ARNaOH, precipitation was the dominant mechanism for phosphate removal, due to the incrase on pH( 8.0) after phosphate removal. The results of both XRD and SEM analysis confirmed CaHPO4·2H2O formation after phosphate removal by AR and AR-NaOH.     

Removal of polycyclic aromatic hydrocarbons from aqueous solution by raw and modified plant residue materials as biosorbents

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.