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Acid buffer capacity of mineral horizons of podzolic and bog-podzolic soils of the Komi Republic

机译:科米共和国的坡地和沼泽坡地土壤矿层的酸缓冲能力

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摘要

The acid buffer capacity of water suspensions and KCl extracts from the main genetic horizons of podzolic and bog-podzolic soils of the Komi Republic was studied by continuous potentiometric titration. Acid titration of eluvial horizons involves the following buffer reactions: displacement of exchangeable bases by protons. dissolution of finely dispersed AI hydroxides, and protonation of pH-dependent exchange positions on Fe and A1 hydroxides. When the degree of hydromorphism increases, the acid buffer capacity of the water suspensions decreases because of the decrease in the pH of the initial titration point and in the content of exchangeable bases and amorphous A1 compounds. In the acid titration of water suspensions from the B and C horizons of the soils studied, the main buffer reaction is the displacement of exchangeable Ca and Mg by protons. A decrease in the basicity of the extracted aluminum hydroxo and aluminum-organic complexes and the protonation of anions of the strongest dissolved organic acids can be the main buffer reactions proceeding during the acid titration of KCl extracts from eluvial horizons of podzolic and bog-podzolic soils. The buffer role of the protonation of organic anions increases with the increasing degree of hydromorphism.
机译:通过连续电位滴定法研究了科米共和国Podzolic和Bog-Podzolic土壤的主要遗传视野中水悬浮液和KCl提取物的酸缓冲能力。洗脱层的酸滴定涉及以下缓冲反应:质子置换可交换碱。细分散的AI氢氧化物的溶解,以及Fe和Al氢氧化物上pH依赖的交换位置的质子化。当氢加氢度增加时,水悬浮液的酸缓冲能力会下降,这是因为初始滴定点的pH值以及可交换碱和无定形A1化合物的含量降低。在从土壤的B和C层对水悬浮液进行酸滴定中,主要的缓冲反应是质子置换可交换的Ca和Mg。在从梯田土壤和沼泽-土壤土壤的坡地中对KCl提取物进行酸滴定时,提取的氢氧化铝和铝-有机配合物的碱度降低以及最强的溶解有机酸阴离子的质子化可能是主要的缓冲反应。 。有机阴离子的质子化的缓冲作用随着氢加成程度的增加而增加。

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