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Activity standards

Activating Standard of comparison Deactivating —R —Ar —CH=CR —H —X (X = F Cl —CH2X (alkyl) (aryl) 2 (alkenyl) (hydrogen) (halogen) Br 1) (halomethyl) Ortho para directing Ortho para directing... [Pg.495]

National Institute of Standards and Technology (NIST). The NIST is the source of many of the standards used in chemical and physical analyses in the United States and throughout the world. The standards prepared and distributed by the NIST are used to caUbrate measurement systems and to provide a central basis for uniformity and accuracy of measurement. At present, over 1200 Standard Reference Materials (SRMs) are available and are described by the NIST (15). Included are many steels, nonferrous alloys, high purity metals, primary standards for use in volumetric analysis, microchemical standards, clinical laboratory standards, biological material certified for trace elements, environmental standards, trace element standards, ion-activity standards (for pH and ion-selective electrodes), freezing and melting point standards, colorimetry standards, optical standards, radioactivity standards, particle-size standards, and density standards. Certificates are issued with the standard reference materials showing values for the parameters that have been determined. [Pg.447]

Activating Standard of comparison Deactivating —R (alkyl) —Ar (aryl) —CH=CR2 (alkenyl) —H (hydrogen) —X (halogen) (X = F, Cl, Br, I) —CH2X (halomethyl) Ortho, para-directing Ortho, para-directing... [Pg.495]

Since Eqs. (5) and (6) are not restricted to the vapor phase, they can, in principle, be used to calculate fugacities of components in the liquid phase as well. Such calculations can be performed provided we assume the validity of an equation of state for a density range starting at zero density and terminating at the liquid density of interest. That is, if we have a pressure-explicit equation of state which holds for mixtures in both vapor and liquid phases, then we can use Eq. (6) to solve completely the equations of equilibrium without explicitly resorting to the auxiliary-functions activity, standard-state fugacity, and partial molar volume. Such a procedure was discussed many years ago by van der Waals and, more recently, it has been reduced to practice by Benedict and co-workers (B4). [Pg.171]

Figure 3.2. Overview of the three states of the active standard [NiFe]-hydrogenase from A. vinosum.The wavelengths indicate the infrared frequencies for the two CN groups and the CO group, respectively. The reactions with hydrogen are fast (thick arrows) or extremely slow (dotted arrow). Protons are not shown, a, active C, C state L, light-induced state R, reduced S, EPR silent , the active site in this state is a S = V2 system (detectable by EPR) 4Fe, [4Ee4S] cluster. Figure 3.2. Overview of the three states of the active standard [NiFe]-hydrogenase from A. vinosum.The wavelengths indicate the infrared frequencies for the two CN groups and the CO group, respectively. The reactions with hydrogen are fast (thick arrows) or extremely slow (dotted arrow). Protons are not shown, a, active C, C state L, light-induced state R, reduced S, EPR silent , the active site in this state is a S = V2 system (detectable by EPR) 4Fe, [4Ee4S] cluster.
R. G. Bates and M. Alfenaar, Activity Standards for Ion-Selective Electrodes,... [Pg.89]

ISEs respond to the activities of ions. To prepare activity standards, the individual activity coefficients of the pertinent ions must be known. However, individual activity coefficients cannot be determined accurately and can only be calculated approximately. For a discussion of conventional activity scales see p. 73-6. [Pg.101]

Figure 5.41 G-X diagram illustrating application of Darken s Quadratic Formalism to a binary join. Although mixing behavior of components 1 and 2 in phases a and ]8 is nonideal (heavy lines), in each of the simple regions it is modeled by an ideal mixing model (light lines) by means of an appropriate choice of the Active standard state potential /x. From Will and Powell (1992). Reprinted with permission of The Mineralogical Society of America. Figure 5.41 G-X diagram illustrating application of Darken s Quadratic Formalism to a binary join. Although mixing behavior of components 1 and 2 in phases a and ]8 is nonideal (heavy lines), in each of the simple regions it is modeled by an ideal mixing model (light lines) by means of an appropriate choice of the Active standard state potential /x. From Will and Powell (1992). Reprinted with permission of The Mineralogical Society of America.
In the study of Tucson (J), at each site whole filter data were analyzed separately. They find factors that are identified as soil, automotive, several secondary aerosols such as (NHjj) SOij and several unknown factors. They also discovered a factor that represented the variation of elemental composition in their aliquots of their neutron activation standard containing Na, Ca, K, Fe, Zn, and Mg. finding illustrates one of the important uses of factor analysis screening the data for noisy variables or analytical artifacts. [Pg.29]

One concludes that to qualify as the rds, it is not which step has the highest activation standard free energy with respect to the energy of the previous state that is important, but which step has the highest standard free energy of the activated state compared with that of the initial state. [Pg.465]

Total Activity)sampie (Total Activity)standard... [Pg.343]

Most of the properties of RNase Ti are summarized in Tables II and IV. It is a very acidic protein, active between pH 4 and 8.5 it is most active at pH 7.5 for RNA digestion (12) and at pH 7.2 for the hydrolysis of guanosine 2, 3 -cyclic phosphate (18). The purified enzyme possesses a specific activity of about 1.6 X 10 units/mg of protein. The molecular activity (standard units/jumole enzyme) has not been determined for the cleavage of a definite dinucleoside monophosphate such as GpC or for the hydrolysis of guanosine 2, 3 -cyclic phosphate. [Pg.213]

The concept of temperature compensation of metabolism at the whole animal level in poikilotherms has been subject to strong criticism by Holeton (1974, 1980) and especially by I.V. Ivleva (1981), who believed that such compensation was an artefact arising from inadequate acclimation. However, Ivleva s own experiments were carried out on aquatic invertebrates, not fish, and the data referred to standard metabolism rather than total or active. Note that total metabolism is that taking place in an animal in nature, active metabolism is that which supplies locomotory activity, standard metabolism is that observed in experiments, and basal metabolism is that in the resting state. Ivlev (1959) found that apparent adaptive reactions of animals are seen mostly in active, not standard or basal, metabolism. However, more recent work (Karamushko and Shatunovsky, 1993 Musatov, 1993) appears rather to favour the concept of I.V. Ivleva, that standard, not active, metabolism illustrates the adaptive reactions. [Pg.9]

Gibbs energy of activation standard Gibbs energy of activation Gibbs energy of activation for forward reaction film thickness... [Pg.222]

We next consider metallic iron whose exergy reference species are oxygen molecules in the atmospheric air and solid iron oxide Fe203, which is the most stable existence of iron in the top layer of the lithosphere. In the atmospheric air metallic iron reacts with oxygen gas to form iron oxide (corrosion of metallic iron). The reaction at the standard state (unit activity, standard pressure 101.3 kJ, and standard temperature 298 K) is expressed in Eq. 10.30 ... [Pg.107]

Protein or peptide content should be well defined by an appropriate physio-chemical test. If the quantity of product can be well correlated to a specific biological activity (standard curve), then an elaborate physiochemical test does not need to be performed. [Pg.32]

Bates and Alfenar (23) proposed that the activity of the chloride ion in NaCl solutions be taken as the activity standard. Using this chloride convention together with the published values of mean activity coefficients, the activity of any simple ionic species can be estimated. The equation used to estimate values of yNo3 and thus aNo3 for nitric acid solutions is... [Pg.331]

Preparations of ionium are used as standards of a-ray activity when a more active standard than urano-uranic oxide is necessary. The production of helium from ionium has been obser ed. Uranium Xj may be used as an indicator for ionium when estimating the latter in terms of the equilibrium quantity contained in uranium minerals. ... [Pg.349]

The daily confrontation of theoretical concepts with production requirements should permit reconciliation of the requirements set by machine performance, manufacturing deadlines, and activity standards to be met. Each product appears to be a unique case, and the result of the characteristics of both the active ingredient and the substrate used. [Pg.353]

Gamma-ray sources for efficiency measurements as standard sources are characterised in terms of photon emission flux in 4tc sr, expressed in s, for each specified gamma-ray. The activity of the source is indicated. When an activity standard is used to determine the efficiency of a y-ray spectrometer as a function of photon energy, certain decay scheme parameters are required (gamma branching ratio, internal conversion coefficient, etc.). In this case, the calibration uncertainty is the combination of the uncertainty on the activity of the standard and of the uncertainties on the parameters of the decay scheme. [Pg.105]

MS/MS spectra with those from known biologically active standards. Thus, previously identified components are rapidly eliminated and do not require time-consuming structure elucidation studies. The savings of effort allow researchers to focus efforts on novel chemistries. Samples of novel compounds can then be infused into an ion trap mass spectrometer, and a multiple stage mass analysis (MS ) fragmentation map is generated. [Pg.3423]

Despite the similarities that sustainability audits have to compliance and EHS management systems verification processes, there are some important yet subtle distinctions to note. Those distinctions include the scope or boundaries of the assurance/verification activities, standards of practice, assurance criteria and evidence, and content of the assurance report. [Pg.264]

Like all laboratory procedures, the PERT assay requires adequate controls to assure the quality of the entire detection procedure. Negative and positive controls must be included for each step of the procedure (i.e., sample preparation, reverse transcription, PCR amplification, and detection of amplified product). In addition, to quantify RT, the PERT assay requires an activity standard. [Pg.309]

Gibbs energy of activation (standard free energy of activation), A4G0 (SI unit kj mol-1) The standard Gibbs energy difference between the transition state of a reaction (either an elementary reaction or a STEPWISE reaction) and the ground state of the reactants. It is calculated from the experimental rate constant k via the conventional form of the absolute rate equation ... [Pg.118]

Standardized extracts" are herbal preparations adjusted within an acceptable tolerance to a given content of constituents with known therapeutic activity standardization is achieved by adjustment of the herbal preparations with inert material or by blending batches of herbal preparations. "Quantified extracts" are herbal preparations adjusted to a defined range of constituents adjustments are made by blending batches of herbal preparations. "Other extracts" are herbal preparations essentially defined by their production process and their specifications. [Pg.404]


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See also in sourсe #XX -- [ Pg.199 ]




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