Further Analysis

All operating parameters and the events or situations such as excess feeding of materials into a reactor, high/low level in process tanks, high/low temperature of reactants, and cooling water supply less/stopped completely shall be considered. 

apply the full study procedure when the design is complete and examine to ensure that all eventualities have been considered. This type of study on a large project may take a long time even many weeks and hence the options to be considered could be  

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Inspection data can be quickly communicated back to the office for further analysis, which helps to support inspectors in the field... 

A. Sandu and T. Schlick. Further analysis of impulse and extrapolation force splitting in molecular dynamics. J. Comp. Phys., 1998. Submitted... 

A molecular dynamics simulation used for a conformational search can provide a quick assessment of low energy conformers suitable for further analysis. Plot the average potential energy of the molecule at each geometry. This plot may also suggest conformational changes in a molecule. 

After dissolving the sample in a beaker, remove any solid impurities by filtering a portion of the solution containing the analyte. Collect and discard the first several milliliters of solution before collecting a sample of approximately 5 mL for further analysis. 

Potential fusion appHcations other than electricity production have received some study. For example, radiation and high temperature heat from a fusion reactor could be used to produce hydrogen by the electrolysis or radiolysis of water, which could be employed in the synthesis of portable chemical fuels for transportation or industrial use. The transmutation of radioactive actinide wastes from fission reactors may also be feasible. This idea would utilize the neutrons from a fusion reactor to convert hazardous isotopes into more benign and easier-to-handle species. The practicaUty of these concepts requires further analysis. 

After a desired clone is obtained and mapped with restriction enzymes, further analysis usually depends on the deterrnination of its nucleotide sequence. The nucleotide sequence of a new gene often provides clues to its function and the stmcture of the gene product. Additionally, the DNA sequence of a gene provides a guidepost for further manipulation of the sequence, for example, lea ding to the production of a recombinant protein in bacteria. 

Commercial Hquid sodium alumiaates are normally analyzed for total alumiaa and for sodium oxide by titration with ethylene diaminetetraacetic acid [60-00-4] (EDTA) or hydrochloric acid. Further analysis iacludes the determiaation of soluble alumiaa, soluble siHca, total iasoluble material, sodium oxide content, and carbon dioxide. Aluminum and sodium can also be determiaed by emission spectroscopy. The total iasoluble material is determiaed by weighing the ignited residue after extraction of the soluble material with sodium hydroxide. The sodium oxide content is determiaed ia a flame photometer by comparison to proper standards. Carbon dioxide is usually determiaed by the amount evolved, as ia the Underwood method. 

Equation 4 estabHshes the relationship between the growth rate, a, and local film parameters. This model provides a reasonable foundation for further analysis of droplet formation. 

Mathematically, the mean value is the desired value for further analysis. 

The end device will be responding to a range of pollutants and be used for rapid, low cost pre-screening of large numbers of samples to determine samples that will then undergo further analysis. 

Further analysis, which is not yet complete, has indicated that dre flow of current should be described as having two effects. The first, the purely... 

Production. When the simulation is equilibrated, the dynamic simulation is considered reliable. Prom this point on, the trajectory generated is stored for further analysis. Typical production runs take from several hundred picoseconds up to tens of nanoseconds (depending on the size of the system and the available computer power). 

Analysis may show one mode of failure to be most likely in which case further analysis conteiunilcs on ihat mode thereby considerably reducing the scope of the analysis. If there are several etiiiallv likely modes, they must all be analyzed. 

This contains two separate requirements one for verifying that the prescribed action has been taken and the other for verifying that the action has been effective in eliminating the original nonconformity. The Corrective Action report should define the corrective action to be taken, the actionee, and the date by which it is to be completed. The action-ee should report when the action has been completed in order that it may be verified. The effectiveness of some actions can be verified at the same time but quite often the effectiveness can only be checked after a considerable lapse of time. Remember it took an analysis to detect the nonconformity therefore it may take further analysis to detect that the nonconformity has been eliminated. In such cases the report should indicate when the checks for effectiveness are to be carried out and provision made for indicating that the corrective action has or has not been effective. 

FIGURE 16.6 Waxymaize ( ) and amylomaize ( ) separated on Sephacryl S-IOOO (95 x 1.6 cm) pooled in 3-ml fractions for further analysis normalized (area = 1.0) eluogram profiles (ev) constructed from an off-line determined mass of carbohydrates for each of the 3 ml fractions flow rate 0.41 ml/ min = 75 ml, V , = 162 ml eluent 0.005 M NaOH. 

Using the standard Bucherer-Lieb variation, a mixture of 9,10-dimethoxy-l,3,4,6,7,llb-hexahydro-pyrido[2,l-fl]isoquinolin-2-one (14, 3 g, 12 mmol), potassium cyanide (1.17 g, 18 mmol) and ammonium carbonate (6.9 g) was dissolved in a 2 1 water-ethanol solution (45 mL). The reaction flask was sealed and heated for 48 h in an oven at 60°C. The cooled reaction mixture left a precipitate, which was filtered to yield 3.7 g (97%) of crude hydantoin 15. Further analysis revealed that it was consisted of 83% of ( )-25,1 lb5 isomer 15a and 9% of ( )-2/ ,llb5 isomer 15b. 

The preseparation utilized a 5 pim cyano column (250 cm X 4.6 mm i.d.) and a 5 p.m silica column (250 cm X 4.6 mm i.d.) in series, followed by GC analysis on an SE-54 column (25 m X 0.2 mm i.d., 0.33 p.m film thickness). The SFC system separated the aviation sample into two peaks, including saturates and single-ring aromatics as the first peak, and two-ring aromatic fractions as the second peak. These fractions were selectively cut and then transferred to the GC unit for further analysis. (Figure 12.20). 

This concept reduces the manual analysis required for each data set. The analyst can scan the documentation that is generated (i.e., the exception report and trend charts) for each of the selected narrowbands to determine if further analysis is required. 

Two concentrations of agonist are chosen for further analysis. These should be two concentrations as widely spread as possible along the... 

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