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Total available phenolic acids

There is, however, a caveat for estimating available total phenolic acid concentrations. The estimates of the total available fraction of phenolic acids in soil extracts represent a crude estimate of what actually occurs in soil, not only because of the range of efficiencies of extraction procedures but also because different phenolic acids at the same concentration generate different absorbances with Folin Ciocalteu s phenol reagent (Fig. 3.7 Blum et al. 1991). In addition soil extracts also contain compounds, other than phenolic acids, that react with (i.e., reduce) the Folin Ciocalteu s phenol reagent (McAllister 1969 Box 1983). The assumption, therefore, was that available total phenolic acid values based on the Folin Ciocalteu s phenol reagent expressed as ferulic acid equivalence were relative values that were consistently related to the acmal total available phenolic acids (hereafter just called total phenolic acid) present in soil extracts. The extraction and quantification by HPLC analysis of available individual phenolic acids in soil do not have these particular problems. [Pg.101]

However, there is one more caveat for both total and individual phenolic acids. Soil extractions recover residual or net concentration, i.e., input - losses, for a point or various points in time. Since both input and losses are unknown between points of time the actual available total or individual phenolic acid concentrations in soil over time are also unknown. The concentrations of available phenolic acids interacting with roots could thus be greater, at times much greater, or lower, at times much lower, than the net concentrations determined from soil extracts. [Pg.101]

In conclusion, the water-autoclave extraction procedure when compared to the EDTA extraction procedure underestimated the total available ferulic acid in the soil by roughly 5% for Cecil A and 22% for Cecil B. In addition to the quantitative difference there also appeared to be a difference in the types of the sorbed ferulic acid recovered. The water-autoclave-procedure recovered some irreversibly sorbed phenolic acids from Cecil A soil since only 55% of the sorbed phenolic acid recovered was utilized by microbes. This difference should not be surprising since the physical and chemical processes of the two extraction procedures, i.e., chelation vs. [Pg.104]

In addition to pore size distribution, the surface chemistry of the activated carbon can have an important influence on the adsorption of certain compounds. As the adsorptive surface of most activated carbons is hydrophobic, they are best suited for the removal of neutral organic molecules, while polar and ionic compounds show much less affinity for adsorption. For the adsorption of polar compounds such as phenol, research has shown that the carbon surface chemistry is more relevant than the total available adsorption capacity or surface area [72-74]. It has been found that the presence of acidic surface oxides, whose concentration can be increased by oxygen adsorption or chemical treatment, leads to a decrease in adsorptive capacity for compounds such as phenols and increases the base adsorption capacity [75 [. [Pg.37]

Creosote bush resin consists of phenolics (eg., flavonoids and nordihydroguaiaretic acid), neutrals (e.g., waxes), basics (e.g., alkaloids), and acidics (e g., phenolic acids). The phenolic portion comprises 83-91% of the total resin. Nordihydroguaiaretic acid accounts for 5-10% of the dry weight of the leaves (Leonforte 1986). No other relevant chemical/physical data are available for creosote bush resin the substance is therefore not addressed further in this profde. [Pg.229]

Thus the summed or average action of extracted available total phenolic acids in soils is just as important as understanding the action of available individual phenolic... [Pg.101]

The use of HPLC for quantification of phenols is often limited to a single class of phenolics and then often only to low-molecular weight compounds that are available as standards. It is, therefore, often necessary to use colorimetric assays such as the Folin-Ciocalteau assay which rely on the reducing ability of phenols to quantify the amount of total phenolics in a sample (Waterman and Mole, 1994 Singleton et al, 1999 Schofield et al, 2001). The degree of condensation of polyphenols can be quantified by colorimetric assays such as the acid-butanol assay and the vanillin assay (Waterman and Mole, 1994 Schofield et al, 2001). [Pg.330]

C12 to C20, primarily Ci6 to ( is), used as surface lubricants in the manufacture of food-contact articles. The method, which uses ethyl palmitate (Eastman Chemicals No. 1575 Red Label) as an internal standard, has been validated at 200 ppm total FAME [185]. Other FAME standards (methyl palmitate, methyl stearate, methyl oleate, methyl linoleate and methyl linolenate) are available (Applied Science Laboratories) [116], Worked out examples of additive determinations are given in the Food Additives Analytical Manual [116], which also describes a great many of indirect food additives, such as BHA, BHT, TBHQ, l-chloro-2-propanol, DLTDP, fatty acid methyl esters, w-heptyl-p-hydroxybenzoate, propyl-gallate, sodium benzoate, sodium stearoyl-2-lactylate, sorbitol and phenolic antioxidants. EPA methods 606 and 8060 describe the CGC separation of phthalate esters (direct injection) (cf. Figure 4.2). [Pg.199]

Recendy, the first total synthesis of taxodone was accomplished via this strategy [152]. Cycloadduct 153, readily available from the Diels-Alder reaction of siloxyfuran 152 and methyl acrylate, was treated with acid to induce ring opening and dehydration to afford phenol 154, Eq. 103. [Pg.45]

Total phenolics, expressed as milligrams of gallic acid equivalents per gram (mg of GAE/g). nd, not detected, na, not available. [Pg.4]

Unlike the common walnut, there is virtually no information available in peer-reviewed literature about the nutritional composition and value of heartnut. The polyphenolic and lipid compositions of the heartnut and how they contribute to the total antioxidant activities have been recently reported [2,3]. This chapter provides a more comprehensive overview about this special tree nut and its potential as a healthy food for consumers and a value-added new crop for growers. Due to lack of information about heartnut, literature reviews on the nutritional composition will mainly be on the common walnut. Furthermore, we will focus our discussions on the phenolic, tocopherol, and fatty acid contents and their contribution to human health through cholesterol reduction and antioxidative properties. [Pg.237]


See other pages where Total available phenolic acids is mentioned: [Pg.24]    [Pg.89]    [Pg.99]    [Pg.161]    [Pg.163]    [Pg.24]    [Pg.89]    [Pg.99]    [Pg.161]    [Pg.163]    [Pg.107]    [Pg.137]    [Pg.161]    [Pg.161]    [Pg.314]    [Pg.364]    [Pg.324]    [Pg.120]    [Pg.243]    [Pg.1043]    [Pg.99]    [Pg.101]    [Pg.161]    [Pg.723]    [Pg.402]    [Pg.97]    [Pg.583]    [Pg.30]    [Pg.50]    [Pg.408]    [Pg.281]    [Pg.168]    [Pg.249]    [Pg.316]    [Pg.23]    [Pg.94]    [Pg.119]    [Pg.95]    [Pg.481]    [Pg.158]    [Pg.60]    [Pg.150]    [Pg.462]    [Pg.154]   
See also in sourсe #XX -- [ Pg.24 , Pg.89 , Pg.99 , Pg.101 , Pg.161 , Pg.163 ]




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Acidic phenols

Available phenolic acids

Phenol acidity

Phenol acids

Phenolic acidity

Phenolic acids

Phenolics phenolic acids

Total acidity

Total phenolics

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