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Phenolic aldehydes

Peroxomonosulfuric acid oxidi2es cyanide to cyanate, chloride to chlorine, and sulfide to sulfate (60). It readily oxidi2es carboxyflc acids, alcohols, alkenes, ketones, aromatic aldehydes, phenols, and hydroquiaone (61). Peroxomonosulfuric acid hydroly2es rapidly at pH <2 to hydrogen peroxide and sulfuric acid. It is usually made and used ia the form of Caro s acid. [Pg.94]

Ozone can be used to completely oxidize low concentrations of organics in aqueous streams or partially degrade compounds that are refractory or difficult to treat by other methods. Compounds that can be treated with ozone include alkanes, alcohols, ketones, aldehydes, phenols, benzene and its derivatives, and cyanide. Ozone readHy oxidizes cyanide to cyanate, however, further oxidation of the cyanate by ozone proceeds rather slowly and may require other oxidation treatment like alkaline chlorination to complete the degradation process. [Pg.163]

Paint and varnish manufacturing Resin manufacturing closed reaction vessel Varnish cooldng-open or closed vessels Solvent thinning Acrolein, other aldehydes and fatty acids (odors), phthalic anhydride (sublimed) Ketones, fatty acids, formic acids, acetic acid, glycerine, acrolein, other aldehydes, phenols and terpenes from tall oils, hydrogen sulfide, alkyl sulfide, butyl mercaptan, and thiofen (odors) Olefins, branched-chain aromatics and ketones (odors), solvents Exhaust systems with scrubbers and fume burners Exhaust system with scrubbers and fume burners close-fitting hoods required for open kettles Exhaust system with fume burners... [Pg.2177]

The phenolics are resinous materials produced by condensation of a phenol, or mixture of phenols, with an aldehyde. Phenol itself and the cresols are the most widely used phenols whilst formaldehyde and, to a much less extent, furfural are almost exclusively used as the aldehydes. [Pg.635]

In Figure 13.2, the intensity of the ion at m/z 170 represents a molecular ion of an aromatic compound. The characteristic losses from the molecular ion (M - 1, M - 28, and M - 29) suggest an aromatic aldehyde, phenol, or aryl ether. The molecular formula of Ci2H 0O is suggested by the molecular ion at m/z 170, which can be either a biphenyl ether or a phenylphenol. The simplest test to confirm the structure is to prepare a TMS derivative, even though m/z 11 strongly indicates the diaryl ether. [Pg.259]

While arthropod defensive secretions often rely for their effect on well-known aliphatic acids, aldehydes, phenols, and quinones, there are many cases in which compounds capable of whetting the appetite of any natural products chemist are utilized. For example, steroids play a... [Pg.40]

One of the more important areas of use of ultraviolet instruments is the identification and determination of biologically active substances. Many components in body fluids can be determined either directly or through colorimetric methods. Drugs and narcotics can be measured both in the body as well as in formulations. Vitamin assay is another related activity. Nearly all metals and nonmetals can be determined through their ultraviolet absorption or by colorimetric methods. In recent years, ultraviolet instruments have been used extensively for the determination of air and water pollutants, such as aldehydes, phenolics, and ozone ... [Pg.1640]

In an analytical experimental series (Fig. 1), the effluent was collected in fractions. These fractions were analyzed with respect to pH, fermentable sugars, furan aldehydes, phenolic compounds, aliphatic acids, sulfate, and ultraviolet (UV) absorption at 280 nm. [Pg.528]

Six different detoxification treatments were performed using both weak and strong anion-exchange resins (Table 1) in an analytical experiment (Fig. 1) and a preparative experiment (Table 2, Fig. 2), in which the fermentability of the fractions was assayed. Figure 1 shows how the pH and the concentrations of glucose, furan aldehydes, phenols, aliphatic acids, and sulfate varied in hydrolysate fractions collected from columns packed with the six different resins in the analytical anion-exchange experiment. [Pg.533]

Juice of the sand pear can also be converted into vermouth (Joshi et al, 1999). The complete process is illustrated in Fig. 8.3. Dry and sweet versions, with various alcohol levels, have been prepared (Attri et al, 1993). TSS, acidity, aldehyde, phenol, and ester contents increase as a... [Pg.268]

Molasses. A large number of volatile and nonvolatile compounds have been identified in the flavor fractions of various types of molasses (51-621. Compound classes identified include aliphatic and aromatic acids, aldehydes, phenols, lactones, amines, esters, furans, pyrazines, and sulfides. Most of these compounds can arise from carbohydrate degradation through a number of traditional pathways especially because residual nitrogen-containing sources are present. [Pg.36]

Puranik includes in his Raman studies the solution systems benz-aldehyde-phenol and ester-phenol. In the former ceise, the 14 cm decrease in i>,(G==0) caused by diluting benzaldehyde with phenol is accompanied by a 7 cm increase in i, (G—G) (at 1197 cm ) (1679). Puranik notes that the corresponding shifts of these two modes are observed for orlAo-substituted aldehydes, such as salicylaldehyde. In the study of the spectral changes brought on by adding phenol to three esters, Puranik found the 23-29 cm" decrease in i, (G==0) to be accompanied by a 17-25 cm" increase in i, (C=0) (1677). [Pg.138]

In addition to these reactions, aldehyde-phenol, aldehyde-urea, aldehyde-melamine and many other aldehyde-based polymers are prepared by polycondensation processes. The first step in a typical reaction of this type is... [Pg.490]

The air-dried leaves gave about 0.5 per cent of a light yellow oil, specific gravity at 15°/15, 0.9181, optical rotation -i-337 , refractive index 1.489, ester value 20, acetyl value 3.5. This oil contained 5 to 10 per cent of ci-pinene, 20 to 25 per cent of h-a-phellandrene, 10 to 15 per cent of cineole, sesquiterpenes 30 to 40 per cent, sesquiterpene alcohols 5 to 10 per with traces of aldehydes, phenols and esters. [Pg.84]

Starch Acetalation with Aldehyde-Amine, Aldehyde-Amide, and Aldehyde-Phenol Resins... [Pg.231]

Figure 1.2-2. Different types of sampling devices for aldehydes, phenols and MDI, 1 = Tenax tube with gas meter and pump 2 = DNPH cartridge 3 = MDI cartridge 4 = Muencke absorber with gas meter and pump. Figure 1.2-2. Different types of sampling devices for aldehydes, phenols and MDI, 1 = Tenax tube with gas meter and pump 2 = DNPH cartridge 3 = MDI cartridge 4 = Muencke absorber with gas meter and pump.

See other pages where Phenolic aldehydes is mentioned: [Pg.179]    [Pg.23]    [Pg.639]    [Pg.188]    [Pg.1061]    [Pg.34]    [Pg.439]    [Pg.129]    [Pg.145]    [Pg.434]    [Pg.186]    [Pg.2427]    [Pg.175]    [Pg.723]    [Pg.130]    [Pg.191]    [Pg.102]    [Pg.2408]    [Pg.17]    [Pg.19]    [Pg.21]    [Pg.23]    [Pg.25]    [Pg.27]    [Pg.29]    [Pg.179]    [Pg.179]   
See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.72 ]




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Phenol aldehydes

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