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JOURNAL OF ALLOYS AND COMPOUNDS · 2017 · IF 3.133

Effects of particle grading on porous gelcasted and solid-state-sintered SiC ceramics with improved connectivity

Haibo Wu,Yinsheng Li,Shan Yun,Xuejian Liu,Zhengren Huang,Dongliang Jiang

Porous gelcasted and solid-state-sintered SiC (S-SiC) ceramics with significantly improved connectivity were successfully prepared through the synergistic pore-forming mechanism of direct foaming and particle packing, using fine (D 50  = 0.5 μm) and coarse (D 50  = 5.0 μm) graded SiC powders as the main raw materials. As the proportion of coarse SiC powder increased, the viscosities of aqueous SiC-B 4 C-C slurries sharply decreased, which thus flourished foaming and enlarged bubble-derived-pore diameter in porous S-SiC ceramics, accompanied with the increased amount and size of window. Moreover, abundant particle-packing pores in struts of bubble-derived pores were also formed and even interconnected with each other at 60 wt% of coarse SiC powder. Besides, there was a remarkable increase in porosity from 61.0% to 81.7% and accordingly a significant decline in density from 1.24 g cm −3 to 0.58 g cm −3 as the content of coarse SiC powder increased. The optimized multiple pore microstructures resulted in an amazing nitrogen gas permeability of 1.78×10 −11  m 2 under the condition of an excellent compressive strength of 10.8 ± 2.7 MPa.

研究领域: 材料科学 · 无机非金属材料 · 多孔陶瓷 · 陶瓷加工 · 结构-功能一体化材料
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF CHEMISTRY · 2011 ·Vol. 29 ·期 4 ·778-782 · IF 0.773

Determination of Glycolate Acid, Mono- and Dichloroacetic Acids in Synthetical Betaine by Anion-exchange Chromatography

Haining Shi,Zonghua Wang,Hui Wang,Rui Zhao,Mingyu Ding

An anion-exchange chromatography method combined solid phase extraction (SPE) was developed for the simultaneous analysis of glycolate acid (GL), monochloroacetic acid (MCA) and dichloroacetic acid (DCA) in synthetical betaine products. The analytes and unknown anionic impurities were well separated on a Metrosep A supp5 anion-exchange column (150 mm×4 mm) with 2.0 mmol/L Na 2 CO 3 +2.0 mmol/L NaHCO 3 solution as eluent. Suppressed conductivity detection was used. A strong cation exchange (SCX) solid phase extraction (SPE) cartridge was used to reduce the concentration of matrix betaine and a Cleanert IC-Ag pretreatment cartridge was used to remove high Cl − concentration. The detection limits of GL, MCA and DCA were 0.09, 0.017 and 0.05 µg/L, respectively. The relative standard deviations (RSDs) of the retention times and peak areas were less than 0.09% and 0.49%, respectively. The recoveries of the three analytes were between 90.6% and 100.8%. The analytical results showed that GL and DCA were present in high concentration and no MCA was found when the proposed ion chromatography method was applied to three synthetical betaine samples. The proposed method is simple, sensitive and timesaving, and is also suitable for routine analysis in quality control of synthetical betaine products.

研究领域: 分析化学 · 药物质量控制 · 分离科学 · 环境分析 · 食品化学
✓ 已验证 DOI 高影响因子
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SOLID STATE IONICS · 2018 · IF 2.751

Preparation and electrochemical performance of F-doped Li4Ti5O12 for use in the lithium-ion batteries

Xue Bai,Wen Li,Aijia Wei,Qian Chang,Lihui Zhang,Zhenfa Liu

Spinel Li 4 Ti 5 O 12 doped with F was synthesized via the solid-state reaction of anatase TiO 2 , Li 2 CO 3 , and NH 4 F. The structural characterization and electrochemical performance evaluation of the prepared materials were carried out utilizing X-ray diffraction, scanning electron microscopy, galvanostatic charge-discharge, electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV) tests. The lattice parameters of all samples were calculated using an internal standard and Rietveld refinement method. The results indicate that the F was successfully doped into the lattice structure of Li 4 Ti 5 O 12 , and this process did not influence the crystal structure and superficial morphology. Moreover, the best-performing material, Li 4 Ti 5 O 11.9 F 0.1 delivers superior rate capacities of 165, 162.1, 160.0, 142.3, 125.1, and 99.2 mAh g −1 , at 0.2 C, 0.5 C, 1 C, 3 C, 5 C, and 10 C, respectively, which is higher than those of Li 4 Ti 5 O 12 (150.0, 135.0, 123.5, 93.7, 76.4, and 56.8 mAh g −1 at the same C-rates), and the cycling retention is 82.7% after 150 cycles at 5 C. Meanwhile, the charge-transfer resistance (R ct ) of Li 4 Ti 5 O 11.9 F 0.1 (56.4 Ω) is lower than that of pure Li 4 Ti 5 O 12 (80.6 Ω), and the lithium-ion diffusion coefficients (D Li + ) of Li 4 Ti 5 O 11.9 F 0.1 (2.505 × 10 −10  cm 2  s −1 ) is higher than that of pure Li 4 Ti 5 O 12 (1.694 × 10 −10  cm 2  s −1 ).

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固体化学
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2012 ·Vol. 39 ·期 5 ·5379-5385 · IF 1.751

Synthesis of Na2FePO4F/C and its electrochemical performance

Jingjing Zhou,Jiefeng Zhou,Yuanhao Tang,Yujing Bi,Chenyun Wang,Deyu Wang,Siqi Shi

Using NaF as the only Na precursor, fluorophosphate Na 2 FePO 4 F/C materials have been synthesized via the solid-state reaction. Na 2 FePO 4 F starts to form at 300   °C, becomes the sole crystalline form between 400 and 600   °C, and decomposes at 650   °C. Comparing with the theoretical capacity of 124   mAh   g −1 , the sample prepared at 600   °C delivered a discharge capacity of 118   mAh   g −1 . The outstanding electrochemical performance is believed to result from the good crystallization and high purity of the synthesized materials . The capacity retentions at 0.5   C and 2   C are 95.8% and 89.8%, respectively, of that at 0.05   C. Furthermore, a discharge capacity of 122   mAh   g −1 is maintained under the cycling between 2.0 and 5.2   V vs. Li/Li + , indicating that the second Na + is not extracted from the Na 2 FePO 4 F lattice.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固体化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS · 2010 ·Vol. 52 ·期 4 ·615-619 · IF 2.453

On-line molecular imprinted solid-phase extraction flow-injection fluorescence sensor for determination of florfenicol in animal tissues

Shenguang Ge,Mei Yan,Xiaoliang Cheng,Congcong Zhang,Jinghua Yu,Peini Zhao,Weiqiang Gao

A simple and convenient on-line molecular imprinted solid-phase extraction flow-injection fluorescence sensor was developed in this study. Florfenicol (FF)-imprinted polymer was prepared by self-assembly with acrylamide (AM) as functional monomer and ethylene glycol dimethacrylate (EGDMA) as cross-linker. The binding characteristics of the imprinted polymer to florfenicol were evaluated by equilibrium binding experiments, and the morphology of the imprinted polymer was studied by scanning electron microscope (SEM). Fluorescence intensity of 3-p-nitrylphenyl-5-(2′-sulfonophenylazo) rhodanine (4NRASP) and bovine serum albumin (BSA) was inhibited by FF. Under optimum conditions the intensity of fluorescence shows a linear relationship with the concentration of FF over the range of 1.2   ×   10 −6 to 2.6   ×   10 −5   g   mL −1 with a regression equation of Δ I   =   23.54   +   17.86 c ( c 10 −6   g   mL −1 ) ( r   =   0.9965, n   =   6). The low detection limit of FF was found to be 3.4   ×   10 −7   g   mL −1 according to 11 parallel determinations for the blank solution. The relative standard deviation for the determination of 2.0   ×   10 −6   g   mL −1 FF solution was 3.5% ( n   =   11). This proposed sensor could be satisfactorily applied to the determination of FF in liver and meat samples.

研究领域: 分析化学 · 药物残留检测 · 食品安全 · 分子识别 · 环境监测 · 兽药代谢
✓ 已验证 DOI 高影响因子
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JOURNAL OF SOLID STATE CHEMISTRY · 2016 · IF 2.265

New oxygen-deficient cationic-ordered perovskites containing turquoise-coloring Mn5+O4 tetrahedral layers

Yifeng Han,Xuanhong Ye,Hong Zhu,Yuexiang Li,Xiaojun Kuang

Ba 6 Na 2 M 2 Mn 2 O 17 (M=Nb, Ta) oxides were synthesized by high-temperature solid-state reaction. The compounds adopt 6-layer perovskite-related structure (referred to as 6C) in P 3 ̅ m 1, analogous to Ba 6 Na 2 Nb 2 P 2 O 17 . The 6C structure consists of cubic ( c ) BaO 3 layers and pseudo-cubic ( c' ) oxygen-vacancy-ordered BaO 2 layers stacked according to a sequence of c'ccccc . Ordering of oxygen vacancies in oxygen-deficient c' -BaO 2 layers leads to two successive isolated tetrahedral layers, which stabilize an unusual +5 oxidation state for Mn cations in the tetrahedral sites. In Ba 6 Na 2 M 2 Mn 2 O 17 , these two Mn 5+ O 4 layers are sandwiched by two single octahedral NaO 6 layers that connected by two successive octahedral NbO 6 layers, forming alternative 2:1-ordered (Ba 3 NaM 2 O 9 ) - and (Ba 3 NaMn 2 O 8 ) + perovskite-like units along the stacking direction. The Mn 5+ O 4 tetrahedral units act as a turquoise chromophore in Ba 6 Na 2 M 2 Mn 2 O 17 , making these two compounds potential turquoise-coloring materials for the cool pigments .

研究领域: 无机化学 · 材料科学 · 固体化学 · 功能材料 · 颜料化学
✓ 已验证 DOI 高影响因子
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MARINE POLLUTION BULLETIN · 2015 ·Vol. 102 ·期 1 ·142-147 · IF 2.991

Determination of diethylstilbestrol in seawater by molecularly imprinted solid-phase extraction coupled with high-performance liquid chromatography

Xiuping He,Xiaoqi Mei,Jiangtao Wang,Ziru Lian,Liju Tan,Wei Wu

An effective and highly selective molecularly imprinted material was prepared by suspension polymerization for the isolation and pre-concentration of synthetic estrogen diethylstilbestrol (DES) in seawater . The obtained MIPMs were proved to have more uniform size and porous structure, with maximum adsorption capacity of 8.43   mg   g −   1 almost two times more than NIPMs (4.43   mg   g −   1 ). The MIPMs showed no significant deterioration of the adsorption capacity after five rounds of regeneration. An off-line molecularly imprinted solid phase extraction (MISPE) method followed by HPLC–DAD was proposed for the detection of DES in seawater , and recoveries were satisfactorily higher than 77%. Four seawater samples in aquaculture area were analyzed and 0.61   ng   mL −   1 DES was detected in one sample. The result demonstrated that this method can be used for the rapid separation and clean up of trace residual of DES in seawater.

研究领域: 环境分析化学 · 海洋环境污染 · 分子印迹技术 · 药物残留检测 · 水体污染物
✓ 已验证 DOI 高影响因子
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CHINESE CHEMICAL LETTERS · 2016 ·Vol. 28 ·期 1 ·49-54 · IF 1.947

Solid-solid phase transition of (1-C14H29NH3)2ZnCl4 in nanopores of silica gel for thermal energy storage

Qi-Feng Li,Chao Wang,Xiao-Zheng Lan

Latent heat storage performance of a layered perovskite-type compound, 1-C 14 H 29 NH 3 ) 2 ZnCl 4 (C 14 Zn), embedded in a series of silica gel (SG) with pore sizes of d   =   15–200   nm is investigated using differential scanning calorimetry (DSC), and powder X-ray diffractions (XRD). C 14 Zn in the nanopores of silica gel shows size-dependent phase transition temperature, enthalpy change and supercooling. They have a stable transition temperature and heat capacity at each size in a short-term thermal cycling. Similar X-ray diffraction patterns are observed for the nano-sized and the bulk C 14 Zn. The encapsulation of a phase change material in nanopores is a new way of tuning its thermal energy storage properties for a wider range of temperature regulation.

研究领域: 材料科学 · 热力学 · 纳米科技 · 能源存储 · 功能材料
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 17 ·7911-7920 · IF 2.7

Large-scale synthesis of LiMn2O4 cathode materials via a rheology-assisted solid-phase method using citric acid

Pengchao Liang,Yuanchao Li,Xiangzhen Xiao,Shumin Fan,Jingjing Ma,Jingjie Liu,Yongqiang Dong,Yuhang Zong,Guangri Xu,Li Yang

Although they possess a high working voltage and environmental compatibility, and are low in cost with abundant resources, the poor cycling performance and rapid capacity attenuation of LiMn2O4 cathodes at high temperature restrict their extensive application. In this study, LiMn2O4 materials are synthesized by a simple rheology-assisted solid-phase method using citric acid as an additive. The citric acid improves the uniformity of the mixed raw materials, resulting in a reduction in particle agglomeration. Consequently, the synthesized LiMn2O4 shows an initial capacity of 117.4 mA h g−1 with a capacity retention of 79.50% at 2C after 300 cycles and 54.78% of the initial discharge capacity at 20C. This work provides a strategy for modifying multicomponent transition metal oxides for advanced lithium-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机固体化学 · 电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY · 2011 ·Vol. 110 ·期 3 ·1437-1442 · IF 1.752

Phase behavior of dodecane—tetradecane binary system confined in SBA-15

Lan X. Z.,Pei H. R.,Yan X.,Liu W. B.

Phase behavior of dodecane–tetradecane ( n -C 12 H 26 –C 14 H 30 , n -C 12 –C 14 ) binary system in bulk and confined in SBA-15 (pore diameters 8 nm; 15.9 nm) has been investigated by differential scanning calorimetry and transmission electron microscopy. The bulk system possesses some special phases relating to the rotator phase in normal alkanes. Dodecane–tetradecane mixtures confined in SBA-15 (8 nm) are a system miscible both in solid and liquid states with a phase diagram of a smooth curve. Dodecane–tetradecane system confined in SBA-15 (15.9 nm) exhibits not only solid–liquid (s–l) in all compositions but solid–solid transition in mole fractions of tetradecane 0.1–0.6, which forms a phase diagram of “loop line” shape. Melting temperatures of n -C 12 –C 14 /SBA-15 (8 nm) are lower than those of n -C 12 –C 14 /SBA-15 (15.9 nm) in all mole fractions. The evolution of the phase diagram of n -C 12 –C 14 confined in 8 nm, 15.9 nm pore sizes of SBA-15 and in bulk, respectively, shows a dramatic effect of confinement on phase behavior of normal alkane mixtures. The s–l phase boundary lines of n -C 12 –C 14 /SBA-15 (8, 15.9 nm) are fitted as \( T_{\text{m,r}}^{x} \) being [ \( xT_{{\text{m} ,r}}^{A} + \left( {1 - x} \right)T_{\text{m,r}}^{B} - D \) ], where D is a polynomial ∑ a i x i , i  = 1, 2,···, n ( A  = C 14 , B  = C 12 ).

研究领域: 物理化学 · 材料科学 · 纳米限域效应 · 热分析 · 软物质物理
✓ 已验证 DOI 高影响因子
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Food Analytical Methods · 2015 ·Vol. 9 ·期 7 ·2026-2035 · IF 1.956

A Novel Molecularly Imprinted Polymer Based on Carbon Nanotubes for Selective Determination of Dioctyl Phthalate from Beverage Samples Coupled with GC/MS

Du Jiaojiao,Gao Ruixia,Mu Hui

Phthalates represent a potential risk for humans, since they are ubiquitous environmental contaminants. Efficient extraction and purification procedures are demanded for the detection of low concentration levels of phthalates. In this work, a novel type of molecularly imprinted polymers coated onto the surface of vinyl functionalized multi-walled carbon nanotubes was synthesized and coupled with gas chromatography–mass spectrometry (GC/MS) for the selective separation and determination of dioctyl phthalate (DOP) in beverage samples. The morphology, structure property, and thermostability of the resultant polymers were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The adsorption properties of the prepared polymers were investigated by equilibrium rebinding and competitive experiments. The resultant imprinted nanomaterials exhibited high capacity and favorable selectivity. In addition, the feasibility of the developed method using the obtained imprinted polymers as a solid-phase sorbent coupled with GC/MS for the selective isolation and determination of DOP in different beverage samples was demonstrated. Under optimal conditions, the limit of detection of the proposed method for DOP was 2.3 ng L −1 . DOP spiked at three levels of concentration in beverage samples was extracted and determined through the application of the present method, with recoveries ranging from 88.6 to 93.0 % with relative standard deviations less than 5.6 %.

研究领域: 分析化学 · 环境毒理学 · 食品安全 · 分子识别 · 材料科学 · 色谱分析
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2015 · IF 4.504

Lithium sodium vanadium phosphate and its phase transition as cathode material for lithium ion batteries

Peng Li,Lianyi Shao,Pengfei Wang,Xi Zheng,Haoxiang Yu,Shangshu Qian,Miao Shui,Nengbing Long,Jie Shu

In this work, Li 2 NaV 2 (PO 4 ) 3 is successfully synthesized by using a simple solid-state reaction method. Structural analysis shows that this sample is a hybrid product consisted of rhombohedral Li 3 V 2 (PO 4 ) 3 phase and rhombohedral Na 3 V 2 (PO 4 ) 3 phase As a cathode material for lithium ion batteries, Li 2 NaV 2 (PO 4 ) 3 exhibits an initial reversible capacity of 108.9   mAh   g −1 at 35   mA   g −1 in the potential range between 3.0 and 4.3   V, with an average working potential at 3.75   V. The lithium-ion diffusion coefficient in Li 2 NaV 2 (PO 4 ) 3 is measured to be 1.86–3.27   ×   10 −15   cm 2   s −1 . In addition, the electrochemical reaction between Li 2 NaV 2 (PO 4 ) 3 and Li is also investigated by various in-situ and ex-situ techniques. Viewed from the in-situ and ex-situ results, it is concluded that the electrochemical reactions of Li 2 NaV 2 (PO 4 ) 3 with Li are associated with the formation of rhombohedral LiV 2 (PO 4 ) 3 phase and rhombohedral NaV 2 (PO 4 ) 3 phase during the lithium ion extraction process and its reverse lithium insertion process is reversible for structural evolution. The highly stable structure ensures the electrochemical reversibility of Li 2 NaV 2 (PO 4 ) 3 cathode material in lithium ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固体化学
✓ 已验证 DOI 高影响因子
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