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The Solid Phase

The aggregates of sedimentary particles are usually arranged before deposition. Within these [Pg.157]

Sediment type % CaCO % clastic and clayey material o/ JO amorphous silica v /o pelagic sed. Composition [Pg.157]

Detrital or epiclastic 30 50 Denudation products of continental rocks [Pg.157]

Biogenic A. Calcareous B. Siliceous 30 30 48 -14 Foraminifera, coccoliths, calcareous algae, molluscs, bryozoa, and corals Diatoms and radiolaria [Pg.157]

Chemogenic Iron-manganese nodules, glauconite, phosphorite, nodules, phillipsite, palagonite, celestobarite, and evaporites [Pg.157]


The performance of fluidized-bed reactors is not approximated by either the well-stirred or plug-flow idealized models. The solid phase tends to be well-mixed, but the bubbles lead to the gas phase having a poorer performance than well mixed. Overall, the performance of a fluidized-bed reactor often lies somewhere between the well-stirred and plug-flow models. [Pg.58]

The solid phase can be considered as a pure substance or a solid solution. [Pg.171]

When pure component i constitutes the solid phase, the liquid-solid equiiibrium obeys the following equation ... [Pg.172]

This study detects the defect of the void and the exfoliation in the solid phase diffusion bonding interface of ductile cast iron and stainless steel with a nickel insert metal using ultrrasonic testing method, and examine the influence of mutual interference of the reflectional wave both the defect and the interface. [Pg.833]

This study was in real time measured that the reflective echo height of the bonding interface in the solid phase diffused bonding process of carbon steel and titanium using ultrasonic testing method. As a result, the following were made discernment. [Pg.848]

On the other hand, the reliability of the product improves, too, if each state of the plasticity deformation, the creep deformation, and the diffusion joint in the solid phase diffusion bonding as the bonding process, is accurately understood, and the bonding process is controlled properly. [Pg.849]

Density functional theory from statistical mechanics is a means to describe the thermodynamics of the solid phase with information about the fluid [17-19]. In density functional theory, one makes an ansatz about the structure of the solid, usually describing the particle positions by Gaussian distributions around their lattice sites. The free... [Pg.334]

Two nucleation processes important to many people (including some surface scientists ) occur in the formation of gallstones in human bile and kidney stones in urine. Cholesterol crystallization in bile causes the formation of gallstones. Cryotransmission microscopy (Chapter VIII) studies of human bile reveal vesicles, micelles, and potential early crystallites indicating that the cholesterol crystallization in bile is not cooperative and the true nucleation time may be much shorter than that found by standard clinical analysis by light microscopy [75]. Kidney stones often form from crystals of calcium oxalates in urine. Inhibitors can prevent nucleation and influence the solid phase and intercrystallite interactions [76, 77]. Citrate, for example, is an important physiological inhibitor to the formation of calcium renal stones. Electrokinetic studies (see Section V-6) have shown the effect of various inhibitors on the surface potential and colloidal stability of micrometer-sized dispersions of calcium oxalate crystals formed in synthetic urine [78, 79]. [Pg.338]

Traditionally one categorizes matter by phases such as gases, liquids and solids. Chemistry is usually concerned with matter m the gas and liquid phases, whereas physics is concerned with the solid phase. However, this distinction is not well defined often chemists are concerned with the solid state and reactions between solid-state phases, and physicists often study atoms and molecular systems in the gas phase. The tenn condensed phases usually encompasses both the liquid state and the solid state, but not the gas state. In this section, the emphasis will be placed on the solid state with a brief discussion of liquids. [Pg.86]

We discuss classical non-ideal liquids before treating solids. The strongly interacting fluid systems of interest are hard spheres characterized by their harsh repulsions, atoms and molecules with dispersion interactions responsible for the liquid-vapour transitions of the rare gases, ionic systems including strong and weak electrolytes, simple and not quite so simple polar fluids like water. The solid phase systems discussed are ferroniagnets and alloys. [Pg.437]

Eleetron energy-loss speetroseopy is used for obtaining speetroseopie data as a eonvenient substitute for optieal speetroseopy, and, taking advantage of diflferenees in seleetion rules, as an adjimet to optieal speetroseopy. In addition, eleetron speetroseopy has many applieations to ehemieal and stnietural analysis of samples in the gas phase, in the solid phase, and at the solid-gas interfaee. [Pg.1322]

Hoover W G and Ree F H 1967 Use of computer experiments to locate the melting transition and calculate the entropy in the solid phase J. Chem. Phys. 47 4873-8... [Pg.2284]

System in which the solid phases consist of the pure components and the components are completely miscible in the liquid phase. We may now conveniently consider the general case of a system in which the two components A and B are completely miscible in the liquid state and the solid phases consist of the pure components. The equilibrium diagram is shown in Fig. 1,12, 1. Here the points A and B are the melting points of the pure components A and B respectively. If the freezing points of a series of liquid mixtures, varying in composition from pure A to pure B, are determined, the two curves represented by AC and BC will be obtained. The curve AC expresses the compositions of solutions which are in equilibrium, at different temperatures, with the solid component A, and, likewise, the curve BC denotes the compositions... [Pg.24]

The separation of the solid phase does not occur readily with some liquid mixtures and supercooling is observed. Instead of an arrest in the cooling curve at /, the cooling continues along a continuation of c/ and then rises suddenly to meet the line f g which it subsequently follows (Fig. 1,13, 1, iii). The correct freezing point may be obtained by extrapolation of the two parts of the curve (as shown by the dotted line). To avoid supercooling, a few small crystals of the substance which should separate may be added (the process is called seeding ) these act as nuclei for crystallisation. [Pg.27]

We shall now exemplify the solid-phase peptide synthesis approach by c )c/o-[-L-Val-[)-Pro-D-Val-L-Pro-]], which was prepared by Merrifield himself, the inventor of the method (B.F. Gisin, 1972). [Pg.235]

The example clearly demonstrates the main advantages of solution chemistry over the solid-phase approach ... [Pg.238]

The protected nucleoside-3-phosphoramidite monomer units such as 671 are used in the solid-phase oligonucleotide synthesis. In the 60mer synthesis, 104 allylic protective groups are removed in almost 100% overall yield by the single Pd-catalyze reaction with formic acid and BuNH2[432], N,(9-protection of uridine derivatives was carried out under pha.se-transfer conditions[433]. [Pg.382]

Quantitative studies of solid-state organic reactions were performed by Glazman (267. 268). Equal amounts of acetic anhydride and 2-aminothiazole (grain diameter 0.15 mm) were mixed for 20 rain, and the mixture was heated in a glycerol bath at 0.5°C per minute. Heating curves showed that the reaction starts in the solid phase the use of an eutectic composition of organic reactants increases the yields. [Pg.52]

Mernfield was awarded the 1984 Nobel Prize in chem istry for developing the solid phase method of pep tide synthesis... [Pg.1141]

Solid phase peptide synthesis does not solve all purification problems however Even if every coupling step m the ribonuclease synthesis proceeded in 99% yield the product would be contaminated with many different peptides containing 123 ammo acids 122 ammo acids and so on Thus Memfield and Gutte s six weeks of synthesis was fol lowed by four months spent m purifying the final product The technique has since been refined to the point that yields at the 99% level and greater are achieved with current instrumentation and thousands of peptides and peptide analogs have been prepared by the solid phase method... [Pg.1142]

FIGURE 27 15 Peptide synthesis by the solid phase method Ammo acid residues are attached sequentially beginning at the C terminus... [Pg.1143]


See other pages where The Solid Phase is mentioned: [Pg.151]    [Pg.171]    [Pg.833]    [Pg.834]    [Pg.848]    [Pg.849]    [Pg.335]    [Pg.547]    [Pg.86]    [Pg.133]    [Pg.1955]    [Pg.2687]    [Pg.26]    [Pg.29]    [Pg.33]    [Pg.33]    [Pg.35]    [Pg.36]    [Pg.129]    [Pg.216]    [Pg.82]    [Pg.1141]    [Pg.1279]    [Pg.1009]   


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Analysis of the Sediments Solid Phase

Analysis of the Solid Phase

Automated Peptide Synthesis The Merrifield Solid-Phase ethod

Axial dispersion in the gas, liquid, and solid phases

Baylis-Hillman Reaction on the Solid Phase

Bridge methods in non-competitive enzyme immunoassays with antigens immobilized on the solid phase

Characterization of the solid phase

Conduction in the solid phase

Dispersion of the solids phase

Fugacity in the Solid Phase

Glass as the solid phase for enzyme immunoassays

Glycopeptide Synthesis in Solution and on the Solid Phase

Glycopeptide Synthesis on the Solid Phase

Glycopeptides synthesis on the solid phase

High-Pressure Domino Cycloaddition Reactions on the Solid Phase

Homogeneous quasi-chemical reactions in the solid phase

Mass Conservation in the Solid Phase

Non-chemical Factors Affecting the Completion of Solid-phase Reactions

Non-competitive assays with antibodies immobilized on the solid phase

Non-competitive assays with complement immobilized on the solid phase

Oxidation in the Solid Phase

Phase Diagrams and the Coexistence of Solids

Phase Transitions and the Chemistry of Solids

Phase Transitions in the Solid Elements

Phase Transitions in the Solid Elements at Atmospheric Pressure

Polyamidation in the solid phase

Polymorphism phase changes in the solid state

Practical Considerations in the Design of Solid Phase FI Optosensing Systems

Properties of the solid phase

Reactions in the Solid Phase

Redox as Eh in the Presence of Solid Phases

Relative Stability of the Solid Phases in Solution

Separation principles for the various solid phases

Solid-Phase Peptide Synthesis The Merrifield Method

Solid-Phase Synthesis of the Blood Group H Determinant

The Idea of Solid-Phase Synthesis

The Principle of Solid Phase Extraction

The Solid-phase Extrusion of Rarely Crosslinked Epoxy Polymers

The Statistical Point of View on Solid Phase Reactions

The initial solid reacts with another phase

The literature of solid phase reactions

The solid Phase References

The use of solid supports and supported reagents in liquid phase organic reactions

Titration with urease on the solid phase

Trapping Phosphorus Ylides with a Ketone Bound to the Solid Phase

Ultrasound-assisted dissolution of the solid phase in heterogeneous samples

Use of Ionic Liquids in the Solid Phase

Water in the solid phase ices

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