A novel route for the synthesis of indium nanoparticles in ionic liquid

In this paper, we report a novel preparation of indium nanoparticles by the reduction of indium chloride in ionic liquid by methanolic solution of NaBH₄. The particles are characterized by means of transmission electron microscopy (TEM), X-ray diffraction and UV-visible studies indicated that the powder consist of the cubic phase of indium. The particle size of indium nanoparticles is in the range of 20 nm mean diameter by Transmission electron microscopy (TEM). The samples display a strong surface plasma absorption band at 231 nm, which indicates that the sample is metal indium and the particle size is less than 20 nm. The thermal analysis of the sample indicate indium not indium oxide. Electrochemical studies show that indium nanoparticles have very good electrical properties.     

Formation of peelable rough gold patterns on an ionic liquid template

The ability to control metal patterns at the micro- and nanoscales, along with the development of a simple fabrication method, is important to many applications in the fields of materials science, biological sensing, electronics, and photonics. Herein, a simple approach to fabricating gold micropatterns with controlled roughness is reported. In this approach, gold is evaporated onto a striped liquid micropattern formed on self-organized microwrinkles. Gold nanoribbons with higher roughness form on the liquid part of the substrate because the deposited gold atoms can diffuse, grow, and aggregate at the liquid-air interface, whereas flat gold films form on the solid part. The rough gold nanoribbons formed on the liquid can then be peeled off through contact with water. The extinction spectrum of the rough gold nanoribbons suggests characteristic surface-plasmon absorption. This shows the possibility of using rough gold nanoribbons with controlled shape in plasmonic technology.     

Microwave green synthesis of PVP-stabilised gold nanoparticles and their adsorption behaviour for methyl orange

In this work, gold nanoparticles (AuNPs) were prepared by the microwave irradiation method and comparative studies on the removal of dye by adsorption on activated carbon (AC) and polyvinylpyrrolidone (PVP)-supported AuNPs-coated AC were made. The uniform and stable AuNPs were prepared by the reduction of gold chloride (HAuCl₄) using glucose as reducing agent and PVP as a stabilising and capping agent. The resulting AuNPs were characterised by transmission electron microscopy (TEM) and UV-Vis spectroscopy. The TEM technique showed the presence of AuNPs with an average size of 20?nm. The effect of various process parameters has been investigated by following the column adsorption technique at room temperature. Percentage removal of dye increased with the decrease in initial concentration and increased with the increase in contact time. Adsorption data were modelled with the Freundlich isotherms. The Freundlich isotherm model has been applied to the equilibrium adsorption data. Desorption studies were made to elucidate recovery of the adsorbate and adsorbent for the economic competitiveness of the removal system. The adsorption capacity of the water-desorbed adsorbate reduced from 97% to 60% for n?=?6 cycles.     

UV-photoactivation technique for size and shape controlled synthesis and annealing of stable gold nanoparticles in micelle

Gold nanoparticles of different sizes and shapes have been prepared by UV-photoactivation technique using the micelle TX-100 (poly(oxyethylene)iso-octylphenyl ether) as reducing agent, stabilizing agent as well as template which has been authenticated from the plasmon absorption band and TEM picture. The heating effect on those gold nanoparticles has also been studied.     

Ionogel-templated synthesis and organization of anisotropic gold nanoparticles

Photochemical reduction of tetrachloroaurate (AuCl4-) ions in the highly constrained aqueous domains of a nanostructured ionogel template, formed via self-assembly of the ionic liquid 1-decyl-3-methylimidazolium chloride (C10mim+Cl-) in water, results in the formation of anisotropic gold nanoparticles with a variety of sizes and morphologies, which include previously unattainable trigonal prismatic nanorods. Unexpectedly, small-angle X-ray scattering studies of the Au-ionogel composite reveal that the in situ formation of the nanoparticles increases the mesoscopic order of the ionogel, which results in its conversion to a near-monodomain structure. The findings demonstrate that nanostructured, ionic liquid-based gels can be used to template the formation of new nanoparticle morphologies with technologically important optical, electronic, and catalytic properties. It may also be possible to design soft templates that permit the fabrication of highly ordered nanoparticle array-hydrogel composites, thereby enabling control and tuning of the collective properties of the encapsulated nanoparticles.     

Facial synthesis of polypyrrole/silver nanocomposites at the water/ionic liquid interface and their electrochemical properties

Polpyrrole (PPy)/silver nanocomposites with their size of around 80-120 nm were successfully synthesized at the interface of water and ionic liquid. High dispersed PPy/silver nanocomposites were obtained in the presence of polyvinylpyrrolidone (PVP) by controlling the reacting conditions. The morphology and structure of the resulting nanocomposites were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction and X-ray photoelectron spectroscopy. It was also found that the electrical conductivity of PPy/silver nanocomposites was much higher than that of pure PPy. Cyclic voltammetric experiments further indicated that the nanocomposite had excellent redox ability: polypyrrole; silver; ionic liquid; interface synthesis; and nanocomposites.     

A task specific basic ionic liquid for synthesis of flower-like ZnO by hydrothermal method

Flower-like ZnO morphology, with different shapes, have been successfully synthesized via a novel and environment-friendly hydrothermal method using zinc acetate and a task specific dicationic dibasic ionic liquid, [mmpim]₂[OH]₂, which plays an important role in fabrication of ZnO structure. The structure and morphology of the product were characterized by X-ray diffraction and scanning electron microscopy, which show different flower-like morphologies. Photoluminescence spectrum of the product exhibits a strong ultraviolet emission at 391 nm and two weak blue-green emissions at about 450 and 500 nm.     

A facile synthesis of monodisperse Au nanoparticles and their catalysis of CO oxidation

Monodisperse Au nanoparticles (NPs) have been synthesized at room temperature via a burst nucleation of Au upon injection of the reducing agent t-butylamine-borane complex into a 1, 2, 3, 4-tetrahydronaphthalene solution of HAuCl₄·3H₂O in the presence of oleylamine. The as-synthesized Au NPs show size-dependent surface plasmonic properties between 520 and 530 nm. They adopt an icosahedral shape and are polycrystalline with multiple-twinned structures. When deposited on a graphitized porous carbon support, the NPs are highly active for CO oxidation, showing 100% CO conversion at −45 °C. This article is published with open access at Springerlink.com     

催化相转化法制备纳米铁酸镍及性质研究

用催化相转化法在不同初始浓度，不同pH值下．在液相中短时间内合成出了纳米铁酸镍微晶．利用XRD、TEM对产物进行了表征，并测定了产物的磁化强度、密度及比表面。结果表明，该方法制备的纳米级铁酸镍具有超顺磁性，粒径小于20nm。     

Thermal expansion of glasses in the solid and liquid phases

In this study, the thermal expansion of a number of mixed oxide glasses was measured in the solid and liquid regions by gamma densitometry. Conventional density measurement techniques are limited to either the solid or the liquid phase; however, with this noncontacting technique, the density and thermal expansion of both the solid and the liquid phases may be investigated as the temperature is varied and the glass viscosity varies over a wide range. This technique allows the continuous measurement of density as the liquid cools to a supercooled glass or to a crystalline solid. Lead borate glasses were examined in the range 27 to 42 mol % PbO. The liquid-phase volumetric thermal expansion coefficient was observed to decrease with increasing PbO content, in contrast to the solid-phase linear thermal expansion coefficients. In soda-baria phosphate glasses (50 mol% P₂O₅), liquid-phase volumetric expansion coefficients were found to vary as the solid-phase linear expansion coefficients. Measurements on a lithia-aluminoscilicate glass ceramic were obtained by this method to approximately 400°C above the limit of conventional dilatometry. The gamma densitometry technique can yield density, thermal expansion, glass transition and crystallization information, and quenching-rate dependence data on glasses to temperatures in excess of 1500°C, and thus provides a means for high-temperature characterization of glasses which complements conventional dilatometry, calorimetry, and thermal analysis.Paper presented at the Ninth Symposium on Thermophysical Properties, June 24–27, 1985, Boulder, Colorado, U.S.A.     

Parametric study of cost-effective synthesis of crystalline copper nanoparticles and their crystallographic characterization

Pure and high-crystalline copper nanoparticles were synthesized at room temperature by reduction of copper nitrate with hydrazine hydrate in cetyltrimethyl ammonium bromide (CTAB) solution without using any extra gases. A parametric study has been carried out in terms of hydrazine concentration, solution pH, and stirring. Pure copper nanoparticles without oxidation were obtained at 0.1–0.2 M N₂H₄ and pH = 10. The growth mechanism of various shaped copper nanoparticles is discussed based on structural analysis by transmission electron microscopy and selected area electron diffraction.     

Temperature and anion responsive self-assembly of ionic liquid block copolymers coating gold nanoparticles

In this paper, double hydrophilic ionic liquid block copolymers (ILBCs), poly poly[1-methyl-3-(2-methacryloyloxy propylimidazolium bromine)]-block-(N-isopropylacrylamide) (PMMPImB-b-PNIPAAm) was first synthesized by reversible addition-fragmentation chain transfer (RAFT) and then attached on the surface of gold nanoparticles (Au NPs) via a strong gold-sulfur bonding for preparing hybrid nanoparticles (PMMPImB-b-PNIPAAm-@-Au NPs). The hybrid NPs had a three layers micelle-like structure, including a gold core, thermo-responsive inner shell and anion responsive outer corona. The self-assembling behavior of thermal- and anion-response from shell and corona were respectively investigated by change of temperature and addition of (CF₃SO₂)₂N^-. The results showed the hybrid NPs retained a stable dispersion beyond the lower critical solution temperature (LCST) because of the space or electrostatic protecting by outer PMMPImB. However, with increasing concentration of (CF₃SO₂)₂N^-, the micellization of self-assembling PMMPImB-b-PNIPAAm-@-Au NPs was induced to form micellar structure containing the core with hydrophobic PMMPImB-(CF₃SO₂)₂N^- surrounded by composite shell of Au NPs-PNIPAAm via the anion-responsive properties of ILBCs. These results indicated that the block copolymers protected plasmonic nanoparticles remain self-assembling properties of block copolymers when phase transition from outer corona polymer.     

硅胶固载酸功能化离子液体催化剂的制备和应用

将带有酸官能团的离子液体固载到具有高表面积的硅胶上,制备的硅胶固载酸功能化离子液体可作为催化剂用于多种有机反应。该新型催化剂具有高效、高选择性、离子液体用量少、产品易分离和催化剂易回收等优点,因有望用于化工过程的固定床反应器而受到关注。     

一种制备ZnO纳米颗粒的新方法

提出了一种制备ZnO纳米颗粒的新方法。在金属钠的液氨溶液中还原硝酸锌,所形成的金属Zn自然氧化而制得ZnO颗粒。为了研究表面修饰对产物形貌、粒径和性能的影响,制备了十二烷基磺酸钠（SDS）修饰的ZnO纳米颗粒。采用X射线粉末衍射仪（XRD）、透射电子显微镜（TEM）、傅立叶变换红外光谱仪（FT-IR）、热重及差热分析仪（TG-DTA）等手段对产物进行了表征。结果表明采用该方法可制得具有六方纤锌矿结构的ZnO颗粒,未修饰ZnO颗粒团聚较为严重;修饰的ZnO纳米颗粒呈棒状,分散较好。红外和热分析表明SDS修饰在了ZnO纳米颗粒表面。测试了所制备ZnO颗粒的紫外可见吸收（UV-Vis）和光致发光（PL）谱,均出现了ZnO的特征谱带。提出的方法也适用于制备其它金属或氧化物纳米材料。     

Medicinal plants mediated the green synthesis of silver nanoparticles and their biomedical applications

The alarming effect of antibiotic resistance prompted the search for alternative medicine to resolve the microbial resistance conflict. Over the last two decades, scientists have become increasingly interested in metallic nanoparticles to discover their new dimensions. Green nano synthesis is a rapidly expanding field of interest in nanotechnology due to its feasibility, low toxicity, eco‐friendly nature, and long‐term viability. Some plants have long been used in medicine because they contain a variety of bioactive compounds. Silver has long been known for its antibacterial properties. Silver nanoparticles have taken a special place among other metal nanoparticles. Silver nanotechnology has a big impact on medical applications like bio‐coating, novel antimicrobial agents, and drug delivery systems. This review aims to provide a comprehensive understanding of the pharmaceutical qualities of medicinal plants, as well as a convenient guideline for plant‐based silver nanoparticles and their antimicrobial activity.     

Self-assembled liquid crystalline nanoparticles as an ophthalmic drug delivery system. Part II: optimization of formulation variables using experimental design

In the field of keratoconus treatment, a lipid-based liquid crystal nanoparticles system has been developed to improve the preocular retention and ocular bioavailability of riboflavin, a water-soluble drug. The formulation of this ophthalmic drug delivery system was optimized by a simplex lattice experimental design. The delivery system is composed of three main components that are mono acyl glycerol (monoolein), poloxamer 407 and water and two secondary components that are riboflavin and glycerol (added to adjust the osmotic pressure). The amounts of these three main components were selected as the factors to systematically optimize the dependent variables that are the encapsulation efficiency and the particle size. In this way, 12 formulas describing experimental domain of interest were prepared. Results obtained using small angle X-rays scattering (SAXS) and cryo-transmission electron microscopy (cryo-TEM) evidenced the presence of nano-objects with either sponge or hexagonal inverted structure. In the zone of interest, the percentage of each component was determined to obtain both high encapsulation efficiency and small size of particles. Two optimized formulations were found: F7 and F1. They are very close in the ternary phase diagram as they contain 6.83% of poloxamer 407; 44.18% and 42.03% of monoolein; 46.29% and 48.44% of water for F7 and F11, respectively. These formulations displayed a good compromise between inputs and outputs investigated.