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At least 1,063 records · Page 59

Electronic absorption spectroscopy of matrix-isolated polycyclic aromatic hydrocarbon cations. II. The phenanthrene cation (C14H10+) and its 1-methyl derivative

The ultraviolet, visible, and near infrared absorption spectra of phenanthrene (C14H10), 1-methylphenanthrene [(CH3)C14H9], and their radical ions [C14H10+; (CH3)C14H9+], formed by vacuum-ultraviolet irradiation, were measured in neon matrices at 4.2 K. The associated vibronic band systems and their spectroscopic assignments are discussed. The oscillator strengths were calculated for the phenanthrene ion and found lower than the theoretical predictions. This study presents the first spectroscopic data for phenanthrene and its methyl derivative trapped in a neon matrix where the perturbation of the isolated species by its environment is minimum; a condition crucial to astrophysical applications.

NASA Discipline Exobiology↗

Properties and Biodegradation of Thermoplastic Starch Obtained from Grafted Starches with Poly(lactic acid)

Properties and biodegradation of thermoplastic starch obtained using granular starches grafted with poly(lactic acid) (St-g-PLA) were studied. The grafting of PLA on the starch granule was verified by the emergence of the carbonyl group in the FTIR spectra and the higher diameter of the grafted starch granule. Thermoplastic starch from ungrafted granular starch (TPS) and grafted granular starch (TPGS) were obtained by mixing ungrafted or grafted starch with water, glycerol or sorbitol in a mixer. TPS and TPGS behave as plastic materials, and their mechanical properties depend on the type of plasticizer used. Materials with glycerol as the plasticizer exhibited less rigidity than the materials obtained using sorbitol. The presence of starch-g-PLA results in an increase in the elongation of the thermoplastic material. TPS and TPGS were hydrolysed by amylolytic enzymes in short-time periods compared to granular PLA-grafted starches.

36 MATERIALS SCIENCE↗

Polymer nanoparticles of N-vinylpyrrolidone loaded with an organic aminonitroxyl platinum (IV) complex. Characterization and investigation of their in vitro cytotoxicity

The conditions for obtaining stable aqueous solutions of a lipophilic aminonitroxyl platinum complex, namely, e-amine-d-(4-amino-2,2,6,6-tetramethylpiperidine 1-oxyl)-a, f-bis(octanoato)-b, c-dichloroplatinum(IV), by means of its encapsulation into nanoparticles of copolymers of N-vinylpyrrolidone with triethylene glycol dimethacrylate with various monomer compositions and topologies were found. Aqueous solutions of the complex encapsulated into polymer particles were investigated by dynamic light scattering, the temperature dependence of nanostructure sizes was studied. Transmission electron microscopy established that the hybrid nanostructures are core—shell particles, in which the platinum complex forms small clusters (∼4 nm). The parameters of ESR spectra of aqueous dispersions indicate a high mobility of nitroxyl contained in hybrid nanostructures. Voltammetric measurements demonstrate a similarity of the redox reactions related to the free radical fragment of the aminonitroxyl Pt{sup IV} complex and of the 4-acetylamino-2,2,6,6-tetramethylpiperidine 1-oxyl radical. Polymer products containing the platinum complex were studied by IR spectroscopy, TGA, and DSC. The cytotoxicity index (IC{sub 50}) of the free and the encapsulated complex was determined for HeLa tumor cells. The cytotoxicity of the latter (IC{sub 50} 47–205 nmol L{sup −1}) depends on the monomeric composition of the nanoparticles and the incubation time.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Investigation of Electrical and Magnetic Properties of La{sup 3+} Substituted M-Type Ba–Ni Nano-Ferrites

In this paper, La{sup 3+} substituted M-type Ba–Ni hexaferrite nanoparticles having composition Ba{sub 0.8}Ni{sub 0.2}Fe{sub 12-x}La{sub x}O{sub 19} (x = 0, 0.2, 0.4, 0.6, and 0.8) were prepared by co-precipitation route. The phase of the grown NPs was confirmed using X-ray diffraction analysis and results reveal the growth of M-type hexaferrite NPs as a major phase. The energy dispersive X-ray spectroscopy (EDX) was employed to determine the elemental composition of prepared samples. The FTIR spectra of synthesized samples confirm the bond formation of M-type hexaferrites. The optical bandgap was determined by UV-Vis spectroscopy and the results exhibit an increase in optical bandgap with decreasing crystallite size. The vibrating sample magnetometry (VSM) technique was used to analyze the effect of dopant on the magnetic properties like coercivity, saturation magnetization, and remanence of the synthesized samples. The electrical resistivity was measured by two probe method and it was observed that the activation energy shows a decreasing trend with increase in La content. The highly resistive nature of prepared nano ferrites indicates the potential to use these ferrites for high-frequency applications.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

A structured framework for predicting sustainable aviation fuel properties using liquid-phase FTIR and machine learning

Sustainable aviation fuels have the potential to improve efficiency, reduce emissions, and enhance energy security. To help identify viable sustainable aviation fuels and accelerate research, machine learning models have been developed to predict relevant physicochemical properties. However, many models have limited applicability, leverage data from complex analytical techniques with confined spectral ranges, or use feature decomposition methods that offer limited interpretability. Using liquid-phase Fourier Transform Infrared (FTIR) spectra, this study presents a structured method for creating accurate and interpretable property prediction models for neat molecules, aviation fuels, and blends. Liquid FTIR spectra can be collected quickly and consistently, offering high reliability, sensitivity, and component specificity using less than 2 ml of sample. The method first decomposes FTIR spectra into fundamental building blocks using non-negative matrix factorization (NMF) to enable scientific analysis of FTIR spectra attributes and fuel properties. The NMF features are then used to create five ensemble models for predicting final boiling point, flash point, freezing point, density at 15°C, and kinematic viscosity at -20°C. All models were trained using experimental property data from neat molecules, aviation fuels, and blends. The models accurately predict key properties across a broad range of neat molecules and representative fuels and blends, while enabling interpretation of relationships between compositional elements, such as functional groups or chemical classes, and their resulting properties. This demonstrates strong potential to support sustainable aviation fuel research and development. The models and data are available on an interactive web tool.

Fourier transform infrared spectroscopy↗

Secular evolution of the vertical column abundances of CHClF2 (HCFC-22) in the Earth's atmosphere inferred from ground-based IR solar observations at the Jungfraujoch and at Kitt Peak, and comparison with model calculations

Series of high-resolution infrared solar spectra recorded at the International Scientific Station of the Jungfraujoch, Switzerland, between 06/1986 and 11/1992, and at Kitt Peak National Observatory, Tucson, Arizona (U.S.A.), from 12/1980 to 04/1992, have been analyzed to provide a comprehensive ensemble of vertical column abundances of CHClF2 (HCFC-22; Freon-22) above the European and the North American continents. The columns were derived from nonlinear least-squares curve fittings between synthetic spectra and the observations containing the unresolved 2 nu(sub 6) Q-branch absorption of CHClF2 at 829.05/cm. The changes versus time observed in these columns were modeled assuming both an exponential and a linear increase with time. The exponential rates of increase at one-sigma uncertainties were found equal to (7.0 +/- 0.35)%/yr for the Junfraujoch data and (7.0 +/- 0.23)%/yr for the Kitt Peak data. The exponential trend of 7.0%/yr found at both stations widely separated in location can be considered as representative of the global increase of the CHClF2 burden in the Earth's atmosphere during the period 1980 to 1992. When assuming two realistic vertical volume mixing ratio profiles for CHClF2 in the troposphere, one quasi constant and the other decreasing by about 13% from the ground to the tropopause, the concentrations for mid-1990 were found to lie between 97 and 111 pptv (parts per trillion by volume) at the 3.58 km altitude of the Jungfraujoch and between 97 and 103 pptv at Kitt Peak, 2.09 km above sea level. Corresponding values derived from calculations using a high vertical resolution-2D model and recently compiled HCFC-22 releases to the atmosphere, were equal to 107 and 105 pptv, respectively, in excellent agreement with the measurements. The model calculated lifetime of CHClF2 was found equal to 15.6 years. The present results are compared critically with similar data found in the literature. On average, the concentrations found here are lower by 15-20% than those derived from in situ investigations; this difference cannot be explained by the absolute uncertainty of +/- 11% assigned presently to the infrared remote measurements.

Zander, R.↗

Improving Prediction of Peroxide Value of Edible Oils Using Regularized Regression Models

We present four unique prediction techniques, combined with multiple data pre-processing methods, utilizing a wide range of both oil types and oil peroxide values (PV) as well as incorporating natural aging for peroxide creation. Samples were PV assayed using a standard starch titration method, AOCS Method Cd 8-53, and used as a verified reference method for PV determination. Near-infrared (NIR) spectra were collected from each sample in two unique optical pathlengths (OPLs), 2 and 24 mm, then fused into a third distinct set. All three sets were used in partial least squares (PLS) regression, ridge regression, LASSO regression, and elastic net regression model calculation. While no individual regression model was established as the best, global models for each regression type and pre-processing method show good agreement between all regression types when performed in their optimal scenarios. Furthermore, small spectral window size boxcar averaging shows prediction accuracy improvements for edible oil PVs. Best-performing models for each regression type are: PLS regression, 25 point boxcar window fused OPL spectral information RMSEP = 2.50; ridge regression, 5 point boxcar window, 24 mm OPL, RMSEP = 2.20; LASSO raw spectral information, 24 mm OPL, RMSEP = 1.80; and elastic net, 10 point boxcar window, 24 mm OPL, RMSEP = 1.91. The results show promising advancements in the development of a full global model for PV determination of edible oils.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Gas phase protonated nicotine is a mixture of pyridine- and pyrrolidine-protonated conformers: implications for its native structure in the nicotinic acetylcholine receptor

The infrared (IR) spectra of gas phase protonated nicotine has been measured in the never-before probed N–H “fingerprint region” (3200–3500 cm -1 ). The protonated molecules generated by an electrospray source are thermalized in the first ion trap with water vapor and He gas at a pre-determined temperature prior to being probed by IR spectroscopy in the second ion trap at 4 K. The IR spectra exhibit two N–H stretching bands which are assigned to the pyridine and pyrrolidine protomers with the aid of high-level electronic structure calculations. This finding is in sharp contrast to previous spectroscopic studies that suggested a single population of the pyridine protomer. The relative populations of the two protomers vary by changing the temperature of the thermalizing trap from 180-300 K. The relative conformer populations at 240 K and 300 K are well reproduced by the theoretical calculations, unequivocally determining that gas phase nicotine is a 3 : 2 mixture of both pyridine and pyrrolidine protomers at room temperature. The thermalizing anhydrous vapor does not result in any population change. It rather demonstrates the catalytic role of water in achieving equilibrium between the two protomers. The combination of IR spectroscopy and electronic structure calculations establish the small energy difference between the pyridine and pyrrolidine protomers in nicotine. Finally, one of the gas phase nicotine pyrrolidine protomers has the closest conformational resemblance among all low-lying energy isomers with the X-ray structure of nicotine in the nicotinic acetylcholine receptor (nAChR).

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Chemical abundances of the young inner-disc open cluster NGC 6705 observed by APOGEE: sodium-rich and not α-enhanced

Previous results in the literature have found the young inner-disc open cluster NGC 6705 to be mildly α-enhanced. We examined this possibility via an independent chemical abundance analysis for 11 red-giant members of NGC 6705. The analysis is based on near-infrared APOGEE spectra and relies on LTE calculations using spherical model atmospheres and radiative transfer. We find a mean cluster metallicity of $\rm [Fe/H] = +0.13 \pm 0.04$, indicating that NGC 6705 is metal-rich, as may be expected for a young inner-disc cluster. The mean α-element abundance relative to iron is $\rm \langle [\alpha /Fe]\rangle =-0.03 \pm 0.05$, which is not at odds with expectations from general Galactic abundance trends. NGC 6705 also provides important probes for studying stellar mixing, given its turn-off mass of M ∼ 3.3 M ⊙ . Its red giants have low 12 C abundances ([ 12 C/Fe] = −0.16) and enhanced 14 N abundances ([ 14 N/Fe] = +0.51), which are key signatures of the first dredge-up on the red giant branch. An additional signature of dredge-up was found in the Na abundances, which are enhanced by [Na/Fe] = +0.29, with a very small non-LTE correction. The 16 O and Al abundances are found to be near-solar. All of the derived mixing-sensitive abundances are in agreement with stellar models of approximately 3.3 M ⊙ evolving along the red giant branch and onto the red clump. As found in young open clusters with similar metallicities, NGC 6705 exhibits a mild excess in the s-process element cerium with $\rm [Ce/Fe] = +0.13\pm 0.07$.

79 ASTRONOMY AND ASTROPHYSICS↗

Adsorption of Iron(III) and Copper(II) by Bacterial Cellulose from Rhodococcus sp. MI 2

Modified cellulose from the pellicle produced by Rhodococcus sp. MI 2 was more efficient at removing Fe(III) and Cu(II) from aqueous solution than similarly modified cellulose from Komagataeibar xylinus TISTR 998. This study first describes the modification of the cellulose to produce mercerized bacterial cellulose (MBC), phosphorylated bacterial cellulose (PBC), acid–base cellulose and diethylenetriamine bacterial cellulose (EABC). Their efficacy as adsorbents to adsorb Fe(III) and Cu(II) was then determined. In aqueous solution at pH 4 at initial Fe(III) concentration of 20 mg/L, PBC reached adsorption equilibrium within 195 min. At pH 5 in an initial Cu(II) concentration of 75 mg/L, EABC reached adsorption equilibrium within 210 min. Molecular structures and chemical bonds were examined by Fourier transform infrared spectroscopy (FT-IR) and physical morphologies by scanning electron microscopy. The adsorption kinetics of MBC, PBC and EABC showed good agreement with the proposed pseudo-second order model and the adsorption isotherm was best described by the Freundlich model. Our study determined optimal conditions, molecular structures, physical morphologies and adsorption kinetics. The cellulose produced by the new strain Rhodococcus sp. MI 2 was highly efficient at adsorbing and removing metal ions from aqueous solution.

36 MATERIALS SCIENCE↗

Novel Environmentally Friendly Superabsorbent Hydrogel Hybrids from Synthesized Star-Shaped Bio-based Monomers and Acrylic Acid

During the past decades, production and applications of petroleum-based superabsorbents have grown dramatically; currently, superabsorbents are produced from acrylic acid, which consequently increase the environmental concerns. The high consumption rate of superabsorbent on the one hand, and their persistence in the environment from the other hand would make the waste of this material a potential hazard for the environment. These materials are not biodegradable, and if degraded hazardous derivatives would be released into soil and water. The current work presents the synthesis and the performance of a novel superabsorbent hydrogel, based on star-shaped bio-based compartments and acrylic acid. Herein, the synthesis of two bio-based star-shaped monomers will be reported based on the condensation reaction between hydroxyl and carboxylic acid end groups of a bio-acid and a bio-alcohol. The first monomer was synthesized from glycerin, succinic acid, lactic acid, itaconic acid, and acrylic acid. The second monomer was synthesized from glycerin, lactic acid, and methacrylic acid. The monomers structures were characterized via FT-IR and {sup 1}HNMR spectroscopies. The different portions of biobased monomers (10, 30, 50, and 70 wt%) were used in combination with the acrylic acid monomer to form hybrid superabsorbents. The swelling properties and the absorbency under load (AUL) of superabsorbents were investigated in turn. The maximum absorption capacities (398.49 and 90.10 g g{sup −1} in water and saline solution, respectively) were observed when 30 wt% of acrylic acid backbone of the superabsorbent was replaced with the bio-based monomer. Moreover, economic and environmental profiles of the hybrid SAPs have been evaluated. The comparative environmental assessment performed using life cycle analysis method, based on the material and energy balances obtained from the available literature. While the economy of the hybrid SAPs production still suffers from the high price of the employed raw biomaterials during manufacturing, the better environmental profiles obtained for the hybrid SAPs.

36 MATERIALS SCIENCE↗

Synthesis and Characterization of Magnetic Halloysite–Alginate Beads for the Removal of Lead(II) Ions from Aqueous Solutions

In this study, alginate (ALG) hybrid spheres supported with magnetic halloysite nanotubes (MHNTs) were synthesized and used effectively in the removal of Pb(II) ions from aqueous solutions. MHNTs were prepared using the “co-precipitation” method. Afterward, magnetic halloysite–alginate (MHNT–ALG) hybrid beads were formed using ALG and MHNTs by the “extrusion dripping” method. The characterization of halloysite nanotubes (HNTs), ALG, MHNTs, and MHNT–ALG hydrogels was performed using FTIR, TGA, particle size analysis, SEM–EDX, TEM, VSM, and BET. According to VSM measurements, the saturation magnetization values of MHNTs and MHNT–ALG hybrid beads at a mass ratio of 1:2 were determined to be 22.7 emu/g and 8.17 emu/g, respectively. The BET surface area of MHNT–ALG hybrid beads was measured to be 81.3 m{sup 2}/g. The adsorption of Pb(II) ions on MHNT–ALG hydrogels was investigated as a function of the pH of the medium, amount of MHNT–ALG, the mass ratio of MHNT to ALG in the composite, and initial Pb(II) concentration in batch stirred vessels. The fit of the adsorption equilibrium of Pb(II) ions on MHNT–ALG hydrogels to the Langmuir type-I and type-II models, Freundlich model, and Redlich–Peterson model was investigated. The fit of the adsorption kinetics to the pseudo-second-order kinetics model was evaluated. Using the Weber and Morris model, the effect of internal and external diffusion limitations was discussed.

36 MATERIALS SCIENCE↗

One-Pot Depolymerization and Polycondensation of PET Based Random Oligo- and Polyesters

The glycolysis of PET is a promising well-developed technique that could be utilized in a wide range of processes. Due to its equilibrial nature, the high ratio of reagents and the purification steps it is an expensive process. In this study our goal was to modify the standard glycolysis to an easily modulateable method (acido-alcoholysis) suited for one-pot oligoester, polyester synthesis. Adipic acid was added to the depolymerization reaction to connect low molecular weighed components into oligoesters. PET depolymerization reaction series were carried out with ethylene–glycol/adipic acid and butane-1,4-diol/adipic acid to demonstrate the tuneability of these systems. The reaction products were thoroughly characterized with NMR, FTIR, TGA, DSC and functional group analysis. One-pot depolymerization-polycondensation reactions were engineered to produce unsaturated and saturated polyesters. The unsaturated polyesters were dissolved in styrene, cross-linked and moulded to be characterized with DMA. A decreasing tendency of the glass transition temperature and cross-link density were found in the function of the ratio of adipic acid used during the depolymerization step. Acido-alcoholysis proved to be a versatile technique that could be used to engineer oligoesters and polyesters. The reagent use can be minimalized, and the raw reaction products can be directly applied as mid-products.

36 MATERIALS SCIENCE↗

Biomass Derived Antimicrobial Hybrid Cellulose Hydrogel with Green ZnO Nanoparticles for Curcumin Delivery and its Kinetic Modelling

Regenerated cellulose obtained from sugarcane bagasse was used for hydrogel preparation using epichlorohydrin (crosslinker) and green zinc oxide nanoparticles (ZNPs) which were phytosynthesised from musk melon seed extract. The synthesised ZNPs were characterised using FESEM and EDAX. The swelling capacity of the hydrogel was determined by swelling measurements. For drug delivery studies from hydrogel, curcumin was selected as the model drug for its appealing anticancer and antimicrobial activity. The presence of ZNPs and curcumin in the hybrid hydrogel was analysed using FTIR, XRD, TGA and SEM analysis. The drug loading efficiency was optimised by Taguchi method. The drug release studies were performed under varying pH and initial drug loading concentration. The kinetic studies showed the best fit with case II type of transport with polymer swelling as the drug release mechanism. Antimicrobial activity for curcumin loaded hybrid hydrogel and pure cellulose hydrogel was performed using Staphylococcus aureus (bacteria) and Trichophyton rubrum (fungi). Thus, the developed curcumin loaded biomass derived hybrid hydrogel could find potential application towards skin infective applications.

36 MATERIALS SCIENCE↗

Waste Eggshells for the Decoration of Carbon Nanotubes and Graphene Nanosheets with Hydroxyapatite for Preparation of LLDPE Nanocomposites

Waste eggshells were used to decorate functionalized carbon nanotubes (CNT) and graphene oxide (GO) by hydroxyapatite (HAP) using in situ synthesis. The HAP decorated CNT and GO were characterized by X-ray diffraction, SEM, and IR spectroscopic techniques. CNT-HAP and GO-HAP were further used to prepare polymer nanocomposites by addition of different percentages of synthesized CNT-HAP and GO-HAP as fillers into linear low density polyethylene (LLDPE). The prepared nanocomposites specimens were utilized for physical and thermo-mechanical analysis. Mechanical properties of the LLDPE nanocomposites were improved with increasing the percentage of CNT-HAP and GO-HAP fillers compared to the pristine LLDPE. Hardness of hybrid-CNT-HAP/LLDPE composite was increased as compared to the GO-HAP/LLDPE, where as tensile strength of the GO-HAP/LLDPE was higher than that of the CNT-HAP/LLDPE composite. Flammability of CNT-HAP and GO-HAP composites was decreased by 32% as compared to the pristine LLDPE. Graphic Abstract: .

36 MATERIALS SCIENCE↗

Gelatin/Gelatinized Sago Starch Biomembranes as a Drug Delivery System Using Rubber Latex as Plasticizer

Preparation and properties of gelatin and gelatin/gelatinized sago starch biomembranes as a drug delivery system are presented. Deproteinized natural rubber latex (DNRL) was chosen to blend as a plasticizer in biomembranes due to its elasticity. The opaque biomembranes were formed, and the effect of DNRL amounts (10–50 part per hundred of gelatin; phg) on mechanical properties of biomembranes was investigated. It was discovered that increasing the amounts of DNRL could decrease the brittleness of biomembranes. However, these DNRL blended biomembranes still swelled, dissolved in water, and eroded within 2 h. The 50 phg DNRL was further chosen for biomembrane preparations. Then, the 5–30 phg gelatinized sago starch which was prepared in-house was added. These gelatin/gelatinized sago starch biomembranes were homogenous and opaque. They portrayed good water uptake properties, and the highest values occurred in 20–30 min, then these biomembranes eroded slowly. Increasing the amounts of sago starch in biomembranes raised the water uptake rates but reduced the erosion properties. Biomembranes with and without starch blends showed the same tensile strengths. Their elongations at break increased when the amounts of starch were raised but still were lower than that of gelatin/DNRL biomembranes. The morphology, scanning electron microscopy, atomic force electron microscopy, Fourier transform infrared spectroscopy, differential scanning calorimeter, and X-ray diffractometer confirmed the compatibility of ingredients in biomembranes. Lidocaine and its hydrochloride salt were successfully incorporated in these biomembranes with good properties. The drug release and permeation of biomembrane showed good drug controlled release and were able to permeate through the pig skin.

36 MATERIALS SCIENCE↗

Synthesis of Carboxyl-Rich Biosorbent by UV-Induced Graft Polymerization Method for High Efficiency Adsorption of Ce{sup 3+} from Aqueous Solution: Activation and Adsorption Mechanism

Developing a cost-effective and highly efficient sorbent for the recovery of rare-earth elements from aqueous solution is still an urgent need. In this study, a novel biosorbent, carboxyl-rich pine bark (CPB), was modified by UV-induced graft polymerization method to increase the carboxyl-containing functional groups and facilitate the adsorption of Ce{sup 3+}. The grafting process was examined by Fourier transform infrared (FTIR) spectroscopy and field emission scanning electron microscopy (FESEM), indicating that high-density carboxyl functional groups are present on the surface of pine bark and the grafting yield of surface polymer brushes reaches up to 128%. Interestingly, the maximum adsorption capacity of Ce{sup 3+} on CPB could reach up to 256.5 mg/g. The adsorption mechanism of Ce{sup 3+} by CPB has been determined by the adsorption models and x-ray photoelectron spectroscopy (XPS), which can be inferred from these results that the high performance of CPB is attributed to the surface coordination between Ce{sup 3+} and hydroxyl or carbonyl groups. This work suggests that engineered surface functional groups of biomass could have an opportunity for the development of high performance rare-earth element adsorbents.

54 ENVIRONMENTAL SCIENCES↗

Effects of Surface Modifications of Kraft Wood Pulp Cellulose Fibres on Improving the Mechanical Properties of Cellulose Fibre/Latex Composites

In this work, three composites with different contents (5, 10, and 15% w/w) of kraft pulp fibre were produced as reinforcing elements for natural latex matrix and the mechanical properties were evaluated. In order to improve the interfacial adhesion between the matrix and the reinforcing element, chemical modifications were carried out on the surface of the fibres using octanoyl and benzoyl chlorides as modifying agents. The extension of chemical modification of the fibres was visualized by the presence of absorption bands in the spectroscopy analyzes of the modified fibre in relation to the crude fibre (ester carbonyl 1700–1740 cm{sup −1}); in addition, the hydroxyl band was preserved, which indicates a modification of surface character. The modified fibres became more hydrophobic due to the decrease in surface energy and the change in the dispersive and polar components. An increase in the storage modulus was observed for the composites with surface-modified fibres, which agrees with the improved dispersion between the surface-modified fibres and the matrix verified by means of scanning electron microscopy images. The incorporation of fibres did not cause changes in the thermal properties of the composites.

36 MATERIALS SCIENCE↗