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Test systems Subject

The air oxidation of aqueous sodium sulfite solutions has had wide use as a test system for evaluating the performance of agitated gas-liquid contactors. As has been noted, gas-liquid processes may involve rate-controlling steps far different from those of the sulfite oxidation system. Green (G2) found it was not useful for application to a hydrogenation problem. Nevertheless, since it is quite convenient to carry out experimentally, sulfite oxidation should always be considered as a possible test system, subject to actual demonstration, in cases where a substitute is needed for the actual process under consideration. For example, Karow et al. (K2) and others have applied sulfite oxidation successfully to fermentation situations. [Pg.167]

The code prescribes minimum requirements for the materials, design, fabrication, assembly, support, erection, examination, inspection, and testing of piping systems subject to pressure or vacuum. The scope of the piping covered by B31.3 is illustrated in Fig. 10-124. It applies to all fluids including fluidized sohds and to all seivdces except as noted in the figure. [Pg.946]

Many different test systems have been used to investigate the ability of chemicals to interact with components of the endocrine system. The usefulness and applicability of the available methods has been the subject of much debate. Four key texts are particularly helpful in reviewing and giving guidance on currently available test methods and strategies for testing EDs. ... [Pg.16]

Test substance (EPA) A substance or mixture administered or added to a test system in a study, in which the substance or mixture 1) is the subject, or contemplated subject, of an application for a research or marketing permit, or 2) is an ingredient or product of a substance as defined above. [Pg.488]

In all the paint systems tested in the atmosphere, the presence of the chloride contaminant at its highest concentration, causes the appearance of small blisters. Such blisters may in time burst due to the oxide built-up inside them, as was seen in the case in the CR system ("Table III.") In the P system ("Table III."), the blistering seen with the third level of chlorides continues after two years outdoor exposure, without rust coming through the coating. This same effect is also seen in salt fog test panels, but it does not appear in those test specimens subjected to accelerated weathering tests. [Pg.97]

From our laboratory cultures of ]P. brevis, we are able to purify to homogeneity and crystallinity two toxins, namely T17 and T34(, ). Both toxins have been subjected to a variety of in vivo and in vitro test systems in order to ascribe specific actions to each(10-13). [Pg.360]

Specific tests of the detonation sensitivity of LP are not very different from those used with liq explosives, but the interpretation of LP sensitivity tests is subject to large uncertainties. This is so, because practical considerations dictate that relatively small amounts of LP be tested, but for many LP systems the increase in sensitivity with increasing test sample amount is not known Tannenbaum Beardell (Ref 30, p 344) suggest the following routine tests ... [Pg.601]

Utility tests. By definition, these are actual food formulations copying accepted food preparations. As mentioned above, when Model Tests are designed, the range of products undergoing the test should be wide enough to include some failures. In some cases, a Utility Test is employed that substitutes objective evaluation systems for sensory ones. This reduces the time of the test and its cost. However, only those objective tests previously found to be well correlated with sensory tests should be employed. Eventually a sensory test has to be performed. No food product should be marketed without a final utility test employing subjective evaluations. [Pg.11]

Incongruities such as the dream character who has the physical attributes of one person that we know and the face of another illustrate an indiscriminate but perhaps functionally significant over-inclusiveness in the categories of unconscious memory systems. We can get at this process by using semantic memory tests of subjects awakened from REM and tested both immediately and later when the sleep inertia is over. Compared to waking and to NREM sleep, we find the expected REM enhancement of weak primes (i.e., loose associations) but, to our surprise, not of strong primes (strong associations). [Pg.121]

Although not yet available, it is likely that Web-based performance testing systems will become available in the near future. Web-based systems will permit selected tasks to be presented on computers equipped with appropriate Web browser software. Hardware requirements include Internet access and appropriate memory and software to support Web-based applications. Depending on the design of the Web-based system, it is could be possible to tailor the specific tasks presented for the performance testing system from a menu of options. Alternatively, testing systems consisting of a standardized array of tasks can also be chosen. As such, the start-up costs of Web-based systems should be lower than with personal or handheld computer systems. Subject identification, date, and time can be recorded at the start of a test, and data from multiple subjects and test occasions can be stored in a central file for easy access to the data. [Pg.105]

Dissolution rate improvement may be beneLcial for producing readily dissolved solids for parenteral or oral administration of drugs subject to hydrolysis. For solid oral dosage forms, the initial rate increase can be sufLcientto alterthe amount of drug that enters the blood and improve the there peutic potency. Unlikan vitro test systems, the concentration in the Gl cavity may never approach... [Pg.540]

Test Account Setup and Approval. The account application is reviewed by the FDA ESG Administrator. The Administrator verifies that a letter of nonrepudiation agreement is on file, that the digital certificate conforms to the X.509 version 3 standard, and that all data fields in the Issuer and Subject fields are completed (see Appendix A, Digital Certificates for more information). The Administrator will also communicate with the Transaction Partner to confirm the application information. If these conditions are met, a test account is set up, and connections to the FDA ESG test system are established before the submitting organization is approved as a Transaction Partner. [Pg.13]

Although the subject is in its infancy, it is already clear that a substantial fraction, possibly a majority, of spontaneous mutations in Drosophila have such a cause. If that turns out to be true and generalizable to mammals (there is reason to believe that such elements are present in mice and humans), it will require a revision in our thinking about mutation and mutagens, and it would mean that the kinds of mutagenic mechanisms discussed in this report account for only a part of the spontaneous-mutation rate. On the one hand, we can conclude optimistically that classical mutagens are relatively less important. On the other hand, we cam assume pessimistically that chemicals not detectable with existing test systems increase the rate of transposon-induced mutations. [Pg.229]


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Test systems

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