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Carbon dots modified hydrange-shaped ZnCo(OH)F used as a flexible electrode for sensitive detection of dopamine and uric acid 碳点修饰的绣球状 ZnCo(OH)F 用作灵敏检测多巴胺和尿酸的柔性电极
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-08 DOI: 10.1016/j.colsurfa.2024.135695
Linghui Cao, Yuanxinyi Zhou, Tianyu Shen, Aijuan Xie , Shiping Luo , Baozhu Yang
Dopamine (DA), widely recognized as the most prevalent catecholamine neurotransmitter in the brain, functions as a vital regulator of various physiological processes within the central nervous system. Meanwhile, uric acid (UA) serves as the terminal product of purine metabolism, and hyperuricemia emerges as a significant risk factor for gout, with a steep escalation in risk as blood uric acid levels surge. Consequently, monitoring the concentrations of DA and UA in biological fluids is crucial not only for the treatment of related disorders but also for enhancing disease prevention strategies. In this work, the blooming hydrangea shaped ZnCo(OH)F/carbon dots (CDs) composite was grown on carbon cloth (CC) substrate by a simple hydrothermal method, which was used as a flexible sensor for the detection of DA and UA. The unique open structure and morphologic adjustment strategy of ZnCo(OH)F/CDs/CC provided a large surface area and highly exposed active site. After screening the experimental variables that affect the sensor performance, the optimal ZnCo(OH)F/CDs/CC flexible electrode achieved individual and simultaneous detection for DA and UA in the concentration ranges of 1.0220.0 µM and 1.0500.0 µM, the detection limits (LOD) of DA and UA were 0.0129 and 0.044 μM, respectively (S/N=3). In addition, the sensor exhibited good repeatability, stability and selectivity, realizing the detection of DA and UA in human serum with recovery rate of 95.20 % 105.3 %. Also, the density functional theory (DFT) calculations were used to explore the interaction between electrode material and detected substrate. A simple hydrothermal method was utilized to grow the ZnCo(OH)F/CDs composite onto the CC substrate. The presence of F in ZnCo(OH)F can increase the charge mobility and improve the conductivity. ZnCo(OH)F/CDs/CC as flexible electrode material can determine DA and UA simultaneously in human serum with a satisfactory recovery rate. This flexible sensor has a broad application prospect in the manufacture of wearable devices.
多巴胺(DA)被公认为大脑中最常见的儿茶酚胺神经递质,是中枢神经系统内各种生理过程的重要调节剂。同时,尿酸(UA)是嘌呤代谢的最终产物,高尿酸血症是痛风的一个重要风险因素,随着血尿酸水平的飙升,风险也会急剧增加。因此,监测生物体液中 DA 和 UA 的浓度不仅对相关疾病的治疗至关重要,对加强疾病预防策略也至关重要。本研究采用简单的水热法在碳布(CC)基底上生长了绣球花状的 ZnCo(OH)F/carbon dots (CDs) 复合材料,并将其用作检测 DA 和 UA 的柔性传感器。ZnCo(OH)F/CDs/CC独特的开放式结构和形貌调整策略提供了较大的比表面积和高度暴露的活性位点。在对影响传感器性能的实验变量进行筛选后,最优的 ZnCo(OH)F/CDs/CC 柔性电极实现了在 1.0220.0 µM 和 1.0500.0 µM 浓度范围内对 DA 和 UA 的单独和同时检测,DA 和 UA 的检出限(LOD)分别为 0.0129 和 0.044 μM(S/N=3)。此外,该传感器还具有良好的重复性、稳定性和选择性,实现了对人血清中 DA 和 UA 的检测,回收率为 95.20 % 105.3 %。此外,还利用密度泛函理论(DFT)计算探讨了电极材料与检测基质之间的相互作用。利用简单的水热法在 CC 基底上生长了 ZnCo(OH)F/CDs 复合材料。ZnCo(OH)F 中 F- 的存在可以增加电荷迁移率并提高导电性。ZnCo(OH)F/CDs/CC 作为柔性电极材料可以同时测定人血清中的 DA 和 UA,且回收率令人满意。这种柔性传感器在可穿戴设备的制造中具有广阔的应用前景。
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引用次数: 0
Surfactant molecules and nano gold on HOPG: Experiment and theory HOPG 上的表面活性剂分子和纳米金:实验与理论
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-08 DOI: 10.1016/j.colsurfa.2024.135664
Imtiaz Ahmad
Excessive surfactant molecules within the solution adhere to highly ordered pyrolytic graphite (HOPG) when a droplet containing gold nanorods evaporates, leading to the emergence of a unique coffee-ring pattern. The combination of surface hydrophobicity and evaporation of the aqueous phase results in a stick-slip motion, which enhances the convective hydrodynamics of suspended particles. This phenomenon initiates interactions that influence the deposition and flow dynamics inside the droplet. High-resolution scanning electron microscopy (HRSEM) does not provide significant insights into regions potentially linked to cetyltrimethylammonium bromide (CTAB) molecules, whereas the atomic force microscope (AFM) displays the presence of gold nanoparticles arranged by CTAB within specific CTAB patches. The layers forms with varying heights and gaps between them, indicating diverse adhesion of CTAB. The analytical focus lies on the quantitative assessment of CTAB molecules, stripe dimensions, and energy profiles influenced by concentration and the effective positioning of CTAB-coated gold nanorods in CTAB-covered regions. AFM examination reveals CTAB molecular stripes on HOPG, showing a binding energy of −20 kJ/mol with the surface, −10 kJ/mol for nitrogen bonding with HOPG, and a total binding energy (BE) of −60 kJ/mol, considering various contributing factors. Completely parallel aligned molecules (CPAM) exhibit higher binding energy than non-perfectly aligned molecules (NPAM) due to maximum Van der Waals (VdW) interactions, ideal electrostatic interactions, and minimal steric repulsion. The difference in binding energy between perfectly and non-perfectly aligned molecules is around 20kJ/mol, emphasizing the importance of molecular orientation. As temperature rises from 298 K to 348 K, the likelihood of NPAM desorption increases significantly, with the binding energy shifting from 2.5kJ/mol to 4.1kJ/mol. Temperature significantly influences the equilibrium of molecules on HOPG surfaces. The emphasis is on elucidating the alterations in energy levels during nanorod aggregation on CTAB areas compared to bare HOPG surfaces, underscoring the impact of nanorods on CTAB micelle deformation energy. Observations on the variation in CTAB desorption rates with temperature changes underscore the dynamic nature of molecular binding energy associated with surface properties, underscoring the importance of molecular configuration and energy transfers in nanoscale systems.
当含有金纳米棒的液滴蒸发时,溶液中过量的表面活性剂分子会附着在高有序热解石墨(HOPG)上,从而形成独特的咖啡环图案。表面疏水性与水相蒸发的结合产生了粘滑运动,从而增强了悬浮颗粒的对流流体力学。这种现象引发的相互作用影响了液滴内部的沉积和流动动力学。高分辨率扫描电子显微镜(HRSEM)无法深入了解可能与十六烷基三甲基溴化铵(CTAB)分子相关联的区域,而原子力显微镜(AFM)则显示在特定的 CTAB 斑块内存在由 CTAB 排列的金纳米颗粒。这些层的高度和间隙各不相同,表明 CTAB 的粘附性多种多样。分析重点在于定量评估 CTAB 分子、条纹尺寸、受浓度影响的能量曲线以及 CTAB 镀金纳米棒在 CTAB 覆盖区域的有效定位。原子力显微镜检查显示,HOPG 上的 CTAB 分子条纹与表面的结合能为 -20 kJ/mol,与 HOPG 的氮键结合能为 -10 kJ/mol,考虑到各种因素,总结合能 (BE) 为 -60 kJ/mol。完全平行排列分子(CPAM)的结合能高于非完全排列分子(NPAM),这是由于范德华(VdW)相互作用、理想的静电相互作用和最小的立体排斥作用达到了最大值。完全排列和非完全排列分子之间的结合能相差约 20kJ/mol,这强调了分子取向的重要性。当温度从 298 K 上升到 348 K 时,NPAM 解吸的可能性显著增加,结合能从 2.5kJ/mol 上升到 4.1kJ/mol。温度对 HOPG 表面的分子平衡影响很大。重点是阐明与裸 HOPG 表面相比,纳米棒在 CTAB 区域聚集时的能级变化,强调纳米棒对 CTAB 胶束变形能的影响。对 CTAB 解吸率随温度变化而变化的观察强调了与表面特性相关的分子结合能的动态性质,突出了纳米级系统中分子构型和能量转移的重要性。
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引用次数: 0
Aqueous-phase synthesis of cationic hydrogel nanoparticles with antibacterial properties 水相合成具有抗菌特性的阳离子水凝胶纳米粒子
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-07 DOI: 10.1016/j.colsurfa.2024.135737
Noriko Yamauchi , Yuka Sue , Tomoya Nagai , Shuntaro Hakozaki , Takeru Saito , Yoichiro Sogame , Yoshio Kobayashi
Antibacterial hydrogel nanoparticles are expected to be used in many biomedical applications, such as drug delivery and the development of antibacterial materials. In this study, we developed a synthesis for hydrogel nanoparticles that are dispersible in liquid media and have antibacterial properties. The particles were synthesized by copolymerizing a hydrophilic monomer (2-hydroxyethyl methacrylate), a cationic monomer containing a quaternary ammonium cation (trimethylaminoethyl methacrylate chloride), and a crosslinker (ethylene glycol dimethacrylate) in an aqueous solution with a cationic polymerization initiator (2,2′-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride) to form a hydrogel. A hydrophobic monomer (methyl methacrylate) was then added and the polymerization was continued. The number average particle diameter by scanning electron microscopy was 122 nm, and the hydrodynamic diameter by dynamic light scattering measurement in water was about 380 nm, suggesting swelling of the particles by water. Furthermore, water was able to penetrate the solidified dry powder, confirming the hydrophilic properties of the particles. The zeta potential of the particles was about +40 mV, and bovine serum albumin, which generally has a high adsorption to positively charged substances, was adsorbed in large amounts to the particle surface, indicating that the particles had sufficient cationicity. The particles maintained stable dispersions even in liquid media with high ionic strength and containing impurities, which is important for nanoparticles used in medical and hygiene applications. The antibacterial activity of the particles was evaluated by incubation with Klebsiella pneumoniae, a Gram-negative bacterium. Almost no K. pneumoniae remained present in the supernatant after incubation, demonstrating the antibacterial properties of the particles.
抗菌水凝胶纳米粒子有望应用于许多生物医学领域,如药物输送和抗菌材料的开发。在这项研究中,我们开发了一种可在液体介质中分散并具有抗菌特性的水凝胶纳米粒子的合成方法。这种颗粒是通过共聚亲水性单体(甲基丙烯酸 2-羟乙基酯)、含季铵阳离子的阳离子单体(甲基丙烯酸三甲胺基乙基氯化物)和交联剂(甲基丙烯酸乙二酯)合成的、和交联剂(乙二醇二甲基丙烯酸酯)的水溶液中与阳离子聚合引发剂(2,2′-偶氮双[2-(2-咪唑啉-2-基)丙烷]二盐酸盐)形成水凝胶。然后加入疏水性单体(甲基丙烯酸甲酯)并继续聚合。通过扫描电子显微镜观察,颗粒的平均直径为 122 nm,而在水中通过动态光散射测量,其水动力直径约为 380 nm,这表明颗粒会被水溶胀。此外,水能够渗透凝固的干粉,这证实了颗粒的亲水性。颗粒的 zeta 电位约为 +40 mV,而牛血清白蛋白通常对带正电荷的物质具有较高的吸附性,它被大量吸附在颗粒表面,这表明颗粒具有足够的阳离子性。即使在高离子强度和含有杂质的液体介质中,颗粒也能保持稳定的分散状态,这对于用于医疗和卫生领域的纳米颗粒来说非常重要。通过与肺炎克雷伯氏菌(一种革兰氏阴性细菌)进行培养,对颗粒的抗菌活性进行了评估。培养后的上清液中几乎没有肺炎克雷伯菌,这证明了颗粒的抗菌特性。
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引用次数: 0
pH-controlled-ion-mobility of Laponite-phosphate dispersion for physical hydrogel with improved mechanical properties and sensitivity to CO2 用于物理水凝胶的磷酸皂石分散体的 pH 值控制离子流动性,具有更好的机械性能和对二氧化碳的敏感性
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-07 DOI: 10.1016/j.colsurfa.2024.135743
Martina Nevoralová , Sonia Bujok , Rafał Konefał , Ewa Mierzwa , Magdalena Konefał , Hynek Beneš , Szczepan Bednarz
Self-assembled physical nanocomposite hydrogels based on bio-based poly(itaconic acid) and Laponite® nanoclays were prepared and tested as possible CO2 sensors in smart food packaging. The structure and mechanical properties of the fabricated hydrogels were controlled by changing the initial pH of the aqueous Laponite® dispersions stabilised by tetrasodium pyrophosphate. The dispersions were studied by SAXS and analysed using circular disc and fractal model to determine clay agglomeration tendency. Sodium and pyrophosphate ions mobility was investigated by 23Na and 31P 1D as well as spin-spin relaxation times T2 NMR measurements. The rheological behaviour of the produced hydrogels was studied by oscillatory shear measurements. It was found that decreasing the pH of the Laponite® nanodispersions up to 8 increases the strength of the physical interactions between the nanoclays, dispersant, and polyelectrolyte chains, which enables production of dimensionally stable and mechanically robust hydrogels. Their potential application as the CO2-sensitive matrix for construction of environmentally friendly colorimetric sensors was demonstrated showing the CO2 sorption capacity of 0.07 mmol CO2/g. A prototype device of hydrogel sensor was built and tested in a food packaging application to monitor the plum fruit respiration processes.
制备并测试了基于生物基聚(衣康酸)和 Laponite® 纳米粘土的自组装物理纳米复合水凝胶,可作为智能食品包装中的二氧化碳传感器。通过改变由焦磷酸钠稳定的 Laponite® 水分散体的初始 pH 值,控制了所制备水凝胶的结构和机械性能。分散体采用 SAXS 进行研究,并使用圆盘和分形模型进行分析,以确定粘土的团聚趋势。通过 23Na 和 31P 1D 以及自旋-自旋弛豫时间 T2 NMR 测量,研究了钠离子和焦磷酸盐离子的流动性。通过振荡剪切测量研究了所制备水凝胶的流变特性。研究发现,将 Laponite® 纳米分散液的 pH 值降至 8 会增强纳米粘土、分散剂和聚电解质链之间的物理相互作用,从而生产出尺寸稳定、机械坚固的水凝胶。水凝胶的二氧化碳吸附能力为 0.07 mmol CO2/g,证明了水凝胶作为二氧化碳敏感基质在构建环境友好型比色传感器方面的潜在应用。水凝胶传感器的原型装置已经建成,并在食品包装应用中进行了测试,以监测李子的呼吸过程。
{"title":"pH-controlled-ion-mobility of Laponite-phosphate dispersion for physical hydrogel with improved mechanical properties and sensitivity to CO2","authors":"Martina Nevoralová ,&nbsp;Sonia Bujok ,&nbsp;Rafał Konefał ,&nbsp;Ewa Mierzwa ,&nbsp;Magdalena Konefał ,&nbsp;Hynek Beneš ,&nbsp;Szczepan Bednarz","doi":"10.1016/j.colsurfa.2024.135743","DOIUrl":"10.1016/j.colsurfa.2024.135743","url":null,"abstract":"<div><div>Self-assembled physical nanocomposite hydrogels based on bio-based poly(itaconic acid) and Laponite® nanoclays were prepared and tested as possible CO<sub>2</sub> sensors in smart food packaging. The structure and mechanical properties of the fabricated hydrogels were controlled by changing the initial pH of the aqueous Laponite® dispersions stabilised by tetrasodium pyrophosphate. The dispersions were studied by SAXS and analysed using circular disc and fractal model to determine clay agglomeration tendency. Sodium and pyrophosphate ions mobility was investigated by <sup>23</sup>Na and <sup>31</sup>P 1D as well as spin-spin relaxation times T<sub>2</sub> NMR measurements. The rheological behaviour of the produced hydrogels was studied by oscillatory shear measurements. It was found that decreasing the pH of the Laponite® nanodispersions up to 8 increases the strength of the physical interactions between the nanoclays, dispersant, and polyelectrolyte chains, which enables production of dimensionally stable and mechanically robust hydrogels. Their potential application as the CO<sub>2</sub>-sensitive matrix for construction of environmentally friendly colorimetric sensors was demonstrated showing the CO<sub>2</sub> sorption capacity of 0.07 mmol CO<sub>2</sub>/g. A prototype device of hydrogel sensor was built and tested in a food packaging application to monitor the plum fruit respiration processes.</div></div>","PeriodicalId":278,"journal":{"name":"Colloids and Surfaces A: Physicochemical and Engineering Aspects","volume":"705 ","pages":"Article 135743"},"PeriodicalIF":4.9,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142653352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Antibacterial double-layer calcium phosphate/chitosan composite coating on metal implants for tissue engineering 用于组织工程的金属植入物抗菌双层磷酸钙/壳聚糖复合涂层
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-07 DOI: 10.1016/j.colsurfa.2024.135652
Anna I. Kozelskaya , Andreas Früh , Sven Rutkowski , Semen I. Goreninskii , Ksenia N. Verzunova , Elena A. Soldatova , Elena V. Dorozhko , Johannes Frueh , Olga V. Bakina , Michael A. Buldakov , Evgeny L. Choinzonov , Leonid K. Brizhan , Artur A. Kerimov , Igor V. Khominets , Denis V. Davydov , Sergei I. Tverdokhlebov
In this study, four different promising two-layer composite coatings on titanium substrates with antibacterial properties were investigated. Two different types of antibacterial agents were used to impart antibacterial properties to the coatings: antibiotic amikacin (in three different concentrations) and zinc. Chitosan, which also has antibacterial properties, was used as a carrier layer for amikacin on a calcium phosphate coating incorporating zinc. This combination should enable long-term antibacterial properties of a bone implant and thus prevent potential complications during wound healing due to bacterial contamination. To examine the physico-chemical properties of the samples, the elemental, chemical and phase compositions, the thickness and the wettability of the coatings were investigated. The release of amikacin from the chitosan coatings was investigated using high-performance liquid chromatography. Antibacterial activity of the prepared coatings was evaluated against five hospital bacteria strains (Staphylococcus aureus, Pseudomonas aeruginosa, Acinetobacter baumannii, Enterococcus faecalis, Klebsiella pneumoniae) and one strain from the microbial strain collection (methicillin-resistant Staphylococcus aureus, ATCC 43300). To investigate the cell toxicity of the composite coating, cell adhesion, proliferation and osteogenic differentiation were tested with mesenchymal stem cells. According to the results, the composite coatings with an amikacin concentration of 5.0 and 7.5 percent by weight have the best biological and antibacterial properties.
本研究调查了四种不同的具有抗菌性能的钛基材双层复合涂层。两种不同类型的抗菌剂被用来赋予涂层抗菌性能:抗生素阿米卡星(三种不同浓度)和锌。壳聚糖也具有抗菌特性,被用作阿米卡星在含锌磷酸钙涂层上的载体层。这种组合可使骨植入物具有长期抗菌特性,从而防止伤口愈合过程中因细菌污染而可能出现的并发症。为了研究样品的物理化学特性,我们对涂层的元素、化学和相组成、厚度和润湿性进行了研究。使用高效液相色谱法研究了壳聚糖涂层中阿米卡星的释放情况。评估了所制备涂层对五种医院菌株(金黄色葡萄球菌、铜绿假单胞菌、鲍曼不动杆菌、粪肠球菌、肺炎克雷伯菌)和一种微生物菌株(耐甲氧西林金黄色葡萄球菌,ATCC 43300)的抗菌活性。为了研究复合涂层的细胞毒性,使用间充质干细胞对细胞粘附、增殖和成骨分化进行了测试。结果表明,阿米卡星浓度为 5.0% 和 7.5% 的复合涂层具有最佳的生物和抗菌性能。
{"title":"Antibacterial double-layer calcium phosphate/chitosan composite coating on metal implants for tissue engineering","authors":"Anna I. Kozelskaya ,&nbsp;Andreas Früh ,&nbsp;Sven Rutkowski ,&nbsp;Semen I. Goreninskii ,&nbsp;Ksenia N. Verzunova ,&nbsp;Elena A. Soldatova ,&nbsp;Elena V. Dorozhko ,&nbsp;Johannes Frueh ,&nbsp;Olga V. Bakina ,&nbsp;Michael A. Buldakov ,&nbsp;Evgeny L. Choinzonov ,&nbsp;Leonid K. Brizhan ,&nbsp;Artur A. Kerimov ,&nbsp;Igor V. Khominets ,&nbsp;Denis V. Davydov ,&nbsp;Sergei I. Tverdokhlebov","doi":"10.1016/j.colsurfa.2024.135652","DOIUrl":"10.1016/j.colsurfa.2024.135652","url":null,"abstract":"<div><div>In this study, four different promising two-layer composite coatings on titanium substrates with antibacterial properties were investigated. Two different types of antibacterial agents were used to impart antibacterial properties to the coatings: antibiotic amikacin (in three different concentrations) and zinc. Chitosan, which also has antibacterial properties, was used as a carrier layer for amikacin on a calcium phosphate coating incorporating zinc. This combination should enable long-term antibacterial properties of a bone implant and thus prevent potential complications during wound healing due to bacterial contamination. To examine the physico-chemical properties of the samples, the elemental, chemical and phase compositions, the thickness and the wettability of the coatings were investigated. The release of amikacin from the chitosan coatings was investigated using high-performance liquid chromatography. Antibacterial activity of the prepared coatings was evaluated against five hospital bacteria strains (<em>Staphylococcus aureus</em>, <em>Pseudomonas aeruginosa</em>, <em>Acinetobacter baumannii</em>, <em>Enterococcus faecalis</em>, <em>Klebsiella pneumoniae</em>) and one strain from the microbial strain collection (<em>methicillin-resistant Staphylococcus aureus</em>, ATCC 43300). To investigate the cell toxicity of the composite coating, cell adhesion, proliferation and osteogenic differentiation were tested with mesenchymal stem cells. According to the results, the composite coatings with an amikacin concentration of 5.0 and 7.5 percent by weight have the best biological and antibacterial properties.</div></div>","PeriodicalId":278,"journal":{"name":"Colloids and Surfaces A: Physicochemical and Engineering Aspects","volume":"705 ","pages":"Article 135652"},"PeriodicalIF":4.9,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142653355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Construction of Au nanoparticles decorated on ZnFe2O4@ZnIn2S4 core-shell structure to enhance photocatalytic hydrogen production 构建装饰在 ZnFe2O4@ZnIn2S4 核壳结构上的金纳米粒子以提高光催化制氢能力
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-07 DOI: 10.1016/j.colsurfa.2024.135705
Jiahui Song , Wen Ge , Sidi Deng , Jiawen Tang , Shukang Deng , Peizhi Yang
Developing effective photocatalysts for water splitting is essential to generating H2 energy sources. Herein, a novel ZnFe2O4@ZnIn2S4/Au ternary composite (abbreviated as ZFO@ZIS/Au) was successfully designed and fabricated by loading Au nanoparticles on the ZFO@ZIS surfaces for effective photocatalytic H2 generation for the first time. Attributed to the synergistic effect of the traditional II-type heterojunction charge transfer and Au nanoparticles as co-catalysts, the ZFO@ZIS/Au heterojunction generated greater amounts of hydrogen under visible light irradiation. The ZFO-7 %@ZIS/Au-2 catalyst displayed the highest H2 production rate of 1145.38 μmol∙g−1∙h−1, which was almost 3.87 times more than the ZIS value. Furthermore, several characterization techniques were performed to investigate the catalysts and evaluate the catalyst's photocatalytic activity when exposed to visible light. Lastly, a detailed discussion of the corresponding photocatalytic H2 production process of the as-prepared ZFO@ZIS/Au heterojunction was provided. The distinctive research might offer a potential approach for modifying zinc ferrate for photocatalytic hydrogen production.
开发有效的光催化剂用于水分离对产生 H2 能源至关重要。在本文中,通过在 ZFO@ZIS 表面负载金纳米颗粒,首次成功设计和制备了新型 ZnFe2O4@ZnIn2S4/Au 三元复合材料(简称 ZFO@ZIS/Au),用于有效光催化产生 H2。由于传统的 II 型异质结电荷转移和金纳米粒子作为辅助催化剂的协同作用,ZFO@ZIS/Au 异质结在可见光照射下产生了更多的氢气。ZFO-7 %@ZIS/Au-2 催化剂的氢气产生率最高,达到 1145.38 μmol∙g-1∙h-1,几乎是 ZIS 值的 3.87 倍。此外,还采用了多种表征技术来研究催化剂,并评估了催化剂在可见光照射下的光催化活性。最后,详细讨论了制备的 ZFO@ZIS/Au 异质结的相应光催化 H2 生成过程。这项独特的研究可能会为改性铁酸锌用于光催化制氢提供一种潜在的方法。
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引用次数: 0
Bio-inspired synthesis of Ag-g-C3N4 nanocomposites and their application for photocatalytic degradation of para-nitrophenol Ag-g-C3N4 纳米复合材料的生物启发合成及其在对硝基苯酚光催化降解中的应用
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-07 DOI: 10.1016/j.colsurfa.2024.135739
Shoaib Mukhtar , Erzsébet Szabó-Bárdos , Ottó Horváth , Éva Makó , Tatjána Juzsakova , Zsombor Molnár
Nanocomposites are promising in advanced materials for environmental applications due to their ability to boost functionality through synergistic effects. Graphitic carbon nitride (g-C3N4) is renowned for its exceptional characteristics in photocatalysis. This work examines the preparation of g-C3N4 from different precursors, and how the presence of silver nanoparticles (Ag NPs) and silver ions (Ag+) in g-C3N4 matrices improve their combined effect on photocatalytic activity, specifically in the degradation of para-nitrophenol (PNP), a persistent organic pollutant. From urea and melamine precursors for the preparation of g-C3N4, the latter provided a much higher yield. Using an easy synthesis approach, Ag NPs were evenly distributed in the g-C3N4 framework, whereas Ag+ ions were incorporated by an apparent physical procedure. A bio-inspired, environmentally friendly method was also applied to prepare Ag NPs. The nanocomposites showed improved light absorption and separation of charge carriers due to the synergistic interaction between g-C3N4 and Ag species. Using UV and Vis LED light sources, we investigated both pure g-C3N4 and Ag-g-C3N4 catalysts. For breaking down para-nitrophenol, the silver-modified catalysts performed significantly better than pure g-C3N4 in both UV and Vis. The study clarified the functions of Ag NPs and Ag+ ions in enhancing photocatalytic activity by examining their involvement in generating reactive oxygen species and degrading pollutants. This work highlights the capability of g-C3N4-based nanocomposites as effective photocatalysts for environmental remediation. It also explores the benefits of adding silver species to improve performance in degrading pollutants.
纳米复合材料能够通过协同效应增强功能,因此在先进材料的环境应用中大有可为。氮化石墨碳(g-C3N4)因其在光催化方面的卓越特性而闻名于世。这项研究探讨了用不同的前驱体制备 g-C3N4 的方法,以及 g-C3N4 基质中银纳米粒子(Ag NPs)和银离子(Ag+)的存在如何提高它们对光催化活性的综合影响,特别是在降解对硝基苯酚(PNP)(一种持久性有机污染物)方面。在制备 g-C3N4 的尿素和三聚氰胺前体中,后者的产率要高得多。通过简便的合成方法,Ag NPs 均匀地分布在 g-C3N4 框架中,而 Ag+ 离子则通过明显的物理过程加入其中。此外,还采用了一种生物启发的环保方法来制备 Ag NPs。由于 g-C3N4 和 Ag 物种之间的协同作用,纳米复合材料显示出更好的光吸收和电荷载流子分离性能。我们使用紫外线和可见光 LED 光源研究了纯 g-C3N4 和 Ag-g-C3N4 催化剂。在紫外和可见光条件下,银修饰催化剂在分解对硝基苯酚方面的性能明显优于纯 g-C3N4。该研究通过研究银纳米粒子和 Ag+ 离子在生成活性氧和降解污染物方面的参与,阐明了它们在增强光催化活性方面的功能。这项工作强调了基于 g-C3N4 的纳米复合材料作为有效光催化剂进行环境修复的能力。它还探讨了添加银物种以提高降解污染物性能的益处。
{"title":"Bio-inspired synthesis of Ag-g-C3N4 nanocomposites and their application for photocatalytic degradation of para-nitrophenol","authors":"Shoaib Mukhtar ,&nbsp;Erzsébet Szabó-Bárdos ,&nbsp;Ottó Horváth ,&nbsp;Éva Makó ,&nbsp;Tatjána Juzsakova ,&nbsp;Zsombor Molnár","doi":"10.1016/j.colsurfa.2024.135739","DOIUrl":"10.1016/j.colsurfa.2024.135739","url":null,"abstract":"<div><div>Nanocomposites are promising in advanced materials for environmental applications due to their ability to boost functionality through synergistic effects. Graphitic carbon nitride (<em>g</em>-C<sub>3</sub>N<sub>4</sub>) is renowned for its exceptional characteristics in photocatalysis. This work examines the preparation of <em>g</em>-C<sub>3</sub>N<sub>4</sub> from different precursors, and how the presence of silver nanoparticles (Ag NPs) and silver ions (Ag<sup>+</sup>) in <em>g</em>-C<sub>3</sub>N<sub>4</sub> matrices improve their combined effect on photocatalytic activity, specifically in the degradation of para-nitrophenol (PNP), a persistent organic pollutant. From urea and melamine precursors for the preparation of <em>g</em>-C<sub>3</sub>N<sub>4</sub>, the latter provided a much higher yield. Using an easy synthesis approach, Ag NPs were evenly distributed in the <em>g</em>-C<sub>3</sub>N<sub>4</sub> framework, whereas Ag<sup>+</sup> ions were incorporated by an apparent physical procedure. A bio-inspired, environmentally friendly method was also applied to prepare Ag NPs. The nanocomposites showed improved light absorption and separation of charge carriers due to the synergistic interaction between <em>g</em>-C<sub>3</sub>N<sub>4</sub> and Ag species. Using UV and Vis LED light sources, we investigated both pure <em>g</em>-C<sub>3</sub>N<sub>4</sub> and Ag<em>-g</em>-C<sub>3</sub>N<sub>4</sub> catalysts. For breaking down para-nitrophenol, the silver-modified catalysts performed significantly better than pure <em>g</em>-C<sub>3</sub>N<sub>4</sub> in both UV and Vis. The study clarified the functions of Ag NPs and Ag<sup>+</sup> ions in enhancing photocatalytic activity by examining their involvement in generating reactive oxygen species and degrading pollutants. This work highlights the capability of <em>g</em>-C<sub>3</sub>N<sub>4</sub>-based nanocomposites as effective photocatalysts for environmental remediation. It also explores the benefits of adding silver species to improve performance in degrading pollutants.</div></div>","PeriodicalId":278,"journal":{"name":"Colloids and Surfaces A: Physicochemical and Engineering Aspects","volume":"705 ","pages":"Article 135739"},"PeriodicalIF":4.9,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142653466","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced microwave absorption in organogels: The synergy of polar molecules and magnetic particles 增强有机凝胶的微波吸收:极性分子和磁性颗粒的协同作用
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-07 DOI: 10.1016/j.colsurfa.2024.135712
Wanting Xu , Jie Li , You Wu , Zhongchen Lu , Tao Wang , Wenbo Ju , Bin Yuan
Herein, wideband microwave absorbing materials with high flexibility are developed by creating a novel layered organogel composite consisting of carbonyl iron particles (CIP) and polyacrylamide (PAM), employing ethylene glycol (EG) as the solvent. The microwave absorbing properties of layered absorbers with different CIP contents are investigated over the 1–18 GHz range. An integrated stratified architecture was obtained using polar EG molecules and magnetic CIP particles, which were the main contributors to magnetic and dielectric losses in the PAM matrix. The results indicated that the minimum reflection loss reaches a value of −48.0 dB at a thickness of 2 mm and a frequency of 15.5 GHz; meanwhile, an effective absorption bandwidth of 3.2 GHz in the C-band can also be obtained. An analysis of the absorption mechanism shows that the combination of an impedance-matching layer composed of CIP magnetic particles and an absorption layer composed of EG polar molecules in the PAM matrix provides strong broadband absorption in the C-band. Overall, the CIP/EG@PAM organogel composites have simple preparation, high flexibility, and it has adhesion. This study provides a new strategy for designing wideband microwave absorbing materials.
本文以乙二醇(EG)为溶剂,通过制造由羰基铁颗粒(CIP)和聚丙烯酰胺(PAM)组成的新型层状有机凝胶复合材料,开发出了具有高柔性的宽带微波吸收材料。研究了不同 CIP 含量的分层吸收体在 1-18 GHz 范围内的微波吸收特性。利用极性 EG 分子和磁性 CIP 颗粒获得了一种集成分层结构,它们是 PAM 矩阵中磁损和介损的主要贡献者。结果表明,在厚度为 2 mm、频率为 15.5 GHz 时,最小反射损耗值达到 -48.0 dB;同时,在 C 波段还能获得 3.2 GHz 的有效吸收带宽。对吸收机制的分析表明,由 CIP 磁性颗粒组成的阻抗匹配层和 PAM 矩阵中由 EG 极性分子组成的吸收层相结合,可在 C 波段提供强大的宽带吸收。总之,CIP/EG@PAM 有机凝胶复合材料具有制备简单、柔韧性高、附着力强等特点。这项研究为设计宽带微波吸收材料提供了一种新策略。
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引用次数: 0
Efficient biochar regeneration for a circular economy: Removing emerging contaminants for sustainable water treatment 高效生物炭再生,促进循环经济:去除新出现的污染物,实现可持续水处理
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-06 DOI: 10.1016/j.colsurfa.2024.135730
Oussama Baaloudj , Serge Chiron , Angelica Rebecca Zizzamia , Vincenzo Trotta , Daniele Del Buono , Debora Puglia , Marco Rallini , Monica Brienza
Biochar is widely known as a highly effective adsorbent for water treatment, capable of removing a wide range of pollutants. However, its saturation point limits its long-term use, but regeneration can extend its applicability. This study aims to develop a sustainable method for removing pollutants from water that aligns with the concept of the circular economy. Biochar derived from forest residue was used to remove emerging pollutants such as fipronil (FIP), venlafaxine (VEN), sulfamethoxazole (SMX) and trimethoprim (TRM). A comparative analysis of the adsorption of the studied pollutants onto biochar was performed by analyzing the kinetics, where it was found that SMX exhibited the lowest adsorption efficiency, prompting further optimization experiments. Under optimal conditions, adsorption isotherms were used to investigate the pollutant removal mechanisms. The results showed that biochar exhibited high adsorption capacities for FIP, VEN, SMX and TRM, which were 3.77, 2.09, 2.71 and 3.88 mg/g, respectively. Regeneration treatments were applied to remove adsorbed contaminants after biochar saturation. Among them, heat-activated persulfate showed the most effective regeneration, maintaining biochar's adsorption capacity after five cycles with no significant loss. Eventual morphological, structural and chemical alterations post-regeneration were assessed using different characterization techniques. The findings of this research highlight the potential of biochar for sustainable water treatment, supporting the circular economy by extending its life cycle through effective regeneration.
众所周知,生物炭是一种高效的水处理吸附剂,能够去除多种污染物。然而,生物炭的饱和点限制了它的长期使用,但再生可以扩大其适用范围。本研究旨在开发一种符合循环经济理念的可持续方法,用于去除水中的污染物。从森林残渣中提取的生物炭被用来去除新出现的污染物,如氟虫腈(FIP)、文拉法辛(VEN)、磺胺甲噁唑(SMX)和三甲氧苄啶(TRM)。通过分析动力学,对所研究的污染物在生物炭上的吸附情况进行了比较分析,发现 SMX 的吸附效率最低,这促使进行进一步的优化实验。在最佳条件下,利用吸附等温线研究污染物的去除机制。结果表明,生物炭对 FIP、VEN、SMX 和 TRM 的吸附容量较高,分别为 3.77、2.09、2.71 和 3.88 mg/g。生物炭饱和后,采用再生处理去除吸附的污染物。其中,热激活过硫酸盐的再生效果最好,经过五个循环后,生物炭的吸附能力保持不变,且没有明显损失。使用不同的表征技术评估了再生后最终的形态、结构和化学变化。这项研究的结果凸显了生物炭在可持续水处理方面的潜力,通过有效再生延长生物炭的生命周期,支持循环经济。
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引用次数: 0
Assessment of three quinolin-8-ol-imidazole hybrids as corrosion carbon steel inhibitors in acidic conditions employing practical and theoretical methodologies 利用实践和理论方法评估三种喹啉-8-醇咪唑杂化物作为酸性条件下碳钢缓蚀剂的性能
IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-06 DOI: 10.1016/j.colsurfa.2024.135690
Z. Amrani , M. El Faydy , Z. Safi , N. Wazzan , A. Boutakiout , F. Benhiba , I. Warad , M. Rbaa , B. Lakhrissi , H. Oudda , Anees A. Khadom , A. Zarrouk
Three hybrids of quinolin-8-ol-imidazole were scrutinized as corrosion inhibitors in 1 M HCl for carbon steel (Cstl). These hybrids are 5-((2-(4-(dimethylamino)phenyl)-4,5-diphenyl-1H-imidazol-1-yl)methyl)quinoline-8-ol (Quin-Amino), 5-((4,5-diphenyl-2-(p-tolyl)-1H-imidazol-1-yl)methyl)quinoline-8-ol (Quin-Tolyl), and 5-((2-(4-bromophenyl)-4,5-diphenyl-1H-imidazol-1-yl)methyl)quinoline-8-ol (Quin-Br). The current research includes a mixture of methods. In addition to computational approaches, several experimental approaches were employed, such as electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM-EDX), UV–vis spectroscopy, and potentiodynamic polarization (PDP). The investigated hybrids' corrosion resistance was encountered to be concerned by the concentration, temperature, and chemical structure, which attained a maximum of 96.1 % for Quin-Amino, 93.4 % for Quin-Tolyl, and 92.5 % for Quin-Br at 10−3 M, respectively. The PDP results illustrated that the studied hybrids performed as mixed-type inhibitors. In addition, the chemisorption of these hybrids on the Cstl surface obeyed the Langmuir adsorption isotherm. SEM-EDX confirmed that the effectiveness of the three hybrids lies in their capability to develop an organic layer on the Cstl surface. The density functional theory (DFT) was employed for theoretical calculations. Molecular dynamics (MD) simulations manifest that hybrids are oriented beneficially on the Fe (110) surface, providing a high surface coverage and thus a high inhibition performance.
研究了三种喹啉-8-醇咪唑混合物,作为碳钢(Cstl)在 1 M HCl 中的缓蚀剂。这些混合物是 5-((2-(4-(二甲基氨基)苯基)-4,5-二苯基-1H-咪唑-1-基)甲基)喹啉-8-醇(Quin-Amino)、5-((4、5-((4,5-二苯基-2-(对甲苯基)-1H-咪唑-1-基)甲基)喹啉-8-醇(Quin-Tolyl)和 5-((2-(4-溴苯基)-4,5-二苯基-1H-咪唑-1-基)甲基)喹啉-8-醇(Quin-Br)。目前的研究包括多种方法。除计算方法外,还采用了多种实验方法,如电化学阻抗光谱法(EIS)、扫描电子显微镜法(SEM-EDX)、紫外可见光谱法和电位极化法(PDP)。结果表明,所研究的杂化物的耐腐蚀性与浓度、温度和化学结构有关,在 10-3 M 时,Quin-Amino、Quin-Tolyl 和 Quin-Br 的耐腐蚀性分别达到 96.1%、93.4% 和 92.5%。PDP 结果表明,所研究的混合物具有混合型抑制剂的性能。此外,这些杂化物在 Cstl 表面的化学吸附符合 Langmuir 吸附等温线。扫描电子显微镜(SEM-EDX)证实,这三种混合物的功效在于它们能在 Cstl 表面形成有机层。理论计算采用了密度泛函理论(DFT)。分子动力学(MD)模拟结果表明,混合物在铁(110)表面具有良好的定向性,提供了高表面覆盖率,因此具有很高的抑制性能。
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引用次数: 0
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Colloids and Surfaces A: Physicochemical and Engineering Aspects
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