Attenuated Total Reflection Spectroscopy Research Articles

Grafting of glycerol methacrylate onto silicone rubber using γ-rays: derivatization to 2-oxoethyl methacrylate and immobilization of lysozyme

Abstract

Controlled release of mitomycin C from PHEMAH–Cu(II) cryogel membranes

Molecular imprinting technique was used for the preparation of antibiotic and anti-neoplastic chemotherapy drug (mitomycin C) imprinted cryogel membranes (MMC-ICM). The membranes were synthezied by using metal ion coordination interactions with N-methacryloyl-(l)-histidine methyl ester (MAH) functional monomer and template molecules (i.e. MMC). The 2-hydroxyethyl methacrylate (HEMA) monomer and methylene bisacrylamide (MBAAm) crosslinker were used for the preparation of mitomycin C imprinted cryogel membranes by radical suspension polymerization technique. The imprinted cryogel membranes were characterized by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET), Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR) and swelling degree measurements. Cytotoxicity of MMC-ICMs was investigated using mouse fibroblast cell line L929. Time-dependent release of MMC was demonstrated within 150 h from cryogel membranes. Cryogels demonstrated very high MMC loading efficiency (70–80%) and sustained MMC release over hours.

Encapsulation of Ionic Liquids with an Aprotic Heterocyclic Anion (AHA-IL) for CO2 Capture: Preserving the Favorable Thermodynamics and Enhancing the Kinetics of Absorption

The performance of an ionic liquid with an aprotic heterocyclic anion (AHA-IL), trihexyl(tetradecyl)phosphonium 2-cyanopyrrolide ([P66614][2-CNPyr]), for CO2 capture has been evaluated considering both the thermodynamics and the kinetics of the phenomena. Absorption gravimetric measurements of the gas-liquid equilibrium isotherms of CO2-AHA-IL systems were carried out from 298 to 333 K and at pressures up to 15 bar, analyzing the role of both chemical and physical absorption phenomena in the overall CO2 solubility in the AHA-IL, as has been done previously. In addition, the kinetics of the CO2 chemical absorption process was evaluated by in situ Fourier transform infrared spectroscopy-attenuated total reflection, following the characteristic vibrational signals of the reactants and products over the reaction time. A chemical absorption model was used to describe the time-dependent concentration of species involved in the reactive absorption, obtaining kinetic parameters (such as chemical reaction kinetic constants and diffusion coefficients) as a function of temperatures and pressures. As expected, the results demonstrate that the CO2 absorption rate is mass-transfer-controlled because of the relatively high viscosity of AHA-IL. The AHA-IL was encapsulated in a porous carbon sphere (Encapsulated Ionic Liquid, ENIL) to improve the kinetic performance of the AHA-IL for CO2 capture. The newly synthesized AHA-ENIL material was evaluated as a CO2 sorbent with gravimetric absorption measurements. AHA-ENIL systems preserve the good CO2 absorption capacity of the AHA-IL but drastically enhance the CO2 absorption rate because of the increased gas-liquid surface contact area achieved by solvent encapsulation.

Atmospheric Pressure Plasma Treatment for Grey Cotton Knitted Fabric.

100% grey cotton knitted fabric contains impurities and yellowness and needs to be prepared for processing to make it suitable for coloration and finishing. Therefore, conventionally 100% grey cotton knitted fabric undergoes a process of scouring and bleaching, which involves the use of large amounts of water and chemicals, in order to remove impurities and yellowness. Due to increased environmental awareness, pursuing a reduction of water and chemicals is a current trend in textile processing. In this study, we explore the possibility of using atmospheric pressure plasma as a dry process to treat 100% grey cotton knitted fabric (single jersey and interlock) before processing. Experimental results reveal that atmospheric pressure plasma treatment can effectively remove impurities from 100% grey cotton knitted fabrics and significantly improve its water absorption property. On the other hand, if 100% grey cotton knitted fabrics are pretreated with plasma and then undergo a normal scouring process, the treatment time is reduced. In addition, the surface morphological and chemical changes in plasma-treated fabrics were studied and compared with the conventionally treated fabrics using scanning electron microscope (SEM), Fourier-transform infrared spectroscopy-attenuated total reflection (FTIR-ATR) and X-ray photoelectron spectroscopy (XPS). The decrease in carbon content, as shown in XPS, reveal the removal of surface impurities. The oxygen-to-carbon (O/C) ratios of the plasma treated knitted fabrics reveal enhanced hydrophilicity.

Zwitterionic molecule layer for inhibiting microbial corrosion of copper alloy

PurposeFor mitigating biocorrosion induced by sulfate-reducing bacteria (SRB) in seawater, the zwitterionic molecule layer (ZML) of poly (sulfobetaine methacrylate) is grafted onto B10 surface by chemical vapor deposition and surface-initiated atom transfer radical polymerization.Design/methodology/approachEnergy-dispersive spectroscopy-attenuated total reflectance Fourier transform infrared spectroscopy and static contact angle measurements are used to characterize the as-formed layer.FindingsAfter surface modification, B10 can significantly reduce SRB adhesion, demonstrating the good antifouling property. Further, the biocorrosion inhibition is investigated by potentiodynamic polarization and electrochemical impedance spectroscopy, indicating that ZML exhibits high resistance to biocorrosion with inhibition efficiency of approximately 90 per cent.Originality/valueZML performs a dual feature, i.e. antifouling film and corrosion inhibitor, for the biocorrosion inhibition.

Unique Hydrogen Bonds in Membrane Protein Monitored by Whole Mid-IR ATR Spectroscopy in Aqueous Solution.

Protein function is coupled to its structural changes, for which stimulus-induced difference Fourier-transform infrared (FTIR) spectroscopy is a powerful method. By optimizing the attenuated total reflection (ATR)-FTIR analysis on sodium-pumping rhodopsin KR2 in aqueous solution, we first measured the accurate difference spectra upon sodium binding in the whole IR region (4000-1000 cm-1). The new spectral window allows the analysis of not only the fingerprint region (1800-1000 cm-1) but also the hydrogen-bonding donor region (4000-1800 cm-1), revealing an unusually strong hydrogen bond of Tyr located in the sodium binding site of KR2. Progress in ATR-FTIR difference spectroscopy provides an approach to investigating stimulus-induced structural changes of membrane proteins under physiological aqueous conditions.

Hygroscopicity of internally mixed particles glycine/NaNO3 studied by FTIR-ATR technique

Internal mixed aerosol particles in atmosphere often take the drastic physical property changes owing to interactions between compositions. Hygroscopicity and phase transition behavior of mixed particles composed of glycine and NaNO3 with different organic to inorganic molar ratios (OIRs) have been investigated by using Fourier transform infrared attenuated total reflection spectroscopy (ATR-FTIR). It is found that pure glycine particles effloresce when the relative humidity (RH) is ∼64.5% and do not deliquesce on humidifying. The efflorescence and deliquescence point for pure NaNO3 particles are ∼54% RH and ∼91.9% RH, respectively. For the internal mixed glycine/NaNO3 particles, there exhibit various hygroscopicities and solid-aqueous phase transitions dependent upon the OIR. When the OIRs are 2:1 and 1:1, NaNO3 particles cannot crystallize. When the OIRs are 1:2, 1:4 and 1:8, crystalline ratios are ~31%, ~45% and 72%, NaNO3 effloresce at ∼44.7% RH, ~35.2% RH and ~35% RH, respectively. For all studied mixture particles, glycine can crystallize. For OIRs of 2:1, 1:1, 1:2, 1:4 and 1:8, the crystalline fractions of glycine are ~78%, 89%, 93%, 94% and 95%, respectively, corresponding to the ERH range of 74% − 42%, 73% − 35.9%, 65.5% − 19.2%, 35.2% − 8.1% and 35% − 3.8%. It shows that both NaNO3 and glycine crystals are favored by more enriched NaNO3. On hydration, the DRHs of NaNO3 for mixtures with OIR of 1:2, 1:4 and 1:8 are ~87.4%, ~87% and 85.4%, respectively. Glycine in mixtures deliquesces at ~99% (incomplete deliquescence), ~98.3%, ~97.3%, ~93.3%, ~85.4% RH, respectively, with decreasing OIR. The results suggest the positive effect of NaNO3 on the deliquescence of glycine and NaNO3.

Differentiation of red lipsticks using the attenuated total reflection technique supported by two chemometric methods

The main challenge for the identification and differentiation of lipsticks for forensic purposes is the fact that they have a similar chemical composition — in particular, samples of the same hue. The objective of the presented research was to solve this problem using a nondestructive analytical technique — attenuated total reflection spectroscopy (ATR). 38 red lipsticks produced by 20 different manufacturers were examined in optimized experimental conditions. To facilitate discrimination and provide more extensive analyses of the obtained data, two chemometric techniques: principal component analysis and cluster analysis were used. Ultimately, nine groups of investigated lipstick samples with comparable chemical compositions were differentiated. Moreover, lipstick smears on six different interfering surfaces were analyzed and spectral subtraction was performed in order to identify individual samples. The established approach succeeded in identifying the index number and the manufacturer of the samples by using an in-lab built ATR spectra library. The developed method demonstrates a great potential for the differentiation and identification of red lipsticks with a very similar hue. It also seems to have good prospects for future application in forensic science investigations.

Predicting the cell-wall compositions of Pinus radiata (radiata pine) wood using ATR and transmission FTIR spectroscopies

Because plant cell walls vary in their polysaccharide compositions and lignin contents, their monosaccharide compositions and lignin contents are often determined, but these analyses are time consuming and laborious. We therefore investigated Fourier transform infrared (FTIR) spectroscopy coupled with partial least squares (PLS) regression analysis as a way of rapidly predicting the monosaccharide compositions and lignin contents of the cell walls of compression wood (CW) and opposite wood (OW) of the gymnosperm Pinus radiata. The effects were investigated of sample moisture content (ambient or dry) and sample particle size (large particles, < 0.422 mm or small particles, < 0.178 mm) of milled wood on attenuated total reflectance (ATR) and transmission FTIR spectra, as well as the PLS-1 models and subsequent predictions. PLS-1 models were built using mixtures of CW and OW as the training set, to provide a linear range of monosaccharide compositions and lignin contents. Models were externally validated by predicting another set of wood mixtures before predicting CW and OW of a separate test set. Most of the monosaccharide amounts in the separate test set were best predicted by ATR spectroscopy of ambient large particles, achieving the lowest standard error values for the monosaccharides arabinose (0.36%), xylose (1.05%), galactose (1.79%), glucose (6.32%), and 4-O-methylglucuronic acid (0.20%). The results show the feasibility of using ATR spectroscopy of ambient large particles for the rapid prediction of monosaccharide compositions and lignin contents of plant cell walls.

Surface modification of model hydrogel contact lenses with hyaluronic acid via thiol-ene "click" chemistry for enhancing surface characteristics.

Discontinuation of contact lens wear as a result of ocular dryness and discomfort is extremely common; as many as 26% of contact lens wearers discontinue use within the first year. While patients are generally satisfied with conventional hydrogel lenses, improving on-eye comfort continues to remain a goal. Surface modification with a biomimetic, ocular friendly hydrophilic layer of a wetting agent is hypothesized to improve the interfacial interactions of the contact lens with the ocular surface. In this work, the synthesis and characterization of poly(2-hydroxyethyl methacrylate) surfaces grafted with a hydrophilic layer of hyaluronic acid are described. The immobilization reaction involved the covalent attachment of thiolated hyaluronic acid (20 kDa) on acrylated poly(2-hydroxyethyl methacrylate) via nucleophile-initiated Michael addition thiol-ene "click" chemistry. The surface chemistry of the modified surfaces was analyzed by Fourier transform infrared spectroscopy-attenuated total reflectance and X-ray photoelectron spectroscopy. The appearance of N (1s) and S (2p) peaks on the low resolution X-ray photoelectron spectroscopy spectra confirmed successful immobilization of hyaluronic acid. Grafting hyaluronic acid to the poly(2-hydroxyethyl methacrylate) surfaces decreased the contact angle, the dehydration rate, and the amount of nonspecific sorption of lysozyme and albumin in comparison to pristine hydrogel materials, suggesting the development of more wettable surfaces with improved water-retentive and antifouling properties, while maintaining optical transparency (>92%). In vitro testing also showed excellent viability of human corneal epithelial cells with the hyaluronic acid-grafted poly(2-hydroxyethyl methacrylate) surfaces. Hence, surface modification with hyaluronic acid via thiol-ene "click" chemistry could be useful in improving contact lens surface properties, potentially alleviating symptoms of contact lens related dryness and discomfort during wear.

Application of ATR spectroscopy for astrobiological investigations aboard planetary landers

We propose the use of infrared attenuated total reflectance (ATR) spectroscopy aboard landers for contact astrobiological soil research on terrestrial planets. The method is based on the absorption bands inherent to biological macromolecules (proteins, DNA/RNA, and carbohydrates). It is also applicable to mineralogical studies of soil, dust, and atmospheric precipitation; the use of balloons (e.g., on Venus) adds aerosols to this list. The optimal spectral range seems to be 2.5–25 μm; the optimal spectral resolution, about 10 cm–1.

Modification of thin-film polyamide membrane with multi-walled carbon nanotubes by interfacial polymerization

Polyamide thin-film composite (TFC) was fabricated on polysulfone (PS-20) base by interfacial polymerization of aqueous m-phenylenediamine (MPD) solution and 1,3,5-benzenetricarbonyl trichloride (TMC) in hexane organic solution. Multi-wall carbon nanotubes (MWCNT) were carboxylated by heating MWCNT powder in a mixture of HNO3 and H2SO4 (1:3 v/v) at 70 °C under constant sonication for different periods. Polyamide nanocomposites were prepared by incorporating MWCNT and the carboxylated MWCNT (MWCNT–COOH) at different concentrations (0.001–0.009 wt%). The developed composites were analyzed by Fourier transform infrared spectroscopy-attenuated total reflection, scanning electron microscopy, transmission electron microscopy, contact angle measurement, determination of salt rejection and water permeate flux capabilities. The surface morphological studies displayed that the amalgamation of MWCNT considerably changed the surface properties of modified membranes. The surface hydrophilicity was increased as observed in the enhancement in water flux and pure water permeance, due to the presence of hydrophilic nanotubes. Salt rejection was obtained between 94 and 99% and varied water flux values for TFC-reference membrane, pristine-MWCNT in MPD, pristine-MWCNT in TMC and MWCNT–COOH in MPD were 20.5, 38, 40 and 43 L/m2h. The water flux and salt rejection performances revealed that the MWCNT–COOH membrane was superior membrane as compared to the other prepared membranes.

Temperature and Copper Concentration Effects on the Formation of Graphene-Encapsulated Copper Nanoparticles from Kraft Lignin.

The effects of temperature and copper catalyst concentration on the formation of graphene-encapsulated copper nanoparticles (GECNs) were investigated by means of X-ray diffraction, Fourier transform infrared spectroscopy-attenuated total reflectance, and transmission electron microscopy. Results showed that higher amounts of copper atoms facilitated the growth of more graphene islands and formed smaller size GECNs. A copper catalyst facilitated the decomposition of lignin at the lowest temperature studied (600 °C). Increasing the temperature up to 1000 °C retarded the degradation process, while assisting the reconfiguration of the defective sites of the graphene layers, thus producing higher-quality GECNs.

Spectroscopic analysis of hot-water- and dilute-acid-extracted hardwood and softwood chips

Hot-water and dilute sulfuric acid pretreatments were performed prior to chemical pulping for silver/white birch (Betula pendula/B. pubescens) and Scots pine (Pinus sylvestris) chips to determine if varying pretreatment conditions on the original wood material were detectable via attenuated total reflectance (ATR) infrared spectroscopy. Pretreatment conditions varied with respect to temperature (130°C and 150°C) and treatment time (from 30min to 120min). The effects of the pretreatments on the composition of wood chips were determined by ATR infrared spectroscopy. The spectral data were compared to those determined by common wood chemistry analyses to evaluate the suitability of ATR spectroscopy method for rapid detection of changes in the wood chemical composition caused by different pretreatment conditions. In addition to determining wood species-dependent differences in the wood chemical composition, analytical results indicated that most essential lignin- and carbohydrates-related phenomena taking place during hot-water and acidic pretreatments could be described by applying this simple spectral method requiring only a small sample amount and sample preparation. Such information included, for example, the cleavage of essential lignin bonds (i.e., mainly β-O-4 linkages in guaiacyl and syringyl lignin) and formation of newly condensed lignin structures under different pretreatment conditions. Carbohydrate analyses indicated significant removal of hemicelluloses (especially hardwood xylan) and hemicelluloses-derived acetyl groups during the pretreatments, but they also confirmed the highly resistant nature of cellulose towards mild pretreatments.

Oxidation of polyacrylonitrile nanofiber webs as a precursor for carbon nanofiber: aligned and non-aligned nanofibers

Carbon nanofibers have a great potential for supercapacitor, battery, photocatalytic applications, and supporting material for light weight composite structures. In addition to use as a carbon fiber precursor, oxidized PAN nanofiber can also be used to produce inherently flame-resistant materials. Temperature and time are the major parameters for oxidation stabilization process and it is possible to examine the oxidation efficiency comparing with the Fourier transform infrared spectroscopy-attenuated total reflection (FTIRATR) spectroscopic results for different temperatures and time intervals. Thus, PAN nanofiber production and oxidation process well examined to fabricate desired featured CNFs. The conventional carbon fiber route which includes oxidation and carbonization can be adapted to obtain carbon nanofibers. In this study, several production parameters for PAN-based nanofiber fabrication were investigated intensely and oxidation studies of PAN-based nanofibers were examined to get an approach to oxidation procedure for carbon nanofiber production. Improved quality of precursor of PAN-based nanofiber webs directly affects the final product, carbon nanofiber properties. Thus, PAN-based nanofiber webs were prepared via electrospinning technique with aligned and non-aligned forms. Rotating and fixed collectors were used to diversify the samples and investigate the physical and chemical changes on the samples. FTIRATR spectroscopy was used to record the characteristic peaks of the nanofiber webs before and after oxidation. Nanofiber webs were characterized using DMA for their mechanical properties. Differential scanning calorimeter was used for thermal analysis. During the thermal treatment, nitrile group of PAN converts to C=N and C–N groups through cyclized structure. For all steps, surface morphology of the fibers was observed with scanning electron microscope and average fiber diameter was calculated through the fabrication steps. In this study, not only mechanical properties of the webs were investigated, but also chemical structure of the oxidized webs was studied. Aligned nanofibers have exhibited superior mechanical properties than the non-aligned ones.

Anti-microbial surfaces: An approach for deposition of ZnO nanoparticles on PVA-Gelatin composite film by screen printing technique

Initially micro-organisms get exposed to the surfaces, this demands development of anti-microbial surfaces to inhibit their proliferation. Therefore, herein, we attempt screen printing technique for development of PVA-GE/ZnO nanocomposite (PG/ZnO) films. The synthesis of PG/ZnO nanocomposite includes two steps as: (i) Coating of Zinc Oxide nanoparticles (ZnO NPs) by poly ethylene glycol in order to be compatible with organic counterparts. (ii) Deposition of coated nanoparticles on the PG film surface. The results suggest the enhancement in anti-microbial activity of PG/ZnO nanocomposite over pure ZnO NPs against both Gram positive Bacillus subtilis and Gram negative Escherichia coli from zone of inhibition. The uniformity in deposition is further confirmed by scanning electron microscopy (SEM) images. The phase identification of ZnO NPs and formation of PG/ZnO nanocomposite has been confirmed by X-ray diffraction (XRD) analysis and UV–vis spectroscopy (UV–vis). The Attenuated total reflection Spectroscopy (ATR) analysis indicates the ester bond between PVA and gelatin molecules. The thermal stability of nanocomposite is studied by thermogravimetric analysis (TGA) revealing increase in crystallinity due to ZnO NPs which could be utilized to inhibit the growth of micro-organisms. The tensile strength is found to be higher and percent elongation is double of PG/ZnO nanocomposite than PG composite film.

Influence of Molecular Aggregation on Electron Transfer at the Perylene Diimide/Indium-Tin Oxide Interface.

Chemisorption of an organic monolayer to tune the surface properties of a transparent conductive oxide (TCO) electrode can improve the performance of organic electronic devices that rely on efficient charge transfer between an organic active layer and a TCO contact. Here, a series of perylene diimides (PDIs) was synthesized and used to study relationships between monolayer structure/properties and electron transfer kinetics at PDI-modified indium-tin oxide (ITO) electrodes. In these PDI molecules, one of the imide substituents is a benzene ring bearing a phosphonic acid (PA) and the other is a bulky aryl group that is twisted out of the plane of the PDI core. The size of the bulky aryl group and the substitution of the benzene ring bearing the PA were both varied, which altered the extent of aggregation when these molecules were absorbed as monolayer films (MLs) on ITO, as revealed by both attenuated total reflectance (ATR) and total internal reflection fluorescence spectra. Polarized ATR measurements indicate that, in these MLs, the long axis of the PDI core is tilted at an angle of 33-42° relative to the surface normal; the tilt angle increased as the degree of bulky substitution increased. Rate constants for electron transfer (ks,opt) between these redox-active modifiers and ITO were determined by potential-modulated ATR spectroscopy. As the degree of PDI aggregation was reduced, ks,opt declined, which is attributed to a reduction in the lateral electron self-exchange rate between adsorbed PDI molecules, as well as the heterogeneous conductivity of the ITO electrode surface. Photoelectrochemical measurements using a dissolved aluminum phthalocyanine as an electron donor showed that ITO modified with any of these PDIs is a more effective electron-collecting electrode than bare ITO.

Polycaprolactone/Amino-β-Cyclodextrin Inclusion Complex Prepared by an Electrospinning Technique.

Electrospun scaffolds of neat poly-ε-caprolactone (PCL), poly-ε-caprolactone/β-cyclodextrin inclusion complex (PCL/β-CD) and poly-ε-caprolactone amino derivative inclusion complex (PCL/β-CD-NH2) were prepared by the electrospinning technique. The obtained mats were analyzed by a theoretical model using the Hartree–Fock method with an STO-3G basis set, and characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR), differential scanning calorimetry (DSC), confocal-Raman spectroscopy, proton nuclear magnetic resonance (1HNMR) and contact angle measure (CA). Different mixtures of solvents, such as dimethylformamide (DMF)-tetrahydrofuran (THF), dichlormethane (DCM)-dimethyl sulfoxide (DMSO) and 2,2,2-Trifluoroethanol (TFE), were tested in the fiber preparation. The results indicate that electrospun nanofibers have a pseudorotaxane structure and when it was prepared using a 2,2,2-Trifluoroethanol (TFE) as solvent, the nanofibers were electrospun well and, with the other solvents, fibers present defects such as molten fibers and bead-like defects into the fiber structure. This work provides insights into the design of PCL/β-CD-NH2 based scaffolds that could have applications in the biomedical field.

Application Of Systems With Total Internal Reflection At Novosibirsk Free Electron Laser For Spectroscopy In The Terahertz Range

Attenuated total reflection (ATR) spectroscopy is widely used in the visible and infrared spectral ranges. Progress in the development of laboratory scale monochromatic sources of terahertz radiation, such as quantum cascade lasers, suggests that in the near future this kind of spectrometers will be widely spread in the terahertz range. For this reason, the development of ATR based methods and devices is highly relevant. In this paper, we discuss the features of the use of ATR spectroscopy in the terahertz range, and describe some of the optical systems, designed for experiments at the Novosibirsk free electron laser (NovoFEL). We show that in the terahertz range the ATR spectroscopy has a number of significant advantages over the absorption spectroscopy. As an example, we are discussing the possibility of using terahertz polarimetry to develop a method for early diagnosis of cancer via the detection of left-handed to right-handed polysaccharide enantiomers ratio. Spectra of selected polysaccharides were recorded with a standard Fourier spectrometer using developed by us an ATR unit. The possibility of studying the polarization characteristics of polysaccharides in aqueous solutions using spectrally selective polarimeter with the NovoFEL as a tunable radiation source was demonstrated.

Influence of acetic acid and calcium hydroxide treatments of rubber waste on the properties of rubberized mortars

The main goal of this study consisted in improving the performance of cementitious materials containing a percentage of rubber particles as a substitution for aggregates. Rubber surface was modified: new chemical and simple treatments based on calcium hydroxide or acetic acid solutions were applied. The effect of the above treatments was compared with that produced by sulphuric acid or sodium hydroxide solutions or by the use of plain rubber particles, already studied and reported in the literature. Fourier transformed infrared spectroscopy-attenuated total reflectance (FTIR-ATR) was used in order to characterize the rubber surface and chemical modifications. The rubber particles were observed by optical microscopy (OM) with the aim of detecting the possible physical changes on their surface. Then, the modified rubber particles were included in the composition of mortar specimens and their properties in the fresh (consistency) and the hardened state (porosity, flexural and compressive strength, capillarity water absorption and ultrasonic pulse velocity, UPV) were examined. Regarding the properties of rubber particles, their surface hydrophilicity, absorption and roughness increased after acid or alkaline treatments. Considering mortars including chemically treated rubber particles, calcium hydroxide gave rise to mortars with lower porosity and acetic acid to mortars with lower density. Mechanical properties of mortars were improved in comparison with these properties in mortars containing plain rubber particles. Alkaline solutions prompted the highest values of compressive strength. A delay in the hardening time for rubberized mortars may be deduced from the mechanical properties evolution. The partial substitution of natural aggregates by chemically treated rubber particles, improves the properties, in terms of flexural and compressive strength, of rubberized mortars.