Yonglin Liu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Yonglin Liu has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Chuanxi Yang
School of Environmental and Municipal Engineering, Qingdao University of Technology, Qingdao 266520, China
1 shared publication - Feng Dang
School of Materials Science & Engineering Shandong University Jinan P.R. China
1 shared publication - Hongmei Liu
Academy of National Food and Strategic Reserves Administration, Beijing 100037, China
1 shared publication - Huimin Zhou
Institute of Environment and Ecology, Shandong Normal University, Jinan 250358, China
1 shared publication - Jin Ye
NFSRA Key Laboratory of Grain and Oil Quality and Safety, Academy of National Food and Strategic Reserves Administration, Beijing 100037, China
1 shared publication - Minghui Zhou
Academy of National Food and Strategic Reserves Administration, Beijing 100037, China
1 shared publication
Latest Publications
- Open Access
Automated and Rapid Easy-to-Use Magnetic Solid-Phase Extraction System for Five Heavy Metals in Cereals and Feeds
A rapid, accurate, and ecofriendly pretreatment plays an extremely important role prior to ICP-MS for heavy metal analysis. In order to improve the pretreatment efficiency, a high-throughput and automatic magnetic solid-phase extraction of five heavy metals (Cd, Pb, Mn, Cu, and Zn) was carried out by a magnet-controlled pretreatment system with an ecofriendly diluted acid as an extracting agent and carboxyl-functionalized magnetic beads as a pretreatment material. Key conditions, including the pH, adsorption time, and eluent solution, were optimized. The time for purification and enrichment was only 8 min. The adsorption capacities of the carboxyl-functionalized magnetic beads were in the range of 152~426 mg g−1. The preconcentration factor of Cu was 40, and others were 200. In the optimal conditions, the limits of detection for Mn, Zn, Cd, Cu, and Pb by ICP-MS were 3.84, 2.71, 0.16, 11.54, and 6.01 ng L−1, respectively. The percentage recoveries were in the range of 80~110%, and the relative standard deviations were less than 3%. The developed method was in good agreement with traditional standard microwave digestion. Additionally, the designed system could simultaneously process up to 24 samples within 22 min, reducing the time to less than 1 min/sample. Thus, the proposed auto-MSPE-ICP-MS method was successfully applied to analyze five heavy metals in cereals and feeds with a simple operation and high precision, safety, and reliability.
Open AccessAutomated and Rapid Easy-to-Use Magnetic Solid-Phase Extraction System for Five Heavy Metals in Cereals and Feeds
A rapid, accurate, and ecofriendly pretreatment plays an extremely important role prior to ICP-MS for heavy metal analysis. In order to improve the pretreatment efficiency, a high-throughput and automatic magnetic solid-phase extraction of five heavy metals (Cd, Pb, Mn, Cu, and Zn) was carried out by a magnet-controlled pretreatment system with an ecofriendly diluted acid as an extracting agent and carboxyl-functionalized magnetic beads as a pretreatment material. Key conditions, including the pH, adsorption time, and eluent solution, were optimized. The time for purification and enrichment was only 8 min. The adsorption capacities of the carboxyl-functionalized magnetic beads were in the range of 152~426 mg g−1. The preconcentration factor of Cu was 40, and others were 200. In the optimal conditions, the limits of detection for Mn, Zn, Cd, Cu, and Pb by ICP-MS were 3.84, 2.71, 0.16, 11.54, and 6.01 ng L−1, respectively. The percentage recoveries were in the range of 80~110%, and the relative standard deviations were less than 3%. The developed method was in good agreement with traditional standard microwave digestion. Additionally, the designed system could simultaneously process up to 24 samples within 22 min, reducing the time to less than 1 min/sample. Thus, the proposed auto-MSPE-ICP-MS method was successfully applied to analyze five heavy metals in cereals and feeds with a simple operation and high precision, safety, and reliability.
- Open Access
Solvothermal Synthesis of ZnO Nanoparticles for Photocatalytic Degradation of Methyl Orange and p-Nitrophenol
The photocatalytic degradation of organic pollutants is an effective method of controlling environmental pollution. ZnO nanoparticles (ZnO NPs) were prepared by the solvothermal method and characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV–visible diffuse reflectance spectroscopy (UV–Vis DRS). The results showed that the ZnO NPs had a uniform size of 25–40 nm, hexagonal wurtzite structure, and a band gap of 2.99 eV. The photocatalytic degradation of methyl orange (MO) and p-nitrophenol (PNP) was used as a model reaction to evaluate the photocatalytic activity of ZnO NPs. The photocatalytic degradation rates (pseudo-first-order kinetics) of MO and PNP were 92% (0.0128 min−1) and 56.2% (0.0042 min−1), respectively, with a 25 W ultraviolet lamp, MO/PNP concentration = 20 mg/L, ZnO NPs dose = 1.5 g/L, and time = 180 min. The photocatalytic mechanism of ZnO NPs and degradation pathways of MO and PNP were also proposed. The results provide valuable information and guidance for the treatment of wastewater via photocatalytic methods.
Open AccessSolvothermal Synthesis of ZnO Nanoparticles for Photocatalytic Degradation of Methyl Orange and p-Nitrophenol
The photocatalytic degradation of organic pollutants is an effective method of controlling environmental pollution. ZnO nanoparticles (ZnO NPs) were prepared by the solvothermal method and characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV–visible diffuse reflectance spectroscopy (UV–Vis DRS). The results showed that the ZnO NPs had a uniform size of 25–40 nm, hexagonal wurtzite structure, and a band gap of 2.99 eV. The photocatalytic degradation of methyl orange (MO) and p-nitrophenol (PNP) was used as a model reaction to evaluate the photocatalytic activity of ZnO NPs. The photocatalytic degradation rates (pseudo-first-order kinetics) of MO and PNP were 92% (0.0128 min−1) and 56.2% (0.0042 min−1), respectively, with a 25 W ultraviolet lamp, MO/PNP concentration = 20 mg/L, ZnO NPs dose = 1.5 g/L, and time = 180 min. The photocatalytic mechanism of ZnO NPs and degradation pathways of MO and PNP were also proposed. The results provide valuable information and guidance for the treatment of wastewater via photocatalytic methods.