Naimah Ibrahim

Dr. Naimah Ibrahim

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 May 2020 in Environmental Science and Pollution Research
Verified
Journal Article
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MHMuhammad Adli Hanif
Muhammad Adli Hanif
NINaimah Ibrahim
Naimah Ibrahim
AJAishah Abdul Jalil
Aishah Abdul Jalil

1 March 2022 in Science of The Total Environment
Verified
Journal Article
Closed access
MHMuhammad Adli Hanif
Muhammad Adli Hanif
NINaimah Ibrahim
Naimah Ibrahim
FDFarrah Aini Dahalan
Farrah Aini Dahalan
UAUmi Fazara Md Ali
Umi Fazara Md Ali
MHMasitah Hasan
Masitah Hasan
AJAishah Abdul Jalil
Aishah Abdul Jalil

1 April 2008 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
MIMohamed Hasnain Isa
Mohamed Hasnain Isa
NINaimah Ibrahim
Naimah Ibrahim
HAHamidi Abdul Aziz
Hamidi Abdul Aziz
MAMohd. Nordin Adlan
Mohd. Nordin Adlan
NSNor Habsah Md Sabiani
Nor Habsah Md Sabiani
SKShamsul Rahman Mohamed Kutty
Shamsul Rahman Mohamed Kutty

21 June 2017 in IOP Conference Series: Materials Science and Engineering
Verified
Conference Paper
Open access
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NZN Z Zulkurnai
N Z Zulkurnai
UAUmi Fazara Md Ali
Umi Fazara Md Ali
NINaimah Ibrahim
Naimah Ibrahim
NMN S Abdul Manan
N S Abdul Manan
In recent years, carbon dioxide (CO2) emission has become a major concern as the amount of the emitted gas significantly increases annually. Consequently, this phenomenon contributes to global warming. Several CO2 capture methods, including chemical adsorption by activated carbon, have been proposed. In this study, activated carbon was prepared from sea mango (Cerbera odollam), which was functionalized with deep eutectic solvent (DES) composed of choline chloride and glycerol to increase the efficiency of CO2 capture. The samples underwent pre-carbonization and carbonization processes at 200 °C and 500 °C, respectively, with nitrogen gas and flowing several gases, namely, CO2 and steam, and then followed by impregnation with 50% phosphoric acid (H3PO4) at 1:2 precursor-to-activant ratio. The prepared activated carbon was impregnated with DES at 1:2 precursor-to-activant ratio. The optimum CO2 adsorption capacity of the activated carbon was obtained by using CO2 gas treatment method (9.851 mgCO2/gsol), followed by the absence of gases (9.685 mgCO2/gsol), steam (9.636 mgCO2/gsol), and N2 (9.536 mgCO2/gsol).

9 November 2023 in Bioengineered
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Journal Article
Open access
NNNik Nor Amirah Mohd Napi
Nik Nor Amirah Mohd Napi
NINaimah Ibrahim
Naimah Ibrahim
MHMuhammad Adli Hanif
Muhammad Adli Hanif
MHMasitah Hasan
Masitah Hasan
FDFarrah Aini Dahalan
Farrah Aini Dahalan
RBRaj Boopathy
Raj Boopathy
Microplastic (MP) is an emerging contaminant of concern due to its abundance in the environment. Wastewater treatment plant (WWTP) can be considered as one of the main sources of microplastics in freshwater due to its inefficiency in the complete removal of small MPs. In this study, a column-based MP removal which could serve as a tertiary treatment in WWTPs is evaluated using granular activated carbon (GAC) as adsorbent/filter media, eliminating clogging problems commonly caused by powder form activated carbon (PAC). The GAC is characterized via N2 adsorption-desorption isotherm, field emission scanning electron microscopy, and contact angle measurement to determine the influence of its properties on MP removal efficiency. MPs (40-48 μm) removal up to 95.5% was observed with 0.2 g/L MP, which is the lowest concentration tested in this work, but still higher than commonly used MP concentration in other studies. The performance is reduced with further increase in MP concentration (up to 1.0 g/L), but increasing the GAC bed length from 7.5 to 17.5 cm could lead to better removal efficiencies. MP particles are immobilized by the GAC predominantly by filtration process by being entangled with small GAC particles/chips or stuck between the GAC particles. MPs are insignificantly removed by adsorption process through entrapment in GAC porous structure or attachment onto the GAC surface.

4 April 2016 in Desalination and Water Treatment
Verified
Journal Article
Open access
SKSu-Huan Kow
Su-Huan Kow
MFMuhammad Ridwan Fahmi
Muhammad Ridwan Fahmi
CAChe Zulzikrami Azner Abidin
Che Zulzikrami Azner Abidin
SOSoon-An Ong
Soon-An Ong
NINaimah Ibrahim
Naimah Ibrahim
Spent activated carbon (SAC) must either be disposed of at a landfill or regenerated and reused in industries. Regeneration of SAC is a more preferable option as it can cut down replacement and disposal cost as well as reduce secondary pollution. Chemical regeneration is more suitable and economically feasible option for small-scale industrial application as compared to thermal regeneration. In this study, SAC is regenerated using sodium hydroxide (NaOH) solution and hot water. The aim of this study is to evaluate the effectiveness of NaOH and hot water regeneration of SAC. The optimal regeneration condition for SAC was determined and the regeneration performance was assessed by iodine and methylene blue (MB) adsorption test. Finding shows the optimal regeneration condition of carbon regeneration is 15 mL of 6 N of NaOH solution per g of carbon with 30 min of contact time. The estimated surface area, micropore volume, and total pore volume of batch and column regenerated SAC were 899.1 m2/g, 0.8702 cm3/g, 0.9521 cm3/g; and 849.0 m2/g, 0.8519 cm3/g, and 0.9450 cm3/g, respectively. The regeneration efficiency of regenerated SAC is comparable to fresh activated carbon with regeneration efficiency more than 90% in iodine adsorption test and 98% in MB adsorption test.