Flexible Humidity and Pressure Sensors Realized by Molding and Inkjet Printing Processes with Sandwich Structure

Flexible and wearable devices are important parts toward the realization of artificial intelligence and have an irreplaceable advantage over traditional rigid sensors. In this work, a film with double surface structure is prepared by using sandpaper and the leather with a rhombic structure as a mold, thereby obtaining a sandwich structure resistive type pressure sensor, which has high sensitivity (77.78 kPa^?1, 24 Pa minimum detection) and wide detection range (0.024–230 kPa). The sensors have fast response time (30 ms) and high reliability over 5000 repetitive cycles. The humidity sensor is printed on the top layer of the sensor by using screen printing and inkjet printing technique, and the sandwich structure humidity and pressure sensor is obtained. The humidity sensors show the sensitivities of 0.137/%, 1.57/%, and 11.145/% in the relative humidity range from 25 to 55%, 55 to 70%, and 70 to 80%, respectively. Such sensors not only have excellent capabilities in pressure and humidity detection, but also avoid the complex process of multiple single‐function devices stacked on each other. The applications of sensors in monitoring artery pulse waves, detecting spatial pressure distribution, and sweat is demonstrated.     

Durable,Sensitive, and Wide‐Range Wearable Pressure Sensors Based on Wavy‐Structured Flexible Conductive Composite Film

Flexible pressure sensors have potential applications in human motion monitoring and electronic skins. To satisfy the practical applications, pressure sensors with a high sensitivity, a low detection limit, a broad response range, and an excellent stability are highly needed. Here, a piezoresistive pressure sensor based on wavy‐structured single‐walled carbon nanotube/graphite flake/thermoplastic polyurethane (SWCNT/GF/TPU) composite film is fabricated by a prestretching process. Due to the random wavy structure, high conductivity, and good flexibility, the prepared sensor displays a low detection limit of 2 Pa, a wide sensing range of 0–60 kPa, and a high sensitivity of 5.49 kPa^?1 for 0–50 Pa. Furthermore, the sensor shows a remarkable repeatability of over 1.1 × 10⁴, 9.0 × 10³, and 2.0 × 10³ pressure loading/unloading cycles at 50 Pa, 500 Pa, and 30 kPa, respectively, and a fast responsibility of 100–150 ms of loading response time and 400–600 ms of relaxation time. Therefore, the pressure sensor is successfully adopted to monitor both the large‐scale human activities (e.g., walk and jump) and the small‐scale signals (e.g., wrist pulse). Furthermore, a sensor array is assembled to map the weight and shape of an object, indicating its various potential applications including human–machine interactions, human health monitoring, and other wearable electronics.     

Preparation and characterization of hybrid thiol‐ene/epoxy UV–thermal dual‐cured systems

Hybrid thiol‐ene/epoxy coatings were prepared by combining thiol‐ene photo‐curable formulations with epoxy monomers, through a dual UV–thermal curing process. An increase in glass transition temperature and in storage modulus was observed for the hybrid thiol‐ene/epoxy coatings when compared with the pristine thiol‐ene UV‐cured system. Also, the bisphenol A moieties introduced into the hybrid networks during the dual‐curing process induced an increase in thermal stability of the cured materials. It has been demonstrated that the addition of epoxy monomer to the thiol‐ene photo‐curable system is a good strategy to follow in order to improve the final properties of thiol‐ene‐based coatings leading to a wide range of possible applications for the hybrid materials. Copyright © 2010 Society of Chemical Industry     

Humidity Sensor Based on PEO/PEDOT:PSS Blends for Breath Monitoring

The discrimination of humidity in exhaled breath is of utmost importance to turn breath analysis into an efficient noninvasive tool for early diagnosis or treatment monitoring of several diseases. Herein, by assembling different ratios of the conductive poly(3,4-ethylenedioxythiophene): polystyrene sulfonate with the polymer matrix polyethylene oxide (PEO), humidity chemiresistor-based sensors are designed and investigated. The testing results display a broad relative humidity detection range (6–92%), repeatability, reproducibility, and good reversibility. Meanwhile, the sensors possess good reliability for distinct temperatures and in the presence of typical volatile organic compounds found in human exhaled air. The hygroscopic idiosyncrasy of PEO is attributed to be the main responsible for the high sensibility toward humidity. In a proof-of-principle for detection of respiration humidity, the outcome shows the ability of the chemiresistors to detect the humidity variation in a real case of breath exposure up to 2 s intervals. The 30 d trial of stability readings shows a standard deviation of only 2.6%. These sensing devices appear as a new array component able to distinguish moisture from biomarkers of diagnosed diseases in breath analysis.     

High‐Performance Flexible Pressure and Temperature Sensors with Complex Leather Structure

The ability of the skin to be pressure‐sensitive has prompted scientists to develop materials and equipment to simulate this function. Recently, flexible and stretchable artificial electronic skin has received increasing attention with its unique ability to detect subtle pressure changes. Pressure sensing is one of the key functions of electronic skin devices. Here, a stretchy and highly sensitive pressure sensor is developed that used a polydimethylsiloxane (PDMS) film with leather composite layer as flexible part. These features enable the sensor to accurately detect a variety of human activities, such as small finger movements and bending, pulse and so on. The sensor is found to have a good sensing signal for temperature. This feature provides great promise for sensors to detect temperature.     

Humidity sensitivity of polypyrrole and polypyrrole/SBA‐15 host–guest composite materials

Polypyrrole (PPY) and PPY/SBA‐15 host–guest composite materials have been prepared using chemical synthesis route and characterized by XRD, IR, N₂ adsorption–desorption isotherms, and SEM. The humidity sensitive properties (HSP) of this kind of materials have been studied by analyzing the variation curve of impedance as a function of relative humidity. It was found that the PPY/SBA‐15 host–guest composites materials exhibit better HSP than that of the corresponding pure PPY. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3301–3305, 2006     

UV‐Cured Interpenetrating Acrylic‐Epoxy Polymer Networks: Preparation and Characterization

Acrylic‐epoxy interpenetrating polymer networks were prepared by means of UV curing. The photopolymerization process was investigated via real‐time FTIR spectroscopy. The hybrid, cured films showed a broad tan δ peak in DMTA demonstrating the high damping properties of the hybrid, cured formulations. A decrease on shrinkage was achieved by increasing the epoxy‐resin content in the photocurable formulation, with a consequent increase in adhesion properties.

     

Trends in Conducting Polymer and Hybrids of Conducting Polymer/Carbon Nanotube: A Review

Several conducting polymers, including polyaniline, polypyrrole, polythiophene, polyvinylpyrrolidone, poly(3,4-ethylenedioxythiophene), poly(m-phenylenediamine), polynaphthylamine, poly(p-phenylene sulfide), and their carbon nanotube reinforced nanocomposites are discussed in this review. The physical, electrical, structural and thermal properties of polymers along with synthesis methods are discussed. A concise note on carbon nanotubes regarding their purification, functionalization, properties and production are reported. Moreover, the article focuses upon synthesis methods, properties and applications of conducting polymer/carbon nanotube nanocomposites are focused. Nanotube dispersion, loading concentration and alignment within conducting polymer/carbon nanotube nanocomposite affect their performance and morphology. The conducting polymer/carbon nanotube nanocomposites are substantially used in sensors, energy storage devices, supercapacitors, solar cells, EMI materials, diodes, and coatings.     

UV‐activated silicone oligomer cross‐linking through photoacid and photobase organocatalysts

Diphenyl iodonium hexafluorophosphate salt and N‐alkyl morpholino acetophenone were shown to be effective photocatalyst generators for the cross‐linking of α,ω‐silanol terminated silicone oligomers. These two photoacid and photobase‐induced polycondensation pathways provided an attractive and efficient alternative to toxic and expensive organometallic catalysts. The utility of this novel UV‐curing process was demonstrated with a combination of time‐resolved infrared spectroscopy to follow the fast reaction kinetics and solid‐state ²⁹Si nuclear magnetic resonance to investigate the polysiloxane network. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39875.     

Flexible and Conductive 3D Printable Polyvinylidene Fluoride and Poly(N,N‐dimethylacrylamide) Based Gel Polymer Electrolytes

In this work, 3D printable gel polymer electrolytes (GPEs) based on N,N‐dimethylacrylamide (DMAAm) and polyvinylidene fluoride (PVDF) in lithium chloride containing ethylene glycol solution are synthesized and their physicochemical properties are investigated. 3D printing is carried out with a customized stereolithography type 3D gel printer named “Soft and Wet Intelligent Matter‐Easy Realizer” and free forming GPE samples having variable shapes and sizes are obtained. Printed PVDF/PDMAAm‐based GPEs exhibit tunable mechanical properties and favorable thermal stability. Electrochemical proprieties of the printed GPEs are carried out via impedance spectroscopy in the temperature range of 25–90 °C by varying PVDF content. Ionic conductivity as high as 6.5 × 10^?4 S cm^?1 is achieved at room temperature for GPE containing low PVDF content (5 wt%) and conductivity of the GPEs is increased as temperature rises.     

Effects of small molecular weight silicon‐containing acrylate on kinetics,morphologies, and properties of free‐radical/cationic hybrid UV‐cured coatings

A series of UV‐curable, silicon‐containing mixtures were prepared by adding different micro amounts of small molecular weight silicon‐containing acrylate KH570 to an interpenetrating polymer network system composed of cycloaliphatic polyurethane acrylate, trimethylolpropane triacrylate, cycloaliphatic epoxy resin, free‐radical photoinitiator Irgacure 754 and cationic photoinitiator Irgacure 250 with a weight ratio of 15 : 15 : 65 : 1 : 4. Hybrid coatings with different addition amounts of KH570 (0.2, 0.6, 1.0 wt %) were cured from the mixtures by UV‐initiated free‐radical/cationic dual curing technique. Final reactant conversions and photopolymerization rates of the hybrid UV‐cured coatings were improved with the increase of KH570 content, as evaluated by conversion profiles. The morphologies and microstructures were characterized by scanning electron micro‐scopic, atomic force micrographic, and fourier transform infrared spectrophotometer measurements. Thermal, mechanical, and surface properties of the hybrid UV‐cured coatings were investigated. The increase in KH570 content caused a decrease in mechanical properties besides the breaking elongation. Thermo‐gravimetric analysis revealed that the incorporation of silicon into cross‐linked network structure resulted in high thermal stability. The surface properties of hybrid UV‐cured coatings, such as hardness, contact angle, flexibility, and glossiness were also examined. It is found that transparent hybrid coating with the addition of 1.0 wt % KH570 exhibited a relatively higher contact angle as a direct result of a relatively higher hydrophobic surface. These researches showed that micro amounts of small molecular weight silicon‐containing acrylate could greatly influence the morphologies of liquid nitrogen quenching cross sections and properties of hybrid UV‐cured coatings and could be used to modify UV‐cured coatings for some superior properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40655.     

Preparation and characterization of UV‐curable MPS‐modified silica nanocomposite coats

A series of UV‐curable nanocomposites were prepared with 3‐(trimethoxysilyl) propyl methacrylate (MPS) modified nanosilica under the initiation of 2,2‐dimethoxy‐1,2‐diphenylethan‐1‐one. It was found that MPS‐modified nanosilica together with free MPS could form transparent nanocomposite coats. As the particle size of nanosilica increased, the photopolymerization rate, final double bond conversion, and tack‐free time of nanocomposites increased while the surface roughness, glass‐transition temperature, and UV absorbance of nanocomposites decreased. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2274–2281, 2005     

Modification of UV‐cured epoxy resins with fluorescent sensors through photopolymerization and click chemistry reactions and preparation of polarity‐sensitive films

In this work, functionalization of epoxy films with dansyl and naphthalimide fluorophores is described. The procedure involves UV‐photopolymerization of an epoxy formulation that includes bromomethyl reactive groups, and their post‐functionalization modification through a click strategy. Quantitative click reaction within the bulk of the film allows one to obtain films in which the fluorophore is uniformly and covalently linked throughout the epoxy network. Depending on the chromophore bounded, the films are sensitive to different stimuli. Evaluation of the fluorescence emission of the films shows a linear response towards changes in polarity but less sensitivity than that of the low‐molecular‐weight chromophore. © 2013 Society of Chemical Industry     

UV‐curing and mechanical properties of polyester–acrylate nanocomposites films with silane‐modified antimony doped tin oxide nanoparticles

Antimony doped tin oxide (ATO) nanoparticles were used as nanofillers to improve mechanical properties of UV‐cured polyester–acrylate films. To improve the dispersion of ATO nanoparticles in the polyester–acrylate resin matrix and to strengthen interfacial interactions between ATO nanoparticles and the resin matrix ATO nanoparticles were first organically modified with 3‐methacryloxypropyltrimethoxysilane (MPS). The modification of ATO nanoparticles with MPS was confirmed by FTIR spectroscopy and thermogravimetric analysis (TGA). UV‐curing behaviors of the nanocomposites films were investigated by FTIR spectroscopy. Compared with the film with neat ATO nanoparticles, the film with the same amount of MPS‐modified ATO nanoparticles showed slightly higher UV‐curing rate and final conversion. The mechanical properties of the nanocomposites films were measured by universal testing machine. The MPS‐modified ATO nanoparticles could improve considerably the mechanical properties of the UV‐cured polyester–acrylate nanocomposites films. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Preparation of silica/polyurethane nanocomposites by UV‐induced polymerization from surfaces of silica

UV‐curable nanocomposites were prepared by the in situ photopolymerizaton with nanosilica obtained from sol–gel process. The photoinitiator 2‐hydroxy‐2‐methyl‐1‐phenylpropane‐1‐one (1173) was anchored onto the surface of the nanosilica with or without methacryloxypropyltrimethoxysilane (MAPS) modification. The photopolymerization kinetics was studied by real‐time Fourier transform IR (RTIR), and the microstructure and properties of the nanocomposite were investigated using transmission electron microscopy and UV–visible (UV–vis) transmistance spectra. RTIR analysis indicated that the nanocomposites without MAPS had higher curing rates and final conversion than those with MAPS. The nanocomposites with an uniformal dispersion of nanosilica had high UV–vis transmittance. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Microgel formation and thermo‐mechanical properties of UV‐curing unsaturated polyester acrylates

The effect of internal and terminal unsaturation on the properties of the acrylated polyester films was investigated. Four types of acrylated polyester resin were prepared using adipic acid, maleic anhydride, neopentyl glycol, trimethylolpropane, and acrylic acid. Terminal and internal double bond content as well as branching was adjusted by the molar quantities of trimethylolpropane and maleic anhydride, respectively. A reactive diluent, trimethylolpropane triacrylate (TMPTA), was also used. A three‐factor, three‐level Box‐Behnken design was used to investigate complex nonlinear relationships. Dynamic mechanical, fracture toughness, and tensile properties were evaluated with respect to the amount of terminal and internal unsaturation, and reactive diluent concentration. It was found that microgel formation extensively affects the final UV‐cured film properties. Small quantities of microgels function as micro‐support units, whereas high extent of microgelation causes phase separation through cluster formation and hence, decreases the mechanical properties. It is essential to control the extent of microgelation and phase separation to optimize product performance. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Preparation and characterization of UV‐cured hybrid coatings by triethoxysilane‐modified dimethacrylate based on bisphenol‐s epoxy

Novel hybrid oligomers based on a UV‐curable bisphenol‐S epoxy dimethacrylate (DBSMA) were synthetized. DBSMA was modified with various amount of (3‐isocyanatopropyl)triethoxysilane coupling agent. The modification degree of the hybrid oligomer was varied from 0 to70 wt %. The photopolymerization kinetics was monitored by a real‐time infrared spectroscopy. The conversion and rate of hybrid coatings increased with the increase in modification degree. UV‐curable, hard, and transparent organic–inorganic hybrid coatings were prepared. They were performed by the analyses of various properties such as surface and mechanical properties. Results from the mechanical measurements showed that the properties of hybrid coatings improved with the increase in modification degree. The thermal behavior of coatings was also investigated. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Properties of nanocomposites based on maleate‐vinyl ether donor—acceptor UV‐curable systems

UV‐curable nanocomposites based on donor–acceptor crosslinking chemistry were prepared containing organically modified montmorillonites. The coatings were characterized for thermal, mechanical, and morphological properties. X‐ray diffraction and transmission electron microscopy showed that nanocomposites were formed in all samples. Results showed that an increase in the percentage of clay caused an increased modulus and glass‐transition temperature. It was also seen that tensile modulus showed dramatic improvement when compared with the unmodified polyester sample. Real time IR kinetic data showed that higher conversions were obtained at higher clay loadings. Pendulum hardness values and tensile modulus values showed different trends in properties depending on the combination of polymer matrix and organomodification. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007