Biobased content analysis is a well-established, analytically independent, standardized method to determine the biobased content of fuels and plastics, based on differences of the specific radiocarbon (14C) activity of fossil and recent biogenic compounds. This biogenic content analysis can be useful for the producers as a quality assurance tool, for the customers as feedback about the truly biobased products and for the control organizations as an independent analytical tool to prove the biological origin. More than 100 commercially available foods, cosmetics, and drug samples have been used for biobased carbon content analysis by accelerator mass spectrometry (AMS) 14C measurement to demonstrate the potential of this technique. Our results show that this measurement technique is a unique tool for the determination of biocontent in foodstuff and medical products. Most of the tested materials were nearly or completely biobased (≥ 98 pMC), and no completely fossil-based final product was detected. The lowest biogenic compound was measured in a vanilla aroma flavor. In 45 of the 102 samples selected a wide range (2–98%) presented fossil-based carbon content. The method can be applied for monitoring raw materials and final products for biobased content in the industry and consumer protection as well.

The biocomponent ratio in liquid fuels as well as the usage of renewable resources for fuel consumption in the transport sector needs to be increased as a result of EU directive 2003/30/EC. Based on radiocarbon (14C) measurements, it should be relatively simple and fast to measure the weight percentage of the fossil and biological sources by accelerator mass spectrometry (AMS) as recommended in the ASTM D 6866-12 and EN 16640 standards. In this study, a relatively easy and fast sample preparation and measurement method based on AMS measurements was developed at the Hertelendi Laboratory of Environmental Studies (HEKAL) using reference samples from the Hungarian MOL Nyrt. oil company. Considering the recent EU regulation for mixing rates of liquid fuels in the transport sector (0.7–2% biofuel content) and the projected higher rates (2–10% biofuel content), the method is applicable to determine fatty acid methyl ester (FAME) and/or hydrotreated vegetable oil (HVO) derived proportions of fuel blends with a 1σ uncertainty better than±0.3% m/m.