Organo-modified clay nanoparticles were mixed at 1 and 5 wt% concentrations with a molten blend of 75 wt% of polylactide (PLA) and 25 wt% poly[(butylene adipate)-co-terephthalate] (PBAT). Three mixing strategies were used to control the localization of nanoclay. Small amplitude oscillatory shear (SAOS) and stress growth tests were conducted to clarify the nanoclay interactions with the blend components and its effect on the molecular relaxation behavior. SAOS and weighted relaxation spectra properties were determined before and after pre-shearing at a rate of 0.01 s−1. Molecular relaxation and its characteristics were influenced by PLA degradation, PBAT droplet coalescence, and nanoclay localization.

Cellprene™ is a recently developed polymeric blend based on poly(lactide-co-glycolide) (PLGA)/polyisoprene (PI) with good biological performance for biomedical applications. However, its potential as fiber scaffold in tissue engineering is still unknown, and the influence of processing parameters is yet to be understood. In this study, several compositions based on PLGA/PI blend mixed with hydroxyapatite (HAp) and polyethylene glycol (PEG) were prepared by solvent casting. Then, the membranes were used to produce micro/nanofibers by centrifugal spinning (CS) and electrospinning (ES). The viscosity's effect was studied to find an ideal viscosity value to produce homogeneous micro/nanofibers. The in vitro bioactivity test was also performed. Rheological results showed that the best viscosity range was (0.105 Pa s > η > 0.138 Pa s) for CS; larger fibers of ES were produced with lower viscosities. The sample with the lowest HAp concentration exhibited thinner and more homogeneous non-beaded fibers and proved its bioactivity response.

The macroscale function of multicomponent polymeric materials is dependent on their phase-morphology. Here, we investigate the morphological structure of a multiblock copolymer consisting of poly(L-lactide) and poly(ε-caprolactone) segments (PLLA-PCL), physically cross-linked by stereocomplexation with a low molecular weight poly(D-lactide) oligomer (PDLA). The effects of blend composition and PLLA-PCL molecular structure on the morphology are elucidated by AFM, TEM and SAXS. We identify the formation of a lattice pattern, composed of PLA domains within a PCL matrix, with an average domain spacing d0 = 12 – 19 nm. The size of the PLA domains were found to be proportional to the block length of the PCL segment of the copolymer and inversely proportional to the PDLA content of the blend. Changing the PLLA-PCL / PDLA ratio caused a shift in the melt transition Tm attributed to the PLA stereocomplex crystallites, indicating partial amorphous phase dilution of the PLA and PCL components within the semicrystalline material. By elucidating the phase structure and thermal character of multifunctional PLLA-PCL / PDLA blends, we illustrate how composition affects the internal structure and thermal properties of multicomponent polymeric materials. This study should facilitate the more effective incorporation of a variety of polymeric structural units capable of stimuli responsive phase transitions, where an understanding the phase-morphology of each component will enable the production of multifunctional soft-actuators with enhanced performance.

Organic light-emitting diodes (OLEDs) have attracted huge concern because of their intrinsic characteristics and ability to reach the pinnacle in the field of high-quality flat-panel displays and energy-efficient solid-state lighting. High-efficiency is always a key crux for OLED devices being energy-saving and longer life-span. OLEDs have encountered enormous difficulties in meeting the requirements for large-sized devices due to a major limitation in vacuum thermal evaporation technology. In multilayered OLED devices, the characteristics of the charge injection/transport layer is a crucial factor for the operating-voltage, power-efficiency and stability of the device. Transition metal oxides have shown great potential owing to their wide range of possible energy level alignments, balanced charge injection, and improvement of carrier mobilities. In this study, we report a solution-processed blend V2O5-PEDOT:PSS hole-injection/hole-transport layer (HIL/HTL) for efficient orange phosphorescent OLEDs. The electroluminescent characteristics of blend V2O5-PEDOT:PSS based devices were studied with the structure ITO/V2O5-PEDOT:PSS/CBP:Ir(2-phq)3/TPBi/LiF/Al. The V2O5-PEDOT:PSS based OLEDs displayed relatively higher device performance and low roll-off than that of the counter PEDOT:PSS device in terms of a maximum luminance of 17,670 cd m-2, power efficiency of 19.4 lm W-1, external quantum efficiency of 8.7%, and more importantly, low turn-on voltage. These results demonstrate an alternative approach based on metal oxide/organic blend HIL/HTL as a substitute of PEDOT:PSS for high-efficiency solution process OLEDs.

Embolic beads for transarterial chemoembolization (TACE) should possess radiopacity and biodegradability at the same time, to be visualized in a body under fluoroscopy and CT scanning to avoid complicating disease. In this study, we fabricated radiopaque and biodegradable beads composed of Lipiodol (LPD) (ethiodized oil) and polycaprolactone (PCL), a biocompatible and biodegradable polymer. LPD/PCL beads were first fabricated with a home-made microfluidic device. By changing the flow-rate ratio in the microfluidic device, the mean diameter of LPD/PCL beads could be well controlled. The radiopacity was evaluated by the fluoroscopic imaging and the CT number measurements. Furthermore, the biodegradability was evaluated by collecting the weight loss data of LPD/PCL immersed in lipase/PBS solution and PBS. The results showed that LPD/PCL beads obtained in this study had sufficient radiopacity and biodegradability, which would be an alternative embolic agent for TACE.

Biodegradable poly(lactide acid) (PLA) has been well-studied as a shape memory polymer in recent years, but the brittleness and relatively high Tg limit its applications. In this study, a series of PLA/poly(ethylene glycol) (PEG) blends were manufactured by using the solvent evaporation method. The thermal behaviors, morphology, hydrophilicity, and mechanical properties of the samples with different contents of PEG have been experimentally studied by differential scanning calorimetry, scanning electronic microscopy, water contact angle, dynamic mechanical analysis, and tensile test. Furthermore, the influence of PEG on the shape memory properties under different loading conditions including the stretch strain, recovery temperature, deformation temperature, and tensile rate were explored systematically. Experimental results reveal that introduction of appropriate contents of the plasticizer PEG into the PLA/PEG systems results in the significant improvement of morphology, hydrophilicity, and mechanical properties while the high shape memory properties are still retained.

Admicellar polymerization, a novel technique for surface modification, was used in this work to enhance the compatibility between polymers with obviously different polarities, e.g., natural rubber (NR) and polylactic acid (PLA). The admicellar polymerization of methyl methacrylate over NR substrates (using potassium peroxodisulfate as an initiator) so-called poly(methyl methacrylate)–natural rubber (PMMA-ad-NR) was prepared and mixed with PLA at different contents (5, 10, and 15 wt%) in comparison to the simple PLA/NR blends. The monomer to initiator ratio was varied: 25:1, 50:1, and 100:1 corresponding to the admicelled PMMA molecular weight of 20,000, 30,000, and 40,000 g/mol, respectively. All PLA/PMMA-ad-NR blends showed good compatibility as evident by FE-SEM results revealing smooth boundary of PMMA-ad-NR domains in the PLA matrix. Moreover, the mechanical properties and thermal stability of PLA/PMMA-ad-NR blends were higher than those of PLA/NR blends, especially with increasing PMMA-ad-NR content up to 10 wt%. It was clear that the lowest molecular weight of the admicelled PMMA gave the highest toughness of PLA/PMMA-ad-NR blends.

Alpha-alumina is a ceramic with excellent chemical stability, mechanical property, high melting point, and insulating property; however, it shows poor workability due to its low fracture toughness. There are a lot of molding processes for α-alumina, such as press molding and extrusion methods. 3D printing is rapidly growing technology to make complex and precious moldings. However, there are still only a few descriptions on 3D ink-jet powder laminating printings for α-alumina due to no self-hydration hardening property. To achieve α-alumina moldings with the 3D ink-jet printers, powder fluidity of α-alumina powders and binders for bonding the powders should be investigated. The powders mixed with α-alumina at 20, 3.4 and 0.4 μm in sizes were adjusted to improve powder fluidity and packing density. Polyvinyl alcohol (PVA) or polyallylamine (PAA) including other additives was used as an ink. The addition of PVA on the adjusted powders made no chemical interaction of powders and no retention of shapes, but that of PAA formed the printed moldings. The relative packing density and compressive strength of the printed moldings were 40 % and 8.2 kPa, which was clearly depended on the printed directions due to the nozzle structure of printer head. Sintering the moldings at 1500°C caused near-net zero shrinkage and improved the maximum compressive strength at 3.6 MPa.

Carboxylated carbon nanotubes (C or cCNTs) were incorporated in polyethersulfone hollow fiber membranes (P HFMs) to improve the gas separation performance, i.e., pure gas permeability and ideal gas selectivity. The developed CP HFMs showed the remarkable improvement in thermal stability and mechanical strength as compared to that of the pristine P HFMs. The pure gas permeability of CO2, CH4, O2, and N2 gases for the HFMs were measured at 3 bar feed pressure and room temperature. It was observed that the presence of cCNTs in HFMs significantly improved the CO2 and O2 permeability for CP HFMs by 10.8-and 11.7- fold, respectively, as compared to that measured for P HFMs. Furthermore, the ideal gas selectivity for CO2/CH4, O2/N2, and CO2/N2 gas pairs for CP HFMs was also remarkably enhanced by almost 8.6-, 10.7-and 9.9-times, respectively, as compared to that measured for P HFMs. CP HFMs exhibited gas separation performance better than or comparable to that of the literature-reported CNTs-based membranes. Remarkably, the gas separation performance of CP HFMs crossed Robeson’s 2008 upper bound curve for O2/N2 gas-pair and was almost closer to the upper bound curves drawn by Robeson in 2008 for CO2/CH4 and CO2/N2 gas pairs. The improved separation performance can be attributed to the presence of cCNTs in HFMs. Thus, the results obtained in this study clearly showed that the CP HFMs can potentially be used as a membrane material for the industrially relevant gas separations.

This work decribes the enhancement of the electrical figures of merit of an Electrolyte Gated Thin-Film Transistor (EG-TFT) comprising a nanocomposite of n-type tungsten disulfide (WS2) nanotubes (NTs) dispersed in a regio-regular p-type poly(3-hexylthiophene-2,5-diyl) (P3HT) polymeric matrix. P3HT/WS2 nanocomposites loaded with different concentrations of NTs, serving as EG-TFTs electronic channel materials have been studied and the formulation has been optimized. The resulting EG-TFTs figures of merit (field-effect mobility, threshold voltage and on-off ratio) are compared with those of the device comprising a bare P3HT semiconducting layer. The optimized P3HT/WS2 nanocomposite, comprising a 60% by weight of NTs, results in an improvement of all the elicited figures of merit with a striking ten-fold increase in the field-effect mobility and the on/off ratio along with a sizable enhancement of the in-water operational stability of the device.

Natural rubber (NR) is expected to enhance impact strength of poly(lactic acid) (PLA). Because the polarity difference of NR and PLA leads PLA/NR blends having phase separation and poor mechanical properties, this research aimed to synthesize NR-graft-PLA (NR–PLA) via esterification of maleated NR (NR-MAH) with PLA. The role of NR–PLA used as a compatibilizer on mechanical and thermal properties of the PLA/NR blends was studied. Maximum grafted PLA level at 66.8% (w/w) was reached when NR-MAH was esterified with PLA [2/1 (w/w) PLA/NR-MAH] catalyzed by 0.05 M 4-dimethylaminopyridine at 140 °C. The addition of 5% (w/w) NR–PLA [36.6% (w/w) grafted PLA content] into PLA/NR blend [80/20 (w/w)] increased Izod impact strength of the neat PLA plate from 28.9 J/m to 62.7 J/m due to partial miscibility of blends attested by morphology analysis and Molau test. Hydrolytic degradation of PLA/NR blends with and without the addition of NR–PLA was also examined.

Poly(L-lactide)/poly(para-dioxanone) (PLLA/PPDO) (85/15 w/w) blends with 0, 1, 3, and 5 wt% poly(para-dioxanone-co-L-lactide) (PDOLLA) as a compatibilizer were prepared by solution coprecipitation. The in vitro hydrolytic degradation (HD) of blend bars with different contents of PDOLLA was studied by immersing the bars in a phosphate buffer solution (PBS) at pH 7.49. To estimate the degradation of blend bars, the weight loss, water absorption, thermal properties, surface morphology, and mechanical properties of blend bars, as well as the pH value changes of the PBS, were studied for 8 wk of HD. By adding 1 and 3 wt% PDOLLA, the weight loss of PLLA/PPDO (85/15 w/w) blends increased from 6.4 to 6.8 and 7.4% after 8 wk of HD, 6.2 and 15.6% increment, respectively, while, the average tensile strength of PLLA/PPDO (85/15 w/w) blends for 2–8 wk of HD increased from 25.8 to 29.0 MPa and 31.0 MPa, 12.4 and 20.2% increment, respectively. Considering their good mechanical properties and HD rate, the PLLA/PPDO (85/15 w/w) blends with 1 and 3 wt% PDOLLA are potential to be used as a medical implant material.

In this work we use a three-dimensional Pauli master equation to investigate the charge carrier mobility of a two-phase system, which can mimic donor-acceptor and amorphous-crystalline bulk heterojunctions. Our approach can be separated into two parts: the morphology generation and the charge transport modeling in the generated blend. The morphology part is based on a Monte Carlo simulation of binary mixtures (donor/acceptor). The second part is carried out by numerically solving the steady-state Pauli master equation. By taking the energetic disorder of each phase, their energy offset and domain morphology into consideration, we show that the carrier mobility can have a significant different behavior when compared to a one-phase system. When the energy offset is non-zero, we show that the mobility electric field dependence switches from negative to positive at a threshold field proportional to the energy offset. Additionally, the influence of morphology, through the domain size and the interfacial roughness parameters, on the transport was also investigated.

Land-Grant Universities including those that were developed under the second Morrill Act in 1890 have historically been a key resource for the best scientifically based information for agricultural production. The University of Maryland Eastern Shore (UMES) is situated on the Eastern Shore of Maryland, a critical area, with small farms and underserved farmers. This unique location serves as an interface between University specialty crop research and those farmers. While prices of crops such as corn and soy, which traditionally have been a major source of income for local farmers, have increased dramatically over the past years, small farms cannot generate enough income from these commodity crops alone, and a need alternatives for extra income. At UMES agricultural, chemical and material research specialists formed a special research and training cluster in which they work jointly on non-traditional and non-food related applications of specialty crops in the field of material research leading to non-traditional applications of such crops. Examples of such research are: (i) blending natural specialty crops extracts with polymers to develop natural and effective anti-foaling coating to prevent biofilm formation on objects including military ships, platforms etc.; (ii) using biocompatible polymeric chitosan-based blends as sorbents for reversible carbon dioxide capturing and controlled release in algae-growing reactors and in the process of transforming biomass into alcohol by fermentation to increase the effectiveness of biomass use. Only about 20% of students-researchers in the cluster are graduate students and the rest are undergraduates. The main focus is to provide undergraduate students with research experience as a powerful tool for their education and career development. Focus on students performing outstanding research through their undergraduate education is the main priority in UMES. Working on the material research projects described above, our material cluster has developed some educational practices for effectively involving undergraduate students into research. These practices include early involvement, the development of special workshops and training settings for fast project starts, working in small groups lead by more experienced students, picking projects that can be easily divided into small tasks suitable to undergraduate student’s schedules, and participation in scientific conferences for undergraduates and others. In this presentation we will review two material research projects for undergraduate students mentioned above and will show how our best practices are implemented in each of these projects.

In the early 1970s, experts predicted that the practical limit of ready-mixed concrete would be unlikely to exceed a compressive strength greater than 90 MPa [1]. Over the past two decades, the development of high-strength concrete has enabled builders to easily meet and surpass this estimate. The primary difference between high-strength concrete and normal-strength concrete relates to the compressive strength that refers to the maximum resistance of a concrete sample to applied pressure. Although there is no precise point of separation between high-strength concrete and normal-strength concrete, the American Concrete Institute defines high-strength concrete as concrete with a compressive strength greater than 45 MPa. Manufacture of high-strength concrete involves making optimal use of the basic ingredients that constitute normal-strength concrete. When selecting aggregates to obtain high-strength concrete, we consider strength, optimum size distribution, surface characteristics and a good bonding with the cement paste that affect compressive strength. Selecting a high-quality Portland cement and optimizing the combination of materials by varying the proportions of cement, water, aggregates, and admixtures is also necessary. Any of these properties could limit the ultimate strength of high-strength concrete. Pozzolans, such as fly ash and silica fume along with silicic acid, are the most commonly used mineral admixtures in high-strength concrete. These materials impart additional strength to the concrete by reacting with Portland cement hydration products to create additional Calcium Silicate Hydrate (CSH) gel, the part of the paste responsible for concrete strength; finally the most important admixture is polycarboxylate ether as super plasticizer. It would be difficult to produce high-strength ready-mixed concrete without using chemical admixtures. In this paper we study the use of high performance concrete (HPC) to obtain very narrow strong pre-fabricated elements for water conducting channels.

The meso-scale hexagonally packed order structures were obtained by solvent casting from the immiscible polymer blend solutions. The order structures were the result of phase separation occurred at the evaporation front during the solvent casting, the so-called dissipative system. The order domains were flat spheres or ellipses on the matrix surface depending on the combination of polymer blends and solvent, the diameter of spheres were tunable from 0.5 to 3 μm by the casting condition, such as the solvent used for mixing and the evaporation rate. Three blend systems, NBR/SBR, NBR/BR and PMMA/BR, formed two dimensional order structures with the domain size in μm-scale by solvent casting from those homogeneous solutions. The conditions to obtain the two dimensional meso-scale order structure were evaluated.

In this study the PANI/PHBV blends were prepared and thermal properties, crystallization behavior, microstructure of the blends were investigated. The PANI/PHBV blends were prepared by dissolution of PANI (emeraldine base doped with dodecylbenzenesulphonic acid, DBSA) and PHBV in chloroform and films were obtained by casting. PANI amount in the blend was varied from 0.1 to 1% wt. PANI/PHBV blends were characterized by FTIR spectroscopy and the thermal behavior were analyzed by differential scanning calorimeter (DSC) and thermogravimetric analysis (TGA). FTIR spectra of the pure PHBV and PANI/PHBV blend had similar peaks. However, blends spectra show an enlargement of bands, due interaction of the chain PANI with PHBV matrix. The crystallization behaviors were investigated using DSC, with at a scanning rate of 10oCmin−1. Curve of pure PHBV showed two melting peaks (159.1°C and 172.3°C). With the increase of PANI amount in the PHBV matrix, both of the melting peaks became wider and shifted to lower temperatures. The decrease trend of first and second melting points with increase of PANI amount, suggests a reduction in the crystallinity of the blends.

Supersulphated cements (SSC) are environmentally friendly binders that incorporate several raw materials, including byproducts. A systematic study was considered opportune considering the wide range of formulations found in the literature. The effect of the type and proportioning of components in the strength of SC was investigated using the Taguchi method to optimize the experimental work and to define the optimal conditions. The factors were: [A] %blast furnace slag (82.5-90%), [B] CaSO4 - alkaline activator ratio (1:0, 3:1, 1:1, 1:3 and 0:1), [C] type of CaSO4 (5 types) and [D] type of alkaline activator (portland cement, Ca(OH)2, KOH and NaCO3 and 2 combinations of these). Pastes were prepared and characterized for up to 28 days at 20°C. In general, for all values of [A] the best strength was for levels of [C] at 3:1, followed by the 1:1 and 1:0 ratios. The optimal conditions using the 28 day strength consisted of [A]= 82.5%, [B]= 3:1, [C]= flyorgypsum and [D] = portland cement, which developed excellent strength from day one and 35MPa. X-ray diffraction showed ettringite and C-S-H formation from the early ages. The microstructures showed dense matrices of reaction products well bonded to partially reacted slag grains, which in some cases showed rims of hydration products.