In order to study the phase transformation between 1nm manganate and 0.7nm manganate, a series of Slum Me^(2+) manganates were made after the synthetic 1nm Na^+ manganate substituted with different kinds of divalent c...In order to study the phase transformation between 1nm manganate and 0.7nm manganate, a series of Slum Me^(2+) manganates were made after the synthetic 1nm Na^+ manganate substituted with different kinds of divalent cations. The X-ray diffraction analysis of wet S1nm Me^(2+) manganates after 24 h room temperature dry showed that their basal d-spacing had been changed, indicating that there was phase transformation between 1nm and 0.7nm manganates. Take 1nm manganates with unstable structure collapsed into 0. 7nm manganate by losing one interlayer OH-H_2O, while those with stable structure still retained the 1nm d-spacing. This factor reminds us that the manganese nodule samples must be kept in wet condition to avoid the misleading results. The structural stabdity of 1nn manganate is mainly controlled by the interlayer divalent cations. There is a possitive correlation between the amount of cations in the interlayer and the structural stability, while the capacity of different canons in stabilizing the structure of 1nm manganate is as follows: Ni > Cu > Co > Zn > Ca>Mg > Na.展开更多
Synthetic Ium manganate has been made in the laboratory at low temperature. The d-spaciug of which shows 1. 002 nm, 0. 501 nm and 0. 34 nm respectively. As the analogue of natural 1nm manganate, it has been used for ...Synthetic Ium manganate has been made in the laboratory at low temperature. The d-spaciug of which shows 1. 002 nm, 0. 501 nm and 0. 34 nm respectively. As the analogue of natural 1nm manganate, it has been used for a serieS of experiments of divalent cations substitution. The results indicate that the 1nm manganate has very strong cation substitution capacity, which probable is the reason of the valuable metal such as Cu, Ni and Co enriched in the manganese nodules. The preference of canons substituting into S 1nm manganate is Cu>Co>Zn≥Ni>Ca>Mg. In the manganese nodules, the content of Ni is usually higher than that of Cu and Co, but in the cation substitution, the latter two are more preference than the former. One can infer from this differentiation that the post-deposition cation substitution is not the sole mechanism by which the valuable metals enter the manganese nodules. It could be the results of combined effects of both original formation and the post-deposition substitution of canons,which leads to the enrichment of valuable metal in the manganese nodules.展开更多
文摘In order to study the phase transformation between 1nm manganate and 0.7nm manganate, a series of Slum Me^(2+) manganates were made after the synthetic 1nm Na^+ manganate substituted with different kinds of divalent cations. The X-ray diffraction analysis of wet S1nm Me^(2+) manganates after 24 h room temperature dry showed that their basal d-spacing had been changed, indicating that there was phase transformation between 1nm and 0.7nm manganates. Take 1nm manganates with unstable structure collapsed into 0. 7nm manganate by losing one interlayer OH-H_2O, while those with stable structure still retained the 1nm d-spacing. This factor reminds us that the manganese nodule samples must be kept in wet condition to avoid the misleading results. The structural stabdity of 1nn manganate is mainly controlled by the interlayer divalent cations. There is a possitive correlation between the amount of cations in the interlayer and the structural stability, while the capacity of different canons in stabilizing the structure of 1nm manganate is as follows: Ni > Cu > Co > Zn > Ca>Mg > Na.
文摘Synthetic Ium manganate has been made in the laboratory at low temperature. The d-spaciug of which shows 1. 002 nm, 0. 501 nm and 0. 34 nm respectively. As the analogue of natural 1nm manganate, it has been used for a serieS of experiments of divalent cations substitution. The results indicate that the 1nm manganate has very strong cation substitution capacity, which probable is the reason of the valuable metal such as Cu, Ni and Co enriched in the manganese nodules. The preference of canons substituting into S 1nm manganate is Cu>Co>Zn≥Ni>Ca>Mg. In the manganese nodules, the content of Ni is usually higher than that of Cu and Co, but in the cation substitution, the latter two are more preference than the former. One can infer from this differentiation that the post-deposition cation substitution is not the sole mechanism by which the valuable metals enter the manganese nodules. It could be the results of combined effects of both original formation and the post-deposition substitution of canons,which leads to the enrichment of valuable metal in the manganese nodules.
