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81.
L. Di Giovacchino F. Angerosa L. Di Giacinto 《Journal of the American Oil Chemists' Society》1996,73(3):371-374
Variable quantities of leaves were added to ripe olives prior to extraction to determine their effect on the quality of the
resulting olive oil. The addition of 1–3% w/w leaves improved the organoleptic quality. An increase intrans-2-hexenal aldehyde content occurred, giving the pleasant flavor of “freshly cut grass.” This compound was produced by the
enzymatic breakdown of 13-L-hydroperoxide of linolenic acid in leaf homogenates. 相似文献
82.
83.
到目前为止TiO2是较为成熟的半导体光催化材料,但因TiO2分散性差、量子利用率低、比表面积小、难回收等问题难以工业化。多孔金属有机框架MOFs的引入可增强TiO2/MOFs复合材料的光吸收性能,提高电子-空穴对分离和提高回收率。基于TiO2/MOFs制备时前驱体添加顺序不同,综述了TiO2/MOFs的三种制备方法(即Ship-in-a-bottle法、Bottle-around-ship法、One-pot法)及TiO2/MOFs光催化机理与性能影响因素,并探讨不同MOFs与TiO2结合的作用机理。最后,对TiO2/MOFs存在的问题提出建议。 相似文献
84.
85.
以NA-5型氨酯胶粘剂作为金属五PU弹性胶料之间的胶粘剂,制作钢/PU橡胶/铝静件。研究了影响制件粘接强度的主要因素,给出了NA-5最佳粘接工艺。 相似文献
86.
It is shown that using transition metals, especially Mn(II) and Ag(I), during ozonation of humic substances in water allows important reductions in the content of organic matter. Characterization of the organic compounds resulting from ozonation was made by concentrating the sample through liquid-liquid extraction or derivation with PFBOA.HCl, along with the GC/MS and GC/ECD techniques. In total, 110 different organic compounds were identified using GC/MS; mainly carboxylic acids, aromatics, hydrocarbons, aldehydes, ketones, and furan-carboxylic acids. The percentages of elimination or formation levels reached during ozonation are discussed. 相似文献
87.
Nanocomposite Ni/ZrO2-AN catalyst consisting of comparably sized Ni metal and ZrO2 nanoparticles is studied in comparison with zirconia- and alumina-supported Ni catalysts (Ni/ZrO2-CP and commercial Ni/Al2O3-C) for steam reforming of methane (SRM) and for combined steam and CO2 reforming of methane (CSCRM). The reactions are performed under atmospheric pressure with stoichiometric amounts of H2O and CH4 or (H2O + CO2) and CH4 at 1073 K. Under a wide range of methane space velocity (gas hourly space velocity of methane GHSVCH4 = 12,000–96,000 ml/(h gcat.), the nanocomposite Ni/ZrO2-AN catalyst always shows higher activity and stability for both SRM and CSCRM reactions. The two supported Ni catalysts (Ni/ZrO2-CP and Ni/Al2O3-C) exhibit fairly stable catalysis under low GHSVCH4 but they are easily deactivated under high GHSVCH4 and become completely inactive when they are reacted for ca.100 h at GHSVCH4 = 48,000 ml/(h gcat.). The CSCRM reaction is carried out with different H2O/CO2 ratios in the reaction feed while keeping the molar ratio (H2O + CO2)/CH4 = 1.0, the results prove that the nanocomposite Ni/ZrO2-AN catalyst can be highly promising in enabling a catalytic technology for the production of syngas with flexible H2/CO ratios (ca. H2/CO = 1.0–3.0) to meet the requirements of various downstream chemical syntheses. 相似文献
88.
本文用量子化学从头算方法对金属离子与碱基活性位点的相互作用及其形成配合物的结构和性质进行理论研究.用HF/6-311G*优化鸟嘌呤及其金属离子(Na 、K 、Mg2 、Ca2 )配合物.在HF水平上,运用6-311G*基组计算Ⅰa和Ⅱa族金属离子(Na 、K 、Mg2 、Ca2 )与鸟嘌吟(Guanine)活性位点的相互作用.结果表明:Mg2 、Ca2 离子引起配位体的变形较Na 、K 离子大;Mg2 、Ca2 离子配合物比Na 、K 离子配合物稳定. 相似文献
89.
原子荧光光谱法测定搪瓷容器中微量溶出锑的研究 总被引:4,自引:0,他引:4
采用氢化物发生-原子荧光光谱法,用L-半胱氨酸预还原锑,对搪瓷容器中微量溶出锑进行了分析,讨论并确定了实验的最佳测定条件.结果表明,锑的检出限为0.235μg/L,回收率为89.0%~104.2%,相对标准偏差为0.8%.该法准确、快速、简便. 相似文献
90.
In drug delivery systems that use silicone elastomers as a diffusion matrix for the active drug, it is common to crosslink the material by the hydrosilylation reaction. In this platinum‐catalyzed reaction, vinyl groups on a polymer add to the methyl siloxane hydride (MHS) groups on a low molecular mass crosslinker. With an excess of crosslinker, a fast curing is achieved and a fully crosslinked material is formed. Unreacted MHS groups were shown to remain in the elastomer after curing because of the excess crosslinker. In this work, a simple procedure was developed to eliminate the unreacted MHS groups from the final product. We found that storage of the product at +40°C and 75% relative humidity for a few weeks will effectively destroy the residual MHS groups in the elastomer. The effects of varying levels of humidity, oxygen, and temperature on this postcuring procedure were studied. The amount of MHS groups was measured with NMR and IR spectroscopy. We also found that the hardness of the material increased by approximately 25% as a consequence of this postcuring treatment. This increase is probably due to a secondary crosslinking reaction between MHS and silanol groups. Heat treatment at higher temperatures led to an even further increase in the hardness and compression modulus. Because no MHS groups remained in the elastomer when this heat treatment was started, it is apparent that another secondary crosslinking reaction is occurring, probably silanol condensation. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2254–2264, 2002 相似文献