Quartz stability

Kerrick D. M. (1972). Experimental determination of muscovite + quartz stability with P(H20) < P (total). Amer. Jour. Set, 272 946-958. 

Khitarov, N.I., 1953. Experimental characteristics of quartz stability and silica migration under hydro-thermal conditions. Trudy IV Soveshchaniya po eksperimentalnoy mineralogii i petrografii (Acta of the Fourth Conference on Experimental Mineralogy and Petrography). Izd. Akad. Nauk S.S.S.R., Moscow, 2 180-186 (in Russian). 

Of the three components, the second is the most important because it depends on the channel number. One can reduce the size of the conversion time by using a clock with higher frequency. Today s ADCs use quartz-stabilized clocks with a... 

Silica O crystallizes from lithium silicate glasses during devitrification at low temperature. It has a crystal lattice similar to quartz and may simply be high quartz" stabilized below 573 C, the normal transition temperature, to low quartz (53, 70) by inclusions of metal ion impurities. The only way pure material can be obtained is by neutron bombardment of quartz. 

The importance of the thin film between the mineral particle and the air bubble has been discussed in a review by Pugh and Manev [74]. In this paper, modem studies of thin films via SFA and interferometry are discussed. These film effects come into play in the stability of foams and froths. Johansson and Pugh have studied the stability of a froth with particles. Small (30-/ m), moderately hydrophobic 6c = 65°) quartz particles stabilized a froth, while more hydrophobic particles destabilized it and larger particles had less influence [75]. 

The numerical values of and a, for a particular sample, which will depend on the kind of linear dimension chosen, cannot be calculated a priori except in the very simplest of cases. In practice one nearly always has to be satisfied with an approximate estimate of their values. For this purpose X is best taken as the mean projected diameter d, i.e. the diameter of a circle having the same area as the projected image of the particle, when viewed in a direction normal to the plane of greatest stability is determined microscopically, and it includes no contributions from the thickness of the particle, i.e. from the dimension normal to the plane of greatest stability. For perfect cubes and spheres, the value of the ratio x,/a ( = K, say) is of course equal to 6. For sand. Fair and Hatch found, with rounded particles 6T, with worn particles 6-4, and with sharp particles 7-7. For crushed quartz, Cartwright reports values of K ranging from 14 to 18, but since the specific surface was determined by nitrogen adsorption (p. 61) some internal surface was probably included. f... 

In the absence of a suitable soHd phase for deposition and in supersaturated solutions of pH values from 7 to 10, monosilicic acid polymerizes to form discrete particles. Electrostatic repulsion of the particles prevents aggregation if the concentration of electrolyte is below ca 0.2 N. The particle size that can be attained is dependent on the temperature. Particle size increases significantly with increasing temperature. For example, particles of 4—8 nm in diameter are obtained at 50—100°C, whereas particles of up to 150 nm in diameter are formed at 350°C in an autoclave. However, the size of the particles obtained in an autoclave is limited by the conversion of amorphous siUca to quartz at high temperatures. Particle size influences the stabiUty of the sol because particles <7 nm in diameter tend to grow spontaneously in storage, which may affect the sol properties. However, sols can be stabilized by the addition of sufficient alkaU (1,33). 

Resins are also used for permanent tooth-colored veneers on fixed prostheses, ie, crown and bridges. Compositions for this application include acryflcs, vinyl—acryflcs, and dimethacrylates, as well as silica- or quartz-microfilled composites. The resins are placed on the metallic substrates of the prostheses and cured by heat or light. These resins are inexpensive, easy to fabricate, and can be matched to the color of tooth stmcture. Acrylic facings do not chemically adhere to the metals and are retained only by curing the resin into mechanical undercuts designed into the metal substrate. They have relatively low mechanical strength and color stability, and poor abrasion and strain resistance they also deform more under the stress of mastication than porcelain veneers or facings. 

It should be noted that, whereas ferroelectrics are necessarily piezoelectrics, the converse need not apply. The necessary condition for a crystal to be piezoelectric is that it must lack a centre of inversion symmetry. Of the 32 point groups, 20 qualify for piezoelectricity on this criterion, but for ferroelectric behaviour a further criterion is required (the possession of a single non-equivalent direction) and only 10 space groups meet this additional requirement. An example of a crystal that is piezoelectric but not ferroelectric is quartz, and ind this is a particularly important example since the use of quartz for oscillator stabilization has permitted the development of extremely accurate clocks (I in 10 ) and has also made possible the whole of modern radio and television broadcasting including mobile radio communications with aircraft and ground vehicles. 

The inductively coupled plasma source (Fig. 20.11) comprises three concentric silica quartz tubes, each of which is open at the top. The argon stream that carries the sample, in the form of an aerosol, passes through the central tube. The excitation is provided by two or three turns of a metal induction tube through which flows a radio-frequency current (frequency 27 MHz). The second gas flow of argon of rate between 10 and 15 L min-1 maintains the plasma. It is this gas stream that is excited by the radio-frequency power. The plasma gas flows in a helical pattern which provides stability and helps to isolate thermally the outside quartz tube. 

Spin orbitals, 258, 277, 279 Square well potential, in calculation of thermodynamic quantities of clathrates, 33 Stability of clathrates, 18 Stark effect, 378 Stark patterns, 377 Statistical mechanics base, clathrates, 5 Statistical model of solutions, 134 Statistical theory for clathrates, 10 Steam + quartz system, 99 Stereoregular polymers, 165 Stereospecificity, 166, 169 Steric hindrance, 376, 391 Steric repulsion, 75, 389, 390 Styrene methyl methacrylate polymer, 150... 

Ceramic materials are typically noncrystalline inorganic oxides prepared by heat-treatment of a powder and have a network structure. They include many silicate minerals, such as quartz (silicon dioxide, which has the empirical formula SiO,), and high-temperature superconductors (Box 5.2). Ceramic materials have great strength and stability, because covalent bonds must be broken to cause any deformation in the crystal. As a result, ceramic materials under physical stress tend to shatter rather than bend. Section 14.22 contains further information on the properties of ceramic materials. 

Heat Stability of 2,3,7,8-Tetrachlorodibenzo- -dioxin. A sample boat containing 1-3 mg of 2,3,7,8-tetrachlorodibenzo-p-dioxin was placed in a Sargent Tube Heater (Model J-807) which contained a 1/2 inch i.d. quartz tube. Air was aspirated through the tube at a velocity of 0.02 ft/sec. This velocity gave a residence time of 21 sec. (Residence time was extended by connecting a second heater in series with the first.)... 

Light Stability of Chlorinated Dibenzo-l -dioxins. A known concentration of chlorinated dibenzo-p-dioxin was placed in a quartz 1-cm path length cell. A General Electric R.S. sunlamp was placed either 0.5 or 1.0 meters from the face of the cell. The stability of the chlorinated dibenzo-p-dioxin was monitored using ultraviolet spectroscopy. 

Changes in thermal stability and mass due to the formation of CdS nanoparticles in LB films were examined [180]. The LB films were formed onto gold-coated quartz oscillators from monolayers of arachidic acid or nonacosa-10,12-diynoic acid on CdCH containing subphases. The films were exposed to H2S gas until the mass change indicated complete conversion of Cd to CdS. The thermal stability of the H2S-treated films was reduced, with significant mass loss initiating at 55°C, compared to minimal mass loss in the untreated films up to at least 80°C under mild vacuum. The average CdS-particle size... 

Besides thermolysis, the photochemical decomposition of solid trihalo-methylmercury compounds RHgCCli, CF3HgOCOCF3 and Hg(OCOCF3)2 has been studied (Scheme 2). The irradiation of samples placed in an evacuated quartz tube, which was connected to a helium cryostat, was carried out at -50 to +10°C. Thus, a desorption into the gas phase of the primary products of the photolysis occurred, and consequent low-temperature matrix stabilization of them was made. As a result, the formation of only the radicals CCI3 (1 3 898 cm" ) and CF3 (vi 1084, V2 702, P2+ V4 1205, r>3 1249 cm ) or of products of their secondary reactions was observed (Mal tsev et al., 1974, 1975, 1977b). 

The experimental procedure employed a capillary viscometer made of quartz as shown in Fig. 26. A solid sample was put in the filtration chamber and the top of the chamber was sealed under a vacuum. Then the sample was heated to melting and filtered into the viscometer and the connecting tube sealed at the middle. The viscometer was settled inside a transparent electric furnace and after the temperature of the melt was stabilized, the furnace containing the viscometer was turned upside down, which transferred the melt into the funnel. Then the tube was turned... 

A solids-stabilized water-in-oil emulsion may be used either as a drive fluid for displacing hydrocarbons from the formation or to produce a barrier for diverting the flow of fluids in the formation. The solid particles may be formation solid particles or nonformation solid particles, obtained from outside the formation (e.g., clays, quartz, feldspar, gypsum, coal dust, asphaltenes, polymers) [228,229]. 

Dam VAT, de Bmijn FA. 2007. The stability of PEMFC electrodes—Platinum dissolution vs. potential and temperature investigated by quartz crystal microbalance. J Electrochem Soc 154 B494-B499. 

It is known [65, 66] that oxygen is observed at the surface of freshly ground quartz in several forms which are characteristic of various conditions of formation, thermal stability, concentration, etc. Jointly with other physical and chemical methods application of semiconductor sen-... 

This latter point was stressed by some of us in a recent report studying NO storage and reduction on commercial LSR (lean storage-reduction) catalysts, in order to catch valuable information about the behaviour of typical NO storage materials in real application conditions. Nature, thermal stability and relative amounts of the surface species formed on a commercial catalyst upon NO and 02 adsorption in the presence and in the absence of water were analysed using a novel system consisting of a quartz infrared reactor. Operando IR plus MS measurements showed that carbonates present in the fresh catalyst are removed by replacement with barium nitrate species after the first nitration of the material. Nitrate species coordinated to different barium sites are the predominant surface species under dry and wet conditions. The difference in the species stabilities suggested that barium sites possess different basicity and, therefore, that they are able to stabilize nitrates at different temperatures. At temperatures below 523 K, nitrite species were observed. The presence of water at mild temperatures in the reactant flow makes unavailable for NO adsorption the alumina sites [181]. 

Direct insertion probe pyrolysis mass spectrometry (DPMS) utilises a device for introducing a single sample of a solid or liquid, usually contained in a quartz or other non-reactive sample holder, into a mass spectrometer ion source. A direct insertion probe consists of a shaft having a sample holder at one end [70] the probe is inserted through a vacuum lock to place the sample holder near to the ion source of the mass spectrometer. The sample is vaporized by heat from the ion source or by heat from a separate heater that surrounds the sample holder. Sample molecules are evaporated into the ion source where they are then ionized as gas-phase molecules. In a recent study, Uyar et al. [74] used such a device for studying the thermal stability of coalesced polymers of polycarbonate, PMMA and polylvinyl acetate) (PVAc) [75] and their binary and ternary blends [74] obtained from their preparation as inclusion compounds in cyclodextrins. 

---