A Controlled Design of Ripple‐Like Polyamide‐6 Nanofiber/Nets Membrane for High‐Efficiency Air Filter

The filtration capacity of fibrous media for airborne particles is restricted by their thick diameter, low porosity, and limited frontal area. The ability to solve this problem would have broad technological implications for various air filtration applications; despite many past efforts, it remains a great challenge to achieve. Herein, a facile and scalable strategy to fabricate the ripple‐like polyamide‐6 nanofiber/nets (PA‐6 NF/N) air filter via combining electrospinning/netting technique with receiving substrate design is demonstrated. This proposed approach allows the scaffold filaments to orderly embed into 2D PA‐6 nanonets layer with Steiner‐tree structures and nanoscale diameter of ≈20 nm, resulting in the ripple‐like membrane with extremely small pore size, highly porous structure, and hugely extended frontal surface, by facilely adjusting its pleat span and pleat pitch. These unique structural advantages enable the ripple‐like PA‐6 NF/N filter to filtrate the ultrafine particles with high removal efficiency of 99.996%, low air resistance of 95 Pa, and robust quality factor of >0.11 Pa^?1; using its superlight weight of 0.9 g m^?2 and physical sieving manner. This approach has the potentialities to give rise to a novel generation of filter media displaying enhanced filtration capacity for various applications thanks to their nanoscale features and designed macrostructures.     

Mineral Oil Barrier Testing of Cellulose‐Based and Polypropylene‐Based Films

Recycled cardboard has been identified as a major source of mineral oil hydrocarbon (MOH) contamination of foods. Identifying and using appropriate functional barriers is a mechanism through which this problem can be addressed. A number of cellulose‐based and biaxially oriented polypropylene (BOPP) films were evaluated as potential functional MOH barriers. The films were tested using a donor material, a paper containing MOH placed on one side of the film barrier and a paper which acted as the receptor on the other. Testing was performed at accelerated conditions of 60°C, the receptor analysed periodically for MOH. The results demonstrated that the cellulose‐based film types provided an MOH barrier of >3.5 years. This contrasted with the BOPP selected films, for which only the proprietary acrylic‐coated BOPP film provided an effective barrier to MOH migration. Further investigation of the MOH barrier properties of the proprietary acrylic‐coated BOPP film was undertaken. Various coating strategies were employed including increasing the coating application weight, increasing the number of coating lay downs and coating one or both surfaces of the film. It was found that an MOH barrier of 1.5 years when tested at 40°C could be achieved for the proprietary acrylic‐coated BOPP film; however, barrier effectiveness was dependent on the coating integrity of the film. Further work with a vertical form filler packaging machine and the use of a staining technique with transmission microscopy proved effective at highlighting and assessing the coating integrity of packets during a typical packaging operation. Copyright © 2014 John Wiley & Sons, Ltd.     

Determination and Prediction of the Lag Times of Hydrocarbons through a Polyethylene Terephthalate Film

Polymeric materials can be used as functional barriers to prevent contamination of food from the environment or from other packaging components, e.g. mineral oil hydrocarbons from printing inks. Polyethylene terephthalate (PET) is such a promising barrier material. From permeation studies found in the scientific literature lag times, diffusion coefficients or permeation rates towards organic chemicals could not derived because of the slow diffusion process of the permeants in PET. Knowledge about lag times or diffusion coefficients for different permeants, however, is essential for the evaluation of the barrier properties of PET films towards organic contaminants, e.g. mineral oil hydrocarbons. The aim of the study was to develop automated permeation testing method in order to determine the lag times of high‐barrier films. From the lag times, the diffusion coefficients as well as the partition coefficients of the alkanes were calculated. In addition, the permeated amounts were simulated by use of diffusion models. Therefore, the lag times can be predicted under different experimental conditions as used in the current study. The results of this study show that the investigated 12 µm PET film is an effective barrier towards mineral oil hydrocarbons. For example, the predicted lag time for n‐octane or n‐dodecane at 40°C is 8.8 and 210 years respectively. Copyright © 2014 John Wiley & Sons, Ltd.     

Investigation of CdTex and Cd1-xZnxTe Schottky Barrier Diode Structure Based γ-Ray Detectors

Cadmium Telluride (CdTe) and Cadmium Zinc Telluride (CdZnTe) based detectors have been developed for hard X-ray and γ -ray detection. These semiconducting materials have high resistivity because of the wide bandgap and also have high photon absorption efficiency because of the large atomic number (Z_Cd = 48, Z_Te = 52). CdTe and CdZnTe substrates (7 mm × 9 mm × 0.5 mm) with different stoichiometry were taken for the fabrication of γ-ray detectors. The substrate was prepared by polishing the bulk crystals grown by the rotational Bridgman method. Crystals with maximum electrical resistivity were grown in this way. For fabrication of Schottky barrier diode structures, the Schottky contacts were made by electroless deposition for gold (Au) and thermal evaporation for Indium (In). The Au/CdTe/In and Au/CdZnTe/In Schottky barrier diodes were linked to the charge sensitive preamplifier by gold wires. Then, I-V measurement and detector efficiency like charge collection performance with energy resolutions were analyzed at room temperature by using ⁵⁷Co and ¹³⁷Cs gamma sources. The good energy resolutions of ⁵⁷Co (122 KeV) and ¹³⁷Cs (662 KeV) sources are obtained for both CdTe and CdZnTe diode detectors.     

Wafer‐Scale Fabrication of High‐Performance n‐Type Polymer Monolayer Transistors Using a Multi‐Level Self‐Assembly Strategy

Wafer‐scale fabrication of high‐performance uniform organic electronic materials is of great challenge and has rarely been realized before. Previous large‐scale fabrication methods always lead to different layer thickness and thereby poor film and device uniformity. Herein, the first demonstration of 4 in. wafer‐scale, uniform, and high‐performance n‐type polymer monolayer films is reported, enabled by controlling the multi‐level self‐assembly process of conjugated polymers in solution. Since the self‐assembly process happened in solution, the uniform 2D polymer monolayers can be facilely deposited on various substrates, and theoretically without size limitations. Polymer monolayer transistors exhibit high electron mobilities of up to 1.88 cm² V^?1 s^?1, which is among the highest in n‐type monolayer organic transistors. This method allows to easily fabricate n‐type conjugated polymers with wafer‐scale, high uniformity, low contact resistance, and excellent transistor performance (better than the traditional spin‐coating method). This work provides an effective strategy to prepare large‐scale and uniform 2D polymer monolayers, which could enable the application of conjugated polymers for wafer‐scale sophisticated electronics.     

New Functional Polymers and Materials Based on 2,2′:6′,2″‐Terpyridine Metal Complexes

New inorganic–organic hybrid structures based on metal complexes have become of increasing interest over the last few decades in the search for new materials. Many different polypyridyl metal complexes have been investigated. Recently, a strong increase in interest regarding 2,2′:6′,2″‐terpyridine has been observed. In particular, octahedral bis‐2,2′:6′,2″‐terpyridine metal complexes offer the advantages of increased symmetry and, in the case of ruthenium(III )/ruthenium(II ) complexation, an entrance to a directed complexation technique. Apart from the combination with polymeric systems, ordered inorganic–organic structures on surfaces are becoming better understood concurrently with the development of sophisticated nanotechnology characterization techniques. There are many ongoing efforts that include terpyridine complex structures, especially concerning photophysical processes such as solar light to energy conversion. This review deals with the incorporation of terpyridine complexes into polymeric structures such as poly(ethylene glycol), poly(styrene), dendrimers, biomacromolecules, micelles, and resins, as well as the combination of terpyridine complexes with surfaces for electrocatalytic, photophysical, and self‐assembly purposes.