Evaluation of two types of polyurethane for the immobilisation of Rhizopus oryzae for copper uptake

2003 ◽  
Vol 47 (9) ◽  
pp. 143-150 ◽  
Author(s):  
M.S. Alhakawati ◽  
C.J. Banks ◽  
D. Smallman

Previous studies have shown that Rhizopus oryzae strain IM 057412 grown in reticulated polyurethane foam demonstrated the same heavy metal adsorption capacity as the free biomass. Immobilisation in other types of polymers was shown to reduce the biomass uptake capacity because of mass transfer limitations due to the restricted porosity of the immobilisation matrices. For practical purposes the growing of biomass in polyurethane support particles to use as a commercial adsorbent is not viable or financially sound. The current work describes a different approach in which dried non-viable cells of R. Oryzae were incorporated into two types of polyurethane carrier matrix during the production process. The polymers used were a conventional hydrophobic polyurethane and a hydrophilic polyurethane, Hypol 2002. Oven-dried and powdered particles (D<150 μm) of R. oryazea were immobilised by mixing the biomass with each of the polymers prior to the reaction in which the polymer was expanded to form a foam: consequently the biomass was uniformly dispersed throughout the porous matrix. The resulting fungi-polyurethane matrices were then cut into cubes (≡4-5 mm dimension) and their adsorptive properties studied with respect to copper. Experiments were conducted in shake flasks to establish the equilibrium time for the reaction for both free and immobilised biomass. The biomass immobilised in Hypol gave the same adsorptive capacity as that of free biomass when compared on a weight basis, but biomass immobilised in conventional polyurethane foam showed no adsorption. To assess fully the effect of pH on copper and to eliminate precipitation as a removal mechanism experiments were conducted at different pHs and different copper concentrations. In each case the solution pH was maintained by acid or base addition in response to measurements using a standard calomel electrode. It was shown that at pH 5 copper concentrations above 100 mg l−1 were likely to precipitate. The amount of precipitation was accounted for within the high concentration adsorption isotherm experiments by using a mass balance approach. Results showed that the adsorption of the Hypol immobilised biomass followed the Langmuir adsorption isotherm model and showed the copper adsorption capacity of the matrix to be between 10 and 13 mg g−1. The copper attached to the immobilised biomass could easily be desorbed by increasing the acidity, allowing the matrix to be used in repetitive sorption-desorption cycles. There was a small decrease in the adsorption capacity after the first desorption cycle that could be explained by a partial loss of biomass as detected by loss of total organic carbon (TOC).

2019 ◽  
Author(s):  
Chem Int

Dodecyltrimethylammonium bromide (DTAB)–modified and unmodified calcium bentonite were both used for the competitive adsorption of aromatics (xylene, ethylbenzene and toluene) and petroleum products (gasoline, dual purpose kerosene and diesel) from their aqueous solution. Infrared spectroscopy (IR) and expansion tests (adsorption capacity and Foster swelling) measurement were performed in order to evaluate the performance of the adsorbents. The Foster swelling index and adsorption capacity of the DTAB modified calcium bentonite in the organic solvents follow the trend: xylene > ethylbenzene > toluene > gasoline > dual purpose kerosene (DPK) > diesel > water. However, the adsorption capacity of the adsorbent in diesel outweighed the adsorption capacity in DPK at high concentration of DTAB indicating that diesel has higher affinity for high DTAB concentration than DPK. The percentage removal of the solvent is directly proportional to the concentration of DTAB used in modifying the bentonite as well as the contact time between the adsorbent and the solvent, hence modified calcium bentonite adsorbed a higher percentage of organic solvents than the unmodified calcium bentonite. The adsorption characteristics of both adsorbents improved remarkably after proper agitation of the organic solvents, the unmodified calcium bentonite however adsorbed more water than the modified bentonite. Data obtained from adsorption isotherm models confirms that Freundlich adsorption isotherm model was favored more than Langmuir adsorption isotherm model with the correlation factor (R2) of the former tending more towards unity. The adsorption of ethylbenzene using DTAB modified and unmodified calcium bentonites follow a pseudo second order kinetics mechanism, suggesting that the rate determining step of adsorption involves both the adsorbent and the organic solvent.


2000 ◽  
Vol 42 (7-8) ◽  
pp. 345-352 ◽  
Author(s):  
M. S. Al-Hakawati ◽  
C. J. Banks

Rhizopus oryzae, strain IMI 057412, was immobilised by inclusion in six different polymers: polyvinlformal, polysulfone, polyurethane, alginate, polyacrylamide, k-carrageenan, polyethyleneimine(PEI). It was also grown on a seventh, polyurethane. The biomass/polymer matrices were formed into equal size units (4 mm spheres or cubes) and the resulting biomass/polymer matrices were used to uptake copper at 2 mg/l from a laboratory-formulated copper solution in shake flask experiments at room temperature and initially neutral pH. Results showed that the copper uptake capacity of immobilised biomass was either equal to or less than that of free biomass. Biomass immobilised in polyurethane gave a capacity equal to that of free biomass, while other matrices hindered the uptake to different degrees. The k-carrageenan matrix proved to be unstable in the copper solution and dissolved during the experiment releasing the biomass and leading to an erroneous result. The polymer matrices without biomass, with theexception of alginate and polysulfone, showed no measurable copper adsorption capacity. All the experiments were conducted in duplicate with a maximum variation between them of 7%.


1997 ◽  
Vol 35 (7) ◽  
pp. 205-211 ◽  
Author(s):  
R. Leyva-Ramos ◽  
J. R. Rangel-Mendez ◽  
J. Mendoza-Barron ◽  
L. Fuentes-Rubio ◽  
R. M. Guerrero-Coronado

The adsorption isotherm of cadmium on activated carbon was measured in a batch adsorber. Effects of temperature and solution pH on the adsorption isotherm were investigated by determining the adsorption isotherm at temperatures of 10, 25, and 40°C and at initial pH values from 2 to 8. Langmuir isotherm better fitted the experimental data since the average percent deviation was lower than with the Freundlich isotherm It was noticed that the amount of Cd2+ adsorbed was reduced about 3 times by increasing the temperature from 10 to 40°C. It was found that Cd2+ was not adsorbed on activated carbon at pH of 2 or lower and that Cd2+ was precipitated out as Cd(OH)2 at pH values above 9. Maximum adsorption capacity was observed at pH of 8 and the adsorption capacity was decreased about 12 times by reducing the initial pH from 8 to 3. According to the cadmium speciation diagram the predominant species below pH of 8 is Cd2+. Thus, cadmium was adsorbed on the activated carbon surface as Cd2+. It was concluded that the adsorption capacity is a strong function of pH and temperature.


2021 ◽  
Vol 10 (1) ◽  
pp. 27-36
Author(s):  
Siti Sarah ◽  
Adisalamun Adisalamun ◽  
Darmadi Darmadi ◽  
Suraiya Kamaruzzaman ◽  
Abrar Muslim ◽  
...  

This paper proposed adsorbent development by synthesizing polyurethane foam (PUF) using a simple method, mixing polyol with isocyanate and adding fillers of bentonite and magnetite to the PUF matrix. The study's main objective was to produce a PUF-based adsorbent with high reactivity to remove Hg2+ in wastewater. This bentonite and magnetite filler-modified polyurethane foam (BMPUF) adsorbent was fixed in a bed column for the adsorption of mercury (II) ions from an aqueous solution. The effect of initial Hg2+ concentration on the removal rate and the effect of contact time on adsorption efficiency was investigated. Langmuir, Freundlich, and BET non-linear models were taken into account to determine the best adsorption isotherm fitting and obtain adsorption capacity, intensity, and pore volume. As a result, it followed the non-linear Freundlich model, and the average adsorption capacity and intensity were 0.466 mg/g and 0.923, respectively. The average BET-based pore volume obtained was 0.782 L/mg. The kinetics study showed that the non-linear pseudo-first-order kinetics model was more suitable for describing the Hg2+ adsorption kinetics. The maximum equilibrium adsorption capacity was 1.770 mg/g with the adsorption rate of 0.0013 min-1 based on the non-linear model. The effect of varying bentonite and magnetite ratio on adsorption isotherm and kinetics was also investigated. Overall, the potential application of BMPUF adsorbent in the adsorption of mercury (II) ions was demonstrated in the current study. 


2016 ◽  
Vol 73 (11) ◽  
pp. 2654-2661 ◽  
Author(s):  
Shuxiong Tang ◽  
Yao Chen ◽  
Ruzhen Xie ◽  
Wenju Jiang ◽  
Yanxin Jiang

Operation experiments were conducted to optimize the preparation of activated carbons from corn cob. The Cr(VI) adsorption capacity of the produced activated carbons was also evaluated. The impact of the adsorbent dosage, contact time, initial solution pH and temperature was studied. The results showed that the produced corn cob activated carbon had a good Cr(VI) adsorptive capacity; the theoretical maximum adsorption was 34.48 mg g−1 at 298 K. The Brunauer–Emmett–Teller and iodine adsorption value of the produced activated carbon could be 924.9 m2 g−1 and 1,188 mg g−1, respectively. Under the initial Cr(VI) concentration of 10 mg L−1 and the original solution pH of 5.8, an adsorption equilibrium was reached after 4 h, and Cr(VI) removal rate was from 78.9 to 100% with an adsorbent's dosage increased from 0.5 to 0.7 g L−1. The kinetics and equilibrium data agreed well with the pseudo-second-order kinetics model and the Langmuir isotherm model. The equilibrium adsorption capacity improved with the increment of the temperature.


Author(s):  
R.A. Herring

Rapid thermal annealing (RTA) of ion-implanted Si is important for device fabrication. The defect structures of 2.5, 4.0, and 6.0 MeV As-implanted silicon irradiated to fluences of 2E14, 4E14, and 6E14, respectively, have been analyzed by electron diffraction both before and after RTA at 1100°C for 10 seconds. At such high fluences and energies the implanted As ions change the Si from crystalline to amorphous. Three distinct amorphous regions emerge due to the three implantation energies used (Fig. 1). The amorphous regions are separated from each other by crystalline Si (marked L1, L2, and L3 in Fig. 1) which contains a high concentration of small defect clusters. The small defect clusters were similar to what had been determined earlier as being amorphous zones since their contrast was principally of the structure-factor type that arises due to the difference in extinction distance between the matrix and damage regions.


J ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 193-205
Author(s):  
Opeyemi A. Oyewo ◽  
Sam Ramaila ◽  
Lydia Mavuru ◽  
Taile Leswifi ◽  
Maurice S. Onyango

The presence of toxic metals in surface and natural waters, even at trace levels, poses a great danger to humans and the ecosystem. Although the combination of adsorption and coagulation techniques has the potential to eradicate this problem, the use of inappropriate media remains a major drawback. This study reports on the application of NaNO2/NaHCO3 modified sawdust-based cellulose nanocrystals (MCNC) as both coagulant and adsorbent for the removal of Cu, Fe and Pb from aqueous solution. The surface modified coagulants, prepared by electrostatic interactions, were characterized using Fourier transform infrared, X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive spectrometry (SEM/EDS). The amount of coagulated/adsorbed trace metals was then analysed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). SEM analysis revealed the patchy and distributed floccules on Fe-flocs, which was an indication of multiple mechanisms responsible for Fe removal onto MCNC. A shift in the peak position attributed to C2H192N64O16 from 2θ = 30 to 24.5° occurred in the XRD pattern of both Pb- and Cu-flocs. Different process variables, including initial metal ions concentration (10–200 mg/L), solution pH (2–10), and temperature (25–45 °C) were studied in order to investigate how they affect the reaction process. Both Cu and Pb adsorption followed the Langmuir isotherm with a maximum adsorption capacity of 111.1 and 2.82 mg/g, respectively, whereas the adsorption of Fe was suggestive of a multilayer adsorption process; however, Fe Langmuir maximum adsorption capacity was found to be 81.96 mg/g. The sequence of trace metals removal followed the order: Cu > Fe > Pb. The utilization of this product in different water matrices is an effective way to establish their robustness.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 399
Author(s):  
Mohammed Umar Abba ◽  
Hasfalina Che Man ◽  
Raba’ah Syahidah Azis ◽  
Aida Isma Idris ◽  
Muhammad Hazwan Hamzah ◽  
...  

High proportion of copper has become a global challenge owing to its negative impact on the environment and public health complications. The present study focuses on the fabrication of a polyvinylidene fluoride (PVDF)-polyvinyl pyrrolidone (PVP) fiber membrane incorporated with varying loading (0, 0.5, 1.0, 1.5, and 2.0 wt%) of titanium dioxide (TiO2) nanoparticles via phase inversion technique to achieve hydrophilicity along with high selectivity for copper removal. The developed fibers were characterized based on scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), permeability, porosity, zeta potential, and contact angle. The improved membrane (with 1.0 wt% TiO2) concentration recorded the maximum flux (223 L/m2·h) and copper rejection (98.18%). Similarly, 1.0 wt% concentration of TiO2 nanoparticles made the membrane matrix more hydrophilic with the least contact angle of 50.01°. The maximum copper adsorption capacity of 69.68 mg/g was attained at 1.0 wt% TiO2 concentration. The experimental data of adsorption capacity were best fitted to the Freundlich isotherm model with R2 value of 0.99573. The hybrid membrane developed in this study has considerably eliminated copper from leachate and the concentration of copper in the permeate was substantially reduced to 0.044 mg/L, which is below standard discharge threshold.


Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 63
Author(s):  
Maria Harja ◽  
Gabriela Buema ◽  
Nicoleta Lupu ◽  
Horia Chiriac ◽  
Dumitru Daniel Herea ◽  
...  

Fly ash/magnetite material was used for the adsorption of copper ions from synthetic wastewater. The obtained material was characterized by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX), X-ray diffractometer (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET) surface area, and vibrating sample magnetometer (VSM). Batch adsorption experiments were employed in order to investigate the effects of adsorbent dose, initial Cu (II) concentration and contact time over adsorption efficiency. The experimental isotherms were modeled using Langmuir (four types of its linearization), Freundlich, Temkin, and Harkins–Jura isotherm models. The fits of the results are estimated according to the Langmuir isotherm, with a maximum adsorption capacity of 17.39 mg/g. The pseudo-second-order model was able to describe kinetic results. The data obtained throughout the study prove that this novel material represents a potential low-cost adsorbent for copper adsorption with improved adsorption capacity and magnetic separation capability compared with raw fly ash.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3718
Author(s):  
Mohammad Azam ◽  
Saikh Mohammad Wabaidur ◽  
Mohammad Rizwan Khan ◽  
Saud I. Al-Resayes ◽  
Mohammad Shahidul Islam

The aim of the research was to prepare low-cost adsorbents, including raw date pits and chemically treated date pits, and to apply these materials to investigate the adsorption behavior of Cr(III) and Cd(II) ions from wastewater. The prepared materials were characterized using SEM, FT-IR and BET surface analysis techniques for investigating the surface morphology, particle size, pore size and surface functionalities of the materials. A series of adsorption processes was conducted in a batch system and optimized by investigating various parameters such as solution pH, contact time, initial metal concentrations and adsorbent dosage. The optimum pH for achieving maximum adsorption capacity was found to be approximately 7.8. The determination of metal ions was conducted using atomic adsorption spectrometry. The experimental results were fitted using isotherm Langmuir and Freundlich equations, and maximum monolayer adsorption capacities for Cr(III) and Cd(II) at 323 K were 1428.5 and 1302.0 mg/g (treated majdool date pits adsorbent) and 1228.5 and 1182.0 mg/g (treated sagai date pits adsorbent), respectively. It was found that the adsorption capacity of H2O2-treated date pits was higher than that of untreated DP. Recovery studies showed maximal metal elution with 0.1 M HCl for all the adsorbents. An 83.3–88.2% and 81.8–86.8% drop in Cr(III) and Cd(II) adsorption, respectively, were found after the five regeneration cycles. The results showed that the Langmuir model gave slightly better results than the Freundlich model for the untreated and treated date pits. Hence, the results demonstrated that the prepared materials could be a low-cost and eco-friendly choice for the remediation of Cr(III) and Cd(II) contaminants from an aqueous solution.


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