采用锰矿从水溶液中吸附铅和镉离子(英文)

采用低成本的本地可得的天然锰矿作为吸附剂,研究吸附工艺从水溶液中脱除铅离子和镉离子。利用伪一级、伪二级动力学和颗粒内扩散模型检验动力学吸附数据,计算和比较这些动力学模型的吸附速率常数,发现用伪二级动力学模型能最佳地描述吸附动力学。将 Langmuir 和 Freundlich 等温吸附模型用来拟合不同温度下的平衡数据,发现实验数据与 Langmuir 模型拟合得更好。采用 Langmuir 等温吸附模型计算出锰矿吸附铅离子和镉离子的最大容量分别为 98 和 6.8 mg/g。计算了热力学参数,如吸附吉布斯自由能的变化、焓变与熵变。结果表明,锰矿作为吸附剂对铅和镉的吸附反应是自发的吸热反应。因此,锰矿作为一种天然的矿物吸附剂,可以替代现有的吸附剂来脱除水溶液中的铅离子和镉离子。     

Simultaneous measurement of mechanical and electrical contact resistances during nanoindentation of NiTi shape memory alloys

The nanoindentation technique can be employed in shape memory alloys (SMAs) to discern the transformation temperatures as well as to characterize their mechanical behavior. In this paper, we use it with simultaneous measurements of the mechanical and the electrical contact resistances (ECR) at room temperature to probe two SMAs: austenite (RTA) and martensite (RTM). Two different types of indenter tips – Berkovich and spherical – are employed to examine the SMAs’ indentation responses as a function of the representative strain, ε_R. In Berkovich indentation, because of the sharp nature of the tip, and in consequence the high levels of strain imposed, discerning the two SMAs on the basis of the indentation response alone is difficult. In the case of the spherical tip, ε_R is systematically varied and its effect on the depth recovery ratio, η_d, is examined. Results indicate that RTA has higher η_d than RTM, but the difference decreases with increasing ε_R such that η_d values for both the alloys would be similar in the fully plastic regime. The experimental trends in η_d vs. ε_R for both the alloys could be described well with a η_d ∝ (ε_R)^?1 type equation, which is developed on the basis of a phenomenological model. This fit, in turn, directs us to the maximum ε_R, below which plasticity underneath the indenter would not mask the differences in the two SMAs. It was demonstrated that the ECR measurements complement the mechanical measurements in demarcating the reverse transformation from martensite to austenite during unloading of RTA, wherein a marked increase in the voltage was noted. A correlation between recovery due to reverse transformation during unloading and increase in voltage (and hence the electrical resistance) was found.     

Combining indentation and diffusion couple techniques for combinatorial discovery of high temperature shape memory alloys

We demonstrate the possibility of accelerated identification of potential compositions for high-temperature shape memory alloys (SMAs) through a combinatorial material synthesis and analysis approach, wherein we employ the combination of diffusion couple and indentation techniques. The former was utilized to generate smooth and compositionally graded inter-diffusion zones (IDZs) in the Ni–Ti–Pd ternary alloy system of varying IDZ thickness, depending on the annealing time at high temperature. The IDZs thus produced were then impressed with an indenter with a spherical tip so as to inscribe a predetermined indentation strain. Subsequent annealing of the indented samples at various elevated temperatures, T_a, ranging between 150 and 550 °C allows for partial to full relaxation of the strain imposed due to the shape memory effect. If T_a is above the austenite finish temperature, A_f, the relaxation will be complete. By measuring the depth recovery, which serves as a proxy for the shape recovery characteristic of the SMA, a three-dimensional map in the recovery–temperature–composition space is constructed. A comparison of the published A_f data for different compositions with the T_a data shows good agreement when the depth recovery is between 70% and 80%, indicating that the methodology proposed in this paper can be utilized for the identification of promising compositions. Advantages and further possibilities of this methodology are discussed.     

Biocidal polymers: Synthesis,antimicrobial activity,and possible toxicity of poly (hydroxystyrene‐co‐methylmethacrylate) derivatives

Functionalized polymers have gained much interest in the last decades. This is due to their functional group and their polymer nature that give them unique properties and more advantages than the corresponding small molecules. In this trend, polyhydroxystyrene‐co‐MMA was modified to introduce amino group in the side chain of the polymer. The amine modified polymer was reacted with two classes of active compounds. The first class is aldehydes such as vanilline, p‐hydroxybenzaldehyde, p‐chlorobenzaldehyde, and anisaldehyde. The second class is phenolic esters such as p‐hydroxymethylbenzoate, 2,4‐dihydroxymethyl benzoate, and methyl salicylate. The antimicrobial activities of the polymer and modified polymer with these two classes were explored with Gram‐negative bacteria (Escherichia coli), Gram‐positive bacteria (Bacillus subtilus), fugus like yeast (Candida albicans SC5314), and pathogenic molds (Aspergillus flavus, Trycophyton rubrum, and F. oxysporium). In vitro studies indicated that the start polymer did not affect on the test microorganisms, in contrary to its derivatives. The diameter of inhibition zone varied according to the active group in the modified polymer, polymer microstructure, and the test microorganism. Derivatives I, II, and III were selected among the most effective antimicrobial compounds. Their inhibitory effects on the ratio of surviving cell number (M/C) increased by increasing derivatives concentrations. Derivatives I and II were inhibitorier to C. albicans and molds than to bacteria while derivative III was only antibacterial. These derivatives seemed toxic to Brine shrimp by increasing their concentrations above 10 ppm, with derivative III being the less toxic, compared to others. To clarify this toxic effect and to decrease the toxicity of these derivatives, more detailed studies are necessary, and this will be focused in the nearest future. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Heterogeneous photo-Fenton oxidation of reactive azo dye solutions using iron exchanged zeolite as a catalyst

The heterogeneous photo-Fenton-type oxidation of reactive azo dye solutions has been investigated in a quartz batch reactor using artificial UVA as a light source. Fe-exchanged zeolite has been used as a heterogeneous catalyst in the process. The effect of various process variables on decolorization performance of the process was evaluated by examining temperature, pH, H₂O₂ dosage, catalyst loading, initial dye concentration and light intensity. The optimal operational parameters were found as follows: 35 °C, pH as solution pH 5.2, 15 mmol H₂O₂ dosage, 1 g/L catalyst loading. Stability and reuse of the catalyst were also tested. Mineralization and comparison with homogenous photo-Fenton process were evaluated by analyzing color removal and total organic carbon (TOC) values.     

Analysis of the Doppler signals using largest Lyapunov exponent and correlation dimension in healthy and stenosed internal carotid artery patients

Nonlinear analysis techniques have been applied for many applications on the physiological systems. In this research, the largest Lyapunov exponent (LLE) and correlation dimension (CD) calculations were performed to evaluate the chaotic behaviour of blood flow obtained from the healthy and stenosed internal carotid artery (ICA) using noninvasive Doppler ultrasonography technique. The Doppler signals were taken from 30 healthy, 8 mild, 8 moderate and 8 serious degree of stenosis ICA subjects. The LLE calculation was performed by using Wolf algorithm. The Grassberger–Procaccia algorithm was used for CD analysis. The calculated LLE and CD values for stenosed ICA Doppler signals were found as significantly high compared to the values belonging to the healthy subjects. It is found that, the LLEs and CDs of stenosed ICA Doppler signals increase with the increasing of the degree of stenosis. The results show that the LLE and CD can be used for diagnosis of the ICA stenosis and to determine the degree of stenosis.     

Modeling and analysis of packing properties through a fuzzy inference system

Packing of manufactured products is important in protecting them from damage during handling and transportation. Several materials and methods are used for packing of products and the optimum level of packing materials should be determined to minimize damage to the product. Design and analysis of experiments (DOE) could be used for this. However, fuzzy logic models can be more suitable than mathematical models derived from DOE due to the error values. This is because fuzzy logic models use several functions instead of a single function. DOE and the adaptive neuro fuzzy inference system (ANFIS) modeling approaches are employed for the modeling and analysis of packing materials with the aim of delivering minimum damage. Although the root of mean square error (RMSE) values of the ANFIS model is 5.7622 × 10⁻⁶, the RMSE value of mathematical model from DOE is 3.57457. This result shows that the ANFIS model is more successful than the DOE model for this purpose.     

Indirect electrochemical treatment of bisphenol A in water via electrochemically generated Fenton's reagent

Bisphenol A (BPA) has been treated with electrochemically generated Fenton's reagent in aqueous medium. Hydroxyl radicals that were formed in Fenton's reagent reacted with the organic substrate producing two different isomers of monohydroxylated product and, upon successive hydroxylation, mainly one dihydroxylated product. Further hydroxylation first degraded one of the aromatic rings, and the side chain thus formed was then cleaved off the other aromatic ring. The second aromatic ring was also degraded upon successive hydroxylations. Small saturated and unsaturated aliphatic acids were the last products prior to mineralization. It was found that use of cuprous/cupric ion pair resulted a faster conversion of BPA and faster mineralization when compared using ferrous/ferric ions, but this happened at the expence of excess electrical charge utilized for an equivalent conversion or mineralization. Degradation by using ferrous/ferric ions was more efficient than cuprous/cupric ions case in terms of total mineralization versus charge utilized, and a mineralization of 82% had been achieved by applying 107.8 mF of charge to a 0.7 mM BPA solution of 0.200 dm3. The rate constant of the monohydroxylation of BPA in the presence of ferrous/ferric ions had been determined as 1.0 x 10(10) M(-1) s(-1) where BPA and salicylic acid competitively reacted with hydroxyl radicals in aqueous medium with the initial concentrations of Fe2+, BPA, and SA of 1.0, 0.5, and 0.5 mM, respectively. In a similar experiment where the initial concentrations of Cu2+, BPA, and SA were 1.0, 0.5, and 0.5 mM, respectively, the corresponding rate constant was determined to be the same as the rate constant obtained for Fe2+ (i.e., 1.0 x 10(10) M(-1) s(-1)). While the use of Cu2+ cannot be advised for processing BPA and similar substrates by using the electro-Fenton technique for both technical and economical reasons, the use of [Fe2+]/[BPA]0 values in the range 3-4 will be sufficient to achieve an efficient mineralization of BPA and similar substrates by the electro-Fenton process in aqueous medium.     

Catalytic behavior of the Fe/Fe system in the electro-Fenton degradation of the antimicrobial chlorophene

The catalytic behavior of the Fe³⁺/Fe²⁺ system in the electro-Fenton degradation of the antimicrobial drug chlorophene has been studied considering four undivided electrolytic cells, where a Pt or boron-doped diamond (BDD) anode and a carbon felt or O₂-diffusion cathode have been used. Chlorophene electrolyses have been carried out at pH 3.0 under current control, with 0.05 M Na₂SO₄ as supporting electrolyte and Fe³⁺ as catalyst. In these processes the drug is oxidized with hydroxyl radical (OH) formed both at the anode from water oxidation and in the medium from electrochemically generated Fenton's reagent (Fe²⁺ + H₂O₂, both of them generated at the cathode). The catalytic behavior of the Fe³⁺/Fe²⁺ system mainly depends on the cathode tested. In the cells with an O₂-diffusion cathode, H₂O₂ is largely accumulated and the Fe³⁺ content remains practically unchanged. Under these conditions, the chlorophene decay is enhanced by increasing the initial Fe³⁺ concentration, because this leads to a higher quantity of Fe²⁺ regenerated at the cathode and, subsequently, to a greater OH production from Fenton's reaction. In contrast, when the carbon felt cathode is used, H₂O₂ is electrogenerated in small extent, whereas Fe²⁺ is largely accumulated because the regeneration of this ion from Fe³⁺ reduction at the cathode is much faster than its oxidation to Fe³⁺ at the anode. In this case, an Fe³⁺ concentration as low as 0.2 mM is required to obtain the maximum OH generation rate, yielding the quickest chlorophene removal. Chlorophene is poorly mineralized in the Pt/O₂ diffusion cell because the final Fe³⁺–oxalate complexes are difficult to oxidize with OH. These complexes are completely destroyed using a BDD anode at high current thanks to the great amount of OH generated on its surface. Total mineralization is also achieved in the Pt/carbon felt and BDD/carbon felt cells with 0.2 mM Fe³⁺, because oxalic acid and its Fe²⁺ complexes are directly oxidized with OH in the medium. Comparing the four cells, the highest oxidizing power regarding total mineralization is attained for the BDD/carbon felt cell at high current due to the simultaneous destruction of oxalic acid at the BDD surface and in the bulk solution.