Melt processing of polyamide 12 and cellulose nanocrystals nanocomposites

The fabrication of nanocomposites of polyamide 12 (PA12) and cellulose nanocrystals (CNCs) isolated from cotton and tunicates is reported. Through a comparative study that involved solution‐cast (SC) and melt‐processed materials, it was shown that PA12/CNC nanocomposites can be prepared in a process that appears to be readily scalable to an industrial level. The results demonstrate that CNCs isolated from the biomass by phosphoric acid hydrolysis display both a sufficiently high thermal stability to permit melt processing with PA12, and a high compatibility with this polymer to allow the formation of nanocomposites in which the CNCs are well dispersed. Thus, PA12/CNC nanocomposites prepared by melt‐mixing the two components in a co‐rotating roller blade mixer and subsequent compression molding display mechanical properties that are comparable to those of SC reference materials. Young's modulus and maximum stress could be doubled in comparison to the neat PA12 by introduction of 10% (CNCs from tunicates) or 15% w/w (CNCs from cotton) CNCs. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42752.     

Electrochemical behavior of multifunctional graphene–polyimide nanocomposite film in two different electrolyte solutions

The effect of solvent on specific capacitance, bulk resistance, and charge/discharge capacity of graphene/polyimide composite films is studied by electrochemical methods. Composite films are synthesized by in situ condensation polymerization of poly (amic acid) in the presence of 50 wt % partly exfoliated graphene sheets followed by thermal curing at 250°C. Raman spectrum of the exfoliated graphene sheets show an increase in the ratio of I_D to I_G peak intensities from 0.167 to 0.222, suggesting increased defects in graphene basal planes. Electrochemical measurements carried out by using 0.4M potassium hexafluorophosphate (KPF₆) dissolved in propylene carbonate and N‐methylpyrrolidone at 25°C show that the composite system exhibits both pseudocapacitance and supercapacitance behaviors, with an average capacitance of 40 and 36.5 F g^?1, respectively. Bulk resistance of the composite obtained by using KPF₆–propylene carbonate electrolyte solution is 300% lower than that obtained in KPF₆–N‐methylpyrrolidone solution, with a fairly stable specific capacity of 85 μAhr g^?1, with 80% retention observed after 30 charge–discharge cycles. Fourier transform infrared spectroscopy measurements show shifts in the cyclic imide carbonyl peak from 1778 to 1774 cm^?1, which suggests that some form of interaction exists between the graphene and polyimide. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42673.     

Palladium‐Based Nanomaterials: A Platform to Produce Reactive Oxygen Species for Catalyzing Oxidation Reactions

Oxidation reactions by molecular oxygen (O₂) over palladium (Pd)‐based nanomaterials are a series of processes crucial to the synthesis of fine chemicals. In the past decades, investigations of related catalytic materials have mainly been focused on the synthesis of Pd‐based nanomaterials from the angle of tailoring their surface structures, compositions and supporting materials, in efforts to improve their activities in organic reactions. From the perspective of rational materials design, it is imperative to address the fundamental issues associated with catalyst performance, one of which should be oxygen activation by Pd‐based nanomaterials. Here, the fundamentals that account for the transformation from O₂ to reactive oxygen species over Pd, with a focus on singlet O₂ and its analogue, are introduced. Methods for detecting and differentiating species are also presented to facilitate future fundamental research. Key factors for tuning the oxygen activation efficiencies of catalytic materials are then outlined, and recent developments in Pd‐catalyzed oxygen‐related organic reactions are summarized in alignment with each key factor. To close, we discuss the challenges and opportunities for photocatalysis research at this unique intersection as well as the potential impact on other research fields.     

大直径重掺硅单晶工艺研究

重掺单晶一些独有的特性,能有效解决目前集成电路面临的一些难题。对大直径重掺硅单晶生长过程中的一些工艺进行了研究,主要包括掺杂方式和拉速设定两个方面,通过实验分析,选取了适宜的掺杂方式与拉速,最终生长出外形良好,符合电阻率目标要求的单晶。     

Preparation of c-axis textured SiC ceramics by a strong magnetic field of 6 T assisted gel-casting process

C-axis textured SiC ceramics were prepared by a strong magnetic field of 6 T assisted gel-casting and subsequent pressureless sintering. The optimal suspension parameters for gel-casting were determined by analyzing the influences of pH value and dispersant content on the stability and dispersibility of suspensions. The effect of sintering conditions on the texture development and properties of SiC ceramics was discussed. It was found that the increasing sintering temperature or holding time promoted the densification process of SiC ceramics. The c-axis of SiC grain was aligned parallel to the magnetic field by applying a strong magnetic field of 6 T. The degree of texture of SiC ceramics showed a slightly increasing trend with the increase of sintering temperature or holding time. When the samples were sintered at 1950 °C for 4 h or 6 h, the large elongated grains were formed in the samples, leading to the extremely evident anisotropic microstructure on different planes. Textured SiC ceramics exhibited the anisotropic bending strength.     

Poly(methyl methacrylate)‐grafted cellulose nanocrystals: One‐step synthesis,nanocomposite preparation,and characterization

Cellulose nanocrystals (CNCs) are ideal reinforcing agents for polymer nanocomposites because they are lightweight and nano‐sized with a large aspect ratio and high elastic modulus. To overcome the poor compatibility of hydrophilic CNCs in non‐polar composite matrices, we grafted poly(methyl methacrylate) (PMMA) from the surface of CNCs using an aqueous, one‐pot, free radical polymerization method with ceric ammonium nitrate as the initiator. The hybrid nanoparticles were characterized by CP/MAS NMR, X‐ray photoelectron spectroscopy, infrared spectroscopy, contact angle, thermogravimetric analysis, X‐ray diffraction, and atomic force microscopy. Spectroscopy demonstrates that 0.11 g/g (11 wt %) PMMA is grafted from the CNC surface, giving PMMA‐g‐CNCs, which are similar in size and crystallinity to unmodified CNCs but have an onset of thermal degradation 45 °C lower. Nanocomposites were prepared by compounding unmodified CNCs and PMMA‐g‐CNCs (0.0025–0.02 g/g (0.25–2 wt %) loading) with PMMA using melt mixing and wet ball milling. CNCs improved the performance of melt‐mixed nanocomposites at 0.02 g/g (2 wt %) loading compared to the PMMA control, while lower loadings of CNCs and all loadings of PMMA‐g‐CNCs did not. The difference in Young's modulus between unmodified CNC and polymer‐grafted CNC composites was generally insignificant. Overall, ball‐milled composites had inferior mechanical and rheological properties compared to melt‐mixed composites. Scanning electron microscopy showed aggregation in the samples with CNCs, but more pronounced aggregation with PMMA‐g‐CNCs. Despite improving interfacial compatibility between the nanoparticles and the matrix, the effect of PMMA‐g‐CNC aggregation and decreased thermal stability dominated the composite performance.     

Sorption of propylene and propane in polyurethane membranes containing silver nanoparticles

The preparation of a facilitated transport membrane of polyurethane (PU) containing silver nanoparticles is reported. The propylene and propane sorption was investigated aiming at the selective separation from C3s mixtures. The silver particles were photogenerated in situ into the polyurethane matrix using UV light radiation and silver triflate (AgCF₃SO₃) as precursor. The morphological properties of these membranes (PUAg) reveled great dispersion of silver particles, which size was smaller than 110 nm. The propylene solubility in PUAg resulted more than four times superior to the one for the pure PU membrane, revealing the high affinity between silver and propylene. Flory–Huggins theory was more accurate to describe the propylene sorption behavior in PUAg than Henry's model. The ideal solubility selectivity of PUAg membrane resulted 24.4, indicating that there is a good potential for an industrial application aiming at the separation of propylene/propane. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42916.     

Dissipative particle dynamics studies on the interfacial tension of A/B homopolymer blends and the effect of Janus nanorods

Janus nanorods are used as a novel rigid compatibilizer to improve the interfacial tension of incompatible A/B homopolymer blends. Dissipative particle dynamics (DPD) methods are preformed to explore the effect of Janus nanorods on the interfacial tension. The results show that Janus nanorods are a good compatibilizer only when the appropriate length is chosen, which is different from the traditional coil compatibilizer (surfactants and block copolymers). The length of the Janus nanorods can significantly influence their orientation through the competition between the entropic and enthalpic effects. The shorter Janus nanorods preferring “standing” have a better efficiency in improving the interfacial tension than the longer ones preferring “lying.” If we can control the orientation of the longer Janus nanorods, they are still a good compatibilizer. This simulation work can widen the application of Janus nanoparticles. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44098.