MACROMOLECULAR CHEMISTRY AND PHYSICS
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2024
·Vol. 225
·期 21
·2400141
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IF 2.5
Lan Li,Yanjun Ren,Rugang Yao,Hong Yang
To solve the downhole problems correlated with clay hydration swelling and dispersion under high-temperature conditions, a 1-aminoethyl-3-vinylimidazolium bromide ([NVim]Br) and a [NVim]Br/acrylamide copolymer (poly([NVim]Br-co-AM)) are synthesized and used as inhibitors. The molecular structures of [NVim]Br and poly([NVim]Br-co-AM) are characterized by FT-IR and 1 H-NMR. The inhibition properties of [NVim]Br and poly([NVim]Br-co-AM) are evaluated by free swelling and dispersion tests, linear swelling, hot roll recovery experiments and thermogravimetric analyses.The inhibition mechanisms were revealed by X-ray diffraction, zeta potential, wettability analysis and ESEM observation. The results showed that both [NVim]Br and poly([NVim]Br-co-AM) has significantly superior inhibition performance compared with the common inhibitors KCl, polyether amine D230 and polyquaternium-7. Both [NVim]Br and poly([NVim]Br-co-AM) can resist 250 °C. [NVim]Br performed excellently in inihibiting both crystalline and osmotic swelling, which depended on the strong electrostatic adsorption and hydrogen bonds of imidazole cations and primary amine in [NVim] + . Poly([NVim]Br-co-AM) exerted excellent inhibition by minimizing osmotic swelling, reducing hydrophilicity and increasing clay bonding. The results are important for understanding the rational design of novel efficient inhibitors for drilling high-temperature shale formation.
研究领域:
化学工程
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材料科学
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产品关联
DOI
高影响因子
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
·
2022
·Vol. 24
·期 39
·24290-24295
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IF 3.945
Jun Guo,Zi-Yuan Wang,Lin Chen,Yu-Ke Zhu,Ying Zhou,Quan Shan,Jing Feng,Zhen-Hua Ge
The hexagonal Bi0.33(Bi6S9)Br intermediate was incorporated to enhance the thermoelectric properties of Bi2S3 by a facile synthesis process. As a result of the increase of carrier concentration caused by Br diffusion doping and the enhancement of phonon scattering caused by pores, point defects, and secondary phase interfaces, a maximum ZT value of 0.64 was achieved at 773 K in Bi2S3 + 5% Bi0.33(Bi6S9)Br. This study provides a strategy for achieving Br doping in the Bi2S3 system by adding the Bi0.33(Bi6S9)Br intermediate alloy, while the nanostructure was maintained in the matrix, which may be also suitable for other thermoelectric materials to obtain higher performance.
研究领域:
材料科学
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物理学
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产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
You Wang,Zhongke Dai,Jiajia Wang,Du Zhang,Fa Zhou,Jiawei Li,Jianhan Huang
Combining inorganic semiconductors with covalent organic frameworks (COFs) to construct excellent hybrid materials is a promising strategy for solar-driven CO 2 reduction, but how to modulate the charge migration to achieve optimal catalytic efficiency remains a great challenge. Herein, we successfully fabricated well-defined core–shell structured HBWO@Br-COFs hybrid materials using the nano-flowered Bi 2 WO 6 (HBWO) as the core and the triazine-based imine-functionalized Br-COF as the shell. The electrostatic attraction between HBWO and Br-COF leads to the formation of C-O covalent bond and a tight and stable interface. Impressively, the Scheme-II heterojunction was favorably formed at the interfacial layer between the core and the shell, and they provided a stable platform for the rapid transfer of the photogenerated charge and efficient separation of the electron-hole pairs, resulting in excellent photocatalytic CO 2 reduction. The resultant HBWO@Br-COF-2 exhibited high CO yield rate of 19.9 μmol·g −1 ·h −1 , about 3.4 times higher than HBWO (5.8 μmol·g −1 ·h −1 ) and 2.6 times greater than Br-COF (7.53 μmol·g −1 ·h −1 ), respectively. This work provides helpful ideas for the optional design and facile fabrication of the novel inorganic–organic hybrid materials for photocatalytic CO 2 reduction.
研究领域:
材料科学
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环境科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
MATERIALS LETTERS
·
2024
·
IF 2.7
Ying Chen,Minghao Li,Jing Huang,Hui Zeng,Linhua Xu,Jing Su
This paper presents the growth of large-sized CsCu(Br, Cl) 3 crystals using the aqueous solution evaporation method. The structure and the components of the crystals were analyzed. It was found that CsCuBr 3 is a direct bandgap material, while CsCuCl 3 is an indirect bandgap material, and the band gap of CsCu(Br, Cl) 3 halides can be adjusted in the range of 2.63–3.63 eV (PBE) by changing the ratio of Br - /Cl - . Besides CsCuCl 3, which has an absorption valley at 654 nm, the other CsCu(Br, Cl) 3 crystals show high absorption in the range of 200–1000 nm. Under UV excitation, the PL spectra show that CsCu(Br, Cl) 3 crystals exhibit red and blue emission.
研究领域:
材料科学
·
光学
✓ 已验证
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Meiying Yang,Tingting Xu,Xueqing Jin,Qi Shen,Chunyan Sun
C Br bond activation is a critical step in the degradation of organic halogenated pollutants. Herein, by introducing oxygen vacancies with different concentration gradients into Bi 2 WO 6 , the CBr bond in decabromodiphenyl ether (BDE209) is activated, so that BDE209 is successfully dehalogenated under visible light. The study shows that the degradation rate of BDE209 on Bi 2 WO 6 is determined by both interface defects and crystallinity. Good crystallinity is conducive to the generation and separation of photogenerated electrons and holes, and an appropriate defect concentration can promote the C-Br activation of BDE209. In addition, through the tracking analysis of the degradation products of BDE209, the content of the meta -debromination products of BDE209 on Bi 2 WO 6 is significantly higher than that of the ortho- and para- debromination products, indicating that the reduction reaction is a position selective multi-electron mechanism. The study shows that oxygen vacancy assisted debromination is an excellent strategy for photocatalytic treatment of halogenated flame retardant pollutants.
研究领域:
环境科学
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材料科学
✓ 已验证
DOI
高影响因子
LANGMUIR
·
2023
·
IF 3.9
Lihong Wei,Yao Zhang,Jinyuan Jiang,Yinbo Yang,Hui Liu
In this work, the Br functional group on the ligand UiO-66-Br was modified with a Bi–O bond through the secondary solvothermal method, and the synthesis method of visible light catalyst UB (UiO-66-BiOBr) with high electron mobility was explored. The findings indicate that the effective charge transfer of the functional group-modified material UB is 2.98 times and 1.22 times that of BiOBr and traditional UiO-66/BiOBr heterojunctions, respectively. Under simulated sunlight irradiation, the removal rate of tetracycline can reach 88.71%, and the photocatalytic performance is 22.73 times higher than that of UiO-66-Br. Moreover, it maintains good adsorption and photocatalytic performance under different laboratory and actual engineering water environment conditions. In the complex water environment of municipal wastewater, the degradation effect reaches more than 80%. Finally, the decomposition pathways of TC and ecotoxicities of the intermediates were analyzed via combining theoretical calculation, LC–MS/MS, and T.E.S.T.
研究领域:
环境科学
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材料科学
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化学工程
✓ 已验证
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Hao Dong,Shefiu Kareem,Xiao Gong,Jian Ruan,Peng Gao,Xuedong Zhou,Xiaoqing Liu,Xiujian Zhao,Yi Xie
Lead halide perovskite (LHP) nanomaterials have attracted tremendous attention owing to their remarkable optoelectronic properties. However, they are extremely unstable under moist environments, high temperatures, and light illumination due to their intrinsic structural lability, which has been the critical unsolved problem for practical applications. To address this issue, we propose a facile and environmentally friendly ligand-free approach to design and synthesize rod-like CsPb2Br5-embedded Pb(OH)Br with excellent stability under various harsh environments such as soaking in water, heating, and ultraviolet (UV) illumination. Plate-like CsPbBr3- and Cs4PbBr6-embedded Pb(OH)Br powders are first formed by evaporating the solvent in a dispersion of ethanol (or methanol, isopropanol), Cs2CO3, and PbBr2. Upon soaking in water, the plate-like sample undergoes phase transformation from CsPbBr3 and Cs4PbBr6 to CsPb2Br5 and shape conversion from nanoplate to a microrod, leading to the formation of rod-like CsPb2Br5-embedded Pb(OH)Br. The stable Pb(OH)Br coating effectively prevents the luminescent CsPb2Br5 nanocrystals from reacting with water, leading to extremely high aqueous stability of the CsPb2Br5-embedded Pb(OH)Br. The photoluminescence (PL) intensity of the representative CsPb2Br5-embedded Pb(OH)Br sample can maintain 92.2% of the initial PL intensity value even after soaking in room-temperature water for 165 days; in the meantime, the phase and shape are preserved. The typical sample also shows outstanding stability under hot water, UV illumination, and annealing conditions. The ultrahigh aqueous stability, thermal stability, and photostability of the CsPb2Br5-embedded Pb(OH)Br nanomaterials suggest an effective, facile, and environmentally friendly technique to grow perovskite-based nanomaterials for promising practical applications in the optoelectronic field.
研究领域:
材料科学
·
光学
✓ 已验证
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2021
·
IF 6.707
Tingting Xu,Meiying Yang,Chuncheng Chen,Ran Duan,Qi Shen,Chunyan Sun
As typical persistent organic pollutants, polybrominated diphenyl ethers (PBDEs) have aroused high environmental concern due to their toxicity and recalcitrant degradation. Herein, the photocatalytic decabromodiphenyl ether (BDE209) removal performance was evaluated firstly on facet-dependent BiOCl with oxygen vacancies under irradiation (>360 nm). The results revealed that BDE209 was rapidly debrominated on {0 0 1} BiOCl with a reaction rate 4.4 times greater than that on {0 1 0} BiOCl under oxygen-free environment. Such a degradation order is completely opposite to that of Rhodamine B (RhB) degradation. This enhanced reduction is mainly attributed to the abundant oxygen vacancies on {0 0 1} facet of BiOCl, which act as adsorption sites for BDE209 to achieve C-Br bond activation efficiently. Meanwhile, debrominated products via meta- position have the highest proportion than that via ortho- and para- position in the first step. Therefore, a position-selective multi-electrons reduction mechanism is hypothesized. This study provides a new sight on C-X bond activation of halogenated aromatics by inducing oxygen vacancies on specific facets.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
NANOTECHNOLOGY
·
2020
·Vol. 31
·期 21
·215605
·
IF 3.551
Yu-Wei Liu,Shao-Hong Guo,Si-Qi You,Chun-Yi Sun,Xin-Long Wang,Liang Zhao,Zhong-Min Su
Halide perovskites have been employed as photocatalysts for CO2 photoreduction due to their excellent optical properties and unique electronic structure. However, their photocatalytic performance is relatively poor. Herein, we demonstrate a new strategy with Mn-doped CsPb(Br/Cl)3 mixed-halide perovskites as catalysts to enhance the efficiency of CO2 photoreduction. By tuning the content of Mn, a series of CsPb(Br/Cl)3:Mn perovskites are obtained and show high efficiency in CO2 conversion to CO and CH4. For the optimum catalyst sample, especially, the yields of CO and CH4 reach 1917 μmol g−1 and 82 μmol g−1 which are 14.2 and 1.4 times higher than those of CsPbBr3. This work provides new insights into improving the reactivity of perovskites in CO2 photoreduction.
研究领域:
材料科学
·
催化化学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Bing Wang,XuXia Zhang,RuiQing Zhang,Zhuo Li,Bin Tian,HaiXia Ma,Zheng Zheng,Bo Zhou,MengTing Ji,ChuanHui Shi,Hong Hao
Developing a simple, low-cost, high-yield, and controllable strategy for preparing various functionalized MoS 2 -based composite materials remains a challenge. This study innovatively utilizes boron subphthalocyanine bromide (SubPc-Br) as a photosensitizer, which self-assembles on MoS 2 via intermolecular π-π stacking, creating a SubPc-Br/MoS 2 organic–inorganic semiconductor system. This addresses a research gap, employing subphthalocyanines as MoS 2 sensitizers. The SubPc-Br/MoS 2 heterojunction exhibited excellent photocatalytic activity for the degradation of antibiotics in water under solar irradiation. The rate constants for the photocatalytic degradation of CTC and CIP by SubPc-Br/MoS 2 were 4.66 and 5.93 times higher than those of pristine MoS 2 , respectively. The significant improvement in photocatalytic performance is attributed to the efficient charge separation and transfer induced by the unique S-Scheme charge transfer mechanism, which has been verified by different theoretical and experimental results. We demonstrate that the photochemical activity of O 2 molecules adsorbed on MoS 2 (1 0 0) is site-sensitive, with O 2 preferentially adsorbing on the Mid-site location with higher electron transport capability. This study provides a new perspective for enhancing photocatalytic performance by constructing an artificial photosynthetic system with an S-scheme heterojunction.
研究领域:
材料科学
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环境科学
·
光催化
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2020
·Vol. 45
·期 1
·208-216
·
IF 3.288
Zhonghua Zhao,Xiang Yuan,Yicheng Huang,Jikui Wang
Conductive hydrogels are promising flexible conductors for human motion monitoring. However, this kind of wearable strain sensor has often shown weak mechanical properties. To overcome the inherent mechanical weakness and improve the electrical conductivity, CNT-Br/PEDOT:PSS/PAAS triple-network penetrating conductive hydrogels (CBP) are fabricated. The n-butylimidazolium bromide salt-functionalized MWCNTs (CNT-Br) as conductive fillers form a three-dimensional conductive path through the crosslinking agent XR-100, penetrating with the skeleton of crosslinking sodium polyacrylate. The conductive liquid PEDOT:PSS is further evenly dispersed in the penetrating double network to further enhance the electrical conductivity of the hydrogels. CNT-Br without obvious agglomeration significantly improved the thermal stability and mechanical properties of CBP. Moreover, CNT-Br enabled the PEDOT:PSS components to be more evenly dispersed in the PAAS matrix. Due to the good conductive paths inside the hydrogels, the maximum electrical conductivity (CBP10) increases to 10.35 mS cm−1, which is 415% higher than that of pure P1. Our work provides a method to prepare conductive hydrogels with high electrical conductivity and excellent mechanical properties, which can be used for human joint motion detection.
研究领域:
材料科学
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生物医学工程
·
可穿戴技术
✓ 已验证
产品关联
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2024
·
IF 3.8
Rui Zhao,Yuan Zong,Guang Li,Ling Zhao,Gance Dai
As emerging green solvents, ionic liquids (ILs) have promising applications in many fields. However, its long reaction time and high price restrict its industrial application. The main reason for this is due to the generation of droplets during the synthesis reaction. Aiming at the process intensification of the 1-methylimidazole (MIM)-based ILs, this paper has studied the evolution behavior of the droplets during its synthesis according to droplet breakage theory. The results show that the droplet size distribution (DSD) and its number density are closely related to the reaction progress. By comparing the Kolmogoroff microscale and droplet size, the synthesis process can be divided into Reaction stage I, when the conversion of MIM is below 60%, and Reaction stage II, when the conversion of MIM is beyond 60%. High stirring speed and temperature increase have been put forward for each stage. The reaction time can be effectively reduced by 43.93%, which is instructive in improving the production efficiency of [BMIM]Br.
研究领域:
化学工程
·
绿色化学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）