scholarly journals Effect of exogenous phosphatase and phytase activities on organic phosphate mobilization in soils with different phosphate adsorption capacities

2012 ◽  
Vol 58 (1) ◽  
pp. 41-51 ◽  
Author(s):  
Hayato Maruyama ◽  
Takuya Yamamura ◽  
Yohei Kaneko ◽  
Hirokazu Matsui ◽  
Toshihiro Watanabe ◽  
...  
Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 283
Author(s):  
Yike Meng ◽  
Yuan Wang ◽  
Chuanyue Wang

Bioretention systems are frequently employed in stormwater treatment to reduce phosphorus pollution and prevent eutrophication. To enhance their efficiency, filter additives are required but the currently used traditional materials cannot meet the primary requirements of excellent hydraulic properties as well as outstanding release and adsorption capacities at the same time. In this research, a polyurethane-biochar crosslinked material was produced by mixing the hardwood biochar (HB) with polyurethane to improve the performance of traditional filter additives. Through basic parameter tests, the saturated water content of polyurethane-biochar crosslinked material (PCB) was doubled and the permeability coefficient of PCB increased by two orders of magnitude. Due to the polyurethane, the leaching speed of phosphorus slowed down in the batching experiments and fewer metal cations leached. Moreover, PCB could adsorb 93–206 mg/kg PO43− at a typical PO43− concentration in stormwater runoff, 1.32–1.58 times more than HB, during isothermal adsorption experiments. In the simulating column experiments, weaker hydropower reduced the PO43− leaching quantities of PCB and had a stable removal rate of 93.84% in phosphate treatment. This study demonstrates the potential use of PCB as a filter additive in a bioretention system to achieve hydraulic goals and improve phosphate adsorption capacities.


2018 ◽  
Vol 10 (12) ◽  
pp. 4578 ◽  
Author(s):  
Yingjie Zhu ◽  
Xiaoli Du ◽  
Can Gao ◽  
Zhenya Yu

Inorganic and organic phosphate adsorption by iron–manganese (Fe–Mn) plaques extracted from reed roots was investigated. Scanning electron microscopy indicated the roots had rough surfaces and fine particles attached. X-ray photoelectron spectra indicated that Fe and Mn in the Fe–Mn plaques were mainly in the +III and +IV oxidation states, respectively. The contact time, initial phosphate concentration, and temperature effects on inorganic and organic phosphate adsorption were investigated by performing batch tests. Pseudo-second-order model described inorganic and organic phosphate adsorption, indicating the chemisorption was the dominant adsorption process. Langmuir and Freundlich isotherm models were fitted to the equilibrium data, and the Langmuir model fitted best. The maximum inorganic and organic phosphate adsorption capacities at 298 K were 7.69 and 3.66 mg/g, respectively. The inorganic and organic phosphate adsorption processes were spontaneous and exothermic. The inorganic phosphate adsorption capacity was higher than the organic phosphate adsorption capacity, and the presence of organic phosphate did not negatively affect adsorption at inorganic to organic phosphate molar ratios between 1:1 and 3:1. Fourier-transform infrared spectra before and after adsorption showed abundant functional groups on Fe–Mn plaques and that phosphate was probably adsorbed via replacement of hydroxyl groups and inner-sphere surface complexation.


2012 ◽  
Vol 476-478 ◽  
pp. 1969-1973 ◽  
Author(s):  
Wei Ya Huang ◽  
Jun Yang ◽  
Yuan Ming Zhang

Ethylenediamine (EDA) functionalized mesoporous MCM-41 particles displaying various functionalization levels have been prepared by one-pot method. The prepared samples were treated with Fe(III) to form cationic complexes inside MCM-41 pores (MCM-41-NN-Fe-x%, x=10, 20 and 30) for trapping phosphate from water. The prepared adsorbents were characterized by XRD, BET, TGA and elemental analysis, and their phosphate adsorption performances were studied. The results showed that the phosphate removal rate of all the prepared adsorbents were higher than 95% at the initial phosphate concentration of 2 ppm. Additionally, the Langmuir model was used to simulate the sorption equilibrium, and the results indicated that the experiment data agreed well with the Langmuir model. The maximum adsorption capacities calculated from the Langmuir model increased with the increase of diamino loadings in adsorbents, and the maximum adsorption capacities of MCM-41-NN-Fe-30% was 52.5 mg/g.


2021 ◽  
Vol 8 (6) ◽  
pp. 201789
Author(s):  
Pengfei Wang ◽  
Mengmeng Zhi ◽  
Guannan Cui ◽  
Zhaosheng Chu ◽  
Shuhang Wang

Metal oxide-loaded biochars are a promising material to remove phosphate from polluted water to ultra-low concentrations. To facilitate preparing the metal oxide-loaded biochar with the best phosphate adsorption performance, five biochars loaded with Al, Ca, Fe, La and Mg oxides, respectively (Al-BC, Ca-BC, Fe-BC, La-BC and Mg-BC) were produced using Phragmites australis pretreated with 0.1 mol AlCl 3 , CaCl 2 , FeCl 3 , LaCl 3 and MgCl 2 , respectively, characterized, and phosphate adsorption kinetics and isotherms of the biochars were determined. The maximum phosphate adsorption capacities ( Q m ) of the biochars ranked as Al-BC (219.87 mg g −1 ) > Mg-BC (112.45 mg g −1 ) > Ca-BC (81.46 mg g −1 ) > Fe-BC (46.61 mg g −1 ) > La-BC (38.93 mg g −1 ). The time to reach the adsorption equilibrium ranked as La-BC (1 h) < Ca-BC (12 h) < Mg-BC (24 h) = Fe-BC (24 h) <Al-BC (greater than 72 h). Q m of Ca-BC, Fe-BC, La-BC and Mg-BC depend on the molar content of metals in the biochars. The small phosphate adsorption rate of Al-BC is due to the slow intra-particle diffusion of phosphate attributed to the undeveloped porosity and dispersed distribution of AlOOH crystals on the Al-BC surface. Mg-BC is suggested for phosphate removal from water considering adsorption rate and capacity. Al-BC is applicable when a long contact time is allowed, e.g. as a capping material to immobilize phosphate in lake sediments.


2018 ◽  
Vol 77 (11) ◽  
pp. 2668-2676 ◽  
Author(s):  
Runjuan Zhou ◽  
Youbao Wang ◽  
Ming Zhang ◽  
Jing Li ◽  
Yanan Gui ◽  
...  

Abstract In the present study, copper tailings were treated at different temperatures (50–650 °C) and for various times (0.5–6 hours) and their phosphate adsorption capacity was investigated. The results showed that heating temperature significantly affected adsorption capacity. The highest capacity was observed in treatments at 310–350 °C. Heating time did not influence phosphate adsorption ability of copper tailings. Scanning electron microscopy, Barrett–Joyner–Halenda (BJH), and Fourier transform infrared spectroscopy (FTIR) were employed to characterize untreated copper tailings (raw CT) and copper tailings heated at 340 °C (CT340). The results showed that CT340 had a rougher surface, more and smaller pores, a larger surface area and higher FTIR transmittance than raw CT. These changes in texture might explain the increased phosphate adsorption of thermally modified copper tailings. Mathematical modeling showed that the Langmuir nonlinear model was the best fit to the current data. The maximum adsorption capacities of raw CT and CT340 were predicted as 2.08 mg/g and 14.25 mg/g at 298 K, pH 6.0, respectively.


2020 ◽  
Vol 2020 ◽  
pp. 1-12
Author(s):  
Trung Thanh Nguyen ◽  
Tri Thich Le ◽  
Phuoc Toan Phan ◽  
Nhat Huy Nguyen

Ferric oxide-amine material was synthesized and applied as a novel adsorbent for nitrate and phosphate removal from aqueous solution. The properties of ferric oxide-amine were examined using TGA, FTIR, BET, SEM, EDX, SEM-mapping, and XRD analysis. The results showed that the adsorption using ferric oxide-amine material reached equilibrium after 30 and 60 min for nitrate and phosphate, respectively. The highest nitrate and phosphate adsorption capacities were 131.4 mg nitrate/g at pH 5-6 and 42.1 mg phosphate/g at pH 6. The effects of adsorbent dosage, initial concentrations of nitrate and phosphate, and adsorption temperature were also investigated. Among the three adsorbents of ferric oxide-amine, ferric oxide, and Akualite A420 ion exchange resin, ferric oxide-amine material had the highest adsorption capacity for nitrate and phosphate removal. These results suggest a great potential use of ferric oxide-amine material for water treatment in practical applications.


2021 ◽  
Vol 8 (8) ◽  
pp. 210428
Author(s):  
Xiaoqiu Ju ◽  
He Cui ◽  
Tao Liu ◽  
Yabing Sun ◽  
Shourong Zheng ◽  
...  

Novel phosphate adsorbents with confined La 2 O 3 inside mesoporous carbon were fabricated by the solid-state grinding method using pristine mesoporous carbon material CMK-3 (PCMK-3) and oxidized CMK-3 (OCMK-3) as the matrixes (denoted as La 2 O 3 @PCMK-3 and La 2 O 3 @OCMK-3). Compared with pure La 2 O 3 , La 2 O 3 @PCMK-3 and La 2 O 3 @OCMK-3 exhibited higher normalized phosphate adsorption capacity, indicative of efficient loading of La 2 O 3 inside the mesopores of the carbon materials. Furthermore, La 2 O 3 loading led to substantially enhanced phosphate adsorption. The adsorption capacities of La 2 O 3 @OCMK-3 samples were higher than those of La 2 O 3 @PCMK-3 samples, possibly owing to the oxygen-containing groups forming in OCMK-3 during HNO 3 oxidation, which enhanced the dispersion of La 2 O 3 in the mesopores of OCMK-3. The adsorption capacities of La 2 O 3 @PCMK-3 and La 2 O 3 @OCMK-3 increased with the La 2 O 3 loading amount. Phosphate adsorption onto La 2 O 3 (14.7)@PCMK-3 followed the pseudo-second-order kinetics with respect to correlation coefficient values (larger than 0.99). As pH increased from 3.4 to 12.0, the phosphate adsorption amounts of La 2 O 3 (14.7)@PCMK-3 and La 2 O 3 (15.7)@OCMK-3 decreased from 37.64 mg g −1 and 37.08 mg g −1 to 21.92 mg g −1 and 14.18 mg g −1 , respectively. Additionally, La 2 O 3 @PCMK-3 showed higher adsorption selectivity towards phosphate than coexisting Cl − , NO 3 − and SO 4 2 − . The adsorbent La 2 O 3 (14.7)@PCMK-3 remained stable after five regeneration cycles.


2019 ◽  
Author(s):  
Chem Int

The study aims to use an adsorbent natural based of Moroccan oil shale of Timahdit area (Y layer) in a physical-chemical adsorption process for treating industrial discharges colorful. The used adsorbent is the insoluble party of the sub-critical extraction of decarbonized oil shale of Timahdit. The tests performed on the methylene blue (MB), showed a strong elimination in the first 10 minutes. The influences of various experimental parameters were studied: mass ratio of adsorbent, time and temperature of thermal treatment, contact time, pH of MB and heating temperature of solution on the parameters of material were studied. The experimental results have shown that the adsorption of methylene blue dye by the adsorbent is more than 90% at initial pH a range 6-7 at room temperature for 30 minutes. The process is simple and the adsorbent produced is a new material with interesting adsorption capacities of moderate cost which does not require an activating agent and can be used as industrial adsorbent for the decontamination of effluents containing organic pollutants.


2017 ◽  
Vol 68 (1) ◽  
pp. 168-171 ◽  
Author(s):  
Letitia Doina Duceac ◽  
Cristina Elena Dobre ◽  
Ioana Pavaleanu ◽  
Gabriela Calin ◽  
Simona Nichitus ◽  
...  

Preventing diseases is deemed to be the major goal of our century especially when an excessive fluoride in drinking water can cause dental fluorosis, bone stiffness, rheumatism and skeletal fluorosis. Fluoride uptake from groundwater implies a worldwide multidisciplinary effort in order to develop renewable, cheap, human friendly materials. Among other materials, hydrotalcites could be good candidates for an efficient fluoride removal from water due to their adsorption, anion exchange and reconstruction properties. These nanostructured materials were synthesized using co-precipitation method in controlled conditions. Presence of anions in the interlayer structure and morphological aspects were performed by FTIR and SEM techniques. Thermal treatment of hydrotalcites showed good adsorption capacities for water defluoridation mostly due to their tendency to restore the original structure.


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