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Formation and Ecotoxicity of N-HeterocyclicCompounds on Ammoxidation of Mono- and Polysaccharides

机译:N-杂环的形成及其生态毒性单糖和多糖氨氧化的化合物

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摘要

Ammoxidation of technical lignins under mild conditions is a suitable approach to artificial humic substances. However, carbohydrates as common minor constituents of technical lignins have been demonstrated to be a potential source of N-heterocyclic ecotoxic compounds. Ethyl acetate extracts of ammoxidation mixtures of the monosaccharides glucose and xylose exhibited considerable growth inhibiting activity in the OECD 201 test, with 4-methyl-1H-imidazole, 4-(hydroxymethyl)-1H-imidazole, and 3-hydroxypyridine being the most active compounds. The amount of N-heterocyclic compounds formed at moderate ammoxidation conditions (70 °C, 0.2 MPa O2, 3 h) was significantly lower for the polysaccharides cellulose and xylan (16–30 μg/g of educt) compared to glucose (15.4 mg). Ammoxidation at higher temperature is not recommendable for carbohydrate-rich materials as much higher amounts of N-heterocyclic compounds were formed from both monosaccharides (100 °C: 122.4–160.5 mg/g of educt) and polysaccharides (140 °C: 5.52–16.03 mg/g of educt).
机译:工业木质素在温和条件下的氨氧化是处理人造腐殖质的合适方法。但是,已证明碳水化合物是工业木质素的常见次要成分,是N杂环生态毒性化合物的潜在来源。单糖葡萄糖和木糖的氨氧化混合物的乙酸乙酯提取物在OECD 201试验中显示出显着的生长抑制活性,其中4-甲基-1H-咪唑,4-(羟甲基)-1H-咪唑和3-羟基吡啶最活跃化合物。与葡萄糖(15.4 mg)相比,在中等氨氧化条件下(70°C,0.2 MPa O2,3 h)形成的N-杂环化合物的量明显低于多糖纤维素和木聚糖(16–30μg/ g的离析物)。 。对于富含碳水化合物的材料,不建议在较高温度下氨氧化,因为单糖(100°C:122.4–160.5 mg / g的离析物)和多糖(140°C:5.52–16.03)都会形成大量的N-杂环化合物毫克/克离析物)。

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