VOC

VOC
  • 文章类型: Journal Article
    二手烟暴露是一种新兴的公共卫生问题,仍未得到充分研究。在这项研究中,收集了ENDS用户(二手)和非ENDS用户(基线)的唾液和呼出排放物,使用自动ENDS气溶胶生成系统生成第一手排放物,该系统被编程为模拟从ENDS用户收集的膨化地形轮廓。表征了颗粒浓度和大小以及挥发性有机化合物。我们揭示了膨化地形指标作为第一手和二手粒子和化学暴露的潜在介体,以及代谢和呼吸健康结果。颗粒沉积模型显示,虽然二手排放显示出较小的沉积质量,总和肺颗粒沉积分数高于第一手沉积水平,可能是由于较小的二手发射粒子直径。最后,由第一手ENDS暴露引起的肺损伤的唾液生物标志物的非靶向代谢组学分析揭示了呼吸窘迫的潜在早期指标,这些指标也可能与暴露于二手烟的旁观者相关.通过利用系统毒理学,我们鉴定出10种代谢物,包括白三烯D4,可能作为ENDS使用的生物标志物,暴露估计,和电子烟相关疾病的预测。这项研究强调了vaping行为的表征是促进我们对ENDS用户和旁观者潜在健康影响的理解的重要组成部分。
    Secondhand vaping exposure is an emerging public health concern that remains understudied. In this study, saliva and exhaled emissions from ENDS users (secondhand) and non-ENDS users (baseline) were collected, firsthand emissions were generated using an automated ENDS aerosol generation system programmed to simulate puffing topography profiles collected from ENDS users. Particulate concentrations and sizes along with volatile organic compounds were characterized. We revealed puffing topography metrics as potential mediators of firsthand and secondhand particle and chemical exposures, as well as metabolic and respiratory health outcomes. Particle deposition modeling revealed that while secondhand emissions displayed smaller deposited mass, total and pulmonary particle deposition fractions were higher than firsthand deposition levels, possibly due to smaller secondhand emission particle diameters. Lastly, untargeted metabolomic profiling of salivary biomarkers of lung injury due to firsthand ENDS exposures revealed potential early indicators of respiratory distress that may also be relevant in bystanders exposed to secondhand vaping scenarios. By leveraging system toxicology, we identified 10 metabolites, including leukotriene D4, that could potentially serve as biomarkers for ENDS use, exposure estimation, and the prediction of vaping-related disease. This study highlights characterization of vaping behavior is an important exposure component in advancing our understanding of potential health effects in ENDS users and bystanders.
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  • 文章类型: Journal Article
    探索了低气态臭氧浓度(300ppb和400ppb)在控制腐败微生物区系和保持陈年TomaPiemontesePDO奶酪质量方面的功效。这项研究整合了消费者测试,气相色谱-质谱(GC-MS)固相微萃取(SPME)纤维和电子鼻(电子鼻)分析进行奶酪的芳香成分的详细评估。结果表明,低臭氧浓度显著影响腐败微生物区系,保持整体质量。通过GC-FID(火焰电离检测)分析,通过GC-MS对所有鉴定的化合物中的22种进行了定量,包括乙酸乙酯(甜味),二乙酰和丙酮(黄油)。与未经处理的样品相比,臭氧处理保持了TomaPiemontesePDO奶酪的独特特征,减少异味相关化合物的形成(即,乙醇)。此外,臭氧处理的样品与消费者给出的正香气评分相关。然而,感官知觉涉及香气化合物之间复杂的相互作用,强调先进方法的重要性。利用12传感器石英天平(QMB)电子鼻在识别香气的细微差异中起着至关重要的作用,有助于对臭氧处理对奶酪感官特征的更细致的理解。总之,这项研究证明了臭氧技术作为提高陈年TomaPiemontesePDO奶酪质量的可行和有效方法的潜力。
    The efficacy of low gaseous ozone concentrations (300 ppb and 400 ppb) in controlling spoilage microflora and preserving the quality of the aged Toma Piemontese PDO cheese was explored. The research integrates consumer tests, Gas Chromatography-Mass Spectrometry (GC-MS) with Solid phase Microextraction (SPME) fiber and Electronic Nose (e-nose) analysis to conduct a detailed assessment of the cheese\'s aromatic composition. Results indicate that low ozone concentrations significantly affected spoilage microflora, preserving the overall quality. Through GC-FID (Flame Ionization Detection) analysis, 22 of all identified compounds by GC-MS were quantified, including ethyl acetate (sweety), diacetyl and acetoin (buttery). Compared with the untreated sample, ozone treatments maintained the distinctive characteristics of Toma Piemontese PDO cheese, reducing the formation of off-flavors-related compounds (i.e., ethanol). Moreover, ozone-treated samples correlated with positive aroma scores given by consumers. However, sensory perception involves complex interactions among aroma compounds, highlighting the importance of advanced approaches. The utilization of a 12-sensor Quartz Microbalance (QMB) e-nose played a crucial role in identifying subtle differences in aroma, contributing to a more nuanced understanding of ozone treatments on the cheese\'s sensory profile. In conclusion, this research demonstrates the potential of ozone technology as a viable and effective method for improving the quality of aged Toma Piemontese PDO cheese.
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  • 文章类型: Journal Article
    SARS-CoV-2的变体由于其增加的传播性和逃避自然免疫的能力而对公共卫生构成重大挑战,疫苗保护,和单克隆抗体疗法。高度传播的Omicron变体和随后的亚变体的出现,特征在于刺突蛋白中超过32个突变的广泛阵列,加剧了对逃避疫苗的担忧。作为回应,多种抗病毒疗法已获得FDA紧急使用批准,靶向SARS-CoV-2RNA依赖性RNA聚合酶(RdRp)和主要蛋白酶(Mpro)区域,已知在新变体中突变相对较少。在这项研究中,我们评估了尼马特雷韦(PF-07321332)和其他具有临床意义的SARS-CoV-2抗病毒药物对多种SARS-CoV-2变体的疗效,包括新鉴定的Omicron亚变体XBB1.5和JN.1,使用活病毒抗病毒测定。我们的发现表明,虽然最后的Omicron亚变体在我们的动物模型中表现出更高的致病性,nirmatrelvir和其他临床相关的抗病毒药物始终保持其对所有测试变体的疗效,包括XBB1.5亚变体。
    Variants of SARS-CoV-2 pose significant challenges in public health due to their increased transmissibility and ability to evade natural immunity, vaccine protection, and monoclonal antibody therapeutics. The emergence of the highly transmissible Omicron variant and subsequent subvariants, characterized by an extensive array of over 32 mutations within the spike protein, intensifies concerns regarding vaccine evasion. In response, multiple antiviral therapeutics have received FDA emergency use approval, targeting the SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) and main protease (Mpro) regions, known to have relatively fewer mutations across novel variants. In this study, we evaluated the efficacy of nirmatrelvir (PF-07321332) and other clinically significant SARS-CoV-2 antivirals against a diverse panel of SARS-CoV-2 variants, encompassing the newly identified Omicron subvariants XBB1.5 and JN.1, using live-virus antiviral assays. Our findings demonstrate that while the last Omicron subvariants exhibited heightened pathogenicity in our animal model, nirmatrelvir and other clinically relevant antivirals consistently maintained their efficacy against all tested variants, including the XBB1.5 subvariant.
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  • 文章类型: Journal Article
    结直肠癌(CRC)检测的常规筛查选择主要是直接可视化和侵入性方法,包括结肠镜检查和柔性乙状结肠镜检查。这必须在临床环境中进行,并且可能与某些患者的不良反应有关。非侵入性CRC诊断测试,例如计算机断层扫描结肠造影和粪便测试,与侵入性测试相比,成本太高或可靠性较低。另一方面,挥发性有机化合物(VOCs)是CRC检测和监测的潜在理想的非侵入性生物标志物。本综述是对当前最先进的基于VOC的CRC诊断的全面介绍,特别关注生物传感器设计和应用的最新进展。其中,概述了基于呼吸的色谱模式分析和采样技术,以及基于纳米粒子的光学和电化学生物传感器方法。还讨论了当前可用技术的局限性,并结合大数据分析和先进仪器进行改进,以及扩大CRC相关挥发性生物标志物的范围和特异性。
    Conventional screening options for colorectal cancer (CRC) detection are mainly direct visualization and invasive methods including colonoscopy and flexible sigmoidoscopy, which must be performed in a clinical setting and may be linked to adverse effects for some patients. Non-invasive CRC diagnostic tests such as computed tomography colonography and stool tests are either too costly or less reliable than invasive ones. On the other hand, volatile organic compounds (VOCs) are potentially ideal non-invasive biomarkers for CRC detection and monitoring. The present review is a comprehensive presentation of the current state-of-the-art VOC-based CRC diagnostics, with a specific focus on recent advancements in biosensor design and application. Among them, breath-based chromatography pattern analysis and sampling techniques are overviewed, along with nanoparticle-based optical and electrochemical biosensor approaches. Limitations of the currently available technologies are also discussed with an outlook for improvement in combination with big data analytics and advanced instrumentation, as well as expanding the scope and specificity of CRC-related volatile biomarkers.
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  • 文章类型: Journal Article
    不可逆吸附,或者脚跟堆积,负面影响活性炭的性能和缩短其寿命。这项研究阐明了流量与解吸吹扫气体的氧杂质之间的相互关系,并在串珠活性炭(BAC)上积累了尾随。探索了九种热解吸方案,变化的氮气吹扫气体氧杂质水平(<5ppmv,10,000ppmv,210,000ppm(21%))和流量(0.1、1、10SLPM或1%,10%,吸附流量的100%)在热解吸过程中。结果表明,增加吹扫气体流量可以提高吸附容量回收率,并减轻吹扫气体氧杂质的不利影响。累积尾随随更高的吹扫气体氧杂质和更低的流速而增加。在最不有效的再生情况下(0.1SLPMN2,21%O2),五个循环后在BAC上形成32.8重量%的累积鞋跟,而最佳情况下(10SLPMN2,<5ppmvO2)仅导致0.3wt%。比较原始和使用过的BAC的孔径分布表明,鞋跟最初形成在狭窄的微孔(<8.5A)中,后来与中孔接合。热重分析(TGA)表明,氧杂质会产生高沸点和/或强结合的鞋跟物质。TGA证实,较高的吹扫气体流量减少了鞋跟量,但在氧气存在下促进了化学吸附鞋跟形成。这些发现可以指导再生条件的优化,提高活性炭在循环吸附过程中的长期性能。
    Irreversible adsorption, or heel buildup, negatively impacts activated carbon performance and shortens its lifetime. This study elucidates the interconnections between flow rate and the oxygen impurity of desorption purge gas with heel buildup on beaded activated carbon (BAC). Nine thermal desorption scenarios were explored, varying nitrogen purge gas oxygen impurity levels (<5 ppmv, 10,000 ppmv, 210,000 ppm (21 %)) and flow rates (0.1, 1, 10 SLPM or 1 %, 10 %, 100 % of adsorption flow rate) during thermal desorption. Results reveal that increasing purge gas flow rate improves adsorption capacity recovery and mitigates adverse effects of purge gas oxygen impurity. Cumulative heel increased with higher purge gas oxygen impurity and lower flow rates. In the least effective regeneration scenario (0.1 SLPM N2, 21 % O2), a 32.8 wt% cumulative heel formed on BAC after five cycles, while the best-case scenario (10 SLPM N2, <5 ppmv O2) resulted in only 0.3 wt%. Comparing the pore size distributions of virgin and used BAC shows that heel initially forms in narrow micropores (<8.5Å) and later engages mesopores. Thermogravimetric analysis (TGA) showed that oxygen impurity creates high boiling point and/or strongly bound heel species. TGA confirmed that higher purge gas flow rates reduce heel amounts but encourage chemisorbed heel formation in oxygen\'s presence. These findings can guide optimization of regeneration conditions, enhancing activated carbon\'s long-term performance in cyclic adsorption processes.
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  • 文章类型: Journal Article
    生物挥发性有机化合物(VOCs)是现代生态系统中气相代谢物的重要组成部分,在调节大气氧化能力方面具有独特的作用。太阳辐射平衡,和气溶胶的形成。从理论上讲,挥发性有机化合物可能是古生界观察到的地质和进化现象的原因。但生物学对早期非甲烷VOC循环的直接贡献仍未被探索。这里,我们提供了最后一个普遍共同祖先(LUCA)代谢的所有潜在VOCs的评估。我们在八个文献来源中鉴定了与LUCA直系同源蛋白质组相关的酶功能,并估计了所有相关底物的挥发性,以鉴定古代的挥发性代谢物。我们磨练了具有保守代谢途径中存在的经证实的现代排放物的挥发性代谢物,并产生了最可能的LUCAVOC的精选列表。我们介绍了与早期生命相关的挥发性有机代谢物,并讨论了它们对早期碳循环和大气化学的潜在影响。
    Biogenic volatile organic compounds (VOCs) constitute a significant portion of gas-phase metabolites in modern ecosystems and have unique roles in moderating atmospheric oxidative capacity, solar radiation balance, and aerosol formation. It has been theorized that VOCs may account for observed geological and evolutionary phenomena during the Archaean, but the direct contribution of biology to early non-methane VOC cycling remains unexplored. Here, we provide an assessment of all potential VOCs metabolized by the last universal common ancestor (LUCA). We identify enzyme functions linked to LUCA orthologous protein groups across eight literature sources and estimate the volatility of all associated substrates to identify ancient volatile metabolites. We hone in on volatile metabolites with confirmed modern emissions that exist in conserved metabolic pathways and produce a curated list of the most likely LUCA VOCs. We introduce volatile organic metabolites associated with early life and discuss their potential influence on early carbon cycling and atmospheric chemistry.
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  • 文章类型: Journal Article
    在这项研究中,探索了一种共催化途径来增强挥发性有机化合物(VOC)的光臭氧催化降解。将NiCo2O4负载到CeO2纳米颗粒的表面上以产生复合催化剂(10%NiCo2O4/CeO2)。NiCo2O4在CeO2上的集成增强了催化剂与甲苯之间的相互作用,代表性的VOC,导致甲苯吸附显着增加,而比表面积没有相应增加。这种集成还改善了电荷载体的利用和臭氧到O2的转化。在可见光照射下,H2O在10%NiCo2O4/CeO2表面积累电荷载流子,促进臭氧利用和甲苯吸附。NiCo2O4负载的另一个好处是其提高太阳能转换效率的能力。因此,与CeO2相比,10%NiCo2O4/CeO2的甲苯去除和矿化效率分别提高了182%和309%,与NiCo2O4相比分别提高了201%和357%。总的来说,这项研究证明了一种新型的助催化剂设计策略,用于增强VOCs的光臭氧催化降解。
    In this study, a co-catalytic route was explored to enhance the photo-ozone catalytic degradation of volatile organic compounds (VOCs). NiCo2O4 was loaded onto the surface of CeO2 nanoparticles to create a composite catalyst (10%NiCo2O4/CeO2). The integration of NiCo2O4 onto CeO2 enhanced the interaction between the catalyst and toluene, a representative VOC, resulting in significantly increased toluene adsorption without a corresponding increase in specific surface area. This integration also improved the utilization of charge carriers and conversion of ozone to O2-. Under visible light irradiation, H2O accumulated charge carriers at 10%NiCo2O4/CeO2\'s surface, facilitating both ozone utilization and toluene adsorption. Another benefit of NiCo2O4 loading was its ability to enhance the conversion efficiency of solar energy. Consequently, the toluene removal and mineralization efficiencies of 10%NiCo2O4/CeO2 were enhanced by 182% and 309% compared to CeO2, and by 201% and 357% compared to NiCo2O4, respectively. Overall, this study demonstrated a novel co-catalyst design strategy for enhancing the photo-ozone catalytic degradation of VOCs.
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  • 文章类型: Journal Article
    一种有前途的污染控制技术是冷等离子体驱动的化学处理。等离子体是在接近大气压-温度的反应器内的脉冲电气体放电。该系统由非常短的高压脉冲的连续流供电。待处理的废气流过反应器。应用的方法涉及开发强大的冷等离子体系统,工业应用和测量技术。在许多工业现场进行了系统测试,涉及控制空气中的VOC(挥发性有机化合物)和气味。电气,用最先进的方法收集化学和气味测量数据。为了解释测试数据,开发了脉冲等离子体化学的整体反应动力学的近似解。它涉及到兰伯特函数,为方便起见,一个简单的近似。后者表明,去除量,在很好的近似中,是单个变量的函数。该变量是电等离子体功率除以气流除以输入浓度。在结果部分中,我们表明,在某些情况下,可以在可接受的能量需求下去除高达99%的挥发性污染。在最后部分中,我们将通过实施(亚)纳秒脉冲等离子体和固态高压技术以及与催化剂技术的集成来探讨未来的效率提高。
    A promising pollution control technology is cold plasma driven chemical processing. The plasma is a pulsed electric gas discharge inside a near atmospheric-pressure-temperature reactor. The system is energized by a continuous stream of very short high-voltage pulses. The exhaust gas to be treated flows through the reactor. The methods applied involve the development of robust cold plasma systems, industrial applications and measuring technologies. Tests of the systems were performed at many industrial sites and involved control of airborne VOC (volatile organic compound) and odor. Electrical, chemical and odor measuring data were collected with state-of-the-art methods. To explain the test data an approximate solution of global reaction kinetics of pulsed plasma chemistry was developed. It involves the Lambert function and, for convenience, a simple approximation of it. The latter shows that the amount of removal, in good approximation, is a function of a single variable. This variable is electric plasma power divided by gas flow divided by input concentration. In the results sections we show that in some cases up to 99% of volatile pollution can be removed at an acceptable energy requirement. In the final sections we look into future efficiency enhancements by implementation of (sub)nanosecond pulsed plasma and solid state high-voltage technology and by integration with catalyst technology.
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  • 文章类型: Journal Article
    在基于钙钛矿的太阳能电池(PSC)的平面异质结构中,氧化锡(SnO2)是经常用作电子传输层(ETL)的材料。SnO2ETL在PSC结构中表现出良好的光学和电学性质。然而,由于SnO2表面上的高氧空位和SnO2的较深导带(CB)能级引起的缺陷,在PSC中发生开路电压(VOC)耗尽。在这项研究中,在SnO2(Ce-SnO2)中引入铈(Ce)掺杂剂以抑制PSC的VOC损失。Ce掺杂后,SnO2的CB最小值更接近钙钛矿的CB最小值。此外,Ce掺杂有效地钝化了SnO2上的表面缺陷,并通过Ce-SnO2提高了电子输运速度。这些结果使得功率转换效率(PCE)能够从PSC(0.09cm2有效面积)的21.1%(SnO2)增加到23.0%(Ce-SnO2),具有约100mV的改进的VOC和减小的滞后。此外,基于Ce-SnO2ETL的大面积(1.0cm2)PSC递送22.9%的最高PCE。此外,1.19V的VOC和23.3%的PCE通过在钙钛矿顶表面上用2-苯乙胺氢碘化物处理的Ce-SnO2ETL基PSC(0.09cm2活性面积)证明。值得注意的是,未包封的基于Ce-SnO2ETL的PSC能够保持其初始PCE的90%以上约2000小时,其在相对湿度为40-50%的室温条件(23-25°C)下储存。
    In the planar heterostructure of perovskite-based solar cells (PSCs), tin oxide (SnO2) is a material that is often used as the electron transport layer (ETL). SnO2 ETL exhibits favorable optical and electrical properties in the PSC structures. Nevertheless, the open circuit voltage (VOC) depletion occurs in PSCs due to the defects arising from the high oxygen vacancy on the SnO2 surface and the deeper conduction band (CB) energy level of SnO2. In this research, a cerium (Ce) dopant was introduced in SnO2 (Ce-SnO2) to suppress the VOC loss of the PSCs. The CB minimum of SnO2 was shifted closer to that of the perovskite after the Ce doping. Besides, the Ce doping effectively passivated the surface defects on SnO2 as well as improved the electron transport velocity by the Ce-SnO2. These results enabled the power conversion efficiency (PCE) to increase from 21.1% (SnO2) to 23.0% (Ce-SnO2) of the PSCs (0.09 cm2 active area) with around 100 mV of improved VOC and reduced hysteresis. Also, the Ce-SnO2 ETL-based large area (1.0 cm2) PSCs delivered the highest PCE of 22.9%. Furthermore, a VOC of 1.19 V with a PCE of 23.3% was demonstrated by Ce-SnO2 ETL-based PSCs (0.09 cm2 active area) that were treated with 2-phenethylamine hydroiodide on the perovskite top surface. Notably, the unencapsulated Ce-SnO2 ETL-based PSC was able to maintain above 90% of its initial PCE for around 2000 h which was stored under room temperature condition (23-25 °C) with a relative humidity of 40-50%.
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  • 文章类型: Journal Article
    这篇综述针对空气污染控制领域的研究人员,旨在了解挥发性有机化合物(VOC)去除的最新进展。实施等离子体催化技术以去除挥发性有机化合物(VOC)导致降解产率和矿化速率显着提高,副产物形成少。等离子体-催化组合可以以两种不同的方式使用:(I)催化剂位于等离子体放电的下游,被称为“后等离子体催化配置”(PPC),和(II)催化剂位于等离子体区并直接暴露于放电,称为“在等离子体催化配置中”(IPC)。将这两种技术结合起来,尤其是对VOCs的消除近年来引起了许多研究者的兴趣。术语“协同作用”在他们的作品中被广泛报道,并与等离子体催化组合的积极作用有关。这篇综述论文研究了新发表的关于催化的论文的最新水平,光催化,非热等离子体,以及它们的组合用于VOC去除应用。重点是了解在等离子体和催化之间相互作用的不同协同源,并将其分为两个主要部分:等离子体放电对催化剂的影响和催化剂对等离子体放电的影响。这种方法具有应用于工业过程或室内环境的空气净化系统的潜力。
    This review is aimed at researchers in air pollution control seeking to understand the latest advancements in volatile organic compound (VOC) removal. Implementing of plasma-catalysis technology for the removal of volatile organic compounds (VOCs) led to a significant boost in terms of degradation yield and mineralization rate with low by-product formation. The plasma-catalysis combination can be used in two distinct ways: (I) the catalyst is positioned downstream of the plasma discharge, known as the \"post plasma catalysis configuration\" (PPC), and (II) the catalyst is located in the plasma zone and exposed directly to the discharge, called \"in plasma catalysis configuration\" (IPC). Coupling these two technologies, especially for VOCs elimination has attracted the interest of many researchers in recent years. The term \"synergy\" is widely reported in their works and associated with the positive effect of the plasma catalysis combination. This review paper investigates the state of the art of newly published papers about catalysis, photocatalysis, non-thermal plasma, and their combination for VOC removal application. The focus is on understanding different synergy sources operating mutually between plasma and catalysis discussed and classified into two main parts: the effect of the plasma discharge on the catalyst and the effect of the catalyst on plasma discharge. This approach has the potential for application in air purification systems for industrial processes or indoor environments.
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