Webometric analysis of Iranian universities of medical sciences

Introduction  There are many researches have been conducted on webometrics, especially the impacts of websites on each other and the web impact factor. However, there are few studies focusing on the websites of Iranian universities. This study analyzed the websites of Iranian universities of medical sciences according to the webometric indicators. Method and materials  In a cross-sectional study, the number of web pages, inlinks, external inlinks and also the overall and absolute web impact factors for Iranian universities of medical sciences with active exclusive websites were calculated and compared using AltaVista search engine. Finally, the websites were ranked based on these webometric indicators. Results  The results showed that the website of Tehran university of medical sciences with 49,300 web pages and 9860 inlinks was ranked first for the size and number of inlinks, while its impact factor was ranked 38th. Rafsanjan UMS with 15 web pages and 211 links had the highest rank for the web impact factor among Iranian universities of medical sciences. Discussions and conclusions  The study revealed that Iranian universities of medical sciences did not have much impact on the web and were not well known internationally. The major reason relies on linguistic barriers. Some of them also suffer from technical problems in their web design.     

Thermal,mechanical, and structural properties of zno/polyethylene membranes made by thermally induced phase separation method

In this study, ZnO/polyethylene membranes were fabricated via thermally induced phase separation method. A set of tests including FE‐SEM, EDX, XRD, DSC, TGA, DMA, mechanical test, and pure water flux (PWF) for characterization of membranes were carried out. The results of EDX, XRD, and TGA analyses confirmed the presence of ZnO nanoparticles in the polymer matrix. The results of DSC analysis revealed that the melting point as well as the crystallinity of the membranes increased slightly with increasing ZnO content. However, glass transition temperature of the membranes was not affected by presence of the particles. Addition of nanoparticles also increased storage modulus, loss modulus. and tensile at break of the membranes due to the stiffness improvement effect of inorganic ZnO. Finally, it was observed that incorporation of the nanoparticles improved PWF of the membranes, whereas humic acid rejection decreased due to the increase in mean pore radius of membranes. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42338.     

Nafion/bio-functionalized montmorillonite nanohybrids as novel polyelectrolyte membranes for direct methanol fuel cells

Polyelectrolyte membranes based on Nafion^® and bio-functionalized montmorillonite (BMMT) with chitosan biopolymer, as polycationic intercalant were fabricated by solvent casting method. X-ray diffraction analysis confirmed the exfoliated structure of clay. Methanol permeability results revealed that the presence of 10 wt% BMMT in synthesized nanohybrid membranes can reduce the permeability to 5.72 × 10⁻⁸ cm² s⁻¹ in comparison with 2.00 × 10⁻⁶ for that of Nafion^® 117. However proton conductivity of nanohybrids was decreasing with increasing BMMT loading, but obtained values were indicating the lower sacrificing of conductivity in comparison with membranes based on unmodified MMT. According to selectivity parameter, membranes containing 2 wt% of BMMT showed optimum properties. It was suggested that improvement of transportation properties could be due to the electrostatic interaction between amino groups of chitosan and Nafion^® sulfone groups. Considering the suitable thermal stability, low methanol crossover and appropriate proton conductivity properties, Nafion^®/BMMT nanohybrid membranes, could be proposed as novel polyelectrolytes for direct methanol fuel cell application.     

Polyampholyte Polymers-Based Sensors: A Review on Stimuli and Applications

Polyampholytes are a specific type of zwitterionic materials composed of monomers with both positive and negative charges. These materials can be synthesized through various methods, such as free radical, anionic, or cationic polymerization, or by modifying existing polymers through postpolymerization processes. Polyampholytes possess unique properties that make them attractive for a wide range of applications, particularly in sensor technology. They can undergo conformational changes in response to external stimuli like pH variations, temperature fluctuations, or changes in salt concentration. These properties have led to their application in biosensors, salt and ion sensors, pH sensors, fluorescence-based sensors, strain sensors, and thermosensitive sensors. It is worth noting that in some cases polyampholytes can respond to multiple stimuli simultaneously. Overall, polyampholytes are drawing great attention for their excellent mechanical properties including self-healing, high toughness, and fatigue resistance. Thus, this review is focused on advances that are made to develop polyampholyte polymer-based sensors in different applications.     

Undesirable effects of heating on hydrogels

Heating is the most conventional drying method for removing water from as‐synthesized hydrogels in laboratory and industry. In this article, the effects of the heating temperature (60–200°C) and time (10 min–24 h) on swelling properties of highly absorbent hydrogels based on 2‐acrylamido‐2‐methylpropane sulfonic acid (AMPS), acrylic acid (AA), potassium acrylate (KA), and acrylamide (AM) were studied. Crosslinkers methylene bisacrylamide (MBA) and poly(ethyleneglycol) dimethacrylate (PEGDMA) were used in the syntheses. Depending on the hydrogel structural composition and its drying temperature and time, the swelling capacities were extremely changed. Generally, AA‐, KA‐, and AM‐based hydrogels showed more hydrolytic‐thermal stability than the corresponding AMPS‐based hydrogels. MBA‐crosslinked hydrogels generally exhibited higher vulnerability against heating. Swelling of PEGDMA‐crosslinked poly(AM‐KA‐AA) hydrogel was greatly increased after heating, whereas its analogousAM‐free sample exhibited huge loss of swelling. PEGDMA‐crosslinked poly(AMPS) samples also exhibited swelling reduction after drying. Rheological studies showed that the storage modulus was highly reduced (～ 5200 Pa) after heating of MBA‐crosslinked poly(AMPS) hydrogels, which reconfirmed the crosslink cleavage. Mechanistic discussions were proposed for the thermal‐induced swelling changes. It was concluded that the chemical nature of both crosslinker and monomer must be taken into consideration to choose the temperature and time of the hydrogel drying. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Residual monomer in superabsorbent polymers: Effects of the initiating system

Minimized residual monomer is an essential requirement particularly in hygienic, pharmaceutical, and food packaging polymer products such as superabsorbent polymers (SAPs). The present article is the first non‐patent report on the study of a highly effective polymerization variable (e.g. initiator) on the residual monomer of SAPs based on partially neutralized acrylic acid. Two persulfate systems, i.e. ammonium persulfate (APS)/sodium metabisulfite (SMBS) and APS/tetramethyl ethylenediamine (TMEDA), were examined to initiate the free‐radical polymerization at room temperature. It was shown that chromatographically measured residual monomer and swelling capacity was strongly dependent on the type and concentration of the initiator. A kinetic model was also derived to describe the experimental results. Dissociation rate of initiation system was recognized to be a key factor to obtain a SAP with low residual monomer. It was found that, in aqueous solution polymerization, the effect of a slowly dissociating system such as APS/TMEDA on decreasing the residual monomer was much higher than that of a rapidly dissociating system like APS/SMBS. Under selected conditions, residual monomer could be reduced up to 5327 ± 138 and 1715 ± 44 ppm for APS/SMBS and APS/TMEDA initiating systems, respectively. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Antipolyelectrolyte superabsorbing nanocomposites: Synthesis and properties

Novel polyampholytic superabsorbing nanocomposites based on the zwitterionic sulfobetaine monomer [3‐(methacrylamido)propyl)]dimethyl(3‐sulfopropyl)ammonium hydroxide were synthesized through in situ polymerization in aqueous solution with different contents of an organo‐modified clay (OMMT, Cloisite 30B). Structural and thermomechanical properties of hydrogels were characterized by FT‐IR, XRD, and DMTA, respectively. Swollen gel strength of hydrogels was determined by a rheological method. Storage modulus of the hydrogels was considerably improved in comparison with its the clay‐free counterpart. The nanocomposite hydrogel containing 15% OMMT possessed the highest gel strength. The glass transition temperature was increased from 58.4 to 67.0°C for the clay‐free and nanocomposite hydrogel containing 8% OMMT, respectively. The swelling behavior of the hydrogel in various salt solutions was investigated. Antipolyelectrolyte behavior was observed with enhancement of concentration of mono‐ and multivalent salts. Swelling in the various pH media was nearly pH‐independent over a wide range of pH. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Chitosan modified MMT‐poly(AMPS) nanocomposite hydrogel: Heating effect on swelling and rheological behavior

Vulnerability of hydrogels against thermal circumstances may be substantially eliminated via incorporating nanoclay to prepare nanocomposite hydrogels. In this research, chitosan‐intercalated montmorillonite (ChitoMMT) was used as a bionanoclay to yield novel nanocomposite hydrogels based on 2‐acrylamido‐2‐methylpropanesulfonic acid. The bionanoclay is suitable especially for preparing biomaterials used in biomedical, food, and pharmaceutical applications, unlike conventional commercial nanoclays (alkyl ammonium‐intercalated MMT) which are not appropriate for bio‐applications due to toxicity of the intercalant particularly where the clay content is high. Two different crosslinkers (i.e., methylene bisacrylamide, and polyethyleneglycol dimethacrylate) were employed to synthesize the nanocomposites. The variations in swelling, rheological and thermal properties of the hydrogels were essentially attributed to thermally induced crosslink cleavage/formation depending upon the crosslinker nature. The nanocomposites comprised superior thermal properties in comparison with the clay‐free hydrogel counterpart. They can preserve substantially their swelling ability for longer heating periods. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Solvent-, ion- and pH-specific swelling of poly(2-acrylamido-2-methylpropane sulfonic acid) superabsorbing gels

Homopolymer hydrogel of 2-acrylamido-2-methylpropane sulfonic acid (AMPS) and its nanocomposite counterpart were prepared to study their swelling properties. The hydrogels showed ability to absorb and retain electrolytes as well as binary mixtures of water and organic solvents (i.e., methanol, ethanol, acetone, ethylene glycol (EG), polyethylene glycol, N-methyl-2-pyrrolidone (NMP), and dimethylsulfoxide (DMSO). The nanocomposite gel exhibited lower swelling in all solvent compositions in comparison with non-composite gel. Unlike conventional acrylic acid-based hydrogels, the poly(AMPS) gels showed superabsorbing capacity in pure ethanol, methanol, EG, DMSO and NMP. Meanwhile, swelling capacity of poly(AMPS) hydrogel in DMSO-water mixtures was surprisingly found to be even higher than that in water. This extraordinary superswelling behavior was explained based on the interactions involved in solvation as well as the solubility parameters. The gels showed pH-independent superabsorbency in a wide range of pH (3–11). Saline-induced swelling transitions were also investigated and the ionic interactions were confirmed by FTIR spectroscopy.