Swendsen‐Wang dynamics for general graphs in the tree uniqueness region

The Swendsen‐Wang (SW) dynamics is a popular Markov chain for sampling from the Gibbs distribution for the ferromagnetic Ising model on a graph G = (V,E). The dynamics is conjectured to converge to equilibrium in O(|V|^1/4) steps at any (inverse) temperature β, yet there are few results providing o(|V|) upper bounds. We prove fast convergence of the SW dynamics on general graphs in the tree uniqueness region. In particular, when β < β_c(d) where β_c(d) denotes the uniqueness/nonuniqueness threshold on infinite d‐regular trees, we prove that the relaxation time (i.e., the inverse spectral gap) of the SW dynamics is Θ(1) on any graph of maximum degree d ≥ 3. Our proof utilizes a monotone version of the SW dynamics which only updates isolated vertices. We establish that this variant of the SW dynamics has mixing time and relaxation time Θ(1) on any graph of maximum degree d for all β < β_c(d). Our proof technology can be applied to general monotone Markov chains, including for example the heat‐bath block dynamics, for which we obtain new tight mixing time bounds.     

Application of ultrasound-assisted physical mixing treatment improves in vitro protein digestibility of rapeseed napin

The in vitro protein digestibility (IVPD) of napin was studied using different pretreatment methods, including ultrasound, mixing napin with lactalbumin, and ultrasound-assisted protein mixing. The relationships between IVPD, molecular structure, and disulfide bonds were explored, showing that the IVPD of napin was the highest compared with the control when treated with 40% ultrasound power. When the proportion of napin to lactalbumin was 5:5, a synergistic influence between the two proteins was observed. Further investigation showed that the IVPD of napin was clearly improved by treatment with ultrasound-assisted protein mixing. Compared with the single protein in the control, the β-sheet content in the secondary structure of the mixed protein after sonication was reduced from 45.02% to 37.16%. The ordered protein structure was also disrupted by ultrasound, as supported by fluorescence intensity and surface hydrophobicity analyses. The decreased number of disulfide bonds and conformational changes indicated that the IVPD of rapeseed napin was closely related to the disulfide bond content. This study provides a theoretical basis for improving protein digestibility by combining ultrasound with physical mixing.     

Bi4Ge3O12:Er3+晶体中的高阶混合效应对EPR g因子的影响

通过对角化364×364完全能量矩阵的理论方法,对掺杂在Bi₄Ge₃O₁₂晶体中的Er³⁺的Stark能级和EPR参数进行了研究,同时,定量分析了高阶晶体场混合效应和J-J混合效应对EPR g因子的影响。研究结果表明:对Er³⁺来说,最主要的J-J混合效应来源于多重态谱项²K_15/2,其对EPR g因子的贡献约占2.5%,而最主要的高阶晶体场混合效应来源于第一激发多重态⁴I_13/2和基态多重态⁴I_15/2之间的晶体场混合,其对各向异性g因子中g_⊥的贡献大致是g_//的两倍(即g_⊥约占 0.21%,g_//约占0.092%),其他更高阶的晶体场混合和J-J混合效应可以忽略不计。因此,对于Er³⁺掺杂的络合物系统来说,只考虑基态多重态⁴I_15/2对EPR g因子的贡献应该是一个很好的近似。     

An optimized mixed‐mode stationary phase based on silica monolith particles for the separation of peptides and proteins in high‐performance liquid chromatography

A phase with both hydrophobic and hydrophilic functionalities has been synthesized by modification of ground silica monolith particles with C18 and 1‐[3‐(trimethoxysilyl)propyl] urea ligands. A series of phases was prepared by changing the ratio of the two ligands to determine the optimal ratio in view of separation efficiency. The resultant optimized stationary phase was packed in narrow‐bore glass‐lined stainless‐steel columns (1 × 300 mm and 2.1 × 100 mm) and used for the separation of synthetic peptides and proteins. The average numbers of theoretical plates (N) of 52 100/column (174 000/m, 5.75 µm plate height) and 35 500/column (118 000/m, 8.47 µm plate height) were achieved with the 300 mm column at a flow rate of 25 µL/min (0.86 mm/s) in 60:40 v/v acetonitrile/30 mM aqueous ammonium formate for the mixture of peptides (Thr‐Tyr‐Ser, Val‐Ala‐Pro‐Gly, angiotensin I, isotocin, and bradykinin) and for the mixture of proteins (myoglobin, human serum albumin, and insulin), respectively. Fast analysis of the peptides and proteins was also carried out at a flow rate of 0.9 mL/min (6.88 mm/s) with the 100 mm column and all the analytes were eluted within 2 min with good separation efficiency.     

基于涡旋光束的超快速角向集束匀滑方案

针对惯性约束聚变装置对激光集束辐照均匀性的需求,提出了一种基于涡旋光束的超快速角向匀滑方案,即利用螺旋相位板使2×2集束中的两子束由超高斯光束变换为涡旋光束,而其余两子束不变,进而通过对子束偏振态和中心波长的调控,使集束中的涡旋光束和超高斯光束在靶面两两相干叠加.相干叠加后的焦斑以皮秒量级为周期超快速旋转,从而在极短时间内快速抹平焦斑强度调制,改善靶面辐照均匀性.通过建立基于螺旋相位板的激光超快速角向集束匀滑方案的物理模型,分析了其角向匀滑特性,并与光谱角色散技术和径向匀滑技术进行了比较分析.结果表明,这一新型激光集束匀滑方案能实现对焦斑的超快速角向匀滑,且能在数皮秒时间内达到最佳辐照均匀性.     

On the boomerang uniformity of a class of permutation quadrinomials over finite fields

Let ${\mathbb{F}}_{2^n}$ be a finite field with $2^n$ elements and $f_{\underset{\_}{c}}(x)=c_0{x}^{2^m(2^k+1)}+c_1{x}^{2^{m+k}+1}+c_2{x}^{2^m+2^k}+c_3{x}^{2^k+1}\in {\mathbb{F}}_{2^n}[x]$, where n, m and k are positive integers with $n=2m$ and $\gcd ?(m,k)=e$. In this paper, motivated by a recent work of Li, Xiong and Zeng (Li et al. (2021) [12]), we further study the boomerang uniformity of $f_{\underset{\_}{c}}(x)$ by using similar ideas and carrying out particular techniques in solving equations over finite fields. As a consequence, we generalize Li, Xiong and Zeng's result from the case of m being odd and $e=1$ to that of both $m/e$ and $k/e$ being odd.     

Detailed experimental study of a highly compressible supersonic turbulent plane mixing layer and comparison with most recent DNS results: “Towards an accurate description of compressibility effects in supersonic free shear flows”

A compressible supersonic mixing layer at convective Mach number (Mc) equal to 1 has been studied experimentally in a dual stream supersonic/subsonic wind-tunnel. Laser Doppler Velocimetry (L.D.V.) measurements were performed making possible a full estimation of the mean and turbulent 3D velocity fields in the mixing layer. The Reynolds stress tensor was described. In particular, some anisotropy coefficients were obtained. It appears that the structure of the Reynolds tensor is almost not affected by compressibility at least up to Mc = 1.The turbulent kinetic energy budget was also experimentally estimated. Reynolds analogies assumptions were used to obtain density/velocity correlations in order to build the turbulent kinetic energy budget from LDV measurements. Results have been compared to other experimental and numerical results. Compressibility effects on the turbulent kinetic energy budget have been detected and commented. A study about thermodynamics flow properties was also performed using most recent DNS results experimentally validated by the present data. A non-dimensional number is then introduced in order to quantify the real effect of pressure fluctuations on the thermodynamics quantities fluctuations.     

Addendum to “Volumetric properties of binary liquid-phase mixture of (water + glycerol) at temperatures of (278.15 to 323.15) K and pressures of (0.1 to 100) MPa” [J. Chem. Thermodyn. 79 (2014) 135–158]: Effect of pressure on excess thermodynamic characteristics of mixture water + glycerol

Experimentally determined volumetric properties of the liquid binary mixture of {water (1) + glycerol (2)} were processed to calculate the changes of the following thermodynamic parameters with pressure: excess molar Gibbs free energy, ${\mathrm{\Delta }}_{P_o\to P}{G}_m^E$, excess molar entropy, ${\mathrm{\Delta }}_{P_o\to P}{S}_m^E$, excess molar enthalpy, ${\mathrm{\Delta }}_{P_o\to P}{H}_m^E$, as well as the enthalpy of mixing of water and glycerol, $H_m^E$, at 100 MPa. The mixing enthalpies of water and glycerol, $H_m^E$, became more exothermic with pressure increasing at all temperatures studied.     

亲水头基大小对正负离子表面活性剂混合体系的影响

<正>负离子表面活性剂混合体系曾被认为是表面活性剂配方的禁忌,但通过增大表面活性剂头基的面积,正负混合体系在很宽的物质的量比下都不会产生沉淀,而且还会产生显著的增效效应。头基大的离子型表面活性剂甚至能够用来增溶难溶的反电荷表面活性剂。     

Natural and artificial light-harvesting systems utilizing the functions of carotenoids

Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced.