Organic contamination

有机污染
  • 文章类型: Journal Article
    蜂蜜是一种天然产品,因其营养和健康特性而在世界范围内广泛消费。然而,农药和环境污染物的残留会损害其质量。出于这个原因,物理化学参数,以及来自阿尔及利亚三个地区的单花和多花蜂蜜的有机污染(Tiaret,Laghouat,和Tindouf)进行监测,以评估蜂蜜的质量及其对消费者的安全性。总的来说,理化分析结果符合欧盟标准.在污染方面,阿尔及利亚农业中授权和使用的农药(甲霜灵-M和cyromazine),以及禁用的农药(西维因),在几乎所有的样本中都有发现.然而,只有环丙嗪的浓度高于相对的欧盟最大残留水平。PCB180,PCB189,蒽,芴,主要检出菲。所有的蜂蜜都显示出DiBP的痕迹,DBP,DEHP,还有DEHT,但没有发现双酚的痕迹.此外,根据饮食暴露评估,少量的阿尔及利亚蜂蜜可以安全食用。总的来说,这项研究的数据应激励阿尔及利亚政府加强其养蜂监测活动,并找到实施与国际立法协调的更可持续农业实践的解决方案。
    Honey is a natural product extensively consumed in the world for its nutritional and healthy properties. However, residues of pesticides and environmental contaminants can compromise its quality. For this reason, the physicochemical parameters, and the organic contamination of monofloral and multifloral honey from three regions of Algeria (Tiaret, Laghouat, and Tindouf) were monitored to evaluate the quality of the honey and its safety for consumers. In general, the results obtained from the physicochemical analyses were in line with the EU standards. In terms of contamination, pesticides authorised and used in Algerian agriculture (metalaxyl-M and cyromazine), as well as a banned pesticide (carbaryl), were found in almost all the samples. However, only the concentration of cyromazine was higher than the relative EU maximum residue levels. PCB 180, PCB 189, anthracene, fluorene, and phenanthrene were mainly detected. All the honey shows traces of DiBP, DBP, DEHP, and DEHT, but no traces of bisphenols were found. Moreover, according to the dietary exposure assessment, a small amount of Algerian honey can be safely consumed. Overall, the data from this study should motivate the Algerian government to enhance their monitoring activities in beekeeping and to find solutions for implementing more sustainable agricultural practices harmonising with international legislation.
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  • 文章类型: Journal Article
    现代社会的主要问题之一是不同有机物对水体的污染,无机,和污染细菌。寻找具有成本效益和高效的材料和方法用于水处理和环境修复是科学家们最重要的考虑因素之一。中空结构纳米材料,包括中空纤维膜,空心球,中空纳米盒,等。,已经显示出一种令人兴奋的废水精制方法的能力,包括膜技术,吸附,和光催化程序,由于其极高的比表面积,高孔隙率,独特的形态,和低密度。多样的中空纳米结构可以消除有机污染物,包括染料,抗生素,油/水乳液,杀虫剂,和其他酚类化合物,无机污染物,如重金属离子,盐,磷酸盐,溴酸盐,和其他离子,和细菌污染。这里,中空纳米结构的制造和改性的全面概述,水污染物分类,并且提供了具有比较态度的中空结构纳米材料在水处理领域的最新研究,表明这类纳米材料的特权和损害。最终,还提出了在炼油厂系统中使用中空纳米材料的未来前景以及扩大规模所面临的挑战。
    One of the major issues of modern society is water contamination with different organic, inorganic, and contaminants bacteria. Finding cost-effective and efficient materials and methods for water treatment and environment remediation is among the scientists\' most important considerations. Hollow-structured nanomaterials, including hollow fiber membranes, hollow spheres, hollow nanoboxes, etc., have shown an exciting capability for wastewater refinement approaches, including membrane technology, adsorption, and photocatalytic procedure due to their extremely high specific surface area, high porosity, unique morphology, and low density. Diverse hollow nanostructures could potentially eliminate organic contaminants, including dyes, antibiotics, oil/water emulsions, pesticides, and other phenolic compounds, inorganic pollutants, such as heavy metal ions, salts, phosphate, bromate, and other ions, and bacteria contaminations. Here, a comprehensive overview of hollow nanostructures\' fabrication and modification, water contaminant classification, and recent studies in the water treatment field using hollow-structured nanomaterials with a comparative attitude have been provided, indicating the privilege abd detriments of this class of nanomaterials. Eventually, the future outlook of employing hollow nanomaterials in water refinery systems and the upcoming challenges arising in scaling up are also propounded.
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  • 文章类型: Journal Article
    在这项研究中,恰纳卡莱海峡(çS)流域河流栖息地水中有机污染压力源的空间分布,并根据人类健康和粘液威胁评估水质。在盆地中定义了七个重要的河流生态系统,这些生态系统流入了高深。在春季(2023年)采集了水样,当浮游植物群落达到最高密度时。然后对它们进行了总共8个血液学参数的测试。应用养分污染指数(NPI)和水质指数(WQI)来评估水域的综合质量特征。应用危害商(HQ)和危害指数(HI)来表明有机应激源的前瞻性非致癌人类健康风险。应用主成分分析(PCA)和聚类分析(CA)对所调查的栖息地进行分类,并定义所调查的污染参数的来源。此外,地理信息系统(GIS)用于通过可视化进行有效评估。确定的ΦS分水岭中测量变量的空间平均值如下:温度为18.21°C,DO为8.51mg/L,4.57NTU用于浊度,3.95mg/L的悬浮固体,NO3-N为1.11mg/L,NO2-N为0.012mg/L;PO4-P为0.173mg/L,BOD为2.32mg/L。已经确定,从上游到下游位置,所调查子盆地的有机污染负荷和水温值都会增加,而恰纳卡莱溪流被记录为严重流域最危险的河流栖息地。根据健康风险评估指标的结果,预计所有年龄组的有机污染物都不会有非致癌风险。
    In this study, the spatial distributions of organic contamination stressors in water of fluvial habitats in the Çanakkale Strait (ÇS) watershed were investigated and the data were assessed in terms of human health and mucilage threat. Seven significant riverine ecosystems flowing into the ÇS were defined in the basin. Water samples were taken in the spring season (2023), when the phytoplankton communities reach their highest densities. Then they were tested for a total of 8 limnological parameters. The Nutrient Pollution Index (NPI) and Water Quality Index (WQI) were applied to assess the comprehensive quality characteristics of waters. The Hazard Quotient (HQ) and Hazard Index (HI) were applied to indicate the prospective non-carcinogenic human health risks of organic stressors. Principal Component Analysis (PCA) and Cluster Analysis (CA) were applied to categorize the investigated habitats and define the sources of investigated contamination parameters. Also, Geographic Information System (GIS) was used to make an effective assessment through visualization. The determined spatial mean values of the measured variables in ÇS watershed as follows: 18.21 °C for temperature, 8.51 mg/L for DO, 4.57 NTU for turbidity, 3.95 mg/L for suspended solids, 1.11 mg/L for NO3-N, 0.012 mg/L for NO2-N; 0.173 mg/L for PO4-P and 2.32 mg/L for BOD. It has been determined that the organic pollution loads and water temperature values of the investigated sub-basins increase from the upstream to the downstream locations and Çanakkale Stream was recorded as the riskiest fluvial habitat for the ÇS watershed. According to the results of health risk assessment indices, non-carcinogenic risks of organic pollutants would not be expected for all age groups.
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  • 文章类型: Journal Article
    金属材料是用于各种医疗器械的一类重要的生物材料,由于其机械性能的适当组合。其表面的(生物)官能化经常进行生物相容性要求,因为它提供了一种强大的方法来控制它们与生物系统的相互作用。当物理化学过程和生物事件发生时,这一点尤为重要。主要涉及蛋白质和细胞,在主体-材料界面处启动。这篇评论针对金属材料的(生物)功能化背景下的“真实界面”状态,以及应对这一问题的必要性,以避免对所使用的程序进行频繁的不当评估。这个问题是,的确,公认但经常被忽视的三个主要问题:(I)有机化合物表面污染的普遍性,(ii)金属表面在生物介质中的反应性,(iii)期望与现实之间(生物)功能化程序的差异。这些干扰了对表面改性所采用的策略的评估,并限制了为其改进提供指导的可能性。为此,X射线光电子能谱(XPS)来拯救。基于方法学发展取得的重大进展,并通过大量的数据编译生成统计上有意义的信息,为了确保选择性,精度和准确度,深入探索“真实接口”的状态,在照顾两个主要成分的同时:(I)生物有机吸附层,其中感兴趣的化合物(锚定分子,偶联剂,蛋白质,等)和有机污染物可以制造,和(ii)金属表面,由于它们的反应性,它们经历了动态过程。此外,通过一种广泛的(生物)功能化策略,作为案例研究,特别注意描述界面在不同阶段的状态(组成,污染物和感兴趣的(生物)化合物的深度分布)和蛋白质保留的模式。它被强调,特别是,生物活性的发生或改善并不能证明化学方案在现实中有效。这些方面对于在选择合适的(生物)功能化策略并提供提高其效率的指南方面取得进展尤其重要。
    Metallic materials are an important class of biomaterials used in various medical devices, owing to a suitable combination of their mechanical properties. The (bio)-functionalization of their surfaces is frequently performed for biocompatibility requirements, as it offers a powerful way to control their interaction with biological systems. This is particularly important when physicochemical processes and biological events, mainly involving proteins and cells, are initiated at the host-material interface. This review addresses the state of \"real interfaces\" in the context of (bio)-functionalization of metallic materials, and the necessity to cope with it to avoid frequent improper evaluation of the procedure used. This issue is, indeed, well-recognized but often neglected and emerges from three main issues: (i) ubiquity of surface contamination with organic compounds, (ii) reactivity of metallic surfaces in biological medium, and (iii) discrepancy in (bio)-functionalization procedures between expectations and reality. These disturb the assessment of the strategies adopted for surface modifications and limit the possibilities to provide guidelines for their improvements. For this purpose, X-ray photoelectrons spectroscopy (XPS) comes to the rescue. Based on significant progresses made in methodological developments, and through a large amount of data compiled to generate statistically meaningful information, and to insure selectivity, precision and accuracy, the state of \"real interfaces\" is explored in depth, while looking after the two main constituents: (i) the bio-organic adlayer, in which the discrimination between the compounds of interest (anchoring molecules, coupling agents, proteins, etc) and organic contaminants can be made, and (ii) the metallic surface, which undergoes dynamic processes due to their reactivity. Moreover, through one of the widespread (bio)-functionalization strategy, given as a case study, a particular attention is devoted to describe the state of the interface at different stages (composition, depth distribution of contaminants and (bio)compounds of interest) and the mode of protein retention. It is highlighted, in particular, that the occurrence or improvement of bioactivity does not demonstrate that the chemical schemes worked in reality. These aspects are particularly essential to make progress on the way to choose the suitable (bio)-functionalization strategy and to provide guidelines to improve its efficiency.
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  • 文章类型: Journal Article
    成功的原位化学氧化(ISCO)应用需要实时监测以评估氧化剂的输送和治疗效果。并支持快速和具有成本效益的决策。在大多数现场条件下,考虑到有限数量的钻孔,现有的监测方法经常遭受较差的空间覆盖。氧化剂的离子性质(例如,高锰酸盐)使延时电阻率层析成像(ERT)成为ISCO的潜在监测工具。然而,延时ERT通常限于定性分析,因为它不能区分离子氧化剂的电响应和来自污染物氧化的离子产物。本研究通过整合延时ERT和基于物理的反应传输模型(RTM),为ISCO提出了一种实时定量监测方法。超越常规做法,ERT调查中的电导率异常与任何离子的浓度大致相关,我们使用PHT3D作为我们的RTM来区分离子氧化剂和离子产物的贡献,并量化所有化学成分的时空演变。通过实验室柱实验对三氯乙烯(TCE)修复进行了评估。通过延时ERT和下游采样来监测该ISCO实验。我们发现反向体电导率的变化,不出所料,由于离子产物,与观察到的高锰酸盐浓度没有很好的相关性。通过集成延时ERT和RTM,所有化学成分的分布都得到了令人满意的表征和量化。发现来自有限位置的测量浓度数据和非侵入性ERT数据是ISCO监测的补充。倒置的体电导率数据有效地捕获了离子物种的空间分布,而浓度数据提供了有关溶解的TCE的信息。通过合并多源数据,ISCO效率的量化误差保持在5%以下,与仅依赖浓度数据时可能高达68%的误差相比。
    Successful in situ chemical oxidation (ISCO) applications require real-time monitoring to assess the oxidant delivery and treatment effectiveness, and to support rapid and cost-effective decision making. Existing monitoring methods often suffer from poor spatial coverage given a limited number of boreholes in most field conditions. The ionic nature of oxidants (e.g., permanganate) makes time-lapse electrical resistivity tomography (ERT) a potential monitoring tool for ISCO. However, time-lapse ERT is usually limited to qualitative analysis because it cannot distinguish between the electrical responses of the ionic oxidant and the ionic products from contaminant oxidation. This study proposed a real-time quantitative monitoring approach for ISCO by integrating time-lapse ERT and physics-based reactive transport models (RTM). Moving past common practice, where an electrical-conductivity anomaly in an ERT survey would be roughly linked to concentrations of anything ionic, we used PHT3D as our RTM to distinguish the contributions from the ionic oxidant and the ionic products and to quantify the spatio-temporal evolution of all chemical components. The proposed approach was evaluated through laboratory column experiments for trichloroethene (TCE) remediation. This ISCO experiment was monitored by both time-lapse ERT and downstream sampling. We found that changes in inverted bulk electrical conductivity, unsurprisingly, did not correlate well with the observed permanganate concentrations due to the ionic products. By integrating time-lapse ERT and RTM, the distribution of all chemical components was satisfactorily characterized and quantified. Measured concentration data from limited locations and the non-intrusive ERT data were found to be complementary for ISCO monitoring. The inverted bulk conductivity data were effective in capturing the spatial distribution of ionic species, while the concentration data provided information regarding dissolved TCE. Through incorporating multi-source data, the error of quantifying ISCO efficiency was kept at most 5 %, compared to errors that can reach up to 68 % when relying solely on concentration data.
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  • 文章类型: Journal Article
    提高污水处理率是维持河流环境中水生生物健康的重要政策。在日本,这个比例还不是100%。消除未经处理的中水排放需要采取两项措施:(1)在有污水系统的地区增加连接污水管线的住户数量,(2)用组合式系统取代单一类型的家庭现场污水处理系统(OWTS)。为了评估提高处置率对河流水质的影响,我们开发了基于水文学的有机污染评估模型,其网格空间分辨率为250m,以估算群马县河流中的生化需氧量(BOD),日本。我们基于2015年70.5%的污水处理率考虑了三种情景。在场景A中,到2030年,通过提高与污水管线的连接率,处理率提高到75.2%。在方案B中,通过从单一类型OWTS转换为组合类型OWTS的额外进展,该比率在2030年增加到88.2%。在方案C中,到2040年,这一比率达到100%。利用星翅目的分类群丰富度评价了河流的生态状况,Plecoptera,和从报告的与BOD的关系估计的毛翅目。根据目前的状态(2015年),群马县被分类为III(差)和IV(非常差)的有机废物污染的地点数量估计为1610,在方案A中减少到1212(减少25%),方案B中的619(减少62%),方案C中的50(减少97%),改善主要在小支河。处理率提高的影响主要在人口密度相对较高的地区,在有污水系统的地区之外使用单一类型的OWTS,在这些领域采取的措施被证明是有效的。
    Improving sewage disposal rates is an important policy for maintaining the health of aquatic organisms in river environments. In Japan, the rate is not yet 100 %. Two measures are necessary to eliminate the discharge of untreated greywater: (1) increase the number of households connected to sewage lines in areas with sewage systems, and (2) replace single-type household onsite wastewater treatment systems (OWTSs) with combined-type systems. To estimate the effect of improving the disposal rate on river water quality, we developed a hydrology-based organic pollution assessment model with a gridded spatial resolution of 250 m to estimate the biochemical oxygen demand (BOD) in rivers in Gunma Prefecture, Japan. We considered three scenarios based on the sewage disposal rate of 70.5 % in 2015. In Scenario A, the disposal rate is increased to 75.2 % in 2030 by increasing the connection rate to sewage lines. In Scenario B, the rate is increased to 88.2 % in 2030 through additional progress in converting from single-to combined-type OWTSs. In Scenario C, the rate reaches 100 % by 2040. The ecological status of rivers was evaluated using taxon richness of Ephemeroptera, Plecoptera, and Trichoptera estimated from its reported relationship to BOD. The number of sites in Gunma Prefecture polluted by organic waste classified as III (poor) and IV (very poor) was estimated to be 1610 under the present state (2015) and decreased to 1212 (25 % reduction) in Scenario A, 619 (62 % reduction) in Scenario B, and 50 (97 % reduction) in Scenario C, with the improvements mainly in small branch rivers. The effects of improved disposal rates were mainly evident in areas with relative high population densities using single-type OWTSs outside of areas with a sewage system, and measures taken in these areas were shown to be effective.
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  • 文章类型: Journal Article
    有限的淡水资源和对清洁水的日益增长的需求要求最大限度地减少废水中的有机污染。水中高水平的生化需氧量(BOD)减少了可用氧,危害生态系统生物多样性,降低水质。这里,建议基于回归的分析模型通过估计与有机分解相关的所需溶解氧(DO)和稀释因子(df)来最大程度地减少有机污染。定义的独立输入的训练数据集(I)最终生化需氧量(UBOD),(ii)最小BODT(BODM),(iii)平均BODT(BODA),(iv)COD,(v)O2消耗(X),和(vi)基于文献收集和/或计算时间(T)。结果表明,应根据BOD5水平指定氧气剂量,注意BOD5和DO5成反比(比例可能因微生物浓度而异)。df的增加以BOD5为主,风暴(STM)为df≈9.2,工业(IND)的df≈12×103,df≈18.5-28.5用于生活(DOM)废水。在训练回归器(包括中树(MT)和集合增强树(EBT))中使用的输入特征之间的混合/匹配对于预测组合显示出>94%的高精度:(i)MT-[UBOD-X],MT-[UBOD-X-T-COD],和EBT-[UBOD-X-T-COD]用于DO5预测,和(Ii)用于df预测的EBT-[BODM-BODA]和EBT-[BODM-BODA-UBOD-X-T-COD],知道一般术语XX-[a-b-c-d-e-f]具有XX=回归量和a,B,C,D,e,f=用作输入的训练参数的预测因子。这些模型能够预测DO5对BOD的变化,偏差为5-10%,而建议的校正因子[公式:见正文]进一步将该偏差降低至<5%,其中i=0,1,2...6是指具有常数α=f(i)的BODM数据点及其对应的UBOD。Theoptimizedcollectivemodels(cticforequesderivedfordfandDO5fromBODMthatisanexponentfunctioninUBOD)wouldenableembilitationqualityevaluationtomanageorganiccontinuation,弥合科学与行业最佳实践之间的差距。
    The limited freshwater resources and increasing demand for clean water require minimizing organic contamination in wastewater. High levels of biochemical oxygen demand (BOD) in water reduce available oxygen, harm ecosystem biodiversity, and degrade water quality. Here, regression-based analytical models are suggested to minimize organic contamination by estimating desired dissolved oxygen (DO) and dilution factors (df) correlated to the organic decomposition. Training datasets of defined independent inputs (i) ultimate biochemical oxygen demand (UBOD), (ii) minimum BODT (BODM), (iii) average BODT (BODA), (iv) COD, (v) O2 consumption (X), and (vi) time (T) were collected and/or calculated based on literature. Results showed that there should be specified oxygen dosing amounts dependent upon BOD5 levels, noting that BOD5 and DO5 are inversely proportional (proportionality might differ based on the microbial concentration). An increase in df is predominated by BOD5, with df≈9.2 for storm (STM), df≈12 × 103 for industrial (IND), and df≈18.5-28.5 for domestic (DOM) wastewaters. Mixing/matching between the input features used in training regressors including medium trees (MT) and ensembles boosted trees (EBT) showed high accuracy > 94% for predictor combinations: (i) MT-[UBOD-X], MT-[UBOD-X-T-COD], and EBT-[UBOD-X-T-COD] for DO5 predictions, and (ii) EBT-[BODM-BODA] and EBT-[BODM-BODA-UBOD-X-T-COD] for df predictions, knowing the general term XX-[a-b-c-d-e-f] has XX = regressor and a,b,c,d,e,f = predictors for the training parameters used as inputs. The models are capable of predicting changes in DO5 against BOD with deviations 5-10%, whereas a suggested correction factor [Formula: see text] further reduced this deviation to < 5%, where i = 0, 1, 2…6 refers to the BODM datapoint and its corresponding UBOD with the constant α = f(i). The optimized collective models (cubic equations derived for df and DO5 from BODM that is an exponent function in UBOD) would enable effluent quality evaluation to manage organic contamination, bridging the gap between science and industry best practices.
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  • 文章类型: Journal Article
    橄榄岩的蛇纹石化为海底生物圈和非生物有机合成提供了重要的能源。蛇纹岩中存在各种各样的微米级有机物,为深入的碳循环和地球上生命的起源提供了见解。在分析蛇纹岩样品时,保持严格的实验室协议至关重要,限制与可能污染蛇纹石并引起误解的有机材料的接触。然而,这些有机材料(例如乳胶手套或尼龙抛光盘)在多大程度上会造成污染,目前尚不清楚。在这里,我们对来自西太平洋雅普海沟的蛇纹岩样品进行了多阶段切割和抛光程序,然后再进行分析。我们从电子显微镜的发现表明,蛇纹岩中的微米级有机物随机分布在样品表面或Cr尖晶石裂缝内。使用拉曼光谱的进一步分析表明,有机物含有几个氢键部分,类似于蛇纹岩样品处理过程中使用的乳胶手套或尼龙抛光盘。我们的结果表明,检测到的有机物可能是由于样品处理过程中涉及的有机材料造成的污染。因此,未来的研究需要仔细评估微米级有机污染,并在分析蛇纹石中的有机化合物时限制有机材料的使用,不仅在地球上,而且在其他岩石行星上。
    Serpentinization of peridotite provides a significant source of energy for the subseafloor biosphere and abiotic organic synthesis. The presence of diverse micrometer-scale organic matter in serpentinites offers insights into deep carbon cycling and the origin of life on Earth. It is critical to maintain stringent lab protocols in analyzing serpentinite samples, limiting the contact with organic materials that could contaminate serpentinites and cause misinterpretations. However, the extent to which these organic materials (e.g. latex gloves or nylon polishing disc) can introduce contamination remains unclear. Here we subject serpentinite samples from the Yap Trench in the western Pacific Ocean to multi-stage cutting and polishing procedures prior to analysis. Our findings from electron microscopy reveal that micrometer-scale organic matter in serpentinites is randomly distributed either on the sample surface or within Cr-spinel fractures. Further analysis using Raman spectroscopy indicates that the organic matter contains several hydrogen bonding moieties, similar to those found in the latex gloves or nylon polishing disc used during the treatment of serpentinite samples. Our results suggest that the detected organic matter is likely due to contamination from the organic materials involved during sample processing. Thus, future studies need to carefully assess micrometer-scale organic contamination and limit the use of organic materials when analyzing organic compounds hosted in serpentinites, not only on Earth but also on other rocky planets.
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  • 文章类型: Journal Article
    在这项研究中,研究了各种清洁方法对涂层形态及其去除有机污染物的有效性的影响。通过在水性电解质和熔融盐中进行等离子体电解氧化,获得了包含氧化钛和羟基磷灰石(HAP)的生物活性涂层。使用高压釜(A)进行涂覆表面的清洁程序,紫外光(UV),射频(RF),空气等离子体(P),和紫外线臭氧清洁剂(O)。使用带有EDS检测器的扫描电子显微镜(SEM)对样品进行表征,X射线光电子能谱(XPS),X射线相分析(XRD),和接触角(CA)测量。所进行的研究表明,与从水性电解质(350nm)获得的样品相比,从熔盐获得的样品表现出更精细的晶体结构形态(275nm)。应用表面清洁方法后,碳含量从5.21at.%至0.11at。%(XPS),其直接对应于如下有机污染物的减少和接触角的减小:A>UV>P>O这对于在熔盐中获得的涂层(25.3°>19.5°>10.5°>7.5°)和在水性电解质中获得的涂层(35.2°>28.3°>26.1°>16.6°)都是如此。最有效和适度的清洁方法是臭氧处理。
    The effect of various cleaning methods on coating morphology and their effectiveness in removing organic contaminants has been studied in this research. Bioactive coatings containing titanium oxides and hydroxyapatite (HAP) were obtained through plasma electrolytic oxidation in aqueous electrolytes and molten salts. The cleaning procedure for the coated surface was performed using autoclave (A), ultraviolet light (UV), radio frequency (RF), air plasma (P), and UV-ozone cleaner (O). The samples were characterized using scanning electron microscopy (SEM) with an EDS detector, X-ray photoelectron spectroscopy (XPS), X-ray phase analysis (XRD), and contact angle (CA) measurements. The conducted studies revealed that the samples obtained from molten salt exhibited a finer crystalline structure morphology (275 nm) compared to those obtained from aqueous electrolytes (350 nm). After applying surface cleaning methods, the carbon content decreased from 5.21 at.% to 0.11 at.% (XPS), which directly corresponds to a reduction in organic contaminations and a decrease in the contact angle as follows: A > UV > P > O. This holds true for both coatings obtained in molten salt (25.3° > 19.5° > 10.5° > 7.5°) and coatings obtained in aqueous electrolytes (35.2° > 28.3° > 26.1° > 16.6°). The most effective and moderate cleaning method is ozone treatment.
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  • 文章类型: Journal Article
    基于过氧单硫酸盐(PMS)活化的高级氧化过程(AOP)已被开发为从水环境中完全根除顽固有机污染物的理想途径。在这里,通过一步热聚合法合理制备了掺杂V的石墨氮化碳(g-C3N4),以激活PMS进行污染净化。结果表明,V原子成功地整合到g-C3N4的骨架中,可以有效地提高光吸收强度并增强电荷分离。V掺杂的g-C3N4对PMS活化表现出优异的催化性能。此外,掺杂量对活化性能有很大影响。自由基猝灭实验证实·O2-,SO4•-,和h+是催化反应中的重要物质。这项工作将为开发有效的g-C3N4基材料用于PMS活化提供可行的策略。
    Advanced oxidation processes (AOPs) based on peroxymonosulfate (PMS) activation have been developed as an ideal pathway for completely eradication of recalcitrant organic pollutants from water environment. Herein, the V-doped graphitic carbon nitride (g-C3N4) is rationally fabricated by one-step thermal polymerization method to activate PMS for contamination decontamination. The results demonstrate the V atoms are successfully integrated into the framework of g-C3N4, which can effectively improve light absorption intensity and enhance charge separation. The V-doped g-C3N4 displays superior catalytic performance for PMS activation. Moreover, the doping content has a great influence on the activation performances. The radical quenching experiments confirm •O2-, SO4•-, and h+ are the significant species in the catalytic reaction. This work would provide a feasible strategy to exploit efficient g-C3N4-based material for PMS activation.
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