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首页> 外文期刊>European Journal of Soil Science >Micropore characteristics of organic matter pools in cemented and non-cemented podzolic horizons
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Micropore characteristics of organic matter pools in cemented and non-cemented podzolic horizons

机译:胶结和非胶结梯形层中有机质池的微孔特征

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摘要

In Podzols, organic matter (OM) is stabilized mainly by interaction with minerals, as a direct consequence of pedogenic processes. Metal-organic associations strongly affect OM surface features, particularly microporosity. Cemented ortstein horizons (CM) may form during podzolization, accompanied by a spatial arrangement of OM on mineral surfaces, which differs from that in non-cemented horizons (N-CM). To investigate the metal-organic associations and their changes during pedogenesis, we selected both N-CM and CM podzolic horizons, isolated NaClO-resistant OM and compared the specific surface area (SSA) before and after OM oxidation. The SSA was assessed by using N-2, to detect the pores in the range of micropores (< 2 nm) and mesopores (2-50 nm), and CO2, to measure a smaller microporosity (< 0.5 nm), which is not accessible to N-2. Only the N-CM samples showed the typical increase in N-2-SSA after the removal of labile OM, while a decrease was found in all CM horizons. The CO2-SSA revealed a large number of small micropores characterizing OM, both before and after oxidation. The smallest micropore classes (< 0.5 nm) were, however, more abundant in NaClO-resistant OM, which had therefore a larger number of N-2-inaccessible surfaces than the labile pool. The N-2-SSA data thus indicated a more homogeneous coverage of mineral surfaces by stabilized OM in CM samples. Because of the abundance of small micropores, OM in these podzolic B horizons had extremely large CO2-SSA values (about 800 m(2) g(-1)), with sharp differences between the NaClO-labile OM (290-380 m(2) g(-1)) and the NaClO-stabilized pool (1380-1860 m(2) g(-1)), thus indicating very reactive illuvial organic materials
机译:在Podzols中,有机物(OM)主要通过与矿物质的相互作用来稳定,这是成岩过程的直接结果。金属-有机缔合会强烈影响OM表面特征,尤其是微孔性。胶结的奥特施泰因层位(CM)可能在地化过程中形成,伴有矿物在矿物表面的空间排列,这与非胶结的层位(N-CM)不同。为了研究成矿过程中的金属-有机缔合及其变化,我们选择了N-CM和CM梯形层,分离了耐NaClO的OM,并比较了OM氧化前后的比表面积(SSA)。通过使用N-2评估SSA,以检测微孔(<2 nm)和中孔(2-50 nm)范围内的孔,以及CO2,以测量较小的微孔(<0.5 nm),这不是N-2可以使用。除去不稳定的OM后,只有N-CM样品显示N-2-SSA的典型增加,而在所有CM视野中均发现N-2-SSA的减少。 CO2-SSA在氧化之前和之后均显示出大量表征OM的小微孔。但是,最小的微孔类别(<0.5 nm)在耐NaClO的OM中更为丰富,因此与不稳定的液池相比,N-2无法进入的表面数量更多。因此,N-2-SSA数据表明通过CM样品中稳定的OM可以更均匀地覆盖矿物表面。由于存在大量的小孔,这些梯形B层中的OM具有非常大的CO2-SSA值(约800 m(2)g(-1)),而NaClO不稳定的OM(290-380 m( 2)g(-1))和NaClO稳定池(1380-1860 m(2)g(-1)),因此表明反应性很强的有机物

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