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Intermediate absorber

Panels of multi-resonator material are made from perforated plate sandwiched with solid plate and an intermediate absorber layer between them. These panels can be built up in enclosures, taking care to seal all junctions adequately. Typically, these enclosures are made to surround small machines (e.g. compressors). They may be fitted together with spring catches to allow for dismantling for maintenance purposes. [Pg.659]

During this study, an intermediate absorbing at 425 m/i was detected and shown in a further study to be a dimer (VOV " ), with nearly two-thirds of the V(IV)-V(II) reaction proceeding via this species in an inner-sphere step, the remainder reacting via an outer-sphere pathway. The mechanism proposed for the reaction was... [Pg.79]

Michael and Hart10 found that the reaction of OH radicals (formed by pulse radiolysis of aqueous solutions saturated with N20) with 1,3- and 1,4-cyclohexadienes leads to formation of an intermediate absorbing at 310 nm. In the case of 1,4-cyclohexadiene, another band at A, < 240 nm was also found. In this system there are both H atoms and OH radicals, however the yield of the OH radicals is 10 times higher than that of the H- atoms. Michael and Hart10 assumed that the band at 310 nm is due to CeWi ... [Pg.328]

The pharmacokinetic profile is different with different compounds. Diazepam after oral administration is completely and rapidly absorbed from the proximal small intestine. Oxazepam is least rapidly absorbed while lorazepam is an intermediately absorbed between these two. They are metabolised in liver by dealkylation and hydroxylation and excreted in urine as glu-curonide conjugates. They cross the placental barrier and are secreted in milk. [Pg.71]

The difference between the RSA process and two-photon absorption is that the two-photon absorption is virtually instantaneous whereas processes involving intermediate absorbing states exhibit certain kinetic behavior,... [Pg.357]

When chloroform was y-ray irradiated in water at pH 6.5 by Getoff [14], formaldehyde was generated with G = 0.025 fimol. 1 1. The formaldehyde concentration increased to a maximum at intermediate absorbed dose, and then decreased with increasing irradiation. Presumably, with continued irradiation it was mineralized to C02 and H20. Only traces of unidentified carboxylic acids were observed as organic products. Similar results were obtained for methylene chloride [14]. [Pg.323]

Conversion II Second pass conversion of S02 to SO3 after reheating the gases from intermediate absorber and subsequent heat removal in a heat exchanger. [Pg.120]

In double absorption plants an intermediate absorber is placed between the second and third (or between the third and fourth) converter beds. By removing S03 from the gas stream at this intermediate point, higher S02 conversions are attained in the downstream converter beds, and the overall S02 conversion is increased. The cooled gas from the intermediate absorber is reheated by hot converter gas in gas-gas heat exchangers before returning to... [Pg.1177]

Fig. 25.11. Sankey energy flow diagram for a 1000ton/day sulfur-burning double absorption sulfuric acid plant (feed gas 10% S02). A Blower B Sulphur furnace C Waste heat boiler D Catalyst bed 1 E Steam superheater F Catalyst bed 2 G Boiler H Catalyst bed 3 J Intermediate heat exchangers K Intermediate absorber L Converter bed 4 M Economizer N Final absorber O Air dryer P Acid coolers. (Courtsey Lurgi GmbH, Frankfurt, Germany.)... Fig. 25.11. Sankey energy flow diagram for a 1000ton/day sulfur-burning double absorption sulfuric acid plant (feed gas 10% S02). A Blower B Sulphur furnace C Waste heat boiler D Catalyst bed 1 E Steam superheater F Catalyst bed 2 G Boiler H Catalyst bed 3 J Intermediate heat exchangers K Intermediate absorber L Converter bed 4 M Economizer N Final absorber O Air dryer P Acid coolers. (Courtsey Lurgi GmbH, Frankfurt, Germany.)...
Chemical in South Korea in 1987.38 39 The process is based on 310 stainless steel, which resists corrosion in 98.5 percent H2S04 at temperatures up to 220°C. The intermediate absorber at Namhae takes 194°C gas from the converter third stage economizer and absorbs the S03 in 199°C, 99 percent acid. Recirculated acid from the absorber is cooled from 220°C in a 10-bar HRS boiler. The added energy recovery for this process is reported to increase the total recovery to 90 percent. Monsanto s proposed Monarch process combines HRS technology with the wet catalytic converter process (Lurgi) to increase heat recovery and shift it to high-pressure steam production for electric power generation.36... [Pg.1179]

Fennentation is an example of a substrate-level phosphorylation process that uses intermediate absorbers such as formaldehyde. Substrate-level phosphorylation is inefhcient and produces only a few molecules of ATP. [Pg.676]

As pointed out earlier, the equivalent circuit shown in Fig. 4A is meant to represent the simplest situation only. It does not take into account factors such as mass transport, heterogeneity of the surface and the occurrence of reaction intermediates absorbed at the surface. Some of these factors are discussed later. Even in the simplest cases, in which this circuit does represent the response of the interphase to an electrical perturbation reasonably well, one should bear in mind that... [Pg.328]

Use Intermediate, absorbent in surgical dressings, rubber compounding. [Pg.1346]

One of the earliest demonstrations by ESR of the peroxidase oxidation of drugs involved the tranquilizer, chlorpromazine [171]. The stoichiometry of the reaction forming the chlorpromazine radical cation (13) was established, and kinetics of the transient radical were shown to be identical to those of an optically detected intermediate absorbing at 530 nm. Measurements were made of the pH-dependent radical dismutation rate and the rate of reaction of compound II with chlorpromazine. At high enzyme concentrations and low dismutation rates, the radical cation undergoes further oxidation by the enzyme, to form the thionium ion. [Pg.106]

The proposed intermediate (189) connecting the 2- and 3-pyridylcarbenes was not observed, but in further studies229,230 a novel intermediate absorbing at 1935 cm-1 was produced on long wavelength irradiation of 3-pyridyl-carbene. This intermediate was assigned the zwitterionic structure 190 and was photochemically converted to 187 and then to 183 without further intermediates being detectable by IR spectroscopy. Thus, 190 occupies the... [Pg.287]

Sundberg and co-workers in 1974 reported results from flash photolysis studies of the reaction of phenyl azide with secondary amines [26]. Irradiation of the azide in hexane solution produced an intermediate absorbing strongly at 366 nm and having a lifetime of about 5 ms. This intermediate was found to react with amines to give, after tautomerization, the 3H-azepine that is obtained in preparative scale reactions. On the basis of these results, De Graff et al. [26] concluded that the detected intermediate is not a nitrene but is a closed-shell intermediate, either benzazirine or dehydroazepine. [Pg.77]

Synthetic Control as a Probe of Mechanism. In certain systems, synthetic control of very subtle power is possible. The oxidation of water to dioxygen by Ru(bpy)3 has long (15-17) been of interest because this process is one putative step in the use of Ru(bpy)3 to mediate the photodecomposition of water into its elements. In the reaction of Ru(bpy)3 with water/hydroxide ion, electron transfer to produce Ru(bpy)3 + OH can be postulated as an elementaiy step. The OH would be expected to add rapidly to the aromatic ring to yield Ru(bpy)2(bpyOH). Studies of the Ru(bpy)3 + OH- reaction by stopped-flow techniques reveal an intermediate absorbing at long wavelengths. To test whether this species might be the OH-radical adduct, pulse radiolysis was used to study the reaction of OH with Ru(bpy)3. ... [Pg.239]

Fig. 46. Electronic absorption spectrum for SHMT in the presence of glycine (curve 1). Note the formation of the quinonoid intermediate absorbing at 495 nm, the extent of which is greatly increased in the presence of THFA (curve 2) (see section on SHMT). Fig. 46. Electronic absorption spectrum for SHMT in the presence of glycine (curve 1). Note the formation of the quinonoid intermediate absorbing at 495 nm, the extent of which is greatly increased in the presence of THFA (curve 2) (see section on SHMT).
Figure 18-9 Precision of replicate absorbance measurements with a diode array spectrometer at 350 nm with a dichromate solution. Filled circles are from replicate measurements in which the sample was not removed from the cuvet holder between measurements. Open circles are from measurements in which the sample was removed and then replaced in the cuvet holder between measurements. Best reproducibility is observed at intermediate absorbance (4 0.3 to 2). Note logarithmic ordinate. Lines are least-squares fit of data to theoretical equations. [Data from J. Galban, S. de Marcos, I. Sanz, C. Ubide, and j. Zuriarrain,/ no/. Chem, 2007, 79,47631. Figure 18-9 Precision of replicate absorbance measurements with a diode array spectrometer at 350 nm with a dichromate solution. Filled circles are from replicate measurements in which the sample was not removed from the cuvet holder between measurements. Open circles are from measurements in which the sample was removed and then replaced in the cuvet holder between measurements. Best reproducibility is observed at intermediate absorbance (4 0.3 to 2). Note logarithmic ordinate. Lines are least-squares fit of data to theoretical equations. [Data from J. Galban, S. de Marcos, I. Sanz, C. Ubide, and j. Zuriarrain,/ no/. Chem, 2007, 79,47631.
Figure 7.9 Typical conversion versus temperature curve for a 3+1 double absorption converter. There are three catalyst beds before the intermediate absorber... Figure 7.9 Typical conversion versus temperature curve for a 3+1 double absorption converter. There are three catalyst beds before the intermediate absorber...

See other pages where Intermediate absorber is mentioned: [Pg.360]    [Pg.105]    [Pg.424]    [Pg.66]    [Pg.287]    [Pg.257]    [Pg.174]    [Pg.1177]    [Pg.1178]    [Pg.156]    [Pg.70]    [Pg.306]    [Pg.76]    [Pg.220]    [Pg.237]    [Pg.237]    [Pg.676]    [Pg.424]    [Pg.190]    [Pg.384]    [Pg.47]    [Pg.105]    [Pg.566]    [Pg.134]    [Pg.323]    [Pg.18]    [Pg.451]    [Pg.7]   
See also in sourсe #XX -- [ Pg.38 ]




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