Preparation of Nanocrystalline Bismuth-Containing Powders through Solution-Phase Reductions

1999 ◽  
Vol 581 ◽  
Author(s):  
Edward E. Foos ◽  
Alan D. Berry ◽  
Arthur W. Snow ◽  
J. Paul Armistead

ABSTRACTIn an attempt to both prepare nanocrystalline bismuth and understand the fundamental chemistry behind the formation of this potentially interesting material, we have examined the reduction of BiCl3 in the presence of strongly coordinating solvents and ligands. These studies have resulted in the formation of bismuth powders with approximate average particle sizes of between 20 and 40 nm which exhibit large size distributions. The simultaneous reduction of both gold and bismuth precursors, done in an attempt to better control the final particle size, instead produces Au2Bi of comparable dimensions. There is no evidence that the ligands utilized in either of these systems remain bound to the final product. These nanocrystalline powders have been characterized through XRD and TEM, and full details of the synthesis are presented.

1996 ◽  
Vol 457 ◽  
Author(s):  
Fatih Dogan ◽  
Shawn O'rourke ◽  
Mao-Xu Qian ◽  
Mehmet Sarikaya

ABSTRACTNanocrystalline powders with an average particle size of 50 nm has been synthesized in two materials systems under hydrothermal conditions below 100°C. Processing variables, such as temperature, concentration and molar ratio of reactants and reaction time were optimized to obtain particles of reduced size and stoichiometric compositions. Hydrothermal reaction takes place between Ba(OH)2 solution and titanium/iron precursors in sealed polyethylene bottles in the BaTiO3 and BaFe12O19 systems, respectively. While crystalline BaTiO3 forms relatively fast within a few hours, formation of fully crystalline and stoichiometric BaFei20i9 require considerably longer reaction times up to several weeks and strongly dependent on the Ba:Fe ratio of the precursors. The structural and compositional evaluation of the nanophase powders were studied by XRD and TEM techniques.


1961 ◽  
Vol 34 (2) ◽  
pp. 433-445 ◽  
Author(s):  
E. Schmidt ◽  
P. H. Biddison

Abstract Knowledge of mass distribution of particle sizes in latex is very important to the latex technologist. Therefore, it is desirable to have available a simple method for the determination of mass distribution of particle sizes. This paper presents a method, based on fractional creaming of latex with sodium alginate, which can be used in any laboratory without special equipment. The method is particularly advantageous for analyzing latexes of very wide particle size distributions. When analyzed with an electron microscope, these latexes require counting a very large number of particles. McGavack found that partial creaming of normal hevea latex with ammonium alginate gives concentrates of larger average particle size than the original latex. He found that the average particle size in the cream approaches that of the original latex as the amount of creaming agent is increased. In a previous paper from this laboratory, Schmidt and Kelsey demonstrated that the phenomenon of fractionation according to particle size with increasing amounts of creaming agent is applicable in a wide variety of anionic latex systems and in colloidal silica. Their results indicated also the existence of a quantitative relationship, independent of the nature of the dispersed particles, between the concentration of creaming agent and size of creamed particles. Maron confirmed fractionation with respect to particle size as a consequence of partial creaming with alginate. He showed that the mass average particle sizes of fractions, determined optically, cumulate to that of the original latex. Although the previous paper by Schmidt and Kelsey implied the basic concept of a method of determining particle size distribution by fractional creaming, it was not exploited at that time. In order to adapt the fractional creaming phenomenon to a quantitative method for particle size determination, we required a more precise knowledge of the relation between creaming agent concentration and size of particles creamed. It was proposed to establish this relationship with the aid of the electron microscope. Various factors influencing the creaming of latex, such as polymer concentration, electrolyte, soap content, and variability of the creaming agent, had to be considered in standardizing the creaming procedure.


1992 ◽  
Vol 271 ◽  
Author(s):  
Barbara Simms ◽  
Tom Gallo

ABSTRACTWe describe a novel precipitation route to silica grain that lies in the interface between sol-gel and Stöber-type silica. The use of acetic acid as a catalyst for TEOS hydrolysis provides access to a precipitation window in which partially hydrolyzed TEOS and TEOS monomer, when reacted with aqueous ammonia, combine to form pumice-like silica particles in up to 90% yield as SlO2. Precipitated particles exhibit narrow particle size distributions that may be controlled for average particle sizes from 50µ to 400 µ. SEM micrographs show that the particles are agglomerates of small particles, which is consistent with the high degree of observed macroporosity.


1998 ◽  
Vol 4 (2) ◽  
pp. 122-127 ◽  
Author(s):  
E. Bruce Nauman ◽  
Timothy J. Cavanaugh

Particle size distributions obtained from a thin section are usually a skewed version of the true distribution. A previous method for determining the parent distribution was questionable because negative particle frequencies could be obtained. Here, we describe a method of determining parent distributions of spherical particles using a model with adjustable parameters. Our calculated distributions are somewhat broader than the distributions obtained with previous methods, but the average particle sizes are nearly identical. The newly developed model is applicable to any type of transmission microscopy.


Polymers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 3047
Author(s):  
Richard D. Sudduth

It has previously been shown that optimum particle size distributions with a maximum packing fraction can be achieved from a straight line plot of the accumulated sum of particle volume fractions versus the square root of particle size. This study addresses practical limits for two dominant fundamental approaches to designing particle size distributions to address the effect on a specific physical property such as viscosity. The two fundamental approaches to obtain such a straight line would include: the first design approach would be generated utilizing the same initial particle size, Dmin, but by using different ultimate particle sizes, Dmax. The second design approach would be generated where each distribution starts with the same initial particle size, Dmin, and ends with the same ultimate particle size, Dmax. The first design approach is particularly useful to identify the possible slopes available based on the smallest and largest particle sizes available. The second design approach can be utilized to identify the preferred ratio between particles, Z, and the number of different particle sizes, n, to be utilized in the final particle blend. The extensive empirical experimental evaluations of particle size distributions generated by McGeary were then utilized to confirm the limits.


Silicon ◽  
2020 ◽  
Author(s):  
Elida Nekovic ◽  
Catherine J. Storey ◽  
Andre Kaplan ◽  
Wolfgang Theis ◽  
Leigh T. Canham

AbstractBiodegradable porous silicon (pSi) particles are under development for drug delivery applications. The optimum particle size very much depends on medical use, and microparticles can outperform nanoparticles in specific instances. Here we demonstrate the ability of sedimentation to size-select ultrasmall (1–10 μm) nanoporous microparticles in common solvents. Size tunability is quantified for 1–24 h of sedimentation. Experimental values of settling times in ethanol and water are compared to those calculated using Stokes’ Law. Differences can arise due to particle agglomeration, internal gas generation and incomplete wetting. Air-dried and supercritically-dried pSi powders are shown to have, for example, their median diameter d (0.5) particle sizes reduced from 13 to 1 μm and from 20 to 3 μm, using sedimentation times of 6 and 2 h respectively. Such filtered microparticles also have much narrower size distributions and are hence suitable for administration in 27 gauge microneedles, commonly used in intravitreal drug delivery.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Xianhai Hu ◽  
Xingyuan Zhang ◽  
Jin Liu

A waterborne polyurethane-based polymeric dye (WPU-CFBB) was synthesized by anchoring 1, 4-bis(methylamino)anthraquinone (CFBB) to waterborne polyurethane chains. The number molecular weight, glass transition temperature, and average emulsion particle size for the polymeric dye were determined, respectively. This polymeric dye exhibited intriguing optical behaviors. The polymeric dye engendered two new absorption bands centered at about 520 nm and 760 nm if compared with CFBB in UV-vis spectra. The 760 nm peak showed hypsochromic shift with the decrease of average particle sizes. The polymeric dye dramatically demonstrated both hypsochromic and bathochromic effects with increasing temperature. The fluorescence intensity of the polymeric dye was much higher than that of CFBB. It was found that the fluorescence intensities would be enhanced from 20°C to 40°C and then decline from 40°C to 90°C. The fluorescence of the polymeric dye emulsion was very stable and was not sensitive to quenchers.


2016 ◽  
Vol 690 ◽  
pp. 236-239
Author(s):  
Oratai Jongprateep ◽  
Rachata Puranasamriddhi

High photocatalytic activity of nanoparticulate titanium dioxide has attracted worldwide attention. Synthesis techniques of the nanoparticles, however, often require high energy supply or costly initial reagents. Solution combustion technique is an energy-effective technique capable of synthesizing nanosized titanium powders. This research aimed at utilizing a less expensive initial reagent in synthesis of nanoparticulate titanium dioxide by the solution combustion technique. The research also examined effects of dissolving agents on chemical composition and particle sizes of the synthesized powders. A low-cost initial reagent, titanium dioxide with average particle size of 154 nanometers, was dissolved in sulfuric acid or dispersed in nitric acid prior to the combustion. Experimental results revealed that the pure anatase phase titanium dioxide was successfully obtained in powders prepared from both sulfuric acid and nitric acid. The average particle size of the powder prepared from sulfuric acid was 77 nanometers, while that of the powder prepared from nitric acid was 117 nanometers. The difference in particle sizes was attributed to solubility of the initial reagent in the acid. Complete solution of initial reagent in sulfuric acid was the main factor attributed to finer particle size.


2013 ◽  
Vol 457-458 ◽  
pp. 131-134 ◽  
Author(s):  
Tao Fan ◽  
Cong Li Xiao ◽  
Yan Rong Sun ◽  
Hong Bo Li

The aim of this study is to investigate the effect of SiC particle pretreatment, aluminum matrix particle size and sintering temperature on relative density, hardness, microstructure and wear resistance to SiC particle einforced aluminum matrix composites. To this end, the amount of 16.7 wt.% SiC with average particle sizes 20μm was used along with pure aluminum of average particle size of 75 μm and 25μm. Powder metallurgy is a method used in the fabrication of this composite in which the powders were mixed using a planetary ball mill. By analyzing SEM micrograph and the Property test, it is concluded that SiC particle pretreatment has significant effect on the morphology of pecimens. pretreatment increase the interface adhesion, improve the wettability. SiC is uniformly distributed in the matrix, with good relation to the substrate, the maximum hardness is 51.1HB, the minimum wear rate is 0.1684%, while the density is 97.3%.For the same SiC content and particle size, the smaller the particle size of aluminum matrix is, the higher wear resistance of composite materials is on condition that others are same, the higher sintering temperature and the higher the wearability of composites, the wear resistance of the composite material is significantly improved after SiC pre-processing.The relative density increases with increasing aluminum matrix particle sizes under the same pressure and the holding time. The actual density of all samples reached the theoretical density over 96%, to a maximum of 98.9%.


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