Adsorption of cefixime from aqueous solutions using modified hardened paste of Portland cement by perlite; optimization by Taguchi method

2016 ◽  
Vol 74 (5) ◽  
pp. 1069-1078 ◽  
Author(s):  
Mohammad Hossein Rasoulifard ◽  
Soghra Khanmohammadi ◽  
Azam Heidari

In the present study, we have used a simple and cost-effective removal technique by a commercially available Fe-Al-SiO2 containing complex material (hardened paste of Portland cement (HPPC)). The adsorbing performance of HPPC and modified HPPC with perlite for removal of cefixime from aqueous solutions was investigated comparatively by using batch adsorption studies. HPPC has been selected because of the main advantages such as high efficiency, simple separation of sludge, low-cost and abundant availability. A Taguchi orthogonal array experimental design with an OA16 (45) matrix was employed to optimize the affecting factors of adsorbate concentration, adsorbent dosage, type of adsorbent, contact time and pH. On the basis of equilibrium adsorption data, Langmuir, Freundlich and Temkin adsorption isotherm models were also confirmed. The results showed that HPPC and modified HPPC were both efficient adsorbents for cefixime removal.

2020 ◽  
Vol 10 (12) ◽  
Author(s):  
Tze Ling Kua ◽  
Muhammad Raziq Rahimi Kooh ◽  
Muhammad Khairud Dahri ◽  
Nur Afiqah Hazirah Mohamad Zaidi ◽  
YieChen Lu ◽  
...  

AbstractIpomoea aquatica (IA) was investigated for its potential as a low-cost adsorbent to remove toxic methyl violet 2B (MV2B) dye in aqueous solutions. Optimising parameters such as the effects of contact time, medium pH and ionic strength (using NaCl, NaNO3, KCl and KNO3) were investigated. The results indicated that 150 min were sufficient for the adsorption to reach an equilibrium state and no adjustment of pH medium was necessary. Batch adsorption experiments such as adsorption isotherm, thermodynamics and kinetics were investigated and the experimental isotherm data were fitted to six isotherm models, namely Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Redlich-Peterson and Sips, with the latter being the best-fit isotherm model showing maximum adsorption capacity (qmax) of 267.9 mg g−1. Thermodynamics studies indicated adsorption of MV2B to be exothermic in nature, occurring spontaneously. The kinetics was best described by the pseudo-second-order model. Regeneration of IA pointed to its reusability, maintaining high adsorption capacity even up until Cycle 5 when treated with acid (HCl) and base (NaOH). Functional groups such as hydroxyl and amine groups which could be involved in the adsorption of MV2B were determined using FTIR spectroscopy, and the point of zero charge of IA was found to be at pH 6.81.


2013 ◽  
Vol 67 (5) ◽  
pp. 983-988 ◽  
Author(s):  
Shuncai Wang ◽  
Rongzhuo Yuan ◽  
Xueyong Yu ◽  
Chaojie Mao

This study explored the feasibility of utilizing lead–zinc tailings for phosphate removal in laboratory experiments. The adsorption isotherm, kinetics and pH effect were examined in batch experiments. The Freundlich and Langmuir isotherm models were used for data fitting. The adsorption kinetics can be best described by the simple Elovich equation. The phosphate adsorption tends to decrease with the increase of pH, from 0.37 mg P/g at pH 2.05 to 0.12 mg P/g at pH 7.01, and tends to increase from 0.12 mg P/g at pH 7.01 to 0.64 mg P/g at pH 12.52. The actual phosphate removal on the tailings could be a consequence of adsorption and precipitation reactions with Fe, Al and Ca. Due to their low cost, this type of tailings has the potential to be utilized for cost-effective removal of phosphate from wastewater.


2018 ◽  
Vol 162 ◽  
pp. 05021
Author(s):  
Alaa Wadie ◽  
Enas Al-Khawaja

The extent of removal of heavy metal ions cadmium Cd(II) and silver Ag(I) in single and binary system by adsorption on alumina has been investigated. Adsorption experiments were performed in batch technique from synthetic solutions using high purity nano activated alumina prepared in laboratory as adsorbent for heavy metals remove. Several experimental parameters that affect the extent of adsorption of the metal ions of interest have been investigated such as adsorbent dosage, concentration of the adsorbate, contact time, agitation speed and pH of the system under study. The equilibrium nature of the adsorption of the metal ions at different concentrations has been followed by Freundlich and Langmuir adsorption isotherms. Correlation coefficients (R2) derived from these plots are (0.965) for cadmium Cd(II) and (0.966) for silver Ag(I). This work proposes a cost-effective method for the efficient removal of Cd(II) and Ag(I) from aqueous solutions. The conditions required for effective removal have been optimized.


2021 ◽  
Vol 11 (22) ◽  
pp. 10722
Author(s):  
Abdelkader Ouakouak ◽  
Messameh Abdelhamid ◽  
Barhoumi Thouraya ◽  
Hadj-Otmane Chahinez ◽  
Grabi Hocine ◽  
...  

This study proposed a novel and low-cost adsorbent prepared from dredging sediment (DSD) for effective removal of dye in aqueous solutions. The adsorption efficiency and behavior of the DSD adsorbent toward the crystal violet (CV), a cationic dye, were investigated via batch experiments. The results showed that DSD samples contain mainly clay minerals (illite and kaolinite) and other mineral phases. In addition, DSD is a mesoporous material (Vmesopore = 94.4%), and it exhibits a relatively high surface area (~39.1 m2/g). Adsorption experiments showed that the solution’s pH slightly affects the adsorption process, and a pH of 11 gave a maximum capacity of 27.2 mg/g. The kinetic data of CV dye adsorption is well described by the pseudo–second-order and the Avrami models. The Langmuir and Liu isotherm models provide the best fit for the adsorption equilibrium data. The monolayer adsorption capacity of Langmuir reached 183.6, 198.0, and 243.6 mg/g at 293, 308, and 323 K, respectively. It was also found that the adsorption process was spontaneous (−ΔG°), exothermic (−∆H°), and increased the randomness (+∆S°) during the adsorption operation. The primary mechanisms in CV dye adsorption were ion exchange and pore filling, whereas electrostatic attraction was a minor contribution. In addition, three steps involving intraparticle diffusion occur at the same time to control the adsorption process. The results of this study highlight the excellent efficiency of DSD material as an ecofriendly sorbent for toxic dyes from water media.


2021 ◽  
Vol 30 (1) ◽  
pp. 86-97
Author(s):  
Saif Alquzweeni ◽  
Rasha Alkizwini ◽  
Afrah Hassan

A novel application of building demolition waste for removal benzene from aqueous solutions. In this research, demolition waste from buildings has been studied for possible use as benzene removal adsorbent from aquatic solution. The effect of adsorbent dosage, contact time, initial benzene concentration, and initial pH on benzene adsorption capacity have been investigated in the batch adsorption experiments. The adsorption effects initially happened very rapidly and achieved equilibrium within 180 min. Benzene removal was observed to decrease by an increase in the initial concentration of benzene of 300–700 mg·L–1, an increase in the adsorbent dose of 0.4–2.4 g per 100 mL, where an optimum adsorbent dose equal to 1.2 g per 100 mL was found. The potential of adsorption increases with pH 3.0–7.0 to reach the maximum removal efficiency at pH 6.0. The findings showed that equilibrium data were adequately adapted and correlated with the Freundlich isotherm models. The average percentage of the removal at room temperature was about 98%. Results suggest that building demolition waste can be used effectively in industrial wastewater treatment for the removal of aromatic hydrocarbon, benzene, as a low-cost option.


2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
Xuan Hoa Vu ◽  
Lan Huong Nguyen ◽  
Huu Tap Van ◽  
Dinh Vinh Nguyen ◽  
Thu Huong Nguyen ◽  
...  

In this study, freshwater snail shells (FSSs) containing CaCO3 were used as a low-cost biosorbent for removing Cr(VI) from aqueous solutions. The characteristics of FSS and mechanism of Cr(VI) adsorption onto FSS were investigated. The FSS biosorbent was characterized using nitrogen adsorption/desorption isotherm, X-ray diffraction, scanning electron microscopy with energy dispersive spectroscopy, and Fourier transform infrared spectroscopy. The adsorption mechanism was determined by conducting various batch adsorption experiments along with fitting experimental data with various adsorption models. Batch adsorption experiments were conducted as a function of solution pH, contact time, biosorbent dose, and initial Cr(VI) concentration. Results indicated that pH = 2, a contact time of 120 min, and an initial Cr(VI) concentration of 30 mg/L at 20°C were the best conditions for adsorption of Cr(VI) onto FSS. The Cr(VI) adsorption onto FSS decreased with an increase in temperature from 20 to 40°C. The obtained maximum adsorption capacity was 8.85 mg/g for 2 g/L of FSS dose with 30 mg/L of initial Cr(VI) at 20°C. The adsorption equilibrium data fit well with the Sips and Langmuir isotherm models at 20°C with a high R2 of 0.981 and 0.975, respectively. Also, a good correlation between the experimental data and the pseudo-second-order model was achieved, with the highest R2 of 0.995 at 20°C. The adsorption mechanisms were electrostatic interaction and ion exchange. Simultaneously, this mechanism was also controlled by film diffusion. The Cr(VI) adsorption process was irreversible, spontaneous (−∆G°), exothermic (∆H° is negative), and less random (∆S° is negative). In conclusion, freshwater snail shells have the potential as a renewable adsorbent to remove toxic metals from wastewater.


Energies ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1771
Author(s):  
Tomasz Kalak ◽  
Ryszard Cierpiszewski ◽  
Małgorzata Ulewicz

In these research studies, fly ash (SW-FA) resulting from the incineration of sunflower (20%) and wood (80%) waste employing the circulating fluidized bed combustion (CFBC) technology was used to analyze the possibility of removing Pb(II) and Cu(II) ions in adsorption processes. Currently, great emphasis is placed on circular economy, zero waste or climate neutrality strategies. The use of low-cost SW-FA waste seems to fit well with pro-ecological, economic and energy-saving trends. Hence, this material was characterized by various techniques, such as granulation analysis, bulk density, SEM-EDX, XRD and XRF analysis, BET, BJH, thermogravimetry, zeta potential, SEM morphology and FT-IR spectrometry. As a result of the conducted research, the factors influencing the effectiveness of the adsorption process, such as adsorbent dosage, initial and equilibrium pH, initial metal concentration and contact time, were analyzed. The maximum removal efficiency were achieved at the level of 99.8% for Pb(II) and 99.6% for Cu(II), respectively. The kinetics analysis and isotherms showed that the pseudo-second-order equation and the Freundlich isotherm models better describe these processes. The experiments proved that SW-FA can act as an appropriate adsorbent for highly effective removal of lead and copper from wastewater and improvement of water quality.


2021 ◽  
Vol 13 (15) ◽  
pp. 8421
Author(s):  
Yuan Gao ◽  
Jiandong Huang ◽  
Meng Li ◽  
Zhongran Dai ◽  
Rongli Jiang ◽  
...  

Uranium mining waste causes serious radiation-related health and environmental problems. This has encouraged efforts toward U(VI) removal with low cost and high efficiency. Typical uranium adsorbents, such as polymers, geopolymers, zeolites, and MOFs, and their associated high costs limit their practical applications. In this regard, this work found that the natural combusted coal gangue (CCG) could be a potential precursor of cheap sorbents to eliminate U(VI). The removal efficiency was modulated by chemical activation under acid and alkaline conditions, obtaining HCG (CCG activated with HCl) and KCG (CCG activated with KOH), respectively. The detailed structural analysis uncovered that those natural mineral substances, including quartz and kaolinite, were the main components in CCG and HCG. One of the key findings was that kalsilite formed in KCG under a mild synthetic condition can conspicuous enhance the affinity towards U(VI). The best equilibrium adsorption capacity with KCG was observed to be 140 mg/g under pH 6 within 120 min, following a pseudo-second-order kinetic model. To understand the improved adsorption performance, an adsorption mechanism was proposed by evaluating the pH of uranyl solutions, adsorbent dosage, as well as contact time. Combining with the structural analysis, this revealed that the uranyl adsorption process was mainly governed by chemisorption. This study gave rise to a utilization approach for CCG to obtain cost-effective adsorbents and paved a novel way towards eliminating uranium by a waste control by waste strategy.


2021 ◽  
Vol 11 (4) ◽  
Author(s):  
Theresa C. Umeh ◽  
John K. Nduka ◽  
Kovo G. Akpomie

AbstractDeterioration in soil–water environment severely contributed by heavy metal bioavailability and mobility on soil surface and sub-surface due to irrational increase in wastewater discharge and agrochemical activities. Therefore, the feasibility of adsorption characteristics of the soil is paramount in curbing the problem of micropollutant contamination in the farming vicinity. Soil from a farming site in a populated area in Enugu, Nigeria was collected and tested to measure the lead and cadmium contents using atomic absorption spectrophotometer (AAS). The adsorption potency of the ultisol soil was estimated for identifiable physicochemical properties by standard technique. The mean activity concentration of Pb2+ and Cd2+ was 15.68 mg/kg and 3.01 mg/kg. The pH, temperature, metal concentration and contact time adsorptive effect on the Pb2+ and Cd2+ uptake was evaluated by batch adsorption technique. The Langmuir, Freundlich and Temkin models were fitted into equilibrium adsorption data and the calculated results depict a better and satisfactory correlation for Langmuir with higher linear regression coefficients (Pb2+, 0.935 and Cd2+, 0.971). On the basis of sorption capacity mechanism of the soil, pseudo-second-order model best described the kinetics of both metal ions retention process. The results of the present study indicated that the soil being a low cost-effective adsorbent can be utilized to minimize the environmental risk impact of these metal ions.


Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1312
Author(s):  
Dereje Tadesse Mekonnen ◽  
Esayas Alemayehu ◽  
Bernd Lennartz

The contamination of surface and groundwater with phosphate originating from industrial and household wastewater remains a serious environmental issue in low-income countries. Herein, phosphate removal from aqueous solutions was studied using low-cost volcanic rocks such as pumice (VPum) and scoria (VSco), obtained from the Ethiopian Great Rift Valley. Batch adsorption experiments were conducted using phosphate solutions with concentrations of 0.5 to 25 mg·L−1 to examine the adsorption kinetic as well as equilibrium conditions. The experimental adsorption data were tested by employing various equilibrium adsorption models, and the Freundlich and Dubinin-Radushkevich (D-R) isotherms best depicted the observations. The maximum phosphate adsorption capacities of VPum and VSco were calculated and found to be 294 mg·kg−1 and 169 mg·kg−1, respectively. A pseudo-second-order kinetic model best described the experimental data with a coefficient of correlation of R2 > 0.99 for both VPum and VSco; however, VPum showed a slightly better selectivity for phosphate removal than VSco. The presence of competitive anions markedly reduced the removal efficiency of phosphate from the aqueous solution. The adsorptive removal of phosphate was affected by competitive anions in the order: HCO3− >F− > SO4−2 > NO3− > Cl− for VPum and HCO3− > F− > Cl− > SO4−2 > NO3− for VSco. The results indicate that the readily available volcanic rocks have a good adsorptive capacity for phosphate and shall be considered in future studies as test materials for phosphate removal from water in technical-scale experiments.


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