金属络合剂在烟气同时脱硫脱硝中的应用

液相络合法是烟气同时脱硫脱硝中广泛应用的方法之一。液相络合法常用的金属络合剂有亚铁络合剂和钴络合剂等。重点介绍了亚铁氨羧络合剂、含-SH的亚铁络合剂和六氨合钴络合剂、乙二胺合钴络合剂等同时脱硫脱硝的基本过程及常用吸收液的再生方法，指出了金属络合剂在烟气同时脱硫脱硝中应用时存在的问题及今后的发展方向。     

Kinetics and thermodynamics studies of cobalt,strontium and caesium sorption on marble from aqueous solution

Adsorption onto solid phases plays an important role in the transport of radionuclides and contaminants in the environment. Radionuclides in radioactive waste have been considered to be hazardous pollutants, and their migration with groundwater is strongly affected by sorption on the geologic media. Therefore, the knowledge of radionuclide sorption is of great importance in the management of radioactive wastes. A series of batch sorption experiments were conducted separately to investigate sorption and transport behaviour of cobalt, strontium and caesium on and through marble. Batch-mode kinetic and equilibrium studies have been carried out at different temperatures. Sorption experimental data were analysed by kinetic and isotherm models. Based on the results obtained, it can be concluded that the marble is an economic and efficient retaining material for environmental hazardous migration and/or leakage of some radionuclides. Therefore, this study could be used as a starting point to establish and consider that rock as a reactive barrier around the disposal facilities at the nuclear activity centres.     

A potentiometric cobalt-based phosphate sensor based on screen-printing technology

A potentiometric cobalt-based screen-pritning sensor was fabricated by electroplating cobalt on the surface of a screen-printing electrode as the sensitive layer for the determination of dihydrogenphosphate （H2PO4） in wastewater samples. The electrochemical performance of this sensor was fully examined to determine its detection calibration, detection limit, response time, selectivity, and interference with pH, various ions, and dissolved oxygen （DO）. The cobalt-based phosphate sensor showed a phosphate-selective potential response in the range of 10 5mol·L^-1 to 10^-1 mol^-1, yielding a detection limit of 3.16 × 10μmol·L^l and a slope of -37.51 mV·decade＇ in an acidic solution （pH 4.0） of H2PO4-. DO and pH were found to interfere with sensor responses to phosphate. Ultimately, the performance of the sensor was validated for detecting wastewater samples from the Xiaojiahe Waste- water Treatment Plant against the standard speetrophotometric methods for HzPO4 analysis. The discrepancy between the two methods was generally ＋5% （relative standard deviation）. Aside from its high selectivity, sensitivity, and stability, which are comparable with conventional bulk Co-wire sensors, the proposed phosphate sensor presents many other advantages, such as low price, compactness, ease of use, and the possibility of integration with other analytical devices, such as flow injectors.     

碳纳米管负载的镍及其氧化物对高毒气体PH3的催化分解性能

采用沉积-沉淀法制备了均一负载于碳纳米管(CNTs)载体的金属Ni和NiO,将其应用于PH3催化分解反应.通过XRD、TEM、XPS、BET等一系列检测手段,对样品的相结构、形貌、组分和比表面积进行了表征.研究结果表明,反应过程中,Ni和NiO很快被磷化为高活性的金属磷化物NiP2,作为反应的活性相.在420℃温度下,两样品对PH3的催化分解率均可达到99.5%以上.将反应中原位生成的NiP2进行催化反应,较钝化-还原的处理方式更有利于样品催化性能的保持.     

Effect of cobalt-supplemented diets on bioaccumulation,digestive enzyme activities and growth of Cyprinus carpio

Experiments were conducted to determine the effects of excess dietary cobalt (Co) on bioaccumulation, digestive enzyme activities, and growth in freshwater Cyprinus carpio. Four isonitrogenous diets (average crude protein: 35%) were formulated to prepare a control diet (T₁) with no Co, and three Co-supplemented diets with 1 (T₂), 1.5 (T₃), or 2 (T₄)% Co. The results showed that C. carpio fed with T₃ diet showed maximal apparent protein digestibility, feed conversion, protein utilization, and growth. Protease and lipase activities were maximal in the fish group given T₃ diet. Accumulation of Co in different soft and hard tissues of fish did not correlate with levels of Co in the diet. The concentration of Co in the water increased with dietary level, being at a disturbing adverse effect level at 2% dietary Co. Evidence indicates that an additional supply of dietary Co up to a level of 1.5% is a viable option to augment growth of C. carpio, but at higher levels of Co it may be detrimental to fish health and the aquatic ecosystem.     

Cobalt speciation assay for human serum,Part II. Method validation in a study of human volunteers ingesting cobalt(II) chloride dietary supplement for 90 days

A new analytical method for determining cobalt (Co) species in human serum by size exclusion chromatography with inductively coupled plasma mass spectrometry (SEC-ICP-MS) was applied to serum samples collected from 12 human volunteers who participated in a Co(II) chloride supplement study involving ingestion of 1 mg Co/day for up to 90 consecutive days. The study protocol included determination of serum total Co by acid digestion followed by ICP-MS. Co speciation assay measurements were conducted for up to 13 time points per individual spanning from one to two weeks before dosing began to two weeks after dosing ceased. The Co speciation assay showed good recovery >91% relative to total Co measurements. Undiluted serum demonstrated uniform fractions of large molecular Co defined as Co bound to albumin and other proteins >50 kDa at 96% and the residual as small molecular Co defined as free Co(II) and <1 kDa Co-complexes for individual serum Co concentrations up to 146 μg/L. There were no dose-related changes in Co distribution. Analysis of the same serum samples with tenfold dilution in 0.1 M acetic acid led to a lower fraction of large molecular Co at 87%, with the difference between diluted and undiluted measurements being 8.4%. The difference noted between undiluted and diluted large molecular Co may be attributed to Co release from albumin. Data demonstrated that large molecular Co was the predominant Co species in both undiluted and diluted human serum over a broad range of in vivo Co concentrations, reflecting high albumin–Co binding capacity. These data validate the Co speciation assay and may be employed in understanding further the toxicokinetics and dose-response relationships for Co species.     

稀土修饰的Co/Hβ催化剂催化分解N_2O

以Hβ分子筛为载体,采用浸渍法制备了一系列以钴为主活性组分,稀土元素为助剂的CoM/Hβ（M=La、Ce、Pr、Nd）催化剂,考察了在含氧条件下直接催化分解N2O的性能.采用X射线衍射、热重-质谱联用系统、H2-TPR、NH3-TPD等方法对催化剂进行了表征.XRD结果表明,Co物种主要以Co3O4尖晶石形态存在.NH3-TPD结果表明,催化剂活性与催化剂的酸性有关.活性评价结果显示,稀土助剂的添加使催化剂活性得到改善,其中以Pr为助剂的催化剂活性最好,N2O转化率达到95%时的反应温度为398℃.     

Removal of toluene from air streams by cobalt-copper bimetallic catalysts supported on sepiolite

Abstract

Oxidative removal of toluene using copper and cobalt bimetallic catalysts with varying molar ratios supported on sepiolite was investigated. The catalysts prepared by a deposition precipitation method and were characterized using X-ray diffraction, nitrogen adsorption-desorption, field emission scanning electron microscopy, H₂-temperature-programmed reduction, transmission electron microscope, and inductive coupled plasma atomic emission spectroscopy. The species supported on sepiolite are Co₃O₄, CuO, and CuCo₂O₄. The activities of the tested catalysts increased in the order 0Co-4Cu/Sep <1Co-3Cu/Sep <4Co-0Cu/Sep <1Co-1Cu/Sep <3Co-1Cu/Sep. The latter exhibiting 90% toluene oxidative degradation at 288?°C within 15?h, having high selectivity towards CO₂, and being stable at 300?°C up to 15?h. In conclusion, this study showed that sepiolite has excellent properties as a support.     

氧化亚铁硫杆菌浸出废旧锂离子电池的工艺条件

考察了接种量、振荡条件、浸出液以及电池原料对氧化亚铁硫杆菌浸出废旧锂离子电池的影响.研究结果表明,浸出10 d,钴浸出率达到48.5%,之后,浸出率不再增加;当接种量在2.5%—12.5%之间时,钴浸出率在第10天都为47.6%,接种量对浸出率无影响;振荡过程中控制温度为35℃时,钴浸出率最佳,并随着振荡速率的升高而增加;浸出液中加入硫磺对浸出影响不大,初始pH值在1.5—2.5范围内,都适合钴酸锂的浸出,而初始亚铁离子浓度在45 g.L-1条件下浸出效果最好;选择固液比为3%最佳,并且钴酸锂粉末的粒度大小对浸出率无影响.     

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。