• Title/Summary/Keyword: Phosphate Adsorption

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A Study on the Mill Scale Pretreatment and Magnetite Production for Phosphate Adsorption (인 흡착을 위한 Mill Scale 전처리 및 Magnetite 제조 연구)

  • Chun, Hyuncheol;Choi, Younggyun
    • Journal of Korean Society of Environmental Engineers
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    • v.37 no.4
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    • pp.246-252
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    • 2015
  • In steel factory, hot roller cleaning process produces a lot of iron oxide particles called as mill scale. Major components of these particles are wustite (FeO), magnetite ($Fe_3O_4$), and hematite ($Fe_2O_3$). In this study, we tried to produce pure magnetite from the mill scale because of the largest phosphate adsorption capacity of the magnetite. The mill scale was treated with acid (HCl+$H_2O_2$), base (NaOH), and acid-base ($H_2SO_4$+NaOH). Batch adsorption tests showed the acid and/or base treatment could increase the phosphate adsorption capacity of the iron oxides from 0.28 to over 3.11 mgP/g. Magnetite, which could be obtained by acid and base treatment of the mill scale, showed the best adsorption capacity. From the kinetic analysis, both Freundlich and Langmuir isotherm well described the phosphate adsorption behavior of the magnetite. In Langmuir model, maximum phosphate adsorption capacity was found to be 5.1 mgP/g at $20^{\circ}C$.

Studies on the Residual Bending Strength of burned Douglas-fir and Western Hemlock soaked with Fire Retardant Chemicals (내화처리(耐火處理) 미송(美松) 및 미삼재(美杉材)의 연소후(燃燒後) 잔유(殘留)휨강도(强度)에 관한 연구(硏究))

  • Lee, Phil-Woo;Park, Heon
    • Journal of the Korean Wood Science and Technology
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    • v.12 no.3
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    • pp.15-24
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    • 1984
  • The $3{\times}3{\times}30\;cm^3$ sized specimens of Douglas-fir(Pseudotsuga menziesii) and western hemlock(Tsuga heterophylla) in this study were soaked in four fire-retardant solutions of ammonium sulfate, monoammonium phosphate, diammonium phosphate, and aluminium chloride for 1, 24, 72, 168, and 336 hours. Subsequently they were air-dried and burned at high temperature of ca. $1,800^{\circ}C$ and for short time of 5 minutes. This study estimated the relationship between the adsorbed chemicals and the residual weight ratio or residual bending strength of these partly burned lumbers. The results were as follows; 1) In average amount of chemical adsorption, diammonium phosphate showed the largest and aluminium chloride the smallest regardless of species but monoammonium phosphate was larger in Douglas-fir than that of western hemlock. 2) The amount of chemical adsorption was larger in western hemlock than Douglas-fir on the whole. 3) The amount of chemical adsorption was increased with the increase of soaking time but the rate of increase began to decrease at 200hrs. 4) Residual weight ratios showed no difference between species but showed differences among the chemicals treated i.e. monoammonium phosphate, diammonium phosphate, ammonium sulfate and aluminium chloride in turn from the largest to the smallest. 5) MOR values showed linear increase with the increase of residual weight ratios but showed no difference in species and chemicals respectively. 6) In the relationship between amount of chemical adsorption and MOR, only diammonium phosphate showed the curve of secondary degree with significance in Douglas-fir. 7) The MOE value of burned Douglas-fir lumber increased and showed significance of 99% as the adsorbed chemical amount increased, but among the chemicals only monoammonium phosphate showed significance. The MOE value of burned western hemlock lumber didn't show significance. 8) In only Douglas-fir, the correlation between adsorbed chemical amount and work to proportional limit showed significance in only monoammonium phosphate. And in both Douglas-fir and western hemlock, the correlation between adsorbed chemicals and work to maximum load showed significance in monoammonium phosphate.

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Highly efficient adsorptive removal of uranyl ions from aqueous solutions using dicalcium phosphate nanoparticles as a superabsorbent

  • Saghatchi, Hadis;Ansari, Reza;Mousavi, H. Zavvar
    • Nuclear Engineering and Technology
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    • v.50 no.7
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    • pp.1112-1119
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    • 2018
  • Dicalcium phosphate nanoparticles (DCP-NPs) was synthesized chemically and used for adsorptive removal of uranyl ions from aqueous solutions in a batch system. A commercial grade of DCP (monetite) was also employed for comparison. The synthesized and commercial adsorbents (S-DCP and C-DCP) were characterized by FT-IR, SEM and XRD techniques. The investigation of adsorption isotherms indicated that the maximum adsorption capacities ($q_m$) for C-DCP and S-DCP were 714.3 and $666.7mg\;g^{-1}$ (at 293 K), respectively. The experimental kinetics were well-described by the pseudo-second-order kinetic and the equilibrium data were fitted with both Langmuir and Freundlich adsorption models. Thermodynamic studies indicated that the adsorption of uranyl ions on the monetite surface was a spontaneous exothermic process. The exhausted adsorbents could be regenerated by washing with $0.10mol\;L^{-1}$ NaOH.

Comparable Influencing Factors to evaluate the Phosphate Removal on the Batch and the fix-bed Column by Converter Slag (회분식과 연속흐름 칼럼에서 전로슬래그에 의한 인제거 영향에 미치는 요소에 관한 연구)

  • Lee, Sang-Ho
    • Journal of Korean Society of Water and Wastewater
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    • v.29 no.5
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    • pp.565-573
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    • 2015
  • The influencing factors to remove phosphate were evaluated by converter slag (CS). Experiments were performed by batch tests using different CS sizes and column test. Solutions were prepared at the different pH and concentrations. The maximum removal efficiency was obtained over 98% with the finest particle size, $CS_a$ within 2 hours in batch tests. The removal efficiency was increased in the order of decreasing size with same amount of CS for any pH of solutions. The adsorption data were well fitted to Freundlich isotherm. From the column experiment, the specific factors were revealed that the breakthrough removal capacity (BRC) $x_b/m_{cs}$, was decreased by increasing the influent concentration. The breakthrough time, tb was lasted shorter as increasing the influent concentration. The pH drop simultaneously led to lower BRC drop during the experimental hours. The relation between the breakthrough time and the BRC to influent concentration was shown in the logarithmic decrease. Results suggested that the large surface area of CS possessed a great potential for adsorptive phosphate removal. Consequently particle size and initial concentration played the major influencing factors in phosphate removal by converter slag.

Adsorption characteristic of Cu(II) and phosphate using non-linear and linear isotherm equation for chitosan bead (비선형과 선형 등온흡착식을 이용한 키토산비드의 구리와 인산염의 흡착특성)

  • Kim, Taehoon;An, Byungryul
    • Journal of Korean Society of Water and Wastewater
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    • v.34 no.3
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    • pp.201-210
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    • 2020
  • 2 (Langmuir, Freundlich, Elovich, Temkin, and Dubinin-Radushkevich) and 3 (Sips and Redlich-Peterson)-parameter isotherm models were applied to evaluated for the applicability of adsorption of Cu(II) and/or phosphate isotherm using chitosan bead. Non-linear and linear isotherm adsorption were also compared on each parameter with coefficient of determination (R2). Among 2-parameter isotherms, non-linear Langmuir and Freundlich isotherm showed relatively higher R2 and appropriate maximum uptake (qm) than other isotherm equation although linear Dubinin-Radushkevich obtained highest R2. 3-parameter isotherm model demonstrated more reasonable and accuracy results than 2-parmeter isotherm in both non-linear and linear due to the addition of one parameter. The linearization for all of isotherm equation did not increase the applicability of adsorption models when error experiment data was included.

Modelling and packed bed column studies on adsorptive removal of phosphate from aqueous solutions by a mixture of ground burnt patties and red soil

  • Rout, Prangya R.;Dash, Rajesh R.;Bhunia, Puspendu
    • Advances in environmental research
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    • v.3 no.3
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    • pp.231-251
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    • 2014
  • The present study examines the phosphate adsorption potential and behavior of mixture of Ground Burnt Patties (GBP), a solid waste generated from cooking fuel used in earthen stoves and Red Soil (RS), a natural substance in fixed bed column mode operation. The characterization of adsorbent was done by Proton Induced X-ray Emission (PIXE), and Proton Induced ${\gamma}$-ray Emission (PIGE) methods. The FTIR spectroscopy of spent adsorbent reveals the presence of absorbance peak at $1127cm^{-1}$ which appears due to P = O stretching, thus confirming phosphate adsorption. The effects of bed height (10, 15 and 20 cm), flow rate (2.5, 5 and 7.5 mL/min) and initial phosphate concentration (5 and 15 mg/L) on breakthrough curves were explored. Both the breakthrough and exhaustion time increased with increase in bed depth, decrease in flow rate and influent concentration. Thomas model, Yoon-Nelson model and Modified Dose Response model were used to fit the column adsorption data using nonlinear regression analysis while Bed Depth Service Time model followed linear regression analysis under different experimental condition to evaluate model parameters that are useful in scale up of the process. The values of correlation coefficient ($R^2$) and the Sum of Square Error (SSE) revealed the Modified Dose Response model as the best fitted model to the experimental data. The adsorbent mixture responded effectively to the desorption and reusability experiment. The results of this finding advocated that mixture of GBP and RS can be used as a low cost, highly efficient adsorbent for phosphate removal from aqueous solution.

Measurement of Langmuir Adsorption Equilibrium by Elution-curve Method and Frontal Analysis (용출곡선법과 Frontal Analysis를 이용한 Langmuir 흡착평형식의 측정)

  • Choi, Yong Seok;Lee, Chong Ho;Row, Kyung Ho
    • Applied Chemistry for Engineering
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    • v.10 no.5
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    • pp.672-676
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    • 1999
  • Adsorption isotherm is the most fundamental information in adsorption separation-process. Directly from the elution profile of a peak, the elution-curve method and frontal analysis(FA) were utilized to measure the adsorption isotherm in this work. Using RP-HPLC, sample and the buffer added in mobile phase were 5'-GMP and sodium phosphate, respectively. In this experimental condition, the retention time was decreased with increase in the injected mass of sample. And the front part of a peak was very stiff, so Langmuir adsorption isotherm might be applied. By the elution-curve method, the parameters used in the isotherm were obtained by optimization method, while by the FA, the concentrations of stationary phase were measured from the elution curve and the isotherm was determined by regression analysis. Compared to FA, the consumption of sample was less, and only one or two injections were needed by the elution-curve method. Finally, the effect of concentration of sodium phosphate in mobile phase on the parameters of the isotherm was investigated.

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Anion Adsorption Properties of Organobentonites Modified by Cationic Polymers (양이온 폴리머를 이용한 유기벤토나이트의 음이온 흡착특성)

  • 윤지해;황진연;이효민;고상모;유장한
    • Journal of the Mineralogical Society of Korea
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    • v.17 no.2
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    • pp.147-155
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    • 2004
  • Anion adsorption properties of organobentonites modified by two cationic polymers, hexadecyltrimmethylammonium (HDTMA) and cetylpyridinum (CP), were investigated. The organobentonites showed the significant expansion of basal spacing to 42.0 $\AA$ at room temperature. The adsorption experiments were conducted for the 0.2 g of organobentonites with 40 mL solutions of various concentrations of anions such as nitrate, sulfate and phosphate. As a result, the organobentonites showed excellent adsorption capacities for those anions whereas untreated bentonite showed very low adsorption capacity. Adsorption rate of HDTMA-bentonite was about 90% for 100 mg/L solutions of nitrate and phosphate, and that of CP-bentonite was 97% for 100 mg/L solution of nitrate. Adsorption behaviors were slightly different for the different organobentonites and anions. Both organobentonites showed relatively higher adsorption rate for nitrate and phosphate than sulfate. Therefore, these organobentonites showing high anion adsorption capacities can be used far the removal of deleterious anions in the treatment of environmental pollution.

Preparation of Calcium Silicate Hydrate Extrudates and Their Phosphate Adsorption Studies

  • Rallapalli, Phani Brahma Somayajulu;Ha, Jeong Hyub
    • Applied Chemistry for Engineering
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    • v.30 no.5
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    • pp.562-568
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    • 2019
  • Cylindrical shape extrudates of calcium silicate hydrate (CSH) were prepared using different percentages of polyvinyl alcohol (PVA) / sodium alginate (SA) mixtures as binders and an aqueous solution containing 6% $H_3BO_3$ and 3% $CaCl_2$ was used as a cross linking agent. As the quantity of alginate increases, the phosphate removal efficiency and capacity were decreased. Among four different extrudate samples, the sample prepared by 8% PVA + 2% SA showed the highest phosphate removal efficiency (59.59%) and capacity (29.97 mg/g) at an initial phosphate concentration of 100 ppm and 2.0 g/L adsorbent dosage. Effects of the adsorbent dosage, contact time and initial phosphate concentration on the sample were further studied. The removal efficiency and capacity obtained by a 4.0 g/L adsorbent dose at an initial phosphate concentration of 100 ppm in 3 h were 79.38% and 19.96 mg/g, respectively. The experimental data of kinetic and isotherm measurements followed the pseudo-second-order kinetic equation and Langmuir isotherm model, respectively. These results suggested that the phosphate removal was processed via a chemisorption and a monolayer coverage of phosphate anions was on the CSH surface. The maximum adsorption capacity ($q_{max}$) was calculated as 23.87 mg/g from Langmuir isotherm model.

Effect of Operating Variables for Phosphate Removal with Cuttlefish Processing Sludge (오징어가공 슬러지를 이용한 인산염인 제거 공정에 미치는 영향인자)

  • 최봉종;이승목;김근한
    • Journal of Environmental Health Sciences
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    • v.24 no.3
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    • pp.87-91
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    • 1998
  • The removal effect of phosphate by sludge from wastewaters prior to discharge into natural waters is an essential measure to prevent eutrophication in receiving waters. There is need for developing low cost, easily and abundantly available, efficient adsorbents for the removal of phosphorus (P as orthophosphate) during the tertiary treatment of wastewaters. The adsorbent carbon which is prepared with fisheries wastes on a laboratory scale has been used to evaluate its performance for phosphate adsorption. Phosphate removal increase with increasing adsorbent dose and temperature, but shows no changes at an adsorbent dose over 8 g/l.

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