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Minjia Meng,Yonghai Feng,Weisheng Guan,Yan Liu,Yanfang Xi,Yongsheng Yan 한국공업화학회 2014 Journal of Industrial and Engineering Chemistry Vol.20 No.6
Highly effective molecularly imprinted nano-polymer on wollastonite (nano-WMIP) was prepared byimprinting technique using oil-in-water emulsion polymerization in the presence of salicylic acid (SA) astemplate. The adsorption behavior of nano-WMIP including adsorption kinetic, isotherms, selectiveadsorption, recognition, and effects of initial pH, ionic strength, initial concentration, adsorptiontemperature, and amount of adsorbents were investigated in detail. Moreover, the selective recognitionof nano-WMIP was further investigated by HPLC toward analogs of SA. The relative selectivitycoefficients for p-HB, MS, and MP were 113.4, 8.049, and 6.239, respectively, showing that much higherselectivity of SA on nano-WMIP was obtained than that of wollastonite-based non-imprinted polymer(nano-WNIP).
Yanhua Cui,Minjia Meng,Dongshu Sun,Yan Liu,Jianming Pan,Xiaohui Dai,Yongsheng Yan 한국화학공학회 2017 Korean Journal of Chemical Engineering Vol.34 No.3
We developed a simple phase inversion technique to prepare molecularly imprinted membrane (MIM) at room temperature for membrane selective adsorption and separation of methyl p-hydroxybenzoate (M4HB). The prepared SMIP-MIM was characterized by SEM, FT-IR, TGA. Compared with non-imprinted membrane (NIM1-5) adsorbent, SMIP-MIM1-5 adsorbent with high specific surface area and showed higher binding capacity, faster kinetic and better selectively adsorption capacity for M4HB. The maximum isotherm adsorption capacity for M4HB of SMIPMIM4 was 3.519mg·g−1, and the experimental data was well fitted to the slips model by multiple analysis. The maximum kinetic adsorption capacity and equilibrium adsorption time for SMIP-MIM4 were 1.335mg·g−1 and 160 min, respectively. The mechanism for dynamic adsorption of M4HB onto SMIP-MIM4 was found to follow pseudo-firstorder model and pseudo-second-order model. Additionally, the permeability separation factor of SMIP-MIM4 for M4HB compared to a structural analogues methyl 2-hydroxybenzoate (M2HB) could reach 2.847. The adsorption capacity of SMIP-MIM4 for M4HB and M2HB was 0.549mg·cm−2 and 1.563mg·cm−2, respectively. The adsorption behavior of M4HB through SMIP-MIM4 followed the retarded permeation mechanism.
Wenlu Guo,Xiangguo Meng,Yan Liu,Liang Ni,Zhaoyong Hu,Rui Chen,Minjia Meng,Yun Wang,Juan Han,Min Luo 한국공업화학회 2015 Journal of Industrial and Engineering Chemistry Vol.21 No.1
The new 8-hydroxyquinoline (8-HQ) modified magnetic mesoporous carbon (8-HQ-Ni-CMK-3) wasprepared and applied for adsorption of multivariate metal ions from aqueous solution. The preparedadsorbent was characterized by Fourier transform infrared, X-ray diffraction, scanning electronmicroscopy, transmission electron microscope, nitrogen adsorption-desorption isotherm, elementalanalysis, and vibrating sample magnetometer. The static adsorption behaviors toward multivariatemetal ions on graphite, the modified graphite by 8-HQ, magnetic mesoporous carbon, and 8-HQ-Ni-CMK-3 were compared, which showed that 8-HQ-Ni-CMK-3 had excellent adsorption capacity. Theremoval of multivariate metal ions using 8-HQ-Ni-CMK-3 by fixed-bed column was further investigated.
Yunlei Zhang,Pei Jin,Minjia Meng,Lin Gao,Meng Liu,Yongsheng Yan 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2018 NANO Vol.13 No.11
The direct synthesis of metal-organic frameworks (MOFs) with acidic and basic active sites is challenging due to the introduction of functional groups by post-functionalization method often jeopardize the framework integrity. Herein, we report the direct synthesis of acid-base bi-functional MOFs with tuning acid-base strength. Employing modulated hydrothermal (MHT) approach, microporous MOFs named UiO-66-NH2 was prepared. Through the ring-opening reaction of 1,3-propanesultone with amino group, UiO-66-NH2-SO3H-type catalysts can be obtained. The synthesized catalysts were well characterized and their catalytic performances were evaluated in one-pot glucose to 5-HMF conversion. Results revealed the acid-base bi-functional catalyst possessed high activity and excellent stability. This work provides a general and economically viable approach for the large-scale synthesis of acid-base bi-functional MOFs for their potential use in catalysis field.
Yanhua Cui,Lili Yang,Minjia Meng,Qi Zhang,Binrong Li,Yilin Wu,Yunlei Zhang,Jihui Lang,Chunxiang Li 한국화학공학회 2019 Korean Journal of Chemical Engineering Vol.36 No.2
A simplified strategy for facilely fabricating antifouling graphite carbon nitride/silver phosphate (g-C3N4/ Ag3PO4) nanocomposite photocatalytic polyvinylidene fluoride (PVDF) porous membranes was developed for effective removal of rhodamine B (RhB). g-C3N4/Ag3PO4 heterojunction was strongly fixed to the interior of the PVDF membranes via phase inversion method. The membrane structure was analyzed by Fourier transform spectrophotometer (FT-IR). The morphology of the prepared membranes was investigated using scanning electron microscopy (SEM), EDX-mapping and atomic force microscopy (AFM), respectively. All prepared nanocomposite photocatalytic PVDF membranes exhibited a typically porous structure, and g-C3N4/Ag3PO4 nanocomposites were well dispersed inside the membranes. The obtained g-C3N4/Ag3PO4 heterojunction nanoparticle decorated PVDF membrane had a lower water contact angle of 79o and higher porosity of 85% than that of other two control membranes. The nanocomposite photocatalytic PVDF porous membranes had extremely high permeation flux over 1,083 L·m−2·h−1, and could be used for the removal of RhB. The removal efficiency of g-C3N4/Ag3PO4-PVDF membranes towards RhB solution under visible light irradiation reached 97%, higher than that of the pure PVDF membranes (41%) and g-C3N4-PVDF membranes (85%). Remarkably, the flux performance and flux recovery ratio (FRR) of membranes revealed that the g-C3N4/Ag3PO4- PVDF membranes could recover high flux after fouling, which presented better fouling resistance. Furthermore, the fabricated antifouling g-C3N4/Ag3PO4 nanocomposite photocatalytic PVDF porous membranes exhibited excellent recyclability. Therefore, it is expected that g-C3N4/Ag3PO4-PVDF membranes could provide an energy-saving strategy for effective removal of organic dyes wastewater and have a great potential for practical wastewater treatment in the future.
Chao Yu,Jian Lu,Qi Zhang,Hougang Fan,Minjia Meng,Shi Zhou,Yinhua Jiang,Yongsheng Yan,Yilin Wu,Chunxiang Li 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2019 NANO Vol.14 No.2
High purity emodin is in great demand with the development of medical treatment. Molecularly imprinted membranes (MIMs) have gained wide attention for selective separation of emodin due to its preferable selectivity. In this work, we describe a simple two-step method for developing emodin-imprinted TiO2@CA (ETMIMs) and emodin-imprinted SiO2@CA (ESMIMs) based on organic–inorganic nanoparticle (SiO2/TiO2) modified cellulose acetate membranes at room temperature. SiO2/TiO2 is used to improve the structural stability and roughness of membranes, and dopamine is used as the functional monomer and crosslinker. Importantly, the as-prepared membranes not only exhibited enhanced rebinding capacity (ETMIMs = 30.73 mg g -1 and ESMIMs = 46.04 mg g -1) but also possessed superior rebinding selectivity (2.76 and 2.99 for physcion and 2.42 and 3.30 for aloe emodin onto ETMIMs and ESMIMs) as well as permselectivity (7.59 and 6.69 for physcion and 5.94 and 5.78 for aloe emodin onto ETMIMs and ESMIMs). The regeneration ability of ETMIMs and ESMIMs still maintained 90.4% and 89.2% of the original rebinding capacity after 10 cycling steps, respectively. The ETMIMs and ESMIMs obtained in this work show potential applications for selective separation and purification of emodin from analogs.
Yanhua Cui,Lili Yang,Yan Yan,Zengkai Wang,Jian Zheng,Binrong Li,Yonghai Feng,Chunxiang Li,Minjia Meng 한국화학공학회 2021 Korean Journal of Chemical Engineering Vol.38 No.2
The photocatalytic efficiency of conventional blending photocatalytic membranes suffers a significant reduction due to effective photocatalyst embedded in membrane matrix. Therefore, in this study, inspired by the bioadhesive technology of polydopamine (pDA), a novel Ti doped bismuth oxyiodide (BiOI)-polydopamine (pDA)-coated cellulose acetate (CA) (Ti/BiOI-pDA/CA) photocatalytic nanocomposite membranes were successfully developed for effective removal of tetracycline (TC). The Ti/BiOI-pDA/CA nanocomposite membranes displayed very high photocatalytic activity toward TC (about 98% after 120 min) under visible light irradiation and superior photodegradation kinetics (k=0.03214 min1). The removal rate of Ti/BiOI/-pDA/CA nanocomposite membranes under dynamic cyclic degradation system could be further improved, giving TC removal efficiency of 91% in 60min. Remarkably, the permeate flux, flux recovery ratio (FRR), reversible fouling (Rr), irreversible fouling (Rir) and the total fouling ratio (Rt) revealed the Ti/BiOI-pDA/CA nanocomposite membranes had excellent antifouling performance. In addition, the Ti/ BiOI-pDA/CA nanocomposite membranes exhibited excellent stability and reusability. Therefore, this work gives insight into the effective removal of TC wastewater and has a great potential for new generation of high-performance photocatalytic membranes for practical wastewater treatment in the future.