Publications by authors named "Huixuan Zhang"

Peracetic acid (PAA)-based advanced oxidation processes (AOPs) have shown broad application prospects in organic wastewater treatment. Alkoxy radicals including CHCOO and CHCOOO are primary reactive species in PAA-AOP systems; however, their reaction mechanism on attacking organic pollutants still remains controversial. In this study, a Co(II)/PAA homogeneous AOP system at neutral pH was constructed to generate these two alkoxy radicals, and their different reaction mechanisms with a typical emerging contaminant (sulfacetamide) were explored.

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In this study, we designed a plain strategy for fabrication of the novel composite ZnO/CuCoO and applied it as catalyst for peroxymonosulfate (PMS) activation to decompose enrofloxacin (ENR) under simulated sunlight. Compared to ZnO and CuCoO alone, the ZnO/CuCoO composite could significantly activate PMS under simulated sunlight, resulting in the generation of more active radicals for ENR degradation. Thus, 89.

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Hydroxyl radical (•OH) and sulfate radical (SO•) produced in advanced oxidation processes (AOPs) have been widely studied for organic contaminants degradation, however, the different radical characteristics and reaction mechanisms on organics degradation are still needed. In this study, a homogeneous Co(II)/peroxymonosulfate activation system was established for caffeine (CAF) degradation, and pH was controlled to regulate the radicals production. The different attack routes driven by SO• and •OH were deeply explored by transformation products (TPs) identification and theoretical calculations.

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Rheum tanguticum is a perennial herb and an important medicinal plant, with anthraquinones as its main bioactive compounds. However, the specific pathway of anthraquinone biosynthesis in rhubarb is still unclear. The accumulation of anthraquinones in different tissues (root, leaf, stem and seed) of R.

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Leaves are essential plant organs with numerous variations in shape and size. The leaf size is generally smaller in plants that thrive in areas of higher elevation and lower annual mean temperature. The Qinghai-Tibetan Plateau is situated at an altitude of >4000 m with relatively low annual average temperatures.

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Poly (lactic acid) (PLA) blends with different toughening agents were prepared by melt compounding, and the effects of toughening agents on the toughness of PLA, especially the low-temperature toughness, were investigated. All blends were immiscible systems, but the rheological Cole-Cole diagram showed that the blends had certain compatibility, and the interfacial bonding of PLA/Ethylene/butyl methacrylate/Glycidyl Methacrylate Terpolymer (GEBMA) blend was the best. With addition of the toughening agents, all blends showed improvement of the tensile and impact toughness both at room temperature and low temperature.

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Poly(L-lactic acid) (PLLA) blends with excellent low-temperature toughness and strength were prepared by melt compounding with acrylic ester based impact resistance agent (AEIR). The morphology, thermal properties, mechanical properties and biodegradability of the blends were investigated. Morphology observations revealed the blend was immiscible but had good compatibility with the dispersed phase size of about 200-300 nm.

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Raab-Straube is a small perennial and polycarpic herb that is distributed on the rocky slopes of the Qinghai-Tibetan plateau (QTP) at an altitude of 3700-5400 meters. It has a chloroplast genome structure similar to that of other species of . It is 152,102 bp in size, including a large single-copy (LSC) region of 83,450 bp, a small single-copy (SSC) region of 18,286 bp and a pair of inverted repeats (IRs) of 25,183 bp.

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Maxim. is a subnival plant of Asteraceae with abundant medicinal and ecological value. Until now, few studies have been conducted on , especially in phylogenetic relationships and species identification.

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Self-healing hydrogels as renewable materials have attracted significant attention recently. However, traditional self-healing hydrogels require a long time for self-healing and cannot be used at low temperatures. Besides, their poor biocompatibility limits the application of hydrogels.

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Article Synopsis
  • A novel BiO/CuNiFe LDHs composite was developed to activate persulfate for degrading the antibiotic lomefloxacin (LOM) under simulated sunlight, achieving 84.6% degradation in 40 minutes.
  • The composite showed excellent reusability for at least four cycles and identified main active radicals involved in the degradation process, including hydroxyl, sulfate, superoxide radicals, and holes.
  • The study also explored the toxicity variations of LOM and its intermediates, alongside proposing a reaction mechanism for the composite's PS activation under sunlight.
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In this study, nanoscale zero-valent iron decorated graphene oxide (NZVI/GO) composite was fabricated through a reduction process in the presence of sodium borohydride (NaBH4) solution. Subsequently, physicochemical properties of the NZVI/GO composites were characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), N2 adsorption/desorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transformation infrared spectroscopy (FT-IR) and Raman spectra. Results indicated that Fe species existed in the form of Fe0, which uniformly dispersed on the surface of GO.

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In this study, magnetic CoFe2O4 nanoparticles were synthesized by hydrothermal method by using ferric nitrate and cobalt nitrate as raw materials. Subsequently, physicochemical properties of the resulting CoFe2O4 nanoparticles were systematically studied by scanning electron microscope, X-ray diffraction, N2 adsorption/desorption, Fourier transformation infrared spectroscopy and Vibration sample magnetometer measurement. Results indicated that CoFe2O4 nanoparticles with cubic spinel structure possessed an average diameter of 6.

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In this study, silver decorated graphene oxide (Ag/GO) composite was fabricated through a reduction process in the presence of potassium borohydride solution. Subsequently, physicochemical properties of the resulting Ag/GO composite were studied by scanning electron microscope, X-ray diffraction, Raman spectra, Fourier transformation infrared spectroscopy and UV-visible diffuse reflectance spectrum. Results indicated that Ag species existed in the form of Ag0, which greatly facilitated the visible light absorbance ability.

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In the present study, silver phosphate/graphene oxide (AgPO/GO) composite was synthesized by ultrasound-precipitation processes. Afterwards, physicochemical properties of the resulting samples were studied through scanning electron microscope, transmission electron microscope, X-ray diffraction, N adsorption/desorption, UV-vis diffuse reflectance spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy, surface photovoltage spectroscopy and photoelectrochemical measurements. Results indicated that spherical AgPO displayed an average diameter of 150 nm and body-centered cubic crystal phase, which was integrated with GO.

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Toughness, strechability and compressibility for hydrogels were ordinarily balanced for their use as mechanically responsive materials. For example, macromolecular microsphere composite hydrogels with chemical crosslinking exhibited excellent compression strength and strechability, but poor tensile stress. Here, a novel strategy for the preparation of a super-tough, ultra-stretchable and strongly compressive hydrogel was proposed by introducing core-shell latex particles (LPs) as crosslinking centers for inducing efficient aggregation of hydrophobic chains.

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In this study, a novel strategy was designed to prepare rapidly recoverable, anti-fatigue, super-tough double-network hydrogels by introducing macromolecular microspheres (MMs) as cross-linking centers for hydrophobic associations. MMs were prepared via emulsion polymerization using butyl acrylate (BA) as a main component and dicyclopentyl acrylate (DCPA) as a cross-linker. Then, a double-network (DN) hydrogel was prepared using gelatin as the first network and a copolymer of acrylamide and hexadecyl methacrylate stabilized by MMs as the second network.

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Particle coagulation is a facile approach to produce large-scale polymer latex particles. This approach has been widely used in academic and industrial research owing to its higher polymerization rate and one-step polymerization process. Our work was motivated to control the extent (or time) of particle coagulation.

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A series of poly (arylene ether ketone sulfone) s containing different amino content (Am-PAEKS) were prepared via direct polycondensation reactions, and then the sulfobutyl groups were grafted onto the Am-PAEKS by amidating reaction between the amide groups in Am-PAEKS and carboxylic acid groups in 4-(N-butane sulfonic) aminobenzoic acid. The structures of the compounds and the polymer were confirmed by FTIR and H-NMR. The new characteristic bands at 1 239 and 1 060 cm(-1) were assigned to O=S=O symmetric stretching vibration and asymmetric stretching vibration of the sulfonic groups in sulfonated poly (arylene ether ketone sulfone) on side chain (S-SPAEKS), and the structures of the polymers were further confirmed by 1H NMR spectra, and the proton peak at 1.

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A series of novel Sulfonted poly(arylene ether sulfone)s (SPAES) containing 1,3,4-oxadiazole are prepared via direct polycondensation reactions to precisely control the degree of sulfonation. The structures of these compounds were confirmed by FTIR, H-NMR and TGA. The characteristic peaks of transmittances spectra of C=N were found at 1 603 cm(-1) and by H-NMR further confirm the structures, which has been successful introducing the oxadiazole ring.

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