Polymer Chemistry
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2017
·Vol. 8
·期 37
·5749-5760
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IF 5.375
Hongcan Zhang,Jian Zhang,Wenxue Dai,Youliang Zhao
The simple and straightforward construction of multi-responsive systems with tunable LCST and UCST dual phase transitions is a great challenge. This study affords an efficient route to tune cloud points via control over the chemical composition of hydroxyl and diethylamino bearing poly(amido thioether)s which were prepared by one-pot thiol–amine–acrylate polyaddition. Owing to the balance of inter/intrachain interactions, various copolymers could exhibit LCST (fOH < 0.84), LCST–UCST (fOH = 0.84–0.89) and UCST (fOH > 0.89) behaviors relying on the hydroxyl fraction in comonomer units. Meanwhile, the thermoresponsive behaviors of copolymer solutions could be efficiently tuned via switching the solvent and solution pH, applying CO2/N2 bubbling, and oxidation. The success of this study further paves the way for the robust synthesis and practical applications of smart polymers with double thermoresponsivity.
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CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Ao Zhou,Dan Zhang,Zhihong Liu,Zhiyong Liu
With the retirement of rechargeable lithium-ion batteries (LIBs) entering peak period, the recycling of LiCoO 2 has become a hot topic. The spent LiCoO 2 batteries are rich in carcinogenic metal Co and high-value metal Li, so they are needed to be recovered in time before causing serious environmental pollution and resource waste. Thus, a clean and efficient process is proposed for the comprehensive recovery of Li, Co, and Mn from the spent LiCoO 2 cathode material. It is an integrated pyro-hydrometallurgical process, mainly consisting of sulfation roasting with NH 4 HSO 4 and selective sulfurizing leaching with (NH 4 ) 2 S solution. Using low melting point ammonium salt as roasting auxiliary, 99.7 %, 99.1 %, and 99.8 % of Li, Co, and Mn in the spent LiCoO 2 powder can be converted into sulfate when roasting under 400 ℃ for 75 min. Then 99.5 % of Li in the sulfation roasting product can be selectively leached with an aqueous (NH 4 ) 2 S solution, which is also a precipitator for Co, Mn, and impurity Al. In addition, 96.4 % of Co and 96.0 % of Mn in the sulfurized precipitate can be separated with impurity elements Al and C via oxidation roasting–water leaching process. Compared to traditional recycling, this method can achieve a higher Li leaching rate at a low roasting temperature, and the recovery of Co and Mn can be realized without adding any acid/base reagents or impurity cations. More importantly, the circulation of NH 3 /NH 4 + and S element in the recycling system has been taken into account, making it an environmental-friendly and economical process. In this study, the sulfation reduction roasting and selective sulfurizing leaching mechanisms were both revealed in details, and the behavior of the valuable elements was also elucidated.
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CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Burenbayaer Borjigin,Lan Ding,Chenghong Liu,Huiqin Li,Xiaojing Wang
The exploration of highly efficient methods for degrading VOCs, with concurrent low energy consumption and lasting reusability, holds significant appeal. In this regard, an S-type CuBi 2 O 4 /CeO 2-x heterojunction with the robust interfacial interactions is presented as an active photocatalyst for the efficient decomposition of gaseous toluene under full-spectrum irradiation. The optimal sample CC15 effectively degrades gaseous toluene at a high concentration of 1800 ppm within 2 h, achieving a notable CO 2 yield of 87.05 %, and a TOC (total organic carbon) removal rate of 89.33 %. Furthermore, CuBi 2 O 4 /CeO 2-x exhibits exceptional stability, maintaining its 100 % degradation capability over 32 cycles for nearly 64 h. Comparative characterization reveals that the superior performance derives from an abundance of oxygen vacancies and effective pre-adsorption capabilities, which facilitate rapid adsorption of VOCs on the catalyst surface, thereby increasing the likelihood of degradation reactions. Additionally, the formation of an S-type heterojunction, valence pairing between Bi 3+ and Ce 3+/4+ ions, and strong interfacial interactions serve as the primary pathways for the efficient separation of photogenerated carriers, contributing to the high CO 2 production rate and prolonged cycle stability. The present investigation underscores the significant potential of vacancy-rich S-type heterojunctions and interfacial interactions between composite components, offering excellent activity and long-term availability for VOCs removal.
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JOURNAL OF MOLECULAR LIQUIDS
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2024
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IF 5.3
Hongmin Zhang,Xiaotong Yang,Xiaona Cui,Hejie Wang,Aixin Song,Xiao Chen,Hong-Guo Liu
Chiral supramolecules have attracted great research interest due to their unique properties and functions. How to assemble them into the ordered superstructures, however, remains a challenge. In this paper, two methods have been developed to fabricate such superstructures. In method I, polystyrene- b -poly (2-vinylpyridine) (PS- b -P2VP) and S-mandelic acid (S-MA) diffused from the oil and aqueous phases respectively to the oil/water interface, combined and self-assembled into helical nanowires and nanospheres with monochirality, and formed parallel-aligned nanowire arrays and close-packed arrays at the liquid/liquid interface. In method II, PS- b -P2VP in DMF droplets was introduced into the aqueous solution of S-MA through a liquid/liquid interfacial phase transfer process. Then the polymer molecules self-assembled into helical nanowires and nanospheres with monochirality in the aqueous phase, which adsorbed at the air/liquid interface and organized into superstructures. The formation of chiral aggregates should be attributed to the induction of S-MA, while the superstructures at the interfaces were considered to result from the modulation by the interfacial pressures. This study has developed one-step techniques to assemble the chiral aggregates and superstructures, which is expected to become universal for fabrication of functional superstructures.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2024
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IF 7.7
Xuedi Yang,Vivian F. Lotfy,Altaf H. Basta,Hao Liu,Shiyu Fu
As biomass, rice straw (RS) is often valorized as a precursor of green products. In this respect, the RS-based carbon quantum dots (CQDs) are synthesized doped with N and S during the preparation. Synergistic doping with lipoic acid and ethylenediamine can vastly increase the yield of CQD from rice straw from 6.14 % to 62.8 %, and sulfur doping plays a more important role on the surface functional groups of the quantum dots. Further assessment is achieved toward the performance of SN-CQDs-hydroxypropyl cellulose nanocomposites. The optical behavior of synthesized SN-CQDs, and the critical concentration of its liquid crystal behaviors, at which the anisotropic phase begins to emerge, is approximately 1 %. Incorporating it into HPC, especially at 5 %, provided nanocomposite films with effective liquid crystal, tensile strength, and thermal stability. This sample's texture reveals a planar structure with colors ranging from yellow to red. The synergistic effect of incorporating SN-CQDs is shown by improving the strength to ~282.1 %, and the activation energy increased from 583.6 kJ.mol −1 to 615.1 kJ/mol. HPC-SN-CQDs can be assembled into an LED device, emitting warm light, of which CIE coordinate is (0.34,0.43).
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PubMed
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2012
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IF 2.237
Liangyan Wang,Xiabin Jing,Haibo Cheng,Xiuli Hu,Lixin Yang,Yubin Huang
The long-chain branched polylactides (LCB-PLAs) prepared by coupling the hydroxyl-terminated two-arm (linear) and triarm PLA prepolymers of identical arm length with hexamethylenediacianate (HDI) were used to improve the melt rheological and crystallization properties of linear polylactide resin, PLA 4032D from NatureWorks. The blends containing LCB-PLA displayed higher zero shear viscosities, more significant shear shinning, more melt elasticity, and much longer relaxation times together with significant strain hardening in elongational deformation. Tg, Tm and crystallinity (Xc) of linear PLA remained virtually unaffected, but the crystallization rate increased obviously, since the branch points of LCB-PLAs could play a role of nucleating agent. High melt strength, fast crystallization, and favorable miscibility improved the foaming ability of the linear/LCB-PLA blends, substantially.
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JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
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2011
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IF 2.733
Lihong Liu,Shenglan Li,Zilin Chen
A simple and selective method was developed for the simultaneous determination of tetrandrine and fangchinoline in herbal medicine by HPLC with electrochemical detection (ECD) on a bare glassy carbon electrode. The HPLC separation and ECD conditions have been optimized. The separation was carried out on a WondaSil ® C18-WR column (4.6 mm × 250 mm, 5 μm), with the mobile phase of acetonitrile–ammonium acetate buffer (pH 6.5; 40 mM) (32:68, v/v) using an isocratic elution at the flow rate of 0.5 mL/min. The electrochemical detection potential was set at +0.9 V. The obtained LODs for tetrandrine and fangchinoline were 0.26 and 0.27 μmol/L, respectively. The method was successfully applied to the analysis of tetrandrine and fangchinoline contents in Stephania tetrandra S. Moore. It has been demonstrated that the LC-ECD method is an excellent technique for analysis of the herbal medicine. The mean recoveries were in the range of 95–105%, while the precision expressed as repetition of peak area was lower than 2.7%.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2024
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IF 7.7
Yanni Li,Yujia Han,Hongxia Li,Xiaohui Niu,Deyi Zhang,Haiyan Fan,Kunjie Wang
In recent years, photocatalytic technology has been introduced to develop a new kind antimicrobial agents fighting antibiotic abusing and related drug resistance. The efforts have focused on non-precious metal photocatalysts along with green additives. In the present work, a novel bis-S heterojunctions based on the coupling of polysaccharide (CS) and wabismuth-based MOF (CAU-17) s synthesized through a two-step method involving amidation reaction under mild conditions. The as prepared photocatalyst literally extended the light response to the near-infrared region. Owing to its double S-type heterostructure, the lifetime of the photocarriers is significantly prolonged and the redox capacity are enhanced. As a result, the as prepared photocatalyst indicated inhibition up to 99.9 % under 20 min of light exposure against Gram-positive ( S. aureus ) and Gram-negative ( E. coli ) bacteria as well as drug-resistant bacteria (MRSA). The outstanding photocatalytic performance is attributed to the effective charge separation and migration due to the unique double S heterostructure. Such a double S heterostructure was confirmed through transient photocurrent response, electrochemical impedance spectroscopy tests and electron spin resonance measurements. The present work provides a basis for the simple synthesis of high-performance heterojunction photocatalytic inhibitors, which extends the application of CAU-17 in environmental disinfection and wastewater purification.
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Energy & Environmental Science
·
2012
·Vol. 5
·期 5
·6966-6972
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IF 9.61
Lichao Yin,Jiulin Wang,Fengjiao Lin,Jun Yang,Yanna Nuli
Polyacrylonitrile/graphene (PAN/GNS) composites have been synthesized via an in situ polymerization method for the first time, which serve as a precursor to prepare a cathode material for high-rate rechargeable Li–S batteries. It is observed from scanning electron microscopy (SEM) and transmission electron microscopy (TEM) that the PAN nanoparticles, less than 100 nm in size, are anchored on the surface of the GNS and this unique structure is maintained in the sulfur composite cathode material. The electrochemical properties of the pyrolyzed PAN-S/GNS (pPAN-S/GNS) composite cathode have been evaluated by cyclic voltammograms, galvanostatic discharge–charge cycling and electrochemical impedance spectroscopy. The results show that the pPAN-S/GNS nanocomposite, with a GNS content of ca. 4 wt.%, exhibits a reversible capacity of ca. 1500 mA hg−1sulfur or 700 mA hg−1composite in the first cycle, corresponding to a sulfur utilization of ca. 90%. The capacity retention is relatively stable at 0.1 C. Even up to 6 C, a competitive capacity of ca. 800 mA hg−1sulfur is obtained. The superior performance of pPAN-S/GNS is attributed to the introduction of the GNS and the even composite structure. The GNS in the composite materials works as a three-dimensional (3-D) nano current collector, which could act not only as an electronically conductive matrix, but also as a framework to improve the electrochemical performance.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2015
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IF 2.999
Yong Cui,Zhe Zhang,Xu Du,Wei Liu,Yulin Deng,Shi Liu,Gang Wang
Ternary metastable wurtzite structure Cu 2 SnS 3 nanocrystals were successfully synthesized via solvothermal way. As-synthesized Cu 2 SnS 3 nanocrystals were characterized in detail by X-ray powder diffraction, energy dispersive X-ray spectrometry, UV–Vis–NIR spectrometry and transmission electron microscopy . Hybrid solution has been obtained by mixing Cu 2 SnS 3 nanocrystals ink and Zn molecule precursor solution. Hybrid solution process was used to fabricate Cu 2 ZnSn(S,Se) 4 thin film .
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JOURNAL OF ALLOYS AND COMPOUNDS
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2024
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IF 5.8
Zhuo Liu,Chao Xiong,Lin Gan,Junhui Yin,Xueying Wang,Jintao Li,Jiayi Wang,Jintong Li,Changyu Lu
In this work, the S-scheme MnFe 2 O 4 /ZnIn 2 S 4 (MFO/ZIS) heterostructure was prepared by hydrothermal method, which can degrade tetracycline (TC) and 2,4,6-trinitrotoluene (TNT) efficiently. Under simulated sunlight irradiation, 88.9 % of TC can be degraded within 75 minutes, and 82.7 % of TNT can be degraded within 120 minutes. The photocurrent response of 3 %MFO/ZIS (0.45 µA cm- 2 ) surpassed that of ZIS (0.15 µA cm −2 ) and MFO (0.08 µA cm −2 ). This is mainly due to the synergistic effect of the S-scheme electron transport pathway and the photothermal effect in MFO/ZIS, which improves its utilization rate of photogenerated electrons. After being used four times, 3 %MFO/ZIS can still degrade 80.2 % of TC, showing excellent stability. In addition, the TC degradation process was analyzed and the low toxicity of TC after degradation was confirmed by LC-MS, ECOSAR and experiments of cultivating mung bean sprouts, demonstrating the potential application value of MFO/ZIS heterojunction in the wastewater treatment field.
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FUEL
·
2024
·
IF 6.7
Yuzhou Xia,Jilong Xiao,Jiacheng Zhang,Renkun Huang,Xiaohui Huang,Guiyang Yan,Liuping Zheng
The construction of step-scheme (S-scheme) heterojunction has become an effective strategy for enhancing photocatalytic CO 2 reduction. In this study, a sunflower-like S-scheme WO 3 /ZnIn 2 S 4 heterostructure is fabricated through the in-situ growth of ZnIn 2 S 4 nanosheets on WO 3 hollow sphere, aimed at improving selective CO 2 reduction. The constructed embedding configuration, featuring a WO 3 hollow sphere core and an outer layer of ZnIn 2 S 4 nanosheet, increases the contact interface and establishes a significant built-in electric field, thereby promoting the migration and separation of photogenerated carriers. The confined internal cavity of the three-dimensional (3D) sunflower-like architecture aids in limiting the free diffusion of CO 2 , and enriching CO 2 molecules at the surface of the photocatalyst, consequently enhancing reaction kinetics. Moreover, S vacancies on ZnIn 2 S 4 nanosheets promote the chemisorption and activation of CO 2 . As a result, the optimized evolution rates for CH 4 and CO of 58.7μmol g –1 h −1 and 51.3μmol g –1 h −1 , respectively, are achieved for WO 3 /ZnIn 2 S 4 heterojunction. The corresponding electron selectivity for CH 4 reaches 82.1 %, which is 13 and 1.5 times higher than those of bare WO 3 and ZnIn 2 S 4 , respectively. This provides valuable insights into the design of muti-functionalized S-scheme heterojunction photocatalysts.
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