163 research outputs found

    Glossary of methods and terms used in analytical spectroscopy (IUPAC Recommendations 2019)

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    Recommendations are given concerning the terminology of concepts and methods used in spectroscopy in analytical chemistry, covering nuclear magnetic resonance spectroscopy, atomic spectroscopy, and vibrational spectroscopy. © 2021 IUPAC and De Gruyter. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. For more information, please visit: http://creativecommons.org/licenses/by-nc-nd/4.0/ 2021

    mass concentration and size distribution of atmospheric particulate matter in an urban environment

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    To investigate the ambient mass concentration, size-distribution and temporal variability of atmospheric particulate matter (PM), a long-term monitoring campaign was undertaken at an urban background site in Como, Northern Italy, from May 2015 to March 2016. A 13-stage Low Pressure Impactor (DLPI) was used for the collection of size-segregated particulates in the 0.028-10 μm size range. The results revealed a good level of agreement between DLPI and a co-located Harvard-type PM_(2.5) Impactor, allowing them to be classified as comparable and characterized by a reciprocal predictability. The PM concentration levels varied greatly between the different 5-days monitoring sessions, with higher mean mass concentrations during the heating season. Appreciable seasonal differences were found for particles between 0.15 and 1.60 μm that, on average, registered concentration levels 3.5 times higher during the heating season (mean: 28.2 μg m^(-3); median: 24.4 μg m^(-3)) compared to the non-heating season (mean: 8.3 μg m^(-3); median: 7.6 μg m^(-3)). No relevant and significant differences were detected for the coarser ranges (> 1.60 μm). Temporal variabilities were influenced by typical PM urban sources (e.g., household heating, traffic), that significantly affected fine and submicrometer particles, and were related to meteorological factors. Ambient air particles exhibited a trimodal distribution: a first and sharp peak more pronounced during the heating season was identified between 0.3 and 0.5 μm and two other slight peaks in the coarse mode were centered on approximately 3 and 8 μm. No relevant differences were found in the shape of the size-distribution between the two investigated seasons. The mean PM_(2.5) (22.4 μg m^(-3)) and PM_(10) (27.7 μg m^(-3)) concentrations monitored in the study area exceeded the annual Air Quality Guideline Values (respectively equal to 10 μg m^(-3) and 20 μg m^(-3)) established by the World Health Organization

    Singular charge fluctuations at a magnetic quantum critical point

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    Strange metal behavior is ubiquitous in correlated materials, ranging from cuprate superconductors to bilayer graphene, and may arise from physics beyond the quantum fluctuations of a Landau order parameter. In quantum-critical heavy-fermion antiferromagnets, such physics may be realized as critical Kondo entanglement of spin and charge and probed with optical conductivity. We present terahertz time-domain transmission spectroscopy on molecular beam epitaxy–grown thin films of YbRh₂Si₂, a model strange-metal compound. We observed frequency over temperature scaling of the optical conductivity as a hallmark of beyond-Landau quantum criticality. Our discovery suggests that critical charge fluctuations play a central role in the strange metal behavior, elucidating one of the long-standing mysteries of correlated quantum matter

    Singular charge fluctuations at a magnetic quantum critical point

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    Strange metal behavior is ubiquitous in correlated materials, ranging from cuprate superconductors to bilayer graphene, and may arise from physics beyond the quantum fluctuations of a Landau order parameter. In quantum-critical heavy-fermion antiferromagnets, such physics may be realized as critical Kondo entanglement of spin and charge and probed with optical conductivity. We present terahertz time-domain transmission spectroscopy on molecular beam epitaxy–grown thin films of YbRh2Si2, a model strange-metal compound. We observed frequency over temperature scaling of the optical conductivity as a hallmark of beyond-Landau quantum criticality. Our discovery suggests that critical charge fluctuations play a central role in the strange metal behavior, elucidating one of the long-standing mysteries of correlated quantum matter.Financial support for this work was provided by the European Research Council (ERC Advanced Grant 227378), the U.S. Army Research Office (ARO W911NF-14-1-0496), the Austrian Science Fund (FWF W1243, P29279-N27, and P29296-N27), and the European Union’s Horizon 2020 research and innovation programme (grant agreement No 824109 – EMP). X.L. and J.K. acknowledge financial support from the National Science Foundation (NSF MRSEC DMR-1720595) and the ARO (W911NF-17-1-0259). Q.S. acknowledges financial support from the NSF (DMR-1920740), the Robert A.Welch Foundation (C-1411), and the ARO (W911NF-14-1-0525), and hospitality of the University of California at Berkeley, the Aspen Center for Physics (NSF grant PHY-1607611), and the Los Alamos National Laboratory (via a Ulam Scholarship from the Center for Nonlinear Studies). This work has also been supported by an InterDisciplinary Excellence Award (IDEA) from Rice University (Q.S., E.R., J.K., S.P.)

    Singular charge fluctuations at a magnetic quantum critical point

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    Strange metal behavior is ubiquitous in correlated materials, ranging from cuprate superconductors to bilayer graphene, and may arise from physics beyond the quantum fluctuations of a Landau order parameter. In quantum-critical heavy-fermion antiferromagnets, such physics may be realized as critical Kondo entanglement of spin and charge and probed with optical conductivity. We present terahertz time-domain transmission spectroscopy on molecular beam epitaxy–grown thin films of YbRh2Si2, a model strange-metal compound. We observed frequency over temperature scaling of the optical conductivity as a hallmark of beyond-Landau quantum criticality. Our discovery suggests that critical charge fluctuations play a central role in the strange metal behavior, elucidating one of the long-standing mysteries of correlated quantum matter

    Oxalic acid in clear and cloudy atmospheres: Analysis of data from International Consortium for Atmospheric Research on Transport and Transformation 2004

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    Oxalic acid is often the leading contributor to the total dicarboxylic acid mass in ambient organic aerosol particles. During the 2004 International Consortium for Atmospheric Research on Transport and Transformation (ICARTT) field campaign, nine inorganic ions (including SO_4^(2−)) and five organic acid ions (including oxalate) were measured on board the Center for Interdisciplinary Remotely Piloted Aircraft Studies (CIRPAS) Twin Otter research aircraft by a particle-into-liquid sampler (PILS) during flights over Ohio and surrounding areas. Five local atmospheric conditions were studied: (1) cloud-free air, (2) power plant plume in cloud-free air with precipitation from scattered clouds overhead, (3) power plant plume in cloud-free air, (4) power plant plume in cloud, and (5) clouds uninfluenced by local pollution sources. The aircraft sampled from two inlets: a counterflow virtual impactor (CVI) to isolate droplet residuals in clouds and a second inlet for sampling total aerosol. A strong correlation was observed between oxalate and SO_4^(2−) when sampling through both inlets in clouds. Predictions from a chemical cloud parcel model considering the aqueous-phase production of dicarboxylic acids and SO_4^(2−) show good agreement for the relative magnitude of SO_4^(2−) and oxalate growth for two scenarios: power plant plume in clouds and clouds uninfluenced by local pollution sources. The relative contributions of the two aqueous-phase routes responsible for oxalic acid formation were examined; the oxidation of glyoxylic acid was predicted to dominate over the decay of longer-chain dicarboxylic acids. Clear evidence is presented for aqueous-phase oxalic acid production as the primary mechanism for oxalic acid formation in ambient aerosols

    Effects of Precursor Concentration and Acidic Sulfate in Aqueous Glyoxal−OH Radical Oxidation and Implications for Secondary Organic Aerosol

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    Previous experiments demonstrated that aqueous OH radical oxidation of glyoxal yields low-volatility compounds. When this chemistry takes place in clouds and fogs, followed by droplet evaporation (or if it occurs in aerosol water), the products are expected to remain partially in the particle phase, forming secondary organic aerosol (SOA). Acidic sulfate exists ubiquitously in atmospheric water and has been shown to enhance SOA formation through aerosol phase reactions. In this work, we investigate how starting concentrations of glyoxal (30−3000 μM) and the presence of acidic sulfate (0−840 μM) affect product formation in the aqueous reaction between glyoxal and OH radical. The oxalic acid yield decreased with increasing precursor concentrations, and the presence of sulfuric acid did not alter oxalic acid concentrations significantly. A dilute aqueous chemistry model successfully reproduced oxalic acid concentrations, when the experiment was performed at cloud-relevant concentrations (glyoxal <300 μM), but predictions deviated from measurements at increasing concentrations. Results elucidate similarities and differences in aqueous glyoxal chemistry in clouds and in wet aerosols. They validate for the first time the accuracy of model predictions at cloud-relevant concentrations. These results suggest that cloud processing of glyoxal could be an important source of SOA

    Atomic spectrometry update – a review of advances in environmental analysis

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