基于生态足迹模型的延边林区可持续发展评价

生态足迹是评价可持续发展状况和能力的重要指标之一。本文以统计年鉴和林业年鉴为主要数据来源,对延边林区1996~2002年的生态足迹进行了计算和分析。结果表明,该区人均生态足迹逐年下降,人均生态承载力波动较小,而人均生态盈余逐年增长。人均万元GDP生态足迹逐年递减,同西部地区相当,而明显高于东部。人均林地生态足迹变化平稳,天然林保护工程实施前后林地生产足迹和林地出口足迹的平均值分别降低了0.341和0.327 hm2.人-1,降幅分别为46.32%和54.94%。延边区域和林业的发展是可持续的,天然林保护工程的实施有助于增强其可持续发展能力,但同林业发达国家相比,仍有很大差距。依靠科技,提高单位面积林地产量和资源利用率,合理经营和管理森林生态系统是今后的工作重点。

以管道理论为基础的林带小钻杨树体结构分析

以管道理论为基础,运用主轴切割的方法,论述不同年龄小钻杨树体的结构特点。结果表明:树干生物量增加与高度的降低呈线性关系;同一层次内的叶量和枝量间存在显著的线性关系,其关系的确定性不受分层方式的影响;树冠不同层次内的累积叶量与支持的枝干总质量存在显著的线性关系;不同层次的总累积生物量与各层内的树干生物量密度之间的线性关系显著,对不同层次累积树干生物量与各层树干生物量密度进行指数回归,系数介于1.1~1.3,指数介于1~2,表明二者的关系是处于线性和指数关系之间的一种形式;在胸高以上,树干边材断面积与侧枝基部断面积总和呈线性关系,胸高之下线性关系不存在。建立不同年龄小钻杨边材与所支持叶量的树体管道模型,同时测得胸径(D1.3)与心材直径(Dx)间的关系为Dx=0.522 exp(0.169 8D1.3),r=0.984 8。

易旱地区褐土P、Zn形态转化特点及其与持续农业的关系

采用田间微区试验和分级提取测定的方法研究了褐土中Ｐ、Ｚｎ形态转化问题．发现褐土中Ｃａ２－Ｐ和Ｃａ８－Ｐ是转化最活跃的Ｐ素形态．而且Ｃａ８－Ｐ的流通容量很大，可超过作物需Ｐ量９倍以上；在Ｚｎ的各种形态中转化最活跃的是ＥＸ－Ｚｎ和ＣＡＲＢ－Ｚｎ，其中ＣＡＲＢ－Ｚｎ的流通容量亦很大，可超过作物需Ｚｎ量１９倍以上．Ｃａ８－Ｐ库和ＣＡＲＢ－Ｚｎ库形成了褐土中调控Ｐ、Ｚｎ养分供蓄以适应旱地水分波动的主要机构．合理施肥和培肥土壤以丰富Ｃａ８－Ｐ和ＣＡＲＢ－Ｚｎ库将有利于增强作物抵御干旱能力，提高水分养分利用效率，促使旱地农业持续向高产优质高效方向发展．

data transformation and attribute subset selection: do they help make differences in software failure prediction?

IEEE, IEEE Comp Soc, Tech Council Software Engn

中国能源保障水平分区初探

在经济高速增长的新形势下,能源保障风险日益凸现。全国能源保障分区研究不仅是能源风险管理的基本要求,也是经济发展对能源产业提出的新要求。本文阐述了全国能源资源的基础形势,并对1996年~2005年间我国一次能源生产和消费情况进行了分析;构建了由能源储量比、对外依存度、库存增减量、能源生产弹性系数、能源消费弹性系数、运输线路长度6个指标组成的能源保障指标体系,采用因子分析法确定各个指标的权重;并根据灰色聚类方法对全国30个省(市、区)"十五"期间的能源保障能力进行了评估与分区。结果表明:我国能源保障水平具有南

Micelle-assisted synthesis of polyaniline/magnetite nanorods by in situ self-assembly process

Polyaniline/magnetite nanocomposites consisting of polyaniline (PANI) nanorods surrounded by magnetite nanoparticles were prepared via an in situ self-assembly process in the presence of PANI nanorods. The synthesis is based on the well-known chemical oxidative polymerization of aniline in an acidic environment, with ammonium persulfate (APS) as the oxidant. An organic acid (dodecylbenzenesulfonic acid, DBSA) was used to replace the conventional strong acidic (1 M HCl) environment. Here, dodecylbenzenesulfonic acid is used not only as dopant, but also as surfactant in our reaction system.

Blends based on sulfonated poly[bis(benzimidazobenzisoquinolinones)] and poly(vinylidene fluoride) for polymer electrolyte membrane fuel cell

A new blend system consisting of an amorphous sulfonated poly[bis(benzimidazobenzisoquinolinones)] (SPBIBI) and the semi-crystalline poly(vinylidene fluoride) (PVDF) was prepared for proton exchange membranes. The miscibility behavior of a series of blends of SPBIBI with PVDF at various weight ratios was studied by WXRD, DSC and FTIR. The properties of the blend membranes were investigated, and it was found that the introduction of PVDF in the SPBIBI matrix altered the morphological structure of the blend membranes, which led to the formation of improved connectivity channels. For instance, the conductivity of the blend membrane containing 10 wt% PVDF displayed the highest proton conductivity (i.e., 0.086 S cm(-1)) at room temperature, a value almost twofold that of the pristine SPBIBI membranes (i.e., 0.054S cm(-1)) under identical conditions.

Investigations of the properties of Mg-5Al-0.3Mn-xCe (x=0-3, wt.%) alloys

Mg-5Al-0.3Mn-xCe (x = 0-3, wt.%) alloys were prepared by metal mould casting method. The microstructures and mechanical properties were investigated. The results revealed that the main phases of as-cast Mg-5Al-0.3Mn alloy consist of alpha-Mg matrix and beta-Mg17Al12 phase. With the addition of Ce element, Al11Ce3 precipitates were formed and mainly aggregated along the grain boundaries. The amount of the Al11Ce3 precipitates increased with increasing addition of Ce, but the amount of beta-Mg17Al12 phase decreased. The highest tensile strength was obtained in Mg-5Al-0.3Mn-1.5Ce alloy. The ultimate tensile strength (UTS), yield strength (YS) and elongation at room temperature are 203 MPa, 88 MPa and 20%, separately.

Effect of cerium on microstructure and electrochemical performance of Ti-V-Cr-Ni electrode alloy

Effect of cerium on the microstructure and electrochemical performance of the Ti0.25V0.35-xCexCr0.1Ni0.3 (x = 0, 0.005) electrode alloy was investigated by X-ray diffraction (XRD), field emission scanning electron microscopy/energy dispersive X-ray spectrometry (FESEM-EDS), and electrochemical impedance spectroscopy (EIS) measurements. On the basis of XRD and FESEM-EDS analysis, the alloy was mainly composed of V-based solid solution with body-centered-cubic structure and TiNi-based secondary phase. Ce did not exist in two phases, instead, it existed as Ce-rich small white particles, with irregular edges, distributed near the grain boundaries of the V-based solid solution phase. Discharge capacity, cycle stability, and high-rate discharge ability of the alloy electrode were effectively improved with the addition of Ce at 293 K. It was very surprising that the charge retention was abnormal with larger discharge capacity after standing at the open circuit for 24 h. EIS indicated that addition of Ce improved the dynamic performance, which caused the charge transfer resistance (R-T) to decrease and exchange current density (I-0) to increase markedly. The exchange current density of the electrochemical reaction on the alloy surface with Ce addition was about 2.07 and 3.10 times larger than that of the alloy without Ce at 303 and 343 K, respectively.

CPE-g-HEA/TDI热塑性弹性体的制备和性能研究

采用氯化原位接枝法合成主链为氯化聚乙烯(CPE)、支链为丙烯酸-2-羟基乙酯（HEA）的官能化接枝聚合 物(CPE-g-HEA),制备CPE-g-HEA/2,4-二异氰酸甲苯酯（TDI）热塑性弹性体,并对其性能进行研究。结果表明, CPE-g-HEA/TDI热塑性弹性体的物理性能较好;与溶液法产物相比,共混法CPE-g-HEA/TDI热塑性弹性体的强度 较大、相对分子质量较小、相对分子质量分布较宽,热行为基本无变化;共混法CPE-g-HEA/TDI热塑性弹性体的反 应温度应控制在60～70℃,共混次数(即打三角包次数) 为150次时拉伸强度较高、80次时拉断伸长率较高,HEA/TDI摩尔比为1/0.5时拉伸强度较高。

Composites of poly(lactide-co-glycolide) and the surface modified carbonated hydroxyapatite nanoparticles

To improve the mechanical properties of the composites of poly(lactide-co-glycolide) (PLGA, LA/GA = 80/20) and the carbonate hydroxyapatite (CHAP) particles, the rice-form or claviform CHAP particles with 30-40 nm in diameter and 100-200 nm in length were prepared by precipitation method. The uncalcined CHAP particles have a coarse surface with a lot of global protuberances, which could be in favor of the interaction of the matrix polymer to the CHAP particles. The nanocomposites of PLGA and surface grafted CHAP particles (g-CHAP) were prepared by solution mixing method. The structure and properties of the composites were subsequently investigated by the emission scanning electron microscopy, the tensile strength testing, and the cell culture. When the contents of g-CHAP were in the range of 2-15 wt %, the PLGA/g-CHAP nanocomposites exhibited an improved elongation at break and tensile strength. At the 2 wt % content of g-CHAP, the fracture strain was increased to 20%) from 4-5% for neat PLGA samples. Especially at g-CHAP content of 15 wt %, the tensile strength of PLGA/g-CHAP composite was about 20% higher than that of neat PLGA materials. The tensile moduli of composites were increased with the increasing of filler contents, so that the g-CHAP particles had both reinforcing and toughening effects on the PLGA composites. The results of biocompatibility test showed that the higher g-CHAP contents in PLGA composite facilitated the adhesion and proliferation properties of osteoblasts on the PLGA/g-CHAP composite film.

Negative differential resistance and memory effect in diodes based on 1,4-dibenzyl C60 and zinc phthalocyanine doped polystyrene hybrid material

Negative differential resistance (NDR) and memory effect were observed in diodes based on 1,4-dibenzyl C60 (DBC) and zinc phthalocyanine doped polystyrene hybrid material. Certain negative starting sweeping voltages led to a reproducible NDR, making the hybrid material a promising candidate in memory devices. It was found that the introduction of DBC enhanced the ON/OFF current ratio and significantly improved the memory stability. The ON/OFF current ratio was up to 2 orders of magnitude. The write-read-erase-reread cycles were more than 10(6), and the retention time reached 10 000 s without current degradation.

Electropolymerization of azure B on a screen-printed carbon electrode and its application to the determination of NADH in a flow injection analysis system

The electrooxidation polymerization of azure B on screen-printed carbon electrodes in neutral phosphate buffer was studied. The poly(azure B) modified electrodes exhibited excellent electrocatalysis and stability for dihydronicotinamide adenine dinucleotide (NADH) oxidation in phosphate buffer (pH 6.9), with an overpotential of more than 400 mV lower than that at the bare electrodes. Different techniques, including cyclic voltammetry, scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy have been employed to characterize the poly (azure B) film. Furthermore, the modified screen-printed carbon electrodes were found to be promising as an amperometric detector for the flow injection analysis (FIA) of NADH, typically with a dynamic range of 0.5 muM to 100 muM.