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Dynamics of Polymeric Fluids 1. The Molecular Theory of Die Swell: A Set of Equation on Swelling Ratio in Extrudates

Mingshi SONG , Guixian HU , Zhihong YANG , Qiang XU , Sizhu WU , null , null , null , null

材料科学技术(英文)

The structural model of the multiple-transient networks and the mechanism of the multiple-reptation entangled chains due to the dynamic reorganization in the entangled sites were extensively applied on the die swell of polymeric liquids in the steady simple shear flow. The total (recoverable and unrecoverable) viscoelastic free energy of deformation and flow, the constitutire equation and the expression of the simple shear (tanψ) were deduced from the conformational probability distribution function of the entangled polymer chains. It found that: (1) the magnitudes of simple shear (tanψ) depended not only on the free recoil (or recoverable strain) but also on the viscous heating (or unrecoverable strain); (2) the total recoil may be resolved into the instantaneous and delayed recoil. Based on these facts, the functions of the partition and two experiential fractions of the recoverable ( ) and the unrecoverable ( ) conformations for the recoil and viscous heating of polymeric liquids were defined correspondingly. Then the correlation of the instantaneously and ultimately (or total) recoverable strains to the (N1/τ12)W and the fraction of trans-form conformation was obtained. After introducing the condition of uniform two-dimensional extension (αx=αy=α, αz=α-2) and the swell ratio (B=α), two sets of equations on the instantaneous and ultimate swelling ratios (BE, BEVT) were obtained, and a method to determine the fraction of the recoverable transform conformation were proposed. The equations of BE and BE5 were verified by the experimental data of HDPE (high denisity polyethylene) at two different high temperatures. It shows that the molecular theory of die swell can be used to predict the correlation of the swelling to the (N1/τ12)W and the fraction of trans-form conformation.

关键词: Die swell , null , null

Dynamics of Polymeric Fluids: Part II The Molecular Theory of Die Swell: Correlation of Ultimate Die Swelling Effect to the Molecular Parameters and the Operational Variables

Mingshi SONG , Qiang XU , Guixian HU , Sizhu WU , null

材料科学技术(英文)

A general expression for the correlation of the simple shear (tan ) to the molecular parameters and the shear rate ( ) was deduced. It shows that the simple shear (tan ) may be resolved into free recoil (recoverable strain) and viscous heating (unrecoverable strain). The magnitudes of the simple shears for recoil (tan E) and (tan V) for viscous heating not only depended on the molecular parameters and the operational variables, but also on the exponential fractions of the recoverable (1- ) and unrecoverable ( ) conformations for recoil and viscous heating. Therefore the magnitudes of the simple shears (tan E) for recoil and (tan V) for viscous heating are, respectively, expressed as the partition function to the (1- )th power and the partition function to the ( )th power. Thus correlations of the total recoil and the ultimately recoverable strains to the molecular parameters [ , a, η0, GN0 and (1- )] and the operational variables ( ), (L=D) and tr) were deduced respectively, which show that at very different shear rates ( ) the polymeric liquids may exhibit a very different viscoelastic behaviors. After introducing the uniform two-dimensional extension, the definition of swelling ratio and the ratio of L to D [De=(L/D)], two expressions for the ultimate die swelling effect and the ultimate extrudate swelling ratio BEVT5 to the molecular parameters [ , a, η0, GN0 and (1- )] and the operational variables ( , (L/D) and tr) were obtained. The two correlation expressions were verified by the experimental data of high-density polyethylene (HDPE) which shows that the two correlation expressions can be used to predict the correlations of the ultimate extrudate swelling behaviors of polymeric liquids to the molecular parameters and the operational variables.

关键词: Die swell , null , null

Part V: A New Molecular Theory of Non-linear Viscoelasticity for Polymeric Suspensions

Mingshi SONG , Wen ZHOU , Guixian HU , Lijiang HU

材料科学技术(英文)

A double-network model is established, which consists of the segments, E and A-constituent chains, the polymeric chains entangled with other ones by multi-entanglement and polymeric chains connected to a great number of destructible particles by multi-adsorption, based on which the E and A-constituent chains can be recreated and released dynamically. The distribution function of the end-to-end vector, the statistical distribution function of conformation for two kinds of chains in the multi-entanglement and multi-adsorption states and their number of polymeric chains are calculated by the combination of statistical mechanics and kinetics. Then the viscoelastic free energies of deformation for two kinds of the networks and suspensions are calculated by Boltzmann's statistical theory. Also, elastic modulus and memory function for two kinds of the network and suspensions are derived. Consequently, a new molecular theory of the non-linear viscoelasticity for polymeric suspensions is proposed, and the constitutive equation and material function with yielding and thinning for the polymeric suspensions in different flow fields are derived from this theory.

关键词:

Rheological Behaviors of Polymer Melts and Concentrated Solutions

Mingshi SONG , Wen ZHOU , Guixian HU , Lijiang HU

材料科学技术(英文)

The memory function and elastic modulus were introduced into the O-W-F type of constitutive equations with the Cauchy-Green and Finger tensors for simple fluid, and then the concrete constitutive equation and material function for polymeric suspensions in the different flow fields were formulated: 1) Viscosity and first normal-stress difference coefficient in the shear flow field; 2) Tensile viscosity at the uni-axial elongation flow field; and 3) Dynamic viscosity and modulus in the dynamic field. Then the dependence of the material function on the deformation rate and weight fraction of fillers was discussed, and the shear flow curves with four characteristic regions ( I-low shear rate plateau region, II-apparent yielding region, III-intermediate rate plateau region, and IV-shear thinning region.) were explained theoretically. Finally, it was verified by a number of experimental values for the rheological suspensions and the viscoelastic and mechanical behaviors can be predicted by the molecular theory of non-linear viscoelasticity for polymeric suspensions.

关键词:

Rheological behavior for polymer melts and concentrated solutions Part VII: A quantitative verification for the molecular theory of non-linear viscoelasticity with entanglement constraints in polymer melts

Mingshi SONG , Chen ZHANG , Guixian HU

材料科学技术(英文)

Based on the molecular theory of non-linear viscoelasticity with constrained entanglements in polymer melts, the material functions in simple shear flow were formulated, the theoretical relations between. eta((gamma) over dot), psi (10)((gamma) over dot) and shear rate ((gamma) over dot), and topologically constrained dimension number n ' and a were derived. Linear viscoelastic parameters (eta (0) and G(N)(0)) and topologically constrained dimension number (n ' a and <()over bar>) as a function of the primary molecular weight (M-n), molecular weight between entanglements (M-C) and the entanglement sites sequence distribution in polymer chain were determined. A new method for determination of viscoelastic parameters (eta (0), psi (10), G(N)(0) and J(e)(0)), topologically constrained dimension number (n ', a and v) and molecular weight (M-n, M-c and M-e) from the shear flow measurements was proposed. It was used to determine those parameters and structures of HDPE, making a good agreement between these values and those obtained by other methods. The agreement affords a quantitative verification for the molecular theory of nonlinear viscoelasticity with constrained entanglement in polymer melts.

关键词:

116HU聚酯亚胺无挥发浸渍树脂的性能及其在风电上的模拟结构试验

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

SAR图像目标识别新方法

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

硝酸羟胺的热稳定性评估及热分解机理研究

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

INVESTIGATION OF HYDROGEN INDUCED DUCTILE BRITTLE TRANSITION IN 7175 ALUMINUM ALLOY

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

基于Android平台的地震云轮廓提取与匹配研究

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 , Android

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