Network structure of fine silica particles

The network structure of silica aerogels heated at 300, 400 and 500°C in dried air have been determined by neutron total scattering measurements using a pulsed spallation neutron source. SANS experiments were also performed to obtain the particle size of the silica constituting aerogel. The elementary particle size obtained is about 13Å in diameter. The distances of the Si-O and O-O interactions in such fine silica particles are 1.61 and 2.64 Å, respectively, which are the same as those of fused silica. The coordination numbers of these pairs are found to be less evident than those of fused silica. In addition, the distances of the Si-Si pairs in the aerogels are slightly longer than that of fused silica. According to the heat treatment temperature, the coordination numbers of the Si-O and O-O interactions increase and the distance of the Si-Si pair decreases. These results indicate that although the network structure of fine silica particles treated at lower temperature is loose and imperfect, such structure can be changed by heating at relatively low temperature. The Raman spectra and the skeletal density measurements of the aerogels support also these results.     

The fine structure of submicron iron particles

Summary High resolution electron micrographs are shown of samples of colloidal alpha iron. According to the conditions of manufacture the samples occur as (1) large, well-formed dendrites, (2) shorter, more fragile dendrites, (3) serrated rods, (4) needles and (5) cubic particulates. The central stem is a line-up of single cubic crystals. Representative dimensions are given for the various measurable units. A fine laminar structure in the cubic particulates, and some of the side branches and main stems is noted. The same laminar structure is observed in some of the background platelet material from the mother liquor. Stereoscopic studies show that the dendrites are three dimensional with their branches and main stem not in the same plane. X-ray diffraction detects alpha iron plus some form of Fe₂O₃ in most samples.

---

Zusammenfassung Es werden elektronenmikroskopische Aufnahmen mit hohem Aufl?sungsverm?gen von kolloiden α-Eisenteilchen gezeigt. Entsprechend den Herstellungsbedingungen fallen die Teilchen als gro\e, gut ausgebildete Dendriten, als kürzere schw?chere Dendriten, als gezackte Stangen, als Nadeln und als kubische Partikeln an. Der zentrale Stamm ist eine lineare Anordnung aus einzelnen kubischen Kristallen. Repr?sentative Dimensionen sind für die verschiedenen me\baren Einheiten eingezeichnet. Eine fein laminierte Struktur der kubischen Teilchen und von einigen Seiten?sten und Hauptachsen ist zu erkennen. Dieselbe Laminarstruktur wird teilweise an dem pl?ttchenartigen Material, das als Untergrund aus der Mutterflüssigkeit dazwischen liegt, beobachtet. Stereoskopische Aufnahmen zeigen, da\ die Dendriten dreidimensional sind und da\ Seitenzweige und Hauptachsen nicht in der gleichen Ebene liegen. R?ntgeninterferenzen lassen aufα-Eisen, sowie eine Form von Fe₂O₃ in den meisten Proben schlie\en.

---

---

The U.S. Navy Department, Bureau of Aeronautics, Industrial Planning Division, is credited with the development and sponsoring of the process for producing these fine powdered irons under contract No a (S) 52–792 C and NO a (S) 54–5190.

---

Presented in part before the Conference and Exhibit on Magnetism and Magnetic Materials held at Pittsburgh, Pennsylvania, June 14, 15 and 16, 1955 and before the annual meeting of the Electron Microscope Society of America, held at State College, Pennsylvania, October 1955; abstract, J. App. Phys.26, 1391 (1955).     

Pore structure study by computer simulation of dense and loose packings of spherical particles

Packings of spherical particles modeling monodisperse silica gels of varying density are constructed by the Monte Carlo method. Each model contains 8000 particles in a cube with periodic boundary conditions. Models with densities (extents of space filling) η = 0.59 and η = 0.37 were studied in detail. For quantitative analysis of the structure of empty interparticle space, Voronoi-Delaunay geometrical constructions are used. By analogy with the mercury porosimetry method, the “intrusion” curves, indicating the fraction of the pore volume accessible for a probe of the given size are built. The results of a standard analysis of these curves and the real arrangement of interparticle space in these models are discussed. The approach using the numerical simulation and the geometrical method suggested for model analysis is a promising trend in structural studies of porous materials.     

Pore structural studies of monodisperse porous polymer particles

Monodisperse polystyrene latex particles with molecular weight on the order of 10⁶ were used as inert diluents for the preparation of monodisperse porous styrene-divinylbenzene copolymer particles via seeded emulsion polymerization techniques. Mercury porosimetry and nitrogen adsorption-desorption isotherms were used to assess pore structure and pore size distribution. Pore size distribution was very sensitive to the molecular weight of the polystyrene latex particles used as inert diluent. Qualitative evidence from the techniques used indicated that the monodisperse porous polymer particles were macroporous (average pore diameter > 500 Å) in nature. As the molecular weight of the linear polymer decreased, the porous structure of the polymer particles ranged in complexity across the spectrum of macro/mesopore structures. Scanning electron microscope results indicated the existence of voids between the microspheres and their agglomerates within the porous polymer particle, and nitrogen adsorption isotherms confirmed that the pores were due to interstices between these crosslinked microspheres and agglomerates.     

Electroless Ni-plating on PTFE fine particles

A Ni electroless plating process was used with polytetrafluoroethylene (PTFE) fine particles (25–500 μm). Using nonionic hydrocarbon surfactant, PTFE particles were dispersed in the plating bath. The PTFE hydrophobicity was sufficiently high that Ni was deposited partly on the PTFE surface in the initial step. The Ni-PTFE particles were formed into the Ni-PTFE plate by heat treatment at 350 °C after pressing. The Ni-PTFE plate had electrical conductivity and gas permeability, which were influenced by the pore distribution in the plate. Pores with 1 μm diameter might be especially important to impart high gas permeability to the Ni-PTFE plate.     

Preparation of composite fine particles by heterocoagulation

To prepare regular composite particles comprised of organic and inorganic compounds, based on heterocoagulation theory, the properties of the mixture of small amphoteric latices (2a=250 nm) and large spherical silica (2a=240–1590 nm) were investigated as a function of pH, particle number ratio, particle size ratio and electrolyte concentration in the medium. It is apparent that under suitable conditions, we may prepare a stable mixed suspension comprising uniform composite particles, which are made up of many latices regularly adsorbed on silica surfaces, and each composite particle is undergoing Brownian motion as an isolated unit. This new composite particle is very stable for electrolyte, base and acid medium, and its surface charges (sign and magnitude) can be controlled by changing the pH of the medium.     

Pore structure of pyrolyzed scrap tires

Internal structure of carbon black produced by pyrolysis (CBp) of rubber samples from the top and bottom parts of sidewall and tread of a passenger car tire was investigated in nitrogen flow at different temperatures. The pore structure (specific surface area, pore size distribution, and porosity) of CBp and commercial CB, was compared. The development of pore structure and the increase of the specific surface area were most intensive during the thermal decomposition at temperatures ranging from 300°C to 500°C. This is caused by the intensive release of volatiles during the pyrolysis. After the pyrolysis was finished, at temperatures above 500°C, further decomposition of solid matter was associated with a slight increase of the specific surface area. Presented at the 34th International Conference of the Slovak Society of Chemical Engineering, Tatranské Matliare, 21–25 May 2007.     

Pore structure of “sivol”

Small-angle x-ray scattering has been used in an investigation of the pore structure of sivol, a material prepared by thermochemical treatment of chrysotile asbestos. It has been shown that sivol has a well-developed pore structure. Pore size distribution curves have been obtained, showing a maximum with a radius of gyration R=2.5–3.0 nm. The data from small-angle scattering are in good agreement with results obtained in previous calculations based on adsorption measurements (for R 2.5 nm). It has been shown that some of the finest pores are not accessible for the molecules being adsorbed.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 978–981, May, 1990.     

Adsorption of large macromolecules on fine colloidal particles

A simple model of adsorption of large macromolecules on ultra-fine colloidal particles is presented. The basic assumption of the model is that the number of particles attached to a single molecule is a random quantity. Both the reversible and irreversible polymerparticle binding is considered. Also, effects of the non-ideal mixing of polymer solution with suspension and of the polymer/particle size ratio on the shape of the adsorption isotherm are examined. The predictions of the model are confronted with experimental results of the study on the adsorption of very high molecular weight polyacrylamide on fine AgI colloidal particles.     

Helical concept of the fine structure of cellulose

The helical concept of the fine structure of cellulose as proposed by Manley is discussed. The deuterium exchange experiments with cotton, cotton crystallites, and regenerated cellulose I, in which accessibility was determined by comparing the ratio of the infrared absorbance of the O? D peak to the O? H peak, revealed that the accessibility of cotton linters decreased on acid hydrolysis, whereas it increased on treatment with ethylamine followed by washing with water. This is in contrast to the finding of Manley, who had evaluated the accessibility by a gravimetric D₂O exchange method and had come to the conclusion that acid hydrolysis did not change the accessibility of cellulose and hence cellulose did not contain crystalline and amorphous phases but was all crystalline. On the basis of Manley's protofibril and the accessibility data obtained in this investigation, a concept of the fine structure of cellulose is proposed, in which the role of Manley's protofibril is analogous to the role of individual molecule in the fringe micellar model. This concept explains the properties of cellulose that are otherwise explainable on the currently accepted fringe micellar theory. In addition, it explains the marked shrinkage in the length of cotton and rayon fibers when placed in 16% sodium hydroxide solution.     

SCR烟气脱硝对PM2.5排放特性的影响机制研究

采用V₂O₅-WO₃/TiO₂催化剂,对选择性催化还原(SCR)烟气脱硝装置出口PM_2.5物性进行分析,考察SO₂氧化与PM_2.5形成的关系,并采用原位漫反射红外光谱(DRIFTS)对SCR脱硝过程中NH₄HSO₄的生成及SCR脱硝温度条件下的NH₄HSO₄热稳定性进行了分析研究。结果表明,经SCR脱硝后,亚微米级细颗粒数浓度明显升高,且形貌特征及元素组成发生变化,形成的细颗粒主要为NH₄HSO₄及少量(NH₄)₂SO₄;SCR烟气脱硝对PM_2.5排放特性的影响主要通过以下途径:一是SO₃与SCR烟气脱硝系统中的NH₃、H₂O反应形成;二是SO₃与逃逸的NH₃、H₂O在SCR脱硝装置后续系统发生反应形成硫酸氢铵与硫酸铵;此外还与SO₃和烟气中游离的CaO等碱土金属氧化物反应形成硫酸盐,随烟气携带出SCR脱硝装置有关。     

Hydrophobic agglomeration kinetics of fine kaolinite particles in aqueous suspensions

The hydrophobic agglomeration kinetics of kaolinite has been studied through the in-situ turbidity meter measurement system. The effects of surfactant dosage, stirring rate and particle size on the hydrophobic agglomeration dynamics have been investigated. Appropriate surfactant concentrations provided the strongest hydrophobicity, modest stirring rate offered a higher agglomerates formation rate and a lower disruption rate, and smaller particles had lower energy barrier and higher attachment efficiency. The best hydrophobic agglomeration conditions have been determined and a kinetic model of hydrophobic agglomeration has been proposed by experimental results. The kinetic model has been turned out to be fitted to the dynamic process well and can characterize as well as assess the hydrophobic agglomeration kinetics appropriately.     

Model of aggregation of colloidal fine particles in the presence of supersized polymer

A simple model of the process of stabilization and destabilization of fine colloidal suspensions induced by supersized linear polymers has been tested by the direct simulation method. In the model, a single polymer molecule may bind a number of colloidal particles and thus form an aggregate. It is assumed that a simultaneous attachment of a few fine particles to one macromolecule does not necessarily destabilize the suspension. The destabilization of the system (occurring if aggregate sedimentation dominates its diffusion ability) takes place only when the number of the attached particles per macromolecule exceeds the critical value which depends on the polymer coil dimension in the dispersion medium. The model permits interpretation of several experimental observations of the behavior of colloidal sols upon introduction of very high molecularweight polymers. The simulation results have been compared with the experimental data on the effect of polyacrylamide on the stability of AgI sol.     

Formation of iron fine particles in a crystal lattice by the computer simulation

The growing up of the fine particles in a sapphire crystal was simulated with a computer and the expected Mössbauer spectra were calculated by considering the influence of the nearest neighbors and next-nearest neighbors to the magnetic hyperfine field of the iron atoms. The simulated spectra were compared with the Mössbauer spectra observed with a Fe-implanted sapphire and the agreement between them was satisfactory on the whole. It is also revealed that an iron atom implanted into a sapphire crystal may interact, before coming to rest, with the iron fine particles situated within 2–3 nm in the crystal.     

On the fracture of composites based on ultrahigh-molecular-weight polyethylene and fine aluminum particles

Mechanical characteristics of polymerization filled composite materials based on ultrahigh-molecular-weight polyethylene and fine aluminum particles are studied. The prepared composites preserve their ability for high plastic deformations even when the volume filler content is φ = 0.57. For the tensile drawing of the composite material with randomly distributed particles, an equation describing the dependence of breaking stress on the volume filler content is derived. For the model of the composite with regularly ordered particles, the Nielsen equation is the approximation of the equation proposed in this work for a material with randomly distributed particles.     

Two-body correlations among particles confined to a spherical surface: packing effects

The two-point correlation functions among particles confined to move within a spherical two-dimensional space are studied here using Monte Carlo simulations in the canonical ensemble and the corresponding liquid theory concepts. This work takes a simple model system with soft-sphere interactions among the particles lying on the spherical surface. We focus this study on the ordering induced by the particle packing and the restrictions imposed by the system topology. The corresponding grand canonical results are obtained from the canonical Monte Carlo data using the standard statistical mechanics formulas. These grand canonical ensemble results show that as the strength of the interactions increases, the system transits between liquidlike states and crystal-like states as the average number of particles on the spherical surface matches certain specific values. The crystal-like states correspond to sharp minima in the plot of the standard deviation in the number of particles on the spherical surface versus the average value of this number. We also test the validity of the integral equation approaches for this kind of closed but boundless systems: It is found that the Percus-Yevick approximation overestimates the correlations for this system in a liquid state, whereas the hypernetted-chain approximation underestimates these correlations.