scholarly journals Evaluation of the Applicability of Concrete Sludge for the Removal of Cu, Pb, and Zn from Contaminated Aqueous Solutions

Metals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 666 ◽  
Author(s):  
Jongchan Yoo ◽  
Heeyoung Shin ◽  
Sangwoo Ji
Keyword(s):  
Aqueous Solutions ◽  
Wastewater Discharge ◽  
Solution Ph ◽  
Precipitated Calcium Carbonate ◽  
Coated Particles ◽  
Solid Ratio ◽  
Metal Carbonates ◽  
Sludge Recycling ◽  
Dried Sludge ◽  
Hydroxide Coprecipitation

In this study, the possibility of using concrete-sludge recycling as an immobilizer, including dried sludge (DS), precipitated calcium carbonate (PCC), and calcite-coated particles (CCP), was evaluated for the remediation of Cu-, Pb-, and Zn-contaminated aqueous solutions. Experimental variables characterizing immobilization, including reaction time, initial solution pH, and immobilizer dosage, were selected. After DS was applied, 98.3% of Cu, 99.9% of Pb, and 95.2% of Zn were removed via metal-hydroxide coprecipitation onto the surface of DS, which increased in pH within the shortened contact time. On the contrary, PCC and CCP removed metals (above 99.9% removal) via the formation of metal carbonates, which was highly dependent on both the pH and the carbonates released from the immobilizers. The acidic solution pH contributed to the dissolution of calcite (leading to an increase in carbonates in solution), thus enhancing the removal of metals. An increase in PCC and CCP dosage (liquid to solid ratio of 1000 to 100) was effective in removing Cu with an increasing final pH and number of carbonates in solution. Our results show that concrete sludge can be recycled to reduce environmental loads, including alkaline wastewater discharge, waste disposal, CO2 emissions, and metal-contaminated aqueous solutions.

scholarly journals Oxytetracycline Adsorption from Aqueous Solutions on Commercial and High-Temperature Modified Activated Carbons

Energies ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3481
Author(s):  
Joanna Lach ◽  
Agnieszka Ociepa-Kubicka ◽  
Maciej Mrowiec
Keyword(s):  
Activated Carbon ◽  
Aqueous Solutions ◽  
Activated Carbons ◽  
Electricity Consumption ◽  
Solution Ph ◽  
Carbon Modification ◽  
Modification Method ◽  
Flow Through ◽  
Proposed Modification ◽  
Modified Activated Carbons

The aim of the work was to evaluate the possibility of using commercial and modified activated carbons for the removal of oxytetracycline from aqueous solutions. The kinetics and statics of adsorption as well as the effect of the activated carbon dose and solution pH on the efficiency of the oxytetracycline adsorption were analyzed. Based on the study of oxytetracycline adsorption isotherms, the activated carbons were ranked in the following order: F-300 > WG-12 > Picabiol > ROW08 > WACC 8 × 30 > F-100 > WAZ 0.6–2.4. The most effective activated carbons were characterized by large specific surfaces. The best matching results were obtained for: Redlich–Peterson, Thot and Jovanovic models, and lower for the most frequently used Freundlich and Langmuir models. The adsorption proceeded better from solutions with pH = 6 than with pH = 3 and 10. Two ways of modifying activated carbon were also assessed. A proprietary method of activated carbon modification was proposed. It uses the heating of activated carbon as a result of current flow through its bed. Both carbons modified at 400 °C in the rotary kiln and on the proprietary SEOW (Joule-heat) modification stand enabled to obtain adsorbents with higher and comparable monolayer capacities. The advantage of the proposed modification method is low electricity consumption.

scholarly journals Adsorption of Pollutants from Aqueous Solutions Using Activated and Non-Activated Oak Shells: Parametric and Fractional Factorial Design Study. Part II. Removal of Phenol and Dyes

2003 ◽  
Vol 21 (2) ◽  
pp. 189-198
Author(s):  
Sameer Al-Asheh ◽  
Fawzi Banat ◽  
Rana Saeidi ◽  
Salam Abu Zaid
Keyword(s):  
Methylene Blue ◽  
Aqueous Solutions ◽  
Factorial Design ◽  
Fractional Factorial Design ◽  
Sorption Process ◽  
Fractional Factorial ◽  
Phenol Concentration ◽  
Blue Dye ◽  
Batch Adsorption ◽  
Solution Ph

As in Part I, non-activated (natural) and chemically activated oak shells were evaluated for their ability to remove phenol and Methylene Blue (as a typical dye component) from aqueous solutions. Batch adsorption experiments were conducted to investigate the effect of contact time, sorbent concentration, phenol concentration and the pH of the solution on the sorption process. Activated oak shells adsorbed more phenol than natural oak shells under the same conditions. A decrease in sorbent concentration or an increase in phenol concentration or solution pH resulted in an increase in phenol uptake by the oak shells. The uptake of Methylene Blue increased with decreasing sorbent concentration and with an increase in the dye concentration, but decreased significantly with solution pH. According to the fractional factorial design technique, the sorbent type employed (natural or activated) had the most significant influence on phenol or Methylene Blue uptake followed by sorbent concentration and then sorbate concentration. Interaction amongst the different operating variables played an important role in the uptake of phenol or Methylene Blue dye by the adsorbent considered.

scholarly journals Photoreduction of Cr(VI) Ions in Aqueous Solutions by UV/ Photocatalytic Processes

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Chih Ming Ma ◽  
Yung Shuen Shen ◽  
Po Hsiang Lin
Keyword(s):  
Aqueous Solutions ◽  
Reaction Rate ◽  
Removal Rate ◽  
Experimental Results ◽  
Order Kinetic ◽  
Solution Ph ◽  
Relationship Of ◽  
The Relationship ◽  
Photocatalytic Processes ◽  
Order Kinetic Equation

This study discussed the photoreduction of Cr(VI) ions in aqueous solutions by UV/TiO2photocatalytic processes under various operational factors. Experimental results showed that the removal rate of Cr(VI) increased with decreasing solution pH values and with increasing dosages of organic compounds, indicating that the recombination rate of electrons and h+can be retarded in the reaction systems by the addition of the scavenger, thus raising the reaction rate of Cr(VI). The relationship of the chemical reaction rate of Cr(VI), TiO2dosage, and changes of Cr(VI) concentration was expressed by the pseudo-first-order kinetic equation. Comparing the experimental results of two different doping metals in modified TiO2photoreduction systems, the removal rate of Cr(VI) by the Ag/TiO2process is larger, possibly because the electron transferring ability of Ag is superior to that of Cu. However, the photoreduction rates of Cr(VI) by modified UV/TiO2processes are worse than those by a nonmodified commercial UV/TiO2process.

scholarly journals Study on Adsorption of Cu and Ba from Aqueous Solutions Using Nanoparticles of Origanum (OR) and Lavandula (LV)

2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Ghadah M. Al-Senani ◽  
Foziah F. Al-Fawzan
Keyword(s):  
Heavy Metals ◽  
Particle Size ◽  
Free Energy ◽  
Aqueous Solutions ◽  
Thermodynamic Parameters ◽  
Solution Ph ◽  
Environment Friendly ◽  
Removal Of Heavy Metals ◽  
Equilibrium Data ◽  
Langmuir And Freundlich Models

Wild herbs (Origanum (OR) and Lavandula (LV)) were used as environment-friendly adsorbents in this study. The adsorbents were used for adsorption of Cu and Ba from water. The adsorption of heavy metals onto OR and LV was dependent on particle size, dose, and solution pH. The diameter of adsorbent particles was less than 282.8 nm. The adsorption follows second-order kinetics. Langmuir and Freundlich models have been applied to describe the equilibrium data, and the thermodynamic parameters, the Gibbs free energy, ∆G°, enthalpy, ∆H°, and entropy, ∆S°, have been determined. The positive value of ∆H° suggests that the adsorption of heavy metals by the wild herbs is endothermic. The negative values of ∆G° at all the studied temperatures indicate that the adsorption is a spontaneous process. It can be concluded that OR and LV are promising adsorbents for the removal of heavy metals from aqueous solutions over a range of concentrations.

scholarly journals Kinetic and Equilibrium Studies on the Zinc Adsorption-desorption Characteristics of Some Promising Biochars in Aqueous Solutions

2021 ◽  
Author(s):  
Masoumeh Faryadi Shahgoli ◽  
Adel Reyhanitabar ◽  
Nosratollah Najafi ◽  
Shahin Oustan
Keyword(s):  
Ionic Strength ◽  
Aqueous Solutions ◽  
Rice Straw ◽  
Pyrolysis Temperature ◽  
Ph Effect ◽  
Solution Ph ◽  
Equilibrium Studies ◽  
Batch Technique ◽  
Adsorption Desorption ◽  
Zinc Adsorption

Abstract The present research aimed at investigating zinc (Zn) sorption capacity of the biochars derived from apple wood (WB) and rice straw (RB) feedstocks at two 300 and 600°C pyrolysis temperatures (WB300, WB600, RB300 and RB600, respectively) in aqueous solutions. Kinetic and equilibrium sorption experiments were conducted via batch technique. In equilibrium adsorption experiments, the study used the concentration range of 5-200 mg Zn L− 1 and focused on the solution pH effect on Zn adsorption in biochars under the following conditions: unadjusted and adjusted pH (4 and 6) and three ionic strength levels (0.01, 0.03, 0.1 M KNO3). Zinc desorption experiments were conducted under all above mentioned conditions but without pH adjustment at five separate stages. Kinetic data analysis indicated that Zn adsorption in biochars reached the near steady state within 24 hours with the sorption rate order of WB300 < WB600 < RB300 < RB600. The best fitness was superior to both Elovich and exponential rate models. Also, Zn adsorption isotherms in the studied biochars were shown to fit quite well to Langmuir, Freundlich and Dubinin-Radushkevich models. Zn sorption maxima were found to be 4.3, 16.4, 17.9 and 33.3 mg g− 1, on average, for WB300, WB600, RB300, and RB600, respectively. The initial increased pH solution from 4 to 6 caused an increase in Zn adsorption in RB600, RB300 and WB600, however the sorption maxima in WB300 was detected at pH 4. The rise in solution ionic strength from 0.01 M to 0.1 M dropped the Zn adsorption capacity in all the studied biochars. Findings suggested that rice straw derived biochars showed a better performance than woody biochars in Zn sorption and retention from aqueous solutions. In addition, this ability increased with increasing pyrolysis temperature in both types of biochars. Finally, the study revealed that rice straw biochars, produced at high pyrolysis temperatures, can serve as economical and efficient absorbents for Zn removal from aqueous solutions.

scholarly journals Effect of Praestol as a Coagulant-Aid to Improve Coagulation-Flocculation in Dye containing Wastewaters

2015 ◽  
Vol 18 (1) ◽  
pp. 38-46 ◽  
Keyword(s):  
Ionic Strength ◽  
Aqueous Solutions ◽  
Removal Efficiency ◽  
Dye Removal ◽  
Settling Time ◽  
Solution Ph ◽  
Polyaluminum Chloride ◽  
Flocculation Process ◽  
Flocculation Time

<div> <p>This study was conducted to investigate the effect of praestol, as a coagulant-aid, to improve coagulation-flocculation process in the removal of disperse red 60 from aqueous solutions. The effect of various parameters including coagulants dose (10-1000 mg l<sup>-1</sup>), praestol dose (0-1000 mg l<sup>-1</sup>), solution pH (3-11), initial dye concentration (100-500 mg l<sup>-1</sup>), flocculation speed (30-60 rpm), flocculation time (15-30 min), settling time (5-60 min) and ionic strength (0-6 mg l<sup>-1</sup>) was evaluated on the dye removal. The dye removal efficiency was substantially increased by using praestol in the concentration of 80 mg l<sup>-1 </sup>and 400 mg l<sup>-1 </sup>for coagulation with alum and polyaluminum chloride (PACl), respectively. The maximum dye removal by alum coupled with praestol (Al-P) and PACl coupled with praestol (PA-P) was found to be 97.8% and 98.7%, respectively that were occurred at pH 7. The results showed that the application of PA-P or Al-P can be effectively used to remove disperse red 60 (DR 60) in aqueous solutions.</p> </div> <p>&nbsp;</p>

scholarly journals Photo-transformation of aqueous nitroguanidine and 3-nitro-1,2,4-triazol-5-one : emerging munitions compounds

2021 ◽  
Author(s):  
Julie Becher ◽  
Samuel Beal ◽  
Susan Taylor ◽  
Katerina Dontsova ◽  
Dean Wilcox
Keyword(s):  
Aqueous Solutions ◽  
Degradation Products ◽  
Pure Water ◽  
Transformation Products ◽  
Water Soluble ◽  
Uv Exposure ◽  
Degradation Pathways ◽  
Solution Ph ◽  
Photo Degradation ◽  
Degradation Rates

Two major components of insensitive munition formulations, nitroguanidine (NQ) and 3-nitro-1,2,4-triazol-5-one (NTO), are highly water soluble and therefore likely to photo-transform while in solution in the environment. The ecotoxicities of NQ and NTO solutions are known to increase with UV exposure, but a detailed accounting of aqueous degradation rates, products, and pathways under different exposure wavelengths is currently lacking. We irradiated aqueous solutions of NQ and NTO over a 32-h period at three ultraviolet wavelengths and analyzed their degradation rates and transformation products. NQ was completely degraded by 30 min at 254 nm and by 4 h at 300 nm, but it was only 10% degraded after 32 h at 350 nm. Mass recoveries of NQ and its transformation products were >80% for all three wavelengths. NTO degradation was greatest at 300 nm with 3% remaining after 32 h, followed by 254 nm (7% remaining) and 350 nm (20% remaining). Mass recoveries of NTO and its transformation products were high for the first 8 h but decreased to 22–48% by 32 h. Environmental half-lives of NQ and NTO in pure water were estimated as 4 and 6 days, respectively. We propose photo-degradation pathways for NQ and NTO supported by observed and quantified degradation products and changes in solution pH.

scholarly journals The Removal of Uranium and Thorium from Their Aqueous Solutions by 8-Hydroxyquinoline Immobilized Bentonite

Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Langmuir Isotherm ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.

Photocatalytic removal of cyanide with illuminated TiO2

2011 ◽  
Vol 64 (7) ◽  
pp. 1383-1387 ◽  
Author(s):  
M. Shirzad Siboni ◽  
M. R. Samarghandi ◽  
J.-K. Yang ◽  
S.-M. Lee
Keyword(s):  
Aqueous Solutions ◽  
Langmuir Isotherm ◽  
Industrial Wastewater ◽  
Photocatalytic Oxidation ◽  
Maximum Adsorption Capacity ◽  
Photocatalytic Reaction ◽  
Solution Ph ◽  
Cyanide Concentration ◽  
Photocatalytic Removal ◽  
Oxidation Efficiency

Effects of TiO2 dosage, pH and initial cyanide concentration on the removal efficiency of cyanide from aqueous solutions with illuminated TiO2 have been investigated. Adsorption and oxidation were recognized as significant processes for the elimination of cyanide. From the Langmuir isotherm, the maximum adsorption capacity was determined as 17.24 mg/g at pH 7. Adsorbed amount of cyanide slightly increased as the TiO2 dosage increased. However, as no significant increase was observed above 1 g/L TiO2, an optimum TiO2 dosage was determined as 1 g/L. Photocatalytic oxidation efficiency of cyanide was greatly affected by the solution pH. It increased as the solution pH decreased. The photocatalytic oxidation efficiency after 120 min was 80.4% at pH 3 while it was only 20.4% at pH 11. Photocatalytic oxidation of cyanide was well described by the second-order kinetics. Photocatalytic reaction with illuminated TiO2 can be effectively applied to treat industrial wastewater contaminated with cyanide.

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