钙、氯对磷酸盐稳定污染土壤中铅的促进作用研究

为探讨促进磷酸盐稳定污染土壤中铅的方法,在全铅含量为517 mg·kg-1的铅冶炼污染土壤中加入5 mmol·kg-1磷酸盐,同时加入10mmol·kg-1硝酸钙或5 mmol·kg-1氯化钾,在15%或30%的含水率下培养40 d,之后种植黑麦草.结果表明,与单独施用磷酸盐相比,采用磷酸盐与钙、氯结合或增加培养期间的土壤含水率后,土壤DTPA-Pb含量下降3.92%~26.1%;对于同一添加剂处理,培养期间土壤含水率从15%增加到30%,土壤有效铅(DTPA-Pb)含量下降8.83%~24.4%.增加土壤含水率后,土壤有效磷(Olsen-P)含量均显著升高(p0.05).土壤铅的EXAFS分析表明,与未施用磷酸盐的对照相比,土壤中加入磷酸盐后矿物态铅的比例由57%上升至81%,加施钙、氯或增加土壤含水率后,多数处理矿物态铅的比例有所下降,而有机结合态铅比例上升.与对照相比,污染土壤中施用磷酸盐后,植物产量大幅增加,但施用钙、氯或增加培养期间含水率后,部分处理植物产量有所下降.以上结果表明,在铅冶炼污染土壤中加入磷酸盐时,加入钙、氯或者增加土壤含水率均有利于铅的稳定,但以上措施可能对植物生长产生不利影响.     

密封消解法测定高氯离子含盐废水COD_(Cr)的探讨

针对国标重铬酸钾法测定高氯离子含盐废水CODCr时的不足,提出用密封消解法来测定高盐废水CODCr的观点,通过丁酮氧化率、氯离子干扰、混配水样和实际水样测定结果的比较,对国标法和密封消解法进行了验证。试验结果表明:在测定高氯离子含盐废水CODCr值时,密封消解法优于重铬酸钾法,能够真实准确地反映废水的CODCr。     

用蒽醌生产中的废硫酸制备硫酸钾

研究了以蒽醌生产中的废硫酸为原料,通过缔合,置换,解缔等步骤,制备硫酸钾的最佳工艺条件。在最佳条件下,可使废硫酸中Ｈ２ＳＯ４的质量分数从２３％降至０．６０％,废硫酸成盐率为８９．０１％,硫酸钾纯度为９５．８５％。     

Sustainable Agriculture: New Paradigms and Old Practices? Increased Production with Management of Organic Inputs in Senegal

Farmers in Sahelian countries are confronted with a variety of soil fertility and management problems. During the last two decades, NGOs have worked with farmers and research institutions to develop and test practices that will increase food production, while at the same time enhance the natural resource base.Since 1987, The Rodale Institute (RI) has worked closely with farmers' associations and government institutions to promote regenerative agriculture-farming systems that prioritize the use of local resources while improving them as they are used to grow food, using agro-ecological methods. The Senegalese Agricultural Research Institute has collaborated in this program as a partner of RI. The Senegal Regenerative Agriculture Resource Center model has been applied as a new and viable approach that builds on traditional knowledge and farmer-to-farmer exchange.Research results on soil conservation and improvement have shown that fields spread with amended animal manure or compost yield greater harvests than fields farmed with traditional methods.     

Fate and availability of glyphosate and AMPA in agricultural soil

The fate of glyphosate and its degradation product aminomethylphosphonic acid (AMPA) was studied in soil. Labeled glyphosate was used to be able to distinguish the measured quantities of glyphosate and AMPA from the background values since the soil was sampled in a field where glyphosate had been used formerly. After addition of labeled glyphosate, the disappearance of glyphosate and the formation and disappearance of AMPA were monitored. The resulting curves were fitted according to a new EU guideline. The best fit of the glyphosate degradation data was obtained using a first-order multi compartment (FOMC) model. DT₅₀ values of 9 days (glyphosate) and 32 days (AMPA) indicated relatively rapid degradation. After an aging period of 6 months, the leaching risk of each residue was determined by treating the soil with pure water or a phosphate solution (pH 6), to simulate rain over a non-fertilized or fertilized field, respectively. Significantly larger (p < 0.05) amounts of aged glyphosate and AMPA were extracted from the soil when phosphate solution was used as an extraction agent, compared with pure water. This indicates that the risk of leaching of aged glyphosate and AMPA residues from soil is greater in fertilized soil. The blank soil, to which 252 g glyphosate/ha was applied 21 months before this study, contained 0.81 ng glyphosate/g dry soil and 10.46 ng AMPA/g dry soil at the start of the study. Blank soil samples were used as controls without glyphosate addition. After incubation of the blank soil samples for 6 months, a significantly larger amount of AMPA was extracted from the soil treated with phosphate solution than from that treated with pure water. To determine the degree of uptake of aged glyphosate residues by crops growing in the soil, ¹⁴C-labeled glyphosate was applied to soil 6.5 months prior to sowing rape and barley seeds. After 41 days, 0.006 ± 0.002% and 0.005 ± 0.001% of the applied radioactivity was measured in rape and barley, respectively.     

Potential environmental impact of dissolution of raw phosphate in sea water of the Gulf of Aqaba

Dissolution of raw phosphate (apatite) in sea water of the Gulf of Aqaba was investigated through lab incubation experiments. Three types from three different sources (Al-Hasa, Al-Abyad and Esh-Shydiya) have been used for these experiments. Impact of quantity, grain size, and source (type) of raw phosphate on dissolution rate were studied. Statistical analysis shows significant differences between the results obtained from comparing each two weights; as weight of apatite increased, dissolved inorganic phosphate-phosphorus (DIP) and fluoride in sea water solution increased. The differences between the dissolution rates of raw phosphate from the three sites were not significant while the differences between the different grain size fractions were significant. Dissolution rates were inversely related to particle size. Using a worst-case scenario, a conservative estimate of the maximum increase in DIP in seawater of the Gulf of Aqaba due to the apatite particles lost to the sea during ship loading resulted in DIP concentrations of 0.03 μM per year. As the residence time of the water in the Gulf of Aqaba is about one year, the DIP concentration will not increase by more than 0.03 μM under the estimated annual quantity of exported phosphate. Fluoride will not increase by more than 0.03 mg/l under the same conditions.     

有效磷含量对硝酸铵溶液热安全性的影响

为了了解硝酸磷肥生产过程中,硝酸铵溶液中加入磷酸一铵的安全性,通过自制实验装置,研究了有效磷含量对质量分数为85%的硝酸铵溶液热分解的影响。结果表明,质量分数为85%的硝酸铵和磷酸一铵混合溶液的临界爆炸温度高于纯质量分数为85%的硝酸铵溶液,稳定性更好;磷酸一铵抑制硝酸铵的热分解,随着有效磷含量的增加,硝酸铵混合溶液临界爆炸温度升高;升温速率对硝酸铵混合溶液的临界爆炸温度影响很大,随着升温速率由2℃/min升高到3℃/min,质量分数为85%的硝酸铵混合溶液的临界爆炸温度升高,不易发生爆炸,安全性更好。研究结果对硝酸磷肥的生产安全有一定的指导意义。     

磷酸银/树脂复合物的制备及其对亚甲基蓝的光催化降解

以聚乙烯吡咯烷酮(PVP)为稳定剂,采用化学沉积法制备了磷酸银/树脂复合物,降解亚甲基蓝,研究其光催化活性,并对样品进行了XRD和SEM表征。探讨了不同的光源、催化剂投加量、PVP含量、p H值等因素对亚甲基蓝降解率的影响。结果表明,在太阳光(夏天早上9点到11点的阳光)下,偏酸介质中,催化剂用量为0.8 g/L,PVP质量分数为0.01%的磷酸银/树脂复合物,液面高度为15 cm的条件下对亚甲基蓝有最佳降解效果。     

新型纳米结构铈锰复合氧化物的磷吸附行为与机制研究

采用共沉淀法制备了一种新型铈锰复合氧化物吸附剂,对其进行了表征,并对磷吸附行为与机制进行了研究.表征结果分析表明,此氧化物由纳米级颗粒组成;铈锰复合氧化物中的铈氧化物有类似水合氧化铈的无定形结构;BET比表面积为157 m2·g-1,等电点为6.5.吸附实验结果表明,Langmuir吸附等温线模型可以更好地拟合铈锰复合氧化物对磷的吸附,最大吸附量为28.6 mg·g-1(p H=7.0);铈锰复合氧化物对磷具有较高的吸附速率,更符合准二级动力学模型;溶液p H对铈锰复合氧化物吸附磷的影响较为明显,随p H升高,吸附量降低;离子强度则影响不大;共存阴离子对吸附影响的大小顺序为Si O2-3CO2-3Cl-≥SO2-4.通过对铈锰复合氧化物吸附磷前后Zeta电位和红外谱图(FTIR)分析,可以推断磷在铈锰复合氧化物表面发生了特性吸附,磷酸根主要通过取代复合氧化物表面的金属羟基而被吸附去除.     

Effect of commercial pesticides on plant growth-promoting activities of Burkholderia sp. strain L2 isolated from rhizosphere of Lycopersicon esculentum cultivated in agricultural soil

The in vitro study was carried out to examine the toxicity of four commercially used pesticides (phorate, mancozeb, chlorpyrifos, and endosulfan) at the recommended dose (1X) and higher field doses (1.5X, 2X, 2.5X, and 3X) on plant growth-promoting activities of Burkholderia sp. strain L2, isolated from pesticide-treated rhizosphere of Lycopersicon esculentum. At the recommended dose, level of toxicity of all the pesticides to phosphate solubilization activity and indole-3-acetic acid (IAA) production was less detrimental as compared to exceeding doses. At maximum dose rate of each pesticide, the percentage decrease in phosphate solubilization and IAA production over control was found in order of chlorpyrifos < mancozeb < endosulfan < phorate. Present study proves that Burkholderia sp. strain L2 could be used as a potential microbial inoculant in the agricultural soil having persistent pesticide residues.