利用离子注入~(15)N靶研究超低能区~(15)N(p,α)~(12)C核反应

描述了利用离子注入固体靶测量15N(p ,α) 12 C核反应微分截面的实验过程和方法 ,给出了在163keV≤Ec≤ 360keV能区 90°方向上的微分截面测量结果和激发函数曲线 ,并对该反应的基本特征进行了分析和描述。

35MeV/u~(36,40)Ar+~(112,124)Sn反应中同位旋自由度的弛豫

35MeV/u 36 ,40　Ar+ 112 ,12 4Sn反应中 ,在前角 5°和 2 0°观测到丰中子核与稳定核的产额比随粒子出射动能的增加而减小 ,而缺中子核与稳定核的产额比随动能的增加而增加 .对于某种元素 ,随着动能的减小 ,其平均中质比逐渐由弹核N/Z向靶核N/Z过渡 .这些现象表明在这样的入射能量下 ,周边或近周边碰撞过程中同位旋自由度没有完全达到平衡 .这种行为对两个靶核系统是相似的 ,但是同位素产额比的绝对值在 5°没有靶核相关性 ,而在 2 0°处却表现出明显的靶核相关性 .

HIRFL-CSR二极磁铁电源的研制；Development of Power Supply for HIRFL-CSR Dipole Magnet

研制了兰州重离子加速器冷却储存环(HIRFL-CSR)二极磁铁电源,提出了一种基于晶闸管相控整流技术和IGBT脉宽调制(PWM)变换技术的同步加速器二极磁铁电源的设计方案,分析、仿真了其工作原理,并设计、生产了1套完整的电源样机。经现场试验、长期运行及测试,电流稳定度<±5×10-5/8h,跟踪精度<±2×10-4,电流纹波<1×10-5。该方案满足HIRFL-CSR二极磁铁对电源技术指标的要求。

12C6+重离子辐照对细胞端粒酶活性表达的影响

端粒是染色体末端由重复DNA序列和相关蛋白组成的一种特殊结构，具有稳定染色体结构及完整性的功能，会随染色体复制与细胞分裂而缩短。端粒酶是一种核糖核蛋白，能以自身RNA模板合成端粒DNA，催化合成TTAGGG重复序列，添加到染色体末端，维持端粒长度不变。端粒酶主要由hTR, TEPl和hTERT组成，一般认为hTERT是端粒酶激活的限速因素。大多数永生化细胞和恶性肿瘤细胞具有端粒酶活性，因而端粒酶目前已成为为细胞持续分裂提供遗传基础的原因。由于端粒酶与细胞衰老、肿瘤发生等关系如此密切，因此已成为肿瘤放射治疗研究热点。目的： 本文利用兰州近代物理研究所重离子研究装置（Heavy Ion Research Facility in Lanzhou,HIRFL）产生的碳离子（31MeV/u 12C6+）对人体细胞、癌细胞进行不同剂量的辐照，探索细胞中端粒酶活性的变化及与之相关的生物学信息。材料与方法： 以人肝细胞HL－7702，肝癌细胞SMMC－7721为实验对象，用不同剂量1Gy、2Gy、3Gy、4Gy的重离子分别对两种细胞进行照射，用多聚酶链式反应-银染端粒重复序列扩增法（PCR- telomeric repeat amplification protocol，TRAP-PCR）检测不同剂量下细胞端粒酶活性的变化。并提取不同剂量下的细胞转入培养皿中，培养10天，固定，染色。统计大于50个细胞的克隆数，绘制细胞存活曲线。结果与讨论： 结果显示，人肝细胞HL-7702自身没有端粒酶活性，经1Gy辐照后也没有端粒酶活性，在2、3Gy处出现端粒酶活性，4Gy处端粒酶活性又消失。肝癌细胞SMMC-7721在1－3Gy处随着剂量的增大端粒酶活性升高，在4Gy处又开始下降；在1－3Gy处随着时间的推移端粒酶活性随着时间而加强（p<0.05）。随着剂量的增大，细胞存活率呈剂量依赖型下降。分析得知，重离子辐射可以诱导人肝细胞产生端粒酶活性，也可以改变肝癌细胞的端粒酶活性。端粒酶参与细胞受辐照后DNA单链损伤的修复；辐照后DNA双链断裂导致端粒酶活性减弱。本实验与其他低LET射线相比，使重离子在辐照治疗中的优势得以体现

Thermochemical and thermal analysis on N-(p-methylphenyl)-N '-(2-pyridyl)urea

Low temperature heat capacities of N-(p-methylphenyl)-N'-(2-pyridyl)urea were determined by adiabatic calorimetry method in the temperature range from 80 to 370 K. It was found that there was not any heat anomaly in this temperature region. Based on the experimental data, some thermodynamic function results were obtained. Thermal stability and decomposition characteristics analysis of N-(p-methylphenyl)-N'-(2-pyridyl)urea were carried out by DSC and TG. The results indicated that N-(p-methylphenyl)-N'-(2-pyridyl)urea started to melt at ca. 426 K (153degreesC) and the melting peak located at 447.01 K (173.86degreesC). The melting enthalpy was 204.445 kJ mol(-1) (899.6 J g(-1)). The decomposition peak of N-(p-methylphenyl)-N'-(2-pyridyl)urea was found at 499.26 K (226.11degreesC) from DSC curve. This result was similar with that from TG and DTG experiment, in which the mass loss peak was determined as 500.4 K (227.2degreesC).

长白山红松阔叶林林隙动态变化对早春草本植物的影响

采用生态学的方法,系统分析了长白山红松阔叶林林冠空隙的动态变化对早春草本层植物的分布密度和生物量的影响以及早春草本层植物对林冠空隙的反应,进而探讨了早春草本层植物在红松阔叶林森林生态系统中所起的生态作用。本研究为全面系统地揭示红松阔叶林森林生态系统的结构与功能及更深入地研究森林循环理论提供科学依据

岷江上游汶川县耕地景观变化及空间驱动力

基于遥感影像和地理信息系统技术,应用景观指数和Kappa指数系列方法对岷江上游耕地景观变化进行研究,并引入二项Logistic逐步回归模型,选择海拔、坡度、坡向、到道路、河流和居民点距离为驱动因子对汶川县耕地景观变化的空间驱动力进行分析.结果表明:研究期间耕地景观面积一直处于增长趋势,1974—1986年间耕地景观面积增幅最大.1986—2000年间耕地面积增加不明显,但是耕地景观与其它景观类型相互转换频繁,空间位置变化剧烈,特别是1994—2000年期间.耕地景观面积变化的驱动力主要为政策变化.耕地景观变化的空间驱动力在不同时间段内存在较大差异.

北京地区气候变化和植被的关系:基于遥感数据和物候资料的分析

气候变化对陆地生态系统的影响及其反馈是全球变化研究的焦点之一。本文利用1951～2000年的气温、降水等气候资料、1982～2000年的NOAA/AVHRR遥感数据和1951～2000年北京春季物候的代表性指标———山桃(Prunusdavidiana)始花的物候数据,分析了在年际和年内时间尺度上北京地区各气候参量与植被变化之间的关系。结果显示:植物生长与温度之间的关系远比其与降水之间的关系密切;各气候参量和植被生长状况之间的关系因时间尺度而不同。1)月际水平上,具有显著生态学意义的气候指标对植被生长状况

饮用水消毒副产物暴露评价研究进展

介绍了饮用水消毒副产物暴露评价的基本定义,对饮用水暴露评价的主要消毒副产物进行了归纳总结,综述了现阶段饮用水消毒副产物暴露评价方法的进展及不足,并结合具体案例对饮用水消毒副产物暴露评价的具体步骤进行较为详细阐述,并对饮用水消毒副产物暴露评价研究的发展趋势及将来研究的重点进行了展望。

Manipulating charge-transfer character with electron-withdrawing main-group moieties for the color tuning of iridium electrophosphors

A new and synthetically versatile strategy has been developed for the phosphorescence color tuning of cyclometalated iridium phosphors by simple tailoring of the phenyl ring of ppy (Hppy=2-phenylpyridine) with various main-group moieties in [Ir(ppy-X)(2)(acac)] (X=B(Mes)(2), SiPh3, GePh3, NPh2, POPh2, OPh, SPh, SO2Ph). This can be achieved by shifting the charge-transfer character from the pyridyl groups in some traditional iridium ppy-type complexes to the electron-withdrawing main-group moieties and these assignments were supported by theoretical calculations.

交联型聚乙烯亚胺智能基因载体的制备及PEG化影响

使用胱胺双丙烯酰胺(CBA)对低分子量聚乙烯亚胺(PEI)进行交联反应制备智能降解型聚阳离子基因载体.通过与聚乙二醇(PEG)反应得到不同程度PEG化的聚阳离子载体.利用核磁、黏度测试、粒度仪、zeta电位仪和凝胶电泳对聚阳离子载体及其与DNA的复合物进行了表征.研究表明随着PEG含量的增加,聚阳离子载体/DNA复合物颗粒粒径变小、表面正电荷降低,PEG具有明显的屏蔽作用,但过多的PEG也使载体与DNA复合能力下降.通过MTT细胞毒性测试和荧光素酶质粒转染实验得出,含二硫键的交联型阳离子聚合物在测试范围内显示了非常低的细胞毒性,最佳转染效率是PEI25k的4倍,PEG化后其细胞毒性得到进一步改善,转染效率却明显降低.

SYNTHESIS AND CHARACTERIZATION OF A CROSSLINKING POLYETHYLENIMINE AS SMART GENE CARRIER AND EFFECTS OF PEGYLATION DEGREE

A smart biodegradable cationic polymer (CBA-PEI) based on the disulfide bond-containing cross-linker cystamine bisacrylamide (CBA) and low molecular weight branched polyethylenimine (1800-Da, PEI1800) was successfully synthesized by Michael addition reaction in our recent study. Furthermore, a series of copolymers (CBA-PEI-PEG) with different PEGylation degree were obtained by the mPEG-SPA (5000-Da) reacting with CBA-PEI at various weight ratios directly. The molecular structures of the resulting polymers CBA-PEI and CBA-PEI-PEG were evaluated by nuclear magnetic resonance spectroscopy (H-1-NMR) and capillary viscosity measurements, all of which had successfully verified formation of the copolymers. The polymer/DNA complexes based on CBA-PEI and CBA-PEI-PEG were measured by dynamic light scattering and gel retardation assay. The results showed that the particle size and zeta potential of complexes were reduced with increasing amount of PEG grafting, even no particle formation. The particle size of CBA-PEI/DNA complexes was in range of 103.1 to 129.1 nm, and the zeta potential was in range of 14.2 to 24.3 mV above the 2:1 weight ratio. In the same measure condition, the particle size of CBA-PEI-PEG complexes was reduced to a range of 32.2 to 55 nm, and the zeta potential was in range of 9.3 to 13.8 mV at the 2:1 weight ratio.

Electrochemistry of hydroquinone derivatives at metal and iodine-modified metal electrodes

The difference in the electrochemical behavior of hydroquinone and pyrocatechol. at platinum and gold surfaces was analyzed using voltammetry and attenuated total reflection Fourier transform infrared spectroscopy. The results show that the hydroquinone derivatives are adsorbed on a gold surface with vertical orientation, which makes the electron transfer between the bulk species and the electrode surface easier than that in the case of flat adsorption of hydroquinone derivatives that occurs at a platinum electrode. The formation of the vertical conformation and the rapid process of electron transfer were also confirmed by quantum chemistry calculations. In addition, the pre-adsorbed iodine on the electrodes played a key role on the adsorbed configuration and. electron transfer of redox species.