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Oxygen exposure

Activated carbons contain chemisorbed oxygen in varying amounts unless special cate is taken to eliminate it. Desired adsorption properties often depend upon the amount and type of chemisorbed oxygen species on the surface. Therefore, the adsorption properties of an activated carbon adsorbent depend on its prior temperature and oxygen-exposure history. In contrast, molecular sieve 2eohtes and other oxide adsorbents are not affected by oxidi2ing or reducing conditions. [Pg.277]

Despite all these safeguards to extend the service life of the antifreeze, fluid replacement is requited periodically. Typically, fluids are replaced because of irreversible damage caused by one of four conditions contamination, gel formation because of glycol/siUcate reaction, extensive glycol degradation caused by overheating or excessive oxygen exposure, or inhibitor depletion. [Pg.190]

Fig. 5.15. STM image of a Si (111)-7x7 surface exposed to 0.2 L of O2 at 300 K. The sample bias voltage was 2 V. Dark and bright sites generated by oxygen exposure are marked with A and B, respectively [5.41]. Fig. 5.15. STM image of a Si (111)-7x7 surface exposed to 0.2 L of O2 at 300 K. The sample bias voltage was 2 V. Dark and bright sites generated by oxygen exposure are marked with A and B, respectively [5.41].
Figure 4.44. Comparison of the oxygen TPD spectra from Ag deposited on YSZ obtained with the three different modes of adsorption, gaseous, electrochemical and mixed, under the same conditions. TadS=300°C, 5.4 kL of oxygen exposure (for gaseous and mixed adsorption), and 4.6x1 O 9 mol O of electrochemically supplied oxygen (for electrochemical and mixed adsorption), i.e. 5 pA for 180 s. (UWR=+0.7 V, A=+1.3 eV).31 Reprinted with permission from Academic Press. Figure 4.44. Comparison of the oxygen TPD spectra from Ag deposited on YSZ obtained with the three different modes of adsorption, gaseous, electrochemical and mixed, under the same conditions. TadS=300°C, 5.4 kL of oxygen exposure (for gaseous and mixed adsorption), and 4.6x1 O 9 mol O of electrochemically supplied oxygen (for electrochemical and mixed adsorption), i.e. 5 pA for 180 s. (UWR=+0.7 V, A<J>=+1.3 eV).31 Reprinted with permission from Academic Press.
Figure 5.21. Experimental setup (inset) showing the location of the working (WE), counter (CE) and reference (RE) electrodes and of the heating element (HE) thermal desorption spectra after gaseous oxygen dosing at 673 K and an 02 pressure of 4x1 O 6 Torr on Pt deposited on YSZ for various exposure times. Oxygen exposure is expressed in kilo-langmuirs (1 kL=l0 3 Torrs). Desorption was performed with linear heating rate, ()=1 K/s.4 S Reprinted with permission from Academic Press. Figure 5.21. Experimental setup (inset) showing the location of the working (WE), counter (CE) and reference (RE) electrodes and of the heating element (HE) thermal desorption spectra after gaseous oxygen dosing at 673 K and an 02 pressure of 4x1 O 6 Torr on Pt deposited on YSZ for various exposure times. Oxygen exposure is expressed in kilo-langmuirs (1 kL=l0 3 Torrs). Desorption was performed with linear heating rate, ()=1 K/s.4 S Reprinted with permission from Academic Press.
Two ferredoxins have been isolated from Desulfomicrobium bacula-tum (Dsm. baculatum) strain Norway 4 (64, 65). Dsm. baculatum ferredoxin I (59 amino acids, 6 cysteines) has one conventional [4Fe-cluster. Dsm. baculatum Fdll, the most acidic, is very unstable toward oxygen exposure and contains 2 X [4Fe-4S] cores in a polypeptide chain of 59 amino acids and 8 cysteines (66, 67). [Pg.371]

After 120 s oxygen exposure (500 C), all of the dynamometer-aged Pd-based catalysts gave oxygen up es that could be accounted for by tfie formation of bulk PdO. [Pg.366]

Figure 2.1 Real-time photoemission study (hv = 6.2 eV) of the interaction of oxygen (Po2 = 10- Torr) with a nickel surface at 300 K. The photocurrent decreases initially (A B), then recovers (B-C), before finally decreasing (CD). Surface reconstruction occurs (B-C) with further support from studies of the work function. The work function measured by the capacitor method15 increases by 1.5 eV with oxygen exposure at 80 K followed by a rapid decrease on warming to 295 K and an increase on further oxygen exposure at 295 K. These observations suggest that three different oxygen states are involved in the formation of the chemisorbed overlayer. (Reproduced from Refs. 15, 42). Figure 2.1 Real-time photoemission study (hv = 6.2 eV) of the interaction of oxygen (Po2 = 10- Torr) with a nickel surface at 300 K. The photocurrent decreases initially (A B), then recovers (B-C), before finally decreasing (CD). Surface reconstruction occurs (B-C) with further support from studies of the work function. The work function measured by the capacitor method15 increases by 1.5 eV with oxygen exposure at 80 K followed by a rapid decrease on warming to 295 K and an increase on further oxygen exposure at 295 K. These observations suggest that three different oxygen states are involved in the formation of the chemisorbed overlayer. (Reproduced from Refs. 15, 42).
At high oxygen exposures at 295 K, the surface consists predominantly of hexagonal structures, but also present as a minor component are square lattice structures (Figure 4.10) reminiscent of the cubic structure associated with MgO smoke formed by the oxidation of magnesium at high temperature.20 Therefore, two pseudomorphic oxide overlayers form at Mg(0001) at room temperature, but what factors control their separate growth are not known. [Pg.59]

Figure 4.10 With increasing oxygen exposure at 295 K, the Mg(0001) surface consists of both hexagonal and square lattice structures the line profiles indicate repeat distances of 0.321 and 0.56 nm in the atom resolved hexagonal and square structures, respectively, the former being the most prevalent structure present. (Reproduced from Ref. 41). Figure 4.10 With increasing oxygen exposure at 295 K, the Mg(0001) surface consists of both hexagonal and square lattice structures the line profiles indicate repeat distances of 0.321 and 0.56 nm in the atom resolved hexagonal and square structures, respectively, the former being the most prevalent structure present. (Reproduced from Ref. 41).
Figure 5.7 STM images (180 x 170 A) taken during the exposure of a Pt(lll)-0 adlayer (oxygen exposure 3 L) to carbon monoxide at 247 K and a pressure of 5 x 10 x Torr. (Reproduced from Ref. 27). Figure 5.7 STM images (180 x 170 A) taken during the exposure of a Pt(lll)-0 adlayer (oxygen exposure 3 L) to carbon monoxide at 247 K and a pressure of 5 x 10 x Torr. (Reproduced from Ref. 27).
L oxygen exposure with a (2 x 1) structure present image (b) is after 42 L oxygen exposure with both (2 x 1) and (3 x 1) states present line profiles of the rows running in the < 100 > direction also shown, inter-row spacings are twice and three times the Cu-Cu distance in the < 110 > direction (c). Also shown is the image of a c(6 x 2) structure present as a minor component (b, d). (Reproduced from Ref. 16). [Pg.110]

Radialene (2) can be stored at —78°C, but undergoes dimerization and polymerization reactions in solution at room temperature neat 2 may even start to burn at this temperature39. It is also very sensitive towards oxygen exposure to air leads to an intractable material containing up to 40% oxygen. [Pg.945]

Figure 6. Peak-to-peak oxygen Auger signal (517 eV) as a junction of oxygen exposure to polycrystalline Pt at 370 K. Oxygen pressures (Pa) are 1.13 X 10 6 1.29 X 10 6 ( 7), 2.93 X... Figure 6. Peak-to-peak oxygen Auger signal (517 eV) as a junction of oxygen exposure to polycrystalline Pt at 370 K. Oxygen pressures (Pa) are 1.13 X 10 6 1.29 X 10 6 ( 7), 2.93 X...
Torr of water vapor or oxygen exposures over 1,000L the 2/2 LEED pattern was observed on Cu(100) and the c(6X2) was observed on Cu(110). There was increased diffuse intensity in these patterns over those resulting from exposure to pure oxygen, but the symmetry was distinct. No elements, other then oxygen and copper, were evidenced by Auger spectroscopy. [Pg.106]

Gelinas, Y., J.A. Baldock, and J.I. Hedges. 2001a. Organic carbon composition of marine sediments Effect of oxygen exposure on oil generation potential. Science 294 (5540) 145-148. [Pg.117]

Fig. 24. Plot of the dependence of the products of CH3OD oxidation on Ag(llO) on the prior exposure of the surface to 02- HjCO and CH3OH form at low oxygen exposures, whereas COj and HCOOCH3 grow in only at higher exposures (137). Reprinted with permission of North-Holland Publishing Company, Amsterdam, 1978. Fig. 24. Plot of the dependence of the products of CH3OD oxidation on Ag(llO) on the prior exposure of the surface to 02- HjCO and CH3OH form at low oxygen exposures, whereas COj and HCOOCH3 grow in only at higher exposures (137). Reprinted with permission of North-Holland Publishing Company, Amsterdam, 1978.
The spectra obtained are completely reversible during observation times of under one hour. For longer time periods of oxygen exposure in the dark, the DC offset signal increases slowly, 5-10 5 of the Langmuir isotherm value per hour. It increases more quickly if the porphyrin films are heated for several minutes with a heat gun, while under oxygen. [Pg.335]

Although CO2 is nontoxic, exposure to a high concentration can cause asphyxiation due to lack of oxygen. Exposure to 5 to 10% volume in air can be fatal. [Pg.186]

Figure 5. Effect of ion bombardment on the decay rate of a 1-D grating of period 17 pm on An (100) at 993C. The ion damage greatly accelerates the decay either by formation of surface defects or by removing the impurities. Similar effects are produced by oxygen exposure. The ordinate is proportional to the grating amplitude. Figure 5. Effect of ion bombardment on the decay rate of a 1-D grating of period 17 pm on An (100) at 993C. The ion damage greatly accelerates the decay either by formation of surface defects or by removing the impurities. Similar effects are produced by oxygen exposure. The ordinate is proportional to the grating amplitude.
The topographs of the Si(lll)-7 X 7 surface after oxygen exposure are studied with a bias of +2 V, that is, probing the unoccupied states. As shown in Fig. 16.9, after an exposure of —0.2 L of oxygen to the clean Si(lll)-7X7 surface, two new sites are observed by STM a dark site such as those... [Pg.334]


See other pages where Oxygen exposure is mentioned: [Pg.428]    [Pg.57]    [Pg.47]    [Pg.364]    [Pg.365]    [Pg.109]    [Pg.59]    [Pg.54]    [Pg.57]    [Pg.90]    [Pg.173]    [Pg.331]    [Pg.10]    [Pg.12]    [Pg.26]    [Pg.112]    [Pg.33]    [Pg.78]    [Pg.78]    [Pg.79]    [Pg.91]    [Pg.328]    [Pg.330]    [Pg.337]    [Pg.316]    [Pg.29]    [Pg.128]    [Pg.135]    [Pg.136]    [Pg.143]   
See also in sourсe #XX -- [ Pg.23 ]

See also in sourсe #XX -- [ Pg.94 ]

See also in sourсe #XX -- [ Pg.23 ]




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