Electromechanical influence of crack velocity at bifurcation for poled ferroelectric materials

The piezoelastodynamic field equations are solved to determine the crack velocity at bifurcation for poled ferroelectric materials where the applied electrical field and mechanical stress can be varied. The underlying physical mechanism, however, may not correspond to that assumed in the analytical model. Bifurcation has been related to the occurrence of a pair of maximum circumferential stress oriented symmetrically about the moving crack path. The velocity at which this behavior prevails has been referred to as the limiting crack speed. Unlike the classical approach, bifurcation will be identified with finite distances ahead of a moving crack. Nucleation of microcracks can thus be modelled in a single formulation. This can be accomplished by using the energy density function where fracture initiation is identified with dominance of dilatation in relation to distortion. Poled ferroelectric materials are selected for this study because the microstructure effects for this class of materials can be readily reflected by the elastic, piezoelectic and dielectric permittivity constants at the macroscopic scale. Existing test data could also shed light on the trend of the analytical predictions. Numerical results are thus computed for PZT-4 and compared with those for PZT-6B in an effort to show whether the branching behavior would be affected by the difference in the material microstructures. A range of crack bifurcation speed upsilon(b) is found for different r/a and E/sigma ratios. Here, r and a stand for the radial distance and half crack length, respectively, while E and a for the electric field and mechanical stress. For PZT-6B with upsilon(b) in the range 100-1700 m/s, the bifurcation angles varied from +/-6degrees to +/-39degrees. This corresponds to E/sigma of -0.072 to 0.024 V m/N. At the same distance r/a = 0.1, PZT-4 gives upsilon(b) values of 1100-2100 m/s; bifurcation angles of +/-15degrees to +/-49degrees; and E/sigma of -0.056 to 0.059 V m/N. In general, the bifurcation angles +/-theta(0) are found to decrease with decreasing crack velocity as the distance r/a is increased. Relatively speaking, the speed upsilon(b) and angles +/-theta(0) for PZT-4 are much greater than those for PZT-6B. This may be attributed to the high electromechanical coupling effect of PZT-4. Using upsilon(b)(0) as a base reference, an equality relation upsilon(b)(-) < upsilon(b)(0) < upsilon(b)(+) can be established. The superscripts -, 0 and + refer, respectively, to negative, zero and positive electric field. This is reminiscent of the enhancement and retardation of crack growth behavior due to change in poling direction. Bifurcation characteristics are found to be somewhat erratic when r/a approaches the range 10(-2)-10(-1) where the kinetic energy densities would fluctuate and then rise as the distance from the moving crack is increased. This is an artifact introduced by the far away condition of non-vanishing particle velocity. A finite kinetic energy density prevails at infinity unless it is made to vanish in the boundary value problem. Future works are recommended to further clarify the physical mechanism(s) associated with bifurcation by means of analysis and experiment. Damage at the microscopic level needs to be addressed since it has been known to affect the macrocrack speeds and bifurcation characteristics. (C) 2002 Published by Elsevier Science Ltd.

Polymorphisms of the estrogen receptor alpha (ESR1) gene and the risk of Alzheimer's disease in a southern Chinese community

Background: Alzheimer's disease (AD) is a neurodegenerative disease with a higher prevalence in women. Expression of estrogen receptor 1 (ESR1) gene has been identified throughout the brain. Owing to the putative neuroprotective effects of estrogen, estro

Positive effects of continuous low nitrate levels on growth and photosynthesis of Alexandrium tamarense (Gonyaulacales, Dinophyceae)

The growth and photosynthesis of Alexandrium tamarense (Lebour) Balech in different nutrient conditions were investigated. Low nitrate level (0.0882 mmol/L) resulted in the highest average growth rate from day 0 to day 10 (4.58 x 10(2) cells mL(-1) d(-1)), but the lowest cell yield (5420 cells mL(-1)) in three nitrate level cultures. High nitrate-grown cells showed lower levels of chlorophyll a-specific and cell-specific light-saturated photosynthetic rate (P-m(chl a) and P-m(cell)), dark respiration rate (R-d(chl a) and R-d(cell)) and chlorophyll a-specific apparent photosynthetic efficiency (alpha(chl a)) than was seen for low nitrate-grown cells; whereas the cells became light saturated at higher irradiance at low nitrate condition. When cultures at low nitrate were supplemented with nitrate at 0.7938 mmol/L in late exponential growth phase, or with nitrate at 0.7938 mmol/L and phosphate at 0.072 mmol/L in stationary growth phase, the cell yield was drastically enhanced, a 7-9 times increase compared with non-supplemented control culture, achieving 43 540 cells mL(-1) and 52 300 cells mL(-1), respectively; however, supplementation with nitrate in the stationary growth phase or with nitrate and phosphate in the late exponential growth phase increased the cell yield by no more than 2 times. The results suggested that continuous low level of nitrate with sufficient supply of phosphate may facilitate the growth of A. tamarense.

黄土高原坡地密植枣园土壤质地与肥力状况分析

采用田间取样与实验室分析相结合的方法,研究了黄土高原坡地密植枣园土壤质地与肥力状况。结果表明,坡地枣园土壤肥力低,氮、磷严重缺乏,钾相对丰富,土壤属于砂壤土,通气性强,保肥、保水性差。0~60 cm土壤有机质含量为1.687~5.002 mg/kg;全氮为0.072~0.316 g/kg;硝酸盐为2.325~16.846 g/kg;铵态氮为1.187~2.146 g/kg,速效磷为0.270~2.480 mg/kg,速效钾为51.9~169.1 mg/kg,并且含量均随剖面向下减少。颗粒组成大部分为粉砂粒,含量一般在65.75%~68.98%;随有机质含量升高,0.25~0.05 mm微团聚体数量呈上升趋势,二者为正相关;<0.05 mm微团聚体含量则逐渐下降,二者呈负相关。黄土高原坡地密植枣园土壤肥力总体水平很低。除了速效钾为中等级外,有机质、全氮、碱解氮、速效磷均为很低等级。

黄土丘陵区植被次生演替灌木种群的土壤养分效应

研究黄土丘陵区植被次生演替灌木群落形成过程中土壤养分的变化情况。【方法】以白羊草群落为对照,选取杠柳、狼牙刺、丁香、虎榛子和柠条5种乡土树种为研究对象,测定其土壤养分含量,计算灌木群落形成变化过程中的土壤养分指数(Soil Nutrient Index,SNI),分析了各养分因子间的线性相关关系。【结果】不同灌木初期对土壤养分的适应能力大小顺序为:柠条(0.072)>狼牙刺(0.114)>杠柳(0.163)>丁香(0.172)>虎榛子(0.292)。不同植被物种群落土壤SNI值大小顺序为:虎榛子群落(0.979)>狼牙刺群落(0.535)>柠条群落(0.457)>丁香群落(0.341)>杠柳群落(0.333)>白羊草群落(0.145)。从不同灌木群落形成过程所产生的土壤养分改善效应来看,各参试群落相对于白羊草群落土壤养分的增幅分别为:虎榛子(4.740倍)、狼牙刺(2.909倍)、柠条(2.661倍)、杠柳(1.169倍)和丁香(1.168倍)。各土壤养分因子间除土壤全磷与有效磷和有效钾的相关性不显著外,其余各土壤养分因子间均表现出极显著的线性相关关系(P<0.01)。【结论】不同灌木种群所需的适宜土...

染料掺杂聚合物薄膜的激光行为研究

自20世纪60年代发展到现在，激光技术发展的速度十分惊人，应用的范围不断拓展，近年来随着有机/聚合物电致发光材料在有机发光二极管上的应用以及有机晶体管和有机太阳能电池的研制成功，科学家们开始了有机/聚合物材料放大自发发射和激光发射行为的研究。到目前为止，已经开发出了这种廉价、可以大面积成膜的、具有更广泛应用范围的有机/聚合物固体激光材料及光泵浦激光器。有机/聚合物激光器的出现不仅向传统激光理论提出了新的挑战，而且具有诸多潜在的应用价值。可以断言，在21世纪知识经济的大潮中，有机/聚合物激光器的研究必将推动传统学科的发展和新兴学科形成，也必将为人类带来巨大的经济效益。新的有机激光材料不断涌现、器件结构不断推陈出新、新的激发原理不断提出并得到修正已经成为有机/聚合物固体激光研究领域的三大特点。本论文进行了利用Förster能量传递对荧光染料DCJTB放大自发发射行为的优化、基于放大自发发射的红光染料DCJTB掺杂聚合物薄膜的白光发射、多孔结构对荧光染料放大自发发射行为的优化以及基于纳米结构的荧光染料DCJTB掺杂聚合物薄膜的激光行为等方面的研究工作，具体研究内容如下: 1、利用Förster能量传递理论，系统地研究了两种或三种染料共掺杂聚合物薄膜的放大自发发射（ASE）行为。研究表明，两种染料共掺杂显著改善了掺杂聚合物薄膜的ASE阈值、增益和损耗特性，而三种染料共掺杂，由于更多的Förster能量传递，使掺杂聚合物薄膜的ASE阈值、增益和损耗性能得到了进一步的改善。将Alq3和C545T两种绿光染料同时掺杂到DCJTB：PS中，通过利用Alq3和C545T同时的能量传递效应，已经使Alq3:C545T:DCJTB：PS薄膜的阈值、增益和损耗分别达到了0.007 mJ/pulse、52 cm-1和7 cm-1。 2、将红色荧光染料DCJTB掺杂到蓝色聚合物PFO中，通过控制DCJTB在PFO中的浓度，我们获得了具有放大自发发射的白光发射，当DCJTB在PFO的掺杂浓度为0.3%时显示了最好的白光ASE特性， 白光中DCJTB和PFO发射的阈值、增益和损耗分别达到了0.072 mJ pulse-1，0.035 mJ pulse-1；36.3 cm-1，22.35 cm-1和7.39 cm-1，15.88 cm-1。我们的结果表明，DCJTB掺杂聚合物PFO体系是实现ASE白光发射的有效方法，拓展了ASE的应用范围。 3、开发出了二维多孔SBA-15和三维TiO2反蛋白石光子晶体两种实现有机ASE有效发射的两种结构，通过利用有序结构的SBA-15的量子限域效应优化了蓝光染料C151的ASE阈值、增益和损耗特性，而通过利用三维TiO2反蛋白石光子晶体的量子限域效应，也使包埋其中的绿光染料C545T的ASE特性得到了明显改善。研究表明，无论是二维SBA-15多孔结构还是三维TiO2反蛋白石光子晶体结构，通过其量子限域效应都能很好地优化包埋其中的荧光染料的ASE特性，为进一步优化有机半导体的ASE特性提供了新的思路。 4、将聚苯乙烯纳米球分散到DCJTB:PS薄膜中和把DCJTB:PS薄膜旋涂在ZnO纳米柱阵列上两种方法，我们已经成功地研制出了多模随机有机激光发射器件。详细研究表明，多模随机有机激光发射特性显著地与聚苯乙烯纳米球的尺寸和浓度以及ZnO纳米柱的疏密程度密切相关，优化后的聚苯乙烯纳米球掺杂DCJTB:PS薄膜的阈值已经达到了0.06 mJ pulse-1cm-2，而ZnO纳米柱包埋DCJTB:PS薄膜的阈值达到了0.375 mJ pulse-1cm-2。我们的结果表明，聚苯乙烯纳米球和ZnO纳米柱都是实现随机有机激光的非常好的散射介质材料。

长白山阔叶红松林冠层光合生产力的模拟研究

森林作为陆地生态系统的主体，在碳的生物地球化学循环中起着关键的作用，因此对森林生态系统生产力的研究具有重要意义。本文以长白山阔叶红松林为研究对象，在2005年7月~9月对其主要优势种红松、紫椴、蒙古栎、水曲柳的生理生态学参数进行了测定，并利用单叶尺度的光合作用-气孔导度-能量平衡耦合模型，以及冠层尺度的多层模型，对单叶尺度以及冠层尺度的光合作用进行了模拟，主要的结论有： （1）长白山阔叶红松林主要优势树种红松、紫椴、蒙古栎、水曲柳的生理生态学参数：光合有效辐射吸收率a、初始量子效率α、光饱和时的最大净光合作用速率Pmax、最大的Rubisco催化反应速率Vcmax、CO2饱和时的最大净光合作用速率Jmax有着明显且不同的季节变化。7、8月水曲柳的α值最大，分别为0.077、0.064，9月紫椴的最大，为0.051。红松的Vcmax值在7、9月为四个树种中最大的，分别为：49.085、43.072μmol•m-2•s-1，8月为水曲柳最大，为66.041μmol•m-2•s-1。 （2）对优势树种单叶尺度的净光合作用速率An和气孔对CO2的导度gsc进行模拟发现：紫椴、蒙古栎、水曲柳的An、gsc的值在7~9月要大于红松，进入植物生长末期的9月则随着生理活性的下降而迅速下降，而红松则表现较为平稳且略有上升。7月蒙古栎的An、gsc的最大值最大分别为15.055μmol•m-2•s-1、0.400 mol•m-2•s-1；8月水曲柳的最大分别为22.944μmol•m-2•s-1、0.567 mol•m-2•s-1；9月紫椴的最大分别为12.045μmol•m-2•s-1、0.249 mol•m-2•s-1。 （3）通过模拟得到：长白山阔叶红松林冠层2005年8月的净光合作用速率An有着明显的日变化特征， 8月林冠的净光合作用速率最大值可以达到44.880μmol•m-2•s-1，该月白天净光合作用速率的总量可以达到23.580 mol•m-2。通过与观测值比较发现模拟结果能够较好地反映冠层光合作用的特征。

森林生态系统健康评估Ⅱ.案例实践

结合样地调查和他人对阔叶红松林生态系统相关指标的研究资料数据,利用健康距离(HD)评估法和上文建立的阔叶红松林生态系统健康评估指标体系框架,对不同人为干扰影响的长白山阔叶红松林生态系统进行系统健康的评估实践.结果按顺序依次为20%强度择伐林021<50%强度择伐林044<白桦中成林067<白桦中幼林072<红松人工林074<人工落叶松林077.

Multi-armed poly(L-glutamic acid)-graft-oligoethylenimine copolymers as efficient nonviral gene delivery vectors

Background The application of polyethylenimine (PEI) in gene delivery has been severely limited by significant cytotoxicity that results from a nondegradable methylene backbone and high cationic charge density. It is therefore necessary to develop novel biodegradable PEI derivates for low-toxic, highly efficient gene delivery.Methods A series of novel cationic copolymers with various charge density were designed and synthesized by grafting different kinds of oligoethylenimine (OEI) onto a determinate multi-armed poly(L-glutamic acid) backbone. The molecular structures of multi-armed poly(L-glutamic acid)-graft-OEI (MP-g-OEI) copolymers were characterized using nuclear magnetic resonance, viscosimetry and gel permeation chromatography. Moreover, the MP-g-OEI/DNA complexes were measured by a gel retardation assay, dynamic light scattering and atomic force microscopy to determine DNA binding ability, particle size, zeta potential, complex formation and shape, respectively. MP-g-OEI copolymers were also evaluated in Chinese hamster ovary and human embryonic kidney-293 cells for their cytotoxicity and transfection efficiency.

The study of synthesis of poly(ethylene oxide)-b-poly(N,N-dimethylacrylamide) by atom transfer radical polymerization and self-assembly in selective solvents

Poly( ethylene oxide)-b-poly(N, N-dimethylacrylamide) (PEO-b-PDMA) was synthesized by successive atom transfer radical polymerization (ATRP) of N, N-dimethylacrylamide (DMA) monomer using PEO-Br macro initiators as initiator, CuBr and 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazamacrocyclotetra decane (Me-6[14] aneN(4)) as catalyst and ligand. PEO-Br macroinitiator was synthesized by esterification of PEO with 2-bromoisobutyryl bromide. GPC and H-1 NMR studies show that the plot of ln([DMA](0)/[ DMA]) against the reaction time is linear, and the molecular weight of the resulting PDMA increased linearly with the conversion. Within 3 h, the polymerization can reach almost 60% of conversion. PEO-b-PDMA copolymer with low polydispersity index (M-w/M-n approximate to 1.1) is obtained. Self-assembly of PEO-b-PDMA in selective solvents is also studied. It could self-assemble into micelles in methanol/acetone (1/10, v/v) solution. TEM analyses of the PEO-b-PDMA micelles with narrow size distribution revealed that their size and shape depend much on the copolymer composition.

Structure of coordination polymer, [Zn(bipy)(H2O)(3)SO4] center dot 2H(2)O (bipy=4,4 '-bipyridine)

The crystal of the title compound (C10H18N2O9SZn M-r=407.69) belongs to the hexagonal system, space group P 6(5) with cell parameters: a=11.411 (2), c=20.908(4) Angstrom, V=2357.7(7) Angstrom(3), Z=6, D-c=1.723g/cm(3), F(000)=1260, mu(MoKa)=1.743mm(-1). The final R and omega R factors are 0.072 and 0.178 respectively for 1335 observed reflections. in the structure, zinc ions are bridged by 4,4'-bipyridine to form infinite chains. The sheets containing parallel chains stack along a 65 screw axis to give a helical staircase motif. The helical structure is mainly controlled by the hydrogen bonds.

Synthesis, properties and crystal structure of organic-inorganic radical salt (DBTTF)(6)HPMo12O40 center dot 2H(2)O

Organic-inorganic radical salt (DBTTF)(6)PMo12O40 . 2H(2)O was synthesized by electrocrystallization and characterized by IR spectrum, electronic spectrum and ESR technology, Its magnetic property, conductivity and crystal structure were determined. The title compound crystallized in a triclinic system with P1 space group, a = 1.378 7(7), b = 1.420 4 (2), c = 1.570 2(2) nm, alpha = 104.57(1)degrees, beta = 103.41(2)degrees, gamma = 95.80(2)degrees, V = 2.853(2) nm(3) Z = 1 and a final R = 0.072 7.

大型藻类在工程治理海水富营养化和抑制病原微生物中的作用

沿海工农业生产的快速发展和人类活动对近海生态系统产生了很大影响，大量化肥的使用和工业污水、生活污水的排放导致近海环境污染，海水富营养化，赤潮频发。另外，由于近海养殖活动的迅猛发展以及养殖的不规范和不科学性导致近海生态系统结构和功能改变，一方面加重了海水富营养化，另一方面养殖动植物病害经常发生，严重影响了海产品的质量和效益。 大型海藻是海区重要的初级生产者，生命周期长、生长快，能通过光合作用吸收固定水体的C、N、P等营养物质来合成自身，同时增加水体溶解氧。因此，大型海藻被称为海洋环境中的生物过滤器。另外，由于大型藻类自身营养成分的复杂性和与藻共生的微生物多样性，大型海藻还可对生态系统中的浮游生物和微生物产生直接和间接影响。 在海洋环境，尤其是海水养殖水体环境存在着两个主要问题：海水富营养化和病源微生物控制，本文针对海洋环境中存在的这两个问题进行了探索研究。 以大型经济藻种长心卡帕藻（Kappaphycus alvarezzi）作为实验材料，分别在实验室内、室外藻类处理系统和海湾养殖现场三种条件下，进行藻类去除海水氮磷的一次性实验、半连续实验和连续实验，研究了其对海水中无机氮、无机磷的吸收速率和去除能力，初步评估了其生态价值。 构建了一种半封闭海域富营养化治理模式，以长心卡帕藻为实验材料，研究了其去除海水富营养化的能力，主要结果如下： （1）室内实验研究发现，长心卡帕藻对氮、磷的吸收速率随底物浓度升高而升高。在氮磷比为10:1，温度28℃条件下，氮浓度为50μmol • L-1时，藻对氮、磷的吸收速率达到最大，分别为0.93µmol • g-1（FW）• h-1和0.072µmol • g-1（FW）• h-1。 （2）人工修建的藻类养殖系统中进行的长心卡帕藻去除氮、磷的半连续实验，结果表明该藻具有连续去除海水DIN、DIP的能力。只要保持足够的底物浓度，长心卡帕藻对无机氮、无机磷的吸收速率达到最大，分别为0.3µmol • g-1（FW） • h-1和0.03µmol • g-1（FW）• h-1。但是对氮磷的吸收速率较室内实验有所降低。 （3）自然条件下，通过调查黎安海湾水质情况发现，长心卡帕藻具有较大的生态效益。在整个海湾大面积养殖卡帕藻，通过收获藻体，每年大约可以从海水中带走33吨氮素，7.5吨磷素。由于在海湾长心卡帕藻的作用，全年海湾水质保持在1-2级国家海水质量标准，产生了明显的生态效益。 另外，我们对大型藻类浒苔（Ulva clathrata）吸收氮磷和抑制鳗弧菌（Vibrio anguillarum）的效果进行了初步探索，结果表明：浒苔不仅对培养系统内无机氮和磷具有明显的去除作用，而且在异养细菌总量没有降低的情况下，对鳗弧菌有显著抑制作用，该抑制作用还受到水体中氮磷营养盐浓度的影响。在10g • L-1海藻的条件下，鳗弧菌以105－107 cfu • mL-1接入2天后，无论是否添加外源氮磷，鳗弧菌密度降到10 cfu • mL-1以下，鳗弧菌去除率几乎达到100%。实验数据还显示，添加氮磷营养盐可以增强浒苔对鳗弧菌的抑制作用，但没有降低其中的异养菌群数量，系统内异养细菌总量均维持在较高水平。进一步研究表明，培养浒苔24h后的海水，也对鳗弧菌65#产生抑制作用，这说明浒苔代谢释放到水体中某种化学成分或与藻共栖的微生物对鳗弧菌生长产生了抑制。

Crystal structure of (5R,10R)-2,7-dibromo-3,8-dihydroxy-5,10-dimethoxy-5,10-dihydrochromeno[5,4,3-cde]chromene sesquihydrate, C16H12Br2O6 center dot 1.5H(2)O

C16H15Br2O7.5, orthorhombic, P2(1)2(1)2 (no. 18), a = 18.483(2) angstrom, b = 9.413(1) angstrom, c = 10.072(1) angstrom, V = 1752.3 angstrom(3), Z = 4, R-gt(F) = 0.083, wR(ref)(F-2) = 0.202, T= 293 K.