Modular Design of Domain Assembly in Porous Coordination Polymer Crystals via Reactivity-Directed Crystallization Process

The mesoscale design of domain assembly is crucial for controlling the bulk properties of solids. Herein, we propose a modular design of domain assembly in porous coordination polymer crystals via exquisite control of the kinetics of the crystal formation process. Employing precursors of comparable chemical reactivity affords the preparation of homogeneous solid-solution type crystals. Employing precursors of distinct chemical reactivity affords the preparation of heterogeneous phase separated crystals. We have utilized this reactivity-directed crystallization process for the facile synthesis of mesoscale architecture which are either solid-solution or phase-separated type crystals. This approach can be also adapted to ternary phase-separated type crystals from one-pot reaction. Phase-separated type frameworks possess unique gas adsorption properties that are not observed in single-phasic compounds. The results shed light on the importance of crystal formation kinetics for control of mesoscale domains in order to create porous solids with unique cooperative functionality.     

Quantitative analysis of microstructures by secondary ion mass spectrometry.

The focus of this review is on trace-element quantitation of microstructures in solids. This review is aimed at the nonspecialist who wants to know how secondary ion mass spectrometry (SIMS) quantitation is achieved. Despite 35 years of SIMS research and applications, SIMS quantitation remains a fundamentally empirical enterprise and is based on standards. The most used standards are "bulk standards"-solids with a homogeneous distribution of a trace element-and ion-implanted solids. The SIMS systematics of bulk standards and ion-implanted solids are reviewed.     

Improved hybrid functional for solids: the HSEsol functional

We introduce the hybrid functional HSEsol. It is based on PBEsol, a revised Perdew-Burke-Ernzerhof functional, designed to yield accurate equilibrium properties for solids and their surfaces. We present lattice constants, bulk moduli, atomization energies, heats of formation, and band gaps for extended systems, as well as atomization energies for the molecular G2-1 test set. Compared to HSE, significant improvements are found for lattice constants and atomization energies of solids, but atomization energies of molecules are slightly worse than for HSE. Additionally, we present zero-point anharmonic expansion corrections to the lattice constants and bulk moduli, evaluated from ab initio phonon calculations.     

Mesoscopic systems

Mesoscopic condensed matter is in the size regime between large clusters and bulk solids. If the linear dimension is considered in relation to various characteristic lengths new phenomena will show up which are absent in the bulk. This is discussed for metal grains in the 10 nm regime and for disordered metallic samples in the 1 µm regime.     

Design of experimental routes and data processing for the determination of the depth-distribution of energy in real solids

No adequate thermodynamic definition of non-equilibrated solids is available at present. In this paper a method is suggested for the energetic characterization of solids by estimation of the distribution of the differential molar internal energies — as they appear during the breakdown of sample e.g. by chemical reaction, i.e. the ‘depth distribution of differential energies’ (DDE) of samples. Thermodynamic considerations are presented for approximating this quantity — and experimental possibilities proposed to attain the needed input information by thermoanalytical methods. Application of the suggested procedure is supposed to contribute to the better understanding of structure — energy — reactivity relations in real solids.     

Exploring the electronic structure of elemental lithium: from small molecules to nanoclusters, bulk metal, and surfaces

Clusters of lithium atoms ranging in size from Li4 to Li40 and bulk metallic solids, including surfaces, are investigated through first principles electronic structure calculations, which are based upon density functional theory and the electron localization function (ELF). It is found that large lithium ppi-type contributions in the electronic wavefunction cause the electrons to localize in interstitial regions, which leads to multicenter bonding for both the clusters and the solids, including their surfaces. For the smaller clusters these stabilizing ppi interactions also lead to short Li-Li interatomic distances, which in conjunction with the longer bonds induces "distance alternation" in the range from 2.45 A to 3.15 A. This consequence of the additional ppi interactions is absent in simple solids due to symmetry. The electronic structure of the clusters is topologically insensitive to deformations that do not affect their general shape, but changes significantly upon isomerization. The ramifications upon dynamic properties is that the clusters are quasi-rigid at low temperatures and retain their shape though the distance alternation pattern is suppressed. The picture which emerges for bonding in the bulk solid is that the metallic state arises from the presence of a large number of partially occupied multicenter bonds. For nanoscale clusters only the surface of these clusters exhibits strong localization, whereas their interiors display localization properties similar to the bulk metallic solid. On the other hand, localized states similar to those of the clusters ("dangling bonds") are found on the (001) surface of body-centered cubic (bcc) and face-centered cubic (fcc) lithium solids.     

THE THEORY OF EXCITON DISTRIBUTION IN ORGANIC SOLIDS

Abstract. The present paper gives an account of the phenomenological theory underlying the three dimensional distribution of excitons in solids. General expressions for the steady state distribution are derived taking into account the bulk and surface and annihilation generation of excitons, the influence of sample geometry and fluorescent reabsorption effects. The wave form of the optical excitation has also been included for purposes of generality. Approximations to the general results are provided for certain special cases which may apply to organic solids.     

Oilfield solids and water-in-oil emulsion stability

Model water-in-hydrocarbon emulsions consisting of toluene, heptane, water, asphaltenes, and native solids were used to investigate the role of native solids in the stability of oilfield emulsions. The solids were recovered from an oil-sands bitumen, a wellhead emulsion, and a refinery slop oil. The solids were clay platelets and fell into two size categories: (1) fine solids 50 to 500 nm in diameter and (2) coarse solids 1 to 10 microm in diameter. Emulsions stabilized by fine solids and asphaltenes were most stable at a 2:1 fractional area ratio of asphaltenes to solids. It appears that when the asphaltene surface coverage is high, insufficient solids remain to make an effective barrier. When the solids coverage is high, insufficient asphaltenes remain on the interface to immobilize the solids. Treatments that weaken the interface, such as toluene dilution, are recommended for emulsions stabilized by fine solids. Emulsions stabilized by coarse solids were unstable at low solids concentrations but became very stable at solids concentrations greater than 10 kg/m(3). At low concentrations, these solids may act as bridges between water droplets and promote coalescence. At high concentrations, layers of coarse solids may become trapped between water droplets and prevent coalescence. Treatments that flocculate the solids, such as heptane dilution, are recommended for emulsions stabilized by high concentrations of coarse solids. It is possible that emulsions containing both types of solids may require more than one treatment, or even process step, for effective water resolution.     

Reversible and Irreversible Chemisorption in Nonporous‐Crystalline Hybrids

The tools of synthetic chemistry allow us to fine‐tune the reactivity of molecules at a level of precision not yet accessible with inorganic solids. We have investigated hybrids that couple molecules to the superior thermal and mechanical properties of solids. Herein we present, to the best of our knowledge, the first demonstration of reactivity between hybrid perovskites and substrates. Reaction with iodine vapor results in a remarkable expansion of these materials (up to 36 % in volume) where new covalent C? I bonds are formed with retention of crystallinity. These hybrids also show unusual examples of reversible chemisorption. Here, solid‐state interactions extend the lifetime of molecules that cannot be isolated in solution. We have tuned the half‐lives of the iodinated structures from 3 h to 3 days. These nonporous hybrids drive substrate capture and controlled release through chemical reactivity. We illustrate the strengths of the hybrid by considering radioactive iodine capture.     

Preparative solid state chemistry. Recent developments

A survey of recent developments in preparative solid state chemistry shows that, with a knowledge of structural chemistry and reactivity patterns of solids, it is possible to synthesize a variety of new solids possessing novel structures. A distinction is made between synthesis ofnew solids and synthesis of solids bynew methods. Three new routes to solid state synthesis are recognized: the precursor method, and topochemical methods involving redox and ion-exchange reactions. The low-temperature topochemical methods enable synthesis of metastable phases that are inaccessible by the high temperature route. Several illustrative examples of solid state synthesis from the recent literature are presented.     

Experimental and theoretical electronic charge densities in molecular crystals

Electronic charge density distribution in molecular systems has been described in terms of the topological properties. After briefly reviewing methods of obtaining charge densities from X-ray diffraction and theory, typical case studies are discussed. These studies include rings and cage systems, hydrogen bonded solids, polymorphic solids and molecular NLO materials. It is shown how combined experimental and theoretical investigations of charge densities in molecular crystals can provide useful insights into electronic structure and reactivity.     

Terminal and Penultimate Reactivity Ratios in the Styrene-Acrylonitrile Free-Radical Copolymerization System in Bulk

ABSTRACT

The terminal and penultimate model reactivity ratios for the styrene-acrylonitrile monomer system in bulk have been investigated by the simplex and scanning method. It has been shown that Mayo-Lewis equation has an unique solution when determining the reactivity ratios according to the terminal model while for the penultimate model the non-uniqueness in determination of the reactivity ratios has been found. The numerical values of the penultimate r-parameters calculated with the simplex method depend on the initial guess for r-parameters.

Several sets of penultimate reactivity ratios for the styrene-acrylonitrile system in bulk have been found to be equal from mathematical point of view. The reactivity ratios with comparable standard deviation have an equivalent graphical representation on the copolymerization diagragm. It has been also confirmed that the penultimate model is a more appropriate of the models considered to describe the variation of the copolymer composition with the monomer feed. Taking into account previous results for the styrene-methyl methacrylate system in bulk it is thereby assumed that the occurrence non-uniqueness in determination of the penultimate model reactivity ratios does not depend on the monomer system.     

Some applications of silica aerogels

Silica aerogels are very highly divided materials which are synthesised through the association of a chemical step, the so-called sol–gel chemistry, with a physical step which is a particular way of drying the wet gel, namely under supercritical conditions with respect to the liquid phase filling its porosity. This drying process preserves the texture of the dry material: in practice it strongly reduces the pore collapse. The resulting hyperporous solids that have bulk densities of the same magnitude as air develop new and very interesting physical and even chemical properties. Owing to their poor chemical reactivity, very large surface areas (of the order of 1,000 m ²/g), unusual porous volumes (greater than 95%), morphologies (monoliths or powders), optical properties (transparent, opaque or translucent), and very low thermal conductivity, they find high added-value applications in the physics of high-energy particles (Cherenkov emitters), transparent and superinsulating double windows, life and space science as well.     

Reintroduced solids increase inhibitor levels in a pretreated corn stover hydrolysate

Following detoxification of the liquid hydrolysate produced in a corn stover pretreatment process, inhibitor levels are seen to increase with the re-addition of solids for the ensuing hydrolysis and fermentation processes. The solids that were separated from the slurry before detoxification of the liquor contain approx 60% (w/w) moisture, and contamination occurs owing to the diffusion of inhibitors from the moisture entrained in the porous structure of the corn stover solids into the bulk fluid. This evidence suggests the need for additional separation and detoxification steps to purge residual inhibitors entrained in the moisture in the solids. An overliming process to remove furans from the hydrolysate failed to reduce total organic acids concentration, so acids were removed by treatment with an activated carbon powder. Smaller carbon doses proved more efficient in removing organic acids in terms of grams of acid removed per gram of carbon powder. Sugar adsorption by the activated carbon powder was minimal.     

冲击波化学

本文综述了冲击波化学研究的最新进展,包括多种气态和凝聚态的无机和有机物质在冲击波作用下发生的物理和化学变化,认为冲击波在固体物质中产生多种缺陷使其化学活性明显提高可能是冲击波化学最重要的特点。     

Modified Ceria-Zirconia Fluorite-Like Catalysts for the Combustion of Methane

For dispersed ceria-zirconia-based solid solutions prepared via the polymerized complex method and annealed at 700℃, effects of bulk doping by Ca, Mn, Co, Bi or Nb cations and surface modification by Mn and Pt on their structural features, surface/bulk oxygen reactivity and catalytic activity in methane combustion are considered. With up to 20 mol% doping, a structural type of homogeneous solid solutions of anion-deficient fluorite with disordered anion vacancies is formed. Doping by transition metal cations or Pt increases the mobility and reactivity of the surface/bulk oxygen. A broad variation in specific rates of methane combustion for the studied systems was observed, suggesting structural sensitivity of this reaction. In general, there is no universal relationship between the oxygen mobility, the reactivity and the catalytic activity in methane combustion, which is explained by the factor of specific methane activation on surface active sites. For the Pt-promoted samples, Pt efficiency in methane activation depends on the Pt-support interaction, and the most favorable ones being mixed Pt/MnOx and Pt/NbOx clusters on the surface of the supports that exhibit high lattice oxygen mobilities.     

Studies on monomer reactivity ratios. I. An electronegativity model

A model based on an electronegativity scheme is proposed for treatment of monomer reactivity ratios in free-radical bulk copolymerization. Values for each monomer are assigned to three parameters: a relative localization (or resonance stabilization) energy, a radical electronegativity, and a monomer electronegativity. Parameters for 17 monomers are given and calculated reactivity ratios are tabulated for a large number of copolymerizations. Agreement with experiment is usually obtained to within experimental error except for systems involving acrylonitrile. Computed parameters are rationalized on the basis of molecular orbital theory.     

Photothermal applications to the thermal analysis of solids

Major application of optically-induced thermal waves to the thermal and thermodynamic analysis of solids are reviewed. The spectrum of available techniques,from the conventional photoacoustic detection to novel photothermal laser probing and frequency multiplexing is discussed, and their utilization for the measurement of thermophysical thermal transport-related parameters of solids is presented. These include the thermal diffusivity, effusivity, conductivity and specific heat. The ability of photothermal methods to perform thermal analysis on large classes of solids, including conducting and insulating bulk materials, crystals, layered porous and coated structures, thin films and inhomogeneous thermal profiles is highlighted. Finally, special capabilities of photothermal analysis, such as the monitoring of surface thermodynamic phenomena and phase transition studies, including high-T _c superconductors, are described in order to give a complete overview of the rich potential of photothermal-based methodologies.     

Modifying the liquid/liquid interface: pores, particles and deposition

The modification of the liquid/liquid interface with solid phases is discussed in this article. Modified interfaces can be formed with molecular assemblies, but here attention is focussed on solid materials such as mesoscopic particles, or microporous and mesoporous membranes. Charge transfer across the modified liquid/liquid interface is considered in particular. The most obvious consequence of the introduction of such modifying components is their effect on the transport to, and the transfer of material across, the liquid/liquid interface, as measured voltammetrically for example. One particularly interesting reaction is interfacial metal deposition, which can also be studied under electrochemical control: the initial formation of metal nuclei at the interface transforms it from the bare, pristine state to a modified state with very different reactivity. Deposition at interfaces between liquids is compared and contrasted with the cases of metal deposition in bulk solution and conventional heterogeneous deposition on conducting solid surfaces. Comparison is also made with work on the assembly of pre-formed micron and nanometre scale solids at the liquid/liquid interface.     

Studies on monomer reactivity ratios. II. A charge-transfer model

A charge-transfer model is proposed for the treatment of monomer reactivity ratios in free-radical bulk polymerization. The procedure involves the assignment of three parameters to each monomer, which can be interpreted as being related to the energies of the highest occupied monomer orbital, the singly occupied radical orbital, and the lowest lying virtual orbital of the monomer. Parameters are found for 17 monomers and computed reactivity ratios for a large number of copolymer systems are tabulated and compared with experiment. Similarities of the present model and the electronegativity scheme are discussed.