• <tr id="yyy80"></tr>
  • <sup id="yyy80"></sup>
  • <tfoot id="yyy80"><noscript id="yyy80"></noscript></tfoot>
  • 99热精品在线国产_美女午夜性视频免费_国产精品国产高清国产av_av欧美777_自拍偷自拍亚洲精品老妇_亚洲熟女精品中文字幕_www日本黄色视频网_国产精品野战在线观看 ?

    E ff ect of sodium tartrate concentrations on morphology and characteristics of anodic oxidefilm on titanium alloy Ti–10V–2Fe–3Al

    2016-11-24 00:50:02KunYuMeiLiuJinhuLiSongmeiWuLingYoWenhui
    CHINESE JOURNAL OF AERONAUTICS 2016年4期

    M Kun,Yu Mei,*,Liu Jinhu,Li Songmei,Wu Ling,Yo Wenhui

    aSchool of Materials Science and Engineering,Beihang University,Beijing 100083,China

    bSchool of Materials Science and Engineering,Chongqing University,Chongqing 400044,China

    E ff ect of sodium tartrate concentrations on morphology and characteristics of anodic oxidefilm on titanium alloy Ti–10V–2Fe–3Al

    Ma Kuna,Yu Meia,*,Liu Jianhuaa,Li Songmeia,Wu Liangb,Yao Wenhuia

    aSchool of Materials Science and Engineering,Beihang University,Beijing 100083,China

    bSchool of Materials Science and Engineering,Chongqing University,Chongqing 400044,China

    The effect of sodium tartrate concentrations on morphology and characteristics of anodic oxidefilm on titanium alloy was investigated.The alloy substrates were anodized in different concentration solutions of sodium tartrate with the addition of PTFE emulsion and their morphology and characteristics were analyzed.The anodic oxidefilm presented a uniform petaloid drums and micro-cracks morphology.Additionally,micro-cracks dramatically swelled with the increase of the tartrate concentrations.The thickness of the anodic oxidefilm increased with the concentrations until the concentration reached 15 g/L.The results of Raman analysis illustrate that all samples have similarity in the crystal structure,consisting of mainly amorphous TiO2,some anatase TiO2and a small amount of rutile TiO2.And the ratios of anatase TiO2and rutile TiO2increase with the concentrations until it reaches 15 g/L.Furthermore,the intensity of the peaks increases with enhanced concentrations until the concentration reaches 15 g/L.The corrosion resistance of the anodic oxidefilm is increased by the sodium tartrate with higher concentrations be fore 15 g/L.The coefficient of friction of the anodic oxidefilm reduces with the concentrations until the concentration reaches 15 g/L,then the coefficient of friction of the anodic oxidefilm increases with the concentrations.

    1.Introduction

    Thick,oxide-based film with potential for protection and functionalization of the surface can be obtained by anodization of titanium.1–3The anodic oxidation of the anodic oxidefilm reveals that their property largely depends on the concentrations,electrical source and temperature.4–6Thesefactors have been widely researched in recent years.7–9

    Due to the specific behavior of the incorporated anions,the morphology and crystallinity of the oxide layer are affected by concentrations in terms of the change of anodizing forming voltage.10Ohtsu et al.reported that high-concentration electrolyte crystallized the oxide layer as a result of thefield crystallization effect.11In addition,electrolyte affected both the surface morphology and the crystallinity of thefabricated oxide layer.12,13Thus,the morphology,microstructure and corrosion resistance of the oxide layer are determined primarily by the electrolyte used.Sodium tartrate is the alkalescent electrolyte that is less destructive to the anodic oxidefilm.There fore,sodium tartrate is the electrolyte widely used for anodic oxidation of Ti and alloys for the strong complexation to Ti.However,the effect of the sodium tartrate concentrations on the anodic oxidefilm is not clear.In this paper,anodic oxidefilm was fabricated on the Ti–10V–2Fe–3Al by using a pulse galvanostatic method.14–17As addition of the sodium tartrate,PTFE particles would obviously improve the corrosion resistance and wear resistance of anodic oxidefilm.

    Thus,the purpose of this paper is to study the effect of sodium tartrate concentrations on morphology and characteristics of anodic oxidefilm on titanium alloy Ti–10V–2Fe–3Al by AC pulse power supply in the sodium tartrate with the addition of PTFE emulsion.And the mechanism of the enhancement of the properties of the anodic oxidefilm has been studied in detail.This paper can of fer a theoretical of basis for the research in thefuture.

    2.Experimental

    2.1.Preparation of anodic oxidefilm

    Titanium alloy Ti–10V–2Fe–3Al was cut into sheets with the dimension of 10 mm×10 mm×2 mm.Prior to anodization,samples were polished with silicon carbide paper which successively grades from 200 to 2000 grit followed by rinsing with acetone and deionized water successively and finally dried in air.

    Anodic oxidation was carried out in a cell with a thermostat water bath and a magnetic stirring apparatus by using a pulse galvanostatic power source(WMY-IV).The output mode of the power source is pulsed power supply,shown in Fig.1.In thefigure,I is the current,t the time of anodization,T the time of pulse cycle,t+the time of pulse working period,and I+the pulse anodic current supplied.The Ti–10V–2Fe–3Al slice sample was used as anode,and a 1Cr18Ni9Ti stainless steel plate was used as cathode.The anode surface was less than 50%that of the cathode.The parameters of anodization process are given in Table 1.After the treatment,the coated samples were rinsed with water and then dried in the air.

    Fig.1 Output mode of power source.

    2.2.Morphology and microstructure of anodic oxidefilm

    The surface morphology and thickness of the anodic oxidefilm were examined by using scanning electron microscopy(FESEM,XL30S,FEI,USA)and atomic force microscope(AFM,Dimension icon,Veeco,USA).The crystalline structure of anodic oxidefilm was determined by Raman spectroscopy(Raman,Horiba-HR800,Yvon Jobin,using a He-Ne laser without filter,633 nm).

    2.3.Corrosion resistance properties of anodic oxidefilm

    Electrochemical tests were progressed in a traditional threeelectrode system(an SCE as reference electrode,a platinum electrode as counter electrode and the oxide sample as working electrode)by using a potentiostat/galvanostat(AES,Parstat 2273,Princeton Applied Research,USA)ina3.5%Na Clsolution.The scanning rate was 0.5 mV·s-1and the scanning range was from-0.5 V to+0.5 V versus the open circuit potential.

    2.4.Wear resistance properties of anodic oxidefilm

    Ball disc wear experiments were progressed by using a micro friction and wear machine(UMT-2,CTER,USA).All experiments were carried out by setting the force 3 N for 500 s and the rotation rate was 200 r/min.The diameter of Si3N4grinding ball was 2 mm while diameter of friction being 8 mm.The results were characterized by coefficients of friction of the anodic oxidefilm.

    3.Results and discussion

    3.1.Effect of concentrations on thickness

    The cross-section images of the anodic oxidefilm fabricated at different concentrations are shown in Fig.2(ρ is the mass of solute per unit volume).

    The corresponding thicknesses of the anodic oxidefilm are 15.7,16.6,19.3,19.4,19.4 μm respectively,when the concentrations are 1,5,15,30,50 g/L(Table 2).It was obvious that the thickness of the anodic oxidefilm would increase with the concentrations until the concentration reached 15 g/L.Thickness of the anodic oxidefilm would be related to ultimate voltage18,19and the rate of the formation and corrosion of the anodic oxidefilm because of the weak alkaline of electrolyte.20At the beginning of the anodic oxidation,the rate of the formation of anodic oxidefilm played a dominant role due to the good conductivity of alloy substrate.At this stage,the rate of formation was obviously fast be fore 5 min according to Fig.3.As the anode oxidation continued,the anodic oxidefilm would be too thick to keep the frequent formation for the insulativity of both the anodic oxidefilm and the PTFE particles.Simultaneously,the anodic oxidefilm would be corroded by the alkalescent electrolyte leading to the dissolution of it.When the rate of formation equaled to the rate of dissolution,the thickness of anodic oxidefilm would no longer increase.

    Table 1 Parameters of fabrication process.

    Fig.2 Cross-section images of anodic oxidefilm surface obtained at different concentrations of sodium tartrate.

    Table 2 Thicknesses of anodic oxidefilm fabricated at different concentrations.

    Fig.3 Anodizing forming voltage with anodizing time relation curves of specimens at different electrolyte concentrations.

    The ultimate voltage of the anode oxidation is shown in Fig.3.As concentrations increased of tartrate,the conductivity of the sodium tartrate increased so that the ultimate voltage would decrease.Thus as the concentration increased,the better conductivity of the sodium tartrate led to more ion’s migration to the surface of the alloy substrate so that the rate of the formation of the anodic oxidefilm would be increased,leading to thicker anodic oxidefilm.In addition of the decreasing ultimate voltage and dissolution of anodic oxidefilm,the thickness of the anodic oxidefilm increased with the concentrations until the concentration reached 15 g/L,and then would no longer increase ultimately.

    3.2.Effect of concentrations on morphology

    Fig.4 shows the scanning electron images of the surface of anodic oxidefilm obtained at different concentrations of sodium tartrate.

    The anodic oxidefilm presented a uniform petaloid drum and micro-cracks morphology.The results of Fig.4 indicate that PTFE particles were enriched on the surface of anodic oxidefilm and preferentially concentrated within internal micro-cracks of thefilm,which was in the circle shown in Fig.4(c),that obviously improved the corrosion resistance of anodic oxidefilm.The petaloid drums showed in Fig.4(a)were probably owe to different rates of the growth of different places due to different topographic features at different zones.6The anodic oxidefilm would befirstly formed as barrier layer and then the barrier layer ruptured because of the high voltage.And outer layer would be preferably formed at the defects of the surface.As the anodization continued,the thickness of the anodic oxidefilm was bigger and bigger at defects of the surface than other places.And the petaloid drums and micro-cracks appeared due to the internal pressure of the anodic oxidefilm.

    Fig.4 SEM of anodic oxidefilm surface obtained at different concentrations of sodium tartrate.

    The results of Fig.4 indicate the presence of anodic oxidefilm on all the samples.As concentrations increased,the surfaces of the anodic oxide film became smoother.According to Fig.4(a),when the concentration was less than 5 g/L,the anodic oxide film obtained was uncompact with the existence of the petaloid drums.The results of Fig.4(b)indicate the presence of electron transport channels appearing as circular spots distributed over the surface of the anodic oxidefilm when the concentration of sodium tartrate was 5 g/L.However,the electron transport channels were almost covered when the concentration increased to 15 g/L and translated to petaloid drums.As shown in Fig.4(c–e),the anodic oxidefilm obtained at concentrations of sodium tartrate more than 5 g/L were compact.As concentrations increased,the number of the petaloid drums increased;on the other hand,the micro-cracks were dramatically swelling.

    The EDS were also detected by using the function of scanning electron microscopy.Fig.5 reveals the distribution of O,Ti and V along the yellow line(Fig.5(a)).It was obvious that the content of O of petaloid drums exceeded other places,indicating that the petaloid drums,preferentially formed anodic oxidefilm,were composed of oxide.Moreover,the distribution of V,representatives of the alloying element,presented an opposite consequence.It was the results of the presence of anodic oxidefilm at the surfaces of substrates,decreasing the content of alloying element.

    Fig.6 shows the AFM three-dimensional topographic representations for the samples at different concentrations.

    The average roughnesses of the surfaces calculated from the AFM images are shown in Fig.7.It was obvious that the surface become rougher with the concentrations until the concentration reached 15 g/L,and then tended to be smoother morphology,in accordance with the results of SEM.

    According to Fig.7,the corresponding roughness values of the anodic oxidefilm are 66.3,275,320,236,294 nm respectively,when the concentrations are 1,5,15,30,50 g/L.The roughness value increased with increased concentrations until it reached 15 g/L,and then the roughness value reduced with increased concentrations.According to the SEM images,the sizes of the petaloid drums increased with increased concentrations.It was obvious that the size of the petaloid drums would affect the roughness value significantly.But when the concentration was more than 15 g/L,the roughness value reduced with increased concentrations.It was probably because of the compaction of the anodic oxidefilm.On the other hand,the roughness value of the surface formed in 1 g/L was remarkably low.It might be due to the imperfection of the anodic oxidefilm and the smaller size of the petaloid drums.When the concentration of the sodium tartrate was less than 5 g/L,the effect of the concentrations on the size of the petaloid drums would be researched in details.

    3.3.Effect of concentrations on crystalline structure

    To investigate the chemical states of Ti,the surface of the anodic oxide film was observed by a Raman micro-scope.The Raman spectra of the anodic oxide film fabricated at different concentrations are shown in Fig.8.The results of Raman analysis illustrate a similarity in the crystal structure of the obtained Ti–10V–2Fe–3Al anodic oxide film with increased concentrations,consisting of mainly amorphous TiO2,some anatase TiO2and a small amount of rutile TiO2.

    An obvious intense band at 152 cm-1was very sharp which represented anatase and another obvious intense band of the anodic oxide film was detected at 632 cm-1which represented rutile.21It was apparent that the anodic oxide film fabricated a tdifferent concentrations would have the same peaks.Furthermore,the intensity of the peaks increased with increased concentration until it reached 15 g/L.The intensity of the peaks would be related to the thickness of anodic oxide film that the thicker layer leaded to high intensity.Consequently,the anodic oxidefilm fabricated at different concentrations had the same crystal structure(anatase and rutile),well the intensity of TiO2anatase and TiO2rutile increased with the increase of concentration until it reached 15 g/L.And the ratio of anatase TiO2and rutile TiO2increased with the concentrations until the concentration was 15 g/L.The Raman spectra of the anodic oxide film fabricated at different concentrations indicate that the increase of the concentrations would promote the trans formation from rutile TiO2to anatase TiO2while affecting the thickness of anodic oxide film,also in accordance with SEM,AFM.

    3.4.Effect of concentrations on corrosion resistance

    The polarizing curves of the anodic oxidefilm are shown in Fig.9.The concrete data are given in Table 3.

    Obviously,the corrosion current density icorrof the anodic oxidefilm decreased with increased concentrations be fore 30 g/L,and then increased with further increased concentrations.

    Fig.5 EDS of anodic oxidefilm obtained when concentration is 1 g/L.

    Fig.6 AFM of three-dimensional anodic oxidefilm obtained at different concentrations of sodium tartrate.

    According to polarizing curves and Table 3,the anodic oxidation potential processing would raise the Ecorras the concentration increased,and reached the maximum at 15 g/L,and then depressed as the concentration further increased.The nyquist diagram of the anodic oxidefilm in a 3.5%NaCl solution are shown in Fig.10 to illustrate the corrosion resistance of anodic oxidefilm.The Zrein Fig.10 expresses resistance which is constant regardless of frequency,and the Zimexpresses reactance which varies with frequency due to capacitance and inductance.

    Fig.7 Roughness of anodic oxidefilm fabricated at different concentrations.

    Fig.8 Raman spectra of anodic oxidefilm fabricated at different concentrations.

    Fig.9 Polarizing curves of anodic oxidefilm at different concentrations.

    The nyquist diagrams presented quadrants for all samples indicating the presence of anodic oxidefilm which was insulative.The radius of quadrants increased with increased concentrations be fore 15 g/L,and then decreased with further increased concentrations,consistent with the results of polarizing curves.

    Fig.10 Nyquist diagram of anodic oxidefilm at different concentrations.

    Fig.11 Coefficient of friction of anodic oxidefilm at different concentrations.

    In general,the corrosion resistance of the anodic oxidefilm would be mainly related to the thickness,the surface states and structure of the anodic oxidefilm.22As anodic oxidefilm had the same crystal structure in the experiment,the key factors would then be the thicknesses and the surface states.According to Fig.4,as the concentrations increased,the number and the sizes of the petaloid drums increased,and the anodic oxidefilm would be more compact.It was agreed with the results of the electrochemical measurement.And when the concentrations were more than 15 g/L,micro-cracks would be dramatically swelling,leading to the decrease of corrosion resistance.

    3.5.Effect of concentrations on friction coefficient

    The coefficients of friction of the anodic oxide film fabricated at different concentrations are shown in Fig.11.All samples show a low coefficient of friction at the beginning of the test,and then increased,indicating the exposure of the Ti substrate.

    Table 3 Properties of anodic oxidefilm fabricated at different concentrations.

    3.6.Mechanism of concentrations’effect

    In conclusion,the sodium tartrate would in fluence the properties of the anodic oxide film as the carrier of the electron.Because of the alternating current,the(C4O6H4)2-would migrate into the oxide film from the solution while the Ti4+migrate into the oxide film from the substrate.The oxide film would be formed with the migration of ions.Thus,at the early stage of the anodization,the barrier layer was formed firstly which was insulative and compact.And then,as the anodization continued,some defects of the surface appeared on the surface of the barrier layer so that the rounded outer layer would be formed afterwards at the defects of the surface.Ultimately,the rounded outer layer would touch and cover each other at different places of the surface of barrier layer as the size of outer layer increased.Hence,the petaloid drums would be formed due to the stress of the extrusion of inhomogeneous outer layer.At this stage,the O2gases would be formed and the size of the petaloid drums would increase,leading to the overloading of the stress of the surface of the petaloid drums.Then micro-cracks would be formed and the PTFE particles would preferentially migrate into the microcracks because of the adsorption.Thus the PTFE particles would preferentially concentrate within internal micro-cracks of thefilm.

    As concentrations of tartrate increased,the resistance of the sodium tartrate would decrease,so that the electroconductivity of the sodium tartrate would be improved.At the beginning of the anodization,more(C4O6H4)2-migration to the substrate led to more chances of the breaking of the barrier layer where the petaloid drums appeared,so that the number of the petaloid drumswould increase as concentrations increased(Fig.4).It was consistent with the results of Fig.6 and Fig.7 that the oxidefilm would become smoother as concentrations increased be fore 15 g/L.As the concentrations further increased,better electroconductivity would lead to the corrosion of the formed anodic oxidefilm.When the concentrations were more than 15–30 g/L,the rate of corrosion would be larger than the rate of formation,and the thicknesses of the anodic oxidefilm would decrease.The micro-cracks of thefilm that were exposed by the corrosion of the concentration contributed to the average roughness and the smoothness.It also contributed to the decrease of the corrosion resistance and wear resistance of the anodic oxidefilm when the concentrations were more than 15 g/L(Table 3 and Fig.11).

    4.Conclusions

    (1)The sodium tartrate would influence the properties of the anodic oxidefilm as the carrier of the electron.Thus,the thicknesses would be related to the rates of formation and dissolution of the anodic oxidefilm at different concentrations.

    (2)The presence of the petaloid drums would be related to different rates of formation of anodic oxidefilm at differentplaces.As concentrations increased,more(C4O6H4)2-migration to the substrate would of fer more chances of the formation of the oxidefilm at the beginning of the anodization,leading to more petaloid drums and smoother surfaces of the anodic oxidefilm.

    (3)PTFE particles would preferentially concentrate within internal micro-cracks of the film because of the adsorption.

    (4)The micro-cracks of thefilm that were exposed by the corrosion of the concentration would contribute to the average roughness,smoothness,corrosion resistance and wear resistance of the anodic oxidefilm.

    Acknowledgements

    The authors thank the anonymous reviewers for their critical and constructive review of the manuscript.This study was supported by the National Natural Science Foundation of China(No.51271012).

    1.Capek D,Gigandet MP,Masmoudi M,Wery M,Banakh O.Long-time anodisation of titanium in sulphuric acid.Surf Coat Technol 2008;202(8):1379–84.

    2.Kumar S,Sankara N,Saravana K.Influence of fluoride ion on the electrochemical behaviour of β-Ti alloy for dental implant application.Corros Sci 2010;52(5):1721–7.

    3.Neupane MP,Park IS,Lee SJ,Kim KA,Lee MH,Bae TS.Study of anodic oxidefilms of titanium fabricated by voltammetric technique in phosphate buffer media.J Electrochem Soc 2009;4(2):197–207.

    4.Frayret JP,Caprani RP.Anodic behaviour of titanium in acidic chloride containing media(HCl-NaCl).Influence of the constituents of the medium-I.Study of the stationary current.Calculation of the overall reaction orders.Electrochim Acta 1981;26(12):1783–8.

    5.Duarte LT,Bolfarini C,Biaggio SR,Rocha-Filho RC,Nascente PA.Growth of aluminum-free porous oxide layers on titanium and its alloys Ti–6Al–4V and Ti–6Al–7Nb by micro-arc oxidation.Mater Sci Eng C 2014;41(1):343–8.

    6.Fan M,Mantia FL.Effect of surface topography on the anodization of titanium.Electrochem Commun 2013;37:91–5.

    7.El-Mahdy G,Kim KB.Monitoring the atmospheric corrosion loss of copper during wet/dry cyclic conditions in oxalic acid solutions.Corrosion 2007;63(2):171–7.

    8.Ohtsuka T,Masuda M,Sato N.Ellipsometric study of anodic oxidefilms on titanium in hydrochloric acid,sulfuric acid,and phosphate solution.J Electrochem Soc 1985;132(4):787–92.

    9.Wang D,Li H,Yang H,Ma J,Li G.Tribological evaluation of surface modified H13 tool steel in warm forming of Ti–6Al–4V titanium alloy sheet.Chin J Aeronaut 2014;27(4):1002–9.

    10.Liu JH,Yi JL,Li SM,Yu M,Wu GL,Wu L.Effect of electrolyte concentration on morphology,microstructure and electrochemical impedance of anodic oxidefilm on titanium alloy Ti–10V–2Fe–3Al.J Appl Electrochem 2010;40(8):1545–53.

    11.Ohtsu N,Ishikawa D,Komiya S,Sakamoto K.Effect of phosphorous incorporation on crystallinity,morphology,and photocatalytic activity of anodic oxide layer on titanium.Thin Solid Films 2014;556:247–52.

    12.Ohtsu N,Komiya S,Kodama K.Effect of electrolytes on anodic oxidation of titanium for fabricating titanium dioxide photocatalyst.Thin Solid Films 2013;534:70–5.

    13.Liu JH,Yang K,Yu M,Li SM,Wu L,Yu XM.Preparation,characterization and fatigue properties of TC18 titanium alloy anodic oxidefilm in sodium hyaluronate system.Acta Aeronaut Astronaut Sin 2014;35(3):902–10[Chinese].

    14.Wu GL,Li SM,Yu M,Yi JL,Wu L.Surface analysis of chemical stripping titanium alloy oxidefilms.J Wuhan Univ Technol-Mater Sci 2012;27(3):399–404.

    15.Komiya S,Sakamoto K,Ohtsu N.Structural changes of anodic layer on titanium in sulfate solution as a function of anodization duration in constant current mode.Appl Surf Sci 2014;296:163–8.

    16.Ou SF,Chou HH,Lin CS,Shih CJ,Wang KK,Pan YN.Effects of anodic oxidation and hydrothermal treatment on surface characteristics and biocompatibility of Ti–30Nb–1Fe–1Hf alloy.Appl Surf Sci 2012;258(17):6190–8.

    17.Tan Y.An overview of techniques for characterizing inhomogeneities in organic surfacefilms and underfilm localized corrosion.Prog Org Coat 2013;76(5):791–803.

    18.Li SM,Yu XM,Liu JH,Yu M,Wu GL,Wu L,et al.Influence of working frequency on structure and corrosion resistance of the anodic oxidefilm on Ti–6Al–4V alloy.Int J Electrochem Sci 2013;8(4):5438–47.

    19.Habazaki H,Fushimi K,Shimizu K,Skeldon P,Thompson GE.Fast migration of fluoride ions in growing anodic titanium oxide.Electrochem Commun 2007;9(5):1222–7.

    20.Ohsaka T,Izumi F,Fujiki YJ.Raman spectrum of anatase TiO2.J Raman Spectrosc 1978;7:321.

    21.Porto S,Fleury P,Damen T.Raman spectra of TiO2,MgF2,ZnF2,FeF2,and MnF2.Phys Rev 1967;154(2):522.

    22.Yu M,Liu YX,Liu JH,Li SM,Xue B,Zhang Y,et al.Effects of cerium salts on corrosion behaviors of Si–Zr hybrid sol–gel coatings.Chin J Aeronaut 2015;28(2):600–8.

    Ma Kun received his B.S.degreefrom Shandong University in 2013 and M.S.degreefrom Beihang University,respectively.His main research interests are corrosion science and protection technology.

    Yu Mei received her Ph.D.degreefrom Beihang University in 2007 and is now an associate prof essor of materials science and engineering at the same university.Her main research interests are nano functional materials,corrosion science and protection technology.

    6 July 2015;revised 25 July 2015;accepted 6 August 2015

    Available online 2 November 2015

    Anodic oxidation;

    Coefficient of friction;

    Concentrations;

    Corrosion resistance;

    Sodium tartrate

    ?2015 The Authors.Production and hosting by Elsevier Ltd.on behalf of Chinese Society of Aeronautics and Astronautics.This is an open access article under the CC BY-NC-ND license(http://creativecommons.org/licenses/by-nc-nd/4.0/).

    *Corresponding author.Tel.:+86 10 82317103.

    E-mail address:yumei@buaa.edu.cn(M.Yu).

    Peer review under responsibility of Editorial Committee of CJA.

    Production and hosting by Elsevier

    http://dx.doi.org/10.1016/j.cja.2015.10.013

    1000-9361?2015 The Authors.Production and hosting by Elsevier Ltd.on behalf of Chinese Society of Aeronautics and Astronautics.

    This is an open access article under the CC BY-NC-ND license(http://creativecommons.org/licenses/by-nc-nd/4.0/).

    一边摸一边抽搐一进一出视频| 满18在线观看网站| 久久九九热精品免费| 大码成人一级视频| 女人爽到高潮嗷嗷叫在线视频| 亚洲精品国产精品久久久不卡| 高清黄色对白视频在线免费看| 国产极品粉嫩免费观看在线| 久久国产亚洲av麻豆专区| 侵犯人妻中文字幕一二三四区| 国产真人三级小视频在线观看| 黑丝袜美女国产一区| 日本一区二区免费在线视频| 久久国产亚洲av麻豆专区| 国产成人欧美| 国产在线免费精品| 国产一区二区在线观看av| av天堂久久9| 美女国产高潮福利片在线看| 美女中出高潮动态图| 男女之事视频高清在线观看| 老司机午夜十八禁免费视频| 亚洲中文日韩欧美视频| 新久久久久国产一级毛片| 五月开心婷婷网| 亚洲熟女精品中文字幕| 中文字幕av电影在线播放| 久久久久久免费高清国产稀缺| 另类亚洲欧美激情| 国产精品成人在线| 夜夜夜夜夜久久久久| 18禁裸乳无遮挡动漫免费视频| 婷婷丁香在线五月| 黄色a级毛片大全视频| 国产av国产精品国产| 99国产精品99久久久久| 国产成人啪精品午夜网站| 中文字幕人妻熟女乱码| 大香蕉久久网| 啦啦啦免费观看视频1| 97人妻天天添夜夜摸| 一级毛片女人18水好多| 国产精品偷伦视频观看了| xxxhd国产人妻xxx| 亚洲五月婷婷丁香| 99精国产麻豆久久婷婷| 欧美av亚洲av综合av国产av| 一区二区三区激情视频| 老司机深夜福利视频在线观看 | 麻豆国产av国片精品| 国产欧美日韩综合在线一区二区| 人人妻人人澡人人看| 狂野欧美激情性xxxx| 伦理电影免费视频| 亚洲精品av麻豆狂野| av不卡在线播放| 侵犯人妻中文字幕一二三四区| 午夜视频精品福利| 久久久国产欧美日韩av| 另类亚洲欧美激情| 女性生殖器流出的白浆| 天堂中文最新版在线下载| 日韩人妻精品一区2区三区| 香蕉国产在线看| 操美女的视频在线观看| 高清av免费在线| 久久综合国产亚洲精品| 丁香六月欧美| 免费在线观看视频国产中文字幕亚洲 | 中文字幕最新亚洲高清| 精品少妇黑人巨大在线播放| 黄片小视频在线播放| 无遮挡黄片免费观看| 久久综合国产亚洲精品| 久久性视频一级片| 欧美日韩成人在线一区二区| 久久精品久久久久久噜噜老黄| 桃花免费在线播放| 亚洲国产中文字幕在线视频| 一级毛片女人18水好多| 亚洲专区字幕在线| 亚洲欧美日韩另类电影网站| 国产欧美日韩一区二区三区在线| 午夜福利视频在线观看免费| 国产主播在线观看一区二区| www.av在线官网国产| 欧美xxⅹ黑人| 两性夫妻黄色片| 国产精品久久久久久人妻精品电影 | 久久久国产成人免费| 国产成人精品无人区| 黄色视频不卡| 久久毛片免费看一区二区三区| 丝瓜视频免费看黄片| 亚洲五月色婷婷综合| 欧美日韩国产mv在线观看视频| 久久午夜综合久久蜜桃| 两人在一起打扑克的视频| 国产av又大| 久久免费观看电影| 男女之事视频高清在线观看| 亚洲激情五月婷婷啪啪| 国产区一区二久久| 9色porny在线观看| 在线十欧美十亚洲十日本专区| 亚洲精品中文字幕在线视频| 男人添女人高潮全过程视频| 五月开心婷婷网| 免费人妻精品一区二区三区视频| 欧美一级毛片孕妇| 一级毛片精品| 一级黄色大片毛片| 国产亚洲精品第一综合不卡| 高清视频免费观看一区二区| 免费观看av网站的网址| 国产av又大| 欧美另类一区| av不卡在线播放| 亚洲精品国产av蜜桃| 国产又色又爽无遮挡免| 性色av乱码一区二区三区2| 99精品久久久久人妻精品| 男女国产视频网站| 高清欧美精品videossex| 丝袜在线中文字幕| 久久亚洲精品不卡| 国产精品自产拍在线观看55亚洲 | 在线观看免费视频网站a站| 性高湖久久久久久久久免费观看| 国产黄色免费在线视频| 精品久久久久久电影网| 人人澡人人妻人| 下体分泌物呈黄色| 91成人精品电影| 亚洲av日韩精品久久久久久密| 制服诱惑二区| 国产亚洲午夜精品一区二区久久| 午夜日韩欧美国产| 蜜桃国产av成人99| 国产av一区二区精品久久| 日韩欧美免费精品| 99热国产这里只有精品6| 搡老乐熟女国产| 99国产精品一区二区三区| 狠狠精品人妻久久久久久综合| 亚洲成人国产一区在线观看| 精品免费久久久久久久清纯 | 男人舔女人的私密视频| 午夜福利乱码中文字幕| 免费高清在线观看日韩| 午夜精品久久久久久毛片777| 亚洲欧洲日产国产| 夜夜骑夜夜射夜夜干| 亚洲精品国产av蜜桃| 亚洲,欧美精品.| 亚洲精品中文字幕一二三四区 | 亚洲avbb在线观看| 咕卡用的链子| 中文字幕制服av| 欧美黄色片欧美黄色片| 一级片免费观看大全| 亚洲成国产人片在线观看| 丁香六月欧美| 妹子高潮喷水视频| 精品人妻在线不人妻| cao死你这个sao货| 爱豆传媒免费全集在线观看| 精品国产国语对白av| 老司机靠b影院| 18禁国产床啪视频网站| 久久久久久久久久久久大奶| 一进一出抽搐动态| 国产成人av激情在线播放| 精品福利观看| 一个人免费看片子| 色94色欧美一区二区| 日韩大码丰满熟妇| 欧美日韩成人在线一区二区| av又黄又爽大尺度在线免费看| 老司机福利观看| 国产精品一区二区在线不卡| www.熟女人妻精品国产| 中文字幕精品免费在线观看视频| 蜜桃国产av成人99| 美女高潮喷水抽搐中文字幕| 免费看十八禁软件| 美女扒开内裤让男人捅视频| 亚洲专区字幕在线| 女人高潮潮喷娇喘18禁视频| 国产三级黄色录像| 男人操女人黄网站| 国产成人av激情在线播放| 亚洲欧美激情在线| 考比视频在线观看| 伊人亚洲综合成人网| 亚洲综合色网址| 高清欧美精品videossex| 人人妻,人人澡人人爽秒播| 岛国毛片在线播放| 波多野结衣一区麻豆| 制服人妻中文乱码| 一级a爱视频在线免费观看| 精品一区二区三卡| 在线看a的网站| 欧美国产精品一级二级三级| 老司机深夜福利视频在线观看 | 国产一区二区在线观看av| 亚洲中文日韩欧美视频| 狠狠精品人妻久久久久久综合| 亚洲精品美女久久久久99蜜臀| 十八禁人妻一区二区| 亚洲精品国产色婷婷电影| 水蜜桃什么品种好| 一区福利在线观看| 久久精品国产亚洲av高清一级| 国产成人欧美在线观看 | 丝袜人妻中文字幕| √禁漫天堂资源中文www| 美国免费a级毛片| 丁香六月天网| 性色av乱码一区二区三区2| 日韩中文字幕视频在线看片| 欧美国产精品va在线观看不卡| 丝袜喷水一区| 国产亚洲精品久久久久5区| 免费不卡黄色视频| 久久精品国产综合久久久| 涩涩av久久男人的天堂| 美女脱内裤让男人舔精品视频| 各种免费的搞黄视频| 老司机亚洲免费影院| 美女中出高潮动态图| 亚洲黑人精品在线| 熟女少妇亚洲综合色aaa.| 曰老女人黄片| h视频一区二区三区| 亚洲av欧美aⅴ国产| √禁漫天堂资源中文www| 精品少妇一区二区三区视频日本电影| 久久精品熟女亚洲av麻豆精品| 纵有疾风起免费观看全集完整版| 中文精品一卡2卡3卡4更新| 亚洲va日本ⅴa欧美va伊人久久 | 一级,二级,三级黄色视频| 欧美少妇被猛烈插入视频| 777久久人妻少妇嫩草av网站| 两个人免费观看高清视频| 中亚洲国语对白在线视频| 亚洲国产中文字幕在线视频| 亚洲精品一卡2卡三卡4卡5卡 | 午夜精品久久久久久毛片777| 国精品久久久久久国模美| 国产欧美日韩一区二区三区在线| 久久精品人人爽人人爽视色| 国产成人一区二区三区免费视频网站| 一级毛片精品| 99国产极品粉嫩在线观看| 欧美激情高清一区二区三区| 精品久久蜜臀av无| 美女国产高潮福利片在线看| 欧美变态另类bdsm刘玥| 一区二区三区精品91| 亚洲 欧美一区二区三区| 久久人人97超碰香蕉20202| 成在线人永久免费视频| 十分钟在线观看高清视频www| 亚洲自偷自拍图片 自拍| 青春草视频在线免费观看| 久久免费观看电影| 国产日韩一区二区三区精品不卡| 久久久国产精品麻豆| 亚洲国产av新网站| av电影中文网址| 男人添女人高潮全过程视频| 免费看十八禁软件| 色视频在线一区二区三区| 午夜视频精品福利| 国产av精品麻豆| 大片电影免费在线观看免费| 九色亚洲精品在线播放| 蜜桃在线观看..| 国产欧美日韩一区二区精品| 男男h啪啪无遮挡| 女人高潮潮喷娇喘18禁视频| 亚洲av日韩在线播放| 成年女人毛片免费观看观看9 | 精品久久久久久久毛片微露脸 | 一二三四在线观看免费中文在| 亚洲成人国产一区在线观看| 午夜精品久久久久久毛片777| 9191精品国产免费久久| 巨乳人妻的诱惑在线观看| 亚洲国产精品一区二区三区在线| 欧美少妇被猛烈插入视频| 妹子高潮喷水视频| 久久女婷五月综合色啪小说| 国产成人欧美在线观看 | 成年女人毛片免费观看观看9 | 一级,二级,三级黄色视频| 青青草视频在线视频观看| 欧美+亚洲+日韩+国产| 国产免费福利视频在线观看| 国产亚洲午夜精品一区二区久久| 亚洲欧美精品综合一区二区三区| 久热这里只有精品99| 俄罗斯特黄特色一大片| 精品欧美一区二区三区在线| 黄色视频在线播放观看不卡| 精品乱码久久久久久99久播| 一进一出抽搐动态| 欧美性长视频在线观看| 国产不卡av网站在线观看| 日韩有码中文字幕| 老司机深夜福利视频在线观看 | av天堂久久9| 天天躁夜夜躁狠狠躁躁| 性色av乱码一区二区三区2| 丰满人妻熟妇乱又伦精品不卡| 亚洲成人免费电影在线观看| 日韩熟女老妇一区二区性免费视频| 狂野欧美激情性xxxx| 久久人人爽人人片av| 在线天堂中文资源库| 十分钟在线观看高清视频www| 九色亚洲精品在线播放| 亚洲国产日韩一区二区| 成年女人毛片免费观看观看9 | 又大又爽又粗| 男男h啪啪无遮挡| 日韩欧美一区视频在线观看| 汤姆久久久久久久影院中文字幕| 91精品国产国语对白视频| 美女午夜性视频免费| 欧美日韩视频精品一区| 一区二区三区乱码不卡18| 久久狼人影院| 免费在线观看黄色视频的| 国产精品熟女久久久久浪| 黄片小视频在线播放| 99热网站在线观看| 97精品久久久久久久久久精品| 久久久水蜜桃国产精品网| 久久久久国产一级毛片高清牌| 欧美成人午夜精品| 大陆偷拍与自拍| 久久久精品94久久精品| 亚洲专区中文字幕在线| 男女下面插进去视频免费观看| 人人澡人人妻人| 一个人免费看片子| 免费高清在线观看视频在线观看| 热re99久久国产66热| 国产av一区二区精品久久| 人人妻人人澡人人看| 亚洲精品一卡2卡三卡4卡5卡 | 两人在一起打扑克的视频| 亚洲五月色婷婷综合| 久久国产精品大桥未久av| 国产精品 欧美亚洲| 久久久久久人人人人人| 99国产精品一区二区蜜桃av | 日韩人妻精品一区2区三区| 国产成人免费无遮挡视频| h视频一区二区三区| bbb黄色大片| 亚洲五月色婷婷综合| 黑丝袜美女国产一区| 国产人伦9x9x在线观看| 亚洲伊人色综图| 久久久久国内视频| 丰满少妇做爰视频| 黄片小视频在线播放| 在线av久久热| 老汉色∧v一级毛片| 亚洲国产精品一区二区三区在线| 日本av手机在线免费观看| 巨乳人妻的诱惑在线观看| 69精品国产乱码久久久| 丝袜脚勾引网站| 久久国产精品大桥未久av| 中文精品一卡2卡3卡4更新| 亚洲精品中文字幕在线视频| 免费观看av网站的网址| 欧美久久黑人一区二区| 少妇精品久久久久久久| 日本av免费视频播放| 国产精品熟女久久久久浪| 日韩,欧美,国产一区二区三区| av又黄又爽大尺度在线免费看| 纯流量卡能插随身wifi吗| 中亚洲国语对白在线视频| 美国免费a级毛片| 精品人妻熟女毛片av久久网站| 免费久久久久久久精品成人欧美视频| 亚洲伊人色综图| 欧美精品一区二区免费开放| 老熟妇乱子伦视频在线观看 | 日韩一卡2卡3卡4卡2021年| 亚洲三区欧美一区| 亚洲黑人精品在线| 又黄又粗又硬又大视频| 欧美日本中文国产一区发布| 法律面前人人平等表现在哪些方面 | 天天添夜夜摸| 2018国产大陆天天弄谢| 2018国产大陆天天弄谢| 一本一本久久a久久精品综合妖精| 精品人妻熟女毛片av久久网站| 老鸭窝网址在线观看| 精品高清国产在线一区| a级片在线免费高清观看视频| 99热网站在线观看| 欧美亚洲日本最大视频资源| 人成视频在线观看免费观看| 一本久久精品| 日韩三级视频一区二区三区| 国产高清videossex| 少妇精品久久久久久久| 免费在线观看黄色视频的| 亚洲精品在线美女| cao死你这个sao货| 咕卡用的链子| av有码第一页| 男女国产视频网站| 国产精品久久久av美女十八| 国产国语露脸激情在线看| 一区二区三区激情视频| 亚洲精华国产精华精| 夜夜骑夜夜射夜夜干| 亚洲人成77777在线视频| 高潮久久久久久久久久久不卡| 亚洲成av片中文字幕在线观看| 中文字幕av电影在线播放| 大陆偷拍与自拍| 老司机亚洲免费影院| 1024视频免费在线观看| 婷婷成人精品国产| 极品人妻少妇av视频| 午夜福利视频在线观看免费| 久久久精品94久久精品| 亚洲精品乱久久久久久| av又黄又爽大尺度在线免费看| 激情视频va一区二区三区| 男女下面插进去视频免费观看| 丰满少妇做爰视频| 一本一本久久a久久精品综合妖精| 久久久久视频综合| 成年av动漫网址| tocl精华| 国产日韩欧美视频二区| 永久免费av网站大全| 中文字幕高清在线视频| 在线精品无人区一区二区三| av一本久久久久| 精品一区二区三卡| 桃花免费在线播放| 欧美+亚洲+日韩+国产| 中文欧美无线码| 国产视频一区二区在线看| 交换朋友夫妻互换小说| 欧美 亚洲 国产 日韩一| videosex国产| av国产精品久久久久影院| 久久天堂一区二区三区四区| 亚洲国产欧美在线一区| 国产野战对白在线观看| 免费在线观看黄色视频的| 欧美日韩黄片免| 黄片大片在线免费观看| 精品少妇一区二区三区视频日本电影| 大型av网站在线播放| 欧美 亚洲 国产 日韩一| 99国产综合亚洲精品| 亚洲成人手机| 欧美激情极品国产一区二区三区| 人人澡人人妻人| 在线永久观看黄色视频| 久久久国产一区二区| 成人av一区二区三区在线看 | 亚洲精华国产精华精| 一本大道久久a久久精品| 捣出白浆h1v1| 搡老乐熟女国产| 啦啦啦免费观看视频1| 亚洲精品乱久久久久久| videos熟女内射| 99久久精品国产亚洲精品| 自线自在国产av| 日韩有码中文字幕| 免费在线观看影片大全网站| 后天国语完整版免费观看| 动漫黄色视频在线观看| 亚洲一区二区三区欧美精品| 在线 av 中文字幕| 狠狠狠狠99中文字幕| 美国免费a级毛片| 日韩欧美免费精品| 夜夜骑夜夜射夜夜干| 免费女性裸体啪啪无遮挡网站| 国产成+人综合+亚洲专区| 国产成人精品在线电影| 少妇猛男粗大的猛烈进出视频| 女性生殖器流出的白浆| 丝袜美足系列| 一个人免费在线观看的高清视频 | 精品一品国产午夜福利视频| 国产av国产精品国产| 久久精品国产亚洲av高清一级| 色婷婷久久久亚洲欧美| 大型av网站在线播放| 日韩中文字幕视频在线看片| 9191精品国产免费久久| 亚洲精品美女久久av网站| 我的亚洲天堂| 亚洲精品美女久久久久99蜜臀| 久久人人爽av亚洲精品天堂| 亚洲国产精品999| 久久午夜综合久久蜜桃| 欧美黄色片欧美黄色片| 久久久久久久久免费视频了| 欧美激情 高清一区二区三区| 亚洲国产精品一区三区| 欧美黄色片欧美黄色片| 91老司机精品| 日韩,欧美,国产一区二区三区| 脱女人内裤的视频| 日韩,欧美,国产一区二区三区| 啦啦啦视频在线资源免费观看| 黄色视频不卡| 色播在线永久视频| 成在线人永久免费视频| 精品久久久精品久久久| 中文字幕另类日韩欧美亚洲嫩草| 免费在线观看视频国产中文字幕亚洲 | 亚洲欧美一区二区三区黑人| 动漫黄色视频在线观看| 亚洲精品乱久久久久久| 十八禁网站免费在线| 热99国产精品久久久久久7| 黄片大片在线免费观看| 午夜福利视频在线观看免费| 黄片播放在线免费| 欧美xxⅹ黑人| 每晚都被弄得嗷嗷叫到高潮| 免费久久久久久久精品成人欧美视频| 欧美激情极品国产一区二区三区| 97人妻天天添夜夜摸| 最新的欧美精品一区二区| 国产亚洲一区二区精品| 国产av又大| 国产一级毛片在线| 欧美精品一区二区免费开放| 久久久久久久大尺度免费视频| 中文字幕人妻熟女乱码| 国产精品影院久久| 一本—道久久a久久精品蜜桃钙片| 午夜影院在线不卡| 亚洲综合色网址| 精品视频人人做人人爽| 法律面前人人平等表现在哪些方面 | 精品免费久久久久久久清纯 | 一进一出抽搐动态| av线在线观看网站| 色婷婷av一区二区三区视频| 99久久人妻综合| 成人国语在线视频| 少妇精品久久久久久久| 午夜激情久久久久久久| 久久精品国产亚洲av香蕉五月 | 国产一区二区三区在线臀色熟女 | 一级毛片电影观看| 日韩欧美一区视频在线观看| 免费av中文字幕在线| 欧美老熟妇乱子伦牲交| 一区二区三区四区激情视频| 日韩三级视频一区二区三区| 黄色毛片三级朝国网站| 美女高潮到喷水免费观看| 啦啦啦视频在线资源免费观看| 大陆偷拍与自拍| 夜夜骑夜夜射夜夜干| 国产精品 国内视频| 婷婷色av中文字幕| 国产国语露脸激情在线看| 99国产极品粉嫩在线观看| 老司机午夜福利在线观看视频 | 国产欧美日韩一区二区三区在线| 菩萨蛮人人尽说江南好唐韦庄| 少妇精品久久久久久久| 亚洲欧洲日产国产| 欧美老熟妇乱子伦牲交| 免费在线观看日本一区| 天天添夜夜摸| 亚洲va日本ⅴa欧美va伊人久久 | 国产片内射在线| 99re6热这里在线精品视频| 国产99久久九九免费精品| 国产成人精品在线电影| 丝袜美足系列| 久久人妻熟女aⅴ| 黄色视频在线播放观看不卡| 成人手机av| 日韩欧美国产一区二区入口| 久久久久视频综合| 午夜免费观看性视频| 久久国产精品人妻蜜桃| 岛国毛片在线播放| 亚洲欧美一区二区三区久久| 亚洲av日韩在线播放| 国产日韩欧美视频二区| 国产熟女午夜一区二区三区| 乱人伦中国视频| 国产亚洲欧美精品永久| 国产av一区二区精品久久| 我的亚洲天堂|