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1.
Gypsum is one of the most universally distributed salts in weathered materials but little is known about the influence of environmental conditions on the damage generated by gypsum in stones. To quantify the damage induced by gypsum crystallization acoustic emission techniques are employed to record the elastic energy released during salt crystallization cycles in a limestone. Different environmental conditions have been established during the cooling and drying periods in traditional salt crystallization cycles. During drying two different temperatures (50 and 25 °C) and relative humidity (low, 25 % at 50 °C and 65 % at 25 °C, and high, 99 %) have been applied. The acoustic emission signals are filtered by a frequency analysis in order to eliminate signals corresponding to external noise or artifacts. Our experimental results show that acoustic emission activity is higher under high relative humidity conditions than under low relative humidity conditions, and also higher when drying at 50 °C than at room temperature. Microscopic observations on the weathered samples indicated that under high relative humidity conditions and at room temperature, gypsum crystallizes not on the sample surface, like in the other samples, but deeper in the inner part of the sample, in good agreement with previously published data. We show that using acoustic emissions as usually done in rock mechanics is also very useful in the study of stone decay and weathering processes in the laboratory.  相似文献   

2.
Coal combustion is the primary anthropogenic source of atmospheric iodine, which has important environmental and health effects. The iodine distribution in Chinese coals and the atmospheric iodine emission factors of coal-fired boilers are studied to estimate the iodine atmospheric flux from coal combustion in China from 1995 to 2009. The national average iodine content weighted by coal yield fluctuated from 2.61 mg kg-1 in 1995 to 2.09 mg kg-1 in 2009, recording an annual decline of 1.42 %. By establishing a monitoring program, iodine distribution in coal by-products after the coal is consumed in combustors is measured, and atmospheric iodine emission factors by sectors are calculated. Based on the coal consumption by sectors, the annual atmospheric iodine emission from coal combustion in China increased at an annual rate of 4.3 % from 3031.1 tons in 1995 to 4872.6 tons in 2009. Anthropogenic atmospheric iodine emission is significantly underestimated, and its environmental and health effects must be given more attention.  相似文献   

3.
Fly ash is a product arising from coal combustion in thermal power plants. It represents a major source of environmental pollution. It is well known by its chemical composition rich of SiO2 and Al2O3. With the aim of preserving the environment against this contamination, fly ash was used along with the starting materials for producing glass cordierite (2MgO, 2Al2O3, 5SiO2). Four formulations were developed by mixing the silica gel, magnesium chloride (MgCl2.6H2O) and fly ash in the percentages enclosing the stoichiometry of cordierite (2MgO, 2Al2O3, 5SiO2). Different experimental techniques (DTA/TGA, X-ray diffraction, FTIR and SEM) were used to characterise the prepared formulations. The results shown that for all formulations, a cordierite phase was obtained at 1200 °C along with several secondary phases such as mullite, cristobalite, silicon oxide, enstatite and spinel. At 1300 °C, pure indialite (α-cordierite) was obtained along with a small amount of spinel. The four formulations sintered at 1200 °C exhibit a homogenous morphology and high porosity. The acicular-shaped indialite grains were observed in both formulations with excess of alumina and excess of magnesia.  相似文献   

4.
Hydrous K-rich kimberlite-like systems are studied experimentally at 5.5–7.5 GPa and 1200–1450?°C in terms of phase relations and conditions for formation and stability of phlogopite. The starting samples are phlogopite–carbonatite–phlogopite sandwiches and harzburgite–carbonatite mixtures consisting of Ol?+?Grt?+?Cpx?+?L (±Opx), according to the previous experimental results obtained at the same P–T parameters but in water-free systems. Carbonatite is represented by a K- and Ca-rich composition that may form at the top of a slab. In the presence of carbonatitic melt, phlogopite can partly melt in a peritectic reaction at 5.5 GPa and 1200–1350?°C, as well as at 6.3–7.0 GPa and 1200?°C: 2Phl?+?CaCO3 (L)?Cpx?+?Ol?+?Grt?+?K2CO3 (L)?+?2H2O (L). Synthesis of phlogopite at 5.5 GPa and 1200–1350?°C, with an initial mixture of H2O-bearing harzburgite and carbonatite, demonstrates experimentally that equilibrium in this reaction can be shifted from right to left. Therefore, phlogopite can equilibrate with ultrapotassic carbonate–silicate melts in a?≥?150?°C region between 1200 and 1350?°C at 5.5 GPa. On the other hand, it can exist but cannot nucleate spontaneously and crystallize in the presence of such melts in quite a large pressure range in experiments at 6.3–7.0 GPa and 1200?°C. Thus, phlogopite can result from metasomatism of peridotite at the base of continental lithospheric mantle (CLM) by ultrapotassic carbonatite agents at depths shallower than 180–195 km, which creates a mechanism of water retaining in CLM. Kimberlite formation can begin at 5.5 GPa and 1350?°C in a phlogopite-bearing peridotite source generating a hydrous carbonate–silicate melt with 10–15 wt% SiO2, Ca# from 45 to 60, and high K enrichment. Upon further heating to 1450?°C due to the effect of a mantle plume at the CLM base, phlogopite disappears and a kimberlite-like melt forms with SiO2 to 20 wt% and Ca#?=?35–40.  相似文献   

5.
Variations in the mechanical properties (compressive strength, elastic modulus, tensile strength, and fracture toughness) of granite were analyzed as functions of temperature. It was found that above 200 °C, tensile strength and fracture toughness tended to decrease with temperature, while variations in the compressive strength and elastic modulus demonstrated decreasing trends when the heating temperature exceeded 400 °C. The temperature ranges of room temperature—200 and above 600 °C—corresponded to an undamaged state and strongly/completely damaged state, respectively. It is suggested that 400 °C might be a critical threshold of thermal damage to granite. Based on results of statistical tests, a sharp decrease in mechanical properties can be recognized, accompanied by a drastic growth in peaking strain and acoustic emission rate. This phenomenon may be associated with the α/β phase transition of quartz.  相似文献   

6.
The selectivity of clinoptilolite toward Pb2+ has stimulated many studies aimed to evaluate the metal uptake. Conversely, the management of a Pb-bearing clinoptilolite has not received the same attention, although it can release a harmful metal. This work aims to evaluate the possibility to control, through thermal treatments, the release of lead from a Pb-clinoptilolite, prepared to simulate the condition of highest dangerousness of an exhausted exchanger. A zeolite-rich rock from Sardinia (Italy) has been processed, obtaining a powder with almost 90 % (wt.) of clinoptilolite. This material has been initially Na- and then Pb-exchanged, reaching a Pb2+ content of 2.28 meq/g. The lead release has been tested before and after 2-h heating at eight different temperatures from 200 to 900 °C. The unheated material releases 64 % of the lead. Heating weakly affects lead release up to 400 °C (54 %), but higher temperatures determine an abrupt reduction from 44 % at 500 °C to 1 % at 700 °C, when the zeolite breakdown occurs. At 800 °C the nucleation of Pb-feldspar and silica polymorphs begins. Basically, the material heated at 900 °C does not release lead (0.03 %), because the metal is trapped in the lead feldspar, whose content attains 42 % (wt.). This solid-state transformation does not involve the emission of lead vapors, another significant environmental aspect.  相似文献   

7.
Fine coal covering for preventing spontaneous combustion of coal pile   总被引：3，自引：1，他引：2  
In order to investigate the effect of fine coal covering around the bottom of coal stockpile on spontaneous combustion prevention, a two-dimensional math model was established to numerically simulate the fine coal covering coal pile and a coal pile temperature-rising experimental system was setup to study the two-dimensional heat and mass transfer characteristics of air diffusion in the horizontal direction and air heat convection in the vertical direction inside coal stockpiles covered by different thicknesses of fine coal. The results showed that (1) the fine coal located at the bottom of the coal pile can effectively inhibit air convection and diffusion, cut off oxygen replenishment, and prevent the temperature rise inside coal pile, and (2) thicker fine coal has more obvious effect. Finally, the field experiments on the fine coal covering coal piles for preventing self-ignition of coal pile were carried out successfully. The results showed that the uncovered or exposed coal piles self-ignited rapidly within a very short period (18 days), while the coal pile covered with 1 m fine coal lasted for 123 days with a maximum coal temperature of only 59.9 °C. The characteristics of temperature distribution and diffusion inside coal stockpile were studied, and the high-temperature region was found in the region 1.3 m high and 2–3 m deep in the coal pile. The effects of environment temperature and precipitation on self-ignition of coal pile were also analyzed in field experiment. The experimental results proved that the fine coal covering technology can effectively prevent the spontaneous combustion of coal stockpiles.  相似文献   

8.
Aquifer thermal energy storage in urban and industrial areas can lead to an increase in subsurface temperature to 70 °C and more. Besides its impacts on mineral and sorption equilibria and chemical reaction kinetics in an aquifer, temperature sensitively influences microbial activity and thus redox processes, such as sulphate reduction. Microorganism species can only operate within limited temperature ranges and their adaptability to temperature is a crucial point for the assessment of the environmental consequences of subsurface heat storage. Column experiments with aquifer sediment and tap water at 10, 25, 40, and 70 °C showed that under the constant addition of acetate sulphate reduction could be initiated after 26–63 pore volumes exchanged at all temperatures. Fastest initiation of sulphate reduction with the highest reduction rates was found at 40 °C. Maximum rate constants during experimental run-time were 0.56 h?1 at 40 °C and 0.33, 0.36, and 0.25 h?1 at 10 and, 25, and 70 °C, respectively. Hence, microbial activity was enhanced by a temperature increase to 40 °C but was significantly lowered at 70 °C. At 25 °C methane was found in solution, indicating the presence of fermenting organisms; at 10, 40, and 70 °C no methane production was observed. It could be shown that redox processes in an aquifer generally can adapt to temperatures significantly higher than in situ temperature and that the efficiency of the reduction process can be enhanced by temperature increase to a certain limit. Enhancement of sulphate reduction in an aquifer due to temperature increase could also allow enhanced degradation of organic ground water contaminants such as BTEX, where sulphate is an important electron acceptor.  相似文献   

9.
To demonstrate the atmospheric emission characteristics of cadmium (Cd), which is considered an important contaminant to human health and environment, a comprehensive emission inventory of Cd has been established by applying the best available emission factors and activity data for the first time. This inventory covers major anthropogenic sources in China and a bottom-up approach is adopted to compile the inventory for the sources where possible. The total emissions of Cd are estimated at about 743.77 metric tons for the year 2009, of which the contributions of industrial processes and combustion sources are approximately 56.6 and 43.4 %, respectively. Nonferrous metals smelting including copper, lead, and zinc, ranks as the leading source accounting for about 40.6 % of the total. The high contribution results from the rapid growth of nonferrous metallurgical industry that reflects a new focus of Cd emission pollution in China. Cd emissions from coal combustion are estimated at approximately 273.69 metric tons, with a share of 36.8 %, in which industrial coal-burning sector is thought to be the primary source. Moreover, Cd emissions are spatially allocated onto grid cells with a resolution of 0.5° × 0.5°, indicating that the emissions are mainly distributed among the regions of eastern, central and southern China. In addition, the uncertainties in the inventory are quantified by using a Monte Carlo simulation, and the overall uncertainty falls within a range of ?15 to 48 %. It implies that more field tests for industrial coal combustion and metals smelting process are very necessary.  相似文献   

10.
Understanding the impact of temperature fluctuations on air quality and public health has gained popularity among environmental and epidemiological researchers. Potentially, increase and decrease in temperature between neighboring days have increased the environmental and health risk worldwide. Based on ordinary least-squares method, this paper aims to examine the impact of temperature fluctuations on air quality index (AQI) and respiratory health outcomes (RHOs) during 2008–2012 in Beijing. Our results show that a drop of more than 3 °C results in the increased impact on AQI and RHO in the heating period. At the same time, a raise of more than 3 °C results in the similar increased impact on AQI in the whole study period and heating period. Furthermore, for a raise of more than 3 °C, a larger impact on RHO is observed in the heating period compared with the whole study period. Additionally, an increase in temperature also results in the increased influence of health risk on females during the heating period. Our results suggest that the air quality and public health in Beijing are significantly influenced by decrease and increase in temperature in the heating period.  相似文献   

11.
Ikram  Maria  Yan  Zhijun  Liu  Yan  Wu  Dan 《Natural Hazards》2015,77(1):153-175

Understanding the impact of temperature fluctuations on air quality and public health has gained popularity among environmental and epidemiological researchers. Potentially, increase and decrease in temperature between neighboring days have increased the environmental and health risk worldwide. Based on ordinary least-squares method, this paper aims to examine the impact of temperature fluctuations on air quality index (AQI) and respiratory health outcomes (RHOs) during 2008–2012 in Beijing. Our results show that a drop of more than 3 °C results in the increased impact on AQI and RHO in the heating period. At the same time, a raise of more than 3 °C results in the similar increased impact on AQI in the whole study period and heating period. Furthermore, for a raise of more than 3 °C, a larger impact on RHO is observed in the heating period compared with the whole study period. Additionally, an increase in temperature also results in the increased influence of health risk on females during the heating period. Our results suggest that the air quality and public health in Beijing are significantly influenced by decrease and increase in temperature in the heating period.

  相似文献   

12.
Sandstone alterations triggered by fire-related temperatures   总被引：1，自引：1，他引：0  
The aim of the study was to identify and describe changes in two different sandstone types when undergoing different environmental and extreme temperature regimes to assess the possibility of finding insolation weathering and how these sandstones would behave during and after a fire. The first step was the simulation in the laboratory of temperature regimes up to 60 °C which would correspond to extreme events that could be found in insolation cycles even in Central Europe and the second one was the temperature above 200 °C simulating in laboratory conditions the thermal regime of a potential fire situation at temperatures up to 200, 400, 600 and 800 °C. Heating the samples above 400 °C led to gradual changes in mineral composition, colour, surface roughness and physical properties reaching, eventually, total rock breakdown through spalling and granular disaggregation. The different behaviour of sandstones exposed to high temperatures is mainly caused by their different mineral composition with various ratios of minerals that are more or less chemically stable at high temperatures as well as by the differences in the porosity.  相似文献   

13.
High temperature damage of rock is a critical problem that must be well known for underground coal gasification, underground storage of nuclear waste, repairment of underground buildings after fire disaster. In order to study the influences of loading rate and high temperature on the tensile strength of sandstone, Brazilian splitting tests were conducted on sandstone disk samples treated with five different temperature levels between 25 and 800 °C at six different loading rates between 0.01 and 10 mm/min. Test results showed that tensile strength of disk samples increases gradually and reaches to the maximum at the temperature level of 400 °C, then drop sharply. The tensile strength of sandstone samples is characterized by obvious rate effect and it increases continuously with the increase of loading rate, meeting a Logarithmic Function. The lower limit tensile strength of sandstone ignoring the influence of rate effect was calculated, and it is helpful for providing some basis for the design of rock engineering.  相似文献   

14.
This paper studies the variation of mass, density, wave velocity and thermal conductivity of concrete after high-temperature heat treatment. The range of temperature to which the concrete specimens are exposed is 25–900 °C, in a heating furnace. The results are summarized as follows: three temperature ranges (20–300 °C, 300–600 °C and above 600 °C) corresponding to the moisture vaporization (i.e., adhered water, combined water or crystal water), decomposition of some minerals (i.e., Ca-hydroxide, Mg-hydroxide) and Ca-carbonate are obviously evident. The physical properties of concrete specimens change most significantly within the temperature range above 300 °C, which may be attributed to the transformation of concrete minerals. Moreover, within the temperature range of 300–900 °C, especially between 400 and 600 °C, the concrete structure has significant chemical changes basing on the variations of surface features, ultimately making the number and width of cracks and mass loss level increased, as well as the wave velocity and thermal conductivity changed.  相似文献   

15.
The evolution of porosity and changes in wave velocity in granite after high-temperature treatment has been experimentally investigated in different studies. Statistical analysis of the test results shows that there is a temperature threshold value that leads to variations in porosity and wave velocity. At a temperature that is less than 200 °C, the porosity of granite slowly increases with increases in temperature, while the wave velocity decreases. When the temperature is greater than 200 °C (especially between 400 and 600 °C), the porosity quickly increases, while the wave velocity substantially decreases. The temperature ranges of room temperature to 200 and 200–400 °C correspond to the undamaged state and the micro-damage state, respectively. The results confirm that there is an important link between the variations of physical and mechanical properties in response to thermal treatment. By studying the relationships among rock porosity, wave velocity and temperature, this provides the basis for solving multi-variable coupling problems under high temperatures for the thermal exploitation of petroleum and safe disposal of nuclear waste.  相似文献   

16.
This study describes changes of surface roughness of semifusinite and fusinite as an indicator of structural alteration resulting from heat treatment at 400–1200 °C. Surface roughness has been investigated by atomic force microscopy of inertinite concentrates from coking coals (vitrinite reflectance Rr = 1.07%–1.41%) from the Upper Silesian Coal Basin of Poland (Namurian C — Westphalian A). Unheated fusinite has a higher surface roughness than semifusinite from the same coal. The average surface roughness of semifusinite decreases with the Swelling Index of the parent coal. Heating increases the surface roughness of semifusinite and fusinite. Increase in the average surface roughness is stronger for semifusinite than fusinite and correlates to increasing reflectance of these macerals. The surface roughness of semifusinite correlates to the relative mass loss of the inertinite concentrates during heating. After heating to 1200 °C fusinite has a lower average surface roughness than semifusinite from the same coal. Consequently, average surface roughness can be used as a measure of structural alteration of inertinite group macerals during heat treatment.  相似文献   

17.
Methane is one of the potential greenhouse gases contributing to global climate change, with a global warming potential of about 25 times than that of carbon dioxide. Aerobic methane oxidation (methanotrophy) is the key process that counteracts emission of methane to atmosphere. In this study, methane oxidation capacity of different methane-oxidizing bacteria (methanotrophs) isolated from six different ecosystems was investigated. Methanotrophic consortium isolated from dumpsite proved to be most effective in oxidizing methane. Initially, methane oxidation rate was found to be 0.72 ± 0.036 mM/day; in course of the study consortium M5 showed an increase in methane oxidation rate up to 1.7 ± 0.016 mM/day. A maximum of 0.78 mol of CO2 production was found during methane oxidation in methanotrophs from dumpsite (M5). While varying temperatures, methane oxidation rate was in the range of 1.3–1.7 mM/day which has been found in the temperature range of 30–40 °C. Even at higher temperature (50 °C), 0.076 ± 0.14 mM of the methane was utilized per day. Methane oxidation was assessed by Michaelis–Menten kinetics. By varying the methane concentration, methane oxidation was studied and kinetic parameters such as V max and K m were derived using Lineweaver–Burk plot and found to be 1.497 mM/day and 2.23 mM, respectively. In methane mitigation approach, Methane soil sink is very essential because a balance between methane production by methanogens and consumption by methanotrophs plays an important role in methane emission reduction. Enhancing the methane soil sink will be a cost-effective method to cut down methane emission.  相似文献   

18.
Differentiation of mantle-derived, hydrous, basaltic magmas is a fundamental process to produce evolved intermediate to SiO2-rich magmas that form the bulk of the middle to shallow continental and island arc crust. This study reports the results of fractional crystallization experiments conducted in a piston cylinder apparatus at 0.7 GPa for hydrous, calc-alkaline to arc tholeiitic magmas. Fractional crystallization was approached by synthesis of starting materials representing the liquid composition of the previous, higher temperature experiment. Temperatures ranged from near-liquidus at 1,170 °C to near-solidus conditions at 700 °C. H2O contents varied from 3.0 to more than 10 wt%. The liquid line of descent covers the entire compositional range from olivine–tholeiite (1,170 °C) to high-silica rhyolite (700 °C) and evolves from metaluminous to peraluminous compositions. The following crystallization sequence has been established: olivine → clinopyroxene → plagioclase, spinel → orthopyroxene, amphibole, titanomagnetite → apatite → quartz, biotite. Anorthite-rich plagioclase and spinel are responsible for a marked increase in SiO2-content (from 51 to 53 wt%) at 1,040 °C. At lower temperatures, fractionation of amphibole, plagioclase and Fe–Ti oxide over a temperature interval of 280 °C drives the SiO2 content continuously from 53 to 78 wt%. Largest crystallization steps were recorded around 1,040 °C and at 700 °C. About 40 % of ultramafic plutonic rocks have to crystallize to generate basaltic–andesitic liquids, and an additional 40 % of amphibole–gabbroic cumulate to produce granitic melts. Andesitic liquids with a liquidus temperature of 1,010 °C only crystallize 50 % over an 280 °C wide range to 730 °C implying that such liquids form mobile crystal mushes (<50 % crystals) in long-lived magmatic systems in the middle crust, allowing for extensive fractionation, assimilation and hybridization with periodic replenishment of more mafic magmas from deeper magma reservoirs.  相似文献   

19.
While the Intergovernmental Panel on Climate Change classifies coal as anthracite, bituminous coal, and sub-bituminous coal, Korea only distinguishes coal as anthracite and bituminous coal while sub-bituminous coal is considered bituminous coal. As a result, Korea conducted research in the CO2 emission factors of anthracite and bituminous coal, but largely ignored sub-bituminous coal. Therefore, the purpose of this research is to develop the CO2 emission factor of sub-bituminous coal by classifying sub-bituminous coal from resources of bituminous coal activities collected in Korea between 2007 and 2011. The 2007–2011 average carbon content of sub-bituminous coal was analyzed to be 69.63 ± 3.11 %, the average hydrogen content 4.97 ± 0.37 %, the inherent moisture 12.60 ± 4.33 %, the total moisture 21.91 ± 5.45 %, and the dry-based gross calorific value was analyzed to be 5,914 ± 391 kcal/kg; using these analyzed values, the as-received net calorific value was found to be 20.75 ± 7.59 TJ/Gg and the CO2 emission factor was found to be 96,241 ± 4,064 kg/TJ. In addition, the 62.7 million ton amount for the 2009 greenhouse gas emission from sub-bituminous coal as estimated with the analyzed value of this study is an amount that is equivalent to 11.1 % of the 2009 total greenhouse gas emission amount of 564.7 million tons, and this amount is larger than the 9.3 % for the industrial processes sector, 3.3 % for the agricultural sector and 2.5 % for the waste sector. Therefore, it is important to reflect the realities of Korea when estimating the greenhouse gas emission from such sub-bituminous coals.  相似文献   

20.
The phosphate content of ancient alkali-glass has been tested as an indicator for biogenic ash, used in glass production. The living tissue of plants and vertebrates accumulates phosphate that remains in native ash as a main component (1 to over 10 wt%) forming together with biologically essential element oxides a complex chemical fingerprint that characterises any glass made with it. If, instead of native plant ash its alkali extract is used, soluble oxides are concentrated in the extract whilst insoluble oxides get depleted, leading to a different elemental fingerprint of the glass. Geogenic raw-materials for glass production like quartz-rich sand, evaporitic natron, or limestone are virtually phosphate free (below detection limit up to ≈0.15 wt%). Several collections of ancient glass stemming from different archaeological excavations, regions and times have been analysed by instrumental methods (WD-XFA, ED-XFA, thermal techniques), i.e. flat- and hollow K–Ca glass dated 1699/1714 N = 340, Na–Ca glass 13th/14th cy N = 94, Na–Ca glass 7th/9th cy N = 110, and alkali-Ca glass La Tène N = 395. Although the phosphate content of native alkali plant ash gets diluted with quartz sand by a factor of roughly two in glass production, it remains a main component of the product glass. Wood-ash glass contains 1–3 wt% phosphate, whilst glass manufactured from halophyte ash contains around 0.2–1 wt%. When processed wood-ash is used, the phosphate content in glass sinks below 1 wt%, the depletion factor amounting to roughly 8–15. Glass made from evaporitic soda displays phosphate contents below 0.2 wt% in the cases examined. The phosphate content of ancient alkali glass thus indicates whether virtually phosphate-free evaporitic soda has been used as a flux, or native ash of halophile plants. Ternary melting diagrams reveal at least three groups of alkali glass: Naturally coloured forest glass displays a broad distributional pattern with minimum melting temperatures ranging from 1200 to ≥1450 °C, colourless potash-extract glass from 900 to ≈1200 °C, and the typical, tight cluster of Roman sodium-calcium glass ranges from 800 to ≈900 °C. The wide-spread sodium-lime glass made with native halophytic ash, contains besides Na2O as the chemical main component always some K2O, and melting temperatures range from 800 to ≈1000 °C.  相似文献   

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