一种HEVC样点自适应补偿快速算法

为解决高性能视频编码标准H.265/HEVC中引入的样点自适应补偿技术的计算复杂度极高导致严重影响编码效率的问题,提出一种HEVC样点自适应补偿快速算法.首先根据编码单元(coding unit, CU)的划分深度确定亮度树形编码块(coding tree block, CTB)中需要提取边缘方向的区域,然后利用边缘方向提取算法获得亮度CTB的边缘方向列表,并根据此列表减少亮度CTB在模式判别过程中遍历的模式数量,最后利用亮度和色度CTB之间的相关性进一步简化色度CTB的模式判别过程.实验结果表明,在性能损失较小的情况下,本算法可以在全I帧(AI)、随机访问(RA)、低延时B帧(LB)、低延时P帧(LP)四种配置下分别节省31.75%、 56.85%、 52.81%、 51.51%的样点自适应补偿编码时间.     

基于模型的汽油机电子节气门控制器设计

摘要： 建立了电子节气门系统模型，并通过系统辨识方法得出模型参数.根据被控电子节气门的摩擦力和非线性回位弹簧模型，设计了前馈非线性补偿控制器.将经过前馈非线性补偿后的电子节气门系统简化成线性系统，并对该线性系统进行H无穷控制器的设计.对设计的H无穷控制器进行离散化，并加入比例控制环节来弥补控制器离散化导致的性能下降.经过试验验证，在前馈非线性补偿器、H无穷控制器和比例控制的作用下，被控电子节气门的性能达到了设计需求.     

梯度网络平稳点集合的Hopfield稳定性与吸引域

给出梯度神经网络模型的电路实现 ,证明了网络平稳点集合的全局 Hopfield稳定性。对各个平稳点吸引域的几何估计得到了相关结果 ,这为网络初始输入的数量与方向判定提供了基本的量度参数准则。     

提高风险投资过程中两级委托—代理效率的思考

本文从对风险投资者与风险投资商、风险投资商与风险企业之间的两层委托代理的简要分析入手 ,首先在诠释委托—代理效率内涵的基础上构建了分析委托—代理效率的一个理论框架 ,并应用此框架对如何提高上述两层委托—代理关系的效率问题进行了探讨     

The controlling factors and distribution prediction of H2S formation in marine carbonate gas reservoir, China

Generally, there are some anhydrites in carbonate reservoir, as H2S is also familiar in carbonate oil and gas reservoirs. Nowadays, natural gas with high H2S concentration is usually considered as TSR origin, so there is close relationship between H2S and anhydrite. On the contrary, some carbonate rocks with anhydrite do not contain H2S. Recently, researches show that H2S is only a necessary condition of H2S formation. The reservoir porosity, sulfate ion content within formation water, reservoir temperature, oil/gas and water interface, hydrocarbon and some elements of reservoir rock have great controlling effects on the TSR occurrence. TSR deoxidizes hydrocarbon into the acidic gas such as H2S and CO2, and the H2S formation is controlled by TSR occurrence, so the relationship among reaction room, the contact chance of sulfate ion and hydrocarbon, the reservoir temperature has great influence on the TSR reaction. H2S has relatively active chemical quality, so it is still controlled by the content of heavy metal ion. Good conditions of TSR reaction and H2S preservation are the prerequisite of H2S distribu- tion prediction. This paper builds a predictive model based on the characteristic of natural gas reservoir with high H2S-bearing. In the porosity reservoir with anhydrite, the formation water is rich in sulfate and poor in heavy metal ion. Oil and gas fill and accumulate in the gas reservoir with good preservation conditions, and they suffered high temperature later, which indicates the profitable area of natural gas with high H2S-bearing.     

实现细粒煤深度脱硫产业化的研究

根据我国高硫煤的赋存特点,提出采用微细介质重介旋流器及细泥选择性絮凝组合工艺实现细粒煤的深度脱硫,无机硫脱除率可大幅度提高,分选下限明显降低,是实现煤炭深度脱硫降灰产业化的有效技术途径.     

硬盘分区链表中结点信息的完全恢复算法

通过对分区链表中结点信息的研究 ,及前后结点中相关数据项比较之后 ,参照磁盘基数表中所记录的相应分区长度 ,给出了其中任一结点或整个分区链表丢失之后的修复算法     

三元酸易溶酸式盐溶液酸碱度的计算

对三元酸易溶酸式盐溶液(铵盐除外)中H^ 离子浓度的计算公式及公式的应用进行讨论。     

Theoretical study on the lithium bond interaction of furan homologues C_4H_4Y (Y=O, S) with LiCH_3 via DFT and MP2

The optimizations geometries and interaction energy corrected by BSSE of the complexes between C4H4Y (Y=O, S) and CH3Li have been calculated at the B3LYP/6-311 G** and MP2/6-311 G** levels. Three complexes were obtained. Abnormally, the calculations showed that all the C10—Li14 bond lengths increased obviously but the blue-shift of C10—Li14 stretching frequency occurred after formed complexes. The calculated binding energy with basis set super-position error (BSSE) and zero-point vibrational energy corrections of complexes I―III is ?45.757, ?35.700 and ?39.107 kJ·mol?1, respectively. The analyses on the combining interaction with the atom-in-molecules theory (AIM) also showed that a relatively strong lithium bond interaction presented in furan homologues C4H4Y---LiCH3 systems. Natural bond orbital theory (NBO) analysis has been performed, and the results revealed that the com- plex I is formed with n-σ type lithium bond interaction between C4H4O and LiCH3, complex II is formed with π-s type lithium bond interaction between C4H4O and LiCH3, and complex III is formed with π-s and n-s type lithium bond interactions between C4H4S and LiCH3, respectively.