Publications by authors named "Weilin Guo"

Heterogeneous electro-Fenton is one of green and promising technologies for removing organic pollutants. In this paper, the FeOOH-CoFe layered double hydroxide carbon felt (LDH/CF) was synthesized by a facile hydrothermal method for an efficient degradation of oxytetracycline (OTC). The structural morphology and elemental composition of the composite electrode were studied by scanning electron microscopy, X-ray diffractometer, and X-ray photoelectron spectroscopy.

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Objective: To describe a novel α-thalassemiadeletion identified from a newborn by third-generation sequencing (TGS).

Case Report: The proband, a newborn subject to neonatal capillary electrophoresis (CE) screening, exhibited suspected α-thalassemia carrier status (Hb Bart's 3.0%).

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In this study, cobalt etched graphite felt electrodes were produced using a simple etching technique. It was used in combination with a solid polymer electrolyte (SPE) for the degradation of the target contaminant Orange II by Electro-Fenton (EF) technique in low conductivity water. In this method, 94% of Orange II in low conductivity water was removed in 90 min.

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Objective: The 4.2 kb deletion (-α/) is a common a-thalassemia with a carrier rate, followed by the South-East Asian deletion (-) and the 3.7 kb deletion (-α/).

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This work presents the role of commercial microfiltration membranes combined with single particle inductively coupled plasma-mass spectrometry (SP-ICP-MS) in removing environmental matrix interference for model silver nanoparticles (AgNPs) determination. The filters with different pore sizes (0.22 μm, 0.

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Objective: To describe the characterization of a novel deletion causing α-thalassemia.

Methods: The proband, a 30-year-old female, displayed mild anemia from thalassemia screening. Gap-PCR was used to detect the four common deletional α-thalassemia, and a PCR-reverse dot blot was performed for the three point mutations of the α-globin gene.

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The removal of phosphate ions by capacitive deionization has become one of the most frontier research topics in the water treatment field in recent years. In this work, hybrid electrodes composed of nickel-iron layered double hydroxide (NiFe-LDH) - anchored on activated carbon fiber (ACF)-were synthesized by a hydrothermal method and subsequently applied in capacitive deionization to remove phosphate ions. The adsorption performance of the two hybrid electrodes on phosphate ions was compared by capacitive deionization experiments.

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A series of FeMn bimetallic ferrocene-based metal-organic frameworks (FeMn-Fc-MOFs) with various molar ratios of Fe and Mn (1:9, 2:8, 4:6, 6:4) were successfully synthesized using a simple hydrothermal synthesis method and employed as an efficient activator on persulfate (PS) activation for water decontamination. Characterizations demonstrated that Fe and Mn were smoothly introduced into ferrocene-based MOFs and various molar ratios of Fe:Mn had some influence on crystallinity and surface structure of FeMn-Fc-MOFs. Within 120 min, FeMn-Fc-MOFs demonstrated the best catalytic activity among the different molar ratios, and acid orange 7(AO7) degradation rate was up to 92.

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The cathode material is critical to the yield of hydrogen peroxide (HO) and electro-Fenton (EF) performance. In this work, bismuth oxychloride (BiOCl) as one of the representatives of ternary oxides was grown in situ on carbon felt (CF) through a simple solvothermal method and employed directly as a self-standing cathode for the EF degradation of the target contaminant tetracycline (TC). TC can be almost completely degraded, up to 95% in 90 min under the heterogeneous EF process.

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Understanding how the morphology of a layered double hydroxide (LDH)-based catalyst alters its catalytic activity provides an available strategy for the rational design and fabrication of high-efficiency catalysts at a micro-scale. Herein, three nickel-iron layered double hydroxide (NiFe-LDH) catalysts including 2D-plate-like hexagon (P-NiFe-LDH), 2D/3D-flower-like solid sphere (FS-NiFe-LDH), and 2D/3D-flower-like hollow sphere (FH-NiFe-LDH) with regulable oxygen vacancies (OVs) were fabricated via a morphological regulation method of Ostwald ripening. The experimental results demonstrated that the three types of NiFe-LDH exhibited different abilities to activate persulfate (PS) for the abatement of acid orange 7 (AO7) with a sequence of FH-NiFe-LDH > FS-NiFe-LDH > P-NiFe-LDH.

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Aims: Alpha-thalassaemia is one of the most common monogenic disorders worldwide. Due to high guanine-cytosine (GC) content and high mutation diversity in α-globin gene cluster, deletional and non-deletional mutations were usually separately detected with different methods. The aim of this study was to develop a novel one-step method for α-thalassaemia genotyping.

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A series of LaNiO perovskite nanoparticles with different morphologies, such as spheres, rods and cubes, were prepared through co-precipitation and hydrothermal methods, and used as the catalysts for peroxydisulfate (PDS) activation. The physical and chemical characterization of LaNiO perovskites was performed, including X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen isotherm absorption (BET), electrochemical impedance spectroscopy (EIS), and X-ray photoelectron spectroscopy (XPS). The LaNiO with different shapes showed different activities in Acid Orange 7 (AO7) degradation.

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Ferrocene-based metal-organic framework with different transition metals (M-Fc-MOFs, M = Fe, Mn, Co) was synthesized by a simple hydrothermal method and used as a heterogeneous catalyst for persulfate activation. The samples were characterized by X-ray diffraction, transmission electron microscopy, X-ray electron spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. Meanwhile, the influences of factors such as catalyst dosage, persulfate concentration, and pH on the degradation of acid orange 7 (AO7) were studied in detail.

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Phosphate residue is a kind of hazardous solid waste and if not properly disposed of, could cause serious environmental contaminations. The abundant iron salt available in phosphate residue can be used to prepare photo-Fenton catalytic reagent for wastewater treatment. In this study, the phosphate residue was effectively purified by a hydrothermal recrystallization method, reaching an iron phosphate purity of 94.

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Goethite is the most ubiquitous iron oxide mineral in soils, and adsorption of organic pollutants on goethite dominates the fate and transportation in the environment. In this study, the facet-dependent adsorption behavior of ciprofloxacin (CIP) on goethite was systematically investigated with in situ attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectra and two-dimensional correlation analysis (2D-COS). The experimental results indicated that the goethite samples with higher facet proportion of {021}/{110} exhibited the better adsorption capacity compared to goethite with lower facet proportion of {021}/{110}.

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Purpose Bile duct injury (BDI) is a catastrophic complication of cholecystectomy, and misidentification of the cystic anatomy is considered to be the main cause. Although several techniques have been developed to prevent BDI, such as the "critical view of safety", the infundibular technique, the rates remain higher during laparoscopic cholecystectomy (LC) than during open surgery. We, here, propose a practical new strategy for ductal identification, that can help to prevent laparoscopic bile duct injury.

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In this work, four novel defective MIL-101(Fe) catalysts with coordinatively unsaturated sites were successfully prepared via a facile synthesis strategy by employing benzoic acid, acetic acid, oxalic acid, or citric acid as a modulator. The modified catalysts were demonstrated the existence of defects in the parent framework by a series of characterizations. As compared to the initial MIL-101(Fe), the electronic structure of defective MIL-101(Fe) catalyst was effectively adjusted; meanwhile, the coordinatively unsaturated Fe sites were efficiently generated and the pore sizes were enlarged.

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To realize the error parameter estimation of strap-down inertial navigation system (SINS) and improve the navigation accuracy for aircraft, a hybrid improved restricted Boltzmann machine BP neural network (IRBM-BPNN) approach, which combines restricted Boltzmann machine (RBM) and BP neural network (BPNN), is proposed to forecast the inertial measurement unit (IMU) instrument errors and initial alignment errors of SINS. Firstly, the error generation mechanism of SINS is analyzed, and initial alignment error model and IMU instrument error model are established. Secondly, an unsupervised RBM method is introduced to initialize BPNN to improve the forecast performance of the neural network.

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In this work, quinone-modified metal-organic framework MIL-101(Fe)(Q-MIL-101(Fe)), as a novel heterogeneous Fenton-like catalyst, was synthesized for the activation of persulfate (PS) to remove bisphenol A (BPA). The synthetic Q-MIL-101(Fe) was characterized via X-ray diffraction, scanning electron microscope, Fourier transform infrared, electrochemical impedance spectroscopy, cyclic voltammetry and X-ray photoelectron spectroscopy. As compared to the pure MIL-101(Fe), Q-MIL-101(Fe) displayed better catalytic activity and reusability.

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Bubble-propelled micromotors with controllable shapes and sizes have been developed by a microfluidic method, which serves for effective wastewater treatment. Using the emulsion from microfluidics as the template, monodisperse micromotors can be fabricated in large quantities based on phase separation and UV-induced monomer polymerization. By adjusting the volume ratio of the two immiscible oils (ethoxylated trimethylolpropane triacrylate/paraffin oil) in the initial emulsion, the geometry of the resulting micromotor can be precisely controlled from nearly spherical, hemispherical to crescent-shaped.

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In this study, a novel and high-performance catalyst was prepared and used as the heterogeneous catalyst to activate persulfate for bisphenol A (BPA) degradation. Ferrocene was anchored to NH-MIL-101(Fe) post-synthetically by the condensation of amine group from NH-MIL-101(Fe) with the carbonyl group of ferrocenecarboxaldehyde. The synthesized ferrocene tethered MIL-101(Fe)-ferrocene was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photo-electron spectra, cyclic voltammetry and electrochemical impedance spectroscopy.

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  In this study, a novel composite containing an iron based metal-organic framework (MOF) and BiOBr was successfully synthesized by a simple method, and was fully characterized by X-ray diffraction patterns, Fourier transform infrared spectra, UV-vis diffuse reflectance spectra, and transmission electron microscopy. Moreover, the photocatalytic activities of BiOBr/MIL-88B(Fe) composites and the pure materials were evaluated by measuring the degradation of Rhodamine B under visible light. The results show that the composite exhibits better photocatalytic activities than pure materials, which can be ascribed to the high adsorption capacity of MIL-88B(Fe) and the enhanced separation of photogenerated charge carriers from assembly of MIL-88B(Fe) on BiOBr.

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Macrophages are key components of the innate immune system and play pivotal roles in immune response, organ development, and tissue homeostasis. Studies in mice and zebrafish have shown that tissue-resident macrophages derived from different hematopoietic origins manifest distinct developmental kinetics and colonization potential, yet the genetic programs controlling the development of macrophages of different origins remain incompletely defined. In this study, we use zebrafish, where tissue-resident macrophages arise from the rostral blood island (RBI) and ventral wall of dorsal aorta (VDA), the zebrafish hematopoietic tissue equivalents to the mouse yolk sac and aorta-gonad-mesonephros for myelopoiesis, to address this issue.

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A novel quinone-modified metal-organic frameworks NH-MIL-101(Fe) was synthesized using a simple chemical method under mild condition. The introduced 2-anthraquinone sulfonate (AQS) can be covalently modified with NH-MIL-101(Fe) and acts as a redox mediator to enhance the degradation of bisphenol A (BPA) via persulfate activation. The obtained AQS-NH-MIL-101(Fe) was characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectra, cyclic voltammetry and electrochemical impedance spectroscopy.

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The efficacies of catalyzed H2O2, activated persulfate, and catalyzed H2O2-persulfate processes for the degradation of ortho-nitrochlorobenzene (o-NCB) in soil were investigated. The application of catalyzed H2O2-persulfate process was promising, and after a careful adjustment of oxidants and activator doses, it demonstrated a considerable improvement in o-NCB degradation compared with activated persulfate process and catalyzed H2O2 process. The degradation of o-NCB in catalyzed H2O2-persulfate process was obviously influenced by the concentration of persulfate and H2O2, the molar ratio between persulfate and H2O2, the concentration of o-NCB, and initial pH.

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