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NANOMETER-SCALE CHEMICAL MODIFICATION OF NANO-BALL ALLOPHANE

机译:纳米球别石的纳米级化学修饰

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Nano-ball allophane is a hydrous Al silicate with a hollow-sphere morphology that contains some defects or pores along the spherule walls. Enlargement of the pore openings by dilute alkali treatment was confirmed by cation exchange capacity determinations using various alkylammonium cations as replacement cations. An allophane sample with a low Si/Al ratio (0.67) was equilibrated with 10 mM CaCl_2 (pH = 6.0) and the Ca~(2+) retained was extracted using aqueous 1 M NH_4Cl or alkylammonium chloride salts. The Ca~(2+) extracted by NH_4~+ was 15.1 cmolc kg~(-1), but CH_3NH_3~+ (mean diameter = 0.38 nm) only extracted 7.9 cmolc kg~(-1) of Ca~(2+). After 10 mM NaOH treatment (0.25 g:100 mL) of the allophane, the Ca~(2+) extracted by NH_4~+ was 29.7 cmolc kg~(-1), 29.6 cmolc kg~(-1) by CH_3NH_3~+, and 29.4 cmolc kg~(-1) by (CH_3)_2NH_2~+. The extraction of Ca~(2+) by the large C_2H_5NH_3~+ cation (mean diameter = 0.46 nm) only decreased to 26.1 cmolc kg~(-1), indicating that pore diameters were enlarged from ~0.35 to 0.45 nm. The significant increase in Ca~(2+) retention after NaOH treatment was attributed to the dissociation of increased numbers of newly exposed silanol groups in the enlarged pores. The low Si/Al ratio of the NaOH-dissolved material (0.35) and the decreased intensity of the 348 cm~(-1) IR band also suggested selective dissolution of the pore region. For allophane with a high Si/Al ratio (0.99) and much accessory polymeric Si, dissolution of polymeric Si and of the pore region occurred simultaneously. Alkali treatment produced a smaller increase in pore size and Ca~(2+) retention for allophanes with large Si/Al ratios than for allophanes with small Si/Al ratios. It was concluded that by altering the dilute alkali treatment conditions and varying the Si/Al ratio of allophane, the extent of structural modification or pore enlargement of the hollow spheres might be controlled.
机译:纳米球铝硅烷基铝是一种具有空心球形态的含水铝硅酸盐,沿球体壁含有一些缺陷或孔。通过使用各种烷基铵阳离子作为替代阳离子的阳离子交换容量测定,证实了通过稀碱处理导致的孔口扩大。用10 mM CaCl_2(pH = 6.0)平衡具有低Si / Al比(0.67)的脲烷样品,并使用1 M NH_4Cl水溶液或氯化烷基铵盐萃取保留的Ca〜(2+)。 NH_4〜+提取的Ca〜(2+)为15.1 cmolc kg〜(-1),CH_3NH_3〜+(平均直径= 0.38 nm)仅提取7.9 cmolc kg〜(-1)的Ca〜(2+) 。经过10 mM NaOH处理(0.25 g:100 mL)的金属铝甲酸酯后,NH_4〜+提取的Ca〜(2+)为29.7 cmolc kg〜(-1),CH_3NH_3〜+提取的Ca〜(2+)为29.6 cmolc kg〜(-1) (CH_3)_2NH_2〜+产生29.4 cmolc kg〜(-1)。大C_2H_5NH_3〜+阳离子(平均直径= 0.46 nm)对Ca〜(2+)的萃取仅降低至26.1 cmolc kg〜(-1),表明孔径从〜0.35 nm增大到0.45 nm。 NaOH处理后,Ca〜(2+)保留量的显着增加归因于在扩大的孔中新暴露的硅烷醇基团数量的增加解离。 NaOH溶解物的Si / Al比值较低(0.35),IR谱带的348 cm〜(-1)强度降低,也提示孔区域选择性溶解。对于具有高Si ​​/ Al比(0.99)和大量辅助聚合物Si的脲丙烷,聚合物Si和孔区域的溶解同时发生。与具有较小Si / Al比率的脲基甲酸酯相比,碱处理对具有大Si / Al比率的脲基甲酸酯产生的孔尺寸和Ca〜(2+)保留的增加较小。结论是,通过改变稀碱处理条件和改变脲丙烷的Si / Al比,可以控制中空球的结构改性程度或孔扩大。

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