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11.
TXRF has been applied in combination with VPD to the analysis of trace impurities in the native oxide layer of Si wafer surfaces down to the range of 10(8) atoms. cm(-2). Proper quantification of VPD/TXRF data requires calibration with microdroplet standard reference wafers. The precision of calibration function has been evaluated and found to allow quantification at a high level of 3 sigma confidence with microdroplet standard reference. 相似文献
12.
Siegfried Noack 《Accreditation and quality assurance》1998,3(11):436-443
An important part of quality assurance in any analytical laboratory is the production of comprehensive results integrating uncertainty measurements. Many testing laboratories face the problem that the expenditure required to evaluate small uncertainties (high precision and high accuracy) is often uneconomic. In most cases an uncertainty of high reliability has to be calculated from only a few data (one calibration, few replications, etc.). This problem can be solved by an expert system. To achieve this the analytical procedure has to be structured into a dialouge and divided into parts. The uncertainty has to be calculated for each part of the procedure. Addition of the individual uncertainties results in the combined and expanded uncertainty. During the dialouge the system should advise the analyst how to get an efficient and effective calculation of uncertainty. All calculations, mathematical and statistical procedures have to be surveyable but running the system should not be too time consuming for economic reasons. Within the scope of the EURECA-project initiated by the Eidgenössische Materialprüfungs- und Forschungsanstalt (EMPA), St. Gallen, Switzerland, expert system software is being developed in cooperation with other research institutes and manufacturers of analytical instruments. Using this software it will be possible to calculate the uncertainty for analytical procedures such as titration, atomic emission spectrometry (ICP-OES), atomic absorption spectrometry (AAS) and gas- and liquid chromatography (GC, HPLC). 相似文献
13.
14.
Summary We start with a measurem on a measurable space (,A), decomposable with respect to an Archimedeant-conorm on a real interval [0,M], which generalizes an additive measure. Using the integral introduced by the second author, a Radon-Nikodym type theorem, needed in what follows, is given.The integral naturally leads to a -decomposable measurem on the space of all measurable functions from to [0, 1]. The main result of the present paper is the converse of this, namely that, under natural conditions, any -decomposable measurem on can be represented as an integral of a certain Markov-kernelK.
We extend this representation to measures
on which have values in a set of distribution functions.These results generalize the work done by the first author in the case of additive measures. 相似文献
15.
Perfluorocongressane was synthesized using elemental fluorine and characterized by mass spectra, (19)F NMR, and X-ray crystallography. 相似文献
16.
Siegfried Steiner 《manuscripta mathematica》1985,52(1-3):21-35
It is well known (and rather trivial to prove) that the square F2 of a Finsler norm F:TM on a differentiable manifold M is differentiable at the zero section if and only if F is the norm function of a Riemannian metric. However, the corresponding question for a general p-areal on M is far less trivial to settle and leads to interesting algebraic and combinatorial problems concerning multiquadratic forms. For p=2, the results are closely related to known properties of the curvature tensor of a Riemannian metric. 相似文献
17.
Fabian Gerson Georg Gescheidt Reinhart Mckel Alexander Aumüller Peter Erk Siegfried Hünig 《Helvetica chimica acta》1988,71(7):1665-1672
The radical anions of 12 N,N′-dicyanoquinone diimines, a new class of electron acceptors, hace been characterized by their hyperfine data with the use of ESR and ENDOR spectroscopy. The largest coupling constant (0.30–0.45 mT), due to the two 14N nuclei in the exocyclic positions, gives rise to a conspicuous broadening of the peripheral ESR lines by an incomplete averaging of the hyperfine anisotropy. The most plausible interpretation of the experimental results for the radical anions of N,N′-dicyano- 1,4-benzoquinone diimine ( 1 ) and N,N′-Dicyano-9,10-anthraquinone diimine ( 9 ) is in terms of both ‘syn’- and ‘anti’-configurations contributing to the ESR and ENDOR spectra and having equal proton- and 14N-coupling constants. The π-spin distribution in the radical anions of N,N′-dicyanoquinone diimines is compared with those in the analogous ions of tetracyanoquinodimethanes and quinones. 相似文献
18.
19.
Jee JE Eigler S Hampel F Jux N Wolak M Zahl A Stochel G van Eldik R 《Inorganic chemistry》2005,44(22):7717-7731
The polyanionic water-soluble and non-mu-oxo-dimer-forming iron porphyrin iron(III) 5(4),10(4),15(4),20(4)-tetra-tert-butyl-5(2),5(6),15(2),15(6)-tetrakis[2,2-bis(carboxylato)ethyl]-5,10,15,20-tetraphenylporphyrin, (P(8-))Fe(III) (1), was synthesized as an octasodium salt by applying well-established porphyrin and organic chemistry procedures to bromomethylated precursor porphyrins and characterized by standard techniques such as UV-vis and (1)H NMR spectroscopy. A single pK(a1) value of 9.26 was determined for the deprotonation of coordinated water in (P(8-))Fe(III)(H(2)O)(2) (1-H(2)()O) present in aqueous solution at pH <9. The porphyrin complex reversibly binds NO in aqueous solution to give the mononitrosyl adduct, (P(8-))Fe(II)(NO(+))(L), where L = H(2)O or OH(-). The kinetics of the binding and release of NO was studied as a function of pH, temperature, and pressure by stopped-flow and laser flash photolysis techniques. The diaqua-ligated form of the porphyrin complex binds and releases NO according to a dissociative interchange mechanism based on the positive values of the activation parameters DeltaS() and DeltaV() for the "on" and "off" reactions. The rate constant k(on) = 6.2 x 10(4) M(-1) s(-1) (24 degrees C), determined for NO binding to the monohydroxo-ligated (P(8-))Fe(III)(OH) (1-OH) present in solution at pH >9, is markedly lower than the corresponding value measured for 1-H(2)O at lower pH (k(on) = 8.2 x 10(5) M(-1) s(-1), 24 degrees C, pH 7). The observed decrease in the reactivity is contradictory to that expected for the diaqua- and monohydroxo-ligated forms of the iron(III) complex and is accounted for in terms of a mechanistic changeover observed for 1-H(2)O and 1-OH in their reactions with NO. The mechanistic interpretation offered is further substantiated by the results of water-exchange studies performed on the polyanionic porphyrin complex as a function of pH, temperature, and pressure. 相似文献
20.
Petra Hoffman Siegfried Hünig Leonhard Walz Karl Peters Hans-Georg von Schnering 《Tetrahedron》1995,51(48):13197-13216
Azo compounds 1 and 3 containing a CC-double bond in a parallel but distant position are quatemized by Me3OBF4 to 1,MeBF4 and 3,MeBF4, whereas MeI produces the cage compounds 2,HX and 4,HX. These [3+2] cycloadducts also are quantitatively formed from 1,MeBF4 and 3,MeBF4 with catalytic amounts of azo compounds. Intermolecular [3+2] cycloadditions occur with a mixture of DBH (5) or DBO (8), MeI and a variety of alkenes (→ HI) salts of (6, 7, 9 — 12). The intermediate azomethineimines, if stabilized by a fluorenylidene group, can be isolated (20, 22,24), but not, however, in the presence of a close parallel CC-bond (25 → 26). 相似文献