Method for analyzing components of organic sample
阅读说明：本技术 有机样品的成分分析方法 (Method for analyzing components of organic sample ) 是由 李群花 高山松 舒歌平 王洪学 王国栋 向春兰 于 2019-09-26 设计创作，主要内容包括：本发明涉及化学分析领域,具体涉及一种有机样品的成分分析方法。包括：(1)采用z值分类法分类并赋值；(2)分析得到核磁共振氢谱谱图；(3)分析得到全二维气相色谱-飞行时间质谱检测谱图；(4)分析得到全二维气相色谱-氢火焰离子化检测器检测谱图,该全二维气相色谱-氢火焰离子化检测器检测谱图与所述全二维气相色谱-飞行时间质谱检测谱图中各成分的出峰位置一一对应；(5)数据分析：进行定性,并用对各成分进行定义；然后根据出峰位置,通过面积归一法计算得到所述有机样品中各成分的含量。本发明的有机样品的成分分析方法能够直观地得到各成分(包括未氢化芳烃和氢化芳烃)的种类和含量。(The invention relates to the field of chemical analysis, in particular to a component analysis method of an organic sample. The method comprises the following steps: (1) classifying and assigning values by adopting a z value classification method; (2) analyzing to obtain a nuclear magnetic resonance hydrogen spectrum; (3) analyzing to obtain a full two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram; (4) analyzing to obtain a detection spectrogram of a full-two-dimensional gas chromatography-hydrogen flame ionization detector, wherein the detection spectrogram of the full-two-dimensional gas chromatography-hydrogen flame ionization detector corresponds to peak positions of components in the detection spectrogram of the full-two-dimensional gas chromatography-flight time mass spectrum one by one; (5) and (3) data analysis: performing qualitative analysis and defining each component; and then calculating the content of each component in the organic sample by an area normalization method according to the peak position. The method for analyzing the components of the organic sample can intuitively obtain the types and the contents of the components (including the unhydrogenated aromatic hydrocarbon and the hydrogenated aromatic hydrocarbon).)
1. A method for analyzing the components of an organic sample, wherein the organic sample contains saturated alkanes, hydrogenated aromatics and unhydrogenated aromatics, the method comprising the steps of:
(1) classifying and assigning the organic components by adopting a z value classification method;
(2) analyzing the organic sample by adopting a nuclear magnetic resonance hydrogen spectrum to obtain a nuclear magnetic resonance hydrogen spectrum of the organic sample;
(3) analyzing the organic sample by adopting a full-two-dimensional gas chromatography-time-of-flight mass spectrometry to obtain a full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram of the organic sample;
(4) analyzing the organic sample by using a full-two-dimensional gas chromatography-hydrogen flame ionization detector to obtain a full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram of the organic sample, wherein the full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram corresponds to peak positions of all components in the full-two-dimensional gas chromatography-flight time mass spectrometry detection spectrogram one by one;
(5) and (3) data analysis:
analyzing the nuclear magnetic resonance hydrogen spectrum to obtain first fixed information containing peak position and peak intensity;
analyzing the full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram to obtain second qualitative information containing retention time;
qualitatively determining each organic component in the organic sample according to the first qualitative information and the second qualitative information, and combining the result of the step (1) to form a qualitative template;
and then applying the qualitative template to data collected by the full-two-dimensional gas chromatography-hydrogen flame ionization detector according to the peak positions of all components in the organic sample in the full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram and the full-two-dimensional gas chromatography-flight time mass spectrometry detection spectrogram, and calculating the content of all components in the organic sample by an area normalization method.
2. The composition analyzing method according to claim 1, wherein, in the step (1), the method of classifying and assigning the organic composition using the z-value classification method comprises: classifying the compounds to obtain family names, and writing the molecular formula of the compounds as CnH2n+zObtaining a z value and naming the compound as a name that is a combination of the family name and the z value; wherein, the classification mode comprises the following steps: saturated alkanes are classified as group S, hydrogenated aromatics as group HA, and unhydrogenated aromatics as group a.
3. The composition analysis method according to claim 2, wherein the hydrogenated aromatic hydrocarbons HAz ═ -12, HAz ═ -14, HAz ═ -16 and HAz ═ -18 are combined in step (4) and step (5) and analyzed.
4. The composition analysis method according to claim 1 or 2, wherein the classifying further comprises: compounds containing heteroatoms are classified as a class named for the element of the heteroatom.
5. The composition analyzing method according to claim 1, wherein in the step (3), the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry include: the one-dimensional column has a column size of (30-80) mx (0.15-0.25) mmx (0.2-0.55) μm, and the two-dimensional column has a column size of (1.5-2.5) mx (0.2-0.3) mmx (0.2-0.3) μm.
6. The composition analyzing method according to claim 1 or 5, wherein in the step (3), the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry include: the sample introduction amount is 0.1-1 mu L, the split ratio is (100-; the one-dimensional temperature program comprises: the initial temperature is 50-60 ℃, the temperature is kept for 0.8-1.5min, and then the temperature is raised to 300-320 ℃ at the speed of 1-2.5 ℃/min and kept for 10-20 min; the two-dimensional program includes: the compensation temperature is 5-15 ℃.
7. The composition analyzing method according to claim 6, wherein in the step (3), the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry include: the sample introduction amount is 0.2-0.4 mu L, the split ratio is (180-; the one-dimensional temperature program comprises: the initial temperature is 50-55 ℃, the temperature is kept for 0.8-1.2min, and then the temperature is increased to 310-315 ℃ at the speed of 1.5-2 ℃/min and kept for 12-18 min; the two-dimensional program includes: the compensation temperature is 8-12 ℃.
8. The composition analyzing method according to claim 6, wherein in the step (3), the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry further include: the bombardment voltage of the electron bombardment ionization source is 68-72eV, the solvent is not delayed, the temperature of the ion source is 240-260 ℃, the temperature of the transmission line is 270-290 ℃, the voltage of the detector is 1350-1450V, the collection mass range is 30-600amu, and the collection frequency is 90-110 spectra/s.
9. The composition analyzing method according to claim 1, wherein in the step (4), the condition of the hydrogen flame ionization detection in the comprehensive two-dimensional gas chromatography-hydrogen flame ionization detection includes: the temperature of the detector is 300-320 ℃, the collection frequency is 95-105spectra/s, the tail gas is blown into inert gas, the flow rate of the tail gas is 45-55mL/min, the air flow rate is 440-460mL/min, and the hydrogen flow rate is 35-45 mL/min.
10. The composition analysis method according to any one of claims 1 to 9, wherein the organic sample is a recycled solvent in a direct coal liquefaction process, in which the content of saturated alkanes is 30 to 60 wt%, the content of hydrogenated aromatics is 30 to 60 wt%, and the content of non-hydrogenated aromatics is 1 to 15 wt%.
Technical Field
The invention relates to the field of chemical analysis, in particular to a component analysis method of an organic sample.
Background
The direct coal liquefaction process is a process for generating liquid products by pyrolyzing and hydrogenating coal at high temperature and high pressure in the presence of a solvent and a catalyst. The circulating solvent plays an important role in the direct coal liquefaction hydrogenation process, such as: the coal slurry is prepared with coal, so that the transportation and the pressurization are convenient; dissolving coal, preventing the polycondensation of free radical fragments of coal pyrolysis; dissolving gas-phase hydrogen, diffusing hydrogen molecules to the surface of coal or a catalyst, and directly supplying hydrogen or transferring hydrogen to free radical fragments; and the like. The components of the circulating solvent in the direct coal liquefaction process are fundamental factors determining the hydrogen supply and transfer capacity of the direct coal liquefaction process, and the accurate representation of the components of the circulating solvent is an important guarantee for adjusting the parameters of the direct coal liquefaction process and improving the oil yield and the coal conversion rate.
Therefore, it is very important to determine the composition of the recycled solvent (or coal direct liquefaction oil) in the coal direct liquefaction process, especially the type and content of the hydrogenated aromatic hydrocarbons therein, for the efficient operation of the coal direct liquefaction process. The analysis of organic solutions is currently common in petroleum, for example, according to the ASTM D3239 standard. However, there are some disadvantages in analyzing the coal direct liquefaction oil by using the petroleum analysis method, for example, first, the content of naphthenes and aromatics in the coal direct liquefaction oil is high, and is significantly different from the petroleum composition, so that there is a limitation in applying the analysis standard of petroleum to the coal direct liquefaction oil; secondly, in the petroleum family composition analysis method, the non-hydrogenated aromatic hydrocarbon and the hydrogenated aromatic hydrocarbon coincide with each other, and the type and the content of the hydrogenated aromatic hydrocarbon cannot be visually judged, so that the demand cannot be met for a direct coal liquefaction process which is expected to pay attention to the type and the content of the hydrogenated aromatic hydrocarbon; third, the pretreatment method in the petroleum analysis standard has poor reproducibility when applied to direct coal liquefaction oil.
Therefore, it is very important for some specific processes to find a new method for analyzing the composition of an organic sample that can obtain the kind and content of the hydrogenated aromatic hydrocarbon.
Disclosure of Invention
The invention aims to overcome the defect that the type and content of hydrogenated aromatic hydrocarbon in an organic sample are difficult to effectively obtain in the prior art when the organic sample is analyzed, and provides a component analysis method of the organic sample. The method for analyzing the components of the organic sample can intuitively obtain the types and the contents of the components (including the unhydrogenated aromatic hydrocarbon and the hydrogenated aromatic hydrocarbon).
In order to achieve the above object, the present invention provides a method for analyzing components of an organic sample, the organic sample containing saturated alkanes, hydrogenated aromatics, and non-hydrogenated aromatics, the method comprising the steps of:
(1) classifying and assigning the organic components by adopting a z value classification method;
(2) analyzing the organic sample by adopting a nuclear magnetic resonance hydrogen spectrum to obtain a nuclear magnetic resonance hydrogen spectrum of the organic sample;
(3) analyzing the organic sample by adopting a full-two-dimensional gas chromatography-time-of-flight mass spectrometry to obtain a full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram of the organic sample;
(4) analyzing the organic sample by using a full-two-dimensional gas chromatography-hydrogen flame ionization detector to obtain a full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram of the organic sample, wherein the full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram corresponds to peak positions of all components in the full-two-dimensional gas chromatography-flight time mass spectrometry detection spectrogram one by one;
(5) and (3) data analysis:
analyzing the nuclear magnetic resonance hydrogen spectrum to obtain first fixed information containing peak position and peak intensity;
analyzing the full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram to obtain second qualitative information containing retention time;
qualitatively determining each organic component in the organic sample according to the first qualitative information and the second qualitative information, and combining the result of the step (1) to form a qualitative template;
and then applying the qualitative template to data collected by the full-two-dimensional gas chromatography-hydrogen flame ionization detector according to the peak positions of all components in the organic sample in the full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram and the full-two-dimensional gas chromatography-flight time mass spectrometry detection spectrogram, and calculating the content of all components in the organic sample by an area normalization method.
Through the technical scheme, the analysis method disclosed by the invention at least has the following advantages:
(1) the method fills the blank that no more universal component analysis method suitable for organic samples except petroleum exists at present;
(2) the types and the contents of the non-hydrogenated aromatic hydrocarbon and the hydrogenated aromatic hydrocarbon can be respectively obtained;
(3) the result is visual;
(4) the accuracy is high;
(5) the method is simple, does not need pretreatment, and greatly shortens the analysis time.
Additional features and advantages of the invention will be set forth in the detailed description which follows.
Drawings
FIG. 1 is a schematic diagram of the structure and operation of an all two-dimensional gas chromatography-time-of-flight mass spectrometry/hydrogen flame ionization detector;
FIG. 2 is a nuclear magnetic resonance hydrogen spectrum of the recycled solvent A analyzed in example 1;
FIG. 3 is a two-dimensional lattice bubble diagram of the recycled solvent A analyzed in example 1;
FIG. 4 is a two-dimensional dot-matrix bubble chart of the recycled solvent B analyzed in example 2.
Description of the reference numerals
1-shunting sample injection port; 2-a one-dimensional column; 3-a first stage modulator; 4-carrier gas inlet;
5-a second stage modulator; 6-two-dimensional column; 7-a separator; 8-a first damping column; 9-a second damping column;
10-a time-of-flight mass spectrometer detector; 11-hydrogen flame ionization detector.
Detailed Description
The endpoints of the ranges and any values disclosed herein are not limited to the precise range or value, and such ranges or values should be understood to encompass values close to those ranges or values. For ranges of values, between the endpoints of each of the ranges and the individual points, and between the individual points may be combined with each other to give one or more new ranges of values, and these ranges of values should be considered as specifically disclosed herein.
The invention provides a component analysis method of an organic sample, wherein the organic sample contains saturated alkane, hydrogenated aromatic hydrocarbon and non-hydrogenated aromatic hydrocarbon, and the component analysis method comprises the following steps:
(1) classifying and assigning the organic components by adopting a z value classification method;
(2) analyzing the organic sample by adopting a nuclear magnetic resonance hydrogen spectrum to obtain a nuclear magnetic resonance hydrogen spectrum of the organic sample;
(3) analyzing the organic sample by adopting a full-two-dimensional gas chromatography-time-of-flight mass spectrometry to obtain a full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram of the organic sample;
(4) analyzing the organic sample by using a full-two-dimensional gas chromatography-hydrogen flame ionization detector to obtain a full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram of the organic sample, wherein the full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram corresponds to peak positions of all components in the full-two-dimensional gas chromatography-flight time mass spectrometry detection spectrogram one by one;
(5) and (3) data analysis:
analyzing the nuclear magnetic resonance hydrogen spectrum to obtain first fixed information containing peak position and peak intensity;
analyzing the full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram to obtain second qualitative information containing retention time;
qualitatively determining each organic component in the organic sample according to the first qualitative information and the second qualitative information, and combining the result of the step (1) to form a qualitative template;
and then applying the qualitative template to data collected by the full-two-dimensional gas chromatography-hydrogen flame ionization detector according to the peak positions of all components in the organic sample in the full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram and the full-two-dimensional gas chromatography-flight time mass spectrometry detection spectrogram, and calculating the content of all components in the organic sample by an area normalization method.
In the present invention, the organic sample includes materials whose main components are organic materials in various forms, such as solid state, powder state, and liquid state. In most cases, the organic sample refers to an organic solution, and the form of the organic sample can be changed according to the needs of the detection mode. According to a preferred embodiment of the present invention, the organic sample is a recycled solvent in a direct coal liquefaction process.
In step (1), the z-value classification can be performed according to a classification concept that is conventional in the art, for example, according to a method described in "application of organic mass spectrometry to petrochemistry" (Suhuan et al, chemical industry Press, page 86).
Preferably, the method for classifying and assigning the organic components by using the z-value classification method comprises the following steps: classifying the compounds to obtain family names, and writing the molecular formula of the compounds as CnH2n+zTo obtain a z value, then the compound is reacted withNamed as the name of the combination of the family name and the z value; wherein, the classification mode comprises the following steps: saturated alkanes are classified as group S, hydrogenated aromatics as group HA, and unhydrogenated aromatics as group a.
In addition, the classification manner of the present invention also preferably includes: compounds containing heteroatoms are classified as a family named for the elements of the heteroatom, e.g., oxygen-containing compounds are classified as group O, sulfur-containing compounds are classified as group S, and the like.
The nomenclature of the z-value classification of common compounds is shown, for example, in tables 1 and 2, and is illustrated as follows:
the designation of saturated alkanes includes, for example: paraffin S z ═ 2, monocycloparaffin S z ═ 0, dicycloalkane S z ═ -2, tricycloalkane S z ═ -4, tetracycloalkane S z ═ -6, and pentacycloalkane S z ═ -8.
The nomenclature for hydrogenated aromatics includes, for example: (ii) the monoalkylbenzene is HA z-8, the bicycloalkylbenzene is HA z-10, and the tricycloalkylbenzene is HA z-12;
for hydrogenated aromatics, HAz-12, HAz-14, HAz-16 and HAz-18 have similar polarities, similar molecular weights and small differences in retention times among the groups, and therefore, the hydrogenated aromatics are preferably synthesized into a small group for testing and analysis without discrimination in the testing and analysis, and the combined small group is referred to as HA z-12141618. Therefore, it is preferable that HAz ═ 12, HAz ═ 14, HAz ═ 16, and HAz ═ 18 hydrogenated aromatic hydrocarbons be combined in step (4) and step (5) and analyzed.
The nomenclature for the unhydrogenated aromatics includes, for example: benzene is A z ═ 6, naphthalene is A z ═ 12, phenanthrene is A z ═ 18, pyrene is A z ═ 22.
For the above classification, when the polarities of 2 or more compounds are similar, the molecular weights of each group are close, the difference in retention times is small, and the combination has little influence on the results, it is possible to combine into a small group to be tested and analyzed as a single body in the later tests and analyses.
In the step (2), nuclear magnetic resonance hydrogen spectrum (A)1H-NMR) analysis of the organic sample to obtain NMR hydrogen of the organic sampleAnd the spectrum spectrogram can acquire information such as peak position, peak intensity and the like from the nuclear magnetic resonance hydrogen spectrum spectrogram, and the information contained in the nuclear magnetic resonance hydrogen spectrum spectrogram is the first fixed information. The organic sample can be characterized by the first qualitative information.
In step (2), the analysis conditions of the nmr hydrogen spectrum may be performed according to the analysis conditions for measuring an organic sample, which are conventional in the art, for example, according to the analysis method for analyzing petroleum. The main aim is to increase the accuracy of the characterization and to exclude functional groups not contained in the recycled solvent.
In the step (3), analyzing the organic sample by using a full-two-dimensional gas chromatography-time-of-flight mass spectrometry to obtain a full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram of the organic sample, wherein information such as retention time can be obtained from the full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram, and the information contained in the full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram is the second qualitative information. The organic sample can be characterized by the second qualitative information.
Preferably, the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry comprise: the one-dimensional column adopts a non-polar chromatographic column, and the two-dimensional column adopts a weak-polar column.
Preferably, the solid phase of the one-dimensional column is dimethylpolysiloxane.
Preferably, the solid phase of the two-dimensional column is (40-60)% phenyl- (40-60)% methylpolysiloxane.
Preferably, the one-dimensional column has a column specification of (30-80) mx (0.15-0.25) mmx (0.2-0.55) μm, more preferably (30-80) mx (0.18-0.22) mmx (0.2-0.52) μm. In one embodiment, the one-dimensional column has a column size of 50m × 0.2mm × 0.5 μm.
Preferably, the two-dimensional column has a column size of (1.5-2.5) mx (0.2-0.3) mmx (0.2-0.3) μm, more preferably (1.9-2.1) mx (0.2-0.27) mmx (0.2-0.27) μm. In one embodiment, the two-dimensional column has a column size of 2m × 0.25mm × 0.25 μm.
Preferably, the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry comprise: the sample introduction amount is 0.1-1 mu L, the split ratio is (100-; the one-dimensional temperature program comprises: the initial temperature is 50-60 ℃, the temperature is kept for 0.8-1.5min, and then the temperature is raised to 300-320 ℃ at the speed of 1-2.5 ℃/min and kept for 10-20 min; the two-dimensional program includes: the compensation temperature is 5-15 ℃.
More preferably, the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry comprise: the sample introduction amount is 0.2-0.4 mu L, the split ratio is (180-; the one-dimensional temperature program comprises: the initial temperature is 50-55 ℃, the temperature is kept for 0.8-1.2min, and then the temperature is increased to 310-315 ℃ at the speed of 1.5-2 ℃/min and kept for 12-18 min; the two-dimensional program includes: the compensation temperature is 8-12 ℃.
Other parameters of the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrum can be set according to the conventional mode in the field, for example, the analysis conditions of the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrum also comprise: the bombardment voltage of the electron bombardment ionization source is 68-72eV, the solvent is not delayed, the temperature of the ion source is 240-260 ℃, the temperature of the transmission line is 270-290 ℃, the voltage of the detector is 1350-1450V, the collection mass range is 30-600amu, and the collection frequency is 90-110spectra/s (the number of spectra sampled per second); according to the arrangement common in the art, typically: the bombardment voltage of the electron bombardment ionization source is 70eV, the solvent is not delayed, the temperature of the ion source is 250 ℃, the temperature of the transmission line is 280 ℃, the voltage of the detector is 1400V, the collection mass range is 35-500amu, and the collection frequency is 100 spectra/s.
In the step (4), analyzing the organic sample by using a full-two-dimensional gas chromatography-hydrogen flame ionization detector to obtain a full-two-dimensional gas chromatography-hydrogen flame ionization detector detection spectrogram of the organic sample.
Preferably, the conditions of the hydrogen flame ionization detection in the comprehensive two-dimensional gas chromatography-hydrogen flame ionization detection include: the temperature of the detector is 300-320 ℃, the collection frequency is 95-105spectra/s, the tail gas is blown into inert gas, the flow rate of the tail gas is 45-55mL/min, the air flow rate is 440-460mL/min, and the hydrogen flow rate is 35-45 mL/min. According to a specific embodiment, the conditions of the hydrogen flame ionization detection in the comprehensive two-dimensional gas chromatography-hydrogen flame ionization detection comprise: the temperature of the detector is 320 ℃, the collection frequency is 100spectra/s, the tail blowing gas is He, the flow rate of the tail blowing gas is 50mL/min, the air flow rate is 450mL/min, and the hydrogen flow rate is 40 mL/min.
Preferably, the conditions of the hydrogen flame ionization detection in the comprehensive two-dimensional gas chromatography-hydrogen flame ionization detection further include: the solvent is not retarded.
In the invention, the apparatus of the comprehensive two-dimensional gas chromatography-time of flight mass spectrometry in the step (3) and the comprehensive two-dimensional gas chromatography-hydrogen flame ionization detector in the step (4) are combined into one apparatus, and the apparatus is named as a comprehensive two-dimensional gas chromatography-time of flight mass spectrometry/hydrogen flame ionization detector (GC x GC-TOF MS/FID). The operation mode of the full two-dimensional gas chromatography-time-of-flight mass spectrometry/hydrogen flame ionization detector is shown in fig. 1, and specifically comprises the following steps: a sample to be detected enters through a shunt sample inlet 1, and carrier gas enters through a
In the step (5), the data analysis is carried out by combining the results obtained in the steps (1) to (4) so as to obtain the types and the contents of the organic components in the organic sample. The data analysis process comprises the following steps: analyzing the nuclear magnetic resonance hydrogen spectrum to obtain first fixed information containing peak position and peak intensity; analyzing the full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram to obtain second qualitative information containing retention time; qualitatively determining each organic component in the organic sample according to the first qualitative information and the second qualitative information, and defining each component by using the assignment of each component obtained in the step (1); and then calculating the content of each component in the organic sample by an area normalization method according to the peak position of each component in the organic sample in the full-two-dimensional gas chromatography detection spectrogram and the full-two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram.
In step (5), the skilled person can determine the specific compound contained in the organic sample by characterizing each organic component in the organic sample according to information such as the peak position and the peak intensity in the first qualitative information and information such as the retention time in the second qualitative information. And the peak position (same as the peak time) of each component in the second qualitative information (namely the comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram) is the same as that in the comprehensive two-dimensional gas chromatography detection spectrogram, so that the specific position of the specific compound obtained qualitatively in the comprehensive two-dimensional gas chromatography detection spectrogram can be determined, and the quantification can be carried out on each component based on the information (including the peak area and the like) obtained by the comprehensive two-dimensional gas chromatography detection spectrogram.
In step (5), the method for quantifying each component is an area normalization method, which is a method conventional in the art. That is, the peak area of each component, which corresponds to the mass of the component, is obtained by performing calculus on the peak corresponding to each component, and the mass content of the component is obtained by dividing the peak area of the component by the sum of the peak areas of all the components, which corresponds to the mass of the component divided by the sum of the masses of all the components.
In the step (5), after a qualitative result is obtained, the components are defined by the assignment of the components obtained in the step (1), and a relative position qualitative template of each group is established (for example, according to the result of fig. 3, fig. 3 can be divided into 3 large regions, namely a paraffin region at the lowest end, a cycloparaffin region at the middle lower part and the right middle part and an aromatic hydrocarbon region at the middle upper part and the left upper part, wherein paraffin series and cycloparaffin series (a series of cycloparaffin series and a series of pentacycloalkane series) are sequentially arranged from low to high along with the extension of two-dimensional retention time, and in the aromatic hydrocarbon region, unhydrogenated aromatic hydrocarbons such as benzene, naphthalene, anthracene \ phenanthrene and the like and hydrogenated aromatic hydrocarbons are staggered in the two-dimensional direction, benzene series, cycloparaffin benzene series and a series from low to high are sequentially arranged according to the z value), and the qualitative template is applied to the full two-dimensional gas chromatography-time-flight mass spectrometry/hydrogen flame ion ionization And (3) transforming the data collected by the detector, and displaying the output result (comprising a full two-dimensional gas chromatography-time-of-flight mass spectrometry detection spectrogram, a full two-dimensional gas chromatography detection spectrogram and the like) in an assignment mode.
The method of the invention does not need the conventional pretreatment step in the petroleum analysis method, and can more quickly and accurately analyze and obtain the types and the contents of all components in the organic sample. The method overcomes the defect that the type and the content of the hydrogenated aromatic hydrocarbon cannot be visually judged by a petroleum analysis method, and can accurately measure the type and the content of the hydrogenated aromatic hydrocarbon.
Therefore, the method of the present invention can be used to effectively and readily measure the types and contents of components in organic samples instead of petroleum analysis methods and other various organic component analysis methods, and in particular, the method of the present invention can be suitably used in the measurement of organic samples in which hydrogenated aromatic hydrocarbons are particularly concerned, for example, in the analysis of a circulating solvent in a direct coal liquefaction process.
Preferably, therefore, the organic sample is a recycled solvent in a direct coal liquefaction process. Generally, the content of saturated paraffins, the content of hydrogenated aromatics and the content of unhydrogenated aromatics in the circulating solvent in the direct coal liquefaction process are in the range of 30 to 60% by weight, 30 to 60% by weight and 1 to 15% by weight.
The present invention will be described in detail below by way of examples.