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The crystals may contain both salts in definite molecular ratio. Their solution will, however, respond to tests for all of the ions originally present. Thus, carnallite, KCl-MgCl2,6H20, gives tests for the ions K+, Mg 1-1", and Cl-. Such salts are called double salts, and their formulas are written, as has just been illustrated, as a series of molecular formulas parted by periods. [Pg.103]

Compound Formula Part-formula based on pentacyclic Ci9H28-NH A req. [Pg.327]

Table 1.4 Rubber compound formulas (parts per hundred rubber, phr) ... Table 1.4 Rubber compound formulas (parts per hundred rubber, phr) ...
Figures 5 and 6 show the increase in carbonyl index for the surface and core of samples aged in 5 ppm chlorine at 95°C. The data for 85 C aging showed similar results. The new formulation and enhanced formulation became extremely oxidized between 119 horn and 380 hours. The original formula did not show this level oxidation until approximately 1124 hours. The new formulation samples show significant oxidation after 2000 hours, while the core of the original formulas do not exhibit any oxidation of the core. At this point the original formula parts have residual life, while the new formula parts are beyond the end of their useful life. Figures 5 and 6 show the increase in carbonyl index for the surface and core of samples aged in 5 ppm chlorine at 95°C. The data for 85 C aging showed similar results. The new formulation and enhanced formulation became extremely oxidized between 119 horn and 380 hours. The original formula did not show this level oxidation until approximately 1124 hours. The new formulation samples show significant oxidation after 2000 hours, while the core of the original formulas do not exhibit any oxidation of the core. At this point the original formula parts have residual life, while the new formula parts are beyond the end of their useful life.
Figure 9 shows the core OIT results for the samples aged in chlorinated water at 95°C. The OIT was measured on the new formulation samples at 180°C in order to get a measurable OIT for the unaged samples. The new formula parts show that the OIT of the surface decreases to near zero between 119 and 380 hours for both the 85°C and 95°C aging tests. The OIT of the lab processed new formula samples mirrored this behavior as shown in Figure 10, with the OIT reaching zero after approximately 164 hours of exposure. [Pg.1950]

These formulas are completely general and may be applied to any material, any form of piece and any coil. in the formula, the conductance is proportional to the amplitude of the part of the flux crossing the coil in phase with the current in the solenoid. [Pg.351]

As already mentioned (Section 5.3), the stored structure information in this type of database makes it possible to search for chemical structures in several ways. One method is to draw a structure (via a molecule editor) and to perform either a precise structure search (full structure search) or a search containing part of the input structure (substructure search) (see Sections 6.2-6.4). The databases also allow the searching of chemical names and molecular formulas (see Section 6.1). The search results are in most cases displayed in a graphical manner. [Pg.262]

This is a simplified formula for tartar emetic, for X-ray crystal analysis and infrared studies indicate that the. Sb is a part of the antimonate anion [Sb(OH)4] and forms part of a cyclic system. [Pg.115]

The comparatively inexpensive long-scale thermometer, widely used by students, is usually calibrated for complete immersion of the mercury column in the vapour or liquid. As generally employed for boiling point or melting point determinations, the entire column is neither surrounded by the vapour nor completely immersed in the liquid. The part of the mercury column exposed to the cooler air of the laboratory is obviously not expanded as much as the bulk of the mercury and hence the reading will be lower than the true temperature. The error thus introduced is not appreciable up to about 100°, but it may amount to 3-5° at 200° and 6-10° at 250°. The error due to the column of mercury exposed above the heating bath can be corrected by adding a stem correction, calculated by the formula ... [Pg.72]

A typical example is total monomers. 100 sodium stearate, 5 potassium persulfate, 0.3 lauryl mercaptan, 0.4 to 0.7 and water, 200 parts. In this formula, 75 parts of 1,3-butadiene and 25 parts of 4-methyl-2-vinylthiazole give 86% conversion to a tacky rubber-like copolymer in 15 hr at 45°C. The polymer contains 62% benzene-insoluble gel. Sulfur analysis indicates that the polymer contains 21 parts of combined 4-methyl-2-vinylthiazole (312). Butadiene alone in the above reaction normally requires 25 hr to achieve the same conversion, thus illustrating the acceleration due to the presence of 4-methyl-2-vinylthiazole. [Pg.398]

Solubility is given in parts by weight (of the formula weight) per 100 parts by weight of the solvent (i.e., percent by weight) and at room temperature. Another unit frequently used is grams per 100 mF of solvent (mF per 100 mF for liquids and gases). The symbols of the common mineral acids represent aqueous solutions of these acids. [Pg.224]

Name Formula Formula weight Density Melting point, °C Boiling point, °C Solubility in 100 parts solvent... [Pg.272]

In general terms, the main function of the magnetic/electric-sector section of the hybrid is to be able to resolve m/z values differing by only a few parts per million. Such accuracy allows highly accurate measurement of m/z values and therefore affords excellent elemental compositions of ions if these are molecular ions, the resulting compositions are in fact molecular formulae, which is the usual MS mode. Apart from accurate mass measurement, full mass spectra can also be obtained. The high-resolution separation of ions also allows ions having only small mass differences to be carefully selected for MS/MS studies. [Pg.157]

Because variations in accurate isotope ratio measurements typically concern only a few parts per 1000 by mass and there are no universal absolute ratios, it is necessary to define some standards. For this purpose, samples of standard substances are produced and made available at two major centers IAEA (International Atomic Energy Authority, U.K.) and NIST (National Institute for Standards and Technology, U.S.). Standards from other sources are also available. These primary standards can be used as such, or alternative standards can be employed if the primary ones are not available. However, any alternative standards need to be related accurately to the primary ones (see formulae below). For example, the material PDB (PeeDee belemnite), used particularly as a standard for the ratio of isotopes, is no longer readily available, and a new standard, VPDB,... [Pg.354]

Haward et al.t have reported some research in which a copolymer of styrene and hydroxyethylmethacrylate was cross-linked by hexamethylene diisocyanate. Draw the structural formula for a portion of this cross-linked polymer and indicate what part of the molecule is the result of a condensation reaction and what part results from addition polymerization. These authors indicate that the crosslinking reaction is carried out in sufficiently dilute solutions of copolymer that the crosslinking is primarily intramolecular rather than intermolecular. Explain the distinction between these two terms and why concentration affects the relative amounts of each. [Pg.339]

In 1885 Balmer was able fo fif fhe discrete wavelengfhs X of part of fhe emission specfrum of fhe hydrogen atom, now called fhe Balmer series and illusfrafed in Figure 1.1, fo fhe empirical formula... [Pg.2]

Here t = (—n2,ni) is the tangential unit vector at T. Integrating by parts, one can obtain the Green formula (Temam, 1983 Khludnev, Sokolowski, 1997)... [Pg.57]

The subscripts D,j denote the integration over the domain D and the boundary 7, respectively. Note that the boundary dfl of is a combination of the sets r,F, r. The formulae (3.15), (3.16) hold true for the domain despite the absence of regularity of dfl. To verify this we can extend the graph F, so that the domain is divided into two parts. For each part the formulae (3.15), (3.16) are valid, hence the statement follows. We should note at this point that the external normals on F, F have opposite directions. [Pg.178]

The boundary dfl of the domain can be represented as the union of the components T, T, and T. In this connection, we note that formulas like (3.124) and (3.125) are also valid for the domain To check this, it suffices to extend the graph T, so that be divided into two parts. On applying formulas (3.124) and (3.125) to both the parts, we can make sure that the formulas are also valid for... [Pg.206]

The formula (4.127) can be written in the form which does not contain the function 9. To show this we choose a ball B, (r) of radius r with the boundary T(r) such that 9 = 1 on Bx, r). In this case the integration by parts in (4.127) yields... [Pg.278]

In this section we find the derivative of the energy functional in the three-dimensional linear elasticity model. The derivative characterizes the behaviour of the energy functional provided that the crack length is changed. The crack is modelled by a part of the two-dimensional plane removed from a three-dimensional domain. In particular, we derive the Griffith formula. [Pg.279]

We have obtained the Griffith formula (4.159). It is not difficult to show that the right-hand side of (4.159) does not depend on 9. To prove this, consider the difference between right-hand sides of (4.159) corresponding to any two functions 9i, 02- Let 9 = 9i — 92- We integrate by parts, which implies that the difference A between the right-hand sides of (4.159) evaluated for is equal to... [Pg.282]

Integrate by parts in the fifth and sixth terms of the left-hand side of (5.152) taking into account the boundary conditions (5.149)-(5.151) and the Green formula like (5.138) for the domain fic- The penalty term is nonnegative and satisfy the equation (5.144). Hence the uniform in the s,5 estimate follows. [Pg.323]

In so doing we have omitted the nonnegative term containing the penalty operator. Using the formula (5.181), the integration by parts can be done in the third and the fifth terms of the left-hand side of (5.189). Also, note that Mij satisfy equation (5.175). Integration of (5.189) in t from 0 to t results in the inequality... [Pg.331]

The characterising, contributory, and differential flavor items are Hsted. The diluent portion of the flavor makes the flavor appHcable and is generally the largest part of every flavor formula. [Pg.17]


See other pages where Formulae parts is mentioned: [Pg.131]    [Pg.314]    [Pg.314]    [Pg.1370]    [Pg.1316]    [Pg.294]    [Pg.14]    [Pg.1536]    [Pg.1482]    [Pg.1536]    [Pg.1314]    [Pg.348]    [Pg.131]    [Pg.314]    [Pg.314]    [Pg.1370]    [Pg.1316]    [Pg.294]    [Pg.14]    [Pg.1536]    [Pg.1482]    [Pg.1536]    [Pg.1314]    [Pg.348]    [Pg.124]    [Pg.20]    [Pg.398]    [Pg.280]    [Pg.1090]    [Pg.1115]    [Pg.1125]    [Pg.266]    [Pg.1105]    [Pg.141]    [Pg.98]    [Pg.222]   
See also in sourсe #XX -- [ Pg.29 ]

See also in sourсe #XX -- [ Pg.29 ]




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