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Journal of Materials Chemistry A · 2018 ·Vol. 7 ·期 11 ·5991-6000 · IF 9.931

A bimetallic thermally regenerative ammonia-based battery for high power density and efficiently harvesting low-grade thermal energy

Weiguang Wang,Hua Tian,Gequn Shu,Dongxing Huo,Fang Zhang,Xiuping Zhu

A bimetallic thermally regenerative ammonia-based battery (B-TRAB) using inexpensive materials efficiently converts low-grade thermal energy into electricity with high power density. Through thermal regeneration of the anolyte, the B-TRAB system realized high-voltage discharge (1.38 V) with redox couples [Cu(II)/Cu and Zn(NH3)42+/Zn] and low-voltage charge (0.72 V) with Zn(II)/Zn and Cu(NH3)42+/Cu. Adding 2 M NH3 to the anolyte of a Cu/Zn-TRAB produced a peak discharge power density of 525 W m−2-electrode (120 W m−2-membrane), and the voltage (or current) and peak power could be doubled by connecting two cells in series (or parallel). In successive regeneration cycles, a maximum power density of 115 W m−2-electrode (26 W m−2-membrane) and a net energy density of 714 W h m−3 were produced at a constant current density of 100 A m−2. The power density was enhanced to 515 W m−2-electrode (118 W m−2-membrane) and maintained in successive cycles by adding acid to the regenerated catholytes, with a net energy density of 299 W h m−3 (discharged at a constant load of 12 Ω and charged at a constant current density of 100 A m−2). A thermal-electricity conversion efficiency of 0.95% (10.7% relative to the Carnot efficiency) was achieved.

研究领域: 能源材料 · 电化学工程 · 热电转换技术 · 可持续能源 · 功能材料
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2019 ·Vol. 44 ·期 12 ·6148-6159 · IF 4.084

Enhanced anhydrous proton conductivity of SPEEK/IL composite membrane embedded with amino functionalized mesoporous silica

Xiaoyu Zhang,Shiyuan Yu,Qian Zhu,Lianhua Zhao

The novel SP/IL/AMS composite membrane doped with amino-functionalized mesoporous silica (AMS) was successfully prepared. Sulfonated poly ether ether ketone (SPEEK, SP) was used as the polymer matrix and the ionic liquid (IL) was N -ethylimidazolium trifluoromethanesulfonate (EIm[Tfo]). Its properties were compared with SP/IL/NMS composite membrane doped with non-functionalized mesoporous silica (NMS). Fourier transform infrared spectroscopy (FT-IR) analysis indicated that the components in the composite membrane were bound by intermolecular forces. In addition, an acid-base interaction was formed between -NH 2 in AMS and -SO 3 H in SPEEK. The acid-base pair is beneficial to proton conduction. The anhydrous proton conductivity of SP/IL/3-AMS-7.5 composite membrane is about 4 times higher than that of the SP/IL/NMS-7.5. In addition, the good interfacial compatibility between AMS and polymer matrix is conducive for creation continuous proton transfer channel. Thermogravimetric analysis (TG) showed that all composite membranes were stable at 270 °C. The leaching of IL data indicated that IL can be effectively retained due to the presence of -OH and -NH 2 on the NMS and AMS surfaces. The SP/IL/AMS composite membrane could be used in proton exchange membrane fuel cells under medium temperature and anhydrous conditions.

研究领域: 材料科学 · 高分子化学 · 能源材料 · 燃料电池 · 膜科学
✓ 已验证 DOI 高影响因子
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REACTIVE & FUNCTIONAL POLYMERS · 2016 · IF 2.725

Application of pH-responsive methylpropargyl leucine polymer in enantioselective crystallization

Jie Zhang,Ningyu Chen,Yuheng Cui,Liqun Zhang,Dongmei Yue

In this study, novel 1-methylpropargyl alcohol derivatives containing leucine side groups on their side chains were successfully synthesized and polymerized using (nbd)Rh + [η 6 -C 6 H 5 B − (C 6 H 5 ) 3 ] as catalyst. Circular dichroism (CD) and ultraviolet–visible (UV–Vis) spectra revealed that the polymers took predominantly one-handed helical structures that were stable under heat. Deprotection of the t-butyloxycarboryl (Boc) groups in the homopolymers under acidic conditions produced polymers with primary amine moieties on the side chains. The polymers were soluble in aqueous medium, and turbidity test revealed that they were pH-responsive. Amino acid-based polymers were further used in the enantionselective crystallization of alanine enantiomers and l -alanine was preferably induced to crystallize with the l -leucine-based polymer.

研究领域: 高分子化学 · 手性分离 · 药物结晶 · 功能材料 · 生物材料 · 有机合成
✓ 已验证 DOI 高影响因子
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RSC Advances · 2016 ·Vol. 6 ·期 35 ·29638-29645 · IF 3.289

Combined experimental/theoretical study of D-glucosamine promoted Ullmann-type C–N coupling catalyzed by copper(I): does amino really count?

Xin Ge,Xinzhi Chen,Chao Qian,Shaodong Zhou

Ullmann type C–N coupling reaction catalyzed by copper(I) with D-glucosamine derivatives as promoters was studied by means of combined experimental/theoretical investigation. The catalytic role of D-glucosamine was addressed. In contrast with previous speculations, the amino group may not count in the catalytic cycle in which the oxidative addition/reductive elimination mechanism works. Experimental results are in good agreement with theoretical findings. Extensive work indicates the wide applicability of the C–N coupling strategy exploited in this work.

研究领域: 有机化学 · 催化化学 · 药物化学 · 计算化学 · 合成方法学 · 生物正交化学 · 金属有机化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF CHEMICAL THERMODYNAMICS · 2016 · IF 2.196

Equilibrium solubility of sodium 2,4-diaminobenzene sulfonate in liquid mixtures (methanol + water, isopropanol + water, and 1,2-propanediol + water) from 273.15 K to 323.15 K

Rongrong Li,Jiaqi Weng,Cuihong Ye,Anguo Ying,Qizhong Zhou,Aiguo Zhong,Hao Chen,Jianguo Yang

The equilibrium solubility of sodium 2,4-diaminobenzene sulfonate in liquid mixtures (methanol   +   water, isopropanol   +   water, and 1,2-propanediol   +   water) were determined at temperatures ranging from (273.15 to 323.15)   K. The solubility of sodium 2,4-diaminobenzene sulfonate increased with temperature increment but decreased with the concentrations of methanol, isopropanol or 1,2-propanediol in liquid mixtures. The obtained solubility data were correlated by Apelblat equation and Sun model. On the base of the measured solubility, the dissolution enthalpy ( Δ H sol o ) of the dissolution process were calculated.

研究领域: 药物化学 · 物理化学 · 药剂学 · 溶解行为研究 · 热力学
✓ 已验证 DOI 高影响因子
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POLYMER · 2015 · IF 3.562

Synthesis of temperature and pH/CO2 responsive homopolymer bearing oligo(ethylene glycol) unit and N,N-diethylamino ethyl group and its solution property

Xue Jiang,Chun Feng,Guolin Lu,Xiaoyu Huang

A homopolymer strategy was developed to synthesize temperature and pH/CO 2 stimulus-responsive homopolymers. A new class of acrylamide monomers bearing oligo(ethylene glycol) unit and N,N -diethylaminoethyl group were designed and prepared through Aza-Michael addition reaction followed by amidation with acryloyl chloride using amino group as a linkage to connect oligo(ethylene glycol), N,N -diethylaminoethyl, and polymerizable double bond groups together. Subsequently, the corresponding homopolymers containing oligo(ethylene glycol) unit and N,N -diethylaminoethyl group in each repeated unit were prepared via RAFT polymerization with controlled molecular weights and relatively narrow molecular weight distributions . The lower critical solution temperature (LCST) of homopolymer was examined to be influenced by molecular weight, salt concentration, and pH value of aqueous solution. The LCSTs of homopolymers could be tuned in a wide temperature window by changing pH value of aqueous solution and it increased with the decrease of pH value. Particularly, CO 2 gas as a unique pH stimulus can also reversibly adjust the solubility of homopolymer without the addition of acids or bases.

研究领域: 高分子化学 · 智能材料 · 药物递送 · 生物医用材料 · 刺激响应材料
✓ 已验证 DOI 高影响因子
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Journal of CO2 Utilization · 2017 · IF 4.292

A green process for production of p-aminophenol from nitrobenzene hydrogenation in CO2/H2O: The promoting effects of CO2 and H2O

Lijun Zhao,Haiyang Cheng,Tong Liu,Yan Li,Zhong Ying,Wenjing Yang,Weiwei Lin,Xiangchun Meng,Chengxue Wang,Fengyu Zhao

An efficient green process was developed for production of p -aminophenol (PAP) from hydrogenation of nitrobenzene (NB) over a traditional Pt/Al 2 O 3 catalyst in a reaction medium of supercritical CO 2 (scCO 2 ) and H 2 O without any additional acid catalyst involved. The combination of scCO 2 and H 2 O was confirmed to be effective for the production of PAP. The acidity, aroused by the in situ formed carbonic acid, increased with CO 2 pressure, which acted as acid catalysis during the reaction, and it can easily self-neutralize by depressurization of CO 2 , resulting in a green and a intensive process for it removed the final neutralization and salts disposal of the traditional liquid acids. Under the optimal reaction conditions, a high yield to PAP (68.9%) was achieved at the high conversion of NB (98.5%). Moreover, the results of in situ diffuse reflectance FTIR spectra revealed that CO was generated by the reverse water-gas shift reaction (CO 2   +   H 2   →   CO   +   H 2 O), it can adsorbed on the surface of Pt/Al 2 O 3 to suppress the undesired deep hydrogenation of N -phenylhydroxylamine (PHA) to aniline (AN), which also contributed to the obtained high selectivity of PAP. Therefore, the present green and efficient catalysis process will arouse the interest of researchers in the fields of the green and sustainable organic synthesis.

研究领域: 绿色化学 · 有机合成 · 催化化学 · 环境友好工艺 · 工业化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY · 2019 · IF 4.027

Synthesis and biological evaluation of 3–(4-aminophenyl)-coumarin derivatives as potential anti-Alzheimer’s disease agents

Yu-Heng Hu,Jie Yang,Yun Zhang,Ke-Chun Liu,Teng Liu,Jie Sun,Xiao-Jing Wang

The work is focused on the design of drugs that prevent and treat Alzheimer’s disease (AD) and its complications. A series of 3–(4-aminophenyl)-coumarin derivatives designed, synthesised, fully characterised and evaluated in vitro/vivo. The biological assay experiments showed that some compounds displayed a clearly selective inhibition for acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). Among all compounds, compound 4m exhibited the highest AChE inhibition with an IC50 value of 0.091 ± 0.011 µM and compound 4k exhibited the highest BuChE inhibition with an IC50 value of 0.559 ± 0.017 µM. A zebrafish behaviour analyser (Zebrobox) was used to determine the behavioural effects of the active compound on the movement distance of the aluminium chloride-induced zebrafish. Compound 4m offered a potential drug design concept for the development of therapeutic or preventive agents for AD and its complications.

研究领域: 药理学 · 神经科学 · 药物设计
✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 139 ·期 1 ·51418 · IF 3.125

High-flux and solvent-selective membranes with aromatic functionalities and dual-layer structures

Lan Hao,Xulin Cui,Xiaoli Wu,Jingtao Wang,Yifan Li,Wenpeng Li,Xingzhong Cao,Haoqin Zhang

Efficient separation of aromatic-aliphatic hydrocarbon mixtures has long been an important topic in chemical industries. Organic nanofiltration (OSN) has been revealing great promise in separating solvent mixtures that has not been effectively resolved by the state-of-the-art technologies. Herein, novel OSN membranes are designed for the separation of toluene and n -heptane. Polyamide active layer with diaminonaphthalene as the aqueous phase monomer is prepared by interfacial polymerization for the first time. The addition of polydimethylsiloxane gutter layer, as well as the combination of spin coating technique and macroporous substrate, renders the membranes with loose and defect-free architectures. The as-designed membranes achieve a rather high selectivity of toluene over n -heptane (>4) together with ultra-high toluene permeance (>180 L m −2 h −1 bar −1 ). These membranes also present excellent stability in the long-term operation.

研究领域: 材料科学 · 膜分离技术 · 化学工程 · 纳米技术 · 高分子化学 · 工业催化 · 绿色化学
✓ 已验证 DOI 高影响因子
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Journal of Environmental Chemical Engineering · 2023 ·Vol. 11 ·期 3 ·110269 · IF 7.7

Mechanochemistry recycling of polyurethane foam using urethane exchange reaction

Jinghua Li,Haofeng Zhu,Dandi Fang,Xusheng Huang,Chaoqun Zhang,Ying Luo

Although the recycling and reuse of polyurethane foam (PUF) is a promising route to deal with this type of waste commodity polymer, highly efficient and green processing protocols are a great challenge due to their stable crosslink structure. In this study, a strategy of urethane exchange reactions was proposed to transform commercial rigid PUF into PUF sheets. The process was composed of the pulverization of the foam, the pretreatment method and the hot pressing. The effects of the pretreatment method on the structure and properties of the recycled commercial PUF were studied. The results show that the ball milling pretreatment method can effectively pulverize the commercial PUF into powder of 74.5 µm and a specific surface area as high as 2991.0 m 2 /kg, which can promote the urethane exchange reaction in close contact with the catalyst. The recycle method of ball milling pretreatment makes the crosslink density and tensile strength of the PUF sheets reach 2236.8 mol/m 3 and 32.6 MPa, which means an increase of 9.9 times and 3.3 times, respectively, compared to the method of other pretreatment. Moreover, PUF sheets can still maintain 71.5% of the tensile strength after two cycles of recycling, indicating the potential of this recycling method for PUF. This simple and efficient method enhances the sustainability of rigid PUF utilization and shows the enormous potential for value-added recycling of thermosets .

研究领域: 高分子材料科学 · 环境科学与工程 · 绿色化学 · 资源循环利用 · 材料再生 · 可持续材料技术 · 功能高分子
✓ 已验证 DOI 高影响因子
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