1. 西北农林科技大学资源环境学院, 陕西 杨凌 712100;
2. 西北农林科技大学理学院, 陕西 杨凌 712100;
3. School of Plant, Environmental and SoilSciences, Louisiana State University Agricultural Center, Baton Rouge, LA 70803, USA;
4. 农业部西北植物营养与农业环境重点实验室, 陕西 杨凌 712100
Phosphate adsorption from solution by metal oxide nanoparticles and the potential on phosphate capture
LIANG Wen1, HE Wei1, LI Man-lin2, HUANG Hui1, Wang Jim J3, ZHANG Zeng-qiang1, LI Rong-hua1,4
1. College of Natural Resources and Environment, Northwest A & F University, Yangling 712100, China;
2. College of Science, Northwest A & F University, Yangling 712100, China;
3. School of Plant, Environmental and Soil Sciences, Louisiana State University Agricultural Center, Baton Rouge, LA 70803, USA;
4. Key Laboratory of Plant Nutrition and the Agri-environment in Northwest China, Ministry of Agriculture, Yangling 712100, China
Effects of four different metal oxide nanoparticles (nMgO,nAl2O3,nTiO2 and nFe2O3) on phosphate adsorption were compared in the batch experiment.The influences of solution pH,contact time and coexist ions on phosphate adsorbed by nMgO were examined.Further,the phosphate adsorption mechanism onto nMgO was evaluated by XRD and XPS analysis.And the potential of recovered phosphate by nMgO from pig breeding wastewater on fertilzer was assessed by pot experiment.The results showed that nMgO had higher phosphate adsorption ability than nAl2O3,nTiO2 and nFe2O3.The phosphate amount reached 40、31.77、15.93 and 13.08mg/g in the range of pH 3.0 to 8.0 for nMgO,nAl2O3,nTiO2 and nFe2O3,respectively.The phosphate adsorption was a inreversible process.The phosphate sorption onto nMgO could reach equilibrium within 0.5h,the adsorption process fitted the pseudo-second order kinetic model.The equal content of coexisted F-,Cl-,NO3-,SO42-,Na+,K+ and NH4+ ions had no negative influence on phosphate adsorbed onto nMgO,while the existence of Mg2+ and Ca2+ ions could promote the phosphate adsorption.Langmuir model could be used to describe the adsorption isotherm,by which the maximum phosphate adsorption capacity was around 139.3mg/g.Based on the results of XRD and XPS analysis,it can be concluded that phosphate adsorption was dominated by chemical precipitation reaction combined with electrostatic attraction process.nMgO particles effectively recovered phosphate from piggery wastewater,in turn the phosphate loaded nMgO nanoparticle could be used as a potential substitute for phosphate-based fertilizer,which significantly improved the cabbage dry biomass from 0.31 to 0.96g/kg soil.
梁文, 何维, 李满林, 黄辉, Wang Jim J, 张增强, 李荣华. 金属氧化物纳米颗粒对磷的吸附及回收潜力[J]. 中国环境科学, 2017, 37(7): 2557-2565.
LIANG Wen, HE Wei, LI Man-lin, HUANG Hui, Wang Jim J, ZHANG Zeng-qiang, LI Rong-hua. Phosphate adsorption from solution by metal oxide nanoparticles and the potential on phosphate capture. CHINA ENVIRONMENTAL SCIENCECE, 2017, 37(7): 2557-2565.
Conley D J. Controlling eutrophication:Nitrogen and phosphorus[J]. Science, 2009,323:1014-1015.
[2]
US Geological Survey. (1950-2013) USGS Minerals Yearbook:Phosphate Rock[R]. 2012.
[3]
Gilbert N. The disappearing nutrient[J]. Nature, 2009,461:716-718.
[4]
Loganathan P, Vigneswaran S, Kandasamy J, et al. Removal and recovery of phosphate from water using sorption[J]. Critical Review of Environmental Science & Technology, 2014,44:847-907.
[5]
Li R H, Wang J J, Zhou B Y, et al. Recovery of phosphate from aqueous solution by magnesium oxide decorated magnetic biochar and its potential as phosphate-based fertilizer substitute[J]. Bioresource Technology, 2016,4:30271-30281.
[6]
Xu K N, Li J Y, Zheng M, et al. The precipitation of magnesium potassium phosphate hexahydrate for P and K recovery from synthetic urine[J]. Water Research, 2015,80:71-79.
[7]
Ye Y Y, Ngo H H, Guo W S, et al. Insight into chemical phosphate recovery from municipal wastewater[J]. Science of The Total Environment, 2017,576:159-171.
[8]
Ye Y Y, Ngo H H, Guo W S, et al. Insight into biological phosphate recovery from sewage[J]. Bioresource Technology, 2016,218:874-881.
[9]
Awual M R, Shenashen M A, Jyo A, et al. Preparing of novel fibrous ligand exchange adsorbent for rapid column-mode trace phosphate removal from water[J]. Journal of Industrial and Engineering Chemistry, 2014,20:2840-2847.
[10]
Liu Q, Hu P, Wang J, et al. Phosphate adsorption from aqueous solutions by Zirconium (IV) loaded cross-linked chitosan particles[J]. Journal of the Taiwan Institute of Chemical Engineers, 2016,59:311-319.
[11]
Huang H M, Zhang D D, Zhao Z J, et al. Comparison investigation on phosphate recovery from sludge anaerobic supernatant using the electrocoagulation process and chemical precipitation[J]. Journal of Cleaner Production, 2017,141:429-438.
[12]
Zong E M, Liu X H, Jiang J H, et al. Preparation and characterization of zirconia-loaded lignocellulosic butanol residue as a biosorbent for phosphate removal from aqueous solution[J]. Applied Surface Science, 2016,387:419-430.
[13]
Li R H, Wang J J, Zhou B Y, et al. Enhancing phosphate adsorption by Mg/Al layered double hydroxide functionalized biochar with different Mg/Al ratios[J]. Science of the Total Environment, 2016,559:121-129.
Li F H, Wu W H, Li R Y, et al. Adsorption of phosphate by acid-modified fly ash and palygorskite in aqueous solution:Experimental and modeling[J]. Applied Clay Science, 2016,132-133:343-352.
Yoon S Y, Lee C G, Park J A, et al. Kinetic, equilibrium and thermodynamic studies for phosphate adsorption to magnetic iron oxide nanoparticles[J]. Chemical Engineering Journal, 2014,236:341-347.
[18]
Mahaninia M H, Wilson L D. Phosphate uptake studies of cross-linked chitosan bead materials[J]. Journal of Colloid and Interface Science, 2017,485:201-212.
He Y H, Lin H, Dong Y B, et al. Simultaneous removal of ammonium and phosphate by alkaline-activated and lanthanumimpregnated zeolite[J]. Chemosphere, 2016,164:387-395.
[21]
Wang Z, W K, Xing M C, et al. A bench-scale study on the removal and recovery of phosphate by hydrous zirconia-coated magnetite nanoparticles[J]. Journal of Magnetism and Magnetic Materials, 2017,424:213-220.
[22]
Ju X Q, Hou J F, Tang Y Q, et al. ZrO2nanoparticles confined in CMK-3as highly effective sorbent for phosphate adsorption[J]. Microporous and Mesoporous Materials, 2016,230:188-195.
[23]
Lai L, Xie Q, Chi L N, et al. Adsorption of phosphate from water by easily separable Fe3O4@SiO2 core/shell magnetic nanoparticles functionalized with hydrous lanthanum oxide[J]. Journal of Colloid and Interface Science, 2016,465:76-82.
[24]
Su Y, Cui H, Li Q, et al. Strong adsorption of phosphate by amorphous zirconium oxide nanoparticles[J]. Water Research, 2013,47:5018-5026.
Cheng G, Xu F, Xiong J, et al. Enhanced adsorption and photocatalysis capability of generally synthesized TiO2-carbon materials hybrids[J]. Advanced Powder Technology, 2016,27(5):1949-1962.
[28]
Xia Y, Zhang L, Wang Y, et al. A facile strategy to fabricate well-defined mesoporous γ-Al2O3, microcubes with good adsorption performance towards Cr(VI) removal[J]. Materials Letters, 2015,143:294-297.
[29]
Asfaram A, Ghaedi M, Hajati S, et al. Synthesis of magnetic γ-Fe2O3-based nanomaterial for ultrasonic assisted dyes adsorption:Modeling and optimization[J]. Ultrasonics Sonochemistry, 2016,32:418-431.
Liang H, Liu K, Ni Y. Synthesis of mesoporous α-Fe2O3, via sol-gel methods using cellulose nano-crystals (CNC) as template and its photo-catalytic properties[J]. Materials Letters, 2015,159:218-220.
[32]
Mor S, Chhoden K, Negi P, et al. Utilization of nano-alumina and activated charcoal for phosphate removal from wastewater[J]. Environmental Nanotechnology Monitoring & Management, 2017,7:15-23.
[33]
Yao Y, Gao B, Chen J, et al. Engineered biochar reclaiming phosphate from aqueous solutions:mechanisms and potential application as a slow-release fertilizer.[J]. Environmental Science & Technology, 2013,47(15):8700-8708.
[34]
Zhang Y, Guo X, Yao Y, et al. Mg-Enriched Engineered Carbon from Lithium-Ion Battery Anode for Phosphate Removal.[J]. Acs Applied Materials & Interfaces, 2016,8(5):2905-2909.
[35]
Xia P, Wang X J, Wang X, et al. Struvite crystallization combined adsorption of phosphate and ammonium from aqueous solutions by mesoporous MgO-loaded diatomite[J]. Colloids and Surfaces A:Physicochemical and Engineering Aspects, 2016,506:220-227.