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QA series

Now we can start iterations by the modified Born series with a quasi-analytical approximation for the anomalous field  [Pg.266]

In this case, the first order QA approximation is equal to [Pg.266]

We will call the first iteration determined by expression (9.171) a modified quasi-analytical approximation (MQA)  [Pg.266]

Taking into account the definition of the modified Green s operator (9.135) and formula (9.170), we obtain [Pg.266]

Equation (9.172) shows that the modified QA approximation is equal to the original QA approximation outside inhomogeneity D  [Pg.266]


We begin with a short review of the method of constructing an always convergent Born series, following mainly Zhdanov and Fang (1997). In the subsequent sections we introduce QL and QA series based on QL and QA approximations. [Pg.256]

We should note that QA series can also be built on TQA and LN approximations for the first iterations. [Pg.267]

This seemingly simple series of events does not address all the requirements. If the device is preparing media does that mean it prepares a buffer to be diluted or only degasses the premixed media When media is dispensed, is there a need to perform a preliminary dispense to assure removal of the previous media If samples are to be read on-line is dilution required prior to reading Systems intended for method development (MD) will have many different requirements than one intended for QA. The value of the automation to the user may be very different for each of these two areas. In fact the MD user may not appreciate the need to automate more than one run at a time and will prefer a semiautomated system, since the MD user may have many different experiments to perform that may be labor intensive. Just a few... [Pg.380]

Study the AG° dependence at different temperatures. This was done by Dutton and co-workers for the electron transfers from Bph to and Qa to (Bchl)2 in Rhodobacter sphaeroides photosynthetic reaction centers [139,140], which take place over about 13 A and 25 A, respectively [18], The rates were measured between 10 K and 300 K in series in which quinone substitutions provide AG° ranges of 0.5 eV and 0.8 eV for the two reactions respectively. The following conclusions were deduced from a thorough analysis of the experimental results ... [Pg.31]

As soon as fraud is suspected, a series of steps needs to be followed which have been thought out and written down as an SOP before any clinical research commenced. Where possible, additional evidence should be obtained, usually by the use of a competent QA auditor. In the meantime, only the minimum key individuals should be made aware of the problem until sufficient evidence has been obtained to establish the truth. The appropriate authorities such as the national drug industry organisation and the regulatory authorities should be informed if fraud has taken place. Sometimes, other sponsors will have reported additional evidence that fraud is taking place at a particular site. The site will need to be closed if study subjects are still being recruited and a full explanation provided to the authorities. Any clinical data collected will need to be reviewed and a decision made as to whether any of the data can be included in an analysis. To a pharmaceutical physician, fraud is never an easy situation. It usually involves a professional colleague and there is always the worry that the established facts have been misinterpreted. However, a fraudulent individual cannot be tolerated in modern clinical research. [Pg.272]

As part of this field study, relevant quality assurance/quality control (QA/QC) criteria and guidelines (SETAC, 1993 JAMP, 1998a,b) have to be set to insure the quality of data generated during the assessments. The development of QA/QC criteria for this study involved conducting a series of replicate bioassays with each of the methods. Samples tested included a control sediment, contaminated sediments and reference toxicants. Based on the results of the bioassay replicates, the variability associated with the tests was quantified and we were able to determine what we considered acceptable QA/QC criteria for these methods. [Pg.14]

Synthesis and Characterization of Lignin-like Model Epoxide. A series of epoxidation reactions were performed with hydroxypropyl guaiacol (HPG) as model compound and ECH. Molar ratios of ECH HPG varied from 1 to 10. Pelletized KOH and a quarternary ammonium salt (QAS) served as catalyst and reagent. Toluene was the solvent. Catalyst concentration and method of addition were varied. Experimental details are given elsewhere (11). [Pg.508]

These benefits make prospective validation a QA tool, but QA is not a stagnant activity. It consists of snapshots of distinct activities, yet when all the snapshots are put together, a kaleidoscope of the life of a process and/or of a series of changes results. It may also include the investigative process, when a deviation occurs, and the corrections implemented to re-establish the validated state. To support such an effort, the trends shown by the data for each batch are documented. Prospective validation should thus be viewed as the anchor for the QA effort. [Pg.809]

While sample documentation and tracking protocols, as well as QA/QC procedures, have been in place and in effect for many years, their application is tailored to the needs and resources of each individual project, with some exploratory or field-feedback studies requiring much less verification than other regulatory or complaint series. Flexibility in experimental design is imperative if a facet of an investigation is to be completed in accordance with its significance and allocated resources. However, since several of our programs are potentially answerable to GLP s, it was deemed important that the laboratories current level of compliance be established so as to accurately measure the full fiscal and scientific impact to be felt if we should attempt to institute a formal GLP structure. [Pg.119]

Eleven 9,10-anthraquinones with various substituents, seven 1,4-naphthoquinones, 1,2-naphthaquinone and five 1,4-benzoquinones were used as QA. These quinones provide a series of RCs with a variation of the reaction exothermicity, - AG , from 0.11 to 0.9 eV. The rates of intraprotein electron transfer from various Qa to (BChl)J were found to be virtually temperature independent from 5 to 100 K and to decrease severalfold from 100 to 300 K. Only a small change of the rate upon the — AG° variation was found when reaction was made more exothermic than in the native RC. As the reaction was made less exothermic, the rate decreased notably without becoming temperature dependent. [Pg.68]

Next, the formal expansion of the S-function into a Taylor s series about the centre of mass qa of the ath macromolecule can be used, retaining only the first two terms of the expansion... [Pg.101]

Table I lists the experimental values of QA for major adatoms such as H, O, N, and C on some close-packed metal surfaces (30-43). Typically, the heat of atomic chemisorption QA decreases while going from the left to right along a transition series and from the top to bottom of a column. This decrease AQA is the least pronounced for monovalent H when, within the series Pt-Ni-W, AQH does not exceed 7 kcal/mol [QH = 61, 63, and 68 kcal/mol for Pt(lll), Ni(lll), and W(110), respectively]. For divalent O and trivalent N, however, the changes in QA from Pt to Ni to W become very large, up to AQA = 40 kcal/mol i.e., Qq = 85-125 kcal/mol and (gN = 115-155 kcal/mol. For tetravalent C, the experimental measurements have been reported only for Ni(lll) and Ni(100), giving Qc = 171 kcal/ mol (43). So, for other metal surfaces we are to use extrapolated estimates of Qc. For C, we assume a somewhat larger spread in QA compared with O and N that is, A<2C = 50 kcal/mol, from Qc = 150 kcal/mol for Pt(l 11)... Table I lists the experimental values of QA for major adatoms such as H, O, N, and C on some close-packed metal surfaces (30-43). Typically, the heat of atomic chemisorption QA decreases while going from the left to right along a transition series and from the top to bottom of a column. This decrease AQA is the least pronounced for monovalent H when, within the series Pt-Ni-W, AQH does not exceed 7 kcal/mol [QH = 61, 63, and 68 kcal/mol for Pt(lll), Ni(lll), and W(110), respectively]. For divalent O and trivalent N, however, the changes in QA from Pt to Ni to W become very large, up to AQA = 40 kcal/mol i.e., Qq = 85-125 kcal/mol and (gN = 115-155 kcal/mol. For tetravalent C, the experimental measurements have been reported only for Ni(lll) and Ni(100), giving Qc = 171 kcal/ mol (43). So, for other metal surfaces we are to use extrapolated estimates of Qc. For C, we assume a somewhat larger spread in QA compared with O and N that is, A<2C = 50 kcal/mol, from Qc = 150 kcal/mol for Pt(l 11)...
By expanding the above dipole moment operators around the origins of qa and qfe, in the Taylor series gives... [Pg.346]

The tetradentate arsine ligand containing three trimethylene linkages, 1,3-propanebis-(3-dimethylarsinopropylphenylarsine) (qas) forms a series of square-pyramidal nickel(II) complexes of the type [Ni(qas)X]BPh (X = Cl, Br, I, NO3) and [Ni(qas)(H20)](C10j2 (35, 46). Similar results have been obtained with the tetraarsine as4ph (28). [Pg.177]

The direction of enohsation of steroid 3-ketones was a subject of much debate from the early 1950 s, for 5a-3-ketones give A2-enols (17), and 5ji -3-ketones give mainly A -enols (18) [12, 128]. The preference for A -enolisation in the 5j8-series was fairly easily explained [128] in terms of relief of non-bonded interactions between the qa-hydrogen and the 7a- and qa-hydrogens when a trigonal centre is formed at C 4) . Recent calculations [ 126] suggest that the A -isomer is favoured by an enthalpy difference of 1.9 kcal/mole. This would result in a A8/A2 ratio of 96 4, compared with the experimentally determined 93.5 6.5. It is interesting that kineticaUy controlled enol acetylation of a 5j5 3-ketone with isopropenyl acetate The preferential Ca-formylation of 5 j -3-ketones is discussed on p. 182. Heferences p. 214... [Pg.330]

It is well known that the conventional Born approximation can be applied iteratively, generating A -th order Born approximations. This approximation can be treated as the sum of N terms of the Born (or Neumann) series. However, the convergence of the Born series is questionable and depends on the norm of the integral equation (Green s) operator. It seems to be very attractive to construct similar series on the basis of the QL and QA approximations. [Pg.256]

The OECD covers a series of activities and personnel. Responsibilities, training, quality assurance (QA), standard operating procedures (SOPs), study plans and study reports, data production and recording, equipment maintenance and calibration, computers and validation, test systems and test substances, and archiving are the primary areas covered by the GLPs. [Pg.1933]


See other pages where QA series is mentioned: [Pg.266]    [Pg.266]    [Pg.45]    [Pg.266]    [Pg.266]    [Pg.45]    [Pg.185]    [Pg.272]    [Pg.739]    [Pg.73]    [Pg.33]    [Pg.269]    [Pg.231]    [Pg.193]    [Pg.188]    [Pg.509]    [Pg.187]    [Pg.208]    [Pg.145]    [Pg.794]    [Pg.809]    [Pg.813]    [Pg.819]    [Pg.414]    [Pg.109]    [Pg.71]    [Pg.113]    [Pg.198]    [Pg.500]    [Pg.258]    [Pg.125]    [Pg.210]    [Pg.90]    [Pg.90]    [Pg.5410]    [Pg.79]   


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