王君
,
邹家桂
,
陈政标
,
高建武
,
刘彦坤
,
张杰元
,
宋莎
绝缘材料
为解决苯乙烯和甲基苯乙烯在VPI浸渍树脂应用于风力发电机中的不足，采用不饱和聚酯亚胺、引发剂和无挥发活性稀释剂研制出116HU聚酯亚胺无挥发浸渍树脂，并对其各项性能进行了研究。结果表明：116HU聚酯亚胺无挥发浸渍树脂的常规性能满足风力发电机的要求，其耐热等级可达H级。用该树脂浸渍的风电模拟线棒具有优异的介电性能、耐湿热交变和高低温循环冲击性能及耐盐雾性能等，能满足风力发电机在极端环境运行的要求。
关键词:
聚酯亚胺
,
无挥发
,
VPI
,
风力发电机
,
耐湿热
,
耐盐雾
王丽
,
魏巍
,
吴林钢
,
王灿进
液晶与显示
doi:10.3788/YJYXS20142903.0429
提出一种SAR图像目标识别新方法.首次引入BM3D方法,用于滤除原始图像中的相干斑噪声,BM3D结合了空间域和变换域去噪的优势,滤波性能优异.在特征提取步骤,将低阶Hu矩与高阶Zernike矩组合,Hu矩描述目标的粗略信息,高阶Zernike矩描述目标的细节信息,因此组合矩能够更加全面而细致地表达目标特性.使用组合矩特征训练SVM分类器,对含噪的SAR图像进行识别实验.实验结果表明:本文方法的识别率高达98.90％,优于已有的SAR目标识别方法.
关键词:
SAR图像
,
目标识别
,
BM3D滤波
,
组合矩
刘建国
,
安振涛
,
张倩
,
杜仕国
,
姚凯
,
王金
材料导报
doi:10.11896/j.issn.1005-023X.2017.04.030
为评估氧化剂硝酸羟胺的热稳定性,使用标准液体铝皿于3 K/min、4 K/min、5 K/min加热速率下进行热分析.借助非等温DSC曲线的参数值,应用Kissinger法和Ozawa法求得热分解反应的表观活化能和指前因子,根据Zhang-Hu-Xie-Li公式、Hu-Yang-Liang-Xie公式、Hu-Zhao-Gao公式以及Zhao-Hu-Gao公式,计算硝酸羟胺的自加速分解温度和热爆炸临界温度,并对热分解机理函数进行了研究.设计了7条热分解反应路径,采用密度泛函理论B3LYP/6-311++G(d,p)方法对硝酸羟胺的热分解进行了动力学和热力学计算.计算结果表明,硝酸羟胺热分解的自加速分解温度TsADT=370.05 K,热爆炸临界温度Te0=388.68K,Tbp0=397.54 K,热分解最可几机理函数的微分形式为f(a) =17×(1-α)18/17.硝酸羟胺热分解各路径中,动力学优先支持路径Path 6、Path 5、Path 4和Path 1生成NO和NO2,其次是Path 2、Path 7和Path 3生成N2和N2O.温度在373 K以下时,Path 1'反应无法自发进行,硝酸羟胺无法进行自发的热分解.从热力学的角度来看,硝酸羟胺在370.05K以下储存是安全的.
关键词:
硝酸羟胺
,
热分析
,
热稳定性
,
热分解机理
,
密度泛函理论
赵洁
,
姚秉华
,
冯逸晨
功能材料
采用共沉淀法制备BiNbO4纳米棒。利用X射线粉末衍射仪（XRD）、透射电镜（TEM）、紫外-可见漫反射光谱（UV-Vis DRS）和热重分析（TG/DTA）对其结构、形貌和性质进行表征,并通过紫外-可见分光光度计分析BiNbO4纳米棒光降解罗丹明B来研究其光催化活性。结果表明以五氧化二铌和五水硝酸铋为原料制备得到正交相结构的BiNbO4纳米棒;BiN-bO4纳米棒具有较高的光催化活性,在紫外光下,pH值=3.05,催化剂用量为2g/L时能够有效地降解罗丹明B,降解率受到光源、催化剂浓度和溶液pH值的影响较大。
关键词:
共沉淀法
,
BiNbO4纳米棒
,
光催化
杨飒
,
郑志硕
量子电子学报
doi:10.3969/j.issn.1007-5461.2015.03.005
针对尺度不变特征变换(Scale-invariant feature transform,SIFT)算法在关键点特征描述向量阶段计算复杂并且维数较高的现象,提出了一种基于压缩感知理论的SIFT算法.通过压缩感知理论的稀疏特征表示方法,对SIFT关键点特征向量进行提取,将高维梯度导数向量降到低维稀疏特征向量,降低了关键点描述向量维度.采用欧式距离作为关键点的相似性度量, Best-Bin-First(BBF)数据结构避免穷举,使数据的运算量大为减少.实验结果表明,新算法对存在仿射变换的医学图像配准性能优于传统SIFT算法,与当前改进型的SIFT算法相比,本文算法的实时性明显增强.
关键词:
图像处理
,
图像配准
,
尺度不变特征变换
,
特征提取
,
稀疏随机投影
李伟国
,
祁超
,
刘立岩
,
赵大庆
应用化学
doi:10.3969/j.issn.1000-0518.2005.11.003
分别研究了二乙三胺五乙酸(DTPA)及2种衍生物二乙三胺五乙酸-双二甲酰胺(DTPA-BDMA)和二乙三胺五乙酸-双(异烟肼)(DTPA-BIN)对乳酸脱氢酶活性及酶促反应动力学的影响.结果表明,它们均可以抑制脱氢酶的活性,其抑制类型为竞争性的抑制作用,抑制常数分别为3.37、7.41、8.52μmol/L.紫外差谱结果表明,DTPA及其衍生物可以和酶分子作用,其羧基部分被包埋到分子内部,在酶分子的结合部位存在芳香族的氨基酸残基.DTPA与脱氢酶作用后使酶分子中的色氨酸荧光强度减弱,对酪氨酸的荧光没有明显影响.
关键词:
二乙三胺五乙酸
,
乳酸脱氢酶
,
酶学动力学
,
紫外差谱
,
荧光光谱
金属学报(英文版)
桑危郑牛樱裕桑牵粒裕桑希巍。希啤。龋伲模遥希牵牛巍。桑危模眨茫牛摹。模眨茫裕桑蹋拧。拢遥桑裕裕蹋拧。裕遥粒危樱桑裕桑希巍。桑巍。罚保罚怠。粒蹋眨停桑危眨汀。粒蹋蹋希?##2##3##4##5INVESTIGATIONOFHYDROGENINDUCEDDUCTILEBRITTLETRANSITIONIN7175ALUMINUMALLOY$R.G.Seng:B.JZhong,MG.ZengandP.Geng(DepartmentofMaterialsScierce,ScienceCollege,NorthearsternUniveisity,Shenyang110006,ChinaMaruscriptreceived4September1995inrevisedform20April1996)Abstrac:Effectsofhydrogenonthemechanicalpropertiesofdifferentlyaged7175aluminumalloyswereinvestigatedbyusingcathodicH-permeation,slowstrainratetensionandsoon.Theresultsindicatethatboththeyieldstressandthepercentagereductionofareadecreasewithincreasinghydrogenchargingtime,andthedegreeofreductiondecreasesasagingtimeincreasesforthesamehydrogenchargingtime.Keywords:hydrogeninducedductile-brittletransition,7175aluminumalloy,mechanicalproperty,cathodicH-permeation1.IntroductionForalongtimehydrogenembrittlementproblemwasthoughttobeabsentinhighstrengthaluminiumalloybecausethesolutiondegreeofhydrogeninaluminumatcommontemperatureandpressureisverysmall.However,hydrogenembrittlementphenomenonwasfoundinaluminumalloyduringtheinvestigationofstresscorrosionandcorrosionfatigue[1-5].Therehavebeenonlyafewreportsofhydrogeninducedsofteningandhardening.Inthispaper,theeffectsofhydrogenonmechanicalpropertiesof7175aluminumalloywereinvestigatedbyusingcathodicalchargingwithhydrogenandslowtensiontests.2.ExperimentalProcedureTheexperimentalmaterialwas7175aluminumalloyforgingintheformofa43mminthicknessandwithcomposition(wt%).5.41Zn,2.54Mg.1.49Cu,0.22Cr,0.1Mn.0.1Ti,0.16Fe.0.11Si,balancedbyA1.Alloyplateof1.5mminthicknesswasobtainedbyhot(465℃)andtoldrollingto83%reductioninthickness.Thelongaxisofhydrogenchargedspecimensisalongtherollingdirection.Allspecimensweresolidsolutionedat480℃for70min,followedtyimmediatequenchinginwaterandthenagedat140℃for6h(A),16h(B)and98h(C).Thetreatmentof6hiscorrespondingtotheunderagedstate.16hthefirstpeak-agedstateand98hthesecondpeak-agedstate.Thespecimenswerepolishedsuccessivelyusingemerypaperbeforehydrogencharging.Thetensilespecimenswerecathodicallychargedina2NH_2SO_4solutionwithasmallamountofAs_2O_3forpromotinghydrogenabsorption,andwithacurrentdensityof20±1mA/cm￣2atroomtemperature.ThehydrogencontentanalysiswascarriedoutonanLT-1Amodelionmassmicroprobeafterthesputteringdepthreached8nm.Theioncurrentsofhydrogenandaluminuminvariousagedstateswererecordedunderthesamecondition.ThetensiletestswereperformedonanAG-10TAmodeltestmachinewhichwascontrolledbycomputer.3.ExperimentalResultsTheratioofioncurrentstrengthofhydrogentoaluminumisrelatedtohydrogenconcentrationinhydrogenchargedspecimen.TheresultswereshowninTable1Thehydrogencontentincreaseswiththeincreaseincharingtime.Ofthethreeagedstates,theunderagedspecimenhasthehighesthydrogencontent.Theratioofyieldstrengthofhydrogenchargedandunchargedspecimenschangeswithhydrogenchargingtime,asshowninFig.1Itcanbeseenthattheyieldstrengthofhydrogenchargedspecimendecreasewithincreasinghydrogenchargingtime.Atthesamechargingtime,theyieldstressdecreasestheleastinthesecondpeak-agedstate,anddecreasesthemostintheunderagedstate.Itindicatesthattheunderagedspecimenismostsensitivetohydrogeninducedsoftening,whichisconsistentwiththeresultsofanotherhighstrengthaluminumalloy[6].TherelativechangesoftheradioofreductionofareawithhydrogenchargingtimearesummarizedinFig.2,whereΨ￣0andΨ￣Harethepercentagereductionofareaofthesamplewithoutandwithhydrogenchargingrespectively.Theradioofreductionofareareduceswhenhydrogenchargingtimeincreases,andthedecreasingdegreeofreductionofareaincreaseswithincreasingagingtime,ie,,theunderagedstateisthemostsensitivetohydrogenembrittlement.4.DiscussionItisknownfromtheresultsabovethatcathodicalchargingwithhydrogenleadstotheobviousdecreaseinthetensilestrengthandplasticityThisisbecausealargeamountofsolidsolutionhydrogenentersthespecimenintheprocessofhydrogenchargingSolidsolutionhydrogenisliabletoenterthecentreofdislocationundertheactionofdislocationtrap,henceraisingthemovabilityofdislocation.Thereforethedislocationsinhydrogenchargedspecimenmoveeasierthaninunchargedspecimen.soresultinginthereductionofyieldstrength[7].Whendislocationstartstomove,thecrystallatticeresistance(P-Nforce)whichitmustovercomeisgivenby:whereμismodulusofshear,visPoissonratio,aisspanofslipplane,bisatomspanofslipdirection.Moreover.theotherresistanceofdislocationmotionmayarisefromtheelasticinteractionofdislocation,theactionwithtreedislocationandetc.,itcanbeexpressedasfollows:whereαisconstant,XisdislocationspanSotheresistanceofdislocationmotioncanbewrittenasfollows:Becausehydrogenatomsreducetheatombondingstrengthafterhydrogencharging,shearmodulusμdecreasesandresultsinthereductionoff,therebytheyieldstressdecreases.Asthecentreofdislocationistheseriousdistortionzoneoflattice.thestresscanberelaxedafterhydrogenatomstuffing,andthesystemenergydecreases.Thusthecentreofdislocationisastrongtrapofhydrogen[8].Therefore,amovabledislocationcaptureshydrogenandmigratestograinboundaries.phaseboundariesorsurfaceofthespecimen,promotingthecrackiesformationandgrowth,thuscausingthelossofplasticity.Sincethelocalenrichmentofhydrogenisrealizedbydislocationtransporting(inthestageofdeformation),thelargerthereductionofyieldstress.theearlierarehydrogenatomstransportedtotheplaceofenrichment.Inaddition,thedamageofatombondingstrengthinducedbyhydrogenmakesthefracturestressdecrease[9]:whereCHishydrogenconcentration.σ_thisfracturestrengthbeforehydrogenchargingandisfracturestrengthafterhydrogencharging.Eq.(4)showsthatthematerialsmaybefracturedatalowerstraini.e.,brittlefractureoccurs.5.Conclusions(1)Hydrogencontentofdifferentlyagedspecimensincreaseswithincreasinghydrogenchargingtimethecapabilityofthealloytoabsorbhydrogeninunderagedstateisthestrongest.(2)Theyieldstressaswellasthepercentagereductionofareaof7175aluminumalloydecreaseashydrogenchargingtimeincreasesundervariousagedstates.(3)Underagedstateismostsensitivetohydrogeninducedsofteningandhardening.(4)Anexplanationwasofferedforthephenomenonofhydrogeninducedsofteninginthestageofdeformation,andhardeninginthestageoffracture.REFERENCES｜｜1G.KKock,Corrosion35(1979)73.2M.K.TsengandH.LMarcus,Scr.Metall.15(1981)427.3PSFao.M.GaoandR.P.Wei,Scr.Metall.19(1985)265.4R.G.SongandM.K.TsengJ.NortheasternUniversity15(1994)5(inChinese).5R.K.Viswanadham,T.S.sunandJ.A.S.Green,Metall.Trans.11A(1980)85.6J.Liu,M.KTsengandB.R.Liu.NonferrousMiningandMetallrgy5(1989)33(inChinese).7LChen,WXChen,ZHLiuandZ.Q.Hu,InFrocofthe1stNationalConfonAl-LiAlloys(Sheryang.China,1991)p.328(inChinese).8Z.HLiuL.ChenW.XChenY.X.ShaoandZ.Q.Hu,InProc.ofthe1stNationalConfonAl-LiAlloys(Shenyang,China,1991)p.334(inChinese).9R.A.OrianiandF.H.Josephic,ActaMetall.22(1974)1065.##61G.KKock,Corrosion35(1979)73.2M.K.TsengandH.LMarcus,Scr.Metall.15(1981)427.3PSFao.M.GaoandR.P.Wei,Scr.Metall.19(1985)265.4R.G.SongandM.K.TsengJ.NortheasternUniversity15(1994)5(inChinese).5R.K.Viswanadham,T.S.sunandJ.A.S.Green,Metall.Trans.11A(1980)85.6J.Liu,M.KTsengandB.R.Liu.NonferrousMiningandMetallrgy5(1989)33(inChinese).7LChen,WXChen,ZHLiuandZ.Q.Hu,InFrocofthe1stNationalConfonAl-LiAlloys(Sheryang.China,1991)p.328(inChinese).8Z.HLiuL.ChenW.XChenY.X.ShaoandZ.Q.Hu,InProc.ofthe1stNationalConfonAl-LiAlloys(Shenyang,China,1991)p.334(inChinese).9R.A.OrianiandF.H.Josephic,ActaMetall.22(1974)1065.##A##BINVESTIGATION OF HYDROGEN INDUCED DUCTILE BRITTLE TRANSITION IN 7175 ALUMINUM ALLOY$$$$R.G.Seng: B.J Zhong, MG. Zeng and P. Geng(Department of Materials Scierce, Science College,Northearstern Univeisity, Shenyang 110006, China Maruscript received 4 September 1995 in revised form 20 April 1996)Abstrac:Effects of hydrogen on the mechanical properties of differently aged 7175 aluminum alloys were investigated by using cathodic H-permeation, slow strain rate tension and so on. The results indicate that both the yield stress and the percentage reduction of area decrease with increasing hydrogen charging time, and the degree of reduction decreases as aging time increases for the same hydrogen charging time.
关键词:
:hydrogen induced ductile-brittle transition
,
null
,
null
,
null
苏琳琳
,
关桂霞
,
赵海盟
,
谭翔
,
徐振亮
,
吕书强
,
马蔼乃
,
晏磊
影像科学与光化学
doi:10.7517/j.issn.1674-0475.2016.01.059
针对当前地震云研究中只能利用长期以来的经验进行目视解译,无法形成系统的研究理论和研究模型的现状,结合目前流行的Android便携式设备,提出在Android平台上对地震云图像进行轮廓提取与匹配的研究思路.采用抗噪性能较好的数学形态学算法,在此基础上得到一种改进算法以提取出感兴趣区域,进而通过构造10个新的不变矩对Hu矩匹配算法进行改进,进行轮廓匹配,识别出地震云图像.在Android平台上则利用NDK(Native Delelopment Kit)通过JNI(Java Native Interface)调用OpenCV库函数,用C++语言实现改进算法.实验结果表明:该方法能够有效地识别时间序列下的地震云,正确率高,并且在Android平台上操作简单方便,为地震云预测地震提供初步研究基础和研究依据.
关键词:
地震云
,
轮廓提取
,
轮廓匹配
,
数学形态学
,
Hu矩
,
Android
张黛
,
范慧俐
,
徐晓伟
,
李永寿
,
李玉萍
人工晶体学报
doi:10.3969/j.issn.1000-985X.2003.01.015
采用氮气加压加温方法,以KBH4和NH4Cl为原料,通过在相同的温度、压力条件下,向反应体系中添加和不添加少量Li3N的对比实验,研究Li3N在KBH4和NH4Cl生成BN反应中的作用.反应产物中有无hBN和cBN生成是依据反应产物的X射线衍射图谱(XRD)和傅立叶变换红外光谱(FTIR)中有无hBN和cBN物相出现确认的.谢乐公式被用于估算生成的BN的粒径.结果表明,在650℃、7MPa的反应条件下,以KBH4和NH4Cl为原料没有生成BN的反应发生.但当在原料中加入Li3N后,反应产物中有大量hBN和少量cBN生成,其中hBN的平均颗粒尺寸约为14nm.分析确认,Li3N在上述由KBH4和NH4Cl合成hBN和cBN的反应中起催化作用.而且加入Li3N后,由KBH4和NH4Cl合成BN的反应压力和时间都明显低于Hu等人的相关报道结果.
关键词:
热气压法
,
合成
,
氮化硼
,
氮化锂
,
催化作用
