scholarly journals Электроды вакуумной камеры под действием дуги в зоне взрывного плавления

2020 ◽  
Vol 90 (7) ◽  
pp. 1209
Author(s):  
А.И. Кудюкин ◽  
М.Н. Махмудов ◽  
Е.Н. Моос ◽  
В.А. Степанов

The floatable systems Cu (60%) - Cr (40%) after repeated influence of the arc vacuum discharge find change of atomic concentration of copper (with 53.7 ат. % to 71.8 ат. %) and, respectively, chromium. The mass-spectrometry showed existence in the residual atmosphere of diffusion instruments fragments of the CxHy molecules and molecules desorbed from all details of the camera, ions of residual gas (CO2, H2O, N2, N and their polyatomic compositions). Inheritance of technological impurity from prior operations in a mass spectrum is revealed.

2021 ◽  
Vol 25 (1) ◽  
pp. 21-28
Author(s):  
Yan Lv ◽  
Laijun Lu ◽  
Mengxue Cao

Because of the interference of mass spectrum and non-mass spectrum, the tracing accuracy of rare earth elements in the surrounding rock of geological formation is low. Pretreatment of test sample reagent, dissolution of test sample residue, characterization of rare earth element doped materials, analysis of mass spectrometry and non-mass spectrometry interference in rare earth element tracking, using three-dimensional positioning algorithm to track rare earth elements in geological strata surrounding rock. In the experiment, five samples of surrounding rock of geological strata are selected as experimental indexes. The experimental results show that the tracking accuracy of four rare earth elements is high.


2009 ◽  
Vol 2009 ◽  
pp. 1-18 ◽  
Author(s):  
Hebe Saraví Cisneros ◽  
Sergio Laurella ◽  
Danila L. Ruiz ◽  
Agustín Ponzinibbio ◽  
Patricia E. Allegretti ◽  
...  

Mass spectrometry is used to evaluate the occurrence of the nitrile-ketenimine tautomerism. Mass spectra of two differently substituted nitriles, ethyl-4,4-dicyano-3-methyl-3-butenoate and diethyl-2-cyano-3-methyl-2-pentenodiate are examined looking for common mass spectral behaviors. Ion fragmentation assignments for specific tautomers allow to predict the presence of the corresponding structures. Additionally, the mass spectrum and nuclear magnetic resonance spectra of ethyl-4,4-dicyano-2,2-diethyl-3-methyl-3-butenoate and that of the corresponding amination product support the occurrence of the ketenimine tautomer in the equilibrium.


1984 ◽  
Vol 39 (2) ◽  
pp. 248-251 ◽  
Author(s):  
Lutz Grotjahn ◽  
Volker B. Koppenhagen ◽  
Ludger Ernst

Hydrogenobalam in (metal-free vitamin B12) and cupribalamin are characterized by their fast atom bombardment (FAB) mass spectra which show molecular ion and characteristic fragment ion peaks. These spectra and the high-resolution FAB mass spectrum of cobalamin (vitamin B12) show that the (M+H)+-CN-59 peak for the latter is due to loss of acetamide and not of the central cobalt atom. In the FAB mass spectrum of cupribalamin metal clusters are observed


1982 ◽  
Vol 35 (7) ◽  
pp. 1365 ◽  
Author(s):  
A Benedetti ◽  
C Preti ◽  
L Tassi ◽  
G Tosi

Substituted benzeneseleninic acids of the type XC6H4SeO2H (X = m-Cl, p-Cl, m-Br, p-Br, p-Me, m-NO2, p-NO2) have been investigated by mass spectrometry. The fragmentation modes and the fragment ions are discussed and compared with those obtained from the mass spectrum of m-nitro-phenyl selenocyanate, O2NC6H4SeCN. Generally, as regards the acids, besides very weak peaks due to the molecular ions, a number of peaks at higher mass numbers and of greater intensity is observed; these peaks are in multiplets typical of the presence of two selenium atoms, and they correspond to the disubstituted diphenyl diselenides of the type XC6H4SeSeC6H4X. m-Nitrophenyl selenocyanate shows an intense molecular ion peak and the relative fragmentation, while the peak due to the diselenide is of very low intensity.


1994 ◽  
Vol 47 (2) ◽  
pp. 229 ◽  
Author(s):  
JW Perich ◽  
I Liepa ◽  
AL Chaffee ◽  
RB Johns

Positive and negative ion fast atom bombardment ( f.a.b .) mass spectrometry were found to be useful methods for the analysis and structural characterization of five Nα-(t- butoxycarbonyl )-O-( diorganylphosphono )-L- serines ( organyl = Ph, Et, Me, Bzl , But), especially in the case of the sensitive benzyl and t-butyl phosphono derivatives. Under positive ion operating conditions, high intensity pseudo-molecular ions were obtained in the f.a.b . mass spectra, and the fragmentation pathway of the phenyl, ethyl and methyl derivatives was established by parent/daughter linked scanning studies to involve (a) the two-step loss of the t- butoxycarbonyl group, (b) loss of the amino acid as the neutral fragment from the [MH]+, [MH-56]+, [MH-100]+ and [MH-146]+ ions by a four- centred β-elimination rearrangement, and (c) cleavage of the phosphono phenyl and ethyl groups from only the [(RO)2P(OH)2]+ and [NH=CHCH2PO3R2+H]+ fragments. Parent/daughter linked scanning studies of the benzyl derivative showed that the prominent fragmentation involved loss of the benzyl group as the tropylium ion and that the 'apparent' [MH-90]+ peak observed in its f.a.b. mass spectrum resulted from cleavage of the phosphono benzyl group in the matrix during the bombardment process. In the case of the t-butyl derivative, parent/daughter linked scanning studies showed that the prominent fragmentation involved successive 'in-flight' loss of the phosphono t-butyl groups as isobutene. Negative ion f.a.b. mass spectrometry of the five derivatives gave f.a.b. mass spectra which displayed distinct [M-H]- anions along with high intensity [M-H-R]- and [(RO)2PO2]- fragment anions, the f.a.b . mass spectrum of the t-butyl derivative containing an additional [M-H-But-But]- fragment anion. Parent/daughter linked scanning studies established that the majority of the observed fragment anions resulted from extensive fragmentation of the Boc -Ser(PO3R2)-OH derivatives in the matrix phase followed by sputtering of the resultant fragments into the gas phase. In addition, positive ion f.a.b . mass spectrometry was found to be useful for the analysis of a series of protected O-( diorganylphosphono ) seryl-containing dipeptides and tripeptides ( organyl = Ph, Et, Me, Bzl ). The obtained spectra showed that β-elimination fragmentation of the Ser(PO3R2) residue was more pronounced with the tripeptide series and indicated that there was increased sensitivity of the O-( diorganylphosphono ) seryl residue with replacement of the Boc group by an amino acyl residue at its N-terminus.


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