scholarly journals The effect of the size of particles on mineralization of Oxycaryum cubense (Poepp. & Kunth) Lye

2006 ◽  
Vol 66 (2b) ◽  
pp. 641-650 ◽  
Author(s):  
I. Bianchini Jr. ◽  
M. B. Cunha-Santino
Keyword(s):  
Dissolved Oxygen ◽  
Aquatic Macrophyte ◽  
Tap Water ◽  
Oxbow Lake ◽  
Order Kinetic ◽  
Dissolved Ions ◽  
Order Kinetic Model ◽  
Mineralization Processes ◽  
Size Of Particles ◽  
Fragmentation Processes

Assays were carried out to evaluate effects of detritus size on the mineralization of an aquatic macrophyte, the Oxycaryum cubense. Samples of plant and water were collected from an oxbow lake, the Infernão lagoon (21° 35' S and 47° 51' W) located at Mogi Guaçu river floodplain. The plants were taken to the laboratory, washed under tap water, dried (50 °C) and fractioned into six groups according to their size, viz. 100, 10, 1.13, 0.78, 0.61 and 0.25 mm. Decomposition chambers were prepared by adding 1.0 g of plant fragments to 4.1 L of water lagoon. In sequence, the incubations were aerated and the concentrations of dissolved oxygen, the pH, the electric conductivity and the temperature were monitored for 120 days. The occurrence of anaerobic processes was avoided by reoxygenating the solutions. The experimental results were fitted to a first order kinetic model and the consumption of dissolved oxygen from mineralization processes was obtained. The physical process of fragmentation of O. cubense detritus is unlikely to promote the consumption of higher quantities of dissolved oxygen in mineralization processes meaning that fragmentation should not interfere in the balance of DO in this aquatic system, however fragmentation processes favored the acidification and increased the liberation of dissolved ions from the Infernão lagoon.

scholarly journals Uranium biosorption from aqueous solution by the submerged aquatic plant Hydrilla verticillata

2016 ◽  
Vol 75 (6) ◽  
pp. 1332-1341 ◽  
Author(s):  
Zheng-ji Yi ◽  
Jun Yao ◽  
Mi-jia Zhu ◽  
Hui-lun Chen ◽  
Fei Wang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Aquatic Macrophyte ◽  
Hydrilla Verticillata ◽  
Hydroxyl Groups ◽  
Order Kinetic ◽  
Experimental Conditions ◽  
Submerged Aquatic Plant ◽  
Isotherm Adsorption ◽  
Order Kinetic Model

The biosorption characteristics of U(VI) from aqueous solution onto a nonliving aquatic macrophyte, Hydrilla verticillata (dry powder), were investigated under various experimental conditions by using batch methods. Results showed that the adsorption reached equilibrium within 60 min and the experimental data were well fitted by the pseudo-first-order kinetic model. U(VI) adsorption was strongly pH dependent, and the optimum pH for U(VI) removal was 5.5. Isotherm adsorption data displayed good correlation with the Langmuir model, with a maximum monolayer adsorption capacity of 171.52 mg/g. Thermodynamic studies suggested that U(VI) adsorption onto H. verticillata was an exothermic and spontaneous process in nature. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy indicated that the amino and hydroxyl groups on the algal surface played an important role in U(VI) adsorption. The mechanisms responsible for U(VI) adsorption could involve electrostatic attraction and ion exchange. In conclusion, H. verticillata biomass showed good potential as an adsorption material for the removal of uranium contaminants in aqueous solution.

scholarly journals Q10 of heterotrophic activity during aerobic decomposition of Utricularia breviscapa and its effect on carbon cycling in a tropical lagoon

2010 ◽  
Vol 70 (2) ◽  
pp. 317-324 ◽  
Author(s):  
MB Cunha-Santino ◽  
I Bianchini Júnior
Keyword(s):  
Dissolved Oxygen ◽  
Temporal Variations ◽  
Summer Temperature ◽  
Order Kinetic ◽  
First Order ◽  
Order Kinetic Model ◽  
Aerobic Decomposition ◽  
Set Up ◽  
Increasing Temperature ◽  
Carbon Concentrations

In this study the Q10 coefficients of heterotrophic activities were measured during aerobic decomposition of Utricularia breviscapa Wright ex Griseb from Óleo lagoon (21° 36' S and 49° 47' W), Luiz Antonio, SP. The bioassays were set up with fragments of U. breviscapa and incubated with lagoon water at distinct temperatures (15.3, 20.8, 25.7 and 30.3 °C). Periodically for 95 days, the concentrations of dissolved oxygen were determined in the bioassays. The results of the temporal variation of dissolved oxygen were fitted to a first-order kinetic model. The stoichiometric relations were calculated on the basis of these fittings. In general, the results allowed us to conclude: i) the oxygen/carbon stoichiometric relations (O/C) varied in function of temperature and time. The temporal variations of the O/C observed in the decomposition of U. breviscapa, suggest that, in the initial phases of the process, low organic carbon concentrations were enough to generate great demands of oxygen, ii) the oxygen consumption coefficients (k d) presented low variation in function of increasing temperature, iii) the increment of the temperature induced a higher consumption of oxygen (COmax) and iv) the simulations indicate that during summer, temperature activates the metabolism of decomposing microbiota.

scholarly journals Implication of anaerobic and aerobic decomposition of Eichhornia azurea (Sw.) Kunth. on the carbon cycling in a subtropical reservoir

2014 ◽  
Vol 74 (1) ◽  
pp. 100-110 ◽  
Author(s):  
I Bianchini Junior ◽  
MB Cunha-Santino ◽  
JU Ribeiro ◽  
DGB Penteado
Keyword(s):  
Mass Loss ◽  
Aquatic Macrophyte ◽  
Aerobic Condition ◽  
Decay Rates ◽  
Order Kinetic ◽  
Reservoir Water ◽  
Eichhornia Azurea ◽  
Order Kinetic Model ◽  
Aerobic Decomposition ◽  
Aerobic And Anaerobic

This study aimed at describing kinetic aspects of aerobic and anaerobic mineralization of Eicchornia azurea. The samples of aquatic macrophyte and water were collected in the Monjolinho Reservoir (22° 00′ S and 47° 54′ W). To determine the leachate potential, dried plant fragments were added to reservoir water, with sampling lasting for 4 months, where the particulate and dissolved organic carbon concentrations were measured. The kinetics of mass loss was obtained with 10 mineralization chambers for both aerobic and anaerobic conditions, with the plant fragments and reservoir water. Two additional chambers were used to monitor the volume of gases produced from anaerobic mineralization, with bioassays to determine oxygen uptake. The results were fitted to a first-order kinetic model, from which 27.21% of detritus corresponded to labile/soluble fractions and 72.62% to the refractory fractions. The decay rates for the global mass losses of the labile/soluble components were 2.07 day–1. DOC mineralization was not verified for either condition. Under aerobic condition, the mass loss constant rate (0.0029 day–1) for the refractory fractions was 2.4 the value for the anaerobic one. Under anaerobic condition, the gases formation occurred in three phases. Based on these results, in the Monjolinho Reservoir, the decomposition of E. azurea that undergo within the water column and in upper layers of sediment is a faster process, favoring the mineralization. In contrast, in the lower layers of sediment the diagenetic processes (i.e. humus production and accumulation of organic matter) are favored.

Chitosan-based Magnetic Composites - Efficient Adsorbents for Removal of Pb(II) and Cu(II) from Aqueous Mono and Bicomponent Solutions

2018 ◽  
Vol 69 (9) ◽  
pp. 2323-2330 ◽  
Author(s):  
Daniela C. Culita ◽  
Claudia Maria Simonescu ◽  
Rodica Elena Patescu ◽  
Nicolae Stanica
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Chemical Properties ◽  
Order Kinetic ◽  
Mass Ratio ◽  
Magnetic Adsorbent ◽  
Magnetic Composites ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Physical And Chemical

A series of three chitosan-based magnetic composites was prepared through a simple coprecipitation method. It was investigated the influence of mass ratio between chitosan and magnetite on the physical and chemical properties of the composites in order to establish the optimum conditions for obtaining a composite with good adsorption capacity for Pb(II) and Cu(II) from mono and bicomponent aqueous solutions. It was found that the microspheres prepared using mass ratio chitosan / magnetite 1.25/1, having a saturation magnetization of 15 emu g--1, are the best to be used as adsorbent for the metal ions. The influence of different parameters such as initial pH values, contact time, initial concentration of metal ions, on the adsorption of Pb(II) and Cu(II) onto the chitosan-based magnetic adsorbent was investigated in details. The adsorption process fits the pseudo-second-order kinetic model in both mono and bicomponent systems, and the maximum adsorption capacities calculated on the basis of the Langmuir model were 79.4 mg g--1 for Pb(II) and 48.5 mg g--1 for Cu(II) in monocomponent systems, while in bicomponent systems were 88.3 and 49.5 mg g--1, respectively. The results revealed that the as prepared chitosan-based magnetic adsorbent can be an effective and promising adsorbent for Pb(II) and Cu(II) from mono and bicomponent aqueous solutions.

Comparison of the fixation of several metal ions onto a low-cost biopolymer

2002 ◽  
Vol 2 (5-6) ◽  
pp. 217-224 ◽  
Author(s):  
Z. Reddad ◽  
C. Gérente ◽  
Y. Andrès ◽  
P. Le Cloirec
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Low Cost ◽  
Operating Conditions ◽  
Order Kinetic ◽  
Adsorption Mechanisms ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Beet Pulp ◽  
Removal Of Metal Ions

In the present work, sugar beet pulp, a common waste from the sugar refining industry, was studied in the removal of metal ions from aqueous solutions. The ability of this cheap biopolymer to sorb several metals namely Pb2+, Cu2+, Zn2+, Cd2+ and Ni2+ in aqueous solutions was investigated. The metal fixation capacities of the sorbent were determined according to operating conditions and the fixation mechanisms were identified. The biopolymer has shown high elimination rates and interesting metal fixation capacities. A pseudo-second-order kinetic model was tested to investigate the adsorption mechanisms. The kinetic parameters of the model were calculated and discussed. For 8 × 10-4 M initial metal concentration, the initial sorption rates (v0) ranged from 0.063 mmol.g-1.min-1 for Pb2+ to 0.275 mmol.g-1.min-1 for Ni2+ ions, with the order: Ni2+ > Cd2+ > Zn2+ > Cu2+ > Pb2+. The equilibrium data fitted well with the Langmuir model and showed the following affinity order of the material: Pb2+ > Cu2+ > Zn2+ > Cd2+ > Ni2+. Then, the kinetic and equilibrium parameters calculated qm and v0 were tentatively correlated to the properties of the metals. Finally, equilibrium experiments in multimetallic systems were performed to study the competition of the fixation of Pb2+, Zn2+ and Ni2+ cations. In all cases, the metal fixation onto the biopolymer was found to be favourable in multicomponent systems. Based on these results, it is demonstrated that this biosorbent represents a low-cost solution for the treatment of metal-polluted wastewaters.

Synthesis of Functionalized Magnetite Titanium Dioxide Nanocomposite for Removal of Acid Fuchsine Dye

2018 ◽  
Vol 21 (8) ◽  
pp. 583-593 ◽  
Author(s):  
Sara Rahnama ◽  
Shahab Shariati ◽  
Faten Divsar
Keyword(s):  
Titanium Dioxide ◽  
Removal Efficiency ◽  
Magnetic Core ◽  
Fractional Factorial ◽  
Order Kinetic ◽  
Sorption Data ◽  
Salt Addition ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir

Objective: In this research, a novel magnetite titanium dioxide nanocomposite functionalized by amine groups (Fe3O4@SiO2@TiO2-NH2) was synthesized and its ability for efficient removal of Acid Fuchsine as an anionic dye from aqueous solutions was investigated. Method: The core-shell structure of Fe3O4@SiO2@TiO2 was prepared using Fe3O4 as magnetic core, tetra ethyl orthosilicate as silica and tetra butyl titanate as titanium source for shell. The synthesized nanocomposites (particle size lower than 44 nm) were characterized by FT-IR, XRD, DRS, SEM and TGA instruments. The various experimental parameters affecting dye removal efficiency were investigated and optimized using Taguchi fractional factorial design. Results: The synthesized adsorbent showed the highest removal efficiency of Acid Fuchsine (99 %) at pH= 3.5, without salt addition and during stirring at contact times less than 10 minutes. The study of kinetic models at two concentration levels showed the fast dye sorption on the surface of proposed nanocomposites with pseudo second order kinetic model (R2=1). Also, the fitting of Acid Fuchsine sorption data to Freundlich, Langmuir and Temkin isotherms suggested that Freundlich model gave a better fitting than other models (R2=0.9936, n=2). Conclusion: Good chemical stability, excellent magnetic properties, very fast adsorption kinetics and high removal efficiency make the synthesized nanocomposite as a proper recoverable sorbent for removal of Acid Fuchsine dye from wastewaters.

scholarly journals Development of Biochars Derived from Water Bamboo (Zizania latifolia) Shoot Husks Using Pyrolysis and Ultrasound-Assisted Pyrolysis for the Treatment of Reactive Black 5 (RB5) in Wastewater

Water ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1615
Author(s):  
Thanh Tam Nguyen ◽  
Hung-Hsiang Chen ◽  
Thi Hien To ◽  
Yu-Chen Chang ◽  
Cheng-Kuo Tsai ◽  
...  
Keyword(s):  
Cost Effective ◽  
Reactive Black 5 ◽  
Order Kinetic ◽  
Sem Images ◽  
Zizania Latifolia ◽  
Surface Areas ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ultrasound Assisted ◽  
Green Technique

Adsorbent made by carbonization of biomass under oxygen-limited conditions has become a promising material for wastewater treatment owing to its cost-effective, simple, and eco-friendly processing method. Ultrasound is considered a green technique to modify carbon materials because it uses water as the solvent. In this study, a comparison of Reactive Black 5 (RB5) adsorption capacity between biochar (BC) generated by pyrolysis of water bamboo (Zizania latifolia) husks at 600 °C and ultrasound-assisted biochar (UBC) produced by pyrolysis at 600 °C assisted by ultrasonic irradiation was performed. UBC showed a greater reaction rate and reached about 80% removal efficiency after 4 h, while it took 24 h for BC to reach that level. Scanning electron microscope (SEM) images indicated that the UBC morphology surface was more porous, with the structure of the combination of denser mesopores enhancing physiochemical properties of UBC. By Brunauer, Emmett, and Teller (BET), the specific surface areas of adsorbent materials were analyzed, and the surface areas of BC and UBC were 56.296 m2/g and 141.213 m2/g, respectively. Moreover, the pore volume of UBC was 0.039 cm3/g, which was higher than that of BC at 0.013 cm3/g. The adsorption isotherms and kinetics revealed the better fits of reactions to Langmuir isotherm and pseudo-second-order kinetic model, indicating the inclination towards monolayer adsorption and chemisorption of RB5 on water bamboo husk-based UBC.

Adsorption Characteristics of Phenol in Aqueous Solution by Pinus massoniana Biochar

2013 ◽  
Vol 295-298 ◽  
pp. 1154-1160 ◽  
Author(s):  
Guo Zhi Deng ◽  
Xue Yuan Wang ◽  
Xian Yang Shi ◽  
Qian Qian Hong
Keyword(s):  
Aqueous Solution ◽  
Ph Value ◽  
Pinus Massoniana ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Adsorbent Dosage ◽  
Salt Ions ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The objective of this paper is to investigate the feasibility of phenol adsorption from aqueous solution by Pinus massoniana biochar. Adsorption conditions, including contact time, initial phenol concentration, adsorbent dosage, strength of salt ions and pH, have been investigated by batch experiments. Equilibrium can be reached in 24 h for phenol from 50 to 250 mg• L-1. The optimum pH value for this kind of biochar is 5.0. The amount of phenol adsorbed per unit decreases with the increase in adsorbent dosage. The existence of salt ions makes negligible influence on the equilibrium adsorption capacity. The experimental data is analyzed by the Freundlich and Langmuir isotherm models. Equilibrium data fits well to the Freundlich model. Adsorption kinetics models are deduced and the pseudo-second-order kinetic model provides a good correlation for the adsorbent process. The results show that the Pinus massoniana biochar can be utilized as an effective adsorption material for the removal of phenol from aqueous solution.

scholarly journals Investigation of Seeds and Peels of Citrullus colocynthis as Efficient Natural Adsorbent for Methylene Blue Dye

Processes ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 1279
Author(s):  
Wafa Mohammed Alghamdi ◽  
Ines El Mannoubi
Keyword(s):  
Methylene Blue ◽  
Kinetic Model ◽  
Langmuir Isotherm ◽  
Order Kinetic ◽  
Citrullus Colocynthis ◽  
Natural Adsorbent ◽  
Spontaneous Process ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Mb Adsorption

Natural adsorbents as low-cost materials have been proved efficient for water remediation and have significant capacity for the removal of certain chemicals from wastewater. The present investigation aimed to use Citrullus colocynthis seeds (CCSs) and peels (CCPs) as an efficient natural adsorbent for methylene blue (MB) dye in an aqueous solution. The examined biosorbents were characterized using surface area analyzer (BET), scanning electron microscope (SEM), thermogravimetric analyzer (TGA) and Fourier transform infra-red (FT-IR) spectroscopy. Batch adsorption experiments were conducted to optimize the main factors influencing the biosorption process. The equilibrium data for the adsorption of MB by CCSs were best described by the Langmuir isotherm followed by the Freundlich adsorption isotherms, while the equilibrium data for MB adsorption by CCPs were well fitted by the Langmuir isotherm followed by the Temkin isotherm. Under optimum conditions, the maximum biosorption capacity and removal efficiency were 18.832 mg g−1 and 98.00% for MB-CCSs and 4.480 mg g−1 and 91.43% for MB-CCPs. Kinetic studies revealed that MB adsorption onto CCSs obeys pseudo-first order kinetic model (K1 = 0.0274 min−1), while MB adsorption onto CCPs follows the pseudo-second order kinetic model (K2 = 0.0177 g mg−1 min−1). Thermodynamic studies revealed that the MB biosorption by CCSs was endothermic and a spontaneous process in nature associated with a rise in randomness, but the MB adsorption by CCPs was exothermic and a spontaneous process only at room temperature with a decline in disorder. Based on the obtained results, CCSs and CCPSs can be utilized as efficient, natural biosorbents, and CCSs is promising since it showed the highest removal percentage and adsorption capacity of MB dye.

scholarly journals Fabrication of the magnetic mesoporous silica Fe-MCM-41-A as efficient adsorbent: performance, kinetics and mechanism

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yige Guo ◽  
Bin Chen ◽  
Ying Zhao ◽  
Tianxue Yang
Keyword(s):  
Mesoporous Silica ◽  
Zero Valent Iron ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Environment And Health ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Neutral Conditions ◽  
Magnetic Mesoporous Silica ◽  
Mcm 41

AbstractAntibiotics are emerging pollutants and increasingly present in aquaculture and industrial wastewater. Due to their impact on the environment and health, their removal has recently become a significant concern. In this investigation, we synthesized nano zero-valent iron-loaded magnetic mesoporous silica (Fe-MCM-41-A) via precipitation and applied the adsorption of oxytetracycline (OTC) from an aqueous solution. The effects of competing ions such as Na+, Ca2+ and Cu2+ on the adsorption process under different pH conditions were studied in depth to providing a theoretical basis for the application of nanomaterials. The characterization of the obtained material through transmission electron microscopy demonstrates that the adsorbent possesses hexagonal channels, which facilitate mass transfer during adsorption. The loaded zero-valent iron made the magnetic, and was thus separated under an applied magnetic field. The adsorption of OTC onto Fe-MCM-41-A is rapid and obeys the pseudo-second-order kinetic model, and the maximum adsorption capacity of OTC is 625.90 mg g−1. The reaction between OTC and Fe-MCM-41-A was inner complexation and was less affected by the Na+. The effect of Ca2+ on the adsorption was small under acidic and neutral conditions. However, the promotion effect of Ca2+ increased by the increase of pH. Cu2+ decreased the removal efficiencies continuously and the inhibitory effects decrease varied with the increase of pH. We propose that surface complexing, ion-exchange, cationic π-bonding, hydrogen bonding, and hydrophobicity are responsible for the adsorption of OTC onto Fe-MCM-41-A.

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