We analyzed the lignin-like polymer we produced to confirm the work is successful. In the first stage of analysis, we started by analyzing the content and structure of our lignin-like polymer by UV-visible spectroscopy. For the second stage, we used NMR spectroscopy and Mass Spectroscopy to analyze information about the molecular structure and molecular weight of our polymer. In the last stage, Thermogravimetric analysis is used to analyze the melting or decomposition point of our product. After the above experiments are completed, we have a deeper understanding of the lignin-like polymer we have made. These experimental data also help us in the application and improvement of the products.

Reaction experiment

   There is a difference between samples of coniferyl alcohol without reacting with enzymes and smaples with Laccase and Peroxidase. From the result, we can prove that the reaction has occurred. The absorption peak shifted to the left, comparing with simulation from study (P. J. Salazar-Valencia et al. 2005), the wavelength of β-5 linkage absorption peak is shorter. Our results are similar to the results of the study, which means our product has β-5 linkage.

Ultraviolet–visible spectroscopy, UV-Vis

Ultraviolet–visible spectroscopy (UV–Vis) refers to absorption spectroscopy or reflectance spectroscopy in the ultraviolet-visible spectral region.The absorption or reflectance in the visible range directly affects the perceived color of the chemicals involved.The wavelengths of absorption peaks can be correlated with the types of bonds in a given molecule and are valuable in determining the functional groups within a molecule.

Nuclear Magnetic Resonance Spectroscopy, NMR

  Nuclear Magnetic Resonance (NMR) is based on quantum magnetic properties at the atomic scale.The method of NMR observation of atoms is to place the sample under a large external magnetic field.Using such a process, molecular science research, such as molecular structure, dynamics, etc., can be performed.

  In the NMR experiment, we measured the commercial lignin, coniferyl alcohol and the products we made.

  First, we first dissolved the coniferyl alcohol in ethanol and measured NMR to obtain the 1H-NMR chart. The chemical shift of each H is derived by the structure of coniferyl alcohol.Then we predict the form of the bonds between each monomer and monomer, and take the product to measure 1H-NMR. Because of some peak changes and the others no changes, we find the most suitable bond to form of the product.

  As a result, our product concentration is too low, peaks are not very obvious, and we can't confirm the correct and proper structural analysis, but there are still some small peaks similar to lignin, which proves that we successfully made similar bonds and indirectly explained our reaction. The successful reaction of the enzymes.

Thermogravimetric analysis, TGA

  Thermogravimetric analysis (TGA) is a method of thermal analysis in which the mass of a sample is measured over time as the temperature changes. A TGA can be used for materials characterization through analysis of characteristic decomposition patterns. It is an especially useful technique for the study of polymeric materials.

  According to the chart, there is a tendency of pyrolysis at 150~160 °C; peroxidase+laccase has a pyrolysis reaction at 340~400 °C; laccase has a pyrolysis reaction at 420~480 °C.

1. The boiling point of coniferyl alcohol is 163~165°C. Compared with the TGA chart, there is a trend change in the range of 150~160°C. It is this temperature that causes the structure to pyrolysis and the slope is more inclined.


2. The product is similar to lignin and has a pyrolysis interval at 200-400 °C.


3. The product of laccase and the product of peroxidase+laccase, which have different phase transition temperatures, can prove that the products are not the same, which indirectly proves that we have a successful reaction, and peroxidase has a effect on the reactants.

Figure1: UV-Visible spectrum of products

Figure2: Simulation of the electronic or ultraviolet spectra for the 3 Coniferyl Alcohol units, with β-O-4 and β-5 linkages. (P. J. Salazar-Valencia et al. 2005)

Figure3: Chemical shift of coniferyl alcohol

   Chemical shift

Figure4: NMR Spectrum of coniferyl alcohol

Figure5: NMR Spectrum of commercial dealkaline lignin

Figure6: NMR Spectrum of Laccase-involved reaction product

Figure7: NMR Spectrum of Laccase & Peroxidase-involved reaction product

Reference

P. J. Salazar-Valencia, S. T. P´erez-Merchancano, and L. E. Bol´ıvar-Marin´ez. (2005). Optical Properties in Biopolymers: Lignin Fragments. Brazilian Journal of Physics, vol. 36, no. 3B.