Displaying publications 1 - 20 of 524 in total

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  1. Recent advances in hybrid wet scrubbing techniques for NOx and SO2 removal: State of the art and future research
    Sharif HMA, Mahmood N, Wang S, Hussain I, Hou YN, Yang LH, et al.
    Chemosphere, 2021 Jun;273:129695.
    PMID: 33524756 DOI: 10.1016/j.chemosphere.2021.129695
    Recently, the discharge of flue gas has become a global issue due to the rapid development in industrial and anthropogenic activities. Various dry and wet treatment approaches including conventional and hybrid hybrid wet scrubbing have been employing to combat against these toxic exhaust emissions. However, certain issues i.e., large energy consumption, generation of secondary pollutants, low regeneration of scrubbing liquid and high efficieny are hindering their practical applications on industrial level. Despite this, the hybrid wet scrubbing technique (advanced oxidation, ionic-liquids and solid engineered interface hybrid materials based techniques) is gaining great attention because of its low installation costs, simultaneous removal of multi-air pollutants and low energy requirements. However, the lack of understanding about the basic principles and fundamental requirements are great hurdles for its commercial scale application, which is aim of this review article. This review article highlights the recent developments, minimization of GHG, sustainable improvements for the regeneration of used catalyst via green and electron rich donors. It explains, various hybrid wet scrubbing techniques can perform well under mild condition with possible improvements such as development of stable, heterogeneous catalysts, fast and in-situ regeneration for large scale applications. Finally, it discussed recovery of resources i.e., N2O, NH3 and N2, the key challenges about several competitive side products and loss of catalytic activity over time to treat toxic gases via feasible solutions by hybrid wet scrubbing techniques.
    Matched MeSH terms: Oxidation-Reduction
  2. Underutilised palm stearin as hard stock for deep-frying medium and its performance for oil uptake in instant noodles
    Ooi EZH, Ab Karim NA, Chan ES, Wang Y, Tang TK, Tong SC, et al.
    J Sci Food Agric, 2024 May;104(7):3958-3970.
    PMID: 38284502 DOI: 10.1002/jsfa.13278
    BACKGROUND: As a by-product of the palm oil industry, palm stearin is often overlooked despite having several beneficial properties, such as excellent stability, which is critically essential to meet the demand of the global food trend in producing safer processed food. Specifically, deep frying of food is often associated with the production of toxic compounds that could potentially migrate into the food system when oils are degraded under continuous heating. The incorporation of palm stearin is regarded as a cost-effective and efficient method to modify the fatty acid composition of oils, enhance the frying qualities and lower the degradation rate.

    RESULTS: This study blended 5% and 10% palm stearin into palm oil to investigate the deep-frying performance and impact on food quality. Increasing the palm stearin content improved the frying oil's oxidative and hydrolytic stability, evidenced by reduction of total polar material, free fatty acid and total oxidation value. Addition of palm stearin increased the slip melting point which improved the oil's oxidative stability but no significant increase in oil content of instant noodles was observed. Scanning electron microscopy and fluorescence microscopy showed the formation of larger pores in the noodle structure that facilitated oil retention.

    CONCLUSION: Blending palm stearin into frying oil enhanced the frying stability and minimally affected the oil uptake in instant noodles. This article presents the viability of blending palm stearin into frying oils to develop longer-lasting frying oils. © 2024 The Authors. Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

    Matched MeSH terms: Oxidation-Reduction
  3. Unlocking the molecular modifications of plasma-activated water-induced oxidation through redox proteomics: In the case of duck myofibrillar protein (Anas platyrhynchos)
    Rao W, Ju S, Sun Y, Xia Q, Zhou C, He J, et al.
    Food Chem, 2024 Nov 15;458:140173.
    PMID: 38943955 DOI: 10.1016/j.foodchem.2024.140173
    Plasma-activated water (PAW) contains multiple active species that alter the structure of myofibrillar protein (MP) to enhance their gel properties. This work investigated the impact of PAW on the oxidation of cysteine in MP by label-free quantitative proteomics. PAW treatment caused the oxidation of 8241 cysteine sites on 2815 proteins, and structural proteins such as nebulin, myosin XVIIIB, myosin XVIIIA, and myosin heavy chain were susceptible to oxidation by PAW. Bioinformatics analysis, including Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway, subcellular localization, and STRING analysis, indicated that these proteins with differential oxidation sites were mainly derived from the cytoplasm and membrane, and were involved in multiple GO terms and KEGG pathways. This is one of the first reports of the redox proteomic changes induced by PAW treatment, and the results are useful for understanding the possible mechanism of PAW-induced oxidation of MP.
    Matched MeSH terms: Oxidation-Reduction*
  4. Electrochemical oxidation of propionaldehyde and butyraldehyde on a gold electrode
    Amirah Ahmad, Mohamed Rozali Othman
    Sains Malaysiana, 2009;38.
    The electrooxidation of propionaldehyde and butyraldehyde on a gold electrode was studied by cyclic voltammetry in alkaline media. Electrooxidation of both aldehydes showed the appearance of two anodic peaks. Another oxidation peak on a newly generated electrode surface was observed after the corresponding reduction peak for both aldehydes.
    Matched MeSH terms: Oxidation-Reduction
  5. An insight into the role of experimental parameters in advanced oxidation process applied for pharmaceutical degradation
    Qutob M, Alshehri S, Shakeel F, Alam P, Rafatullah M
    Environ Sci Pollut Res Int, 2024 Apr;31(18):26452-26479.
    PMID: 38546921 DOI: 10.1007/s11356-024-33040-3
    The advanced oxidation process (AOP) is an efficient method to treat recalcitrance pollutants such as pharmaceutical compounds. The essential physicochemical factors in AOP experiments significantly influence the efficiency, speed, cost, and safety of byproducts of the treatment process. In this review, we collected recent articles that investigated the elimination of pharmaceutical compounds by various AOP systems in a water medium, and then we provide an overview of AOP systems, the formation mechanisms of active radicals or reactive oxygen species (ROS), and their detection methods. Then, we discussed the role of the main physicochemical parameters (pH, chemical interference, temperature, catalyst, pollutant concentration, and oxidant concentration) in a critical way. We gained insight into the most frequent scenarios for the proper and improper physicochemical parameters for the degradation of pharmaceutical compounds. Also, we mentioned the main factors that restrict the application of AOP systems in a commercial way. We demonstrated that a proper adjustment of AOP experimental parameters resulted in promoting the treatment performance, decreasing the treatment cost and the treatment operation time, increasing the safeness of the system products, and improving the reaction stoichiometric efficiency. The outcomes of this review will be beneficial for future AOP applicants to improve the pharmaceutical compound treatment by providing a deeper understanding of the role of the parameters. In addition, the proper application of physicochemical parameters in AOP systems acts to track the sustainable development goals (SDGs).
    Matched MeSH terms: Oxidation-Reduction*
  6. Fulltext Qualitative analyses of the antimicrobial effect of ozonated water on supragingival plaque and salivary microbes
    Sadatullah S, Mohamed N, Razak F
    Ann Med Health Sci Res, 2014 Jul;4(4):526-31.
    PMID: 25221698 DOI: 10.4103/2141-9248.139301
    Ozone is an unstable gas, capable of oxidizing any biological entity. It is an effective bactericide in its gaseous as well as aqueous form.
    Matched MeSH terms: Oxidation-Reduction
  7. Synthesis, characterization and physicochemical properties of oleic acid ether derivatives as biolubricant basestocks
    Salimon J, Salih N, Yousif E
    J Oleo Sci, 2011;60(12):613-8.
    PMID: 22123242
    Petroleum is a finite source as well as causing several environmental problems. Therefore petroleum needs to be replaced by alternative and sustainable sources. Plant oils and oleochemicals derived from them represent such alternative sources; the use of oleochemicals as biobased lubricants is of significant interest. This article presents a series of chemical modification on oleic acid to yield synthetic biolubricant basestocks. Measuring of density, volatility, cloud point (CP), pour point (PP), flash point (FP), viscosity index (VI), onset temperature (OT) and signal maximum temperature (SMT) was carried out for each compound. Furthermore, the friction and wear properties were measured using high-frequency reciprocating rig (HFRR). The results showed that octadecyl 9-octadecyloxy-10-hydroxyoctadecanoate exhibited the most favorable low-temperature performance (CP %ndash;26°C, PP %ndash;28°C) and the lowest ball wear scan diameter (42 µm) while propyl 9-propyloxy-10-hydroxyoctadecanoate exhibited the higher oxidation stability (OT 156°C).
    Matched MeSH terms: Oxidation-Reduction
  8. Oxidation of p-cresol by ozonation
    Muhammad Ridwan Fahmi, Che Zulzikrami Azner Abidin, Ong Sa, Abdul Haqi Ibrahim, Siti Nasuha Sabri, Nur Aqilah Razali, et al.
    Sains Malaysiana, 2018;47:1085-1091.
    Oxidation of p-Cresol was investigated by using ozonation process. The aim of this research is to assess the effectiveness
    of ozonation on oxidation of micropollutant such as p-Cresol. Ozonation performance was evaluated based on p-Cresol
    concentration reduction and chemical oxidation demand (COD) reduction. It was found ozonation at pH11 achieved
    the highest p-Cresol degradation, with 95.8% of p-Cresol reduced and 96.0% of COD reduced, for an initial 50 mgL-1
    of p-Cresol. The degradation of p-Cresol could be expressed by second-order of kinetic model. The second-order rate
    constant k increases as the initial pH increased, but decreases with the increasing of initial p-Cresol concentrations.
    Besides, the absorption spectra of p-Cresol over ozonation time were analyzed by spectrophotometry. The evolution of
    absorption spectra of p-Cresol degradation suggests that the oxidation of p-Cresol follows three stages mechanisms
    with cycloaddition as the first step to produce aromatic intermediates followed by ring-opening reactions, degradation
    of the intermediates, and subsequently achieved mineralization.
    Matched MeSH terms: Oxidation-Reduction
  9. Evaluation of quality parameters for fresh, used and recycled palm olein
    Khor YP, Sim BI, Abas F, Lai OM, Wang Y, Nehdi IA, et al.
    J Sci Food Agric, 2019 Dec;99(15):6989-6997.
    PMID: 31414493 DOI: 10.1002/jsfa.9989
    BACKGROUND: Recycled oil has emerged as a significant food safety issue and poses a major threat to public health. To date, very limited studies have been conducted aiming to detect the adulteration of used and recycled palm olein in refined, bleached and deodorized palm olein (RBDPO). In the present study, oil samples that underwent controlled heating and deep-frying studies were refined using the common oil refining procedure to simulate the production of recycled oil. Polymerized triacylglycerol (PTG), oxidized monomeric triacylglycerols (oxTAGs), such as epoxy, keto and hydroxy acids, and caprylic acid have been proposed as potential indicators for tracking the adulteration of recycled oil.

    RESULTS: For PTG, triacylglycerol oligomers and dimers showed a significant increase (P 

    Matched MeSH terms: Oxidation-Reduction
  10. Recent trends in advanced oxidation process-based degradation of erythromycin: Pollution status, eco-toxicity and degradation mechanism in aquatic ecosystems
    Ashraf A, Liu G, Yousaf B, Arif M, Ahmed R, Irshad S, et al.
    Sci Total Environ, 2021 Jun 10;772:145389.
    PMID: 33578171 DOI: 10.1016/j.scitotenv.2021.145389
    Wide spread documentation of antibiotic pollution is becoming a threat to aquatic environment. Erythromycin (ERY), a macrolide belonging antibiotic is at the top of this list with its concentrations ranging between ng/L to a few μg/L in various global waterbodies giving rise to ERY-resistance genes (ERY-RGs) and ERY- resistance bacteria (ERY-RBs) posing serious threat to the aquatic organisms. ERY seems resistant to various conventional water treatments, remained intact and even increased in terms of mass loads after treatment. Enhanced oxidation potential, wide pH range, elevated selectivity, adaptability and greater efficiency makes advance oxidation processes (AOPs) top priority for degrading pollutants with aromatic rings and unsaturated bonds like ERY. In this manuscript, recent developments in AOPs for ERY degradation are reported along with the factors that affect the degradation mechanism. ERY, marked as a risk prioritized macrolide antibiotic by 2015 released European Union watch list, most probably due to its protein inhibition capability considered third most widely used antibiotic. The current review provides a complete ERY overview including the environmental entry sources, concentration in global waters, ERY status in STPs, as well as factors affecting their functionality. Along with that this study presents complete outlook regarding ERY-RGs and provides an in depth detail regarding ERY's potential threats to aquatic biota. This study helps in figuring out the best possible strategy to tackle antibiotic pollution keeping ERY as a model antibiotic because of extreme toxicity records.
    Matched MeSH terms: Oxidation-Reduction
  11. Aerobic oxidation of 5-hydroxymethylfurfural into 2,5-diformylfuran using manganese dioxide with different crystal structures: A comparative study
    Lin KA, Oh WD, Zheng MW, Kwon E, Lee J, Lin JY, et al.
    J Colloid Interface Sci, 2021 Jun 15;592:416-429.
    PMID: 33691223 DOI: 10.1016/j.jcis.2021.02.030
    Aerobic oxidation of 5-Hydroxymethylfurfural (HMF) to 2,5-Diformylfuran (DFF) using O2 gas represents a sustainable approach for valorization of lignocellulosic compounds. As manganese dioxide (MnO2) is validated as a useful oxidation catalyst and many crystalline forms of MnO2 exist, it is critical to explore how the crystalline structures of MnO2 influence their physical/chemical properties, which, in turn, determine catalytic activities of MnO2 crystals for HMF oxidation to DFF. In particular, six MnO2 crystals, α-MnO2, β-MnO2, γ-MnO2, δ-MnO2, ε-MnO2, and λ-MnO2 are prepared and investigated for their catalytic activities for HMF oxidation to DFF. With different morphologies and crystalline structures, these MnO2 crystals possess very distinct surficial chemistry, redox capabilities, and textural properties, making these MnO2 exhibit different catalytic activities towards HMF conversion. Especially, β-MnO2 can produce much higher DFF per surface area than other MnO2 crystals. β-MnO2 could achieve the highest CHMF = 99% and YDFF = 97%, which are much higher than the reported values in literature, possibly because the surficial reactivity of β-MnO2 appears to be highest in comparison to other MnO2 crystals. Especially, β-MnO2 could exhibit YDFF > 90% over 5 cycles of reusability test, and maintain its crystalline structure, revealing its advantageous feature for aerobic oxidation of HMF to DFF. Through this study, the relationship between morphology, surface chemistry, and catalytic activity of MnO2 with different crystal forms is elucidated for providing scientific insights into design, application and development of MnO2-based materials for aerobic oxidation of bio-derived molecules to value-added products.
    Matched MeSH terms: Oxidation-Reduction
  12. Arsenic removal in aqueous solutions using FeS2
    Fu D, Kurniawan TA, Lin L, Li Y, Avtar R, Dzarfan Othman MH, et al.
    J Environ Manage, 2021 May 15;286:112246.
    PMID: 33667817 DOI: 10.1016/j.jenvman.2021.112246
    This study tested the technical feasibility of pyrite and/or persulfate oxidation system for arsenic (As) removal from aqueous solutions. The effects of persulfate on As removal by the pyrite in the integrated treatment were also investigated. Prior to the persulfate addition into the reaction system, the physico-chemical interactions between As and the pyrite alone in aqueous solutions were explored in batch studies. The adsorption mechanisms of As by the adsorbent were also presented. At the same As concentration of 5 mg/L, it was found that As(III) attained a longer equilibrium time (8 h) than As(V) (2 h), while the pyrite worked effectively at pH ranging from 6 to 11. At optimum conditions (0.25 g/L of pyrite, pH 8.0 and 5 mg/L of As(III) concentration), the addition of persulfate (0.5 mM) into the reaction promoted a complete removal of arsenic from the solutions. Consequently, this enabled the treated effluents to meet the arsenic maximum contaminant limit (MCL) of <10 μg/L according to the World Health Organization (WHO)'s requirements. The redox mechanisms, which involved electron transfer from the S22- of the pyrite to Fe3+, supply Fe2+ for persulfate decomposition, oxidizing As(III) to As(V). The sulfur species played roles in the redox cycle of the Fe3+/Fe2+ of the pyrite by giving its electrons, while the As(III) oxidation to As(V) was attributed to the pyrite. Overall, this work reveals the applicability of the pyrite as an adsorbent for water treatment and the importance of persulfate addition to promote a complete As removal from aqueous solutions.
    Matched MeSH terms: Oxidation-Reduction
  13. Effective toluene oxidation under ozone over mesoporous MnOx/γ-Al2O3 catalyst prepared by solvent deficient method: Effect of Mn precursors on catalytic activity
    Reddy KHP, Kim BS, Lam SS, Jung SC, Song J, Park YK
    Environ Res, 2021 04;195:110876.
    PMID: 33592225 DOI: 10.1016/j.envres.2021.110876
    In this study, the role of manganese precursors in mesoporous (meso) MnOx/γ-Al2O3 catalysts was examined systematically for toluene oxidation under ozone at ambient temperature (20 °C). The meso MnOx/γ-Al2O3 catalysts developed with Mn(CH3COO)2, MnCl2, Mn(NO3)2.4H2O and MnSO4 were prepared by an innovative single step solvent-deficient method (SDM); the catalysts were labeled as MnOx/Al2O3(A), MnOx/Al2O3(C), MnOx/Al2O3(N), and MnOx/Al2O3(S), respectively. Among all, MnOx/Al2O3(C) showed superior performance both in toluene removal (95%) as well as ozone decomposition (88%) followed by acetate, nitrate and sulphated precursor MnOx/Al2O3. The superior performance of MnOx/Al2O3(C) in the oxidation of toluene to COx is associated with the ozone decomposition over highly dispersed MnOx in which extremely active oxygen radicals (O2-, O22- and O-) are generated to enhance the oxidation ability of the catalysts greatly. In addition, toluene adsorption over acid support played a vital role in this reaction. Hence, the properties such as optimum Mn3+/Mn4+ ratio, acidic sites, and smaller particle size (≤2 nm) examined by XPS, TPD of NH3, and TEM results are playing vital role in the present study. In summary, the MnOx/Al2O3 (C) catalyst has great potential in environmental applications particularly for the elimination of volatile organic compounds with low loading of manganese developed by SDM.
    Matched MeSH terms: Oxidation-Reduction
  14. Morphology-Controlled Synthesis of α-Fe2O3 Nanocrystals Impregnated on g-C3N4-SO3H with Ultrafast Charge Separation for Photoreduction of Cr (VI) Under Visible Light
    Balu S, Chen YL, Juang RC, Yang TC, Juan JC
    Environ Pollut, 2020 Dec;267:115491.
    PMID: 32911336 DOI: 10.1016/j.envpol.2020.115491
    Surface functionalization and shape modifications are the key strategies being utilized to overcome the limitations of semiconductors in advanced oxidation processes (AOP). Herein, the uniform α-Fe2O3 nanocrystals (α-Fe2O3-NCs) were effectively synthesized via a simple solvothermal route. Meanwhile, the sulfonic acid functionalization (SAF) and the impregnation of α-Fe2O3-NCs on g-C3N4 (α-Fe2O3-NCs@CN-SAF) were achieved through complete solvent evaporation technique. The surface functionalization of the sulfonic acid group on g-C3N4 accelerates the faster migration of electrons to the surface owing to robust electronegativity. The incorporation of α-Fe2O3-NCs with CN-SAF significantly enhances the optoelectronic properties, ultrafast spatial charge separation, and rapid charge transportation. The α-Fe2O3-HPs@CN-SAF and α-Fe2O3-NPs@CN-SAF nanocomposites attained 97.41% and 93.64% of Cr (VI) photoreduction in 10 min, respectively. The photocatalytic efficiency of α-Fe2O3-NCs@CN-SAF nanocomposite is 2.4 and 2.1 times higher than that of pure g-C3N4 and α-Fe2O3, respectively. Besides, the XPS, PEC and recycling experiments confirm the excellent photo-induced charge separation via Z-scheme heterostructure and cyclic stability of α-Fe2O3-NCs@CN-SAF nanocomposites.
    Matched MeSH terms: Oxidation-Reduction
  15. A review on advances in green treatment of glycerol waste with a focus on electro-oxidation pathway
    Ahmad MS, Ab Rahim MH, Alqahtani TM, Witoon T, Lim JW, Cheng CK
    Chemosphere, 2021 Aug;276:130128.
    PMID: 33714877 DOI: 10.1016/j.chemosphere.2021.130128
    Over the past decades, research efforts are being devoted into utilizing the biomass waste as a major source of green energy to maintain the economic, environmental, and social sustainability. Specifically, there is an emerging consensus on the significance of glycerol (an underutilised waste from biodiesel industry) as a cheap, non-toxic, and renewable source for valuable chemicals synthesis. There are numerous methods enacted to convert this glycerol waste to tartronic acid, mesoxalic acid, glyceraldehyde, dihydroxyacetone, oxalic acid and so on. Among these, the green electro-oxidation technique is one of the techniques that possesses potential for industrial application due to advantages such as non-toxicity process, fast response, and lower energy consumption. The current review covers the general understanding on commonly used techniques for alcohol (C1 & C2) conversion, with a specific insight on glycerol (C3) electro-oxidation (GOR). Since catalysts are the backbone of chemical reaction, they are responsible for the overall economy prospect of any processes. To this end, a comprehensive review on catalysts, which include noble metals, non-noble metals, and non-metals anchored over various supports are incorporated in this review. Moreover, a fundamental insight into the development of future electrocatalysts for glycerol oxidation along with products analysis is also presented.
    Matched MeSH terms: Oxidation-Reduction
  16. Elucidation of stoichiometric efficiency, radical generation and transformation pathway during catalytic oxidation of sulfamethoxazole via peroxymonosulfate activation
    Bao Y, Oh WD, Lim TT, Wang R, Webster RD, Hu X
    Water Res, 2019 03 15;151:64-74.
    PMID: 30594091 DOI: 10.1016/j.watres.2018.12.007
    In this work, nano-bimetallic Co/Fe oxides with different stoichiometric Co/Fe ratios were prepared using a novel one-step solution combustion method. The nano-bimetallic Co/Fe oxides were used for sulfamethoxazole (SMX) degradation via peroxymonosulfate (PMS) activation. The stoichiometric efficiencies of the as-prepared nano-bimetallic catalysts were calculated and compared for the first time. The radical generation was identified by electron paramagnetic resonance (EPR) as well as chemical quenching experiments, in which different scavengers were used and compared. The catalytic PMS activation mechanism in the presence of catalyst was examined by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The results showed that besides SO4•- and •OH, •OOH was also detected in the PMS/CoFeO2.5 system. Meanwhile, in addition to the previously proposed radical oxidation pathway, the results showed that SMX degradation also involved a non-radical oxidation, which could be verified by the degradation experiment without catalyst as well as the detection of 1O2. In the PMS activation process, cobalt functioned as the active site on CoFeO2.5 while Fe oxide functioned as the adsorption site. The electron transfer mechanism was proposed based on the XPS and metal leaching results. Additionally, via the detection of transformation products, different SMX transformation pathways involving nitration, hydroxylation and hydrolysis in the PMS/CoFeO2.5 system were proposed.
    Matched MeSH terms: Oxidation-Reduction
  17. Fulltext Chemical constituents and antioxidant activity of cinnamomum microphyllum
    Norazah, M.A., Rahmani, M., Khozirah, S., Ismail, H.B.M., Sukari, M.A., Ali, A.M., et al.
    Pertanika Journal of Science & Technology, 2010;18(2):-.
    MyJurnal
    The extract of Cinnamomum microphyllum showed strong antioxidant activity when it was tested against auto-oxidation of linoleic acid, superoxide, and DPPH radical scavenging activity. Further detailed investigations of the plant constituents and bioactivity studies led to the isolation and identification of known compounds consisting of three lignans, a coumarin, an ester and β-sitosterol. The structures of the compounds were determined using detailed spectroscopic analysis. The lignans were found to possess a significant antioxidant activity when tested against the three assay systems.
    Matched MeSH terms: Oxidation-Reduction
  18. Antioxidant properties of methanolic extract of Canarium odontophyllum fruit
    Azrina, A., Nurul Nadiah, M.N., Amin, I.
    International Food Research Journal, 2010;17(2):319-326.
    MyJurnal
    The antioxidant properties of skin, flesh and kernel of Canarium odontophyllum fruit were determined. The methanolic extracts of the fruit were screened for their total phenolic content and antioxidant properties. The averaged antioxidant properties (mM TE/g FM) in skin, flesh, and kernel of Canarium odontophyllum were 16.46 ± 0.24, 20.54 ± 0.35, and 8.89 ± 0.29, respectively by DPPH assay; 151.24 ± 9.75, 70.58 ± 2.98, and 5.65 ± 0.02, respectively by FRAP assay; and 47.9 ± 0.00, 11.61 ± 1.14, and 3.00 ± 0.00, respectively by β-Carotene bleaching method. The averaged OH scavenging activity (mg DMSOE/mg FM) in skin, flesh, and kernel of Canarium odontophyllum were 43.33 ± 13.85, 7.81 ± 1.42, and 3.31 ± 0.80, respectively. While averaged total phenolic content (mg GAE/100g FM) were 387.5 ± 33.23, 267.0 ± 4.24, and 51.0 ± 0.00 for skin, flesh, and kernel respectively. Antioxidant activities were positively correlated with the total phenolic content (0.71 ≤ r ≤ 0.84).
    Matched MeSH terms: Oxidation-Reduction
  19. Fulltext Effect of microwave pretreatment on stability of kenaf (Hibiscus cannabinus L.) seed oil upon accelerated storage
    Nyam, K.L., Tan, C.H., Long, K.
    International Food Research Journal, 2015;22(5):1898-1905.
    MyJurnal
    The aim of this study was to investigate the oxidative stability, antioxidant activity and fatty acid composition of 2 minutes microwave pre-treated kenaf seed oil (MKSO) in comparison with the untreated kenaf seed oil (KSO) under accelerated storage for 24 days. Results obtained on oxidative stability for both KSO and MKSO by the end of storage with PV were 9.83 meq O2 /kg and 8.97 meq O2 /kg, respectively; p-Anv were 17.28 and 13.48, respectively; TOTOX value of 36.94 and 31.42, respectively; IV value were measured 84.50 g of I2 / 100 g and 84.34 g of I2 / 100 g oil, respectively; FFA value of 5.67 mg KOH/100g oil and 5.14 mg KOH/100g oil, respectively. Aside from that, the antioxidant activity in MKSO was better than KSO. For the fatty acid composition, the oleic and linoleic acids were affected significantly throughout storage for both KSO and MKSO. MKSO presented a better overall oxidative stability, antioxidant activity and retained higher content of MUFA and PUFA significantly (p< 0.05) upon accelerated storage.
    Matched MeSH terms: Oxidation-Reduction
  20. Fulltext Properties of canned mengkudu (Morinda citrifolia L.) extract during storage
    Noor Hafizah, Y, Maskat, M. Y., Wan Aida, W. M., Maaruf, A. G.
    International Food Research Journal, 2012;19(3):1211-1215.
    MyJurnal
    Storage study of mengkudu (Morinda citrifolia L.) extract was carried out to determine the effects
    of canning and storage period on pH, total polyphenol content, antioxidant activity, intensity of off-odour and aroma acceptance. Uncanned (control) and canned extract were stored for 0, 8, 16 and 24 weeks under room temperature. Results showed canning resulted in a significant (p
    Matched MeSH terms: Oxidation-Reduction
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