超声波辅助提取竹叶黄酮的研究

以青竹叶为原料、乙醇为萃取剂,利用超声波辅助提取其中的黄酮类物质。研究了溶剂浓度、料液比、搅拌速度、超声波功率、萃取时间、萃取次数等因素对产物得率的影响。结果表明:常温下,乙醇浓度为75%,料液比为1∶15(g/mL),搅拌速度为80r/min,超声功率为30 W,单次萃取时间为25 min,萃取3次,黄酮提取率最高为2.91%。与常规提取方法相比,超声波法具有省时节能、提取率高等优势。对油脂氧化抑制作用研究表明,竹叶黄酮具有良好的抗氧化性,可以作为天然绿色的抗氧剂进行开发。     

基于热诱导的绿咖啡油氧化过程解析及活性成分变化规律研究

绿咖啡油是一种富含生物活性成分的功能性油脂,贮藏过程中极易氧化酸败影响产品品质。本文以海南地区兴隆咖啡为原料提取绿咖啡油,系统研究在60 ℃加速贮藏36 d内氧化指标、生物活性成分及表征氧化的光谱特征峰变化。结果表明：过氧化值、茴香胺值、硫代巴比妥酸、总氧化值初始值分别为0.97±0.04 meq/kg、4.19±0.14、55.08± 1.98 nmol/mL、8.05±0.06,经过36 d的氧化分别显著升高到28.56±0.15 meq/kg、19.19±0.13、102.38±2.18 nmol/mL、133.43± 0.45。本研究中共鉴定出11种脂肪酸,在绿咖啡油氧化过程中,饱和脂肪酸与不饱和脂肪酸比值由1.14上升至1.49。利用高效液相色谱测定绿咖啡油中的二萜类物质和生育酚,咖啡豆醇、咖啡醇的初始含量分别为21.01±0.31 mg/g、23.44±0.52 mg/g,在氧化24 d后升高至8.21±0.10 mg/g、8.99±0.02 mg/g,随后含量趋于稳定。共定性出α、δ和γ-生育酚,总生育酚含量由初始的49.75±0.88 mg/100 g在氧化18 d达到最大值53.70±1.72 mg/100 g,在氧化结束时降至34.58± 0.05 mg/100 g。利用傅里叶变换红外光谱（FTIR）从特征官能团的角度分析绿咖啡油的氧化过程,油脂在3008、2927、2854、1745、1461、1375、1238、1164、721 cm^-1处有特征吸收峰。采用拉曼光谱技术表征绿咖啡油加速贮藏中的氧化变质,在1000~1800 cm^-1波段的峰强度有明显减弱趋势。本研究表明绿咖啡油在热诱导下的贮藏过程中发生了明显的氧化反应,可为提升绿咖啡油贮藏稳定性提供理论参考。     

Current Status of DIMOX in Synthesizing Al/Al2O3 by Aluminum Alloy

The processes, microstructures, properties and mechanisms of DIMOX in synthesizing Al/Al 2O 3 by Al-Mg-Si alloy are reviewed and their problems are considered mainly as following:non_homogeneous oxidation growth of Al/Al 2O 3 at the surface of melts and the porosity of Al/Al 2O 3 limites structural application of Al/Al 2O 3 composite. The mechanisms and models of microchannel,magnesium action,silicon action,and induction are outlined. Several problems which need to be noticed are pointed out,which are diffusion and transfer of oxygen in aluminium melts;the role of MgO and MgAl 2O 4 at outer layer;the reaction feature of solid_gas in the oxidation microstructures of Al_Mg_Si alloy;SiO 2 induction mechanism of silicon and its correlation with the mechanism of magnesium action in Al_Mg_Si alloy.     

秦川牛腿骨油的脂质组成分析

为了实现畜禽骨副产物的有效利用,本研究采用超声波辅助溶剂浸出法提取秦川牛腿骨油,应用高效液相色谱(HPLC)、气相色谱-质谱联用(GC-MS)法和基于多维质谱“鸟枪法”脂质组学技术(MDMS-SL)综合分析牛腿骨油的脂质组成,并对牛腿骨油的氧化稳定性、酸价和过氧化值等理化性质以及酚类化合物进行测定。结果表明,秦川牛腿骨油中含有丰富的甘油酯,其中甘油三酯(TAG)含量为93.85%,同时含有少量的甘油二酯(DAG)。在秦川牛腿骨油中共检测出24种脂肪酸,单不饱和脂肪酸和多不饱和脂肪酸含量分别为62.85%和2.18%;24种酰基肉碱,总含量为1.18 nmol·g^-1;17种鞘磷脂,总含量为35.36 nmol·g^-1;38种磷脂酰胆碱,总含量为22.16 nmol·g^-1。样品具有较强的氧化稳定性,酸价和过氧化值分别为16.43 mg KOH·g^-1和5.22 mmol·kg^-1,含有α-生育酚、α-三烯酚及γ-三烯酚3种酚类化合物。丰富的TAG、不饱和脂肪酸及鞘磷脂含量使秦川牛腿骨油在促进营养吸收、降血糖血脂及抗炎等方面具有较大的利用潜力。本研究为秦川牛腿骨油相关高附加值产品的开发提供了理论基础。     

Studies on the Oxidation of Weathered Coal with Nitric Acid

A raseach has been done on the possibility of producing nitriochumic acid fromweathered coal of Nantong,Sichuan,oxidised by nithic acid.The optimun reacting conditions,whichare found through the way of orthogonal experiment,are suggested as follows:concentration ofHON3 35%,rate of HON3 to coal 3.5,reacting take 15 min,and reaction temperature 369 K. Thecomposition of product is Wf 2. 91 %;Ag 14.06%;HAg 78.28%;Ng 1.62%.     

预氧丝原位炭化无粘结剂C/C复合材料氧化动力学研究

采用恒温热重法测定了在空气中，０．１ＭＰａ，６７３Ｋ到９７３Ｋ下预氧丝（即预氧化聚丙烯腈纤维）原位炭化无粘结剂Ｃ／Ｃ复合的氧化失重率；并利用扫描电镜分析了这种复合材料氧化前后的结构，氧化动力学测定结果表明：该材料在氧化开始时，其氧化速率随时间的增长而增大，然后随时间的延长而减小，并趋向恒定，研究表明：该材料中预氧丝与基体炭界面结合处是空气中氧的扩散通道，杂质为空气中氧的吸附起到了有附活性中心的催化     

改良型氧化沟工艺调试与运行

介绍了娄底市第一污水处理厂一期工程设计概况和采用的改良型氧化沟脱氮除磷工艺,分析了该污水处理厂调试、培菌过程中出现的问题,并针对性地采取了一系列改进措施.在进水远低于设计值的不利条件下,通过合理培菌,不到一个月系统启动成功.监测结果表明:该工艺运行可靠,出水水质稳定、达标.     

日粮添加酵母硒对鸡肉线粒体氧化损伤及细胞凋亡的影响

旨在研究日粮中添加酵母硒对白羽肉鸡宰后成熟过程中线粒体氧化损伤及细胞凋亡的影响。以饲喂不同酵母硒添加量日粮肉鸡的胸肉为研究对象,测定宰后成熟过程中鸡肉线粒体氧化损伤程度、抗氧化酶活性、Caspase-3和Caspase-9活性及肉嫩度的变化。结果表明,宰后成熟过程中,酵母硒饲喂组活性氧（reactive oxygen species,ROS）水平、线粒体膜通透性转换孔（mitochondrial permeability transition pore,MPTP）开放程度、线粒体膜通透性、Caspase-3以及Caspase-9活性均显著低于对照组（P<0.05）;硒含量、胞浆细胞色素c （cytochrome c,Cyt-c）还原水平、线粒体膜电位及谷胱甘肽过氧化物酶（glutathione peroxidase,GSH-Px）活性显著高于对照组（P<0.05）。酵母硒饲喂组总抗氧化能力（total antioxidant capacity,T-AOC）在宰后成熟初期显著高于对照组（P<0.05）,而在其他时间点虽有提高但差异不显著（P>0.05）。此外,酵母硒饲喂组肌原纤维小片化指数（myofibrillar fragmentation index,MFI）在宰后成熟过程中显著低于对照组,相对应的剪切力显著高于对照组（P<0.05）。由此可见,饲喂酵母硒通过降低鸡肉线粒体的氧化损伤进而抑制了细胞凋亡,最终减弱了肌原纤维蛋白的降解。     

Determination of nitrobenzene oxidation products by GC and1H-NMR spectroscopy using 5-iodovanillin as a new internal standard

The nitrobenzene oxidation method was modified to obtain more reproducible data and more structural information about lignin, not only by gas chromatography (GC) but also by proton nuclear magnetic resonance (¹H-NMR) spectroscopy for quantitative determination of the oxidation products and to simplify the procedures. The nitrobenzene oxidation mixture was directly extracted after acidification without preextraction of by-products. The direct extraction made the extractive step easy and gave reproducible data. 5-Iodovanillin was selected as a new internal standard. The reason for this selection was that 5-iodovanillin did not exist in the nitrobenzene oxidation products from any plant species and had an aldehyde group whose peak did not overlap with the other aldehyde peaks on an¹H-NMR spectrum. Thus, the use of 5-iodovanillin enabled us to quantifyp-hydroxybenzaldehyde, vanillin, and syringaldehyde in oxidation products on the basis of¹H-NMR analysis as well as GC. Furthermore, more information about the condensed structure of lignin was derived by comparing the¹H-NMR and GC analyses.Part of this work was presented at the 42nd Annual Meeting of the Lignin Symposium, Sapporo, October 1997     

Semi-quantitative method to evaluate the α-carbonyl content in lignin

A method to estimate the content of -carbonyl structures in lignin was developed. This method consists of two successive treatments: NaBD₄ treatment of pulp to reduce an -carbonyl structure in lignin, and nitrobenzene oxidation. NaBD₄ was used to convert an -carbonyl structure to a deuterium-labeled hydroxymethine structure. The ratio of D-vanillin [(HO)(H₃CO)C₆H₃CDO] to H-vanillin [(HO)(H₃CO)C₆H₃CHO] or that of their syringyl analogues obtained by nitrobenzene oxidation was used as the measure of the content of -carbonyl structure. Model experiments demonstrated that when sodium hydroxide was used as alkali for the nitrobenzene oxidation, the retention of deuterium at the side chain -position was very low due to the displacement of deuterium with hydrogen by an unknown reaction mechanism. In order to depress this unexpected displacement, the reaction conditions of the nitrobenzene oxidation were modified. The modified nitrobenzene oxidation employs 0.5mol/l of lithium hydroxide as a reaction medium instead of 2.0mol/l sodium hydroxide. By this modification, this method could successfully trace the formation and the degradation of the -carbonyl structure in milled wood lignins.This paper was presented in part at the 11th International Symposium on Wood and Pulping Chemistry, Nice, France, June 2001 and at the 46th Lignin Symposium, Kyoto, Japan, November 2001