Changes in physical properties of methacrylonitrile (MAN)-grafted silk fibers

Changes in physical properties of silk fibers, grafted with methacrylonitrile (MAN), were investigated as a function of the weight gain. The weight gain increased steadily during the first 60 min of reaction and gradually attained an equilibrium value (60%) after about 4 h. The initial tensile resistance of silk fibers decreased by MAN grafting. The crystalline structure of silk fibers remained unchanged, regardless of MAN grafting, however. a minor and broad peak appeared in the X-ray diffraction curves of MAN-grafted silk fibers with a weight gain of 60%, corresponding to the unoriented MAN polymer attached inside the fibers. Molecular orientation of silk fibroin chains in the crystalline regions, evaluated from X-ray diffraction curves, did not change significantly, while both birefringence and isotropic refractive index decreased as the weight gain increased, implying that MAN polymer attached preferentially to the amorphous and not to the crystalline regions. Dynamic vis-coelastic measurements showed that the position at which the E′ value began to decrease shifted to a lower temperature as the weight gain increased. These findings suggest that the thermal movement of silk fibroin molecules was accelerated by the presence of the poly-MAN chains attached to the amorphous regions of silk fibroin fibers. © 1993 John Wiley & Sons, Inc.     

Effects of acidic fibroblast growth factor on neuronal activity of the parvocellular part in rat paraventricular nucleus

The effects of acidic fibroblast growth factor (aFGF) and its amino-terminal and carboxyl-terminal fragments (aFGF(1-15) and aFGF(114-140), respectively were examined on the neuronal activity in the parvocellular part of the paraventricular nucleus. As well known, this part contains a lot of corticotropin-releasing factor (CRF)-immunoreactive neurons. Application of 1 pg/ml and 2 pg/ml aFGF produced responses in 29.7% and 46.7% of neurons tested, respectively. Half or more than half of the responding neurons increased their discharge rate. Application of 0.2 ng/ml and 0.4 ng/ml aFGF(1-15) (1-15) also elicited response in 46.2% and 68.8% of neurons tested, respectively. Of these responding neurons, more than two third increased their firing rate. However, most of neurons tested for 0.67 ng/ml and 1.33 ng/ml aFGF(114-140) did not respond. Results suggest that aFGF and aFGF(1-15) promote the release of CRF through the activation of CRF-containing neurons.     

Room‐Temperature Printing of Organic Thin‐Film Transistors with π‐Junction Gold Nanoparticles

Printing semiconductor devices under ambient atmospheric conditions is a promising method for the large‐area, low‐cost fabrication of flexible electronic products. However, processes conducted at temperatures greater than 150 °C are typically used for printed electronics, which prevents the use of common flexible substrates because of the distortion caused by heat. The present report describes a method for the room‐temperature printing of electronics, which allows thin‐film electronic devices to be printed at room temperature without the application of heat. The development of π‐junction gold nanoparticles as the electrode material permits the room‐temperature deposition of a conductive metal layer. Room‐temperature patterning methods are also developed for the Au ink electrodes and an active organic semiconductor layer, which enables the fabrication of organic thin‐film transistors through room‐temperature printing. The transistor devices printed at room temperature exhibit average field‐effect mobilities of 7.9 and 2.5 cm² V^?1 s^?1 on plastic and paper substrates, respectively. These results suggest that this fabrication method is very promising as a core technology for low‐cost and high‐performance printed electronics.     

Effect of spark plasma sintering temperature on the phase equilibria and dielectric properties of BaTi2O5 ceramics

The effect of sintering temperature (ranging from 1055 to 1200 °C) on the phase ingredient and dielectric property of the nominal BaTi₂O₅ ceramics (starting with the Ba/Ti of 1:2) fabricated by a spark plasma sintering method were systematically studied. At the first stage, BaTi₂O₅ component was enhanced in the sintering temperature range of 1055–1120 °C; it turned out to be the dominant phase. For these BaTi₂O₅ phase dominated ceramics, the Curie temperature T _c rised on increasing the sintering temperature and saturated around 440 °C with the maximum dielectric constant of 500. Further increasing the sintering temperature, the decomposition of the obtained BaTi₂O₅ into BaTiO₃ extensively happened; the ceramics turned to be the BaTi₂O₅ and BaTiO₃ coexisting state. These ceramics can be characterized by two dielectric anomalies. One at ~420 °C stood for the phase transition of BaTi₂O₅ while the other at ~150 °C stood for the transition of BaTiO₃, which is exceptionally high as the normal BaTiO₃ ceramics. Further increasing the sintering temperature (until 1200 °C) would dramatically enhance the BaTiO₃ phase; the ceramics showed T _c at 130 °C with the maximum dielectric constant of 1800.     

Physical properties and dyeability of NaOH-treated silk fibers

Domestic (Bombyx mori) and wild (tussah, Antheraea pernyi) silk fabrics were treated with diluted NaOH solutions by the pad/batch method. The equillbrium moisture regain of tussah silk fibers increased steadily with alkaline treatment, while that of B. mori did not change. B. mori tensile strenght and elongation at break were slightly impaired. The average molecular orientation and crystallinity of both kinds of silk remained unchanged. Differential scanning calorimetry (DSC) and thermomechanical analysis(TMA) showed that the thermal behavior of B. mori silk was almost unaffected, while that of tussah exhibited slight changes in the temperature range 250–300°C. By dynamic mechanical measurements (DMA) it was elucidated that both storage and loss moduli of B. mori silk fibers decreased following NaOH treatment. On the other hand, tussah silk exhibited a noticeable upward shift of the major loss peak. Alkali-treated tussah silk fibers, dyed with an acid dyestuff, attained a lower degree of dye-bath exhaustion. © 1995 John Wiley & Sons, Inc.     

Grafting of vinyl monomers onto silk using redox systems. Yellowing of silk

The aim of this study is to investigate the influence of temperature, initiator concentration, and vinyl monomer on silk yellowing during grafting. A series of silk fabrics was treated at four different temperatures (70, 75, 80, and 88°C), with different concentrations of initiator in the range 1–4% owf, with and without methacrylamide (MAA) or 2-hydroxyethyl methacrylate (HEMA). By treating silk with ammonium persulphate (APS), in the absence of a monomer, the degree of silk yellowing increased linearly with increasing both initiator concentration and treatment temperature, indicating that the initiator plays a specific role in enhancing silk yellowing through macroradical formation. The graft copolymerization of MAA (with APS as the initiator) caused only slight changes in the intensity of silk yellowing compared to blank-treated fabrics. On the other hand, the use of HEMA resulted in a deeper yellowing of silk fabrics, especially in the 70–80°C temperature range, due to its higher reactivity and to the tendency to form a homopolymer, leaving unreacted macroradicals on silk fibroin backbone. Compared to APS, other initiators, such as 2,2′-azobis(isobutyronitrile) (AIBN) and 2–2′-azobis-(2-amidino propane) dihydrochloride (ADC), caused a significantly lower degree of silk yellowing when tested in the absebce of a monomer. The yellowness of silk fabrics tended to increase by grafting with HEMA, while decreased by grafting with MAA. The use of variable amounts of monomer (25–150% owf) did not influence the degree of yellowing with ADC as the initiator. The results reported in this study show that the extent of yellowing induced on silk fabrics by grafting MAA and HEMA with APS as the initiator can be limited by a suitable selection of the processing parameters (initiator concentration, temperature). Moreover, the use of both AIBN and ADC appears promising, owing to their negligible effect on silk yellowing. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 239–246, 1998     

Properties of poly(styrene)-“grafted” silk fibers and molecular weight of poly(styrene)

Poly(styrene) was grafted onto silk fibers in an aqueous medium, using ammonium persulphate initiator. Add-ons of up to 100% were achieved. The add-on increased linearly with the monomer concentration of the grafting system, all other factors remaining constant. The yield of the reaction attained about 80% and the extent of homopolymerization was negligible. The equilibrium moisture regain decreased noticeably with increasing add-on. Breaking load showed a tendency to increase in the 0–55% range of poly(St) content, while elongation at break and work of rupture decreased. The DSC endothermal peak at 315°C slightly shifted towards higher temperature by graft—copolymerization, and a new endothermal transition appeared beyond 400°C. TG measurements showed an increase of weight retention beyond 300°C for poly(St)-“grafted” silk fibers. The dynamic mechanical behavior was characterized by a shift to lower temperature of the loss modulus peak. The transverse dimension of the fibers increased with increasing add-on. The polymeric residue remaining after alkaline dissolution of silk fibroin showed a porous texture with a sponge-like morphology. The molecular weight of poly(St) removed from silk increased up to 120 kDa in the 0–55% add on range and then remained constant. The “Poly(St)/Silk” molar ratio increased linearly over the add-on range examined. © 1996 John Wiley & Sons, Inc.