外源Mo降低As(Ⅲ)和As(Ⅴ)对水稻的毒性及As的积累

通过溶液培养试验,研究外源添加Mo对2种价态砷(As(Ⅲ)和As(Ⅴ))胁迫下水稻吸收积累Mo和As的影响。结果表明,这2种价态的As对水稻生长均有抑制作用,As(Ⅲ)比As(Ⅴ)对水稻毒害更明显,添加Mo可缓解As对水稻的毒害。As添加可影响水稻根系和茎叶对Mo的吸收积累,但是不同价态As对Mo积累量的影响不一致。同时,Mo的添加也可以显著地降低水稻根系和茎叶对2个价态As的吸收积累。在100μmol·L~(-1)As(Ⅲ)处理下,添加0.1和0.5 mg·L~(-1)的Mo可导致水稻根系As积累量分别比对照处理降低38.8%和52.8%,茎叶As积累量分别降低5.1%和10.6%;当As(V)浓度为100μmol·L~(-1)时,添加0.1和0.5 mg·L~(-1)的Mo可导致水稻根系As积累量分别比对照处理降低15.4%和62.4%,茎叶As积累量分别降低11.9%和23.7%。Mo的添加还能显著地降低2种价态As在水稻根系和茎叶中的富集系数。因此,通过施用适量的Mo肥可以用来防治农田As污染,降低As对人体健康的危害。     

碱熔法回收废催化剂中的钴、钼和铝

采用碱熔法从废钴钼催化剂中回收钴、钼和铝。该方法的工艺过程为 :将废催化剂与纯碱按质量比 1∶1 8混合 ,在焙烧温度 90 0℃条件下 ,焙烧 2h ;用 2倍于熔块的沸水浸取30min ;用稀硫酸调浸取液 pH至 6 ,浸取液中的铝形成氢氧化铝被回收 ;然后除盐并回收钼酸钠 ;使酸浸黑渣中的钴形成氢氧化钴并脱水氧化成为氧化钴。用该工艺回收铝、钼和钴 ,其回收率可达 95 %以上 ,回收产品的纯度可达 97%以上。     

MoS2/g-C3N4纳米纤维光催化降解柴油机苯系排放污染物

采用同轴静电纺丝法制备了MoS_2/g-C_3N_4纳米纤维,采用XRD、FTIR、XPS、UV-Vis和Raman等光谱分析技术表征了催化剂相组成和微观形貌,评价了催化剂表面化学形态和吸光特性,探讨了催化剂对甲苯的光催化降解机理,研究了MoS_2含量、光源条件、温度和催化稳定性对降解甲苯的影响规律.结果表明,在MoS_2/g-C_3N_4中掺杂适宜的MoS_2有助于提高催化剂活性,改善催化剂比表面积和孔容积.在可见光条件下,催化剂(10%MoS_2)对甲苯的降解率为90.24%.由汽车尾气中苯系污染物光催化降解应用可知,在柴油机转速为2000 r·min~(-1),油门开度(负荷)分别为25%、50%、75%和100%的条件下,10%MoS_2对苯、甲苯、乙苯、对二甲苯、间二甲苯和邻二甲苯的平均降解率分别为88.12%、90.03%、86.25%、87.12%、87.07%和87.23%,表明MoS_2/g-C_3N_4纳米纤维具有较强的光催化降解苯系物能力.     

石墨炉原子吸收法测定电子废弃物处理场地附近植物中的钼

利用预烘干一湿法酸化消解方法处理植物并获得消解液,然后采用涂层石墨管,在探索不同原子化温度与灰化温度的多种优化试验条件基础上,对电子废弃物处理场地附近植物体内的钼进行了测定,样品进行平行试验,相对标准偏差（n=11）〈2．3％。     

芦苇和香蒲对重金属钼的吸收特性研究

研究了水生植物芦苇和香蒲对重金属钼的吸收特性.通过短期室内水培实验,对比考察了2种植物对重金属钼的耐毒性、动态去除率、吸收过程及富集情况,并对在不同浓度营养液中植物对重金属钼吸收的影响进行了分析.结果表明,2种植物钼中毒导致其茎叶发黄、蒸腾能力下降,在钼浓度为2～20 mg.L-1时,香蒲对重金属钼的耐毒性较芦苇强.香蒲对重金属钼的去除率高于芦苇,在钼浓度为2 mg.L-1时,香蒲和芦苇去除率分别为87%和62%.2种植物对重金属钼的吸收是一个动态平衡过程,且以被动吸收为主.香蒲对钼的富集量较芦苇高,且植物地上部重金属积累量大于根部,符合超积累植物特征之一.营养液浓度的增加不会提高植物对重金属钼的吸收量,反而会因离子竞争等因素使去除率有所下降.芦苇和香蒲对溶液中钼的吸收均具有显著效果,香蒲吸收效果较芦苇好.     

Recovery of molybdenum from fly ash by gibbsite

The effectiveness of gibbsite (GB), an amorphous aluminum oxide, for the recovery of Mo(VI) from eluates of fly ash of two coal-fired thermal power stations and of roof tile waste was investigated. Upon the qualitative analysis of an eluate of fly ash, 16 elements were detected. Greater amounts of these elements were eluted under acidic conditions (pH 2) than from the neutral or basic eluate of fly ash. GB was used for the adsorption of Mo(VI). Equilibrium adsorption was reached within 1?min. Optimal solution acidity for the adsorption of Mo(VI) onto GB400 (calcined at 400°C) was pH 2. The main adsorption mechanism was ion exchange with a number of hydroxyl groups of GB400. For repeated ad- and desorption of Mo(VI), GB400 could be used at least four times and the recovery percentage of Mo(VI) with sodium hydroxide solution as eluent surpassed 90%. Our results showed that GB400 was very effective for the recovery of Mo(VI) from fly ash.     

钼尾矿制备硅微粉

以钼尾矿为原料,采用酸溶—碳酸钾沉淀法制备硅微粉。考察了反应温度、反应时间、K₂CO₃质量分数对产品中SiO₂质量分数和SiO₂产率的影响。得到的优化工艺条件为：钼尾矿粒径小于74 μm,反应温度50 ℃,反应时间60 min,K₂CO₃质量分数50%。在此工艺条件下,SiO₂产率可达98.92%,产品硅微粉的SiO₂质量分数达98.44%,粒径为100~200 nm,超过中华人民共和国黑色冶金行业标准《不定型耐火材料用二氧化硅微粉》（YB/T 115—2004）中SF96指标（SiO₂质量分数≥96.0%）的要求。     

高浊度钼矿浮选废水的混凝沉淀

针对某钼矿选矿厂浮选废水,以PAC、PFS和FeCl3为凝聚剂,以APAM-A和APAM-N为絮凝剂,以H2SO4和NaOH为pH调整剂,研究了不同混凝剂、不同pH值和不同水力条件下废水处理后的浊度和COD.实验结果表明,在最佳水力条件下,原水pH不调整,以APAM-A为絮凝剂,以PAC为凝聚剂,其用量分别为15 g/t,750g/t时,处理后上清液浊度为25 NTU,COD小于30 mg/L.浮选废水经处理后回用于选矿浮选流程,大大改善了选矿指标.     

SYNTHESIS OF DATA FROM STUDIES BY THE NATIONAL IRRIGATION WATER-QUALITY PROGRAM1

ABSTRACT: From 1986 to 1993, the National Irrigation Water-Quality Program (NIWQP) of the U.S. Department of the Interior studied whether contamination was induced by irrigation drainage in 26 areas of the Western United States. In 1992, a study to evaluate and synthesize data collected during these 26 investigations began. Selenium, boron, and molybdenum are the trace elements and DDT the pesticide most commonly found in surface water at concentrations exceeding chronic criteria for the protection of aquatic life. In six of the areas, the median selenium concentration exceeded the criterion. Aquatic-life criteria have not been developed for uranium, but the median uranium concentration exceeded the proposed Maximum Contaminant Level for drinking water in seven areas. A principal components analysis indicates that severity of selenium contamination is not related to the severity of contamination by boron, molybdenum, and arsenic. Arsenic, boron, molybdenum, and selenium concentrations are nearly the same in both filtered and unfiltered samples, which indicates that contaminant concentrations in filtered samples can be directly compared with biological-effects data developed using unfiltered samples. At a given site, selenium concentrations in surface water can change by an order of magnitude during the course of a year and from one year to another.     

Recovery of molybdenum, phosphorus and arsenic fromleaching solution of molybdenum residues by solvent extraction with primary amine and tributylphosphate

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