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几种新兴XRF技术在地质与地球化学分析中的应用
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作者 袁静 张华 +4 位作者 时磊 黄海波 谭桂丽 刘建坤 于俊杰 《光谱学与光谱分析》 北大核心 2025年第9期2401-2409,共9页
X射线荧光光谱分析技术(XRF)凭借操作简便、分析快速、绿色环保、分析精度高以及无损检测等特点,在地质与地球化学分析领域已得到广泛应用。然而,近年来地学领域的研究重心逐步向地球系统科学转变,研究范畴涵盖全球气候变化、地球圈层... X射线荧光光谱分析技术(XRF)凭借操作简便、分析快速、绿色环保、分析精度高以及无损检测等特点,在地质与地球化学分析领域已得到广泛应用。然而,近年来地学领域的研究重心逐步向地球系统科学转变,研究范畴涵盖全球气候变化、地球圈层的相互作用及人类活动引发的环境变化等领域。这些领域的蓬勃发展对元素分析提出了新需求,例如:元素空间分布特征及赋存形态的解析、野外现场地球化学数据的实时获取、低原子序数元素的准确快速定量,以及仪器分辨率、灵敏度和检出限的进一步优化等。这些需求又推动了XRF新技术新方法的研究和进步及其在地学领域的应用拓展。同步辐射微区X射线荧光光谱(SR-μ-XRF)和X射线吸收谱(XAFS)依托同步辐射光源的优越性,能够在亚微米尺度对物质进行原位微区分析,实现元素分布成像、化学形态、氧化态和配位环境解析;新型实验室光源的μ-XRF通过对X射线光管、探测器及聚焦光学系统的升级改进,在兼顾省时、便利的同时,显著提升了低原子序数元素的分析精度;便携式X射线荧光技术(PXRF)以其小型化、样品处理简单的特性,满足了野外现场分析及动态过程样品的分析需求;X射线荧光岩芯扫描仪(XRF core scanner)克服了传统实验室分析的周期限制,可对大批量岩芯进行高精度连续原位扫描,实现主量和微量元素的快速分析。本文回顾了上述几类XRF技术近年来在地质与地球化学分析中的应用,旨在为地学研究者与XRF技术人员提供一些研究思路与技术参考。 展开更多
关键词 微区X射线荧光(μ-xrf) X射线吸收谱(XAFS) 便携式X射线荧光(Pxrf) X射线荧光岩芯扫描仪(xrf core scanner) 地质与地球化学分析
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基于PRE-PLS的XRF煤炭灰分智能预测算法
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作者 孙明 廖祥国 +6 位作者 王邵康 高单 孙嘉悦 黄筱俊 何光明 李博昊 吴威辰 《金属矿山》 北大核心 2025年第9期176-183,共8页
煤炭灰分值是衡量煤炭质量的关键指标之一,灰分含量和性质对燃烧设备、环境、后续的加工利用都有着极大影响。针对目前煤炭灰分检测方法的滞后性、劳动密集型问题,提出了一种基于XRF光谱的预处理(Preprocessing,PRE)与偏最小二乘法(Part... 煤炭灰分值是衡量煤炭质量的关键指标之一,灰分含量和性质对燃烧设备、环境、后续的加工利用都有着极大影响。针对目前煤炭灰分检测方法的滞后性、劳动密集型问题,提出了一种基于XRF光谱的预处理(Preprocessing,PRE)与偏最小二乘法(Partial Least Squares,PLS)相结合的XRF煤炭灰分智能预测算法。通过将XRF技术获取煤炭样品的光谱数据输入PLS主模型初步预测灰分,再将相关校正参数输入补偿优化模型中,最终将两者相加得到预测灰分值。试验结果表明:相对于偏最小二乘法回归、神经网络回归模型,PRE-PLS模型决定系数为0.9951,均方根误差为0.9411,平均绝对误差为0.7332%,表明该模型具备较高的精度,能够胜任现场检测工作,为生产提供可靠指导。 展开更多
关键词 X射线荧光光谱(xrf) 煤炭 灰分预测 偏最小二乘法(PLS) 光谱预处理
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基于PIEspline的土壤XRF光谱背景扣除方法研究
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作者 李唐虎 甘婷婷 +4 位作者 赵南京 殷高方 叶紫琪 汪颖 盛若愚 《光谱学与光谱分析》 北大核心 2025年第5期1364-1372,共9页
XRF光谱法作为重金属现场快速检测的重要技术手段,当其用于土壤重金属检测时,受土壤基质影响XRF光谱中存在强度较高且复杂的背景光谱,严重影响重金属特征谱峰信息的准确获取及定量分析准确性。针对该问题,提出一种极值法峰谷识别与惩罚... XRF光谱法作为重金属现场快速检测的重要技术手段,当其用于土壤重金属检测时,受土壤基质影响XRF光谱中存在强度较高且复杂的背景光谱,严重影响重金属特征谱峰信息的准确获取及定量分析准确性。针对该问题,提出一种极值法峰谷识别与惩罚项修正的三次平滑样条曲线拟合相结合(PIEspline)的土壤XRF光谱背景扣除方法,该方法首先通过极值法对土壤完整XRF光谱中的峰谷点进行识别,获取光谱中对背景具有代表性的数据点,再对一系列峰谷点进行惩罚项修正的三次平滑样条曲线拟合形成背景基线,从而实现土壤XRF光谱中复杂背景的扣除;并通过与自适应迭代重加权惩罚最小二乘法(airPLS)、迭代小波变换法(IWT)、统计敏感的非线性迭代剥峰算法(SNIP)三种传统光谱背景扣除方法对比,进一步验证了PIEspline方法的性能。结果表明:对于模拟的土壤XRF光谱,PIEspline方法所获取的背景谱线与光谱真实背景谱线间的均方根误差(RMSE)分别为0.4258和0.6441,均低于其他三种方法,并且具有最快的背景扣除运行效率;对于栗钙土、盐碱土和黄土三种不同类型土壤及农用、工业、建筑三种不同用途土壤,PIEspline方法背景拟合所获得的XRF光谱中10个特征谷点处荧光强度的平均相对误差为10.87%,与三种传统方法相比分别降低了84.88%、76.30%和16.51%;且PIEspline方法用于上述6种土壤中Cr、Pb、Cd定量分析的平均相对误差分别为4.01%、2.50%和5.20%,与airPLS、IWT、SNIP三种方法相比分别降低了22.39%~84.07%、60.15%~71.92%和79.18%~84.07%,且当土壤类型和用途发生变化时,PIEspline方法的相对误差波动最小,展现出了最好的稳定性,表明PIEspline方法在不同类型及不同用途土壤多种重金属同时XRF定量分析中具有最好的普适性。因此该研究所提出的PIEspline方法能够实现不同类型与不同用途土壤XRF光谱背景的精准扣除,有利于提高重金属XRF定量分析准确性。该研究为土壤重金属XRF现场快速准确检测提供了重要的方法基础。 展开更多
关键词 X射线荧光 背景扣除 重金属检测 光谱解析 土壤
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基于WPS-GMM的土壤XRF光谱重叠峰解析方法研究
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作者 李唐虎 甘婷婷 +5 位作者 赵南京 殷高方 汪颖 李星池 盛若愚 叶紫琪 《光谱学与光谱分析》 北大核心 2025年第10期2737-2746,共10页
X射线荧光(XRF)光谱法作为重金属现场快速检测的重要技术,当用于土壤重金属检测时,由于土壤所含元素较多,XRF光谱中存在部分元素特征谱峰交叉重叠问题,影响重金属特征谱峰提取及定量分析准确性。针对该问题,提出一种基于小波峰锐化-高... X射线荧光(XRF)光谱法作为重金属现场快速检测的重要技术,当用于土壤重金属检测时,由于土壤所含元素较多,XRF光谱中存在部分元素特征谱峰交叉重叠问题,影响重金属特征谱峰提取及定量分析准确性。针对该问题,提出一种基于小波峰锐化-高斯混合模型(WPS-GMM)的土壤XRF光谱重叠峰解析方法。该方法通过离散小波变换对重叠峰进行峰锐化,以增强信号中的重要局部特征,明确子峰峰位,并以其作为先验约束条件,对重叠峰构建高斯混合模型,进一步通过最大化似然估计模型参数,获得重叠峰中各子峰中心峰位、积分面积等相关信息,实现重叠峰的解析。将所建WPS-GMM方法用于土壤XRF光谱中Ni Kα-Co Kβ、Cu Kα-Ni Kβ、Zn Kα-Cu Kβ三组典型重叠峰解析及重叠峰中主峰对应重金属Ni、Cu、Zn的定量分析,并将结果与传统仅基于高斯混合模型(GMM)的重叠峰解析方法对比,验证所建方法的准确性。结果表明:与GMM方法相比,所建WPS-GMM方法对土壤XRF光谱三组重叠峰中Ni Kα、Ni Kβ、Cu Kα、Cu Kβ和Zn Kα子峰峰位解析的准确率平均分别提高了77.55%、47.03%、52.65%、22.07%和8.43%,积分面积解析准确率平均分别提高了74.05%、80.17%、61.62%、28.29%和43.59%;用于Ni、Cu、Zn定量分析的准确率平均分别提高了73.23%、68.47%、47.62%;并且用于工业用土、农用土、建筑用土三种不同用途土壤中Ni、Cu、Zn准确定量分析均具有更好的普适性。因此所建WPS-GMM方法能够更准确获取不同土壤XRF光谱中重叠峰的子峰信息,更有利于提高土壤重金属XRF定量分析准确性。该研究为土壤重金属XRF现场快速准确检测提供了重要的方法基础。 展开更多
关键词 X射线荧光 重叠峰解析 重金属检测 土壤 光谱分析
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手持式XRF和实验室分析在土壤污染与修复实验课程中的比较和应用
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作者 付志平 雷畅 +1 位作者 龙来寿 胡月 《广东化工》 2025年第13期176-178,共3页
利用手持式XRF与实验室分析法,对比分析了不同污染程度土壤重金属含量的测试效果。结果表明,手持式XRF对不同污染程度土壤Pb以及轻度污染土壤中Zn和As的测试效果都较好,但是对中度和重度污染土壤的Zn和As的分析效果则较差,尤其不适用于C... 利用手持式XRF与实验室分析法,对比分析了不同污染程度土壤重金属含量的测试效果。结果表明,手持式XRF对不同污染程度土壤Pb以及轻度污染土壤中Zn和As的测试效果都较好,但是对中度和重度污染土壤的Zn和As的分析效果则较差,尤其不适用于Cd等低背景值元素的分析。因此,土壤污染与修复实验课程选取手持式XRF的分析样品时,首选Pb污染土壤,其次为Zn、As轻度污染土壤,可为其中的“土壤淋洗修复实验”提供较准确的重金属含量,丰富“土壤重金属快速检测与筛查”实验内容,提高学生实验效率,培养学生的实践操作能力和创新意识。 展开更多
关键词 手持式xrf 实验室分析 实验教学 土壤污染 土壤修复
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Recent application of near-infrared fluorescence probes in food safety detection
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作者 Lei Li Zhongrui Peng +1 位作者 Yun Zeng Gang Liu 《Journal of Innovative Optical Health Sciences》 2025年第3期45-59,共15页
Fluorescent probes have wide applications in biological and environmental analysis due to their advantages of simple operation, convenient flexibility, high sensitivity and efficiency. They are considered to be promis... Fluorescent probes have wide applications in biological and environmental analysis due to their advantages of simple operation, convenient flexibility, high sensitivity and efficiency. They are considered to be promising tools for accurate analysis of agriculture- and food-related hazardous substances. In this review, the types and characteristics of the near-infrared fluorescence probes (NIFPs) are briefly described. The recent advances of NIFPs for precisely detecting various hazardous substances including heavy metals, sulfite and related sulfiting agents and hydrogen peroxide are summarized. Finally, the present challenges and future perspectives faced by NIFPs in food safety analysis are discussed. 展开更多
关键词 Near-infrared fluorescence probes food safety food analysis AGRICULTURE
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Sensitive fluorescence detection of baicalin in biological samples using Eu^(3+)-based metal-organic frameworks
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作者 Hao Zhang Yutong Chen +2 位作者 Runnan Wang Fanxu Meng Dawei Lou 《Journal of Rare Earths》 2025年第8期1703-1710,I0005,共9页
Baicalin,a major flavonoid compound found in Scutellariae radix,is the first SARS-CoV-23CLpro virus inhibitor.Therefore,developing an accurate and reliable strategy to detect baicalin in biological systems is vital.He... Baicalin,a major flavonoid compound found in Scutellariae radix,is the first SARS-CoV-23CLpro virus inhibitor.Therefore,developing an accurate and reliable strategy to detect baicalin in biological systems is vital.Herein,we report the first indolyl-lanthanide metal-organic framework(MOF)materials and their application as baicalin sensors.The results of this study indicate that the new crystal structure has good stability and luminous performance.The detection limits of baicalin in serum and urine are 0.05 and 0.04μmol/L,respectively,suggesting high sensitivity and selectivity.Various background substances present in practical samples,such as anions,cations,and amino acids,do not interfere with the photoluminescence analytical signal of Eu^(3+).We identified that the quenching of the Eu-MOF is due to the inner filter effect,absorption energy competition,and photoinduced electron transfer among the baicalin,ligand,and MOF through powder X-ray diffraction analysis,Fourier transform infrared spectroscopy,luminescence lifetimes,ultraviolet studies,and computational analysis.Thus,we designed a convenient,sensitive,and facile detection method using the Eu-MOF and demonstrate that Eu^(3+)-based materials are promising sensors for baicalin detection in actual serum and urine.Additionally,the prepared Eu-MOF@polyvinyl alcohol composite matrix membrane test film has considerable practical application value for the portable detection of baicalin. 展开更多
关键词 Lanthanide metal-organic frameworks Luminescent materials Rare earths BAICALIN Fluorescent analysis
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Laparoscopic hepatectomy using indocyanine green attenuates postoperative inflammatory response for hepatocellular carcinoma:A propensity score matching analysis
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作者 Wei-Xun Wu Ming-Bin Huang +3 位作者 Mei-Xia Wang Li-Hua Chen Bo Hu Zhen-Bin Ding 《World Journal of Gastrointestinal Surgery》 2025年第1期193-202,共10页
BACKGROUND Improving the intraoperative and postoperative performance of laparoscopic hepatectomy was quite a challenge for liver surgeons.AIM To determine the benefits of indocyanine green(ICG)fluorescence imaging in... BACKGROUND Improving the intraoperative and postoperative performance of laparoscopic hepatectomy was quite a challenge for liver surgeons.AIM To determine the benefits of indocyanine green(ICG)fluorescence imaging in patients with hepatocellular carcinoma(HCC)who underwent laparoscopic hepatectomy during and after surgery.METHODS We retrospectively collected the clinicopathological data of 107 patients who successfully underwent laparoscopic hepatectomy at Zhongshan Hospital(Xiamen),Fudan University from June 2022 to June 2023.Whether using the ICG fluorescence imaging technique,we divided them into the ICG and non-ICG groups.To eliminate statistical bias,a 1:1 propensity score matching analysis was conducted.The comparison of perioperative outcomes,including inflammationrelated markers and progression-free survival,was analyzed statistically.RESULTS Intraoperatively,the ICG group exhibited lower blood loss,a shorter surgical time,lower hepatic inflow occlusion(HIO)frequency,and a shorter total HIO time.Postoperatively,the participation of ICG resulted in a shorter duration of hospitalization(6.5 vs 7.6 days,P=0.03)and postoperative inflammatory response attenuation(lower neutrophil-lymphocyte ratio on the first day after surgery and platelet-lymphocyte ratio on the third day,P<0.05).Although the differences were not significant,the levels of all inflammation-related markers were lower in the ICG group.The rates of postoperative complications and the survival analyses,including progression-free and overall survivals showed no significant difference between the groups.CONCLUSION The involvement of ICG fluorescence imaging may lead to improved perioperative outcomes,especially postoperative inflammatory response attenuation,and ultimately improve HCC patients’recovery after surgery. 展开更多
关键词 Hepatocellular carcinoma Laparoscopic hepatectomy Indocyanine green fluorescence Postoperative inflammatory response attenuation Propensity score matching analysis
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基于XRF法建立云浮市南药品种重金属及有害元素含量快速测定方法
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作者 黎莉莉 黄海珍 区梓聪 《广东化工》 2025年第5期143-145,共3页
目的:采用便携式X射线荧光元素分析仪(XRF)建立云浮市南药品种重金属及有害元素含量的快速检测方法。方法收集云浮市辖区内种植的17批次样品采用便携式XRF对上述中药材进行测定,将测试结果与电感耦合等离子体质谱法(ICP-MS)的测定结果对... 目的:采用便携式X射线荧光元素分析仪(XRF)建立云浮市南药品种重金属及有害元素含量的快速检测方法。方法收集云浮市辖区内种植的17批次样品采用便携式XRF对上述中药材进行测定,将测试结果与电感耦合等离子体质谱法(ICP-MS)的测定结果对比,报告其重金属及有害元素含量情况并评价其实用性。结果采用ICP-MS测定17批次中药材的5种元素(铅、砷、镉、汞、铜)的含量均低于限值水平,与XRF的测定结果对比,相对平均偏差(RD%)均小于10%。便携式XRF测定5种元素的检测限,分别为20 ppm、16 ppm、30 ppm、20 ppm、8 ppm;重复性(RSD%)均小于6%;检测范围分别为20 mg/L~1000 mg/L、20 mg/L~1000 mg/L、20 mg/L~1000 mg/L、30 mg/L~1000 mg/L、10 mg/L~1000 mg/L。结论:云浮市辖区内种植的牛大力、广藿香、三丫苦、肉桂、巴戟天5个南药品种均无出现重金属及有害元素污染的情况,品质较佳。便携式XRF具有较好的实用性、稳定性和耐用性。该方法适用于云浮市南药品种重金属及有害元素含量的快速检测,可在中药材重金属及有害元素初筛阶段进行半定量分析测试。 展开更多
关键词 电感耦合等离子体质谱法 便携式X射线荧光元素分析法 重金属及有害元素 含量测定 南药
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FLUORESCENCE SPECTRUM ANALYSIS OF ETHER-WATER SOLUTION BASED ON GAUSSIAN DECOMPOSITION METHOD 被引量:1
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作者 韩彩芹 宋春元 +3 位作者 吴斌 刘莹 骆晓森 倪晓武 《Transactions of Nanjing University of Aeronautics and Astronautics》 EI 2010年第1期70-75,共6页
The fluorescence spectrum of the ether-water solution excited by the ultraviolet light with the wavelength of 245 nm is experimentally detected. Based on the second derivative analysis, the fluorescence spectrum of th... The fluorescence spectrum of the ether-water solution excited by the ultraviolet light with the wavelength of 245 nm is experimentally detected. Based on the second derivative analysis, the fluorescence spectrum of the ether-water solution is used as Gaussian decomposition and seven Gaussian spectral lines are obtained. The center wavelength, the peak intensity and the half peak bandwidth of each Gaussian spectral line are measured, and the multi-peak fitting is made by using Gaussian primitive parameters. The highest and the lowest oscillation energy level differences in the ground state of each Gaussian spectrum are calculated. It is found that there are seven types of luminescent association molecules formed by ether and water molecules in different configurations existed in the solution. The location of each optimum absorption wavelength and the half peak bandwidth of the Gaussian spectral line is different. The energy level difference with the central wavelength of 304 nm attains the maximum value The result can contribute to the study of the molecular association in ether-water solution. 展开更多
关键词 fluorescence spectrum analysis ether-water solution Gaussian decomposition
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Characterization of dissolved organic matter in urban sewage using excitation emission matrix fluorescence spectroscopy and parallel factor analysis 被引量:41
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作者 Weidong Guo Jing Xu +3 位作者 Jiangping Wang Yingrou Wen Jianfu Zhuo Yuchao Yan 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2010年第11期1728-1734,共7页
Wastewater dissolved organic matter (DOM) from different processing stages of a sewage treatment plant in Xiamen was characterized using fluorescence and absorption spectroscopy. Parallel factor analysis modeling of... Wastewater dissolved organic matter (DOM) from different processing stages of a sewage treatment plant in Xiamen was characterized using fluorescence and absorption spectroscopy. Parallel factor analysis modeling of excitation-emission matrix spectra revealed five fluorescent components occurring in sewage DOM: one protein-like (C1), three humic-like (C2, C4 and C5) and one xenobiotic-like (C3) components. During the aerated grit chamber and primary sedimentation tank stage, there was only a slight decrease in fluorescence intensity and the absorption coefficient at 350 nm (a 350 ). During the second aeration stage, high concentration of protein-like and short-wavelength-excited humic-like components were significantly degraded accompanied by significant loss of DOC (80%) and a 350 (30%), indicating that C1 and C2 were the dominant constituents of sewage DOM. As a result, long-wavelength- excited C4 and C5 became the dominant humic-like components and the DOM molecular size inferred from the variation of spectral slope S (300–650 nm) and specific absorption (a 280 /DOC) increased. Combination use of F max of C1 and the ratio of C1/C5, or a 350 may provide a quantitative indication for the relative amount of raw or treated sewage in aquatic environment. 展开更多
关键词 dissolved organic matter SEWAGE fluorescence EEM parallel factor analysis
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Quantitative energy-dispersive X-ray fluorescence analysis for unknown samples using full-spectrum least-squares regression 被引量:6
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作者 Yong-Li Liu Qing-Xian Zhang +2 位作者 Jian Zhang Hai-Tao Bai Liang-Quan Ge 《Nuclear Science and Techniques》 SCIE CAS CSCD 2019年第3期149-159,共11页
The full-spectrum least-squares(FSLS) method is introduced to perform quantitative energy-dispersive X-ray fluorescence analysis for unknown solid samples.Based on the conventional least-squares principle, this spectr... The full-spectrum least-squares(FSLS) method is introduced to perform quantitative energy-dispersive X-ray fluorescence analysis for unknown solid samples.Based on the conventional least-squares principle, this spectrum evaluation method is able to obtain the background-corrected and interference-free net peaks, which is significant for quantization analyses. A variety of analytical parameters and functions to describe the features of the fluorescence spectra of pure elements are used and established, such as the mass absorption coefficient, the Gi factor, and fundamental fluorescence formulas. The FSLS iterative program was compiled in the C language. The content of each component should reach the convergence criterion at the end of the calculations. After a basic theory analysis and experimental preparation, 13 national standard soil samples were detected using a spectrometer to test the feasibility of using the algorithm. The results show that the calculated contents of Ti, Fe, Ni, Cu, and Zn have the same changing tendency as the corresponding standard content in the 13 reference samples. Accuracies of 0.35% and 14.03% are obtained, respectively, for Fe and Ti, whose standard concentrations are 8.82% and 0.578%, respectively. However, the calculated results of trace elements (only tens of lg/g) deviate from the standard values. This may be because of measurement accuracy and mutual effects between the elements. 展开更多
关键词 Energy-dispersive X-ray fluorescence analysis Full-spectrum LEAST-SQUARES METHOD Effective atomic number Mass attenuation coefficient Fundamental parameter METHOD
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Geochemical analysis of marine sediments using fused glass disc by X-ray fluorescence spectrometry 被引量:8
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作者 夏宁 张勤 +1 位作者 姚德 李国会 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2008年第4期475-479,共5页
A method was developed for content determination of Na, Mg, A1, Si, P,S, C1, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Nb, Zr, Y, Sr, Rb, Ba, La and Ce etc. covering 26 major, minor, and trace elements in marine sedim... A method was developed for content determination of Na, Mg, A1, Si, P,S, C1, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Nb, Zr, Y, Sr, Rb, Ba, La and Ce etc. covering 26 major, minor, and trace elements in marine sediment samples using fused glass disc by X-ray Fluorescence spectrometry. Calibration was made using marine sediment certified reference materials and the synthetic standard samples prepared by mixing several marine sediments with stream sediment and carbonate standard samples in different proportions. The matrix effect was corrected using theoretical alpha coefficients, experience coefficients and the scattered radiation as the internal standard (for the trace elements). The accuracy of the method was evaluated by analysis of certified reference materials GBW07314, GBW07334 and GSMS6. The results are in good agreement with the certified values of the standards with RSD less than 2.60%, except for Y, Cr, Ga, Ce, La, Nb, Rb, and V with RSD less than 9.0% (n=12). 展开更多
关键词 marine sediment X-ray fluorescence spectrometry geochemical analysis multi-element analysis
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Elemental and proximate analysis of coal by x-ray fluorescence assisted laser-induced breakdown spectroscopy 被引量:6
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作者 Zhihui TIAN Xiaolin LI +9 位作者 Gang WANG Lei ZHANG Jiaxuan LI Shuqing WANG Yu BAI Wanfei ZHANG Han YUE Xiaofei MA Wangbao YIN Suotang JIA 《Plasma Science and Technology》 SCIE EI CAS CSCD 2022年第8期55-63,共9页
Although laser-induced breakdown spectroscopy(LIBS),as a fast on-line analysis technology,has great potential and competitiveness in the analysis of chemical composition and proximate analysis results of coal in therm... Although laser-induced breakdown spectroscopy(LIBS),as a fast on-line analysis technology,has great potential and competitiveness in the analysis of chemical composition and proximate analysis results of coal in thermal power plants,the measurement repeatability of LIBS needs to be further improved due to the difficulty in controlling the stability of the generated plasmas at present.In this paper,we propose a novel x-ray fluorescence(XRF) assisted LIBS method for high repeatability analysis of coal quality,which not only inherits the ability of LIBS to directly analyze organic elements such as C and H in coal,but also uses XRF to make up for the lack of stability of LIBS in determining other inorganic ash-forming elements.With the combination of elemental lines in LIBS and XRF spectra,the principal component analysis and the partial least squares are used to establish the prediction model and perform multi-elemental and proximate analysis of coal.Quantitative analysis results show that the relative standard deviation(RSD) of C is 0.15%,the RSDs of other elements are less than 4%,and the standard deviations of calorific value,ash content,sulfur content and volatile matter are 0.11 MJ kg,0.17%,0.79% and 0.41%respectively,indicating that the method has good repeatability in determination of coal quality.This work is helpful to accelerate the development of LIBS in the field of rapid measurement of coal entering the power plant and on-line monitoring of coal entering the furnace. 展开更多
关键词 laser-induced breakdown spectroscopy(LIBS) x-ray fluorescence spectrometry(xrf) high repeatability measurement spectral calibration instability analysis
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Fluorescence Microscopic Image Analysis of Nucleic Acids Based on The Capillary Flow Directed Assembly Ring of Neutral Red-nucleic Acid Supramolecular Complexes 被引量:6
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作者 LI Yuan fang HUANG Cheng zhi 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2003年第3期275-279,共5页
It is critical to establish a direct and precise method with a high sensitivity and selectivity in analytical chemistry. In this research, making use of a well known phenomenon of capillary flow, we have proposed an... It is critical to establish a direct and precise method with a high sensitivity and selectivity in analytical chemistry. In this research, making use of a well known phenomenon of capillary flow, we have proposed an image analysis method of nucleic acids at the price of a small amount of sample. When a droplet of the supramolecular complex solution, formed by neutral red and nucleic acids(NA) under an approximate neutral condition, was placed on the hydrophobic surface of dimethyl dichlorosilane pretreated glass slides, and it was evaporated, the supramolecular complex exhibited the periphery of the droplet due to the capillary effect, and accumulated there to form a red capillary flow directed assembly ring(CFDAR). A typical CFDAR has an outer diameter of (2 r ) about 1.18 mm and a ring width(2 δ ) of about 41 μm. Depending on the experimental conditions, a variety of CFDAR can be assembled. The experimental results are in agreement with our former theoretical discussion. It was found that when a droplet volume is 0.1 μL, the fluorescence intensity of the CFDAR formed by the NR NA is in proportion to the content of calf thymus DNA in the range of 0-0.28 ng, fish sperm DNA of 0-0.24 ng and yeast RNA of 0-0.16 ng with the limit of detection(3 σ ) of 1 7, 1.4 and 0.9 pg, respectively for the three nucleic acids. 展开更多
关键词 Nuclei acids(NA) Neutral red(NR) Ring assembly Solid support surface fluorescence imaging analysis
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手持式XRF在土壤调查修复项目中应用的可靠性分析 被引量:3
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作者 孙中瑾 张莹莹 +6 位作者 叶小瑭 李新元 满伟慧 刘超 史瑞 刘敬兵 王子鸣 《环境工程技术学报》 CAS CSCD 北大核心 2024年第3期1005-1014,共10页
为确定手持式X射线荧光光谱仪(XRF)测量精度和准确度是否能够满足土壤环境快速检测要求,以山东省济宁市某地块土壤污染状况调查项目为背景,分别采用XRF快速检测仪检测和实验室检测方法对浅层土层(0.2~0.5 m)和深层土层(1.5~2.0 m)样品中... 为确定手持式X射线荧光光谱仪(XRF)测量精度和准确度是否能够满足土壤环境快速检测要求,以山东省济宁市某地块土壤污染状况调查项目为背景,分别采用XRF快速检测仪检测和实验室检测方法对浅层土层(0.2~0.5 m)和深层土层(1.5~2.0 m)样品中砷(As)、铜(Cu)、铅(Pb)、锌(Zn)和镍(Ni)5种元素浓度进行检测。结果表明:浅层土层重金属As的XRF检测值普遍高于实验室检测值,Cu、Pb、Zn、Ni的XRF检测值普遍低于实验室检测值,误差普遍在±30%以内;浅层土层的重金属元素XRF检测值与实验室检测值普遍相对偏差(RD为−33.82%~23.53%)及总体相对偏差标准差(6.79~19.52)小于深层土层(分别为−30.26%~98.36%、9.53~49.77),相对偏差的离散程度小于深层土层;浅层土层的重金属的决定系数(R^(2)为0.7762~0.9549)普遍高于深层土层(R^(2)为0.7762~0.9549),相关性高于深层土层。野外使用XRF对土壤样品中重金属进行检测时,所取的土壤样品尽量避免大颗粒,对样品待测面进行压实、压平处理,对于含水率高的样品应适当进行干燥处理,以降低检测误差。虽然手持式XRF检测存在一定误差,但在土壤污染状况调查项目中可以较好地反映土壤元素浓度范围,具有较高的可靠性,可以满足项目土壤快速检测需求。 展开更多
关键词 X射线荧光光谱仪(xrf) 重金属 土壤污染状况 快速检测 可靠性
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Discrimination of marine algal taxonomic groups based on fluorescence excitation emission matrix, parallel factor analysis and CHEMTAX 被引量:1
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作者 CHEN Xiaona SU Rongguo +2 位作者 BAI Ying SHI Xiaoyong YANG Rujun 《Acta Oceanologica Sinica》 SCIE CAS CSCD 2014年第12期192-205,共14页
An in vivo three-dimensional fluorescence method for the determination of algae community structure was developed by parallel factor analysis (PARAFAC) and CHEMTAX. The PARAFAC model was applied to fluo-rescence exc... An in vivo three-dimensional fluorescence method for the determination of algae community structure was developed by parallel factor analysis (PARAFAC) and CHEMTAX. The PARAFAC model was applied to fluo-rescence excitation-emission matrix (EEM) of 60 algae species belonging to five divisions and 11 fluorescent components were identified according to the residual sum of squares and specificity of the composition profiles of fluorescent. By the 11 fluorescent components, the algae species at different growth stages were classified correctly at the division level using Bayesian discriminant analysis (BDA). Then the reference fluo-rescent component ratio matrix was constructed for CHEMTAX, and the EEM-PARAFAC-CHEMTAX method was developed to differentiate algae taxonomic groups. The correct discrimination ratios (CDRs) when the fluorometric method was used for single-species samples were 100% at the division level, except for Bacil-lariophyta with a CDR of 95.6%. The CDRs for the mixtures were above 94.0% for the dominant algae species and above 87.0% for the subdominant algae species. However, the CDRs of the subdominant algae species were too low to be unreliable when the relative abundance estimated was less than 15.0%. The fluorometric method was tested using the samples from the Jiaozhou Bay and the mesocosm experiments in the Xiaomai Island Bay in August 2007. The discrimination results of the dominant algae groups agreed with microscopy cell counts, as well as the subdominant algae groups of which the estimated relative abundance was above 15.0%. This technique would be of great aid when low-cost and rapid analysis is needed for samples in a large batch. The fluorometric technique has the ability to correctly identify dominant species with proper abundance both in vivo and in situ. 展开更多
关键词 CHEMTAX fluorescence excitatiqn-emission matrices in vivo fluorescent components parallel factor analysis PHYTOPLANKTON
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Comparison of three-dimensional fluorescence analysis methods for predicting formation of trihalomethanes and haloacetic acids 被引量:4
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作者 Nicolás M.Peleato Robert C.Andrews 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2015年第1期159-167,共9页
This work investigated the application of several fluorescence excitation–emission matrix analysis methods as natural organic matter(NOM) indicators for use in predicting the formation of trihalomethanes(THMs) an... This work investigated the application of several fluorescence excitation–emission matrix analysis methods as natural organic matter(NOM) indicators for use in predicting the formation of trihalomethanes(THMs) and haloacetic acids(HAAs). Waters from four different sources(two rivers and two lakes) were subjected to jar testing followed by 24 hr disinfection by-product formation tests using chlorine. NOM was quantified using three common measures: dissolved organic carbon, ultraviolet absorbance at 254 nm, and specific ultraviolet absorbance as well as by principal component analysis, peak picking,and parallel factor analysis of fluorescence spectra. Based on multi-linear modeling of THMs and HAAs, principle component(PC) scores resulted in the lowest mean squared prediction error of cross-folded test sets(THMs: 43.7(μg/L)^2, HAAs: 233.3(μg/L)^2). Inclusion of principle components representative of protein-like material significantly decreased prediction error for both THMs and HAAs. Parallel factor analysis did not identify a protein-like component and resulted in prediction errors similar to traditional NOM surrogates as well as fluorescence peak picking. These results support the value of fluorescence excitation–emission matrix–principal component analysis as a suitable NOM indicator in predicting the formation of THMs and HAAs for the water sources studied. 展开更多
关键词 Natural organic matter fluorescence Principal component analysis PARAFAC Disinfection byproducts Drinking water
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Impact of Different Grinding Aids on Standard Deviation in X-Ray Fluorescence Analysis of Cement Raw Meal 被引量:3
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作者 Andrew Aondoaver Tyopine Aondo Joseph Wangum Edwin Ameh Idoko 《American Journal of Analytical Chemistry》 2015年第5期492-494,共3页
X-ray fluorescence (XRF) analysis utilizes particle size which is resulted from milling of a material. The milling ensures uniform and fine grained powder. The finer and more uniform the particle size is, the better t... X-ray fluorescence (XRF) analysis utilizes particle size which is resulted from milling of a material. The milling ensures uniform and fine grained powder. The finer and more uniform the particle size is, the better the result and easier it is for material quality control. To ensure uniformity in particle size and finer powder, a comparative analysis was conducted with different grinding aids and pressed pellet method was used in obtaining analysis results. Pressed pellets of cement raw meal sample milled with different grinding aids (graphite, aspirin and lithium borate) were subjected to XRF. Graphite produced better particle size uniformity with a corresponding standard deviation that made quality control of raw meal easier and better than aspirin and lithium borate. 展开更多
关键词 X-Ray fluorescence Pressed PELLETS Standard Deviation GRINDING AID Particle Size UNIFORMITY Comparative analysis Cement RAW MEAL Quality Control
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Evaluation of Dissolved Organic Carbon Using Synchronized Fluorescence Emission Spectra and Unsupervised Method of Principal Component Analysis (PCA) and Independent Component Analysis (ICA) 被引量:1
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作者 Tais Cristina Filippe Luana Mayumi Takahasi Marques +2 位作者 Heloise G. Knapik Júlio César Rodrigues de Azevedo Jorge Costa Pereira 《Journal of Water Resource and Protection》 2019年第3期244-279,共36页
Dissolved organic matter (DOM) can be originated from autochthonous or allochthonous sources, where allochthonous DOM can be from pedogenic sources (humic substances—HSs) or anthropogenicsources (wastewater). The ana... Dissolved organic matter (DOM) can be originated from autochthonous or allochthonous sources, where allochthonous DOM can be from pedogenic sources (humic substances—HSs) or anthropogenicsources (wastewater). The analysis of fluorescence emission, excitation, synchronous or excitation-emission matrix (EEM) have been used to identify the main source or probable contribution of dissolved compounds, such as humic acids (HA), fulvic acids (FA) and dissolved organic carbon (DOC) from sewage, but does not quantify. Fluorescence emission is a powerful technique to detect and qualify organic dissolved compounds but fails in quantitative aspects. In this work, we propose an in situ method for direct determination of DOC using synchronous fluorescence spectra with independent component analysis (ICA). Well known standard solutions were used for method development and validation. In this work, we show that it is possible to predict the number of independent contributions using an unsupervised method based on iterative Principal Component Analysis and Independent Component Analysis (PCA-ICA) approach over combined matrix results. Within these results it’s also possible to see that with a very small amount of independent components it is possible to describe environmental samples of HA, FA and primary productivity (PP). 展开更多
关键词 INDEPENDENT Component analysis Dissolved ORGANIC Carbon SPECTRA DECONVOLUTION Synchronized fluorescence
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