3,564 research outputs found
A new specifically designed calix[8]arene for the synthesis of functionalized, nanometric and subnanometric Pd, Pt and Ru nanoparticles
A new thioester functionalized calix[8]arene derivative is used for the synthesis of metallic Pd, Pt and Ru nanoparticles, exhibiting several interesting features such as stability and remarkable surface functionalization. Crystalline particles of very small dimensions and good dispersion have been obtained
Нові документи про родину Лисянських
Het lijkt een wet van Meden en Perzen: in tijden van
crisis duikt ook steeds een roep om ingrijpende
verandering op. Constante in deze dynamiek is het
concept van de rechtvaardige stad. Hoewel al in de
jaren zeventig geïntroduceerd, is het nog steeds
onderdeel van verhit debat. In deze AGORA een
historische en theoretische refl ectie en een analyse
van rechtvaardigheid in de stedelijke praktijk
In-Situ Investigation of Gas Phase Radical Chemistry in the Catalytic Partial Oxidation of Methane on Pt
The catalytic partial oxidation of methane on platinum was studied in situ under atmospheric pressure and temperatures between 1000 and 1300 °C. By combining radical measurements using a molecular beam mass spectrometer and threshold ionization with GC, GC-MS and temperature profile measurements it was demonstrated that a homogeneous reaction pathway is opened at temperatures above 1100 °C, in parallel to hetero-geneous reactions which start already at 600 °C. Before ignition of gas phase chemistry, only CO, H2, CO2 and H2O are formed at the catalyst surface. Upon ignition of gas chemistry, CH3⋅ radicals, C2 coupling products and traces of C3 and C4 hydrocarbons are observed. Because the formation of CH3⋅ radicals correlates with the formation of C2 products it can be concluded that C2 products are formed by coupling of methyl radicals in the gas phase followed by dehydrogenation reactions. This formation pathway was predicted by numerical simulations and this work presents an experimental confirmation under high temperature atmospheric pressure conditions
Role of dispersion of vanadia on SBA-15 in the oxidative dehydrogenation of propane
A series of vanadia catalysts supported on the mesoporous silica SBA-15 are synthesized using an automated laboratory reactor. The catalysts contain from 0.6 up to 13.6V atoms/nm2 and are structurally characterized by various techniques (BET, XRD, SEM, TEM, Raman, IR, UV/Vis). Samples containing up to 3.1V/nm2 are structurally rather similar. They all contain a mixture of tetrahedral (VOx)n species, both monomeric and oligomeric. The ratio of monomeric and oligomeric species depends on the vanadia loading. At the highest loading of 13.6V/nm2, in addition to tetrahedral (VOx)n, also substantial amounts of three-dimensional, bulk-like V2O5 are present in the catalyst. The structural similarity of the low-loaded catalysts is reflected in their alike catalytical activity during the oxidative dehydrogenation (ODH) of propane between 380 and 480 °C. Propene, CO, and CO2 are formed as reaction products, while neither the formation of ethene nor acrolein or acrylic acid is observed in other than trace amounts. The activation energy for ODH of propane is not, vert, similar140 kJ/mol. The catalyst with the highest loading yields varying activation energies for different reaction conditions, which is probably related to rearrangements between bulk-like and dispersed, two-dimensional (VOx)n. Rather than the monomer to oligomer ratio, the ratio of two-dimensional to three-dimensional vanadia seems to be crucial for the catalytic properties of silica supported vanadia in the ODH of propane
Quadrupole transitions and quantum gates protected by continuous dynamic decoupling
Dynamical decoupling techniques are a versatile tool for engineering quantum states with tailored properties. In trapped ions, nested layers of continuous dynamical decoupling (CDD) by means of radio-frequency field dressing can cancel dominant magnetic and electric shifts and therefore provide highly prolonged coherence times of electronic states. Exploiting this enhancement for frequency metrology, quantum simulation or quantum computation, poses the challenge to combine the decoupling with laser-ion interactions for the quantum control of electronic and motional states of trapped ions. Ultimately, this will require running quantum gates on qubits from dressed decoupled states. We provide here a compact representation of nested CDD in trapped ions, and apply it to electronic S and D states and optical quadrupole transitions. Our treatment provides all effective transition frequencies and Rabi rates, as well as the effective selection rules of these transitions. On this basis, we discuss the possibility of combining CDD and Mølmer-Sørensen gates
Quadrupole transitions and quantum gates protected by continuous dynamic decoupling
Dynamical decoupling techniques are a versatile tool for engineering quantum
states with tailored properties. In trapped ions, nested layers of continuous
dynamical decoupling by means of radio-frequency field dressing can cancel
dominant magnetic and electric shifts and therefore provide highly prolonged
coherence times of electronic states. Exploiting this enhancement for frequency
metrology, quantum simulation or quantum computation, poses the challenge to
combine the decoupling with laser-ion interactions for the quantum control of
electronic and motional states of trapped ions. Ultimately, this will require
running quantum gates on qubits from dressed decoupled states. We provide here
a compact representation of nested continuous dynamical decoupling in trapped
ions, and apply it to electronic and states and optical quadrupole
transitions. Our treatment provides all effective transition frequencies and
Rabi rates, as well as the effective selection rules of these transitions. On
this basis, we discuss the possibility of combining continuous dynamical
decoupling and M{\o}lmer-S{\o}rensen gates
Significant Conditions on the Two-electron Reduced Density Matrix from the Constructive Solution of N-representability
We recently presented a constructive solution to the N-representability
problem of the two-electron reduced density matrix (2-RDM)---a systematic
approach to constructing complete conditions to ensure that the 2-RDM
represents a realistic N-electron quantum system [D. A. Mazziotti, Phys. Rev.
Lett. 108, 263002 (2012)]. In this paper we provide additional details and
derive further N-representability conditions on the 2-RDM that follow from the
constructive solution. The resulting conditions can be classified into a
hierarchy of constraints, known as the (2,q)-positivity conditions where the q
indicates their derivation from the nonnegativity of q-body operators. In
addition to the known T1 and T2 conditions, we derive a new class of
(2,3)-positivity conditions. We also derive 3 classes of (2,4)-positivity
conditions, 6 classes of (2,5)-positivity conditions, and 24 classes of
(2,6)-positivity conditions. The constraints obtained can be divided into two
general types: (i) lifting conditions, that is conditions which arise from
lifting lower (2,q)-positivity conditions to higher (2,q+1)-positivity
conditions and (ii) pure conditions, that is conditions which cannot be derived
from a simple lifting of the lower conditions. All of the lifting conditions
and the pure (2,q)-positivity conditions for q>3 require tensor decompositions
of the coefficients in the model Hamiltonians. Subsets of the new
N-representability conditions can be employed with the previously known
conditions to achieve polynomially scaling calculations of ground-state
energies and 2-RDMs of many-electron quantum systems even in the presence of
strong electron correlation
Molecular Beam Mass Spectrometer Equipped with a Catalytic Wall Reactor for In Situ Studies in High Temperature Catalysis Research
International audienc
Heterogeneous–Homogeneous Catalytic Partial Oxidations Investigated by Molecular Beam Mass Spectrometry
Heterogeneous catalytic reactions are often insufficiently described by surface reaction steps only; gas phase contributions are neglected. Surface and gas phase reaction steps can take place simultaneously and are coupled by exchange of energy and reaction intermediates. Catalytic partial oxidations are suspected to proceed via combined heterogeneous–homogeneous mechanisms because of high reaction temperatures and the diradical oxygen as reactant. Gas phase radicals are thought to be key intermediates, but there is little understanding of mechanistic details [1]. To study the mechanism of such reactions we have developed a Molecular Beam Mass Spectrometer (MBMS) equipped with a high temperature catalytic wall reactor
Probabilistic tractography in the ventrolateral thalamic nucleus: cerebellar and pallidal connections
The ventrolateral thalamic nucleus (VL), as part of the ‘motor thalamus’, is main relay station of cerebellar and pallidal projections. It comprises anterior (VLa) and posterior (VLpd and VLpv) subnuclei. Though the fibre architecture of cerebellar and pallidal projections to of the VL nucleus has already been focus in a numerous amount of in vitro studies mainly in animals, probabilistic tractography now offers the possibility of an in vivo comparison in healthy humans. In this study we performed a (a) qualitative and (b) quantitative examination of VL-cerebellar and VL-pallidal pathways and compared the probability distributions between both projection fields in the VL after an (I) atlas-based and (II) manual-based segmentation procedure. Both procedures led to high congruent results of cerebellar and pallidal connectivity distributions: the maximum of pallidal projections was located in anterior and medial parts of the VL nucleus, whereas cerebellar connectivity was more located in lateral and posterior parts. The median connectivity for cerebellar connections in both approaches (manual and atlas-based segmentation) was VLa > VLpv > VLpd, whereas the pallidal median connectivity was VLa ~ VLpv > VLpd in the atlas-based approach and VLpv > VLa > VLpd in the manual approach.Peer reviewe
- …