Publications by authors named "Guohao Cheng"

Metal-organic frameworks (MOFs) are used as novel adsorption materials owing to their large surface area and tunable pore size. However, the lack of selectivity considerably limits their application. Consequently, designing functionalized MOFs with specific recognition abilities is essential for enhancing their adsorption performance.

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Molecularly imprinted polymers (MIPs) synthesized from chain functional monomers are restricted by spatial extension and exhibit relatively poor affinity and selectivity; this results in unsatisfactory applications in complex media. In this study, we prepared unique spherical carbonized polymer dots (CPDs-OH) via the incomplete carbonization of 1-allyl-3-vinylimidazolium bromide and ethylene glycol, and used it as a functional monomer to prepare a newly imprinted polymer (CPDs-OH@MIP) in aqueous media. As a result, the CPDs-OH@MIP exhibited effective recognition of oxytetracycline with an impressive imprinting factor of 6.

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The demand for the removal of pollutants in aqueous solution has triggered extensive studies to optimize the performance of adsorbents, but the adsorption rate and selectivity of adsorbents have been overlooked. Hierarchically ordered porous vinyl-functionalized UIO-66 was used as supporter to prepare a surface molecular imprinted polymer (MIP-IL@UIO-66). The UIO-66 with large specific surface area significantly increased the number of active site of polymer, and so the MIP-IL@UIO-66 can achieve the rapid and highly selective adsorption of sulfamethoxazole (SMZ) in water.

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The effective analysis of cephalosporin antibiotics in food animals has attracted considerable attention. Herein, a high-performance liquid chromatograph equipped with a UV method based on molecularly imprinted-solid phase extraction (MISPE-HPLC-UV) was developed for preconcentration, cleanup and determination of ceftiofur sodium (CTFS) in food samples. In this method, an eco-friendly molecularly imprinted polymer (MIP) was synthesized and employed as an adsorbent, which exhibited excellent selectivity towards CTFS in water, and adsorption equilibrium could be reached within 1 h.

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The widespread occurrence of sulfathiazole (STZ) in the environment has raised concerns regarding the potential risks to ecosystem and human health. Thus, there is a need to develop facile and efficient methods for monitoring STZ. In this study, a novel fluorescent probe, based on N, B, F co-doped carbon dots (N, B, F-CDs), was developed for the highly sensitive and selective determination of STZ.

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Functional metal organic framework composite can effectively remove antibiotics from environmental water samples. However, designing excellent adsorbents with multiple active sites via a rapid one-step method is still a challenging problem. A novel metal organic framework composite (UiO-66-NH-AMPS) was synthesized through one-step polymerization by adding functional monomer 2-acrylamide-2-methylpropanesulfonic acid (AMPS) during the preparation of UiO-66-NH.

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A novel green hydrophilic levofloxacin imprinted polymer was presented via one-step polymerization in water using ionic liquid 1,6-hexa-3,3'-bis-1-vinylimidazolium bromine with multiple hydrophilic groups and 2-hydroxyethyl methacrylate as a co-functional monomer. Adsorption experiment revealed that the ionic liquid significantly improved the water compatible of imprinted polymer, and the excellent recognition of molecularly imprinted polymer for levofloxacin in water corresponds to the synergetic effect of H-bonding and the electrostatic and π-π interactions between the levofloxacin and co-functional monomer. Furthermore, the adsorption process of the imprinted material towards levofloxacin fitted the Langmuir model, and the maximum binding amount of levofloxacin onto the imprinted and corresponding non-imprinted polymer were 16.

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A novel water compatible ciprofloxacin imprinted polymer is synthesized in water via a green, non-toxic and environmentally friendly polymerization process. Hydrophilic groups, including anionic chlorine, hydroxyl, and carbonyl oxygen provided by a bifunctional monomer comprising 1-allyl-3-vinylimidazole chloride and 2-hydroxyethyl methacrylate, are introduced into the imprinted material, which allows the polymer to interact strongly with imprinting molecule via hydrogen bonds, electrostatic and π-π dipole interactions in aqueous solution. Rebinding experiments show that the obtained molecularly imprinted polymer (MIP) presents special molecular recognition towards quinolone antibiotics (ciprofloxacin, levofloxacin and pefloxacin mesylate) in aqueous matrices.

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An ionic liquid functionalized polymer (IL-P) was prepared feasibly and simply by grafting1-butyl-3-vinylimidazolium bromide onto the silica surface. The IL-P was fully characterized, and the results showed that IL-P has a rough surface with a lower specific surface area (205.49 m g), and the involvement of ionic liquid significantly improved the adsorption performance of IL-P.

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Toward improving the selective adsorption performance of molecularly imprinted polymers in strong polar solvents, in this work, a new ionic liquid functional monomer, 1-butyl-3-vinylimidazolium bromide, was used to synthesize sulfamethoxazole imprinted polymer in methanol. The resulting molecularly imprinted polymer was characterized by Fourier transform infrared spectra and scanning electron microscopy, and the rebinding mechanism of the molecularly imprinted polymer for sulfonamides was studied. A static equilibrium experiment revealed that the as-obtained molecularly imprinted polymer had higher molecular recognition for sulfonamides (e.

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