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Absorbance, determination

ABP = 2-amino-5-bromophenyl(pyridin-2-yl)methanone 226,227 Absorbance, determination of 31 Absorption, measurement of 9,17,31 molar coefficient 36, 40 quantitative relationship 35, 36 recording of spectra 30, 31 -bathochromic/hypsochromic shift 31 -comparison to spectra of solutions 31 scanning curves 17,31,32 ACB = 2-amino-5-chlorobenzophenone 227... [Pg.231]

The same considerations will apply to other nonspecific methods of detection, such as fluorescence or UV absorbance determinations. Particularly with these methods, it must be appreciated that many of the cells used to form mono-layers secrete a variety of products such as lipids and proteins into both the donor and receiver compartments. These substances can result in a variable background in solutions and may interfere with solute quantitation. Even if a chromatographic method is used with fluorescence or UV detection, these products can still interfere with the separation unless specifically accounted for. [Pg.248]

An ultraviolet spectrophotometric method based on the absorbance of a periodate oxidation product of pseudoephedrine hydrochloride will be the official method of analysis in the USP XX.19,20 A portion of tablets or syrup in water is placed in a separatory funnel. Sodium bicarbonate and sodium metaperiodate are added. After standing for 15 minutes, 1 N HC1 is added. The solution is extracted with hexane. The hexane extract is filtered and its absorbance determined at 242 nm in 1 cm cells. The amount of the oxidation product of pseudoephedrine hydrochloride is determined by comparison of the sample absorbance against the absorbance of a Pseudoephedrine Hydrochloride Reference Standard treated in the same manner. [Pg.500]

The law summarized by Equation (9.10) only holds for absorbances determined with monochromatic light. [Pg.443]

The Rayleigh ratio as defined by Equation (24) has a precise meaning, yet it is a quantity somewhat difficult to visualize physically. After we have discussed the experimental aspects of light scattering, we shall see that Re is directly proportional to the turbidity of the solution when turbidity is the same as the absorbance determined spectrophotometrically. [Pg.207]

Aluminum Oxide Moisture Sensor. This type of sensor is a capacitor, formed by depositing a layer of porous aluminum oxide onto a conductive substrate, and then coaling the oxide with a thin film of gold The conductive base and the gold layer become the capacitor s electrodes. Water vapor penetrates the gold layer and is absorbed by the porous oxidation layer The number of water molecules absorbed determines the electrical impedance of the capacity, which is. m turn, a measure of water vapor pressure. [Pg.814]

All but one of the seven laboratories that recently participated in a intercomparison of niacin assays chose to use microbiological assays (42). The results from the lone HPLC determi-nation/UV absorbance determination were rejected due to lack of chromatographic resolution. [Pg.430]

Ultraviolet Absorbance Determine as directed under Ultraviolet Absorbance of Citrus Oils, Appendix VI, using about 50 mg of sample, accurately weighed. The absorbance maximum occurs at 315 3 nm. [Pg.48]

Use this solution to zero your spectrophotometer at both 550 nm and 420 nm in the absorbance determinations described below. [Pg.133]

Ash contained in carbons, especially of plant origin, causes their alkalinity. Adsorption capacity may be increased even up to 30% (SO), depending on kind and concentration of substance removed, by washing out ashes. Table 2 shows content of ash in carbons. Values of absorbability determined for tested carbons are in the range of 0.4—2 cm /gi The parameter is useful for evaluation of total volume of pores and may be correlated... [Pg.449]

Procedures and standardization. Reagents I and II. After collection, the samples were transferred immediately to photometer tubes and the absorbances determined. [Pg.95]

Samples in 10 ml. of the alkaline iodide reagent were rapidly acidified and mixed with 2.0 ml. of phosphoric acid reagent. The mixture (in a stoppered container) was cooled to room temperature in a water bath, and the absorbance determined 5 to 10 minutes after acidification. [Pg.95]

The specific agent, the route of exposure and the dose absorbed determine the onset and severity of symptoms (14). Onset can range from a few minutes to 18h, depending on the extent of exposure. To best remember the clinical presentation, it helps to divide the cholinergic symptoms into three categories central effects, muscarinic effects, and nicotinic effects. [Pg.121]

Based on preliminary studies, it was determined that a 10-tray column is appropriate for an absorption operation. The overall tray efficiency is estimated at 60%. For the indicated feed gas and absorbent, determine the expected flow rates and compositions of the products using the Kremser method. [Pg.523]

Into a 10 mL volumetric calibrated tube, 1 mL of EHC (1.00X 10 4 mol/L) and 0.5 mL of buffer solution were transferred and diluted to 10 mL with water, and then the absorbance determined. [Pg.398]

Increasing inflow rates decrease compound A concentrations by decreasing rebreathing of gas, that has passed through the absorbent, thereby decreasing the amount of CO2 that reaches the absorbent. The amount of CO2 absorbed determines the temperature of the absorbent, since CO2 absorption is an exothermic reaction [65, 66]. [Pg.376]

Time-dependent offline sampling of 1 ml aliquots was performed aseptically during fermentations. Samples were mixed immediately before dilution in deionized water, and then subjected to duplicate absorbance determination in a spectrophotometer at 600 nm. Diluted cell-free medium was used to establish background readings and set zero absorbance levels. Values were averaged and corrected for dilution. Protein concentration in cell-free extracts was determined by Bradford method [21], using bovine serum albumin as a standard. [Pg.704]

Figure 6. Elution profiles for platinum polymers. One milliliter of a polymer solution in dimethyl sulfoxide was loaded onto a 2.0 X 20 cm Sephacryl S-200 column. Fractions of 0.5 ml were collected and the absorbances determined. Elution profiles for (a) a 0.1% solution of polymer 18 (folic acid) and (b) a 0.05% solution of polymer 21 (tilorone) are shown. Figure 6. Elution profiles for platinum polymers. One milliliter of a polymer solution in dimethyl sulfoxide was loaded onto a 2.0 X 20 cm Sephacryl S-200 column. Fractions of 0.5 ml were collected and the absorbances determined. Elution profiles for (a) a 0.1% solution of polymer 18 (folic acid) and (b) a 0.05% solution of polymer 21 (tilorone) are shown.
Hantash, J., Bartlett, A., Oldfield, R, Denes, G., O Rielly, R., Roudiere, D., Menduni, S. (2006). Use of an on-line imprinted polymer pre-column, for the liquid chromatographic-UV absorbance determination of carbaryl and its metabolite in complex matrices,... [Pg.651]

The apparent permeability value is determined from the concentration of compound in the acceptor compartment after a given incubation time. Equation (15.8) has been derived from the differential equation (15.2), which describes diffusion kinetics under non-sink conditions. Experiments performed under non-sink conditions allow one to work with substantially higher concentrations in the acceptor compartment. This makes optical (UV) detection possible and greatly simplifies analytics when LC-MS is used. In (15.8) below r is the ratio of the absorbance in the acceptor chamber divided by the theoretical equilibrium absorbance (determined independently), Vr is the volume of the acceptor compartment, Vd is the donor volume, A is the accessible filter area (total filter area multiplied by porosity), and t is the incubation time. Equation 1 is obtained from the differential equation... [Pg.393]

Figure 24. Psuedo first order kinetic treatment of convoluted Nb, Nb-TBE, and MAH (total area from 670 to 725 cm ) absorbances determined via in situ FTIR. Figure 24. Psuedo first order kinetic treatment of convoluted Nb, Nb-TBE, and MAH (total area from 670 to 725 cm ) absorbances determined via in situ FTIR.
Whereas the absorbance measured with the concentration sets 1 and 2b are overlapping, the absorbance determined with set Ic are nearly 1 order of... [Pg.170]

In double-beam systems (Figure 3B), the light from the radiation source is split by a beam splitter into two beams - a sample beam directed through the sample cell and a reference beam directed around the sample cell. The reference beam serves as a monitor of the lamp intensity and the response characteristics of electronic circuitry. The observed absorbance, determined from the ratio of sample beam and reference beam readings, is thus free of effects due to drifting lamp intensities. [Pg.164]


See other pages where Absorbance, determination is mentioned: [Pg.477]    [Pg.122]    [Pg.539]    [Pg.272]    [Pg.209]    [Pg.540]    [Pg.824]    [Pg.45]    [Pg.34]    [Pg.497]    [Pg.766]    [Pg.215]    [Pg.397]    [Pg.152]    [Pg.63]    [Pg.1594]    [Pg.483]    [Pg.734]   
See also in sourсe #XX -- [ Pg.31 ]




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