POLYMER
·
2022
·
IF 4.432
Ling-jie Zhang,Jian Liu,Long-bo Luo,Xiang-yang Liu,Xu Wang
The combination of high breakdown strength and low dielectric loss has always been a challenge for the preparation of high energy storage density dielectric films . In this work, in order to optimize their dielectric performances, we develop a series of all-organic PI composite films by introducing perchlorinated hexa-peri-hexabenzocoronene (Cl-HBC) molecules with a concentration (0.01–0.1mol%) into PI film. Even at an ultra-low concentration, the Cl-HBC molecule with a quasi-two-dimensional structure would successfully induce the in-plane orientation of PI macromolecular chains and reduce their orientation confusion and molecular cavity. Thus, the existence of Cl-HBC obviously limits the chain mobility of PI in PI-Cl-HBC film under the electric field, which is supposed to reduce the dielectric loss of resulted films. Moreover, Cl-HBC molecules are equipped with a low Lowest Unoccupied Molecular Orbital (LUMO) of about −3.52eV and could work as an electron trap and block the conduction of electrons in the PI composite film. Here, the breakdown strength of the composite film was improved from 442 kV/mm (pure PI) to 539 kV/mm and the dielectric loss was reduced to 0.002. To our best knowledge, it is the first time to significantly enhance the dielectric strength and largely reduce its dielectric loss simultaneously by preparing PI composite film. Meanwhile, compared with pure PI, the energy storage density of composite film increases by 43% and 96% at room temperature and 150 °C, respectively.
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Nanomaterials
·
2021
·Vol. 11
·期 12
·3242
·
IF 5.076
Yu Sun,Jin Chen,Fengchao Wang,Yi Yin,Yan Jin,Jun Wang,Xiaogai Peng,Ruiyi Han,Canyun Zhang,Jinfang Kong,Jing Yang
Nowadays, Mn-doping is considered as a promising dissolution for the heavy usage of toxic lead in CsPbX3perovskite material. Interestingly, Mn-doping also introduces an additional photoluminescence band, which is favorable to enrich the emission gamut of this cesium lead halide. Here, a solution spraying strategy was employed for the direct preparation of CsPbxMn1−x(Br,Cl)3film through MnCl2doping in host CsPbBr3material. The possible fabrication mechanism of the provided approach and the dependences of material properties on Mn-doping were investigated in detail. As the results shown, Pb was partially substituted by Mn as expected. With the ratio of PbBr2:MnCl2increasing from 3:0 to 1:1, the obtained film separately featured green, cyan, orange-red and pink-red emission, which was caused by the energy transferring process. Moreover, the combining energy of Cs, Pb, and Mn gradually red-shifted resulted from the formation of Cs-Cl, Pb-Cl and Mn-Br coordination bonding as MnCl2doping increased. In addition, the weight of short decay lifetime of prepared samples increased with the doping rising, which indicated a better exciton emission and less defect-related transition. The aiming of current work is to provide a new possibility for the facile preparation of Mn-doping CsPbX3film material.Keywords:MnCl2doping;CsPbxMn1−x(Br,Cl)3;thin films;solution spraying
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PubMed
高影响因子
CHEMICAL PHYSICS LETTERS
·
2021
·
IF 2.328
Xi Wang,Jiali Yan,Hao Wang,Daoli Yang,Jinli Zhai,Xiaoya Gao,Chao Gong,Wenjie Zhu,Yongming Luo
To use solar energy effectively, BiOX (Cl, Br, I) nanosheets with reasonable band gap structure were prepared by ultrasonic assisted hydrothermal method. The prepared BiOX (Cl, Br, I) nanosheets removed 90% of CBZ within 5 min, showing rapid degradation kinetic of 0.3858 min −1 . The improved photocatalytic activities can be due to the reduced recombination of photoinduced electron-hole pairs, strong visible-light absorption ability, large surface area and pore. Radicals experiments indicated that the BiOX (Cl, Br, I) generated main holes ( h + ) and minor electrons ( e − ) to degrade CBZ. These results demonstrated the good feasibility of BiOX (Cl, Br, I) nanosheets in the degradation of CBZ under simulated solar light irradiation.
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JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2023
·
IF 2.6
Jie Yang,Huan Zhou,Jie Li,Cunbing Xu,Yifan Li,Sifan Wang,Jiangbo Chen
The solid–liquid phase equilibria of the Ba2+//Cl–, S2–, and OH––H2O quaternary system and its three subternary systems at 298.15 K are studied via the isothermal solubility phase equilibrium method. The solubility data, liquid properties of density and pH, and phase diagrams of the ternary and quaternary systems are obtained. Solid species of Ba(OH)2·8H2O, BaCl2·2H2O, Ba(OH)Cl·2H2O, and BaS exist in the quaternary system and corresponding ternary systems at 298.15 K. The four solid species build up two invariant points, one disproportionate and one proportionate, and four phase regions. The largest phase area is covered by Ba(OH)·8H2O, and the lowest water point is the proportionate invariant point saturated by BaCl2·2H2O, Ba(OH)Cl·2H2O, and BaS.
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ACS Omega
·
2020
·
IF 2.87
Hao Xu,Lijie Huang,Mingzi Xu,Minghui Qi,Tan Yi,Qi Mo,Hanyu Zhao,Chongxing Huang,Shuangfei Wang,Yang Liu
1-Ally-3-methylimidazolium chloride ([Amim]Cl), dimethyl sulfoxide (DMSO), and CaCl2 were selected to construct dissolution systems to produce value-added products from pretreatment of waste corrugated cardboards (P-WCCs). The dissolution behaviors of P-WCCs before and after ball milling were studied in different dissolution systems. The regenerated cellulose films were quickly and efficiently prepared via dissolving, regenerating, and pressurized drying. When 4 wt % waste corrugated cardboard was dissolved in [Amim]Cl for 4 h at 90 °C, the regenerated cellulose films featured tensile strengths as high as 59.00 MPa. Adding 40% DMSO and 2 wt % CaCl2 increased the tensile strength of the film to a maximum value of 85.86 MPa. This demonstrates that DMSO improves the ability of WCC to dissolve in ionic liquids; Ca2+ improves the tensile strength and thermal stability of the regenerated cellulose film but reduces its transparency. This work provides a new, simple, and highly efficient way to use WCCs for packaging and wrapping.
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高影响因子
JOURNAL OF NANOPARTICLE RESEARCH
·
2020
·Vol. 22
·期 6
·1-11
·
IF 2.132
Zhao Yubin,Xie Cong,Song Yuxiang,Yang Ping
The photoluminescence (PL) of doped ions is depended strongly on the position of the ion in the substrate. Ion doping endows semiconductor nanocrystals with novel properties. In this paper, Mn:CsPb(Cl/Br) 3 nanocrystals (NCs) with different halogen ratios were obtained by one-pot hot injection synthesis and halogen ion exchange. The emission of Mn 2+ from 4 T 1g - 6 A 1g d-d transition was observed in the case of changing the molar ratio of Cl/Br for Mn:CsPb(Cl/Br) 3 NCs. In the case of a Cl/Br ratio of 4/1, the PL peak of perovskite became weak and Mn 2+ emission was enhanced. After I − ion exchange, the emission of Mn 2+ was observed in Mn:CsPb(Cl/Br) 3 with Cl/Br ratio of 1/4, in which the PL efficiency of the nanocrystals reached 55.74%. Thus, Cl − ions increase the band gap and effectively promote the emission of Mn 2+ . At the same time, the morphology of the samples after ion exchange always remains cube. The lifetimes of the nanocrystals were short aged with increasing Cl − ions and prolonged with increasing I − ions. Because these Mn:CsPbX 3 (x = Cl, Br, I) NCs with different halogen ratios revealed highly stabile blue to red emission, the nanocrystals would be utilizable for further applications.
Graphical abstract
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FUEL PROCESSING TECHNOLOGY
·
2019
·
IF 4.507
Haotian Li,Feng Liu,Shuhui Wang,Fengjia Wang,Xin Qian,Caiduan Zhang,Yongliang Ma,Lidong Wang
Based on advanced oxidation technology, a new method for the simultaneous removal of SO 2 and NO x from industrial flue gas using Na 2 S 2 O 8 /MgO was proposed. The method does not require the body structure of the wet desulfurization device is changed but adds Na 2 S 2 O 8 to the original equipment to realize simultaneous desulfurization and denitrification. After determining Cl − was additive, the effects of various reaction factors on the simultaneous removal of SO 2 and NO x were investigated, including the Cl − concentration, the initial concentration of the oxidant, the initial pH value of the solution, and the reaction temperature. According to the characterization of removal products and the types of free radicals involved in the reaction by XRD , XPS , and EPR , the reaction mechanism was elucidated. The experimental results indicated that the removal products were mainly sulfates and nitrates. The free radicals involved in the reaction were SO 4 ·− , ·OH, and Cl·, and the key free radical was Cl·.
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JOURNAL OF THE ENERGY INSTITUTE
·
2018
·
IF 4.217
Shuai-wei Liu,Rui-tang Guo,Xiao Sun,Jian Liu,Wei-guo Pan,Zhi-ling Xin,Xu Shi,Zhong-yi Wang,Xing-yu Liu,Hao Qin
In present study, the poisoning mechanism of Cl on V/TiO 2 catalyst for SCR removal of NOx using NH 3 as the reductant was explored by in situ DRIFT technique. The experimental results revealed that the existence of Cl did not change the SCR reaction mechanism over V/TiO 2 catalyst, which was mainly under the control of both E-R and L-H mechanisms. The deactivation of V/TiO 2 catalyst by Cl was mainly resulted from the inhibited adsorption of NH 3 and NOx species, accompanied by the decrease of the reactivity of adsorbed NH 3 species.
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高影响因子
RSC Advances
·
2019
·Vol. 9
·期 25
·14400-14406
·
IF 3.049
Rong-xiang Zhao,Xiu-ping Li,Chun-feng Mao,Liangpei Hou,Xiaohan Gao
N,N-Dimethylformamide hydrochloric acid/XMCln ([HDMF]Cl/XMCln, M = Zn or Fe, n = 2 or 3) was synthesized by stirring the mixture of [HDMF]Cl and metal chloride. [HDMF]Cl-based DES was characterized by FT-IR spectroscopy, ESI-MS and 1H-NMR spectroscopy. The oxidative desulfurization activity was investigated using [HDMF]Cl/0.2FeCl3 and [HDMF]Cl/ZnCl2 as the extractant and catalyst, and hydrogen peroxide (H2O2) as the oxidant. The desulfurization rate can reach up to 98.08% and 99.2% for DBT using [HDMF]Cl/0.2FeCl3 and [HDMF]Cl/ZnCl2, respectively. After recycling for 7 times, the removal rate of DBT still can reach more than 97%.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Wenfeng Han,Jinchao Wang,Lulu Chen,Luteng Yang,Shucheng Wang,Miao Xi,Haodong Tang,Wucan Liu,Weiyu Song,Jianjun Zhang,Ying Li,Huazhang Liu
Trifluoromethane is one of the most potent and stable greenhouse gases with global warming potential of 14,800 times higher than CO 2 (100-year time horizon). At present, it is destroyed by incineration or plasma at temperatures above 1200 K. For the first time, this work report that CHF 3 can be reverted to HCFC-22 via the intermolecular Cl/F exchange reaction of CHF 3 with CHCl 3 over AlF 3 catalyst under moderate conditions. As CHF 3 is produced during the manufacture of HCFC-22 via the fluorination of CHCl 3 in liquid phase, no additional feedstock and products are involved for the treatment of CHF 3 in this proposed process. At 593 K and atmospheric pressure, CHF 3 conversion levels of about 18%–20% are achieved and no significant deactivation is observed following time on stream of 100 h. In addition, the catalytic reaction mechanism is proposed. According to the experiments and DFT calculation, the intermolecular Cl/F exchange reaction of CHF 3 with CHCl 3 is mainly initiated by the breakage of C Cl. The present work provides a potential resource utilization route for the treatment of CHF 3 and other hydrofluorocarbons (HFCs).
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Materials Science & Engineering C-Materials for Biological Applications
·
2015
·
IF 3.088
Manqing Yan,Hongjun Yang,Guangzhao Zhang
A novel biocompatible and biodegradable copolymer was synthesized by one-step hybrid copolymerization of ε -caprolactone (CL) and 2-( N , N -dimethylamino) ethyl methacrylate (DMAEMA) employing (1-tert-butyl-4,4,4-tris(dimethylamino)-2,2-bis[tris(dimethylamino)phophoranylidenamino]-2Λ5,Λ5-catenadi(phosphazene) ( t -BuP 4 ) as a catalyst. The as-synthesized copolymer was betainizated resulting in a zwitterionic copolymer poly (CL- co - z DMAEMA) and the structure of the zwitterionic copolymer was confirmed by the FT-IR, NMR, and XPS measurements. The results of dynamic light scattering (DLS) show that this zwitterionic copolymer can self-assemble into stable micelles. The results of quartz crystal microbalance with dissipation (QCM- D ) analysis and MTT measurement suggest that this zwitterionic copolymer possess better protein resistance and lower cell cytotoxicity in vitro in comparison with the cationic copolymer. The pyrene solubilization measurement of copolymers poly (CL- co - z DMAEMA) indicates an excellent pyrene solubilization capacity. These zwitterionic polymer micelles can release drugs in response to specific signals, such as temperature, pH, and enzymes and have a potential application in drug delivery and gene therapy due to their good antifouling, low cytotoxicity and high pyrene solubilization.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2016
·
IF 2.567
Fan Tian,Huiping Zhao,Zan Dai,Gang Cheng,Rong Chen
Cl-incorporated BiOI nanostructures with different Cl/I molar ratios have been successfully fabricated via a facile room-temperature method in H2O/EG mixture solvent. Combined with FT-IR, Raman spectrum, XRD Rietveld refinements, and DFT calculation, the incorporated Cl ions are found mainly occupied on I sites, resulting in a hybrid valence band consisting of I 5p, O 2p, and Cl 3p orbitals, which deepens the valence band location of the materials and induces photogenerated holes with higher oxidation power. The incorporated Cl ions into the lattice also change the evolution of photogenerated electrons and holes, inducing the broadening of the bandgap but efficient production of photogenerated carriers. The enhanced oxidation power of Cl-incorporated BiOI products was evaluated by photocatalysis degradation of methylene blue, an organic dye for which pure BiOI shows negligible direct oxidation efficiency. Ascribed to the relatively low valence band maximum (VBM) and efficient generation of photoinduced electrons and holes, the incorporated products show distinct enhancement photocatalytic activities.
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