Impurity emission

Details of nitrobenzene photochemistry reported by Testa are consistent with the proposal that the lowest triplet excited state is the reactive species. Photoreduction, as measured by disappearance quantum yields of nitrobenzene in 2-propanol is not very efficient = (1.14 0.08) 10 2 iD. On the other hand, the triplet yield of nitro benzene in benzene, as determined by the triplet-counting method of Lamola and Hammond 28) is 0.67 0.10 2). This raises the question of the cause of inefficiency in photoreduction. Whereas Lewis and Kasha 29) report the observation of nitrobenzene phosphorescence, no long-lived emission from carefully purified nitrobenzene could be detected by other authors i4,3o). Unfortunately, the hterature value of Et for nitrobenzene (60 kcal mole i) is thus based on an impurity emission and at best a value between 60 and 66 kcal mole can be envisaged from energy-transfer experiments... 

Filters or monochromators are generally used for the selection of either excitation and/or emission. Other, undesired sources of radiation (Raman scattering, Rayleigh scattering, solvent impurity emission) must not reach the photomultiplicator. 

The polymers obtained from linear starting materials (di-, tri and tetrasilane halides) exhibit neither a significant fluorescence emission nor noticeable optical absorption in the visible. However, a weak blue-ultraviolet fluorescence is observed, which we attribute to impurity emission centers. As expected, the products fi om cyclic silanes show quite strong fluorescence emission accompanied by an optical absorption in the visible range. The fluorescence spectra of the cyclic materials are depicted in Fig. 2 and Fig. 3. 

Figure 1. Extreme UV (EUV) spectrum, from the PDX tokamak, showing prominent impurity emission lines. (Reproduced with permission from Ref. 12. Copyright 1982,...

N. Pradhan et ah, An alternative of CdSe nanocrystal emitters Pure and tunable impurity emissions in ZnSe nanocrystals, journal of the American Chemical Society, 127(50), 17586-17587 (2005). 

Figure Cl.5.9. Vibrationally resolved dispersed fluorescence spectra of two different single molecules of terrylene in polyetliylene. The excitation wavelengtli for each molecule is indicated and tlie spectra are plotted as the difference between excitation and emitted wavenumber. Each molecule s spectmm was recorded on a CCD detector at two different settings of tire spectrograph grating to examine two different regions of tlie emission spectmm. Type 1 and type 2 spectra were tentatively attributed to terrylene molecules in very different local environments, although tlie possibility tliat type 2 spectra arise from a chemical impurity could not be mled out. Furtlier details are given in Tchenio [105-1071.

The emission spectrum from a hollow cathode lamp includes, besides emission lines for the analyte, additional emission lines for impurities present in the metallic cathode and the filler gas. These additional lines serve as a potential source of stray radiation that may lead to an instrumental deviation from Beer s law. Normally the monochromator s slit width is set as wide as possible, improving the throughput of radiation, while being narrow enough to eliminate this source of stray radiation. 

Short-lived gamma-ray Emission from impurities... 

The products manufactured are predominantiy paraffinic, free from sulfur, nitrogen, and other impurities, and have excellent combustion properties. The very high cetane number and smoke point indicate clean-burning hydrocarbon Hquids having reduced harmful exhaust emissions. SMDS has also been proposed to produce chemical intermediates, paraffinic solvents, and extra high viscosity index (XHVI) lubeoils (see Lubrication and lubricants) (44). 

Inductively coupled plasma (icp) emission, direct current plasma (dcp), and inductively coupled plasma mass spectrometry (icp/ms) have taken over as the methods of choice for the simultaneous detection of metallic impurities in hafnium and hafnium compounds (29,30). 

In determining the purity or percentage of lead in lead and lead-base alloys, the impurities or minor components are deterrnined and the lead content calculated by difference. Quality control in lead production requires that the concentration of impurities meet standard ASTM specifications B29 (see Table 7). Analyses of the individual impurities are performed using various wet chemical procedures and instmmental methods such as emission spectroscopy. 

GaP N, is clearly evident. The addition of N shifts the peak to longer wavelengths and broadens the spectral emission. The curves for the AIGalnP LEDs represent devices of three different alloy compositions, all exhibiting recombination for the conduction band direct minimum. The emission spectmm of the blue InGaN LED exhibits uniquely broad emission, most likely as a result of recombination via deep Zn impurities levels (23). 

Spectroscopic methods for the deterrnination of impurities in niobium include the older arc and spark emission procedures (53) along with newer inductively coupled plasma source optical emission methods (54). Some work has been done using inductively coupled mass spectroscopy to determine impurities in niobium (55,56). X-ray fluorescence analysis, a widely used method for niobium analysis, is used for routine work by niobium concentrates producers (57,58). Paying careful attention to matrix effects, precision and accuracy of x-ray fluorescence analyses are at least equal to those of the gravimetric and ion-exchange methods. 

Rubidium metal is commeicially available in essentially two grades, 99 + % and 99.9 + %. The main impurities ate other alkali metals. Rubidium compounds are available in a variety of grades from 99% to 99.99 + %. Manufacturers and suppliers of mbidium metal and mbidium compounds usually supply a complete certificate of analysis upon request. Analyses of metal impurities in mbidium compounds are determined by atomic absorption or inductive coupled plasma spectroscopy (icp). Other metallic impurities, such as sodium and potassium, are determined by atomic absorption or emission spectrograph. For analysis, mbidium metal is converted to a compound such as mbidium chloride. 

The sodium hydroxide is titrated with HCl. In a thermometric titration (92), the sibcate solution is treated first with hydrochloric acid to measure Na20 and then with hydrofluoric acid to determine precipitated Si02. Lower sibca concentrations are measured with the sibcomolybdate colorimetric method or instmmental techniques. X-ray fluorescence, atomic absorption and plasma emission spectroscopies, ion-selective electrodes, and ion chromatography are utilized to detect principal components as weU as trace cationic and anionic impurities. Eourier transform infrared, ft-nmr, laser Raman, and x-ray... 

Chiral separations have become of significant importance because the optical isomer of an active component can be considered an impurity. Optical isomers can have potentially different therapeutic or toxicological activities. The pharmaceutical Hterature is trying to address the issues pertaining to these compounds (155). Frequendy separations can be accompHshed by glc, hplc, or ce. For example, separation of R(+) and 5 (—) pindolol was accompHshed on a reversed-phase ceUulose-based chiral column with duorescence emission (156). The limits of detection were 1.2 ng/mL of R(+) and 4.3 ng/mL of 3 (—) pindolol in semm, and 21 and 76 ng/mL in urine, respectively. 

Commercially produced barium is analyzed for metallic impurities by means of emission spectroscopy. Carbon content can be deterrnined by combustion, and nitrogen by the Kjeldahl method. Total barium can best be deterrnined gravimetricaHy by precipitation as the sulfate. 

MetaUic impurities in beryUium metal were formerly determined by d-c arc emission spectrography, foUowing dissolution of the sample in sulfuric acid and calcination to the oxide (16) and this technique is stUl used to determine less common trace elements in nuclear-grade beryUium. However, the common metallic impurities are more conveniently and accurately determined by d-c plasma emission spectrometry, foUowing dissolution of the sample in a hydrochloric—nitric—hydrofluoric acid mixture. Thermal neutron activation analysis has been used to complement d-c plasma and d-c arc emission spectrometry in the analysis of nuclear-grade beryUium. 

Commercially produced calcium metal is analyzed for metallic impurities by emission spectroscopy. Carbon content is determined by combustion, whereas nitrogen is measured by Kjeldahl determination. 

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