热门站点| 世界资料网 | 专利资料网 | 世界资料网论坛
收藏本站| 设为首页| 首页

ANSI ISO/IEC 13818-7-2003 信息技术.移动图像和相关有声信息的通用编码.第7部分:被INCITS采用的高级音频编码(AAC)

作者:标准资料网 时间:2024-05-19 08:18:17  浏览:8309   来源:标准资料网
下载地址: 点击此处下载
【英文标准名称】:InformationtechnologyGenericcodingofmovingpicturesandassociatedaudioinformationPart7:AdvancedAudioCoding(AAC)AdoptedbyINCITS
【原文标准名称】:信息技术.移动图像和相关有声信息的通用编码.第7部分:被INCITS采用的高级音频编码(AAC)
【标准号】:ANSIISO/IEC13818-7-2003
【标准状态】:现行
【国别】:美国
【发布日期】:2003-08-01
【实施或试行日期】:
【发布单位】:美国国家标准学会(US-ANSI)
【起草单位】:ANSI
【标准类型】:()
【标准水平】:()
【中文主题词】:
【英文主题词】:
【摘要】:DescribestheMPEG-2audionon-backwardscompatiblestandardcalledMPEG-2AdvancedAudioCoding,AAC[1],ahigherqualitymultichannelstandardthanachievablewhilerequiringMPEG-1backwardscompatibility.ThisMPEG-2AACaudiostandardallowsforITU-R&8216;indistinguishable&8217;qualityaccordingto[2]atdataratesof320kbit/sforfivefull-bandwidthchannelaudiosignals.
【中国标准分类号】:L71;L81
【国际标准分类号】:33_160_60;35_040
【页数】:
【正文语种】:英语


下载地址: 点击此处下载
【英文标准名称】:ULStandardforSafetyAttachmentPlugsandReceptaclesCOMMENTSDUE:MARCH31,2008
【原文标准名称】:连接插头和插座的UL安全的标准(评审到期日:2008年3月31日)
【标准号】:UL498BULLETIN-2008
【标准状态】:现行
【国别】:美国
【发布日期】:2008-07-23
【实施或试行日期】:
【发布单位】:美国保险商实验所(US-UL)
【起草单位】:UL
【标准类型】:()
【标准水平】:()
【中文主题词】:
【英文主题词】:
【摘要】:Thefollowingisbeingproposedforpreliminaryreviewandcommentonly:1.ForPreliminaryReviewOnly:ProposedAdoptionoftheStandardforApplianceCouplersforHouseholdandSimilarGeneralPurposes-Part1:GeneralRequirements,IEC60320-1withHarmonizedNationalDifferencesastheProposedSecondEditionoftheStandardforApplianceCouplersforHouseholdandSimilarGeneralPurposes-Part1:GeneralRequirements,UL60320-1.
【中国标准分类号】:K30
【国际标准分类号】:29_120_30
【页数】:132P.;A4
【正文语种】:英语


【英文标准名称】:StandardGuideforMechanicalandFunctionalCharacterizationofNucleusDevices
【原文标准名称】:核装置的机械和功能特征表示的标准指南
【标准号】:ASTMF2789-2010
【标准状态】:现行
【国别】:美国
【发布日期】:2010
【实施或试行日期】:
【发布单位】:美国材料与试验协会(US-ASTM)
【起草单位】:F04.25
【标准类型】:(Guide)
【标准水平】:()
【中文主题词】:
【英文主题词】:dynamictests;nucleusdevice;spinalimplants;statictests
【摘要】:Nucleusdevicesaregenerallydesignedtoaugmentthemechanicalfunctionofnativedegeneratednucleusmaterialortoreplacetissuethathasbeenremovedduringasurgicalprocedure.Thisguideoutlinesmethodsforevaluatingmanydifferenttypesofdevices.Comparisonsbetweendevicesmustbemadecautiouslyandwithcarefulanalysis,takingintoaccounttheeffectsthatdesignandfunctionaldifferencescanhaveonthetestingconfigurationsandoverallperformance,andthepossibilitythatmechanicalfailuremaynotberelatedtoclinicalfailureandinversely,thatmechanicalsuccessmaynotberelatedtoclinicalsuccess.Thesetestsareconductedinvitrotoallowforanalysisofthemechanicalperformanceofthenucleusdeviceunderspecifictestingmodalities.Theloadsappliedmaydifferfromthecomplexloadingseeninvivo,andthereforetheresultsfromthesetestsmaynotdirectlypredictinvivoperformance.Thesetestsareusedtoquantifythestaticanddynamicpropertiesandperformanceofdifferentimplantdesigns.Themechanicaltestsareconductedinvitrousingsimplifiedloadsandmoments.Fatiguetestinginasimulatedbodyfluidorsalinemayhavefretting,aging,corroding,orlubricatingeffectsonthedeviceandtherebyaffecttherelativeperformanceoftesteddevices.Hence,thetestenvironmentandtheeffectofthatenvironment,whetherasimulatedbodyfluid,normalsalinebath(9gNaClper1000mLH2O),ordry,isanimportantcharacteristicofthetestandmustbereportedaccurately.Dynamictestingmethodsshouldbedesignedtoanswerthefollowingquestions,includingbutnotlimitedto:Doesthedevicestillfunctionasintendedaftercycling?Doesitretainadequateperformancecharacteristics(forexample,mechanicalandkinematicpropertiessuchasROM)?Didthedevicewearordegrade?Ifthereisevidenceofwearordegradationofthedevice,itshouldbeidentifiedandquantifiedwithreasonablemethodsgenerallyavailable.Theusershalldistinguishbetweenparticulatesgeneratedbythedeviceandparticulatesgeneratedbythetestmodelandfixturesiftechnicallyfeasible.1.1Thisguidedescribesvariousformsofnucleusreplacementandnucleusaugmentationdevices.Itfurtheroutlinesthetypesoftestingthatarerecommendedinevaluatingtheperformanceofthesedevices.1.2Biocompatibilityofthematerialsusedinanucleusreplacementdeviceisnotaddressedinthisguide.However,usersshouldinvestigatethebiocompatibilityoftheirdeviceseparately(seeX1.1).1.3Whileitisunderstoodthatexpulsionandendplatefracturesrepresentdocumentedclinicalfailures,thisguidedoesnotspecificallyaddressthem,althoughsomeofthefactorsthatrelatetoexpulsionhavebeenincluded(seeX1.3).1.4Multipletestsaredescribedinthisguide;however,theuserneednotusethemall.Itistheresponsibilityoftheuserofthisguidetodeterminewhichtestsareappropriateforthedevicesbeingtestedandtheirpotentialapplication.Sometestsmaynotbeapplicableforalltypesofdevices.Moreover,somenucleusdevicesmaynotbestableinalltestconfigurations.However,thisdoesnotnecessarilymeanthatthetestmethodsdescribedareunsuitable.1.5Thescienceofnucleusdevicedesignisstillveryyoungandincludestechnologythatischangingmorequicklythanthisguidecanbemodified.Therefore,theusermustcarefullyconsidertheapplicabilityofthisguidetotheuserx2019;sparticulardevice;theguidemaynotbeappropriateforeverydevice.Forexample,atthetimeofpublication,thisguidedoesnotaddressthenucleusreplacementandnucleusaugmentationdevi......
【中国标准分类号】:F60
【国际标准分类号】:11_040_40
【页数】:10P.;A4
【正文语种】:英语



版权声明:所有资料均为作者提供或网友推荐收集整理而来,仅供爱好者学习和研究使用,版权归原作者所有。
如本站内容有侵犯您的合法权益,请和我们取得联系,我们将立即改正或删除。
京ICP备14017250号-1