JOURNAL OF CHEMICAL AND ENGINEERING DATA
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2019
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IF 2.298
Yameng Wan,Pengshuai Zhang,Haixia He,Jiao Sha,Kunpeng Yang,Tao Li,Baozeng Ren
Solubility of phenylphosphonic acid (PPOA) in 15 solvents (methanol, ethanol, n-propanol, isopropyl alcohol, 1-butanol, 1-pentanol, 1-hexanol, 1-heptanol, 1-octanol, 2-methoxyethanol, 2-ethoxyethanol, 2-propoxyethanol, 2-butoxyethanol, acetone, and 1,4-dioxane) was measured by the isothermal saturation method under 0.1 MPa. Solubility of PPOA increased with increasing temperature. The interaction energies between PPOA and selected solvents were calculated by molecular simulation to explain the solubility order. Experimental solubility was correlated by five thermodynamic models including the modified Apelblat equation, uniquac, the nonrandom two-liquid (NRTL)-segment activity coefficient (SAC), NRTL, and the Wilson model. The modified Apelblat equation, NRTL, and NRTL-SAC were more applicable for fitting of solubility data of PPOA. Thermodynamic properties of the mixing process including the mixing Gibbs energy (ΔmixG), mixing enthalpy (ΔmixH), and mixing entropy (ΔmixS) were investigated by the Wilson equation. The mixing process was spontaneous, exothermic, and entropy-driven.
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Journal of the Taiwan Institute of Chemical Engineers
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2023
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IF 5.7
Yanxi Zhao,Shiyan Huang,Chengchao Liu,Yuhua Zhang,Longsheng Wang,Aihua lin,Jinlin Li
Background The design and synthesis of catalysts with high stability, activity and selectivity in Fischer–Tropsch synthesis (FTS) have been attracting extensive research attention. Maintaining high catalytic stability and activity is the best strategy for improving the catalyst efficiency and economic benefits. Methods In this study, graphitic carbon nitride (g-C 3 N 4 )-coated SBA-15 was utilised as a support material to prepare cobalt-based FTS catalysts. The catalysts coated with g-C 3 N 4 were studied via TEM, XPS, XRD, H 2 -TPR, TG, N 2 adsorption–desorption, and tested in a fixed-bed reactor. Significant findings The catalysts coated with g-C 3 N 4 were considerably more stable than the Co/SBA-15 catalyst without g-C 3 N 4 coating during a 100 h test period. Furthermore, the CO-conversion performance of the Co/SBA-15 catalyst decreased continuously. Notably, the activity of the Co/ [email protected] 3 N 4 catalyst with a low g-C 3 N 4 loading was higher than that of the Co/SBA-15@1C 3 N 4 catalyst with a relatively high g-C 3 N 4 loading. g-C 3 N 4 can significantly strengthen the interaction between the cobalt species and the support, thereby increasing the catalyst stability. Therefore, a highly stable catalyst with good activity can be achieved by employing a small amount of g-C 3 N 4 for surface modification. The results highlight the effectiveness of the proposed strategy for preparing highly stable, cobalt-based catalysts with good activity.
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APPLIED ORGANOMETALLIC CHEMISTRY
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2019
·Vol. 33
·期 6
·e4874
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IF 3.259
Yingpeng Huo,Jiwen Hu,Shudong Lin,Xingming Ju,Yanlong Wei,Zhenzhu Huang,Yangfei Hu,Yuanyuan Tu
Reported herein is an easy-to-prepare novel heterogeneous catalyst of platinum complexes bearing binary ligands of bidentate naphthalenolimine and cyclo-1,5-octadiene that are anchored onto mesoporous silica SBA-15. The presence of the binary ligands not only stabilized the platinum, but also enabled the platinum atoms to form nanoclusters with diameters of ca 1 nm, and led to high platinum loading (8.69 wt%). Moreover, the platinum catalyst exhibited high catalytic activity towards hydrosilylation of terminal alkenes and styrene with silanes under mild and solvent-free conditions, with excellent regioselectivity.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2018
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IF 3.909
Yongcun Song,Li-Ye Yang,Yang-guang Wang,Di Yu,Jiafeng Shen,Xiao-kun Ouyang
In this work, amino-functionalized Santa Barbara Amorphous-15/calcium alginate (ASBA-15@CA) microspheres were fabricated and characterized by FTIR, SEM, XRD, TGA , and XPS analyses. The Pb(II) adsorption properties of the ASBA-15@CA microspheres were studied in terms of the effects of the adsorption time, adsorbent dose, solution pH, temperature, and initial concentration of Pb(II) on the adsorption capacity. At pH 6 and 298 K, the adsorption reached equilibrium after 100 min and the sample exhibited a good adsorption effect, affording a maximum adsorption capacity of 1029.58 mg/g and a removal rate as high as 98.99%. The adsorption process conformed to the Langmuir model ( R 2 = 0.9937) and followed the pseudo-second-order kinetics model ( R 2 = 0.9995). Regeneration experiments showed that the removal rate of the sample reached 75% even after 6 cycles. Overall, this study provides new insights into the development of novel, highly efficient, and repeatable degradation materials for the removal of Pb(II).
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PubMed
高影响因子
MICROCHEMICAL JOURNAL
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2019
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IF 3.206
Xiang-Dong Qing,Huai-Bo Zhou,Xiao-Hua Zhang,Hai-Long Wu,Chang-Ya Chen,Su-Wen Xu,Shuang-Shuang Li
Polycyclic aromatic hydrocarbons (PAHs) are of worldwide environmental concern because of their properties of carcinogenicity, mutagenicity and teratogenicity. In the work, a smart combination of gel permeation chromatography-diode array detector and second-order calibration based on alternating trilinear decomposition (ATLD-GPC-DAD) is proposed for simultaneous targeted identification and quantification of 15 PAHs in atmospheric pollution sources such as flue-dust and greasy-dirt samples. No need of tedious sample pretreatment and specific PAHs separation column, severely overlapped chromatograph peaks are successfully resolved by the ATLD-GPC-DAD method even with only 3 s of difference in retention times. Accurate quantitative results of 15 PAHs are achieved by using the developed method even in the presence of unexpected interferents. The limits of detection range from 0.94 ng mL −1 to 48.86 ng mL −1 , and the average recoveries are in the range of (81.2 ± 1.0)% to (108.9 ± 11.6)% for flue-dust samples and (89.7 ± 3.4)% to (107.5 ± 8.0)% for greasy-dirt samples. The sensitivity and selectivity of analytes is significantly improved with the aid of “mathematical separation” of the method. These results indicate that it opens a promising analytical strategy for control of PAHs emissions and management of urban air quality.
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JOURNAL OF HAZARDOUS MATERIALS
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2016
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IF 4.836
Jun Cheng,Qing Ye,Zongbo Yang,Weijuan Yang,Junhu Zhou,Kefa Cen
The response mechanisms of microalgal mutant Chlorella PY-ZU1 cells were investigated in their removal of antibiotic tilmicosin from wastewater under 15% CO 2 . Low concentrations (0.01–2 mg L −1 ) of tilmicosin in wastewater stimulated the growth of microalgal cells, whereas high concentrations (5–50 mg L −1 ) of tilmicosin significantly inhibited cell growth. When initial tilmicosin concentration increased from 0 to 50 mg L −1 , fractal dimension of microalgal cells monotonically increased from 1.36 to 1.62 and cell size monotonically decreased from 4.86 to 3.75 μm. In parallel, malondialdehyde content, which represented the degree of cellular oxidative damage, monotonically increased from 1.92 × 10 −7 to 7.07 × 10 −7 nmol cell −1 . Superoxide dismutase activity that represented cellular antioxidant capacity first increased from 2.59 × 10 −4 to the peak of 6.60 × 10 −4 U cell −1 , then gradually decreased to 2.39 × 10 −4 U cell −1 . The maximum tilmicosin removal efficiency of 99.8% by Chlorella PY-ZU1 was obtained at the initial tilmicosin concentration of 50 mg L −1 .
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RSC Advances
·
2017
·Vol. 7
·期 11
·6605-6614
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IF 3.108
Ce Gao,Qingda An,Zuoyi Xiao,Shangru Zhai
Nowadays, processing of ultra-low sulfur fuel oil has been a hot topic of research all over the world; hence, an efficient adsorption process to tackle this issue is eliciting increasing attention. However, the preparation of high-performance adsorbents is still a challenge. Herein, zirconium-substituted mesoporous SBA-15 with highly dispersed active Cu(I) species has been successfully synthesized by our group at 493 K via a mild vapor-reduction method. The as-prepared material was characterized by powder X-ray diffraction (XRD), nitrogen adsorption and desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-vis diffuse reflectance (DRUV) spectroscopy. All characterization methods demonstrated that the Cu(I) species were highly dispersed in an ordered mesoporous framework with short channels rather than piled on the surface. The as-prepared materials also exhibited an excellent adsorption capacity for thiophene (up to 29.86 mg g−1 at 323 K). Pseudo-second-order kinetics model and Freundlich isotherm can well describe the adsorption kinetics and isotherm data, respectively. More remarkably, an ultrasound-assisted treatment can be effectively employed to regenerate adsorbent, with only a slight reduction in the adsorption capacity after five cycles.
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JOURNAL OF SOLID STATE CHEMISTRY
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2012
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IF 2.159
Yan-Jing Gu,Bing Yan,Yan-Yan Li
Novel organic–inorganic mesoporous luminescent polymeric hybrid materials containing europium(III) complexes incorporated to mesoporous silica SBA-15/SBA-16 have been prepared by simple physical doping (impregnation) methods, followed by the addition polymerization reaction of the monomer 4-vinylpyridine (vpd) extending along the mesoporous channels. The precursor europium(III) complexes are synthesized by β-diketonate (β-diketonate=2-thenoyltrifluoroacetonate (tta), hexafluoroacetylacetonate (hfac), trifluoroacetylacetonate (taa)) and monomer 4-vinylpyridine (vpd) coordinated to Eu 3+ , and SBA-15/SBA-16 are obtained via a sol–gel process. After the physical doping and the polymerization reaction , the final ternary materials Eu(β-diketonate) 3 pvpd-SBA-15/Eu(β-diketonate) 3 pvpd-SBA-16 (β-diketonate=tta, hfac, taa) are received. The physical properties and espeically the photoluminescence of these hybrids are characterized, and the XRD and BET results reveal that all of these hybrid materials have uniformity in the mesostructure. The detailed luminescence investigation on all the materials show that Eu(tta) 3 pvpd-SBA-16 have the highest luminescence intensity and the materials with taa ligands have longer lifetimes.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2025
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IF 9
Xianyu Sun,Shiqin Xu,Yuelin Jin,Tao Cai,Xiaodong Wang,Hongqing Niu,Dezhen Wu
Global demand for lithium (Li) is experiencing a significant growth. A green and effective solution has been devised to address the increasing demand for resource recovery of Li from recycled Li-ion batteries. The objective of this study was to chemically graft 4′-Aminobenzo-15-crown-5-ether (AB15C5) onto polyimide (PI) fiber through a three-step method, resulting in the successful fabrication of AB15C5-functionalized PI fiber (PI-g-AB15C5). The PI-g-AB15C5 fiber exhibits a specific surface area of 2.69 m 2 g −1 as determined by Brunauer-Emmett-Teller analysis. The textiles derived from PI-g-AB15C5 are particularly significant. The textiles exhibit a higher specific surface area and elevated free pore volume, which enhance the full exposure of crown ethers and the adsorption of Li + . The PI-g-AB15C5 fiber exhibits advantageous hydrophilicity, has a significant equilibrium adsorption capacity for Li + (qmax = 21.09 mg g −1 ), demonstrates remarkable repeatability in cycling tests, displays excellent tensile properties, and maintains its fabric morphology during the adsorption process. PI-g-AB15C5 fiber effectively retrieved Li + in an acidic setting. When four interfering ions (Na + , K + , Co 2+ , and Mn 2+ ) were present, the PI-g-AB15C5 fiber demonstrated a remarkable ability to adsorb Li + selectively. The selective separation factors of Li + for Na + , K + , Co 2+ , and Mn 2+ were 8.47, 18.88, 6.99, and 9.85, respectively. A literature survey revealed that PI-g-AB15C5 fiber had better selective separation factors. The selectivity of PI-g-AB15C5 fiber towards Li + is supported by Density Functional Theory (DFT) calculations, which show that the greater Gibbs free energy change of the PI-g-AB15C5–Li + complex (−1008.82 kcal mol −1 ) is responsible for this exceptional selectivity. In summary, the functionality of this study’s polymer fiber material provides an effective method for recovering Li + from recycled Li-ion batteries. It can efficiently adsorb Li + , facilitating their selective separation from other heavy metals.
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JOURNAL OF MEMBRANE SCIENCE
·
2024
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IF 8.4
Taipu Chen,Lei Chen,Yutong Zhao,Jinkai Hao,Zhigang Shao
To tackle the challenges of phosphoric acid (PA) leakage and suboptimal proton transfer efficiency in PA-polybenzimidazole (PBI) high-temperature proton exchange membranes (HTPEMs), this research has pioneered the development of a novel porous silicon material, DP/S15, which has been tailored through organic phosphonic acid modification. S15 or DP/S15 was utilized to fabricate PBI composite membranes and subjected these membranes to a thorough examination of their properties. The integration of DP/S15 into the membrane matrix notably enhanced acid uptake and facilitated the formation of a robust and extensive proton transportation network. This was largely attributable to the synergistic interaction between the organic phosphonic acid groups in DP/S15 and PA. As a result, the membranes incorporating DP/S15 exhibited a host of commendable properties, most notably their substantial mechanical strength , which registered at 89.80 MPa with undoped PA and 13.10 MPa with doped PA. Furthermore, theoretical analyses lent credence to the efficient adsorption between DP/S15 and phosphoric acid. Consequently, the composite membranes delivered superior performance metrics, evident in their high conductivity (reaching 57.7 mS cm −1 at 160 °C) and excellent PA retention capabilities (up to 89.5 %). Of paramount significance was the performance of the single fuel cell equipped with the PA-DP/S15-PBI composite membrane, which achieved a peak power density of 672.29 mW cm −2 . This figure impressively surpassed that of the pure PBI membrane by 262.23 mW cm −2 . In light of these promising outcomes, the PA-DP/S15-PBI composite membrane harbors significant potential for deployment in HT-PEMFCs.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2024
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IF 3.8
Chi Sun,Yudong Xia,Xue Ye,Wenlin Xu,Hui Shi,Xinhua Gao,Jinghao Yu,Lisheng Guo,Jie Li
The direct dimethyl ether (DME) synthesis reaction via CO2 hydrogenation typically requires a bifunctional catalyst that effectively combines a methanol synthesis catalyst with a methanol dehydration catalyst, but the effect of the relationship between the two catalysts on the catalytic performance has not been as well studied. In this study, we developed a CuZnZr/Al–S(10)-PG bifunctional catalyst physically mixed with Al-modified SBA-15 and the traditional CuZnZr catalyst for the hydrogenation of CO2 to DME. A pivotal discovery is that the modulation of interaction intensity between these two constituents significantly influences the electronic configuration of each component. Through X-ray photoelectron spectroscopy characterization and methanol dehydration experiments, it was confirmed that diminishing the synergistic interplay between CuZnZr and Al-modified SBA-15, which regulated the electronic structure of the Cu–Zn interface and enhanced the Cu–Zn interfacial interaction, played a crucial role in enhancing the catalyst’s performance in CO2 hydrogenation to DME. This finding contests established beliefs about the necessity of strong synergistic interactions in such systems and provides new insights for designing rational bifunctional catalysts.
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APPLIED CATALYSIS A-GENERAL
·
2025
·
IF 4.8
Yifan Liu,Jiangang Wang,Yuhan Liu,Yuan Zhang,Hongzi Tan,Hongyou Cui
Herein, a series of Sn-based catalysts supported on SBA-15 with temperature responsive ability to in situ construct acidic and basic sites are reported for efficient conversion of biomass-derived sugars into ethyl lactate (EL). Based on the investigation on the effects of the molar ratio of Cl/OH in Sn(OH) x Cl 2-x and the support types, it is found that Sn(OH) 0.5 Cl 1.5 @SBA-15 is an excellent catalyst in catalytic conversion of various sugars to EL, achieving a maximum EL yield of 68.1 % from sucrose. The in situ generated basic SnO sites play important roles in accelerating the retro-aldol condensation reaction, while the concomitantly released acidic sites (Sn 2 + , SnCl + and H + ) could catalyze the reactions of hydrolysis, isomerization, intermolecular rearrangement and esterification to EL. Benefiting from the temperature responsive effect, not only can the reaction pathways be regulated toward high EL selectivity, but also the catalyst can be recycled easily. This research paves an avenue for exploring efficient catalysts for biomass valorization.
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