限盐降压策略面临的挑战

详细叙述了限盐降压策略面临的三大挑战,是否要全民普遍限盐,是否血压降得越低越好,是否要吃得淡些更淡些。现有流行病学调查和临床试验结果表明,我国成人高血压盐敏感者约占相应总人口的三分之一强,约有7亿人不必严格限盐;降压治疗中可能存在J形曲线现象,血压降得过低,结局危险增大;每天摄入7~13 g食盐对健康较为有益,吃得＂淡些更淡些＂并不科学。     

试谈中国特色的现代微量元素研究

中国微量元素研究取得了处于国际前沿的研究成果,逐渐形成了具有中国特色的微量元素医学的完整体系,形成了元素基础医学学派、元素形态分析学派和元素组学研究学派。微量元素知识普及、期刊论文和会议论文、学位论文、专利项目、基金资助项目、图书出版、元素形态分析、微量元素组学等8个方面发生了翻天覆地的变化。首创微量元素组学研究,成功地破解了临床医学和中药传统理论中一系列关键问题,发现微量元素的双面效应。     

中国硒研究历史回顾（上）

过去50年中,中国微量元素科学和营养科学中最重要的发现,就是认识了硒对人体健康的重要性。在诸多微量元素中,没有哪一个元素能像硒那样对人类产生如此深刻而又广泛的影响。从硒的生物必需性、硒的生物效应两面性、硒的抗癌性、硒的延寿作用及富硒产品开发五个方面回顾了中国的硒研究历程。     

Experimental study on combustion characteristics of diesel–hydrogen dual-fuel engine

As a clean and sustainable energy source, hydrogen is widely considered as an engine fuel by top researchers. In view of the fact that the uneven fuel mixture of diesel fuel deteriorated the combustion and emissions process, it is expected to adopt diesel and hydrogen dual-fuel combustion technology to optimize combustion and heat release of diesel engine. In this study, experiments are carried out on a diesel engine and the combustion characteristics of the engine with different hydrogen ratios (RH) are compared. It has been found that hydrogen addition is conducive to accelerate the heat release rate and improve the thermal efficiency. Specifically, compared with pure diesel conditions, the peak pressure increased by 7.7% and the cumulative heat release rate increased by 3.7% under the condition of RH of 20%. Moreover, although the effect on the ignition delay period is not clear, the higher RH brings about earlier heat release center and more cumulative heat release while enhancing the heat release of premixed combustion reducing the diffusion combustion and post-combustion.

     

固定化多酶级联反应器

多酶级联反应在生命活动过程中发挥着重要作用。固定化多酶级联反应器是将不同功能的酶通过物理化学或生物手段固定于特定载体上,以之模拟生物体内多种酶协同作用方式促使底物发生降解和转化等反应的新型仿生催化技术。该技术具有固定化酶的稳定性、可重复利用以及酶级联的高效协同催化等优点,近年来在生物传感、模拟生物学以及生物转化等领域得到越来越多的关注。本文从多酶级联反应原理、反应器制备、级联反应的影响因素及应用等方面对近年来固定化多酶级联反应器的进展进行详细评述,并展望其发展前景。     

(+)‐Tartaric Acid‐Catalyzed High Regio‐ and Stereoselective Aminobromination of Olefins

(+)‐Tartaric acid‐catalyzed aminobromination of α,β‐unsaturated ketones, α,β‐unsaturated esters and simple olefins utilizing TsNH₂/NBS as the nitrogen/halogen sources at room temperature without protection of inert gases achieved good yields (up to 92% yield) of vicinal haloamino products with excellent regio‐ and stereoselectivity, even just 10% of (+)‐tartaric acid was used as catalyst. The regio‐ and stereochemistry was unambiguously confirmed by X‐ray structural analysis of products 2b and 12c . The electron‐rich and deficient olefins show significant differences in activity to the aminobromination reaction and give the opposite regioselectivities. The 21 cases have been investigated which indicated that our protocol has the advantage of a large scope of olefins. Additionally, tartaric acid as catalyst has the advantage of avoiding any hazardous metals retained in products.     

中国的中药微量元素研究Ⅴ.微量元素:中药质量控制不可或缺的特征参数

从中药鉴定、分类、组方解析、疗效相似药物筛选、质量控制5个方面综述了中国的中药微量元素质控研究概况.     

Visible‐Light‐Driven Overall Water Splitting Boosted by Tetrahedrally Coordinated Blende Cobalt(II) Oxide Atomic Layers

Directly splitting water into H₂ and O₂ with solar light is extremely important; however, the overall efficiency of water splitting still remains extremely low. Two types of ultrathin semiconductor layers with the same elements and the same thicknesses were designed to uncover how different atomic arrangements influence water‐splitting efficiency thermodynamically and kinetically. As an example, tetrahedrally coordinated blende and octahedrally coordinated rocksalt CoO atomic layers with nearly the same thicknesses were synthesized for the first time. The blende CoO atomic layers have a smaller E_g and abundant d–d internal transition features relative to the rocksalt CoO atomic layers, which ensure enhanced visible‐light harvesting ability. Density functional theory calculations reveal that the Bader charge for Co atoms in blende CoO atomic layers is larger than that of the rocksalt CoO atomic layers, which facilitates photocarrier transfer kinetics, as verified by photoluminescence spectra and time‐resolved fluorescence emission decay spectra. In situ FTIR spectra and energy calculations reveal that the *OOH dissociation step is the rate‐limiting step, where the blende CoO atomic layers possess a smaller *OOH dissociation energy thanks to their higher Bader charge and stronger steric effect, as confirmed by the elongated Co?OOH bonds. The blende CoO atomic layers exhibit visible‐light‐driven H₂ and O₂ formation rates of 4.43 and 2.63 μmol g^?1 h^?1, roughly 3.7 times higher than those of the rocksalt CoO atomic layers.     

Kinetic Control over Morphology of Nanoporous Graphene on Surface

On-surface synthesis of high-quality nanoporous graphene (NPG) for application in nanotechnology and nanodevices remains challenging. Rational design of molecular precursors and proper kinetic control over the reaction process are the two key factors to tune the synthesis. Herein, we report a detailed study of the coupling reactions of a planar halogen-substituted nanographene molecular precursor, hexaiodo-peri-hexabenzocoronene (I₆-HBC), on the Au(111) surface in the synthesis of NPG. The influence of three basic kinetic processes – molecular adsorption, migration, and coupling – on the synthesis was investigated. The results show that the HBC molecules deposited at low temperature predominantly desorb from the Au(111) surface during the annealing process, whereas depositing the precursor molecules onto a hot surface (700 K) can lead to the formation of NPG. However, at such a high surface temperature, simultaneous intermolecular dehydrogenative coupling between HBC monomers can hinder the ordered growth of NPG through Ullmann coupling. Moreover, the deposition rate of the precursors greatly influences the growth morphology of the NPG nanostructures.