
Susan Shahab Ahmed
Research InterestsWater and Wastewater Treatment
Biochar
Adsorption
Gender | FEMALE |
---|---|
Place of Work | Technical Engineering College/ Kirkuk |
Position | Non |
Qualification | Ph.d |
Speciality | Environmental Engineering |
Susan.ahmed@ntu.edu.iq | |
Phone | 07511176815 |
Address | Imam Kasim, Al tamim, Kirkuk, Iraq |
Languages
Arabic (97%)
English (95%)
Kurdish (75%)
Turkish (70%)
Skills
Research & Technical Writing: Writing reports, research papers, and environmental impact assessments. (95%)
Planning and executing environmental projects (85%)
Academic Qualification
Bachelor in Environmental Engineering
Sep 1, 1994 - Jul 1, 1999Al Mustansriyah University
Master Degree in Environmental Engineering
Sep 1, 2000 - Dec 1, 2003Almustansriyah University
Ph.D in Environmantal Engineering
Jun 12, 2016 - Nov 20, 2020University of Southern Queensland, Australia
Publications
Bone char as a green sorbent for removing health threatening fluoride from drinking water
Jun 1, 2019Journal Environment International
publisher ELSEVIER
DOI https://doi.org/10.1016/j.envint.2019.03.065
Volume 127
Millions of people around the world suffer from or prone to health problems caused by high concentration of fluoride in drinking water sources. One of the environmentally friendly and cost-effective ways for removing fluoride is the use of bone char. In this review, the structural properties and binding affinity of fluoride ions from different water sources was critically discussed. The effect of experimental conditions on enhancing the adsorption capacity of fluoride ions using bone char samples was addressed. It appears that surface properties, and conditions of the bone char production such as temperature and residence time play an important role in designing the optimal fluoride removal process. The optimum temperature for fluoride removal seems to be in the range of 500–700 °C and a residence time of 2 h. Applying various equilibrium adsorption isotherms for understanding fluoride adsorption mechanism was presented. The effect of bone char modification with different elements were discussed and recommendations for a further increase in the removal efficiency was proposed. Cost of bone char production and large-scale treatment systems were also discussed based on information available from scientific and commercial sources. Challenges with existing domestic defluoridation designs were highlighted and suggestions for new conceptual designs were provided.
Biochar versus bone char for a sustainable inorganic arsenic mitigation in water: What needs to be done in future research?
Jun 1, 2019Journal Environment International
publisher ELSEVIER
DOI https://doi.org/10.1016/j.envint.2019.03.012
Volume 127
Arsenic (As) is an emerging contaminant on a global scale posing threat to environmental and human health. The relatively brief history of the applications of biochar and bone char has mapped the endeavors to remove As from water to a considerable extent. This critical review attempts to provide a comprehensive overview for the first time on the potential of bio- and bone-char in the immobilization of inorganic As in water. It seeks to offer a rational assessment of what is existing and what needs to be done in future research as an implication for As toxicity of human health risks through acute and chronic exposure to As contaminated water. Bio- and bone-char are recognized as promising alternatives to activated carbon due to their lower production and activation cost. The surface modification via chemical methods has been adopted to improve the adsorption capacity for anionic As species. Surface complexation, ion exchange, precipitation and electrostatic interactions are the main mechanisms involved in the adsorption of As onto the char surface. However, arsenic-bio-bone char interactions along with their chemical bonding for the removal of As in aqueous solution is still a subject of debate. Hence, the proposed mechanisms need to be scrutinized further using advanced analytical techniques such as synchrotron-based X-ray. Moving this technology from laboratory phase to field scale applications is an urgent necessity in order to establish a sustainable As mitigation in drinking water on a global scale.
Effect of pyrolysis conditions on bone char characterization and its ability for arsenic and fluoride removal
Jul 1, 2020Journal Environmental Pollution
publisher ELSEVIER
DOI https://doi.org/10.1016/j.envpol.2020.114221
Volume 262
This study examined arsenite [As(III)], arsenate [As(V)] and fluoride (F−) removal potential of bone char produced from sheep (Ovis aries) bone waste. Pyrolysis conditions tested were in the 500 °C–900 °C range, for a holding time of 1 or 2 h, with or without N2 gas purging. Previous bone char studies mainly focused on either low or high temperature range with limited information provided on As(III) removal. This study aims to address these gaps and provide insights into the effect of pyrolysis conditions on bone char sorption capacity. A range of advanced chemical analyses were employed to track the change in bone char properties. As pyrolysis temperature and holding time increased, the resulting pH, surface charge, surface roughness, crystallinity, pore size and CEC all increased, accompanied by a decrease in the acidic functional groups and surface area. Pyrolysis temperature was a key parameter, showing improvement in the removal of both As(III) and As(V) as pyrolysis temperature was increased, while As(V) removal was higher than As(III) removal overall. F− removal displayed an inverse relationship with increasing pyrolysis temperature. Bone char prepared at 500 °C released significantly more dissolved organic carbon (DOC) then those prepared at a higher temperature. The bone protein is believed to be a major factor. The predominant removal mechanisms for As were surface complexation, precipitation and interaction with nitrogenous functional groups. Whereas F− removal was mainly influenced by interaction with oxygen functional groups and electrostatic interaction. This study recommends that the bone char pyrolysis temperature used for As and F− removal are 900 °C and 650 °C, respectively.
Inorganic arsenic species removal from water using bone char: A detailed study on adsorption kinetic and isotherm models using error functions analysis
Mar 5, 2021Journal Journal of Hazardous Materials
publisher ELSEVIER
DOI https://doi.org/10.1016/j.jhazmat.2020.124112
Volume 405
The removal of inorganic arsenic (As) species from water using bone char pyrolyzed at 900 °C was investigated. Results revealed that the Sips model resulted in the best As(III) experimental data fit, while As(V) data were best represented by the Langmuir model. The adsorption rate and mechanisms of both As species were investigated using kinetic and diffusional models, respectively. At low As(III) and As(V) concentrations of 0.5 and 2.5 mg/L, the removal was due to intra-particle interactions and pore diffusion following Pseudo-first-order kinetics. However, at higher concentrations of 5 and 10 mg/L, the pore diffusion mechanism was ineffective, and the adsorption was best described by Pseudo-second-order and Elovich models. The goodness of the fit of linearized and nonlinear forms of all models against experimental data was thoroughly tested using error function analysis. Nonlinear regressions produced lower error values, so they were utilized to calculate the parameters of the models. The changes in bone char surface chemistry were examined using FTIR and Energy-dispersive X-ray spectroscopy (EDS). Arsenic oxide and complexes with metals were the confirmed immobilized forms of As on the bone-char surface. To the authors’ knowledge, this study is the first attempt at As(III) adsorption analysis using bone char.
Evaluating the Ability of Bone Char/nTiO2 Composite and UV Radiation for Simultaneous Oxidation and Adsorption of Arsenite
Dec 22, 2021Journal Sustainable Chemistry
publisher MDPI
DOI https://doi.org/10.3390/suschem3010002
Volume 3
first_pagesettingsOrder Article Reprints Open AccessArticle Evaluating the Ability of Bone Char/nTiO2 Composite and UV Radiation for Simultaneous Oxidation and Adsorption of Arsenite by Susan Alkurdi 1,2ORCID,Raed Al-Juboori 3,Jochen Bundschuh 1,4,* andAlla Marchuk 5 1 School of Civil Engineering and Surveying, Faculty of Health, Engineering and Sciences, University of Southern Queensland, West Street, Toowoomba, QLD 4350, Australia 2 Engineering Technical College, Northern Technical University, Kirkuk 36001, Iraq 3 Water Engineering Research Group, Department of Civil and Environmental Engineering, Aalto University, P.O. Box 15200, Aalto, FI-00076 Espoo, Finland 4 Doctoral Program in Science, Technology, Environment, and Mathematics, Department of Earth and Environmental Sciences, National Chung Cheng University, 168, University Rd., Min-Hsiung, Chia-Yi 62102, Taiwan 5 Centre for Sustainable Agricultural Systems, University of Southern Queensland, Toowoomba, QLD 4350, Australia * Author to whom correspondence should be addressed. Sustain. Chem. 2022, 3(1), 19-34; https://doi.org/10.3390/suschem3010002 Submission received: 28 October 2021 / Revised: 15 December 2021 / Accepted: 22 December 2021 / Published: 8 January 2022 Downloadkeyboard_arrow_down Browse Figures Versions Notes Abstract The reuse of waste materials for water treatment purposes is an important approach for promoting the circular economy and achieving effective environmental remediation. This study examined the use of bone char/titanium dioxide nanoparticles (BC/nTiO2) composite and UV for As(III) and As(V) removal from water. The composite was produced via two ways: addition of nTiO2 to bone char during and after pyrolysis. In comparison to the uncoated bone char pyrolyzed at 900 °C (BC900), nTiO2 deposition onto bone char led to a decrease in the specific surface area and pore volume from 69 to 38 m2/g and 0.23 to 0.16 cm3/g, respectively. However, the pore size slightly increased from 14 to 17 nm upon the addition of nTiO2. The composite prepared during pyrolysis (BC/nTiO2)P had better As removal than that prepared after pyrolysis with the aid of ultrasound (BC/nTiO2)US (57.3% vs. 24.8%). The composite (BC/nTiO2)P had higher arsenate oxidation than (BC/nTiO2)US by about 3.5 times. Arsenite oxidation and consequent adsorption with UV power of 4, 8 and 12 W was examined and benchmarked against the composite with visible light and BC alone. The highest UV power was found to be the most effective treatment with adsorption capacity of 281 µg/g followed by BC alone (196 µg/g). This suggests that the effect of surface area and pore volume loss due to nTiO2 deposition can only be compensated by applying a high level of UV power.
Innovative capacitive deionization-degaussing approach for improving adsorption/desorption for macadamia nutshell biochar
Jun 1, 2022Journal Journal of Water Process Engineering
publisher ELSEVIER
DOI https://doi.org/10.1016/j.jwpe.2022.102786
Volume 47
Adsorption is a well known effective technology for water treatment. Although limited capacities of adsorbents and regeneration issues are two common challenges. This study proposed and tested innovative approaches for improving adsorption/desorption of biochar made from macadamia nutshell (MBC). These approaches are capacitive deionization (CDI) and degaussing (full process detailed in methods), for the respective enhancement of adsorption and desorption of MBC. Nitrate was used as a model contaminant. It was found that CDI could extend the saturation time of MBC by increasing the bed specific throughput by 10 fold. Modeling of the breakthrough curves showed that the modified dose-response model fits well the experimental data. The regeneration of MBC with degaussing and deionized water backwash was compared with conventional tap and deionized water backwash. Degaussing increased the maximum nitrate recovery for deionized water from 50% to 73%. In comparison, the maximum nitrate recovery with tap water was 23%. The degaussing improvement of nitrate desorption holds for only the first 60 min. The obtained charge efficiency for MBC-CDI was slightly higher than literature values for the same applied voltage (78,6%). The degaussing system was also proven to be efficient with energy consumption of 43,7 J/mmol of NO3−. The possible mechanism behind degaussing improvement of nitrate desorption is the removal of the static charges on nitrate ion hydration. The regenerated MBC with degaussing and deionized water was tested with CDI for nitrate adsorption and compared to fresh MBC. The regenerated MBC-CDI exhibited better nitrate adsorption than fresh MBC for two cycles.