In order to improve the solubility of C60 fullerene in conventional solvents, grafting of hydrophilic poly(ethylene oxide) (PEO) by utilizing the radical-trapping nature of C60 fullerene was investigated. Macroazo initiators containing a poly(ethylene oxide) unit, known as Azo-PEO, were prepared at various molecular weights by the reaction of 4,4′-azobis(4-cyanopentanoyl chloride) with poly(ethylene glycol) methyl ether. PEO radicals formed by thermal decomposition of Azo-PEO were successfully trapped by C60 fullerene to give PEO-grafted C60 fullerene. Their structures were confirmed by FT-IR spectroscopy, size exclusion chromatography, UV-vis spectroscopy, and differential scanning calorimetry. When Azo-PEO with low-molecular weight was reacted with C60 fullerene, a bis-adduct, C60-(PEO)2, and a tetrakis-adduct, C60-(PEO)4, were formed. In contrast, in reactions with Azo-PEO of higher molecular weight, only the bis-adduct was formed, and no formation of the tetrakis-adduct was observed. The structure of bis-adduct was found to be 1,4-type. The solubility of C60 fullerene in water, THF, methanol, and other conventional organic solvents was remarkably improved by grafting of PEO. In addition, the thermal stability of PEO was dramatically increased by grafting onto C60 fullerene. 相似文献
Summary: Silk fibroin cast film was prepared using a ternary solvent system of CaCl2/CH3CH2OH/H2O (1/2/8 in mole ratio). A drying temperature at casting influenced crystal structure of fibroin. When a drying temperature was set lower than 9 °C, the cast film became amorphous. When a drying temperature was set higher than 40 °C, a fibroin film of silk‐II structure was obtained. In order to produce a fibroin film of silk‐I structure, a preferable temperature range was from 20 to 26 °C. The crystal transformation from random coil structure into silk‐I could be made through exposure of an amorphous film to water vapor. As for the crystal transformation from silk‐I into silk‐II, the treatment with a glycerin solution was effective. In the course of the treatment a film showed self‐thinning and self‐expanding. The expansion ratio exceeded 40% at maximum. The film produced accompanying self‐expansion was ductile in nature.
The apparent self‐expansion percentage as a function of initial thickness of the film. The ductility of the film was classified into four stages from the observation of recovery behavior after folding: ?, very soft; ?, soft; ?, middle; ?, hard (see Figure 5 ). 相似文献
A soluble and stable one-handed helical conjugated polymer without the coexistence of any other chiral moieties was successfully synthesized by asymmetric-induced polymerization of a chiral monomer having two hydroxyl groups followed by desubstitution of the chiral groups in a solid membrane state. The reason for the success was the polymer reaction was carried out in the membrane state. This is an alternative method to obtain such a unique chiral polymer which was obtained only by the helix-sense-selective polymerization (HSSP) we reported before. In addition the efficiency of the chiral induction was higher than that of the HSSP. It is interesting that the “Membrane state” acted like as if a protecting group. 相似文献
The effect of citric acid (CA) addition was studied on the HDS of thiophene over Co–Mo/(B)/Al2O3 catalysts. The catalysts were characterized by means of LRS, Mo K-edge EXAFS, NO adsorption capacity measurements, and UV–vis spectra. The catalysts were subjected to a chemical vapor deposition (CVD) technique using Co(CO)3NO as a precursor of Co in order to get deeper insights into the effect of citric acid addition. It was shown that the HDS activity was enhanced by the citric acid addition up to the CA/Mo mole ratio of around 1 and leveled off with further addition. The amount of Co anchored by the CVD was increased by the addition of citric acid, suggesting an increase in the dispersion of MoS2 particles on the catalyst by the simultaneous presence of Co, Mo and citric acid, in conformity with the increase in the NO adsorption capacity. In contrast to Co–Mo catalysts, the edge dispersion of MoS2 particles in Mo/B/Al2O3 was not affected by the addition of citric acid. The LRS, UV–vis spectra and Mo K-edge EXAFS showed that Co–CA and Mo–CA surface complexes are formed by the addition of citric acid. The Co–CA surface complex is more preferentially formed on CoMo/Al than on CoMo/B/Al, in agreement with a greater promoting effect of citric acid at a lower CA/Mo mole ratio for CoMo/Al than for CoMo/B/Al. 相似文献
Metallurgical and Materials Transactions B - The dissolution and passivation of pure Cu and Cu-5 wt pct Ag anodes in H2SO4-CuSO4 electrolyte were investigated by a direct... 相似文献
Food-borne outbreaks caused by Listeria monocytogenes have been recognized in US and European countries. Only sporadic cases, of neonatal listeriosis, have been reported in Japan. Since L. monocytogenes has been often isolated from foods in Japan, food-borne outbreaks potentially could have occurred. In February 2001, L. monocytogenes serotype 1/2b was isolated from a washed-type cheese during routine Listeria monitoring of 123 domestic cheeses. Further samples from products and the environments at the plant that produced the contaminated cheese were examined for L. monocytogenes. L. monocytogenes serotype 1/2b was detected in 15 cheese samples, at most probable number that ranged from <30 to 4.6 x 10(9)/100 g, and in environmental samples. Studies with people who had consumed cheese from the plant revealed 86 persons who had been infected with L. monocytogenes. Thirty-eight of those people had developed clinical symptoms of gastroenteritis or the common cold type after the consumption of cheese. Isolates from those patients exhibited the same serotype, pathogenicity for mice and HeLa cells, DNA fingerprinting patterns and PCR amplification patterns. From the epidemiological and genetic evidence, it appeared that the outbreak was caused by cheese. This is the first documented incidence of food-borne listeriosis in Japan. 相似文献
Intrinsically disordered proteins (IDPs) that lack stable conformations and are highly flexible have attracted the attention of biologists. Therefore, the development of a systematic method to identify polypeptide regions that are unstructured in solution is important. We have designed an “indirect/reflected” detection system for evaluating the physicochemical properties of IDPs using nuclear magnetic resonance (NMR). This approach employs a “chimeric membrane protein”-based method using the thermostable membrane protein PH0471. This protein contains two domains, a transmembrane helical region and a C-terminal OB (oligonucleotide/oligosaccharide binding)-fold domain (named NfeDC domain), connected by a flexible linker. NMR signals of the OB-fold domain of detergent-solubilized PH0471 are observed because of the flexibility of the linker region. In this study, the linker region was substituted with target IDPs. Fifty-three candidates were selected using the prediction tool POODLE and 35 expression vectors were constructed. Subsequently, we obtained 15N-labeled chimeric PH0471 proteins with 25 IDPs as linkers. The NMR spectra allowed us to classify IDPs into three categories: flexible, moderately flexible, and inflexible. The inflexible IDPs contain membrane-associating or aggregation-prone sequences. This is the first attempt to use an indirect/reflected NMR method to evaluate IDPs and can verify the predictions derived from our computational tools. 相似文献
This article presents a consistent techno-economic assessment and comparison of CO2 capture technologies for key industrial sectors (iron and steel, cement, petroleum refineries and petrochemicals). The assessment is based on an extensive literature review, covering studies from both industries and academia. Key parameters, e.g., capacity factor (91-97%), energy prices (natural gas: 8 €2007/GJ, coal: 2.5 €2007/GJ, grid electricity: 55 €/MWh), interest rate (10%), economic plant lifetime (20 years), CO2 compression pressure (110 bar), and grid electricity CO2 intensity (400 g/kWh), were standardized to enable a fair comparison of technologies. The analysis focuses on the changes in energy, CO2 emissions and material flows, due to the deployment of CO2 capture technologies. CO2 capture technologies are categorized into short-mid term (ST/MT) and long term (LT) technologies. The findings of this study identified a large number of technologies under development, but it is too soon to identify which technologies would become dominant in the future. Moreover, a good integration of industrial plants and power plants is essential for cost-effective CO2 capture because CO2 capture may increase the industrial onsite electricity production significantly.For the iron and steel sector, 40-65 €/tCO2 avoided may be achieved in the ST/MT, depending on the ironmaking process and the CO2 capture technique. Advanced LT CO2 capture technologies for the blast furnace based process may not offer significant advantages over conventional ones (30-55 €/tCO2 avoided). Rather than the performance of CO2 capture technique itself, low-cost CO2 emissions reduction comes from good integration of CO2 capture to the ironmaking process. Advanced smelting reduction with integrated CO2 capture may enable lower steel production cost and lower CO2 emissions than the blast furnace based process, i.e., negative CO2 mitigation cost. For the cement sector, post-combustion capture appears to be the only commercial technology in the ST/MT and the costs are above 65 €/tCO2 avoided. In the LT, a number of technologies may enable 25-55 €/tCO2 avoided. The findings also indicate that, in some cases, partial CO2 capture may have comparative advantages. For the refining and petrochemical sectors, oxyfuel capture was found to be more economical than others at 50-60 €/tCO2 avoided in ST/MT and about 30 €/tCO2 avoided in the LT. However, oxyfuel retrofit of furnaces and heaters may be more complicated than that of boilers.Crude estimates of technical potentials for global CO2 emissions reduction for 2030 were made for the industrial processes investigated with the ST/MT technologies. They amount up to about 4 Gt/yr: 1 Gt/yr for the iron and steel sector, about 2 Gt/yr for the cement sector, and 1 Gt/yr for petroleum refineries. The actual deployment level would be much lower due to various constraints, about 0.8 Gt/yr, in a stringent emissions reduction scenario. 相似文献
Conventional highwall mining extracts coal with an auger machine or a continuous miner from exposed seams at the base of opencut or strip operations. However, under poor strata and high stress conditions, highwall mining cannot be conducted due to pillar and roof failures. In such cases, punch highwall mining is more effective than the conventional highwall mining. This paper describes conventional highwall mining and punch highwall mining systems and discusses the stability of the highwall due to punch highwall mining at opencut coal mines. 相似文献