Gas chromatography experiments were carried out with a GC 6890 gas chromatograph coupled with a Hewlett Packard GC 5975B mass spectrometer (Agilent 5975B, Santa Clara, CA, USA). The GC-MS operation was performed according to the procedure described by (Chen et al., 2020 (link)). To obtain the resin component content, 0.05 g resin was dissolved in 0.5 mL of ethyl alcohol containing 50 µL tetramethylammonium hydroxide. The GC column temperature conditions were as follows: the initial column temperature was 60°C, held for 2 min, increased at 8°C min-1 to 80°C, and reached a maximum of 280°C at a rate of 2°C per min for 5 min. The helium gas flow was set at 1 ml min-1. The temperature of the injector was 260°C, and the volume was 1 µL with a 1/50 split ratio. Mass spectra were recorded under electron impact ionization at an electron energy of 70 eV in the range from m/z 30 to 600 along with solvent delay for 3 min.
Resin compositions were identified by matching experimental fragmentation patterns in mass spectra with the NIST08 database through the data processing system of Agilent Chem Station and then comparing with the relevant literature. Monoterpene and sesquiterpene content were determined by isobutylbenzene content, and diterpene content was determined by heptadecanoic acid content. We calculated the resin component content by comparing their peak areas.
Resin compositions were identified by matching experimental fragmentation patterns in mass spectra with the NIST08 database through the data processing system of Agilent Chem Station and then comparing with the relevant literature. Monoterpene and sesquiterpene content were determined by isobutylbenzene content, and diterpene content was determined by heptadecanoic acid content. We calculated the resin component content by comparing their peak areas.
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