Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Stability strict

For microporous compounds with special compositions, calcination effects are even more severe. As compared with zeolites, these compounds have lower thermal stability. Strictly speaking, most of them are nonporous since removal of the occluded guest molecules by calcination usually results in collapse. This is due to strong H-bonds with the framework, coordination bonds, and sometimes the templating molecule is shared with the inorganic polyhedra. Relevant examples of low-stability microporous compounds with interesting structural features are zeolitic open-framework phosphates made of Ga [178], In [179], Zn [180], Fe [181],... [Pg.133]

All the residues involved in important functions in the catalytic mechanism are strictly conserved in all homologous GTPases with one notable exception. Ras does not have the arginine in the switch 1 region that stabilizes the transition state. The assumption that the lack of this catalytically important residue was one reason for the slow rate of GTP hydrolysis by Ras was confirmed when the group of Alfred Wittinghofer, Max-Planck Institute,... [Pg.260]

Having determined tlie stability class. Figs. 12.6.2. and 12.6.3. may be used to evaluate ay and a as a function of downwind distance from tlie source. Figures 12.6.2. and 12.6.3. apply strictly to open, level country and probably underestimate tlie plume dispersion potential from low level sources in built-up areas. Altliough tlie vertical spread may be less than tlie values for class F witli... [Pg.375]

Because of the differing focus of interest in these elements their chemistries have not developed in parallel and the data on which strict comparisons might be based are not always available. Nevertheless many of the similarities and contrasts expected in the chemistry of transition elements are evident in this triad. The relative stabilities of different oxidation states in aqueous, acidic solutions are summarized in Table 24.2 and Fig. 24.1. [Pg.1044]

The reaction is strictly intramolecular the migrating group R is never completely released from the substrate. The driving force is the formation of the more stable rearranged carbenium ion 4, that is stabilized by the hydroxy substituent. The... [Pg.229]

EDTA is a very unselective reagent because it complexes with numerous doubly, triply and quadruply charged cations. When a solution containing two cations which complex with EDTA is titrated without the addition of a complex-forming indicator, and if a titration error of 0.1 per cent is permissible, then the ratio of the stability constants of the EDTA complexes of the two metals M and N must be such that KM/KN 106 if N is not to interfere with the titration of M. Strictly, of course, the constants KM and KN considered in the above expression should be the apparent stability constants of the complexes. If complex-forming indicators are used, then for a similar titration error KM/KN z 108. [Pg.312]

What are they like to eat Humans are particular about the organoleptic properties of their food. Microbial cells may have little taste or smell, or even smell or taste unpleasantly to some people. The texture may not be the same as in conventional foods, particularly with unicellular organisms. These draw-backs can be overcome by adding a proportion of SCP to manufactured foods. However, even when SCP is incorporated into manufactured foods it may not have suitable characteristics such as stability, ability to bind water or fats, or ability to form gels, emulsions or foams. SCP for feed does not have to meet such strict requirements. [Pg.64]

An alternative mechanism by which additives may protect polymers from photo-oxidation is radical trapping. Additives which operate by this mechanism are strictly light stabilizers rather than antioxidants. The most common materials in this class are the hindered amines, which are the usual additives for the protection of poly (ethylene) and poly (propylene). The action of these stabilisers is outlined in Reactions 8.3-8.5. [Pg.124]

Research reports—Research reports such as stability reports, method validation and transfer reports, and pharmaceutical development reports are key documents used for NDA/MAA filings. These documents are strictly version controlled. [Pg.63]

IV, CCR and oxidation stability are three strictly co-related parameters. As a general rale, the reduction of IV (on the same feedstock) dramatically improves the oxidation stability. On the contrary the distillation step removes the main part of naturally occurring antioxidants. For this reason, even after hydrogenation the Rancimat induction time (as measured according to the EN 14112 standard) of the hydrogenated sample does not fulfill the EN 14214 requirement for oxidation stabihty (6 hours at 110°C), 4 hours being the measured induction period. [Pg.275]

It was shown that complexes 19 of the zwitterionic precursors of ortho-quinone methides and a bis(sulfonium ylide) derived from 2,5-di hydroxyl 1,4 benzoquinone46 were even more stable than those with amine N-oxides. The bis(sulfonium ylide) complexes were formed in a strict 2 1 ratio (o-QM/ylide) and were unaltered at —78 °C for 10 h and stable at room temperature under inert conditions for as long as 15—30 min (Fig. 6.18).47 The o-QM precursor was produced from a-tocopherol (1), its truncated model compound (la), or a respective ortho-methylphenol in general by Ag20 oxidation in a solution containing 0.50-0.55 equivalents of bis(sulfonium ylide) at —78 °C. Although the species interacting with the ylide was actually the zwitterionic oxidation intermediate 3a and not the o-QM itself, the term stabilized o-QM was introduced for the complexes, since these reacted similar to the o-QMs themselves but in a well defined way without dimerization reactions. [Pg.181]


See other pages where Stability strict is mentioned: [Pg.119]    [Pg.119]    [Pg.325]    [Pg.182]    [Pg.10]    [Pg.306]    [Pg.123]    [Pg.161]    [Pg.364]    [Pg.777]    [Pg.219]    [Pg.132]    [Pg.342]    [Pg.13]    [Pg.584]    [Pg.1006]    [Pg.141]    [Pg.822]    [Pg.847]    [Pg.652]    [Pg.442]    [Pg.386]    [Pg.75]    [Pg.203]    [Pg.253]    [Pg.43]    [Pg.153]    [Pg.474]    [Pg.309]    [Pg.584]    [Pg.1006]    [Pg.38]    [Pg.209]    [Pg.163]    [Pg.337]    [Pg.183]    [Pg.218]    [Pg.259]    [Pg.57]    [Pg.278]    [Pg.27]   
See also in sourсe #XX -- [ Pg.157 ]




SEARCH



Strict

Strictly

© 2024 chempedia.info