JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2021
·Vol. 32
·期 22
·26291-26305
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IF 2.478
Qi Lu,Zhiheng Wang,Yimin Dai,Ling Chen,Chengqian Fang,Shengyun Wang,Yue-fei Zhang,Yan Li,Li Wan
Using a simple dipping method, a novel the magnetically driven hydrophobic polyurethane sponge (MHPS) was synthesized in this work. The isodecyl alcohol with longer carbon chain is grafted onto the sponge surface through substitution reaction and condensation reaction, and Fe 3 O 4 nanoparticles are adhered to the sponge to give it magnetism and make it easy to collect. MHPS were characterized by Fourier transformed infrared, X-ray diffraction, scanning electron microscopy and energy dispersive spectrometers. The maximum adsorption capacity for various oils/organic solvents was 24–50 times its own weight. MHPS shows excellent reusability after ten absorption–extrusion-heating cycles. Moreover, it can selectively absorb and continuously remove oil in a wide range of water due to the combination of its high porosity, hydrophobicity and lipophilicity. The magnetism of MHPS makes it easy to collect with magnets. It is believed that MHPS has potential application prospects in oil purification and oil spill removal industry wastewater.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
·
IF 8.128
Yunjin Yao,Hongwei Hu,Hongyu Yin,Zhenshan Ma,Zhongming Tao,Yongjie Qiu,Shaobin Wang
FeS 2 -embedded in porous carbon (FeS 2 /C) was prepared by simultaneous sulfidation and carbonization of an iron-based metal–organic framework precursor, and subsequently immobilized in polyvinylidene fluoride membranes (FeS 2 /C@PVDF) for organics removal via peroxymonosulfate (PMS) activation. The composition , structure, and morphology of the FeS 2 /C@PVDF membrane were extensively characterized. Scanning electron microscopy images manifest that the FeS 2 /C nanoparticles with an average diameter of 40 nm are assembled on the external and internal membrane surface. The as-prepared FeS 2 /C@PVDF membrane exhibits excellent performances over a wide pH range of 1.53–9.50, exceeding carbon-free syn -FeS 2 @PVDF. The effective degradation could be improved by inner pyrite FeS 2 cores and thus enhanced the electron transfer between carbon shell and PMS. Electron paramagnetic resonance and quenching experiments elucidated that radical ( HO ∙ , SO 4 ∙ - ) and nonradical ( 1 O 2 ) species were the predominant reactive oxidants. In addition, FeS 2 /C@PVDF exhibited high stability with low Fe leaching (0.377 mg/L) owing to the effective protection of the outer carbon skeleton. Plentiful porosity of PVDF membranes not only affords a controlled size and confined uniform distribution of the immobilized FeS 2 /C nanoparticles, but also enables a persistent exposure of active sites and enhanced mass transfer efficiency. Our findings demonstrate a promise for utilizing the novel FeS 2 /C@PVDF membrane as an efficient catalyst for the environmental cleanup.
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ACS Applied Nano Materials
·
2021
·
IF 5.097
Mengdan Guan,Yameng Zhu,Xiaoping Yue,Yan Liang,Huixiang Sheng,Jin Wang,Chengyu Zhang,Qiming Peng,Gang Lu
The plasmon-mediated coupling reaction of nitroaromatic compounds is an effective strategy to synthesize the aromatic azo compounds that are widely applied in material science, pharmacy, and agricultural chemistry. Nonetheless, the reaction rate can be further improved since the lifetime of the plasmon-generated hot carriers is limited to femtoseconds or picoseconds. Herein, using in situ plasmon-enhanced Raman spectroscopy, we reveal that the adsorbed positively charged methyl violet molecules on the silver nanoparticle (Ag NP)–graphene oxide (GO) composite structure act as simple and cost-effective molecular cocatalysts, largely boosting the coupling of p-nitrothiophenol to p,p′-dimercaptoazobenzene. This boosting is attributed to the promoted separation of the plasmon-generated hot carriers at the Ag NP–GO interface. In addition, the reduction of laser power will help to promote the efficiency of the MV-induced acceleration. This work provides a highly simple, efficient, and cost-effective strategy to accelerate the coupling reaction of nitroaromatic compounds, and this strategy can be extended to the acceleration of many other plasmon-mediated chemical reactions.
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JOURNAL OF POLYMER SCIENCE
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2021
·Vol. 59
·期 11
·1065-1071
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IF 0
Yi-Ning Hu,Qiao-Mei Li,Yan-Feng Guo,Li-Jing Zhu,Zhi-Xiang Zeng,Zhu Xiong
Here, polyvinylidene fluoride (PVDF) membranes were fabricated via non-solvent induced phase separation (NIPS) using dopamine (DA) and polyethyleneimine (PEI) as the hydrophilic additives, which has a loose surface and somewhat improved hydrophilicity. Then nanofiltration (NF)-like thin-film composite forward osmosis (TFC FO) membrane with a loose polyamide (PA) active layer on the blend membrane was synthesized via the interfacial polymerization. The as-prepared NF-like TFC FO membrane exhibited a high water flux ( J w ) of 29.98 L m −2 h −1 and a much low specific salt flux ( J s /J w ) of 0.018 g/L, when 0.6 M NaCl was used as draw solution (DS). It had a superior rejection of malachite green (99.6% ± 0.1%) and a low rejection of NaCl (27.4% ± 4.2%), when filtrated malachite green/NaCl mixture solution in active layer-facing draw solution (AL-FS) mode. The results provide new insights on the design and preparation of FO membranes of selective separation for dyes from salty water. Graphical
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ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Lipei Ren,Guomeng Zhao,Luqi Pan,Bei Chen,Yali Chen,Qian Zhang,Xingfang Xiao,Weilin Xu
Adsorption techniques have been successfully applied in water purification because of their flexibility, simplicity of design, and effectiveness. Activated carbon is an effective absorbent using for dye adsorption; however, the powder structure is not conducive for practical applications and cannot be used to filter dye solutions which are challenges that still need to be addressed. Herein, a natural cellulose-based absorbent, activated carbon-Juncus effusus fiber (AC-JE fiber), demonstrates the removal of all kinds of dyes without selectivity and humic substances and humic-like organics from wastewater. The combined macroporous structures of JE fibers and the microporous and mesoporous structures of activated carbon particles enhance their adsorption properties. These composite absorbents have excellent adsorption and continuous filtration effect. The rejection rate is approximately 100% not only on acidic and anionic dyes but also on basic and cationic dyes. Moreover, the dye solution adsorbed by AC-JE fibers exhibits an ideal freshwater quality (almost no bacteria), similar to that of the deionized water. The AC-JE fibers prove their potential for dye removal, in both adsorption and filtration. Their sterilization ability substantiates their potential in the field of water purification as they can be used as ideal absorbents based on cellulose for removing dyes and purifying wastewater.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2021
·
IF 6.953
Jiying Men,Hongxing Shi,Chengya Dong,Yuanyuan Yang,Yuanrui Han,Ruixin Wang,Yiqing Zhang,Ting Zhao,Jun Li
A novel adsorbent with high adsorption capacity to remove cationic dyes was synthesized. Sodium 4-styrene sulfonate (SSS) was grafted polymerization on the surface of magnetic chitosan microspheres via -NH 2 /S 2 O 8 2− surface initiating system, obtaining MCS-g-PSSS microspheres. The grafted microsphere was characterized by Fourier transforms infrared spectroscopy , X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, vibration sample magnetometer and the Brunauer-Emmett-Teller. Cationic dyes were adsorbed by MCS-g-PSSS and methylene blue(MB) was acted as a typical example. The adsorption performance was explored by varying experimental conditions. The results showed the maximal adsorption capacity was 989 mg/g at pH 1 at 25 °C. The pseudo-second order model was found to be applicable for the adsorption kinetics . The adsorption capacity increased with rising temperature and it decreased owing to adding of ions. The adsorption isotherms were the best fitted by Langmuir. MCS-g-PSSS for MB showed high adsorption capacity due to the strong electrostatic interactions and π-π stacking, which was explained by FTIR and XPS and was verified by DFT calculations. The degree of adsorption spontaneity increased with rising the temperature. The grafted MCS-g-PSSS microspheres had high adsorption capacity for various kinds of cationic dyes and excellent for remove MB in the aqueous solution.
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Molecular Catalysis
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2021
·
IF 5.062
Ruixue Wu,Caifeng Bi,Xia Zhang,Jinmiao Wang,Lulu Wang,Chuanbin Fan,Mei Wang,Feng Shao,Nana Li,Ziao Zong,Yuhua Fan
Two novel Co-MOFs constructed from aromatic polycarboxylic acid named {[Co(tib) 2 (bimb) 2 ]·4H 2 O} n (tib = 3-((4-(1H-1,2,4-triazol-1-yl)benzyl)oxy)benzoic acid, bimb = 1,4-bis(imidazole-1-ylmethy) benzene) and {[Co 2 (bipa) 4 (bibp) 6 ]} n (bipa = 2-(4-carboxy-2-nitrophenoxy)-6-nitroterephthalic acid, bibp = 4,4′-bis(imidazolyl) biphenyl), have been synthesized under solvothermal conditions and characterized by single-crystal X-ray diffraction, elemental analysis, IR spectra, powder X-ray diffraction (PXRD), thermogravimetric analysis (TG) as well as electrochemistry. The single-crystal X-ray diffraction analysis indicates that Co-MOF 1 exhibits an uninodal net with a (6 5 ·8) topology, whereas Co-MOF 2 exhibits an uninodal 4-connected framework with a (4 4 ·6 2 ) topology. The electrochemistry studies demonstrate that both of the two Co-MOFs can behave as the efficient electrocatalysts for water oxidation in a mild neutral system at the potential around 1.20 V vs. NHE with comparatively low overpotential ( η ) for Co-MOF 1 and 2 of 337–541 mV vs. NHE. Moreover, the two Co-MOFs also show good photocatalytic degradation capabilities toward MB/MV dyes under UV irradiation, and the mechanism studies demonstrate that the main active species are · OH radicals. Therefore, these bi-functional Co-MOFs materials can be treated as convenient and efficient catalysts for the oxygen evolution reaction and aromatic dyes degradation.
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Frontiers in Chemistry
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2021
·
IF 5.221
Chen Kaiwei,Du Linlin,Gao Peng,Zheng Junli,Liu Yuanli,Lin Hua
The carboxylate-functionalized passion fruit peel (PFPCS) was an efficient and rapid biosorbent for wastewater treatment. The PFPCS exhibited excellent selectivity to the cationic dyes, where the maximum adsorption capacities for methylene blue (MB) and methyl violet (MV) were 1,775.76 mg g−1 and 3,756.33 mg g−1, respectively. And the adsorption process of MB and MV on PFPCS reached equilibrium within 20 min. Moreover, the adsorption conditions and mechanisms were investigated. The adsorption process was in good agreement with the pseudo-second-order and Langmuir isotherm models. The adsorption mechanism was also proposed to be electrostatic interaction and hydrogen bond. After six cycles of desorption-adsorption, the removal efficient of MB and MV could be kept above 95%. Thus, PFPCS was considered as a highly efficient absorbent for removing cationic dyes from polluted water due to excellent adsorption characteristics, low cost and environmental friendliness.
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CHEMICAL ENGINEERING JOURNAL
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2021
·
IF 13.273
Ling Cai,Guangxue Chen,Bin Su,Minghui He
Ultra-tough transparent conductive elastomers (TCEs) with self-healing performance are of great significance for research in the fields of soft robotics, optical display electronics, wearable electronic equipment and human–computer interaction. However, their limitation, such as the desolventizing process, low polymerization rate or balance between toughness and self-healing performance, cause difficulty in manufacturing by the 3D printing technique. Here, we propose a novel preparation strategy for 3D printed TCEs based on the photopolymerization of maleic acid (MA)/choline chloride (ChCl) and acrylamide (AAm)/choline chloride type polymerizable deep eutectic solvents (PDESs). PDES can polymerize into a tough and rich in hydrogen bonds poly(PDES) in a few seconds without solvent evaporation. The printed TCEs with precision of 10 µm have high transparency (95.6%) and stable electrical signals at 50% compression for 10,000 cycles. In addition, efficient self-healing performance due to the dynamic hydrogen bonds of poly(PDES) provides broad application prospects for 3D printed TCEs in long-term pressure-resistant intelligent applications.
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ANALYST
·
2021
·Vol. 146
·期 6
·1996-2008
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IF 4.616
Taotao Fan,Zongcheng Yan,Chanyuan Yang,Shunguo Qiu,Xiong Peng,Jianwei Zhang,Lihua Hu,Li Chen
A series of natural, environmentally friendly and low-cost menthol-based hydrophobic deep eutectic solvents (DES) were synthesized to extract and concentrate solutes from dilute aqueous solutions, especially triphenylmethane (TPM) dye micropollutants. The system has excellent extraction performance for TPM. Density functional theory (DFT) and molecular dynamics (MD) simulation were used to quantitatively analyze the effect of the DES composition and TPM structure on the distribution of target molecules in two phases. The solvation free energy of ethyl violet (EV) in DES (−17.128 to −21.681 kcal mol−1) is much larger than that in water (−0.411 kcal mol−1), and increases with the increase of the HBD chain length, which is proportional to the extraction rate, indicating that the TPM molecules are more inclined to the DES environment, especially long-chain DES, than aqueous solution. For the same C12DES, the extraction efficiency of the TPM dyes follows the order: ethyl violet (EV) (99.9%) > crystal violet (CV) (99.6%) > methyl violet (MV) (98.8%). EV has the smallest positive charge and the smallest dipole moment (9.109 D), and the Flory–Huggins parameters of EV (χEV–C12DES 0.053) relative to MV and CV are the smallest in C12DES, and are also the largest in water (χEV–H2O 0.053), indicating that EV has the largest polarity difference with H2O and is more easily detached from water and compatible with the long-chain DES phase. The motion of EV and MV on the phase interface of DES and water was calculated to further analyze from the molecular level. At the same time, EV tends to move into the DES phase. In summary, the excellent extraction ability of DES for TPM is verified through experiments and simulations, providing solid theoretical support in terms of separation in other fields.
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Journal of the Taiwan Institute of Chemical Engineers
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2021
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IF 5.876
Junli Zheng,Linlin Du,Peng Gao,Kaiwei Chen,LiLi Ma,Yuanli Liu,Shaohong You
The excessive discharge of dye wastewater is a great threat to human health and environment with the development of industry. And it is of great significance to use biomass materials to remove dyes from wastewater with the low cost, renewability and environmental friendliness. In this study, the amine-modified passion fruit peel (ACPFP) was prepared by amination reaction, which exhibited highly efficient removal for anionic dyes (methyl orange (MO) and amaranth (ART)). The adsorption capacities of ACPFP for MO and ART were 1530.81 and 970.87 mg⋅g −1 , respectively. And the adsorption conditions (pH, ionic strength, temperature, initial dye concentration, and contact time) and mechanism (kinetic and isotherm models) were investigated. The results revealed that 99% of MO and ART was removed in the best adsorption conditions: pH=5, an adsorbent dose of 1 g⋅L −1 , 600 mg⋅L −1 of MO and ART initial concentration. The adsorption process correlated well with the pseudo-second-order kinetic model and the Langmuir isotherm. And ACPFP had good adsorption selectivity, stability and recyclability for anionic dyes. In conclusion, ACPFP has broad application prospects in actual water treatment.
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CANADIAN JOURNAL OF CHEMICAL ENGINEERING
·
2020
·
IF 1.687
Hucheng Ge,Ze Zhang,Xiaowei Zhao,Hai Li,Jingyi Sun,Xiaojun Jv
Since organic dyes are poorly biodegradable and completely soluble, they are difficult to be efficiently and rapidly removed. Therefore, a poly(itaconic acid)/magnetite sepiolite composite (PIA/MSEP) is prepared via a simple and environmentally friendly approach. The resulting adsorbent is employed for adsorption of methylene blue (MB) and methyl violet (MV). Factors influencing dyes adsorption efficiency are systemically researched, such as pH, contact time, temperature, and initial concentration of dye. Under optimal experimental conditions, the adsorption behaviour is satisfactorily modelled by the Langmuir model, and the maximum adsorption capacity reaches 196.08 and 175.44 mg · g −1 for MB and MV, respectively. Adsorption is a fast process, well represented by pseudo-second-order rate expression, and being the equilibrium reached as short as 30 minutes for both MB and MV. The thermodynamic parameters suggest a favourable, spontaneous, and endothermic process. Fast, kinetic, and convenient magnetic separation, and a high adsorption capacity, make PIA/MSEP composite an impressive adsorbent for adsorption of organic dyes.
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