University of Rostock, Institute of Land Use, Justus-von-Liebig Weg 6, D-18051 Rostock, Germany.
Environ Sci Technol. 2010 Mar 15;44(6):2092-7. doi: 10.1021/es902963c.
Little is known about P species in agro-industrial byproducts from developing countries, which may be either pollutants or valuable soil amendments. The present study speciated P in dry (COD) and wet (COW) coffee, sisal (SIS), barley malt (BEB) and sugar cane processing (FIC) byproducts, and filter cakes of linseed (LIC) and niger seed (NIC)with sequential fractionation, solution (31)P nuclear magnetic resonance (NMR) spectroscopy, and P K- and L(2,3)-edge X-ray absorption near-edge structure (XANES) spectroscopy. The sequential P fractionation recovered 59% to almost 100% of total P (P(t)), and more than 50% of P(t) was extracted by H(2)O and NaHCO(3) in five out of seven samples. Similarly, the NaOH + EDTA extraction for solution (31)P NMR recovered 48-94% of P(t). The (31)P NMR spectra revealed orthophosphate (6-81%), pyrophosphate (0-10%), and orthophosphate monoesters (6-94%). Orthophosphate predominated in COD, COW, SIS, and FIC, whereas BEB, UC, and NIC were rich in orthophosphate monoesters. The concentrations of P(i), and P(o) determined in the sequential and NaOH + EDTA extractions and (31)P NMR spectra were strongly and positively correlated (r = 0.88-1.00). Furthermore, the P K- and L(2,3)-edge XANES confirmed the H(2)SO(4)--P(i) detected in the sequential fractionation by unequivocal identification of Ca--P phases in a few samples. The results indicate that the combined use of all four analytical methods is crucial for comprehensive P speciation in environmental samples and the application of these byproducts to soil.
关于发展中国家农业工业副产物中的 P 物种知之甚少,它们可能是污染物,也可能是有价值的土壤改良剂。本研究采用连续分级、溶液(31)P 核磁共振(NMR)光谱和 P K- 和 L(2,3)-边 X 射线吸收近边结构(XANES)光谱法对干燥(COD)和湿(COW)咖啡、剑麻(SIS)、大麦麦芽(BEB)和甘蔗加工(FIC)副产物以及亚麻籽(LIC)和尼日尔种子(NIC)的滤饼中的 P 进行了形态分析。连续分级回收了 59%至接近 100%的总磷(P(t)),在七种样品中的五种中,超过 50%的 P(t)可被 H(2)O 和 NaHCO(3)提取。同样,NaOH+EDTA 提取溶液(31)P NMR 回收了 48-94%的 P(t)。(31)P NMR 光谱显示正磷酸盐(6-81%)、焦磷酸盐(0-10%)和正磷酸盐单酯(6-94%)。COD、COW、SIS 和 FIC 中以正磷酸盐为主,而 BEB、UC 和 NIC 则富含正磷酸盐单酯。连续分级和 NaOH+EDTA 提取以及(31)P NMR 光谱中测定的 P(i)和 P(o)浓度之间呈强烈正相关(r = 0.88-1.00)。此外,P K- 和 L(2,3)-边 XANES 证实了连续分级中检测到的 H(2)SO(4)-P(i),通过在少数样品中对 Ca-P 相的明确鉴定得到证实。结果表明,综合使用所有四种分析方法对于环境样品中全面的 P 形态分析以及这些副产物在土壤中的应用至关重要。