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Condensation of H2O

Sulfur tolerances of the zeolite SCR catalysts (20/50 mesh size) were determined in a fixed-bed flow reactor system with a reaction mixture containing 500 ppm of NO, 1,000 ppm of C2H4 or 2,000 ppm of C3HJ, 4.2% of Oj, 1,000 ppm SO2 and He (balance). To observe the simultaneous effect of both SOj and HjO on the removal reaction, 7.3% H2O was also fed to the reaction system in addition to die reactants described above. H2O was injected to the feed gas stream by bubbling He into a water saturator with a small-pore frit immers in deionized water. To avoid condensation of H2O vapor after the bubbler, reactor lines were heated to a temperature higher than the saturation temperature of the feed gas stream including H2O. A gas flow rate of 300 cmVmin was employed for the present study, corresponding to a space velocity of 13,200 h . [Pg.214]

C8H10N4O2. An alkaloid occurring in tea, coffee and guarana, from which it may be prepared by extraction, It is also manufactured by the methylation of theobromine and by the condensation of cyanoacetic acid with urea. Crystallizes with H2O or anhydrous from organic solvents. M.p. (anhydrous) 235"C, sublimes at 176 C. Odourless, and with a very bitter taste. Caffeine acts as a stimulant and diuretic, and is a constituent of cola drinks, tea and coffee. [Pg.75]

LY311727 is an indole acetic acid based selective inhibitor of human non-pancreatic secretory phospholipase A2 (hnpsPLA2) under development by Lilly as a potential treatment for sepsis. The synthesis of LY311727 involved a Nenitzescu indolization reaction as a key step. The Nenitzescu condensation of quinone 4 with the p-aminoacrylate 39 was carried out in CH3NO2 to provide the desired 5-hydroxylindole 40 in 83% yield. Protection of the 5-hydroxyl moiety in indole 40 was accomplished in H2O under phase transfer conditions in 80% yield. Lithium aluminum hydride mediated reduction of the ester functional group in 41 provided the alcohol 42 in 78% yield. [Pg.150]

A synthesis of 2-alkyl-2,3-dihydro-y-pyrones (187) from methoxybutenyne and aldehydes has been described (83TL4551). The condensation of lithiomethoxy-butenyne (184) with aldehydes at -78°C leads to the secondary alcohols 185, which form the dihydropyrones 187 via hydration of the acetylenic bond and hydrolysis of the methoxyethenyl group to the ketoenol 186 (0°C, p-TSA, THF, H2O or 30% HCIO4, 20 min) folowed by intramolecular cycloaddition. [Pg.206]

We see from this diagram that partial pressures of H2O at ordinary conditions range from very small values to perhaps 30 or 40 mbar. This corresponds to a mass concentration range up to about 25 g H20/m. In typical clouds, relatively little of this is in the condensed phase. Liquid water contents in the wettest of cumulus clouds are around a few grams per cubic meter ordinary mid-latitude stratus clouds have 0.3-1 g/m. ... [Pg.144]

Chemical interactions also occur in the condensed phases. Some of these are expected to be quite complex, e.g., the reactions of free radicals on the surfaces of or within aerosol particles. Simpler sorts of interactions also exist. Perhaps the best understood is the acid-base relationship of NH3 with strong acids in aerosol particles and in liquid water (see Chapter 16). Often, the main strong acid in the atmosphere is H2SO4, and one may consider the nature of the system consisting of H2O (liquid), NH3, H2SO4, and CO2 under realistic atmospheric conditions. Carbon dioxide is not usually important to the acidity of atmospheric liquid water (Charlson and Rodhe, 1982) the dominant effects are due to NH3 and H2SO4. The sensitivity the pH of cloud (or rainwater produced from it) to NH3 and... [Pg.152]

Methyl levulinate 679 condenses with silylated y9-alanine 680 in the presence of catalytic amounts of TsOH-H20 to give hexamethyldisiloxane 7 and the Schiff-base 681, whose O-trimethylsilyl groups are saponified by water (derived from TsOH H2O) to give, via 682, the intermediate enamine 683. Subsequent condensation of 683 with the Schiff base 681 affords, via 684, and subsequent saponification, a 4 1 mixture of olefins 685 and 686 [201, 202] (Scheme 5.64). [Pg.118]

Although the most recent modifications of the Prelog condensation of 1,3-dike-tones and 1,3,5-triketones, for example that of acetylacetone with dimethyl 1,3-acetonedicarboxylate in the presence of NaOH in H2O, afford substituted benzenes such as 1486 in up to 94% yield (Scheme 9.22) and coumarins [40], these condensations of highly substituted polyketones with the corresponding aromatic systems might also be effected in the presence of HMDS 2/TCS 14 or TMSOTf... [Pg.226]

The formation of dew and fog are consequences of this variation in relative humidity. Warm air at high relative humidity may cool below the temperature at which its partial pressure of H2O equals the vapor pressure. When air temperature falls below this temperature, called the dew point, some H2 O must condense from the atmosphere. Example shows how to work with vapor pressure variations with temperature, and our Chemistry and the Environment Box explores how variations in other trace gases affect climate. [Pg.330]

The recently discovered Ugand precursor HOB[OSi(O Bu)3]2 was prepared by the hydrolysis of BuOB[OSi(O Bu)3]2 (in CeHe) with one equiv of H2O [64]. After stirring for 1 h, the solution is frozen and the solvent is removed via lyophiUzation under reduced pressure. Purification can be achieved via subUmation (ca. 50 °C) of the dry powder under reduced pressure to give yields in excess of 85%. Although not stable in solution for extended periods (due to condensation processes), HOB[OSi(O Bu)3]2 is stable indefinitely in the solid state imder an inert atmosphere. [Pg.75]

Typical characterization of the thermal conversion process for a given molecular precursor involves the use of thermogravimetric analysis (TGA) to obtain ceramic yields, and solution NMR spectroscopy to identify soluble decomposition products. Analyses of the volatile species given off during solid phase decompositions have also been employed. The thermal conversions of complexes containing M - 0Si(0 Bu)3 and M - 02P(0 Bu)2 moieties invariably proceed via ehmination of isobutylene and the formation of M - O - Si - OH and M - O - P - OH linkages that immediately imdergo condensation processes (via ehmination of H2O), with subsequent formation of insoluble multi-component oxide materials. For example, thermolysis of Zr[OSi(O Bu)3]4 in toluene at 413 K results in ehmination of 12 equiv of isobutylene and formation of a transparent gel [67,68]. [Pg.90]

Tetraethoxysilane-water-alcohol-hydrochloric acid solutions of appropriate compositions become viscous and spinnable in the course of hydrolysis and condensation of SiCCX Hs). Fig.l shows the time change of the viscosity of a Si(0C2H5)4 solution with the [H2O]/... [Pg.346]

By using the classical theory of ion induced nucleation to describe the growth of radon daughters from the free activity mode to the nucleation mode, we loose information about the size of the subcritical clusters. These clusters are all lumped together between the size of a pure H2O ion cluster at 75% r.h. and the size of the critical H2O-H2SO4 cluster. The model only does keep track of the growth by condensation of the radon daughters once they arrived in the nucleation mode. [Pg.332]

The synthesis of other biologically active thiazoles was described by Ohsumi et al. [50] and is shown in Scheme 16. Condensation of phosphonium bromide and 4-methoxy-3-nitrobenzaldehyde gave a 1 1 mixture of (Z)- and (-E)-stilbenes. ( )-stilbene 64 was purified by crystallization and then converted to bromohydrin 65 by NBS-H2O. Oxidation of the bromohydrin by DMSO-TFAA gave the bromoketone intermediate 66, which was condensed with thiocarbamoyl compounds in the presence of Na2C03 in DMF to give the corresponding 2-substituted thiazole derivatives (67a and b). Compound 67a... [Pg.33]

The first modern hydrophilic nonspecific iodinated CA was diatrizoic acid, which, formulated as a sodium and/or meglumine salt, is still used. This agent was first synthesized in 1953 [1]. Osmolality for this compound, at concentrations compatible with imaging (ie. 300-370 mgl mL" ), is about 5-7 times that of plasma (1500-2100 mOsm kg H2O). Other HOCA such as iothalamate, metrizoate and ioxithalamate, were synthesized and marketed over the next few years. In an attempt to reduce the osmolality of the injected solution and thus reduce pain and haemodynamic disturbances, metrizamide, a compound resulting from the condensation of metrizoic acid and glucosamine, was synthesized. It was the first nonionic CA. [Pg.153]

The aldol formed by the aldol reaction, especially if heated, can react further. The heating causes dehydration (loss of H2O), and the overall reaction involving an aldol reaction followed by dehydration is the aldol condensation. The product of an aldol condensation, favored by the presence of extended conjugation, is an a,(3-unsaturated aldehyde (an enal) or ketone. The mechanism for dehydration (Figure 11-13) begins where the mechanism of the aldol reaction (Figure 11-12) ends. This process works better if extended conjugation results. The aldol reaction and condensation are reversible. [Pg.169]

Nature has long used reactions such as these to produce interesting solids such as cotton (seed pod), hemp (grass), and silk (cocoons for worms while they develop into moths) as fibers that we can strand into rope or weave into cloth. Chemists discovered in the early twentieth century that cellulose could be hydrolyzed with acetic acid to form cellulose acetate and then repolymerized into Rayon, which has properties similar to cotton. They then searched for manmade monomers with which to tailor properties as replacements for rope and sdk. In the 1930s chemists at DuPont and at ICl found that polyamides and polyesters had properties that could replace each of these. [Linear polyolefins do not seem to form in nature as do condensation polymers. This is probably because the organometaUic catalysts are extremely sensitive to traces of H2O, CO, and other contaminants. This is an example where we can create materials in the laboratory that are not found in nature.]... [Pg.461]


See other pages where Condensation of H2O is mentioned: [Pg.5]    [Pg.187]    [Pg.228]    [Pg.123]    [Pg.106]    [Pg.5]    [Pg.187]    [Pg.228]    [Pg.123]    [Pg.106]    [Pg.297]    [Pg.353]    [Pg.6]    [Pg.86]    [Pg.346]    [Pg.767]    [Pg.150]    [Pg.38]    [Pg.39]    [Pg.40]    [Pg.73]    [Pg.328]    [Pg.352]    [Pg.76]    [Pg.118]    [Pg.123]    [Pg.212]    [Pg.314]    [Pg.309]    [Pg.42]    [Pg.43]    [Pg.90]    [Pg.120]    [Pg.38]    [Pg.675]    [Pg.130]    [Pg.92]    [Pg.199]    [Pg.247]   
See also in sourсe #XX -- [ Pg.43 ]

See also in sourсe #XX -- [ Pg.43 ]




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