Search results for "X-Ray Absorption Spectroscopy"
showing 9 items of 129 documents
The complementary structural studies of the double metal cyanide type catalysts for the ring opening polymerization of the oxiranes
2016
Przeprowadzono badania strukturalne katalizatorów dimetalocyjankowych (DMC) z dwoma rodzajami ligandów organicznych. Zaproponowano wyjaśnienie etapów przebiegu krzywych otrzymanych metodą analizy termograwimetrycznej i różnicowej kalorymetrii skaningowej (TG/DSC) badanych katalizatorów. Wykazano obecność kilku stopni związania ligandów w kompleksach DMC. Na podstawie wyników badań z wykorzystaniem absorpcji rentgenowskiej (XAS) stwierdzono, że centrum aktywne katalizatora stanowi atom cynku. W bezpośrednim sąsiedztwie atomów Zn wykryto obecność atomów Cl, natomiast w najbliższych sferach koordynacyjnych atomu Zn nie wykryto atomów tlenu.
Effect of Pre-Reduction on the Properties and the Catalytic Activity of Pd/Carbon Catalysts: A Comparison with Pd/Al2O3
2013
The effect of pre-reduction in solution with chemical reagents on the catalytic performance and catalyst properties of Pd/carbon catalysts was systematically investigated with a multitechnique approach. The results are critically discussed in comparison to those recently obtained on analogous Pd/alumina catalysts. It was proved that the Pd phase on the carbon surface is characterized by a high mobility, opposite to what occurs on alumina. As a result, the Pd particles on carbon aggregate together during pre-reduction, with a consequent decrease in available metal surface. Pd particles remain aggregated also in reaction conditions; the decreased Pd dispersion negatively affects the catalyst …
Concave π-prismand hydrocarbon [2.2.2]cyclophanes and their crystalline Ag-triflate complexes
1999
New small concave hydrocarbon cyclophanes were prepared via the well-known HD-2SO2-method. The cyclophanes obtained are isomers of the very well-known [2.2.2]p,p,p-cyclophane, C24H24, a π-prismand efficiently complexing Ag+-ion. X-ray crystal structure determinations showed the bis-sulfide 7 (1,10-dithia[3.3.2]m,p,p-cyclophane) to be helically chiral and that the conformation of the parent hydrocarbon cyclophane 13 ([2.2.2]m,p,p-cyclophane) does not change dramatically upon complexation with the Ag+-ion. The 16- and 17-membered [2.2.2]m,m,p- and [2.2.2]m,p,p-cyclophane (15 and 16) also act as π-prismands and form surprisingly similar crystalline 1:1 Ag-triflate complexes (π-prismates) as th…
Cover Feature: Towards Atomically Precise Supported Catalysts from Monolayer‐Protected Clusters: The Critical Role of the Support (Chem. Eur. J. 31/2…
2020
New insights for materials science characterisation using different complementary techniques combined with X-ray absorption Spectroscopy
2005
The combination of x-ray absorption spectroscopy (XAS) with UV-Vis and Raman spectroscopies or with Differential Scanning Calorimetry (DSC) has been recently carried out on the D44 beamline of DCI-LURE. The different set-ups used to perform such combinations are described and examples of combined investigations belonging to different field of materials science (coordination chemistry, sol-gel and catalysis) are presented.
Local Structure Studies of Ti for SrTi16O3 and SrTi18O3 by Advanced X-ray Absorption Spectroscopy Data Analysis
2015
Strontium titanate is a model quantum paraelectric in which in the region of dominating quantum statistics the ferroelectric instability is inhibited due to nearly complete compensation of the harmonic contribution into ferroelectric soft mode frequency by the zero-point motion contribution. The enhancement of atomic masses by the substitution of 18O for 16O decreases the zero-point atomic motion and low-T ferroelectricity in SrTi18O3 is realized. In this study we report on the local structure of Ti in SrTi16O3 and SrTi18O3 by Ti K-edge extended x-ray absorption fine structure measurements in temperature range 6 – 300 K.
ODS tērauda izejmateriālu lokālās struktūras analīze izmantojot Ti un Y K-malas rentgenabsorbcijas spektroskopiju
2017
Šajā darbā tika izmantota rentgenstaru absorbcijas spektru analīze oksīdu stiprinātam tēraudam (ODS), kas ir perspektīvs materiāls dažādās jomās, piemēram, saules elektrostacijās, reaktīvos dzinējos, ķīmiskos reaktoros un kodolreaktoros, jo materiālam piemīt tādas īpašības kā laba siltumvadītspēja un zema termiskās izplešanās apvienojumā ar augstu temperatūras izturību, korozijas un radiācijas pretestību. Darbā tiek iegūta informācija par ar dažādām metodēm izgatavotu ODS tēraudu lokālās atomārās struktūras izmaiņu ap itrija (Y) un titāna (Ti) atomiem, analizējot Y un Ti absorbcijas K-malu.
ODS tērauda izejmateriālu lokālās struktūras analīze, izmantojot rentgenabsorbcijas spektroskopiju
2015
Oksīdu stiprināts tērauds (ODS) ir perspektīvs kodolsintēzes reaktoru materiāls, kuram ir lieliska siltumvadītspēja un zema termiskās izplešanās, apvienojumā ar augstu temperatūras izturību, korozijas un radiācijas pretestību. Tamdēļ šo materiālu var izmantot arī daudzos citos pielietojumos, piemēram, saules elektrostacijās, reaktīvos dzinējos, ķīmiskos reaktoros, kā arī ūdeņraža ražošanā. Šajā darbā ar rentgenabsorbcijas spektroskopijas metodi tika analizētas ferīta un austentisko ODS tēraudu lokālās atomārās struktūras izmaiņas ap dzelzs (Fe) un hroma (Cr) atomiem dažādos tēraudu izgatavošanas posmos, analizējot Fe un Cr absorbcijas K-malas spektrus.
Revealing the local structure of CuMo1−xWxO4 solid solutions by multi-edge X-ray absorption spectroscopy
2022
I.P. and A.K. would like to thank the support of the Latvian Council of Science project No. lzp-2019/1-0071. I.P. acknowledges the L’OREAL Baltic “For Women In Science Program” with the support of the Latvian National Commission for UNESCO and the Latvian Academy of Sciences. The experiment at the Elettra synchrotron was performed within project No. 20150303. Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2.