有机物料对石灰性土壤磷素形态转化及吸附特性的影响研究

利用石灰性土壤,对猪粪(DR)、夏玉米秸秆(MR)和冬小麦秸秆(WR)单施或者与磷肥混施(在等磷量条件下)对土壤磷的吸附特性及其形态转化进行了为期15周的室内模拟培养研究.结果表明,无论是DR、MR和WR单施,还是有机物料与磷肥混施,都可以减少土壤对磷的吸附量,增加土壤磷的活性,其中有机物料单施处理的用NaHCO3或者NaOH提取的活性无机磷(Pi)和有机磷(Po)提高较大,顺序为:猪粪>夏玉米秸秆>冬小麦秸秆.夏玉米秸秆处理与对照(CK)相比NaHCO3提取的Pi、Po增加的量分别为6 0mg·kg-1,5 6mg·kg-1,NaOH提取的Po增加的量为12 7mg·kg-1,而猪粪处理与CK相比NaHCO3提取的Pi、Po增加的量分别为7 1mg·kg-1,5 4mg·kg-1,NaOH提取的Po增加的量为14 1mg·kg-1.通过Langmuir方程求得磷的最大吸附量(b)、磷吸附结合能常数(k)、磷素最大缓冲量(MPBC)、标准需磷量(SPR)的值,进一步说明了3种有机物料均可使土壤对磷的吸附能力降低,增加土壤中磷的活性.     

Recovery of seven kinds of cfc and cfc replacements on high‐surface area activated carbon

The adsorption isotherms, the constants of the Dubinin—Radushkevich plots, and the constants of the Langmuir plots of chlorofluorocarbon (CFC) and CFC replacements on high‐surface area activated carbon were investigated to estimate the recovery efficiency of CFC and CFC replacements. The adsorption and desorption of HFC134a on a high‐surface area activated carbon was much easier than that of CFC 113 and the CFC replacements. The recovery efficiency of CFC replacements depends on the hydrogen atoms in molecule. It is possible that the saturated amount adsorbed in the pores or on the surface of the activated carbon could be evaluated by the W_s constant of the the Langmuir equation and the W_o constant of the Dubinin‐Radushkevich equation. The a constant of the Langmuir equation and the BE_o constant of the Dubinin‐Radushkevich equation depend on the molecular composition.     

Platinum (IV) recovery from chloride solution by functionalized acrylic copolymers

Two acrylic adsorbents with different morphological structures and bearing amidoethylenamine and thiol groups were obtained and used for platinum sorption from chloride solution by the batch method. Physico-chemical parameters that influence adsorption such as initial Pt(IV) concentration, stirring time, pH, and adsorbent amount were investigated. The thermodynamic parameters of Pt(IV) sorption on the synthesized adsorbent were also evaluated based on Langmuir and Freundlich isotherms. Thermodynamic parameters estimated from Langmuir constants indicated that the adsorption is spontaneous, exothermic and there is a disordered state at the molecular level. The models used to analyze the sorption rate led to the conclusion that the most important step in the sorption of Pt(IV) could be both particle diffusion and chemical reaction of [PtCl₆]⁻ with amine functional groups. Thus, both the ion exchange and complex formation mechanisms can occur via nitrogen atoms in the recovery of Pt(IV) on the studied adsorbent.     

Biosorption of nickel(II) from aqueous solution by Aspergillus niger: Response surface methodology and isotherm study

In the present study, the effects of biosorbent Aspergillus niger dosage, initial solution pH and initial Ni(II) concentration on the uptake of Ni(II) by NaOH pretreated biomass of A. niger from aqueous solution were investigated. Batch experiments were carried out in order to model and optimize the biosorption process. The influence of three parameters on the uptake of Ni(II) was described using a response surface methodology (RSM) as well as Langmuir and Freundlich isotherm models. Optimum Ni(II) uptake of 4.82 mg Ni(II) g⁻¹ biomass (70.30%) was achieved at pH 6.25, biomass dosage of 2.98 g L⁻¹ and initial Ni(II) concentration of 30.00 mg L⁻¹ Ni(II). Langmuir and Freundlich were able to describe the biosorption isotherm fairly well. However, prediction of Ni(II) biosorption using Langmuir and Freundlich isotherms was relatively poor in comparison with RSM approaches. The biosorption mechanism was also investigated by using Fourier transfer infrared (FT-IR) analysis of untreated, NaOH pretreated, and Ni(II) loaded A. niger biomass.     

Adsorption of glyphosate on Brazilian subtropical soils rich in iron and aluminum oxides

Abstract

We investigated the adsorption of glyphosate onto five subtropical soils of Paraná and São Paulo states, Brazil, a region of intense agricultural activities, aiming at the determination of kinetic and isotherm adsorption parameters which enable the evaluation of the potential leaching of the herbicide. The adsorption was fast, being described by the pseudo-second order and intraparticle diffusion models, thus suggesting that mixed mechanisms are involved. The Oxisol containing the highest concentrations of metal oxides (209.5?g kg^?1 Fe₂O₃ and 160.2?g kg^?1 Al₂O₃) was the sample with the highest rate constant, indicating the adsorption sites are readily available. All the soils are rich in aluminum and iron oxides, explaining the Freundlich coefficients (K_F) between 642 and 1360?mg^1-1/n kg^?1 L^1/n, which are higher than most of the coefficients described for other soils around the world. The maximum desorption (15% of the adsorbed amount) was observed for the Oxisol. For the other soils, desorption ranged from 2 to 7%. These results suggest that the leaching of free glyphosate to nearby surface and groundwaters is unlikely unless excessive doses are used. The adsorption parameters are useful for managing the right doses applied to the crops, thus avoiding contamination of adjacent areas.     

Partial characterization of the exopolysaccharide from Oscillatoria trichoides Szafer and the role of released polysaccharide in sequestration of Cr6+

The structural investigation and the chromium adsorptive potential of an exopolysaccharide (EPS) released during the growth of an indigenous cyanobacterium, Oscillatoria trichoides Szafer, were investigated in a laboratory‐scale study. The results showed that, of the total EPS produced, 410.53 milligrams/gram (mg g^?1) were released polysaccharides (RPS) and 11.36 mg g^?1 were capsular polysaccharides (CPS). The sorption of hexavalent chromium (Cr⁶⁺) by the RPS achieved a maximum amount of metal removal (q_max) value of 76.92 mg g^?1 of polysaccharide dry weight. The highest coefficient of determination (0.9742) for the Langmuir adsorption model indicates best fitness of the model in explaining the sorption as a unilayer process. Equilibrium studies indicated that 30 to 40 milligrams per liter initial chromium concentration and a pH of 2 were optimal for biosorption of chromium by the RPS. Scanning electron microscopy with energy‐dispersive X‐ray spectroscopy analysis of Cr⁶⁺‐treated RPS showed the presence of 3.76% bound chromium. Compositional analysis of the EPS showed the presence of carbohydrates, proteins, pyruvic acid, and hexosamines. High‐performance liquid chromatography analysis demonstrated the presence of hexoses, as neutral sugars and glucuronic acid as an acidic sugar. The presence of carboxylic groups was also detected by infrared spectroscopy. The presence of these chemical constituents may serve as binding sites for the metal ions; therefore, the RPS of this species appears to be a promising biosorbent for Cr⁶⁺.     

2,4-dichlorophenoxyacetic acid (2,4-D) micropollutant herbicide removing from water using granular and powdered activated carbons: a comparison applied for water treatment and health safety

Abstract

Activated carbons are well-known porous materials as an effective adsorbent used for the removal of emerging contaminants, such as herbicides, which are increasingly present in water bodies. Most water treatment plants, specially in Brazil, are unable to completely remove such contaminants by the conventional process and advanced treatment using activated carbons is required. The aim of this paper was to verify the influence of the activated carbons granulometry and specific surface area on the 2,4-dichlorophenoxyacetic acid (2,4-D) herbicide removal efficiency using distilled-deionized water and filtered water collected from a conventional Water Treatment Plant. Commercial activated carbons samples used in this work were obtained from two different manufacturers. Activated carbons were analyzed by the specific surface area, pore size and volume distribution, nuclear magnetic resonance, infrared and x-ray spectroscopy, moisture, volatile matter and ash contents. Batch adsorption isotherms experiments were used and performed by Langmuir and Freundlich models. Granular and powdered activated carbons removed over 99% of 2,4-D in distilled water and near to 99% using filtered water. The activated carbons evaluated in this work presented high performance and played a key role in water treatment by removing 2,4-D herbicide, ensuring the protection of human health and the ecosystem.     

Thermodynamics of tetracycline adsorption on silica

The adsorption of antibiotic tetracycline onto silica particles was investigated. The effects of pH, electrolyte concentration and temperature on the adsorption equilibrium were examined and the data correlated with a dual site adsorption model. Adsorption of tetracycline onto approximately 9% of the adsorption sites was found to be irreversible, whereas the rest exhibited Langmuir behaviour. Increasing pH of the solution had a strong negative effect on the adsorbed amounts. Adsorption decreased also with increasing ionic strength and temperature. The enthalpy and entropy of adsorption were found to be approximately −16 and −25 J/mol, respectively.     

Sorption of organic compounds to activated carbons. Evaluation of isotherm models

Sorption to ‘hard carbon’ (black carbon, coal, kerogen) in soils and sediments is of major importance for risk assessment of organic pollutants. We argue that activated carbon (AC) may be considered a model sorbent for hard carbon. Here, we evaluate six sorption models on a literature dataset for sorption of 12 compounds onto 12 ACs and one charcoal, at different temperatures (79 isotherms in total). A statistical analysis, accounting for differences in the number of fitting parameters, demonstrates that the dual Langmuir equation is in general superior and/or preferable to the single and triple Langmuir equation, the Freundlich equation, a Polanyi–Dubinin–Manes equation, and the Toth equation. Consequently, the analysis suggests the presence of two types of adsorption sites: a high-energy (HE) type of site and a low-energy (LE) type of site. Maximum adsorption capacities for the HE domain decreased with temperature while those for the LE domain increased. Average Gibbs free energies for adsorption from the hypothetical pure liquid state at 298 K were fairly constant at −15 ± 4 and −5 ± 4 kJ mol⁻¹ for the HE and LE domain, respectively.