A conceptual approach to model sand–gravel extraction from rivers based on a game theory perspective

Sand–gravel mining is a significant parameter of economic development and social welfare function in modern societies. As demand for aggregate increases in construction industry, conflicts for the availability of the resource and environmental impacts become more intense. The present paper describes the contested status quo in riverbed sand–gravel mining activities with an example from Greece, as a case study. The scope is to propose a methodology about good governance of the mining sector that promotes a sustainable sharing of aggregate resource by securing environment and safekeeping revenues in the mining trade market.     

萃取法分离回收不锈钢酸洗污泥硫酸浸出液中的重金属

采用非皂化P204和皂化P204萃取剂对不锈钢酸洗污泥的硫酸浸出液进行萃取。在浸出液pH为0.80、非皂化P204体积分数为25%、萃取剂与浸出液体积比为1∶2、萃取时间为5 min的条件下,Fe~(3+)萃取率达99.64%,Cr~(3+)和Ni~(2+)萃取率为3.98%和6.99%,一次萃余液pH为0.64。采用皂化P204对除Fe~(3+)后的一次萃余液进行萃取,在P204体积分数为25%、萃取剂与浸出液体积比为1∶2、萃取剂皂化率为60%、一次萃余液pH为1.50、萃取时间为5 min的条件下,Ni~(2+)萃取率为93.12%,Cr~(3+)萃取率为20.69%,二次萃余液pH为2.63。     

Variability of pesticide residues in cauliflower units collected from a field trial and market places in Greece

To estimate the variability of pesticide residue levels present in cauliflower units, a total of 142 samples were collected from a field trial of a cooperative farmer, and 120 samples were collected from different market places in Thessaloniki, Greece. The collected samples were extracted using the quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction technique, and the residues were determined by liquid chromatography–tandem mass spectrometry. The developed method was validated by evaluating the accuracy, precision, linearity, limit of detection (LOD), and limit of quantification (LOQ). The average recoveries for all the analytes, derived from the data of control samples fortified at 0.01, 0.05, 0.1, and 0.2 mg/kg, ranged from 74 to 110% with a relative standard deviation of ≤8%. The correlation coefficient (R²) was ≥0.997 for all the analytes using matrix-matched calibration standards. The LOD values ranged from 0.001 to 0.003 mg/kg, and the LOQ was determined at 0.01 mg/kg for all the sought analytes. The matrix effect was found to be at a considerable level, especially for cypermethrin and deltamethrin, amounting to +90% and +145%, respectively. For the field samples, the unit-to-unit variability factors (VFs) calculated for cypermethrin and deltamethrin were 2.38 and 2.32, respectively, while the average VF for the market basket samples was 5.11. In the market basket samples, residues of cypermethrin, deltamethrin, chlorpyrifos, and indoxacarb were found at levels ≥LOQ and their respective VFs were 7.12, 5.67, 5.28, and 2.40.     

丹江口水库表层沉积物不同形态氮的赋存特征及其生物有效性

为了揭示丹江口水库沉积物氮空间分布特征及其生物有效性,采用连续分级提取法研究了表层沉积物中可交换态氮(Exchangeable nitrogen,EN)、酸解态氮(Acid hydrolysable nitrogen,HN)及残渣态氮(Residue nitrogen,RN)的赋存特征,同时结合生物可利用态氮的含量,探讨了各形态氮对生物可利用态氮的贡献。结果表明,丹江口水库沉积物中总氮(Total nitrogen,TN)在425~5796 mg/kg之间,平均为1 319.32 mg/kg,其中EN、HN和RN的平均值相对比例为2.15∶1.95∶1,且各形态氮含量的空间分布呈入库河流大于库区开阔区域的特征,尤其在丹江、老灌河以及犟河-堵河入库口的含量较大。潜在矿化氮(Potential mineralized nitrogen,PMN)含量在40.20~1 468.95 mg/kg之间,平均为275.06 mg/kg,其中EN对丹江口水库沉积物PMN的贡献较大,比例在19.85%~90.80%之间,平均为63.47%。各形态氮在不同的水环境条件下发生迁移转化,保持着水-沉积物界面氮的动态平衡。     

高效液相色谱-串联质谱法同时检测地表水中13种药物及个人护理品

采用高效液相色谱-串联质谱(HPLC-MS/MS)检测,建立了地表水中13种药物及个人护理品的测定方法。水样用盐酸与氢氧化钠溶液调p H值至7.0左右,过固相萃取小柱进行富集,用14 m L甲醇洗脱。以C18柱为分离柱,0.01%甲酸的甲醇-0.01%甲酸水溶液为流动相,目标物在10 min内分离,在0.50~250μg/L范围内,13种化合物峰面积与内标物质峰面积之比与质量浓度的线性关系良好(0.99),检出限在0.05~0.5 ng/L范围内。基质加标实验结果表明,13种化合物在水中的回收率分别在56.2%~123.2%之间(加标水平5 ng/m L)和58.0%~107.8%(加标水平50 ng/m L),相对标准偏差在1.60%~19.9%(n=6)之间。应用该方法测定了从2条纳污河流采集的10份水样,结果表明,除美托诺尔和普洛萘尔未被检出外,其余11药物的检出频率在30%~100%之间。在13种目标物质中,咖啡因的检测浓度最高达287.5ng/L,舒必利次之,为277.5 ng/L。本方法快速、准确,适用于地表水中PPCPs类的快速测定。     

β-环糊精接枝羧甲基壳聚糖吸附剂的制备及其性能

采用γ-氨丙基三乙氧基硅烷化学修饰活化后的硅胶,以戊二醛为交联剂,接上羧甲基壳聚糖,继而接枝上β-环糊精作为功能单体,制备了一种用于分离富集水样中Cu(Ⅱ)的固相萃取新材料。利用红外光谱(FT-IR)、比表面分析(BET)、X射线衍射光谱(XRD)以及热重分析(TG)等方法对吸附剂进行结构表征。采用火焰原子吸收(FAAS)作为检测手段,考察了溶液p H、振荡时间、吸附剂用量、样品流速、洗脱液浓度和体积等对吸附剂吸附Cu(Ⅱ)的影响。吸附剂饱和吸附容量为9.37 mg/g,最大富集倍数高达350。吸附过程能用准二级动力学模型和Langmuir等温吸附方程进行很好的拟合。应用于环境水样中Cu(Ⅱ)的分离富集与测定,回收率在96.8%~105.2%之间,效果较好。     

盐效萃取法从电子产品清洗废液中回收异丙醇

用盐效萃取法从电子产品清洗废液中回收片丙醇,考察了碳酸钾水溶液与该清洗废液的质量比对脱水率的影响,测定了异丙醇-水-碳酸钾体系存40℃时的液液相平衡数据,用Pitzer理论和NRTL方程对液液相平衡数据进行了理论计算。结果表明：当质量分数为60．00％的碳酸钾水溶液与该废液的质晕比为2．00时,脱水率高达90．00％;将有机相进行精馏可得到质量分数为99．50％的异丙醇;计算值与实测值接近,水相和有机相的绝对平均偏差分别为0．62％和0．46％。     

Aquafluor藻细胞活体分析法在三峡库区次级河流回水区Chla测定中的校准及应用

从三峡库区次级河流大宁河、小江、汤溪河及梅溪河139m回水区中段采集水样,经实验室培养后,用丙酮萃取分光光度法和Aquafluor藻细胞活体分析法测定Chla浓度.通过对Chla萃取值(y)和活体值(x)进行回归分析,得到其回归方程为y=4.15x 2.48,t检验显示回归方程具有线性.在库区次级河流139m回水区富营养化监测中,Chla模拟值与萃取值基本吻合,相对误差＜±7%,故可以采用Chla模拟值对水体富营养化程度进行评价.     

固相萃取和高效液相色谱联用测定污水中的五氯苯酚

采用固相萃取和高效液相色谱相结合的方法对污水中五氯苯酚的含量进行定量检测。结果表明,污水的pH值为4,流速控制在4mL/L以内,C18固相萃取柱对五氯苯酚有良好的吸附保留性能,以2mL的甲醇洗脱,洗脱效率在85%~95%之间。与传统的液液萃取相比,固相萃取的优势在于操作时间缩短、有机溶剂的使用量减少。     

玄武湖沉积物中磷的形态分布特征

利用分级提取法分析了玄武湖的沉积磷形态,在玄武湖沉积物中,铝结合态磷的含量较低,平均值为64 mg/kg,其余形态磷中,铁结合态磷为241 mg/kg,有机磷为335 mg/kg,钙结合态磷为394 mg/kg.在环境变化的条件下,铁结合态磷可以释放到间隙水和上层水体中,是湖泊产生富营养化的重要因素;铝结合态磷由于含量少,对湖泊富营养化影响很小;钙结合态磷相对稳定且很难被生物利用,对湖泊富营养化影响不大;有机磷对水体有机负荷影响较大,并影响水体富营养化程度.