LD7铝合金热变形行为的实验研究

在G1eeble-1500热模拟试验机上对LD7铝合金试样在变形程度为60％，变形温度为360～480℃、变形速率为0．0l～1s^-1的条件下进行等温压缩试验，然后对其进行固溶处理。根据试验结果分析热变形参数对合金流动应力和固溶之后显微组织的影响，可以得到如下结论：LD7铝合金是动态回复型合金，合金的流动应力随温度的升高而降低，随应变速率的升高而升高；合金的晶粒尺寸随温度的升高而增大，随变形程度和变形速率的增大而减小。     

LD7铝合金时效工艺的研究

通过试验系统地研究了ＬＤ７铝合金的单级和两级时效工艺。结果表明，与传统的单级时效相比，两级时效在不降低室温强度，硬度的前提下，可显著提高合金的电导率及高温性能。     

用相变方法制取高纯度超细钽粉的研究

报导了通过相变热处理使Ｋ２ＴａＦ７晶体参数发生变化，以利于制取高纯度超细钽粉的实验依据和结果。结果表明，Ｋ２ＴａＦ７在２００～２５０℃发生可逆相变；相变后Ｋ２ＴａＦ７晶体的粒径可由原来的１３５１．８μｍ减小至７０．８μｍ，极大地提高了比表面积；相变后，杂质极大挥发，提高了Ｋ２ＴａＦ７的纯度。     

稀土Y对纳米粉90W-Ni-Fe合金性能和微观结构的影响

采用SEM和金相仪器对添加不同Y量的纳米粉90W-7Ni-3Fe合金试样断口进行形貌观察和W晶粒测试：并对烧结态试样的相对密度、抗拉强度、延伸率等性能进行测定与分析。结果表明：当Y量在0．2％～0．6％（质量百分数，下同）时，试样相对密度为99.2％～99．6％，抗拉强度为1000MPa-1100MPa，延伸率为16％-19．5％：添加0．4％Y后，W晶粒从原来的20μm～25μm减小到12μm，W晶粒形状由不加稀土时的球形变为近球形或多边形。添加0．4％Y后，在界面上形成了W13．07Ni2.96Fe1.52Y23．65Ox（摩尔数比）的中间相，其阻止了W原子在粘结相中的扩散，阻止了W晶粒长大，细化了W晶粒，提高了合金的性能。     

Na2B4O7对镁合金旧料组织和性能的影响

利用等离子发射光谱仪、电镜、X衍射、万能材料试验机、腐蚀试验等手段研究了不同Na2B4O7含量的熔剂对镁合金废旧料的力学性能、相组成、断口形貌以及腐蚀行为的影响.研究表明,使用含Na2B4O7的熔剂可以使镁合金旧料中Fe的质量分数降低到0.004%以下,同时提高材料的抗拉强度和伸长率.腐蚀试验表明含Na2B4O7的质量分数为20%的熔剂可以使材料的腐蚀速率从15.1 mg*cm-2*d-1降低到0.4 mg*cm-2*d-1.电镜观察和X衍射表明,净化处理对断口形貌和相组成没有明显影响.最后分析了Na2B4O7除铁的机理,认为Fe与B形成某种化合物沉淀下来是主要原因.     

7-氨基-6-氰基-5-(3-硝基苯基)吡喃并嘧啶-2,4-二酮的合成

报道了常温、超声辐射、水中、无催化剂条件下，以3-硝基苯甲醛、丙二腈和巴比妥酸为原料合成标题化合物的方法。考察了超声技术、反应时间及反应温度对反应的影响。最佳反应条件为：室温、超声辐射2h，收率为86．2％。     

A carboxyalkanethiol monolayer modified electrode for blocking of ascorbic acid oxidation and its application to a biosensor

Upon the application of amperometric biosensor to the biological fluid, ascorbic acid interferes the amperometric determination of analytes, because the oxidative potential of ascorbic acid is lower than that of electro active substances such as H₂O₂ produced by the enzymatic reaction. In this study we propose a method to block ascorbic acid based on the electrostatic interaction with self-assembled monolayer (SAM) and its application of the surface modified electrode to biosensor. In order to form SAM on the gold electrode with carboxyl group, 7-carboxy-heptanethiol (7-CHT) was used. The 7-CHT modified electrode did not show anodic response to ascorbic acid, but oxidized phenanthroline cobalt complex [Co(phen)₃²⁺], which can be used as a mediator of biosensor. Thus, the 7CHT-modified electrode was applied to biosensor mediated with Co(phen)₃²⁺. Fructose dehydrogenase (FDH) was immobilized to the 7-CHT modified electrode. Fructose was determined selectively with the FDH/7-CHT modified electrode at the range of 0.2-2 mM.     

重组B7-H1IgV融合蛋白的表达、纯化及活性鉴定

目的以B7-H1为靶点,研制肿瘤免疫治疗蛋白疫苗。方法将人B7-H1胞外片段IgV区基因插入pQE-30原核表达载体,转化大肠杆菌,经IPTG诱导表达。Ni2+-NTA亲和层析纯化蛋白,Westernblot鉴定。用纯化的rhB7-H1IgV蛋白免疫昆明小鼠,经ELISA、流式细胞术、免疫组化技术和CDC试验测定融合蛋白及其抗血清的生物学活性。结果所构建的pQE-30-TT-B7-H1IgV表达载体,能稳定表达rhB7-H1IgV蛋白,经纯化后免疫昆明小鼠,可获得高滴度抗B7-H1抗血清。经流式细胞术和免疫组化检测显示,其抗血清可与HT-29/B7-H1+及SP2/0肿瘤细胞结合,且在CDC试验中,可依赖补体杀伤HT-29/B7-H1+及SP2/0肿瘤细胞。结论rhB7-H1IgV融合蛋白不仅可引发小鼠体液免疫应答,而且其抗体还能与表达B7-H1的肿瘤细胞相结合,并介导补体依赖的体外杀伤作用。     

用酰胺缩醛合成1,4,7,10-四氮杂十二烷的研究

用甲苯作溶剂,使三乙烯四胺和N,N-二甲基甲酰胺二甲基缩醛在85℃反应2h,得到中间体双咪唑啉,产率90.4%,在乙腈溶剂中,碳酸钾存在下,双咪唑啉和1,2-二溴乙烷进行扩环反应,得到环状中间体一溴盐,产率78.7%,一溴盐经碱性水解2h,得到1,4,7,10-四氮杂十二烷,产率74.2%。用元素分析、质谱和核磁共振氢谱对目标化合物进行了表征。     

FA composition and regiospecific analysis of Acer saccharum (sugar maple tree) and Acer saccharinum (silver maple tree) seed oils

GC analysis was performed to determine regiospecific distribution and FA composition in seed oils of the Aceraceae species, Acer saccharum and A. saccharinum. The oil content in the seeds was low at 5.0% in A. saccharum and 5.8% in A. saccharinum, and the main FA were linoleic (30.8 and 29.4%), oleic (21.3 and 27.6%), palmitic (10.1 and 10.5%), and cis-vaccenic (9.4 and 7.9%) acids, respectively. In addition, both oils contained long-chain monoenes of the n−9 and n−7 groups, including 11-eicosenoic, 13-docosenoic, 15-tetracosenoic, 13-eicosenoic, and 15-docosenoic acids, whereas γ-linolenic acid accounted for 0.8% of total FA in A. saccharum, and 0.5% in A. saccharinum. Regiospecific analysis, performed using the methodology of dibutyroyl derivatives of MAG, indicated that linoleic, oleic, and linolenic acids were mainly esterified at the internal position of TAG in both seed oils, whereas long-chain monoenes of the n−7 group were almost exclusively esterified on the external positions.