Volatile percentage, calculation

Nonvolatile Matter. Evaporate 100ml of the sample on a steam bath in a tared dish (preferably platinum) and dry the residue to constant weight in an oven, maintained at 105 to 110°C. The increase in weight of dish shall be calcd as percentage non-volatile residue. Calculate as follows ... 

Fixed carbon, the residue left after the volatile matter is driven off, is calculated by subtrac ting from 100 the percentages of moisture, volatile matter, and ash of the proximate analysis. In addition to carbon, it may contain several tenths of a percent of hydrogen and oxygen, 0.4 to 1.0 percent nitrogen, and about half of the sulfur that was in the coal. 

Determine the loss in weight, and calculate the loss as the percentage of volatiles in the propellant specimen. 

Calculate the percentage of total volatiles in each of the 2-gm specimens using the equation given below. The results of calculations... 

Separating the three macerals from the dull coal was difficult. The petro-graphical purity of the exinite is 86% and that of the micrinite 94%. For both macerals, vitrinite is the main impurity. Since the vitrinite has a petrographi-cal purity of 99%, it is not difficult to calculate the values for the pure exinite and pure micrinite from the experimental data on the highly enriched maceral fractions. All values reported in the tables are corrected ones. Table I summarizes the results of elementary analysis (maf) and the percentage of volatile matter. 

The estimation of individual components and different synthetics was effectively achieved by gas chromatography after simple silylation (10). Figure 2 shows the separation obtained, clearly away from other volatiles in a capsicum extract. The individual capsaicinoids were quantitated in relation to vanillyl octanamide as the internal standard chosen, because it eluted just prior to the capsaicinoids and the response factors of the capsaicinoids with reference to this standard were close to unity. The standardised conditions were as follows Silylation with N,0-bis (trimethylsilyl)-trifluoroacetamide in tetrahydrofuran gave clear rapid reaction at room temperature. The silylated extracts were injected directly on to a stainless steel column of 2 m x 3 mm, filled with 3% SE-30 on Chromosorb-GHP, (100-120 mesh) the column temperature was programmed from 170° to 215°C at 4°/min. and held at 215°C for 10 minutes. The injection port temperature was important for rapid volatilisation of all the components without decomposition, and was fixed at 200°C. The flame ionisation detector temperature was kept at 250°C, and nitrogen flow at 20 ml/min. The percentages of the individual capsaicinoids were calculated from the areas of the peaks, the response factors, and the weight and area of the reference compound. 

Pipet a 10-mL sample into a 100-mL cassia flask fitted with a stopper, and add 50 mL of a freshly prepared 30 in 100 solution of sodium sulfite. Add 2 drops of phenolphthalein TS, and neutralize with 50% (by volume) acetic acid solution. Heat the mixture in a boiling water bath, and shake the flask repeatedly, neutralizing the mixture from time to time by the addition of a few drops of the 50% acetic acid solution, stoppering the flask to prevent loss of volatile material. After no coloration appears upon the addition of a few more drops of phenolphthalein TS and heating for 15 min, cool to room temperature. When the liquids have separated completely, add sufficient sodium sulfite solution to raise the lower level of the oily layer within the graduated portion of the neck of the flask. Calculate the percentage, by volume, of the aldehyde or ketone by the equation... 

When distillation is complete, allow the contents of the collection tube to settle until the oil and water layers are separated completely. Allow the distillate to cool to room temperature, read its volume, and calculate therefrom the percentage of volatile oil. 

Figure 6.2 The relationship between percentage loss of a nonreactive POP to volatilization versus washoff from surface film as a function of Kqa calculated using MUM-Fate. Summer and winter conditions were estimated assuming 25 and 5 °C, respectively...

Fig. 4.5 Extent of hydrolysis of glycoside of different volatile compounds during MLF with four strains of malolactic bacteria (MLB). Values are calculated as a percentage ratio between the concentration of glycosides in MLF samples and in a non-MLF control. Sum of 1-hexanol, trans- and CM-3-hexenol, trans- and c/i-2-hexenol sum of isoamyl alcohols, heptanol, and 4-hydroxy-4-methyl-2-pentanol sum of benzyl alcohol and 2-phenylethanol sum of vanillin and benzaldehyde sum of 4-vinylphenol and 4-vinylguaiacol sum of Unalool and a-terpineol sum of nerol and geraniol sum of cis- and rrani-linalool oxides (pyranic and furanic) sum of 3,7-dimethyl-l,5-octadien-3,7-diol and the two 2,7-dimethyl-2,7-octadien-l,6-diol isomers (from Ugliano and Moio 2006, reproduced with permission)...

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