Source spectrophotometry

Hodgson B W and Keene J P 1972 Some characteristics of a pulsed xenon lamp for use as a light source in kinetic spectrophotometry Rev. Sol. Instnim. 43 493-6... 

In contrast to spectrophotometry, hght-scattering experiments are generally conducted at constant wavelength. Mercury vapor lamps are the most widely used light sources, since the strong lines at 436 and 546 nm are readily isolated by filters to allow monochromatic illumination. Polarizing filters are also included for both the incident and scattered beams so that depolarization can... 

The quantitative phenylation of pyridine has been studied by two groups of workers. Dannley and Gregg showed that 2-, 3-, and 4-phenylpyridine are formed in relative amounts 58 28 14 in the phenylation of pyridine with dibenzoyl peroxide, as estimated by infrared spectrophotometry. Hey and his co-workers obtained the ratios shown in Table I for the phenylation of pyridine using four different sources of phenyl radicals. ... 

A molecular absorption spectrophotometry method, using a sharp-line irradiation source, has been developed for the determination of sulfide (as hydrogen sulfide) in water and sludge samples. The method was tested with measurements of real waste-water samples. The limit of detection was 0.25 g (1-10 mL sample volume). 

Figure 5.3. Zinc reactor column for generation of arsine by electrothermal atomic absorption spectrophotometry. Source Author s own files... 

Nalidixic acid has been determined spectrophotometri-cally in tablets after chloroform extraction at a wavelength maximum of 258 nm.(l)(2) Another source reported 259 nm as the maximum for chloroform and 258 nm for 0.1 N NaOH.( ) The infrared spectrum has also been used to identify nalidixic acid in tablets.( )... 

Programming a CAM for fluorometry is far more complex than for spectrophotometry. Spectrophotometry is simple because it is based on the ratio of light in to light out. But fluorometry creates many of the problems associated with true radiometry—measuring the emission spectrum of an unknown source. The logic may become circular. Radiometry to determine an emission spectrum requires the relative spectral sensitivity of the photometer to be known, but how can this be determined without a source with a known emission spectrum Fortunately, physicists in our national standardization organizations provide us with calibrated sources and photometers. 

One often unsuspected source of error can arise from interference by the substances originating in the sample which are present in addition to the analyte, and which are collectively termed the matrix. The matrix components could enhance, diminish or have no effect on the measured reading, when present within the normal range of concentrations. Atomic absorption spectrophotometry is particularly susceptible to this type of interference, especially with electrothermal atomization. Flame AAS may also be affected by the flame emission or absorption spectrum, even using ac modulated hollow cathode lamp emission and detection (Faithfull, 1971b, 1975). 

In a search for sources of alkaline materials in rural air and rain, we have sampled and performed multi-element analyses on ambient particulate matter and potential source materials. Ambient aerosols were sampled daily using single Nuclepore filters or Florida State University "streakers." Samples of soil and unpaved road materials were also collected and analyzed. The samples were analyzed by various multi-element methods, including ion-and proton-induced X-ray emission and X-ray fluorescence, as well as by atomic absorption spectrophotometry. Visual observations, as well as airborne elemental concentration distributions with wind direction and elemental abundances in aerosols and source materials, suggested that soil and road dust both contribute to airborne Ca. Factor analysis was able to identify only a "crustal" source, but a simple mass balance suggested that roads are the major source of Ca in rural central Illinois in summer. 

The NADH-forming activity described here is different from the classical malic enzyme activity found by London et al. (95) in Lacto-badUus casei. In their system, NADH is a major end product and detectable by spectrophotometry while lactic acid is only a minor product. L. casei uses malic acid as an energy source with carbon dioxide, acetate, and ethanol as the main fermentation products. The optimal pH... 

For the purposes of chemical oceanography, spectrophotometry is limited to wavelengths from the UV to near-IR (250 to 1500 nanometers). The various forms of spectrophotometer differ primarily in combinations of light sources, dispersive elements, and detectors. 

This experiment provides students with the opportunity to isolate a biomolecule from its natural source, followed by its purification and identification. In addition, students will follow a procedure that is typical of the general extraction and characterization of lipids. However, unlike most lipids, the plant pigments are highly colored and may be characterized and quantified by visible spectrophotometry. Several types of plant tissue may be used. Some recommendations are fresh leaves (tree, plant, grass, spinach), green algae, or mosses. For variety, students may be asked to bring their own samples for analysis. 

One of the most challenging aspects of atomic spectrometry is the incredibly wide variety of sample types that require elemental analysis. Samples cover the gamut of solids, liquids, and gases. By the nature of most modem spectrochemical methods, the latter two states are much more readily presented to sources that operate at atmospheric pressure. The most widely used of these techniques are flame and graphite furnace atomic absorption spectrophotometry (FAAS and GF-AAS) [1,2] and inductively coupled plasma atomic emission and mass spectrometries (ICP-AES and MS) [3-5]. As described in other chapters of this volume, ICP-MS is the workhorse technique for the trace element analysis of samples in the solution phase—either those that are native liquids or solids that are subjected to some sort of dissolution procedure. 

Emphasis was therefore put on analytical procedures able to determine many elements in parallel and/or requiring almost no previous separation. procedures preferred were X-ray fluorescence using a Am source and Si(Li)-detector, atomic absorption spectrophotometry, gamma spectrometry using tracer isotopes and Ge(Li)-detector and acid-base titrations with recording of the pH-volume derivative. Table 2 summarises the use of these methods for the different elements, and it also gives a rough indication of interferences, sensitivity and accuracy obtained. 

Source From W.J. Price and J.T.H. Roos, Analysis of Fruit Juice by Atomic Absorption Spectrophotometry. 

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