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221.
Here we report iron (Fe) isotopic data of three pure Fe solution standards (IRMM-014, GSB Fe, and NIST 3126a) and five widely used geological reference materials (RMs) from the United States Geological Survey and Geological Survey of Japan obtained on a Neptune Plus multi-collector–inductively coupled plasma–mass spectrometer (MC-ICP-MS) in our laboratory over the past 3 years. The instrumental mass bias was corrected by three independent methods: sample-standard bracketing (SSB), Ni doping?+?SSB, and 57Fe–58Fe double spike?+?SSB. Measurements reveal that both the Ni doping and double spike methods helped calibrate short-term fluctuations in mass bias. Collectively, almost all measurements of RMs yielded δ56Fe within?±?0.05 of recommended values, provided that each sample was measured four times on MC-ICP-MS. For the first time, new recommended values for NIST SRM3126a are reported (δ56Fe?=?0.363?±?0.006, 2SE, 95% CI; and δ57Fe?=?0.534?±?0.010, 2SE). 相似文献
222.
Calcite was synthesized by four methods, and the luminescence decay-time was measured for nine samples before and after heating
hydrothermally in the temperature range 200–400°C. Decay-time data were collected between room temperature and approximately
15 K. The decay time at room temperature is approximately 50 ms, with little difference between a given calcite before and
after hydrothermal treatment. The decay time at 15 K is always greater than at room temperature as the effect of thermal quenching
diminishes. Differences in decay time before and after heating are more apparent at low temperature owing to this reduction
in thermal quenching. The decay time decreased significantly in two samples, and an increase in decay time was observed in
the remaining seven samples following heating. Among the latter group, the change in decay time was insignificant in three
samples. The results are compared with previous data in which it was shown that the effect of heating is to increase the intensity
of luminescence. 相似文献
223.
Adsorption of antimony(V) on kaolinite as a function of pH,ionic strength and humic acid 总被引:1,自引:0,他引:1
The present work investigated the adsorption and mobility (desorption) of Sb(V) on kaolinite using batch experiments. The
adsorption of Sb(V) on kaolinite was studied as a function of contact time, pH, ionic strength, humic acid (HA), initial Sb(V)
concentration and temperature. Kinetic studies suggest that the equilibrium is achieved within 24 h. The adsorption of Sb(V)
was strongly affected by changes in I at low ionic strength and unaffected at high ionic strength. The adsorption is weakly
dependent on the presence of humic acid, but is strongly dependent on pH. Within the range tested, the optimal pH for Sb(V)
adsorption is 3.6, and close to 75% removal can be achieved. Desorption is dependent on the original suspension pH. The addition
sequence of Sb(V)/HA do not influence the adsorption of Sb(V) on kaolinite. The adsorption data fit both the Freundlich and
Langmuir isotherm. The thermodynamic parameters (ΔH
0, ΔS
0 and ΔG
0) were calculated from the temperature dependence, and the results suggest the endothermic and spontaneous nature of the process. 相似文献
224.
Hamid El Maanaoui Fabian Wilangowski Aditya Maheshwari Hans-Dieter Wiemhöfer Rainer Abart Nicolaas A. Stolwijk 《Physics and Chemistry of Minerals》2016,43(5):327-340
We measured the ion conductivity of single-crystal alkali feldspar originating from two different locations in the Eifel/Germany, named Volkesfeld and Rockeskyller sanidine and having potassium site fractions \(C_\mathrm{K}\) of 0.83 and 0.71, respectively. The dc conductivities resulting from electrochemical impedance spectroscopy over the temperature range of 300–900 \(^{\circ }\hbox {C}\) show a weak composition dependence but pronounced differences between the b-direction [\(\perp (010)\)] and \(c^{*}\)-direction [\(\perp (001)\)] of the monoclinic feldspar structure. Conductivity activation energies obtained from the observed linear Arrhenius plots are close to 1.2 eV in all cases, which is closely similar to the activation energies of the \(^{22}\mathrm{Na}\) tracer diffusivity in the same crystals. Taking into account literature data on K tracer diffusion and diffusion correlation effects, the present results point to a predominance of the interstitialcy mechanism over the vacancy mechanism in mass and charge transport on the alkali sublattice in potassium-rich alkali feldspar. 相似文献
225.
Sandstones of Jhuran Formation from Jara dome, western Kachchh, Gujarat, India were studied for major, trace and rare earth element (REE) geochemistry to deduce their paleo-weathering, tectonic setting, source rock characteristics and provenance. Petrographic analysis shows that sandstones are having quartz grains with minor amount of K-feldspar and lithic fragments in the modal ratio of Q 89:F 7:L 4. On the basis of geochemical results, sandstones are classified into arkose, sub-litharenite, wacke and quartz arenite. The corrected CIA values indicate that the weathering at source region was moderate to intense. The distribution of major and REE elements in the samples normalized to upper continental crust (UCC) and chondrite values indicate similar pattern of UCC. The tectonic discrimination diagram based on the elemental concentrations and elemental ratios of Fe2O3 + MgOvs. TiO2, SiO2 vs. log(K2O/Na2O), Sc/Cr vs. La/Y, Th–Sc–Zr/10, La–Th–Sc plots Jhuran Formation samples in continental rift and collision settings. The plots of Ni against TiO2, La/Sc vs. Th/Co and V–Ni–Th ?10 reveals that the sediments of Jhuran Formation were derived from felsic rock sources. Additionally, the diagram of (Gd/Yb) N against Eu/Eu ? suggest the post-Archean provenance as source possibly Nagar Parkar complex for the studied samples. 相似文献
226.
Prosper Rakotovao Andrianjakavah Stefano Salvi Didier Béziat Michel Rakotondrazafy Gaston Giuliani 《Mineralium Deposita》2009,44(7):817-835
The Ianapera emerald deposit is located in the Neoproterozoic Vohibory Block of southern Madagascar. The local geology consists
of intercalated migmatitic gneissic units and calcareous metasedimentary rocks, containing boudinaged metamorphosed mafic/ultramafic
lenses, all intruded by pegmatite veins. These units occur near the hinge of the tightly folded Ianapera antiform, within
a few kilometers of the Ampanihy shear zone. Emerald mineralization is hosted by metasomatic phlogopite veins, and bodies
developed within the mafic/ultramafic rocks. Based on field and textural relationships, we distinguish proximal and distal
styles of mineralization. Proximal mineralization occurs at the contact of pegmatite veins with mafic/ultramafic units; in
the distal style, pegmatites are not observed. Three types of emeralds could be distinguished, mainly on the basis of color
and mineral zoning. Some of these emeralds have the most Al-depleted and Cr-rich composition ever recorded. Another characteristic
feature to the Ianapera deposit and, to our knowledge, yet unreported, is the association of some emeralds with scapolite
in metasomatised mafic rocks. Mineral inclusions are common in most emeralds and include phlogopite, carbonates, barite, K-feldspar,
quartz, pyrite, zircon, monazite, bastnaesite, phenakite, plus Fe and Cr oxides. However, feldspar and rare earth element-bearing
minerals occur predominantly in proximal emeralds, which also have a more incompatible trace-element signature than distal
emeralds. We propose a model related to syn- to post-tectonic magmatic-hydrothermal activity. Pegmatitic bodies intruded units
of the Ianapera antiform probably during tectonic relaxation. Exsolution of fluids rich in halogens and incompatible elements
from the cooling pegmatites caused hydrothermal metasomatism of Cr-bearing mafic/ultramafic rocks in direct contact with the
pegmatites. Local fracturing favored fluid infiltration, permitting the formation of distal mineralization. Emerald composition
was controlled by the chemistry of the host rock. The presence of carbonate mineral inclusions in the emeralds and the high
F-activity indicated by elevated F-contents in newly formed minerals suggest transport of Be as a fluoride-carbonate complex.
It seems likely that beryl formation was triggered by precipitation of F-rich phlogopite, which removed the complexing ligand
from the fluid. 相似文献
227.
Tin deposits are often closely associated with granitic intrusions. In this study, we analyzed tin partition coefficients between different fluids and melts (\({\text{D}}_{Sn}^{aq.fl./melt}\)) as well as various crystals and melts \({\text{D}}_{Sn}^{aq.fl./melt}\)(\({\text{D}}_{Sn}^{crystal/melt}\)) from the Furong tin deposit associated with the Qitianling A-type granite. Our experimental results indicate that tin partition behavior is affected by the chemical compositions of fluids, melts, and minerals. Tin is prone to partitioning into the residual magma in fractional crystallization or other differential magmatic processes if the magma originated from crustal sources with high alkali content, high volatile content, and low oxygen fugacity. Highly evolved residual peralkaline granitic magma enriched in tin can lead to tin mineralization in a later stage. Furthermore, the volatiles F and Cl in the magma play important roles in tin partitioning behavior. Low F contents in the melt phase and high Cl content in the aqueous fluid phase are favorable factors for tin partitioning in the aqueous fluid phase. High Cl content in the aqueous fluid catalyzes water–rock interaction and leads to the extraction of tin from tin-bearing minerals. All these findings support a hydrothermal origin for the tin deposits. In light of the geotectonic setting, petrochemical characteristics, and mineralizing physicochemical conditions of the Furong tin deposit, it is inferred that the ore-forming fluid of the Furong tin ore deposit could have derived from the Qitianling peralkaline intrusion. 相似文献
228.
This study provided a picture of the spatial and temporal distributions of Cr, Co, Ni Cu, Zn, As, Cd and Pb in bottom sediments
of Tolo Harbour. The concentrations of the eight heavy metals differed significantly between sites due to the poor tidal flushing
in Tolo Harbour. The levels of Cu, Zn, Cd and Pb were generally enriched in sediments from inner Tolo Harbour, while sediments
from outer Tolo Harbour (Tolo Channel) had higher levels of Cr, Co and Ni. The redox sensitive element arsenic showed no distinct
spatial pattern in Tolo Harbour. The decreasing levels of Cu, Zn, Pb and Cd in sediments with increasing distance from land
demonstrated a typical diffusion pattern from land to the direction of sea. Two hot spots of Cu, Zn, Pb and Cd in sediments
were located near Tai Po and Sha Tin new town, indicating that Cu, Zn, Pb and Zn were from land-derived sources. The sites
with relatively high levels of Cr, Co and Ni in sediments were located in areas close to waste spoil in sea floor. The natural
and anthropogenic inputs from Sha Tin and Tai Po to Tolo Harbour were mostly responsible for Cu, Zn, Cd and Pb enrichment
in sediments from inner Tolo Harbour. The waste spoil in sea floor was believed to contribute to the Cr, Co and Ni in outer
Tolo Harbour. The results of correlation coefficient between the eight heavy metals showed that Cu, Zn, Cd and Pb were strongly
positively correlated, and Cr, Co and Ni were also significantly correlated with each other. The best explanation of strong
correlation was their similar source. As, however, is not well correlated with the other seven heavy metals. The average concentrations
of Cu and Zn displayed general increasing trends from 1978 to 2006 in Tolo Harbour, while the mean levels of Cr and Pb displayed
a substantial decrease from 1978 to 1987, then a slight increase after 1987. No distinct temporal trends of the concentrations
of Ni and As were observed from 1978 due to the inconsecutive data. On the other hand, the increasing trends of Cr, Cu, Zn,
Cd and Pb were observed since 1996. 相似文献
229.
Naguleswaran Niroshan Nagaratnam Sivakugan Ryan Llewellyn Veenstra 《Geotechnical and Geological Engineering》2018,36(4):2261-2272
Cemented paste backfill (CPB) is primarily used for backfilling underground voids at George Fisher Mine (Mount Isa, Australia). The objective of this paper is to summarise the geotechnical characterisation of the tailings and the rheological properties of the CPB as determined from a laboratory testing program undertaken at James Cook University. Two binders were examined [a General Purpose cement and a slag blend cement] over a range of dosages from 0 to 6% and CPB mix solids content in the range of 72–78%. The slump tests were carried out using the standard cone (ASTM C 143) used for concrete and a cylinder with 110 mm (diameter) × 110 mm (height), whereas the yield stress was measured using a shear vane (Brookfield vane spindle V-73). The index characteristics of the tailings including the grain size distribution, liquid limit, plastic limit, specific gravity were determined as per ASTM standards. This paper will then discuss the interrelationships among the solid content, slump, saturated density and the yield stress of the CPB. It is shown that there is strong correlation between the two different slump test devices used in this study. The smaller cylindrical device appears to have good potential for slurries like mine tailings or dredged mud that have high water content for slump test. There is also strong inter-relationship among solid content, slump, yield stress, and bulk density. Increasing the solid content increases the bulk density and yield stress, but reduces the slump. While there is hardly any difference between the two binder types used in this study in terms of flow parameters, namely the yield stress and slump, the binder dosage has an effect. At any specific solid content, higher binder dosages lead to a drop in the slump and increase in the yield stress. The difference is more pronounced in dense slurries. It is also strongly believed that the trends and relationships developed in this study may be valuable for the other mining operations using CPB. 相似文献
230.
A palygorskite unit was discovered in a road cut of undifferentiated Tertiary limestone between the villages of El Pariso
and San Roman (18°49.309N, 88°37.861W) in the southeastern Yucatán Peninsula, Mexico. This is the southern most locality of
a clay-rich sedimentary unit reported in the literature for the Tertiary carbonates of the Yucatán Peninsula. This occurrence
indicates a much wider range of palygorskite-rich clay deposition than previously recognized. The lithology is 99% clay and
1% sand to silt size diagenetic quartz grains. The clay consists of approximately 85% palygorskite, 15% montmorillonite and
trace amounts of titanium oxides. EDS analyses on palygorskite are largely consistent with sedimentary palygorskites from
other coastal marine settings, however palygorskite has a low total Fe content (average = 0.40 wt% expressed as Fe2O3) compared to many other sedimentary palygorskites. Montmorillonite chemical compositions are typical and compared to the
palygorskite have substantially higher Fe2O3 concentrations (average = 3.90 wt%). The low percentage of coarse grains in the lithology combined with a high proportion
of palygorskite and lack of detrimental trace minerals suggest the deposit is of industrial grade; however, it has limited
reserves (6,000 m3). The unit could be potentially used in a wide array of environmental applications which are needed in the region including
liners for landfills and constructed wetlands. The unit is in a geographic location which would serve the expanding economy
of the region. This resource has the potential to have great impact on the quality of the local environment and the economy
of a region under great environmental threat. 相似文献