Microwave

微波炉
  • 文章类型: Journal Article
    通过微波辅助液相剥离(LPE)从1-甲基-2-吡咯烷酮(NMP)或乙腈(ACN)1-甲基-2-吡咯烷酮(NMP)溶剂中的散装粉末中产生的剥离MoS2的X射线分析,揭示了散装粉末和微波剥离样品之间明显的结构差异。具体来说,我们进行了X射线衍射(XRD)和X射线光电子能谱(XPS)测量,以确定通过滴注沉积在Si衬底上的剥落样品的元素,以及它们的化学状态和结构结晶相。在剥落的样品中,峰值模式仅部分类似于MoS2的理论Miller指数。相比之下,散装粉末的光谱显示MoS2的2H多型的特征峰,但有一些加宽。值得注意的是在剥离后阶段保留了部分结晶度,特别是在法线到平面的方向上,因此证明了微波辅助技术在生产2DMoS2和获得材料所需性能方面的有效性。XPS测量证实剥离程序的成功,并且剥离的样品保持其原始结构。已对剥离过程进行了优化,以保持MoS2的结构完整性,同时增强其表面积和电化学性能,从而使其成为环境条件下从能量存储到传感设备的高级电子和光电应用的有前途的材料。
    An X-ray analysis of exfoliated MoS2, produced by means of microwave-assisted liquid-phase exfoliation (LPE) from bulk powder in 1-methyl-2-pyrrolidone (NMP) or acetonitrile (ACN) + 1-methyl-2-pyrrolidone (NMP) solvents, has revealed distinct structural differences between the bulk powder and the microwave-exfoliated samples. Specifically, we performed X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) measurements to identify the elements of our exfoliated sample deposited on a Si substrate by drop-casting, as well as their chemical state and its structural crystalline phase. In the exfoliated sample, the peaks pattern only partially resemble the theoretical Miller indices for MoS2. In contrast, the bulk powder\'s spectrum shows the characteristic peaks of the 2H polytype of MoS2, but with some broadening. Notable is the retention of partial crystallinity in the post-exfoliation phases, specifically in the normal-to-plane orientation, thus demonstrating the effectiveness of microwave-assisted techniques in producing 2D MoS2 and attaining desirable properties for the material. XPS measurements confirm the success of the exfoliation procedure and that the exfoliated sample retains its original structure. The exfoliation process has been optimized to maintain the structural integrity of MoS2 while enhancing its surface area and electrochemical performance, thereby making it a promising material for advanced electronic and optoelectronic applications ranging from energy storage to sensing devices under ambient conditions.
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  • 文章类型: Journal Article
    微波炉已经成为现代厨房的重要组成部分,但是它们作为细菌定植的储库和其中的微生物组成的潜力在很大程度上仍未被开发。在这项研究中,我们调查了微波炉中的细菌群落,并比较了家用微波炉的微生物组成,在共享的大空间中使用的微波,和实验室微波,使用下一代测序和培养技术。微波炉细菌种群以变形杆菌为主,Firmicutes,放线菌,和拟杆菌,类似于人体皮肤的细菌成分。与其他环境的比较表明,家用微波炉的细菌组成与厨房表面的细菌组成相似,而实验室微波具有较高的类群,以它们承受微波辐射的能力而闻名,高温和干燥。这些结果表明,不同的选择压力,比如人类接触,营养可用性和辐射水平,可以解释观察到的家用和实验室微波之间的差异。总的来说,这项研究为微波炉细菌群落及其潜在的生物技术应用提供了有价值的见解。
    Microwaves have become an essential part of the modern kitchen, but their potential as a reservoir for bacterial colonization and the microbial composition within them remain largely unexplored. In this study, we investigated the bacterial communities in microwave ovens and compared the microbial composition of domestic microwaves, microwaves used in shared large spaces, and laboratory microwaves, using next-generation sequencing and culturing techniques. The microwave oven bacterial population was dominated by Proteobacteria, Firmicutes, Actinobacteria, and Bacteroidetes, similar to the bacterial composition of human skin. Comparison with other environments revealed that the bacterial composition of domestic microwaves was similar to that of kitchen surfaces, whereas laboratory microwaves had a higher abundance of taxa known for their ability to withstand microwave radiation, high temperatures and desiccation. These results suggest that different selective pressures, such as human contact, nutrient availability and radiation levels, may explain the differences observed between domestic and laboratory microwaves. Overall, this study provides valuable insights into microwave ovens bacterial communities and their potential biotechnological applications.
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  • 文章类型: Journal Article
    作为食物系统的重要组成部分之一,淀粉经胃肠消化后可水解成葡萄糖,因此,调节其消化特性对于保持健康至关重要。微波可以促进淀粉分子内结构的重排,从而改善其物理化学性质,增强其缓慢消化的特征,并扩大其应用范围。这篇综述描述了有关微波处理对淀粉的多尺度结构和理化性质的影响的最新研究成果,并总结了这些变化的模式。此外,淀粉结构的变化,抗性淀粉含量,指出了消化后的血糖指数,以深入了解微波处理对淀粉缓慢消化特性的增强。淀粉对酶消化的抗性可能很大程度上取决于微波处理期间形成的特定结构。淀粉在消化过程中的多层次结构演变赋予其抵抗消化和降低血糖指数的能力。淀粉的性质决定了它的应用,这些特性与它的结构高度相关。因此,了解微波改性淀粉的结构变化有助于制备具有多样化品种和功能性复合材料的改性淀粉。
    As one of the crucial components of the food system, starch can be hydrolyzed into glucose after gastrointestinal digestion, so regulating its digestive properties is vital for maintaining health. Microwaves can promote the rearrangement of intramolecular structure of starch, thus improving its physicochemical properties, enhancing its slowly digestible features, and expanding its scope of application. This review zooms in describing recent research results concerning the effects of microwave treatment on the multi-scale structure and physicochemical properties of starch and summarizing the patterns of these changes. Furthermore, the changes in starch structure, resistant starch content, and glycemic index after digestion are pointed out to gain an insight into the enhancement of starch slowly digestible properties by microwave treatment. The resistance of starch to enzymatic digestion may largely hinge on the specific structures formed during microwave treatment. The multi-level structural evolutions of starch during digestion endow it with the power to resist digestion and lower the glycemic index. The properties of starch dictate its application, and these properties are highly associated with its structure. Consequently, understanding the structural changes of microwave-modified starch helps to prepare modified starch with diversified varieties and functional composites.
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  • 文章类型: Journal Article
    微波气体传感器在挥发性有机化合物(VOC)检测中具有高灵敏度和选择性,已引起人们的关注。然而,传统的气体传感器通常依赖于敏感材料,这些材料会随着时间的推移而降解,并且容易受到环境的影响,损害其稳定性和准确性。本研究提出了一种基于冷凝效应的微波VOC气体传感器。传感器采用新颖的设计,没有敏感材料,利用冷凝效应检测丙酮气体。传感器系统由微波传感器和温度控制装置组成。当传感器温度低于丙酮的沸点时,实现了丙酮气体在传感器表面的冷凝,能够准确检测丙酮气体。实验结果表明,丙酮在传感器表面的累积量与其响应呈正相关,3000ppm丙酮气体的最大响应达到0.34dB。此外,本研究研究了添加敏感材料MXene后传感器的检测机理,并比较了传感器在不同温度(-10°C,0°C,和60°C)。结果表明,在-10℃时,传感器主要通过物理吸附捕获丙酮,在25和60°C时,它主要通过化学吸附反应,最大响应为0.29dB。基于不含敏感材料的冷凝效应的VOC传感器不仅具有与传统微波传感器相同的灵敏度,而且具有更强的稳定性和抗干扰能力。
    Microwave gas sensors have garnered attention for their high sensitivity and selectivity in the detection of volatile organic compounds (VOCs). However, traditional gas sensors generally rely on sensitive materials that degrade over time and are easily affected by the environment, compromising their stability and accuracy. This study proposes a microwave VOC gas sensor based on the condensation effect. The sensor adopts a novel design without sensitive materials, utilizing the condensation effect to detect acetone gas. The sensor system consists of a microwave sensor and a temperature control device. As the sensor temperature is lowered below the boiling point of acetone, the condensation of acetone gas on the sensor surface is achieved, enabling accurate detection of acetone gas. Experimental results indicate that the accumulated amount of acetone on the sensor surface is positively correlated with its response, with the maximum response of 3000 ppm acetone gas reaching 0.34 dB. Additionally, this study investigated the detection mechanism of the sensor after adding the sensitive material MXene and compared the performance of the sensor at different temperatures (-10 °C, 0 °C, and 60 °C). The results show that at -10 °C the sensor mainly captures acetone through physical adsorption, while at 25 and 60 °C, it primarily responds through chemical adsorption, with a maximum response of 0.29 dB. The VOC sensor based on the condensation effect without sensitive materials not only achieves the same sensitivity as traditional microwave sensors but also demonstrates stronger stability and anti-interference capabilities.
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  • 文章类型: Journal Article
    杂环分子在制药和材料科学领域有许多不同的应用,这使得它们成为一个重要的化合物家族。在这些杂环化合物中,含氮杂环(N-杂环)化合物由于其在各个领域的各种应用而引起了研究人员的极大兴趣。在过去的几年中,已经进行了许多研究,以研究在不同反应条件下合成N-杂环,如无溶剂,催化,固定在固体支持物上的反应物,一锅法合成,和微波辐射。我们的研究小组已经证明,微波可用于快速有效地合成生物活性化合物。在这次审查中,我们提供了微波辅助的非催化和催化制备含氮杂环的概述,主要是多环N-杂环,五元N-杂环,六元N-杂环,和稠合的N-杂环。在这篇文章中,我们探索了微波辅助制备生物重要化合物,例如嘧啶,噻唑,亚胺,四唑,类固醇衍生物,喹啉,吲哚嗪,三唑类,β-内酰胺,吡咯和喹喔啉。
    There are many different applications of heterocyclic molecules in the pharmaceutical and materials science fields, which make them an important family of compounds. Among these heterocyclic compounds, nitrogen-containing heterocyclic (N-heterocyclic) compounds have attracted a lot of interest among researchers due to their various applications across a wide variety of fields. Many studies have been performed over the past few years to study the synthesis of N-heterocycles under different reaction conditions, such as solvent-free, catalytic, reactants immobilized on a solid support, one-pot synthesis, and microwave irradiation. It has been demonstrated by our research group that microwaves can be utilized for rapid and efficient synthesis of biologically active compounds. In this review, we provide an overview of the microwave-assisted non-catalytic and catalytic preparation of nitrogen-containing heterocycles, mostly polycyclic N-heterocycles, five-membered N-heterocycles, six-membered N-heterocycles, and fused N-heterocycles. Mostly in this article, we explore the microwave-assisted preparation of biologically important compounds, such as pyrimidines, thiazoles, imines, tetrazoles, steroidal derivatives, quinolines, indolizine, triazoles, beta-lactams, pyrroles and quinoxalines.
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  • 文章类型: Journal Article
    微藻越来越被认为是天然生物活性化合物的有希望的来源。然而,使用挥发性有机溶剂(VOCs)的传统提取方法存在环境风险。这项研究探索了可再生的低共熔溶剂(DES)作为从微藻生物质中提取生物活性化合物的可持续替代品,专注于普通小球藻和大叶栅藻。四个DES系统,包含氯化胆碱(ChCl)和甘油,柠檬酸,尿素,和葡萄糖,与三种常规溶剂(乙醇,甲醇,和水)。基于总酚含量(TPC)评估提取效率,类黄酮含量,和单宁含量,然后使用DPPH进行抗氧化活性评估,CAT,和FRAP测定。此外,DES提取物的抗菌活性测定对大肠杆菌(ATCC25922),铜绿假单胞菌(ATCC27853),金黄色葡萄球菌(ATCC29213),和枯草芽孢杆菌(ATCC3366)使用圆盘扩散和微孔板稀释方法确定最小抑制浓度(MIC)和最小杀菌浓度(MBC)。结果表明,DES,特别是氯化胆碱:柠檬酸,在多酚提取效率方面优于常规溶剂,抗氧化活性,和抗革兰氏阴性菌和革兰氏阳性菌的抗菌活性。例如,柠檬酸基DES(SIDES2)的TPC为4.98mg/g,而常规溶剂乙醇表现出3.27mg/g的TPC。此外,SIDES2表现出75%的最高DPPH清除活性,相比之下,乙醇为60%。此外,SIDES2对金黄色葡萄球菌的MIC为0.5mg/ml。这项研究强调了DES从微藻生物质中可持续提取天然抗氧化剂的潜力,有助于在各个行业开发环保的提取工艺。
    Microalgae are increasingly recognized as promising sources of natural bioactive compounds. However, traditional extraction methods using volatile organic solvents (VOCs) pose environmental risks. This study explores renewable deep eutectic solvents (DES) as sustainable alternatives for extracting bioactive compounds from microalgae biomass, focusing on Chlorella vulgaris and Scenedesmus incrassatulus. Four DES systems, comprising choline chloride (ChCl) and glycerol, citric acid, urea, and glucose, were compared with three conventional solvents (ethanol, methanol, and water). Extraction efficiency was assessed based on total phenolic content (TPC), flavonoid content, and tannin content, followed by antioxidant activity evaluation using DPPH, CAT, and FRAP assays. Additionally, antibacterial activity of the DES extracts was determined against Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), Staphylococcus aureus (ATCC 29213), and Bacillus subtilis (ATCC 3366) using disc diffusion and microplate dilution methods to determine minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). Results reveal that DES, particularly choline chloride: citric acid, outperform conventional solvents in terms of polyphenol extraction efficiency, antioxidant activity, and antibacterial activity against both Gram-negative and Gram-positive bacteria. For instance, the citric acid-based DES (SIDES2) showed a TPC of 4.98 mg/g, while the conventional solvent ethanol exhibited a TPC of 3.27 mg/g. Additionally, SIDES2 exhibiting the highest DPPH scavenging activity of 75 %, compared to 60 % for ethanol. Furthermore, SIDES2 showed an MIC of 0.5 mg/ml against Staphylococcus aureus. This study underscores the potential of DES for sustainable extraction of natural antioxidants from microalgae biomass, contributing to the development of environmentally friendly extraction processes in various industries.
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  • 文章类型: Journal Article
    目标:在这项工作中,我们展示了在离体动物模型上用微波辐射人工诱导白内障后,用低能量皮秒超短激光脉冲进行晶状体碎裂的第一个实验室研究结果。背景:将使用新型超短皮秒激光系统代替超声超声乳化术或明显更复杂的飞秒激光破碎来评估晶状体破碎的进一步发展。方法:我们使用死后猪眼作为样本。将镜片解剖,然后在微波炉中照射用于人工白内障诱导。随后的计算机驱动的镜头碎片以12ps进行,具有100µJ脉冲能量的1064nm脉冲激光源,和10kHz脉冲重复率。结果:人工白内障诱导和晶状体碎裂均得到证实。诱导白内障时,用不同的辐照时间和方法可以实现不同程度/阶段的不透明性和硬度。12ps脉冲的碎片导致了关于消融深度和速率的良好结果。特别是对于较软的镜片。结论:可以证明,低能量皮秒超短激光脉冲在人工白内障诱导的离体动物模型上用于白内障晶状体破碎是可行的。因此,这项技术可能会影响未来的白内障手术,因为它可能是最先进方法的替代或扩展。这将通过进一步的测试和研究进行评估。
    Objectives: In this work we demonstrate the first laboratory study results of lens fragmentation with low-energy picosecond ultrashort laser pulses after artificial induction of cataract with microwave radiation on an ex vivo animal model. Background: This method will be evaluated with regard to the further development of lens fragmentation with novel ultrashort picosecond laser systems instead of ultrasonic phacoemulsification or the significantly more complex femtosecond laser fragmentation. Methods: As samples we used postmortem porcine eyes. The lenses were dissected and then irradiated in a microwave oven for artificial cataract induction. Subsequent computer-driven lens fragmentation was performed with a 12 ps, 1064 nm pulsed laser source with 100 µJ pulse energy, and 10 kHz pulse repetition rate. Results: Both the artificial cataract induction and the lens fragmentation were demonstrated. When inducing cataract, different degrees/stages of opaqueness and hardness could be achieved with different irradiation times and methods. The fragmentation with 12 ps pulses led to good results with regard to ablation depth and rate, especially for the softer lenses. Conclusions: As could be shown, low-energy picosecond ultrashort laser pulses are feasible for cataractous lens fragmentation on an ex vivo animal model with artificial cataract induction. Thus, this technique may influence future cataract surgeries by possibly being an alternative or extension to state-of-the-art methods. This will be evaluated with further tests and studies.
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  • 文章类型: Journal Article
    在这里,存在微波促进的游离伯芳胺与重氮化合物在水中的串联反应,用于清洁合成2,2-二取代的3-羟吲哚。水在整个级联过程中起着重要作用:O-H插入重氮,空气氧化,邻位C-H官能化,环化和1,2-酯迁移。特别是,水在位点选择性邻位C-H添加中起中介作用。
    Herein, a microwave promoted tandem reaction of free primary arylamines with diazo compounds in water for clean synthesis of 2,2-disubstituted 3-oxindoles is present. Water plays important roles in the whole cascade process: O-H insertion to diazo, air oxidation, ortho C-H functionalization, cyclization and 1,2-ester migration. In particular, water plays a mediation role in the site selective ortho-C-H addition.
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  • 文章类型: Journal Article
    新醋在销售前需要较长的成熟时间来改善其不良风味,这大大增加了其生产成本。因此,迫切需要探索促进醋风味成熟的调控技术。根据文献和我们的研究,本文介绍了醋的风味调节技术的最新进展,包括微生物强化/多发酵剂发酵,关键生产工艺优化和新颖的物理加工技术。微生物强化或多发酵剂发酵通过增强总酸加速醋风味成熟,醋中的酯类和香气前体含量。调整原材料成分,发酵温度,和氧气流量合理增加酒精,有机酸,多酚和酯水平通过在醋中产生更多相应的前体,从而改善其风味。此外,新型加工技术极大地促进了醋中醇向酸和酯的转化,缩短风味成熟时间超过六个月。同时,讨论了相应的机制,并提出了未来的研究方向。
    New vinegar needs a long maturing time to improve its poor flavor before sale, which greatly increases its production cost. Therefore, it is urgent to explore regulation technologies to accelerate vinegar flavor maturation. Based on literature and our research, this review introduces the latest advances in flavor regulation technologies of vinegar including microbial fortification/multi starters fermentation, key production processes optimization and novel physical processing technologies. Microbial fortification or multi starters fermentation accelerates vinegar flavor maturation via enhancing total acids, esters and aroma precursors content in vinegar. Adjusting raw materials composition, fermentation temperature, and oxygen flow reasonably increase alcohols, organic acids, polyphenols and esters levels via generating more corresponding precursors in vinegar, thereby improving its flavor. Furthermore, novel processing technologies greatly promote conversion of alcohols into acids and esters in vinegar, shortening flavor maturation time for over six months. Meanwhile, the corresponding mechanisms are discussed and future research directions are addressed.
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  • 文章类型: Journal Article
    两种微波(MW)响应异质结纳米复合催化剂,即,α-Bi2O3/CoFe2O4(BO/CFO)和ZnO/CoFe2O4(ZO/CFO),通过顺序热分解和共沉淀方法合成了重量百分比为70/30、50/50、30/70的,并用于在MW辐射下降解四环素(TC)。通过XRD的表征结果证实了所需催化剂的形成,FT-IR,SEM,VSM,UV-DRS,XPS,BET,等。使用批量MW实验,催化剂剂量,pH值,初始TC浓度,反应温度,和MW功率进行了优化以去除TC。在以下反应条件下:催化剂剂量~1g/L,初始TC浓度~1mg/L,温度90ºC,MW~450W,BO/CFO,ZO/CFO的TC降解率为97.55%和88.23%,分别,5分钟后。对TC降解的催化响应的差异表明这两种催化剂之间的反射损失(RL)的差异。由于清除作用,其他竞争性阴离子的存在会影响TC的去除效率。自由基捕获研究揭示了在ZO/CFO的情况下,羟基自由基对TC降解的显着贡献,而对于BO/CFO来说,超氧化物(●O2-)和羟基自由基(●OH)均起影响作用。BO/CFO的Z方案异质结允许形成●O2-,但由于价带位置,在ZO/CFO的II型异质结中也受到抑制。介电损耗,磁损耗,界面极化,和高导电性,“热点”在催化剂表面上产生,同时在异质结处电子-空穴分离,负责活性氧的产生。此外,Co3+/Co2+和Fe3+/Fe2+氧化还原循环促进了过硫酸盐施用过程中O2-和硫酸根的产生。在两种MW响应催化剂中,BO/CFO可能是一种在MW辐射下无需使用其他氧化性化学物质即可快速破坏废水中新兴有机污染物的潜在材料。
    Two microwave (MW) responsive heterojunction nanocomposite catalysts, i.e., α-Bi2O3/CoFe2O4 (BO/CFO) and ZnO/CoFe2O4 (ZO/CFO), with weight% ratio of 70/30, 50/50, 30/70 were synthesized by sequential thermal decomposition and co-precipitation methods, and used for the degradation of tetracycline (TC) under MW irradiation. The formation of desired catalysts was confirmed through the characterization results of XRD, FT-IR, SEM, VSM, UV-DRS, XPS, BET, etc. Using batch MW experiments, the catalyst dose, pH, initial TC concentration, reaction temperature, and MW power were optimized for TC removal. Under the following reaction conditions: catalyst dose ∼1 g/L, initial TC concentration ∼1 mg/L, temperature ∼90 °C, MW ∼450 W, BO/CFO, and ZO/CFO showed ∼97.55% and 88.23% TC degradation, respectively, after 5 min. The difference in the catalytic response against TC degradation indicated the difference in reflective loss (RL) between these two catalysts. The presence of other competitive anions has affected the removal efficiency of TC due to the scavenging effect. The radical trapping study revealed the significant contribution of TC degradation by hydroxyl radicals in the case of ZO/CFO, whereas for BO/CFO, superoxide (●O2-) and hydroxyl radicals (●OH) both played influential roles. The Z-scheme heterojunction of BO/CFO allowed the formation of ●O2- but the same was inhibited in type-II heterojunction of ZO/CFO due to the valance band position. The dielectric loss, magnetic loss, interfacial polarization, and high electrical conductivity, \'hotspots\' were produced over the catalyst surface alongside electron-hole separation at heterojunctions, which were responsible for the generation of reactive oxygen species. In addition, Co3+/Co2+ and Fe3+/Fe2+ redox cycles have promoted ●O2- and sulfate radical production during persulfate application. Among the two MW responsive catalysts, BO/CFO could be a potential material for rapidly destroying emerging organic pollutants from wastewater without applying other oxidative chemicals under MW irradiation.
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