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11.
12.
多金属结核中二氧化锰的测定 总被引:1,自引:0,他引:1
用过量的含有H2SO4的(NH4)2Fe(SO4)2溶液分解多金属结核的同时,还原了试样中的MnO2,然后以K2Cr2O7标准溶液滴定测定了多金属结核中的MnO2。就样品分解过程中的加热温度和时间对测定结果的影响及标准溶液的标定等问题进行了讨论,经多次测定,方法重现性好。应用此方法为新研制的多金属结核标准物质提供了MnO2的定值数据,其结果与初定值相符,无剔除值,精密度(RSD,n=8)小于06%。 相似文献
13.
痕量铁和锰的化学发光检测 总被引:5,自引:1,他引:5
评述了国内外有关铁、锰的化学发光分析进展。从发光体系、操作方式、最佳条件、干扰离子、检测限等各个方面对化学发光法测定铁、锰及其它们与其它组分同时测定中的应用进行分类评述。 相似文献
14.
我国现有锰矿资源状况,不能满足钢铁工业发展的需要。寻找低磷低铁低硅富锰矿,是解决锰矿资源短缺的重要途径。城口锰矿具有较大的找矿前景,锰矿层产出稳定,锰含量高,铁含量低,烧失量大。加强城口矿区勘查,扩大矿床规模,可望成为我国锰矿的重要生产基地。 相似文献
15.
南宁、百色盆地红土风化壳的地球化学特征及其环境意义* 总被引:4,自引:0,他引:4
本文以广西南宁盆地那桐风化壳,及百色盆地江泽风地壳的大量土体化学分析数据为依据,进行了第四纪红土的确认、形成、分布和土壤肥力状况。以及通过地球化学强度、硅铁系数、硅铝系数等指标进行了两风化壳的对比研究。同时,还探讨了风化壳的发育过程及其与环境的关系。 相似文献
16.
湘西南区氧化锰矿以锰帽型氧化锰矿为主,赋矿地层为震旦系下统湘锰组。其特点是含锰点多,分布面广,矿体在地壳贫化,往下3~7m开始富集,氧化深度40m左右。 相似文献
17.
催化褪色光度法测定痕量锰的研究及应用 总被引:2,自引:0,他引:2
本研究了在PH=4.0醋酸-醋酸钠缓冲溶液中,锰催化KIO4氧化5-Br-PADAP的褪色反应及其动力学条件,建立了一个痕量锰的高灵敏度新方法,方法灵敏度为1.32×10^-10g/ml,测定范围Mn^2+浓度为0 ̄1.5μg/ml,用于测定人发,自来水,茶叶中痕量锰,结果满意。 相似文献
18.
M. Roy-Barman C. Jeandel M. Souhaut M. Rutgers van der Loeff I. Voege N. Leblond R. Freydier 《Earth and Planetary Science Letters》2005,240(3-4):681-693
230Th, 232Th and 234Th were analyzed in sinking particles collected by moored and drifting sediment traps in the NE Atlantic Ocean (POMME experiment) in order to constrain the phase(s) carrying Th isotopes in the water column. It reveals a contrasted behaviour between 234Th and 230Th. 234Th is correlated to the particulate organic carbon suggesting that it is primarily scavenged by organic compounds in the surface waters. 230Thxs is correlated with Mn, Ba and the lithogenic fraction that are enriched in small suspended particles and incorporated in the sinking particulate flux throughout the water column. The lack of correlation between 230Thxs and CaCO3 or biogenic silica (bSi) indicates that CaCO3 and bSi are not responsible for 230Th scavenging in the deep waters of this oceanic region. 230Th is generally correlated with the lithogenic content of the trapped material but this correlation disappears in winter during strong atmospheric dust inputs suggesting that lithogenic matter is not directly responsible for 230Th scavenging in the deep waters or that sufficient time is required to achieve particle–solution equilibration. MnO2 could be the prevalent 230Thxs-bearing phase. The narrow range of Kd_MnO2Th obtained for very contrasted oceanic environments supports a global control of 230Thxs scavenging by MnO2 and raises the possibility that the 230Th–231Pa fractionation is controlled by the amount of colloidal MnO2 in seawater. 相似文献
19.
Abstract. Chemistry and sulfur isotopes are analyzed for a series of rocks in the chert‐dominant sequence around the stratiform manganese ore deposit of the Noda‐Tamagawa mine in the northern Kitakami Terrane, northeast Japan. The sequence is litholog‐ically classified into six units in ascending order: lower bedded chert, lower black shale, massive chert, manganese ore, upper black shale, and upper bedded chert. The rocks around the manganese ore deposit exhibit anomalous enrichment in Ni (max. 337 ppm), Zn (102) and U (30) in the upper part of lower bedded chert, Mo (122), Tl (79) and Pb (33) in the lower black shale, MnO, Cu (786) and Co (62) in the manganese ore, and As (247) and Sb (17) in the upper black shale. The aluminum‐normalized profiles reveal zonal enrichment of redox‐sensitive elements around the manganese bed: Zn‐Ni‐Fe‐Mo‐U(‐Co), Tl‐Pb(‐Mo), Mn‐Fe‐Cu‐V‐Cr‐Co(‐Zn) and As‐Sb in ascending order. The uppermost part of the lower bedded chert and black shale exhibit negative Ce/Ce* values, whereas the massive chert, manganese ore and lower part of the upper bedded chert display positive values. The isotopic δ34S values are 0±6 % in the lower part of the lower bedded chert, ‐19 to ‐42 % in the upper part of the lower bedded chert, ‐36 to ‐42 % in the lower black shale, ‐28 to ‐35 % in the massive chert, manganese ore and upper black shale, and ‐23±5 % in the upper bedded chert. Thus, there is a marked negative shift in δ34S values in the lower bedded chert, and an upward‐increasing trend in δ34S through the manganese ore horizon. The present data provide evidence for a change in the paleoceanographic environmental resulting from inflow of oxic deepwater into the stagnant anoxic ocean floor below the manganese ore horizon. This event is likely to have triggered the precipitation of manganese oxyhydroxides. The redistribution of redox‐sensitive elements through the formation of metalliferous black shale and manganese carbonate ore may have occurred in association with bacterial decomposition of organic matter during early diagenesis of initial manganese oxyhydroxides. 相似文献
20.
Abstract. Inorganic chemical compositions are determined for a series of rocks crossing an Early Jurassic stratiform manganese ore deposit in a chert‐dominant sequence at Katsuyama, in the Mino Terrane of central Japan. The lithology in the vicinity of the manganese ore bed is classified into lower bedded chert, black shale, massive chert, manganese ore and upper bedded chert, in ascending order. The rocks surrounding the manganese deposit are anomalously high in certain elements: Pb (max. 29 ppm), Ni (1140) and Co (336) in the lower bedded chert, Mo (438), As (149), Tl (29) and U (12) in the black shales, V (210) and Cr (87) in the massive chert, and MnO and W (24) in the manganese ore. The aluminum‐normalized profiles reveal a distinct zonation of redox‐sensitive elements: Pb‐Zn, Ni‐Co‐Cu(‐Zn) and U‐Cr in the lower bedded chert, Mo‐As‐Tl in the black shale, V(‐Cr) in the massive chert, and Mn‐Fe‐Ba‐W in the manganese ore, in ascending order. The lower and upper bedded cherts and manganese ore generally exhibit flat rare earth element patterns with positive Ce anomalies, whereas the uppermost part of the lower bedded chert, the black shale and massive chert have flat patterns with weak or nonexistent negative Ce anomalies and weak positive Eu anomalies. The strong enrichment in Ni, Co, W, Tl and As detected in the Katsuyama section is not recognized in other sediments, including those of anoxic deposition origin, but is identified in modern ferromanganese nodules, suggesting that metal enrichment in the Katsuyama section is essentially due to the formation of ferromanganese nodules rather than to deposition in an anoxic environment. The observed elemental zonation is well explained by equilibrium calculations, reflecting early diagenetic formation and associated gradual reduction with depth. The concentration profiles in combination with litho‐ and biostratigraphical features suggest that formation of these bedded manganese deposits was triggered by an influx of warm, saline and oxic water into a stagnant deep ocean floor basin in Panthalassa at the end of the middle Early Jurassic. Paleoceanographic environmental controls thus appear to be important factors in the formation and preservation of this type of stratiform manganese deposit. 相似文献