Publications by authors named "Sanyuan Zhu"

Beyond its economic value, copper (Cu) serves as a valuable tracer of deep magmatic processes due to its close relationship with magmatic sulfide evolution and sensitivity to oxygen fugacity (fO). However, determining Cu's oxidation state (+ 1 or + 2) in silicate melts, crucial for interpreting its behavior and reconstructing fO in the Earth's interior, has long been a challenge. This study utilizes X-ray Absorption Near Edge Structure spectroscopy to investigate the Cu oxidation state in hydrous mafic silicate melts equilibrated under diverse fO (- 1.

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Aerosol black carbon (BC) is a short-lived climate pollutant. The poorly constrained provenance of tropical marine aerosol BC hinders the mechanistic understanding of extreme climate events and oceanic carbon cycling. Here, we collected PM samples during research cruise NORC2016-10 through South China Sea (SCS) and Northeast Indian Ocean (NEIO) and measured the dual-carbon isotope compositions (δC-C) of BC using hydrogen pyrolysis technique.

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Article Synopsis
  • - The study investigates the sources and atmospheric behaviors of organic carbon aerosol (OC) in Guangzhou, China, highlighting that about 60% of OC originates from non-fossil sources like biomass burning and biogenic emissions.
  • - Non-fossil secondary organic carbon (SOC) was identified as the main contributor to OC, making up approximately 39%, followed by fossil SOC (26%), fossil primary OC (14%), biomass burning OC (13%), and cooking OC (8%).
  • - The research also examines how the aging of OC impacts its characteristics, finding that OC particles from non-fossil sources exhibit a higher degree of aging (86%) when influenced by emissions from northern regions.
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Incomplete understanding of the sources of secondary organic aerosol (SOA) leads to large uncertainty in both air quality management and in climate change assessment. Chemical reactions occurring in the atmospheric aqueous phase represent an important source of SOA mass, yet, the effects of anthropogenic emissions on the aqueous SOA (aqSOA) are not well constrained. Here we use compound-specific dual-carbon isotopic fingerprints (δC and ΔC) of dominant aqSOA molecules, such as oxalic acid, to track the precursor sources and formation mechanisms of aqSOA.

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Article Synopsis
  • Black carbon (BC) aerosol is a significant contributor to air quality issues and global warming, with petroleums combustion identified as the leading source in Guangzhou, China (39%).
  • The study utilized a dual-carbon isotope method via a Bayesian Markov chain Monte Carlo (MCMC) approach to analyze BC sources, highlighting the influence of regional air mass transport on BC contribution patterns.
  • The research indicates that fossil fuel combustion is responsible for 84% of the total BC reduction from 2013-2018, and predicts it will take about 6 years to meet the WHO PM guideline values if current emission controls remain unchanged.
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  • Black Carbon (BC) impacts air quality and climate, but its emission sources in Southeast Asia are not well understood; this study analyzes BC in Malaysia to determine the contributions from biomass and fossil fuels over one year.
  • The findings indicate a roughly equal contribution from biomass burning and fossil fuels overall, with seasonal variations revealing up to 70% of BC from biomass burning during the dry spring season.
  • The study highlights the need to address and reduce vegetation fires during the dry season in SE Asia to improve air quality and mitigate climate change effects.
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Naphthalene (NAP), as a surrogate of intermediate-volatility organic compounds (IVOCs), has been proposed to be an important precursor of secondary organic aerosol (SOA). However, the relative contribution of its emission sources is still not explicit. This study firstly conducted the source apportionment of atmospheric NAP using a triple-isotope (δC, δH, and ΔC) technique combined with a Bayesian model in the Beijing-Tianjin-Hebei (BTH) region of China.

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We report the surface exploration by the lunar rover Yutu that landed on the young lava flow in the northeastern part of the Mare Imbrium, which is the largest basin on the nearside of the Moon and is filled with several basalt units estimated to date from 3.5 to 2.0 Ga.

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Determination of oxidation states of solid-phase arsenic in bulk sediments is a valuable step in the evaluation of its bioavailability and environmental fate in deposits, but is difficult when the sediments have low arsenic contents and heterogeneous distribution of arsenic species. As K-edge X-ray absorption near-edge spectroscopy (XANES) was used to determine quantitatively the oxidation states of arsenic in sediments collected from different depths of boreholes in the Pearl River Delta, China, where the highest aquatic arsenic concentration is 161.4 μg/L, but the highest solid arsenic content only 39.

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Tetrabromobisphenol A (TBBPA), a widely used brominated flame retardant, could negatively affect various aspects of mammalian and human physiology, which triggers effective techniques for its removal. In this work, the degradation characteristics of TBBPA in heterogeneous UV/Fenton reaction catalyzed by titanomagnetite (Fe(3-x)Ti(x)O₄) were studied. Batch tests were conducted to evaluate the effects of titanomagnetite dosage, H₂O₂ concentration and titanium content in magnetite on TBBPA degradation.

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This study investigated the methylene blue (MB) decolorization through heterogeneous UV-Fenton reaction catalyzed by V-Ti co-doped magnetites, with emphasis on comparing the contribution of V and Ti cations on improving the adsorption and catalytic activity of magnetite. In the well crystallized spinel structure, both Ti(4+) and V(3+) occupied the octahedral sites. Ti(4+) showed a more obvious effect on increasing specific surface area and superficial hydroxyl amount than V(3+) did, resulting in a significant improvement of the adsorption ability of magnetite to MB.

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The catalytic activity of natural vanadium-titanium magnetite was investigated in the decolorization of Acid Orange II by non-homogeneous Fenton process. The natural catalysts purified by magnetic separation were characterized using X-ray diffraction (XRD), polarizing microscope, X-ray absorption fine structure (XAFS) analysis and Mössbauer spectroscopy. The obtained results show that the natural samples after magnetic separation mainly contain titanomagnetite, with a small amount of ilmenite and chlorite.

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