简介：Onenewsesquiterpenecompound,namely,illihenlactoneA（1）,andonenewprenylatedC6–C3compound,illihenryioneH（2）,alongwiththreeknownsesquiterpenes（3–5）wereisolatedfromthestemsofIlliciumhenryi.Thestructuresof1and2wereelucidatedbyspectroscopicevidenceincludingNMR,HRESIMSandcirculardichroism（CD）.Compound2exhibitedaweakinhibitoryratioforbglucuronidasereleaseinducedbyplatelet-activatingfactor（PAF）inratpolymorphonuclearleukocytes（PMNs）invitro.

简介：Inthispaper,weintroduceaconditionweakerthantheLpdifferentiability,whichwecallCpcondition.Weprovethatifafunctionsatisfiesthisconditionatapoint,thenthereexiststhebestlocalapproximationatthatpoint.WealsogiveanecessaryandsufficientconditionforthatafunctionbeLpdifferentiable.Inaddition,westudytheconvexityofthesetofclusterpointsofthenetofbestappoximationsoff,{Pe(f)}ase→0.

简介：Inthispaper,weapplythecontractionmappingtheoremtoestablishsomeboundedandunboundedadditiveperturbationtheoremsconcerninglocalC-semigroups.SomegrowthconditionsofperturbationsoflocalC-semigroupsarealsoestablished.

简介：ThefirststarsintheearlyUniversewereformedabout400millionyearsafterthebigbang.VerificationoftheexistenceofthesestarsisimportantforourunderstandingoftheevolutionoftheUniverse[1].IthasbeenpredictedthatforPopulation-IIIstellarproductionyields,theabundancesofodd-Zelementsareremarkablydeficientcomparedtotheiradjacenteven-Zelements[2].Astronomersaresearchingforlong-lived,lowmassstarswiththeuniquenucleosyntheticpatternmatchingthepredictedyields[3].

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简介：TheeffectofacidcomponentincludingvariousconventionalacidsandtungsticcompoundsonglucosehydrogenationoveraseriesofbinarycatalystsystemcontainingRu/Ccatalystwasinvestigated.TheresultsshowedthatHCl,H2SO4,H3BO3,H3PO4,andHNO3hadnegligibleeffect,whileallthetungsticcompoundsimposedinhibitingeffectsonthehydrogenationofglucoseoverRu/Ccatalyst,andthesuppressingeffectfollowedtheorderofH2WO4>HPW>WO3>AMT>HSiW.Thisorderisthesameastheorderofethyleneglycol(EG)yieldsintheone-potconversionofglucosetoEG,suggestingtheimportantroleofcompetitionbetweenglucosehydrogenationandretro-aldolcondensationincontrollingtheselectivityofEG.

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简介：纸的目的是估计Wasserstein测量的密度功能或分发功能公制的，统计距离的一种典型类型，它通常在统计学习被要求。基于古典伯恩斯坦近似，一个计划被介绍。得到计划的错误估计，到为单调C1功能估计伯恩斯坦近似的L1标准的问题拐弯，它是很少在古典近似理论讨论了。最后，我们由统计距离得到概率估计。

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简介：Inthispaper,weintroducegeneralizedcyclicC-contractionsthroughpnumberofsubsetsofaprobabilisticmetricspaceandestablishtwofixedpointresultsforsuchcontractions.InourfirsttheoremweusetheHadzictypet-norm.InournexttheoremweuseLukasiewiczt-norm.OurresultsgeneralizetheresultsofChoudhuryandBhandari[11].Acontrolfunction[3]hasbeenutilizedinoursecondtheorem.Theresultsareillustratedwithsomeexamples.

简介：Arylhalidesareakindofextremelyvaluablecompoundsusedintransition-metal-catalyzedcouplingreactions,aswellasimportantstructuremotifsinmanynaturalproductsandmanufactureddrugs[1,2].Theclassicalapproachforpreparationofhaloarenesiselectrophilicaromaticsubstitution(EAS)usingvarioushalogenatingreagentsoroxidativehalogenationswithhalogenatingreagentgeneratedinsitufromhalidesandoxidants,suchasperoxide,oxygenandmeta-cholorperoxybenzoicacid(mCPBA)[3,4].However,harshreactionconditionsarerequiredforhalogenationoflessactivearomatics.orthoMetalationfollowedbyhalogenquenchingisanotherapproachforhalogenationofaromatics[5].However,thereareobviousdrawbacksforthesemethods,suchaslowregioselectivity,harshconditionsandevendangerousprocedures.Therefore,thedevelopmentofanalternativeandpracticalwayremainschallengeinorganicsynthesis.

简介：Toeffectivelysolvetheagglomerationproblemsinthesolidstatereactionprocess,pre-addingglucoseisadoptedtothesynthesisofLiFePO4/CenergymaterialsusingFe–Pwasteslag.Theaverageparticle&grainsizeofLiFePO4/Cdecreases,andtheimpuritiesinLiFePO4/Ccompositesreducetoagreatextent.Itmakesgreatsensetothemassindustrialproduction.Theoptimumsynthesisconditionsdeterminedinthisworkarebasedontheorthogonalexperiments.Thesamplessynthesizedinascaleof500gexhibithighpurity,excellentelectrochemicalperformance,highreactionactivity,goodreversibility,andlowpolarizationlevel.Thedischargecapacitiesare145,134,117,and102mAh/gatthecurrentdensitiesof0.1C,0.2C,0.5Cand1C,respectively.ThisworkputsforwardapracticalsuggestionformassproducingenvironmentalbenignandlowcostLiFePO4/Cascathodematerialsoflithiumionbatteries.

简介：若无限长均匀带电直导线（线电荷）与接地平板系统的电场是二维静电场,当求解区域可视为为多边形时,则可应用S-C映射法和电像法为统一模型,求解出线电荷在求解区域所激发的电势。

简介：Theroleofpulseparametersonnanoparticlepropertyisinvestigatedself-consistentlybasedonacoupleoffluidmodelandaerosoldynamicsmodelinacapacitivelycoupledparallel-plateacetylene(C2H2)discharge.Inthismodel,themasscontinuityequation,momentumbalanceequation,andenergybalanceequationforneutralgasaretakenintoaccount.Thus,thethermophoreticforceariseswhenagastemperaturegradientexists.Thetypicalresultsofthismodelarepositiveandnegativeiondensities,electronimpactcollisionsrates,nanoparticledensity,andchargedistributions.Thesimulationisperformedfordutyratio0.4/0.7/1.0,aswellaspulsemodulationfrequencyfrom40kHzto2.7MHzforpureC2H2dischargesatapressureof500mTorr.Wefindthatthepulseparameters,especiallythedutyratio,haveagreataffectonthedissociativeattachmentcoefficientandthenegativedensity.Moreimportantly,bydecreasingthedutyratio,nanoparticlesstarttodiffusetothewall.Undertheactionofgasflow,nanoparticledensitypeakiscreatedinfrontofthepulseelectrode,wherethegastemperatureissmaller.

简介：本文讨论矩阵方程ATX＋xTA=C的一般解及其最佳逼近解的正交投影迭代解法．首先，利用矩阵的结构特点及相关性质，并借助矩阵空间的相关理论，给出求该矩阵方程一般解正交投影迭代算法；其次，根据奇异值分解、F-范数正交变换不变性证明算法的收敛性并推导出算法的收敛速率估计式，当方程相容时，该算法收敛于问题的极小范数解，且对该算法稍加修改，就可得到相应最佳逼近解；最后，用数值实例验证算法的有效性．

简介：本文证明第二种服务可选的M/M/1排队模型的主算子的点谱包含一个区间（-α,0）,α〉0.此结果表明该主算子生成的C_0-半群不是紧算子,甚至不是最终紧算子.本文的结果与我们以前的结果合并后得到：（i）该C_0-半群的本质增长界为0.从而,该C_0-半群不是拟紧算子.（ii）该模型的时间依赖解不可能指数收敛于其稳态解.（iii）该C_0-半群的本质谱半径等于1.

简介：Theoreticalmodelsofstellarevolutionpredictnegligiblequantitiesof6Li,9Be,and11Binthehydrogenburningphasesofastar’sevolution[1].TheprimordialBig-Bangnucleosynthesis(BBN)modelmightbemoregenerousinitsproductionoftheseelements[2].Theradiative-capturecrosssectionforprotoncaptureon11Bleadingto12CissmallatastrophysicallyinterestingenergiesbecauseofthelargeCoulombbarrier.

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简介：Pt/WO3/CnanocompositeswithparallelWO3nanorodsweresynthesizedandappliedasthecathodecatalystforprotonexchangemembranefuelcells(PEMFCs).Electrochemicalresultsandsinglecelltestsshowthatanenhancedactivityfortheoxygenreductionreaction(ORR)isobtainedforthePt/WO3/CcatalystcomparedwithPt/C.ThehighercatalyticactivitymightbeascribedtotheimprovedPtdispersionwithsmallerparticlesizes.ThePt/WO3/Ccatalystalsoexhibitsagoodelectrochemicalstabilityunderpotentialcycling.Thus,thePt/WO3/CcatalystcanbeusedasapotentialPEMFCcathodecatalyst.

简介：Radiotherapyisacommontreatmentmodalityforheadandneckcancers,nasopharyngealcancers,primarybraintumorsandbrainmetastases.Alargenumberofpatientsintheworldwithprimaryormetastaticbraintumorswillrequirelargevolumeorwholebrainirradiationeveryyear.However,therapeuticirradiationnotonlykillstumorcells,butalsoinjuresnormalbraintissue,whichiscommonlyassociatedwithsignificantfunctionalmorbidityanddecreasedqualityoflifeinpatientstreatedwithbrainradiotherapy[1].