Abstract
Pseudoestrogene bisphenol A (BPA) can be important ingredient of thermochromic inks, increasingly used materials in thermal printing paper, security printing, advertising, design and as temperature indicators in medicine and food industry. BPA mass fraction in thermochromic inks can be up to several percent. Hence, disposal of items with thermochromic prints pose a risk of environmental pollution. In this work BPA mass fraction was monitored during anaerobic degradation of papers with thermochromic prints in soil in both matrices: papers and soil. The degradation conditions simulated deeper layers of waste at a landfill site. Six types of papers with prints of thermochromic ink containing 2% of BPA were subjected to anaerobic degradation over up to 150 days. Initial mass fractions of BPA in papers decreased form (126–460) μg/g to (<QL – 45) μg/g after 150 days. BPA amounts were reduced 10 to 50 times depending on the paper type: least for synthetic paper and most for wood-free coated. For soil analysis new HPLC-UV method was developed and validated. The method was linear from 0.75 ng/g to 0.6 μg/g of BPA in soil with correlation coefficient of 0.9994. Method precision was 4.4%, accuracy 83% and detection limit 0.9 ng/g. Expectedly, amount of BPA in soil was increasing during the experiment. Mass fractions of BPA in soil were from not detected in earlier stage of degradation to (4.9–23.2) ng/g after 150 days. Final BPA amounts in soil were similar to those found in industrial, urban and agricultural soils worldwide. Hence, BPA from papers with thermochromic prints was notably decomposed, and contaminated soil had the capacity to absorb and decompose BPA even under anaerobic conditions. After 150 days of anaerobic degradation, only up to 1.86% of BPA contained in paper prints was found in soil, whilst, on average, 4% of initial BPA remained in paper.
Published Version
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