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PARTICLE & PARTICLE SYSTEMS CHARACTERIZATION · 2020 ·Vol. 37 ·期 3 ·2000008 · IF 3.099

Self-Assembly of Chiral Nematic Liquid Crystalline Phases of AgNR@SiO2@Cysteine@CsPbBr3 Hybrid Nanorods with Plasmon-Dependent Photoluminescence

Zhen Li,Huali Liu,Fei Li,Jiaqi Zhao,Yu Wang

The direct synthesis of a chiral nematic liquid crystalline phase of AgNR@SiO 2 @cysteine@CsPbBr 3 hybrid nanorods (HNRs) is reported. The circular dichroism spectra can be divided into three components: (1) the interband absorption–enhanced optical activity of structural arrangement of cysteine (cys) molecules, 200–320 nm, (2) the chiral nematic liquid crystalline arrangement of the Ag nanorods (AgNRs), 350–450 nm, and (3) the exciton adsorption edge of the perovskite, 500–550 nm. The polarizing optical microscope images indicate that the chiroptical response of perovskite arises from chiral nematic crystalline arrangement rather than cys-induced electronic coupling between a chiral ligand and otherwise achiral perovskite quantum dots (QDs). The luminescent intensity of CsPbBr 3 QDs in AgNR@SiO 2 @cys@CsPbBr 3 HNRs is boosted 87-fold due to the local surface plasmon resonance field enhancement effect. Furthermore, the high-performance green light emitting diode is constructed employing AgNR@SiO 2 @cys@CsPbBr 3 complexes, which exhibit excellent luminescent properties. This work contributes insights into structure–property relationships and this strategy promisingly provides guidance for the other inorganic chiral semiconductor suprastructures.

研究领域: 材料科学 · 纳米技术 · 光学 · 光子学
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2021 · IF 5.302

Influence of Ca/Al ratio on physical and dielectric properties of Al2O3/CaO-B2O3-SiO2 glass-ceramics composite coatings prepared by high enthalpy atmospheric plasma spraying

Qi Li,Jianliang Xie,Jin Hu,Xin Wang,Chengyong Yu,Shaoliang Jiang,Peng Liu,Chengli Sun,En Li,Longjiang Deng

The dielectric layer plays a key role in regulating electromagnetic wave broadband scattering based on meta-surface technology. Herein, the physical properties of composite powder, prepared by spray drying of CaO-B 2 O 3 -SiO 2 (CBS) glass-ceramic powder and Al 2 O 3 in different mass ratios, are systematically investigated. Meanwhile, a high enthalpy atmospheric plasma spraying equipment is utilized to prepare CBS/Al 2 O 3 composite coatings , and the morphology, physical properties and dielectric properties of the composite coating are analyzed. The XRD and DSC data of the composite coating reveal that the crystallization behavior of β-CaSiO 3 and CaB 2 O 4 gradually disappear with the increase of Al 2 O 3 content. Hence, only CaAl 2 Si 2 O 8 phase is observed during heat treatment. The experimental results confirm that the dielectric properties of CBS/Al 2 O 3 composite coating conform to the rule of mixture for composite materials. Also, the dielectric properties are affected by porosity and crystallization rate.

CAS / MDL: 3458-72-8 9002-98-6
研究领域: 材料科学 · 电磁工程 · 涂层与薄膜 · 复合材料
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2024 · IF 3.8

Unraveling the Coking and Deactivation Behavior of Al–Cs/SiO2 Catalyst in the Aldol Condensation of Methyl Propionate with Formaldehyde

Ran Ran,Wei Zhu,Guoliang Zhang,Lei Wang,Gongying Wang,Jie Li

The loaded acid–base bifunctional catalysts exhibit good catalytic performance in the synthesis of methyl methacrylate via aldol condensation of methyl propionate with formaldehyde, but they still suffer from deactivation caused by coke deposition. In this paper, coke deposition as well as consequential deactivation behavior of Cs/SiO2 catalyst loaded with various amounts of Al was investigated under different reactant compositions by using nuclear magnetic resonance, thermogravimetric, Brunauer–Emmett–Teller, and Raman analysis. As a result, coke on the catalyst was characterized by amorphous coke deposition, which was mainly composed of polycyclic aromatic hydrocarbons and aliphatic substances. Al added to the 10Cs/SiO2 catalyst significantly reduced the amount of coke deposition and inhibited the C/H ratio of coke. Appropriate amounts of Al and reactant compositions could ultimately increase the stability of the catalyst. Moreover, the kinetics of coke deposition observed on the Al–Cs/SiO2 catalyst was studied. It was found that the Voorhies equation modified using the variables of reaction temperature and reactants composition could accurately forecast coke accumulation on the 3.5Al-10Cs/SiO2 catalyst under specific conditions.

CAS / MDL: 67-56-1
研究领域: 催化化学 · 化工工程 · 物理化学
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CHEMICAL ENGINEERING JOURNAL · 2015 · IF 4.321

Preparation and characterization of molecular imprinted polymer functionalized with core/shell magnetic particles (Fe3O4@SiO2@MIP) for the simultaneous recognition and enrichment of four taxoids in Taxus × media

Jie-Ping Fan,Xiao-Kang Xu,Rui Xu,Xue-Hong Zhang,Jian-Hang Zhu

In this work, the superparamagnetic Fe 3 O 4 particles prepared by the coprecipitation method were coated successively by SiO 2 , vinyl end groups and molecularly imprinted polymer (MIP) shells to afford a pomegranate-like core/shell superparamagnetic particle (Fe 3 O 4 @SiO 2 @MIP), and the MIP shell preparation conditions were optimized by multi-objective response surface methodology. In order to simultaneously enrich and separate the four taxoids (10-DAB, baccatin III, cephalomannine and paclitaxel), cephalomannine was selected as the template because of its similar chemical structure to other three taxoids and relative inexpensiveness. Especially, to avoid template leaking which may influence the accuracy of identification and quantitation of the analytes, we selected paclitaxel as the target molecular during the investigation of the adsorption property of Fe 3 O 4 @SiO 2 @MIP particles. This strategy was similar to the dummy molecular imprinting technique in which the dummy molecularly imprinted polymer was prepared by using a dummy template, structural analog of the target analyte. The as-prepared Fe 3 O 4 @SiO 2 @MIP particles were characterized by transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), and Fourier transform infrared spectroscopy (FTIR). The adsorption kinetics, isotherms and reusability were also investigated. Finally, the Fe 3 O 4 @SiO 2 @MIP particles were successfully applied to simultaneously enrich and separate these four taxoids in the extract of Taxus   ×   media ( T.   ×   media ).

CAS / MDL: 97-90-5
研究领域: 分析化学 · 材料科学 · 药学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2020 · IF 3.573

Catalytic Hydrodeoxygenation of Methyl Stearate and Microbial Lipids to Diesel-Range Alkanes over Pd/HPA-SiO2 Catalysts

Huifang Liu,Jianyu Han,Qitian Huang,Hongwei Shen,Lijun Lei,Zhipeng Huang,Zhixin Zhang,Zongbao K. Zhao,Feng Wang

Catalytic hydrotreating of renewable oils is a promising way to get diesel alkanes, with the use of microbial lipids further facilitating scalable production of green diesel. The core issue of triglyceride hydrodeoxygenation (HDO) research is still to develop efficient catalysts under mild reaction conditions. Herein, we demonstrate that the heteropolyacid (HPA)-modified SiO2 supported Pd catalysts showed high activity for the HDO reaction of methyl stearate and soybean oil to diesel alkanes (C15∼C18, >90 wt % at 200 °C). Characterizations show that the Brønsted acid sites introduced by grafting heteropolyacid on SiO2 and metal sites of small Pd particles contribute to the high HDO activity of this bifunctional catalyst. Additionally, lipids produced by Rhodosporidium toruloides Y4 from glucose or corn stover were also transformed to about 75 wt % of diesel-range alkane products. This integration of microbial lipid production with chemical catalysis should facilitate the engineering of green diesel production from lignocellulosic biomass.

研究领域: 化学工程 · 催化 · 生物能源 · 绿色化学 · 可再生能源
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Potential application of novel amphiphilic Janus-SiO2 nanoparticles stabilized O/W/O emulsion for enhanced oil recovery

Han Jia,Jiajun Dai,Lingchun Miao,Xin Wei,Hongtao Tang,Pan Huang,Haidong Jia,Juan He,Kaihe Lv,Dexin Liu

The Janus nanoparticles stabilized Pickering emulsions showed great application potential in various fields, including enhanced oil recovery (EOR). In this study, the amphiphilic Janus-SiO 2 nanoparticles (Janus-C12) are successfully synthesized by the Pickering emulsion method and characterized by Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), ζ-potential and contact angle measurements. The phase inversion from oil-in-water (O/W), multiple oil-in-water-oil (O/W/O) emulsion, to water-in-oil (W/O) emulsions was observed with the delicate control for the modification degrees of Janus-C12. The possible emulsification mechanisms for various Janus-C12 stabilized emulsions were proposed. The multiple O/W/O emulsion stability in harsh conditions and the influence factors (nanoparticles concentration, water/oil volume ratio and NaCl concentration) were studied systematically. Moreover, the Janus-C12–79% stabilized multiple O/W/O Pickering emulsions exhibited excellent EOR performance (additional oil recovery of 27.2%) in core flooding tests, and the possible EOR mechanism was explored via microscopic visualization experiments.

研究领域: 化学工程 · 材料科学 · 石油工程
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2020 · IF 4.192

Competitive Lateral Flow Immunoassay Relying on Au–SiO2 Janus Nanoparticles with an Asymmetric Structure and Function for Furazolidone Residue Monitoring

Lihong Su,Lulu Wang,Jingke Xu,Zonghan Wang,Xiaolin Yao,Jing Sun,Jianlong Wang,Daohong Zhang

Gold nanoparticles (AuNPs) are the most commonly used signal materials in lateral flow immunoassay (LFIA). However, the assay sensitivity of traditional AuNP-based LFIA is usually limited by the incomplete competition between free target analytes and immobilized antigens for the binding of AuNP-labeled antibodies. To unfreeze this limitation, here, asymmetric Au–SiO2 Janus NPs (about 66 nm) were designed and synthesized. Au–SiO2 Janus NPs can assemble into snowman-like anisotropic structures and combine two different physicochemical properties at their opposite sides, where the AuNP side mainly possesses the antibody conjugating and signal providing functions and the SiO2 side primarily offers the stable function. In virtue of the unique asymmetric nanostructure, only the AuNP side can interact with target analytes by specific antigen–antibody interactions, which could significantly improve the efficiency of competition. Selecting furazolidone as a model analyte, the immunoassay biosensor showed a limit of detection as low as 0.08 ng/mL, 10-fold decreased than that of the AuNPs-LFIA. Moreover, the Au–SiO2 Janus NP lateral flow immunoassay was well applied in chicken, pork, honey, and beef food samples with visual detection limits of 0.8 ng/g, 0.16 ng/g, 0.4 ng/mL, and 0.16 ng/g, respectively. The Au–SiO2 Janus NPs possess the advantages of both materials, which will broaden their applications as a potential alternative in the rapid and sensitive detection of antibiotic residues.

研究领域: 分析化学 · 纳米技术 · 食品安全 · 生物技术
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ACS Applied Materials & Interfaces · 2020 · IF 8.758

Biodegradable Multifunctional Nanotheranostic Based on Ag2S-Doped Hollow BSA-SiO2 for Enhancing ROS-Feedback Synergistic Antitumor Therapy

Ziliang Zheng,Rong Dai,Zhuo Jia,Xiaorong Yang,Yufei Qin,Shuo Rong,Xiaoyang Peng,Xianmei Xie,Yanyan Wang,Ruiping Zhang

Stimuli-responsive silica nanoparticles are an attractive therapeutic agent for effective tumor ablation, but the responsiveness of silica nanoagents is limited by intrastimulation level and silica framework structure. Herein, a biodegradable hollow SiO2-based nanosystem (Ag2S-GOx@BHS NYs) is developed by a novel one-step dual-template (bovine serum albumin (BSA) and cetyltrimethylammonium bromide (CTAB)) synthetic strategy for image-guided therapy. The Ag2S-GOx@BHS NYs can be specifically activated in the tumor microenvironment via a self-feedback mechanism to achieve reactive oxygen species (ROS)-induced multistep therapy. In response to the inherent acidity and H2O2 at the tumor sites, Ag2S-GOx@BHS would accelerate the structural degradation while releasing glucose oxidase (GOx), which could efficiently deplete intratumoral glucose to copious amounts of gluconic acid and H2O2. More importantly, the sufficient H2O2 not only acts as a reactant to generate Ag+ from Ag2S for metal-ion therapy and improves the oxidative stress but also combines with gluconic acid results in the self-accelerating degradation process. Moreover, the released Ag2S nanoparticles can help the Ag2S-GOx@BHS NYs realize the second near-infrared window fluorescence (NIR-II FL) and photoacoustic (PA) imaging-guided precise photothermal therapy (PTT). Taken together, the development of a self-feedback nanosystem may open up a new dimension for a highly effective multistep tumor therapy.

研究领域: 纳米技术 · 癌症治疗 · 材料科学 · 生物医学工程 · 诊疗学
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Talanta Open · 2024 · IF 4.1

Europium-based core-shell materials for fluorescence and colorimetric dual-mode sensing of alkaline phosphatase activity

Chen-Xi Zhao,Xiao-Xia Li,Yang Shu

Abnormal alkaline phosphatase levels have been associated with several diseases, including tumor growth, diabetes, liver dysfunction and so on. Generally, the occurrence and prognosis of these diseases can be reflected by the serum alkaline phosphatase level. In this work, Eu/DBM@SiO 2 @SiO 2 is prepared to protect the internal Eu complex from the external environment by wrapping Eu/DBM inside the silica shell. Then, Eu/DBM@SiO 2 @SiO 2 /MnO 2 , a sensor consists of Eu/DBM@SiO 2 @SiO 2 and MnO 2 , is prepared and applied for alkaline phosphatase detection. MnO 2 is used as the response part of alkaline phosphatase, which can be degraded to Mn 2+ by ascorbic acid. Ascorbic acid is the hydrolysate of alkaline phosphatase. In the process of this reaction, UV–vis absorption of Eu/DBM@SiO 2 @SiO 2 /MnO 2 is reduced and fluorescence is turned on. Alkaline phosphatase concentration is linearly correlated with the logarithmic value of fluorescence enhancement in the range of 10.0–100.0 U/L with linear equation of Lg(F/F 0 )=0.008C-0.030 (R 2 =0.99). For fluorescence method, the LOQ is 10.0 U/L and the LOD is 4.4 U/L. For colorimetric method, the concentration of alkaline phosphatase is linearly correlated with the decrease of absorption intensity in the range of 20.0–90.0 U/L with the linear equation of A/A 0 =-0.012C+1.148 (R 2 =0.99). The LOQ is 20.0 U/L and the LOD is 7.2 U/L. The detection system has good selectivity and can detect alkaline phosphatase in human serum samples, the accuracy of the detection system is verified by the experiment of spike-in experiment. The RSD of alkaline phosphatase concentration in serum samples is in the range of 1.4–8.4 %. This method has potential application in the detection of ALP activity in biological samples.

CAS / MDL: 120-46-7 10031-53-5
研究领域: 生物化学 · 医学诊断
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Molecular Catalysis · 2024 · IF 3.9

PDA/SiO2 microspheres immobilize dual enzymes to increase temperature tolerance and catalyze the production of D-ribulose and D-xylulose from D-xylose

Yuqiu Wu,Fanjin Meng,Jiaolong Fu,Yuyang Zhou,Huan Fan,Xin Ju,Liangzhi Li

D-xylose, a biomass derivative, is used as a substrate to generate D-xylulose and D-ribulose with high-added value through a cascade reaction. During this process, the thermal stability and catalytic efficiency of rate-limiting enzymes during cascade reactions are important issues that must be addressed in industrial applications. In this study, we prepared and validated PDA/SiO 2 microspheres as highly loaded immobilization carriers by oxidative self-polymerization of polydopamine (PDA) on silica (SiO 2 ) microspheres. D-xylose was successfully catalyzed by the co-immobilized D-5-phosphate ribose isomerase B (RpiB) and D-tagatose-3-epimerase (DTE), denoted PDA/SiO 2 -RpiB-DTE, to produce D-ribulose and D-xylulose. After immobilization, the K m of co-immobilized RpiB and DTE decreased, which suggested increased substrate affinity. The half-life of the co-immobilized enzymes was 3.5–8 fold higher than that of the free enzymes at 50–70 °C, and the inactivation rate constant was reduced, demonstrating that immobilization improved significantly the thermal stability. The conversion of D-xylose at 10 mM was 29.98% under optimal conditions, which contained 9.85% D-ribulose and 20.13% D-xylulose. PDA/SiO 2 -RpiB-DTE showed up to 89.10% initial enzyme activity after 3 recycle runs. The thermal stability and recovery aspects were improved by immobilization, which facilitates the use of biomass to produce high-value-added products and further exploitation.

研究领域: 生物技术 · 酶工程 · 生化工程
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SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

A novel self-enhanced electrochemiluminescence sensor based on PEI-CdS/Au@SiO2@RuDS and molecularly imprinted polymer for the highly sensitive detection of creatinine

Nian Cao,Faqiong Zhao,Baizhao Zeng

In this work, a novel self-enhanced solid state electrochemiluminescence (ECL) platform, based on polyethyleneimine (PEI) capped CdS quantum dots (PEI-CdS QDs) as coreactant and [email protected] 2 @Ru(bpy) 3 2+ doped silica ( [email protected] 2 @RuDS) nanocomposite as ECL emitter, was constructed. The PEI-CdS QDs integrated double coreactant of PEI and CdS QDs, thus significantly promoted the ECL of [email protected] 2 @RuDS. Polyaniline hydrogel was introduced to boost the electron transfer and to improve the immobilization of PEI-CdS/ [email protected] 2 @RuDS. In addition, creatinine imprinted poly(o-aminophenol) film was electrodeposited on the PEI-CdS/ [email protected] 2 @RuDS surface as recognition element. Thus, the obtained sensor possessed high sensitivity, stability, reproducibility and selectivity for creatinine sensing. The change of ECL intensity and logarithm of creatinine concentration showed a good linear relationship in the range of 0.05 nM to 5 μM, and the detection limit was low to 0.02 nM. The sensor was applied to detect creatinine in human serum and urine samples, and the results were in good agreement with those of commercial enzyme-linked immunosorbent assay kit.

研究领域: 分析化学 · 纳米技术 · 生物传感器 · 材料科学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2020 · IF 3.573

Slurry-Phase Hydrocracking of a Decalin–Phenanthrene Mixture by MoS2/SiO2–ZrO2 Bifunctional Catalysts

Yongde Ma,Yanru Wang,Wenquan Wu,Jiayin Zhang,Yanning Cao,Kuan Huang,Lilong Jiang

Slurry-phase hydrocracking is one of the most advanced technologies for the conversion of inferior heavy oil to light fuel oil. In this work, MoS2 was combined with SiO2–ZrO2 mixed oxides to offer a new class of bifunctional catalysts for slurry-phase hydrocracking. In the bifunctional catalysts, SiO2–ZrO2 mixed oxides with abundant mesopores and acid sites act as cracking catalysts. They were presynthesized by a sol–gel-hydrothermal method and systematically characterized by X-ray diffraction (XRD), N2 adsorption, Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), NH3-temperature programed desorption (NH3-TPD), and in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). The effect of Si/Zr molar ratios on the chemical structure, especially the acid properties of SiO2–ZrO2 mixed oxides were examined. Subsequently, a mixture of decalin–phenanthrene was selected as the model system to investigate the performance of bifunctional catalysts. It was found that the conversions of decalin and phenanthrene were significantly improved for MoS2/SiO2–ZrO2 bifunctional catalysts. Further analysis indicated that the Brønsted acid sites of SiO2–ZrO2 mixed oxides played an important role in the improvement of decalin and phenanthrene conversions.

研究领域: 化学工程 · 催化 · 石油炼制
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