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Total residual oxidant

This is an indirect method of analysis because the chlorine-containing species do not react with the titrant. Instead the total chlorine residual oxidizes l to l3 , and the amount of 13 is determined by the redox titration with Na282 03. [Pg.340]

Stairs comments that this p value is strongly dependent on the temperature but his data have been criticised by Duffin and Tucker ", who prefer their method of observing the rate of formation of the adduct to that of estimating total residual oxidising power employed by Stairs, and they find p (25°) to be —2.32+0.10 as compared to a value of —2.20+0.07 at 40 °C. These values are considerably more negative than those found for chromic acid oxidation of diphenylmethanes (— 1.17) and toluenes (-1.12). [Pg.296]

Cow feces (di sulfoton and 5 metabolites as total residue) Extraction with chloroform concentration then oxidation with m-chioroperbenzoi c acid clean-up by column chromatography GC/FPD 1ng/kga 74 Bowman and Beroza 1969... [Pg.158]

Based on analyses of well water from Suffolk County, New York, which show aldlcarb sulfoxide and sulfone, (and generally 0 or <10% parent aldlcarb) to be the only compounds In well water, and In an approximate 50 50 ratio. Onion Carbide decided to analyze all ground water samples using a total residue method, l.e., by oxidizing all residues present to the sulfone. [Pg.301]

Baquiloprim is extensively metabolized in the target animals to a variety of metabolites including desmethylbaquiloprim, bis-desmethylbaquiloprim, baquiloprim- 1-A-oxide, baquiloprim-3-A-oxide, and 6-hydroxybaquiloprim. A high percentage of the total residues in liver, kidney, and injection site is covalently bound. [Pg.93]

In all target species, trimethoprim is rapidly and almost completely absorbed, and widely distributed throughout the body after oral administration. A significant proportion of the residues in tissues consists of unmetabolized trimethoprim, but several metabolites including the 1-A-oxide, 3-A-oxide, 3-hydroxy, 4-hydroxy, and the -hydroxy metabolites are also present, each metabolite comprising less than 5% of the total residues. [Pg.94]

Tin total residue obtained from 50 er. ui Ihe original tannin solution, and dried at 105" (, is also usn-rlniiied. On now ealeulating the residue lor 2110 ev. of tmuiin. -.011111011. and deducting this from tlx tolnl residue left from 11 u liinniu solution (j-euted with the aluminum oxide, tin result should show that 1 gm. of nlmuiuuni oxide absorbs I), It) to 0.50 gm. of tannin. [Pg.50]

Figure 11.13. General scheme of breakpoint chlorination difference between total residual Cl and chlorine dose reflects chlorine demand, primarily from ammonium and amines. Before breakpoint, most Cl is in combined forms, primarily mono- and dichloramine after the breakpoint, the combined residual consists of slow-reacting organic chloramines. Added Cl remains in free form after the breakpoint. Sharpness of breakpoint and minimum observed Cl concentration depend on pH, temperature, and time of reaction. Loss of residual Cl at breakpoint is caused by oxidation of di- and trichloramines to Nj according to reactions 33a and 33b and other reactions. (Adapted from Brezonik, 1994.)... Figure 11.13. General scheme of breakpoint chlorination difference between total residual Cl and chlorine dose reflects chlorine demand, primarily from ammonium and amines. Before breakpoint, most Cl is in combined forms, primarily mono- and dichloramine after the breakpoint, the combined residual consists of slow-reacting organic chloramines. Added Cl remains in free form after the breakpoint. Sharpness of breakpoint and minimum observed Cl concentration depend on pH, temperature, and time of reaction. Loss of residual Cl at breakpoint is caused by oxidation of di- and trichloramines to Nj according to reactions 33a and 33b and other reactions. (Adapted from Brezonik, 1994.)...
Saturated Zone Degradation. Because of the rapid oxidation process in the root zone, parent aldicarb is rarely detected in the saturated zone. In rare instances where transport from the soil surface is rapid, aldicarb may be present at less than five percent of the total residues found. In the saturated zone, residues are usually a mixture of aldicarb sulfoxide and aldicarb sulfone in an average ratio of 3 2. [Pg.201]

The residual oxide was carefully isolated and weighed. The difference in weight before and after burning gave another independent measure of the total amount of carbon present on the sample at that point in the preparative process. The data from these experiments over twelve cycles are displayed graphically in Figure 3. [Pg.345]

Products of incomplete combustion have been shown to increase as the catalyst deactivates. Agarwal et al. report that the oxidation of a mixed stream of trichloroethylene and C5-C9 hydrocarbons over a chromia alumina catalyst produced CO equal to 32% of the total CO + CO2 with fresh catalyst. With a deactivated catalyst, CO had risen to 54% of the total carbon oxides produced. Pope et al. report products of incomplete combustion for the oxidation of 1,1,1-trichloroethane over a cobalt oxide catalyst. The cause of the catalyst deactivation has not been established, but both Agarwal et al. and Michalowiczl reference evidence of carbonaceous deposits on the catalyst after oxidation of halogenated hydrocarbons. ESCA studies by Hucknall et al. O have always shown a carbon residue on palladium alumina catalysts in addition to adsorbed halogen. [Pg.170]

Oxidant residuals in the form of total residual chlorine were first reported by the New York State Department of Environmental Conservation in rainfall and lake waters of the Western Adirondacks of New York State in 1976-77. Chlorine residuals analyzed by the orthotoline colorimetric procedure developed by Palin (1957) were detected in rainfall at Boonville and Stillwater, New York and in Echo Lake, Hinckley Reservoir and Stillwater Reservoir (Figure 2. Total residual chlorine in rainfall near Boonville, New York... [Pg.373]

The smelter treats all of the zinc plant residues, which constitute approximately 45-50% of the charge. The percentage of zinc plant residues is a function of the smelter elemental limits and maintains a specific heat balance in the KIVCET furnace. Residues fiom the oxide leach plant and sulphide leach plant are blended and pumped to the feed plant at a specific gravity of 1.75. The residues are filtered through two Ingersoll-Rand Lasta plate filter presses. The total residue filtering capacity is 825 dry t/d, with the filter cake containing 20-22% moisture. [Pg.172]

In a DAFC the total electro-oxidation to CO2 of an aliphatic mono-alcohol, CxHyO, involves the participation of water (H2O) or of its adsorbed residue (OHads) provided by the cathodic reaction (electro-reduction of dioxygen). [Pg.322]

Bromine is not as effective as chlorine in combating algae and oxidizing organic matter in the water. It sometimes causes a green color in the pool and occasionally imparts a brown discoloration to pool walls. Where local authorities permit bromination, the normal range for total residual bromine varies between 2.0 and 4.0 ppm (NSPI, 2002A). [Pg.149]

The chlorine demand is the difference between the chlorine added and the residual concentration after a designated reaction time of approximately 10 min. Total residual chlorine is determined by the oxidation of AA -diethyl-p-phenylenediamine (DPD) to produce a red-colored product Addition of iodine then catalyzes further reaction with chloramines, and it is possible to obtain concentration values for aU chloramines and free chlorine. [Pg.267]

As long as the condition l/j//o,jl 1 is fulfilled, the electrode reaction j may be treated as if it were in equilibrium. The exchange currents o,v> o,H and Iq j are a measure of the reactivity of the electrode material with respect to the Volmer, Heyrovsky or Tafel reaction. The electrode functions as hydrogen electrode at pn = diXm if either 7o,v> f o,T I rI o,v o,h I rI Here 7r designates the total residual current resulting from oxidation and reduction of impurities, anodic metal dissolution, and cathodic reduction of molecular oxygen. [Pg.25]

One of the most important applications of redox titrimetry is in evaluating the chlorination of public water supplies. In Method 9.3 an approach for determining the total chlorine residual was described in which the oxidizing power of chlorine is used to oxidize R to 13 . The amount of 13 formed is determined by a back titration with 8203 . [Pg.344]

The methods described earlier for determining the total, free, or combined chlorine residual also are used in establishing the chlorine demand of a water supply. The chlorine demand is defined as the quantity of chlorine that must be added to a water supply to completely react with any substance that can be oxidized by chlorine while also maintaining the desired chlorine residual. It is determined by adding progressively greater amounts of chlorine to a set of samples drawn from the water supply and determining the total, free, or combined chlorine residual. [Pg.345]

Correcting for Residual Current In any quantitative analysis the signal due to the analyte must be corrected for signals arising from other sources. The total measured current in any voltammetric experiment, itot> consists of two parts that due to the analyte s oxidation or reduction, and a background, or residual, current, ir. [Pg.521]


See other pages where Total residual oxidant is mentioned: [Pg.58]    [Pg.198]    [Pg.399]    [Pg.58]    [Pg.198]    [Pg.399]    [Pg.489]    [Pg.1141]    [Pg.80]    [Pg.129]    [Pg.139]    [Pg.678]    [Pg.420]    [Pg.276]    [Pg.99]    [Pg.258]    [Pg.114]    [Pg.485]    [Pg.106]    [Pg.42]    [Pg.138]    [Pg.118]    [Pg.379]    [Pg.22]    [Pg.257]    [Pg.109]    [Pg.138]    [Pg.569]    [Pg.570]    [Pg.266]    [Pg.1000]    [Pg.340]    [Pg.396]   
See also in sourсe #XX -- [ Pg.198 ]




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Oxidation residues

Total oxidations

Total residue

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