| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 61 | 基于傅里叶变换中红外光谱识别正常食用植物油和精炼潲水油的方法 | CN201310629904.6 | 2013-11-29 | CN103592256A | 2014-02-19 | 屠大伟; 李红; 赵博; 冉晓鸿; 李沿飞; 吴彦蕾; 周彦伶 |
| 本发明公开了一种基于傅里叶变换中红外光谱快速识别正常食用植物油和精炼潲水油的方法。该方法包括以下步骤：先取已知的正常食用油和精炼潲水油样品，在4000-450cm–1的光谱波长范围内，对样品进行扫描，采集光谱谱图，光谱谱图进行光谱预处理后结合偏最小二乘判别法建立区分正常食用油和精炼潲水油的PLS-DA分析模型标准；再对未知油样进行扫描，采集未知油样光谱谱图，对未知油样光谱谱图进行同样的光谱预处理后结合偏最小二乘判别法分析，将分析结果与上述分析模型标准对比，确定未知油样样品是正常食用油还是精炼潲水油。本发明方法操作简单、方便，使用该方法能快速筛查出可疑油脂样品，非常适合在食用油生产、流通环节实施潲水油现场筛查。 | ||||||
| 62 | 一种基于傅里叶变换红外光谱定量分析的变压器油浸气体分析系统及其分析方法 | CN201010520324.X | 2010-10-26 | CN101975761A | 2011-02-16 | 汤晓君; 刘君华; 孟永鹏; 姚建军; 成永红 |
| 本发明公开了一种基于傅里叶变换红外光谱定量分析的变压器油浸气体分析系统及其分析方法，所述系统包括第一变压器油阀、第二变压器油阀、一台油气分离装置、一台带有气室的傅里叶变换红外光谱仪、一台电脑、进油管、回油管和气输送管道。该分析方法首先对变压器绝缘油进行油气分离，然后用傅里叶变换红外光谱仪对所分离出来的气体进行定量分析，以实现多组分气体的快速定量分析。所分析气体除了常规变压器油浸气体分析所涉及的甲烷、乙烷、丙烷、乙烯、乙炔、二氧化碳以外，还包括异丁烷、正丁烷、一氧化碳、丙烯、丙炔、六氟化硫和水汽。由于本方法所分析的气体种类多、速度快、分辨率高、运行成本低、安全可靠，因此是一种有广阔应用前景的变压器油浸气体分析方法。 | ||||||
| 63 | 结合傅里叶变换红外光谱和化学计量学分析鉴别生前死后骨折的方法 | CN202010442559.5 | 2020-05-22 | CN111707636B | 2021-07-13 | 王振原; 于凯; 魏昕; 王功绩; 吴迪; 刘睿娜 |
| 本发明公开了一种结合傅里叶变换红外光谱和化学计量学分析鉴别生前死后骨折的方法：利用傅里叶变换红外光谱采集骨折断面样本的光谱信息，利用化学计量学对选定的光谱信息进行处理，根据均值中心化和标准正态变量变换处理后的光谱数据，利用偏最小二乘法判别分析建立生前死后骨折鉴别模型，利用该模型客观、快速、准确的鉴别生前死后骨折。 | ||||||
| 64 | 结合傅里叶变换红外光谱和化学计量学分析鉴别生前死后骨折的方法 | CN202010442559.5 | 2020-05-22 | CN111707636A | 2020-09-25 | 王振原; 于凯; 魏昕; 王功绩; 吴迪; 刘睿娜 |
| 本发明公开了一种结合傅里叶变换红外光谱和化学计量学分析鉴别生前死后骨折的方法：利用傅里叶变换红外光谱采集骨折断面样本的光谱信息，利用化学计量学对选定的光谱信息进行处理，根据均值中心化和标准正态变量变换处理后的光谱数据，利用偏最小二乘法判别分析建立生前死后骨折鉴别模型，利用该模型客观、快速、准确的鉴别生前死后骨折。 | ||||||
| 65 | 傅里叶变换红外光谱分析仪的控制方法、装置、存储介质和计算机设备 | CN201710993511.1 | 2017-10-23 | CN107894406A | 2018-04-10 | 邓仕发; 潘奕; 何坚兵; 丁庆 |
| 本发明涉及一种傅里叶变换红外光谱分析仪的控制方法、装置、存储介质和计算机设备。获取红外信号启动参数的峰值，动镜与定镜相互垂直时，红外信号启动参数的峰值为预设最大峰值，得到此时激光信号启动参数，获取音圈电机的预设运行扫描频率，根据预设运行扫描频率获取温湿度数据实时值、激光信号运行参数以及红外信号运行参数，将温湿度数据实时值与其预设值进行比较，激光信号运行参数与激光信号启动参数之差与预设差值进行比较；当温湿度数据实时值等于其预设值，且激光信号运行参数与激光信号启动参数之差等于预设差值时，输出红外信号运行参数，这样可以确保运行时动镜与定镜相互垂直，提高输出的红外信号运行参数进行光谱分析时的分辨率。 | ||||||
| 66 | 一种基于漫反射傅里叶变换红外光谱的多晶型碳酸钙定量分析方法 | CN201611192865.8 | 2016-12-21 | CN106596455A | 2017-04-26 | 施晓旦; 刘莹; 傅斌 |
| 本发明公开了一种基于漫反射傅里叶变换红外光谱的多晶型碳酸钙定量分析方法，利用漫反射中红外傅立叶变换红外光谱分析技术结合偏最小二乘回归算法PLS定量分析算法，基于CO32‑面外弯曲振动吸收峰建立定量分析模型，采用此模型对碳酸钙样品进行定量分析，取得了和X射线粉末衍射法(XRD)基本一致的结果。采用本发明分析方法建好的定量分析模型可以作为标准模型长期使用，避免反复建立定量模型，相对于常规晶型分析方法XRD，本方法具有制样简单、分析快、误差小、费用低的特点。 | ||||||
| 67 | 基于衰减全反射傅里叶变换红外光谱技术的糙米中黄曲霉毒素含量的快速检测方法 | CN201510447345.6 | 2015-07-27 | CN105445217A | 2016-03-30 | 沈飞; 吴启芳 |
| 本发明提供一种基于衰减全反射傅里叶变换红外光谱技术的糙米中黄曲霉毒素含量的快速检测方法，包括以下步骤：样品准备，收集不同黄曲霉侵染程度的糙米样品，将糙米样品粉碎得到样品粉末，并冷藏待测；光谱检测，采用傅里叶变换近红外光谱仪扫描样品的光谱信息，并取部分过筛样品，测定糙米样品粉末中黄曲霉毒素B1、B2、G1、G2及其总量的水平；数据预处理，对样品粉末的原始光谱信息进行预处理，消除干扰；定量预测分析，基于偏最小二乘回归分析方法(PLSR)，依据糙米样品中黄曲霉毒素B1、B2、G1、G2及其总量的水平与其相应光谱吸收值的对应关系，建立糙米样品中黄曲霉毒素真实含量水平与预测水平的相关关系模型；快速测定，利用前述建立的模型，基于待测的糙米的光谱信息而输出其黄曲霉毒素B1、B2、G1、G2及其总量水平。 | ||||||
| 68 | 傅里叶变换衰减全反射红外光谱在线测定挥发有机水污染物的方法 | CN201310422025.6 | 2013-09-17 | CN103439290B | 2015-09-23 | 覃爱苗; 李庄杰 |
| 本发明公开了一种傅里叶变换衰减全反射红外光谱在线测定挥发有机水污染物的方法。利用挥发有机水污染物如反1,2-二氯乙烯在1155—1238cm-1处有Cl-C-H弯曲振动及顺1,2-二氯乙烯在840-860cm-1处有C-Cl振动的红外特征吸收峰，而水在此无吸收峰，采用衰减全反射红外光谱法、并用MacroBasic/OMNIC软件进行较正来测定水溶液中水污染挥发有机物的含量。测定结果表明,水中有机物的含量均与其红外吸收峰的峰高和峰面积在一定实验浓度范围内皆有良好的线性关系。本发明方法操作步骤简单、快速，测定结果令人满意。 | ||||||
| 69 | DIFFUSE REFLECTANCE INFRARED FOURIER TRANSFORM SPECTROSCOPY FOR CHARACTERIZATION OF EARTH MATERIALS | PCT/US2012050703 | 2012-08-14 | WO2013025679A2 | 2013-02-21 | HERRON MICHAEL M; HERRON SUSAN; CHARSKY ALYSSA; AKKURT RIDVAN |
| The subject disclosure relates to the evaluation of lithology, mineralogy and organic content of earth materials. More particularly, the subject disclosure relates to evaluating lithology, mineralogy and organic content of earth materials using diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). | ||||||
| 70 | 식물 DNA의 적외선 분광 스펙트럼 분석을 이용한 유전자 변이 식물체를 구별하는 방법 | KR1020130108816 | 2013-09-11 | KR1020150029871A | 2015-03-19 | 김석원; 안명숙; 지은이; 박종미; 유장렬; 장혜림 |
| 본 발명은 (a) 야생형 식물 및 유전자 변이 식물체, F1 잡종 식물체 또는 식물의 세포질 융합체로부터 DNA를 추출하는 단계; (b) 상기 (a)단계의 추출된 DNA에 적외선 분광 스펙트럼을 조사하여 적외선 분광 스펙트럼 프로파일을 얻는 단계; (c) 상기 (b)단계의 적외선 분광 스펙트럼 프로파일을 이용하여 다변량 통계분석 (multivariate analysis)을 수행하는 단계; 및 (d) 상기 (c)단계의 적외선 분광 스펙트럼 프로파일의 다변량 통계 분석 결과를 비교하여 야생형 식물 및 유전자 변이 식물체, F1 잡종 식물체 또는 식물의 세포질 융합체를 구별하는 단계를 포함하는 DNA에 적외선 분광 스펙트럼을 조사하여 유전자 변이 식물체, F1 잡종 식물체 또는 식물의 세포질 융합체를 구별하는 방법에 관한 것이다.
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| 71 | METHOD FOR THE DETECTION OF CELLULAR ABNORMALITIES USING FOURIER TRANSFORM INFRARED SPECTROSCOPY | EP96940389.0 | 1996-11-12 | EP0873506A1 | 1998-10-28 | COHENFORD, Menashi, A.; BHANDARE, Prashant S.; CAHN, Frederick; KRISHNAN, Krishnaswamy; RIGAS, Basil |
| This invention teaches a method to identify cellular abnormalities which are associated with disease states. In one aspect, the invention is a method to distinguish premalignant and malignant stages of cervical cancer from normal cervical cells. The method utilizes infrared (IR) spectra of exfoliated cervical cells which are dried on an infrared transparent matrix and scanned at the frequency range from 3000-950 cm-1. The identification of samples is based on establishing a calibration using a representative set of spectra of normal, dysplastic and malignant specimens. During the calibration process, multivariate techniques such as Principal Component Analysis (PCA) and/or Partial Least Squares (PLS) are used. PCA and PLS reduce the data based on maximum variations between the spectra, and generate clusters in a multidimensional space representing the different populations. The utilization of Mahalinobis distances, or linear regression (e.g., Principle Component Regression on the reduced data from PCA) form the basis for the discrimination. This method is simple to use and achieves statistically reliable distinction between the following groups of cervical smears: normal (individuals with no prior history of dysplasia), dysplasia and malignant samples. Further, this invention discloses a method to obtain the IR spectrum of individual cervical cells fixed on an infrared transparent matrix and to use the spectra of the individual cells in the method described above. In an additional aspect, the invention is a method for using vibrational spectroscopic imaging to distinguish between normal and diseased cells. | ||||||
| 72 | 一般的な、固有の特性の分析法皮膚発がんのＦＴＩＲ顕微フーリエ変換赤外分光法 | JP2014558002 | 2013-02-21 | JP2015508166A | 2015-03-16 | アイキエ，ナタリア |
| 発明は人間の皮膚腫瘍における変換赤外 (FTIR) 顕微分光発癌の一般的および特定の特性のためのフーリエのメソッドを示します。発明を提供し、ユーザーには、メソッドを分析し内と間の分子間相互作用の核酸とタンパク質の赤外線(IR)スペクトルの人間の皮膚表皮癌を理解する分子、細胞、組織変更が発生する時に皮膚癌発生します。特に、詳細は、特に提案解析手法は同時に観察する DNA ・ RNA、DNA、蛋白質 DNA および蛋白質蛋白質の相互作用 1 型腫瘍と腫瘍の種類間の中で表現された相互作用の活動レベルによって一般的、具体的には、良性、前癌および悪性の皮膚組織の細胞の活動のグレードの更なる徴候と利点があります。 | ||||||
| 73 | Method and apparatus for process control using fourier transform infrared spectroscopy | US09636560 | 2000-08-11 | US06539285B1 | 2003-03-25 | Wilfried Hartmann; Arno Simon |
| The invention concerns a method and a device for process control of reaction processes using Fourier transform infrared spectroscopy. In accordance with the invention, an interferogram is generated before or after interaction with the compositions. Subsequent thereto, the interferogram is inspected in segments for externally introduced intensity fluctuations. The intensity fluctuations are subjected to an analysis procedure involving integration, differentiation, or the like, and on the basis of this evaluation, a decision is made as to whether or not the interferogram has an acceptable degree of interfering signals. The interferogram is labeled with this evaluation result and the procedure is repeated a plurality of times. After a sufficient number of acceptable interferograms have been collected, the acceptable interferograms are summed and subjected to a Fourier transform process to extract the frequency dependence. In this manner, Fourier transformation infrared spectroscopy techniques can be applied for process control of processes which would otherwise be impossible due to unacceptably large degrees of interference caused primarily by bubble formation. | ||||||
| 74 | Apparatus and method for real-time spectral alignment for open-path fourier transform infrared spectrometers | US743295 | 1996-11-04 | US5790250A | 1998-08-04 | C. David Wang; Robert Howard Kagann |
| An improved open-path fast Fourier infrared spectrometer includes a circuit or algorithm which performs real-time, spectral alignment on measured interferograms to reduce measuremental errors. The improved spectrometer measures selected water vapor lines in a measurement path and compares the centerline of these measured water vapor lines to a reference library. From two or more such comparisons within the spectrometer bandwidth, the spectrometer calculates correction factors for the entire bandwidth. The improved spectrometer performs an overlap and add algorithm which applies the correction factors to perform bandwidth segment-specific shifts on subsequently measured interferograms. | ||||||
| 75 | Apparatus and method for real-time spectral alignment for open-path fourier transform infrared spectrometers | US992227 | 1997-12-17 | US5959730A | 1999-09-28 | Chung-Tao David Wang; Robert Howard Kagann |
| An improved method for use with an open-path fast Fourier infrared spectrometer performs real-time, spectral alignment on measured interferograms to reduce measuremental errors. The improved method includes the step of selecting a plurality of water-vapor lines in a defined spectral region and comparing the centerline of these measured water vapor lines to a reference library. From these comparisons, the spectrometer calculates correction factors to apply to the spectrometer bandwidth. The improved spectrometer performs transform functions on selected segments of the spectrometer bandwidth which introduce integer-continuous corrective shifts on subsequently measured interferogram data. | ||||||
| 76 | Method for the detection of cellular abnormalities using Fourier transform infrared spectroscopy | US851776 | 1997-05-06 | US6146897A | 2000-11-14 | Menashi A. Cohenford; Prashant S. Bhandare; Basil Rigas |
| This invention teaches a method to identify cellular abnormalities which are associated with disease states. The method utilizes infrared (IR) spectra of cell samples which are dried on an infrared-transparent matrix and scanned at the frequency range from 3000-950 cm.sup.-1. The identification of samples is based on establishing a reference using a representative set of spectra of normal and/or diseased specimens. During the reference assembly process, multivariate techniques such as Principal Component Analysis (PCA) and/or Partial Least Squares (PLS) are used. PCA and PLS reduce the data based on maximum variations between the spectra, and generate clusters in a multidimensional space representing the different populations. The utilization of Mahalinobis distances, or linear regression (e.g., Principle Component Regression on the reduced data from PCA) form the basis for the discrimination. In one embodiment, the invention is a method to distinguish premalignant and malignant stages of cervical cancer from normal cervical cells. This method is simple to use and achieves statistically reliable distinction between the following groups of cervical smears: normal (individuals with no prior history of dysplasia), dysplasia and malignant samples. Further, this invention discloses a method to obtain the IR spectrum of individual cervical cells fixed on an infrared-transparent matrix and to use the spectra of the individual cells in the method described above. In another aspect, the invention is a method for using vibrational spectroscopic imaging to distinguish between normal and diseased cells. In another aspect, the invention is a method to identify women at a high risk for developing cervical dysplasia. | ||||||
| 77 | Method for the detection of cellular abnormalities using fourier transform infrared spectroscopy | US09433655 | 1999-11-03 | US06620621B1 | 2003-09-16 | Menashi A. Cohenford; Prashant S. Bhandare; Frederick R. Cahn; Krishnaswamy Krishnan; Basil Rigas |
| This invention teaches a method to identify cellular abnormalities which are associated with disease states. The method utilizes infrared (IR) spectra of cell samples which are dried on an infrared-transparent matrix and scanned at the frequency range from 3000-950 cm−1. The identification of samples is based on establishing a reference using a representative set of spectra of normal and/or diseased specimens. During the reference assembly process, multivariate techniques such as Principal Component Analysis (PCA) and/or Partial Least Squares (PLS) are used. PCA and PLS reduce the data based on maximum variations between the spectra, and generate clusters in a multidimensional space representing the different populations. The utilization of Mahalinobis distances, or linear regression (e.g., Principle Component Regression on the reduced data from PCA) form the basis for the discrimination. In one embodiment, the invention is a method to distinguish premalignant and malignant stages of cervical cancer from normal cervical cells. This method is simple to use and achieves statistically reliable distinction between the following groups of cervical smears: normal (individuals with no prior history of dysplasia), dysplasia and malignant samples. Further, this invention discloses a method to obtain the IR spectrum of individual cervical cells fixed on an infrared-transparent matrix and to use the spectra o the individual cells in the method described above. In another aspect, the invention is a method for using vibrational spectroscopic imaging to distinguish between normal and diseased cells. In another aspect, the invention is a method to identify women at a high risk for developing cervical dysplasia. | ||||||
| 78 | Apparatus and process for monitor and control of an ammoxidation reactor with a fourier transform infrared spectrometer | US10624022 | 2003-07-21 | US20040023407A1 | 2004-02-05 | Hector L. Casal; Nazaneen Asker; Michael J. Seely; Linda L. Nero; Jean A. Baldwin |
| The present invention is a method and an apparatus for identifying and quantifying components in an effluent stream from an ammoxidation reactor, the apparatus comprising a microprocessor; and a Fourier Transform infrared spectrometer having a sample cell through which may flow a portion of the effluent stream, an infrared source to emit infrared radiation and pass the infrared radiation through the effluent stream, an infrared detector to detect transmitted infrared radiation at the selected infrared wavelengths and to generate absorbance data due to absorbance of the infrared radiation by the components, wherein each of the components absorbs infrared radiation at one or more of the infrared wavelengths, and an output apparatus to provide the absorbance data to the microprocessor; wherein the microprocessor is programmed to identify and quantify each of the plurality of components based upon the absorbance data and calibration data, the calibration data being obtained from recovery run analyses and calibration analyses in the sample cell. The method may be applied to utilize the apparatus to provide real-time control of the operation of an ammoxidation reactor, based on the analytical results obtained by the FT-IR spectrometer and the calibration model developed therefor. | ||||||
| 79 | Continuous flow apparatus and method for interfacing liquid chromatograph and fourier transform infrared spectrometer | US434306 | 1995-05-02 | US5538643A | 1996-07-23 | George J. Kallos; Richard R. Papenfuss |
| Apparatus for interfacing a liquid chromatograph (LC) with a spectrometer such as a Fourier transform infrared spectrometer, the LC having an eluant, the eluant containing a solvent and a component of interest. The apparatus includes five basic parts. The first is a means for generating a stream of droplets of the eluant, such as a nebulizer. The second is a means for removing most of the solvent from the stream of droplets of the eluant to thereby generate a stream of particles, the particles containing the component of interest and any residual solvent, such as a membrane solvent separator/momentum separator combination. The third is a cryogenic receiving surface, such as a gold drum. The forth is a means for focusing the stream of particles onto the cryogenic receiving surface so that the particles adhere to the cryogenic receiving surface, such as a one and two-tenths millimeter inside diameter stainless steel tube positioned with a gap between the distal end of the tube and the cryogenic receiving surface of one-quarter millimeter. The fifth is a means for controlling the temperature of the cryogenic receiving surface, such as a helium refrigerator. In operation, the cryogenic receiving surface is maintained at a temperature effective to cause the particles to adhere to the cryogenic receiving surface to form a region of adhered particles, such as a temperature of between seventy and one hundred and five degrees Kelvin, the cryogenic receiving surface being maintained in a partial vacuum. Then, the cryogenic receiving surface is warmed, e.g., to between one hundred and five and two hundred degrees Kelvin, to volatilize essentially all of any remaining solvent from the region of adhered particles prior to spectroscopic analysis of the region of adhered particles. | ||||||
| 80 | Method and apparatus for determining mirror position in a fourier-transform infrared spectrometer | US175513 | 1988-03-31 | US4847878A | 1989-07-11 | Robert R. Badeau |
| The position of the moving mirror (20) in a Fourier-transform infrared spectrometer is monitored with a circuit which has an incremental counter formed of a plurality of cascaded up/down counters (82, 84, and 86) that count the pulses received by a laser detector (42) to yield a relative position count. A microprocessor (100) maintains an absolute position count by reading the counters (82, 84, and 86) and updating its absolute position count at regular intervals. A portion of the circuit is dedicated to discriminating the direction of the moving mirror (20) by gating circuitry connected to the digitized output of the laser detectors (42, 44). | ||||||
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