Treatment of wastewater is becoming a concern of an increasing prominence. Trace amounts of toxic metalloids and heavy metals (HMs) would contaminate large volumes of water. Being present as traces, removal of these ultratrace contaminants from wastewater is challenging. Adsorption of HMs onto raw (RPP) and burnt (BPP) potato peels (PP) is presented in the current treatise. Both adsorbents (RPP and BPP) proved to be efficient in removing Cd(II), Co(II), Cu(II), Fe(II), La(III), Ni(II), and Pb(II) from aqueous solutions. BPP was a more efficient adsorbent compared to RPP. Ecodesign of a model, green adsorbent was structured executing a multivariate approach, design of experiments (DoE). The purpose of using DoE is to maximize the efficiency of BPP (carbonaceous biomass) as a versatile adsorbent. Plackett–Burman design (PBD) was used as a screening phase. Four factors were considered: pH, contact time (CT), heavy metal concentration (HMC), and the adsorbent dose (AD). The Pareto chart of standardized effects shows that the most influential factor is the HMC. These data were confirmed by analysis of variance (ANOVA). Derringer’s function was operated to find the best factorial blend that maximizes the adsorption process. The percentage (%) removal of Cd(II), for example, was maximized hitting 100%. Adsorbent surface characterization was performed using FTIR, BET, SEM, TGA/dTG, and EDX analyses. Adsorption was found to be physisorption that follows Temkin isotherm with sorption energy 66 kJ/mole. Adsorption kinetics was found to be pseudo-first-order. Adsorption capacity (qm) for BPP was 239.64 mg/g. The diffusion inside the particles was very limited, while the initial rate of the adsorption was extremely high as shown by the Elovich plot.
Date pits (DPs) have been recycled into a low-cost adsorbent for removing of selected heavy metals (HMs) from artificially contaminated aqueous solutions. Adsorption of targeted HMs, both by raw date pits (RDP) and burnt date pits (BDP) was tested. Results showed that BDP is more efficient as an adsorbent and mostly adsorbing Cu(II). A novel approach; fractional factorial design (2 k − p – FrFD) was used to build the experimental pattern of this study. The effects of four factors on the maximum percentage (%) of removal (Y) were considered; pH, adsorbent dose (AD), heavy metal concentration (HMC), and contact time (CT). Statistically significant variables were detected using Pareto chart of standardized effects, normal and half-normal plots together with analysis of variance (ANOVA) at 95.0 confidence intervals (CI). Optimizing ( maximizing ) the percentage (%) removal of Cu(II) by BDP, was performed using optimization plots. Results showed that the factors: pH and adsorbent dose (AD) affect the response positively. Scanning electron microscopy (SEM) was used to study the surface morphology of both adsorbents while fourier-transform infrared spectroscopy (FTIR) was employed to get an idea on the functional groups on the surface and hence the adsorption mechanism. Raman spectroscopy was used to characterize the prepared adsorbents before and after adsorption of Cu(II). Equilibrium studies show that the adsorption behavior differs according to the equilibrium concentration. In general, it follows Langmuir isotherm up to 155 ppm, then Freundlich isotherm. Free energy of adsorption (Δ G ad ) is −28.07 kJ/mole, when equilibrium concentration is below 155 ppm, so the adsorption process is spontaneous, while (Δ G ad ) equals +17.89 kJ/mole above 155 ppm, implying that the process is non-spontaneous. Furthermore, the adsorption process is a mixture of physisorption and chemisorption processes, which could be endothermic or exothermic reactions. The adsorption kinetics were described using a second order model.
Titan yellow (TY), a triazene azo dye, was removed from contaminated wastewater samples using a green adsorbent recycled from Aloe vera leaves (AV) waste. Two adsorbents were developed—air-dried Aloe vera (ADAV) and thermally treated Aloe vera (TTAV). Adsorption efficacy of both adsorbents was assessed in terms of percent removal (%R) of TY and adsorption capacity (qe). ADAV had a better performance compared to TTAV. Plackett–Burman design (PBD) was exploited to establish the experimental pattern of the study. Four variables were studied: pH, adsorbent dose (AD), dye concentration (DC), and stirring time (ST). Analysis of variance (ANOVA) at 95.0 confidence interval (CI), control, and quality charts helped establish regression model(s). Characterization of both adsorbents was performed using FT-IR/Raman spectroscopy together with TGA/dTGA and SEM/energy dispersive X-ray spectroscopy (EDX) analyses. Textural properties were determined using nitrogen adsorption isotherms at 77 K. Results showed that the surface areas of ADAV and TTAV300 were 3.940 and 7.076 m2/g, respectively. Raman analysis showed that the TTAV had clear D- and G-bands. Equilibrium studies revealed that data were well fitted to Freundlich isotherm with a maximum adsorption capacity of 55.25 mg/g using Langmuir equation, and the adsorption was physisorption. Adsorption followed a pseudo-second order that occurred in two steps—diffusion and then adsorption.
Non-magnetic and magnetic low-cost biochar (BC) from date pits (DP) were applied to remove tigecycline (TIGC) from TIGC-artificially contaminated water samples. Pristine biochar from DP (BCDP) and magnetite-decorated biochar (MBC-DP) were therefore prepared. Morphologies and surface chemistries of BCDP and MBC-DP were explored using FT-IR, Raman, SEM, EDX, TEM, and BET analyses. The obtained IR and Raman spectra confirmed the presence of magnetite on the surface of the MBC-DP. SEM results showed mesoporous surface for both adsorbents. BET analysis indicated higher amount of mesopores in MBC-DP. Box–Behnken (BB) design was utilized to optimize the treatment variables (pH, dose of the adsorbent (AD), concentration of TIGC [TIGC], and the contact time (CT)) and maximize the adsorptive power of both adsorbents. Higher % removal (%R), hitting 99.91%, was observed using MBC-DP compared to BCDP (77.31%). Maximum removal of TIGC (99.91%) was obtained using 120 mg/15 mL of MBC-DP for 10 min at pH 10. Equilibrium studies showed that Langmuir and Freundlich isotherms could best describe the adsorption of TIGC onto BCDP and MBC-DP, respectively, with a maximum adsorption capacity (qmax) of 57.14 mg/g using MBC-DP. Kinetics investigation showed that adsorption of TIGC onto both adsorbents could be best-fitted to a pseudo-second-order (PSO) model.
Biosorptive removal of basic fuchsin (BF) from wastewater samples was achieved using the recycled agro-wastes of pistachio nut shells (PNS). Seven adsorbents were developed; raw shells (RPNS) and the thermally activated biomasses at six different temperatures (250–500 °C). Two measures were implemented to assess the performance of utilized adsorbents; %removal (%R) and adsorption capacity (qe). RPNS proved to be the best among the tested adsorbents. A smart approach, definitive-screening design (DSD) was operated to test the impact of independent variables on the adsorption capacity of RPNS. pH, adsorbent dose (AD), dye concentration (DC), and stirring time (ST), were the tested variables. Analysis of variance (ANOVA), control, and quality charts helped establishing regression model. Characterization was performed using Fourier- transform infrared (FT-IR)/Raman spectroscopies together with thermogravimetric analysis (TGA) and scanning electron microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDX) analyses. The surface area and other textural properties were determined using the Brunauer Emmett-Teller (BET) analysis. Removal of 99.71% of BF with an adsorption capacity of 118.2 mg/g could be achieved using a factorial blend of pH 12, 100 mg/50 mL of RPNS, and 250 ppm BF for 20 min. Equilibrium studies reveal that the adsorption is physisorption with adsorption energy of 7.45 kJ/mol as indicated by Dubinin-Radushkevich (DR) and Langmuir isotherms. Moreover, adsorption follows pseudo-second-order kinetics with respect to BF and is controlled by the adsorption rate.
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