A Method for Constructing the Average Molecular Structure Model of Complex Organic Macromolecules
A technology of organic macromolecules and macromolecular structures, applied in molecular design, material separation, material analysis, etc., can solve the problems of unclear understanding of complex organic macromolecular structures
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0119] 1. Taking coal sample 1 as an example, conduct elemental analysis on dry ash-free coal sample 1 to obtain the content of each element, N element: 1.2602%, C element: 65.6475%, H element: 4.9053%, S element: 2.207%, O * element: 25.98%, where O* is obtained by subtraction. Assume that the molecular weight of coal sample 1 is about 3000, and the molecular formula is C 169 h 152 o 50 N 3 S 2 .
[0120] 2. Peakfit split peak analysis; Figure 1 is the Peakfit split peak fitting curve of coal sample 1, and the aromatic hydrogen rate, hydrogen-carbon atomic ratio, methyl methylene ratio, and aromatic carbon ratio are obtained from the peak split data.
[0121] (1) Aromatic hydrogen rate
[0122] h al / H ar =A al / A ar = 6.8982 / 2.1356 = 3.2301
[0123] h ar / H=0.2364
[0124] (2) Hydrogen to carbon atomic ratio
[0125] H / C=H m / (C m / 12)=0.8963
[0126] (3) ratio of methyl methylene to
[0127] CH 3 / CH 2 =[A(2881cm -1 )+A(2950cm -1 )] / [A(2850cm -1 )+A(2...
Embodiment 2
[0144] 1. Coal sample 2. Carry out elemental analysis on coal sample 2 to obtain the content of each element, N element: 0.931%, C element: 63.72%, H element: 4.251%, S element: 0.979%, O* element: 30.12%, where O* is determined by the difference Get by subtraction. Assuming that the relative molecular mass of the average molecular structure of coal sample 2 is about 3000, the molecular formula of the average molecular structure model is obtained as C 159 h 128 o 56 N 2 S.
[0145] 2. Peakfit split peak analysis; Figure 5 is the coal sample 2Peakfit peak split fitting curve, and the structural parameters are obtained through the peak split data: aromatic hydrogen ratio, hydrogen-carbon atomic ratio, methyl methylene ratio, and aromatic carbon ratio.
[0146] (1) Aromatic hydrogen rate
[0147] Har / H=Aar / (Aar+Aal)=0.785 / (0.785+4.339)=0.1532
[0148] (2) Hydrogen to carbon atomic ratio
[0149] H / C=(H m / 1) / (C m / 12)=0.8006
[0150] (3) ratio of methyl methylene to
...
Embodiment 3
[0169] 1. Coal sample3. Firstly, elemental analysis is carried out to obtain the content of each element, N element: 0.75%, C element: 51.42%, H element: 3.78%, S element: 0.65%, O* element: 43.40%, where O* is obtained by subtraction. It is determined that the relative molecular weight of coal sample 3 is about 2000. The molecular formula obtained from the average molecular structure model is C 98 h 96 NO 44 , Mr=1990.
[0170] 2. Peakfit split peak analysis; Figure 9 is the coal sample 3Peakfit peak split fitting curve, and the structural parameters are obtained through the peak split data: aromatic hydrogen ratio, hydrogen-carbon atomic ratio, methyl methylene ratio, and aromatic carbon ratio.
[0171] (1) Aromatic hydrogen rate
[0172] Har / H=Aar / (Aar+Aal)=27.14 / (027.14+83.729)=0.2448
[0173] (2) Hydrogen to carbon atomic ratio
[0174] H / C=(H m / 1) / (C m / 12)=0.9860
[0175] (3) ratio of methyl methylene to
[0176] CH 3 / CH 2 =[A(2871cm -1 )+A(2889cm -1 )+...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


