scholarly journals Removal of Paracetamol from Wastewater by Calcined Gypsum: Adsorption and Kinetics Study

2020 ◽  
Vol 3 (1) ◽  
pp. 11-18
Author(s):  
Hossam Al-Itawi

It has been established that the presence of paracetamol in wastewaters can cause a potential risk to the environment. This work examined the possibility of using calcined gypsum in removing paracetamol from aqueous solutions. At neutral pH conditions, calcined gypsum was successful in removing paracetamol via adsorption, from aqueous solutions with a removal efficiency that ranged between 56.8 to 65.3 % of an initial concentration of 600 ppm. Increased temperature (from 20 to 500C) had a minor effect on the removal % of paracetamol while increasing the initial calcined gypsum dose (from 0.5 gm to 3 gm) and contact time (up to 15 min) increased by the removal % of paracetamol. Thermodynamically, the adsorption of paracetamol by calcined gypsum process was found to be spontaneous and endothermic, and more likely a physical process, while kinetically; the Pseudo-Second order model was found to be the best fit compared to the Elovich model. The removal process mainly consists of two stages, and it could be deduced from the kinetic behavior of paracetamol adsorption that the recrystallization process can be another rate-limiting step in the process.

2003 ◽  
Vol 48 (4) ◽  
pp. 217-220 ◽  
Author(s):  
H.M. El-mashad ◽  
G. Zeeman ◽  
W.K.P. van Loon ◽  
G.P.A. Bot ◽  
G. Lettinga

The anaerobic digestion of solid animal wastes has been studied in an accumulation system (AC) at a filling time of 60 days followed by about 50 days batch digestion at 40 and 50°C. Poor mixing conditions during anaerobic digestion of solid wastes promote stratification of the substrate and intermediate products along the reactor height. The effect of layers stratification has also been followed in the AC system. The results showed a pronounced stratification of both CODdis and VFA concentrations along the AC system height. The temperature had a minor effect on the methane yield. The results also showed that methanogenesis was rate limiting in the AC system while the hydrolysis was the rate-limiting step during batch digestion.


1989 ◽  
Vol 92 (3) ◽  
pp. 341-344
Author(s):  
W. Engstrom ◽  
O. Larsson ◽  
W. Sachsenmaier

The effects of two inhibitors of 3-hydroxy 3-methyl glutaryl-coenzyme A reductase (tunicamycin and mevinolin) on nuclear division in the myxomycete Physarum polycephalum were examined. Tunicamycin exerted a minor effect on division in synchronized cultures, whereas mevinolin delayed the second, third and fourth nuclear divisions with increasing efficiency. Mevinolin also appeared to be the more potent inhibitor of HMG-CoA reductase, which catalyses the rate-limiting step in the biosynthesis of cholesterol and other isoprene derivatives. These effects of mevinolin could be partially reversed by the addition of mevalonate, suggesting that mevinolin exerts its inhibitory effects on Physarum nuclear division by decreasing the activity of HMG-CoA reductase.


1998 ◽  
Vol 38 (8-9) ◽  
pp. 77-84 ◽  
Author(s):  
M. Majone ◽  
P. Massanisso ◽  
R. Ramadori

In various activated sludge systems, the biomass grows under transient (unbalanced) conditions and the storage response (formation of internal polymers as the fastest adaptation to the changing environment) becomes important. Till now the role of storage on population dynamics has been deeply investigated under anaerobic (EBPR processes) or aerobic (bulking control) conditions. Little attention has been given to processes including anoxic conditions even though in many of them storage phenomena are likely to occur (anoxic selectors, nitrogen removal processes with addition of an external source of readily biodegradable COD or with aerobic contact/anoxic stabilization). For these reasons, the aim of the present work was to investigate storage and succeeding use of stored products under anoxic and mixed (anoxic/aerobic) conditions. Batch experiments have shown that a mixed culture selected under aerobic conditions and intermittent feed (acetate-limited medium), was also able to take up acetate (90–100 mgCOD/gCOD h) and store it as PHB (35–40 mgCOD/gCOD h) under anoxic conditions. After acetate depletion, the stored PHB was used for growth and maintenance. The NUR on acetate in the presence of storage was 20 mgN/gVSS h (which corresponded to a COD removal of 6.9 mgCOD/mgN) while it dropped to 10–3 mgN/gVSS h in the “endogenous phase” when denitrification was on the stored PHB. The presence of aerobic conditions instead of anoxic ones had a major positive effect on the rate and yield of PHB storage while it had only a minor effect on the rate of PHB consumption. The latter observation can be explained by assuming that the hydrolysis of the stored product is the rate limiting step of the “endogenous” metabolism and that the hydrolysis rate is not highly dependent on aerobic-anoxic conditions. Cross-comparison of PHB storage and consumption under aerobic/anoxic conditions made it possible to determine that, in the particular mixed culture under investigation, all aerobic heterotrophs able to store were also able to denitrify.


Clay Minerals ◽  
2012 ◽  
Vol 47 (1) ◽  
pp. 81-92 ◽  
Author(s):  
S. Tomić ◽  
N. Rajić ◽  
J. Hrenović ◽  
D. Povrenović

AbstractNatural zeolitic tuff from Brus (Serbia) consisting mostly of clinoptilolite (about 90%) has been investigated for the reduction of the Mg concentration in spring water. The sorption capacity of the zeolite is relatively low (about 2.5 mg Mg g-1for the initial concentration of 100 mg Mg dm-3). The zeolitic tuff removes Mg from water solutions by ion exchange, which has been demonstrated by energy dispersive X-ray analysis (EDS). The extent of ion exchange was influenced by the pH and the initial Mg concentration. Kinetic studies revealed that Lagergen's pseudo-second order model was followed. Intra-particle diffusion of Mg2+influenced the ion exchange, but it is not the rate-limiting step. Rather than having to dispose of the Mg-loaded (waste) zeolite, a possible application was tested. Addition to a wastewater with a low concentration of Mg showed that it could successfully make up for the lack of Mg micronutrient and, accordingly, enabled the growth of phosphate-accumulating bacteriaA. Junii, increasing the amount of phosphate removed from the wastewater.


Author(s):  
Elisha A. Adeniji ◽  
Temitope O. Abodunrin ◽  
Temitope A. Ogunnupebi ◽  
Babatunde A. Koiki ◽  
Abimbola M. Olatunde ◽  
...  

AbstractThis research enthusiastically highlights the bio-adsorption of methylene blue (MB) by local, poultry, NaOH and citric acid modified ubiquitous eggshell (LES, NLES, CLES, PES, NPES and CPES) adsorbents. The microstructures of these adsorbents indicated that they had some surface functional moieties that were responsible for the adsorption of MB. The Langmuir isotherm and PSO model best fit the experiment data. The largest Langmuir monolayer adsorption capacity${q_{max}}$, was 242.47 mg/g, with the largest MB initial concentration of 400 mg/L. This was a clear indication and a confirmation that MB adsorption by the powdered eggshells was chemisorptive. Moreover, the values of$F$, the thickness of the boundary layer/film were$\gt 0$, showing that the rate limiting step for the adsorption process was controlled by more than one diffusion mechanism. The values of$\Delta {G^\circ }$for the adsorption of MB by the adsorbents indicated that the adsorption reactions were all non-feasible and non-spontaneous. The values for$\Delta {S^\circ }$(J/K/mol) for LES, NLES and CPES for the uptake of MB showed decrease in the chaos or degree of randomness of the adsorption reactions, and the reverse was the case for PES, NPES and CLES for the uptake of MB, which showed increase in the chaos or degree of randomness of the adsorption. The adsorption of MB by LES, NLES and CPES gave$\Delta {H^\circ }$(kJ/mol) values which were indicative of endothermic nature of the adsorption systems, and the reverse was the case for the uptake of MB by PES, NPES and CLES, which was indicative of the exothermic nature of the adsorption systems.


Author(s):  
Dorota Kołodyńska ◽  
Aleksandra Łyko ◽  
Marzena Gęca ◽  
Zbigniew Hubicki

<p>Lately there has been observed the increased presence of chlorates(VII) in the natural environment which can affect human health negatively. Therefore the removal of chlorate(VII) ions using the gel type resin functionalized with the tri-n-butyl ammonium (Dowex<sup>™</sup>PSR-2) from waters was studied. The main aim was to evaluate the effects of experimental conditions including contact time, initial solution concentration, pH and temperature on chlorate(VII) ions removal as well as the anion exchanger properties on chlorate(VII) ions sorption. It was found that only the pseudo second order model described the experimental data well and the intraparticle diffusion was not the rate-limiting step. According to the Freundlich model, the q<sub>e</sub> value was to be 69.26 mg/g at optimum conditions (pH 7.0 at 25 <sup>o</sup>C).<strong></strong></p>


2020 ◽  
Vol 81 (3) ◽  
pp. 436-444
Author(s):  
Wen Huang ◽  
Min Zhang ◽  
Yinhai Wang ◽  
Jiao Chen ◽  
Jianqiang Zhang

Abstract Biochar was prepared from rabbit faeces (RFB550) at 550 °C through pyrolysis and was characterised using elemental analysis, scanning electron microscopy, Brunauer–Emmett–Teller analysis and Fourier transform infrared spectroscopy (FTIR). The related factors, kinetics, isothermal curves and thermodynamics of the adsorption behaviours were investigated by conducting batch experiments. The results revealed the adsorption equilibrium of rhodamine B (RhB) and Congo red (CR) onto RFB550 with initial concentrations of 30 mg · L−1 at 25 °C and 210 min, and the best adsorption was observed when the pH of the RhB and CR solutions was 3 and 5, respectively. Pseudo-second-order kinetics was the most suitable model for describing the adsorption of RhB and CR onto RFB550, indicating that the rate-limiting step was mainly chemical adsorption. The isotherm data were best described by the Freundlich model, and the adsorption process was multi-molecular layer adsorption. Thermodynamic parameters revealed the spontaneous adsorption of RhB and CR onto RFB550. According to the results of the FTIR analysis, the oxygen-containing functional groups and aromatic structures on the surface of RFB550 provided abundant adsorption sites for RhB and CR, and the adsorption mechanism was potentially related to the hydrogen bonds and π–π bonds.


It has been widely assumed that the rate-limiting step in actomyosin ATPase activity during contraction is a single-stage attachment of the myosin head to a site on the thin filament. This assumption leads to a rate of energy liberation that increases monotonically with speed of shortening, in agreement with pre-war estimates of the output of work and heat; it does not explain the fall in energy release at high speeds that has been found more recently. This fall can be explained by assuming that the attachment is a two-stage process.


Molecules ◽  
2019 ◽  
Vol 24 (20) ◽  
pp. 3685 ◽  
Author(s):  
Abdulaziz Ali Alghamdi ◽  
Abdel-Basit Al-Odayni ◽  
Waseem Sharaf Saeed ◽  
Mohammed S. Almutairi ◽  
Fahad A. Alharthi ◽  
...  

The adsorption of methyl orange (MO) from aqueous solutions onto a KOH-activated polypyrrole-based adsorbent (PACK) was investigated using batch and fixed-bed column techniques. The structural, thermal, and morphological properties of the PACK, analyzed by various methods, support its applicability as an adsorbent. An adsorption kinetic study revealed a preferably pseudo-second-order (R2 = 0.9996) and rate-limiting step controlled by both film and intra-particle diffusions. The thermodynamic adsorption tests resulted in negative ΔG°, ΔH°, and ΔS° values, which decreased as the temperature and concentration increased, indicating the spontaneous and exothermic adsorption over 25–45 °C. The adsorption isotherms fit the experimental data in the order of Langmuir ≈ Freundlich > Temkin, with evidence of adsorption operating well via the monolayer physical adsorption process, and maximum monolayer adsorption ranging from 520.8 to 497.5 mg/g. The breakthrough curve of the fixed-bed column experiment was modeled using the Thomas, Yoon–Nelson, and Hill models, resulting in an equilibrium capacity of 57.21 mg/g. A 73% MO recovery was achieved, indicating the possibility of column regeneration. Compared to other adsorbents reported, PACK had comparable or even superior capacity toward MO. For cost-effectiveness, similar nitrogen-containing polymeric wastes could be exploited to obtain such excellent materials for various applications.


2020 ◽  
Vol 148 ◽  
pp. 02002 ◽  
Author(s):  
Rodel Guerrero ◽  
Catherine Acibar ◽  
Christine Marie Alarde ◽  
Jane Maslog ◽  
Christine Joy Pacilan

This study examined the removal of Pb2+ ions from aqueous solution with two different lead concentrations using a hydrogel-forming polymer based on hydroxypropyl cellulose (HPC) and sodium alginate (SA). The feasibility of the adsorption behavior of SA/HPC beads has been investigated with three varying ratios of 50:50, 75:25 and 100:0 under a stir condition. The adsorption experiments were done to determine the effects of contact time, lead concentration and SA-HPC ratio to the adsorption capacity of SA-HPC hydrogel beads. The results showed that the ratio 75:25 showed higher adsorption capacity compared to 100:0 and 50:50. It showcased 47.72 mg/g adsorption capacity and 95.45% adsorption percentage after three hours of contact time. The adsorption kinetic model indicated that the adsorption of Pb2+ ions onto the beads followed a pseudo-second order kinetic equation. This means that the adsorption mechanism shows a chemisorption process and its sole rate-limiting step is intraparticle diffusion.


Sign in / Sign up

Export Citation Format

Share Document