Preparation of Gold Nanorods of High Quality and High Aspect Ratio

We report the synthesis of gold nanorods (NRs) by seed-mediated growth method. A small amount of different shapes such as triangles, hexagons and a large amount of rods are obtained by varying the proportion of seed to metal salt, adding NaOH to growth solution as well as using the seed solution of CTAB-capped agent. The gold nanorod (NR) formation yield is improved. Meanwhile, the growth mechanism of high yield gold NRs is discussed. The high quality single size NRs can be separated from polydisperse sampl...     

招远玲珑金矿废石模拟淋滤试验分析

为了分析降雨淋滤对水质化学组分的影响状况、研究玲珑金矿区废石经降水淋滤对环境带来的影响,进行了金矿废石模拟淋滤试验.通过对比分析淋滤前后水的化学成分发现,淋滤效果与降雨量大小和降雨强度有关,降雨量越大淋滤效果越明显,在同一降雨量条件下,降雨强度越小,则淋滤效果越明显;淋滤后绝大部分组分(离子)浓度呈现不同程度的增大趋势,淋滤液中Pb、Mn2+、NO2-、F-、Ca2+、NO3-、耗氧量淋失较多.结合淋滤试验结果和当地水质环境综合分析,废石经降雨淋滤使水中NO2-、Pb含量升高是造成该区水环境污染的主要因素之一.最后结合玲珑金矿区金矿废石的实际情况,提出了防治措施.     

含铁低镍白色金合金镍渗出及抗变色性能

研究Fe元素部分取代镍对白色金合金镍渗出以及抗变色性能影响.指出当Fe等元素取代合金中的部分Ni元素后,由于镍含量降低,合金的镍释放率出现下降,镍降低导致表面镍钝化膜的破坏.当镍质量分数低于2.5%时,合金的镍释放量反而升高.Fe对合金的漂白效果弱于镍,Fe的加入会导致合金抗变色性能降低.均匀化退火热处理对该实验系列金合金材料的抗变色性能影响不大,但可减少合金成分的偏析,有效降低合金的镍渗出量.     

The influence of pH on reaction pathways for O2 reduction on the Au(100) face

Oxygen reduction on the Au(100) face was studied by the rotating disk-ring electrode technique in solutions of anions which adsorb strongly on gold (HSO₄⁻/SO₄²⁻ and/or OH⁻) over the entire pH range. The specific adsorption of OH⁻ anions, which is a pH dependent process, is found to play the key role in determining the reaction pathways. In the absence of OH⁻ adsorption, for pHs below 6, the reduction of O₂ begins as a 2e-process. Due to the increase in local pH during O₂ reduction, the reaction pathway turns into a 4e-reduction at a certain potential depending on the pH of the solution. For pHs higher than 6, O₂ reduction begins as a 4e-process in the potential region where specifically adsorbed OH⁻ anions are present.     

大孔强酸树脂吸附硫脲金

研究了D072大孔强酸性阳离子交换树脂从硫脲[Tu=CS(NH2)2]浸金液中吸附Au(Tu)2+的性能和机理. 结果表明，pH=2.0时，树脂对Au(Tu)2+有优良的吸附性能，金的交换容量为78.95 mg/g (Au/干树脂)，吸附的硫脲金可用乙醇-硫酸水溶液洗脱，洗脱率可达96.5%. D072树脂对Au(Tu)2+的吸附符合Langmuir吸附模型.     

Acetylene Hydrogenation on Au-Based Catalysts

Hydrogenation of acetylene has been investigated on Au/TiO₂, Pd/TiO₂ and Au-Pd/TiO₂ catalysts at high acetylene conversion levels. The Au/TiO₂ catalyst (avg. particle size: 4.6 nm) synthesized by the temperature-programmed reduction-oxidation of an Au-phosphine complex on TiO₂ showed a remarkably high selectivity to ethylene formation even at 100% acetylene conversion. Au/TiO₂ prepared by the conventional incipient wet impregnation method (avg. particle size: 30 nm), on the other hand, showed negligible activity for acetylene hydrogenation. Although the Au catalysts showed a high selectivity for ethylene, the acetylene conversion activity and catalyst stability were inferior to the Pd-based catalysts. Au-Pd catalysts prepared by the redox method showed high acetylene conversions as well as high selectivity for ethylene. Interestingly Au-Pd catalysts prepared by depositing Pd via the incipient wetness method on Au/TiO₂ showed very poor selectivity (comparable to mono-metallic Pd catalysts) for ethylene. High-resolution transmission electron microscopy (TEM) studies coupled with energy dispersive X-ray spectroscopy (EDS) showed that while the redox method produced bimetallic Au-Pd catalysts, the latter method produced individual Pd and Au particles on the support.     

Aromatization of n-hexane on Mo2C catalysts

The deposition-precipitation method was used to prepare gold catalysts based on different supports. Their catalytic activities for combustion of carbon monoxide (CO) and formaldehyde (HCHO) were investigated. All these catalysts showed good activity for the two reactions and the Au/CeO₂-a catalyst exhibited the highest activity for the two reactions. Furthermore, catalysts derived from the as-precipitate hydroxides exhibited higher activity than that from corresponding oxide supports. The BET, XRD, TEM and XPS were carried out. The results indicated that the gold dispersed more homogeneous on the as-precipitate hydroxide supports than that on the corresponding oxide supports.     

人血清淀粉样蛋白A1原核表达及胶体金检测方法的建立

通过胶体金免疫层析技术建立一种特异、便捷、快速的SAA1定量检测新方法.利用大肠杆菌BL21(DE3)原核表达人血清淀粉样蛋白A1(SAA1),根据BL21(DE3)表达偏好性设计并合成SAA1蛋白基因片段,构建表达载体pET-28a-SAA1,采用CaCl2法制备BL21(DE3)感受态,热激转化法将pET-28a-SAA1转入到BL21(DE3).经表达条件优化,获得重组蛋白最佳诱导表达条件:温度30℃,时间6h,转速180rpm/min,培养基pH 7.0,IPTG浓度0.4mM,诱导表达后目的蛋白经SDS-PAGE电泳鉴定,Ni柱纯化、透析、浓缩从而获得浓度为8.09mg/ml,纯度为85%的SAA1.同时,结合胶体金标记技术,建立了SAA1胶体金免疫层析试纸检测方法,线性范围0.16~500μg/ml,最低检测限0.16μg/ml,该研究为临床体外诊断SAA1快速检测提供技术基础.     

金矿堆浸中废水治理的工艺研究

从低品位（0．5—3g／t）含金矿石中提取黄金会产生大量高体积质量（〉350mg／L）剧毒氰化物废水,为了减少含氰废水对人类健康和对环境造成的污染,有效地保护生态平衡,论述了含氰废水的4种治理工艺,即碱性氯化法、酸化法、自然净化法和二氧化硫．空气法的除氰原理、反应过程、工艺流程和治理效果,并分析了其优缺点、结合宁夏中卫金矿在实际生产中采用碱性氯化法治理含氰废水的试验和工艺研究,重点对碱性氯化法进行了分析．研究表明,该方法简捷、快速、安全、经济,易于掌握,治理效果好,完全达到中华人民共和国《污水综合排放标准GB8979-88》中的规定和环保要求．该方法较适宜在宁夏各矿山黄金生产中推广和应用．     

Catalytic activity of Au/Fe-PILC and Au/Fe-oxide catalysts for catalytic combustion of formaldehyde

Iron polymeric hydroxygroups pillared clays （Fe-PILC） were prepared by Na^＋-montmorillonite with iron pillaring agent. 2.01Au/Fe-PILC catalyst was obtained by deposited-precipitation （DP） method. 2.52Au/Fe-oxide catalyst was prepared by co-precipitation method. The catalytic activity of these catalysts was measured by catalytic combustion of formaldehyde. The catalyst of 2.01Au/Fe-PILC exhibits the high catalytic activity. The catalytic combustion reaction of formaldehyde proceeds at considerable rates at 20 ℃ and complete burn-off of formaldehyde is achieved at 120 ℃. The structure of catalysts, the valence state of gold and the size of gold particles were investigated by means of X-ray powder diffractometry, X-ray photoelectron spectroscopy and transmission electron microscopy. The results show that gold atoms with partially positive charge exist in the catalyst and play an important role in the catalytic activity. In addition, nano-sized, well-dispersed gold particles and good adsorption properties of support are necessary to obtain high activity Au catalysts for catalytic combustion of formaldehyde.