简介:Thepreparationofcalciumphosphate(CP)coatingonaluminaceramicsusingelectricpulsestimulatingmethodhasbeeninvestigated.Thecup-shapedaluminaceramicsweresoakedinasimulatedbodyfluid(SBF),andasquarepulsepotentialwithfrequencyof1Hzandvoltageof110Vwasappliedbetweentheinnerandoutersurfacesofthealuminacup.SurfacemorphologyofCPcoatingsduringdifferentdepositionperiodswasobservedbyaPhilipsXL-30scanningelectronmicroscope(SEM).CompositionalanalysiswasexaminedbyEDAX.ThemechanismofnucleationandgrowthofCPcoatingwasdiscussed.SEMresultindicatesthatthecoatingcomprisesofalargenumberoftinyneedle-likegrainsandhasaporousmicrostructure.ThereisastrongbondbetweenthedepositedlayerandAl2O3substrate,whichmaybeduetothegentlegrowthofthebiomimeticmethod.TheEDAXanalysisindicatesthatmaincompositionofthecoatingiscalciumandphosphor.TheformationofCPcoatingmaybecontributedtothestimulationofelectricpulseandthehighionsconcentrationwhichis1.5timesoftheconcentrationofSBFsolution(1.5SBFsolution).SuchsurfacefunctionalizationmethodbyelectricpulsepotentialcanbeusedtoprepareCPcoatingonvariouselectric-insulatingbioinertmaterialsforimprovingtheirbioactivecharacter.
简介:EnvironmentalfriendlyrecyclingprocessforNd-Fe-Bsinteredmagnetsludgesgeneratedinthemanufacturingprocess,whichcontainlargeamountofrareearth,includingNd,PrandDy,isbadlyneededsofar.Inpresentstudy,wehavedevelopedaneffectiveroutetoobtainrecycledsinteredmagnetsfromNd-Fe-Bsinteredmagnetsludgesbycalciumreduction-diffusion(RD)process.Comparedtoconventionalrecyclingprocess,ourresearchisfocusedonrecoveringmostoftheusefulelements,includingNd,Pr,Dy,Co,andFetogetherinsteadofjustrareearthelements.Toimprovetherecyclingefficiencyandreducepollution,theco-precipitatingparametersweresimulatedandcalculatedusingMATLABsoftware.Mostofusefulelementswererecoveredbyaco-precipitationmethod,andtheobtainedcompositepowderswerethendirectlyfabricatedasrecycledNd-Fe-Bpowdersbyacalciumreduction-diffusion(RD)method.Therecoveryratesare98%,99%,99%,93%,and99%,forNd,Pr,Dy,Co,andFe,respectively.Theamountofusefulelementscontainedintherecoveredcompositepowdersisgreaterthan99.71wt%.TheprocessofRDforsynthesizingNd2Fe14BandsubsequentlyremovingCaOwasthoroughlyinvestigated.Furthermore,therecycledNd-Fe-Bmagnetexhibitsaremanenceof1.1T,acoercivityof1053kA/m,andanenergyproductof235.6kJ/m3,respectively,indicatingthatrecycledNd-Fe-Bsinteredmagnetwassuccessfullyrecoveredfromtheseverelycontaminatedsludgesviaaneffectiverecyclingroute.
简介:ObjectivesToinvestigateeffectofAngll,captoprilonsingleguineamyocytesonL-typecalciumcurrentandsodiumcurrent.MethodsMembranepatchclampwholecellrecordingtechniquewasusedtoinvestigateeffectofangll,captoprilonL-Camaximumcurrentdensityandsodiummaximumcurrentdensity.ResutlsAngllincreasedthemaximumcurrentdensitycomparedwithcontrolafterperfused5min,357.7±219.7Vs279.5±240.5PA/PF,increaserateis27.9%,theshapeofcurrent-voltagerelationshipcurvewasunchanged,peakedat+10mv,indicatedthatangllincreasedL-Cacurrentdensityinvoltage-dependent.Afterperfusedwithcaptopril,captopril+angll3,5min,L-Cacurrentwasrecorded,resultssuggestL-Camaximumcurrentdensitydecreasedsignificantlycomparedwithcontrol,incaptoprilgroup,128.4±92.6Vs286.2±89.7,66.7±68.3Vs286.2±89.7,respectively,rateofinhibitionis55.1%,76.6%,respectively.L-Cacurrentfurtherdecreasedincaptoprilpe
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简介:Theinfluencesofmagnesiumandferricionsintheirdifferentratiosontherateofgypsumcrystallizationwerestudiedundertheconditionssimilartothoseofwetflue-gasdesulfurization(WFGD).TheresultsshowthatadditionofbothMg2+andFe3+increasedinductiontimeanddecreasedthegrowthefficiencyupto50%comparedwiththebaseline(withoutimpurities)dependingontheconcentrationandthetypeofimpurity.TheeffectsofMg2+andFe3+onthesurfaceenergyandtherateofnucleationwereestimatedbyemployingtheclassicalnucleationtheory.Thesurfaceenergydecreasedby8%and14%withtheadditionof0.02mol/Lmagnesiumorferricions,respectively,comparedtothebaseline.Mg2+andFe3+madethegrowthrateofthe(020),(021)and(040)facesofgypsumcrystalamuchgreaterreduction,whichleadstotheformationofneedlecrystalscomparedtothebaselinewhichfavorstheformationofplateorflakes.Furthermore,anedgedetectionprogramwasdevelopedtoquantifytheeffectsofimpuritiesonthefiltrationrateofgypsumproduct.Theresultsshowthattheinhibitionefficiencyofthepresenceof0.02mol/LMg2+andFe3+onthefiltrationrateofgypsumcrystalrangesfrom22%to39%.
简介:Objective:Tostudytheeffectofnitricoxide-inducedtyrosinephosphorylationoflarge-conductancecalcium-activatedpotassium(BKCa)channelαsubunitonvascularhyporesponsivenessinrats.Methods:Atotalof46Wistarratsofeithersex,weighing250g±20g,wereusedinthisstudy.Modelsofvascularhyporesponsivenessinducedbyhemorrhagicshock(30mmHgfor2hours)invivoandbyL-arginineinvitrowereestablishedrespectively.Thevascularresponsivenessofisolatedsuperiormesentericarteriestonorepinephrinewasobserved.TyrosinephosphorylationofBKCaαsubunitwasevaluatedwithmethodsofimmunoprecipitationandWesternblotting.Results:Inthesmoothmusclecellsofthesuperiormesentericarteries,theexpressionofBKCaαsubunittyrosinephosphorylationincreasedfollowinghemorrhagicshock,andL-argininecouldinduceBKCachannelαsubunittyrosinephosphorylationinatime-anddose-dependentmanner.L-NAME(Nω-nitro-L-arginine-methyl-ester),anitricoxidesynthetaseinhibitor,couldpartlyrestorethedecreasedvasoresponsivenessofthesuperiormesentericarteriesafterhemorrhagicshockinrats.Down-regulatingtheproteintyrosinephosphorylationwithgenistein,awidely-usedspecialproteintyrosinekinaseinhibitor,couldpartlyimprovethedecreasedvasoresponsivenessofthesuperiormesentericarteriesinducedbyL-arginineinvitro,whileup-regulatingtheproteintyrosinephosphorylationwithNa3VO4,aproteintyrosinephosphataseinhibitor,couldfurtherdecreasethenitricoxide-inducedvascularhyporesponsiveness,whichcouldbepartlyamelioratedby0.1mmol/Ltetrabutylammoniumchloride(TEA),aselectiveBKCainhibitoratthisconcentration.Conclusions:NitricoxidecaninducethetyrosinephosphorylationofBKCaαsubunit,whichinfluencesthevascularhyporesponsivenessinhemorrhagicshockratsorinducedbyL-arginineinvitro.
简介:SimultaneousBiparametricDeterminationofTotalCalciumandPotassiuminBiologicalFluidsbyFlowInjectionAnalysis──UseofPowell'sMethod...
简介:hard-core/soft-shell钙碳酸盐(CaCO3)的合成/poly(甲基methacrylate)(PMMA)混合结构化的nanoparticles(<100nm)由把分裂成原子的微乳液聚合,过程被报导。聚合物链通过acoupling代理人的使用被抛锚到nano-CaCO3的表面上,triethoxyvinylsilane(TEVS)。铵persulfate(APS),钠dodecyl硫酸盐(SDS)和n-pentanol分别地被用作开始者,表面活化剂和cosurfactant。coreshell乳胶粒子的聚合机制被讨论。由PMMA的nano-CaCO3的封装用一台传播电子显微镜(TEM)被证实。coreshell粒子的grafting百分比被thermogravimetric分析(TGA)调查。nano-CaCO3/PMMAcoreshell粒子被Fourier变换描绘红外线(FTIR)光谱学和微分扫描热量测定(DSC)。FTIR结果在nano-CaCO3粒子和PMMA的接口揭示了一个强壮的相互作用的存在,它成功地暗示聚合物链是grafted到通过联合代理人的连接的nano-CaCO3粒子的表面上。另外,TGA和DSC结果与纯nano-PMMA的相比显示了coreshell材料的热稳定性的改进。nano-CaCO3/PMMA粒子被混合进聚丙烯(PP)矩阵由融化处理。它能也用扫描PMMA锁住的电子显微镜学(SEM)被观察grafted在聚合物矩阵(PP矩阵)防碍到CaCO3nanoparticles上CaCO3的聚集并且因此与PP矩阵改进CaCO3nanoparticles的相容性。