纳米激光粒度仪在生物药品团聚物测试中的应用

探讨了纳米激光粒度仪测定生物药品团聚物质量浓度的方法。以SALD–7500nano颗粒测试仪为例,介绍其在测量纳米级颗粒物粒度范围方面的应用。通过进一步分析颗粒浓度与光强度成正比的关系获得以质量浓度形式给出的粒度分布数据。通过牛血清蛋白(BSA)团聚物测量的实例,验证了颗粒物质量浓度的测试方法。该方法可用于生物制药领域对团聚物的监控测量以及评价药品药效、安全性能等。     

The impact of asymptomatic individuals on the strength of public health interventions to prevent the second outbreak of COVID-19

Nonlinear Dynamics - The pandemic of coronavirus disease 2019 (COVID-19) has threatened the social and economic structure all around the world. Generally, COVID-19 has three possible transmission...     

Sound attenuation of a periodic array of micro-perforated tube mufflers

The wave propagation in a periodic array of micro-perforated tube mufflers is investigated theoretically, numerically and experimentally. Because of the high acoustic resistance and low mass reactance due to the sub-millimeter perforation, the micro-perforated muffler can provide considerable sound attenuation of duct noise. Multiple mufflers are often used to enhance attenuation performance. When mufflers are distributed periodically in a duct, the periodic structure produces special dispersion characteristics in the overall sound transmission loss. The Bloch wave theory and the transfer matrix method are used to study the wave propagation in periodic micro-perforated tube mufflers and the dispersion characteristics of periodic micro-perforated mufflers are examined. The results predicted by the theory are compared with finite element method simulation and experimental results. The results indicate that the periodic structure can influence the performance of micro-perforated mufflers. With different periodic distances, the combination of the periodic structure and the micro-perforated tube muffler can contribute to the control of lower frequency noise with a broader frequency range or improvement of the peak transmission loss around the resonant frequency.     

Quantum speedup via engineering multiple environments

Evolution speed of an open quantum system is vividly influenced by the structure of environments. The strong system‐environment coupling is found to be able to accelerate quantum evolution. In this work, we propose a different method of governing the quantum speedup via engineering multiple environments. It is shown that, with a judicious choice of the number of coupling environments, the quantum speedup of an open system can be achieved even under weak system‐environment coupling conditions. The mechanism for the speedup is due to the switch between Markovian and non‐Markovian regions by manipulating the number of the surrounding environments. In addition, we verify the above phenomena by using quantum dots embedded in a planar photonic crystal under current technologies. These results provide a new degree of freedoms to accelerate quantum evolution of open systems. The strong system‐environment coupling can speed up the quantum evolution process. This work shows that, via engineering multiple environments, one can speed up the evolution process even under weak coupling conditions.     

First-principles study on electronic structures of BaWO4 crystals containing F-type color centers

The electronic structures of BaWO₄ crystals containing F-type color centers are studied within the framework of the fully relativistic self-consistent Dirac-Slater theory, using a numerically discrete variational (DV-Xα) method. It is concluded that F and F⁺ color centers have donor energy level in the forbidden band. The optical transition energies are 2.449 and 3.101 eV, which correspond to the 507 and 400 nm absorption bands, respectively. It is predicted that 400-550 nm absorption bands originate from the F and F⁺ color centers in BaWO₄ crystals.     

Redox-Active Two-Dimensional Covalent Organic Frameworks (COFs) for Selective Reductive Separation of Valence-Variable,Redox-Sensitive and Long-Lived Radionuclides

We report the first example of 2D covalent organic framework nanosheets (Redox-COF1) for the selective reduction and in situ loading of valence-variable, redox-sensitive and long-lived radionuclides (abbreviated as VRL nuclides). Compared with sorbents based on chemical adsorption and physical adsorption, the redox adsorption mechanism of Redox-COF1 can effectively reduce the impact of functional group protonation under the usual high-acidity conditions in chemisorption, and raise the adsorption efficiency from the monotonous capture by pores in physisorption. The adsorption selectivity for UO₂²⁺ reaches up to unprecedented ca. 97 % at pH 3, more than for any analogous adsorbing material.