CN110646375A - Camellia oil adulteration identification method - Google Patents

Camellia oil adulteration identification method Download PDF

Info

Publication number
CN110646375A
CN110646375A CN201910842272.9A CN201910842272A CN110646375A CN 110646375 A CN110646375 A CN 110646375A CN 201910842272 A CN201910842272 A CN 201910842272A CN 110646375 A CN110646375 A CN 110646375A
Authority
CN
China
Prior art keywords
adulteration
samples
camellia oil
oil
identification
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201910842272.9A
Other languages
Chinese (zh)
Inventor
王伟
郭笑欢
鹿瑶
宋淑仙
金奇
钟斌
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gannan Medical University
Original Assignee
Gannan Medical University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gannan Medical University filed Critical Gannan Medical University
Priority to CN201910842272.9A priority Critical patent/CN110646375A/en
Publication of CN110646375A publication Critical patent/CN110646375A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/35Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
    • G01N21/359Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light using near infrared light
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/35Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
    • G01N21/3577Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light for analysing liquids, e.g. polluted water
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/12Circuits of general importance; Signal processing
    • G01N2201/129Using chemometrical methods

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)

Abstract

The invention relates to the technical field of food quality safety, in particular to a camellia oil adulteration identification method, which comprises the following steps of establishing a camellia oil adulteration grade identification model: the method comprises the following steps: collecting spectral data; preparing a plurality of samples doped with other oil products in different proportions, and collecting data of the samples by adopting a near-infrared spectrometer; step two: removing head and tail noises to obtain an original spectrum curve; step three: establishing a principal component-support vector machine discrimination model; (1) selecting a main component; performing dimensionality reduction on the spectral data by adopting a principal component analysis method to obtain key principal components; (2) establishing a adulteration grade discrimination model by taking the main components obtained in the step (1) as a support vector machine; step four: model application, adulteration identification. The method can realize the detection of the adulteration degree of the camellia oil, is simple to operate, and can realize the requirements of rapidness, no damage and the like.

Description

Camellia oil adulteration identification method
Technical Field
The invention relates to the technical field of food quality safety, in particular to a camellia oil adulteration identification method.
Background
The camellia oil is edible vegetable oil prepared from camellia seeds, is rich in unsaturated fatty acids such as oleic acid, linoleic acid and linolenic acid, is rich in nutrition, has fragrant smell and health-care function, is widely favored by consumers, and has very wide market prospect. However, because the camellia oil has high price and great profit, the phenomenon that illegal merchants blend other grease in the camellia oil to obtain violence is frequently seen in the society. Therefore, the identification of the adulterated camellia oil is significant for guaranteeing the rights and interests of consumers and maintaining the reputation of enterprises.
In the prior art, the quality of camellia oil is often detected by adopting some physicochemical methods. For example, in the chemical aspect, a chemical reagent is added to observe the color change reaction of the adulteration reagent, so that the qualitative detection of the adulteration is realized. The quality of the camellia oil can be quantitatively detected by a gas chromatography instrument, a liquid chromatography instrument and the like. However, the methods all have pollution to samples or are complex to operate, and cannot meet the requirements of rapidness, no damage and the like.
In view of this, an adulteration identification method is established by combining the near infrared spectrum technology with the chemometrics method, and camellia oil doped with other oil products can be distinguished and the adulteration degree can be judged.
Disclosure of Invention
The invention aims to solve the technical problem of providing a camellia oil adulteration identification method for detecting the adulteration degree.
In order to solve the problems, the technical scheme adopted by the invention is as follows:
the key technology of the camellia oil adulteration identification method is that a camellia oil adulteration grade identification model is established, and the camellia oil adulteration grade identification method comprises the following steps:
the method comprises the following steps: collecting spectral data; preparing a plurality of samples doped with other oil products in different proportions, and collecting data of the samples by adopting a near-infrared spectrometer;
step two: removing head and tail noises to obtain an original spectrum curve;
step three: establishing a principal component-support vector machine discrimination model;
(1) selecting a main component; performing dimensionality reduction on the spectral data by adopting a principal component analysis method to obtain key principal components;
(2) establishing a adulteration grade discrimination model by taking the main components obtained in the step (1) as a support vector machine;
step four: model application, adulteration identification.
Furthermore, the other oil products in the step one adopt sunflower oil.
Further, by taking the sunflower oil content of 1% as a gradient, 6 samples with the mass fraction range of 0-5% are prepared and marked as a group A, and 5 samples with the mass fraction range of 6-10% are prepared and marked as a group B; taking the sunflower oil content of 5% as a gradient, preparing 6 samples with the mass fraction range of 15-40%, and marking as a group C; taking the sunflower oil content of 10% as a gradient, preparing 6 samples with the mass fraction range of 50-100%, marking as group D, and dividing each camellia oil sample with different adulteration proportions into 9 parts.
Further, the spectral data is divided into a training set and a verification set; the training set and the verification set are respectively divided randomly according to the ratio of 2:1 by the spectrum data measured by the four groups of samples.
Further, the spectrometer is an AvaSpec-NIR256 near infrared spectrometer.
Furthermore, the spectral range of the spectral data acquisition is 1000-2500nm, the resolution is 4.4-77nm, the spectrometer integration time is 0.0319ms, and the scanning times are 100 times.
Further, the original spectral curve in the second step is the spectral curve after the head and tail noise is removed, and the intercepted wavelength range is 1000-2300 nm.
Further, the identification standard of the fourth step is the judgment accuracy.
Adopt the produced beneficial effect of above-mentioned technical scheme to lie in:
the camellia oil adulteration identification method provided by the invention establishes a principal component-support vector machine discrimination model by utilizing a near infrared spectrum technology in combination with a chemometrics method, can discriminate the camellia oil adulterated with other oil products and judge the adulteration degree of the camellia oil, is simple to operate, and can meet the requirements of rapidness, no damage and the like. The discrimination model is adopted to discriminate the training set and the verification set of the sample, the discrimination accuracy of the training set and the verification set is respectively 96.38 percent and 94.20 percent, and the adulteration grade can be discriminated well.
Detailed Description
The present invention will be described in further detail with reference to the following embodiments. In the following description, numerous details are set forth in order to provide a better understanding of the present application. However, those skilled in the art will readily recognize that some of the features may be omitted or replaced with other elements, materials, methods in different instances. In some instances, certain operations related to the present application have not been shown or described in detail in order to avoid obscuring the core of the present application from excessive description, and it is not necessary for those skilled in the art to describe these operations in detail, so that they may be fully understood from the description in the specification and the general knowledge in the art.
Furthermore, the features, operations, or characteristics described in the specification may be combined in any suitable manner to form various embodiments. Also, the various steps or actions in the method descriptions may be transposed or transposed in order, as will be apparent to one of ordinary skill in the art. Thus, the various sequences of the specification are for clarity only to describe certain embodiments and are not meant to imply a required sequence unless otherwise stated where a certain sequence must be followed.
The method for identifying the adulteration of the camellia oil is characterized in that an identification model of the adulteration grade of the camellia oil is established, and the method comprises the following steps:
the method comprises the following steps: and (6) collecting spectral data. Preparing a plurality of samples doped with other oil products in different proportions, and collecting data of the samples by adopting a near-infrared spectrometer. The other oil product can be sunflower oil, soybean oil, rapeseed oil, etc., and the sunflower oil is adopted in the step.
The prepared samples are characterized in that 1% of sunflower oil content is used as a gradient, 6 samples with the mass fraction range of 0-5% are marked as group A, and 5 samples with the mass fraction range of 6-10% are marked as group B; taking the sunflower oil content of 5% as a gradient, preparing 6 samples with the mass fraction range of 15-40%, and marking as a group C; taking the sunflower oil content of 10% as a gradient, preparing 6 samples with the mass fraction range of 50-100%, marking as group D, dividing each camellia oil sample with different adulteration proportions into 9 parts, and finally obtaining 207 parts of samples. For ease of testing, the samples prepared in different gradients were designated as group a, group B, group C, and group D, respectively.
In order to ensure the accuracy of the test and the subsequent verification, the spectral data are divided into a training set and a verification set. The training set and the verification set are respectively randomly divided according to a ratio of 2:1, 138 samples form the training set, and 69 samples form the verification set.
Step two: and removing head and tail noises to obtain an original spectrum curve. The spectrometer adopted in the invention is an AvaSpec-NIR256 near infrared spectrometer. The spectral range of the spectral data acquisition is 1000-2500nm, and the resolution is 4.4-77 nm. Before spectrum collection, the spectrometer integration time is set to 0.0319ms, the scanning times are 100 times, and special white board information and the dark current of the spectrometer are collected to realize correction. Finally, the sample is placed in a quartz cuvette and placed on a special cuvette support to collect absorption spectra, and spectral data are obtained by matching software Avasoft.
And because the head and tail noises of the spectrometer are relatively large, the original spectrum curve in the second step is the spectrum curve without the head and tail noises, and the intercepted wavelength range is 1000-2300 nm. The 207 original spectral curves of the samples with the head and tail noises removed are very similar, and the adulteration degree of the samples cannot be directly judged from the original spectral curves, so that the samples need to be further analyzed and judged by other methods.
Step three: and establishing a principal component-support vector machine discrimination model. (1) Selecting a main component; and performing dimensionality reduction on the spectral data by adopting a principal component analysis method to obtain key principal components. And 2, the data obtained in the step two is large in size and easy to cause information redundancy, so that the principal component analysis method is adopted to reduce the dimension of the data, and the key principal component score is utilized to represent the internal characteristics and clustering information of the sample. Through analysis, the model established by selecting 4 principal components as input has higher accuracy, so that 4 principal components are finally selected.
(2) And (3) establishing a adulteration grade discrimination model by taking the principal components obtained in the step (1) as a support vector machine. On the basis of principal component analysis, a support vector machine is utilized to establish an adulterated camellia oil identification model. And determining a penalty parameter and a kernel function parameter by using a grid optimization method by using a radial basis kernel function as a support vector machine kernel function.
Step four: model application, adulteration identification. And the identification standard of the step four is the judgment accuracy. The established model is adopted to distinguish the training set and the verification set, the distinguishing accuracy of the training set and the verification set is respectively 96.38% and 94.20%, and adulteration grade can be distinguished well.
Finally, it should be noted that: the present invention has been described in terms of specific examples, which are provided to aid understanding of the invention and are not intended to be limiting. For those skilled in the art to which the invention pertains, numerous and varied variations and substitutions may be made in accordance with the spirit of the invention, and these simple variations and combinations should also be considered as within the scope of the invention disclosed herein.

Claims (8)

1. The camellia oil adulteration identification method is characterized in that a camellia oil adulteration grade identification model is established, and the method comprises the following steps:
the method comprises the following steps: collecting spectral data; preparing a plurality of samples doped with other oil products in different proportions, and collecting data of the samples by adopting a near-infrared spectrometer;
step two: removing head and tail noises to obtain an original spectrum curve;
step three: establishing a principal component-support vector machine discrimination model;
(1) selecting a main component; performing dimensionality reduction on the spectral data by adopting a principal component analysis method to obtain key principal components;
(2) establishing a adulteration grade discrimination model by taking the main components obtained in the step (1) as a support vector machine;
step four: model application, adulteration identification.
2. The method for identifying the adulteration of camellia oil as claimed in claim 1, wherein the other oil products in the first step are sunflower oil.
3. The method for identifying the adulteration of the camellia oil as claimed in claim 2, wherein 6 samples with the mass fraction range of 0-5% are prepared by taking the content of the sunflower oil as a gradient and are marked as a group A, and 5 samples with the mass fraction range of 6-10% are prepared and are marked as a group B; taking the sunflower oil content of 5% as a gradient, preparing 6 samples with the mass fraction range of 15-40%, and marking as a group C; taking the sunflower oil content of 10% as a gradient, preparing 6 samples with the mass fraction range of 50-100%, marking as group D, and dividing each camellia oil sample with different adulteration proportions into 9 parts.
4. The method for identifying camellia oil adulteration according to claim 3, wherein the spectral data is divided into a training set and a validation set; the training set and the verification set are respectively divided randomly according to the ratio of 2:1 by the spectrum data measured by the four groups of samples.
5. The method for identifying the adulteration of camellia oil as claimed in claim 1, wherein the spectrometer is an AvaPec-NIR 256 near infrared spectrometer.
6. The method as claimed in claim 1, wherein the spectral range of the spectral data acquisition is 1000-2500nm, the resolution is 4.4-77nm, the spectrometer integration time is 0.0319ms, and the scanning times are 100 times.
7. The method as claimed in claim 1, wherein the original spectral curve in the second step is a spectral curve obtained after removing noise from the head and tail, and the cut wavelength range is 1000-2300 nm.
8. The method for identifying the adulteration of camellia oil as claimed in claim 1, wherein the identification criterion of the fourth step is the accuracy of discrimination.
CN201910842272.9A 2019-09-06 2019-09-06 Camellia oil adulteration identification method Pending CN110646375A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910842272.9A CN110646375A (en) 2019-09-06 2019-09-06 Camellia oil adulteration identification method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910842272.9A CN110646375A (en) 2019-09-06 2019-09-06 Camellia oil adulteration identification method

Publications (1)

Publication Number Publication Date
CN110646375A true CN110646375A (en) 2020-01-03

Family

ID=68991650

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910842272.9A Pending CN110646375A (en) 2019-09-06 2019-09-06 Camellia oil adulteration identification method

Country Status (1)

Country Link
CN (1) CN110646375A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107121406A (en) * 2017-05-24 2017-09-01 福州大学 A kind of adulterated discrimination method of grape-kernel oil based near infrared spectrum
CN107894408A (en) * 2017-11-24 2018-04-10 中国农业科学院油料作物研究所 A kind of edible oil based near infrared spectrometer is polynary to mix pseudo- discrimination method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107121406A (en) * 2017-05-24 2017-09-01 福州大学 A kind of adulterated discrimination method of grape-kernel oil based near infrared spectrum
CN107894408A (en) * 2017-11-24 2018-04-10 中国农业科学院油料作物研究所 A kind of edible oil based near infrared spectrometer is polynary to mix pseudo- discrimination method

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
褚璇 等: "近红外光谱和特征光谱的山茶油掺假鉴别方法研究", 《光谱学与光谱分析》 *

Similar Documents

Publication Publication Date Title
US10948407B2 (en) Method for detecting multivariate adulteration of edible oil based on near-infrared spectroscopy
Esslinger et al. Potential and limitations of non-targeted fingerprinting for authentication of food in official control
Cozzolino et al. Can spectroscopy geographically classify Sauvignon Blanc wines from Australia and New Zealand?
Šmejkalová et al. High-power gradient diffusion NMR spectroscopy for the rapid assessment of extra-virgin olive oil adulteration
Ogrinc et al. The application of NMR and MS methods for detection of adulteration of wine, fruit juices, and olive oil. A review
Cai et al. An expert system based on 1H NMR spectroscopy for quality evaluation and adulteration identification of edible oils
Pan et al. a simple and portable screening method for adulterated olive oils using the hand‐held FTIR spectrometer and chemometrics tools
Furlan et al. Investigating the oxidation of biodiesel from used vegetable oil by FTIR spectroscopy: used vegetable oil biodiesel oxidation study by FTIR
CN103472094A (en) Olfactory analog instrument and on-site analysis method for odor grade of specific substance
Zhao et al. Detection of adulteration of sesame and peanut oils via volatiles by GC× GC–TOF/MS coupled with principal components analysis and cluster analysis
Souayah et al. Discrimination of olive oil by cultivar, geographical origin and quality using potentiometric electronic tongue fingerprints
CN104502320A (en) Method for identifying strong flavor Baijiu by combining three-dimensional fluorescence spectrum with PCA-SVM
KR101965293B1 (en) Developement of metabolic biomarkers and discrimination model for determining origin of white rice
KR101432543B1 (en) Method to identify sesame oil using nuclear magnetic resonance spectroscopy
CN105548027A (en) Analytical model and method for determining content of tea oil in blend oil based on near infrared spectroscopy
Qian et al. Differentiation and classification of Chinese Luzhou‐flavor liquors with different geographical origins based on fingerprint and chemometric analysis
Chiavaro et al. Application of a multidisciplinary approach for the evaluation of traceability of extra virgin olive oil
CN112033911A (en) Method for rapidly identifying grade of tea based on chromatic aberration and ultraviolet spectrum
Majchrzak et al. Classification of Polish wines by application of ultra-fast gas chromatography
Soni et al. A review of conventional and rapid analytical techniques coupled with multivariate analysis for origin traceability of soybean
CN113324987B (en) Method for detecting sesame oil adulteration
Teye et al. Nondestructive authentication of cocoa bean cultivars by FT-NIR spectroscopy and multivariate techniques
Wu et al. Geographical origin traceability and authenticity detection of Chinese red wines based on excitation-emission matrix fluorescence spectroscopy and chemometric methods
CN112485216B (en) Multi-source information fusion Thailand jasmine rice adulteration identification method
Monteiro et al. 1H NMR and multivariate calibration for the prediction of biodiesel concentration in diesel blends

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
CB03 Change of inventor or designer information
CB03 Change of inventor or designer information

Inventor after: Wang Wei

Inventor after: Zhong Bin

Inventor after: Guo Xiaohuan

Inventor after: Lu Yao

Inventor after: Song Shuxian

Inventor after: Jin Qi

Inventor before: Wang Wei

Inventor before: Guo Xiaohuan

Inventor before: Lu Yao

Inventor before: Song Shuxian

Inventor before: Jin Qi

Inventor before: Zhong Bin

WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20200103