提高Li/MnO2扣式电池质量的研究

探索了提高ＭｎＯ２ 电化学活性的方法,正极材料和电解液的配比和用量,以及工艺过程中应注意的问题。     

The Composite Effect of Nanometer MnO2 Mixed with the Electrolytic MnO2

The nanometer MnO2 has outstanding electrochemical performance theoretically, but it is not suitable for actual utilization, which may result in capacity decrease and resource waste. In this study we have utilized the characterizations of the nanometer material, synthesized a type of nanometer α-MnO2 through KMnO4 and KNO3 with hydrothermal method, and mixed the products into micron electrolytic manganese dioxide （EMD） to enhance the electrochemical performance of the electrode.The cyclic voltammogram and galvanostatical discharge measurements of the samples were investigated. It is found that the 50﹪ nanometer MnO2 mixed electrode has the best electrochemical performance. The electrochemical performance improvement mechanism of the sample nanometer MnO2 mixed into micron EMD was discussed. With the existence of electrolyte, the nanometer MnO2 particles filled into the interspaces of the micron EMD particles, the mass and charge transfer conditions of the electrode reaction were improved, and the electrode polarization was diminished.     

Adsorption behaviors of Cd^2＋ on Fe2O3/MnO2 and the effects of coexisting ions under alkaline conditions

This study describes the adsorption features of cadmium on Fe2O3 and MnO2 in alkaline saline conditions. The adsorption reached equilibrium in 6 hours under alkaline conditions. The absorption of cadmium on Fe2O3 and MnO2 was consistent with Freundlich absorption isotherms, and the corresponding adsorption capacities were 16.3 and 16.7 mg·g-1, respectively. Moreover, the adsorption quantity of cadmium on Fe2O3 and MnO2 rose with increasing pH from acidic to neutral, and reached the maximum at pH= 9. The coexisting chlorides reduced the adsorption capacity of Fe2O3 and MnO2. The influence intensities of different cations follow the order of CaCl2>>KCl>NaCl. However, the influence of sodium salts on the capacities of Fe2O3 and MnO2 to adsorb cadmium appeared more complicated: the relatively low concentrations of sodium salts could reduce the adsorption capacity; with increasing concentrations of sodium salts, e.g. NaCl and NaNO3. The adsorption capacity decreased continually. Moreover, due to the competition adsorption and precipitation effects, the adsorption capabilities of Na2CO3, NaH2PO4 and Na2HSO4 could also be reduced and cadmium concentrations in the solution were reduced as well.     

Metamorphic evolution of the Georgetown Inlier,northeast Queensland,Australia; evidence for an accreted Palaeoproterozoic terrane?

Mineral textures, coupled with thermodynamic modelling in the MnO–Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O (MnNCKFMASH) model system, of mid‐amphibolite facies metapelites from the Georgetown Inlier, northeast Australia, point to the recording of two separate and unrelated metamorphic events. The first occurred contemporaneously with Palaeo‐ to Mesoproterozoic orogenesis and involved heating and burial to temperatures and pressures of approximately 600–650 °C and 6.0–7.0 kbar. Textural evidence for the up‐temperature (and pressure) prograde part of this path is inferred from the inclusion of garnet in biotite and staurolite. The second metamorphic event resulted in a low‐pressure thermal overprint that is equated with the advective addition of heat to the terrane via the emplacement of the Forsayth Batholith (c. 1550 Ma). This event is inferred from subsequent growth of andalusite and randomly orientated fibrolitic sillimanite after garnet, biotite and staurolite. This two stage metamorphic evolution, when coupled with a number of other distinct geological characteristics, suggests that the Georgetown Inlier is dissimilar to the other Australian Palaeoproterozoic terranes with which it is commonly correlated.     

东疆哈尔里克变质带中石榴子石的特征

石榴子石为东疆哈尔里克变质带中的常见矿物。从外形上可分为两种 类型,一种是晶形发育较好的石榴子石,为断裂区域变质作用形成;另一种是破碎状、裂纹 发育的石榴子石,为早期热变质作用形成,呈残留状出现。二者在空间上共存。对于晶形较 好的石榴子石的化学成分研究表明,石榴子石发育生长环带,在晶体粒径与核部MnO的含量 之间存在着相关关系。其峰期MnO的含量反映了递增变质带变质温度变化的趋势。     

Room-temperature compressibilities of MnO and CdO: further examination of the role of cation type in bulk modulus systematics

Room-temperature volume measurements up to 8.1 GPa reveal that rock-salt structured MnO and CdO have identical compressibility in the pressure range studied. In the plot of bulk modulus vs unit-cell volume, CdO plots well above the trend of the 3d transition metal monoxides, a behavior that deviates from empirical predictions of constant K ₀ V ₀. The present observations are in favor of our earlier suggestion that, for isostructural solids, the empirically predicted bulk modulus-volume relationship may be limited to their subsets that share the same valence electron character (i.e., s vs 3d vs 4d). For cations forming transition metal monoxides, variations of Pauling electronegativity with ionic radius show differences that are qualitatively similar to the observed trends of bulk modulus, suggesting that bond covalency differences may contribute to the different behaviors between the 3d and 4d transition metal monoxides. Received: 23 November 1998 / Revised, accepted: 1 April 1999     

X-射线荧光光谱法定量分析海山富钴结壳中MnO2与MnO的含量之比值

通过普通X-射线荧光光谱仪,结合PeakFit谱峰处理软件,对不同比例的MnO和MnO₂的混合样品的K_β谱峰参数进行了研究,用数学方法将实测的谱峰分解为各个单一的谱峰参数(峰位、峰高、半高宽、子峰面积),找出了各个谱峰参数与不同价态锰的含量之间的关系,并据此确定了中太平洋海山区大量富钴结壳样品中不同价态锰的相对含量.分析结果显示,富钴结壳中+4价锰从核心向外有增高的趋势,可以认为这与该区第三纪以来南极底流活动的增强有关.     

The effect of whole-rock MnO content on the stability of garnet in pelitic schists during metamorphism

Garnet-bearing mineral assemblages are commonly observed in pelitic schists regionally metamorphosed to upper greenschist and amphibolite facies conditions. Modelling of thermodynamic data for minerals in the system Na₂O–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O, however, predicts that garnet should be observed only in rocks of a narrow range of very high Fe/Mg bulk compositions. Traditionally, the nearly ubiquitous presence of garnet in medium- to high-grade pelitic schists is attributed qualitatively to the stabilizing effect of MnO, based on the observed strong partitioning of MnO into garnet relative to other minerals. In order to quantify the dependence of garnet stability on whole-rock MnO content, we have calculated mineral stabilities for pelitic rocks in the system MnO–Na₂O–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O for a moderate range of MnO contents from a set of non-linear equations that specify mass balance and chemical equilibrium among minerals and fluid. The model pelitic system includes quartz, muscovite. albite, pyrophyllite, chlorite, chloritoid, biotite, garnet, staurolite, cordierite, andalusite, kyanite. sillimanite, K-feldspar and H₂O fluid. In the MnO-free system, garnet is restricted to high Fe/Mg bulk compositions, and commonly observed mineral assemblages such as garnet–chlorite and garnet–kyanite are not predicted at any pressure and temperature. In bulk compositions with X_Mn= Mn/(Fe + Mg + Mn) > 0.01, however, the predicted garnet-bearing mineral assemblages are the same as the sequence of prograde mineral assemblages typically observed in regional metamorphic terranes. Temperatures predicted for the first appearance of garnet in model pelitic schist are also strongly dependent on whole-rock MnO content. The small MnO contents of normal pelitic schists (X_Mn= 0.01–0.04) are both sufficient and necessary to account for the observed stability of garnet.