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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 37 records · Page 2
All sourcesNASA NTRSDOE OSTI
DOE OSTI2020

Tensile testing and fracture mechanism analysis of polyvinyl alcohol nanofibrous webs

Abstract A tensile properties testing study was conducted to understand the influence of thickness, cross‐head speed (speed of testing), gauge length (GL; specimen test length), and sample shape on important tensile properties of polyvinyl alcohol (PVA) nanofiber webs. The effects of each testing parameter on load at break, extension at break, Young's modulus, and tensile stress–strain curve of PVA nanofiber webs are analyzed. The Welch two sample t ‐tests show the significant difference among tested data. Using interaction plots, two‐way analysis of variance, and margin mean plots, the interaction effects among testing parameters have been analyzed. Of all the factors, cross‐head speed, the interaction among GL, and sample thickness (GL: Thickness) and the interaction among GL, testing speed and sample thickness (GL: Speed: Thickness) have significant influence on the tensile properties of PVA nanofiber webs. Moreover, the hypothesized model of mechanism of tensile strain–stress curve of PVA nanofiber webs has been proposed. Based on the model, the tensile strain–stress curve can be split into three stages: linear elastic, partial break up, and complete breakage. This study will provide a better understanding of tensile testing parameters' effects and their interaction effects on the tensile properties of nanowebs.

Lou, Lihua↗
DOE OSTI2013

MRI Assessment of Uterine Artery Patency and Fibroid Infarction Rates 6 Months after Uterine Artery Embolization with Nonspherical Polyvinyl Alcohol

Purpose: We have observed significant rates of uterine artery patency after uterine artery embolization (UAE) with nonspherical polyvinyl alcohol (nsPVA) on 6 month follow-up MR scanning. The study aim was to quantitatively assess uterine artery patency after UAE with nsPVA and to assess the effect of continued uterine artery patency on outcomes. Methods: A single centre, retrospective study of 50 patients undergoing bilateral UAE for uterine leiomyomata was undertaken. Pelvic MRI was performed before and 6 months after UAE. All embolizations were performed with nsPVA. Outcome measures included uterine artery patency, uterine and dominant fibroid volume, dominant fibroid percentage infarction, presence of ovarian arterial collaterals, and symptom scores assessed by the Uterine Fibroid Symptom and Quality of Life questionnaire (UFS-QOL). Results: Magnetic resonance angiographic evidence of uterine artery recanalization was demonstrated in 90 % of the patients (64 % bilateral, 26 % unilateral) at 6 months. Eighty percent of all dominant fibroids demonstrated >90 % infarction. The mean percentage reduction in dominant fibroid volume was 35 %. No significant difference was identified between nonpatent, unilateral, and bilateral recanalization of the uterine arteries with regard to percentage dominant fibroid infarction or dominant fibroid volume reduction. The presence of bilaterally or unilaterally patent uterine arteries was not associated with inferior clinical outcomes (symptom score or UFS-QOL scores) at 6 months. Conclusion: The high rates of uterine artery patency challenge the current paradigm that nsPVA is a permanent embolic agent and that permanent uterine artery occlusion is necessary to optimally treat uterine fibroids. Despite high rates of uterine artery recanalization in this cohort, satisfactory fibroid infarction rates and UFS-QOL scores were achieved.

62 RADIOLOGY AND NUCLEAR MEDICINE↗
DOE OSTI2017

Bariatric Arterial Embolization with Non-spherical Polyvinyl Alcohol Particles for Ghrelin Suppression in a Swine Model

PurposeTo evaluate the effect of bariatric arterial embolization (BAE) with non-spherical polyvinyl alcohol (PVA) particles on systemic ghrelin levels, weight change, and gastric ulceration risk in a swine model.Materials and MethodsFrom March 2014 to February 2015, ten healthy swine were used in the study (mean weight 31.5 kg; range 24.0–41.5 kg). The animals were randomly assigned to two groups: the embolized group (n = 5) in which BAE was performed and the control group (n = 5). In the embolized group, BAE was performed by selectively infusing 150–250 or 50–150 μm PVA into the gastric arteries that supplied the fundus of the stomach. In the control group, a sham procedure was performed with saline infusion. Plasma ghrelin levels were prospectively obtained at baseline and every 2 weeks thereafter. Endoscopy was performed 3 weeks after BAE to see whether any gastric ulcer occurred. To determine the durability of the occluded arteries, repeated celiac trunk angiography was performed 8 weeks after BAE. Then, all the swine were killed and necropsies were performed.ResultsThe mean post-procedure ghrelin value decreased by 370.0 pg/mL in the embolized group at week 3 (mean 536.0 ± 334.3 pg/mL) and week 5 (mean 515.0 ± 150.0 pg/mL, p < 0.05) relative to baseline (880.0 ± 559.5 pg/mL), respectively, but ghrelin levels were not significantly decreased between the embolized and control groups. There was a significant body weight change as follows: 35.1 ± 9.5 to 46.6 ± 15.7 kg and 31.8 ± 5.8 to 41.2 ± 6.6 kg at baseline and endpoint in the control and embolized groups, respectively (p < 0.05). However, the difference between groups was not significant at endpoint. In the embolized group, ulcerations were identified in three animals (60%) and the recanalization of the embolized arteries was noted on follow-up angiography in three animals (60%), respectively.ConclusionBAE with PVA particles can transiently suppress ghrelin levels in embolized animals, but levels are not significantly different compared to controls. Stomach ulcerations were identified in 60% of the embolized animals.

62 RADIOLOGY AND NUCLEAR MEDICINE↗
DOE OSTI2019

Preparation and characterization of nanocellulose–polyvinyl alcohol multilayer film by layer-by-layer method

Nanofibrillated cellulose (NFC) and polyvinyl alcohol (PVA) were alternately deposited on a NFC/polyethylene terephthalate (PET) substrate by the use of layer-by-layer (LBL) self-assembly technique. The results reveal that by adding a single PVA layer on the NFC/PET substrate, the surface exhibited more hydrophilic properties showing reduced contact area and excellent surface wettability. Moreover, the common FT-IR band for a carboxylic group was observed at 1535 cm –1 , which indicates that NFC treated by TEMPO oxidation was attached to the surface layer of cellulose mats. Moreover, the 10 layer LBL assembly of the NFC and PVA were spread out into a reticulate structure during the drying process, resulting in a much rougher surface than that of 1 LBL assemble on the NFC/PET film. Lastly, the thermal stability of the multilayer films had been significantly improved.

42 ENGINEERING↗
DOE OSTI2018

Photochemical Kinetic Modeling of Degradation of Aqueous Polyvinyl Alcohol in a UV/H{sub 2}O{sub 2} Photoreactor

This study presents a photochemical kinetics model to describe the degradation of water-soluble PVA (Polyvinyl Alcohol) polymer in a UV/H{sub 2}O{sub 2} batch reactor. Under the effect of UV light, the photolysis of hydrogen peroxide into hydroxyl radicals can generate a series of polymer scission reactions. For a better understanding and analysis of the UV/H{sub 2}O{sub 2} process in the cracking of the PVA macromolecules, a chemical reaction mechanism of the degradation process and a relevant photochemical kinetics model are developed to describe the disintegration of the polymer chains. Taking into account the probabilistic fragmentation of the polymer, the statistical moment approach is used to model the molar population balance of live and dead polymer chains. The model predicts the PVA molecular weight reduction, the acidity of the solution, and hydrogen peroxide residual. In addition to previously published data collected in this laboratory, a new set of experiments were conducted using a 500 mg/L PVA aqueous for different hydrogen peroxide/PVA ratios for model validation. Measurements of average molecular weights of the polymer, hydrogen peroxide concentrations and pH of the PVA solution were determinant factors in constructing a reliable photochemical model of the UV/H{sub 2}O{sub 2} process. Experimental data showed a decrease in the PVA molecular weight and a buildup of the solution acidity. The experimental data also served to determine the kinetics rate constants of the PVA photochemical degradation and validate the model whose predictions are in good agreement with data. The model can provide a comprehensive understanding of the impact of the design and operational variables.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Investigation of Photodegradation Preventing of Polyvinyl Alcohol/Nanoclay Composites

The effects of UV irradiation on chemical, thermal, mechanical, and morphological properties of polyvinyl alcohol (PVOH)/2 wt.% of nanoclay(NC) filler were investigated. PVOH composite films were prepared from PVOH blend with fixed content (2%) of NC via the solution casting method. Pure PVOH and PVOH composites were exposed to 340 nm fluorescent UV lamps and assessed for 50 h, 100 h, and 200 h UV exposue. The experimental results such as Fourier transform infrared (FTIR) confirmed that 2% wt. NC filler is efficient and can resist chemical degradation that is caused by ultraviolet irradiation (UV). The carbonyl and hydroxyl indices were increased with increasing the UV exposure irradiation times of both PVOH and PVOH composite. However, the PVOH nanocomposites exhibited more resistant to increasing the indices after exposure to UV irradiation with a longer exposure time. The thermal results (TGA) indicated that PVOH nanocomposite is exhibited more resistance to thermal degradation after UV irradiation exposure compared to that of pure PVOH sample. From DMA results, the storage of modulus was reduced after exposure to UV irradiation of PVOH and PVOH nanocomposites. The results of T{sub g} of PVOH nanocomposites increased after the incorporation of 2% wt. NC into PVOH after exposure to UV irradiation. PVOH nanocomposite exhibited more resistance to reduce the tensile strength after exposure to 200 h UV irradiation. XRD tests showed that PVOH/2 wt.% NC nanocomposites have more resistant to increase intensity after exposure to 200 h UV irradiation compared to that of PVOH sample. The morphology micrographs showed that no obvious cracks on the PVOH nanocomposite after UV irradiation exposure by comparing to that of pure PVOH.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Impact of Blend Proportion on the Miscibility and Thermal Characteristics of Synthetic Plastic-Derived Polypentapeptide with Commercially Available Polyvinyl Alcohol

Plastic-based polypeptides are versatile entities formed to conceive a broad range of scaffold biomaterials. They possess distinct, repetitive, hydrophobic sequences that confer conservation, reversibility, temperature-dependent self-association and dissociation properties. The repeating sequence of plastic-based peptides, poly(AVGVP) have been synthesized by the solution phase method and characterized by {sup 13}C and {sup 1}H-NMR spectroscopy. The intermolecular interactions between poly(AVGVP) and polyvinyl alcohol (PVA) was explored in solution and solid phase by diverse analytical methods. The interaction parameters, namely; α, β, µ and ∆[η]{sub m} obtained from the dilute solution viscometric approach, unveiled that the two polymers were miscible up to 40% of the polypeptide in the blends. Besides, Fourier transform infrared (FTIR) spectroscopy authenticated the formation of strong intermolecular hydrogen bonds connecting blend networks. Further, other analytical techniques such as DSC, SEM and XRD probes advocated the miscibility results. Thermogravimetric investigation of the blends confirmed the proportionate decrease of the thermal stability with the increase of polypentapeptide, attributable to the intermolecular amalgamation between the polypeptide and PVA. The blends and plain poly(AVGVP) degraded completely at about 700 °C, whereas the virgin PVA was about only 60% at this temperature. Graphic Abstract: .

36 MATERIALS SCIENCE↗
DOE OSTI2019

Polyvinyl Alcohol (PVA)–Azadirachta indica (Neem) Nanofibrous Mat for Biomedical Application: Formation and Characterization

The present study provides credence to the formation of polyvinyl alcohol (PVA)–Azadirachta indica (neem) nanofibrous mat (PNNM) under optimum processing conditions of electrospinning technique from a mixer of PVA and neem extract to utilize the inherent medicinal properties of this herb for biomedical application. The bonding behavior, orientation of fibers, thermal behavior, and moisture management properties were evaluated by Fourier transforms infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermo gravimetric analysis (TGA) and moisture management tester (MMT) reports respectively. The antibacterial activity of the developed sample at the maximum mixing ratio of neem extract (80%) was tested against Gram-positive (S. aureus) bacteria using agar disc diffusion method. The results reveal that the prepared nanofibrous mat exhibited better thermal and moisture management properties in comparison with PVA nanofiber alone. The formation of smooth fibers was confirmed by SEM images having average diameter of 185 nm under 5k, 10k and 15k magnifications. The characteristic peaks of PVA and neem constituents in FTIR spectra of the developed mat confirmed the presence of both components. Bacterial resistance was reached up to 20 mm due to the antibacterial constituents of neem extract. Thus the developed mat could be used as a biocompatible and bio based in biomedical applications. Graphic Abstract: .

36 MATERIALS SCIENCE↗
DOE OSTI2019

Magnetic Evaluation of the Nanoparticles Coated with Polyvinylpyrrolidone and Polyvinyl Chloride Nanoparticles Synthesized by Electro-deposition Method for Hyperthermia Application

Fe{sub 3}O{sub 4} nanoparticles, coated with polyvinylpyrrolidone (PVP) + polyvinyl chloride (PVC), were synthesized using cathodic electrochemical deposition (CED) technique. Physical properties of the uncoated and PVP + PVC-coated nanoparticles were investigated using several methods including X-ray diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), Fourier transform infrared (FT-IR), and AC susceptometer. In both the samples, single-phase formation in cubic spinel structure is detected in the XRD analysis. In this study, the mean crystallite size of the prepared specimens is found to be varied from 10.2 to 8.7 nm after PVP + PVC coating. The results of the FT-TR test thoroughly verified the existence of PVP/PVC layer onto the surface of the electrodeposited NPs, and magnetic results also confirmed a superparamagnetic (SPM) behavior at room temperature for both of them. Coercivity and magnetization saturation reduction have also been observed, despite having lower grain size. Also, weak magnetic interactions of inter-particle and a superspin glass-like behavior at low temperatures are confirmed. In addition, increasing of PVP + PVC content on the surface coating of the magnetic nanoparticles has decreased the inter-particle interactions.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Evaluation of polyvinyl toluene scintillators for fast neutron imaging

We evaluated here polyvinyl toluene (PVT) scintillators fabricated with different emitting dopants and scintillator optical configurations for fast neutron imaging. A neutron imaging apparatus was constructed to study scintillators under MeV neutron exposure. PVT with 2% Xylyl Flrpic emitter was identified as the brightest. The addition of a black backing to the scintillator, compared with a specular reflector film backing, improved the resolution of the neutron image obtained with the PVT scintillator by about 2 ×. It is concluded that a PVT imaging screen with 2% Xylyl Flrpic, configured with a black backing, provides the best quality fast neutron image of the scintillators tested.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Strain hardening magnesium-silicate-hydrate composites (SHMSHC) reinforced with short and randomly oriented polyvinyl alcohol microfibers

Magnesium-silicate-hydrate (M-S-H) cement has emerged as an alternative binder with potentially lower energy requirements and emissions. Due to the intrinsically low pH values of its matrix, however, normal steel reinforcement is not appropriate for M-S-H system. To toughen the matrix and to overcome the brittle nature of the material, a new strain hardening magnesium-silicate-hydrate composite (SHMSHC) is developed for the first time by incorporating 2 vol% short and randomly oriented polyvinyl alcohol (PVA) microfibers. The resulting SHMSHC exhibits significant strain hardening with a tensile strain capacity of more than 3%, a compressive strength beyond 50 MPa and a tensile strength of around 3 MPa. Remarkably, saturated multiple cracking with a tight crack width less than 10 μm invisible to the human naked eyes was observed. The newly developed SHMSHC addresses the fundamental challenge of M-S-H binder and is expected to widen possible application areas of M-S-H system.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Electromagnetic wave absorption of multifunctional cementitious composites incorporating polyvinyl alcohol (PVA) fibers and fly ash: Effects of microstructure and hydration

Highlights: • The cementitious composite shows excellent wide-band electromagnetic wave absorption in a frequency range of 2–18 GHz. • The PVA fibers and the fly ash change the dielectric properties of the cementitious composite by Debye polarization. • The iron oxide of the cementitious binders contributes to the magnetic properties of the composites. • The impacts of the microstructure and the hydration of the cementitious composite on its microwave absorption are analyzed. This paper devises a novel method for the adjustment of the pore structure and the hydration of cement to improve the electromagnetic wave absorption of the cementitious composites incorporating polyvinyl alcohol (PVA) fibers and fly ash in a frequency range of 2–18 GHz. The underlying mechanism of the absorption is investigated to explore the possibility of the structural and functional integration of these composites. The electromagnetic parameters of the prepared cementitious composites and those of the raw materials are analyzed in a frequency range of 0.5–18 GHz. Moreover, the pore structure and the chemical environment of the cementitious composites are examined by mercury intrusion porosimetry (MIP), back-scattered electron detector (BSE), and X-ray photoelectron spectroscopy (XPS). The results indicate that the PVA fibers and the high-volume fly ash have a positive effect on electromagnetic wave absorption of the cementitious composites through the adjustment of their pore structure and hydration.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Molecular dynamics and experimental study on the adhesion mechanism of polyvinyl alcohol (PVA) fiber in alkali-activated slag/fly ash

This paper aims to study the adhesion mechanism of polyvinyl alcohol (PVA) fiber within alkali-activated slag/fly ash (AASF) matrix using molecular dynamics (MD) simulation in combination with systematic experimental characterization. The adhesion of PVA to C-(N-)A-S-H gel with different Ca/(Si+Al) and Al/Si ratios was modeled using MD simulation, with the related adsorption enthalpy calculated and the adhesion mechanism explored. The experimentally attained chemical bonding energy of PVA fiber in AASF coincides well with the simulation results. In both cases, the adhesion enhances primarily with increasing Ca/(Si+Al) ratio of C-(N-)A-S-H gel. Additionally, MD simulation indicates preferential element distributions of Ca around PVA molecule, which was confirmed experimentally by the detection of the Ca-rich C-(N-)A-S-H gel in the interfacial transition zone (ITZ). }This study provides further insights into the adhesion mechanism of PVA fiber to C-(N-)A-S-H gel formed in AASF, which is particularly valuable for the future development of PVA-based high-performance alkali-activated composites.

36 MATERIALS SCIENCE↗
DOE OSTI2025

Electrocatalytic grafting of polyvinyl chloride plastics

Polyvinyl chloride (PVC) plastics require high loadings of plasticizers and stabilizers to achieve commercially useful bulk properties. However, these non-covalent additives leach from PVC over time, resulting in the loss of their tailored functionality. This work details the electrocatalytic functionalization of PVC to covalently graft plasticizing additives directly onto the polymer backbone. Here, mechanistic insights guided the design of electrocatalysts capable of modifying C–Cl bonds of PVC under mild conditions with high selectivity while suppressing side reactions such as elimination and chain scission. Functional groups that mimic PVC plasticizers are covalently installed into the backbone of PVC to create new materials with distinct bulk properties from the original polymer. The degree of polymer grafting is easily controlled by simply changing the redox capacity that is passed during electrolysis. This strategy is employed to create chemically- and leach-resistant PVC materials by directly electrolyzing mixtures of consumer PVC products

Zackasee, Jordan L.S.↗
DOE OSTI2018

Characterization and flux assessment of airborne phthalates released from polyvinyl chloride consumer goods

Highlights: • Enhanced levels of semi-volatile organic compounds (SVOCs) can affect human health. • The major SVOCs like phthalates are released into indoor by many sources like plasticizers. • This study investigated the emission characteristics of diverse phthalates from plastic/rubber products. • Emission behavior of phthalates is described in relation to several key variables, e.g., types of PVC. The concentrations and fluxes of airborne phthalates were measured from five types of polyvinyl chloride (PVC) consumer products (vinyl flooring, wallcovering, child's toy, yoga mat, and edge protector) using a small chamber (impinger) system. Airborne phthalates released from each of those PVC samples were collected using sorbent (Tenax TA) tubes at three temperature control intervals (0, 3, and 6 h) under varying temperature conditions (25, 40, and 90 °C). A total of 11 phthalate compounds were quantified in the five PVC products examined in this study. To facilitate the comparison of phthalate emissions among PVC samples, their flux values were defined for total phthalates by summing the average fluxes of all 11 phthalates generated during the control period of 6 h. The highest flux values were seen in the edge protector sample at all temperatures (0.40 (25 °C), 9.65 (40 °C), and 75.7 μg m{sup −2} h{sup −1} (90 °C)) of which emission was dominated by dibutyl isophthalate. In contrast, the lowest fluxes were found in wallcovering (0.01 (25 °C) and 0.05 μg m{sup −2} h{sup −1} (40 °C)) and child's toy (0.23 μg m{sup −2} h{sup −1} (90 °C)) at each temperature level. The information regarding phthalate composition and emission patterns varied dynamically with type of PVC sample, controlled temperature, and duration of control.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2017

A durable polyvinyl butyral-CsH 2 PO 4 composite electrolyte for solid acid fuel cells

We report a composite electrolyte membrane composed of polyvinyl butyral (PVB) and CsH 2 PO 4 has been prepared via a facile and cost-effective method for solid acid fuel cells. The effect of PVB content on conductivity, mechanical integrity, and fuel cell performance is investigated. A minimum amount of 3 wt% PVB in the CsH 2 PO 4 -based composite electrolyte not only offers the required mechanical integrity but also allows high conductivity (~28 mS cm -1 at 260 °C). Single cells based on the composite electrolytes demonstrate a peak power density of 108 mW cm -2 at 260 °C. Almost no degradation in electrochemical performance could be observed during the stability test for 10 h and three thermal-cycling test in H 2 /O 2 fuel cell, indicating the promising application of the composite electrolyte in solid acid fuel cells.

25 ENERGY STORAGE↗
DOE OSTI2018

Effect of BiFeO3 nanoparticle on electrical, thermal and magnetic properties of polyvinyl alcohol (PVA) composite film

Highlights: • Conductivity increases with increasing of BFO in PVA nanocomposite. • The resistivity of the films increases with lowering temperature. • Characteristic relaxation time increases with BFO contents in composites. • The Current-voltage characteristics of the film samples show nonlinearity. • A transformation from antiferromagnetic to diamagnetic behaviour is observed. - Abstract: Synthesis of BiFeO{sub 3} (BFO) nanoparticles (NPs) is demonstrated by sol-gel method. The fabrication of the flexible nanocomposite films based on different wt. % of BFO NPs and Polyvinyl alcohol (PVA) has been done by solution casting method. Conductivity as well as thermal stability tends to increase with the increase in wt. % of BFO filler in PVA matrix. Current-voltage characteristics of the composite films show nonlinearity which invokes the concept of back to back Schottky diode. Due to generation of recombination current and high leakage current, large value of ideality factor arises in the BFO-PVA nanocomposite film. Activation energies from dc conductivity and dielectric response have been evaluated and a decreasing trend in activation energy is observed with the increase in wt. % of BFO nanoparticle insertion in the PVA matrix. At room temperature, BFO NPs exhibit antiferromagnetic behaviour whereas BFO-PVA composite films show diamagnetism.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2022

Polyvinyl alcohol coating induced preferred crystallographic orientation in aqueous zinc battery anodes

The development of rechargeable aqueous zinc batteries is mainly hindered by the Zn anode, which suffers from dendrite growth, corrosion, hydrogen evolution, and surface passivation. Herein, a thin polyvinyl alcohol (PVA) coating layer on Zn anode has enabled dendrite-free, long-life aqueous Zn batteries by effectively regulating the interfacial ion diffusion and inducing the homogeneous Zn nucleation and deposition of stacked plates with preferentially crystallographic orientation along (002) Zn planes. The PVA@Zn anode achieved an ultralong cycle lifespan of thousands of hours at 0.25 and 1 mA cm -2 . Outstanding durability under a deep cycling capacity (5 mA h cm -2 ), high current density (10 mA cm -2 ), and long duration conditions were achieved. The superior cyclability of PVA@Zn anode was also demonstrated in PVA@Zn//V 2 O 5 full cells. In conclusion, the insights of PVA induced Zn deposition with preferred crystal orientation and interfacial regulation shed light on the future development of stable Zn anodes.

Crystallographic orientation↗