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Total ordinary

Impurities are typically resolved from the drug by a chromatographic procedure and quantified by comparison to an external standard, often the drug itself, rather than by comparison to standards of the individual impurities. Pharmacopoeial methods must be suitable for pharmaceuticals produced by different manufacturers that may contain different types and amounts of impurities. Pharmacopoeias typically view 1.0-2.0% as the general limit for total ordinary impurities, unless there is documentation to support a higher or lower level. Concomitant components, toxic or signal impurities are not included in the estimate of ordinary impurities and separate limits may be set for these, as necessary. [Pg.3625]

Harmonics of given total (ordinary) angular momentum / = / + / > (not to be confused with the grand orbital momentum L) are constructed by Clebsch-Gordan coupling of the HH (5.10). One should further restrict the expansion (5.6) to these HH having the desired permutation properties. [Pg.32]

Although it is hard to draw a sharp distinction, emulsions and foams are somewhat different from systems normally referred to as colloidal. Thus, whereas ordinary cream is an oil-in-water emulsion, the very fine aqueous suspension of oil droplets that results from the condensation of oily steam is essentially colloidal and is called an oil hydrosol. In this case the oil occupies only a small fraction of the volume of the system, and the particles of oil are small enough that their natural sedimentation rate is so slow that even small thermal convection currents suffice to keep them suspended for a cream, on the other hand, as also is the case for foams, the inner phase constitutes a sizable fraction of the total volume, and the system consists of a network of interfaces that are prevented from collapsing or coalescing by virtue of adsorbed films or electrical repulsions. [Pg.500]

The ordinary BO approximate equations failed to predict the proper symmetry allowed transitions in the quasi-JT model whereas the extended BO equation either by including a vector potential in the system Hamiltonian or by multiplying a phase factor onto the basis set can reproduce the so-called exact results obtained by the two-surface diabatic calculation. Thus, the calculated hansition probabilities in the quasi-JT model using the extended BO equations clearly demonshate the GP effect. The multiplication of a phase factor with the adiabatic nuclear wave function is an approximate treatment when the position of the conical intersection does not coincide with the origin of the coordinate axis, as shown by the results of [60]. Moreover, even if the total energy of the system is far below the conical intersection point, transition probabilities in the JT model clearly indicate the importance of the extended BO equation and its necessity. [Pg.80]

Hydrolysis of p-tolunitrile to p-toluic acid. Boil a mixture of 5 g. of p-tolunitrile, 80 ml. of 10 per cent, aqueous sodium hydroxide solution and 15 ml. of alcohol under a reflux condenser. (The alcohol is added to prevent the nitrile, which volatUises in the steam, from crystalhsing in the condenser it also increases the speed of hydrolysis. The alcohol may be omitted in the hydrolysis of nitriles which are hquid at the ordinary temperature, e.g., benzo-nitrUe.) The solution becomes clear after heating for about 1 hour, but continue the boiling for a total period of 1 - 5 hours to ensure complete hydrolysis. Detach the condenser and boil the solution for a few minutes in the open flask to remove dissolved ammonia and incidentally some of the alcohol CAUTION /). Cool, and add concentrated hydrochloric acid until precipitation of the p-toluic acid is complete. When cold, filter off the p-toluic acid with suction and wash with a little cold water. Recrystallise from a mixture of equal volumes of water and alcohol (methylated spirit) or from benzene. The yield of p-toluic acid, m.p. 178°, is 5-5 g. [Pg.608]

The routes by which mineral phosphates are processed into finished fertilizers are outlined in Eigure 7. World and U.S. trends in the types of products produced are shown in Eigures 8 and 9, respectively. Most notable in both instances is the large, steady increase in the importance of monoammonium and diammonium phosphates as finished phosphate fertilizers at the expense of ordinary superphosphate, and to some extent at the expense of triple superphosphate. In the United States, about 65% of the total phosphate appHed is now in the form of granular ammonium phosphates, and additional amounts of ammonium phosphates are appHed as integral parts of granulated mixtures and fluid fertilizers. [Pg.222]

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]

Biosynthesis of Protein. The dynamic equilibrium of body protein was confirmed by animal experiments using A/-labeled amino acids in 1939 (104). The human body is maintained by a continuous equilibrium between the biosynthesis of proteins and their degradative metabolism where the nitrogen lost as urea (about 85% of total excreted nitrogen) and other nitrogen compounds is about 12 g/d under ordinary conditions. The details of protein biosynthesis in living cells have been described (2,6) (see also Proteins). [Pg.282]

The success of preheater kiln systems led to precalciaer kiln systems. These units utilize a second burner to carry out calciaation ia a separate vessel attached to the preheater. The flash furnace (57), eg, utilizes preheated combustion air drawn from the clinker cooler and kiln exit gases and is equipped with an oil burner that bums about 60% of the total kiln fuel. The raw material is calciaed almost 95%, and the gases continue their upward movement through successive preheater stages ia the same manner as ia an ordinary preheater. [Pg.293]

Special purpose and blended Portland cements are manufactured essentially by the same processes as ordinary Portland cements but have specific compositional and process differences. White cements are made from raw materials of very low iron content. This type is often difficult to bum because almost the entire Hquid phase must be furnished by calcium aluminates. As a consequence of the generally lower total Hquid-phase content, high burning-zone temperatures may be necessary. Past cooling and occasionally oil sprays are needed to maintain both quaHty and color. [Pg.293]

The XeroX Copier Machine Model A was announced in 1949, and involved compHcated manual operation. Copies of acceptable quaUty were operator dependent. The Copyflo printer, introduced in 1955, was the first automated xerographic machine and enabled the production of copies on a continuous web of ordinary paper. Early electrophotographic products used paper coated with dye-sensitized zinc oxide Electrofax which had met market resistance in terms of aesthetics and cost, so that in 1958 the total market was only about 100 million (1—3,5). [Pg.128]

Optimum Reflux Ratio The general effecl of the operating reflux ratio on fixed costs, operating costs, and the sum of these is shown in Fig. 13-39. In ordinary situations, the minimum on the total-cost cui ve wih geueraUy occur at an operating reflux ratio of from 1.1 to 1.5 times the minimum R = Lv + i/D value, with the lower value corresponding to a value of the relative volatility close to 1. [Pg.1270]

Dividing equation 3.4.4-1 by the total number of trials T and letting T go to infinity, probability in the von Misesian sense results in equation 3.4.4-2. It is important to note that the symbols -i- and in this equation represent the operations of union and intersection using the rules of combining probability -not ordinary algebra (Section 2.1). [Pg.103]

Fuller claims that an auxiliary cupboard has better performance than an ordinary cupboard, if properly designed and used. The auxiliary flow rate should be 50% to 75% of the total exhaust flow from the cupboard. Below 50% there is no beneficial effect and above 75% the auxiliary air will aspirate contaminants out of the cupboard. The auxiliary air should enter the hood through the upper one-half to two-thirds of the opening. This should fill the volume between the cupboard operator and the opening and assist in the containment. The auxiliary air should be distributed uniformly across the length of the cupboard for a vertically sliding sash or above only the open sash of a cupboard with a horizontally sliding sash. It should also have a temperature within 1.5 °C of the room temperature and have a constant flow rate without pulsations. [Pg.996]

It is an ordinary differential equation (time dependenee only) where the zeroth moment (/io) is the total erystal number (per unit volume of suspension), the first (/ii) the total erystal length (lined up end to end), the seeond (7 2) is related to total surfaee area, the third (7 3) total volume (and lienee mass) and so on. [Pg.55]

In the CHS model only nearest neighbors interact, and the interactions between amphiphiles in the simplest version of the model are neglected. In the case of the oil-water symmetry only two parameters characterize the interactions b is the strength of the water-water (oil-oil) interaction, and c describes the interaction between water (oil) and an amphiphile. The interaction between amphiphiles and ordinary molecules is proportional to a scalar product between the orientation of the amphiphile and the distance between the particles. In Ref. 15 the CHS model is generalized, and M orientations of amphiphiles uniformly distributed over the sphere are considered, with M oo. Every lattice site is occupied either by an oil, water, or surfactant particle in an orientation ujf, there are thus 2 + M microscopic states at every lattice site. The microscopic density of the state i is p.(r) = 1(0) if the site r is (is not) occupied by the state i. We denote the sum and the difference of microscopic oil and water densities by and 2 respectively and the density of surfactant at a point r and an orientation by p (r) = p r,U(). The microscopic densities assume the values = 1,0, = 1,0 and 2 = ill 0- In close-packing case the total density of surfactant ps(r) is related to by p = Ylf Pi = 1 - i i. The Hamiltonian of this model has the following form [15]... [Pg.721]

Estimating the total release of flammable material within a reasonable amount of time (generally 2 to 5 minutes) and multiplying this by the heat of combustion of the material times an efficiency factor (generally in the range of 1% to 5% for ordinary hydrocarbons). [Pg.126]

All ordinary ferrous structural materials, mild steels, low-alloy steels and wrought irons corrode at virtually the same rate when totally immersed in natural waters. Wrought iron may be slightly more resistant than mild steel in a test in sea-water at Gosport, Scottish wrought-iron specimens lost about 15% less weight after 12 months immersion than specimens of ordinary mild steel. As shown in Table 3.5, the process of manufacture and the composition of mild steel do not affect its corrosion rate appreciably . [Pg.498]

The excellent resistance of zinc to corrosion under natural conditions is largely responsible for the many and varied applications of the metal. In fact nearly half the world consumption of zinc is in the form of coatings for the prevention of corrosion of steel fabrications exposed to the atmosphere and to water. For its varied applications zinc is obtainable in a number of grades. Ordinary commercial (G.O.B.) zinc contains up to about I -5% total of lead, cadmium and iron. Electrolytic zinc has a minimum zinc content of 99-95% and contains small amounts of the same impurities. Special high-purity zinc has a minimum of 99-99% zinc. Even purer zincs are commercially available. [Pg.812]

Low-alloy steels usually contain small percentages of alloying elements, such as copper, chromium and nickel, up to a total of 1-2%. Under favourable conditions they tend to corrode less rapidly than the ordinary carbon steels when exposed freely in air. Under sheltered conditions, or in crevices, they may well corrode at the same rate as mild steels ... [Pg.46]

We have now discussed three types of intermolecular forces dispersion forces, dipole forces, and hydrogen bonds. You should bear in mind that all these forces are relatively weak compared with ordinary covalent bonds. Consider, for example, the situation in HzO. The total intermolecular attractive energy in ice is about 50 kj/mol. In contrast, to dissociate one mole of water vapor into atoms requires the absorption of928 kj of energy, that is, 2(OH bond energy). This explains why it is a lot easier to boil water than to decompose it into the elements. Even at a temperature of 1000°C and 1 atm, only about one H20 molecule in a billion decomposes to hydrogen and oxygen atoms. [Pg.240]

The first orbital X is very closely related to the ordinary SCF function, which is also shown by comparing the total energy of the wave function (xx)2 with the Hartree-Fock energy ... [Pg.281]

In the ordinary Hartree-Fock scheme, the total wave function is approximated by a single Slater determinant and, if the system possesses certain symmetry properties, they may impose rather severe restrictions on the occupied spin orbitals see, e.g., Eq. 11.61. These restrictions may be removed and the total energy correspondingly decreased, if instead we approximate the total wave function by means of the first term in the symmetry adapted set, i.e., by the projection of a single determinant. Since in both cases,... [Pg.293]

If the temperature is changed the miscibility of the liquids alters, and at a particular temperature the miscibility may become total this is called the critical solution temperature. With rise of temperature the surface of separation between the liquid and vapour phases also vanishes at a definite temperature, and we have the phenomenon of a critical point in the ordinary sense. According to Pawlewski (1883) the critical temperature of the... [Pg.407]

Although the first reaction is of an ordinary sort, the next two are unusual in that one propagating intermediate is converted into two. These are branching reactions. As each occurs, the total rate speeds up. When that happens, even more branching occurs, and so on. If unchecked, the exponential growth of chain carriers leads to explosion, just as in nuclear chain reactions. [Pg.189]


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Total ordinary differential equation

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