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1.
The thermal modified rectorite (TR) was prepared and characterized by x-ray diffraction, scanning electron microscopy, and Fourier transform infrared spectroscopy. The structure of TR was destroyed gradually with increasing the calcination temperature, and the adsorption capacity for methylene blue (MB) of the rectorite can be improved by thermal modification in appropriate temperature ranges. The equilibrium data were well described by the Langmuir model. The kinetic studies indicated that the adsorption process was fitted well with the pseudo-second-order kinetic model. Thermodynamic studies indicated that adsorption of MB was endothermic in nature and favorable with the positive ΔH 0 value of 25.90 kJ/mol.  相似文献   

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The wide use of lithium ion batteries (LIBs) has created much waste, which has become a global issue. It is vital to recycle waste LIBs considering their environmental risks and resource characteristics. Anode graphite from spent LIBs still possess a complete layer structure and contain some oxygen-containing groups between layers, which can be reused to prepare high value-added products. Given the intrinsic defect structure of anode graphite, copper foils in LIB anode electrodes, and excellent properties of graphene, graphene oxide–copper composite material was prepared in this work. Anode graphite was firstly purified to remove organic impurities by calcination and remove lithium. Purified graphite was used to prepare graphene oxide–copper composite material after oxidation to graphite oxide, ultrasonic exfoliation to graphene oxide (GO), and Cu2+ adsorption. Compared with natural graphite, preparing graphite oxide using anode graphite consumed 40% less concentrated H2SO4 and 28.6% less KMnO4. Cu2+ was well adsorbed by 1.0 mg L?1 stable GO suspension at pH 5.3 for 120 min. Graphene oxide–copper composite material could be successfully obtained after 6 h absorption, 3 h bonding between GO and Cu2+ with 3/100 of GO/CuSO4 mass ratio. Compared to CuO, graphene oxide–copper composite material had better catalytic photodegradation performance on methylene blue, and the electric field further improved the photodegradation efficiency of the composite material.  相似文献   

4.
In this study, an amidoximated chelating ion exchange resin was prepared by poly-acrylonitrile (PAN) grafted potato starch. The adsorbent characterizations such as specific surface area, pore volume, average pore radius, and Fourier transform infrared (FTIR) spectrum of the resin were measured. The effects of pH, adsorbent dosage, contact time, initial concentration of thorium ion, and temperature on adsorption of thorium ion from aqueous solutions were investigated. Four isotherm models including Langmuir, Freundlich, Dubinin-Radushkevich, and Temkin were applied to analyze the equilibrium isotherm data. The results showed that Langmuir and Temkin models had a good agreement with experimental data. The maximum capacity of the adsorbent using the Langmuir isotherm model was 227.27 mg · g?1. The kinetic models like pseudo-first-order, pseudo-second-order, Elovich, and intraparticle were examined to describe the adsorption process. The kinetics of the adsorption process was found to follow the pseudo-second-order kinetic model. The thermodynamic parameters (ΔG°, ΔH°, ΔS°) were also calculated using equilibrium constant values at various temperatures (25, 35, 45, 55°C) and the positive value for ΔH° showed an endothermic adsorption process. The study suggests that the prepared adsorbent has promising potential for the removal of thorium from wastewaters.   相似文献   

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Response surface methodology (RSM) in conjunction with central composite rotatable design (CCRD) was employed to find out the influence of preparation properties of walnut oil/water nanoemulsion namely ultrasonic time (5–15 minutes), walnut oil content (4–10% w/w) and concentration ratio of Span 80 to Tween 80 (K 0, 0.55–0.80) on response variables including emulsion capacity, cloudiness, density and surface tension. The calculated regression models with high value of coefficient of determination (0.910–0.973) and insignificant lack of fit test indicated satisfactory agreement of empirical models with experimental observations. The results revealed linear term of walnut oil concentration was the most significant (p < 0.05) parameter on the all responses. The overall optimum region to achieve the ideal characteristics was ultrasonic time of 11.74 minutes, walnut oil content of 4.00% (w/w) and K 0 of 0.80.  相似文献   

7.
The adsorption kinetics of Quercus infectoria natural dye on cotton in the absence and presence of the cationic (cetyl trimethyl ammonium bromide; CTAB) and anionic (sodium lauryl sulfate; NaLS) surfactants has been investigated at three temperatures, namely, 40°C, 50°C, and 60°C. On increasing the surfactant content in the surfactant-dye mixture, the initial rate of adsorption (h i) and the adsorption capacity at equilibrium (q e) were found to increase while pseudo-second-order rate constant (k 2) was found to decrease. The retarding effect of surfactant on k 2 was in order of CTAB > NaLS. The activation parameters for adsorption process have been evaluated in each case, and the mechanism of adsorption process has been discussed.  相似文献   

8.
Iron oxide particles were micronized by supercritical carbon dioxide (CO2) as an antisolvent in a batch gas antisolvent (GAS) process. In the present study, the feasibility of GAS process to micronize the iron oxide particles using dimethyl sulfoxide (DMSO) as a solvent was investigated. In this direction, particle size and morphology changes were investigated with changing solution pressure (80–150 bar), temperature (308.15–328.15 K), and concentration (1.5–6 g/l). Based on the different experimental conditions, the particle size of the original iron oxide was decreased in the range of 17.25 to 4.23 µm, which shows a the success of the GAS process to reduce the particle size of the intact iron oxide particles. Simultaneously, morphology changes were observed starting from the irregular morphology for synthesized particles to more regular shapes that included fused and spherical-fused particles.  相似文献   

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以棒状石墨为原料,采用改良的Hummers法与热处理制备得到膨胀氧化石墨(E-GO),利用在酸性水溶液中归中化学反应的方法合成纳米尺寸的硫颗粒,使其嵌入到膨胀氧化石墨的内部,制备了膨胀氧化石墨-硫复合材料。采用红外光谱,X-射线光电子能谱表征了膨胀氧化石墨表面官能团的存在和种类;X-射线衍射分析结果表明生成的硫属于斜方晶结构;扫描电子显微镜和透射电镜分析证明了材料中硫的均匀分布。恒电流充放电结果表明该复合正极材料的首次放电容量为1 020 mAh.g-1,100周循环之后其容量还保持在650 mAh.g-1左右;材料的倍率性能和库伦效率优异,这可能得益于小尺寸的硫在材料中均匀分布,以及表面官能团对硫的固定化作用。  相似文献   

10.
In the present study, adsorption of Bismarck Brown (BB) dye onto iron oxide nanospheres (IONs) and modified IONs by HCl from aqueous solution was investigated. The IONs was synthesized by solvothermal method and then modified by HCl. The high magnetic properties of both adsorbents lead to facial separation from aqueous solution by an external magnet. The results show that the modification of adsorbent cause higher adsorption capacity for removal of BB from aqueous solution. The prepared adsorbents were characterized by SEM, XRD, FTIR, and ATR-IR techniques. The adsorption kinetic and equilibrium data were fitted with different models. The results show that the equilibrium and kinetic data were best fitted with Langmuir–Freundlich isotherm and fractal-like pseudo-second-order kinetic model, respectively. The effects of pH and temperature have also been investigated.  相似文献   

11.
Equisetum arvense supercritical CO2 extracts (EAE) contained an initial antioxidant activity of 10.3 mM TEAC that suffered a sharp first order kinetics decay characterized by half-life time (t1/2) of 1.05 ± 0.03 and 0.86 ± 0.03 weeks at 25 and 4°C, respectively. The aim of the present work was to develop a nanoemulsion formulation for providing EAE protection against deleterious environmental factors and extending its shelf-life functionality. The nanoemulsion area was identified by constructing pseudoternary phase diagrams and response surface methodology was used to optimize the preparation conditions. The best formulation achieved an EAE encapsulation efficiency of 97.5 ± 0.5% and antioxidant activity half-life time (t1/2) was extended to 12.32 ± 0.40 and 14.56 ± 0.60 weeks at 25 and 4°C, respectively.   相似文献   

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In this work, nine monostearic esters of ethoxylated dialkyle-amine (group I) and ethoxylated polyalkylenepolyamine (group II) nonionic surfactants were prepared and characterized by FTIR spectroscopy and nitrogen content. The 1,4-diaminobutane (DAB), 1,6 diamino hexane (DAH), 1,8-diamino-octane (DAO), diethylenetriamine (DETA), triethylenetetramine (TETA), and tetraethylenepentamine (TEPA) were ethoxylated at 50, 100, 150 ethylene oxide units individually. The ethoxylated products of (group I) reacted with stearic acid to give the monostearate products. The surface tension of the prepared compounds were measured at 25°C and 60°C. The thermodynamic parameters of micellization and adsorption were also calculated. The surface active properties, such as critical micelle concentration (CMC), maximum surface excess concentration (Γmax), effectiveness of surface tension reduction (πcmc), and minimum area per molecule at the aqueous solution-air interface (Amin), have been calculated. The surface active and thermodynamic properties of the prepared compounds were correlated to their chemical structure. It was found that CMC decreases when increasing the molecular weight of polyethylene oxide units. Furthermore, the data show that the synthesized surfactants favor adsorption than micellization, so that they can be used as demulsifiers for waxy crude oil emulsion (BSW 18%). In this respect, the demulsification test was carried out and the results of demulsification efficiency were correlated to the chemical composition of the investigated compounds. Some factors that affect the demulsification efficiency were also considered such HLB, concentration and time. The maximum demulsification efficiency (100%) was obtained by DAOE150-M and TEPAE150 at 60 and 45 minutes (300 ppm), respectively.  相似文献   

14.
Two series of cationic dimeric (gemini) surfactants are prepared with respect to key surfactants properties, such as surface activity and solubilization. The influence of both the dimerization and the spacer group is examined in order to establish structure-property relationships. The surface tension and critical micelle concentration can be markedly reduced compared to the monomeric surfactants in the pure state. The critical micelle concentration (cmc) of each series has been determined using equilibrium surface tension measurements. Furthermore, air/water interface parameters including effectiveness (πcmc), efficiency (PC20), maximum surface excess (Γ max ), and minimum surface area (A min ) have been also derived using Gibb's adsorption equation at 25°C. Standard free energies of micellization and adsorption were calculated. Solubilization behaviors of the synthesized surfactants were measured towards paraffin oil as solubilized material using light transmission technique.  相似文献   

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A nanocomposite of activated carbon and iron oxide was prepared and characterized by x-ray diffraction and scanning electron microscopy methods. The prepared magnetic nanocomposite can be separated easily from water by an external magnet. The prepared magnetic nanocomposite was used as adsorbent for removal of Bismarck Brown (B.B.) as a dye pollutant from water. The adsorption studies include both equilibrium and kinetic aspects, and the results were modeled with different equations. The obtained results indicate that the prepared magnetic nanocomposite of iron oxide and activated carbon is one of the best adsorbents for the removal of B.B. from aqueous solution.  相似文献   

17.
Eggshell particles (ESP), a solid bio-waste, treated with sodium dodecylsulfate (SDS) have been examined for the adsorption of some tailor-made cationic styrylpyridinium dyes. The adsorbent is characterized through Fourier transform infrared spectroscopy and scanning electron microscopy. The anionic headgroups of the surfactant bilayer on the SDS-treated ESP (SDS-ESP) provide avenue for binding with the dye molecules. Dependence of equilibrium adsorption capacity on various adsorption parameters and effects of substituent and hydrophobic tail of the adsorbate on adsorption are enumerated. Physical adsorption obeying pseudo-second order kinetics has been proposed. (Supplemental materials are available for this article. Go to the publisher's online edition of Journal of Dispersion Science and Technology to view the free supplemental file.)  相似文献   

18.
The dilational rheological behaviors of absorbed films of p-(n-alkyl)-benzyl polyoxyethylene ether carboxybetaine CxBE2CB (x = 8, 10, 12) at the water–decane interface have been investigated by the drop-shape analysis method. The influences of time, oscillation frequency, and bulk concentration on dilational modulus and phase angle have been expounded. The experimental results show that the phase angle of CxBE2CB (x = 10, 12) decreases with the increase of time, the slope of the log ? ? log ω curve and phase angle of CxBE2CB (x = 10, 12) decrease in a wide concentration range. These phenomena become more and more apparent with the increase of hydrocarbon chain length and it cannot be attributed to the diffusion-exchange process between the bulk and the interface. It is reasonable to consider that ethylene oxide groups are flexible and can be compressed and expanded, just like a spring. Therefore, the compression and expansion of the ethylene oxide groups in the interfacial layer and the exchange between interface and sublayer play a more important role for CxBE2CB (x = 10, 12) adsorption film. The dependence of dilational modulus on interfacial pressure can support our provided mechanism strongly.  相似文献   

19.

A simple, sensitive and accurate method was developed for solid-phase extraction and preconcentration of trace levels of gold in various samples. It is based on the adsorption of gold on modified oxidized multi-walled carbon nanotubes prior to its determination by graphite furnace atomic absorption spectrometry. The type and volume of eluent solution, sample pH value, flow rates of sample and eluent, sorption capacity and breakthrough volume were optimized. Under these conditions, the method showed linearity in the range of 0.2–6.0 ng L−1 with coefficients of determination of >0.99 in the sample. The relative standard deviation for seven replicate determinations of gold (at a level of 0.6 ng L−1) is ±3.8 %, the detection limit is 31 pg L−1 (in the initial solution and at an S/N ratio of 3; for n = 8), and the enrichment factor is 200. The sorption capacity of the modified MWCNTs for gold(III) is 4.15 mg g−1. The procedure was successfully applied to the determination of gold in (spiked) water samples, human hair, human urine and standard reference material with recoveries ranging from 97.0 to 104.2 %.

A sorbent based on modified carbon nanotubes was prepared and used to extract gold ion from various samples prior to its determination by graphite furnace atomic absorption spectrometry

  相似文献   

20.
The adsorption and corrosion inhibition behavior of mild steel in 0.1 M H2SO4 in presence of L-cystine and L-cystine in combination with surfactants sodium dodecyl sulfate and cetyltrimethyl ammonium bromide at 30–60°C was investigated using weight loss and potentiodynamic polarization measurements. Inhibition efficiency of L-cystine is synergistically enhanced on addition of surfactants. Surface morphology of corroded steel samples was evaluated using scanning electron microscopy and atomic force microscopy, which further confirmed the existence of an adsorbed protective film on the mild steel surface. Calculated thermodynamic parameters reveal that adsorption process is spontaneous and obey Langmuir adsorption isotherm.  相似文献   

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