Spray coating thin polymeric sensor films for Au3+

A novel polymeric sensor of the poly(sodium-4-styrenesulfonate) (PSS)-modified rhodamine B derivative (Rho) was synthesized using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)/N,N′-dimethylpyridin-4-amine (DMAP) as coupling reagents to obtain PSS-Rho4 in 21% yield. The characterization and “Off–On” sensing phenomena were established through UV–Vis, fluorescence, NMR, and FTIR techniques. The PSS-Rho4 showed high selectivity and sensitivity for Au³⁺ over other metal ions. Upon the addition of Au³⁺, significant color change and “Off–On” fluorescence were observed due to a cation Au³⁺ induced spirolactam ring-opening process with detection limit down to micromolar values (1.2 μM). In addition, spray coating thin polymeric sensor films were produced onto the surface of material (PSS-Rho4-ITO and PSS-Rho4-filtered paper) providing a fast, portable, and easy-to-use molecular device for the detection of Au³⁺ in the real system. Reversibility was evaluated by rinsing with EDTA solution under basic condition. We believe that, this approach provides a sensitive and accurate method for the detection of Au³⁺ in environmental and biological applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48273.     

Novel fabrication route for porous silicon carbide ceramics through the combination of in situ polymerization and reaction bonding techniques

For the first time, an in situ polymerization technique was applied to produce mullite‐bonded porous SiC ceramics via a reaction bonding technique. In this study, SiC microsized particles and alumina nanopowders were successfully coated by polyethylene (PE), which was synthesized from the particle surface in a slurry phase reactor with a Ziegler–Natta catalyst system. The thermal studies of the resulting samples were performed with differential scanning calorimetry and thermogravimetric analysis. The morphology analysis obtained by transmission electron microscopy and scanning electron microscopy (SEM) confirmed that PE was successfully grafted onto the particle surface. Furthermore, the obtained porous ceramics were characterized in terms of their morphologies, phase composition, open porosity, pore size distribution, and mechanical strength. SEM observations and mercury porosimtery analysis revealed that the quality of the dispersion of nanosized alumina powder into the microsized SiC particles was strongly enhanced when the particles were coated by polymers with in situ polymerization. This resulted in a higher strength and porosity of the formed ceramic porous materials with respect to the traditional process. In addition, the X‐ray diffraction results reveal that the amount of mullite as the binder increased significantly for the samples fabricated by this novel method. The effects of the sintering temperature, forming pressure, and polymer content on the physical and mechanical properties of the final porous ceramic were also evaluated in this study. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40425.     

New method for fabricating an α‐fetoprotein affinity monolithic polymer array

Bisphenol A based epoxy acrylate (BABEA), a commercial UV‐curable material, was introduced as a crosslinker for the fabrication of an epoxy‐functionalized monolithic polymer array through UV‐initiated copolymerization with glycidyl methacrylate as the functional monomer and poly(ethylene glycol) 200 as the porogen. Scanning electron microscopy images showed that the monolithic poly(bisphenol A based epoxy acrylate‐co‐glycidyl methacrylate) [poly(BABEA‐co‐GMA)] exhibited a well‐controlled skeletal and well‐distributed porous structure. The α‐fetoprotein (AFP) immunoaffinity monolithic polymer array prepared by the immobilization of AFP on epoxy‐functionalized monolithic arrays was used as an immunosensor for chemiluminescent AFP detection. X‐ray photoelectron spectroscopy results indicate that the AFP antibody was successfully immobilized on the monolithic poly(BABEA‐co‐GMA) array. With a noncompetitive immune‐response format, the proposed AFP immunoaffinity array was demonstrated as a low‐cost, flexible, homogeneous, and stable array for AFP detection. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41792.     

3D-Printed thermoplastic polyurethane/graphene composite with porous segregated structure: Toward ultralow percolation threshold and great strain sensitivity

Low-percolation threshold and large deformation capacity are two critical attributes of the strain sensor, which determine its sensitivity and stability respectively. However, endowing these two attributes to the strain sensor simultaneously is still a great challenge in this field. In this work, the strain sensor with the three-dimensional porous segregated structure constructed by graphene wrapped thermoplastic polyurethane (TPU) particles was fabricated successfully through the selective laser sintering technology. Results demonstrated that the percolation threshold of the composite is only 0.2 wt% and the strain gage factor can reach as high as 668.3, which represents the excellent sensitivity of the strain sensor. Furthermore, after 10 circles of stretching at the 15% strain, resistance-strain behavior of the strain sensor shows great repeatable, which represents the remarkable stability. Therefore, the highly sensible and stable strain sensor was fabricated successfully, which will provide the guidance for the manufacture of the high-performance strain sensor.     

Synthesis and characterization of novel hyperbranched fluorescent polymers that can be precisely used for metal ion detection and quantification

Four novel hyperbranched polymers with 4 or 5 ring-closed rhodamine units in each were achieved through RAFT polymerization followed by modification with rhodamine moieties. The solubility, thermostability, and photophysical properties of the polymers were studied. The polymers showed high selectivity and sensitivity to Fe³⁺ among various metal ions in CH₃CN/H₂O (75/25, v/v) and could signal Fe³⁺ through multichannels: emerging a new absorption around 558 nm, over 30 nm fluorescence redshift and significant fluorescence enhancement (including 33–37 folds in intensity and 8.3–12.8 folds in quantum yield), accompanied by visual and fluorescent color changes. The polymers could be applied in the analysis of Fe³⁺ in real water samples. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48933.     

Fabrication of imprinted photonic films via predesigned multiple UV-polymerizations and their ability to detect solvents and metal ions in aqueous solution

To synthesize photonic films without a chiral dopant, a predesigned multiple photopolymerization process was carried out. The photonic films were prepared by the photopolymerization of a mixture of chiral nematic liquid crystals. After polymerization, the chiral dopant, CB15, was removed and recycled. The imprinted photonic polymer films showed Bragg reflection without the presence of the chiral dopant. Upon the sensing of solvents in aqueous solution, significant color changes and peak shifts were observed by the naked eye and ultraviolet–visible spectroscopy, respectively. A linear calibration curve between the central wavelength of the reflection band of the fabricated imprinting film and the volume ratio of 1,4-dioxane in water was observed. Furthermore, the sensing of chloroform content in methanol, ethanol, and acetone via the imprinted film were also investigated. The results suggest that the synthesized imprinted photonic films can detect different kinds of mixed solvents. The sensing properties of the photonic films were further improved by copolymerization with a rhodamine-derived monomer. The synthesized modified photonic films can detect heavy metal ions in aqueous solution. This study reports a novel, recyclable, and easy approach to detect organic solvents and copper ions in aqueous solution.     

Optical sensor based on fluorescent PMMA/PFO electrospun nanofibers for monitoring volatile organic compounds

The development of polymeric materials with superior electrical and/or optical properties is highly demanded for designing optical gas sensors, where conjugated polymers play an important role due to their π‐electron conjugation. However, usually the low processability and high cost of these materials hinder technological applications. Here we report on a simple route to develop highly fluorescent electrospun nanofibers of poly(methyl methacrylate) (PMMA) containing low contents of polyfluorene (PFO). The PMMA_PFO nanofibers were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis, while the luminescence properties changes were evaluated by exposing the PMMA_PFO nanofibers to distinct volatile organic compounds (VOCs) including ethanol, toluene, tetrahydrofuran, acetone, dichloromethane, and chloroform. The changes in luminescence properties, specifically fluorescence quenching, of PMMA_PFO nanofibers were analyzed in terms of conformational changes from glassy‐phase to β‐phase of PFO when the nanofibers were exposed to the VOCs. The developed nanostructured platform showed a suitable response to detect chloroform, with linear responses in the concentration range from 10 to 300 ppm and from 350 to 500 ppm and limits of detection of 47.9 and 15.4 ppm, respectively. The results suggest the PMMA_PFO electrospun nanofibers are highly potential materials for optical gas sensor applications based on luminescence quenching. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46128.     

Determination of moisture content of polyamide 66 directly from combination region near‐infrared spectra

The hygroscopic nature of polyamide (PA) polymers motivates the development of analysis tools for use in assessing their moisture content. Among possible analysis techniques, near‐infrared (near‐IR) spectroscopy is non‐destructive, requires little or no sample preparation, and is compatible with sample thicknesses on the order of mm. The work reported here makes use of transmission near‐IR spectroscopy in the combination region (5000–4000 cm^?1) to develop a protocol for assessing the moisture content of PA 66 samples directly from their spectral intensities after preprocessing with the standard normal variate transform and partial least‐squares. The method is compatible with online or continuous monitoring applications and can be calibrated without the use of destructive reference measurements such as thermogravimetric analysis. The long‐term calibration performance of the technique is evaluated, and on a scale of 0–100% moisture uptake, the standard error of prediction is found to average 1.4% over 6 months. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40645.     

Outstanding performance of parylene polymers as electrets for energy harvesting and high-temperature applications

Parylene C is used in many applications due to its high properties but it remains a material with moderate performance as long as it is intended for use as an electret. Hence, the generally accepted idea, rightly so, in the scientific and industrial community not to necessarily select parylene (i.e., parylene C) for applications where the endurance of the electret is a strong criterion. Our study provided a new perspective on the performance of parylenes as electret. In this case, we will talk about fluorinated Parylenes of the VT-4 type and especially AF-4 variant. Their thermal stability is outstanding and a charge stability is almost total up to 100 °C. A 50% reduction in the charge is recorded at a temperature as high as of 220 °C (9 μm thick Parylene AF-4), making it one of the most efficient polymer electrets to date. Negatively and positively charged Parylene AF-4 electrets presented similar performance over long durations, which is out of ordinary for the commonly employed polymeric electrets. Finally, these fluorinated polymers are therefore particularly promising new candidates for applications in electret-based converters for energy harvesting. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48790.     

Graphene/poly(styrene‐b‐isoprene‐b‐styrene) nanocomposite optical actuators

This article presents an optomechanical actuator, which is driven by infra red (IR) radiation. The actuator is a nanocomposite‐containing graphene platelets embedded in poly(styrene‐b‐isoprene‐b‐styrene) (SIS) matrix. 0.1 mm thick free‐standing nanocomposite films are fabricated by a simple process of solvent casting. We demonstrate that graphene/SIS nanocomposite contracts on irradiation with IR radiation under strained conditions, whereas expansion behavior was exhibited by them when no prestrain is applied. A maximum photomechanical stress of 28.34 kPa and strain upto 3.1% was obtained for these nanocomposite actuators. We have also studied the mechanical characteristics and thermal degradation of these nanocomposite actuators. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3902–3908, 2013     

Fabrication of porous thick films using room-temperature aerosol deposition

A novel technique for the rapid room-temperature deposition of porous ceramic, glass, or metal thick films using the aerosol deposition (AD) method is presented. The process is based on the co-deposition of the desired film material and a second water-soluble constituent, resulting in a ceramic-ceramic composite. Following the subsequent removal of water-soluble end member, a network of pores is retained. To demonstrate the process, porous BaTiO₃ thick films were fabricated through co-deposition with NaCl. Microstructural images show the clear development of a porous structure, which was found to enhance the dielectric properties over dense thick films, possibly related to the lower extent of internal residual stress. This simple but highly effective porous structure fabrication can be applied to any film and substrate material stable in water and is promising for the application of AD-processed films in gas sensors, solid oxide fuel cells, and humidity sensors.     

Poly(N‐isopropylacrylamide) microgel‐based etalons for determining the concentration of ethanol in gasoline

A device composed of a poly (N‐isopropylacrylamide)‐based microgel layer sandwiched between two thin gold layers was used as a platform for determining the amount of ethanol in gasoline (octane number of 87). This device, also known as an etalon, has unique optical properties, which depend on the diameter of the microgels that make up the device. We show that the optical properties of the device depend on the concentration of the ethanol in gasoline samples. Specifically, as the reflectance peaks shift to higher wavelength, the visual color of the device changes from green to red up to 12% (v/v) ethanol. We show that the response was consistent from sample to sample and that the devices are reusable at least three times. We went on to show that the response did not depend on the source of the gasoline, and that the etalon's response is specific to ethanol compared to other common solvents found in gasoline. The performance of these devices make them potentially useful for detecting ethanol in gasoline at the time of gasoline purchase, to determine if the gas being purchased has been adulterated. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42106.     

A novel type of waterborne fluorescent nanofiber membranes with effectively suppressed ACQ phenomenon: Fabrication,properties, and applications

In this research, a novel type of waterborne fluorescent nanofiber membranes (WNFM) based on fluorescent acrylic latex (FAL) has been developed by electrospinning method using environment-friendly water as the spinning solvent. FALs are synthesized by doping Rhodamine B (Rh B) into acrylate monomers through emulsion polymerization, and then polyvinyl alcohol (PVA) is added to fabricate a series of WNFM via electrospinning process. As the hydrophilic emulsifier sodium dodecyl sulfate enriches on the surface of the latex, a portion of Rh B can be adsorbed onto the surface of FAL and form an electrical double layer to prevent its aggregation, which accounts for the enhancement in fluorescence of FALs. The relationships between the preparation conditions, morphology and properties of WNFM have been studied with a combination of techniques including fluorometry and microscopies. The developed waterborne fluorescent nanofiber membranes demonstrate a good water-resistant property with a linear response of photoluminescence intensity to temperature for many cycles. The study points a new direction to develop the nanofiber membrane using environment-friendly water as a spinning solvent in electrospinning and realize its fluorescent functionalization.     

A versatile radiochromic dosimeter for low‐medium gamma radiation and its application to food irradiation

This article presents a novel radiochromic film for selective detection of low‐medium (0–10 kGy) gamma radiation (⁶⁰Co) doses. This dosimeter is based on a printed fluorescent multilayer structure comprising a paper substrate having layers of copper phthalocyanine (DY220) (a green emitter material) on the bottom, and layers of poly[2‐methoxy‐5(2′‐ethylhexyloxy)‐p‐phenylenevinylene] (MEH‐PPV) (a green‐light absorber, red emitter, and radiation sensitive polymer) on the top. The effect of gamma radiation on the optical properties of DY220/MEH‐PPV was described: it was observed as a strong correlation between radiation dose and fluorescent, color coordinates for CIE (1931) chromatic diagram, and Pantone color reference of the dosimeter. The rate of these changes can be altered by manipulation of top–bottom layers to represent easily the radiation dose to be determined in a wide range. This versatile dosimeter has many uses in the field of food radiation for monitoring, quality assurance, and control of the gamma radiation process. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45729.     

Piezoelectric polymer microfiber-based composite for the flexible ultra-sensitive pressure sensor

This study presents a new type of composite consisting of piezoelectric poly(γ-benzyl-α, l -glutamate) (PBLG) polymer fibers, which contain a large dipole moment, and the elastomer polydimethylsiloxane (PDMS) as the matrix material. PBLG microfibers were fabricated and polarized using the electrospinning method and cast in PDMS to form a unidirectional continuous-fiber composite. The PBLG/PDMS composite was characterized based on various aspects such as crystalline structure, mechanical properties, piezoelectricity, and electromechanical response. The piezoelectric charge constants in the transverse and longitudinal modes were measured to be 10.2 and 54 pC/N, respectively, which are the largest piezoelectric coefficients of biocompatible polymers up to date. The thin PBLG/PDMS composite film can produce up to 200 mV peak-to-peak under sinusoidal actuation and exhibit ultra-sensitivity up to 615 mV N⁻¹. These results show the great potential of the highly flexible piezoelectric polymer fiber-based composite for use in a variety of applications such as energy harvesting devices, biomechanical self-powered structures, and force sensors. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48884.     

Additive-free,robust and superelastic dual-network graphene/melamine composite sponge for motion sensing

Graphene aerogel (GA) has a large potential in many fields such as energy storage, catalyst support, and sensors. However, its poor mechanical property has restricted the wide application. In this work, superelastic and robust melamine/graphene composite sponges are prepared by constructing a dual-network structure of melamine and graphene without any chemical additives. The strength of as-prepared composite sponge at 50% strain can reach 40 times higher than that of controlled GA. After 50 compressive cycles, the strain and strength recovery ratios of composite sponge are about 97% and 90%, respectively. More importantly, the excellent compression performance combines with the good electrical conductivity of the graphene network enable it as a dynamic piezo-resistive material, which can provide immediate responses to dynamic stresses and strains with different frequencies. Benefitting by these excellent performances, the dual-network composite sponge shows a great potential application in the field of motion sensing.     

Impact damage sensing of multiscale composites through epoxy matrix containing carbon nanotubes

Carbon nanotubes are used to provide increased electrical conductivity for polymer matrix materials, thus offering a method to monitor the structure's health. This work investigates the effect of impact damage on the electrical properties of multiscale composite samples, prepared with woven fiberglass reinforcement and epoxy resin modified with as‐received multi‐walled carbon nanotubes (MWCNTs). Moreover, this study addresses potential bias from manufacturing, and investigates the effectiveness of resistance measurements using two‐ and four‐point probe methods. Transmission electron microscopy and static tensile tests results were used to evaluate, respectively, the dispersion of MWCNTs in the epoxy resin and the influence of the incorporation of these nanoparticles on the static tensile properties of the matrix, and interpret results from the resistance measurements on impacted specimens. In this study, the four‐point probe method is shown to be much more repeatable and reliable than the two‐point probe method. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis of a polymeric sensor containing an occluded pyrylium salt and its application in the colorimetric detection of trimethylamine vapors

A dense membrane (MS) based on vinyl polymers and containing a pyrylium salt [2,6‐diphenyl‐4(p‐methacryloyloxy)phenylpyryliumtetrafluoroborate] was prepared. The MS has hydrophilic and sensory properties that make it a good material for the selective colorimetric detection of trimethylamine (TMA) vapors, a biogenic amine of great importance in food safety. The polymeric sensor changes from yellow to an intense pink color with increasing concentrations of TMA. The material could be reused in the presence of HCl vapors for at least 10 times. The detection and quantification limits were determined by ultraviolet–visible absorption spectroscopy (4.42 and 13.40 ppm, respectively) and by the RGB parameters of digital color (3.37 and10.22 ppm, respectively). © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46185.     

Self-adhesive plasticized regenerated silk on poly(3-hydroxybutyrate-co-3-hydroxyvalerate) for bio-piezoelectric force sensor and microwave circuit design

This study shows that regenerated silk (RS), a natural biodegradable and biocompatible polymer, can behave as a self-adhesive thermoplastic material with multifunctional properties. In particular, Ca ions-plasticized RS hybrids with gold nanorods have been produced. It has been found that at mild conditions of temperature and pressure, RS hybrids undergo to the loss of the β-sheet content and forms a tough self-adhesive material on poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) substrate. The structure-dependent piezoelectricity of such RS adhesives on PHBV films was investigated and it was demonstrated that this forms a RS/PHBV piezoelectric sensor that can be used for the monitoring of force. The constitutive parameters (i.e., permittivity and loss tangent) of both PHBV and RS/PHBV were measured in view of their use as dielectric substrates in microwave circuit design. Being fully made of biodegradable and biocompatible materials, this self-adhesive material can be used in tissue engineering for different applications.     

Preparation and characterization of porous titanium dioxide sulfonated polystyrene composite microspheres with amphiphilicity

Porous particles with amphiphilicity were prepared by a nonpolymeric pore‐formation process with the sulfonation of polystyrene microspheres. Nano titanium dioxide (TiO₂) particles were then grafted onto the surface via a sol–gel method to finally form the composite particles. The effects of the mass ratio of ethanol (EtOH) to water, temperature, and solubility parameter on the pore‐formation process is discussed in detail. The morphology, porous structure, and wetting properties of the particles were studied by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared (FTIR) spectroscopy, and contact angle measurement. The results show that porous sulfonated polystyrene (SP) microspheres could be fabricated at 60°C with a 1 : 1 mass ratio of EtOH–water and a solubility parameter of 29.69 MPa^1/2. The TiO₂ particles were determined to be grafted onto the SP microspheres by physical‐bond interaction on the basis of FTIR analysis. The contact angles for both water (aqueous‐phase) and various organic solvent (oil‐phase) droplets with different polarities on the surface of compressed tablets of TiO₂–SP powder were all lower than 30°; this indicated excellent amphiphilicity in the composite particles. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013