基于单字提示特征的中文命名实体识别快速算法

近年来条件随机场(CRF)模型在自然语言处理中的应用越来越广泛。标准的线性链(Linear-chain)模型一般采用L—BFGS参数估计方法，收敛速度慢。本文在分析模型复杂度的基础上提出了一种改进的快速CRF算法。该算法通过引入小规模单字特征降低特征的规模，并通过在推理过程中引入任务相关的人工知识压缩Viterbi和Baum-Welch格搜索空间，提高了训练的速度。在中文863命名实体识别评测语料和SIGHAN06语料集上进行的实验表明，该算法在不影响中文命名实体识别精度的同时，有效地降低了模型的训练代价。

一种基于JMX的远程作业管理系统设计与实现

文章提出了一种新型远程作业管理系统框架.该框架基于JMX架构,融合了基于企业权限映射模型的安全机制、JSF（Java Server Face）的可视化框架等多项技术,有效地改进了传统的作业管理系统的可扩展性差、安全机制不足和缺乏统一、完善的系统管理三点不足.并基于该框架实现了国家863项目“远程作业管理系统”,实现了灵活的系统组件动态配置,基于企业权限映射模型的高安全和可视化管理界面,比较了实现系统和传统系统的优点,讨论了其中涉及到的关键技术.

波浪能海水淡化的应用研究

简要介绍了“十五”期问在广东省汕尾市研建的波浪能海水淡化系统的组成和工作原理。为了验证波浪能海水淡化装置运行的实用性和可靠性，在国内外波浪能海水淡化研究的基础上，对汕尾波浪能海水淡化装置进行了不同操作压力情况下的试验研究。研究结果表明，随着高压海水压力的升高，产出淡水量会明显增加，淡水质量提高，装置产出淡水的能耗较低。

中国海洋能专利研究

专利是除论文外的又一非常重要的科技成果。目前专利申请工作并未得到足够重视，并且文献中对专利技术成果的反映甚少。文章对中国国家知识产权局（SIPO）专利数据库中海洋能专利授权情况进行了分类统计。介绍了波浪能、潮汐能、温差能的最新专利，并指出了该领域专利申请的热点和空白领域。最后根据统计数据从专利的角度分析了中国海洋能研究的进展和前景。

小型水产养殖热泵试验数据的采集及计算机处理

本文叙述了小型水产养殖热泵试验数据采集的特点及其仪表，并利用R22工质的数据库程序块及计算框图，采用计算机数据处理的方法进行计算，精度高，速度快，对工质为R22的空气—水型热泵系统的数据处理提供了一种较好的计算方法。

Effect of Ru addition to CO/SiO2/HZSM-5 catalysts on Fischer-Tropsch synthesis of gasoline-range hydrocarbons

Microporous HZSM-5 zeolite and mesoporous SiO2 supported Ru-Co catalysts of various Ru adding amounts were prepared and evaluated for Fischer-Tropsch synthesis (FTS) of gasoline-range hydrocarbons (C-5-C-12). The tailor-made Ru-Co/SiO2/HZSM-5 catalysts possessed both micro- and mesopores, which accelerated hydrocracking/hydroisomerization of long-chain products and provided quick mass transfer channels respectively during FTS. In the same time. Ru increased Cor reduction degree by hydrogen spillover, thus CO conversion of 62.8% and gasoline-range hydrocarbon selectivity of 47%, including more than 14% isoparaffins, were achieved simultaneously when Ru content was optimized at 1 wt% in Ru-Co/SiO2/HZSM-5 catalyst.

Design and operation of integrated pilot-scale dimethyl ether synthesis system via pyrolysis/gasification of corncob

The integrated pilot-scale dimethyl ether (DME) synthesis system from corncob was demonstrated for modernizing utilization of biomass residues. The raw bio-syngas was obtained by the pyrolyzer/gasifier at the yield rate of 40-45 Nm(3)/h. The content of tar in the raw bio-syngas was decreased to less than 20 mg/Nm(3) by high temperature gasification of the pyrolysates under O-2-rich air. More than 70% CO2 in the raw bio-syngas was removed by pressure-swing adsorption unit (PSA). The bio-syngas (H-2/CO approximate to 1) was catalytically converted to DME in the fixed-bed tubular reactor directly over Cu/Zn/Al/HZSM-5 catalysts. CO conversion and space-time yield of DME were in the range of 82.0-73.6% and 124.3-203.8 kg/m(cat)(3)/h, respectively, with a similar DME selectivity when gas hourly space velocity (GHSV, volumetric flow rate of syngas at STP divided by the volume of catalyst) increased from 650 h(-1) to 1500 h(-1) at 260 degrees C and 4.3 MPa. And the selectivity to methanol and C-2(+) products was less than 0.65% under typical synthesis condition. The thermal energy conversion efficiency was ca. 32.0% and about 16.4% carbon in dried corncob was essentially converted to DME with the production cost of ca. (sic) 3737/ton DME. Cu (111) was assumed to be the active phase for DME synthesis, confirmed by X-ray diffraction (XRD) characterization.

Study on the hydrolysis/precipitation behavior of Keggin Al-13 and Al-30 polymers in polyaluminum solutions

The hydrolysis/precipitation behaviors of Al3+, Al-13 and Al-30 under conditions typical for flocculation in water treatment were investigated by studying the particulates' size development, charge characteristics, chemical species and speciation transformation of coagulant hydrolysis precipitates. The optimal pH conditions for hydrolysis precipitates formation for AlCl3, PAC(A113) and PAC(A130) were 6.5-7.5, 8.5-9.5, and 7.5-9.5, respectively. The precipitates' formation rate increased with the increase in dosage, and the relative rates were AlCl3 >> PAC(A130) > PACA113. The precipitates' size increased when the dosage increased from 50 mu M to 200 mu M, but it decreased when the dosage increased to 800 AM. The Zeta potential of coagulant hydrolysis precipitates decreased with the increase in pH for the three coagulants. The isoelectric points of the freshly formed precipitates for AlCl3, PAC(A113) and PAC(A130) were 7.3, 9.6 and 9.2, respectively. The Zeta potentials of AlCl3 hydrolysis precipitates were lower than those of PAC(A113) and PAC(A130) when pH > 5.0. The Zeta potential of PAC(A130) hydrolysis precipitates was higher than that of PACA113 at the acidic side, but lower at the alkaline side. The dosage had no obvious effect on the Zeta potential of hydrolysis precipitates under fixed pH conditions. The increase in Zeta potential with the increase in dosage under uncontrolled pH conditions was due to the pH depression caused by coagulant addition. Al-Ferron research indicated that the hydrolysis precipitates of AlCl3 were composed of amorphous AI(OH)3 precipitates, but those of PACA113 and PACA130 were composed of aggregates of Al-13 and Al-30, respectively. Al3+ was the most un-stable species in coagulants, and its hydrolysis was remarkably influenced by solution pH. Al-13 and Al-30 species were very stable, and solution pH and aging had little effect on the chemical species of their hydrolysis products. The research method involving coagulant hydrolysis precipitates based on Al-Ferron reaction kinetics was studied in detail. The Al species classification based on complex reaction kinetic of hydrolysis precipitates and Ferron reagent was different from that measured in a conventional coagulant assay using the Al--Ferron method. The chemical composition of Al-a, Al-b and Al-c depended on coagulant and solution pH. The Al-b measured in the current case was different from Keggin Al-13, and the high Alb content in the AlCl3 hydrolysis precipitates could not used as testimony that most of the Al3+ Was converted to highly charged Al-13 species during AlCl3 coagulation.

Kinetic Model Study on Enzymatic Hydrolysis of Cellulose Using Artificial Neural Networks

Enzymatic hydrolysis of cellulose was highly complex because of the unclear enzymatic mechanism and many factors that affect the heterogeneous system. Therefore, it is difficult to build a theoretical model to study cellulose hydrolysis by cellulase. Artificial neural network (ANN) was used to simulate and predict this enzymatic reaction and compared with the response surface model (RSM). The independent variables were cellulase amount X-1, substrate concentration X-2, and reaction time X-3, and the response variables were reducing sugar concentration Y-1 and transformation rate of the raw material Y-2. The experimental results showed that ANN was much more suitable for studying the kinetics of the enzymatic hydrolysis than RSM. During the simulation process, relative errors produced by the ANN model were apparently smaller than that by RSM except one and the central experimental points. During the prediction process, values produced by the ANN model were much closer to the experimental values than that produced by RSM. These showed that ANN is a persuasive tool that can be used for studying the kinetics of cellulose hydrolysis catalyzed by cellulase.

Isolation and Characterization of a Methomyl-Degrading Paracoccus sp mdw-1

Methomyl, an extremely toxic pesticide, is widely used in agriculture. A strain named mdw-1 capable of degrading methomyl rapidly was successfully isolated from activated sludge in this study. It could utilize methomyl as the sole carbon or nitrogen source. The optimal temperature and medium pH for its growth and methomyl biodegradation were 30 degrees C and 7.0, respectively. It was identified as a Paracoccus sp. according to its morphological features, physiological and biochemical characteristics, and phylogenetic analysis based on the sequence of 16S rDNA. Gas chromatography-mass spectrometry (GC-MS) analysis showed that methomyl could be completely transformed to S-methyl-N-hydroxythioacetamidate in 10 h of incubation with the isolate mdw-1.

Low potential detection of glutamate based on the electrocatalytic oxidation of NADH at thionine/single-walled carbon nanotubes composite modified electrode

A glutamate biosensor based on the electrocatalytic oxidation of reduced nicotinamide adenine dinucleotide (NADH), which was generated by the enzymatic reaction, was developed via employing a single-walled carbon nanotubes/thionine (Th-SWNTs) nanocomposite as a mediator and an enzyme immobilization matrix. The biosensor, which was fabricated by immobilizing glutamate dehydrogenase (GIDH) on the surface of Th-SWNTs, exhibited a rapid response (ca. 5 s), a low detection limit (0.1 mu M), a wide and useful linear range (0.5-400 mu M), high sensitivity (137.3 +/- 15.7) mu A mM(-1) cm(-2), higher biological affinity, as well as good stability and repeatability. In addition, the common interfering species, such as ascorbic acid, uric acid, and 4-acetamidophenol, did not cause any interference due to the use of a low operating potential (190 mV vs. NHE). The biosensor can be used to quantify the concentration of glutamate in the physiological level. The Th-SWNTs system represents a simple and effective approach to the integration of dehydrogenase and electrodes, which can provide analytical access to a large group of enzymes for wide range of bioelectrochemical applications including biosensors and biofuel cells.

基于Vif-APOBEC3G相互作用的抗HIV-1药物研究

载脂蛋白B mRNA编辑酶催化多肽样蛋白3G(apolipoprotein B mRNA-editing enzyme catalyticpolypeptidelike3G,APOBEC3G或A3G)是人体天然抗病毒分子,可以使病毒逆转录形成的cDNA的胞嘧啶(C)脱氨为尿嘧啶(U),产生鸟嘌呤(G)→腺嘌呤(A)超突变,导致病毒转录产物突变,从而达到抑制病毒复制的作用。HIV-1的辅助蛋白Vif,可与APOBEC3G相互作用并导致其被降解,使得这一天然抗病毒机制失效,进而增强了HIV的感染力。Vif与APOBEC3G这种相互作用为抗HIV药物提供了新靶点。针对Vif-APOBEC3G相互作用的抗HIV抑制剂已经成为研究热点。本文综述了Vif和APOBEC3G的结构、二者的相互作用,以及基于这一相互作用的抗HIV-1抑制剂研究进展。

纳米银体外抗HIV 活性的研究

［ 目的］ 制备纳米银颗粒并检测其抗人类免疫缺陷病毒（HIV） 活性及其体内外毒性， 探讨纳米银体外抗 HIV 的作用机制。［ 方法］ 在体外培养C8166 细胞中加入不同浓度的纳米银， 检测其体外细胞毒性CC50； 不同病毒株 感染细胞， 同时加入不同浓度的纳米银， 孵育后检测细胞病变及病毒抗原， 检测纳米银对HIV 的抑制作用。纳米银滴鼻 处理小鼠， 检测小鼠体重变化， 并进行病理切片， 观察纳米银滴鼻处理小鼠的肝、肾及肺组织的病理变化。［ 结果］ 纳米银颗粒对C8166 细胞毒性的CC50 为105.73 μg ／ ml， 抑制HIV 实验株HIV-1IIIB， HIV-2CBL-20 诱导细胞病变的 EC50 分别为26.56 μg ／ ml 和35.47 μg ／ ml； 抑制HIV-1IIIB p24 抗原产生的EC50 为9.80 μg ／ ml； 直接杀病毒作用的EC50 为 12.08 μg ／ ml。纳米银经滴鼻处理的小鼠， 其体重及肝、肾及肺组织切片与对照组比较， 均无明显改变。［ 结论］ 纳米 银有较好的抗HIV 活性， 作用机制可能主要通过直接杀病毒来抑制HIV 的复制； 纳米银在呼吸道黏膜局部应用无明显 的毒副作用， 作为黏膜表面抗病毒药物， 值得进一步深入研究。

PASSIVATION OF THE INP(100) SURFACE USING (NH4)(2)S-X

InP(100) surface treated with (NH4)(2)S-x has been investigated by using photoluminescence(PL), Auger electron spectroscopy and X-ray photoelectron spectroscopy. It is found that PL intensity increased by a factor of 3.3 after (NH4)(2)S-x passivation and the sulfur remained on the surface only bonded to indium, not to phosphorus. This suggests that the sulfur atoms replace the phosphorus atoms on the surface and occupy the phosphorus vacancies.

基于silica波导光栅的单纤三向器的混合集成研究

通过有源实时监控系统,采用手动和自动相结合的方法,将光纤、silica基阵列波导光栅(AWG)、1310 nm激光器(LD)平台和1490 nm、1550 nm探测器(PD)平台用紫外同化胶混合集成为一新型单纤三向器.在耦合集成过程中,LD在15 mA偏置电流下,三向器的上行出纤功率大约为-4 dBm,LD和波导的耦合效率大约40%;当三向器输入1 550 nm光功率为1 mW,PD在2.6 V反向偏压下,下行输出光电流大约为76 μA,波导和PD的耦合效率大约为42%.三向器中采用了对管PD集成方法.