Mohammad W. Kadi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Mohammad W. Kadi has a total of 40 co-authors. Here are the top co-authors by number of shared publications:
A. Abd El-Mohty
Hot Labs Center, Atomic Energy Authority
2 shared publications- Abdallah A. Shaltout
Spectroscopy Department, Physics Research Institute, National Research Centre, El Behooth St., 12622 Dokki, Cairo, Egypt
2 shared publications - Mohammad Soror El-Shahawi
Department of Chemistry, Faculty of Science, Damietta University, New Damietta, 34517 Damietta, Egypt
2 shared publications N. E. A. Eweda
Nuclear Research Center, Atomic Energy Authority
2 shared publications- Nadeem Ali
Centre of Excellence in Environmental Studies, King Abdulaziz University, Jeddah, Saudi Arabia
2 shared publications - Reda M. Mohamed
Department of Chemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia
2 shared publications
Latest Publications
- 22 August 2023
- Published by Springer Nature in Archives of Environmental Contamination and Toxicology
- Vol. 85 (4) , 451-465
Temporal and Spatial Variations of Potentially Toxic Elements in PM10 Collected in Jeddah City, Saudi Arabia
Air pollution causes environmental and health problems around the world. In this study, ambient particulate matter with an aerodynamic diameter equal to or less than 10 microns (PM10) has been collected at three different locations in Jeddah city, Saudi Arabia. The locations are characterized by differences in terms of traffic, residential intensity, industrial, and non-road mobile machinery activities. The monthly and annual mass concentration of the PM10 exceeds the recommended annual limit of the World Health Organization (15 µg/m3) and the European air quality standard (40 µg/m3) at the three locations. The collected PM10 samples as well as a certified reference material of atmospheric particulates (NIST 1678a) were digested in aqua regia using microwave digestion. The quantitative elemental analysis was carried out using inductively coupled plasma mass spectrometry. The variations of the elemental concentration in terms of workdays, weekends, seasons, and annual were determined at the three locations. The spatial and temporal elemental variations were found to be different between the three sites, pointing to local influences that should be further evaluated. The concentration of Cd was found to be high and may cause health problems.
- 22 August 2023
- Published by Springer Nature in Archives of Environmental Contamination and Toxicology
- Vol. 85 (4) , 451-465
Temporal and Spatial Variations of Potentially Toxic Elements in PM10 Collected in Jeddah City, Saudi Arabia
Air pollution causes environmental and health problems around the world. In this study, ambient particulate matter with an aerodynamic diameter equal to or less than 10 microns (PM10) has been collected at three different locations in Jeddah city, Saudi Arabia. The locations are characterized by differences in terms of traffic, residential intensity, industrial, and non-road mobile machinery activities. The monthly and annual mass concentration of the PM10 exceeds the recommended annual limit of the World Health Organization (15 µg/m3) and the European air quality standard (40 µg/m3) at the three locations. The collected PM10 samples as well as a certified reference material of atmospheric particulates (NIST 1678a) were digested in aqua regia using microwave digestion. The quantitative elemental analysis was carried out using inductively coupled plasma mass spectrometry. The variations of the elemental concentration in terms of workdays, weekends, seasons, and annual were determined at the three locations. The spatial and temporal elemental variations were found to be different between the three sites, pointing to local influences that should be further evaluated. The concentration of Cd was found to be high and may cause health problems.
- Open Access
- 30 April 2021
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 18 (9) , 4803
Semi-Volatile Organic Compounds in Car Dust: A Pilot Study in Jeddah, Saudi Arabia
People may spend a significant amount of their daily time in cars and thus be exposed to chemicals present in car dust. Various chemicals are emitted from during car use, contaminating the car dust. In this study, we compiled published and unpublished data on the occurrence of phthalates, flame retardants (FRs), polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs) in Saudi car dust. Phthalates, a class of chemical commonly used as plasticizers in different car parts, were the major pollutants found in car dust, with a median value of ∑phthalates 1,279,000 ng/g. Among other chemicals, organophosphate flame retardants (OPFRs) were found to be between 1500–90,500 ng/g, which indicates their use as alternative FRs in the car industry. The daily exposure to Saudi drivers (regular and taxi drivers) was below the respective reference dose (RfD) values of the individual chemicals. However, the estimated incremental lifetime cancer risk (ILCR) values due to chronic exposure to these chemicals was >1 × 10−5 for taxi drivers for phthalates and PAHs, indicating that the long-term exposure to these chemicals is a cause of concern for drivers who spend considerable time in cars. The study has some limitations, due to the small number of samples, lack of updated RfD values, and missing cancer slope factors for many studied chemicals. Despite these limitations, this study indicates the possible range of exposure to drivers from chemicals in car dust and warrants further extensive studies to confirm these patterns.
- 30 April 2021
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 18 (9) , 4803
Open AccessSemi-Volatile Organic Compounds in Car Dust: A Pilot Study in Jeddah, Saudi Arabia
People may spend a significant amount of their daily time in cars and thus be exposed to chemicals present in car dust. Various chemicals are emitted from during car use, contaminating the car dust. In this study, we compiled published and unpublished data on the occurrence of phthalates, flame retardants (FRs), polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs) in Saudi car dust. Phthalates, a class of chemical commonly used as plasticizers in different car parts, were the major pollutants found in car dust, with a median value of ∑phthalates 1,279,000 ng/g. Among other chemicals, organophosphate flame retardants (OPFRs) were found to be between 1500–90,500 ng/g, which indicates their use as alternative FRs in the car industry. The daily exposure to Saudi drivers (regular and taxi drivers) was below the respective reference dose (RfD) values of the individual chemicals. However, the estimated incremental lifetime cancer risk (ILCR) values due to chronic exposure to these chemicals was >1 × 10−5 for taxi drivers for phthalates and PAHs, indicating that the long-term exposure to these chemicals is a cause of concern for drivers who spend considerable time in cars. The study has some limitations, due to the small number of samples, lack of updated RfD values, and missing cancer slope factors for many studied chemicals. Despite these limitations, this study indicates the possible range of exposure to drivers from chemicals in car dust and warrants further extensive studies to confirm these patterns.
- Open Access
- 11 May 2020
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 17 (9) , 3339
Spectroscopic Assessment of Platinum Group Elements of PM10 Particles Sampled in Three Different Areas in Jeddah, Saudi Arabia
Platinum group elements (PGE) including Ru, Rh, Pt and Pd have been quantified in air particulate matter with an aerodynamic diameter equal or less than 10 microns (PM10) using inductively coupled plasma mass spectrometry (ICP-MS). PM10 aerosols have been collected from three sites representing various activities in Jeddah city, Saudi Arabia. These locations are residential site with heavy traffic, industrial site and heavy traffic and a light traffic site outside the city. To obtain reasonable data of the PGE concentrations, a group from 10 to 15 PM10 samples were collected every month. The annual and seasonal variation of the mass concentration of the PGE were demonstrated. In all locations, Pt and Pd were relatively higher than Ru and Rh possibly because their main use is in automobile catalytic converters. Concentrations of observed PGE in PM10 could be arranged in ascending order as: Rh < Ru < Pd < Pt. In case of Ru and Pt, there are clear similarities in terms of the overall mean concentrations at the sampling locations. Due to the high concentration of Ru, Rh and Pd at low traffic site, there are certainly other sources of these elements rather than vehicle catalytic converters. However, at the industrial/heavy traffic location, high concentrations of Ru were detected during February 2015. In addition, high Pt concentrations were also detected at the light traffic site during May 2015. Results indicate that Pt source in PM10 is mainly the automobile catalytic converters.
- 11 May 2020
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 17 (9) , 3339
Open AccessSpectroscopic Assessment of Platinum Group Elements of PM10 Particles Sampled in Three Different Areas in Jeddah, Saudi Arabia
Platinum group elements (PGE) including Ru, Rh, Pt and Pd have been quantified in air particulate matter with an aerodynamic diameter equal or less than 10 microns (PM10) using inductively coupled plasma mass spectrometry (ICP-MS). PM10 aerosols have been collected from three sites representing various activities in Jeddah city, Saudi Arabia. These locations are residential site with heavy traffic, industrial site and heavy traffic and a light traffic site outside the city. To obtain reasonable data of the PGE concentrations, a group from 10 to 15 PM10 samples were collected every month. The annual and seasonal variation of the mass concentration of the PGE were demonstrated. In all locations, Pt and Pd were relatively higher than Ru and Rh possibly because their main use is in automobile catalytic converters. Concentrations of observed PGE in PM10 could be arranged in ascending order as: Rh < Ru < Pd < Pt. In case of Ru and Pt, there are clear similarities in terms of the overall mean concentrations at the sampling locations. Due to the high concentration of Ru, Rh and Pd at low traffic site, there are certainly other sources of these elements rather than vehicle catalytic converters. However, at the industrial/heavy traffic location, high concentrations of Ru were detected during February 2015. In addition, high Pt concentrations were also detected at the light traffic site during May 2015. Results indicate that Pt source in PM10 is mainly the automobile catalytic converters.
- 3 July 2018
- Published by Springer Nature in Applied Nanoscience
- Vol. 8 (6) , 1587-1596
Decoration of mesoporous graphite-like C3N4 nanosheets by NiS nanoparticle-driven visible light for hydrogen evolution
- 3 July 2018
- Published by Springer Nature in Applied Nanoscience
- Vol. 8 (6) , 1587-1596
Decoration of mesoporous graphite-like C3N4 nanosheets by NiS nanoparticle-driven visible light for hydrogen evolution
- 14 December 2015
- Published by Elsevier in Chinese Journal of Catalysis
- Vol. 36 (12) , 2103-2108
Enhanced photocatalytic hydrogen generation of mesoporous rutile TiO2 single crystal with wholly exposed {111} facets
- 14 December 2015
- Published by Elsevier in Chinese Journal of Catalysis
- Vol. 36 (12) , 2103-2108
Enhanced photocatalytic hydrogen generation of mesoporous rutile TiO2 single crystal with wholly exposed {111} facets
- Open Access
- 1 January 2014
- Published by Hindawi Limited in The Scientific World Journal
- Vol. 2014, 1-7
Elemental Spatiotemporal Variations of Total Suspended Particles in Jeddah City
Elements associated with total suspended particulate matter (TSP) in Jeddah city were determined. Using high-volume samplers, TSP samples were simultaneously collected over a one-year period from seven sampling sites. Samples were analyzed for Al, Ba, Ca, Cu, Mg, Fe, Mn, Zn, Ti, V, Cr, Co, Ni, As, and Sr. Results revealed great dependence of element contents on spatial and temporal variations. Two sites characterized by busy roads, workshops, heavy population, and heavy trucking have high levels of all measured elements. Concentrations of most elements at the two sites exhibit strong spatial gradients and concentrations of elements at these sites are higher than other locations. The highest concentrations of elements were observed during June–August because of dust storms, significant increase in energy consumption, and active surface winds. Enrichment factors of elements at the high-level sites have values in the range >10~60 while for Cu and Zn the enrichment factors are much higher (~0–>700) indicating that greater percentage of TSP composition for these three elements in air comes from anthropogenic activities.
- 1 January 2014
- Published by Hindawi Limited in The Scientific World Journal
- Vol. 2014, 1-7
Open AccessElemental Spatiotemporal Variations of Total Suspended Particles in Jeddah City
Elements associated with total suspended particulate matter (TSP) in Jeddah city were determined. Using high-volume samplers, TSP samples were simultaneously collected over a one-year period from seven sampling sites. Samples were analyzed for Al, Ba, Ca, Cu, Mg, Fe, Mn, Zn, Ti, V, Cr, Co, Ni, As, and Sr. Results revealed great dependence of element contents on spatial and temporal variations. Two sites characterized by busy roads, workshops, heavy population, and heavy trucking have high levels of all measured elements. Concentrations of most elements at the two sites exhibit strong spatial gradients and concentrations of elements at these sites are higher than other locations. The highest concentrations of elements were observed during June–August because of dust storms, significant increase in energy consumption, and active surface winds. Enrichment factors of elements at the high-level sites have values in the range >10~60 while for Cu and Zn the enrichment factors are much higher (~0–>700) indicating that greater percentage of TSP composition for these three elements in air comes from anthropogenic activities.
- 1 January 2014
- Published by Elsevier in Ceramics International
- Vol. 40 (1) , 227-232
Synthesis and optimization of cubic NiFe2O4 nanoparticles with enhanced saturation magnetization
- 1 January 2014
- Published by Elsevier in Ceramics International
- Vol. 40 (1) , 227-232
Synthesis and optimization of cubic NiFe2O4 nanoparticles with enhanced saturation magnetization
- Open Access
- 7 March 2013
- Published by Hindawi Limited in International Journal of Photoenergy
- Vol. 2013, 1-7
Enhanced Photocatalytic Activity of ZrO2-SiO2Nanoparticles by Platinum Doping
ZrO2-SiO2mixed oxides were prepared via the sol-gel method. Photo-assisted deposition was utilized for doping the prepared mixed oxide with 0.1, 0.2, 0.3, and 0.4 wt% of Pt. XRD spectra showed that doping did not result in the incorporation of Pt within the crystal structure of the material. UV-reflectance spectrometry showed that the band gap of ZrO2-SiO2decreased from 3.04 eV to 2.48 eV with 0.4 wt% Pt doping. The results show a specific surface area increase of 20%. Enhanced photocatalysis of Pt/ZrO2-SiO2was successfully tested on photo degradation of cyanide under illumination of visible light. 100% conversion was achieved within 20 min with 0.3 wt% of Pt doped ZrO2-SiO2.
- 7 March 2013
- Published by Hindawi Limited in International Journal of Photoenergy
- Vol. 2013, 1-7
Open AccessEnhanced Photocatalytic Activity of ZrO2-SiO2Nanoparticles by Platinum Doping
ZrO2-SiO2mixed oxides were prepared via the sol-gel method. Photo-assisted deposition was utilized for doping the prepared mixed oxide with 0.1, 0.2, 0.3, and 0.4 wt% of Pt. XRD spectra showed that doping did not result in the incorporation of Pt within the crystal structure of the material. UV-reflectance spectrometry showed that the band gap of ZrO2-SiO2decreased from 3.04 eV to 2.48 eV with 0.4 wt% Pt doping. The results show a specific surface area increase of 20%. Enhanced photocatalysis of Pt/ZrO2-SiO2was successfully tested on photo degradation of cyanide under illumination of visible light. 100% conversion was achieved within 20 min with 0.3 wt% of Pt doped ZrO2-SiO2.
- 28 September 2012
- Published by Springer Nature in Journal of Radioanalytical and Nuclear Chemistry
- Vol. 295 (3) , 1873-1880
Retention profile and selective separation of 90Y from 89Sr using zirconium-vanadate gel packed column
- 28 September 2012
- Published by Springer Nature in Journal of Radioanalytical and Nuclear Chemistry
- Vol. 295 (3) , 1873-1880
Retention profile and selective separation of 90Y from 89Sr using zirconium-vanadate gel packed column
- 3 July 2012
- Published by Springer Nature in Journal of Radioanalytical and Nuclear Chemistry
- Vol. 295 (1) , 15-22
Separation of Y from Sr by zirconium vanadate gel ion-exchanger sorbent: kinetics and thermodynamic study
- 3 July 2012
- Published by Springer Nature in Journal of Radioanalytical and Nuclear Chemistry
- Vol. 295 (1) , 15-22
Separation of Y from Sr by zirconium vanadate gel ion-exchanger sorbent: kinetics and thermodynamic study