Cation-Selective Actuator-Sensor Response of Microcrystalline Cellulose Multi-Walled Carbon Nanotubes of Different Electrolytes Using Propylene Carbonate Solvent.

Microcrystalline cellulose (MC) with 50 wt.% multi-walled carbon nanotube (MCNT) composites is obtained through extrusion, forming MC-MCNT fiber. In this study, we concentrate on three different electrolytes in propylene carbonate (PC) which have the same anions (TF-, trifluoro-methanesulfonate CF3SO3-) but different cations, EDMI+ (1-ethyl-2,3-dimethylimidazolium), Li+ (lithium ion), and TBA+ (tetrabutylammonium). Cyclic voltammetry and square wave potential steps, in combination with linear actuation measurements in a potential range of 0.7 V to -0.2 V, were conducted. Our goal in this work was to establish a cation-selective actuator-sensor device capable of distinguishing different cations. The linear actuation of MC-MCNT fiber had its main expansion at discharge due to the incorporation of TF- in the MC-MCNT fiber with the cations. In the following order, TBA+ > EDMI+ > Li+ had the best stress, strain, charge density, diffusion coefficients, and long-term stability. Chronopotentiometric measurements revealed that the cations in the PC solvent can be differentiated by their ion sizes. Further characterization of the MC-MCNT fiber was completed using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and FTIR and Raman spectroscopy.

Polypyrrole with Embedded Carbide-Derived Carbon with and without Phosphor Tungsten Acid: Linear Actuation and Energy Storage.

Researchers have focused on incorporating porous carbon particles such as carbon-derived carbon (CDC) into polypyrrole (PPy), preferably on the surface, to achieve high-capacitive electrodes. Less attention is afforded to their linear actuation properties. Therefore, in this work, we chose two different electropolymerization processes using the typical PPy doped with dodecylbenzene sulfonate (DBS-) and added CDC particles, compared with CDC with phosphotungstic acid (PTA), forming CDC-PT4- dopants. The resulting PPy/DBS-CDC (PPyCDC) and PPy/DBS-CDC-PT (PPyCDC-PT) films showed different morphologies, with PPyCDC having the most CDC particles on the surface with less surrounding PPy, while in PPyCDC-PT, all the CDC particles were covered with PPy. Their linear actuation properties, applying electrochemical techniques (cyclic voltammetry and square wave potential steps), were found to enhance the PPyCDC-PT films in organic (2-times-higher strain) and aqueous electrolytes (2.8-times-higher strain) in an applied potential range of 0.8 V to -0.5 V. The energy storage capability found for the PPyCDC was favorable, with 159 ± 13 F cm-3 (1.2 times lower for PPyCDC-PT) in the organic electrolyte, while in the aqueous electrolyte, a result of 135 ± 11 F cm-3 was determined (1.8 times lower for PPyCDC-PT). The results showed that PPyCDC was more favorable in terms of energy storage, while PPyCDC-PT was suitable for linear actuator applications. The characterization of both the film samples included scanning electron microscopy (SEM), Raman, FTIR, and energy-dispersive X-ray (EDX) spectroscopy.

Role of Polyoxometalate Contents in Polypyrrole: Linear Actuation and Energy Storage.

A combination of polyoxometalates with polypyrrole is introduced in this work. Our goal was to include phosphotungstic acid (PTA) in different molar concentrations (0.005, 0.01, and 0.05 M) in the electropolymerization of pyrrole doped with dodecylbenzene sulfonate (DBS) and phosphotungstinates (PT), forming PPy/DBS-PT films. Scanning electron microscopy (SEM) revealed that the PPy/DBS-PT films became denser and more compact with increasing PTA concentrations. The incorporation of PT in PPy/DBS was analyzed using Fourier-transform infrared (FTIR) and energy dispersive X-ray (EDX) spectroscopy. The linear actuation in cyclic voltammetry and potential square wave steps in an organic electrolyte revealed increasing mixed actuation, with major expansion upon oxidation found for PPy/DBS-PT films with a PTA concentration of 0.005 M. Best results of a strain of 12.8% and stress at 0.68 MPa were obtained for PPy/DBS-PT (0.01 M). The PPy/DBS-PT films polymerized in the presence of 0.05 M of PTA and showed main expansion upon reduction, changing the actuation direction. Chronopotentiometric measurements of PPy/DBS-PT samples were conducted to determine the specific capacitance optimal for a 0.01 M PTA concentration in the range of 80 F g-1 (±0.22 A g-1).

Electrochemical performance of composite electrodes based on rGO, Mn/Cu metal-organic frameworks, and PANI.

Benzendicarboxylic acid (BDC)-based metal-organic frameworks (MOFs) have been widely utilized in various applications, including supercapacitor electrode materials. Manganese and copper have solid diamond frames formed with BDC linkers among transition metals chosen for MOF formation. They have shown the possibility to enlarge capacitance at different combinations of MOFs and polyaniline (PANI). Herein, reduced graphene oxide (rGO) was used as the matrix to fabricate electrochemical double-layer SCs. PANI and Mn/Cu-MOF's effect on the properties of electrode materials was investigated through electrochemical analysis. As a result, the highest specific capacitance of about 276 F/g at a current density of 0.5 A/g was obtained for rGO/Cu-MOF@PANI composite.

Antagonist Concepts of Polypyrrole Actuators: Bending Hybrid Actuator and Mirrored Trilayer Linear Actuator.

Following the natural muscle antagonist actuation principle, different adaptations for "artificial muscles" are introduced in this work. Polypyrrole (PPy) films of different polymerization techniques (potentiostatic and galvanostatic) were analyzed and their established responses were combined in several ways, resulting in beneficial actuation modes. A consecutive "one-pot" electrosynthesis of two layers with the different deposition regimes resulted in an all-PPy bending hybrid actuator. While in most cases the mixed-ion activity of conductive polymers has been considered a problem or a drawback, here for the first time, the nearly equal expansions upon oxidation and reduction of carefully selected conditions further allowed to fabricate a "mirrored" trilayer laminate, which behaved as a linear actuator.

Polypyrrole with Phosphor Tungsten Acid and Carbide-Derived Carbon: Change of Solvent in Electropolymerization and Linear Actuation.

Linear actuators based on polypyrrole (PPy) are envisaged to have only one ion that triggers the actuation direction, either at oxidation (anion-driven) or at reduction (cation-driven). PPy doped with dodecylbenzenesulfonate (PPy/DBS) is the most common applied conducting polymer having cation-driven actuation in aqueous solvent and mainly anion-driven actuation in an organic electrolyte. It is somehow desired to have an actuator that is independent of the applied solvent in the same actuation direction. In this research we made PPy/DBS with the addition of phosphorus tungsten acid, forming PPyPT films, as well with included carbide derived carbon (CDC) resulting in PPyCDC films. The solvent in electropolymerization was changed from an aqueous ethylene glycol mixture to pure EG forming PPyPT-EG and PPyCDC-EG composites. Our goal in this study was to investigate the linear actuation properties of PPy composites applying sodium perchlorate in aqueous (NaClO4-aq) and propylene carbonate (NaClO4-PC) electrolytes. Cyclic voltammetry and square potential steps in combination with electro-chemo-mechanical-deformation (ECMD) measurements of PPy composite films were performed. The PPyPT and PPyCDC had mixed ion-actuation in NaClO4-PC while in NaClO4-aq expansion at reduction (cation-driven) was observed. Those novel PPy composites electropolymerized in EG solvent showed independently which solvent applied mainly expansion at reduction (cation-driven actuator). Chronopotentiometric measurements were performed on all composites, revealing excellent specific capacitance up to 190 F g-1 for PPyCDC-EG (best capacitance retention of 90 % after 1000 cycles) and 130 F g-1 for PPyPT-EG in aqueous electrolyte. The films were characterized by scanning electron microscopy (SEM), Raman, Fourier-transform infrared (FTIR) and energy dispersive X-ray spectroscopy (EDX).

The Use of Laminates of Commercially Available Fabrics for Anti-Stab Body-Armor.

Modern personal protective armor has been generally based on the Kevlar fabrics, with the main goal to offer defense against bullets. In addition to the high cost and poor processability, Kevlar has the disadvantage of limited stab-proofing capability. On the other hand, a large number of crimes involving deadly injures represent knife attacks. Our goal in this work was to investigate composites based on traditional commercially available fabrics of linen and silk, using different adhesives-polymers for forming laminates. The silk composites also contained different amounts of in-woven polyester. Three different water-based adhesives of polyurethane, urea formaldehyde and polyvinyl alcohol were considered. It was found, that besides the strength of the fabrics themselves, the adhesives polymers played a crucial role in the obtained performance of the laminates. The laminates were characterized in their mechanical properties, as well as with scanning electron microscopy and FTIR spectroscopy.

Radon and radium concentrations in drinkable water supplies of the Thu Duc region in Ho Chi Minh City, Vietnam.

The results of (222)Rn and (226)Ra activity measurements in drinkable water supplies of the Thu Duc region in Ho Chi Minh City, Vietnam, are presented in this paper. The measurements were performed using a RAD 7 radon detector manufactured by Durridge Company, Inc. Mean concentrations of (222)Rn and (226)Ra were found to be 0.11±0.01Bql(-1) and 0.11±0.02Bql(-1) in 14 drinking water samples. They are 0.12±0.01Bql(-1) and 0.10±0.02Bql(-1) in 15 tap water samples, respectively. The mean (222)Rn concentration of 1.40±0.03Bql(-1) in the 20 groundwater samples of this study is also lower than the WHO advised level of 100Bql(-1). Fifty percent of groundwater samples analysed have (226)Ra levels in excess of the USEPA recommended maximum contaminant level of 0.185Bql(-1). The occurrence of elevated concentrations of (226)Ra in groundwater samples was explained by pH and alkaline conditions.