The damage effects of water sorption on the mechanical properties of the hydroxyapatite particle reinforced Bis-GMA/TEGDMA copolymer （HA/Bis-GMA/TEGDMA） h-ave been predicted using 3D finite cell models. The plastici...The damage effects of water sorption on the mechanical properties of the hydroxyapatite particle reinforced Bis-GMA/TEGDMA copolymer （HA/Bis-GMA/TEGDMA） h-ave been predicted using 3D finite cell models. The plasticizer effect on the polymer matrix was considered as a variation of its Young＇s modulus. Three different cell models were used to determine the influence of varying particle contents, interphase strength and moisture concentration on the debonding damage. The stress distribution pattern has been examined and the stress transfer mode clarified. The Young＇s modulus and fracture strength of the Bis-GMA/TEGDMA composite were also predicted using the model with and without consideration of the damage. ine Iormer results with consideration of the debonding damage are in good agreement with existing literature experimental data. The shielding effect of our proposed model and an alternative approach were discussed. The FCC cell model has also been extended to predict the critical load for the damaged and the undamaged composite subject to the 3-point flexural test.展开更多
Electrochemical impedance spectra （EIS） technique was adopted to evaluate the water sorption behaviour of an epoxy freestanding film in a 0.5 mol/L sodium chloride solution at 20℃. The methods for obtaining the cap...Electrochemical impedance spectra （EIS） technique was adopted to evaluate the water sorption behaviour of an epoxy freestanding film in a 0.5 mol/L sodium chloride solution at 20℃. The methods for obtaining the capacitance data from EIS data were compared. The Brasher-Kingsbury （BK） and corresponding modified version （Modi-BK） models were used to calculate the water uptake in film and the gravimetric results were presented for comparisons. According to the discussion of the discrepancy of water content in film obtained from two models, a new method was proposed to indicate the organic film structure.展开更多
Novel SiO_(2)-LiBr microcapsules for water-retaining pavement were prepared and firstly characterized by scanning electron microscope(SEM),particle size analysis,and Fourier transform infrared spectroscopy(FT-IR).The ...Novel SiO_(2)-LiBr microcapsules for water-retaining pavement were prepared and firstly characterized by scanning electron microscope(SEM),particle size analysis,and Fourier transform infrared spectroscopy(FT-IR).The water vapor sorption and desorption of the formulated microcapsules was then experimentally studied using dynamic vapor sorption(DVS),with the results fitted to three kinds of adsorption kinetics models.In addition,the specific surface area(SSA)was also calculated based on BET theory;and the thermal performance was investigated by laser flash analysis(LFA).Experimental results show a change of 103%in mass of the microcapsule sample under 90%relative humidity(RH)at 30℃after water vapor sorption.The fitting of results indicates that the adsorption process is mainly governed by the intra-particle diffusion mechanism,followed by the pseudo-first-order adsorption process.In comparison with most conventional pavement materials,it is found that the SSA of the formulated microcapsules is much larger while the thermal conductivity is lower.The unique properties of the formulated SiO_(2)-LiBr microcapsules have significant potential to take the edge off the urban heat island effect and reduce rutting when applied to water-retaining pavement materials.展开更多
Connate water strongly restricts shale gas enrichment and production,and most artificially injected water is confined in shale pore networks owing to low water recovery during hydraulic fracturing,which leads to a mor...Connate water strongly restricts shale gas enrichment and production,and most artificially injected water is confined in shale pore networks owing to low water recovery during hydraulic fracturing,which leads to a more complex pore water distribution.However,previous studies have focused on the water vapor sorption of gas shales rather than liquid pore water.This study clarifies the occurrence and distribution of pore water and the controlling factors by conducting thermogravimetry(TGA)under liquid water saturation and water vapor sorption experiments on four gas shales from the Wufeng Formation in South China.Nuclear magnetic resonance(NMR)T_(2)and T_(1)-T_(2)technologies were used to monitor the dynamic changes and states of moisture,and the microscopic pore structures during water vapor sorption were detected using low-temperature nitrogen adsorption-desorption.The results indicate that TGA is adequate for determining the adsorbed,bound,and movable water contents.These four gas shales are characterized by high adsorbed and movable water contents,and some bound water.The adsorbed water primarily occurs in tiny pores(<100 nm),controlled by organic matter,followed by clay mine rals.The movable water,typically associated with quartz,primarily exists in pores of>100 nm,particularly macropores of>1000 nm.The bound water predominantly correlates with pores ranging from 10 to 2000 nm in clay minerals.The water vapor sorption process of the gas shale is well clarified.Water molecules primarily adsorb on the clay mineral's hydrophilic surface,followed by oxygen functional groups in the organic matter.Therefore,clay mine rals control water vapor sorption at low relative humidity(RH<0.75),whereas organic matter primarily affects vapor sorption at high RH.The TGA of liquid wate r-saturated gas shales can clarify the water distributions in full-scale pore networks,whereas the water vapor sorption method primarily discloses the moisture in small nanopores(<100 nm)but ignores most bound and movable water.This paper provides insight into liquid water distribution and occurre nce states within shale pore netwo rks,contributing to a better understanding of gas-wate r-rock interaction systems in-situ and hydraulic fracturing shale gas formations.展开更多
Woods from Korean Larch, Chinese Fir, Aspens, Manchumian, and Fortunes Paulownia were chosen for investigation. Specimens cut from the air-dried woods had a cubic shape with nominal air-dried size of 17.0 mm and 8.5 m...Woods from Korean Larch, Chinese Fir, Aspens, Manchumian, and Fortunes Paulownia were chosen for investigation. Specimens cut from the air-dried woods had a cubic shape with nominal air-dried size of 17.0 mm and 8.5 mm. Oven-died specimens were put in containers filled with water and water sorption was implemented at atmospheric pressure and room temperature. Results from the experiment could not described exactly by the model of steady state flow from Darcy' law. An empirical equation is put forward fo...展开更多
Natural arsenic (As) contamination of groundwater which provides drinking water and/or irrigation supplies remains a major public health issue,particularly in South and Southeast Asia.A number of studies have evaluate...Natural arsenic (As) contamination of groundwater which provides drinking water and/or irrigation supplies remains a major public health issue,particularly in South and Southeast Asia.A number of studies have evaluated various aspects of the biogeochemical controls on As mobilization in aquifers typical to this region,however many are predicated on the assumption that key biogeochemical processes may be deduced by sampled water chemistry.The validity of this assumption has not been clearly established even though the role of sorption/desorption of As and other heavy metals onto Fe/Mn (hydr) oxides is an important control in As mobilization.Here,selective chemical extractions of sand-rich and clay-rich sediments from an As-affected aquifer in Kandal Province,Cambodia,were undertaken to explore the potential role of partial re-equilibrium through sorption/desorption reactions of As and related solutes (Fe,Mn and P) between groundwater and the associated solid aquifer matrix.In general,groundwater As is strongly affected by both pH and Eh throughout the study area.However,contrasting sorption behaviour is observed in two distinct sand-dominated (T-Sand) and clay dominated (T-Clay) transects,and plausibly attributed to differing dominant lithologies,biogeochemical and/or hydrogeological conditions.Sorption/desorption processes appear to be re-setting groundwater As concentrations in both transects,but to varying extents and in different ways.In T-Sand,which is typically highly reducing,correlations suggest that dissolved As may be sequestered by sorption/re-adsorption to Fe-bearing mineral phases and/or sedimentary organic matter;in T-Clay Eh is a major control on As mobilization although binding/occlusion of Fe-bearing minerals to sedimentary organic matter may also occur.Multiple linear regression analysis was conducted with groups categorised by transect and by Eh,and the output correlations support the contrasting sorption behaviours encountered in this study area.Irrespective of transect,however,the key biogeochemical processes which initially control As mobilization in such aquifers,may be “masked” by the re-setting of As concentrations through in-aquifer sorption/desorption processes.展开更多
An integrative technology including the surfactant enhanced sorption and subsequentdesorption and biodegradation of phenanthrene in the soil-water system was introduced and tested. For slightly contaminated agricultur...An integrative technology including the surfactant enhanced sorption and subsequentdesorption and biodegradation of phenanthrene in the soil-water system was introduced and tested. For slightly contaminated agricultural soils, cationic-nonionic mixed surfactant- enhanced sorption of organic contaminants onto soils could reduce their transfer to plants, therefore safe-guarding agricultural production. After planting, residual surfactants combined with added nonionic surfactant could also promote thedesorption and biodegradation of residual phenanthrene, thus providing a cost-effective pollution remediation technology.0ur results showed that the cationic-nonionic mixed surfactantsdodecylpyridinium bromide （DDPB） and Triton X-100 （TX100） significantly enhanced soil retention of phenanthrene. The maximum sorption coefficient Kd＊ of phenanthrene for contaminated soils treated by mixed surfactants was about24.5 times that of soils without surfactant （Kd ） and higher than the combined effects of DDPB and TX100 individually, which was about 16.7 and 1.5 times Kd , respectively.0n the other hand, TX100 could effectively remove phenanthrene from contaminated soils treated by mixed surfactants, improving the bioavailability of organic pollutants. Thedesorption rates of phenanthrene from these treated soils were greater than 85% with TX100 concentration above2000 mg/L and approached 100% with increasing TX100 concentration. The biodegradation rates of phenanthrene in the presence of surfactants reached over 95% in30days. The mixed surfactants promoted the biodegradation of phenanthrene to some extent in 10-22days, and had no obvious impact on phenanthrene biodegradation at the end of the experiment. Results obtained from this study provide some insight for the production of safe agricultural products and a remediation scheme for soils slightly contaminated with organic pollutants.展开更多
In this contribution, we review and critically compare the results of the analyses we have previously performed on water sorption thermodynamics in a series of polyimides. The experimental investigation was performed ...In this contribution, we review and critically compare the results of the analyses we have previously performed on water sorption thermodynamics in a series of polyimides. The experimental investigation was performed by combining gravimetric tests and in situ vibrational spectroscopy. A non-equilibrium theory, based on a compressible lattice framework accounting for the glassy state of the polymer and for the occurrence of hydrogen bonding interactions, has been used to interpret data. Information at a molecular level gained by vibrational spectroscopy has been used to tailor the model equations. The main features of water sorption thermodynamics are well captured, qualitatively and quantitatively, by the adopted model which displays a remarkable agreement with experimental results.展开更多
Preliminary research was conducted about how to incorporate sorption/desorption of organic pollutants with suspended solids and sediments into single-chemical and one-dimensional water quality model of Jinghang Canal....Preliminary research was conducted about how to incorporate sorption/desorption of organic pollutants with suspended solids and sediments into single-chemical and one-dimensional water quality model of Jinghang Canal. Sedimentation-resuspension coefficient k 3 was deduced; characteristics of organic pollutants, concentrations and components of suspended solids/sediments and hydrological and hydraulic conditions were integrated into k 3 and further into river water quality model; impact of sorption/desorption of organic pollutants with suspended solids and sediments on prediction function of the model was discussed. Results demonstrated that this impact is pronounced for organic pollutants with relatively large K oc and K ow, especially when they are also conservative and f oc of river suspended solids/sediments is high, and that incorporation of sorption/ desorption of organic pollutants into river water quality model can improve its prediction accuracy.展开更多
In this paper we are describing a green cycle process. The first step was a novel hydrotalcite-like compound (HTLC) synthesized by a co-precipitating method, under standard ambient temperature and pressure, using chem...In this paper we are describing a green cycle process. The first step was a novel hydrotalcite-like compound (HTLC) synthesized by a co-precipitating method, under standard ambient temperature and pressure, using chemical industry wastewater rich in divalent and trivalent cations, activated by a thermal treatment and finally characterized by scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDS) and thermogravimetric analysis (TGA). The second step was a series of batch sorption tests performed with this activated HTLC and untreated underground sulfurous water from the state of Puebla, México. The HTLC calcined at 500°C/3 h exhibited the best sorption ability for ions, demonstrated a decrease of the hardness and sulfate ions to below the regional legal standards for drinking water. Once inactive after being used in water treatment, the sorbed ions were removed by ion exchange in a carbonate-containing solution, resulting in an 80% recycling of the material which upon activation demonstrated a retained capacity for water treatment. This recyclability suggests the exciting possibility of this novel compound as an efficient “green” technology in water treatment processes.展开更多
For the assessment of the carbon dioxide (CO2) storage potential of water-filled reservoir rocks (i.e., saline aquifers), it should be first important step for a thorough understanding of the effect of water content o...For the assessment of the carbon dioxide (CO2) storage potential of water-filled reservoir rocks (i.e., saline aquifers), it should be first important step for a thorough understanding of the effect of water content on CO2/water/rock interactions during CO2 injection. The purpose of this study is to examine the CO2 sorption amount for Kimachi sandstone and Berea sandstone at different water content using the manometric method at temperature of 50?C and pressures of up to 20 MPa. Our results document that a significant quantity of CO2 was sorbed on the two types of sandstone on all water-saturated bases, which corresponded to the amount adsorbed on the air-dry basis. Also, all the wet samples had significantly higher sorption capacity than the theoretical values calculated from the solubility model based on dissolution of CO2 in pore water and the pore-filling model, which assumes that the pore volume unoccupied by water is filled with CO2. Furthermore, the observations indicated a certain degree of correlation between the sorbed amount and the water content, except at pressures below the critical point for Berea sandstone. This investigation points out that CO2 sorption is a possible mechanism in CO2 geological storage even under water-saturated conditions and that the mechanism of sorption on silica and silicate minerals plays an essential role in the reliable and accurate estimation of the CO2 storage capacity of water-saturated reservoirs.展开更多
Denatonium benzoate is an aversive agent proposed for use in certain anti-freeze formulations to reduce poisoning events of pets and humans. Unfortunately, the sorption properties of denatonium cations to soil and/or ...Denatonium benzoate is an aversive agent proposed for use in certain anti-freeze formulations to reduce poisoning events of pets and humans. Unfortunately, the sorption properties of denatonium cations to soil and/or soil components have not been investigated. In this paper, denatonium sorption to reference kaolinite clay under varied pH, ionic strength, and cation identity is described. The data clearly indicate that the nature of the background electrolyte cation modulates denatonium sorption with enhanced sorption occurring the presence of potassium ions versus minimal sorption occurring in a calcium chloride electrolyte at each pH studied as estimated using Dubinin-Raduskevich (D-R) isotherms. The effect of background electrolyte concentration on sorption was consistent with an ion-exchange process wherein the sorption capacity increased with decreased background electrolyte concentration. An interesting and unexpected observation of increased sorption capacity (estimated using the D-R model) with decreasing pH was observed in 10 mM CaCl2 in contrast to an observed and expected increase in denatonium sorption to kaolinite in the presence of either of 10 mM NaCl or 10 mM KCl. Estimates of the mean sorption energy using D-R isotherms ranging from 2.65 kJ/mol in 10 mM CaCl2 at pH 4 to 4.68 kJ/mol at pH 10 suggesting that the sorption process is not exclusively ion-exchange.展开更多
Fe/Al drinking water treatment residuals（WTRs）, ubiquitous and non-hazardous by-products of drinking water purification, are cost-effective adsorbents for glyphosate. Given that repeated glyphosate applications coul...Fe/Al drinking water treatment residuals（WTRs）, ubiquitous and non-hazardous by-products of drinking water purification, are cost-effective adsorbents for glyphosate. Given that repeated glyphosate applications could significantly decrease glyphosate retention by soils and that the adsorbed glyphosate is potentially mobile, high sorption capacity and stability of glyphosate in agricultural soils are needed to prevent pollution of water by glyphosate.Therefore, we investigated the feasibility of reusing Fe/Al WTR as a soil amendment to enhance the retention capacity of glyphosate in two agricultural soils. The results of batch experiments showed that the Fe/Al WTR amendment significantly enhanced the glyphosate sorption capacity of both soils（p 〈 0.001）. Up to 30% of the previously adsorbed glyphosate desorbed from the non-amended soils, and the Fe/Al WTR amendment effectively decreased the proportion of glyphosate desorbed. Fractionation analyses further demonstrated that glyphosate adsorbed to non-amended soils was primarily retained in the readily labile fraction（Na HCO3-glyphosate）. The WTR amendment significantly increased the relative proportion of the moderately labile fraction（HCl-glyphosate） and concomitantly reduced that of the Na HCO3-glyphosate, hence reducing the potential for the release of soil-adsorbed glyphosate into the aqueous phase. Furthermore, Fe/Al WTR amendment minimized the inhibitory effect of increasing solution p H on glyphosate sorption by soils and mitigated the effects of increasing solution ionic strength. The present results indicate that Fe/Al WTR is suitable for use as a soil amendment to prevent glyphosate pollution of aquatic ecosystems by enhancing the glyphosate retention capacity in soils.展开更多
The sorption and phase distribution of 20% ethanol and butanol blended gasoline （E20 and B20） vapours have been examined in soils with varying soil organic matter （SOM） and water contents via laboratory microcosm ...The sorption and phase distribution of 20% ethanol and butanol blended gasoline （E20 and B20） vapours have been examined in soils with varying soil organic matter （SOM） and water contents via laboratory microcosm experiments. The presence of 20% alcohol reduced the sorption of gasoline compounds by soil as well as the mass distribution of the compounds to soil solids. This effect was greater for ethanol than butanol. Compared with the sorption coefficient （Kd） of unblended gasoline compounds, the Kd of E20 gasoline compounds decreased by 54% for pentane, 54% for methylcyclopentane （MCP） and 63% for benzene, while the Kd of B20 gasoline compounds decreased by 39% for pentane, 38% for MCP and 49% for benzene, The retardation factor （R） of E20 gasoline compounds decreased by 53% for pentane, 53% for MCP and 48% for benzene, while the R of B20 gasoline compounds decreased by 39% for pentane, 37% for MCP and 38% for benzene. For all SOM and water contents tested, the Kd and R of all gasoline compounds were in the order of unblended gasoline 〉 B20 〉 E20, indicating that the use of high ethanol volume in gasoline to combat climate change could put the groundwater at greater risk of contamination,展开更多
To explore the formation process and mechanism of organic matter and organic-mineral complex under humification and mineralization conditions, a series of samples including humic acid, kaolin, and humic acid-kaolin co...To explore the formation process and mechanism of organic matter and organic-mineral complex under humification and mineralization conditions, a series of samples including humic acid, kaolin, and humic acid-kaolin complex were prepared using a subcritical water treatment method（SWT） under specific temperature, pressure and reaction time conditions. HA was used as a surrogate for natural organic matter because it has a similar abundant pore structure,variety of carbon types, and chemical components. These samples were used in carbamazepine（CBZ） sorption experiments and characterized by a variety of techniques. The polymerization of humic acid under the conditions of increased temperature and pressure resulted in an increase in specific surface area and molecular quantity. In addition, the degree of aromaticity rose from59.52% to 70.90%. These changes were consistent with the transformation from ‘soft carbon＇ to‘hard carbon＇ that occurs in nature. The results of sorption experiments confirmed the interaction between humic acid and kaolin from the difference between the predicted and actual Qevalues. The conceptual model of humic acid-kaolin complex could be deduced and described as follows. Firstly, the aromatic components of humic acid preferentially combine with kaolin through the intercalation effect, which protects them from the treatment effects.Next, the free carboxyl groups and small aliphatic components of humic acid interact on the surface of kaolin, and these soft species transform into dense carbon through cyclization and polymerization. As a result, humic acid-kaolin complex with a mineral core and dense outer carbonaceous patches were formed.展开更多
Surface inlets are installed in subsurface drainage systems to reduce ponding duration and surface runoff, but can contribute to water quality concerns by allowing water to directly enter buried drains. Blind inlets c...Surface inlets are installed in subsurface drainage systems to reduce ponding duration and surface runoff, but can contribute to water quality concerns by allowing water to directly enter buried drains. Blind inlets consist of perforated pipes covered with gravel and are separated from an overlying sand layer by a geotextile membrane and have been shown to be more effective in reducing losses of sediment, nutrients, and pesticides than typical tile line risers. In this study, we investigated whether the effectiveness of blind inlets to sorb pollutants, with emphasis on the herbicide atrazine, could be further improved by amended them with materials other than limestone. The media, shredded tires (tire chips), electric arc steel furnace slag (steel slag), and oak-derived biochar were chosen because they are readily available, inexpensive, and do not present environmental concerns. Kinetic sorption and isotherms were determined to ascertain atrazine sorption by these materials, in addition to testing for potential metal leaching using the Synthetic Precipitation Leaching Procedure (SPLP) and the Toxicity Characteristic Leaching Procedure (TCLP). The kinetic data were fitted using pseudo first- and second-order reaction equations and indicated that atrazine sorption rate was 38 times faster and equilibrium was reached 5 times earlier for biochar than tire chips. The 24-h sorption isotherm data were fitted to the Freundlich sorption equation. The sorption coefficient for biochar was higher than for tire chips, steel slag, and limestone. Per the SPLC and TLCP tests, there was no leaching of heavy metals at levels of environmental concern. Our results suggested that the effectiveness of blind inlets as well as other conservation practices that include filter media such as rain gardens and filter socks could be improved by incorporating more reactive materials than sand and gravel with biochar being a particularly effective alternative.展开更多
Geosmin is one of the major causative compounds of earthy-musty odor and taste (off-flavor) in drinking water (lakes) and in farmed fish. In this study, the sorption of cyclodextrin polymers (CDPs) towards geosmin in ...Geosmin is one of the major causative compounds of earthy-musty odor and taste (off-flavor) in drinking water (lakes) and in farmed fish. In this study, the sorption of cyclodextrin polymers (CDPs) towards geosmin in aqueous solution was investigated. Sorption kinetics, the effect of solution pH and contact time on the sorption capability of α-, β- and γ-cyclodextrin polymers was discussed. Results disclosed that the sorption of geosmin by the CDPs followed the Ho and McKay kinetic mechanism with the liquid film diffusion as the rate-determining step. Both β-CDP and γ-CDP exhibit high removal efficiencies of 93.4% and 96%, respectively, within 240 minutes at 25°C and pH 7, whilst α-CDP was not effective, removing only 40% geosmin, at an initial concentration of 5 μg·L—1and 5 g·L—1of CDP dose. The cyclodextrin polymers can adapt to a wide range of pH from 3.0 to 11.0 for geosmin adsorption with pH 7.0 as optimum. Results indicate that these sorbents demonstrate significant potential in reducing the concentration of geosmin in water that presents taint problems in both drinking water and fish.展开更多
基金Project supported by the Research Committee of the Hong Kong Polytechnic University (No.G-U042).
文摘The damage effects of water sorption on the mechanical properties of the hydroxyapatite particle reinforced Bis-GMA/TEGDMA copolymer （HA/Bis-GMA/TEGDMA） h-ave been predicted using 3D finite cell models. The plasticizer effect on the polymer matrix was considered as a variation of its Young＇s modulus. Three different cell models were used to determine the influence of varying particle contents, interphase strength and moisture concentration on the debonding damage. The stress distribution pattern has been examined and the stress transfer mode clarified. The Young＇s modulus and fracture strength of the Bis-GMA/TEGDMA composite were also predicted using the model with and without consideration of the damage. ine Iormer results with consideration of the debonding damage are in good agreement with existing literature experimental data. The shielding effect of our proposed model and an alternative approach were discussed. The FCC cell model has also been extended to predict the critical load for the damaged and the undamaged composite subject to the 3-point flexural test.
文摘Electrochemical impedance spectra （EIS） technique was adopted to evaluate the water sorption behaviour of an epoxy freestanding film in a 0.5 mol/L sodium chloride solution at 20℃. The methods for obtaining the capacitance data from EIS data were compared. The Brasher-Kingsbury （BK） and corresponding modified version （Modi-BK） models were used to calculate the water uptake in film and the gravimetric results were presented for comparisons. According to the discussion of the discrepancy of water content in film obtained from two models, a new method was proposed to indicate the organic film structure.
基金financial support of The National Scholarship Foundation of China,China Scholarship Council([2018]3101)。
文摘Novel SiO_(2)-LiBr microcapsules for water-retaining pavement were prepared and firstly characterized by scanning electron microscope(SEM),particle size analysis,and Fourier transform infrared spectroscopy(FT-IR).The water vapor sorption and desorption of the formulated microcapsules was then experimentally studied using dynamic vapor sorption(DVS),with the results fitted to three kinds of adsorption kinetics models.In addition,the specific surface area(SSA)was also calculated based on BET theory;and the thermal performance was investigated by laser flash analysis(LFA).Experimental results show a change of 103%in mass of the microcapsule sample under 90%relative humidity(RH)at 30℃after water vapor sorption.The fitting of results indicates that the adsorption process is mainly governed by the intra-particle diffusion mechanism,followed by the pseudo-first-order adsorption process.In comparison with most conventional pavement materials,it is found that the SSA of the formulated microcapsules is much larger while the thermal conductivity is lower.The unique properties of the formulated SiO_(2)-LiBr microcapsules have significant potential to take the edge off the urban heat island effect and reduce rutting when applied to water-retaining pavement materials.
基金This study was financially supported by the National Natural Science Foundation of China(42302160)the PhD Scientific Research and Innovation Foundation of the Education Department of Hainan Province Joint Project of Sanya Yazhou Bay Science and Technology City(HSPHDSRF-2024-07-001)Educational Reform of Hainan Higher Education Institutions(Hnjg2024-276)。
文摘Connate water strongly restricts shale gas enrichment and production,and most artificially injected water is confined in shale pore networks owing to low water recovery during hydraulic fracturing,which leads to a more complex pore water distribution.However,previous studies have focused on the water vapor sorption of gas shales rather than liquid pore water.This study clarifies the occurrence and distribution of pore water and the controlling factors by conducting thermogravimetry(TGA)under liquid water saturation and water vapor sorption experiments on four gas shales from the Wufeng Formation in South China.Nuclear magnetic resonance(NMR)T_(2)and T_(1)-T_(2)technologies were used to monitor the dynamic changes and states of moisture,and the microscopic pore structures during water vapor sorption were detected using low-temperature nitrogen adsorption-desorption.The results indicate that TGA is adequate for determining the adsorbed,bound,and movable water contents.These four gas shales are characterized by high adsorbed and movable water contents,and some bound water.The adsorbed water primarily occurs in tiny pores(<100 nm),controlled by organic matter,followed by clay mine rals.The movable water,typically associated with quartz,primarily exists in pores of>100 nm,particularly macropores of>1000 nm.The bound water predominantly correlates with pores ranging from 10 to 2000 nm in clay minerals.The water vapor sorption process of the gas shale is well clarified.Water molecules primarily adsorb on the clay mineral's hydrophilic surface,followed by oxygen functional groups in the organic matter.Therefore,clay mine rals control water vapor sorption at low relative humidity(RH<0.75),whereas organic matter primarily affects vapor sorption at high RH.The TGA of liquid wate r-saturated gas shales can clarify the water distributions in full-scale pore networks,whereas the water vapor sorption method primarily discloses the moisture in small nanopores(<100 nm)but ignores most bound and movable water.This paper provides insight into liquid water distribution and occurre nce states within shale pore netwo rks,contributing to a better understanding of gas-wate r-rock interaction systems in-situ and hydraulic fracturing shale gas formations.
文摘Woods from Korean Larch, Chinese Fir, Aspens, Manchumian, and Fortunes Paulownia were chosen for investigation. Specimens cut from the air-dried woods had a cubic shape with nominal air-dried size of 17.0 mm and 8.5 mm. Oven-died specimens were put in containers filled with water and water sorption was implemented at atmospheric pressure and room temperature. Results from the experiment could not described exactly by the model of steady state flow from Darcy' law. An empirical equation is put forward fo...
基金funded by a NERC(Natural Environment Research Council, UK) Standard Research Grant(NE/J023833/1)to DAP, BEvD and C.J.Ballentine(now at University of Oxford)a NERC PhD studentship(NE/L501591/1) to DM+1 种基金receipt of a University of Cadiz(UCA) Postdoctoral Bridge Contract awardthe support of The Leverhulme Trust (UK)(ECF2015-657)
文摘Natural arsenic (As) contamination of groundwater which provides drinking water and/or irrigation supplies remains a major public health issue,particularly in South and Southeast Asia.A number of studies have evaluated various aspects of the biogeochemical controls on As mobilization in aquifers typical to this region,however many are predicated on the assumption that key biogeochemical processes may be deduced by sampled water chemistry.The validity of this assumption has not been clearly established even though the role of sorption/desorption of As and other heavy metals onto Fe/Mn (hydr) oxides is an important control in As mobilization.Here,selective chemical extractions of sand-rich and clay-rich sediments from an As-affected aquifer in Kandal Province,Cambodia,were undertaken to explore the potential role of partial re-equilibrium through sorption/desorption reactions of As and related solutes (Fe,Mn and P) between groundwater and the associated solid aquifer matrix.In general,groundwater As is strongly affected by both pH and Eh throughout the study area.However,contrasting sorption behaviour is observed in two distinct sand-dominated (T-Sand) and clay dominated (T-Clay) transects,and plausibly attributed to differing dominant lithologies,biogeochemical and/or hydrogeological conditions.Sorption/desorption processes appear to be re-setting groundwater As concentrations in both transects,but to varying extents and in different ways.In T-Sand,which is typically highly reducing,correlations suggest that dissolved As may be sequestered by sorption/re-adsorption to Fe-bearing mineral phases and/or sedimentary organic matter;in T-Clay Eh is a major control on As mobilization although binding/occlusion of Fe-bearing minerals to sedimentary organic matter may also occur.Multiple linear regression analysis was conducted with groups categorised by transect and by Eh,and the output correlations support the contrasting sorption behaviours encountered in this study area.Irrespective of transect,however,the key biogeochemical processes which initially control As mobilization in such aquifers,may be “masked” by the re-setting of As concentrations through in-aquifer sorption/desorption processes.
基金supported by the National Natural Science Foundation of China(No.21137003,20890111)the Natural Science Foundation of Zhejiang Province(No.Z5090031)the Key Innovation Team for Science and Technology of Zhejiang Province,China(No.2009R50047)
文摘An integrative technology including the surfactant enhanced sorption and subsequentdesorption and biodegradation of phenanthrene in the soil-water system was introduced and tested. For slightly contaminated agricultural soils, cationic-nonionic mixed surfactant- enhanced sorption of organic contaminants onto soils could reduce their transfer to plants, therefore safe-guarding agricultural production. After planting, residual surfactants combined with added nonionic surfactant could also promote thedesorption and biodegradation of residual phenanthrene, thus providing a cost-effective pollution remediation technology.0ur results showed that the cationic-nonionic mixed surfactantsdodecylpyridinium bromide （DDPB） and Triton X-100 （TX100） significantly enhanced soil retention of phenanthrene. The maximum sorption coefficient Kd＊ of phenanthrene for contaminated soils treated by mixed surfactants was about24.5 times that of soils without surfactant （Kd ） and higher than the combined effects of DDPB and TX100 individually, which was about 16.7 and 1.5 times Kd , respectively.0n the other hand, TX100 could effectively remove phenanthrene from contaminated soils treated by mixed surfactants, improving the bioavailability of organic pollutants. Thedesorption rates of phenanthrene from these treated soils were greater than 85% with TX100 concentration above2000 mg/L and approached 100% with increasing TX100 concentration. The biodegradation rates of phenanthrene in the presence of surfactants reached over 95% in30days. The mixed surfactants promoted the biodegradation of phenanthrene to some extent in 10-22days, and had no obvious impact on phenanthrene biodegradation at the end of the experiment. Results obtained from this study provide some insight for the production of safe agricultural products and a remediation scheme for soils slightly contaminated with organic pollutants.
文摘In this contribution, we review and critically compare the results of the analyses we have previously performed on water sorption thermodynamics in a series of polyimides. The experimental investigation was performed by combining gravimetric tests and in situ vibrational spectroscopy. A non-equilibrium theory, based on a compressible lattice framework accounting for the glassy state of the polymer and for the occurrence of hydrogen bonding interactions, has been used to interpret data. Information at a molecular level gained by vibrational spectroscopy has been used to tailor the model equations. The main features of water sorption thermodynamics are well captured, qualitatively and quantitatively, by the adopted model which displays a remarkable agreement with experimental results.
文摘Preliminary research was conducted about how to incorporate sorption/desorption of organic pollutants with suspended solids and sediments into single-chemical and one-dimensional water quality model of Jinghang Canal. Sedimentation-resuspension coefficient k 3 was deduced; characteristics of organic pollutants, concentrations and components of suspended solids/sediments and hydrological and hydraulic conditions were integrated into k 3 and further into river water quality model; impact of sorption/desorption of organic pollutants with suspended solids and sediments on prediction function of the model was discussed. Results demonstrated that this impact is pronounced for organic pollutants with relatively large K oc and K ow, especially when they are also conservative and f oc of river suspended solids/sediments is high, and that incorporation of sorption/ desorption of organic pollutants into river water quality model can improve its prediction accuracy.
文摘In this paper we are describing a green cycle process. The first step was a novel hydrotalcite-like compound (HTLC) synthesized by a co-precipitating method, under standard ambient temperature and pressure, using chemical industry wastewater rich in divalent and trivalent cations, activated by a thermal treatment and finally characterized by scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDS) and thermogravimetric analysis (TGA). The second step was a series of batch sorption tests performed with this activated HTLC and untreated underground sulfurous water from the state of Puebla, México. The HTLC calcined at 500°C/3 h exhibited the best sorption ability for ions, demonstrated a decrease of the hardness and sulfate ions to below the regional legal standards for drinking water. Once inactive after being used in water treatment, the sorbed ions were removed by ion exchange in a carbonate-containing solution, resulting in an 80% recycling of the material which upon activation demonstrated a retained capacity for water treatment. This recyclability suggests the exciting possibility of this novel compound as an efficient “green” technology in water treatment processes.
文摘For the assessment of the carbon dioxide (CO2) storage potential of water-filled reservoir rocks (i.e., saline aquifers), it should be first important step for a thorough understanding of the effect of water content on CO2/water/rock interactions during CO2 injection. The purpose of this study is to examine the CO2 sorption amount for Kimachi sandstone and Berea sandstone at different water content using the manometric method at temperature of 50?C and pressures of up to 20 MPa. Our results document that a significant quantity of CO2 was sorbed on the two types of sandstone on all water-saturated bases, which corresponded to the amount adsorbed on the air-dry basis. Also, all the wet samples had significantly higher sorption capacity than the theoretical values calculated from the solubility model based on dissolution of CO2 in pore water and the pore-filling model, which assumes that the pore volume unoccupied by water is filled with CO2. Furthermore, the observations indicated a certain degree of correlation between the sorbed amount and the water content, except at pressures below the critical point for Berea sandstone. This investigation points out that CO2 sorption is a possible mechanism in CO2 geological storage even under water-saturated conditions and that the mechanism of sorption on silica and silicate minerals plays an essential role in the reliable and accurate estimation of the CO2 storage capacity of water-saturated reservoirs.
文摘Denatonium benzoate is an aversive agent proposed for use in certain anti-freeze formulations to reduce poisoning events of pets and humans. Unfortunately, the sorption properties of denatonium cations to soil and/or soil components have not been investigated. In this paper, denatonium sorption to reference kaolinite clay under varied pH, ionic strength, and cation identity is described. The data clearly indicate that the nature of the background electrolyte cation modulates denatonium sorption with enhanced sorption occurring the presence of potassium ions versus minimal sorption occurring in a calcium chloride electrolyte at each pH studied as estimated using Dubinin-Raduskevich (D-R) isotherms. The effect of background electrolyte concentration on sorption was consistent with an ion-exchange process wherein the sorption capacity increased with decreased background electrolyte concentration. An interesting and unexpected observation of increased sorption capacity (estimated using the D-R model) with decreasing pH was observed in 10 mM CaCl2 in contrast to an observed and expected increase in denatonium sorption to kaolinite in the presence of either of 10 mM NaCl or 10 mM KCl. Estimates of the mean sorption energy using D-R isotherms ranging from 2.65 kJ/mol in 10 mM CaCl2 at pH 4 to 4.68 kJ/mol at pH 10 suggesting that the sorption process is not exclusively ion-exchange.
基金supported by the National Natural Science Foundation of China (Nos.51278055, 51179008)the National Key Technology R&D Program (No.2012BAJ21B08)the National Public Benefit (Environmental) Research Foundation of China (No.201109009)
文摘Fe/Al drinking water treatment residuals（WTRs）, ubiquitous and non-hazardous by-products of drinking water purification, are cost-effective adsorbents for glyphosate. Given that repeated glyphosate applications could significantly decrease glyphosate retention by soils and that the adsorbed glyphosate is potentially mobile, high sorption capacity and stability of glyphosate in agricultural soils are needed to prevent pollution of water by glyphosate.Therefore, we investigated the feasibility of reusing Fe/Al WTR as a soil amendment to enhance the retention capacity of glyphosate in two agricultural soils. The results of batch experiments showed that the Fe/Al WTR amendment significantly enhanced the glyphosate sorption capacity of both soils（p 〈 0.001）. Up to 30% of the previously adsorbed glyphosate desorbed from the non-amended soils, and the Fe/Al WTR amendment effectively decreased the proportion of glyphosate desorbed. Fractionation analyses further demonstrated that glyphosate adsorbed to non-amended soils was primarily retained in the readily labile fraction（Na HCO3-glyphosate）. The WTR amendment significantly increased the relative proportion of the moderately labile fraction（HCl-glyphosate） and concomitantly reduced that of the Na HCO3-glyphosate, hence reducing the potential for the release of soil-adsorbed glyphosate into the aqueous phase. Furthermore, Fe/Al WTR amendment minimized the inhibitory effect of increasing solution p H on glyphosate sorption by soils and mitigated the effects of increasing solution ionic strength. The present results indicate that Fe/Al WTR is suitable for use as a soil amendment to prevent glyphosate pollution of aquatic ecosystems by enhancing the glyphosate retention capacity in soils.
文摘The sorption and phase distribution of 20% ethanol and butanol blended gasoline （E20 and B20） vapours have been examined in soils with varying soil organic matter （SOM） and water contents via laboratory microcosm experiments. The presence of 20% alcohol reduced the sorption of gasoline compounds by soil as well as the mass distribution of the compounds to soil solids. This effect was greater for ethanol than butanol. Compared with the sorption coefficient （Kd） of unblended gasoline compounds, the Kd of E20 gasoline compounds decreased by 54% for pentane, 54% for methylcyclopentane （MCP） and 63% for benzene, while the Kd of B20 gasoline compounds decreased by 39% for pentane, 38% for MCP and 49% for benzene, The retardation factor （R） of E20 gasoline compounds decreased by 53% for pentane, 53% for MCP and 48% for benzene, while the R of B20 gasoline compounds decreased by 39% for pentane, 37% for MCP and 38% for benzene. For all SOM and water contents tested, the Kd and R of all gasoline compounds were in the order of unblended gasoline 〉 B20 〉 E20, indicating that the use of high ethanol volume in gasoline to combat climate change could put the groundwater at greater risk of contamination,
基金supported by the Fundamental Research Funds for the Outstanding Teachers in the Central Universities(No.35832015023)
文摘To explore the formation process and mechanism of organic matter and organic-mineral complex under humification and mineralization conditions, a series of samples including humic acid, kaolin, and humic acid-kaolin complex were prepared using a subcritical water treatment method（SWT） under specific temperature, pressure and reaction time conditions. HA was used as a surrogate for natural organic matter because it has a similar abundant pore structure,variety of carbon types, and chemical components. These samples were used in carbamazepine（CBZ） sorption experiments and characterized by a variety of techniques. The polymerization of humic acid under the conditions of increased temperature and pressure resulted in an increase in specific surface area and molecular quantity. In addition, the degree of aromaticity rose from59.52% to 70.90%. These changes were consistent with the transformation from ‘soft carbon＇ to‘hard carbon＇ that occurs in nature. The results of sorption experiments confirmed the interaction between humic acid and kaolin from the difference between the predicted and actual Qevalues. The conceptual model of humic acid-kaolin complex could be deduced and described as follows. Firstly, the aromatic components of humic acid preferentially combine with kaolin through the intercalation effect, which protects them from the treatment effects.Next, the free carboxyl groups and small aliphatic components of humic acid interact on the surface of kaolin, and these soft species transform into dense carbon through cyclization and polymerization. As a result, humic acid-kaolin complex with a mineral core and dense outer carbonaceous patches were formed.
文摘Surface inlets are installed in subsurface drainage systems to reduce ponding duration and surface runoff, but can contribute to water quality concerns by allowing water to directly enter buried drains. Blind inlets consist of perforated pipes covered with gravel and are separated from an overlying sand layer by a geotextile membrane and have been shown to be more effective in reducing losses of sediment, nutrients, and pesticides than typical tile line risers. In this study, we investigated whether the effectiveness of blind inlets to sorb pollutants, with emphasis on the herbicide atrazine, could be further improved by amended them with materials other than limestone. The media, shredded tires (tire chips), electric arc steel furnace slag (steel slag), and oak-derived biochar were chosen because they are readily available, inexpensive, and do not present environmental concerns. Kinetic sorption and isotherms were determined to ascertain atrazine sorption by these materials, in addition to testing for potential metal leaching using the Synthetic Precipitation Leaching Procedure (SPLP) and the Toxicity Characteristic Leaching Procedure (TCLP). The kinetic data were fitted using pseudo first- and second-order reaction equations and indicated that atrazine sorption rate was 38 times faster and equilibrium was reached 5 times earlier for biochar than tire chips. The 24-h sorption isotherm data were fitted to the Freundlich sorption equation. The sorption coefficient for biochar was higher than for tire chips, steel slag, and limestone. Per the SPLC and TLCP tests, there was no leaching of heavy metals at levels of environmental concern. Our results suggested that the effectiveness of blind inlets as well as other conservation practices that include filter media such as rain gardens and filter socks could be improved by incorporating more reactive materials than sand and gravel with biochar being a particularly effective alternative.
文摘Geosmin is one of the major causative compounds of earthy-musty odor and taste (off-flavor) in drinking water (lakes) and in farmed fish. In this study, the sorption of cyclodextrin polymers (CDPs) towards geosmin in aqueous solution was investigated. Sorption kinetics, the effect of solution pH and contact time on the sorption capability of α-, β- and γ-cyclodextrin polymers was discussed. Results disclosed that the sorption of geosmin by the CDPs followed the Ho and McKay kinetic mechanism with the liquid film diffusion as the rate-determining step. Both β-CDP and γ-CDP exhibit high removal efficiencies of 93.4% and 96%, respectively, within 240 minutes at 25°C and pH 7, whilst α-CDP was not effective, removing only 40% geosmin, at an initial concentration of 5 μg·L—1and 5 g·L—1of CDP dose. The cyclodextrin polymers can adapt to a wide range of pH from 3.0 to 11.0 for geosmin adsorption with pH 7.0 as optimum. Results indicate that these sorbents demonstrate significant potential in reducing the concentration of geosmin in water that presents taint problems in both drinking water and fish.
