Total Atomic Scattering Factors of 1s^23s ~2S States for Lithium Isoelectronic Sequence

Total atomic scattering factors for the 1s^23s ^2S stages for the lithium isoelectronic sequence from Z = 3 - 10 are calculated by using the full core plus correlation wave function. The influence of electron correlation on total atomic scattering factors is considered sufficiently in our calculation. For the 1s^2 3s ^2S states of the lithium isoelectronic sequence, the general functional behaviour of total atomic scattering factors is analyzed together for each state of the isoelectronic sequence.

Determination of Proteins by Measuring Total Internal-reflected Resonance Light Scattering Signals on Water/Tetrachloromethane Interface with Evans Blue and Cetyltrimethylammonium Bromide

A sensitive and selective assay of proteins is proposed based on measuring the total internal-reflected resonance light scattering(TIR-RLS) signals produced on the water/tetrachloromethane(H_2O/CCl_4) interface. In an aqueous medium with pH value in the range of 3.29—3.78, electrostatic attraction occurs between the negatively charged Evans Blue(EB) and positively charged proteins, forming hydrophobic ion associates and resulting in EB-protein adsorption on H_2O/CCl_4 interface. The presence of cetyltrimethylammonium bromide prompts this adsorption, resulting in strongly enhanced TIR-RLS signals. The intensity of the enhanced TIR-RLS at 360—370 nm was found to be proportional to the concentration of proteins. For bovine serum albumin and human serum albumin, the linear range of detection is 0.07—1.2 μg/mL and the limits of detection are 6.68 and 6.30 ng/mL(3σ), respectively, while for lysozyme, the linear range of detection is 0.06—1.0 μg/mL and the limit of detection is 6.0 ng/mL(3σ). The content of the total albumin in a human urine sample could be directly determined by using the standard addition method with a percent recovery of 97.6%—104.1%, and the RSD ranging from 1.9% to 4.2%.

Mechanisms of Proton-Proton Inelastic Cross-Section Growth in Multi-Peripheral Model within the Framework of Perturbation Theory.Part 3

We develop a new method for taking into account the interference contributions to proton-proton inelastic cross-section within the framework of the simplest multi-peripheral model based on the self-interacting scalar φ3 field theory, using Laplace’s method for calculation of each interference contribution. We do not know any works that adopted the inter- ference contributions for inelastic processes. This is due to the generally adopted assumption that the main contribution to the integrals expressing the cross section makes multi-Regge domains with its characteristic strong ordering of secon- dary particles by rapidity. However, in this work, we find what kind of space domains makes a major contribution to the integral and these space domains are not multi-Regge. We demonstrated that because these interference contributions are significant, so they cannot be limited by a small part of them. With the help of the approximate replacement the sum of a huge number of these contributions by the integral were calculated partial cross sections for such numbers of secondary particles for which direct calculation would be impossible. The offered model qualitative agrees with experimental dependence of total scattering cross-section on energy with a characteristic minimum in the range ≈ 10 GeV. However, quantitative agreement was not achieved;we assume that due to the fact that we have examined the simplest diagrams of theory.

A new semi-empirical formula for total cross sections of electron scattering from triatomic molecules at 30—5000 eV

Total cross sections （TCSs） of electrons scattering from triatomic molecules over the energy range from 30 to 5000 eV are investigated employing a new semi-empirical formula. The TCSs of electrons scattering from triatomic molecules SO2, NO2, and CO2 are calculated. The quantitative TCSs are in good agreement with those obtained by experiments. It is shown that the results derived from the semi-empirical formula are much closer to the measurements than other calculations.

Long-and short-range orders in 10-component compositionally complex ceramics

Neutron diffraction and total scattering are combined to investigate a series of single-phase 10-component compositionally complexfluorite-based oxides,[(Pr_(0.375)Nd_(0.375)Yb_(0.25))2(Ti_(0.5)Hf_(0.25)Zr_(0.25))_(2)O_(7)]_(1-x)[(DyHoErNb)O_(7)]_(x),denoted as 10CCFBOxNb.A long-range order-disorder transition(ODT)occurs at x=0.81±0.01 from the ordered pyrochlore to disordered defectfluorite.In contrast to ternary oxides,this ODT occurs abruptly without an observable two-phase region;moreover,the phase stability in 10CCFBOs deviates from the well-established criteria for simpler oxides.Rietveld refinements of neutron diffraction patterns suggest that this ODT occurs via the migration of oxygen anions from the position 48f to 8a,with a smallfinal jump at the ODT;however,the 8a oxygen occupancy changes gradually(without an observable discontinuous jump).We further discover diffuse scattering in Nb-rich compositions,which suggests the presence of short-range order.Using small-box modelling,four compositions near ODT(x=0.75,0.8,0.85,and 1)can be betterfitted by C2221 weberite ordering for the local polyhedral structure at nanoscale.Interestingly,10CCFBO_(0.75)Nb and 10CCFBO_(0.8)Nb possess both long-range pyrochlore order and short-range weberite-type order,which can be understood from severe local distortion of the pyrochlore polyhedral structure.Thus,weberite-type short-range order emerges before the ODT,coexisting and interacting with long-range pyrochlore order.After the ODT,the long-range pyrochlore order vanishes but the short-range weberite-type order persists in the long-range disordered defectfluorite structure.Notably,a drop in the thermal conductivity coincides with emergence of the short-range order,instead of the long-range ODT.