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1.
Surface Acidity of Amorphous Aluminum Hydroxide   总被引：3，自引：0，他引：3  
The surface acidity of synthetic amorphous AI hydroxide was determined by acid/base titration with several complementary methods including solution analyses of the reacted solutions and XRD characterization of the reacted solids. The synthetic specimen was characterized to be the amorphous material showing four broad peaks in XRD pattern. XRD analyses of reacted solids after the titration experiments showed that amorphous AI hydroxide rapidly transformed to crystalline bayerite at the alkaline condition （pH〉10）. The solution analyses after and during the titration Ksp=^aAl^3＋/aH^＋^3 ,was 10^10.3. The amount of consumption of added acid or base during the titration experiment was attributed to both the protonation/deprotonation of dissolved AI species and surface hydroxyl group. The surface acidity constants, surface hydroxyl density and specific surface area were estimated by FITEQL 4.0.  相似文献   

2.
In order to study the damage mechanism of mineral dusts on the pulmonary alveolar macrophage （AM）, the changes in their death ratio, malandialdthyde （MDA） content and activities of lactate dehydrogenase （LDH） and superoxide dismutase （SOD） were measured, and the technique of cell culture in vitro was used to investigate the cytotoxicity of six mineral dusts （twelve crystal habits） from twelve mineral deposits. The results show that woUastonite and clinoptilolite have no AM cytotoxicity, while other fibrous and grainy mineral dusts damage pulmonary AM in various degrees. The cytotoxicity of fibrous mineral dusts was greater than that of the grainy ones, and the cytotoxicity of dusts was positively correlated with the active OH- content in dusts, but not necessarily so with its SiO2 content. The high pH values produced by dust was unfavorable for the survival of cells and the dusts with low bio-resistance were safe for cells. The content of variable valence elements in dusts might influence their cytotoxicity and the surface charge of dusts was not a stable factor for their toxicity. It is demonstrated that the shape of mineral dusts was one of the factors affecting cytotoxicity, and that the cytotoxicity of mineral dusts depends mainly on their properties.  相似文献   

3.
A comprehensive study on the chemical composition of wet precipitation was carried out from January 2004 to December 2004 at Jinhua, China. All samples were analyzed for pH, electrical conductivity and major ions （F, Cl, NO3,. SO4^2-, K^＋, Na^＋, Ca^2＋, Mg^2＋. and NH4^＋）. The results showed that SO4^2- is one of the dominant anions, accounting for 66.1% of the measured anions in precipitation, while NH4^＋ and Ca^2＋ account for 56.6% and 33.4% of the measured cations, respectively. Even though the concentrations of SO4^2- and NO3^- were not high relative to those in the northern areas of China, rainwater in the studied area is typically acidic with a volume-weighted mean pH of 4.54 due to the lack of neutralization in precipitation. The fractional acidity value suggested that about 76% of acid was neutralized by alkaline constituents. On the other hand, H^＋ showed no significant correlation with other ionic species, which indicates that its acidity might be attributed to the comprehensive effect of all the acidifying and neutralizing ions rather than one major ion in precipitation. A good correlation between Ca^2＋ and Mg^2＋, as well as between Na^＋ and Cl^-, indicated these ions are commonly of crustal and marine origin, respectively. Other relatively good correlations were observed between NH4^＋ and SO4^2-, Ca^2＋ and SO4^2-, Mg^2＋ and SO4^2-, Mg^2＋ and NO3^-, and Mg^2＋ and Cl^-. These results were attributed to the atmospheric chemical reactions of the acids H2SO4, HNO3 and HCl with alkaline compounds such as NH3 and/or carbonate materials. High enrichment factor of marine source for SO4^2-, Ca^2＋ and K^＋ indicated that large amounts of these ions came mainly from a non-marine source. Similarly, a high enrichment factor of soil for SO4^2-, NO3^- and CI also suggested that most of these ions did not come from soil source.  相似文献   

4.
Tenorite is an oxide of cupper which has been well documented on its structure,force constants and spectrum.Based on the isotopic shifts of its spectrum calculated from the force constants of tenorite,its reduced partition function ratios were calculated,from which an oxygen isotopic fractionation curve between tenorite and water was obtained:10^3lnα=2.51X^2-14.87X 6.31(X=10^3/T)Oxygen isotopic fractionation of tenorite was also calculated with the modified increment method of Zheng(1991),and another equation was obtained:10^3lnα=2.89X^2-13.10X 3.92(X=10^3/T) Calculated results of the two different models were fitted and possible deviation involved in the calcuation was also discussed.  相似文献   

5.
A systematic research was performed about diffusion kinetics of adsorbing F^- dissolved in water for carbonate hydroxyapatite （CHAP） from the natural hydroxyapatite which was modified by adulterating with CO3^2-. The result shows that the speed of F^- adsorption is controlled by membrane diffusion when F^- concentration is relatively low, which is expressed by the kinetic equation of diffusion Q=0.0005（Ci-C）（t-ti）＋0.3967, or by vacancy diffusion when F^- concentration is relatively high, which is expressed by the kinetic equation of diffusion In[C（o, t）]=8.4718-0.5048Int. Based on the feature of CHAP for adsorbing F^- dissolved in water and its special channel of the structure of CO3^3- modified hydroxyapatite, models of vacancy diffusion and membrane diffusion were established.  相似文献   

6.
Although hydrotalcite, or layered double hydroxides （LDHs）, is not a common mineral, it is an important material that can be easily synthesized in laboratory. In this study, structural evolvement and BET surface area changes of heat treated Mg/AI-LDH is evaluated by XRD, TEM and N2-BET analyses. The results indicate that the magnesium-aluminum LDH with carbonate as interlayer anion, periclase-like oxides was formed at temperatures of 400-800℃. Meanwhile, 2-3 nanometer mesoporous were formed during decomposition of LDH. However, the heat treated samples still preserve the morphology of the original LDH plates. Periclase-like formed from LDH heat treatment may re-hydrolyze and recover the structure of LDH. However, crystallinity of the recovered LDH is lower than that of the original LDH. This heat treatment will result in formation of （Mg, Al）-oxide nano-crystals and nanopores among the nano-crystals. When heating temperature exceeds 1000, the periclase-like （Mg, Al）-oxide is transformed into a composite with periclase （MgO） and spinel phases. The periclase can be re-hydrolyzed and dissolved in HCl solution. After acid treatment, the sample with a high surface area is composed of spinel nano-crystals and nanopores among them. Our results will provide a new and economic way to synthesize mesoporous materials through pathways of phase transformation of precursor materials with different composition.  相似文献   

7.
We investigated in more detail the adsorption phenomenon which was described earlier. It was clearly established that the hydroxyl apatite was not participated in P adsorption. This phenomenon takes place because of ferric hydroxide film. Modem sediments from the Southem Basin of Lake Baikal were taken and stirred with Baikal water. Carrier-free [^32p]-orthophosphate was added in this system. Similar experiments were made with carrier-free [^35S]-sulphate. Sulphate stayed in supematant completely. The influence of pH on the system with inorganic phosphate was also studied. In low alkali conditions phosphate migrated in supematant, in low acid, in sediments. Baikal sediment was stripped of iron-hydroxous film by treatment with 1% oxalic acid. Investigation of striped sediment shown that phosphate stays in supematant only. Hence, hydroxyl apatite cannot be the phase of the sediments of Lake Baikal which binds phosphate. This all showed by our group before. Now we have found the limit of phosphate sorption in Lake Baikal sediments and the stehiometry of the sorption. The sorption limit of Lake Baikal sediments was studied. An experiment with inorganic ^31P phosphate was made. 0.025% K2HPO4 solution with adding ^32P radioactive mark into it was prepared. 100 μL of mixture of ^31PO4^3- and ^32PO4^3- seven times were added in a ＂Baikal water-Baikal sediment＂ system and blank （100 ml BW only）. Concentrations of inorganic ^31PO4^3- were very low so the bend dot on the diagram was found and sorption limit of sediment was estimated. Baikal sediment stopped assimilating phosphate in the bend dot. The stehiometry of sorption was estimated by supematant-sediment radioactive ratio, which equals 3, that is, three Fe （Ⅲ） atoms associate one PO4^3- anion. The only Fe （Ⅲ） substance which could associate P is -Fe-O-Fe- polymer film. It also dissolves in acid conditions.  相似文献   

8.
Spectral Reflectance Features of Rocks and Ores and Their Applications   总被引：2，自引：0，他引：2  
The spectral reflectance features of rocks and minerals are correlated with their composition,col-or,grain size and surface state.Different wall rocks,altered rocks and ores have their spectral reflectance features,which are very helpful for the explanation of remote sensing data and searching for mineral deposits by remote sensing.After the treatment of spectrum data and searching for mineral deposits by remote sensing.After the treatment of spectrum data of rocks and ores and physical and chemical parameters in the mathematical statistics,we analyzed the laboratorial spectrum dataand put forward better wave bands(520-590,650-710,730-760,770-860,1560-1760,2200 and 2300-2400nm) for distinguishing rocks and ores.  相似文献   

9.
邓华兴 《地球化学》1980,(4):368-374
Experimental data on cathodeluminescence of 34 individual specimens of naturallyoccurring apatite differring in the mode of occurrence are presented in this paper.In accordance with the characteristic distribution of the bands and lines of apatite specimens,it has been confirmed that RE ions Sm^2 ,Dy^3 ,En^2 ,etc.,are the main activators for the cathodeumineseence of apatite.In conjunction with the crystallological study.a priliminary investigation into the mechanism for apatite cathodelnminescence has been made as well.The author has suggested that the cathodelumineseence of apatite may be attributed to the replacement of Mn at the site of Can by Mn^2 ,and the luminous colour seems to have no direct,simple correlation with that of the crystal itsself.  相似文献   

10.
Obtained new data on major element contents, trace and REE concentrations of sedimentary bedrock and groundwaters in Lastochka spa, along with isotope data, allow solving the problem of origin and evolution of these groundwaters. In the Lastochka area, located in Primorye region （Far East of Russia）, two types of groundwater are found： groundwater （TDS 0.2-0.4 g/L, pH 7.3-7.5） with lower pCO2 levels and groundwater with higher dissolved mineral content （TDS 3.7-4.7 g/L, pH 5.8-6.4） and high pCO2 levels. Our studies proved that both types of groundwaters originated from meteoric water and water-sedimentary stratum interaction has played a main role in forming chemical composition of waters. The main gas composition in the high pCO2 groundwater is CO2, which may as high as 98% of the total amount of all gas. The pressure of CO2, calculated using the water analysis data is at about 0.6 bar, while one measured in the field could reach 2.6 bar. The pressure of CO2 in groundwater with low TDS is 10.2 bar. Our δ^13C data [δ^13C （gas）=-6.22 versus PDB] indicate that most of the ^13C in the free CO2 of Lastochka spa is of upper mantle origin. Sedimentary bedrock is mainly sandstone with a good permeability. Dominate minerals are K-feldspar, quartz and plagioclase and secondary minerals are calcite, limonite, cericite and kaolinite. Our results indicate that the role of mantle CO2 gas is crucial for highly mineralized groundwater. This type of groundwater evolved only during water-rock-gas interaction. Extreme dissolution of albite in the presence of CO2 gas leads to the formation of lower pH and drastic accretion TDS and Na content in high pCO2 water. The violent difference in the trace element concentration in waters is caused by more intensive weathering of primary minerals in the presence of CO2 gas.  相似文献   

11.
Coals from Guizhou Province, Southwest China, attract many researchers＇ attention for their high concentrations of hazardous trace elements, sulphur and mineral components. Trace elements in coals have diverse modes of occurrence that will greatly influence their migration in the process of coal preparation. Mode of occurrence is also important in determining the partitioning during coal combustion. The coal floatation test by progressive release was used to study the migration of trace elements and mineral components in the process of froth floatation. Inductively coupled plasma mass spectrometry （ICP-MS） was used to determine the absolute concentrations of trace elements including As, Be, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Sb, Se, Th, U, V and Zn in the parent coals and the floatation fractions. Precise determination of the mineral matter percentage in coals was obtained by low-temperature ashing. The mineral compositions in coals were quantified using Rietveld-based X-ray diffraction analysis package on low-temperature ash. Scanning electron microscope equipped with energy dispersive X-ray detector was used to provide information on the forms of occurrence of mineral components in coal. Five floatation fractions were obtained from the pulverized coal samples. The contents of trace elements and mineral components decrease from the first tailings to the last cleaned coal. The concentrations of trace elements and mineral components in parent coals and different floatation samples show that trace elements and mineral components are mainly concentrated in the first tailings samples. Nearly 60% of mineral components are enriched in the first tailings, whereas less than 1.3% remains in the cleaned coal. The ratio of sixteen trace elements concentrations in the first tailings to the corresponding concentrations in the cleaned coal ranges from 1.6 to 22.7. Quantitative mineralogical analysis results using the full-profile general structure analysis system （GSAS） showed that the main compositions of LTA include quartz, calcite, kaolinite, pyrite, chlorite, montmorillonite, illite, anatase and pyrite.  相似文献   

12.
Decoloration of acidic scarlet GR by pyrolusite is studied in this paper. The effects of pH in solution, dosage and granularity of pyrolusite, reaction temperature, and vibration speed on decoloration efficiency are discussed. According to experiment results, the decoloration efficiency may exceed 95% for 40 mg/L GR solution by pyrolusite. pH is most important among all factors which impact the decoloration of acidic scarlet GR. Dosage and granularity of pyrolusite, reaction temperature, and vibration speed have a little benitfit on decoloration. The high decoloration efficiency and low removal efficiency of COD as well as FT-IR spectra of products between pyrolusite and acidic scarlet GR indicate that acidic scarlet GR undergoes the redox reaction on the interface of mineral and its chromophore is oxidated and decolored, but it is not removed thoroughly by oxidation.  相似文献   

13.
The Holocene lacustrine diatomaceous earth of Fayium,South West of Cairo,has been studied to define its minerals,chemistry,petrography and physical properties.Minerals were processed by way of calcination at 550℃ ,followed by acid leaching to reduce levels of mineral impurities.The diatomite is of biogenic opal A.with calcite as the main ganue mineral,quartz and clay minerals(smectite followed by kaolinite in abundance and a trace amount of illite).Silica in the diatomaceous earth accounts for about 63% on average.Positive correlation between CaO and CO2 indicates that Ca is present mainly as calcite.Al2O3,Fe2O3,MgO and K2O are attributed mainly to clay minerals.However,the physical properties of the diatomaceous earth as filter-aids and filler for paints and plastics are poor because of general high levels of impurities.The technological performances of the diatomaceous earth have been significantly improved owing to upgrading of diatoms through mineral processing trical.  相似文献   

14.
34samples of loess-paleosol from the Luochuan and Xifeng sections in the Loess Plateau,northern China were eparated into sand,silt and clay fractions and analyzed for their mineral compositions.The results indicate that there is almost no difference between loess and paleosol in mineral composition.Major mineral species are quartz,mica,feldspar and chlorite,accounting for about 88-92% of the total;other minerals are kandite,smectite,vermiculite and a few heavy minerals.The calcite,magnetite and hematite were not taken into consideration because of their removal in the process of sample preparation.The main difference with respect to the mineral composition of samples collected from different sections and different statigraphic levels lies in the amount and grain size of minerals hosted.Comparisons between the Luochuan section and the Xifeng section,between paleosol and loess and between the upper part and the lower part of some paleosol layers show that the formers contain less feldspar but more mica and vermiculite and are finer in grain size,indicating the co-occurrence of both biochemical weathering process responsible for mineral change and physical weathering process leading to grain-size change during the soil-forming processes.This result favours such an explanation of the soil-forming mechanism that loess deposition and paleosol development occurred synchronously,though the rate of soil formation was greater than that of loess deposition,thus leading to soil development.  相似文献   

15.
The Ningqiang meteorite is a fall carbonaceous chondrite, containing various Ca-, Al-rich inclusions that usually escaped from secondary events such as high-temperature heating and low- temperature alteration. However, it has not yet been classified into any known chemical group. In order to address this issue, 41 elements of the bulk Ningqiang meteorite were analyzed using inductively coupled plasma mass spectrometry （ICP-MS） and inductively coupled plasma atom emission spectrometry （ICP-AES） in this study. The Allende （CV3） carbonaceous chondrite and the Jilin （H5） ordinary chondrite were also measured as references, and our analyses are consistent with the previous results. Rare earth and other refractory lithophile elements are depleted in Ningqiang relative to both Allende and mean CK chondrites. In addition, the REE pattern of Ningqiang is nearly flat, while that of Allende shows slight enrichment of LREE relative to HREE. Siderophile elements of Ningqiang are close to those of mean CK chondrites, but lower than those of Allende. Our new analyses indicate that Ningqiang cannot be classified into any known group of carbonaceous chondrites, consistent with previous reports.  相似文献   

16.
Sorption of hydrophobic organic chemicals by various components influences their behavior and fate in environment. In the natural environment, mineral components, organic matter and microorganism didn＇t exist alone. They combined or reacted one another and formed the mineral-humic, mineral-microorganic and mineral- humic- microorganic complexes. A clear understanding of the sorption of organic chemicals by the complexes of mineral and humic acid and/or microorganism will help to determine their sorptive mechanisms in environment. In this paper, the sorption patterns of phenanthrene on the complexes of kaolinite and different organic component （humic acid and microorganism） have been carried on. The results show that the combination of HA and kaolinite not only changed the structure of HA, but also modified the surface chemistry of clay mineral. Interaction between HA and kaolinite is presumably ascribable to coulombic interactions and ligand exchange between the -COOH groups of HA and OH groups at the kaolinite surface. During the sorption on mineral surface, aliphatic fractions of HA were preferentially sored by kaolinite while aromatic fractions were left in the solution. More linear isotherms and higher Koc values were observed for kaolinite-HA complex in comparison of the pure HA. The sorption capacity of kaolinite-HA complex increased with increasing ionic strength and pH, and showed more nonlinear character. Kaolinite, microorganism and kaolinite-microorganism complex can all sorb phenanthrene, but the sorption capacity significantly differed. Bacterial cell sorbed more phenanthrene than kaolinite. The biofllm coating of kaolinite affected its sorption to phenanthrene. Kaolinite with biolfilm coating sorbed more phenanthrene than that without biofilm coating. The sorption capacity of kaolinite-microorganism complex decreased with increasing ionic strength and decreasing pH, but showed more nonlinear character. Both HA and microorganism can alter the nature of kaolinite sorbing phenanthrene respectively.  相似文献   

17.
The relationship between trace elements in coal and organic functional groups of coal,also some of aromatic structure,was investigated by using curve fitting of infrared spectra.Cluster analysis was also performed according to the degree of affinity of organic groups to the trace elements.The results show that there is a possibility that trace elements,especially LREE,were bound to peripheral organic functional groups of middle rank coal macromolecule.The most possible functional group that binds trace element is the hydroxyl,and to the less degree,the asymmetric-CH_3andCH_2 stretching,-CH_3 stretching,etc.The degree of affinity of trace elements to different functional groups varies.The tendency obeys the natural structural changing law of trace elements—the periodic law.The deviation of some trace elements from this regular trend is attributed to the deviation of intrinsic"confusion degree"(conventional molar entropy)of the matter system of coal basin,which is affected by the inner and outer factors during the evolution.  相似文献   

18.
According to 73 snow samples collected in the southeast and southwest of Tibetan Plateau in January,2021,the characteristics of hydrogen and oxygen stable isotopes（δD and δ18O）fractionation in dry season and the influence of water vapor migration on the chemical composition change of snow profile were revealed by measuring the stable isotopes of hydrogen and oxygen and soluble inorganic ions in snow,and the relationship between stable isotopes of hydrogen and oxygen and climate and the composition and source of soluble inorganic ions were discussed. The results show that the local meteoric waterline of snowpack in the whole study area is δD=7. 86δ18O+11. 8（R2=0. 95）,which is close to the Lhasa winter meteoric waterline,and the slope and inter⁃ cept of the meteoric waterline in the southeast are slightly lower than those in the southwest. δD and δ18O fluctu⁃ ates from -178. 11% to -68. 07% and -23. 80% to -9. 61%,respectively,and the d-excess values fluctuate from 11. 03% to 23. 49%,showing low values of δD and δ18O in winter,and high d-excess values. The surface layer is relatively enriched in heavy isotopes,and the isotope values are higher than those of the lower snow sam⁃ ples,and the water vapor migration inside the snow makes the slope of the relationship between δD and δ18O dif⁃ ferent. The concentration sequence of the main soluble inorganic ions is Ca2+>SO42->Na+>NO3->Cl->K+>Mg2+> NH4+,of which Ca2+（42. 47%）,SO42-（23. 53%）accounted for the largest proportion of cation and anion,re⁃ spectively,and the average concentration of ions in the southeast was higher than that in the southwest. The re⁃ sults of principal component analysis show that terrigenous sources are the main source of ions in snow,and NH4+ and some NO3- are related to human activities. The backward air mass trajectory shows that the source of water vapor is related to the water vapor transport controlled by the upper-altitude westerly circulation,and most of the ions are terrestrial mineral dust carried by westerly winds in winter. © 2023 The Author(s).  相似文献   

19.
周维全 《地球化学》1977,(3):227-234
Alkali amphibole asbestus is widely distributed in a Mesozoic terrestrial redbed.Preliminary mineralogical study shows that it belongs to magnesian riebeckite asbestus. The mineral contains higher Na, Mg and Fe^3 , lower Al, and is well comparable with that of typical magnesian riebeckite asbestus in chemical composition. A comparasion between the methods used for calculating the crystallochemical formula of amphibole indicatesthat the structural characteristics of amphibole can be best brought out if a total catian number of 15, i.e., x y z=15, is taken as the factor for magnesian riebeckite. The infrared spectra for fibrous magnesian riebeckite exhibit two definite absorption bands. The firat one is at 850--1250 cm^-1, involving several minor bands due to the valency vibration of Si--O, with maximum values of 975,1025, 1080cm^-1 respectively. The second absorption band which is attributable to the distortional vibration of Si--O--Si, is detected at 350--600cm^-1, with a maximum value of 440cm^-2. Optically, its refractien iadices bacrease with increasing transition elements, especiany the ratio of Mg/Mg Fe^2 Fe^3 Mn. A distinct exothermic effect is observed between 350--400℃, indicating the oxidation of Fe^3 to Fe^3 . A deep endothermic valley between 970--1020℃ can be attributed to the melting of magnesian riebeckite and the formation of new minerals. The auther oonsideres that fibrous magnesian riebeckite is crystallized in favorable accumulation strata from a Na-, Mg-, Fe-rich silicate colloidal solution that has been derived from country rocks by some alkline ground water duringg the process of sedimentation and diagenesis in terrestrial saline carbonate muds. Magnesian riebeckite formed at terrestrial carbonate saline formations promises to be a potentially important genesis type for alkali amphiboles.  相似文献   

20.
Soils contain about twice the amount of carbon presented in the atmosphere, so a small change in the soil carbon will influence atmospheric chemistry and heat balance. The soil carbon ultimately exchanged with the atmospheric CO2 as soil CO2, which mainly exists at the depth of 0-20 cm. The transport of soil CO2 is affected by the sources of soil CO2. Thus, separation of the contributions of sources of soil CO2 is a fundamental need to understand and predict implications of environmental change on soil carbon cycling and sequestration. It is a complicated task, so that a number of different methodological approaches such as component integration, root removal, and gap analyses have been developed. However, these methods could not avoid changing soil characteristics such as air-filled porosity, soil temperature and soil water contents. Consequently, fractional contributions of respiration of living root and decomposition of soil organic matter to the total soil CO2 cannot be estimated correctly. In this study, based on mass balance theory of both concentrations and δ^13C of soil CO2, a trenching method with a stable-isotope technique was used to determine both soil CO2 sources at the depth of 3-13 cm in a Japanese larch forest area during 30 May to 7 October 2005 and fractional contributions of these sources. Experimental results showed that the amount of atmospheric CO2 invaded the soil air was not significantly variable while its percent rate in the total soil CO2 had significantly temporal variations with the lower values between 5 August and 1 September. The litter-layer decomposition was very small. The soil CO2 derived from the respiration of living root and the decomposition of soil organic matter showed significantly temporal variations with increase from 30 May to 5 Aug. and decrease from 1 September to 7 October, 2005; and it accounted for 82%-98% of the total soil CO2 in which the respiration of living root was in the range from 32% to 62%.  相似文献   

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