聚乙烯醇缩-5-甲酰基-2,4-二羟基苯偶氮安替比林液-固萃取和光度测定镍的研究

本文报道了2,4-二羟基-5-安替比林偶氮苯甲醛(DAP)及DAP与聚乙烯醇(PVA)的缩合产物(PV·DAP)的合成.并利用PV·DAP做萃取剂,析相萃取和光度测定了铝合金和环境水样中的镍.实验结果还表明,高分子显色剂与相应的小分子试剂相比,在液-固萃取方面表现为易获得高萃取率且不受萃合物电性的影响,在光度测定方面则表现出较高的灵敏度和稳定性.从而说明试剂的高分子化可改善其性能.     

Bimetallic atomic site catalysts for CO2 reduction reactions: a review

Environmental Chemistry Letters - Carbon neutral becomes one of the most important environmental goals due to the excessive emission of CO2. The reduction of CO2 into valuable chemicals or fuels is...     

Impact of anthropogenic heat emissions on meteorological parameters and air quality in Beijing using a high-resolution model simulation

• The Large scale Urban Consumption of energY model was updated and coupled with WRF. • Anthropogenic heat emissions altered the precipitation and its spatial distribution. • A reasonable AHE scheme could improve the performance of simulated PM_2.5. • AHE aggravated the O₃ pollution in urban areas. Anthropogenic heat emissions (AHE) play an important role in modulating the atmospheric thermodynamic and kinetic properties within the urban planetary boundary layer, particularly in densely populated megacities like Beijing. In this study, we estimate the AHE by using a Large-scale Urban Consumption of energY (LUCY) model and further couple LUCY with a high-resolution regional chemical transport model to evaluate the impact of AHE on atmospheric environment in Beijing. In areas with high AHE, the 2-m temperature (T₂) increased to varying degrees and showed distinct diurnal and seasonal variations with maxima in night and winter. The increase in 10-m wind speed (WS₁₀) and planetary boundary layer height (PBLH) exhibited slight diurnal variations but showed significant seasonal variations. Further, the systematic continuous precipitation increased by 2.1 mm due to the increase in PBLH and water vapor in upper air. In contrast, the precipitation in local thermal convective showers increased little because of the limited water vapor. Meanwhile, the PM_2.5 reduced in areas with high AHE because of the increase in WS₁₀ and PBLH and continued to reduce as the pollution levels increased. In contrast, in areas where prevailing wind direction was opposite to that of thermal circulation caused by AHE, the WS₁₀ reduced, leading to increased PM_2.5. The changes of PM_2.5 illustrated that a reasonable AHE scheme might be an effective means to improve the performance of PM_2.5 simulation. Besides, high AHE aggravated the O₃ pollution in urban areas due to the reduction in NO_x.     

Hygroscopicity of particles generated from photooxidation of α-pinene under diferent oxidation conditions in the presence of sulfate seed aerosols

Smog chamber experiments were conducted to investigate the hygroscopicity of particles generated from photooxidation of α-pinene/NOx with diferent sulfate seed aerosols or oxidation conditions. Hygroscopicity of particles was measured by a tandem diferential mobility analyzer(TDMA) in terms of hygroscopic growth factor(Gf), with a relative humidity of 85%. With sulfate seed aerosols present, Gf of the aerosols decreased very fast before notable secondary organic aerosols(SOA) formation was observed, indicating a heterogeneous process between inorganic seeds and organic products might take place as soon as oxidation begins, rather than only happening after gas-aerosol partition of organic products starts. The final SOA-coated sulfate particles had similar or lower Gf than seed-free SOA. The hygroscopicity of the final particles was not dependent on the thickness but on the hygroscopicity properties of the SOA, which were influenced by the initial sulfate seed particles. In the two designed aging processes, Gf of the particles increased more significantly with introduction of OH radical than with ozone. However, the hygroscopicity of SOA was very low even after a long time of aging, implying that either SOA aging in the chamber was very slow or the Gf of SOA did not change significantly in aging. Using an aerosol composition speciation monitor(ACSM) and matrix factorization(PMF) method, two factors for the components of SOA were identified, but the correlation between SOA hygroscopicity and the proportion of the more highly oxidized factor could be either positive or negative depending on the speciation of seed aerosols present.     

河南省平顶山市大气降尘的化学特征及其来源解析

为系统反映河南省平顶山市大气降尘的特征,选取平顶山市5个典型功能区(工业区、交通区、居民区、文教区、居民商业混合区),于2008年5月-2009年4月用圆筒型集尘缸采集60个大气降尘样品,应用电感耦合等离子体原子发射光谱法(ICP-AES)和离子色谱法(IC)分别对其中的20种元素浓度和14种离子浓度进行了分析.结果表...     

Carbon dioxide capture under ambient conditions using 2-chloroethylamine

This is the first case applying 2-haloethylamine to CO₂ capture. The prospect of global warming and the urgent need to reduce atmospheric concentration of carbon dioxide has prompted actions at many levels. The conventional capture of carbon dioxide is predominantly based on chemical absorption using ethanolamine. Recent developments of carbon dioxide capture focus on new materials, such as ionic liquids, zeolites, membranes, carbonaceous absorbents, and metal–organic frameworks. However, no unique solution exists currently to solve the problem of carbon dioxide capture. In order to examine the efficiency of 2-chloroethylamine as an absorbent of CO₂, we treated an aqueous solution of 2-chloroethylamine hydrochloride with CO₂ in the presence of an alkali, e.g., NaOH, under ambient conditions. The absorption was complete within 30 min, seemingly following first-order reaction kinetics. Furthermore, we succeeded in capturing CO₂ from ambient air using 2-chloroethanolamine. The efficiency of 2-chloroethylamine as an absorbent of CO₂ could be attributed to the production of stable 2-oxazolidinone, therefore, this reaction is favored thermodynamically. Compared with previously reported absorbents, this novel system is capable of capturing CO₂ with an extremely high efficiency of 1 mol per mol absorbent under ambient conditions, even from the atmosphere. This potential method could be used to capture CO₂ particularly from small, mobile, or low-concentration emission sources.