JOURNAL OF ALLOYS AND COMPOUNDS
·
2013
·
IF 2.39
Hongtao Cui,Yunan Zhao,Wanzhong Ren,Minmin Wang,Yan Liu
In this work, α-Co(OH) 2 and β-Co(OH) 2 nanosheets were selectively synthesized through an epoxide precipitation reaction under mediation of fluoride ions. The protonation and ring opening reaction of propylene oxide promoted the hydrolysis [Co(H 2 O) 6 ] 2+ to form a mixed phase of α-Co(OH) 2 and Co 2 (OH) 3 Cl in the condition of no existence of fluoride ions. Due to the enhanced hydrolysis of [Co(H 2 O) 6 ] 2+ under function of fluoride ions, pure phases of α-Co(OH) 2 and β-Co(OH) 2 were formed respectively at different concentration of fluoride ions. The mild reaction condition of this route allows for large scale synthesis of cobalt hydroxide nanosheets, which is only limited by volume of the vessel used as reactor.
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Russian Journal of Physical Chemistry A
·
2025
·Vol. 98
·期 13
·3009-3016
·
IF 0.8
Zhe Wang,Li Junzhi,Zhao Wei,Li Xiao Liang
The isobaric vapor-liquid equilibrium data for the four systems consisting of 1-octene + 2-methyl-thiophene, cyclohexene + 2-methylthiophene, 2,3-dimethyl-1-butene + 2-methylthiophene, and 2,3-dimethyl-2-butene + 2-methylthiophene were determined by using a modified Rose-Williams equilibrium still at 90.00 kPa. All the vapor-liquid equilibrium data measurements passed the thermodynamic consistent test by employing the Herington method. The azeotropic behavior was observed in the 1-octene + 2-methyl-thiophene system. Additionally, the experimental data were correlated by the Wilson model, and they were also compared with the original UNIFAC and UNIFAC Dortmund predictive models. All the results indicated that the measured data were in good agreement with the calculated values obtained from the Wilson. Meanwhile, the UNIFAC Dortmund model can provide better prediction result than the original UNIFAC model.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Chao Liu,Guohua Jing,Zongqiang Zhu,Yinming Fan,Shengpeng Mo,Yanan Zhang,Dunqiu Wang,Bihong Lv,Mingming Fu,Xiaobin Zhou
Diamines or polyamines with two or more amino groups are suitable for formulating non-aqueous absorbents (NAAs) with high CO 2 loading capacity and low regeneration energy consumption. However, these two types of amines in NAAs are prone to produce insoluble gelatinous products after absorbing CO 2 , resulting in difficult operation of the CO 2 capture system. In this study, by using 2-amino-2-methyl-1-propanol (AMP) as an inhibitor, the insoluble gelatinous products of the aminoethylethanolamine (AEEA)-N-methyl-2-pyrrolidone (NMP) (A-A-N) and 3-(methylamino)propylamine (MAPA)-NMP (M-A-N) NAAs were successfully eliminated. The experimental results showed that the AMP-regulated NAAs possessed a high absorption rate, high CO 2 loading capacity, excellent desorption efficiency, and stable recyclability. The reaction mechanism of CO 2 absorption and the inhibitory mechanism of AMP on the formation of gelatinous products were comprehensively elucidated. Taking the A-A-N system as a representative, AEEA reacted with CO 2 to form zwitterionic protonated carbamate species (AEEACO 2 − (P) H + (S) ), which tended to self-aggregate via hydrogen-bond interaction, resulting in the formation of insoluble gelatinous products. With the introduction of AMP, the AMP-derived products could combine easily with AEEACO 2 − (P) H + (S) via strong electrostatic attraction to form ion pairs, preventing the AEEACO 2 − (P) H + (S) molecules from self-aggregating to form insoluble gelatinous products. The regeneration heat duty of the A-A-N system was 1.89 GJ∙ton −1 CO 2 , which was 49.9 % lower than that of the benchmark 30 wt% MEA. Overall, introducing AMP as a gelatinous product inhibitor was beneficial for the development of NNAs with high CO 2 absorption capacity and low-energy consumption.
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CHEMISTRY OF MATERIALS
·
2024
·
IF 7.2
Yi-Gang Chen,Xiwei Hu,Yao Guo,Sangen Zhao,Bingbing Zhang,Xia Zhang,Xian-Ming Zhang
A challenging topic for tetrahedra-based deep-ultraviolet (deep-UV, wavelength λ < 200 nm) birefringence crystals is how to generate both large birefringence and high deep-UV transmittance. Edge-sharing tetrahedra can induce large structural distortion and thus could produce strong optical polarization anisotropy to realize the challenging topic, but edge-sharing tetrahedra frequently require extreme synthesis conditions to overcome large repulsion interaction between tetrahedra. Herein, under mild hydrothermal conditions, an α-Be3(H2O)2(PO4)2 crystal with edge-sharing BeO4 and its polymorph β-Be3(H2O)2(PO4)2 with common corner-sharing BeO4 were synthesized, both featuring a three-dimensional stable structure constructed by BeO4, BeO2(H2O)2, and PO4 tetrahedral units. Remarkably, α-Be3(H2O)2(PO4)2 manifests superior birefringence of 0.101 and high deep-UV transmittance of 167 nm, with the largest birefringent quality factor (BQF) of 0.75 among the known tetrahedra-based deep-UV materials. By contrast, β-Be3(H2O)2(PO4)2 manifests a small birefringence of 0.019 and 160 nm deep-UV transmittance, with only a mediocre BQF of 0.15. Further, computational investigations reveal that edge-sharing BeO4 makes a dominant contribution to the great birefringence. This study could push the synthesis of edge-sharing-tetrahedra materials and offers an alternative strategy toward designing high-performance tetrahedra-based deep-UV birefringence materials.
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ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Haoyang Liu,Yue Zhu,Weixu Chen,Renwang Sheng,Chuanquan Liu,Yuzhi Sun,Jia Liu,Mingyue Wang,Jun Lu,Jialin Chen,Wei Zhang
The advancement of nanomedicine requires a thorough understanding of the intrinsic bioactivity and molecular interactions of nanomaterials for safe and effective clinical applications, which remains lacking for most currently developed nanomaterials. Here, we uncover the unique intrinsic bioactivity and regulatory mechanisms of carbon-based fullerol nanomaterials through high-throughput molecular analysis and explore their therapeutic potential for tissue regeneration using tissue engineering approaches. Fullerol exhibits intrinsic pro-differentiation and antioxidant properties that enhance the osteogenesis and chondrogenesis of MSCs. Mechanistically, proteomic analysis combined with small-molecule inhibition studies reveals that fullerol is internalized by MSCs via clathrin-mediated endocytosis and activates NRF2 signaling, thereby exerting antioxidant effects that restore impaired MSC viability and differentiation under oxidative stress. Leveraging these unique bioactivities, we develop a fullerol-functionalized hydrogel with feasible physicochemical properties and triple biological functions in antioxidant, pro-osteogenic, and pro-chondrogenic effects and confirm its great regenerative capacity for both cartilage and subchondral bone by promoting structural restoration and improving functional recovery in a rat osteochondral defect model. Our findings offer new insights into the intricate interactions between stem cells and nanomaterials at the cellular and molecular levels and broaden the potential biomedical applications of fullerol for future cartilage and bone regeneration therapies.
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ENVIRONMENTAL POLLUTION
·
2020
·
IF 6.793
Cui Ma,Shengyong Jia,Pengfei Yuan,Zhengguang He
Composite magnetic oxide at cow dung ash, nano-Fe 3 O 4 @cow dung ash (nano-Fe 3 O 4 @CDA), was used as catalytic material for the degradation of 2, 2′-methylenebis (4-methyl-6-tert-butylphenol) (AO 2246) in real biologically pretreated landfill leachate . The Fe 3 O 4 @CDA composite exhibited catalytic ozonation activity and allowed material separation and magnetic recovery. The effects of several operating parameters including O 3 concentration, catalyst dosage, temperature and scavengers were evaluated in parallel. Over 70% of AO 2246 were removed by the nano-Fe 3 O 4 @CDA/O 3 system under optimum conditions within 120min reaction time. The EPR, GC–MS and free-radical quenching experiments expatiated the mechanism of this degradation process. It was confirmed that the AO 2246 was degraded efficiently in this catalytic micro-ozonation process, Additionally, GC–MS analysis state clearly that the 3,5-bis(1,1-dimethylethyl)phenol, 4-(1,5-dihydroxy-2,6,6-trimethylcyclohex-2-enyl)but-3-en-2-one, ethanone, 1-(1,4-dimethyl-3-cyclohexen-1-yl)-, 5-tert-butyl-6-3, 5-diene-2-one, 2-hydroxyhexanoic acid, 2-propenoic acid 1,1-dimethylethyl ester, butanoic acid, 2-methyl-, methyl ester and propanoic acid, 2, 2-dimethyl- were the dominant oxidation products (OPs) during the degradation of the AO 2246. The EPR results showed that the catalytic ozonation over Fe 3 O 4 @CDA led to produce more hydroxyl radicals , which were in favor of AO 2246 degradation. The toxicity evolution was also performed through a QSAR analysis calculated by the ECOSAR program which further demonstrated the different responses toward the AO 2246 and its OPs.
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2017
·
IF 3.154
Lukai Ma,Guoqin Liu
A group of toxic aldehydes such as, malondialdehyde (MDA), 4-hydroxy-2-hexenal (HHE), and 4-hydroxy-2-nonenal (HNE) have been found in various vegetable oils and oil-based foods. Then simultaneous determination of them holds a great need in both the oil chemistry field and food field. In the present study, a simple and efficient analytical method was successfully developed for the simultaneous separation and detection of MDA, HHE, and HNE in vegetable oils by reversed-phase-high-performance liquid chromatography (RP-HPLC) coupled with photodiode array detector (PAD) at dual-channel detection mode. The effect of various experimental factors on the extraction performance, such as coextraction solvent system, butylated hydroxytoluene addition, and trichloroacetic acid addition were systematically investigated. Results showed that the linear ranges were 0.02–10.00 μg/mL for MDA, 0.02–4.00 μg/mL for HHE, and 0.03–4.00 μg/mL for HNE with the satisfactory correlation coefficient of >0.999 for all detected aldehydes. The limit of detection (LOD) and limit of quantification (LOQ) of MDA, HHE, and HNE were ∼0.021and 0.020 μg/mL, ∼0.009 and 0.020 μg/mL, and ∼0.014 and 0.030 μg/mL, respectively. Their recoveries were 99.64–102.18%, 102.34–104.61%, and 98.87–103.04% for rapeseed oil and 96.38–98.05%, 96.19–101.34%, and 96.86–99.04% for French fries, separately. Under the selected conditions, the developed methods was successfully applied to the simultaneous determination of MDA, HHE, and HNE in different tested vegetable oils. The results indicated that this method could be employed for the quality assessment of vegetable oils.
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GREEN CHEMISTRY
·
2015
·Vol. 17
·期 7
·3992-3999
·
IF 8.02
Shujing Zhu,Xiaoqiang Ma,Erzheng Su,Dongzhi Wei
From an environmental perspective, utilizing nonconventional solvents (i.e. green solvents) with low ecological footprints is a highly beneficial alternative to using conventional organic solvents to form a reaction system. The nitrile hydratase (NHase, EC 4.2.1.84) catalyzed hydration of 2-amino-2,3-dimethylbutyronitrile (ADBN) to 2-amino-2,3-dimethylbutyramide (ADBA) in various green solvent–aqueous reaction systems was investigated in this study. After systematically optimizing the reaction conditions, the HFE-7100/H2O (v/v, 10%) biphasic system was ultimately identified as a promising reaction system for reducing product inhibition, avoiding substrate hydrolysis, and facilitating product separation and solvent recovery. The average ADBA yield of an entire batch reaction was 97.3%, which is obviously higher than those obtained with previously reported chemical or enzymatic methods. This is the first attempt to apply a fluorous solvent–aqueous biphasic system to a biocatalytic process, and the results suggest that the fluorous solvent employed in the biphasic system satisfies the requirements for green chemistry.
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CHEMISTRY-A EUROPEAN JOURNAL
·
2019
·Vol. 25
·期 55
·12842-12848
·
IF 5.16
Hong Li,Xiao-Fang Jia,Qing Zhao,Ju-Ping Ma,Jian-Dang Liu,Bang-Jiao Ye,Yoshihiro Kuroiwa,Chikako Moriyoshi,Zhi-Yong Li,Qi Liu,Jun-Ying Zhang,Hong-Tao Sun
Graphical Beyond ferroelectricity : The defective [Bi 2 O 2 ] 2+ layers in Aurivillius phases show broadband near-IR luminescence that covers the telecommunication and biological optical windows (see figure). The luminescence was identified to stem from oxygen vacancies and defect complexes. This offers a probe for the examination of defect states in Aurivillius-phase ferroelectrics and possibilities for coupling both physical behaviors. Aurivillius phases have been routinely known as excellent ferroelectrics and have rarely been deemed as materials that luminesce in the near-infrared (NIR) region. Herein, it is shown that the Aurivillius phases can demonstrate broadband NIR luminescence that covers telecommunication and biological optical windows. Experimental characterization of the model system Bi 2.14 Sr 0.75 Ta 2 O 9− x , combined with theoretical calculations, help to establish that the NIR luminescence originates from defective [Bi 2 O 2 ] 2+ layers. Importantly, the generality of this finding is validated based on observations of a rich bank of NIR luminescence characteristics in other Aurivillius phases. This work highlights that incorporating defects into infinitely repeating [Bi 2 O 2 ] 2+ layers can be used as a powerful tool to space-selectively impart unusual luminescence emitters to Aurivillius-phase ferroelectrics, which not only offers an optical probe for the examination of defect states in ferroelectrics, but also provides possibilities for coupling of the ferroelectric property with NIR luminescence.
研究领域:
材料科学
·
光学
·
物理学
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Zijun Zhou,Qizhen Zhuo,Lejia Wang,Chao Ying,Wangyang Lu,Baohong Guan
To address the issue of tap water safety caused by the seasonal increase in odor, a novel fluorine-doped ceramic has been prepared and employed in catalytic ozonation for the removal of 2-methylisoborneol (2-MIB), a typical odorant compound in tap water. Fluorine was incorporated into the ceramic framework through the solid-phase addition of CaF 2 , leading to the concurrent formation of Lewis acid sites (LAS) and oxygen vacancies (OVs). These sites substantially promote the generation of reactive oxygen species (ROS). The optimal catalyst doped with 1.0 wt% CaF 2 exhibits an appropriate pore structure and the highest density of acid sites, enabling the complete removal of 2-MIB (100 ng/L) within 6 min during the catalytic ozonation process. This catalytic ozonation, in which the singlet oxygen ( 1 O 2 ) and superoxide radicals (·O 2 − ) dominate the oxidative degradation of 2-MIB, exhibits an approximately 4-fold higher reaction rate constant than ozonation. This work demonstrates that catalytic ozonation using a CaF 2 -doped ceramic catalyst is a highly feasible and efficient method for 2-MIB removal, offering a promising strategy for odor control in tap water.
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BIOCHEMICAL PHARMACOLOGY
·
2026
·
IF 6.5
Zeyuan Wang,Chaoying Yang,Yanpeng Wang,Zhiming Guo,Ruibo Jin,Ling Xiao,Jing Liu,Hui Zhou,Xiaojuan Xiao,Xu Han
Multiple myeloma (MM) is a malignant hematological disorder characterized by the neoplastic proliferation of plasma cells. Hypercalcemia is a common complication in MM and is often considered a secondary consequence of disease progression. When calcium levels are severely elevated, it can lead to coma in affected patients. However, whether hypercalcemia plays a direct role in MM progression remains unclear. Herein we found that high calcium concentrations promote MM cell proliferation and it was associated with calpain-2 (CAPN2). We also observed that CAPN2 expression is significantly increased in MM patients and correlates with poor prognosis. Furthermore, knockdown of CAPN2 inhibited MM cell proliferation both in vitro and in vivo via upregulation of FN14 and induction of apoptosis. Importantly, treatment with ALLN, a CAPN2 inhibitor, substantially suppressed MM cell proliferation in vitro and in vivo by inducing apoptosis. Notably, ALLN significantly enhanced the sensitivity of MM cells to commonly used clinical drugs bortezomib and doxorubicin, while exhibiting no obvious cytotoxicity in normal cells. These findings establish CAPN2 as a promising therapeutic target in MM, with its inhibitor serving as a potential lead compound for further clinical evaluation. Our study also elucidates the relationship between hypercalcemia, CAPN2, and malignant proliferation in MM cells, and expands the therapeutic landscape for MM patients.
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
·
2026
·Vol. 27
·期 11
·4759
·
IF 5.6
Kadireya Tuerxun,Zhuoling Ding,Xueqing Luo,Shishui Zhou
2-Phenylethanol (2-PE) is a key aromatic alcohol contributing to the rose-like odor in brewed wines, primarily synthesized by yeast metabolism with a typical yield of less than 100 mg/L. To enhance the 2-PE content in brewed wines, this study used CRISPR-Cas9 gene editing technology to delete the ARO8 gene (encoding aromatic transaminase I) in Saccharomyces cerevisiae SY. The single-factor experiments were performed to optimize the fermentation process, and the 2-PE content in the brewed wine was measured by high-performance liquid chromatography. The results demonstrated that the 2-PE content in whisky fermented by the SY-A8 was 0.73 g/L, increasing 23.73% compared to SY. The fermentation conditions of SY-A8 were optimized through single-factor experiments and the Box–Behnken design. The optimal conditions were a sugar concentration of 46.30 g/L, a fermentation time of 6 days, and an L-phenylalanine concentration of 1.43 g/L. The high 2-phenylethanol aroma whisky was brewed with a higher 2-phenylethanol content of 3.68 g/L in a 1 L fermenter at the optimal conditions. In conclusion, the modification of Saccharomyces cerevisiae by CRISPR-Cas9 gene editing combined with fermentation process optimization provides an effective technical strategy for improving the 2-PE content in whisky, thereby providing a research perspective for the flavor enhancement of whisky and other brewed wines.
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