Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Rocks, first

The CDM has two additional features that allow it to represent fracture in rocks. First, there is a brittle/ductile transition pressure. Above this pressure, the rock behaves as an elastic/plastic ductile solid, the failure surface is independent of the level of damage, and the damage is not allowed to increase, even if the failure surface is exceeded. Second, the CDM allows for non-vanishing plastic volume strain to approximate the dilatancy observed in certain laboratory experiments on oil shale. [Pg.24]

Barth AP, Dorais MJ (2000) Magmatic anhydrite in granitic rocks first occrrrrence and potential petrologic consequences. Am Mineral 85 430-435... [Pg.287]

Mew, M. C. 1994. Phosphate Rock - first Green Shoots of Recovery, Engineering and Mining Journal, 195(3) 50-53. [Pg.155]

GB started commercial manufacture of white P from bones Concluded phosphate of lime was the important nutrient in bones Condensed polyphosphoric acids prepared P-containing Lecithin first isolated from egg yolk Phosphate rock first mined in Suffolk, England Discovered thiophosphoric esta-s Inosinic acid isolated from beef muscle Existence of trimethylphosphine, PMe, reported First preparation of red phosphorus... [Pg.7]

Igneous phosphate rock first mined in Norway Commercial production of red P started in GB First phosphoryl complex prepared Introduction of safety matches containing red P Finally established that phosphates were essential for plant growth US patent - first use of phosphates in baking powder formulations Norwegian phosphate ore imported by GB for fertiUser manufacture Early reports of complexes with metal-P-carbon bonds... [Pg.7]

Phosphate rock first mined in Ontario, Canada... [Pg.8]

Several conditions need to be satisfied for the existence of a hydrocarbon accumulation, as indicated in Figure 2.1. The first of these is an area in which a suitable sequence of rocks has accumulated over geologic time, the sedimentary basin. Within that sequence there needs to be a high content of organic matter, the source rock. Through elevated temperatures and pressures these rocks must have reached maturation, the condition at which hydrocarbons are expelled from the source rock. [Pg.9]

The basics of the method are simple. Reflections occur at all layers in the subsurface where an appreciable change in acoustic impedance is seen by the propagating wave. This acoustic impedance is the product of the sonic velocity and density of the formation. There are actually different wave types that propagate in solid rock, but the first arrival (i.e. fastest ray path) is normally the compressional or P wave. The two attributes that are measured are... [Pg.18]

The relationship was based on a number of observations, firstly that the conductivity (Cq) of a water bearing formation sample is dependent primarily upon pore water conductivity (C ) and porosity distribution (as the rock matrix does not conduct electricity) such that ... [Pg.147]

Reservoir engineers describe the relationship between the volume of fluids produced, the compressibility of the fluids and the reservoir pressure using material balance techniques. This approach treats the reservoir system like a tank, filled with oil, water, gas, and reservoir rock in the appropriate volumes, but without regard to the distribution of the fluids (i.e. the detailed movement of fluids inside the system). Material balance uses the PVT properties of the fluids described in Section 5.2.6, and accounts for the variations of fluid properties with pressure. The technique is firstly useful in predicting how reservoir pressure will respond to production. Secondly, material balance can be used to reduce uncertainty in volumetries by measuring reservoir pressure and cumulative production during the producing phase of the field life. An example of the simplest material balance equation for an oil reservoir above the bubble point will be shown In the next section. [Pg.185]

Variational RRKM theory is particularly important for imimolecular dissociation reactions, in which vibrational modes of the reactant molecule become translations and rotations in the products [22]. For CH —> CHg+H dissociation there are tlnee vibrational modes of this type, i.e. the C—H stretch which is the reaction coordinate and the two degenerate H—CH bends, which first transfomi from high-frequency to low-frequency vibrations and then hindered rotors as the H—C bond ruptures. These latter two degrees of freedom are called transitional modes [24,25]. C2Hg 2CH3 dissociation has five transitional modes, i.e. two pairs of degenerate CH rocking/rotational motions and the CH torsion. [Pg.1016]

Tolbert S H and Aiivisatos A P 1994 Size dependence of a first order solid-solid phase transition the wurtzite to rock salt transformation in CdSe nanocrystais Science 265 373... [Pg.2924]

Since Know can be measured by a variety of methods, equation (3) is easily solved. For example, if Ar/ Knovy, is 0.05, then the time (f) is approximately 6x10 years, viz, the rocks were first formed (or previously melted) some 600 million years previously. [Pg.368]

By using K/Ar isotope ratios, potassium-containing rocks can be dated to their first formation, even through millions of years. [Pg.368]

Triple (Concentrated) Superphosphate. The first important use of phosphoric acid in fertilizer processing was in the production of triple superphosphate (TSP), sometimes called concentrated superphosphate. Basically, the production process for this material is the same as that for normal superphosphate, except that the reactants are phosphate rock and phosphoric acid instead of phosphate rock and sulfuric acid. The phosphoric acid, like sulfuric acid, solubilizes the rock and, in addition, contributes its own content of soluble phosphoms. The result is triple superphosphate of 45—47% P2 s content as compared to 16—20% P2 5 normal superphosphate. Although triple superphosphate has been known almost as long as normal superphosphate, it did not reach commercial importance until the late 1940s, when commercial supply of acid became available. [Pg.226]

Resources of Sulfur. In most of the technologies employed to convert phosphate rock to phosphate fertilizer, sulfur, in the form of sulfuric acid, is vital. Treatment of rock with sulfuric acid is the procedure for producing ordinary superphosphate fertilizer, and treatment of rock using a higher proportion of sulfuric acid is the first step in the production of phosphoric acid, a production intermediate for most other phosphate fertilizers. Over 1.8 tons of sulfur is consumed by the world fertilizer industry for each ton of fertilizer phosphoms produced, ie, 0.8 t of sulfur for each ton of total 13.7 X 10 t of sulfur consumed in the United States for all purposes in 1991, 60% was for the production of phosphate fertilizers (109). Worldwide the percentage was probably even higher. [Pg.245]

The earliest record of human usage of iron dates to ca 2000 BC (5) in Egypt, Asia Minor, Assyria, China, and India. It is almost certain, however, that the first iron to be used was not processed but was obtained from meteorites (1). One of the few places where native iron is found is in Greenland, where it occurs as very small grains or nodules in basalt (an iron-bearing igneous rock) that empted through beds of coal. [Pg.412]

Thermal stabihty of the foaming agent in the presence of high temperature steam is essential. Alkylaromatic sulfonates possess superior chemical stabihty at elevated temperatures (205,206). However, alpha-olefin sulfonates have sufficient chemical stabihty to justify their use at steam temperatures characteristic of most U.S. steamflood operations. Decomposition is a desulfonation process which is first order in both surfactant and acid concentrations (206). Because acid is generated in the decomposition, the process is autocatalytic. However, reservoir rock has a substantial buffering effect. [Pg.193]


See other pages where Rocks, first is mentioned: [Pg.69]    [Pg.48]    [Pg.6]    [Pg.27]    [Pg.394]    [Pg.8]    [Pg.2022]    [Pg.304]    [Pg.1768]    [Pg.69]    [Pg.48]    [Pg.6]    [Pg.27]    [Pg.394]    [Pg.8]    [Pg.2022]    [Pg.304]    [Pg.1768]    [Pg.49]    [Pg.2913]    [Pg.64]    [Pg.79]    [Pg.391]    [Pg.12]    [Pg.216]    [Pg.232]    [Pg.137]    [Pg.224]    [Pg.432]    [Pg.270]    [Pg.271]    [Pg.272]    [Pg.274]    [Pg.412]    [Pg.169]    [Pg.225]    [Pg.286]    [Pg.394]    [Pg.396]    [Pg.242]    [Pg.193]   
See also in sourсe #XX -- [ Pg.55 , Pg.86 ]




SEARCH



© 2024 chempedia.info