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Photo examination

In methods involving image formation there is a common factor. Radiation normally propagated in rectilinear fashion, such as light or an electron beam, is interrupted by the particles under examination, and the pattern of the interruption can be observed in different ways, eg, optically or photo-electrically... [Pg.531]

Flares. A flare compn is described in Refs 15 16 contg powd Mg, Na perchlorate, and a binder which can be cast and cured, and which has a luminous intensity of 50,500 candle-secs/g Incendiaries. A mixt of 1 OOg of Na perchlorate and 58.7g of powd Al has a Qr of 2751cal/g and can be used as a filler for incendiary bombs (Ref 6). A proc is described in Ref 14 for coating Na perchlorate with Al, and the use of the coated material in incendiaries Photo flash Compositions. Mixts of 80% Ca metal and 20% Na perchlorate and 80% Ca, 10% Na perchlorate, and 10% Na nitrate have been examined as expl photoflash compns for both sea level and high altitude use (Ref 13) Refs 1) Gmelin, System No 21 (1928), 408 Supp Part 1 (1964), 180 2) H.H. Willard ... [Pg.645]

PBE dendrons bearing a focal bipyridine moiety have been demonstrated to coordinate to Ru + cations, exhibiting luminescence from the metal cation core by the excitation of the dendron subunits [28-30]. The terminal peripheral unit was examined (e.g., phenyl, naphthyl, 4-f-butylphenyl) to control the luminescence. The Ru +-cored dendrimer complexes are thought to be photo/redox-active, and photophysical properties, electrochemical behavior, and excited-state electron-transfer reactions are reported. [Pg.200]

The (photo)electrochemical behavior of p-InSe single-crystal vdW surface was studied in 0.5 M H2SO4 and 1.0 M NaOH solutions, in relation to the effect of surface steps on the crystal [183]. The pH-potential diagram was constructed, in order to examine the thermodynamic stability of the InSe crystals (Fig. 5.12). The mechanism of photoelectrochemical hydrogen evolution in 0.5 M H2SO4 and the effect of Pt modification were discussed. A several hundred mV anodic shift of the photocurrent onset potential was observed by depositing Pt on the semiconductor electrode. [Pg.257]

Tinnemans et al.132 have examined the photo(electro)chemical and electrochemical reduction of C02 using some tetraazamacrocyclic Co(II) and Ni(II) complexes as catalysts. CO and H2 were the products. Pearce and Pletcher133 have investigated the mechanism of the reduction of C02 in acetonitrile-water mixtures by using square planar complexes of nickel and cobalt with macrocyclic ligands in solution as catalysts. CO was the reduction product with no significant amounts of either formic or oxalic acids... [Pg.369]

Examination of Eqs. (2.9-2.11) suggests that having frequency domain lifetimes measured at a variety of frequencies is desirable, as it will allow a mixture of fluorophores to be determined. With this in mind, two approaches may be taken to obtain multifrequency results. The first of these is simply to make a series of FLIM measurements while stepping through a predetermined set of frequencies. In practice, this is of limited utility for biological systems because of photo-induced damage to the specimen. [Pg.83]

Collins and Williams [30] have recently described a modification of Ehr-hardt s earlier photochemical method [57], which offers the practical advantages of speed, convenience, and the potential for real-time analyses. However, until the accuracy of the results is established, the method will not receive general acceptance. Collins and Williams [30] examined the completeness of oxidation of their photo-oxidation system using three independent methods, but pointed out that while essentially complete oxidation was indicated, definitive proof was lacking. A more satisfactory solution to the problem might be found through comparison of results of the photo-oxidation method with the dry-combustion method, which most analysts are willing to accept as complete [96]. [Pg.493]

In Section I the sensitivity of conjugated systems to possible photo-dissociation (PD) was mentioned. If this PD is conducted in the ionization chamber of a mass spectrometer, a PDPI/MS (photo-dissociation, photo-ionization/mass spectrometry) can be measured7. The examination of the PDPI/MS spectra of hexa-1,3-, 1,4-, 1,5- and 2,4-dienes using 9.68 and 10.49 eV photo-ionization (PI) is summarized in Table 1. [Pg.496]

Accident facts Make detailed examinations with photos, inspections, and interviews. Establish origin of accident and facts relevant to layered causes and recommendations. Record extent of damage, and hypothesize the sequence of events. Resist development of potential causes to maintain momentum and objectivity while collecting data. [Pg.519]

Several Ru(III) salen complexes of the type Ruin(salen)(X)(NO) (X=C1-, ONO-, H20 salen = N,AP-bis(salicylidene)-ethylenediamine dianion) have been examined as possible photochemical NO precursors (19). Photo-excitation of the Rum(salen)(NO)(X) complex labilizes NO to form the respective solvento species Ruin(salen)(X)(Sol). The kinetics of the subsequent back reactions to reform the nitrosyl complexes (e.g. Eq. (8)) were studied as a function of the nature of the solvent (Sol) and reaction conditions. The reaction rates are dramatically dependent on the identity of Sol, with values of kNO (298 K, X = C1-) varying from 5 x 10-4 M-1 s-1 in acetonitrile to 4 x 107 M-1 s-1 in toluene, a much weaker electron donor. In this case, Rum Sol bond breaking clearly... [Pg.207]

In this section, results of Photo Electron Spectroscopy (PES) as well as infrared spectroscopy shall be examined in terms of n— a interactions. [Pg.183]

We next examine the possible fates of the alkoxy radical produced as a result of hydroperoxide fragmentation. It should be noted that the other fragment produced in this process, an hydroxy radical (not shown), would be an extremely reactive species. Since it is not attached to a polymer chain end, it is also capable of more readily diffusing through the polymer matrix than most of the radicals discussed to this point. This also makes the photo-oxidation of the glycol potentially more destructive. [Pg.633]

Try to obtain a sample of your material, to examine its physical properties. If this is not possible, find illustrations or photos of the material from books, magazines, or the Internet. You will need materials for your presentation, which may include charts, a poster, models, pictures, or pamphlets. [Pg.212]

Finally these compounds may also present in the future some interest in the area of novel anti-tumor drugs, or in photochemotherapy [12], Up to now the mechanism of action of the Pt complexes as antineoplastic agents has been extensively examined [13]. In spite of their successful applications, there is a need in compounds that are less toxic than the Pt derivatives. Therefore novel photo-active metallic compounds could offer future possibilities for cancer treatment. The fact that a drug would become active exclusively under illumination might represent an advantage. [Pg.28]

It should be stressed that for the TAP and HAT Ru(II) complexes, although their modes of binding has been examined by luminescence spectroscopy, the nature of the excited species responsible for the photo-electron transfer (i.e. intercalated or surface bound) and the site specificity of these photoreactions, is not known at present. [Pg.53]


See other pages where Photo examination is mentioned: [Pg.311]    [Pg.404]    [Pg.507]    [Pg.280]    [Pg.193]    [Pg.26]    [Pg.242]    [Pg.269]    [Pg.283]    [Pg.195]    [Pg.27]    [Pg.295]    [Pg.408]    [Pg.410]    [Pg.427]    [Pg.697]    [Pg.55]    [Pg.47]    [Pg.206]    [Pg.860]    [Pg.46]    [Pg.47]    [Pg.52]    [Pg.192]    [Pg.207]    [Pg.217]    [Pg.3]    [Pg.353]    [Pg.110]    [Pg.215]    [Pg.183]    [Pg.499]    [Pg.195]    [Pg.105]    [Pg.192]   


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