Synthesis and electrochromic properties of aromatic polyimides bearing pendent triphenylamine units

A series of aromatic polyimides with pendent triphenylamine group were synthesized from equimolar mixtures of 4,4′-oxydianiline (ODA) and 4-(3,5-diaminobenzamido)triphenylamine (4), 4-(3,5-diaminobenzamido)-4′,4″-di-tert-butyltriphenylamine (t-Bu-4) or 4-(3,5-diaminobenzamido)-4′,4″-dimethoxytriphenylamine (MeO-4) with two aromatic tetracarboxylic dianhydrides (DSDA or 6FDA) via a conventional two-step procedure that included a ring-opening polyaddition to give poly(amic acid)s, followed by chemical imidization. These polyimides exhibited good solubility in polar organic solvents and could be solution-cast into flexible and strong films. They showed excellent thermal stability, with T_g values in the range of 284–309 °C. The polyimides derived from diamines t-Bu-4 and MeO-4 exhibited reversible electrochemical oxidation, accompanied by strong color changes with high contrast ratio and electrochromic stability. For the polyimides derived from diamine 4, the coupling reaction between the triphenylamine radical cations occurred during the oxidative process forming a tetraphenylbenzidine structure, which resulted in an additional oxidation state and color change together with enhanced near-IR absorption at fully oxidized state.     

Electrochemical Performance of PrBaCo2O5+δ and Sm0.5Sr0.5CoO3−δ Infiltrated Ce0.9Gd0.1O1.95 Cathodes

Cathodes with PrBaCo₂O_5+δ (PBC) and Sm_0.5Sr_0.5CoO_3−δ (SSC) infiltrated on Ce_0.9Gd_0.1O_1.95 (CGO) backbones are prepared using metal nitrates as precursors and ethanol as wetting agent. Electrochemical impedance spectra (EIS) are measured from cathode/CGO/cathode symmetrical cells in 400–650 °C under humidified air. The results indicate that interfacial area specific resistance (ASR) value decreases and then increases with infiltrate loading and minimum values occur at 50 wt.% loading (relative to sum of infiltrate and backbone) for both PBC and SSC infiltrates. ASR values of PBC infiltrated cathodes are lower than that of corresponding SSC infiltrated cathodes in general, and in particular ASR values as low as 1.36 × 10⁻² and 2.27 × 10⁻² Ω cm² are obtained at 650 °C in air for 50 wt.% PBC and 50 wt.% SSC infiltrated cathodes, respectively. Conductivity values of CGO electrolyte increase with infiltrate loading and agree with the reported values when the loading reaches 50 wt.%.     

FAK in Cancer: From Mechanisms to Therapeutic Strategies

Focal adhesion kinase (FAK), a non-receptor tyrosine kinase, is overexpressed and activated in many cancer types. FAK regulates diverse cellular processes, including growth factor signaling, cell cycle progression, cell survival, cell motility, angiogenesis, and the establishment of immunosuppressive tumor microenvironments through kinase-dependent and kinase-independent scaffolding functions in the cytoplasm and nucleus. Mounting evidence has indicated that targeting FAK, either alone or in combination with other agents, may represent a promising therapeutic strategy for various cancers. In this review, we summarize the mechanisms underlying FAK-mediated signaling networks during tumor development. We also summarize the recent progress of FAK-targeted small-molecule compounds for anticancer activity from preclinical and clinical evidence.     

Fabrication and Thermal Dissipation Properties of Carbon Nanofibers Derived from Electrospun Poly(Amic Acid) Carboxylate Salt Nanofibers

Polyimides (PIs) possess excellent mechanical properties, thermal stability, and chemical resistance and can be converted to carbon materials by thermal carbonization. The preparation of carbon nanomaterials by carbonizing PI‐based nanomaterials, however, has been less studied. In this work, the fabrication of PI nanofibers is investigated using electrospinning and their transformation to carbon nanofibers. Poly(amic acid) carboxylate salts (PAASs) solutions are first electrospun to form PAAS nanofibers. After the imidization and carbonization processes, PI and carbon nanofibers can then be obtained, respectively. The Raman spectra reveal that the carbon nanofibers are partially graphitized by the carbonization process. The diameters of the PI nanofibers are observed to be smaller than those of the PAAS nanofibers because of the formation of the more densely packed structures after the imidization processes; the diameters of the carbon nanofibers remain similar to those of the PI nanofibers after the carbonization process. The thermal dissipation behaviors of the PI and carbon nanofibers are also examined. The infrared images indicate that the transfer rates of thermal energy for the carbon nanofibers are higher than those for the PI nanofibers, due to the better thermal conductivity of carbon caused by the covalent sp² bonding between carbon atoms.     

Making reusable reaction-bonded silicon nitride crucibles for silicon casting from kerf-loss silicon waste

Silicon kerf loss during wafer slicing and the broken quartz crucibles after silicon casting are two major solid wastes from photovoltaic (PV) industry. Especially, the recycle of kerf-loss silicon has become an urgent issue because near 100 000 t of solid wastes are generated every year. One of the most meaningful recycle routes of the kerf-loss silicon is to make silicon nitride crucibles to replace the quartz crucibles. In this study, we demonstrated how this is feasible through acid leaching refining, slip casting, and nitridation. The reaction-bonded silicon nitride (RBSN) crucibles after oxidation were found pure enough for silicon ingot growth. More importantly, they could be reused after ingot growth. With the present examples, the potential of using the kerf-loss silicon for fine ceramics is prominent.     

The bone‐protective effect of a Taiwanese yam (Dioscorea alata L. cv. Tainung No. 2) in ovariectomised female BALB/C mice

BACKGROUND: Yam products have been marketed for treating postmenopausal syndromes. This study investigated the effects of Dioscorea alata L. cv. Tainung No. 2 (TNG yam) on the bone density of ovariectomised (OVX) female BALB/c mice and the mechanism whereby TNG yam exerted this effect. Sham and OVX control groups were fed a control diet while remaining OVX mice were randomly allocated into experimental diets, i.e. yam (630 g TNG powder kg^?1), E2 (20 mg 17β‐oestradiol kg^?1), or genistein (2 g genistein kg^?1) diet. After 12 weeks of feeding, the uterine weight, indices of bone mass and caecal short chain fatty acids were determined. RESULTS: Neither a yam nor genistein diet restored the OVX‐induced uterine atrophy as did the E2 diet. The femoral and lumbar bone mineral density (BMD) of mice fed the yam diet was greater than those of the sham group, respectively (P < 0.05 vs OVX control), while the lumbar BMD of yam and sham groups were similar (P > 0.05 vs sham). The femoral ash and calcium content in the yam group was significantly greater than that in the OVX control group, respectively (P < 0.05 vs OVX control). The total short chain fatty acid content in the caecum, only enhanced in the yam group, was not correlated with the calcium content of either bone or the plasma calcium level. CONCLUSION: TNG yam prevented loss of BMD and improved bone calcium status without stimulating uterine hypertrophy in OVX BALB/c mice. TNG yam may be beneficial for postmenopausal women for preventing bone loss. Copyright © 2008 Society of Chemical Industry     

Fabrication of cellulose nanofiber‐based ultrafiltration membranes by spray coating approach

Ultrafiltration membranes containing a cellulose nanofiber barrier layer were fabricated by the spray coating method, where the thickness and uniformity of the barrier layer were systematically investigated as a function of air pressure, flow rate and concentration of the cellulose nanofiber suspension. In specific, the surface morphology of the barrier layer was studied by scanning electron microscopy and its uniformity was examined by the fluorescence dye imaging method. The ultrafiltration performance of the membranes fabricated by the spray coating method was also compared with that of the membranes made by the knife coating approach using dextran molecules as probe, where the former consistently exhibited significantly higher permeation flux while remaining the same rejection ratio. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44583.     

Compatibilization of Poly(ethylene terephthalate)/Polypropylene Blends with Maleic Anhydride Grafted Polyethylene-Octene Elastomer

Blends of poly(ethylene terephthalate) (PET) and polypropylene (PP) at composition 80/20 with and without a compatibilizing agent were studied. Both materials are widely used in the soft drink bottle industry. The compatibilizing agent was a maleic anhydride grafted polyethylene-octene elastomer (POE-g-MA). The olefinic segment of POE is compatible with PP, whereas the maleic anhydride is affined with PET carbonyl groups. The effectiveness of the compatibilizing agent was evaluated using different techniques, such as Fourier transform IR spectroscopy, mechanical analysis, scanning electron microscopy, dynamic mechanical analysis, and rheological analysis. The results show that the addition of POE-g-MA promotes a fine dispersed-phase morphology, and improves process ability and toughness of these blends. Shifts in the glass-transition temperature of the PET phase and the increase in the melt viscosity of the compatibilized blends indicated enhanced interactions between the discrete PET and PP phases induced by the functional compatibilizer.     

Synthesis and properties of organosoluble polyimides based on 1,1-bis[4-(4-amino-2-trifluoromethylphenoxy)phenyl]cyclohexane

New aromatic diamine with cyclohexane cardo group substituted with trifluoromethyl group in the side chain, 1,1-bis[4-(4-amino-2-trifluoromethylphenoxy)phenyl]cyclohexane (II), was prepared through the nucleophilic substitution reaction of 1,1-bis(4-hydroxyphenyl)cyclohexane and 2-chloro-5-nitrobenzotrifluoride in the presence of potassium carbonate, to yield the intermediate dinitro compound I, followed by catalytic reduction with hydrazine and Pd/C to afford the diamine II. Fluorinated polyimides (IVa-g) were prepared from the II with various aromatic dianhydrides via thermal or chemical imidization of poly(amic acid). These polyimides had inherent viscosity ranging from 0.72 to 1.16 dl/g and showed excellent solubility in a variety of organic solvents. They were soluble in a concentration of 10% in the amide polar solvent, and 1-5% in the other testing solvents. IV films showed good mechanical properties, excellent thermal stability. The 10% weight loss temperature was above 476 °C in nitrogen or air, and the glass transition temperature was recorded at 214-278 °C. In comparison of the IV series with the analogous nonfluorinated polyimides (V series) based on 1,1-bis[4-(4-aminophenoxy)phenyl]cyclohexane (II′), IV series revealed better solubility, lighter-colored and lower dielectric constants and moisture absorptions. Their films had cut-off wavelengths in the range of 364-414 nm, b^* value (a yellowness index) ranging from 3.3 to 66.3, dielectric constants of 3.02-3.55 (1 MHz), with moisture absorption of 0.16-0.36 wt%.