Hydroliquefaction of subbituminous coal Effectiveness of pretreatment by organic reduction with Na or k

Hydroliquefaction of subbituminous Taiheiyo coal, without any pretreatment and after organic reduction, was carried out in the presence of tetralin using fine iron powder as catalyst. Two pretreatment procedures were used (A) reduction of coal with Na in liquid ammonia solution and (B) treatment with K in refluxing THF. Samples of treated coal with well-dispersed iron powder were prepared by co-reduction of coal coated with FeBr₂ using both procedures. Non-catalytic liquefaction of coal treated by A showed double the yield of hexane-solubles compared with that from liquefaction of the original coal while non-catalytic liquefaction of the coal treated by B roughly tripled the hexane-solubles yield and consumed the same amount of hydrogen. The presence of iron powder increased hexane-solubles by 5 wt% while increasing benzene-solubles by 13 wt% compared with non-catalytic liquefaction of treated coal by procedure B. The coals prepared by co-reduction (A and B) showed highest conversion (73 and 77%) along with highest yield of HS (38 and 43%). This significant effect on hydroliquefaction could be correlated with a slight increase of hydrogen atoms added to coal organic materials and the loosening of clusters of aromatic sheets.     

Effectiveness of both ZnCl2- and SnCl2-containing molten salt catalysts for hydrogenation of Big Ben coal in the absence of a solvent

Hydrogenation of Big Ben coal (Australian bituminous coal) with 9.8 MPa H₂ for 3h at 400 °C has been carried out using a batch autoclave system in the presence of a molten salt catalyst such as ZnCl₂, SnCl₂, ZnCl₂-KCl-NaCl (3:1:1 mol ratio) and SnCl₂-KCl (3:2). The hexane-soluble (HS) yield decreases in the order: SnCl₂-KCl, SnCl₂, ZnCl₂-KCl-NaCl, ZnCl₂. The use of SnCl₂-containing melt is characterized by higher yields of both HS and benzene-soluble (BS) fractions and the suppression of gas yield compared with the use of ZnCl₂. The average aromatic unit and the molecular weight of HS increase in the order: ZnCl₂, ZnCl₂-KCl-NaCl, SnCl₂, SnCl₂-KCl. Chromatographic separation of HS fractions indicates that the saturate content is lowest and polar-material content is highest with the SnCl₂-KCl melt: this fact coupled with the structural parameters suggests that HS material with SnCl₂-KCl melt has, on average, a reasonably-high-molecular-weight skeleton which has more alkyl chains and heteroatoms. Micrographs of resulting benzene-insoluble (Bl) materials clearly indicated that the Bl particles were larger when ZnCl₂ was used than when the other melts were used, the Bl particles in these cases being of similar size. Lewis acidity and the viscosity of the molten salt appear to be related, in part, to the size of the Bl particles.     

5mm厚铝合金双面搅拌摩擦焊接

对5mm厚的1050-H24铝合金板材进行了双面搅拌摩擦焊接(FSW)，重点研究了接头的拉伸性能和断裂部位及其影响因素。研究结果表明，一次焊接参数、二次焊接参数和焊接方向对双面FSW接头的拉伸性能和断裂部位有不同程度的影响。一次焊接参数的影响较小，而二次焊接参数的影响显著并且存在最佳取值。同向焊接的接头强度较高且断在前进侧(AS)或后退侧(RS)，而异向焊接的接头强度较低且只断在AS。在文中的试验条件下，1500r／min的旋转速度、400mm／min的二次焊速和同向焊接方式是最佳的工艺组合，接头最高强度达到母材强度的78％。     

Effects of phorbol esters,A23187 and vasopressin on oleate metabolism in isolated rat hepatocytes

Studies were conducted to compare the metabolic effects of vasopressin, 4β-phorbol-12-myristate-13-acetate (PMA) and A23187 on ketogenesis and oleate metabolism in isolated hepatocytes from fed rats. Vasopressin inhibited the formation of acid-soluble products from [1-¹⁴C]oleate (0.25 mM, 0.5 mM and 1 mM), the inhibition being most marked at low (0.25 mM) concentration of oleate. Conversion of [1-¹⁴C]oleate into¹⁴CO₂ and esterified products was stimulated by vasopressin. The stimulatory effect of this hormone on¹⁴CO₂ production was most marked at high (1 mM) concentration of oleate, whereas that on [1-¹⁴C]-oleate esterification was most marked at low (0.25 mM) concentration of oleate. These vasopressin actions were abolished when hepatocytes were incubated in the absence of calcium in the medium. Our results strongly suggest that both increase in esterification and increase in oxidation to CO₂ contribute to the anti-ketogenic action of vasopressin when oleate is added as substrate, although the relative extent of their contribution varies according to the oleate concentration. The anti-ketogenic action of vasopressin was mimicked by PMA but not by A23187. PMA also caused a stimulation of [1-¹⁴C]oleate esterification although the effect was diminished at 1 mM [1-¹⁴C]oleate. A23187 failed to affect [1-¹⁴C]oleate esterification. The metabolic effects of PMA were elicited in the absence of extracellular calcium, too. Conversion of [1-¹⁴C]oleate into¹⁴CO₂ was only slightly increased by both PMA and A23187 when 1 mM [1-¹⁴C]oleate was added as substrate. The marked stimulatory effect of vasopressin on¹⁴CO₂ production from [1-¹⁴C]oleate was not reproduced even by the combination of PMA and A23187. The possible involvement of protein kinase C and calcium mobilization in the regulation of oleate metabolism is discussed.     

Relationship between postmortem changes and browning of boiled, dried, and seasoned product made from Japanese common squid (Tedarodes pacificus) mantle muscle

ABSTRACT:  To clarify the process that possibly causes discoloration in boiled, dried, and seasoned squid products ("sakiika" or "ikakun" in Japanese), we investigated the relationship of squid freshness with the rate of browning using the boiled, freeze-dried, and ground squid product model. ATP and its related compounds in Japanese common squid ( Tedarodes pacificus ) decomposed gradually during storage, yielding hypoxanthine and ribose at 24 h postmortem. The browning rate of the model during preservation as revealed by the increase of the b * value showed a high coefficient in the linear regression against ribose content ( R² = 0.767). Only the model made from the squid stored for 24 h postmortem turned brown. These results strongly suggest that ribose produced during storage plays a major role in the browning of dried and seasoned squid products.     

Distribution of aflatoxin-producing Aspergillus flavus and Aspergillus parasiticus in sugarcane fields in the southernmost islands of Japan

The distribution of Aspergillus flavus and Aspergillus parasiticus in sugarcane field soils and on harvested sugarcane stems was studied on seven islands of Okinawa and Kagoshima Prefectures, the southernmost prefectures in Japan. With the use of a combination of dilution plate and plant debris plate techniques, the fungi were detected on all seven islands studied and in 74% of 53 soil samples. The fungi were also found on the cut surfaces of sugarcane stems from one of the islands. A. parasiticus was the predominant fungus, although many atypical A. parasiticus isolates that produced metulated conidial heads were also obtained. The proportions of isolates testing positive for aflatoxin production were ca. 89% (146 of 164) of all isolates and ca. 69% of A. flavus isolates. More than 40% of A. flavus isolates also produced G aflatoxins. Scanning electron microscopic observation of conidial wall texture was useful in distinguishing A. parasiticus from A. flavus. Cyclopiazonic acid, an indole mycotoxin, was never synthesized by any of the A. parasiticus or G aflatoxin-producing A. flavus isolates tested.     

Nitric acid-based partial-digestion method for selective determination of inorganic arsenic in hijiki and application to soaked hijiki

Because there is a great difference between the toxicity of inorganic arsenic (As) and organic As in food, the JECFA has set a PTWI value for inorganic As (iAs) rather than for total As. The difference in As toxicity makes it necessary to extract iAs completely from food samples for toxicological analysis, but complete extraction of As from most foods including seaweed has not been achieved to date. We developed a partial-digestion method that uses nitric acid as a solvent in order to extract almost all arsenicals from the solid matrix of hijiki (Hizikia fusiforme, a brown alga) samples. In this method, organic As species were not converted into iAs. HPLC/ICP-MS was then used to determine the concentration of iAs. Total As was measured by hydride generation-atomic absorption spectrometry. The adopted conditions for 0.1 g of ground fine powder sample were: 2 mL of 0.3 mol/L nitric acid; heating, 80 degrees C for 1 hr. Intra-laboratory validation of the method showed good precision and accuracy. The repeatability and intermediate precision for iAs were 1.5% and 1.5%, respectively. The LOD and LOQ for iAs were 0.14 and 0.46 mg/kg dry weight, respectively. Recovery studies performed by spiking 0.5 mg/kg dry weight as the LOQ level and by spiking 3 mg/kg dry weight as the iAs concentration of an un-spiked hijiki sample showed good accuracy. The method was applied to hijiki samples after a water soaking process and a water soaking and simmering process. The results suggested that the As concentration in hijiki after both processes was lower than that before the treatments and that the water soaking and simmering process reduced the iAs concentration much more effectively than the water soaking process.     

Microstructure and plasma corrosion behavior of yttria coatings prepared by the aerosol deposition method

Particle contamination arising from inner ceramic components of the plasma etching equipment has become a serious issue. Yttria (Y₂O₃) coatings prepared via aerosol deposition (AD) have demonstrated superior plasma resistance in the reduction of particle contamination. The superior particle contamination performance of Y₂O₃ coatings prepared by AD has been speculatively attributed to its unique microstructure; however, the relationship between the coatings’ microstructure and plasma corrosion behavior has been insufficiently clarified. Herein, we investigated the relationship between the microstructure and plasma corrosion behavior of Y₂O₃ coatings prepared by the AD method and compared the results with those for coatings prepared by other coating methods. When internal pores are present, these internal pores were selectively plasma corroded; plasma corrosion marks reflecting their pore shape were formed, and the surface roughness increased with increasing plasma exposure time. However, when no internal pores were present, as in the case of the AD coating, the surfaces were homogeneously corroded and maintained their initial surface. As the risk of particle contamination caused by the corrosion of the plasma-resistant coatings is greatly increased with surface roughness, we concluded that the Y₂O₃ coating prepared via AD will contribute greatly to reducing particle contamination.