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ACS Applied Nano Materials · 2020 · IF 0

TiO(OH)2 Nanoparticle Composite Membranes for Enhancing the Hot Potash Process

Ebrahim Ataeivarjovi,Yubing Liu,Zhigang Tang,Hao Ding,Dong Guo,Xiaofei Song,Guoxun Ben,Mengyue Zhou

The desorption process of CO2 absorbed by the hot-potash-alkali method was studied in this paper. In a traditional hot-potash-alkali process, the temperatures of KHCO3 aqueous solutions are high, moisture vaporization is serious, and energy consumption is high. We proposed that membrane desorption can be used instead of heating desorption and conducted relevant research. PDMS-PTFE-PVDF/PET was used as a composite membrane. The water evaporation considerably declined, and the decomposition conversion rate reduced to 25.5% as the equilibrium liquid-phase concentration decreased. Results show that the PDMS-PTFE-PVDF/PET composite membrane loaded with 1 wt % TiO(OH)2 nanoparticles can be used for membrane desorption, while the decomposition conversion rate of the KHCO3 aqueous solution decreased by only 4.2% after 10 cycles, and the effect was considerably improved. The comprehensive capture energy consumption was about 65% lower than that of the absorption-heating desorption process on account of the positive effect of TiO(OH)2 nanoparticles. Brief calculation, which is based on CO2 concentration tested by a gas analyzer and the linear fitting of the Arrhenius equation, demonstrates that the reaction activation energy can be reduced (Supporting Information).

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MACROMOLECULAR RESEARCH · 2017 ·Vol. 25 ·期 11 ·1070-1075 · IF 1.405

Kinetics of Sn(Oct)2-catalyzed ring opening polymerization of ε-caprolactone

Wu Dan,Lv Yin,Guo Rui,Li Jiahui,Habadati Aerman,Lu Bowen,Wang Heyun,Wei Zhong

To evaluate the effects of different alcohols (primary, secondary, and two different tertiary alcohols) as initiators on the structure of polycaprolactone (PCL) in ring-opening polymerization (ROP), four experiments were conducted in toluene with tin(II) 2-ethylhexanoate (Sn(Oct) 2 ) as the catalyst. The kinetics of ε -caprolactone ( ε -CL) ROP at different temperatures and monomer concentrations were studied with n -butanol as the initiator and Sn(Oct) 2 as the catalyst. The kinetic plot of ln(M 0 /M t ) vs. time ( t ) seems a linear, which indicates that the propagation rate is in the first order with respect to monomer concentration. When the reaction temperature increased, the reaction rate and the final relative maximum monomer conversions also increased. The molecular weight of PCL initially increased and then decreased as monomer conversion increased. This behavior can be attributed to the high viscosity of the system, which affected monomer diffusion and polymer chain propagation. In addition, prolonging reaction time caused inter-/intramolecular transesterification. However, when monomer concentration decreased, the reaction rate decreased. The actual activation energy of Sn(Oct) 2 -catalyzed ROP of ε -CL in toluene was -75 kJ/mol.

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CHEMISTRY-A EUROPEAN JOURNAL · 2025 · IF 3.7

MXene Loaded With Cu(2-x)Se Nanozyme for Nanocatalytic Tumor Therapy

Mengtian Lu,Tianye Zhang,Yue Yang,Xin Lin,Jin Huang,Yuan Sun,Tiedong Sun

Graphical The study innovatively combines etched/stripped monolayer Ti 3 C 2 MXene with Cu (2- x ) Se nanoparticles in a one-pot method. The synthesized Ti 3 C 2 /Cu (2- x ) Se nanocomposite has catalase (CAT) and peroxidase (POD) -like activities combined with the excellent photothermal properties of MXene, which enhances the catalytic performance of Cu (2- x ) Se under near infrared (NIR) irradiation, and realizes the synergic photothermal catalytic treatment. Traditional tumor treatments (surgery, radiotherapy, chemotherapy, etc.) have certain limitations and can have serious negative effects, such as difficulty in cutting out tumors, damage to normal tissues, and complications. Ordinary nanozymes have low catalytic activity and require higher doses for treatment, which can increase in vivo toxicity and side effects. To address these limitations, we developed a Ti 3 C 2 MXene-based nanocomposite (Ti 3 C 2 /Cu (2- x ) Se) integrating Cu (2- x ) Se nanozymes with dual enzyme-mimicking activities (catalase and peroxidase) and MXene's photothermal properties. The Cu (2- x ) Se component catalyzes the decomposition of tumor-overexpressed H 2 O 2 into O 2 and cytotoxic ·OH, alleviating hypoxia while inducing oxidative stress. Simultaneously, MXene's high surface area and photothermal capability enhance nanozyme stability, biocompatibility, and catalytic efficiency under near-infrared irradiation. Notably, the photothermal effect amplifies enzymatic activity, enabling synergistic nanocatalytic-photothermal therapy. This synergy not only degrades glutathione to suppress tumor antioxidant defenses but also achieves targeted tumor ablation with reduced dosage requirements. Our work highlights a rational design of MXene-based nanozymes for enhanced multimodal tumor therapy, offering a paradigm for nanocomposite-driven disease treatment.

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JOURNAL OF MATERIALS SCIENCE · 2022 ·Vol. 57 ·期 44 ·20580-20588 · IF 4.682

Co(OH)2 nanosheets anchored on CoB nanochains with enhanced electrochemical performance

Yan Jingjing,Zhu Chengwei,Liu Baohua,Shu Ruiwen

A facile synthetic route based on the assistance of magnetic field is reported to fabricate core–shell CoB@Co(OH) 2 nanochains for purpose of the high conductive pathway and enhanced pseudocapacitance in 3 M LiOH electrolyte. By adjusting the loading amount of the shell Co(OH) 2 nanosheets anchored on the core CoB alloy surface, the typical core–shell CoB@Co(OH) 2 is endowed with the appropriate pore volume of 0.27 cm 3  g −1 and the high accessible electrode/electrolyte interfacial area (62.3 m 2  g −1 ) and the fast conductive highway; meanwhile taking advantages of core–shell structure can be favor for fast ion transport between the electrode/electrolyte interphase and rapid electron transfer. Benefiting from the advantageous properties, the typical CoB@Co(OH) 2 electrode exhibits a high specific capacitance of 492.8 F g −1 in three-electrode device together with good cyclic stability (90.4% capacitance retention) during continuously 5000 cycles at 2 A g −1 . This work can provide an inspiring strategy for rational designing of core–shell CoB@Co(OH) 2 , and indicate their potential energy application in alkaline electrolyte. Graphical abstract Core–shell CoB@Co(OH) 2 electrode with rapid conductive highway achieves the broaden voltage of 0.8 V and the enhanced supercapacitive performance.

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JOURNAL OF PHYSICS D-APPLIED PHYSICS · 2022 ·Vol. 55 ·期 42 ·424005 · IF 3.409

Nonlinear optical absorption of Co3(PO4)2·4H2O nanosheets in broadband spectra

Chang Wang,Ran Duan,Xingcheng Xiao,Yingwei Wang,Zhihui Chen,Yejun Li,Si Xiao,Jun He

Long hexagonal Co3(PO4)2·4H2O nanosheets were synthesized using a hydrothermal method, where their nonlinearity was probed via a femtosecond Z-scan system. The results show that the Co3(PO4)2·4H2O nanosheets exhibit saturable absorption when the incident photon energy is greater than the forbidden band width, while optical limiting is found when the incident photon energy is smaller than the forbidden band width. In particular, the obtained Co3(PO4)2·4H2O nanosheets demonstrate the best optical limiting properties at 600 nm. The present study suggests the cobalt phosphates nanosheets as a promising candidate for optical limiters.

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2018 · IF 2.829

The hydrophobic mechanism of di(2-ethylhexyl) phosphoric acid to hemimorphite flotation

Jingqin Qin,Guangyi Liu,Hongli Fan,Wen Tan

In this paper, the flotation separation of hemimorphite from quartz was investigated by using di(2-ethylhexyl) phosphoric acid (DEHPA) as a collector. The results elucidated that DEHPA exhibited better flotation performances to hemimorphite than dibutyl phosphoric acid (DBP), tributyl phosphate (TBP), octanoic acid (OA) and palmitic acid (PA). And DEHPA also possessed good selectivity against quartz flotation and could realize the effective flotation separation of hemimorphite from quartz under pH 6.0–10.0. The adsorption and contact angle findings clearly indicated that DEHPA selectively adsorbed on hemimorphite, hardly on quartz. After DEHPA treatment, the hydrophobicity of hemimorphite was dramatically improved. Zeta potential suggested that DEHPA anion anchored on hemimorphite surfaces mainly through chemical bonds. FTIR inferred that DEHPA chemisorbed on to hemimorphite surfaces by formation of the Zn O bonds between the O atoms of the P( O)(OH) group and the surface zinc atoms, simultaneously with splitting the O H bonds of the P O H group. XPS gave clear evidences that the adsorbed DEHPA combined with Zn(II) species on hemimorphite surfaces to generate the Zn(II)-DEHPA surface complexes.

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AICHE JOURNAL · 2017 ·Vol. 63 ·期 9 ·3955-3965 · IF 2.836

Fabrication of supported Pd–Ir/Al2O3 bimetallic catalysts for 2-ethylanthraquinone hydrogenation

Runrun Hong,Yufei He,Junting Feng,Dianqing Li

A series of χ wt % Pd-(1-χ) wt % Ir (χ = 0.75, 0.50, and 0.25) catalysts supported on γ-Al 2 O 3 have been prepared by co-impregnation and calcination-reduction, and subsequently employed in the hydrogenation of 2-ethylanthraquinone—a key step in the manufacture of hydrogen peroxide. Detailed studies showed that the size and structure of the bimetallic Pd–Ir particles vary as a function of Pd/Ir ratio. By virtue of its small metal particle size and the strong interaction between Pd and Ir, the 0.75 wt % Pd–0.25 wt % Ir/Al 2 O 3 catalyst afforded the highest yield of H 2 O 2 , some 25.4% higher than that obtained with the monometallic 1 wt % Pd catalyst. Moreover, the concentration of the undesired byproduct 2-ethyl-5,6,7,8-tetrahydroanthraquinone (H 4 eAQ) formed using the Pd–Ir bimetallic catalysts was much lower than that observed with the pure Pd catalyst, which can be assigned to the geometric and electronic effects caused by the introduction of Ir. © 2017 American Institute of Chemical Engineers AIChE J , 63: 3955–3965, 2017

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International Journal of Medical Sciences · 2025 ·Vol. 22 ·期 8 ·1773-1790 · IF 3.2

Integrated Phenotypic and Transcriptomic Analyses of Osteoporosis in Type 2 Diabetic Mice

Xing Shu-Juan,Gao Ying-Feng,Liu Lu,Sui Bing-Dong,Da Ning-Ning,Liu Jin-Yu,Wang Hao,Yuan Yuan,Qin Yuan,Liu Pei-Sheng,Ying Si-Qi,Zhang Kai,Liu Jie-Xi,Chen Ji,Liu Yi-Han,Xie Xin,Jin Yan,Zhang Sha,Zheng Chen-Xi

Background: Type 2 diabetes (T2D) is a global metabolic condition associated with complications of multiple organs, including the bone. However, the exact impact of T2D on bone along the disease progression, particularly in the early phase, remains largely unknown.Methods: Four-week and sixteen-week high-fat diet (HFD) feeding-induced T2D mouse models were established, and the glucose metabolic status was examined. Bone mass was evaluated by micro-computed tomography (micro-CT), and immunofluorescent (IF) staining was performed for bone histomorphometry with enzyme-linked immunosorbent assay (ELISA) determining serum markers. RNA sequencing analysis was performed to examine the transcriptome of bone, and single-cell RNA-sequencing (scRNA-seq) analysis was further applied. Bone marrow mesenchymal stem cells (BMMSCs) were isolated and analyzed for functional behaviors.Results: The occurrence of glucose metabolic disorders was confirmed at both four weeks and sixteen weeks of HFD feeding, showing increased blood glucose levels with impaired glucose tolerance and insulin sensitivity. Notably, early T2D osteoporosis symptoms were detected at four weeks, especially in the trabecular bone, demonstrating reduced bone mass and mineral density. Histological analysis confirmed that bone remodeling and immune-related inflammation were also altered in T2D mice, remarkably at the early phase, mainly reflected by suppressed bone formation, stimulated bone resorption, increased macrophages, and elevated tumor necrosis factor-alpha (TNF-α) levels. Transcriptomic sequencing further demonstrated significant yet distinct changes in the gene expression profile of bone during T2D progression, which confirmed the histological findings. Notably, overlapping genes with altered expression at four weeks and sixteen weeks of T2D compared to the respective control were identified, and bone marrow scRNA-seq analysis indicated many of them were expressed in BMMSCs, suggesting BMMSCs critically involved in T2D osteoporosis. Dysregulated molecular profiles and functional abnormalities of BMMSCs in T2D mice were validated by ex vivo assays, showing early and persistent occurrence of impaired colony-forming and proliferative capacities with biased differentiation potential.Conclusions: These findings elucidate the bone lesion phenotype in T2D, particularly at the early phase, uncover changes in gene expression profiles of bone during T2D progression, and clarify the functional alterations in bone stem cells, providing a basis for subsequent research and the development of treatment strategies.

CAS / MDL: 65-86-1
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BIOTECHNOLOGY LETTERS · 2019 ·Vol. 41 ·期 6 ·789-799 · IF 2.154

Biocatalytic synthesis and characterization of sn-1/3 and sn-2 monoacylglycerols

Wang Xiuwen,Cheng Yang,Jin Qingzhe,Wei Wei,Wang Xingguo

Objectives To investigate the lipase-catalyzed synthesis of high purity sn -1/3 and sn -2 monoacylglycerols (1/3-MAG and 2-MAG) of different fatty acids (FAs). Results The 1/3-MAGs of three FAs (16:0, 17:0, 16:1) were synthesized using lipase-catalyzed esterification of glycerol with FAs. The 2-MAGs were obtained from the ethanolysis of synthetic triacylglycerols using sn -1,3 regiospecific lipase. The effects of lipase types, substrate ratio, temperature, reaction time and lipase load on the MAG conversion were studied. Under the optimal conditions, high purities (96.74%, 95.44%, 92.96%) with acceptable isolated yields (51.00%, 54.28%, 46.00%) were obtained for 1/3-16:0-MAG, 1/3-17:0-MAG, and 1/3-16:1-MAG, respectively. For 2-16:0-MAG, 2-17:0-MAG, and 2-16:1-MAG, the purities were 92.64, 95.04, and 96.48%, with isolated yields of 50.64, 52.16, and 26.12%, respectively. The molecular structures of the synthetic compounds were confirmed by 1 H NMR, and MS and the melting points were characterized by DSC. Conclusions High purity MAG isomers can be synthesized via lipase-catalyzed reactions to be building blocks for production of functional lipids, the melting points of which are largely governed by the hydrophobic interactions among the alkanyl chains.

CAS / MDL: 506-12-7 75-65-0
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Ca(OH)2 nanosheets fabricated by carbide residue for effective dry desulfurization

Panpan Wang,Meiyu Shi,Bochen Zhao,Yuan Shu,Qiang Niu,Pengfei Zhang

Carbide residue, a highly alkaline industrial solid waste generated during acetylene production, is primarily composing of Ca(OH) 2 . In this study, a top-down solid-state redispersion strategy. By synergizing mechanochemical activation with surfactant capping, we achieving the recycling of carbide residue to synthesize Ca(OH) 2 -CTAB anosheet-based desulfurization agent. The resultant material exhibits a significantly enhancing BET specific surface area (30.2 m 2 ·g −1 ) and abundant pore architecture. Comparative evaluations with Ca(OH) 2 -P123 and raw carbide residue revealing the superior performance of the Ca(OH) 2 -CTAB adsorbent, demonstrating a sulfur dioxide adsorption capacity of 2.57 mmol·g −1 is a 2-fold improvement over untreating carbide residue. Furthermore, significantly extends the fixed-bed penetration time to 43869 seconds. Comprehensive characterization through TG, FTIR, BET, SEM, TEM, and AFM elucidating the relationship between the nanosheet morphology and its exceptional desulfurization performance. This work provides a green methodology for upcycling industrial alkaline waste into functional nanomaterials for environmental remediation.

CAS / MDL: 57-09-0 9003-11-6
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MATERIALS LETTERS · 2019 · IF 3.019

β-Ba(PO3)2 with DUV cut-off edge and large birefringence

Na Li,Xuefang Lu,Qun Jing,Ping Wei,Lu Qi,Zhongqi Jiang,Zhaohui Chen

Phosphates are another new family of exploring deep-ultraviolet nonlinear optical materials. As one material, the simpler the composition is the more favorable synthesis and application is. In this work, a simple alkaline earth metal phosphate β -Ba(PO 3 ) 2 was synthesized by high temperature solid phase method. It is worth mentioning that it has short cut-off edge (<190 nm) and relatively large birefringence (Δn = 0.032 @ 1064 nm) in phosphates and the optical anisotropy and birefringence can be enhanced by optimizing the basic anion arrangement. Combining with theoretical analysis, the relationship between structure and performance is further elaborated. In additional, thermal properties, linear optical and nonlinear optical properties for β -Ba(PO 3 ) 2 were also investigated.

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JOURNAL OF MOLECULAR STRUCTURE · 2023 · IF 3.8

Synthesis, characterization, crystal structure, and cholinesterase inhibitory activity of 2-phenylthiazole derivatives

Jing-Jing Qian,Jing-Pei Zou,Shan-Ming Liu,Xiao-Qing Zhang,Rui Li,Zhao-Yuan Zhang,Wei-Weil Liu,Shao-Jie Ma,Da-Hua Shi

ABSTRACT A series of 2-phenylthiazole derivatives were synthesized, characterized, and appraised as cholinesterase inhibitors. The structures of the 2-phenylthiazole derivatives were characterized by FT-IR, HRMS, 1 H NMR, 13 C NMR spectroscopy, and single-crystal X-ray diffraction studies. Compound 5a is a monoclinic crystal system with space group P2 1 . Compound 5c has an orthorhombic crystal system with the space group P2 1 2 1 2 1 . The cholinesterase inhibitory effects of synthetic 2-phenylthiazole derivatives were determined by Ellman's method. Most 2-phenylthiazole compounds possessed potent acetylcholinesterase inhibitory effects and weak butyrylcholinesterase inhibitory activities. Compound 5a has the best inhibitory effect on acetylcholinesterase, with an IC 50 of 0.031 µM which was comparable to that of donepezil (IC 50  = 0.039 µM). Molecular docking, molecular dynamics simulation, and binding free energy calculation/MM-GBSA revealed that compound 5a interacts with the peripheral anion site (PAS) of acetylcholinesterase stably. In conclusion, compound 5a is promising as an acetylcholinesterase inhibitor, which can be used as a leading compound for Alzheimer's disease in-depth research and development.

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