Correspondence between colour and odour for women in pre‐menopause and post‐menopause

Cross‐modal correspondences in the human sensory systems often appear for different levels of sensory inputs, such as colour and odour. However, whether there is hormonal modification of such colour‐odour correspondence has remained unclear. Here, we experimentally investigated the influence of hormonal changes in menopausal women by conducting evaluations of colour and odour impressions, matching tasks between colour and odour, and odor identification tasks, comparing two groups of women: premenopausal and postmenopausal. The results showed that both premenopausal and postmenopausal women had similar impressions and images of colours for odors, while postmenopausal women had significantly lower abilities of odor identification than premenopausal women. This suggested that the degree of conviction about an odor's identification might slightly affect the subjects’ impressions of odors and their corresponding colour choices. Menopause might not directly affect cognitive aspects regarding colour or odor, but might instead affect their perceptions.     

Fire performance and post‐fire mechanical properties of polymer composites coated with hybrid carbon nanofiber paper

In this study, glass fiber reinforced polyester composites were coated with carbon nanofiber/clay/ammonium polyphosphate (CCA) paper and carbon nanofiber/exfoliated graphite nanoplatelets/ammonium polyphosphate (CXA) paper. The composites were exposed to a heat flux of 35 kW/m² during the cone calorimeter testing. The testing results showed a significant reduction in both heat release rates and mass loss rates. The peak heat release rate (PHRR) of CCA and CXA composite samples in the major decomposition period are 23 and 34% lower than the control sample, respectively. The time to reach the PHRR for the CCA and CXA composite samples are ～ 125% longer than the control sample. After the composite samples were exposed to heat for different time periods, their post‐fire mechanical properties were determined by three‐point bending testing. The three‐point bending testing results show that the composite samples coated with such hybrid papers exhibit more than 20% improvement in mechanical resistance at early stages of combustion. The mechanism of hybrid carbon nanofiber paper protecting the underlying laminated composites is discussed. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Influence of alcohol pre‐infusion on the quality of VARTM composites

In the vacuum assisted resin transfer molding (VARTM) process, part‐to‐part variations such as the uncertainty in the permeability and race tracking phenomenon make it difficult to achieve consistent mold filling and ensure part quality of composites. Alcohol pre‐infusion was presented in this study as a novel real‐time monitoring and control approach for the flow process in the VARTM process, alcohol test fluid is infused before the actual resin infusion to locate the potential dry spots without using the large quantity of sensors. Then corresponding process control strategy is designed, such as opening the auxiliary gate at specific moment on those predicted dry spot locations to compensate flow defects. Moreover, alcohol can be easily removed by heat without changing the local permeability. The influence of alcohol pre‐infusion on the quality of VARTM composites were investigated in this study. The mechanical tests were conducted to verify that the alcohol pre‐infusion approach has no significant effect on composite properties because alcohol can be removed from fiber by heat and air flow. Specifically, DMA, TGA, and FTIR spectrum proved that negligible difference existed on the resin–fiber interface between the composites with or without alcohol pre‐infusion. Finally, the microscopy results revealed a similar failure path in a resin matrix. TMA results also demonstrated similar dimension stability. This alcohol pre‐infusion approach was effective when compared with computer simulation and could eliminate the occurrence of dry spots and voids without using sensors or data‐acquisition system. The control schemes were shown in a case study to be capable of compensating the flow defects and achieving desired fill patterns in the face of permeability uncertainty. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Green composites of organic materials and recycled post‐consumer polyethylene

Addition of organic fillers to post‐consumer recycled plastics can give rise to several advantages. First of all, the cost of these fillers is usually very low, the organic fillers are biodegradable contributing to an improved environmental impact and, last but not least, some mechanical and thermomechanical properties can be enhanced. Organic fillers are not widely used in the plastic industry although their use is increasing. Bad dispersion into the polymer matrix at high‐level content and poor adhesion with the matrix are the more important obstacles to this approach. In this work various organic fillers have been used with a post‐consumer plastic material originating from films for greenhouses. The properties of these green composites have been compared with those of materials filled with a conventional inorganic filler. The organic fillers cause slightly worse processability, due to an increase of viscosity, an enhancement of the rigidity and of the thermomechanical resistance similar to that measured for the inorganic filler, while a reduction of the impact strength is observed. Copyright © 2004 Society of Chemical Industry     

Development of semitransparent wood‐polymer composites

A new material has been developed consisting of pieces of wood embedded within a matrix of acrylic polymer, resulting in a transparent or semitransparent wood‐based product. This material presents quite appealing aesthetic features, thereby opening new possibilities for decorative applications. Because acrylic and methacrylic monomers are in the liquid state at room temperature, it is possible to introduce wood (in the current case, walnut wood) into a mixture of acrylic (hydroxypropyl acrylate) and/or methacrylic monomers (methyl methacrylate and 2‐hydroxyethyl methacrylate) along with a plasticizer (dioctyl phthalate) in the presence of a chemical initiator (benzoyl peroxide). A transparent polymeric matrix with dispersed wood is then obtained through bulk free‐radical polymerization. Introducing this reaction mixture along with pieces of wood into a mold results in a wood‐polymer composite. A 2^4?1 experimental fractional factorial design was implemented to study the importance of the composition of these materials on several relevant properties. The sheets produced were characterized by tensile testing, dynamic mechanical thermal analysis, thermal gravimetric analysis, and heat deflection temperature. The models obtained for predicting each property pointed to valuable insights regarding the influential constituents. In particular, our results suggested that monomers to be used in future applications of this material should be selected in terms of their cost and the desired flexibility for the final product, not in terms of their polarity. J. VINYL ADDIT. TECHNOL., 2012. © 2012 Society of Plastics Engineers     

An improved pull‐out model for the carbon nanotube/nanofiber‐reinforced polymer composites with interfacial defects

The procedure of pulling a carbon nanotube/nanofiber (CNT/CNF) with interfacial defect out from a polymer matrix is studied in this article. By ignoring the fiber–matrix interaction and the stress concentration in the zone of interfacial defect, an analytical model is proposed to describe the pull‐out behavior of the CNT/CNF. The accuracy and rationality of the model is validated by comparing to the pull‐out experiment and the finite element simulation. The results from the parametric study indicate that the geometric parameters of the interfacial defect have pronounced influences on the pull‐out behavior of the CNT/CNF. The influence of the defect on the strength and toughness of the composites is discussed in detail. POLYM. COMPOS., 229–240, 2016. © 2014 Society of Plastics Engineers     

Non‐isothermal crystallization kinetics of cork‐polymer composites for injection molding

The non‐isothermal crystallization behavior of cork–polymer composites (CPC) based on polypropylene (PP) matrix was studied. Using differential scanning calorimetry (DSC), the crystallization behavior of CPC with 15 wt % cork powder at different cooling rates (5, 10, 15, and 20 °C/min) was studied. The effect of a coupling agent based on maleic anhydride was also analyzed. A composite (PPg) containing polypropylene grafted maleic anhydride (PPgMA) and PP was prepared for comparison purposes. Crystallization kinetic behavior was studied by Avrami, Ozawa, Liu, and Kissinger methods. The Ozawa method fails to describe the behavior of these composites. Results show that cork powder surface acts as a nucleating agent during non‐isothermal crystallization, while the addition of PPgMA decreases the crystallization rate. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44124.     

Photofabrication of biofiber‐based polymer matrix composites

The novel development of a photofabrication process of biofiber composites, based on oil palm empty fruit bunch fibers, is reported. The process consists of the following steps: (1) the preparation by a wet process of nonwoven mat of biofiber, either alone or in combination with glass and nylon; (2) drying the mat; (3) preparation of photocurable resin matrix, consisting of vinyl ester and photoinitiator; (4) impregnation of the mat by photocurable resin; and (5) irradiation of the impregnated mat by UV radiation to effect the cure of the composite. The nonwoven mat was formed in a “headbox” into which was poured a slurry of fibers. A wet mat was formed by after dewatering of the slurry. Biofiber, glass, and nylon fibers were mixed in different proportions. A “mixture experimental design” was used to generate experimental compositions of the reinforcing fibers and to model dependency of the response variables on the components through mathematical relationships. These relationships were meant to (1) determine the effect of composition of the reinforcing fibers on the physical and mechanical properties, (2) predict the response for any unknown composition of fibers, and (3) determine the optimum values of any identified properties. Because the product was characterized by multiple responses, simultaneous maximization of all properties was not feasible. The product must be considered in the definition of the trade‐off or compromise of properties to obtain overall satisfactory performance. Such an optimization was carried out and the results are reported. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 95: 1493–1499, 2005     

Influence of polymer microstructure on the performance of post‐treated latex‐based pressure sensitive adhesives

Latex‐based butyl acrylate (BA)/acrylic acid (AA)/2‐hydroxyethyl methacrylate (HEMA) pressure sensitive adhesive (PSA) films with various microstructures were heated to improve their performance. The treated PSA films showed significantly better performance than original latex‐based PSA films with similar polymer microstructures. The effect of the heat treatment depended on the polymer microstructure of the untreated PSA films (or corresponding latices). Decreasing the amount of very small sol polymers (i.e., M_x < 2M_e) in gel‐free untreated PSA films, or both very small (i.e., M_x < 2M_e) and very large sol polymers (i.e., M_x > 20M_e) in gel‐containing untreated PSA films led to treated PSA films with significantly better performance. (Note: M_e is the molecular weight between two adjacent entanglement points in a polymer material.) In addition, simultaneously increasing the sol polymer molecular weight (M_w) as well as the size of the chain segments between two adjacent cross‐linking points (M_c) of the gel polymer in the original PSAs resulted in treated PSA films with better performance. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Fabrication and applications of cellulose nanoparticle‐based polymer composites

The impressive mechanical properties, reinforcing capability, abundance, low weight, low filler load requirements, and biodegradable nature of nanoparticles from bioresources such as cellulose, make it an ideal candidate for the development of green polymer nanocomposites. Significant amount of research in this area is primarily focused on the extraction, qualitative surface modification, and evaluation of mechanical performance after filling in polymer matrixes at different ratios. The extreme agglomeration tendency, hydrophilic nature, difficult dispersion in many organic solvents of cellulose nanoparticles are the challenging obstacles when fabrication of such nanocomposites is concerned. Traditional processing of polymer composites mainly through extrusion and melt compounding, is not easily possible in case of cellulose nanocomposites due to higher possibility of poor dispersion and degradation of nanofibers. Therefore, issues related to the fabrication of nanofiber‐based products and their application appears to be one of the most important areas in order to enhance their competitiveness with other nanoparticles. This review is aimed to summarize the recent accomplishments and issues involving the use of cellulose nanoparticles in the development of new polymeric materials. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Preparation and characterization of polyamide‐leather wastes polymer composites

Chrome tanning of leather improves its appearance, but at the same time, it emits both solid and liquid wastes. These solid wastes mainly after shaving process present in large amount causing hazard to the environment. Leather wastes were disintegrated to prepare hide powder and mixed with polyamide (nylon 6) in different ratios. The physical, mechanical and thermal properties of different composites were investigated, which showed enhancement in physical characters but decreasing in mechanical properties. The charred residue increases by increasing the presence of leather waste filler. Morphological studies were performed on the fractured surface of composites showed uniform and fine particles dispersion. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Optimization of thermoelectric properties of metal‐oxide‐based polymer composites

Thermoelectric modules can be used for thermal energy harvesting. Common rigid thermoelectric stacks usually contain heavy metal alloys such as Bi₂Te₃. In order to substitute conventional materials and to reduce manufacturing costs, nontoxic, inexpensive and abundant materials using low‐cost processes are first choice. This study deals with polymer composites consisting of a polysiloxane matrix filled with thermoelectric Sn_0.85Sb_0.15O₂ particles in micrometer scale. Thin composite sheets have been prepared by doctor blade technique and the Seebeck coefficient, the electrical and thermal conductivity, and the porosity were measured. Platelet‐type particles, consisting of Sn_0.85Sb_0.15O₂‐coated insulating mica substrate and globular Sn_0.85Sb_0.15O₂ particles have been varied in size, coating thickness and were mixed with each other in different ratios. The filler content was varied in order to maximize the figure of merit, ZT, to 1.9 × 10^?5 ± 4 × 10^?6. Owing to their low raw material costs and the high degree of design freedom of polymer composites, one may use these materials in thermoelectric generators for remote low‐power demanding applications. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 40038.     

Conducting polymer composites of zinc‐filled nylon 6

The present work is concerned with the effect of processing variables and filler concentration on the electrical conductivity, hardness, and density of composite materials prepared by compression molding of a mixture of zinc powder and nylon 6 powder. The electrical conductivity of the composites is <10^?12 S/cm, unless the metal content reaches the percolation threshold at a volume fraction of about 0.18, beyond which the conductivity increases markedly by as much as 10 orders of magnitude. The density of the composites was measured and compared with values calculated by assuming different void levels within the samples. Furthermore, it is shown that the hardness increases with the increase of metal concentration, but for values of filler volume fraction higher than about 0.30 the hardness of samples remains almost constant. Two parameters of molding process, temperature and time, were shown to have a notable effect on the conductivity of composites, whereas pressure has no influence on this property in the pressure range considered. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 1449–1454, 2001     

Load bearing properties of three‐component polymer composites

Metal or solid polymer anchors are used as the load transfer components for foam and foam composites when they are used as the structural elements in design. The traditional method of fixation of these components is by fastening and adhesion. In this study, anchors were created in the form of inserts and were imbedded in the sandwich composite during the foaming process, resulting in the manufacture of three‐component composite. Flexure tests were conducted to study the effect of different geometries (rectangular, cylindrical, tapered/wedge shaped) and lengths of metal inserts on the strengths of sandwich composites. The stress strain response, mode of fracture of sandwich composite with metallic anchors was elucidated. The results showed that long tapered inserts imbedded in sandwich composite provide better load bearing and adhesion properties than other geometries. A model is presented that describes the relationship between stiffness reduction and progressive crack length of sandwich composite. Finite element analysis (FEA) of the interactions between the inserts and sandwich composites under different loads were carried out. FEA modeling and experimental results were in good agreement, thus validating the model. POLYM. COMPOS., 31:1731–1737, 2010. © 2010 Society of Plastics Engineers.     

Insert injection molding of high‐density polyethylene single‐polymer composites

A process for making high‐density polyethylene (HDPE) single‐polymer composites (SPCs) by insert injection molding was investigated. HDPE SPCs with relatively good tensile and interfacial properties were prepared within a short cycle time within a temperature range of 40°C. Melt‐spun HDPE fibers were made from the same resin as the matrix. The fibers were heat treated in silicone oil, with and without tension, to study the changes of fiber properties upon exposure to high temperature. HDPE SPCs containing about 30 wt% lab‐made HDPE fabric achieved a tensile strength of 50 MPa, 2.8 times that of neat HDPE. The peel strength of HDPE SPCs increased with increasing injection temperature and achieved a maximum value of 16.7 N/cm. Optical micrographs of polished transverse cross‐sections of the SPC samples showed that higher injection temperature is beneficial to the wetting and permeation properties of the matrix. Scanning electronic microscope photographs suggested good bonding and compatibility between the fibers and the matrix. POLYM. ENG. SCI., 55:2448–2456, 2015. © 2015 Society of Plastics Engineers     

Electrical conductivity modeling of carbon‐filled liquid‐crystalline polymer composites

Electrically conductive resins are needed for bipolar plates used in fuel cells. Currently, the materials for these bipolar plates often contain a single type of graphite powder in a thermosetting resin. In this study, various amounts of two different types of carbon, carbon black and synthetic graphite, were added to a thermoplastic matrix. The resulting single‐filler composites were tested for electrical conductivity, and electrical conductivity models were developed. Two different models, the Mamunya and additive electrical conductivity models, were used for both material systems. It was determined how to modify these models to reduce the number of adjustable parameters. The models agreed very well with experimental data covering a large range of filler volume fractions (from 0 to 12 vol % for the carbon black filled composites and from 0 to 65 vol % for the synthetic graphite filled composites) and electrical conductivities (from 4.6 × 10^?17 S/cm for the pure polymer to 0.5 S/cm for the carbon black filled composites and to 12 S/cm for the synthetic graphite filled composites). © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3293–3300, 2006     

Application of homogenization method on the evaluation and analysis of the effective stiffness for noncontinuous carbon nanotube/polymer composites

The effective stiffness of noncontinuous carbon nano‐tubes (CNTs)/polymer composites are predicted by the homogenization method with exact periodic boundary conditions. Numerical calculations for regular and staggered array models are performed by the macro–microscopic finite element methods. The results are compared with those from Mori–Tanaka and Halpin–Tsai theories, which show that the stiffness of CNTs composites are not only related to aspect ratio and CNTs volume fraction as described in the earlier theories, but also sensitive to the space between CNTs ends, the distribution of CNTs within the selected representative volume element, and the geometrical shape of CNTs. The results from the two empirical approaches are included in the present results with special spacing ratios of horizontal and vertical fiber ends (T_f/H_f). It is proved that the homogenization method is an efficient method to predict the effective stiffness of CNTs/polymer composites with periodic microstructure. POLYM. COMPOS., 28:688–695, 2007. © 2007 Society of Plastics Engineers     

Conducting polymer composites of zinc‐filled urea–formaldehyde

This article is concerned with the preparation and characterization of composite materials prepared by the compression molding of mixtures of zinc powder and urea–formaldehyde embedded in cellulose powder. The morphologies of the constituent, filler, and matrix were investigated by optical microscopy. The elaborated composites were characterized by density, which was compared with calculated values, and the porosity rate was deduced. Further, the hardness of samples remained almost constant with increasing metal concentration. The electrical conductivity of the composites was less than 10^?11 S/cm unless the metal content reached the percolation threshold at a volume fraction of 18.9%, beyond which the conductivity increased markedly, by as much as eight orders of magnitude. The obtained results interpreted well with the statistical percolation theory. The deduced critical parameters, such as the threshold of percolation, the critical exponent t, and the packing density coefficient were in good accord with earlier studies. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 2011–2015, 2005     

Graphene‐based molecularly imprinted polymer for separation and pre‐concentration of trace polycyclic aromatic hydrocarbons in environmental water samples

A composite of reduced graphene oxide and pyrene‐imprinted polymer was synthesized and employed as a solid phase for extraction of five selected polycyclic aromatic hydrocarbons (PAHs) from water samples. Gas chromatography‐time of flight/mass spectrometry was employed in the analysis of the extracts. The composite was prepared by a free radical polymerization of methacrylic acid and 4‐vinylpyridine as monomers and ethylene glycol dimethacrylate as a crosslinker. The adsorption studies were carried out through batch binding studies. The binding capacity for the imprinted and non‐imprinted composite was 101.83 and 68.21 µg g^?1, respectively. The adsorption followed the pseudo 2nd order and well fitted the Langmuir isotherm. Mean recoveries ranging from 73% to 105.4% for both spiked deionized water and environmental water samples were obtained when the imprinted composites were employed in solid phase extraction of the PAHs. The composites could be re‐used for five times without a significant loss in recoveries. The proposed method was employed for the analysis of spiked environmental water samples and did not show significant changes in the recoveries showing there were no matrix interferences. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45300.     

Viscoelastic properties and characterization of inorganic particulate‐filled polymer composites

To identify effects of glass bead (GB) content on the dynamic mechanical properties of filled low‐density‐polyethylene (LDPE) composites, the storage modulus, loss modulus, glass transition temperature, and mechanical damping of these composites were measured using a Du Pont dynamical mechanical analysis instrument in temperature range from ?150 to 100°C. It was found that the storage modulus increased nonlinearly with an increase of the GB volume fraction. On the basis of Eshelby's method and Mori's work, an equation describing the relationship between the relative storage modulus (E′_R) and filler volume fraction for polymeric composites was proposed, and the E′_R of LDPE/GB composites were estimated by means of this equation at temperatures of ?25, 0, and 25°C, and the calculations were compared with the experimental data, good agreement was showed between the predictions and the measured data. Furthermore, this equation was verified by the experimental from Al(OH)₃ filled EPDM composites at glassy state reported in a reference. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009