Deposition of sulfur dioxide to building stones: the influence of the ambient concentration on the deposition velocity

We report on extensive deposition measurements of sulfur dioxide (SO₂) on three types of commonly used building stones (Obernkirchen sandstone, Sand sandstone, Ihrlerstein sandstone). The deposition velocities on the three materials were determined in a number of measuring campaigns at different sites with different levels of air pollution. The measurements clearly imply that there is a strong influence of SO₂ concentration on the deposition velocity. With increasing concentration there is a strong decrease in the deposition velocity. To understand this deposition behavior a simple model with a single rate constant as the only adjustable parameter was established. Rate constants for the three stone materials were determined by least squares analysis and good agreement between experimental and calculated deposition velocities was obtained. According to the model treatment the surface resistance of stone materials increases with increasing SO₂ concentration due to a decrease of the pH in surface films. It follows from the concentration dependence of the deposition velocity that emission control measures for the reduction of ambient SO₂ concentrations do not lead to a proportional reduction of the SO₂ deposition. At low SO₂ concentrations the differences in the deposition behavior of different stone materials diminish and stone surfaces behave like ideal absorbers under such conditions, i.e., the deposition velocity is controlled by the aerodynamic resistance.     

Analysis of the surface of different marbles by X-ray photoelectron spectroscopy (XPS) to evaluate decay by SO2 attack

Atmospheric pollution is one of the main agents of decay in monuments and other works of art located in industrialised urban centres. SO₂ is a permanent and abundant component of air pollution and, although it does not have an immediate visual effect, after continuous exposure, it can cause irreversible damage to building materials. Marble is one of the most commonly used ornamental stones in historical monuments and its mineralogical composition makes it very susceptible to damage caused by exposure to SO₂. To measure the chemical reactions caused on marble by the action of atmosphere rich in SO₂, selected calcitic and dolomitic samples were altered by weathering accelerated test. For this, seven marble types (four calcitic and three dolomitic) were exposed to high concentration of sulphur dioxide for 24 h in a climate chamber under controlled temperature and humidity conditions (20 °C and > 90 % HR). Changes on marble surfaces caused by reactions of SO₂ with calcite and dolomite were studied using two non-destructive techniques: chromatic change by means of colorimetry and chemical analysis using X-ray photoelectron spectroscopy (XPS). The development of new mineral phases was also observed by scanning electron microscopy. Colorimetric analysis revealed a decrease in lightness and chromatic parameters suggesting that these changes were due to the development of new mineral phases in all marbles. The XPS technique, which is generally used in the analysis of metals, is relatively new in the field of stone deterioration. It enabled us to recognise the development of sulphites and sulphates on marble surfaces with high precision, after just 24 h of exposure to high SO₂ concentrations and to distinguish different decay paths for calcitic and dolomitic marbles.     

Preparation of carbon molecular sieves and its impregnation with Co and Ni for CO<Subscript>2</Subscript>/N<Subscript>2</Subscript> separation

The carbon molecular sieves (CMSs) prepared by carbonaceous materials as precursors are effective in CO₂/N₂ separation. However, selectivity of these materials is too low, since hydrocarbon cracking for developing the desired microporosity in carbonaceous materials has not been done effectively. Hence, in this study, cobalt and nickel impregnation on the precursor was conducted to introduce catalysts for hydrocarbon cracking. Cobalt and nickel impregnation, carbonization under N₂ atmosphere, and chemical vapor deposition (CVD) by benzene were conducted on the extruded mixtures of activated carbon and coal tar pitch under different conditions to prepare CMSs. The best CMS prepared by carbon deposition on the cobalt-impregnated samples exhibited CO₂ adsorption capacity of 54.79 mg/g and uptake ratio of 28.9 at 0 °C and 1 bar. In terms of CO₂ adsorption capacity and uptake ratio, CMSs prepared by carbon deposition on non-impregnated and cobalt-impregnated samples presented the best results, respectively. As benzene concentration and CVD time increased, equilibrium adsorption capacity of CO₂ decreased, and uptake ratio increased. Cobalt was found to be the best catalyst for benzene cracking in the CVD process.     

Phase transition of potassium sulfate,K2SO4 (II); dielectric constant and electrical conductivity

The phase transition of K₂SO₄ has been investigated by measurements of the dielectric constant and electrical conductivity, correlated with the structural point of view. Using single crystals, the temperature dependences of the dielectric constants and electrical conductivities were measured at frequencies of 0.3, 1, 3, and 5 MHz in the temperature range from 20° to 640 °C. Within this range, the dielectric constant does not reach a maximum, but near the phase-transition temperature at 587° C, the dielectric constant along the c axis shows a larger discontinuity than those along the a and b axes. The temperature dependence of the dielectric constant is consistent with the disordered structure of the high temperature form. Based on the parabolic increase of the dielectric constant in the temperature range from 582° to 587° C, it is likely that the phase transition propagates through an intermediate state. The electrical conductivity coefficients of K₂SO₄ increase with increasing temperature, exhibiting semiconducting character above the phase-transition temperature. In the high-temperature form, the electrical conductivity along the a axis exceeds that along the c axis. Since the electrical conductivity of K₂SO₄ is mainly ionic in character, the migration of K⁺ ions makes a major contribution to the conduction process.     

Geochemical alterations in surface waters of Govind Ballabh Pant Sagar,Northern Coalfield,India

Major ions showed high concentrations, ionic strength and chemical activity in the surface waters of Govind Ballabh Pant Sagar reservoir. Various geochemical ratios showed the dominance of silicate over carbonate weathering and major ions such as Na⁺ + K⁺ account for about 52 % of the cation budget. The high Na⁺ and K⁺ showed sedimentation of rock/coal particles consisting of highly weathered silicate minerals contributed by the discharge of mine water, fly ash mixing during transportation, etc. Further, Ca²⁺ + Mg²⁺/Na⁺ + K⁺ ratio was <1 (0.92) indicating the occurrence of silicate weathering in the reservoir catchment. The comparative assessment showed that the proportion of Ca²⁺ + Mg²⁺/Na⁺ + K⁺ tends to be lower along the coal mining belts compared to non-coal mining regions in the world. The Ca²⁺/SO₄ ^2? ratio <1 revealed not only H₂CO₃ but H₂SO₄ also acting as a source of protons for rock weathering. The cause underlying these differences can be related directly to geological substrate and anthropogenic activities.     

Single-crystal elastic properties of alunite, KAl3(SO4)2(OH)6

The single-crystal elastic constants of natural alunite (ideally KAl₃(SO₄)₂(OH)₆) were determined by Brillouin spectroscopy. Chemical analysis by electron microprobe gave a formula KAl₃(SO₄)₂(OH)₆. Single crystal X-ray diffraction refinement with R ₁ = 0.0299 for the unique observed reflections (|F _o| > 4σ _F) and wR ₂ = 0.0698 for all data gave a = 6.9741(3) Å, c = 17.190(2) Å, fractional positions and thermal factors for all atoms. The elastic constants (in GPa), obtained by fitting the spectroscopic data, are C ₁₁ = 181.9 ± 0.3, C ₃₃ = 66.8 ± 0.8, C ₄₄ = 42.8 ± 0.2, C ₁₂ = 48.2 ± 0.5, C ₁₃ = 27.1 ± 1.0, C ₁₄ = 5.4 ± 0.5, and C ₆₆ = ½(C ₁₁–C ₁₂) = 66.9 ± 0.3 GPa. The VRH averages of bulk and shear modulus are 63 and 49 GPa, respectively. The aggregate Poisson ratio is 0.19. The high value of the ratio C ₁₁/C ₃₃ = 2.7 and of the ratio C ₆₆/C ₄₄ = 1.6 are characteristic of an anisotropic structure with very weak interlayer interactions along the c-axis. The basal plane (001) is characterized by 0.1% longitudinal acoustic anisotropy and 0.9–1.1% shear acoustic anisotropy, which gives alunite a characteristic pseudo-hexagonal elastic behavior, and is related to the pseudo-hexagonal arrangement of the Al(O,OH)₆ octahedra in the basal layer. The elastic Debye temperature of alunite is 654 K. The large discrepancy between the elastic and heat capacity Debye temperature is also a consequence of the layered structure.     

Measurements of volcanic SO2 and CO2 fluxes by combined DOAS,Multi-GAS and FTIR observations: a case study from Turrialba and Telica volcanoes

Over the past few decades, substantial progress has been made to overcome the technical difficulties of continuously measuring volcanic SO₂ emissions. However, measurements of CO₂ emissions still present many difficulties, partly due to the lack of instruments that can directly measure CO₂ emissions and partly due to its strong atmospheric background. In order to overcome these difficulties, a commonly taken approach is to combine differential optical absorption spectroscopy (DOAS) by using NOVAC scan-DOAS instruments for continuous measurements of crateric SO₂ emissions, and electrochemical/NDIR multi-component gas analyser system (multi-GAS) instruments for measuring CO₂/SO₂ ratios of excerpts of the volcanic plume. This study aims to quantify the representativeness of excerpts of CO₂/SO₂ ratios measured by Multi-GAS as a fraction of the whole plume composition, by comparison with simultaneously measured CO₂/SO₂ ratios using cross-crater Fourier transform infrared spectroscopy (FTIR). Two study cases are presented: Telica volcano (Nicaragua), with a homogenous plume, quiescent degassing from a deep source and ambient temperature, and Turrialba volcano (Costa Rica), which has a non-homogeneous plume from three main sources with different compositions and temperatures. Our comparison shows that in our “easier case” (Telica), FTIR and Multi-GAS CO₂/SO₂ ratios agree within a factor about 3 %. In our “complicated case” (Turrialba), Multi-GAS and FTIR yield CO₂/SO₂ ratios differing by approximately 13–25 % at most. These results suggest that a fair estimation of volcanic CO₂ emissions can be provided by the combination of DOAS and Multi-GAS instruments for volcanoes with similar degassing conditions as Telica or Turrialba. Based on the results of this comparison, we report that by the time our measurements were made, Telica and Turrialba were emitting approximately 100 and 1,000 t day^?1 of CO₂, respectively.     

Exceedance of air quality standards resulting from pyro-metallurgical production of copper: a case study, Bor (Eastern Serbia)

This study represents air quality data of SO₂ and As concentrations around the mining–metallurgical complex Bor (Serbia) from 1994 to 2008. Daily and annual SO₂ concentrations greatly exceed current air quality standards in the studied area. The “hot spot” with the highest SO₂ and As annual concentrations during 15 years was the urban-industrial area (the town core). Daily SO₂ concentrations and meteorological parameters during the period from 2005 to 2008 were statistically analysed to develop suitable prediction equations for daily SO₂ concentrations. Anode copper production is an important but not the only factor that has influence on SO₂ concentrations. By stepwise multiple linear regression analysis, it was determined that daily SO₂ concentrations are most influenced by maximum wind gust, relative humidity and air temperature at all the measuring sites. The prediction equations of daily SO₂ concentrations represent a good model with regression coefficients from 0.854 to 0.926 at all the measuring sites. Correlation analysis showed that eastern and western winds increase SO₂ concentrations, thus increasing the health risk of the inhabitants in the study area.     

PGE mineralization and melt composition of chromitites in Proterozoic ophiolite complexes of Eastern Sayan,Southern Siberia

The Ospino-Kitoi and Kharanur ultrabasic massifs represent the northern and southern ophiolite branches respectively of the Upper Onot ophiolitic nappe and they are located in the southeastern part of the Eastern Sayan(SEPES ophiolites).Podiform chromitites with PGE mineralization occur as lensoid pods within dunites and rarely in harzburgites or serpentinized peridotites.The chromitites are classified into type I and type Ⅱ based on their Cr~#.Type I(Cr~# = 59-85) occurs in both northern and southern branches,whereas type Ⅱ(Cr~# = 76-90) occurs only in the northern branch.PGE contents range from ∑PGE 88-1189 ppb,Pt/Ir0.04-0.42 to ∑PGE 250-1700 ppb,Pt/Ir 0.03-0.25 for type I chromitites of the northern and southern branches respectively.The type Ⅱ chromitites of the northern branch have ∑PGE contents higher than that of type Ⅰ(468-8617 ppb,Pt/Ir 0.1-0.33).Parental melt compositions,in equilibrium with podiform chromitites,are in the range of boninitic melts and vary in Al_2O_3,TiO_2 and FeO/MgO contents from those of type I and type Ⅱ chromitites.Calculated melt compositions for type Ⅰ chromitites are(Al_2O_3)_(melt) = 10.6—13.5 wt.%,(TiO_2)_(melt) = 0.01-0.44 wt.%,(Fe/Mg)_(melt) = 0.42-1.81;those for type Ⅱ chromitites are:(Al_2O_3)_(melt) = 7.8-10.5 wt.%,(TiO_2)_(melt) = 0.01-0.25 wt.%,(Fe/Mg)_(melt) = 0.5-2.4.Chromitites are further divided into Os-Ir-Ru(Ⅰ) and Pt-Pd(Ⅱ) based on their PGE patterns.The type Ⅰ chromitites show only the Os-Ir-Ru pattern whereas type Ⅱ shows both Os-Ir-Ru and Pt-Pd patterns.PGE mineralization in type Ⅰ chromitites is represented by the Os-Ir-Ru system,whereas in type Ⅱ it is represented by the Os-Ir-Ru-Rh-Pt system.These results indicate that chromitites and PGE mineralization in the northern branch formed in a suprasubduction setting from a fluid-rich boninitic melt during active subduction.However,the chromitites and PGE mineralization of the southern branch could have formed in a spreading zone environment.Mantle peridotites have been exposed in the area with remnants of mantle-derived reduced fluids,as indicated by the occurrence of widespread highly carbonaceous graphitized ultrabasic rocks and serpentinites with up to 9.75 wt.%.Fluid inclusions in highly carbonaceous graphitized ultrabasic rocks contain CO,CO_2,CH4,N_2 and the δ~(13)C isotopic composition(-7.4 to-14.5‰) broadly corresponds to mantle carbon.     

Compressive and Tensile Behavior of Polymer Treated Sulfate Contaminated CL Soil

In this study, the compressive and tensile behavior of polymer treated sulfate contaminated CL soil was investigated. Based on the information in the literature, a field soil was contaminated with up to 4 % (40,000 ppm) of calcium sulfate in this study. In addition to characterizing the behavior of sulfate contaminated CL soil, the effect of treating the soil with a polymer solution was investigated and the performance was compared to 6 % lime treated soil. In treating the soil, acrylamide polymer solution (15 g of polymer dissolved in 85 g of water) content was varied up to 15 % (by dry soil weight). Addition of 4 % calcium sulfate to the soil decreased the compressive and tensile strengths of the compacted soils by 22 and 33 % respectively with the formation of calcium silicate sulfate [ternesite Ca₅(SiO₄)₂SO₄)], magnesium silicate sulfate (Mg₅(SiO₄)₂SO₄) and calcium-magnesium silicate (merwinite Ca₃Mg(SiO₄)₂). With the polymer treatment the strength properties of sulfate contaminated CL soil was substantially improved. Polymer treated sulfate soils had higher compressive and tensile strengths and enhanced compressive stress–strain relationships compared to the lime treated soils. Also polymer treated soils gained strength more rapidly than lime treated soil. With 10 % of polymer solution treatment, the maximum unconfined compressive and splitting tensile strengths for 4 % of calcium sulfate soil were 625 kPa (91 psi) and 131 kPa (19 psi) respectively in 1 day of curing. Similar improvement in the compressive modulus was observed with polymer treated sulfate contaminated CL soil. The variation of the compacted compressive strength and tensile strength with calcium sulfate concentrations for the treated soils were quantified and the parameters were related to calcium sulfate content in the soil and polymer content. Compressive stress–strain relationships of the sulfate soil, with and without lime and polymer treatment, have been quantified using two nonlinear constitutive models. The constitutive model parameters were sensitive to the calcium sulfate content and the type of treatment.     

An automatic system for continuous monitoring of CO2, H2S, SO2 and meteorological parameters in the atmosphere of volcanic areas

An automatic system for the continuous monitoring of CO₂, H₂S, SO₂ and meteorological parameters in atmosphere has been developed. The system has been tested in the laboratory in order to verify the stability and reliability of each sensor and of the whole system. A field test for a period of one month, at the Solfatara of Pozzuoli has also been carried out. The acquired data during the field test reveal a correlation between the wind speed and the concentrations of CO₂, H₂S, and SO₂ in the atmosphere. With a wind speed of over 4 ms^-1 the concentration of the three gases reached constant background values of 600 ppm for CO₂ and about 2 ppm vol. for H₂S and SO₂. The different ratios of H₂S/SO₂ measured in the fumaroles (~100) and in the atmosphere (1–0.1) clearly indicate that H₂S is oxidized to SO₂ during the transport.     

The effect of air pollution on stone decay: the decay of the Drachenfels trachyte in industrial, urban, and rural environments—a case study of the Cologne, Altenberg and Xanten cathedrals

Severe stone deterioration is evident at the Cologne cathedral. In particular, the “Drachenfels” trachyte, which was the building material of the medieval construction period, shows significant structural deterioration as well as massive formation of gypsum crusts. The present article investigates crust formation on limestone, sandstone, and volcanic rock from the Cologne cathedral as well as from the Xanten and Altenberg cathedrals. These three buildings, showing varying degrees of deterioration, are located in different areas and exposed to varying industrial, urban, and rural pollution. Thin laminar and black framboidal crusts form on calcareous as well as silicate stone. The lack of a significant intrinsic calcium and sulfur source for the formation of the gypsum crusts on the Drachenfels trachyte indicates major extrinsic environmental impact: a sufficient offer of SO _x from pollutant fluxes as well as external calcium sources (e.g., pollution, mortars, neighboring calcite stones). Chemical analyses reveal strong gypsum enrichment within the crusts as well as higher concentrations of lead and other pollutants (arsenic, antimony, bismuth, tin, etc.), which generally can be linked to traffic and industry. The formation of weathering crusts in an industrial environment is clearly distinguishable from that in rural areas. Scanning electron microscopy observations confirm that the total amount of pollution is less at the Altenberg cathedral than at the Cologne and Xanten cathedrals. XRF analyses show that the formation of gypsum occurs in lower amounts at Altenberg. This correlates well with the measured SO₂ content and the intensity of the decay at the different locations. Furthermore, the different types of crusts, e.g., framboidal and laminar, can be differentiated and assigned to the different locations. The black weathering crusts on the silicate Drachenfels trachyte contribute to the degradation of the historic building material. They enhance mechanical moisture-related deterioration processes and the decay by chemical corrosion of rock-forming minerals. Although SO₂ concentrations in air have shown a strong decrease over the past 30 years, degradation in connection with weathering crusts is still observed. This indicates that not only contemporary or recent emissions, but also past pollutant concentrations have to be considered.     

Weathering Processes in the Min Jiang: Major Elements, {}^{87}{\text{Sr/}}{}^{86}{\text{Sr}},\;\delta {}^{34}{\text{S}}_{{\text{SO}}_{\text{4}} } ,\;{\text{and}}\;\delta {}^{18}{\text{O}}_{{\text{SO}}_{\text{4}} }

We investigated the dissolved major elements, $ {}^{87}{\text{Sr/}}{}^{86}{\text{Sr}},\;\delta {}^{34}{\text{S}}_{{\text{SO}}_{\text{4}} } ,\;{\text{and}}\;\delta {}^{18}{\text{O}}_{{\text{SO}}_{\text{4}} } $ composition of the Min Jiang, a headwater tributary of the Chang Jiang (Yangtze River). A forward calculation method was applied to quantify the relative contribution to the dissolved load from rain, evaporite, carbonate, and silicate reservoirs. Input from carbonate weathering dominated the major element composition (58–93%) and that from silicate weathering ranged from 2 to 18% in unperturbed Min Jiang watersheds. Most samples were supersaturated with respect to calcite, and the CO₂ partial pressures were similar to or up to ～5 times higher than atmospheric levels. The Sr concentrations in our samples were low (1.3–2.5 μM) with isotopic composition ranging from 0.7108 to 0.7127, suggesting some contribution from felsic silicates. The Si/(Na^* + K) ratios ranged from 0.5 to 2.5, which indicate low to moderate silicate weathering intensity. The $ \delta {}^{34}{\text{S}}_{{\text{SO}}_{\text{4}} } \;{\text{and}}\;\delta {}^{18}{\text{O}}_{{\text{SO}}_{\text{4}} } $ for five select samples showed that the source of dissolved sulfate was combustion of locally consumed coal. The silicate weathering rates were 23–181 × 10³ mol/km²/year, and the CO₂ consumption rates were 31–246 × 10³ mol/km²/year, which are moderate on a global basis. Upon testing various climatic and geomorphic factors for correlation with the CO₂ consumption rate, the best correlation coefficients found were with water temperature (r ² = 0.284, p = 0.009), water discharge (r ² = 0.253, p = 0.014), and relief (r ² = 0.230, p = 0.019).     

Effects of the external carbon sources on the microbes in the simultaneous biological removal of SO2 and NO x process

Effects of sodium acetate and glucose on the microbes from the simultaneous flue gas desulfurization and denitrogenation tandem biotrickling process were respectively investigated. For the acidophiles, although the impacts of the carbon sources on the total microbial growth and nitrogen conversion in the medium were slight, the sulfite oxidation rate was obviously improved. The highest sulfite ion oxidation ratio in 48 h was up to 47.2 % as 258.08 mmol L^?1 sodium acetate was added in the medium. For the neutrophiles, the two carbons promoted the total microbial growth, but only sodium acetate could enhance the nitrite consumption significantly. The best nitrite consumption rate in 48 h could reach to 86.7 % with 258.08 mmol L^?1 sodium acetate. It provides valuable information for the development of biological SO₂ and NO _x simultaneous purification process.     

Geochemical evolution and quality assessment of water resources in the Sarcheshmeh copper mine area (Iran) using multivariate statistical techniques

Hydrochemical data were gathered throughout the last 12 years from 57 sampling stations in the drainage basin of the Sarcheshmeh copper mine, Kerman Province, Iran. The mean values of these data for each sampling station were used to evaluate water quality and to determine processes that control water chemistry. Principal component analyses specified the oxidation of sulfide minerals, dissolution of carbonate and sulfate minerals and weathering of silicate minerals as the principal processes responsible for the chemical composition of water in the study area. Q-mode cluster analysis revealed three main water groups. The first group had a Ca-HCO₃–SO₄ composition whereas the second and third groups had Ca–SO₄ and Ca–Mg–SO₄ composition, respectively. The results of this study clearly indicated the role of sulfide minerals oxidation and the buffering processes in the geochemical evolution of water in the Sarcheshmeh area. Due to these processes, extensive changes occurred in the chemical composition of water by passage through the mining area or waste and low-grade dumps, so that the fresh water of the peripheral area of the pit evolved to an acid water rich in sulfate and heavy metals at the outlet of the pit and in the seepages of waste and low-grade dumps.     

Hydrogeological processes controlling the release of arsenic in parts of 24 Parganas district,West Bengal

A study was conducted to understand the hydrogeological processes dominating in the North 24 Parganas and South 24 Parganas based on representative 39 groundwater samples collected from selected area. The abundance of major ions was in the order of Ca²⁺ > Na⁺ > Mg²⁺ > K⁺ > Fe²⁺ for cations and HCO₃ ^? > PO₄ ^3? > Cl^? > SO₄ ^2? > NO₃ ^? for anions. Piper trilinear diagram was plotted to understand the hydrochemical facies. Most of the samples are of Ca-HCO₃ type. Based on conventional graphical plots for (Ca + Mg) vs. (SO₄ + HCO₃) and (Na + K) vs. Cl, it is interpreted that silicate weathering and ion exchange are the dominant processes within the study area. Previous studies have reported quartz, feldspar, illite, and chlorite clay minerals as the major mineral components obtained by the XRD analysis of sediments. Mineralogical investigations by SEM and EDX of aquifer materials have shown the occurrence of arsenic as coating on mineral grains in the silty clay as well as in the sandy layers. Excessive withdrawal of groundwater for irrigation and drinking purposes is responsible for fluctuation of the water table in the West Bengal. Aeration beneath the ground surface caused by fluctuation of the water table may lead to the formation of carbonic acid. Carbonic acid is responsible for the weathering of silicate minerals, and due to the formation of clay as a product of weathering, ion exchange also dominates in the area. These hydrogeological processes may be responsible for the release of arsenic into the groundwater of the study area, which is a part of North 24 Parganas and South 24 Parganas.     

Thermal phase transition of potassium sulfate,K2SO4

The thermal phase transition of K₂SO₄ has been investigated by high temperature polarized light microscopy. K₂SO₄ undergoes a first-order transition at 587° C where the orthorhombic low temperature form (Pmcn) transforms into a hexagonal high temperature modification (P6₃/mmc). Prior to the beginning of the phase transition, K₂SO₄ shows an anomalous optical behavior. The crystal apparently becomes optically uniaxial twice at 338° and 425° C, respectively, and truly optically uniaxial at 587° C. The phase transition propagates through an intermediate temperature form, which is sandwiched between the low and the high temperature forms and moves in a definite direction, 〈130〉 (orthorhombic indices), in the vicinity of the phase transition. Passing through the phase transition point on cooling, dark belts crossing each other are observed which are a result of the transformation twins parallel to {110} and {130}.     

Assessment of groundwater quality for irrigation purposes and identification of hydrogeochemical evolution mechanisms in Pengyang County, China

Groundwater is an important water source for agricultural irrigation in Penyang County. Some traditional methods such as irrigation coefficient, sodium adsorption ratio, total alkalinity, total salinity and total dissolved solids were employed to assess groundwater quality in this area. In addition, an improved technique for order preference by similarity to ideal solution model was applied for comprehensive assessment. The origin of major ions and groundwater hydrogeochemical evolution was also discussed. Groundwater in Penyang County contains relative concentrations of dominant constituents in the following order: Na⁺ > Ca²⁺ > Mg²⁺ > K⁺ for cations and HCO₃ ^? > SO₄ ^2? > Cl^? > CO₃ ^2? for anions. Groundwater quality is largely excellent and/or good, suggesting general suitability for agricultural use. Calcite and dolomite are found saturated in groundwater and thus tend to precipitate out, while halite, fluorite and gypsum are unsaturated and will dissolve into groundwater during flow. Groundwater in the study area is weathering-dominated, and mineral weathering (carbonate and silicate minerals) and ion exchange are the most important factors controlling groundwater chemistry.     

Assessment of chemical properties and hydro-geochemical coefficients at the Qareh Sou Basin,Golestan Province,Iran

This paper focuses on the Qareh Sou Basin in Golestan Province, Iran. Golestan Province is the third largest cereal producer in Iran and water scarcity and salinity are major problems in this area. This study attempts to facilitate the comprehension of system behavior with respect to water quality issues and hydro-geochemical coefficients within the Qareh Sou Basin. This study was carried out during the year 2010. Various parameters, such as pH, EC, chloride, sulfate, bicarbonate, sodium, potassium, calcium and magnesium have been determined for evaluation purposes. Then, Ca/Mg, Na/Cl, Mg/(Ca + Mg), Ca/HCO₃, (Ca + Mg)–(HCO₃ + SO₄), (Na + K)–Cl, (Ca + Mg + Na + K)–Cl, HCO₃ + SO₄, Ca + Mg and chloro-alkaline indices (CAI) were calculated. Results show that cation exchange probably is an important factor in the hydrochemistry and silicate mineral weathering. Also, CAI-1 plot against CAI-2 demonstrates that most of samples have positive values which suggest normal ion exchange in the system. The carbonic acid is the main agent of calcite, limestone and dolomite weathering which occurs in some stations. According to Chadha’s diagram, the type of water is determined as Ca–Mg–HCO₃.