Home Physical Sciences A brief insight into the prediction of water vapor transmissibility in highly impermeable hybrid nanocomposites based on bromobutyl/epichlorohydrin rubber blends
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A brief insight into the prediction of water vapor transmissibility in highly impermeable hybrid nanocomposites based on bromobutyl/epichlorohydrin rubber blends

  • Kumar Sankaran , Partheban Manoharan , Sofana Reka S and Santanu Chattopadhyay EMAIL logo
Published/Copyright: December 4, 2018

Abstract

The present work proposes a schematic model for predicting the water vapor transmissibility in hybrid nanocomposites based on bromobutyl (BIIR)/epichlorohydrin (CO) rubber blends. Morphology study reveals the exfoliation of nanoclay and development of hybrid nanostructures in the rubber nanocomposites. A unique correlation between water vapor transmissibility and gas (oxygen) permeability through the rubber nanocomposites has been systematically derived. The prediction of relative water vapor transmissibility was achieved by considering the polar path along with the existing tortuous path and has been validated. Interestingly, it is found that the water vapor transmissibility (TW) directly depends on the weight fraction of the polar rubber (ΦP) in the rubber blend and permeability to gas (PG) of the nanocomposites.

1 Introduction

Barrier properties are the prime requisite for rubber membranes, bladders, tubes, and tubeless tires. A low barrier property significantly affects the performance and durability of the rubber product. In particular, the water vapor transport potentially causes degradation mechanism like hydrolysis and corrosion affecting the electrical conductivity and mechanical properties of the composites considerably [1]. Water vapor barrier is of significant value for tire inner liner material asit prevents the liner material from corroding steel belts and bead wires. It also increases the adhesion strength with ply compounds. It is, therefore, important to analyze the water vapor transmission characteristics and to develop a highly impermeable rubber compound. Diffusion and permeation of gas and vapors in rubbers were briefly discussed in earlier literature [2, 3, 4, 5]. However, modeling, theoretical prediction, and the correlation between water vapor transmissibility and gas permeability in the rubber nanocomposites were hardly found in literature and needs exploration.

Layered silicates due to their high aspect ratio and platelet like structure, offers low permeability in the nanocomposites. The dispersion of the nanoclay is the key factor in reinforcing the rubber and to improve the properties of the rubber nanocomposites. BIIR (bromobutyl) is the most favored rubber for the construction of tire inner liners, heat resistant tubes, bladders and pharmaceutical ware due to lower permeability to gases [6]. Polyepichlorohydrin rubber (CO) also offers excellent resistance to gas permeability [7], which is even lower than that of the butyl rubber. Frank et.al claimed that blending of epicholorohydrin rubber with brominated butyl rubber and having delaminated talc in the rubber composite has lower air permeability [8]. It finds potential application in tire inner liners with low permeability. Hence, CO rubber is suitably blended with BIIR in order to further reduce the permeability of the rubber nanocomposites.

This present work discusses in detail the effect of the polar fraction of rubber blends, and nanoclay, on the permeation characteristics of the unique BIIR-CO hybrid nanocomposites. A unique schematic has been modelled to determine the relative moisture transmissibility. An equation has been derived based on the model to correlate water vapor transmissibility with the gas permeability of the nanocomposite.

2 Experimental

2.1 Materials

Hydrin H 55 (specific gravity of 1.37), which is a homopolymer of epicholorohydrin (CO) and Zisnet F-PT (2,4,6 trimercapto-sym-triazine) chemical was kindly provided by M/S Zeon Chemicals, Louisville KY. Bromobutyl rubber (BIIR-2255) was purchased from M/S Exxon Mobil. The organically modified montmorillonite (OMMT) nanoclay (Cloisite 20A) was purchased from M/S Southern Clay Products Inc. Gonzales TX. Carbon black (GPF N 660 grade) was procured from M/S Philips Carbon Black Limited (PCBL), India. Nytex 810 (Naphthenic oil) was supplied by M/S Nynas. Span-60, an anti mill-sticking agent, was procured from M/S Sigma-Aldrich, USA. Other chemicals were supplied by the local vendors.

2.2 Preparation of rubber blend nanocomposites

Rubber nanocomposites were mixed in an internal mixer, Brabender Plasticorder. Mixing was performed in two stages for achieving better dispersion of nanoclay in the rubber matrix. The first stage mixing (master batch) includes melt mixing of BIIR rubber and pre-blended CO-Zisnet F-PT stock, followed by the addition of nanoclay, process aids, carbon black, oil and other functional additives. Nanoclay was added at the beginning of the mix to have better dispersion in the rubber matrix. The addition of the curing agent and accelerators in the second stage mixing constituted the final batch. Compounding temperature was set at 55°C and the rotor speed was maintained around 50 rpm. The total mixing time of the rubber nanocomposites was 10 minutes. Cure characteristics of the samples were obtained by using an oscillating disc rheometer (ODR, Monsanto Rheometer 100) equipped with a digital thermologger operated at 170°C. The samples were cured for characterization based on the optimum cure time (OCT) obtained from ODR. Compound formulations are listed in Table 1. B100H0CB50NC0 is the standard BIIR compound. The effect of nanoclay is analyzed in B100H0CB50NC5. The combined effect of polar fraction and nanoclay is analyzed in B90H10CB50NC5 and the effect of an increase in the polar weight fraction is studied in B80H20CB50NC5.

Table 1

Compound formulation[a] (all ingredients are measured in phr, parts per 100 g of rubber).

Chemical IngredientsB100H0CB50NC0B100H0CB50NC5B90H10CB50NC5B80H20CB50NC5
BIIR 22551001009080
Hydrin H-55-01020
Stearic Acid2---
Calcium stearate-1.51.51.5
Process Promoter15151515
CI Resin2222
CB N 66050505050
Cloisite 20A-555
Zisnet F-PT--0.20.2
Cure Package[b]4.84.84.84.8

3 Characterization

Structural analysis of nanofillers and rubber vulcanizates with different dosages of nanoplatelets were determined by X-ray diffraction (XRD, X-PERT PRO) using Cu anode target (λ = 0.154 nm) with a scan step size of 0.02 °. The d-spacing of nanoplatelets was calculated using the Bragg’s law and structural aspects (intercalation or exfoliation) of the nanoplatelets in the rubber matrix were determined from the peak intensities. The samples were placed vertically in front of the X-ray source. The detector was allowed to move at an angle of 2θ, while the sample was allowed to move at an angle θ, to pick up the diffracted rays by the detector.

The samples for high-resolution transmission electron microscopy (HRTEM) analysis were carefully made by ultra cryo-microtome using a Leica ultracut. Since the samples were elastomeric in nature, ultramicrotome was performed below the glass transition temperature of the blended rubbers (-75±5°C) using sharpened glass knives with a cutting edge of 45°. Dispersion of nanoclay in the nanocomposites was extensively analyzed by using HRTEM. The cryotomed sections were supported on a copper grid for capturing photomicrographs. The microscopy was performed using JEM-2100, JEOL, Japan.

Blend compatibility of the rubber blends were analyzed by dynamic mechanical analyzer (DMA) using Metravib 50 N, France, using tension mode. The samples were subjected to sinusoidal displacements with varying temperature sweeps (-100 to +80°C) at a frequency of 10 Hz and a strain of 0.15%. Tan delta was measured for each sample in above mentioned temperature sweep.

Oxygen has been used as the test gas throughout the permeability experiment and is referred as gas permeability. Gas permeability of the nanocomposites was measured following GB 1038 standard using Labthink permeability tester at 40±1°C. By measuring the pressure differences, the gas transmission rate (GTR) of the specimen was measured, and average values are reported.

Water vapor transmissibility was determined on a thin sheet (1mm thickness) using WVTR SG 3/33, MOCON, USA referring ASTM F 1249-06 at temperature around 40±0.5°C and RH 90±3%.

Surface hydrophilicity/hydrophobicity was measured using water droplet with Rame-Hart standard goniometer (Model 260, F4 series, USA) using Dropimage Advanced V2.7 software.

Ethical approval: The conducted research is not related to either human or animals use.

4 Results and Discussion

4.1 Determination of nanostructural morphology

Morphology of the nanocomposites has been analyzed using XRD and TEM measurements. XRD spectra of the OMMT clay and BIIR-CO nanocomposites are shown in Figure 1. The XRD of OMMT clay exhibits a sharp peak (001) at around 2θ = 3.67 (d-spacing of around 2.406 nm) but the nanocomposites, housing 5 phr of OMMT clay, do not display any sharp peaks over the entire range of 2θ studied. The pattern of the diffractogram is similar to all the samples revealing exfoliated state of dispersion of nanoclay in the rubber matrix. XRD analysis discusses the gallery spacing of the nanoclay. However, it is not a useful tool to understand the spatial distribution and structural heterogeneities of the nanoclay in the rubber matrix.

Figure 1 XRD reveals complete exfoliation of the nanoclay in the rubber nanocomposites.
Figure 1

XRD reveals complete exfoliation of the nanoclay in the rubber nanocomposites.

Dispersion of the nanoclay and the formation of hybrid nanostructures in the rubber nanocomposite are analyzed by using HRTEM. All the nanocomposites display a good level of dispersion of nanoclay in the rubber matrix. The nanocomposites also exhibit the formation of hybrid nanostructures with the development of nanounit and halo. The bending of the nanoclay around the carbon black particle (yellow dotted circle in Fig 2(a-c)) reveals the signature of ‘nano unit’ whereas the entrapment of nanoclay within the black particles corresponds to the halo (red circle in Fig 2(a-c)). The development of those hybrid nanostructures (NC-CB) and good dispersion of nanoclay channels the overall improvement in the filler connectivity as well as the properties of the nanocomposites [9, 10, 11].

Figure 2 TEM Photomicrographs confirms development of hybrid nanostructures in the nanocomposites (a) B100H0CB50NC5 (b) B90H 10CB50NC5 (c) B80H20CB50NC5.
Figure 2

TEM Photomicrographs confirms development of hybrid nanostructures in the nanocomposites (a) B100H0CB50NC5 (b) B90H 10CB50NC5 (c) B80H20CB50NC5.

4.2 Water vapor transmissibility

The diffusion coefficient of the water vapor in nanocomposites significantly contributes to its permeation path. A water vapor transmissibility model has been developed, which significantly explains the possible paths of the diffusion of water vapor in the nanocomposites based on rubber blends.

4.2.1 The Model

The gas barrier of the nanocomposite corresponds to the tortuous path offered by the layered clay platelets [12]. The diffusion rate of the water vapor is relatively more than that of the gas molecule (O2) due to the lower kinetic diameter of the water molecule [13,14]. However, the process of restriction to diffusion due to the tortuosity remains the same irrespective of the size of the gas molecule in the rubber nanocomposites. To understand the effect of the polar component on vapor transmissibility in the rubber nanocomposites, different ratios of rubber blends were mixed. The water vapor transmissibility in the rubber nanocomposite depends on the tortuous path and the polar tunnels. The tortuous path in the nanocomposite corresponds to the presence of nanoclay in the rubber matrix. The polar capillary corroborates the polar nature of the rubber blend nanocomposites. The two paths which possibly occur in the water vapor transmission process are schematically presented in Scheme 1. Tortuous route occurs due to the formation of nanoclay induced hybrid nanostructures. The polar route constitutes through the polar capillary of the rubber.

Scheme 1 A schematic model explaining plausible water vapor transmissibility mechanism in the rubber nanocomposite.
Scheme 1

A schematic model explaining plausible water vapor transmissibility mechanism in the rubber nanocomposite.

The polar chains act as a capillary, absorbing the vapor molecules. The effect is more pronounced if the polar fraction is more as many such capillaries arise. The formation of polar tunnels can be better explained by understanding the effect of CO domain in BIIR-CO rubber blends (Figure 3). Typically, the nanocomposites based on BIIR-CO blends were analyzed. It is noted that an increase in the addition of CO rubber (B80H20CB50NC5) clearly displays two peaks at around -30°C and -9°C. It corresponds to the glass transition temperature of BIIR and CO respectively. This confirms that the higher dosage of CO rubber predominantly phase separate the BIIR-CO blend in the nanocomposite. However, the effect is minimal for the rubber blend having a lower dosage of CO rubber (B90H10CB50NC5). The influential presence of CO domain in the BIIR-CO rubber blend, therefore, essentially corroborates the existence of polar pathways or capillaries in the hybrid nanocomposite. Hence, the water vapor transmission is considerably dependent on the volume fraction of the clay and the weight fraction of polar rubber in the rubber blend nanocomposite.

Figure 3 Loss factor (tan delta) as a function of temperature for the nanocomposites.
Figure 3

Loss factor (tan delta) as a function of temperature for the nanocomposites.

4.2.2 Analysis of water vapor transmissibility in the rubber nanocomposite

From the above figure, the prediction of water vapor transmissibility in the rubber nanocomposites can be evaluated. Figure 4 depicts the variation of water vapor transmissibility and gas permeability with an increase in the polar fraction of the rubber blend nanocomposites. From the figure, it is observed that the gas permeability of the nanocomposites decreases as the weight fraction of the polar rubber increases. The formation of hybrid nanostructures also contributes to a significant reduction in the gas permeability in the rubber nanocomposites (see bottom inset in Figure 4). It is also clear that the water vapor transmissibility significantly changes with the weight fraction of the polar rubber and tortuosity offered by clay platelets. Water vapor transmissibility in the rubber nanocomposites is directly proportional to the polar fraction and permeability to gas. It can be obtained by using the following equation:

Figure 4 A Comparison of water vapor transmissibility and oxygen permeability with an increase in the polar weight fraction of the samples. Top inset: Formation of polar capillaries increases water vapor transmissibility (Polar path). Bottom inset: Formation of hybrid nanostructures decreases gas permeability (Tortuous path).
Figure 4

A Comparison of water vapor transmissibility and oxygen permeability with an increase in the polar weight fraction of the samples. Top inset: Formation of polar capillaries increases water vapor transmissibility (Polar path). Bottom inset: Formation of hybrid nanostructures decreases gas permeability (Tortuous path).

(1)TWΦPPC

Where TW represents water vapor transmissibility, ΦP is the weight fraction of the polar rubber in the rubber blend, and PC is the permeability to gas of the rubber blend nanocomposites.

The figure depicts some interesting water vapor permeation characteristics which can be explained as follows:

  1. The water vapor transmissibility is predominantly dependent upon the permeability of the gas molecule for the non-polar rubber blend nanocomposites (B100H0CB50NC5). It is dependent only on the tortuous path offered by the clay platelets as there is no polar path. Therefore, the above equation can be written as follows:

    (2)TWPC
  2. There is a crossover point at B90H10CB50NC5. At this point, TW is dependent on weight fraction of the polar constituent as well as the permeability of the nanocomposites. In this case, equation 1 holds good.

    (1)TWΦPPC
  3. After the cross-over point, the water vapor transmissibility shoots up in the nanocomposite B80H20CB50NC5. It signifies that TW is predominantly dependent on polar weight fraction of the nanocomposite after the crossover point (see top inset of Figure 4).

    (3)TWΦP
  4. Hence for non-polar rubber blend nanocomposites, TW is dependent on permeability (PC), whereas, for polar rich rubber blend nanocomposites, TW is dependent on polar weight fraction (ΦP) of the rubber blends predominantly.

4.2.3 Prediction of relative water vapor transmissibility

From the schematic model and subsequent equations, the relative water vapor transmissibility in the rubber blend nanocomposites can be predicted. It is derived considering the relative gas permeability accounting to the tortuous path as well as the polar factor or polar component. The relative water vapor transmissibility (RWT) in a rubber blend nanocomposites can be given as:

Table 2

Comparison of relative water vapor transmissibility obtained from model and experimental data.

CompoundRWT
TheoreticalExperimental
B100H0CB50NC50.700.59
B90H10CB50NC50.780.76
B80H 20CB50NC50.980.95
(4)RWT=k×RGP

Where k is the polar component and RGP is the relative permeability of the rubber nanocomposite, Bharadwaj model [12] for clay platelets. The component is determined using the following equation:

(5)k=PF×ΦP

Where PF is the polar factor and ΦP is the weight fraction of the polar rubber in the rubber blend. The polar factor is due to the polar surface formed by the polar component of a molecule (http://www.chemicalize.org/structure/#!mol=epichlorohydrin). The polar factor is a good indicator of the water transport properties of the material. The polar factor (PF) of epichlorohydrin rubber is around 12.53. As the polar factor decreases, k decreases and this polar effect is not considered for non-polar rubber blend nanocomposites B100H0CB50NC5, as mentioned in equation 2. The weight fraction (ΦP) of the polar rubber (CO) in the rubber blend for B90H10CB50NC5 and B80H20CB50NC5 is 0.1 and 0.2 respectively. The relative gas permeability (RGP) is theoretically determined using Bharadwaj equation [12] as follows,

(6)RGP=PC/PP=1-Φ/1+(αΦ2S+1

Where PC and PP represent the gas permeability of nanocomposite and neat polymer respectively, Φ is the volume fraction of nanoclay, α is the aspect ratio, and S is the order parameter. The theoretical prediction of the relative water vapor transmissibility is compared against the experimental data. The relative water vapor transmissibility values have been tabulated in Table 1, and the comparison between theoretical values and experimental data is shown in Figure 5. The theoretical calculations are done by employing the equations (4), (5), and (6). Experimental values are determined directly from the permeability tester.

Figure 5 Comparison of theoretical relative water vapor transmissibility against the experimental data of the samples.
Figure 5

Comparison of theoretical relative water vapor transmissibility against the experimental data of the samples.

From the Figure 5, it is noticed that the theoretical values fit close with the experimental data for the rubber blend nanocomposites with the polar constituent. The relative water vapor transmissibility of the nanocomposites increases as the polar constituent increases. It signifies the impact of the polar fraction on water vapor transmissibility in the rubber blend nanocomposites.

4.3 Surface hydrophilicity analysis

The surface hydrophilicity of the samples is analyzed using contact angle measurements and is shown in Figure 6. The water droplet is used to determine the hydrophilicity or hydrophobicity of a surface. The surface is said to be hydrophilic if interaction force between water and surface is greater than that of the cohesive force associated with water droplet [16]. The surface is hydrophilic if the contact angle is below 90° and hydrophobic if it is above 90°.

Figure 6 Surface hydrophilicity of the samples using contact angle measurement.
Figure 6

Surface hydrophilicity of the samples using contact angle measurement.

It is noticed that B100H0CB50NC0 composite tends to be hydrophobic, and all nanocomposites exhibit surface hydrophilicity. B100H0CB50NC5 nanocomposite displays a marginal hydrophilic nature due to the presence of the nanoclay. The contact angles for all other samples remain well below 90°. The surface tends to be more hydrophilic with an increase in the polar nature of the rubber. It invokes that the water molecules are potentially imbibed towards the polar chain of the rubber.

5 Conclusions

The nanocomposites are prepared using melt compounding techniques. TEM photomicrograph confirms well-dispersed nanoclay within the blend matrix and the formation of hybrid nanostructures in the nanocomposites. The development of hybrid nanostructures considerably increases the barrier properties of the rubber nanocomposites. A successful attempt has been made to predict the water vapor transmissibility in a rubber nanocomposite using a schematic model. The relative water vapor transmissibility, derived theoretically, is compared and found to fit the experimental data. Thus, it signifies the dependency of the water vapor transmission characteristics on the polar fraction of the composites in addition to the tortuous permeation offered by the nanoclay platelets. Surface hydrophilicity of the nanocomposites confirms the same.

Acknowledgements

The authors acknowledge gratefully the management of CEAT LIMITED, Vadodara for funding this work. Special thanks to Mr.C.Cable (Zeon Chemicals, USA) for supplying free samples of CO rubber and Zisnet F-PT chemicals in this work.

  1. Conflict of interest: Authors state no conflict of interest.

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Received: 2017-08-31
Accepted: 2018-05-07
Published Online: 2018-12-04

© 2018 Kumar Sankaran et al., published by De Gruyter

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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  67. DMFDMA catalyzed synthesis of 2-((Dimethylamino)methylene)-3,4-dihydro-9-arylacridin-1(2H)-ones and their derivatives: in-vitro antifungal, antibacterial and antioxidant evaluations
  68. Production of Methanol as a Fuel Energy from CO2 Present in Polluted Seawater - A Photocatalytic Outlook
  69. Study of different extraction methods on finger print and fatty acid of raw beef fat using fourier transform infrared and gas chromatography-mass spectrometry
  70. Determination of trace fluoroquinolones in water solutions and in medicinal preparations by conventional and synchronous fluorescence spectrometry
  71. Extraction and determination of flavonoids in Carthamus tinctorius
  72. Therapeutic Application of Zinc and Vanadium Complexes against Diabetes Mellitus a Coronary Disease: A review
  73. Study of calcined eggshell as potential catalyst for biodiesel formation using used cooking oil
  74. Manganese oxalates - structure-based Insights
  75. Topological Indices of H-Naphtalenic Nanosheet
  76. Long-Term Dissolution of Glass Fibers in Water Described by Dissolving Cylinder Zero-Order Kinetic Model: Mass Loss and Radius Reduction
  77. Topological study of the para-line graphs of certain pentacene via topological indices
  78. A brief insight into the prediction of water vapor transmissibility in highly impermeable hybrid nanocomposites based on bromobutyl/epichlorohydrin rubber blends
  79. Comparative sulfite assay by voltammetry using Pt electrodes, photometry and titrimetry: Application to cider, vinegar and sugar analysis
  80. MicroRNA delivery mediated by PEGylated polyethylenimine for prostate cancer therapy
  81. Reversible Fluorescent Turn-on Sensors for Fe3+ based on a Receptor Composed of Tri-oxygen Atoms of Amide Groups in Water
  82. Sonocatalytic degradation of methyl orange in aqueous solution using Fe-doped TiO2 nanoparticles under mechanical agitation
  83. Hydrotalcite Anchored Ruthenium Catalyst for CO2 Hydrogenation Reaction
  84. Production and Analysis of Recycled Ammonium Perrhenate from CMSX-4 superalloys
  85. Topical Issue on Agriculture
  86. New phosphorus biofertilizers from renewable raw materials in the aspect of cadmium and lead contents in soil and plants
  87. Survey of content of cadmium, calcium, chromium, copper, iron, lead, magnesium, manganese, mercury, sodium and zinc in chamomile and green tea leaves by electrothermal or flame atomizer atomic absorption spectrometry
  88. Biogas digestate – benefits and risks for soil fertility and crop quality – an evaluation of grain maize response
  89. A numerical analysis of heat transfer in a cross-current heat exchanger with controlled and newly designed air flows
  90. Freshwater green macroalgae as a biosorbent of Cr(III) ions
  91. The main influencing factors of soil mechanical characteristics of the gravity erosion environment in the dry-hot valley of Jinsha river
  92. Free amino acids in Viola tricolor in relation to different habitat conditions
  93. The influence of filler amount on selected properties of new experimental resin dental composite
  94. Effect of poultry wastewater irrigation on nitrogen, phosphorus and carbon contents in farmland soil
  95. Response of spring wheat to NPK and S fertilization. The content and uptake of macronutrients and the value of ionic ratios
  96. The Effect of Macroalgal Extracts and Near Infrared Radiation on Germination of Soybean Seedlings: Preliminary Research Results
  97. Content of Zn, Cd and Pb in purple moor-grass in soils heavily contaminated with heavy metals around a zinc and lead ore tailing landfill
  98. Topical Issue on Research for Natural Bioactive Products
  99. Synthesis of (±)-3,4-dimethoxybenzyl-4-methyloctanoate as a novel internal standard for capsinoid determination by HPLC-ESI-MS/MS(QTOF)
  100. Repellent activity of monoterpenoid esters with neurotransmitter amino acids against yellow fever mosquito, Aedes aegypti
  101. Effect of Flammulina velutipes (golden needle mushroom, eno-kitake) polysaccharides on constipation
  102. Bioassay-directed fractionation of a blood coagulation factor Xa inhibitor, betulinic acid from Lycopus lucidus
  103. Antifungal and repellent activities of the essential oils from three aromatic herbs from western Himalaya
  104. Chemical composition and microbiological evaluation of essential oil from Hyssopus officinalis L. with white and pink flowers
  105. Bioassay-guided isolation and identification of Aedes aegypti larvicidal and biting deterrent compounds from Veratrum lobelianum
  106. α-Terpineol, a natural monoterpene: A review of its biological properties
  107. Utility of essential oils for development of host-based lures for Xyleborus glabratus (Coleoptera: Curculionidae: Scolytinae), vector of laurel wilt
  108. Phenolic composition and antioxidant potential of different organs of Kazakh Crataegus almaatensis Pojark: A comparison with the European Crataegus oxyacantha L. flowers
  109. Isolation of eudesmane type sesquiterpene ketone from Prangos heyniae H.Duman & M.F.Watson essential oil and mosquitocidal activity of the essential oils
  110. Comparative analysis of the polyphenols profiles and the antioxidant and cytotoxicity properties of various blue honeysuckle varieties
  111. Special Issue on ICCESEN 2017
  112. Modelling world energy security data from multinomial distribution by generalized linear model under different cumulative link functions
  113. Pine Cone and Boron Compounds Effect as Reinforcement on Mechanical and Flammability Properties of Polyester Composites
  114. Artificial Neural Network Modelling for Prediction of SNR Effected by Probe Properties on Ultrasonic Inspection of Austenitic Stainless Steel Weldments
  115. Calculation and 3D analyses of ERR in the band crack front contained in a rectangular plate made of multilayered material
  116. Improvement of fuel properties of biodiesel with bioadditive ethyl levulinate
  117. Properties of AlSi9Cu3 metal matrix micro and nano composites produced via stir casting
  118. Investigation of Antibacterial Properties of Ag Doped TiO2 Nanofibers Prepared by Electrospinning Process
  119. Modeling of Total Phenolic contents in Various Tea samples by Experimental Design Methods
  120. Nickel doping effect on the structural and optical properties of indium sulfide thin films by SILAR
  121. The effect mechanism of Ginnalin A as a homeopathic agent on various cancer cell lines
  122. Excitation functions of proton induced reactions of some radioisotopes used in medicine
  123. Oxide ionic conductivity and microstructures of Pr and Sm co-doped CeO2-based systems
  124. Rapid Synthesis of Metallic Reinforced in Situ Intermetallic Composites in Ti-Al-Nb System via Resistive Sintering
  125. Oxidation Behavior of NiCr/YSZ Thermal Barrier Coatings (TBCs)
  126. Clustering Analysis of Normal Strength Concretes Produced with Different Aggregate Types
  127. Magnetic Nano-Sized Solid Acid Catalyst Bearing Sulfonic Acid Groups for Biodiesel Synthesis
  128. The biological activities of Arabis alpina L. subsp. brevifolia (DC.) Cullen against food pathogens
  129. Humidity properties of Schiff base polymers
  130. Free Vibration Analysis of Fiber Metal Laminated Straight Beam
  131. Comparative study of in vitro antioxidant, acetylcholinesterase and butyrylcholinesterase activity of alfalfa (Medicago sativa L.) collected during different growth stages
  132. Isothermal Oxidation Behavior of Gadolinium Zirconate (Gd2Zr2O7) Thermal Barrier Coatings (TBCs) produced by Electron Beam Physical Vapor Deposition (EB-PVD) technique
  133. Optimization of Adsorption Parameters for Ultra-Fine Calcite Using a Box-Behnken Experimental Design
  134. The Microstructural Investigation of Vermiculite-Infiltrated Electron Beam Physical Vapor Deposition Thermal Barrier Coatings
  135. Modelling Porosity Permeability of Ceramic Tiles using Fuzzy Taguchi Method
  136. Experimental and theoretical study of a novel naphthoquinone Schiff base
  137. Physicochemical properties of heat treated sille stone for ceramic industry
  138. Sand Dune Characterization for Preparing Metallurgical Grade Silicon
  139. Catalytic Applications of Large Pore Sulfonic Acid-Functionalized SBA-15 Mesoporous Silica for Esterification
  140. One-photon Absorption Characterizations, Dipole Polarizabilities and Second Hyperpolarizabilities of Chlorophyll a and Crocin
  141. The Optical and Crystallite Characterization of Bilayer TiO2 Films Coated on Different ITO layers
  142. Topical Issue on Bond Activation
  143. Metal-mediated reactions towards the synthesis of a novel deaminolysed bisurea, dicarbamolyamine
  144. The structure of ortho-(trifluoromethyl)phenol in comparison to its homologues – A combined experimental and theoretical study
  145. Heterogeneous catalysis with encapsulated haem and other synthetic porphyrins: Harnessing the power of porphyrins for oxidation reactions
  146. Recent Advances on Mechanistic Studies on C–H Activation Catalyzed by Base Metals
  147. Reactions of the organoplatinum complex [Pt(cod) (neoSi)Cl] (neoSi = trimethylsilylmethyl) with the non-coordinating anions SbF6– and BPh4
  148. Erratum
  149. Investigation on Two Compounds of O, O’-dithiophosphate Derivatives as Corrosion Inhibitors for Q235 Steel in Hydrochloric Acid Solution
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