Preparation and study of colloid-chemical and optical properties of the nanocrystals of zinc sulfide modified with amino acids

The effect of some amino acids: cysteine, methionine, glycine, lysine, and aspartic acid, on the formation of nanoparticles of zinc sulfide in aqueous solutions at pH 5.5–10.0 was investigated. A method of obtaining stable sols of ZnS particles of 2–4 nm size with narrow distribution of the particle size was developed. The investigated nanoparticles are shown to be sphalerite, the cubic modification of zinc sulfide. The ZnS sols modified with methionine and glycine show intense luminescence at 415–425 nm.     

半导体硫化锌纳米微粒的合成与表征

采用液相均沉淀法,用不同原料(采用不同硫源或金属离子螯合剂)从3个途径合成了不同粒径的半导体ZnS纳米粒子,并用透射电子显微镜、X射线粉末衍射仪对粒子进行表征.     

Preparation of copper and zinc sulfide nanoparticles and their modification with cysteine

A new method for the preparation of copper and zinc sulfides nanoparticles in homogeneous aqueous solutions using cysteine as a surface modifier was proposed. The size of the particles obtained is 5–7 and 1.5–3 nm for copper and zinc sulfides, respectively, depending on the concentration of the reactants. Associates of the nanoparticles 10–30 nm in size are formed in the system with an increase in the total concentrations of the sulfides. Sols of the nanoparticles obtained in cysteine solutions are resistant to oxidation and coagulation within several weeks. The variation of the synthesis conditions makes it possible to obtain zinc sulfide particles with optical properties related to size effects.     

Regularities of the retention of aminopyridines by silica gel modified with gold nanoparticles

New sorbents based on silica gel and gold nanoparticles stabilized by L-cysteine and its methyl ester are synthesized. Regularities of the retention of various substituted aminopyridines by the synthesized sorbents are examined in the normal-phase mode of high-performance liquid chromatography upon elution by a binary mobile phase (hexane-isopropanol). Quantum-chemical simulations of L-cysteine and its derivative adsorptions on the surface of a gold cluster are performed, along with simulations of subsequent adsorptions of substituted pyridines on the modified gold surface. It is shown that the Snyder-Soczewinski and Scott-Kucera displacement models can be used to describe the experimental data on the synthesized sorbents.     

Formation of zinc sulfide and hydroxylapatite nanoparticles in polyelectrolyte-modified microemulsions

The paper is focused on the formation of nanoparticles, i.e., zinc sulfide (ZnS) and hydroxylapatite, in a microemulsion template phase consisting of heptanol, water, and a surfactant with a sulfobetaine head group in the absence and presence of an added polyelectrolyte. In the absence of a polyelectrolyte, beside larger particles, spherical ZnS nanoparticles with a diameter below 10 nm can be redispersed after solvent evaporation. In the presence of the synthetic cationic polyelectrolyte poly(diallyldimethylammonium chloride), a reloading of the particle surface is observed, and cationic charged ZnS nanoparticles, of about 5 nm in size, can be redispersed as a main fraction. When hydroxylapatite is formed in the presence of the more stiff biopolymer chitosan hydroxylapatite, hybrid structures were formed. Transmission electron micrographs show fiber-like aggregate structures, consisting of individual small nanoparticles ordered along the polymer chain.     

Investigation of structural,optical and photoluminescence properties of non-essential amino acid capped zinc sulfide nanoparticles for optoelectronic applications

The objective of the study is to synthesize Zinc Sulphide nanoparticles (ZnS) with different amino acid capping agents in aqueous solution by a simple and cost effective facile chemical co precipitation method and analyze their optoelectronic features. Bio compatibility with less toxic amino acids such as l-Glutamic acid, l-Alanine and l-Asparagine were used as capping agents. These amino acids are from Non-essential amino acid group and its capping behavior suitable for semiconducting nanoparticles like ZnS. The role of non essential amino acids were to stabilize the nanoparticle against agglomeration and also to provide chemical passivation that leads to a significant influence on the improved structural, optical and photoluminescence properties of ZnS nanoparticles. The detailed structural analysis of Zinc Sulphide nano particles revealed by X-ray diffraction method (XRD). From this analysis observed the formation of Cubic ZnS nanoparticles with an average crystallite size in the range of 2.08–2.22 nm.The morphology of the nano particles studied by Field emission scanning electron microscope (FESEM). Particle size examined by Dynamic Light scattering studies (DLS) and which revealed that particle size ranges are below 50 nm. The functional groups of nanoparticles were identified by Fourier transform Infrared spectroscopy (FT-IR) studies. Photoluminescence studies attributed that the considerable emission bands. The UV–Vis analysis disclosed the optical band gap range from 3.77 eV to 3.95 eV.     

Sorbent for the separation of enantiomers of amino acids based on silica gel modified with stabilized Au nanoparticles

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Regularities of the formation of silver nanoparticles with oligostyrylmonocarboxylate ligands in ED-20 oligomer

Regularities of the formation of silver nanoparticles according to the reduction reaction of silver oligostyrylmonocarboxylate with ED-20 resin in the absence of hardening agent were studied at 60–75°C by UV/Vis spectroscopy and IR spectroscopy, transmission electron microscopy, and viscosimetry. Spherical silver nanoparticles with oligostyrylcarboxylate ligands characterized by diameter equal to 1.8 ± 0.2 nm and tendency toward ordered disposition in space were obtained. The process of formation of nanoparticles includes consecutive formation of diphilic complexes of silver carboxylate with epoxy resin, Ag⁺ → Ag⁰ reduction, and formation of (Ag⁰) _n nuclei at the ends of the diexpoxy component and/or along the oligomer chain. The activation energy values of formation of nanoparticles during the “inductive period” and at the stage of accumulation as well as the activation energy of viscous flow of ED-20 were measured. The threshold temperature of formation of narrow-size silver nanoparticles in epoxy oligomer ED-20 equals 75°C.     

Synthesis of cationic porphyrin modified amino acids

Derivatives of amino acids bearing a porphyrin moiety on a side chain were synthesized by coupling a porphyrin to a glutamic acid side chain; the utility of these compounds was demonstrated by their use in solid-phase synthesis of a peptide bearing a cationic porphyrin and by studying its DNA-binding properties.     

Study on the preparation and formation mechanism of barium sulphate nanoparticles modified by different organic acids

This paper reports a simple method to prepare barium sulphate nanoparticles by use of tetradecanoic acid, hexadecanoic acid and stearic acid as modifier. The barium sulphate nanoparticles obtained are characterized by using Fourier transform infra-red spectroscopy (FT-IR), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic laser light scatter (DLLS) and thermogravimetric analysis (TGA), respectively. The results show that the BaSO₄ particles are all spherical and in the nano-scale. Our method has a better dispersion and controllable diameter dependent on the length of the chain of organic acid and the pH value of the system. A possible mechanism is also discussed.     

有机修饰氧化硅对抗紫外纳米ZnO的原位表面修饰

以正硅酸乙酯和二甲基二乙氧基硅烷作为共前驱体,通过溶胶-凝胶反应得到有机修饰氧化硅;用有机修饰氧化硅对碱式碳酸锌进行原位表面改性,通过对表面改性碱式碳酸锌进行热处理得到表面改性纳米ZnO;分析了表面改性纳米ZnO的结构和性能.结果表明,经有机修饰氧化硅改性处理的纳米ZnO具有强憎水性,与有机相的相容性较强,光催化活性得...     

Specific ionic effect for simple and rapid colorimetric sensing assays of amino acids using gold nanoparticles modified with task-specific ionic liquid

In this study, a novel task-specific ionic liquid functionalized gold nanoparticle (TSIL-GNP) was successfully prepared and applied in the recognition of amino acids. Particularly, the surface of GNP was modified with the ionic liquid containing carbamido and ester group via thiol, which was characterized by Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). The stability of this material in aqueous solution improves apparently and can remain unchanged for more than three months. The effect of pH was also discussed in this study. Attractive ionic interaction would effectively weaken intensity of the covalent coupling between the metal ion and the functional groups of amino acids. Thus, TSIL-GNP was successfully applied to recognizing serine, aspartic acid, lysine, arginine, and histidine in the presence of Cu²⁺ through distinctive color changes. Suspension would be generated once a spot of cysteine was added into the GNPs solution. Results indicated that it had a good linear relationship between extinction coefficients and concentration of amino acids in a wide range of 10⁻³–10⁻⁶ M. Moreover, the proposed strategy was successfully used to analyze the histidine in urinary samples. In brief, TSIL-GNP is a suitable substrate for discrimination of five amino acids in a rapid and simple way without sophisticated instruments.     

Regularities of silver atom formation in gamma-irradiated aluminium silicate modified by yttrium

The ESR method was used to study the regularities of formation of silver atoms in gamma-irradiated aluminium silicate modified by yttrium and containing¹⁰⁹Ag istope ions introduced by various techniques. The existence of two types of silver atoms and an Ag ₂ ¹ complex stabilized an the surface of a gamma-irradiated carrier has been established. g-Factors and superfine structure constants of spectral lines of paramagnetic silver particles belonging to various types observed on the surface have been calculated. Quantitative correlations of paramagnetic silver particles and the nature of their kinetic dependences in a broad temperature range (from 77 to 353 K) are determined by the number of silver ions introduced into the carrier and by the mode of introduction, thermal and vacuum pretreatment of the samples, irradiation dose and the temperature of investigating the gamma-irradiated surface.     

Formation of zinc sulfide nanorods and nanoparticles in ternary W/O microemulsions

A simple, easy approach to the synthesis of semiconductor ZnS nanorods and nanoparticles exhibiting versatile morphology-formation ability is reported. Water-insoluble zinc sulfide nanocrystals were synthesized in ternary water-in-oil (w/o) microemulsion systems stabilized by either nonionic or, in contrast, cationic surfactant. Products were visualized by transmission electron microscopy (TEM) and identified by energy-dispersive X-ray spectroscopy (EDAX); electron diffraction (ED) was also performed for individual nanorods. With varying molar ratios of water to surfactant (omega0) in solution, hence changing droplet sizes of water pool of microemulsions consequently, several morphologies with different size spans were encountered in the formation of ZnS, such as nanorods and spherical or ellipsoidal particles. Meanwhile, product morphology was also found to be sensitive to the absolute reactant concentration and concentration ratio of [Zn2+] to [S2-], the incubation time, and the ambient temperature. A schematic mechanism for the formation of ZnS nanocrystals and their morphological diversity is described. It is feasible to extend this method to the synthesis of one-dimensional nanocrystals of other semiconductors, given suitable formulae of microemulsions and other appropriate reaction conditions.     

Miscibility of zinc sulfide and zinc phosphide

Solid solutions in the system zinc sulfide/zinc phosphide (Zn(2+)(x)S(2-2xP(2x)) were investigated using the cyclic cluster model within the semiempirical MSINDO method. Results of cyclic cluster calculations for binding energies of the perfect ZnS and Zn(3)P(2) are presented and compared with the experimental data. The miscibility of ZnS and Zn(3)P(2) over the whole composition range of 0 < x < 1 was investigated by calculating the Gibbs free energy of mixing Delta(M)G for different values of x. A miscibility gap was found at both ends of the composition range and compared with experimental data.     

Colorimetric detection of thiol-containing amino acids using gold nanoparticles

This paper reports findings of an investigation of the unusual colorimetric change of gold nanoparticles in the presence of thiol-containing amino acids such as homocysteine, cysteine and glutathione. The colorimetric change for homocysteine exhibits a rate that is about two orders of magnitude higher than that for cysteine, and at least five orders of magnitude higher than that for glutathione. The reactivity is effectively reduced or suppressed by the coexistence of either cysteine or glutathione. It is believed that the reactivity involves encapsulation of the particles by the thiol-containing amino acids which is followed by crosslinking at the encapsulating shells. In comparison with cysteine and glutathione, homocysteine has a slower encapsulating rate but a faster crosslinking rate. Implications of the findings of the interfacial encapsulation and crosslinking reactivities of gold nanoparticles to potential nanoparticle-enhanced analytical detection of thiol-containing amino acids are also briefly discussed.     

The mechanism of particle formation during homogeneous precipitation of zinc sulfide

Monodisperse zinc sulfide particles were prepared by homogeneous precipitation from zinc sulfate solutions. Particle size could be adjusted in the range of 1 to 5 microns by changing the viscosity of the reaction medium. From electron micrographs of particles prepared in high viscosity media subparticles up to 50 nm in diameter could be observed. From these results it was concluded that particle growth took place predominantly by Brownian coagulation.Furthermore, it was established that stirring the reactor content during the initial phase of particle formation alone did not influence particle size, nor did it promote coagulation of micron-sized spheres. We were able to prepare this material in amounts up to 2 kg of solid material from a reactor with a working volume of 36 l.     

Water-soluble zinc porphyrins as artificial receptors for amino acids

The binding of amino acids to water-soluble zinc porphyrins in basic aqueous solution was spectrophotometrically analyzed. The amino acids were bound to the porphyrins through the coordination of the N atom with the central zinc ion. Additional attractions arise due to Coulomb interactions between the -COO(-) anion of the amino acids and the -N(CH(3))(3)(+) cation of the porphyrin substituents and due to hydrophobic interactions between the porphyrin plane and the hydrophobic substituents of the amino acids. These attractions could be explained based on the binding data. The compensatory relationships of DeltaS and DeltaH were also discussed.     

Aqueous pathways for the formation of zinc oxide nanoparticles

We examine the effect of reactant concentrations, temperatures and feeding methods on the morphology of ZnO formed when reacting solutions of ZnSO(4) and NaOH. The catalytic effect of hydroxide in excess relative to the stoichiometric ratio is considered. It is shown that, having fixed other reaction conditions, the end-products, particle structures and size strongly depend on the mole ratio of the precursors. The presence of zinc salt hydroxide species was confirmed at sub-stoichiometric ratios in slightly acidic conditions. At the stoichiometric ratio both zinc hydroxide and zinc oxide are formed, while only zinc oxide forms in an excess of hydroxide. The method of feeding the reactants into the reaction vessel also has a strong influence on the end-product properties, as does the reaction temperature. By control of these parameters the specific surface area could be varied from 10 to 33 m(2) g(-1), the particle shape could be varied from equiaxed, through to star-like and needle-like, and the particle size may be varied from 50 to over 300 nm.