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Process standardization

It will be the responsibihty of industry to suggest alternative control approaches and demonstrate satisfactorily that the proposal is equivalent in pollution reduction, enforceabihty, and environmental impact to existing individual process standards. [Pg.2158]

Key Terms enthalpy, H free energy of formation, AG standard entropy change, AS° entropy, S spontaneous process standard free energy change, AG° free energy, G... [Pg.472]

For the basic evaluation of a linear calibration line, several parameters can be used, such as the relative process standard deviation value (Vxc), the Mandel-test, the Xp value [28], the plot of response factor against concentration, the residual plot, or the analysis of variance (ANOVA). The lowest concentration that has been used for the calibration curve should not be less than the value of Xp (see Fig. 4). Vxo (in units of %) and Xp values of the linear regression line Y = a + bX can be calculated using the following equations [28] ... [Pg.249]

The national organic certification bodies will also provide useful information on food processing standards in organic food production. In addition, there are publications that have reviewed decontamination processes and disinfection procedures used in the fresh produce industry. Some of these are also listed below. [Pg.448]

Lactose USP—hydrous spray process standard, McKesson Chemical. cFast-flo lactose USP, McKesson Chemical. [Pg.295]

The specific requirements for organic pigments in terms of heat stability result from the temperature levels at which individual polyolefins are processed. Standards have been developed to test the heat stability of pigments in polyolefins [33] (see also Sec. 1.6.7). [Pg.166]

Process Standard output Linked processing cost... [Pg.26]

As an example, the results obtained for method precision and capability are presented in Table 10 for a Gage R R study performed for an oral film-coated tablet in four different labs, using six sample batches, and analyzed in replicate by two analysts in each lab. The %P/T metric was calculated according to the Ph. EUR specifications 95-105% and according to the USP specifications 90-110%. The method standard deviation (apart from the process standard deviation) is also presented, together with average assay results and confidence intervals thereof per lab and for all labs together. [Pg.181]

The correlation coefficient does not indicate the quality. If we divide the residual standard deviation by the sensitivity (the slope of the function) we get the process standard deviation and the process variation coefficient respectively. [Pg.189]

The formula for the residual standard deviation is a bit different. This reflects that the degrees of freedom are one less. The slope of the function and therefore also the sensitivity is concentration dependent. So usually the sensitivity in the middle of the working range is reported. We may also calculate the process standard deviation and process variation coefficient in the middle of the working range. [Pg.189]

In the middle ofthe working range E x) = b+2c x Process standard deviation... [Pg.189]

The common values of constants c4 and A3 are tabulated in Table 4 for sample sizes from 2 to 10. Like other control charts, the values of x and s should be periodically verified to assure that they can be used to derive good estimators for the process average and process standard deviation. [Pg.298]

Since only individual measurements are available, moving ranges need to be calculated for the estimation of process standard deviation o. A -point moving range, MR, can be calculated as... [Pg.301]

For m individual measurements, there are m - MR available, and the process standard deviation can be estimated as... [Pg.301]

The parameter is called the allowance and is usually determined as the magnitude of the shift to be detected in terms of c If either C,+ or Q exceeds a decision interval h, the process is considered out of control. In other words, the value of h is considered a UCL and -h is considered an LCL. Its centerline is always at zero. A reasonable value for h is five times the process standard deviation o. [Pg.302]

In terms of breaching the warning and control limits, it will take a long time for a Shewhart means chart to show that the process mean has shifted by a small fraction of the process standard deviation. The ARL for deviation of half a standard deviation from the mean is 155 (table 4.1), so on average 155... [Pg.121]

We will examine three synthetic fuel scenarios and compare their implications regarding sulfur availability with the current and projected market for sulfur to the year 2000. The analysis will consider three production levels of synthetic fuels from coal and oil shale. A low sulfur Western coal will be utilized as a feedstock for indirect liquefaction producing both synthetic natural gas and refined liquid fuels. A high sulfur Eastern coal will be converted to naphtha and syncrude via the H-Coal direct liquefaction process. Standard retorting of a Colorado shale, followed by refining of the crude shale oil, will round out the analysis. Insights will be developed from the displacement of imported oil by synthetic liquid fuels from coal and shale. [Pg.84]

I have three categories of regulation, Anti-trust, Economic, and Product or Process Standards. The latter category requires a further sub-division into specifications and judgmental standards. This, of course, is not meant to be a complete list of all the types of regulations we have. This categorization is simply those major regulation types that have been reported to have an impact on innovation. [Pg.34]

Social justice and social rights are an integral part of organic agriculture and processing. Standards shall require that ... [Pg.338]

Microdialysis sampling. Sampling frequency of 15 h 1. Around 20% decrease in the signal in 20 h of continuous operation for both the glucose and L-lactate electrodes. During the on-line monitoring of the fermentation process standard injections were made intermittently to check the decrease in the responses of the electrodes. The decrease in the responses were taken into account. [Pg.287]

AS= change in thermodynamic disorder for a process Standard Entropy, S° ... [Pg.4]

Real process standards, but reference concentrations obtained from process sampling/lab analysis or temporary on-line method... [Pg.310]

User Clinical Analytical EPA/Process Standards Organic Synth. [Pg.138]

Federal Information Processing Standards http //www.itl.nist.goc/fipspubs/... [Pg.41]

FIPS 81, DES Modes of Operation, Federal Information Processing Standards Publication 81, U.S. Department of Commerce / National Bureau of Standards, National Technical Information Service, Springfield, Virginia, 1980. [Pg.314]

Another method of validation is the use of standard samples from an approved source but such sources and tissue are not currently available. The use of consensus positive and negative tissue in the form of tissue microarrays is a possible substitute (Fitzgibbons et al, 2006). Alternatively, tissue samples from cases accessioned by your own laboratory known to harbor the target protein by non-IHC means can be used, but in all these situations it has to be remembered that there is no fixation or processing standard so that agreement between laboratories and between samples is subject to pre-analytical variables discussed previously. Clearly the ideal validation procedure would be against patient outcome but this is a costly exercise and often not practical as they require appropriate numbers of patients and a prospective study. [Pg.101]

Internal standards are used to correct for errors in sample preparation or sample introduction and to help determine solute recoveries. They are added to the sample at the earliest possible introduction point in the analytical process. Standards solutions containing the solutes of interest are prepared, preferably at two or three different, known concentrations but with a constant concentration of internal standard. The same concentration of internal standard is also added to each sample. All the standards and samples receive the same treatment from sample preparation, through the sample introduction and separation processes, to detection. [Pg.235]

Astd = activity of the standard added to the processed standard solution, in Bq... [Pg.117]


See other pages where Process standardization is mentioned: [Pg.229]    [Pg.16]    [Pg.37]    [Pg.435]    [Pg.435]    [Pg.478]    [Pg.174]    [Pg.473]    [Pg.47]    [Pg.19]    [Pg.259]    [Pg.221]    [Pg.344]    [Pg.306]    [Pg.749]    [Pg.11]    [Pg.208]    [Pg.250]    [Pg.549]    [Pg.216]    [Pg.351]    [Pg.438]    [Pg.150]   
See also in sourсe #XX -- [ Pg.63 ]




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