Publications by authors named "Shouyong Zhou"

The Cadmium contamination in paddy soils significantly threatens soil health and food safety. This study addresses the urgent need for cost-effective and sustainable remediation methods by evaluating the efficacy of green-synthesized hydroxyapatite (GHAP) in immobilizing Cd in paddy soils. The investigation focused on the effects of applying GHAP, commercial hydroxyapatite (CHAP), and pure hydroxyapatite (CK) on soil physicochemical properties, as well as Cd mobility and transfer within the soil-rice system.

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Semicarbazide, as a derivative of urea, constitutes a great variety of functional molecules for different needs. Herein, novel stationary phases with an incorporated semicarbazide group were proposed. Using aliphatic (docosanoyl, C22) and aromatic (benzoyl, Bz) hydrazides, the semicarbazide-embedded ligands were synthesized before chemical modification of the silica gel, allowing for an accurate interpretation of the chromatographic properties of the corresponding packings.

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Hydrogel-based evaporators are a promising strategy to obtain freshwater from seawater and sewage. However, the time-consuming and energy-consuming methods used in hydrogel preparation, as well as their limited scalability, are major factors that hinder the development of a hydrogel-based evaporator. Herein, a facile and scalable strategy was designed to prepare a hydrogel-coated evaporator to realize efficient solar-driven water evaporation.

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Article Synopsis
  • Lithium metal batteries hold great potential for energy storage but face challenges with uneven growth of Li dendrites.
  • Researchers created a leaf-inspired membrane separator made from natural attapulgite nanorods that promotes uniform Li growth and exhibits beneficial properties like high thermal stability and ion-selectivity.
  • The new Li//PLIM battery design demonstrates impressive performance, including long cycle life, minimal capacity decay, and high efficiency at elevated temperatures, suggesting a promising path for improving battery technology.
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Non-enzymatic electrochemical sensors with significant advantages of high sensitivity, long-term stability, and excellent reproducibility, are one promising technology to solve many challenges, such as the detection of toxic substances and viruses. Among various materials, perovskite oxides have become a promising candidate for use in non-enzymatic electrochemical sensors because of their low cost, flexible structure, and high intrinsic catalytic activity. A comprehensive overview of the recent advances in perovskite oxides for non-enzymatic electrochemical sensors is provided, which includes the synthesis methods of nanostructured perovskites and the electrocatalytic mechanisms of perovskite catalysts.

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The harmful effects on the human body from p-phenylenediamine (PPD) in hair dyes can cause allergies and even cancer. Therefore, it is particularly important to accurately control and detect the content of PPD in our daily products and environment. Here, a small amount of non-metallic elemental P doped in perovskite oxide of SrCoO (SC) forms a good catalytic material, SrCoPO (SCP), for PPD detection.

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Terphenyls are important building blocks for a wide range of functional molecules. Among the three isomers, p-terphenyl (CH) is particularly useful for the construction of optical devices on account of its unique structure. Herein, two rigid stationary phases bearing p-terphenyl as an external moiety and variable embedded carbamate groups (p-TerC with one embedded carbamate group and p-TerC with two embedded carbamate group) were presented.

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A highly efficient carbonylative coupling method for the preparation of alkyl stationary phases with variable numbers of carbamate groups was established. The effectiveness of such method was verified through elemental analysis, X-ray photoelectron spectroscopy and solid-state C nuclear magnetic resonance spectroscopy of three as-synthesized stationary phases bearing different alkyl chains and different numbers of carbamate groups (octadecyl/one carbamate group, C18C; docosyl/three carbamate groups, C22C; triacontyl/two carbamate groups, C30C). The comparative evaluation of these stationary phases using a great variety of analytes, including three sets of isomers of alkylbenzenes, two sets of standard mixtures of polycyclic aromatic hydrocarbons (SRM 1647e and 869b), nine polychlorinated biphenyls, fiveteen N-substituted ureas, ten sulfonylureas, five xanthines and some other phytonutrients, revealed their remarkable applicability in reversed-phase liquid chromatography.

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A convenient synthetic approach to a linear alkyl-polyamine amphiphilic chromatographic selector was proposed. Successive immobilization of the amphiphile onto silica gel afforded a multimodal stationary phase for high-performance liquid chromatography (HPLC). The as-prepared silica material was studied comparatively with a conventional octadecyl (C18) and an amide-embedded C18 stationary phase.

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Flue gas desulphurization gypsum (FGD) is a major solid waste in coal-fired energy plants, and the appropriate reuse of this resources is still a major challenge. In this study, the feasibility of FGD as a calcium source to produce hydroxyapatite (FGD-HAP) for the immobilization of lead (Pb) and cadmium (Cd) in spiked soil was investigated. The effects of FGD and FGD-HAP on soil properties and redistribution, bioaccessibility and plant uptake of Pb and Cd were examined.

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Biocatalytic upgrading of biomass-derived 5-hydroxymethylfurfural (HMF) into high-value derivatives is of great significance in green chemistry. In this study, we disclosed the successful utilization of whole-cell F18 for its switchable catalytic performance in the on-demand catalysis of HMF to different value-added derivatives, namely, selective reduction to 2,5-bis(hydroxymethyl)furan (BHMF) or oxidation to 5-hydroxymethyl-2-furancarboxylic acid (HMFCA). Based on the fine-tuning of biochemical properties, the biocatalyst can proceed an efficient hydrogenation reaction toward HMF with a good selectivity of 97.

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An alternative method for efficient synthesis of urea-functionalized silanes was proposed on the basis of an N, N'-carbonyldiimidazole-mediated acyl-transfer reaction between various amino-containing building blocks. The employment of different parent aminosilanes and alkylamines afforded an array of urea-containing silanes, which were subsequently immobilized onto silica gel to form corresponding urea-embedded alkyl stationary phases for high-performance liquid chromatography. The different substituents on the silicon core of the derivatized silane were found to significantly influence the final chromatographic behaviors.

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The present work described two triacontyl-bonded silica adsorbents containing different polar embedded groups (i.e. amide- and carbamate-type) for high performance liquid chromatography, which were prepared by covalent surface modification of silica gel with respective pre-synthesized polar-embedded triacontyl (C30) silane.

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Distiller waste (DW), a common by-product of soda ash plants, was used as the unique calcium source to produce low-cost hydroxyapatites (HAPs) for the first time. The DW-derived HAPs were characterized by SEM, TEM, XRD and BET methods and investigated as amendments for soil Pb immobilization. The DW-derived HAPs displayed relatively smaller particle size (30-80 nm) and larger BET specific surface areas (60.

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Aromatic stationary phases showing complementary selectivity to their alkyl counterparts are extremely useful for certain challenging separation tasks. Herein, a series of polar-embedded aryl stationary phases were synthesized from reactive derivatives of large polycyclic aromatic hydrocarbons (PAHs), including anthracene (three-ring, catacondensed), pyrene (four-ring, pericondensed) and triphenylene (four-ring, fully-benzenoid). These PAHs were functionalized with hydroxymethyl group (PAH-CHOH), then catalytically converted to carbamates (PAH-CHOC(=O)NH-R) using isocyanate, and finally covalently grafted onto silica to produce corresponding carbamate-embedded PAH stationary phases.

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TMC-incorporated carbon nitride (CN) with hexagonal and quadrangle honeycomb-like structure and having periodic lattice defects linked by -CONH- bond was synthesized through combining the high calcination with the chemical condensation of melamine and 1,3,5-benzenetricarbonyl trichloride. The obtained CN has a tri-s-triazine ring and benzene ring skeleton, which makes it have excellent mechanical and thermal stability. The BET specific surface area was enhanced to about 125.

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A new polar-embedded aromatic stationary phase has been prepared by covalently attaching p-biphenylacetamide silane to silica spheres. The retention behavior of this phase was compared with an alkylamide counterpart and octadecyl phases using different classes of analytes, including geometric isomers and congeners from Standard Reference Materials 869b, 870 and 1647e, positional isomers of electron-deficient benzenes, as well as alkylbenzenes and alkylbiphenyls. The relationship between shape selectivity and surface chemistry of stationary phase was comparatively studied.

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New poly(N-isopropylacrylamide) brushes grafted with ZrO2 (PNIPAAm-g-ZrO2) composite membranes, which had been prepared in our laboratory, were used for humic acid (HA) removal. We found that the fluxes associated with such membranes, when compared to those obtained from unmodified ZrO2 membranes, declined slightly at both 25 °C and 35 °C. The PNIPAAm-g-ZrO2 membrane achieved a high rejection, of 98.

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The amine moiety has an important function in many applications, including, adsorption, catalysis, electrochemistry, chromatography, and nanocomposite materials. We developed an effective adsorbent for aqueous reactive dye removal by modifying attapulgite with an amino-terminated organosilicon (3-aminopropyltriethoxysilane, APTES). Surface properties of the APTES-modified attapulgite were characterized by the Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption-desorption.

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Article Synopsis
  • Polyacrylamide/attapulgite (PAM/ATP) was created by polymerizing acrylamide onto modified attapulgite and was analyzed with FTIR and XPS.
  • The study examined the effects of contact time, adsorbent dosage, and pH on the adsorption of mercury ions (Hg(2+)), finding that 88% of adsorption happens in just 5 minutes and reaches equilibrium in about 40 minutes.
  • The maximum capacity for Hg(2+) adsorption was determined to be 192.5 mg g(-1), indicating that chemical processes likely limit the rate of adsorption, while the material can be regenerated effectively, maintaining 95% of its capacity after six cycles.
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