Concept for automated computer-aided identification and evaluation of potentially non-compliant food products traded via electronic commerce

The online marketplace for food products is continually expanding and all types of food and beverages can now be purchased over the internet. It is primarily the responsibility of the food business operator to ensure compliance with food safety law. However, the competent authorities are tasked with controlling the e-food sector as part of their regulatory duties to protect consumer health and to prevent fraud, regardless of the sales channel being used. For this purpose, a new software prototype concept was developed that automatically identifies and evaluates potentially non-compliant e-food products. The prototype was developed using a modular architecture comprising a research tool, an image analysis tool, and a monitoring tool. User-defined thresholds are applied to assess the reliability of the retrieved data. Results that are not deemed reliable enough can be reworked using a computer-aided evaluation interface. The research tool utilizes both internet search engines and customized search algorithms. A multi-stage filtering process is performed to limit the sites according to defined criteria (e.g. food product merchants only). The data acquisition module stores all matching data from webpages for later analysis and preservation of evidence. In another module, automatic recognition of a site's legal notice (impressum) is carried out for the respective vendor within whose online shop a potentially non-compliant food product is being offered. The image analysis tool performs logo recognition to enrich the text-based information of websites, thus providing additional visual information. The monitoring tool performs regular automated monitoring of e-food vendors, products and ingredients. The proof of principle of the prototype was achieved by conducting a web search for hazardous food products containing synephrine and caffeine. In total, 1242 product offerings on the internet for suspicious food products were identified among the 8683 search results. The software prototype has potential to enhance consumer protection and food safety with respect to e-foods.     

High performance carbon nanotube spun yarns from a crosslinked network

We report a new method to create covalent crosslinks between carbon nanotubes (CNTs) with reduced intertube and interbundle spaces, for improving the mechanical properties of CNT spun yarns. This is achieved through the pretreatment of a CNT yarn with 4-carboxybenzenediazonium tetrafluoroborate to form reactive carboxyphenyl groups on the CNT sidewalls. These carboxyphenyl groups are then reacted with a multifunctional crosslinker hexa(methoxymethyl) melamine, leading to a highly crosslinked network within the yarn. The CNT yarns were characterized by X-ray photoelectron spectroscopy, focused ion beam scanning electron microscope, and also assessed for their mechanical properties. The results showed that the method developed effectively improved mechanical properties of CNT yarns: we are able to produce CNT yarns with a tensile strength up to 2.5 GPa and Young’s modulus 121 GPa.     

温度场对iPP/CAB体系形态结构的影响

利用扫描电子显微镜研究了温度场对iPP/CAB共混物样品形态结构的影响,研究发现共混物样品在150℃的硅油或者140℃的真空烘箱中放置时,随着热处理时间的增加,分散相尺寸会不断增大;并且样品在硅油中放置时,分散相尺寸增大的速度更快.     

Preparation,morphology and properties of acid and amine modified multiwalled carbon nanotube/polyimide composite

The precursor of polyimide, polyamic acid, was prepared by reacting 4,4′-oxydianiline (ODA) with 3,3′,4,4′-benzophenone tetracarboxylic dianhydride (BTDA). Unmodified, acid-modified and amine-modified multiwall carbon nanotubes (MWCNT) were separately added to the polyamic acid and heated to 300 °C to produce polyimide/carbon nanotube composite. Scanning electron microscopic (SEM) and transmission electron microscopic (TEM) microphotographs reveal that acid-modified MWCNT and amine-modified MWCNT were dispersed uniformly in the polyimide matrix. The effect of the acid and amine-modified MWCNTs on the surface and volume electrical resistivities of MWCNT/polyimide composites were investigated . The surface electrical resistivity of the nanocomposites decreased from 1.28 × 10¹⁵ Ω/cm² (neat polyimide) to 7.59 × 10⁶ Ω/cm² (6.98 wt% unmodified MWCNT content). Adding MWCNTs influenced the glass transition temperatures of the nanocomposites. Modified MWCNTs significance enhanced the mechanical properties of the nanocomposites. The tensile strength of the MWCNT/polyimide composite was increased from 102 MPa (neat polyimide) 134 MPa (6.98 wt% acid modified MWCNT/polyimide composites).     

Highly ordered graphene architectures by duplicating melamine sponges as a three-dimensional deformation-tolerant electrode

In this study, macroscopic graphene-wrapped melamine foams (MF-G) were fabricated by an MF-templated layer-by-layer (LBL) assembly using graphene oxide as building blocks, followed by solution-processed reduction. By concisely duplicating sponge-like, highly ordered three-dimensional architectures from MF, the resulting MF-G with an interconnected graphene-based scaffold and tunable nanostructure was explored as compressible, robust electrodes for efficient energy storage. A thin layer of pseudocapacitive polypyrrole (PPy) was then attached and uniformly coated on MF-G, resulting in a well-defined core–double-shell configuration of the MF-G-PPy ternary composite sponges. The as-assembled devices exhibited enhancement of supercapacitor performance, with a high specific capacitance of 427 F·g^?1 under a compressive strain of 75% and an excellent cycling stability with only 18% degradation after 5,000 charge–discharge cycles. Besides, the MF-G-PPy electrode maintained stable capacitance up to 100 compression–release cycles, with a compressive strain of 75%. These encouraging results thus provide a new route towards the low-cost, easily scalable fabrication of lightweight and deformation-tolerant electrodes.

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Hydrophilic bismuth sulfur nanoflower superstructures with an improved photothermal efficiency for ablation of cancer cells

Nanomaterials with intense near-infrared (NIR) absorption exhibit effective photon-to-thermal energy transfer capabilities and can generate heat to ablate cancer cells, thus playing a pivotal role in photothermal cancer therapeutics. Herein, hydrophilic flower-like bismuth sulfur (Bi₂S₃) superstructures with uniform size and improved NIR absorption were controllably synthesized via a facile solvothermal procedure assisted by polyvinylpyrrolidone (PVP), which could adjust the product morphology. Induced by an 808-nm laser, the as-prepared Bi₂S₃ nanoflowers exhibited much higher photothermal conversion efficiency (64.3%) than that of Bi₂S₃ nanobelts (36.5%) prepared in the absence of PVP. This can be attributed not only to the Bi₂S₃ nanoflower superstructures assembled by 3-dimensional crumpled-paper-like nanosheets serving as many laser-cavity mirrors with improved reflectivity and absorption of NIR light but also to the amorphous structures with a lower band gap. Thus, to achieve the same temperature increase, the concentration or laser power density could be greatly reduced when using Bi₂S₃ nanoflowers compared to when using Bi₂S₃ nanobelts, which makes them more favorable for use in therapy due to decreased toxicity. Furthermore, these Bi₂S₃ nanoflowers effectively achieved photothermal ablation of cancer cells in vitro and in vivo. These results not only supported the Bi₂S₃ nanoflowers as a promising photothermal agent for cancer therapy but also paved an approach to exploit new agents with improved photothermal efficiency.

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Brown ceramic pigments based on chromium(III)-doped titanite obtained by spray pyrolysis

Cr-doped titanite (CaTiSiO₅) pigments were synthesized through spray pyrolysis of aerosols generated from aqueous solutions containing colloidal silica, calcium chloride, titanium(IV) oxychloride and chromium(III) nitrate. This process yielded amorphous powders with spherical morphology and broad size distribution (<10 μm) after thermal decomposition at 600 °C. The titanite phase was obtained by further calcination at 800 °C without any addition of flux agents. The brown color of the pigments can be attributed mainly to the existence of Cr(IV) ions occupying both, octahedral positions of Ti(IV) and tetrahedral position of Si(IV), together with a small amount of Cr(III) present as Cr₂O₃. The optimum pigment obtained by this method corresponded to a Cr/titanite mole ratio of 0.04.     

Effects of superfine silk protein powders on mechanical properties of wet‐spun polyurethane fibers

Mechanical measurements were employed to investigate the effects of three types of superfine silk protein powder on tensile strength, elongation, and elasticity of wet‐spun Pellethane^® 2363‐80AE polyurethane (PU) fiber. These superfine silk protein powders included undegummed silk (with both native silk fibroin and sericin, water insoluble), native silk fibroin (with native silk fibroin only, water insoluble), and regenerated silk fibroin (with regenerated silk fibroin only, water soluble) in powder form. Experimental data derived from the mechanical measurements illustrated that the miscibility between the PU and regenerated silk fibroin were superior to that between PU and the other two silk proteins. This may be attributed to the similar chemical structure and microphase separation of PU and regenerated silk fibroin with lower molecular weight than native silk fibroin. This preliminary work may provide some information for biomimetic processing of silk‐inspired PU biofibers, which combine elasticity of synthetic PU with biofunction of natural silk fibroin for special biomedical applications. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Quantitative effects of synthesis conditions on oil absorptive properties of oil gels based on EPDM/4‐tert‐Butylstyrene

The oil absorption properties of porous polymeric gels are dependent on their synthesis conditions. In this work, we have investigated whether it is feasible to find a quantitative relationship between the synthesis conditions of porous poly(EDPM/4‐tert‐Butylstyrene) gels and their behavior in the kerosene absorption through a factorial design of experiments. For this purpose, a series of such oil gels have been synthesized in toluene with various divinylbenzene (DVB) and EPDM contents. The kerosene absorbency and kerosene‐absorption kinetics of oil gels were determined. Finally, empirical models correlating the synthesis conditions with the kerosene absorbency (Q_eq) and kerosene‐absorption kinetic constant (K) were calculated; it was observed that lower the DVB concentration and higher the EPDM fraction in the monomeric mixtures, the higher the kerosene absorbency. With regard to the kerosene‐absorption kinetics, the largest K value was achieved with the lowest DVB concentration and the highest EPDM fraction. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009