Displaying publications 61 - 80 of 1023 in total

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  1. Synthesis of bioinspired sorbent and their exploitation for methylene blue remediation
    Haq F, Kiran M, Chinnam S, Farid A, Khan RU, Ullah G, et al.
    Chemosphere, 2023 Apr;321:138000.
    PMID: 36724851 DOI: 10.1016/j.chemosphere.2023.138000
    In this research article, novel starch phosphate grafted polyvinyl imidazole (StP-g-PIMDZs) was synthesized. Firstly, a phosphate group was attached to starch polymer via a phosphorylation reaction. Next, 1-vinyl imidazole (VIMDZ) was grafted on the backbone of starch phosphate (StP) through a free radical polymerization reaction. The synthesis of these modified starches was confirmed by 1H NMR, 31P NMR and FT-IR techniques. The grafting of vinyl imidazole onto StP diminished the crystallinity. Due to the insertion of the aromatic imidazole ring, the StP-g-PIMDZs demonstrated greater thermal stability. The StP and StP-g-PIMDZs were used as sorbents for the adsorption of methylene blue dye (MBD) from the model solution. The maximum removal percentage for starch, StP, StP-g-PIMDZ 1, StP-g-PIMDZ 2 and StP-g-PIMDZ 3 was found to be 60.6%, 66.7%, 74.2%, 85.3 and 95.4%, respectively. The Pseudo second order kinetic model and Langmuir adsorption isotherm were best suited to the experimental data with R2 = 0.999 and 0.99, respectively. Additionally, the thermodynamic parameters showed that the adsorption process was feasible, spontaneous, endothermic and favored chemi-sorption mechanism.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  2. Angiotensin converting enzyme (ACE) inhibitors activity from purified compounds Fructus Phaleria macrocarpa (Scheff) Boerl
    Eff ARY, Huri HZ, Radji M, Mun'im A, Suyatna FD, Eden Y
    BMC Complement Med Ther, 2023 Feb 20;23(1):56.
    PMID: 36803524 DOI: 10.1186/s12906-023-03889-x
    BACKGROUND: Mahkota Dewa [Phaleria macrocarpa (Scheff) Boerl.] fruit in vitro and in- vivo can decrease and prevent elevation of the blood pressure, lower plasma glucose levels, possess an antioxidant effect, and recover liver and kidney damage in rats. This study aimed to determine the structure and inhibitory activity of angiotensin-converting enzyme inhibitors (ACE) from the Mahkota Dewa fruit.

    METHODS: The fruit powder was macerated using methanol and then partitioned by hexane, ethyl acetate, n-butanol, and water. The fractions were chromatographed on the column chromatography and incorporated with TLC and recrystallization to give pure compounds. The structures of isolated compounds were determined by UV-Visible, FT-IR, MS, proton (1H-NMR), carbon (13C-NMR), and 2D-NMR techniques encompassing HMQC and HMBC spectra. The compounds were evaluated for their ACE inhibitory activity, and the strongest compound was determined by the kinetics enzyme inhibition.

    RESULTS: Based on the spectral data, the isolated compounds were determined as 6,4-dihydroxy-4-methoxybenzophenone-2-O-β-D-glucopyranoside (1), 4,4'-dihydroxy-6-methoxybenzophenone-2-O-β-D-glucopyranoside (2) and mangiferin (3). IC50 values of the isolated compounds 1, 2 and 3 were 0.055, 0.07, and 0.025 mM, respectively.

    CONCLUSION: The three compounds have ACE inhibitor and mangiferin demonstrated the best ACE inhibitory activity with competitive inhibition on ACE with the type of inhibition kinetics is competitive inhibition.

    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  3. UV-blocking and photocatalytic properties of Ag-coated cotton fabrics with Si binders for photo-degradation of recalcitrant dyes in aqueous solutions under sunlight
    Amjad M, Mohyuddin A, Ulfat W, Goh HH, Dzarfan Othman MH, Kurniawan TA
    J Environ Manage, 2024 Feb 27;353:120287.
    PMID: 38335595 DOI: 10.1016/j.jenvman.2024.120287
    Textile wastewater laden with dyes has emerged as a source of water pollution. This possesses a challenge in its effective treatment using a single functional material. In respond to this technological constraint, this work presents multifunctional cotton fabrics (CFs) within a single, streamlined preparation process. This approach utilizes the adherence of Ag NPs (nanoparticles) using Si binder on the surface of CFs, resulting in Ag-coated CFs through a pad dry method. The prepared samples were characterized using scanning electron microscope-energy dispersive X-ray electroscopy (SEM-EDS), thermal gravimetric analysis (TGA), Fourier transformation infrared (FT-IR). It was found that the FT-IR spectra of Ag NPs-coated CFs had peaks appear at 3400, 2900, and 1200 cm-1, implying the stretching vibrations of O-H, C-H, and C-O, respectively. Based on the EDX analysis, the presence of C, O, and Ag related to the coated CFs were detected. After coating the CFs with varying concentrations of Ag NPs (1%, 2% and 3% (w/w)), they were used to remove dyes. Under the same concentration of 10 mg/L and optimized pH 7.5 and 2 h of reaction time, 3% (w/w) Ag-coated CFs exhibited a substantial MB degradation of 98 %, while removing 95% of methyl orange, 85% of rhodamine B, and 96% of Congo red, respectively, following 2 h of Vis exposure. Ag NPs had a strong absorption at 420 nm with 2.51 eV of energy band gap. Under UV irradiation, electrons excited and produced free radicals that promoted dyes photodegradation. The oxidation by-products included p-dihydroxybenzene and succinic acid. Spent Ag-coated CFs attained 98% of regeneration efficiency. The utilization of Ag-coated CFs as a photocatalyst facilitated treated effluents to meet the required discharge standard of lower than 1 mg/L mandated by national legislation. The integration of multifunctional CFs in the treatment system presents a new option for tackling water pollution due to dyes.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  4. Synergistic effect of Hylocereus polyrhizus (dragon fruit) peel on physicomechanical, thermal, and biodegradation properties of thermoplastic sago starch/agar composites
    Taharuddin NH, Jumaidin R, Mansor MR, Hazrati KZ, Hafila KZ, Md Yusof FA
    Int J Biol Macromol, 2024 Oct;277(Pt 1):133852.
    PMID: 39025171 DOI: 10.1016/j.ijbiomac.2024.133852
    The potential of Hylocereus polyrhizus peel (HPP) as a new eco-friendly reinforcement for thermoplastic sago starch/agar composite (TPSS/agar) was investigated. The integration of HPP into TPSS/agar composite aimed to enhance its mechanical and thermal characteristics. The study employed Fourier transform-infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), Thermogravimetric analysis (TGA), and Differential Scanning Calorimetry (DSC), as well as mechanical, physical properties and soil burial testing to analyse the composites. The results showed a favourable miscibility between the matrix and filler, while at higher concentrations of HPP, the starch granules became more visible. The tensile and impact properties of the composites improved significantly after incorporating HPP at 20 wt%, with values of 12.73 MPa and 1.87 kJ/m2, respectively. The glass transition temperature (Tg) and initial decomposition temperature (Ton) decreased with the addition of HPP. The density of the composites reduced from 1.51 ± 0.01 to 1.26 ± 0.01 g/cm3 as the HPP amount increased. The environmental properties indicated that the composites can be composted, with weight loss accelerating from 35 to 60 % and 61 to 91 % by the addition of HPP in 2- and 4-weeks' time, respectively. The study demonstrates the potential of TPSS/agar/HPP composites as eco-friendly materials for various applications.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  5. Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) microfilled anhydride-modified crude lignin blend biodegradable materials
    Bairwan RD, Sukeksi L, Khalil HPSA, Hosny KM, Baradwan M, Rizg WY, et al.
    Int J Biol Macromol, 2025 Apr;304(Pt 2):140985.
    PMID: 39952528 DOI: 10.1016/j.ijbiomac.2025.140985
    This study explores the potential of crude lignin, extracted from coir fibers, an agricultural byproduct, as a sustainable filler in Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) biodegradable blends. To enhance compatibility with the PHBV matrix, lignin was chemically modified using acetic anhydride (AL) and propionic anhydride (PL). These modifications were confirmed through FTIR, XRD, FE-SEM, EDX, and TGA analyses. The blends were prepared via melt compounding in a twin-screw extruder, followed by compression molding, with lignin microfillers incorporated at 1, 3, 5, and 7 wt% of dried PHBV. The addition of modified lignins improved the physical, mechanical, and thermal properties of the blends, with the optimal performance observed at 5 wt%, attributed to enhanced interfacial bonding. Two-way ANOVA with Tukey tests (p ≤ 0.05) confirmed statistical significance. However, at 7 wt%, all blends exhibited reduced performance due to lignin agglomeration, confirmed by morphology and tensile tests. Both modifications provided desirable multi-functional properties, but propionylated lignin-based blends outperformed those with acetylated and raw lignins, due to more effective substitution of non-polar groups, which improved filler-matrix miscibility. Fracture surface analysis, topography, and thermal evaluations validated these observations. These findings highlight chemically modified lignins, as effective, sustainable fillers for eco-friendly biopolymer composites suitable for packaging applications.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  6. Biochar and activated carbon derived from oil palm kernel shell as a framework for the preparation of sustainable controlled release urea fertiliser
    Vejan P, Abdullah R, Ahmad N, Khadiran T
    Environ Sci Pollut Res Int, 2023 Mar;30(13):38738-38750.
    PMID: 36585594 DOI: 10.1007/s11356-022-24970-x
    The oil palm kernel shell biochar (OPKS-B) and oil palm kernel shell activated carbon (OPKS-AC) were used as a framework to entrap urea using adsorption method. Batch adsorption studies were performed to gauge the influence of contact time on the adsorption of urea onto both OPKS-B and OPKS-AC. To evaluate the physicochemical traits of the studied materials, energy dispersive X-ray spectrometer (EDS), N2-sorption, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), elemental analysis, differential thermal gravity (TG/DTG) and thermal gravity were applied. Result shows OPKS-AC has a better sorption capacity for urea compared to OPKS-B. The Langmuir isotherm model better justified the sorption isotherms of urea. For the adsorption process for both OPKS-B and OPKS-AC, the pseudo-second-order kinetic model was picked as it best fitted the experimental sorption outcome with the superior R2 values of > 65.1% and > 74.5%, respectively. The outcome of the experiments showcased that the maximum monolayer adsorption capacity of the OPKS-AC towards urea was 239.68 mg/g. OPKS-AC has showed promising attributes to be picked as an organic framework in the production of controlled release urea fertiliser for a greener and environmentally friendly agricultural practices.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  7. Insight into microwave-assisted synthesis of the chitosan-MOF composite: Pb(II) adsorption
    Gul Zaman H, Baloo L, Kutty SR, Aziz K, Altaf M, Ashraf A, et al.
    Environ Sci Pollut Res Int, 2023 Jan;30(3):6216-6233.
    PMID: 35989404 DOI: 10.1007/s11356-022-22438-6
    Heavy metal contamination has increased over the globe, causing significant environmental issues owing to direct and indirect releases into water bodies. As a result, metal removal from water entities must be addressed soon. Various adsorbents such as MOFs and chitosan have demonstrated promising results in water treatment. The present study prepared a composite material (chitosan-UiO-66-glycidyl methacrylate MOF) by a microwave-assisted method. The structure and morphology of the chitosan-MOF composite were studied using FE-SEM, EDX, XRD, BET, FT-IR, and TGA techniques. In addition, the adsorption of Pb(II) from aqueous solution onto the chitosan-MOF composite was analyzed in a batch study concerning pH, contact time, initial metal ion concentration, and adsorbent dosage. The composite has a large surface area of 867 m2/g with a total pore volume of 0.51 cm3/g and thermal stability of up to 400 [Formula: see text]. Following an analysis of the adsorption isotherms, kinetics, and thermodynamics, the Langmuir model showed an excellent fit with the adsorption data (R2 = 0.99) and chi-squared (X2 = 3.609). The adsorption process was a spontaneous exothermic reaction and the pseudo-second-order rate equation fitted the kinetic profile well. Moreover, the composite is recyclable, retaining 83.45% of its removal effectiveness after 5 consecutive cycles, demonstrating it as a sustainable adsorbent for metal recovery. This study introduces a novel synthesized composite with enhanced recyclability and a higher potential for eliminating pollutants from industrial wastewater.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  8. Microplastics in facial cleanser: extraction, identification, potential toxicity, and continuous-flow removal using agricultural waste-based biochar
    Hanif MA, Ibrahim N, Dahalan FA, Md Ali UF, Hasan M, Azhari AW, et al.
    Environ Sci Pollut Res Int, 2023 May;30(21):60106-60120.
    PMID: 37017846 DOI: 10.1007/s11356-023-26741-8
    Microplastic (MP) is an emerging contaminant of concern due to its ubiquitous quantity in the environment, small size, and potential toxicity due to strong affinity towards other contaminants. In this work, MP particles (5-300 μm) were extracted from a commercial facial cleanser and determined to be irregular polyethylene (PE) microbeads based on characterization with field emission scanning electron microscopy (FESEM) and Raman spectroscopy. The potential of extracted MP acting as toxic pollutants' vector was analyzed via adsorption of methylene blue and methyl orange dye where significant dye uptake was observed. Synthetic wastewater containing the extracted MP was subjected to a continuous-flow column study using palm kernel shell and coconut shell biochar as the filter/adsorbent media. The prepared biochar was characterized via proximate and ultimate analysis, FESEM, contact angle measurement, atomic force microscopy (AFM), and Fourier transform infrared (FTIR) spectroscopy to investigate the role of the biochar properties in MP removal. MP removal performance was determined by measuring the turbidity and weighing the dry mass of particles remaining in the effluent following treatment. Promising results were obtained from the study with highest removal of MP (96.65%) attained through palm kernel shell biochar with particle size of 0.6-1.18 mm and continuous-flow column size of 20 mm.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  9. New porous amine-functionalized biochar-based desiccated coconut waste as efficient CO2 adsorbents
    Zakaria DS, Rozi SKM, Halim HNA, Mohamad S, Zheng GK
    Environ Sci Pollut Res Int, 2024 Mar;31(11):16309-16327.
    PMID: 38315341 DOI: 10.1007/s11356-024-32285-2
    Climate change caused by the greenhouse gases CO2 remains a topic of global concern. To mitigate the excessive levels of anthrophonic CO2 in the atmosphere, CO2 capture methods have been developed and among these, adsorption is an especially promising method. This paper presents a series of amine functionalized biochar obtained from desiccated coconut waste (amine-biochar@DCW) for use as CO2 adsorbent. They are ethylenediamine-functionalized biochar@DCW (EDA-biochar@DCW), diethylenetriamine-functionalized biochar@DCW (DETA-biochar@DCW), triethylenetetramine-functionalized biochar@DCW (TETA-biochar@DCW), tetraethylenepentamine-functionalized biochar@DCW (TEPA-biochar@DCW), and pentaethylenehexamine-functionalized biochar@DCW (PEHA-biochar@DCW). The adsorbents were obtained through amine functionalization of biochar and they are characterized using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy, Brunauer-Emmett-Teller (BET), and thermogravimetric analysis (TGA). The CO2 adsorption study was conducted isothermally and using a thermogravimetric analyzer. From the results of the characterization analyses, a series of amine-biochar@DCW adsorbents had larger specific surface area in the range of 16.2 m2/g-37.1 m2/g as compare to surface area of pristine DCW (1.34 m2/g). Furthermore, the results showed an increase in C and N contents as well as the appearance of NH stretching, NH bending, CN stretching, and CN bending, suggesting the presence of amine on the surface of biochar@DCW. The CO2 adsorption experiment shows that among the amine modified biochar adsorbents, TETA-biochar@DCW has the highest CO2 adsorption capacity (61.78 mg/g) when using a mass ratio (m:m) of biochar@DCW:TETA (1:2). The adsorption kinetics on the TETA-biochar@DCW was best fitted by the pseudo-second model (R2 = 0.9998), suggesting the adsorption process occurs through chemisorption. Additionally, TETA-biochar@DCW was found to have high selectivity toward CO2 gas and good reusability even after five CO2 adsorption-desorption cycles. The results demonstrate the potential of novel CO2 adsorbents based on amine functionalized on desiccated coconut waste biochar.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  10. CO2 adsorption and CO2/CH4 separation using fibrous amine-containing adsorbents: isothermal, kinetic, and thermodynamic behaviours
    Mohamad NA, Nasef MM, Abdullah TAT, Ahmad A, Ting TM
    Environ Sci Pollut Res Int, 2023 Nov;30(55):116906-116920.
    PMID: 37121947 DOI: 10.1007/s11356-023-26913-6
    A series of fibrous aminated adsorbents for CO2 adsorption were prepared by covalent incorporation of poly (glycidyl methacrylate) (PGMA) by graft copolymerization of GMA onto electron beam (EB) irradiated polyethylenepolypropylene (PE/PP) fibrous sheets and subsequent amination with ethylenediamine (EDA), diethylenetriamine (DETA), or tetraethylenepentamine (TEPA). The physico-chemical properties of the adsorbents were evaluated using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermogravimetric (TGA), X-ray diffraction (XRD), and Brunauer-Emmett-Teller (BET) analysis. All the adsorbents displayed typic primary and secondary amine features combined with a decrease in both of crystallinity and surface area of PE/PP, and such a decrease was higher in adsorbents with longer aliphatic chain of the amine. Of all adsorbents, TEPA-containing fibres showed the highest CO2 adsorption capacity and thus was further investigated for CO2 capture from CO2/CH4 mixtures of different gas ratios under various pressures and temperatures. The selectivity of CO2 over CH4 and equilibrium isotherms, kinetics, and thermodynamics of the adsorption on the fibrous aminated adsorbent were all investigated. The Sips model was found to best fit the isotherm of CO2 adsorption suggesting the presence of a combination of monolayer and multilayer adsorptions. The adsorption kinetic data was found to best fit Elovich model reflecting chemisorption. The ΔG°, ΔS°, and ΔH° showed positive values suggesting that the adsorption of CO2 on the present fibrous adsorbent was non-spontaneous with an increase in randomness implying that the process was endothermic. Overall, it can be suggested that PE/PP-g-PGMA/TEPA adsorbent has a strong potential for separation of CO2 from NG.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  11. Fulltext Statistical Optimization for Acid Hydrolysis of Microcrystalline Cellulose and Its Physiochemical Characterization by Using Metal Ion Catalyst
    Karim MZ, Chowdhury ZZ, Hamid SBA, Ali ME
    Materials (Basel), 2014 Oct 13;7(10):6982-6999.
    PMID: 28788226 DOI: 10.3390/ma7106982
    Hydrolyzing the amorphous region while keeping the crystalline region unaltered is the key technology for producing nanocellulose. This study investigated if the dissolution properties of the amorphous region of microcrystalline cellulose can be enhanced in the presence of Fe(3+) salt in acidic medium. The process parameters, including temperature, time and the concentration of metal chloride catalyst (FeCl₃), were optimized by using the response surface methodology (RSM). The experimental observation demonstrated that temperature and time play vital roles in hydrolyzing the amorphous sections of cellulose. This would yield hydrocellulose with higher crystallinity. The factors that were varied for the production of hydrocellulose were the temperature (x₁), time (x₂) and FeCl₃ catalyst concentration (x₃). Responses were measured in terms of percentage of crystallinity (y₁) and the yield (y₂) of the prepared hydrocellulose. Relevant mathematical models were developed. Analysis of variance (ANOVA) was carried out to obtain the most significant factors influencing the responses of the percentage of crystallinity and yield. Under optimum conditions, the percentage of crystallinity and yield were 83.46% and 86.98% respectively, at 90.95 °C, 6 h, with a catalyst concentration of 1 M. The physiochemical characteristics of the prepared hydrocellulose were determined in terms of XRD, SEM, TGA and FTIR analyses. The addition of FeCl₃ salt in acid hydrolyzing medium is a novel technique for substantially increasing crystallinity with a significant morphological change.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  12. Fulltext Biosynthesis of Silver Nanoparticles Using Brown Marine Macroalga, Sargassum Muticum Aqueous Extract
    Azizi S, Namvar F, Mahdavi M, Ahmad MB, Mohamad R
    Materials (Basel), 2013 Dec 18;6(12):5942-5950.
    PMID: 28788431 DOI: 10.3390/ma6125942
    Biological synthesis of nanoparticles is a relatively new emerging field of nanotechnology which has economic and eco-friendly benefits over chemical and physical processes of synthesis. In the present work, for the first time, the brown marine algae Sargassum muticum (S. muticum) aqueous extract was used as a reducing agent for the synthesis of nanostructure silver particles (Ag-NPs). Structural, morphological and optical properties of the synthesized nanoparticles have been characterized systematically by using FTIR, XRD, TEM and UV-Vis spectroscopy. The formation of Ag-NPs was confirmed through the presence of an intense absorption peak at 420 nm using a UV-visible spectrophotometer. A TEM image showed that the particles are spherical in shape with size ranging from 5 to 15 nm. The nanoparticles were crystalline in nature. This was confirmed by the XRD pattern. From the FTIR results, it can be seen that the reduction has mostly been carried out by sulphated polysaccharides present in S. muticum.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  13. Fulltext Utilization of an Ionic Liquid/Urea Mixture as a Physical Coupling Agent for Agarose/Talc Composite Films
    Shamsuri AA, Daik R
    Materials (Basel), 2013 Feb 22;6(2):682-698.
    PMID: 28809334 DOI: 10.3390/ma6020682
    An ionic liquid, 1-n-butyl-3-methylimidazolium chloride (BmimCl) was blended with urea at 1:1 mole ratio to create a BmimCl/Urea mixture. The agarose/talc composite films containing the BmimCl/Urea mixture were then acquired through a gelation method. The weight ratio of agarose and talc was fixed at 4:1, while the content of BmimCl/Urea was varied from 0 to 10 wt % relative to the overall weight of the composite films. The tensile stress and modulus results showed the optimum BmimCl/Urea content in the composite film lies at 8 wt %. The talc particles are embedded in the agarose matrix and there are no pullouts for the composite films containing BmimCl/Urea as demonstrated by SEM micrographs. The addition of BmimCl/Urea increased the glass transition temperature of the composite films, however, the thermal decomposition temperature decreased drastically. FTIR and FT-Raman spectra indicated the existence of interaction between agarose and talc, which improves their interfacial adhesion. As a conclusion, a BmimCl/Urea mixture can be utilized as a coupling agent for agarose/talc composite films.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  14. Fulltext Evaluation of Biological Pretreatment of Rubberwood with White Rot Fungi for Enzymatic Hydrolysis
    Nazarpour F, Abdullah DK, Abdullah N, Zamiri R
    Materials (Basel), 2013 May 15;6(5):2059-2073.
    PMID: 28809260 DOI: 10.3390/ma6052059
    e effects of biological pretreatment on the rubberwood (Hevea brasiliensis), was evaluated after cultivation of white rot fungi Ceriporiopsis subvermispora, Trametes versicolor, and a mixed culture of C. subvermispora and T. versicolor. The analysis of chemical compositions indicated that C. subvermispora had greater selectivity for lignin degradation with the highest lignin and hemicellulose loss at 45.06% and 42.08%, respectively, and lowest cellulose loss (9.50%) after 90 days among the tested samples. X-ray analysis showed that pretreated samples had a higher crystallinity than untreated samples. The sample pretreated by C. subvermispora presented the highest crystallinity of all the samples which might be caused by the selective degradation of amorphous components. Fourier transform infrared (FT-IR) spectroscopy demonstrated that the content of lignin and hemicellulose decreased during the biological pretreatment process. A study on hydrolysis of rubberwood treated with C. subvermispora, T. versicolor, and mixed culture for 90 days resulted in an increased sugar yield of about 27.67%, 16.23%, and 14.20%, respectively, as compared with untreated rubberwood (2.88%). The results obtained demonstrate that rubberwood is a potential raw material for industrial applications and white rot fungus C. subevermispora provides an effective method for improving the enzymatic hydrolysis of rubberwood.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  15. Fulltext A Novel Hydrazinecarbothioamide as a Potential Corrosion Inhibitor for Mild Steel in HCl
    Al-Amiery AA, Kadhum AAH, Mohamad AB, Junaedi S
    Materials (Basel), 2013 Apr 02;6(4):1420-1431.
    PMID: 28809218 DOI: 10.3390/ma6041420
    2-(1-methyl-4-((E)-(2-methylbenzylidene)amino)-2-phenyl-1H-pyrazol-3(2H)-ylidene)-hydrazineecarbothioamide (HCB) was synthesized as a corrosion inhibitor from the reaction of 4-aminoantipyrine, thiosemicarbazide and 2-methylbenzaldehyde. The corrosion inhibitory effects of HCB on mild steel in 1.0 M HCl were investigated using potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS). The results showed that HCB inhibited mild steel corrosion in acidic solution and inhibition efficiency increased with an increase in the concentration of the inhibitor. The inhibition efficiency was up to 96.5% at 5.0 mM. Changes in the impedance parameters suggested that HCB adsorbed on the surface of mild steel, leading to the formation of a protective film. The novel corrosion inhibitor synthesized in the present study was characterized using Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) spectral data.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  16. Trichoderma asperellum cultured in reduced concentrations of synthetic medium retained dye decolourization efficacy
    Marcharchand S, Ting ASY
    J Environ Manage, 2017 Dec 01;203(Pt 1):542-549.
    PMID: 28693968 DOI: 10.1016/j.jenvman.2017.06.068
    Trichoderma asperellum (Ta) was first cultured in synthetic medium (Potato Dextrose Broth, PDB) of various concentrations (100, 75, 50, 25%). The biomass was harvested and inoculated into dye solutions (crystal violet, CV; methyl violet, MV; malachite green, MG; and cotton blue, CB). Reduced concentrations (20, 50, 75%) affected growth rate but their decolourization efficacies remained unaffected. This was attributed to similar numbers and types of functional groups (hydroxyl, amine, ester-lipid, alkane groups) found on the surface of fungal biomass, as revealed by the Fourier transformed infrared spectroscopy (FTIR) analysis. Their production of NADH-reductase for degradation, and their biosorption activities were also unaffected. In general, Ta cultured in reduced concentrations (20, 50, 75%) retained the ability to perform biosorption and biodegradation, similar to cultures from control (100% PDB). This suggested that reduced nutrient levels (as a cost-feasible strategy) could be used to cultivate biomass of Ta for dye removal activities.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  17. Fulltext Impact of Sulfuric Acid Treatment of Halloysite on Physico-Chemic Property Modification
    Gaaz TS, Sulong AB, Kadhum AAH, Nassir MH, Al-Amiery AA
    Materials (Basel), 2016 Jul 26;9(8).
    PMID: 28773741 DOI: 10.3390/ma9080620
    Halloysite (HNT) is treated with sulfuric acid and the physico-chemical properties of its morphology, surface activity, physical and chemical properties have been investigated when HNT is exposed to sulfuric acid with treatment periods of 1 h (H1), 3 h (H3), 8 h (H8), and 21 h (H21). The significance of this and similar work lies in the importance of using HNT as a functional material in nanocomposites. The chemical structure was characterized by Fourier transform infrared spectroscopy (FTIR). The spectrum demonstrates that the hydroxyl groups were active for grafting modification using sulfuric acid, promoting a promising potential use for halloysite in ceramic applications as filler for novel clay-polymer nanocomposites. From the X-ray diffraction (XRD) spectrum, it can be seen that the sulfuric acid breaks down the HNT crystal structure and alters it into amorphous silica. In addition, the FESEM images reveal that the sulfuric acid treatment dissolves the AlO₆ octahedral layers and induces the disintegration of SiO₄ tetrahedral layers, resulting in porous nanorods. The Bruncher-Emmett-Teller (BET) surface area and total pore volume of HNTs showed an increase. The reaction of the acid with both the outer and inner surfaces of the nanotubes causes the AlO₆ octahedral layers to dissolve, which leads to the breakdown and collapse of the tetrahedral layers of SiO₄. The multi-fold results presented in this paper serve as a guide for further HNT functional treatment for producing new and advanced nanocomposites.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  18. Fulltext Parametric Studies of Titania-Supported Gold-Catalyzed Oxidation of Carbon Monoxide
    Chong S, Yang TC
    Materials (Basel), 2017 Jul 05;10(7).
    PMID: 28773110 DOI: 10.3390/ma10070756
    This paper remarks the general correlations of the shape and crystallinity of titanium dioxide (TiO₂) support on gold deposition and carbon monoxide (CO) oxidation. It was found that due to the larger rutile TiO₂ particles and thus the pore volume, the deposited gold particles tended to agglomerate, resulting in smaller catalyst surface area and limited gold loading, whilst anatase TiO₂ enabled better gold deposition. Those properties directly related to gold particle size and thus the number of low coordinated atoms play dominant roles in enhancing CO oxidation activity. Gold deposited on anatase spheroidal TiO₂ at photo-deposition wavelength of 410 nm for 5 min resulted in the highest CO oxidation activity of 0.0617 mmol CO/s.gAu (89.5% conversion) due to the comparatively highest catalyst surface area (114.4 m²/g), smallest gold particle size (2.8 nm), highest gold loading (7.2%), and highest Au⁰ content (68 mg/g catalyst). CO oxidation activity was also found to be directly proportional to the Au⁰ content. Based on diffuse reflectance infrared Fourier transform spectroscopy, we postulate that anatase TiO₂-supported Au undergoes rapid direct oxidation whilst CO oxidation on rutile TiO₂-supported Au could be inhibited by co-adsorption of oxygen.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  19. Fulltext Rapid investigation of α-glucosidase inhibitory activity of Phaleria macrocarpa extracts using FTIR-ATR based fingerprinting
    Easmin S, Sarker MZI, Ghafoor K, Ferdosh S, Jaffri J, Ali ME, et al.
    J Food Drug Anal, 2017 Apr;25(2):306-315.
    PMID: 28911672 DOI: 10.1016/j.jfda.2016.09.007
    Phaleria macrocarpa, known as "Mahkota Dewa", is a widely used medicinal plant in Malaysia. This study focused on the characterization of α-glucosidase inhibitory activity of P. macrocarpa extracts using Fourier transform infrared spectroscopy (FTIR)-based metabolomics. P. macrocarpa and its extracts contain thousands of compounds having synergistic effect. Generally, their variability exists, and there are many active components in meager amounts. Thus, the conventional measurement methods of a single component for the quality control are time consuming, laborious, expensive, and unreliable. It is of great interest to develop a rapid prediction method for herbal quality control to investigate the α-glucosidase inhibitory activity of P. macrocarpa by multicomponent analyses. In this study, a rapid and simple analytical method was developed using FTIR spectroscopy-based fingerprinting. A total of 36 extracts of different ethanol concentrations were prepared and tested on inhibitory potential and fingerprinted using FTIR spectroscopy, coupled with chemometrics of orthogonal partial least square (OPLS) at the 4000-400 cm-1 frequency region and resolution of 4 cm-1. The OPLS model generated the highest regression coefficient with R2Y = 0.98 and Q2Y = 0.70, lowest root mean square error estimation = 17.17, and root mean square error of cross validation = 57.29. A five-component (1+4+0) predictive model was build up to correlate FTIR spectra with activity, and the responsible functional groups, such as -CH, -NH, -COOH, and -OH, were identified for the bioactivity. A successful multivariate model was constructed using FTIR-attenuated total reflection as a simple and rapid technique to predict the inhibitory activity.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
  20. Synthesis and characterization of magnetic graphene oxide for arsenic removal from aqueous solution
    Sherlala AIA, Raman AAA, Bello MM
    Environ Technol, 2019 May;40(12):1508-1516.
    PMID: 29300679 DOI: 10.1080/09593330.2018.1424259
    A magnetic graphene oxide (MGO) was developed for the adsorption of As(III) from aqueous solution. The characteristics of MGO were investigated using Fourier-transform infrared (FTIR), X-ray diffraction and field emission scanning electron microscope-E/energy-dispersive X-ray analyses. Batch adsorption experiments were designed using central composite design, and the effects of adsorbent dosage, pH, contact time and concentration of As(III) were investigated. The MGO showed an excellent performance, removing up to 99.95% of As(III) under the following condition: initial As(III) concentration = 100 mg/L, pH = 7, adsorbent dosage = 0.3 g/L and contact time = 77 min. MGO dosage and initial pH were the most significant parameters influencing the process performance. FTIR analysis of the used adsorbent confirms the adsorption of As(III) through complexation between surface functional groups of the MGO and the oxyanions of As(III). The adsorbent maintained a significant level of performance even after four cycles of adsorption. Thus, the developed MGO has the potential to be used for the abatement of arsenic pollution.
    Matched MeSH terms: Spectroscopy, Fourier Transform Infrared
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