This work mainly studies the effect of fluid phase momentum transfer mechanisms on the acidizing results,including the retardation effect of the porous structure and the interaction between the fluid phase,such as vis...This work mainly studies the effect of fluid phase momentum transfer mechanisms on the acidizing results,including the retardation effect of the porous structure and the interaction between the fluid phase,such as viscous dissipation and inertial effect.The results show that the acid fluid momentum transfer is influenced by the complex porous structure and fluid viscous dissipation.Eventually,the Stokes-Darcy equation is recommended to be adopted to describe the fluid phase momentum transfer in the following numerical simulation studies of the carbonate acidizing process.Based on this model,a parametric research is carried out to investigate the impact of acid on rock physical characteristics in the stimulation process.Increasing the acid concentration appears to minimize the quantity of acid consumed for the breakthrough.The acid surface reaction rate has a considerable impact on the pore volume to breakthrough and the optimum acid injection rate.The influence of permeability on the acidizing results basically shows a negative correlation with the injection rate.The difference between the acidizing curves of different permeability gradually becomes insignificant with the decrease in injection rate.The existence of isolated fracture and vug significantly reduces acid consumption for the breakthrough.展开更多
Acidizing treatment is considered as a significant process in the oil well stimulations to form wormholes in carbonate formation in order to enhance the reservoir fluid production.Obtaining the number of pore volumes ...Acidizing treatment is considered as a significant process in the oil well stimulations to form wormholes in carbonate formation in order to enhance the reservoir fluid production.Obtaining the number of pore volumes to breakthrough is an important objective in matrix acidizing,for it contributes to determining the wormhole characteristics such as type,shape,and size.Finding this number in experimental works requires a considerable amount of time,energy and cost.Therefore,this study aimed to establish an analytical method in which a reasonable result is achieved for the number of pore volumes to breakthrough.This purpose is accomplished by solely implementing acid and formation properties without performing any experimental works.The process of wormhole creation is done through developing a numerical model by utilizing the conservation of mass law method in which the carbonate core is considered as a closed system and the overall mass in the system as constant during the acid injection process.Furthermore,a constant number is added to the mathematical part of the model in order to eliminate the dimensionless Damk鰄ler number which is supposed to be calculated experimentally.The results of the numerical procedure of the model are further compared to four other experimental works,which led to calculating the average accuracy of this model that is shown to be 95.98%.This study puts forward a comprehensive numerical model to estimate the number of pore volumes to breakthrough with an acceptable accuracy rate merely through implementing known acid and core properties.展开更多
Polymers play an important role in hybrid enhanced oil recovery (EOR), which involves both a polymer and low-salinity water. Because the polymer commonly used for low-salinity polymer flooding (LSPF) is strongly sensi...Polymers play an important role in hybrid enhanced oil recovery (EOR), which involves both a polymer and low-salinity water. Because the polymer commonly used for low-salinity polymer flooding (LSPF) is strongly sensitive to brine pH, its efficiency can deteriorate in carbonate reservoirs containing highly acidic formation water. In this study, polymer efficiency in an acidic carbonate reservoir was investigated experimentally for different salinity levels and SO42− concentrations. Results indicated that lowering salinity improved polymer stability, resulting in less polymer adsorption, greater wettability alteration, and ultimately, higher oil recovery. However, low salinity may not be desirable for LSPF if the injected fluid does not contain a sufficient number of sulfate (SO42−) ions. Analysis of polymer efficiency showed that more oil can be produced with the same polymer concentration by adjusting the SO42− content. Therefore, when river water, which is relatively easily available in onshore fields, is designed to be injected into an acidic carbonate reservoir, the LSPF method proposed in this study can be a reliable and environmentally friendly method with addition of a sufficient number of SO42− ions to river water.展开更多
Aqueous zinc-ion hybrid capacitors(ZIHCs)are promising electrochemical energy storage systems with advantages of high-energy density,low cost,safety and environmental friendliness.However,application of carbon-based c...Aqueous zinc-ion hybrid capacitors(ZIHCs)are promising electrochemical energy storage systems with advantages of high-energy density,low cost,safety and environmental friendliness.However,application of carbon-based cathodes is limited by their low-energy density due to the lack of active sites.Herein,a chemisorption sites modulating strategy is proposed to construct nitrogen-doped polyimide carbon nanoflowers with abundant oxygen vacancies and carbonyl functionalization via high-temperature calcination and subsequent acid processing.The synergistic effect of oxygen vacancies,carbonyl groups,enhanced surface area and porous structure enables stable zinc-ion storage with high capacity.Remarkably,the carbon materials can circulate 20,000 cycles stably at a current density of 2 A·g^(-1).After 10,000 cycles at a high rate of 3 A·g^(-1),a capacity retention rate of 64%can still be achieved.The as-prepared ZIHCs provide an energy density of 65.61 Wh·kg^(-1)at the power density of 197.82 W·kg^(-1).Current research shows that polyimide-derived carbon material synthesized by acid activation provides a new idea for developing cathodes in aqueous ZIHCs.展开更多
A carbon solid acid catalyst was prepared by the sulfonation of partially carbonized peanut shell with concentrated H2SO4. The structure and acidity of the catalyst were characterized by Fourier transform infrared spe...A carbon solid acid catalyst was prepared by the sulfonation of partially carbonized peanut shell with concentrated H2SO4. The structure and acidity of the catalyst were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, X‐ray diffraction, thermogravimetric analysis, X‐ray photoelectron spectroscopy, and elemental analysis, which showed that it was an amorphous carbon material composed of aromatic carbon sheets in random orientations. Sulfonic acid groups were present on the surface at a density of 0.81 mmol/g. The carbon solid acid catalyst showed better performance than HZSM‐5 for the esterification of cyclohexene with formic acid. At a3：1 molar ratio of formic acid to cyclohexene, catalyst loading of 0.07 g/mL of cyclohexene, and reaction time of 1 h at 413 K, the cyclohexene conversion was 88.4% with 97.3% selectivity to cyclohexyl formate. The carbon solid acid catalyst showed better reusability than HZSM‐5 because its large pores were minimally affected by the accumulation of oligomerized cyclohexene, which deactivated HZSM‐5. The activity of the carbon solid acid catalyst decreased somewhat in the first two recycles due to the leaching of polycyclic aromatic hydrocarbon containing –SO3H groups and then it remained constant in the following reuse.展开更多
Study of the thermodynamic behaviour of CaCl2-H2O-CO2 systems is important in different scientific areas in the chemical and petroleum engineering fields. For example, a system including salt- H20-CO2 is a common syst...Study of the thermodynamic behaviour of CaCl2-H2O-CO2 systems is important in different scientific areas in the chemical and petroleum engineering fields. For example, a system including salt- H20-CO2 is a common system in CO2 geological storage. During carbonate matrix acidizing, this mixture also appears as the spent acid. Hence, study of the behaviour of this system and the solubility of CO2 in CaCl2 brine in different thermodynamic conditions is critical. In this study, CO2 solubility in 0, 1.90 and 4.80 mol/L CaCl2 solutions at 328.15 to 375.15 K and 68.9 to 206.8 bar were measured. These values are normal for oil reservoirs. A popular thermodynamic model is available in the literature for estimating the CO2 solubility in pure water and NaC1 solutions. In this paper, the available model was modified by experimental work to be applicable for CaCl2 as well. Based on the measured data, the component interaction parameters in the base model were adjusted for a CaCl2-H2O-CO2 system. The developed model could predict CO2 solubility in different conditions with remarkable accuracy, particularly for high concentration solutions and at high pressures. This improvement is up to 65% better than in the base model. This model can be used in Darcy scale models for predicting wormhole propagation during carbonate matrix acidizing.展开更多
Revegetation is a traditional practice widely used for soil protection. We evaluated the effect of natural revegetation succession on soil chemical properties and carbon fractions （particulate organic carbon （POC）,...Revegetation is a traditional practice widely used for soil protection. We evaluated the effect of natural revegetation succession on soil chemical properties and carbon fractions （particulate organic carbon （POC）, humus carbon （HS-C）, humic acid carbon （HA-C） and fulvic acid carbon （FA-C）） on the Loess Plateau of China. The vegetation types, in order from the shortest to the longest enclosure duration, were： （a） abandoned overgrazed grassland （AbG3; 3 years）; （b） Hierochloe odorata Beauv. （HiO7; 7 years）; （c） Thymus mongoficus Ronnm （ThM15; 15 years）; （d） Artemisia sacrorum Ledeb （AtS25; 25 years）; （e） Stipa bungeana Trin Ledeb （StB36; 36 years） and （f） Stipa grandis P. Smirn （StG56; 56 years）. The results showed that the concentrations of soil organic carbon, total nitrogen and available phosphorus increased with the increase of restoration time except for ThM15. The concen- tration of NH4-N increased in the medium stage （for ThM15 and AtS25） and decreased in the later stage （for StB36 and StG56） of vegetation restoration. However, NO3-N concentration significantly increased in the later stage （for StB36 and StG56）. Carbon fractions had a similar increasing trend during natural vegetation restoration. The con- centrations of POC, HS-C, FA-C and HA-C accounted for 24.5%-49.1%, 10.6%-15.2%, 5.8%-9.1% and 4.6%-6.1% of total carbon, respectively. For AbG3, the relative changes of POC, HS-C and FA-C were significantly higher than that of total carbon during the process of revegetation restoration. The higher relative increases in POC, HS-C and FA-C confirmed that soil carbon induced by vegetation restoration was sequestrated by higher physical and chemical protection. The increases of soil C fractions could also result in higher ecological function in semiarid grassland ecosystems.展开更多
Works on exploring an environmentally clean method for producing an Mg,Al-hydrotalcite(Mg6Al2(OH) 16CO3·4H2O) layer and/or calcium carbonate(CaCO3) layer on Mg alloy in a carbonic acid solution system(aqueous HCO...Works on exploring an environmentally clean method for producing an Mg,Al-hydrotalcite(Mg6Al2(OH) 16CO3·4H2O) layer and/or calcium carbonate(CaCO3) layer on Mg alloy in a carbonic acid solution system(aqueous HCO3-/CO3 2-or Ca 2+ /HCO3-) at 50℃ were reviewed.Conversion treatment for the Mg,Al-hydrotalcite conversion coating was as follows.Mg alloy was treated first in acidic HCO3-/CO3 2-aqueous for precursor layer formation on Mg alloy surface and then in alkaline HCO3-/CO3 2-aqueous to form a crystallized Mg,Al-hydrotalcite coating.Duration of an Mg,Al-hydrotalcite coating on Mg alloy surface was reduced from 12 h to 4 h by the conversion treatment.On the other hand,for reducing the formation time of CaCO3 coating on Mg alloy,the aqueous Ca 2+ /HCO3-with a saturated Ca 2+ content was employed for developing a CaCO3 coating on Mg alloy.A dense CaCO3 coating could yield on Mg alloy surface in 2 h.Corrosion rate(corrosion current density,Jcorr) of the Mg,Al-hydrotalcite-coated sample and CaCO3-coated AZ91D sample was 7-10μA/cm 2,roughly two orders less than the Jcorr of the as-diecast sample(about 200μA/cm 2) . No corrosion spot on the Mg,Al-hydrotalcite-coated sample and CaCO3-coated sample was observed after 72 h and 192 h salt spray test,respectively.展开更多
Soil humic carbon is an important component of soil organic carbon （SOC） in ter- restrial ecosystems. However, no study to date has investigated its geographical patterns and the main factors that influence it at a ...Soil humic carbon is an important component of soil organic carbon （SOC） in ter- restrial ecosystems. However, no study to date has investigated its geographical patterns and the main factors that influence it at a large scale, despite the fact that it is critical for exploring the influence of climate change on soil C storage and turnover. We measured levels of SOC, humic acid carbon （HAC）, fulvic acid carbon （FAC）, humin carbon （HUC）, and extractable humus carbon （HEC） in the 0-10 cm soil layer in nine typical forests along the 3800-km North-South Transect of Eastern China （NSTEC） to elucidate the latitudinal patterns of soil humic carbon fractions and their main influencing factors. SOC, HAC, FAC, HUC, and HEC increased with increasing latitude （all P〈0.001）, and exhibited a general trend of tropical 〈 subtropical 〈 temperate. The ratios of humic C fractions to SOC were 9.48%-12.27% （HAC）, 20.68%-29.31% （FAC）, and 59.37%-61.38% （HUC）. Climate, soil texture, and soil microbes jointly explained more than 90% of the latitudinal variation in SOC, HAC, FAC, HEC, and HUC and interactive effects were important. These findings elucidate latitudinal patterns of soil humic C fractions in forests at a large scale, and may improve models of soil C turnover and storage.展开更多
Two kinds of mesoporous carbon solid acids(LDMCE-SO3H and LDMCS-SO3H)were successfully prepared using masson pine alkali lignin as carbon source by evaporation-induced self-assembly(EISA)and salt-induced selfassembly(...Two kinds of mesoporous carbon solid acids(LDMCE-SO3H and LDMCS-SO3H)were successfully prepared using masson pine alkali lignin as carbon source by evaporation-induced self-assembly(EISA)and salt-induced selfassembly(SISA)followed by sulfonation,respectively.In terms of preparation process,SISA(self-assembly in water and preparation time of 2 days)is greener and simpler than EISA(self-assembly in ethanol and preparation time of 7 days).The prepared LDMCE-SO3H and LDMCS-SO3H exhibit obvious differences in structural characteristics such as pore channel structure,specific surface area,mesopore volume and the density of-SO3H groups.Furthermore,the catalytic performances of LDMCE-SO3H and LDMCS-SO3H were investigated in the hydrolysis of microcrystalline cellulose in water,and the glucose yields of 48.99%and 54.42%were obtained under the corresponding optimal reaction conditions.More importantly,the glucose yields still reached 28.85%and 30.35%after five runs,and restored to 39.02%and 45.98%through catalysts regeneration,respectively,demonstrating that LDMCE-SO3H and LDMCS-SO3H have excellent recyclability and regenerability.展开更多
The synthesis of 2, 4-diisopropyl-5,5-dimethy1- 1.3-dioxane through the acetalization of isobutyraldehyde with 2, 2, 4-trimethy1-1,3-pentanediol （TMPD） catalyzed by the novel carbon based acid was first carried out....The synthesis of 2, 4-diisopropyl-5,5-dimethy1- 1.3-dioxane through the acetalization of isobutyraldehyde with 2, 2, 4-trimethy1-1,3-pentanediol （TMPD） catalyzed by the novel carbon based acid was first carried out. High conversion （≥98%） and specific selectivity were obtained using the novel carbon based acid, which kept high activity after it was reused 5 times. Moreover. the catalyst could be used to catalyze the acetalization and ketalization of different aldehydes and ketones with superior yield. The yield of several products was over 90%. The novel heterogeneous catalyst has the distinct advantages of high activity, strikingly simple workup procedure, non-pollution, and reusability, which will contribute to the success of the green process greatly.展开更多
The dissolution of carbon steel in 5% HCl in the temperature range of 30~90℃ was inhibited by two organic compounds having the general formula: ClR NH2(CH2)n NH2 RCl where R is a benzyl group. The behaviour of these ...The dissolution of carbon steel in 5% HCl in the temperature range of 30~90℃ was inhibited by two organic compounds having the general formula: ClR NH2(CH2)n NH2 RCl where R is a benzyl group. The behaviour of these inhibitors in acidic medium were investigated using weight loss method, open circuit potential and linear polarization technique. These inhibitors provided satisfactory corrosion inhibition for carbon steel in hydrochloric acid solutions even at higher temperature and acid concentration (10%). The electrochemical results showed that the polarization resistance (Rp) values increased with increasing inhibitor concentration, also the corrosion current decreased and a higher inhibition efficiency was obtained. The protective properties of these two organic inhibitors were attributed to the chemisorption mechanism展开更多
One driver for steel development over recent decades has been the engineering requirements of improved strength and toughness,combined with weldability,for the safe and cost effective recovery and transmission of oil ...One driver for steel development over recent decades has been the engineering requirements of improved strength and toughness,combined with weldability,for the safe and cost effective recovery and transmission of oil and gas.This has been achieved through refinement of grain size by microalloy precipitation and thermomechanical processing.However,little attention has been paid to these significant changes in steel chemistry and processing on corrosion resistance,despite the dominance of economic carbon steel for construction in the oil and gas industries.The more common forms of corrosion are associated with the presence of H 2 S or CO 2.CO 2 in aqueous solution forms a weak acid sufficient to promote significant localized corrosion in transmission gas/oil pipelines and in well-head applications (’down-hole’).Systematic study has identified the influence of a wide range of alloying elements and different processing conditions on the resistance of low-carbon steels to CO 2 corrosion;strong carbide-forming microalloying elements such as Ti,Nb and V,along with Cr additions,and different levels of Mn,Si,Cu,Mo and Ni,have been explored,along with treatments simulating different processing conditions.The present study also emphasizes the role of V and Ti microalloying in improving the resistance of Cr-containing carbon steel to corrosion in carbonic acid and how this is influenced by microstructure and the metallurgical condition of the microalloying addition,in particular,the extent of precipitation.It is noted that some commercially available corrosion inhibitors contain V as a vanadate compound to interfere with the corrosion process and so it is suggested that V microalloying may also be beneficial if present in an appropriate form in the steel.That Ti also seems to play a role in corrosion in the steels studied is judged to be compatible with the thermodynamics of transition metal anions in the Ti-V-Cr group.展开更多
The reaction between carbonic acid and montmorillonite minerals was studied in order to provide a theoretical basis for analyzing changes in the physical properties of coal seams after CO_(2)injection and for optimizi...The reaction between carbonic acid and montmorillonite minerals was studied in order to provide a theoretical basis for analyzing changes in the physical properties of coal seams after CO_(2)injection and for optimizing CO_(2) pumping parameters.A single montmorillonite mineral of purity[90%was selected and subjected to reactions at 25,35,and 45℃in carbonic acid solutions of varying acidity.The Si and Al concentrations in the solutions and the structure and elemental compositions of the montmorillonite before and after the reactions were analyzed using a spectrophotometer,an X-ray diffractometer,and an energy-dispersive X-ray spectrometer;kinetic reaction models were established for the dissolution of Si and Al in carbonic acid solutions in order to estimate the apparent activation energy of Si dissolution under different acidity conditions.The results indicate that Al dissolved rapidly and soon reached solubility equilibrium.On the other hand,Si concentration in the solutions increased rapidly and then gradually declined with vibrations,with maximum values at 25,35,and 45℃,which were observed at approximately 96,72,and 48 h,respectively.In addition,Si dissolution fitted the diffusion-controlled reaction model well;as the pH value decreased,the apparent activation energy of Si dissolution decreased,and Si became easier to dissolve.Furthermore,it was concluded that as a weak acid,carbonic acid causes little damage to the mineral structure of montmorillonite.展开更多
A batch experiment was conducted to investigate the adsorption of an acid dye(Acid Orange 51) and a basic dye(Safranine) from aqueous solutions by the sludge-based activated carbon(SBAC). The results show that the ads...A batch experiment was conducted to investigate the adsorption of an acid dye(Acid Orange 51) and a basic dye(Safranine) from aqueous solutions by the sludge-based activated carbon(SBAC). The results show that the adsorption of Acid Orange 51 decreases at high p H values, whereas the uptake of Safranine is higher in neutral and alkaline solutions than that in acidic conditions. The adsorption time needed for Safranine to reach equilibrium is shorter than that for Acid Orange 51. The uptakes of the dyes both increase with temperature increasing, indicating that the adsorption process of the dyes onto SBAC is endothermic. The equilibrium data of the dyes are both best represented by the Redlich-Peterson model. At 25 °C, the maximum adsorption capacities of SBAC for Acid Orange 51 and Safranine are 248.70 mg/g and 525.84 mg/g, respectively. The Elovich model is found to best describe the adsorption process of both dyes, indicating that the rate-limiting step involves the chemisorption. It can be concluded that SBAC is a promising material for the removal of Acid Orange 51 and Safranine from aqueous solutions.展开更多
Li_(4)Ti_(5)O_(12)(LTO) anode material demonstrates superior cycling performance due to its stable spinel structure and high lithiation/de-lithiation potential.Herein,a novel energy-saving solid-phase synthesis route ...Li_(4)Ti_(5)O_(12)(LTO) anode material demonstrates superior cycling performance due to its stable spinel structure and high lithiation/de-lithiation potential.Herein,a novel energy-saving solid-phase synthesis route for LTO has been successfully designed,employing the cheap industrial intermediate product of metatitanic acid (HTO) as titanium source.Through the in-situ Fourier transform infrared spectroscopy (FTIR)and ex-situ X-ray diffraction (XRD),it is revealed for the first time that the amorphous crystal structure of HTO is more conducive for the Li+insertion,making it possible to prepare LTO at a relatively lower sintering temperature.Utilizing the dehydration carbonization reaction between glucose and sulfuric acid,an ingenious strategy of glucose pre-coating is adopted to avoid the generation of Li_(2)SO_(4) impurity caused by the residual sulfuric acid on the surface of HTO,which meanwhile enhances the conductivity and inhibits the particle growth of LTO.The obtained ALTO@C anode material consequently exhibits excellent electrochemical performance that 132.0 m Ah g^(-1)is remained even at 20 C,and ultra low decay rate of 0.015% per cycle is achieved during 1000 cycles at 2 C.Remarkably,LiCoO_(2)//ALTO@C full cell delivers conspicuous low-temperature property (130.7 m Ah g^(-1)at 0.5 C and almost no attenuation after 300 cycles under-20℃).展开更多
A carbon paste electrode（CPE） chemically modified with multiwall carbon nanotubes and ferrocene（FC） was used as a selective electrochemical sensor for the simultaneous determination of trace amounts of cysteamine...A carbon paste electrode（CPE） chemically modified with multiwall carbon nanotubes and ferrocene（FC） was used as a selective electrochemical sensor for the simultaneous determination of trace amounts of cysteamine（CA） and folic acid（FA）.This modified electrode showed very efficient electrocatalytic activity for the anodic oxidation of CA.The peak current of differential pulse voltammograms of CA and FA increased linearly with their concentration in the ranges of 0.7-200μmol/L CA and 5.0- 700μmol/L FA.The detection limits for CA and FA were 0.3μmol/L and 2.0μmoI/L,respectively.The diffusion coefficient（D） and transfer coefficient（α） of CA were also determined.These conditions are sufficient to allow determination of CA and FA both individually and simultaneously.展开更多
Humic acid(HA)was carbonized at 300,400 and 500℃ and then functionalized with 1 wt%–12 wt%Fe(Ⅲ)respectively[CHA300/400/500-Fe(Ⅲ)].Adsorption of such Fe(III)-functionalized carbonized HA as adsorbents to aqueous te...Humic acid(HA)was carbonized at 300,400 and 500℃ and then functionalized with 1 wt%–12 wt%Fe(Ⅲ)respectively[CHA300/400/500-Fe(Ⅲ)].Adsorption of such Fe(III)-functionalized carbonized HA as adsorbents to aqueous tetracycline(TC:25 mg·L^-1)was studied.The adsorption equilibrium time for CHA400-Fe(Ⅲ)to TC was 6 h faster and the adsorption removal efficiency(Re)was two times higher than that of HA/CHA.The adsorption Reof CHA400-Fe(Ⅲ)loaded 10%iron[CHA400-(10%)Fe(Ⅲ)]to TC could reach 99.8%at 8 h and still kept80.6%after 8 cycles.The adsorption kinetics were well fitted to the pseudo-second-order equation and the adsorption isotherms could be well delineated via Langmuir equations(R^2N 0.99),indicating that the homogeneous chemical adsorption of TC occurred on the adsorbents.The main adsorption mechanisms of TC were complexation Fe(III)and hydrophobic distribution.Electropositive and electronegative repulsion between TC and CHA400-(10%)Fe(Ⅲ)at lowly p H(2)and highly p H(8–10)respectively,leaded to the relatively low adsorption capacity and more notable influence of ion concentration.When the p H was between 4 and 8,TC mainly existed in neutral molecules(TCH2),so the influence of ion concentration was not obvious.The dynamic adsorption results showed that the CHA400-(10%)Fe(Ⅲ)could continuously treat about 2.4 L TC(27 mg·L^-1)wastewater with the effluent concentration as low as 0.068 mg·L^-1.Our study suggested a broad application prospect of a new,effective,lowcost and environment-friendly adsorbent CHA400-(10%)Fe(Ⅲ)for treatment of low-concentration TC polluted wastewater.展开更多
In the present work, the behavior of folic acid （FA） molecule adsorbed onto single-walled carbon nanotube （SWCNT） was examined using the DFT-B3LYP/6-31G＊ level. In order to obtain information about the binding fe...In the present work, the behavior of folic acid （FA） molecule adsorbed onto single-walled carbon nanotube （SWCNT） was examined using the DFT-B3LYP/6-31G＊ level. In order to obtain information about the binding features of SWCNT as adsorbent with FA molecule, several studies, including the structural and electronic parameters and also the Atoms in Molecules （AIM） analysis, were performed. It was observed that the FA molecule via hydrogen bond prefers to adsorb on SWCNT with adsorption energy of about -18.70 kcal/mol. The molecular orbitals （HOMO and LUMO）, natural bond orbital （NBO）,analysis, and density of states （DOS） plot indicated that a charge about 0.032 [ e [ is transferred from the FA molecule to the nanotube. After solvation energy calculations, it was found that the presence of a polar solvent causes an increase in FA adsorption on the single-walled carbon nanotube. Topological features such as electron energy density （Hc） and Laplacian of the electron density （V2p~） demonstrate partial covalent nature for H（ll6）...O（10） interaction in the FA/SWCNT complex. According to the calculated results, the single-walled carbon nanotubes are expected to be a potential efficient adsorbent for the adsorption of folic acid drug and also can be used as a suitable drug delivery vehicle within biological systems.展开更多
In this work, a new sample pretreatment method prior to HPLC separations was developed for the determination of auxins in plant samples, Owing to its large surface area and high adsorption capacity, multi-walled carbo...In this work, a new sample pretreatment method prior to HPLC separations was developed for the determination of auxins in plant samples, Owing to its large surface area and high adsorption capacity, multi-walled carbon nanotube （MWCNT） was chosen as the adsorbent for the extraction of auxins from plant samples. In this study, two important auxins were selected as model analytes, namely indole-3- butyric acid （IBA） and 1-naphthylacetic acid （NAA）. They could be extracted and concentrated due to their π-π stacking interactions with MWCNT. Then HPLC-UV was introduced to detect IBA and NAA after sample pretreatment. Factors that may affect the enrichment efficiency were investigated and optimized. Comparative studies showed that MWCNT was superior to CI 8 for the extraction of the two analytes. Validation experiments showed that the optimized method had good linearity （0.9998 and 0.9960）, high recovery （81.4%-85.4%）, and low detection limits （0.0030 mg/L and 0.0012 mg/L）. The results indicated that the novel method had advantages of convenience, good sensitivity, high efficiency, and it was feasible for the determination of auxins in plant samples.展开更多
基金financial support from the Key Project of the National Natural Science Foundation of China(No.52034010)the China Scholarship Council(201906450038)
文摘This work mainly studies the effect of fluid phase momentum transfer mechanisms on the acidizing results,including the retardation effect of the porous structure and the interaction between the fluid phase,such as viscous dissipation and inertial effect.The results show that the acid fluid momentum transfer is influenced by the complex porous structure and fluid viscous dissipation.Eventually,the Stokes-Darcy equation is recommended to be adopted to describe the fluid phase momentum transfer in the following numerical simulation studies of the carbonate acidizing process.Based on this model,a parametric research is carried out to investigate the impact of acid on rock physical characteristics in the stimulation process.Increasing the acid concentration appears to minimize the quantity of acid consumed for the breakthrough.The acid surface reaction rate has a considerable impact on the pore volume to breakthrough and the optimum acid injection rate.The influence of permeability on the acidizing results basically shows a negative correlation with the injection rate.The difference between the acidizing curves of different permeability gradually becomes insignificant with the decrease in injection rate.The existence of isolated fracture and vug significantly reduces acid consumption for the breakthrough.
文摘Acidizing treatment is considered as a significant process in the oil well stimulations to form wormholes in carbonate formation in order to enhance the reservoir fluid production.Obtaining the number of pore volumes to breakthrough is an important objective in matrix acidizing,for it contributes to determining the wormhole characteristics such as type,shape,and size.Finding this number in experimental works requires a considerable amount of time,energy and cost.Therefore,this study aimed to establish an analytical method in which a reasonable result is achieved for the number of pore volumes to breakthrough.This purpose is accomplished by solely implementing acid and formation properties without performing any experimental works.The process of wormhole creation is done through developing a numerical model by utilizing the conservation of mass law method in which the carbonate core is considered as a closed system and the overall mass in the system as constant during the acid injection process.Furthermore,a constant number is added to the mathematical part of the model in order to eliminate the dimensionless Damk鰄ler number which is supposed to be calculated experimentally.The results of the numerical procedure of the model are further compared to four other experimental works,which led to calculating the average accuracy of this model that is shown to be 95.98%.This study puts forward a comprehensive numerical model to estimate the number of pore volumes to breakthrough with an acceptable accuracy rate merely through implementing known acid and core properties.
基金supported by the Energy Efficiency&Resources(No.20212010200010)the“Development of Intelligential Diagnosis,Abandonment Process and Management Technology for Decrepit Oil and Gas Wells”(No.20216110100010)of the Korea Institute of Energy Technology EvaluationPlanning(KETEP)grant funded by the Korean Government Ministry of Trade,Industry&Energy.
文摘Polymers play an important role in hybrid enhanced oil recovery (EOR), which involves both a polymer and low-salinity water. Because the polymer commonly used for low-salinity polymer flooding (LSPF) is strongly sensitive to brine pH, its efficiency can deteriorate in carbonate reservoirs containing highly acidic formation water. In this study, polymer efficiency in an acidic carbonate reservoir was investigated experimentally for different salinity levels and SO42− concentrations. Results indicated that lowering salinity improved polymer stability, resulting in less polymer adsorption, greater wettability alteration, and ultimately, higher oil recovery. However, low salinity may not be desirable for LSPF if the injected fluid does not contain a sufficient number of sulfate (SO42−) ions. Analysis of polymer efficiency showed that more oil can be produced with the same polymer concentration by adjusting the SO42− content. Therefore, when river water, which is relatively easily available in onshore fields, is designed to be injected into an acidic carbonate reservoir, the LSPF method proposed in this study can be a reliable and environmentally friendly method with addition of a sufficient number of SO42− ions to river water.
基金supported by the National Natural Science Foundation of China(Nos.52272211 and 52072145)the Funding of Jilin Province Development and Reform Commission(Nos.2024C018-11 and 2020C026-2)+3 种基金the Scientific and Technological Developing Project of Jilin Province(Nos.20230508046RC,20240602023RC,YDZJ202101ZYTS185 and YDZJ202201ZYTS372)Jilin Talent Development Funding(No.2021Y027)the Funds for Special Projects of the Central Government in Guidance of Local Science and Technology Development(No.202002017JC)the Research Program on Science and Technology from the Education Department of Jilin Province(Nos.JJKH20220439KJ and JJKH20210550KJ).
文摘Aqueous zinc-ion hybrid capacitors(ZIHCs)are promising electrochemical energy storage systems with advantages of high-energy density,low cost,safety and environmental friendliness.However,application of carbon-based cathodes is limited by their low-energy density due to the lack of active sites.Herein,a chemisorption sites modulating strategy is proposed to construct nitrogen-doped polyimide carbon nanoflowers with abundant oxygen vacancies and carbonyl functionalization via high-temperature calcination and subsequent acid processing.The synergistic effect of oxygen vacancies,carbonyl groups,enhanced surface area and porous structure enables stable zinc-ion storage with high capacity.Remarkably,the carbon materials can circulate 20,000 cycles stably at a current density of 2 A·g^(-1).After 10,000 cycles at a high rate of 3 A·g^(-1),a capacity retention rate of 64%can still be achieved.The as-prepared ZIHCs provide an energy density of 65.61 Wh·kg^(-1)at the power density of 197.82 W·kg^(-1).Current research shows that polyimide-derived carbon material synthesized by acid activation provides a new idea for developing cathodes in aqueous ZIHCs.
基金supported by the National Natural Science Foundation of China(2123600121176056)+1 种基金the Programme for 100 Excellent Talents in Universities of Hebei Province(II)(BR2-208)the Natural Science Foundation of Hebei Province(B2015202228)~~
文摘A carbon solid acid catalyst was prepared by the sulfonation of partially carbonized peanut shell with concentrated H2SO4. The structure and acidity of the catalyst were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, X‐ray diffraction, thermogravimetric analysis, X‐ray photoelectron spectroscopy, and elemental analysis, which showed that it was an amorphous carbon material composed of aromatic carbon sheets in random orientations. Sulfonic acid groups were present on the surface at a density of 0.81 mmol/g. The carbon solid acid catalyst showed better performance than HZSM‐5 for the esterification of cyclohexene with formic acid. At a3：1 molar ratio of formic acid to cyclohexene, catalyst loading of 0.07 g/mL of cyclohexene, and reaction time of 1 h at 413 K, the cyclohexene conversion was 88.4% with 97.3% selectivity to cyclohexyl formate. The carbon solid acid catalyst showed better reusability than HZSM‐5 because its large pores were minimally affected by the accumulation of oligomerized cyclohexene, which deactivated HZSM‐5. The activity of the carbon solid acid catalyst decreased somewhat in the first two recycles due to the leaching of polycyclic aromatic hydrocarbon containing –SO3H groups and then it remained constant in the following reuse.
文摘Study of the thermodynamic behaviour of CaCl2-H2O-CO2 systems is important in different scientific areas in the chemical and petroleum engineering fields. For example, a system including salt- H20-CO2 is a common system in CO2 geological storage. During carbonate matrix acidizing, this mixture also appears as the spent acid. Hence, study of the behaviour of this system and the solubility of CO2 in CaCl2 brine in different thermodynamic conditions is critical. In this study, CO2 solubility in 0, 1.90 and 4.80 mol/L CaCl2 solutions at 328.15 to 375.15 K and 68.9 to 206.8 bar were measured. These values are normal for oil reservoirs. A popular thermodynamic model is available in the literature for estimating the CO2 solubility in pure water and NaC1 solutions. In this paper, the available model was modified by experimental work to be applicable for CaCl2 as well. Based on the measured data, the component interaction parameters in the base model were adjusted for a CaCl2-H2O-CO2 system. The developed model could predict CO2 solubility in different conditions with remarkable accuracy, particularly for high concentration solutions and at high pressures. This improvement is up to 65% better than in the base model. This model can be used in Darcy scale models for predicting wormhole propagation during carbonate matrix acidizing.
基金supported by the National Natural Science Foundation of China (41171226)the Program for New Century Excellent Talents in University (NCET-12-0479)the Foundation for Youths Teacher by Northwest A&F University
文摘Revegetation is a traditional practice widely used for soil protection. We evaluated the effect of natural revegetation succession on soil chemical properties and carbon fractions （particulate organic carbon （POC）, humus carbon （HS-C）, humic acid carbon （HA-C） and fulvic acid carbon （FA-C）） on the Loess Plateau of China. The vegetation types, in order from the shortest to the longest enclosure duration, were： （a） abandoned overgrazed grassland （AbG3; 3 years）; （b） Hierochloe odorata Beauv. （HiO7; 7 years）; （c） Thymus mongoficus Ronnm （ThM15; 15 years）; （d） Artemisia sacrorum Ledeb （AtS25; 25 years）; （e） Stipa bungeana Trin Ledeb （StB36; 36 years） and （f） Stipa grandis P. Smirn （StG56; 56 years）. The results showed that the concentrations of soil organic carbon, total nitrogen and available phosphorus increased with the increase of restoration time except for ThM15. The concen- tration of NH4-N increased in the medium stage （for ThM15 and AtS25） and decreased in the later stage （for StB36 and StG56） of vegetation restoration. However, NO3-N concentration significantly increased in the later stage （for StB36 and StG56）. Carbon fractions had a similar increasing trend during natural vegetation restoration. The con- centrations of POC, HS-C, FA-C and HA-C accounted for 24.5%-49.1%, 10.6%-15.2%, 5.8%-9.1% and 4.6%-6.1% of total carbon, respectively. For AbG3, the relative changes of POC, HS-C and FA-C were significantly higher than that of total carbon during the process of revegetation restoration. The higher relative increases in POC, HS-C and FA-C confirmed that soil carbon induced by vegetation restoration was sequestrated by higher physical and chemical protection. The increases of soil C fractions could also result in higher ecological function in semiarid grassland ecosystems.
基金Project supported by the Ministry of Education Under the ATU Plan
文摘Works on exploring an environmentally clean method for producing an Mg,Al-hydrotalcite(Mg6Al2(OH) 16CO3·4H2O) layer and/or calcium carbonate(CaCO3) layer on Mg alloy in a carbonic acid solution system(aqueous HCO3-/CO3 2-or Ca 2+ /HCO3-) at 50℃ were reviewed.Conversion treatment for the Mg,Al-hydrotalcite conversion coating was as follows.Mg alloy was treated first in acidic HCO3-/CO3 2-aqueous for precursor layer formation on Mg alloy surface and then in alkaline HCO3-/CO3 2-aqueous to form a crystallized Mg,Al-hydrotalcite coating.Duration of an Mg,Al-hydrotalcite coating on Mg alloy surface was reduced from 12 h to 4 h by the conversion treatment.On the other hand,for reducing the formation time of CaCO3 coating on Mg alloy,the aqueous Ca 2+ /HCO3-with a saturated Ca 2+ content was employed for developing a CaCO3 coating on Mg alloy.A dense CaCO3 coating could yield on Mg alloy surface in 2 h.Corrosion rate(corrosion current density,Jcorr) of the Mg,Al-hydrotalcite-coated sample and CaCO3-coated AZ91D sample was 7-10μA/cm 2,roughly two orders less than the Jcorr of the as-diecast sample(about 200μA/cm 2) . No corrosion spot on the Mg,Al-hydrotalcite-coated sample and CaCO3-coated sample was observed after 72 h and 192 h salt spray test,respectively.
基金National Key Research Project of China,No2016YFC0500202STS of Chinese Academy of Sciences,No.KFJ-SW-STS-167+1 种基金National Natural Science Foundation of China,No.31290221,No.31570471Youth Innovation Research Team Project,No LENOM2016Q0005
文摘Soil humic carbon is an important component of soil organic carbon （SOC） in ter- restrial ecosystems. However, no study to date has investigated its geographical patterns and the main factors that influence it at a large scale, despite the fact that it is critical for exploring the influence of climate change on soil C storage and turnover. We measured levels of SOC, humic acid carbon （HAC）, fulvic acid carbon （FAC）, humin carbon （HUC）, and extractable humus carbon （HEC） in the 0-10 cm soil layer in nine typical forests along the 3800-km North-South Transect of Eastern China （NSTEC） to elucidate the latitudinal patterns of soil humic carbon fractions and their main influencing factors. SOC, HAC, FAC, HUC, and HEC increased with increasing latitude （all P〈0.001）, and exhibited a general trend of tropical 〈 subtropical 〈 temperate. The ratios of humic C fractions to SOC were 9.48%-12.27% （HAC）, 20.68%-29.31% （FAC）, and 59.37%-61.38% （HUC）. Climate, soil texture, and soil microbes jointly explained more than 90% of the latitudinal variation in SOC, HAC, FAC, HEC, and HUC and interactive effects were important. These findings elucidate latitudinal patterns of soil humic C fractions in forests at a large scale, and may improve models of soil C turnover and storage.
基金financial support from the National Natural Science Foundation of China(grant No.21706085)Subsidized Project for Postgraduates’Innovative Fund in Scientific Research of Huaqiao Universitythe Foundation of Key Laboratory of Pulp and Paper Science and Technology of Ministry of Education/Shandong Province of China(grant No.KF201804)。
文摘Two kinds of mesoporous carbon solid acids(LDMCE-SO3H and LDMCS-SO3H)were successfully prepared using masson pine alkali lignin as carbon source by evaporation-induced self-assembly(EISA)and salt-induced selfassembly(SISA)followed by sulfonation,respectively.In terms of preparation process,SISA(self-assembly in water and preparation time of 2 days)is greener and simpler than EISA(self-assembly in ethanol and preparation time of 7 days).The prepared LDMCE-SO3H and LDMCS-SO3H exhibit obvious differences in structural characteristics such as pore channel structure,specific surface area,mesopore volume and the density of-SO3H groups.Furthermore,the catalytic performances of LDMCE-SO3H and LDMCS-SO3H were investigated in the hydrolysis of microcrystalline cellulose in water,and the glucose yields of 48.99%and 54.42%were obtained under the corresponding optimal reaction conditions.More importantly,the glucose yields still reached 28.85%and 30.35%after five runs,and restored to 39.02%and 45.98%through catalysts regeneration,respectively,demonstrating that LDMCE-SO3H and LDMCS-SO3H have excellent recyclability and regenerability.
基金the National Key Project ofScientific and Technical SupportingPrograms Funded by the Ministry of Science & Technology of China (No.2006BAE03B06)the Shanghai International Cooperation of Science and Technology Project (No.06SR07101).
文摘The synthesis of 2, 4-diisopropyl-5,5-dimethy1- 1.3-dioxane through the acetalization of isobutyraldehyde with 2, 2, 4-trimethy1-1,3-pentanediol （TMPD） catalyzed by the novel carbon based acid was first carried out. High conversion （≥98%） and specific selectivity were obtained using the novel carbon based acid, which kept high activity after it was reused 5 times. Moreover. the catalyst could be used to catalyze the acetalization and ketalization of different aldehydes and ketones with superior yield. The yield of several products was over 90%. The novel heterogeneous catalyst has the distinct advantages of high activity, strikingly simple workup procedure, non-pollution, and reusability, which will contribute to the success of the green process greatly.
文摘The dissolution of carbon steel in 5% HCl in the temperature range of 30~90℃ was inhibited by two organic compounds having the general formula: ClR NH2(CH2)n NH2 RCl where R is a benzyl group. The behaviour of these inhibitors in acidic medium were investigated using weight loss method, open circuit potential and linear polarization technique. These inhibitors provided satisfactory corrosion inhibition for carbon steel in hydrochloric acid solutions even at higher temperature and acid concentration (10%). The electrochemical results showed that the polarization resistance (Rp) values increased with increasing inhibitor concentration, also the corrosion current decreased and a higher inhibition efficiency was obtained. The protective properties of these two organic inhibitors were attributed to the chemisorption mechanism
文摘One driver for steel development over recent decades has been the engineering requirements of improved strength and toughness,combined with weldability,for the safe and cost effective recovery and transmission of oil and gas.This has been achieved through refinement of grain size by microalloy precipitation and thermomechanical processing.However,little attention has been paid to these significant changes in steel chemistry and processing on corrosion resistance,despite the dominance of economic carbon steel for construction in the oil and gas industries.The more common forms of corrosion are associated with the presence of H 2 S or CO 2.CO 2 in aqueous solution forms a weak acid sufficient to promote significant localized corrosion in transmission gas/oil pipelines and in well-head applications (’down-hole’).Systematic study has identified the influence of a wide range of alloying elements and different processing conditions on the resistance of low-carbon steels to CO 2 corrosion;strong carbide-forming microalloying elements such as Ti,Nb and V,along with Cr additions,and different levels of Mn,Si,Cu,Mo and Ni,have been explored,along with treatments simulating different processing conditions.The present study also emphasizes the role of V and Ti microalloying in improving the resistance of Cr-containing carbon steel to corrosion in carbonic acid and how this is influenced by microstructure and the metallurgical condition of the microalloying addition,in particular,the extent of precipitation.It is noted that some commercially available corrosion inhibitors contain V as a vanadate compound to interfere with the corrosion process and so it is suggested that V microalloying may also be beneficial if present in an appropriate form in the steel.That Ti also seems to play a role in corrosion in the steels studied is judged to be compatible with the thermodynamics of transition metal anions in the Ti-V-Cr group.
基金This research was supported by the National Science and Technology Special Foundation for Major Large Oil and Gas Fields and Coal Bed Methane Development(2011ZX05042-003)the Provincial Ministry of State Key Laboratory Breeding Base of Open Projects Henan Gas Geology and Gas Control Laboratory(WS2013B06).
文摘The reaction between carbonic acid and montmorillonite minerals was studied in order to provide a theoretical basis for analyzing changes in the physical properties of coal seams after CO_(2)injection and for optimizing CO_(2) pumping parameters.A single montmorillonite mineral of purity[90%was selected and subjected to reactions at 25,35,and 45℃in carbonic acid solutions of varying acidity.The Si and Al concentrations in the solutions and the structure and elemental compositions of the montmorillonite before and after the reactions were analyzed using a spectrophotometer,an X-ray diffractometer,and an energy-dispersive X-ray spectrometer;kinetic reaction models were established for the dissolution of Si and Al in carbonic acid solutions in order to estimate the apparent activation energy of Si dissolution under different acidity conditions.The results indicate that Al dissolved rapidly and soon reached solubility equilibrium.On the other hand,Si concentration in the solutions increased rapidly and then gradually declined with vibrations,with maximum values at 25,35,and 45℃,which were observed at approximately 96,72,and 48 h,respectively.In addition,Si dissolution fitted the diffusion-controlled reaction model well;as the pH value decreased,the apparent activation energy of Si dissolution decreased,and Si became easier to dissolve.Furthermore,it was concluded that as a weak acid,carbonic acid causes little damage to the mineral structure of montmorillonite.
基金Project(51008106)supported by the National Natural Science Foundation of China
文摘A batch experiment was conducted to investigate the adsorption of an acid dye(Acid Orange 51) and a basic dye(Safranine) from aqueous solutions by the sludge-based activated carbon(SBAC). The results show that the adsorption of Acid Orange 51 decreases at high p H values, whereas the uptake of Safranine is higher in neutral and alkaline solutions than that in acidic conditions. The adsorption time needed for Safranine to reach equilibrium is shorter than that for Acid Orange 51. The uptakes of the dyes both increase with temperature increasing, indicating that the adsorption process of the dyes onto SBAC is endothermic. The equilibrium data of the dyes are both best represented by the Redlich-Peterson model. At 25 °C, the maximum adsorption capacities of SBAC for Acid Orange 51 and Safranine are 248.70 mg/g and 525.84 mg/g, respectively. The Elovich model is found to best describe the adsorption process of both dyes, indicating that the rate-limiting step involves the chemisorption. It can be concluded that SBAC is a promising material for the removal of Acid Orange 51 and Safranine from aqueous solutions.
基金financial support from the Major Science and Technology Projects of Sichuan Province(2019KJT0078)the National Natural Science Foundation of China(51904193)the Fundamental Research Funds for the Central Universities。
文摘Li_(4)Ti_(5)O_(12)(LTO) anode material demonstrates superior cycling performance due to its stable spinel structure and high lithiation/de-lithiation potential.Herein,a novel energy-saving solid-phase synthesis route for LTO has been successfully designed,employing the cheap industrial intermediate product of metatitanic acid (HTO) as titanium source.Through the in-situ Fourier transform infrared spectroscopy (FTIR)and ex-situ X-ray diffraction (XRD),it is revealed for the first time that the amorphous crystal structure of HTO is more conducive for the Li+insertion,making it possible to prepare LTO at a relatively lower sintering temperature.Utilizing the dehydration carbonization reaction between glucose and sulfuric acid,an ingenious strategy of glucose pre-coating is adopted to avoid the generation of Li_(2)SO_(4) impurity caused by the residual sulfuric acid on the surface of HTO,which meanwhile enhances the conductivity and inhibits the particle growth of LTO.The obtained ALTO@C anode material consequently exhibits excellent electrochemical performance that 132.0 m Ah g^(-1)is remained even at 20 C,and ultra low decay rate of 0.015% per cycle is achieved during 1000 cycles at 2 C.Remarkably,LiCoO_(2)//ALTO@C full cell delivers conspicuous low-temperature property (130.7 m Ah g^(-1)at 0.5 C and almost no attenuation after 300 cycles under-20℃).
文摘A carbon paste electrode（CPE） chemically modified with multiwall carbon nanotubes and ferrocene（FC） was used as a selective electrochemical sensor for the simultaneous determination of trace amounts of cysteamine（CA） and folic acid（FA）.This modified electrode showed very efficient electrocatalytic activity for the anodic oxidation of CA.The peak current of differential pulse voltammograms of CA and FA increased linearly with their concentration in the ranges of 0.7-200μmol/L CA and 5.0- 700μmol/L FA.The detection limits for CA and FA were 0.3μmol/L and 2.0μmoI/L,respectively.The diffusion coefficient（D） and transfer coefficient（α） of CA were also determined.These conditions are sufficient to allow determination of CA and FA both individually and simultaneously.
基金financially supported by the National Natural Science Foundation of China(No.51641209)。
文摘Humic acid(HA)was carbonized at 300,400 and 500℃ and then functionalized with 1 wt%–12 wt%Fe(Ⅲ)respectively[CHA300/400/500-Fe(Ⅲ)].Adsorption of such Fe(III)-functionalized carbonized HA as adsorbents to aqueous tetracycline(TC:25 mg·L^-1)was studied.The adsorption equilibrium time for CHA400-Fe(Ⅲ)to TC was 6 h faster and the adsorption removal efficiency(Re)was two times higher than that of HA/CHA.The adsorption Reof CHA400-Fe(Ⅲ)loaded 10%iron[CHA400-(10%)Fe(Ⅲ)]to TC could reach 99.8%at 8 h and still kept80.6%after 8 cycles.The adsorption kinetics were well fitted to the pseudo-second-order equation and the adsorption isotherms could be well delineated via Langmuir equations(R^2N 0.99),indicating that the homogeneous chemical adsorption of TC occurred on the adsorbents.The main adsorption mechanisms of TC were complexation Fe(III)and hydrophobic distribution.Electropositive and electronegative repulsion between TC and CHA400-(10%)Fe(Ⅲ)at lowly p H(2)and highly p H(8–10)respectively,leaded to the relatively low adsorption capacity and more notable influence of ion concentration.When the p H was between 4 and 8,TC mainly existed in neutral molecules(TCH2),so the influence of ion concentration was not obvious.The dynamic adsorption results showed that the CHA400-(10%)Fe(Ⅲ)could continuously treat about 2.4 L TC(27 mg·L^-1)wastewater with the effluent concentration as low as 0.068 mg·L^-1.Our study suggested a broad application prospect of a new,effective,lowcost and environment-friendly adsorbent CHA400-(10%)Fe(Ⅲ)for treatment of low-concentration TC polluted wastewater.
文摘In the present work, the behavior of folic acid （FA） molecule adsorbed onto single-walled carbon nanotube （SWCNT） was examined using the DFT-B3LYP/6-31G＊ level. In order to obtain information about the binding features of SWCNT as adsorbent with FA molecule, several studies, including the structural and electronic parameters and also the Atoms in Molecules （AIM） analysis, were performed. It was observed that the FA molecule via hydrogen bond prefers to adsorb on SWCNT with adsorption energy of about -18.70 kcal/mol. The molecular orbitals （HOMO and LUMO）, natural bond orbital （NBO）,analysis, and density of states （DOS） plot indicated that a charge about 0.032 [ e [ is transferred from the FA molecule to the nanotube. After solvation energy calculations, it was found that the presence of a polar solvent causes an increase in FA adsorption on the single-walled carbon nanotube. Topological features such as electron energy density （Hc） and Laplacian of the electron density （V2p~） demonstrate partial covalent nature for H（ll6）...O（10） interaction in the FA/SWCNT complex. According to the calculated results, the single-walled carbon nanotubes are expected to be a potential efficient adsorbent for the adsorption of folic acid drug and also can be used as a suitable drug delivery vehicle within biological systems.
基金supported by National Natural Science Foundation of China(Nos.20975056,21275082 and 81102411)Natural Science Foundation of Shandong(Nos. ZR2011BZ004,ZR2011BQ005)+2 种基金JSPS and NSFC under the Japan-China Scientific Cooperation Program(No.21111140014)State Key Laboratory of Analytical Chemistry for Life Science(No. SKLACLS1110)the National Key Basic Research Development Program of China(973 Special Preliminary Study Plan,No. 2012CB722705)
文摘In this work, a new sample pretreatment method prior to HPLC separations was developed for the determination of auxins in plant samples, Owing to its large surface area and high adsorption capacity, multi-walled carbon nanotube （MWCNT） was chosen as the adsorbent for the extraction of auxins from plant samples. In this study, two important auxins were selected as model analytes, namely indole-3- butyric acid （IBA） and 1-naphthylacetic acid （NAA）. They could be extracted and concentrated due to their π-π stacking interactions with MWCNT. Then HPLC-UV was introduced to detect IBA and NAA after sample pretreatment. Factors that may affect the enrichment efficiency were investigated and optimized. Comparative studies showed that MWCNT was superior to CI 8 for the extraction of the two analytes. Validation experiments showed that the optimized method had good linearity （0.9998 and 0.9960）, high recovery （81.4%-85.4%）, and low detection limits （0.0030 mg/L and 0.0012 mg/L）. The results indicated that the novel method had advantages of convenience, good sensitivity, high efficiency, and it was feasible for the determination of auxins in plant samples.
