Microbial decolorization and degradation of crystal violet dye by <Emphasis Type="Italic">Aspergillus niger</Emphasis>

Two fungi were isolated and examined to decolorize crystal violet dye, frequently used as textile dye and in microorganism staining, using basal salt medium under static condition at 30 °C. The more effective fungus gave less dry weight and lower pH indicating that the process was directed toward the decolorization process giving acidic products rather than microbial growth. The effective fungus was identified as Aspergillus niger and was used in the rest of experiments. Increasing the incubation period more than 10 days did not improve the decolorization process, while the best pH was 5.5. The decolorization process was effective (up to 84.6 %) with the examined range of dye concentrations (10–40 ppm). Sucrose content, as a carbon source, more than 1 % did not improve the decolorization process (80.9 %). Using ammonium sulfate as a nitrogen source, instead of sodium nitrate in the original basal medium, lowered the decolorization process, while using corn steep liquor enhanced the biodegradation up to 96.1 %. Although the dye violet color vanishes in acid medium because of decreasing the possibility of extending the benzene chromophore as a result of binding the nitrogen lone pair in the ammonium ion, the UV–Vis spectra and LC–MS–ESI analysis of the bioassay products proved that the decolorization is due to the biodegradation of the dye rather than the resonance factor in acidic medium or biosorption by fungus mycelia.     

Response surface methodology mediated optimization of Remazol Orange decolorization in plain distilled water by Pseudomonas aeruginosa BCH

The bacterium Pseudomonas aeruginosa BCH decolorized and degraded the sulphonated azo dye Remazol Orange in plain distilled water. The effects of different parameters, i.e. pH, temperature and cell mass concentration on the biodegradation of dye in aqueous phase was evaluated using response surface methodology. Optimization was carried out using three-level Box–Behnken design. Predicted values were found to be in good agreement with experimental values (R ² 0.9997 and pred R ² 0.9984), which indicated suitability of the employed model and the success of response surface methodology. Optimum dye decolorization was maximized and the favourable conditions were pH 7.43, temperature 29.39 °C and cell mass concentration 2.88 g l^?1, which resulted in 96.01 % decolorization within 5 h. It was validated from the predicted response (97.37 %). According to the analysis of variance results, the proposed model can be used to navigate the design space. 3D plot analysis disclosed the significant interaction between all three tested factors on decolorization process. The combinations of the three variables predicted during response surface methodology were confirmed through confirmatory experiments. Observations indicated that higher cell mass accelerated the decolorization process. Degradation of the dye was verified through high performance liquid chromatography analysis. Phytotoxicity studies carried out with dye and dye metabolites using Phaseolus mungo, Triticum aestivum and Sorghum vulgare indicated the detoxification of dye.     

Kinetics of Mn(II) oxidation by Leptothrix discophora SS1

The kinetics of Mn(II) oxidation by the bacterium Leptothrix discophora SS1 was investigated in this research. Cells were grown in a minimal mineral salts medium in which chemical speciation was well defined. Mn(II) oxidation was observed in a bioreactor under controlled conditions with pH, O₂, and temperature regulation. Mn(II) oxidation experiments were performed at cell concentrations between 24 mg/L and 35 mg/L, over a pH range from 6 to 8.5, between temperatures of 10°C and 40°C, over a dissolved oxygen range of 0 to 8.05 mg/L, and with L. discophora SS1 cells that were grown in the presence of Cu concentrations ranging from zero to 0.1 μM. Mn(II) oxidation rates were determined when the cultures grew to stationary phase and were found to be directly proportional to O₂ and cell concentrations over the ranges investigated. The optimum pH for Mn(II) oxidation was approximately 7.5, and the optimum temperature was 30°C. A Cu level as low as 0.02 μM was found to inhibit the growth rate and yield of L. discophora SS1 observed in shake flasks, while Cu levels between 0.02 and 0.1 μM stimulated the Mn(II) oxidation rate observed in bioreactors. An overall rate law for Mn(II) oxidation by L. discophora as a function of pH, temperature, dissolved oxygen concentration (D.O.), and Cu concentration is proposed. At circumneutral pH, the rate of biologically mediated Mn(II) oxidation is likely to exceed homogeneous abiotic Mn(II) oxidation at relatively low (≈μg/L) concentrations of Mn oxidizing bacteria.     

Biosorption of ammoniacal nitrogen from aqueous solutions with low-cost biomaterials: kinetics and optimization of contact time

The biosorption of ammoniacal nitrogen (N-NH₄ ⁺) from aqueous solutions by dead biomass of brown seaweed Cystoseira indica and Jatropha oil cake (JOC), which is generated in the process of biodiesel recovery from its seeds, was studied under diverse experimental conditions. The N-NH₄ ⁺ biosorption was strictly pH dependent, and maximum uptake capacity of C. indica (15.21 mg/g) and JOC (13.59 mg/g) was observed at initial pH 7 and 3, respectively. For each biosorbent–N-NH₄ ⁺ system, kinetic models were applied to the experimental data to examine the mechanisms of sorption and potential rate-controlling steps. The generalized rate model and pseudo-second-order kinetic models described the biosorption kinetics accurately, and the sorption process was found to be controlled by pore and surface diffusion for these biosorbents. Results of four-stage batch biosorber design analysis revealed that the required time for the 99 % efficiency removal of 40 mg/L N-NH₄ ⁺ from 500 L of aqueous solution were 76 and 96 min for C. indica and JOC, respectively. The Fourier transform infrared spectroscopy analysis before and after biosorption of ammonium onto C. indica and JOC revealed involvement of carboxylic and hydroxyl functional groups.     

Effects of pH on ferri-cyanide uptake and assimilation by several plants

This paper presents an investigation of the capacity of four different plants to remove and assimilate ferri-cyanide at different pH conditions. Detached roots of weeping willows (Salix babylonica L.), rice (Oryza sativa L. cv. JY 98), soybean (Glycine max L. cv. WH) and maize (Zea mays L. var. HK) were hydroponically exposed to ferri-cyanide in a closed system at 25?±?0.5°C for 24?h kept under darkness. Almost all applied ferri-cyanide was in the complex form in the hydroponic solution at pH????7.0 in the absence of light, while dissociation of ferri-cyanide to free cyanide and iron in solution was detected at pH????6.5. All plant species used were found to be able to remove and assimilate ferri-cyanide efficiently. The uptake and assimilation rates appeared to be inversely related to the pH, in which positive effects were observed at pH 6.0 and 6.5. Remarkable decreases in the assimilation rates were found at pH 8.0. Results presented here suggest that changes in solution pH have a substantial influence on not only the speciation of ferri-cyanide in the plant growth media, but also the uptake and assimilation mechanisms of ferri-cyanide by plants.     

Characterization of bioflocculants produced by bacteria isolated from crude petroleum oil

The aim of this study was to look for high efficient bioflocculant-producing microorganisms. Among 36 bacterial colonies isolated from a crude petroleum oil sample, three of them as Bacillus subtilis and Pseudomonas spp. exhibited flocculation activity exceeding 90 % after 3 days of cultivation. They were identified by 16 S rDNA sequence analysis as Bacillus subtilis and Pseudomonas sp. Spectroscopic analysis of the polymers by nuclear magnetic resonance and fourier-transform infrared revealed that the polymers were glycoproteins. These polymers were soluble in water and insoluble in any organic solvents tested. The effects of bioflocculant dosage, temperature and pH on the flocculation activity were evaluated. The maximum bioflocculation activities were observed at an optimum bioflocculant dosage of 3.5 mg/L (strains Bacillus subtilis and Pseudomonas) and 5.0 mg/L (strain CPO14), respectively. In addition, these biopolymers were able to flocculate kaolin suspension (5 g/L) over a wide range of pH (pH 3–9) and temperature (5–50 °C) tested in the presence of CaCl₂. The highest flocculation activities of strains CPO8, CPO13 and CPO14 were 96.03 %, 92.17 % and 97.59 %, respectively in the early stationary phase (at 24 h), while the cell production reached its maximum in the stationary phase (at 72 h). Their efficient flocculation capabilities suggest potential applications in industries.     

Co-metabolic decolorization of a textile reactive dye by <Emphasis Type="Italic">Aspergillus fumigatus</Emphasis>

In the present study, a widely used reactive dye, Color Index (C.I.) Reactive Blue 268 was utilized for mycoremediation by Aspergillus fumigatus isolated from textile effluent. Complete decolorization of the test dye (0.1 g L^?1) was recorded within 6 days of static incubation at 27 °C in Czapek Dox broth (CDB). However, the isolate was unable to utilize the dye as a sole source of energy in Czapek Dox agar and CDB in absence of sucrose and obligate requirement of a labile carbon source, i.e., sucrose needed for induction of decolorization. Biosorption seems to play the pivotal role in decolorization as evident by coloring of the fungal biomass as that of dye color. The optimal conditions for the highest decolorization were found at 30 °C and pH 6.0 with 6-day-old inoculums supplemented with sucrose (10 g L^?1) and ammonium chloride (2 g L^?1) as a carbon and nitrogen source, respectively. The response of the isolate to increasing dye concentrations was found to be growth inhibitory. Surprisingly, about 65 % of dye decolorization was recorded with heat-inactivated biomass powder within 6 days of static incubation supporting the fact of fungal biosorption. Results of this study have established the candidature of the isolate for biotechnological removal of dyes from disreputable dying effluents.     

Effect of leachate loading rate and incubation period on the treatment efficiency by T. versicolor immobilized on foam cubes

This study focuses on treatment of landfill leachate in column experiments by immobilized Trametes versicolor on polyurethane foam, collected from Nonthaburi landfill site, Thailand. In this study, glucose was used as a co-substrate. The effect of biomass growth on color removal was observed by immobilizing fungi on polyurethane foam. The same immobilized fungi were used for four cycles of 5 days each to find the reuse of fungi. Leachate was diluted to see the effect of organic loading on color removal. At optimum pH of 4 and in 20 days with 3 g/L of glucose, the fungi could decolorize 78 % and 63 % for 5-times dilution and concentrated leachate, respectively, using immobilized fungi after 4 days initial growth. Fungi could also reduce biological oxygen demand and chemical oxygen demand of 52 % and 42 % (with initial biological oxygen demand and chemical oxygen demand of 48,900 and 96,512 mg/L), respectively, with glucose 3 g/L in concentrate leachate and with 4 days initial immobilization of fungi on polyurethane foam. About 1–6% higher color removal was observed on day 20 with 15 days fungi immobilization initially as compared to 4 days immobilization. Higher removal efficiency was observed for the same leachate after dilution due to reduction in organic loading. Addition of co-substrate enhances significantly removal of color, biological oxygen demand and chemical oxygen demand. Chemical oxygen demand removal reached to 0.6 mg/mg of biomass with the co-substrate. Therefore, white rot fungi can be considered as potentially useful microorganisms in landfill leachate treatment.     

天然金红石光催化降解藏红T实验研究

以低压汞灯为光源研究了天然金红石悬浆体系中藏红T的脱色条件及其光催化反应动力学，讨论了溶液初始pH值、催化剂投入量、光强、气流量、催化剂粒径、反应气氛等实验条件对藏红T脱色速率的影响，阐述了实验过程中无机离子的生成情况。结果表明，该反应基本上符合一级反应动力学；在酸性条件下尤其是当溶液初始pH值为2．5时，藏红T的脱色速率要比在碱性和中性条件下快得多；增加光强度能较大地提高反应的降解速率；催化剂最佳投入量为1．3g／L；在氧化气氛下该反应比在非氧化气氛快得多；通入气体的流量在40L／h最合适；反应溶液中有氯离子溶出说明有机物中的含氯部分被降解。本研究为光催化作用降解有机污染物提供了新的途径。     

Response surface methodology (RSM) optimization approach for degradation of Direct Blue 71 dye using CuO–ZnO nanocomposite

The present study highlights the synthesis of CuO–ZnO nanocomposite via facile hydrothermal method at 150 °C and autogenous pressure. The structural and textural features of prepared composite material was characterized by several characterization techniques such as X-ray powder diffraction, Fourier transform infrared spectroscopy, Scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The optimized prepared nanocomposite was utilized for photocatalytic degradation of aromatic Direct Blue 71 dye (DB71) under natural sunlight conditions. The catalytic activity results by CuO–ZnO nanocomposite were observed to be higher than the reagent-grade zinc oxide under visible light conditions. The response surface methodology protocol (RSM) with central composite design was optimized by different photodegradation operational parameters such as pH, dye concentration, catalyst amount, and reaction time. The optimized RSM results demonstrated that a quadratic polynomial model was found suitable to define the relation between the photocatalytic activity and operational parameters. Moreover, the observed high R ² value (0.9786) confirms a strong evaluation of experimental data. To achieve maximum DB71 degradation, optimized condition was found at 177.13 min of contact time, 3.93 solution pH, and 24.34 mg/L of dye concentration with 1.85 g/L of catalyst dose The identical optimum conditions resulted maximum 89.58% DB71 degradation.     

Biodegradation of Cypermethrin by a newly isolated actinomycetes HU-S-01 from wastewater sludge

A new cypermethrin degrading strain was isolated from wastewater sludge using enrichment technique. On the basis of morphological, physiological, biochemical characteristics tests and 16S rDNA sequence analysis, the strain was determined to be a Streptomyces species, probably a strain of Streptomyces parvulus, so it was designated as Streptomyces sp. HU-S-01. The strain Streptomyces sp. HU-S-01 is aerobic and optimum growth temperature for the strain was found to be 26–28 °C with initial pH range 6.0-9.0 and pH 7.5 was found to be the optimum. This strain can also completely degrade 3-phenoxybenzoic acid within 96 h at the concentration of 50 mg/L. The kinetic constants Vmax, Km, Kcat and Kcat/ Km of enzyme for cypermethrin were 1.236 ?mol/min, 6.418 ?mol/mL, 13.493 min and 2.102 mL/mol.min, respectively. The degradation products of cypermethrin were identified using gas chromatographmass spectrometric (GC-MS) analysis. The degradation pathway followed by HU-S-01 involves oxidative as well as hydrolyzing. Biodegradation ability of strain Streptomyces sp. HU-S-01 without toxic byproducts reveals its potential for further study as a biological agent for the remediation of soil, water or crops, contaminated with cypermethrin.     

NaOH-treated dead leaves of <Emphasis Type="Italic">Ficus racemosa</Emphasis> as an efficient biosorbent for Acid Blue 25 removal

A novel biosorbent synthesized from Ficus racemosa leaves based on the treatment using NaOH was applied for removal of Acid Blue 25 from aqueous solution. The synthesized biosorbent was characterized using scanning electron microscopy, Fourier transform infrared spectroscopy and Brunauer–Emmett–Teller analysis. NaOH treatment was demonstrated to remove lignin content from the biomass and to induce the development of significant pores. Batch experiments were performed to evaluate the effect of important operating parameters such as pH (range of 2–10), biosorbent dose (range of 1–10 g/L), contact time (range of 0–5 h), initial dye concentration (range of 50–400 mg/L) and temperature (range of 293–323 K) on the extent of removal of Acid Blue 25. The established optimum conditions were pH of 2, biosorbent dose of 4 g/L, contact time of 3 h and temperature of 323 K, yielding maximum removal of dye. Pseudo-second-order model was found to best fit the kinetic data. Langmuir and Temkin isotherm models were found to best fit the equilibrium data. The obtained thermodynamic parameters confirmed endothermic and spontaneous nature of adsorption. The study established the utility of novel biosorbent for removal of Acid Blue 25 with higher adsorption capacities (83.33 mg/g) as compared to the more commonly used adsorbents. Desorption-adsorption  studies conducted for seven cycles indicated potential reusability of synthesized biosorbent for the treatment of dye effluents.     

Biosorption of fluoride by water lettuce (<Emphasis Type="Italic">Pistia stratiotes</Emphasis>) from contaminated water

Phytoremediation is a proven low-cost and sustainable method for the removal of toxic pollutants from water. This green technology has been practiced for the past several years all over the world. In the present study, the interaction of fluoride on the surface of the floating aquatic plant water lettuce (Pistia stratiotes) during fluoride removal was investigated. Batch kinetic studies were performed to examine the fluoride uptake capacity of the plant with different initial fluoride concentrations such as 3, 5, 10, and 20 mg/L. The effects of various process parameters on fluoride uptake dynamics such as pH, plant biomass, initial fluoride concentration, and time were examined. Freundlich’s isotherm model was found to (R ² = 0.957) fit well to the experimental data. The nature of reaction order followed pseudo-first-order kinetics, when the initial fluoride level in the solution was 5 mg/L. The experimental findings showed that the removal mechanism was driven by biosorption phenomenon. High fluoride concentration in the solution reduced the growth ratio of P. stratiotes. The lowest growth ratio of this aquatic macrophyte was found to be 76.80 ± 3.73% at 20 mg/L fluoride concentration. At lower fluoride concentrations such as 3 and 5 mg/L, the growth ratio of the plant was not reduced significantly.     

Removal of heavy metals from paint industry’s wastewater using Leca as an available adsorbent

The ability of light expanded clay aggregate to remove lead and cadmium from paint industry’s effluents was studied at different levels of adsorbent, contact time and pH in April 2008. For this purpose, lead and cadmium removal from paint industry effluents were studied in batch reactors. lead and cadmium measurements have been taken with non-flame atomic absorption techniques and test methods were adapted from 19^th. Ed. of standard methods for the examination of water and wastewater. In this study, different amounts of Leca (1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 g/L) were investigated. The amount of adsorbed lead and cadmium exposure to Leca increased from 1.41 to 3 mg/g and 0.22 to 0.75 mg/g, respectively. The maximum removal efficiency for Pb was 93.75 % at pH = 7 and exposure to 10 g/L of Leca, while for cadmium, it was nearly 89.7 % at the same condition. In this study, adsorption process of lead and cadmium was fitted with Freundlich adsorption isotherm (R² _Pb = 0.97 and R² _Cd = 0.98). The sufficient contact time was deemed 1–2 h for lead and cadmium. According to the results, Leca is recommended as a low cost and available adsorbent to remove lead and cadmium from industrial wastewater.     

Sodium-cadmium and sodium-zinc exchangeability in montmorillonite

A sodium montmorillonite from Ivan?ice (Czech Republic) was treated with solutions containing various molar concentrations of Zn and Cd for the purpose of determining ion exchange equilibria. The sorption isotherms for Zn and Cd exhibit a rather similar shape, which depends on pH; the maxima for Zn and Cd sorbed on Na-montmorillonite are very close to each other (e.g., 0.419?mmol/1?g and 0.440?mmol/1?g, respectively, for pH=5). It is a characteristic of both elements that a high level of sorption is reached at low concentration in solution. The leachability of Zn and Cd in deionized water from fully saturated montmorillonites is very similar, but a different results were observed for Na leached from fully saturated Na-montmorillonite. The total amount of leached Na was 21.7% (after four consecutive leaching runs). However, only 2.1% and 1.6% were found for Cd and Zn, respectively. Different quantities of Cd and Zn exchanged in Na-montmorillonite influence significantly the shape and position of maximum of the 001 XRD profile. Experimental XRD profiles of montmorillonites, fully saturated with Na, Cd and Zn, corrected for instrumental and physical factors exhibit maxima at 12.59, 14.86, and 14.77?Å, respectively. When the d ₀₀₁ spacing is determined from a corrected profile, it varies systematically with the percentage of exchanged Zn and Cd and the relationships seem to be linear for both elements. For montmorillonites, not fully saturated with one element, the peak shift and peak broadening, characteristic for mixed layered structures with random layer sequences, has been observed.     

Synergistic degradation of diazo dye Direct Red 5B by Portulaca grandiflora and Pseudomonas putida

Plants and bacterial consortium of Portulaca grandiflora and Pseudomonas putida showed complete decolorization of a sulfonated diazo dye Direct Red 5B within 72 h, while in vitro cultures of P. grandiflora and P. putida independently showed 92 and 81 % decolorization within 96 h, respectively. A significant induction in the activities of lignin peroxidase, tyrosinase, 2,6-dichlorophenol indophenol reductase and riboflavin reductase was observed in the roots of P. grandiflora during dye decolorization; whereas, the activities of laccase, veratryl alcohol oxidase and 2,6-dichlorophenol indophenol reductase were induced in the cells of P. putida. Plant and bacterial enzymes in the consortium gave an enhanced decolorization of Direct Red 5B synergistically. The metabolites formed after dye degradation analyzed by UV–Vis spectroscopy, Fourier transformed infrared spectroscopy and high performance liquid chromatography confirmed the biotransformation of Direct Red 5B. Differential fate of metabolism of Direct Red 5B by P. grandiflora, P. putida and their consortium were proposed with the help of gas chromatography–mass spectroscopy analysis. P. grandiflora metabolized the dye to give 1-(4-diazenylphenyl)-2-phenyldiazene, 7-(benzylamino) naphthalene-2-sulfonic acid, 7-aminonaphthalene-2-sulfonic acid and methylbenzene. P. putida gave 4-hydroxybenzenesulfonic acid and 4-hydroxynaphthalene-2-sulfonic acid and benzamide. Consortium showed the formation of benzenesulfonic acid, 4-diazenylphenol, 6-aminonaphthalen-1-ol, methylbenzene and naphthalen-1-ol. Consortium achieved an enhanced and efficient degradation of Direct Red 5B. Phytotoxicity study revealed the nontoxic nature of metabolites formed after parent dye degradation. Use of such combinatorial systems of plant and bacteria could prove to be an effective and efficient strategy for the removal of textile dyes from soil and waterways.     

Optimization of aqueous methylparathion biodegradation by Fusarium sp in batch scale process using response surface methodology

Biotreatment of methylparathion (O,O-dimethyl-O-4-nitrophenyl phosphorothioate) was studied in aqueous mineral salts medium containing fungal culture to demonstrate the potential of the pure culture (monoculture) of Fusarium sp in degrading high concentration of methylparathion. A statistical Box–Behnken design of experiments was performed to evaluate the effects of individual operating variables and their interactions on the methylparathion removal with initial concentration of 1,000 mg/L as fixed input parameter. A full factorial Box–Behnken design of experiments was used to construct response surfaces with the removal, the extent of methylparathion biodegradation, removal of chemical oxygen demand and total organic carbon, and the specific growth rate as responses. The temperature (X ₁), pH (X ₂), reaction time (X ₃) and agitation (X ₄) were used as design variables. The result was shown that experimental data fitted with the polynomial model. Analysis of variance showed a high coefficient of determination value of 0.99. The maximum biodegradation of methylparathion in terms of the methylparathion removal (Y ₁), chemical oxygen demand removal (Y ₂) and total organic carbon removal (Y ₃) were found to be 92, 79.2 and 57.2 % respectively. The maximum growth in terms of dry biomass (Y ₄) was 150 mg/L. The maximum biodegradation corresponds to the combination of following factors of middle level of temperature (X ₁ = 30 °C), pH (X ₂ = 6.5), agitation (X ₄ = 120 rpm) and the highest level of reaction time (X ₃ = 144 h). The removal efficiency of methylparathion biodegradation was achieved 92 %. It was observed that optimum biotreatment of methylparathion can be successfully predicted by response surface methodology.     

Ni(II) sorption on natural chlorite

Sorption of Ni(II) onto chlorite surfaces was studied as a function of pH (5–10), ionic strength (0.01–0.5 M) and Ni concentration (10⁻⁸–10⁻⁶ M) in an Ar atmosphere using batch sorption with radioactive ⁶³Ni as tracer. Such studies are important since Ni(II) is one of the major activation products in spent nuclear fuel and sorption data on minerals such as chlorite are lacking. The sorption of Ni(II) onto chlorite was dependent on pH but not ionic strength, which indicates that the process primarily comprises sorption by surface complexation. The maximum sorption was at pH ∼ 8 (K_d = ∼10⁻³ cm³/g). Desorption studies over a period of 1–2 weeks involving replacement of the aqueous solution indicated a low degree of desorption. The acid–base properties of the chlorite mineral were determined by titration and described using a non-electrostatic surface complexation model in FITEQL. A 2-pK NEM model and three surface complexes, Chl_OHNi²⁺, Chl_OHNi(OH)⁺ and Chl_OHNi(OH)₂, gave the best fit to the sorption results using FITEQL. The high K_d values and low degree of desorption observed indicate that under expected groundwater conditions, a large fraction of Ni(II) that is potentially leachable from spent nuclear fuel may be prevented from migrating by sorption onto chlorite surfaces.     

Biotite weathering and nutrient uptake by ectomycorrhizal fungus, Suillus tomentosus, in liquid-culture experiments

Ectomycorrhiza-forming fungi (EMF) alter the nutrient-acquisition capabilities of vascular plants, and may play an important role in mineral weathering and the partitioning of products of weathering in soils under nutrient-limited conditions. In this study, we isolated the weathering function of Suillus tomentosus in liquid-cultures with biotite micas incubated at room temperature. We hypothesized that the fungus would accelerate weathering by hyphal attachment to biotite surfaces and transmission of nutrient cations via direct exchange into the fungal biomass. We combined a mass-balance approach with scanning electron microscopy (SEM) and atomic force microscopy (AFM) to estimate weathering rates and study dissolution features on biotite surfaces. Weathering of biotite flakes was about 2-3 orders of magnitude faster in shaken liquid-cultures with fungus compared to shaken controls without fungus, but with added inorganic acids. Adding fungus in nonshaken cultures caused a higher dissolution rate than in inorganic pH controls without fungus, but it was not significantly faster than organic pH controls without fungus. The K⁺, Mg²⁺ and Fe²⁺ from biotite were preferentially partitioned into fungal biomass in the shaken cultures, while in the nonshaken cultures, K⁺ and Mg²⁺ was lost from biomass and Fe²⁺ bioaccumulated much less. Fungal hyphae attached to biotite surfaces, but no significant surface changes were detected by SEM. When cultures were shaken, the AFM images of basal planes appeared to be rougher and had abundant dissolution channels, but such channel development was minor in nonshaken conditions. Even under shaken conditions the channels only accounted for only 1/100 of the total dissolution rate of 2.7 × 10⁻¹⁰ mol of biotite m⁻² s⁻¹. The results suggest that fungal weathering predominantly occurred not by attachment and direct transfer of nutrients via hyphae, but because of the acidification of the bulk liquid by organic acids, fungal respiration (CO₂), and complexation of cations which accelerated dissolution of biotite. Results further suggest that both carbohydrate source (abundant here) and a host with which nutrients are exchanged (missing here) may be required for EMF to exert an important weathering effect in soils. Unsaturated conditions and physical dispersal of nutrient-rich minerals in soils may also confer a benefit for hyphal growth and attachment, and promote the attachment-mediated weathering which has been observed elsewhere on soil mineral surfaces.     

Optimization of ammonia removal by ion-exchange resin using response surface methodology

The ability of ion-exchange resin for ammonia removal from aqueous solution was studied. The results showed that Amberlite ion-exchange resin was effective in removing ammonia from aqueous solution. Factorial design and response surface methodology were applied to evaluate and optimize the effects of pH, resin dose, contact time, temperature and initial ammonia concentration. Low pH condition was preferred with the optimum pH found to be 6. High resin dose generated high removal rate and low exchange capacity. Results of factorial design and response surface methodology showed that temperature was not a significant parameter. The model prediction was in good agreement with observed data (R ² = 0.957). The optimum Q _e was 28.78 mg/g achieved at pH = 6 and initial TAN concentration of 3000 mg/L. The kinetics followed the pseudo-second-order kinetic model (R ² = 0.999). Equilibrium data were fitted to Langmuir and Freundlich isotherm models with Langmuir model providing a slightly better predication (R ² = 0.996). The resin was completely regenerated by 2 N H₂SO₄.