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An economical and flexible chip using surface-enhanced infrared absorption spectroscopy for pharmaceutical detection:Combining qualitative analysis and quantitative detection
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作者 Jikai Wang Pengfei Zeng +3 位作者 Haitao Xie Suisui He Xilin Xiao Cuiyun Yu 《Journal of Pharmaceutical Analysis》 2025年第2期474-476,共3页
Infrared(IR)spectroscopy,a technique within the realm of molecular vibrational spectroscopy,furnishes distinctive chemical signatures pivotal for both structural analysis and compound identification.A notable challeng... Infrared(IR)spectroscopy,a technique within the realm of molecular vibrational spectroscopy,furnishes distinctive chemical signatures pivotal for both structural analysis and compound identification.A notable challenge emerges from the misalignment between the mid-IR light wavelength range and molecular dimensions,culminating in a constrained absorption cross-section and diminished vibrational absorption coefficients(Supplementary data). 展开更多
关键词 pharmaceutical detection quantitative detection structural analysis surface enhanced infrared absorption spectroscopy qualitative analysis chemical signatures infrared spectroscopy molecular vibrational spectroscopyfurnishes
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Qualitative and quantitative analysis of four different polarity fractions from Huang-Lian-Jie-Du-Decoction by HPLC-DAD-ESI-MS/MS and their related neuroprotective effects 被引量:6
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作者 杨阳 赵海誉 +4 位作者 王宏洁 宋建芳 杨健 司南 边宝林 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2013年第4期334-341,共8页
Huang-Lian-Jie-Du-Decoction (HLJDD) has been widely used for the treatment of Alzheimer's disease (AD) in clinic. However, the relationship between its chemical profile and neuroprotective bioactivity was not cle... Huang-Lian-Jie-Du-Decoction (HLJDD) has been widely used for the treatment of Alzheimer's disease (AD) in clinic. However, the relationship between its chemical profile and neuroprotective bioactivity was not clearly clarified yet. In present study, the water extract of HLJDD and subsequent three polarity fractions divided by different reagents were investigated. A total of 17 chromatographic peaks were confirmed by comparison with standards and their UV, MS spectra. Among them, 11 major compounds were determined by HPLC-DAD method with good linear regression relationship (r2, 0.9994-0.9999), precisions (inter-day precision RSD, 0.79%-1.07%; intra-day precision RSD, 1.59%-2.10%), repeatability (RSD, 1.66%-3.67%), stability (RSD, 1.26%-4.77%) and recovery (95.24%-105.41%, RSD, 0.29%-2.69%). Furthermore, PC12 cells and primary neurons cells were used for the neuroprotective effective assessment of aforementioned four samples from HLJDD. 3"he total aqueous extract and n-butanol extract of HLJDD presented more significant effects than the other two parts. According to their quality and quantity determination results, iridoids and alkaloids have a positive correlation with the neuroprotective effectiveness of HLJDD. 展开更多
关键词 Huang-Lian-Jie-Du-Decoction qualitative and quantitative analysis Neuroprotective effects
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Qualitative and Quantitative Analysis of Alkaloids in Cortex Phellodendri by HPLC-ESI-MS/MS and HPLC-DAD 被引量:20
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作者 ZHU Shuang-lai DOU Sheng-shan +6 位作者 LIU Xin-ru LIU Run-hui ZHANG Wei-dong HUANG Hong-lin ZHANG Yi HU Yao-hua WANG Shu-ping 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2011年第1期38-44,共7页
A combined method of high performance liquid chromatograph-elecrtrospray-ionization mass spectrometer(HPLC-ESI-MS/MS) coupled with a photodiode array detector(HPLC-DAD) and principal component analysis(PCA) was ... A combined method of high performance liquid chromatograph-elecrtrospray-ionization mass spectrometer(HPLC-ESI-MS/MS) coupled with a photodiode array detector(HPLC-DAD) and principal component analysis(PCA) was applied to the qualitative and quantitative analyses of alkaloids in Cortex Phellodendri(CP) samples, and to the differentiation of two species of CP, Cortex Phellodendri Chinensis(CPC) and Cortex Phellodendri Amurensis(CPA). Twenty-two peaks appeared in the HPLC-MS base peak chromatogram of CP detected by the HPLC-ESI-MS/MS analysis, and the alkaloids were identified according to the MSn data, the known MS fragmentation rules and the literature data. Five alkaloids including berberine, palmatine, jatrorrhizine, phellodendrine and magnoflorine were simultaneously determinated by the HPLC-DAD. Berberine was the primary component in all CP samples, and the contents of berberine and palmatine were exploited to be two critical parameters for effective discrimination between the two species of CP. The average content of berberine in CPC(58.75 mg/g) was higher than that in CPA(9.16 mg/g), while the content of palmatine was less, only 0.25 mg/g in CPC and 4.19 mg/g in CPA. With the use of PCA, samples datasets were separated successfully into two different clusters corresponding to the two species, and berberine, pahnatine, phellodendrine and magnoflorine contribute most to the above mentioned calssifying . The proposed method oroved to be a useful tool in the aualitv control of Chinese herbal medicines. 展开更多
关键词 Cortex Phellodendri ALKALOID HPLC-ESI-MS/MS quantitative analysis qualitative analysis Principal component analysis
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Qualitative and Quantitative Analysis of Linoleic Acid in Polygonati Rhizoma 被引量:2
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作者 ZHOU Zhun YUAN Han-Wen +8 位作者 PENG Cai-Yun JIAN Yu-Qing ZHOU Xu-Dong LI Bin SHENG Wen-Bing GONG Li-Min HE Shu-Jin WANG Wei LIU Chang-Xiao 《Digital Chinese Medicine》 2020年第3期180-187,共8页
Objective To explore the major compound in Polygonati Rhizoma(Huang Jing,黄精)for quality control.Methods The major compound was isolated and analyzed by liquid chromatography-mass spectrometry(LC-MS),and subsequently... Objective To explore the major compound in Polygonati Rhizoma(Huang Jing,黄精)for quality control.Methods The major compound was isolated and analyzed by liquid chromatography-mass spectrometry(LC-MS),and subsequently further identified by nuclear magnetic resonance(NMR).Thin layer chromatography(TLC)was optimized based on the previous methods reported in the Chinese Pharmacopeia(2015 edition).Results The major compound was isolated from the natural material and identified as linoleic acid.A high performance liquid chromatography(HPLC)method with robust linearity(R2=0.9997),specificity,precision,stability,repeatability and recovery was developed for linoleic acid determination.TLC chromatogram was improved significantly after optimization for qualitative analysis.Conclusions The optimized TLC method is practical and can be adopted for quality control of Polygonati Rhizoma(Huang Jing,黄精).The levels of linoleic acid vary between species of Polygonati Rhizoma(Huang Jing,黄精),with Polygonatum cyrtonema Hua(Jiang Xing Huang Jing,姜型黄精)showing the highest contents.This study provides valuable information for quality control of Polygonati Rhizoma(Huang Jing,黄精). 展开更多
关键词 Polygonati Rhizoma(Huang Jing 黄精) Linoleic acid qualitative analysis quantitative analysis Thin layer chromatography(TLC) High performance liquid chromatography(HPLC)
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Qualitative and quantitative analysis ofβ-sitosterol marker in virgin camellia oil and virgin olive oil 被引量:2
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作者 李阳 吴旻谕 +2 位作者 翟量 张辉 沈立荣 《Food Quality and Safety》 SCIE CAS CSCD 2023年第4期579-587,共9页
Camellia oil and olive oil with superior economic value are easily adulterated with other,cheaper oils.It is difficult to identify both oils by traditional methods because of their similar fatty acid profiles.In the p... Camellia oil and olive oil with superior economic value are easily adulterated with other,cheaper oils.It is difficult to identify both oils by traditional methods because of their similar fatty acid profiles.In the present study,a novel method for qualitative and quantitative analysis ofβ-sitosterol using GC/MS and GC/FID was developed to identify camellia oil and olive oil.The method validation ofβ-sitosterol analysis showed good linearity and satisfactory values for recovery,accuracy,precision,and repeatability.The linear regression coefficient(R^(2))of the calibration curve was 0.9985.An acceptable limit of detection(0.36 mg/100 g)and limit of quantification(1.20 mg/100 g)were achieved.The spiked recoveries were 95.0%to 100.3%.The relative standard deviation(RSD)of within-day precision was less than 3.26%,and the RSD of retention times and peak areas for repeatability were within 0.03%and 1.08%,respectively.The contents ofβ-sitosterol in virgin camellia oil and virgin olive oil were in the range of 14.1–30.2 mg/100 g and 94.3–173.2 mg/100 g,respectively,indicating that theβ-sitosterol content in the former is seven times that in the latter,andβ-sitosterol could be a potential marker for the authentication and adulteration detection of both oils. 展开更多
关键词 Β-SITOSTEROL virgin camellia oil(VCO) virgin olive oil(VOO) qualitative analysis quantitative analysis
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Qualitative and quantitative analysis of atmospheric methanol using a continuous-wave terahertz spectrometer 被引量:2
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作者 Han Zhang Zhaohui Zhang +4 位作者 Xiaoyan Zhao Xiaotong Zhang Tianyao Zhang Can Cao Yang Yu 《Chinese Optics Letters》 SCIE EI CAS CSCD 2018年第10期74-78,共5页
We present a specific-window method to subtract the interference of water vapor on terahertz frequency-domain spectroscopy(THz-FDS) at ambient temperature and pressure. A continuous-wave spectrometer based on photom... We present a specific-window method to subtract the interference of water vapor on terahertz frequency-domain spectroscopy(THz-FDS) at ambient temperature and pressure. A continuous-wave spectrometer based on photomixing was utilized to obtain THz-FDS of methanol vapor in the range of 50–1200 GHz. The distinctly spaced absorption features in the neighborhood of atmospheric windows of transparency were selected to perform linear fitting versus the calculated absorption cross section and obtain the concentration of methanol. Furthermore, the gradually decreased methanol vapor was quantified to demonstrate the reliability of the method. 展开更多
关键词 THz qualitative and quantitative analysis of atmospheric methanol using a continuous-wave terahertz spectrometer
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Qualitative and semi-quantitative analysis of health-care pharmaceutical products using laser-induced breakdown spectroscopy 被引量:1
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作者 Sobia Nisar Ghulam Dastgeer +1 位作者 Muhammad Shafiq Muhammad Usman 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2019年第1期20-24,共5页
Laser-induced breakdown spectroscopy(LIBS) is a sensitive optical technique that is capable of rapid multi-elemental analysis. The development of this technique for elemental analysis of pharmaceutical products may ev... Laser-induced breakdown spectroscopy(LIBS) is a sensitive optical technique that is capable of rapid multi-elemental analysis. The development of this technique for elemental analysis of pharmaceutical products may eventually revolutionize the field of human health. Under normal circumstances, the elemental analysis of pharmaceutical products based on chemical methods is time-consuming and complicated. In this investigation, the principal aim is to develop an LIBS-based methodology for elemental analysis of pharmaceutical products. This LIBS technique was utilized for qualitative as well as quantitative analysis of the elements present in Ca-based tablets. All the elements present in the tablets were detected and their percentage compositions were verified in a single shot, using the proposed instrument. These elements(e.g., Ca, Mg, Fe, Zn, and others) were identified by the wavelengths of their spectral lines, which were verified using the NIST database. The approximate amount of each element was determined based on their observed peaks and the result was in exact agreement with the content specification. The determination of the composition of prescription drug for patients is highly important in numerous circumstances. For example, the exploitation of LIBS may facilitate elemental decomposition of medicines to determine the accuracy of the stated composition information. Moreover, the approach can provide element-specific, meaningful, and accurate information related to pharmaceutical products. 展开更多
关键词 LASER-INDUCED BREAKDOWN spectroscopy Elements identification HEALTH-CARE PHARMACEUTICS qualitative analysis quantitative analysis
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Consequences of Insufficient Selectivity in Quantitative and Qualitative Chemical Analysis
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作者 Mats Larsson Göran Nilsson 《Journal of Analytical Sciences, Methods and Instrumentation》 2023年第2期13-25,共13页
A problem in chemical analysis in connection with measurements of a substance normally occurring in a sample, or identification of a substance which should not exist in a sample, is insufficient selectivity. In this a... A problem in chemical analysis in connection with measurements of a substance normally occurring in a sample, or identification of a substance which should not exist in a sample, is insufficient selectivity. In this article, we analyze this problem and propose remedies. We use a real doping case to illustrate how chemical noise causes a serious selectivity problem, probably causing a false positive outcome. 展开更多
关键词 Chemical analysis quantitative and qualitative Selectivity Chemical Measurement Procedures Measurement Errors Chemical Noise
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Meta-analysis evidence supporting foot reflexology for nausea and vomiting management:Additional insights to recent systematic review
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作者 Vaishnu Karthik KAMARAJ Yeswanth Kumaran VENKATACHALAM +1 位作者 Deenadayalan BOOPALAN Maheshkumar KUPPUSAMY 《Journal of Integrative Nursing》 2025年第3期179-180,共2页
Dear Editor,We read with a great interest the recently published systematic review by Shamsikhani and Hosseini titled,“Foot reflexology on nausea and vomiting:A systematic review.”[1]While the authors provided a com... Dear Editor,We read with a great interest the recently published systematic review by Shamsikhani and Hosseini titled,“Foot reflexology on nausea and vomiting:A systematic review.”[1]While the authors provided a comprehensive qualitative synthesis of six studies meeting their inclusion criteria,we believe that additional quantitative analysis would strengthen the evidence base for foot reflexology in managing nausea and vomiting.We conducted a complementary meta-analysis to provide quantitative evidence supporting the qualitative findings presented in the systematic review. 展开更多
关键词 qualitative synthesis NAUSEA meta analysis foot reflexology systematic review quantitative analysis evidence base
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The research of mine rock burst hazard identification based on fault tree analysis
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作者 李文 纪洪广 +1 位作者 程久龙 蔡嗣经 《Journal of Coal Science & Engineering(China)》 2007年第4期544-546,共3页
In order to identify the rock burst hazard in coalmine and thus to give a credible forecast, firstly, analyzed such effect factors as natural geological factors and mining technological conditions based on the investi... In order to identify the rock burst hazard in coalmine and thus to give a credible forecast, firstly, analyzed such effect factors as natural geological factors and mining technological conditions based on the investigation of more than one hundred mine rock burst cases. Secondly, adopted the fault tree analysis (FTA) technology to the mine rock burst hazard identification for the first time and confirmed twelve kinds of basic events, that is, the large mining depth, the burst-orientation coal seams, the solid strata of roof and bottom, near the faults with bigger fall, the folds, the change of seam thickness, other regional tectonics transformation or stress strip, the drilling, blasting and extracting operation, the unscientific extracting methods, the illogical extracting sequence, the residual pillars and the too close distance between the working face and the residual areas or the stopping extracting lines. Moreover, worked out the fault tree of mine rock burst. At last, it made qualitative analysis and quantitative analysis and forecasted the rock burst hazard according to the characteristic of geologic structure and exploitation technology conditions in certain mine of Shandong Province, China, the rock burst accidents happened in the following exploitation validated that it is of feasibility and veracity adopting FTA to identify the mine rock burst hazard. 展开更多
关键词 rock burst fault tree qualitative analysis quantitative analysis
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On Improving Students' Listening Proficiency From Correlation Analysis Between English Listening and Other English Skills
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作者 ZHAI Yong-li 《Sino-US English Teaching》 2013年第4期334-338,共5页
Researches have proved that in human beings' actual languange communication, listening is the most important part. However, in English learning, listening seems always to be a weakness for many Chinese students. Engl... Researches have proved that in human beings' actual languange communication, listening is the most important part. However, in English learning, listening seems always to be a weakness for many Chinese students. English learning is a systematic process, during which, English listening proficience is influeced by many factors. Therefore, from the systematicness and inner relations in English learning and based on qualitative analysis and quantitative analysis between English listening and other English skills in English listening, this paper tries to give the correlation analysis and accordingly give some suggestions to improve listening proficiency for ESL (English as a second language) learners 展开更多
关键词 English listening quantitative analysis qualitative analysis language skills
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Advantages and Disadvantages of Quantitative and Qualitative Information Risk Approaches
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作者 Stroie Elena Ramona 《Chinese Business Review》 2011年第12期1106-1110,共5页
Due to rapidly development of information systems, risk and security issues have increased and became a phenomenon that concerns every organization, without considering the size of it. To achieve desired results, mana... Due to rapidly development of information systems, risk and security issues have increased and became a phenomenon that concerns every organization, without considering the size of it. To achieve desired results, managers have to implement methods of evaluating and mitigating risk as part of a process well elaborated. Security risk management helps managers to better control the business practices and improve the business process. An effective risk management process is based on a successful IT security program. This doesn't mean that the main goal of an organization's risk management process is to protect its IT assets, but to protect the organization and its ability to perform their missions. During this process, managers have to take into consideration risks that can affect the organization and apply the most suitable measures to minimize their impact. The most important task is choosing the best suited method for analyzing the existing risk properly. Several methods have been developed, being classified in quantitative and qualitative approaches of evaluating risk. The purpose of this paper is to present the advantages and disadvantages of each approach taking current needs and opportunities into consideration. 展开更多
关键词 risk management risk analysis risk assessment quantitative approach qualitative approach
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气相色谱-质谱联用法检测减肥保健食品中非法添加的氯卡色林
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作者 李想 蔺婉轩 +4 位作者 宋辉 夏鑫鑫 朱昱 于蔚常 张睿文 《中国药物依赖性杂志》 2025年第3期185-190,共6页
目的建立气相色谱-质谱联用(GC/MS)法对可疑减肥片剂和减肥饮品中的氯卡色林进行定性定量检测,并进行方法学考察。方法选择HP-5MS色谱柱,柱温120℃,保持1 min,以10℃/min升温至170℃,保持1 min,再以30℃/min升温至280℃,保持10 min,氯... 目的建立气相色谱-质谱联用(GC/MS)法对可疑减肥片剂和减肥饮品中的氯卡色林进行定性定量检测,并进行方法学考察。方法选择HP-5MS色谱柱,柱温120℃,保持1 min,以10℃/min升温至170℃,保持1 min,再以30℃/min升温至280℃,保持10 min,氯卡色林及内标物色谱峰色谱行为良好。结果空白片剂添加氯卡色林浓度在2.0~100.0μg/mg范围内均呈良好线性,空白饮品添加浓度在2.0~100.0μg/mL范围内均呈良好线性,片剂和饮品回归方程相关系数r^(2)都在0.9991以上,检出限为1.5μg/mL,定量限为5.0μg/mL,空白片剂粉末添加回收率在82.5%~113.4%之间,相对标准偏差(RSD)为4.2%~6.7%。饮品空白添加回收率在82.9%~104.0%之间,RSD为3.9%~6.2%。结论所建方法适用于法庭科学领域同类检材当中氯卡色林的定性定量检验鉴定。 展开更多
关键词 气相色谱-质谱联用 保健食品 氯卡色林 定性定量分析
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基于核磁共振法对阿立哌唑片定性及定量分析
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作者 杨娜 方洁芸 +2 位作者 朱俊麟 席坤强 郝海军 《化学研究与应用》 北大核心 2025年第12期3825-3830,共6页
采用核磁共振法(NMR)对阿立哌唑片同时进行定性鉴别及定量分析。采用CDCl3提取阿立哌唑片成分,分别测试氢谱(^(1)H NMR)、碳谱(13C NMR)及异核单量子相关谱(HSQC)。选择对苯二甲酸二甲酯化学位移δ:8.05~8.22处质子峰为内标峰,阿立哌唑... 采用核磁共振法(NMR)对阿立哌唑片同时进行定性鉴别及定量分析。采用CDCl3提取阿立哌唑片成分,分别测试氢谱(^(1)H NMR)、碳谱(13C NMR)及异核单量子相关谱(HSQC)。选择对苯二甲酸二甲酯化学位移δ:8.05~8.22处质子峰为内标峰,阿立哌唑化学位移δ:6.28~6.41处为定量峰,采集定量核磁共振氢谱(^(1)H qNMR),对内标峰和定量峰积分后计算阿立哌唑片含量。结果显示,阿立哌唑片提取成分的核磁共振信息与阿立哌唑一致。建立的^(1)H qNMR定量峰和内标峰不受其他质子峰干扰,专属性高,精密度和稳定性良好,阿立哌唑线性范围是2.58~16.68 mg·mL^(-1),平均回收率为100.38%,RSD为1.61%。^(1)H qNMR法与HPLC法的测定结果基本一致。因此,核磁共振法可对阿立哌唑片同时进行定性及定量分析,为生产、检验提供了一种简便快捷的分析方法。 展开更多
关键词 阿立哌唑 对苯二甲酸二甲酯 核磁共振法 定性鉴别 定量分析
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多种气相色谱定量分析方法同步应用于中药制剂中有效成分的测定
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作者 彭淑女 李华敏 +1 位作者 陈招斌 王翊如 《大学化学》 2025年第10期243-249,共7页
本文改进了一个用气相色谱法分离分析中药制剂中五种主要成分桉叶油醇、樟脑、薄荷醇、水杨酸甲酯、丁香酚含量的本科仪器分析实验。提出同时用内标法、外标法、归一化法对同一组数据文件进行定量并判断定量结果的准确性,使学生能在有... 本文改进了一个用气相色谱法分离分析中药制剂中五种主要成分桉叶油醇、樟脑、薄荷醇、水杨酸甲酯、丁香酚含量的本科仪器分析实验。提出同时用内标法、外标法、归一化法对同一组数据文件进行定量并判断定量结果的准确性,使学生能在有限的教学时间内掌握色谱基础的定性定量方法,了解不同定量分析方法的适用范围,学会计算理论塔板数及分离度等。本实验将基本的色谱理论知识融入生活用品风油精等中药制剂的主成分分析中,使学生真切感受学以致用,且绿色环保,有利于培养学生分析实验数据的能力。 展开更多
关键词 气相色谱 风油精 仪器分析实验 定性定量方法
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基于近红外结合化学计量学构建甘草二氧化硫残留量分析模型
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作者 张怀辉 马睿 +3 位作者 张云蓉 唐小涵 孟从燕 侯英 《云南化工》 2025年第5期117-122,共6页
目的:实现甘草二氧化硫残留的准确快速无损定性和定量分析。方法:基于有无二氧化硫残留甘草近红外光谱差异性信息,结合偏最小二乘判别和偏最小二乘回归,分别建立了甘草二氧化硫残留的定性识别和定量模型,并用模型内部参数和外部测试集... 目的:实现甘草二氧化硫残留的准确快速无损定性和定量分析。方法:基于有无二氧化硫残留甘草近红外光谱差异性信息,结合偏最小二乘判别和偏最小二乘回归,分别建立了甘草二氧化硫残留的定性识别和定量模型,并用模型内部参数和外部测试集样品预测结果对模型的准确性和稳定性进行了评价。结果:1)有无二氧化硫残留甘草近红外光谱波数在7231.8、7162.3、7112.2、6946.3 cm^(-1)(亚甲基的C—H,脂肪烃)、6047.7、5962.8 cm^(-1)(羰基相连甲基的C—H,酮)、5881.8 cm^(-1)(与醚相连甲基的C—H,醚或醇)、5797.0 cm^(-1)(亚甲基的C—H,烃、亚甲基)、5287.9、5183.7、4948.5、4855.9 cm^(-1)(酰胺的HN…O C,蛋白质)、4763.3 cm^(-1)[聚合体(C O和C—O伸缩)C O—O,多糖]、4485.6、4385.3 cm^(-1)[淀粉(·C—H和CH_(2))的C—H,多糖]、4312.1 cm^(-1)[支链烃RC(CH_(3))3或RCH(CH_(3))_(2)亚甲基的C—H,烃类、脂肪烃]、4173.2、4049.8cm^(-1)(支链烃亚甲基的C—H,蛋白质、脂肪烃)处存在差异,与甘草多糖、黄酮类化合物和香豆素类化合物含量变化相关。2)建立的是否有二氧化硫残留甘草的近红外PLS-DA模型的R^(2)X、R^(2)Y和Q^(2)分别为0.999、0.979和0.985,200次交互验证表明模型未出现过拟合。3)建立的甘草二氧化硫残留近红外PLS模型决定系数R^(2)为0.973,校正标准误差为2.670 mg/kg,交互验证均方根误差(Root Mean Square Error of Cross Validation,RMSECV)为3.042 mg/kg;在0.05显著水平下,14个外部测试样品的模型预测值与参考方法测定值间的配对t检验表明,两种方法的测定结果间无明显差异,测试集样品的预测平均相对误差为4.68%。结论:研究建立的甘草二氧化硫残留定性和定量模型具有较好的稳定性和准确性,为甘草二氧化硫残留的定性定量检测提供了一种准确、快速、无损的检测方法。 展开更多
关键词 甘草 二氧化硫残留 近红外 定性分析 定量分析
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反复加卸荷煤体氧化特性研究 被引量:1
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作者 陈雷 周福宝 +3 位作者 郭再富 张晴 阎露璐 潘荣锟 《矿业安全与环保》 北大核心 2025年第2期30-38,共9页
为研究采动载荷煤体因力学特性和孔裂隙变化发生初期氧化的演化规律,采用煤岩三轴蠕变、程序升温实验和FTIR、AFM技术对易自燃原煤样、反复加卸荷煤样进行氧化宏微观参数对比分析。研究表明,加卸荷煤样升温氧化过程中耗氧量和CO产生速... 为研究采动载荷煤体因力学特性和孔裂隙变化发生初期氧化的演化规律,采用煤岩三轴蠕变、程序升温实验和FTIR、AFM技术对易自燃原煤样、反复加卸荷煤样进行氧化宏微观参数对比分析。研究表明,加卸荷煤样升温氧化过程中耗氧量和CO产生速率均较前一实验条件增加,低温阶段,指标性气体参数值“骤降”和“陡升”点对应的临界温度值逐渐减小,加卸荷3次和加卸荷2次煤样较前一实验条件煤样增幅减小。随着加卸荷次数增加,氧化煤样中芳香烃含量逐渐增多,脂肪烃含量逐渐减少,羟基先减少后增多,羧基—COOH和羰基—C=O波峰呈“马鞍”状,由此判断出煤样氧化进程加快。煤体BJH比表面积、孔容值和吸附—脱附差量逐渐增大,可表征加卸荷作用致煤样中微孔增加,中孔、大孔塌陷裂变。加卸荷前3次较前一实验条件煤样的微观孔隙结构参数值增幅先增大后减小最终趋为0,综合加卸荷4次实验分析结果,推断出,随着加卸荷次数的增加,煤体的微观孔隙结构参数值有减小的趋势,可证实存在最优的加卸荷次数(≥3次)和BJH比表面积(≥27.002 m^(2)/g)使煤体氧化自燃能力最强。采掘工作面前方、煤层保护层及相邻近煤层受重复采动的影响,煤体孔裂隙再发育贯通性增强,破碎程度升高,氧化自燃的潜在危险性增大。 展开更多
关键词 深部开采 原煤氧化 反复加卸荷 微观结构 定性定量分析
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基于近红外光谱技术的文冠果油人工掺杂快速分析研究 被引量:2
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作者 陈启文 向超群 +3 位作者 李欣怡 余丹华 王乐琪 肖雪 《分析测试学报》 北大核心 2025年第2期253-258,共6页
该研究以文冠果油为例,以5%为梯度,人工制备文冠果油含量为0%~100%的文冠果油掺杂样品并采集其近红外光谱图。针对文冠果油掺杂油的鉴别问题,采用偏最小二乘法-判别分析(PLS-DA)构建不同品种掺杂油的识别方法,结合不同预处理方法比较优... 该研究以文冠果油为例,以5%为梯度,人工制备文冠果油含量为0%~100%的文冠果油掺杂样品并采集其近红外光谱图。针对文冠果油掺杂油的鉴别问题,采用偏最小二乘法-判别分析(PLS-DA)构建不同品种掺杂油的识别方法,结合不同预处理方法比较优选并优化了模型性能。采用偏最小二乘回归法(PLSR)构建掺杂油的掺杂比例预测模型,结合不同光谱预处理方法和不同波长选择方法优选并优化了模型性能。结果表明,通过卷积一阶导数预处理(1^(st) Dec),PLS-DA模型鉴别不同品种掺杂油达到了98%的准确率;结合1^(st) Dec和竞争自适应重加权采样变量选择(CARS),文冠果油中不同品种掺杂油的近红外光谱模型的相对分析误差(RPD)分别为5.90、40.00、5.20和4.90,显示出良好的预测性能。该研究实现了文冠果油样品在不同掺杂品种和比例下的定性定量分析,为文冠果油掺杂的质量快检开展了探索性研究。 展开更多
关键词 文冠果油 掺杂 近红外光谱 定性分析 定量分析
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基于定性、定量及化学模式识别分析的蒙药森登-4质量评价 被引量:2
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作者 周枫叶 李君 +5 位作者 张谦 李荣杰 张微 刘静 王芳 李胜男 《中国药房》 北大核心 2025年第9期1040-1045,共6页
目的基于定性、定量及化学模式识别分析对蒙药森登-4进行质量评价,以期为其质量控制提供参考。方法采用高效液相色谱-四极杆/静电场轨道阱高分辨质谱(HPLC-Q-Exactive-MS)技术对森登-4中化学成分进行定性分析;采用高效液相色谱串联质谱(... 目的基于定性、定量及化学模式识别分析对蒙药森登-4进行质量评价,以期为其质量控制提供参考。方法采用高效液相色谱-四极杆/静电场轨道阱高分辨质谱(HPLC-Q-Exactive-MS)技术对森登-4中化学成分进行定性分析;采用高效液相色谱串联质谱(HPLC-MS/MS)技术定量分析15批森登-4样品(S1~S15)中16个成分(没食子酸甲酯、没食子酸乙酯、表儿茶素、二氢杨梅素、京尼平-1-O-β-D-龙胆双糖苷、咖啡酸、儿茶素、柯里拉京、去乙酰车叶草苷酸甲酯、芦丁、栀子苷、木犀草素、杨梅素、槲皮素、阿魏酸、川楝素)的含量;对15批样品进行聚类分析、主成分分析、正交偏最小二乘-判别分析,并以变量重要性投影(VIP)值大于1为标准筛选差异性成分。结果在森登-4中共鉴定出73个化学成分,包括20个黄酮类、16个鞣质类、14个有机酸类成分等。定量分析结果显示,上述16个成分的含量分别为3.683~7.730、2.391~6.952、2275.538~4377.491、2699.188~3537.924、858.266~1377.393、3.366~11.003、140.624~315.683、414.629~978.334、285.501~1510.457、27.799~48.325、3625.415~6309.563、0.506~0.656、442.337~649.283、47.093~59.736、12.942~15.822、127.738~326.649μg/g。聚类分析和主成分分析结果显示,15批森登-4样品可聚为2类:S1~S3、S5~S6、S9~S10、S13样品聚为一类,S4、S7~S8、S11~S12、S14~S15样品聚为另一类;表儿茶素、京尼平-1-O-β-D-龙胆双糖苷、去乙酰车叶草苷酸甲酯、栀子苷的VIP值大于1。结论本研究采用HPLC-Q-Exactive-MS和HPLC-MS/MS技术对森登-4进行了定性、定量分析,并结合化学模式识别分析筛选出了栀子苷、表儿茶素、去乙酰车叶草苷酸甲酯、京尼平-1-O-β-D-龙胆双糖苷4个差异性成分。 展开更多
关键词 森登-4 定性分析 定量分析 化学模式识别分析 含量测定 质量评价 差异性成分
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山楂果实生长期挥发性成分变化趋势及评价
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作者 刘天祎 王玉春 +1 位作者 李存满 任杰 《药物分析杂志》 北大核心 2025年第3期417-425,共9页
目的:探究生长时期山楂果实中挥发性成分的生长变化趋势。方法:采用气相色谱-质谱联用法(GC-MS)对不同生长阶段山楂果实中的挥发性成分进行定量定性分析,考察其动态变化并进行统计分析。色谱柱为HP-5(30 m×0.32 mm,0.25μm),柱温... 目的:探究生长时期山楂果实中挥发性成分的生长变化趋势。方法:采用气相色谱-质谱联用法(GC-MS)对不同生长阶段山楂果实中的挥发性成分进行定量定性分析,考察其动态变化并进行统计分析。色谱柱为HP-5(30 m×0.32 mm,0.25μm),柱温为程序升温(初温60℃,以10℃·min^(-1)的速率升温至250℃,保持33 min),进样口温度为280℃。离子源为电子轰击源(EI),离子源温度为230℃。结果:果实中共测出57个代表性挥发性成分,其中16个成分在生长前期存在,后期消失;有12个成分在生长前期不存在。11-癸基-二十四烷含量最高且逐渐升高,丙烯酸十六酯含量逐渐降低。结论:本文对山楂成分在生长期的动态变化的考察,为进一步合理开发和利用山楂果实提供参考。 展开更多
关键词 山楂果实 挥发性成分 气相色谱质谱联用 生长期 定性定量分析 统计分析
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