掺铁二氧化钛薄膜的自组装制备、表征与光催化性能研究

采用自组装方法于低温液相反应体系中成功制备出大尺寸二维纳米二氧化钛薄膜和掺铁二氧化钛薄膜。样品通过荧光发射光谱、拉曼光谱、高分辨透射电镜等方法进行表征,并研究了紫外光和可见光下Fe3+/TiO2纳米薄膜对甲基橙溶液(MO)的光催化降解过程,探讨了Fe3+对TiO2的光催化活性的影响。结果表明,此方法不需要高温煅烧即可得到高催化活性的金红石和锐钛矿混合型二氧化钛薄膜,以金红石为主。Fe3+掺杂明显提高了TiO2对甲基橙溶液的光催化降解效率:掺杂Fe3+浓度为0.5 mmol/L时光催化效果最优,且更利于较低浓度甲基橙溶液的降解,在紫外光和可见光下对初始浓度5 mg/L甲基橙溶液的降解率分别达到98.62%和89.24%。     

静电自组装制备斜发沸石负载纳米TiO2吸附及光催化降解甲基橙染料研究

为了实现纳米TiO2的固定化负载,提高材料对污染物的光催化效率,采用静电自组装方法制备了天然斜发沸石负载纳米TiO2光催化材料。采用硅烷偶联剂(OCH3)3Si(CH2)3SH干法改性斜发沸石,采用30%H2O2/HOAc氧化剂将偶联剂巯基基团(—SH)氧化为易电离的磺酸基基团(—SO3H),带负电荷的沸石与钛聚合阳离子在静电引力的作用下自发地组装在一起,经一定温度的焙烧得到斜发沸石负载纳米TiO2光催化材料。采用XRD和SEM对材料进行分析和表征,采用甲基橙染料评价材料的吸附和光催化性能,结果表明:沸石负载纳米TiO2对甲基橙染料具有吸附与光催化的协同作用,静电自组装方法制备的材料的光催化性能较传统方法有所提高。     

氨基酸作用下碳酸钙各种晶型自组装形貌的研究

生物矿化作用是指生物在生命活动中形成无机矿物的过程,它与传统地质意义上的矿化作用明显不同的是生物体内的有机质对矿物的晶型和晶向有严格的控制作用[1].碳酸钙是自然界分布最广泛的一类生物矿物.在生物体系中,碳酸钙常见的多型体有:方解石,文石,球文石,非晶质碳酸钙,水合碳酸钙等.     

自组装制备掺铁锐钛矿型二氧化钛薄膜及光催化性能研究

<正>近年来,利用过渡金属离子掺杂改性TiO2被证实具有很好的效果。由于Fe3+掺杂可同时具有降低电子空穴的复合几率和拓展TiO2的吸收阈值的作用,且价格低廉、制备方法多样,因而具     

洛川黄土纳米尺度观察：纳米棒状方解石

本文对洛川黄土剖面典型样品进行了透射电镜分析，发现黄土中存在纳米棒状方解石。此类方解石直径30～50nm，长度几百纳米至几微米。纳米棒状晶体有圆滑地粗细变化和弯曲现象，偶见晶体连接成树枝状或晶体直角连接形成框架状形态。X-射线能谱分析显示方解石有少量的镁、磷和硫，这种纳米棒状方解石在国内外文献中鲜有报道。根据纳米尺度研究结果推测，这种纳米棒状方解石形成与生物衍生物诱导的定向结晶有关。纳米棒状方解石是一种重要的黄土堆积时期干旱环境指示矿物，其碳、氧稳定同位素组成代表黄土堆积时气候参数。纳米棒状方解石的发现，对环境中纳米矿物研究、黄土中碳酸盐碳成因及古气候研究具有重要价值。     

纳米多孔TiO2薄膜的合成及其光电化学性能

采用溶胶-凝胶、水热合成、旋转涂覆等方法制备了纳米多孔TiO2薄膜。以扫描电镜、X射线衍射等手段，分析了不同纳米多孔TiO2薄膜的结构。通过比较不同薄膜制作的染料敏化太阳能电池性能，寻求不同方法所制备薄膜对DSC性能的影响因素。实验结果表明，旋转涂覆法所制备的染料敏化太阳能电池具有较高的光电化学性能，在50mW／cm^2的模拟光照下（AM1．5）开路电压为0．696V，短路电流为6．19mA／cm^2，填充因子为0．584。     

蒙脱石基纳米FeOOH/TiO2复合材料的制备与光催化活性研究

以蒙脱石为基底,采用溶胶-凝胶法制备二氧化钛/蒙脱石(TiO2/Mmt)复合光催化材料,通过Fe(NO3)3-HNO3体系水解生长纳米FeOOH,从而制备出负载型羟基氧化铁/二氧化钛/蒙脱石(FeOOH/TiO3/Mmt)复合光催化材料以改善材料在可见光下的光催化性能.高分辨透射电镜的表征结果显示,FeOOH/TiO2复合薄膜厚度约为10～40 nm,TiO2为晶粒粒径约为5～10nm的锐钛矿,FeOOH为长10～30 nm,宽约4 nm的针铁矿.以甲基橙为目标物,对FeOOH/TiO2/Mmt复合材料的光催化性能进行初探,在甲基橙初始浓度为5 mg/L,催化剂用量为1.875 g/L,H2O2初始浓度为2 mmol/L,pH值为6.5,350 W氙灯照射1 h,甲基橙脱色率达到99%,明显优于相同条件下TiO2/Mint对甲基橙的45%脱色率;同时甲基橙残液的红外光谱图显示FeOOH/TiO2/Mmt/H2O2/UV体系比FeOOH/TiO2/Mint/H2O2/Visible light体系具备更好的光催化氧化苯环的能力,降解更为彻底.     

利用尾矿砂制备镁铁氢氧化物实验研究

以金川铜镍矿尾矿酸浸液为原料,根据矿物沉淀pH值区间的不同,分步分离Fe、Mg的沉淀物以及有价金属Al、Co、Ni、Cu的混合沉淀物,进而制备具有高附加值的Fe(OH)3和Mg(OH)2,同时富集Co、Ni、Cu等有价金属。结果表明,当溶液pH值为3.8时可沉淀分离出主要成分为施威特曼石(schwertmannite)的氢氧化铁前驱体,pH值达到9.8时沉淀富集出Al、Co、Ni、Cu的混合氢氧化物,随即得到只含有Mg离子的溶液。在60℃条件下,将施威特曼石在pH值为12的NaOH溶液中老化36h,可以得到Fe(OH)3。同时,以NaOH调节只含有Mg离子的溶液至pH值为12.4时可获得Mg(OH)2。本研究为金属矿山尾矿的资源化综合利用提供了新的思路与方法。     

共存铁和锰氧化物氧化和固定Ce(Ⅲ)的机制

该研究通过批次和动态实验,考查含锰褐铁矿和合成针铁矿对Ce(Ⅲ)的氧化和固定作用,并在此基础上探讨共存铁和锰氧化物氧化和固定Ce的机制及地质意义。批次实验结果显示,含锰褐铁矿对Ce的氧化和固定有重要促进作用,在初始Ce浓度为6000μg/L,含锰褐铁矿添加量为1 g/L时,可在48 h实现对Ce的完全固定;初始Ce(Ⅲ)浓度在300～4500μg/L时,含锰褐铁矿对Ce(Ⅲ)氧化和沉淀的促进作用与Mn含量正相关,而合成针铁矿相对于无矿体系体现出抑制效应。动态实验结果显示,对高锰褐铁矿固定的Ce,其分布不受锰氧化物的制约,与铁氧化物的分布一致。对结果的分析表明Ce氧化和沉淀的过程为：吸附—氧化—CeO₂沉淀生成—CeO₂自催化氧化Ce(Ⅲ);锰和铁氧化物共存时,对Ce氧化和固定的贡献分别是：前者促进Ce氧化,后者通过静电吸附作用促进CeO₂的固定。研究对于解释“锰氧化物氧化Ce(Ⅲ)的能力强于铁氧化物,但二者共存时铁氧化物更易于固定Ce”这一地质现象有一定启示意义。     

铜陵新桥矿田褐铁矿矿物组成及成因

褐铁矿是铁帽型金矿和铁矿的重要矿产类型,但目前对其从矿物学的微观角度研究较少。本文采用粉晶X射线衍射(XRD)以及场发射扫描电镜(SEM)矿物学研究手段,对铜陵矿集区新桥矿田褐铁矿的矿物组成、微结构进行研究。根据矿物组成及微结构将新桥褐铁矿分为两种成因类型:Ⅰ型褐铁矿,该类型褐铁矿主要起源于黄铁矿矿石,矿石多具蜂窝状构造。主要组成矿物为针铁矿,次要矿物为赤铁矿,含有少量石英,针铁矿晶体长度一般介于500 nm~2μm,长度/半径比值(长径比)较大;Ⅱ型褐铁矿,由原生菱铁矿矿石风化而成,矿石多具肾状构造。矿物组成主要为针铁矿,其次为赤铁矿、锰氧化物和伊利石等粘土矿物,针铁矿晶体长度一般小于500 nm,具有较小的长径比。褐铁矿矿物学和微结构不仅可以初步确定原生矿物和矿石类型,而且对寻找铁帽金矿床也具有重要指示意义。     

几种不同类型的FeOOH吸附水溶液中铬离子研究

采用两种显微结构不同的螺旋状和管状构造的天然铁细菌矿化针铁矿和化学合成的α—FeOOH及两种有机高分子模板矿化结晶的β-FeOOH作为吸附材料，分别在pH=5和6时对含Cr^3 和Cr(Ⅵ)废水进行了吸附实验研究，结果表明，天然生物矿化针铁矿对金属阳离子和阴离子均有明显的吸附作用，其显微结构、大小和形态影响其吸附能力；纯化学合成的针铁矿对铬离子的吸附能力较低；通过有机模板合成的纳米微晶β-FeOOH对Cr^3 和Cr(Ⅵ)均有极高的去除率，这与其表面存在与有机分子络合作用、增大了其表面对金属离子和铬酸根的化学亲合力有关。     

Feroxyhyte,a new modification of FeOOH

Two modifications of the delta-hydroxide of iron have been synthesized under laboratory conditions. Both are formed topotactically by the rapid course of the abiogenic reaction of the oxidation of Fe⁺² at the expense of Fe(OH)₂. Natural δ'-FeOOH, for which the authors propose the name "feroxyhyte," was found as yellowish-brown deposits in iron-manganese nodules from the bottom of the Pacific Ocean, Baltic, White, and Kara seas, and in gley soils. Feroxyhyte is an unstable hydrous oxide of iron, apparently transformed spontaneously into goethite, the stable modification of FeOOH. Its theoretical composition is Fe₂O₃ - 89.86, H₂O - 10. 147%.     

Model biomimetic studies of templated growth and assembly of nanocrystalline FeOOH

We studied biomimetic mineralization of self-assembling polymer matrices in order to develop a model for biomineralization of iron oxides in nature. High-resolution transmission electron microscopy (HRTEM), rheology, and fluorescence probe analyses show self-assembly of acidic polysaccharide alginic acid (Alg) to form fibrils in dilute solutions. The resulting Alg fibrils are subsequently mineralized by FeOOH in a biomimetically controlled process. Experiments were conducted in pH 9.2 solutions containing millimolar concentrations of iron at 38°C. The unperturbed state of the hybrid mineral-organic structures was studied by characterization of samples of interfacial films collected from an inorganic-organic interface. Progress of mineralization over a 4-week period was followed by HRTEM, energy-dispersive X-ray analysis, and selected area electron diffraction. Morphologies of hybrid structures determined by HRTEM, X-ray powder diffraction, Fourier transform infrared spectroscopy, energy-dispersive X-ray analysis, and selected area electron diffraction suggest formation of iron (III) oxyhydroxide phases and their assembly through a variety of mechanisms, possibly occurring simultaneously. An initial step involves precipitation of nanometer-scale amorphous particles and two-line ferrihydrite in bulk solution. Some nanoparticles assemble into chains that recrystallize to form akaganeite (β-FeOOH), presumably via a solid-state transformation pathway. Small organic molecules may mediate this process by stabilizing the akaganeite structure and controlling particle assembly. Ferrihydrite particles also bind to acidic polysaccharide fibrils and are transformed to ordered arrays of akaganeite. The parallel orientation of adjacent akaganeite nanocrystals may be inherited from the orientation of precursor ferrihydrite, possibly conferred during attachment of ferrihydrite to the polyacid fibrils. Alternatively, particle-particle interactions may induce orientation, leading to recrystallization. Subsequently, akaganeite is transformed to goethite that is characterized by nanoscale porosity and fine-scale twinning on {021}. Dislocation, twin, and nanopore microstructures are consistent with coarsening by nanoparticle assembly, possibly templated by the substrate. Nanoparticle assembly to generate biomimetic hybrid materials may be relevant to formation of complex natural biominerals in natural systems where mineral nanoparticles, small organic molecules, and more complex polymers coexist.     

硅藻土负载羟基氧化铁对铬（VI）吸附的固体浓度效应研究

利用硅藻土负载羟基氧化铁颗粒作吸附剂对六价铬进行吸附和解吸附实验,探讨了硅藻土负载羟基氧化铁对六价铬的吸附机制和固体浓度效应。实验结果表明：在实验条件下,当吸附剂的用量从0.05 g增加到0.2 g时,六价铬的吸附量从23940.124μg/g降低到8575.415μg/g,吸附剂对Cr6＋的吸附存在明显的固体浓度（Cs）效应。吸附滞后角随着Cs 的增加而减小,吸附反应的可逆性增大。将实验数据分别用Languir和Freundlich吸附模型进行拟合,发现Freundl-ich吸附模型对实验数据拟合效果较好,表明该吸附反应以单分子层吸附为主。     

Sorption of uranyl and arsenate on SiO2, Al2O3, TiO2 and FeOOH

Migration of uranium and arsenic in aquatic environments is often controlled by sorption on minerals present along the water flow path. To investigate the sorption behaviour, batch experiments were conducted for uranium and arsenic as single components and also solutions containing both uranium and arsenic in the presence of SiO₂, Al₂O₃, TiO₂ and FeOOH at a pH ranging from 3 to 9. In solutions containing only U(VI) or As(V) with the minerals, the sorption of U(VI) was low at acidic pH range and increases with increasing pH, whereas As(V) showed opposite sorption behaviour to Al₂O₃, TiO₂ and FeOOH from acidic pH range to alkaline condition. For the As(V)–SiO₂ system, the sorption was low for almost all pH. Sorption of U(VI) and As(V) on SiO₂ and FeOOH is almost similar in solutions containing either U(VI) or As(V) separately, or both together. In the U(VI)–As(V)–Al₂O₃ system, a significant retardation in uranyl sorption and an enhancement in arsenate sorption on Al₂O₃ were observed for a wide range of pH. The sorption behaviour of U(VI) and As(V) was changed when Al₂O₃ was replaced by TiO₂, where an increase in sorption was observed for both elements. The sorption behaviour of uranyl and arsenate in the U(VI)–As(V)–TiO₂ system gives evidence for the formation of uranyl–arsenate complexes. The change in sorption retardation/enhancement of U(VI) and As(V) could be explained by the formation of uranyl–arsenate complexes or due to the competitive sorption between uranyl and arsenate species.     

Laser-Induced Dissociation of the Monolayer of Adsorbed Methanol Molecules

Astronomy Reports - Astronomical observations indicate a high abundance of methanol molecules in the gas phase of molecular-cloud dense cores, which cannot be explained by gas-phase chemical...     

一种仿金刚石膜的研究

针对客户声称的表面覆金刚石膜（DF）的合成立方氧化锆进行常规宝石学检测,结果发现,样品为覆膜合成立方氧化锆,但样品表面的覆膜层硬度低、光滑平整,与多晶金刚石膜的粒状结构及单晶金月1石膜表面定向排列的突起等特征均不相同。为了确定表面覆膜层的成分,采用小角X射线衍射仪、X射线光电子能谱仪和红外光谱仪对样品表面的覆膜层进行了物相分析、化学成分分析及谱学测试。X射线衍射分析表明样品表面的覆膜层属于非晶物相;X射线光电子能谱分析表明样品的膜层主要化学成分为C,F。结合薄膜材料资料分析,初步确定其表面覆膜层可能属于非晶氟化碳（a—C：F）膜;红外光谱分析结果显示样品表面的膜层所导致的1068cm-1处的特征峰,进一步验证了X射线衍射分析结论。综合结果表明,该样品表面的覆膜层为非晶氟化碳（a—C：F）膜,是一种仿金刚石膜。     

A Review on Hydraulic Fracture Height Growth for Layered Formation

Geotechnical and Geological Engineering - The fracture vertical stretching distance and fracture morphologies have great impact on the stimulated reservoir volume and well production in layered...