Atomic emission spectroscopy hydrogen

The Bi-promoted catalysts were prepared by consecutive deposition of Bi onto a commercial 5 wt% Pt/alumina (Engelhard E 7004, Pt dispersion 0.30 determined by TEM) [7]. The reduction of bismuth-nitrate was carried out in a dilute aqueous acidic solution O10"6 M, pH = 3-4) by hydrogen. The metal content of the catalysts was determined by inductive coupled plasma atomic emission spectroscopy (ICP-AES). Preferential deposition of Bi onto Pt particles has been confirmed by TEM, combined with energy dispersive X-ray analysis (EDX) [7]. Pb-, Sn- and Ag-promoted catalysts were prepared similarly. 

Phosphorus can serve as a benehcial adjunct or as a deleterious agent. There are several test methods for the determination of phosphorus. In addition to the three test methods described here, reference should also be made to multielement analysis methods such as inductively coupled plasma atomic emission spectroscopy (ICPAES) (ASTM D-4951, ASTM D-5185) and X-ray fluorescence (XRF) (ASTM D-4927, ASTM D-6443) described above in this guide. Phosphorus can also be determined by a photometric procedure (IP 148) or by a test method (ASTM D-1091) in which the organic material in the sample is destroyed, phosphorus in the sample is converted to phosphate ion by oxidation with sulfuric acid, nitric acid, and hydrogen peroxide, and the magnesium pyrophosphate is determined gravimetrically. Another method (ASTM D-4047, IP 149) in which the phosphorus is converted to quinoline phosphomolybdate is also available. 

Actual metal contents were determined by inductively coupled plasma-atomic emission spectroscopy (ICP-AES). Metal particles were examined by X-ray diffraction, transmission electron microscopy and CO chemisorption. Details about the procedures used can be found elsewhere [9]. In the case of Pd-Ag/C catalysts, the combination of these three techniques enabled us to obtain the metal particles size and their bulk and surface composition [9, 13]. Finally, the Pt/C catalysts were tested for benzene hydrogenation, and the Pd-Ag/C catalysts were used to study mass transfer in the support during a well-known reaction the selective hydrodechlorination of 1,2-diehloroethane into ethylene. 

The combination of gas chromatography and atomic emission spectroscopy has been used for element selective investigations. The measurements were carried out with an HP G2350A Atomic emission detector (Hewlett Packard Inc.). For structural elucidation the channels carbon (C), hydrogen (H), arsenic (As), chlorine (Cl), oxygen (O) and sulfur (S) have been investigated. Spectral background correction was performed for elimination of interferences. 

Tin compounds are converted to the corresponding volatile hydride (SnH4, CH3 SnH3, (CH3 )2 SnH2, and (CH3 >3 SnH) by reaction with sodium borohydride at pH 6.5 followed by separation of the hydrides and then atomic absorption spectroscopy using a hydrogen-rich hydrogen-air flame emission type detector (Sn-H band). 

Elemental composition Li 31.85%, B 49.66%, H 18.50%. The compound is dissolved in water cautiously and the evolved hydrogen is measured by GC using a TCD. The aqueous solution is treated with nitric acid and the diluted nitric acid extract is analyzed for lithium by atomic absorption or emission spectroscopy (See Lithium). 

This system forms highly ionized so-called Penning mixtures [12,13]. The higher excited states of Hj are partly stable and partly unstable, depending on the quantum numbers of the electron present. The stable excited states have, however, only very shallow minima of the potential curves [14]. That is the reason why no spectrum of Hj is observed for the helium plasma jet. The argon excited neutrals, on the other hand, cannot ionize hydrogen atoms or molecules, but could produce excited H2 molecules, which can be detected by optical emission spectroscopy. 

Impurities in zirconium and zirconium alloys and compounds are often determined by emission spectroscopy. Both carrier distillation techniques and poiat-to-plane methods are available (91,92). Several metaUic impurities can be determined instantaneously by this method. Atomic absorption analysis has been used for iron, chromium, tin, copper, nickel, and magnesium (93). The interstitial gases, hydrogen, nitrogen, and oxygen are most often determiaed by chromatography (81). Procedures for carbon, chloride, fluoride, phosphorus, siUcon, sulfur, titanium, and uranium in zirconium are given in the hteiatuie (81,94—96). 

The discussion of emission spectroscopy will be concluded by a description of a rather unusual application. Bay and Steiner have measured atomic hydrogen concentrations in the presence of molecular hydrogen by microwave excitation of the atomic hydrogen line spectrum. With low power fed into the gas (ca. 5 watts), there is not enough energy available for the dissociation of molecular hydrogen and subsequent excitation. Thus the measured intensities of the atomic hydrogen lines correspond to the concentrations of atoms already present in the reaction mixture. The method is curiously similar to that adopted to detect atoms and free radicals by mass spectrometry (see Section 3). 

Every line in the hydrogen spectrum corresponds to a transition between electron energy levels. Spectral lines from hydrogen emission spectroscopy are shown at right and in the table below. Please see Skill 17.7 for additional information on atomic spectra. 

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