简介:Rare-earthcompoundsolidsuperacidSO42-/TiO2/La3+wasprepared.Itscatalyticactivitywasexaminedunderdifferentsyntheticconditionsfortheesterificationofpropanoicacidandn-butylalcoholasprobingreaction.Theoptimumconditionswerealsofound,whichwerethepH=8,thedepositingtimewas24h,themassfractionofLa(NO3)3usedinsolidsuperacidwas5%,theconcentrationofH2SO4was1.25mol/L,thesoakingtimeinH2SO4was16handthecalciningtemperaturewas500°C.TheethyloleatewassynthesizedfromoleicacidandethanolinthepresenceofSO42-/TiO2/La3+.Theoptimumreactionconditionswereobtainedwhichwerethereactiontimewas6h,molarratioofoleicacidtoethanolwas1:4andthemassfractionofcatalystwas4%.
简介:将SO4^2-/TiO2-HZSM-5负载镧制备了新型催化剂SO4^2-/La2O3-TiO2-HZSM-5,以对羟基苯甲酸和丙醇的酯化反应为探针,考察了不同制备条件对催化剂性能的影响。结果表明:la^3+浸渍浓度为0.07mol/L,经110℃烘干后于500℃焙烧3h所得催化剂活性最好。对影响酯化反应的因素进行考察,最佳实验条件为n(醇)∶n(酸)=5∶1,反应时间4h,催化剂用量3.0%(总物料),酯化率可达96.0%。且该催化剂具有良好的重复使用和再生能力,适宜合成对羟基苯甲酸酯。
简介:Weperformfirst-principlecalculationsforthestudyoftheorthorhombicRb2Cd2(SO4)3structure.Electronicenergybands,totalandpartialdensitiesofstatesarereportedandanalysed.Itisfoundthatoxygenatomic2pelectronsstronglyhybridizewithRb/orCd4dandS2pstates,resultingintwo-typeionicgroupswithweakcouplings.Itisshownthatmacroscopicdomainwallsoriginatefromsuchweak-couplingionicgroups,arisingatthecellboundaries.Theasymmetriccationbonds(Rb-OandCd-O)andthesubsequentrotationsoftheS04tetrahedracanleadtothedrivingforceoftheferroelectricbehaviour.Thepredictedpyroelectriccurrenteffectsareobservedexperimentallyintheferroelectricphase.
简介:在H2SO4-Fe2(SO4)3体系中研究载金黄铁矿的浸出动力学,探讨反应温度、Fe3+浓度、硫酸浓度、搅拌速度等对黄铁矿浸出的影响规律。结果表明:在H2SO4-Fe2(SO4)3体系中,在30~75°C下黄铁矿浸出过程主要受化学反应控制Fe3+浓度与黄铁矿的浸出呈正相关,通过Arrhenius经验公式求得浸出表观活化能为51.39kJ/mol。EDS与XPS分析结果表明:黄铁矿氧化过程中硫的氧化经一系列中间形态,最终被氧化成硫酸根,并伴有部分元素硫生成,符合硫代硫酸根氧化路径机理。
简介:本文研究了以TiO2-Sb2O3/SO4^2-为催化剂,催化假性紫罗兰酮合成紫罗兰酮。探索了反应温度、反应时间、催化剂用量、溶剂用量等因素对环化反应的影响。最佳合成条件:6mL假性紫罗兰酮,催化剂用量为1.8g,溶剂用量为6mL,环化反应温度为30℃,反应时间为3.0h,紫罗兰酮产率约为70%。
简介:Kineticsofchloride/sulfate,chloride/nitrateandnitrate/sulfateforwardexchangesandreverseexchangesatsolutionconcentrationsof1N,0.2Nand0.02Non201×7strongbaseanionexchangeresin,respectively,havebeenexaminedat25℃.Itisfoundthattheforwardandthereverseexchangeratesofthetwogivenionsatlowsolutionconcentration,respectively,underidenticalconditionscanbecontrolledbydifferentmechanisms,whilethoseathighsolutionconcentrationareallcontrolledbyparticlediffusion.Theternaryexchangeratesofsulfate/(chloride+nitrate)andnitrate/(chloride+sulfate)havealsobeenexamined.
简介:One-potachievementofethyllevulinatefromcassavawasconductedinethanol-watersystemoverseveralsimplesulfatesaltcatalysts.Al2(SO4)3catalysthadthebestperformanceinsynthesizingethyllevulinatecomparingwiththoseofaseriesofsulfatesalts.Thehighestyieldsofethyllevulinatewasupto39.27%aswellas7.78%levulinateacidwhencassavawascatalyzedinethanolmediumbyadding10wt%water.13Cand1HNMRspectroscopicinvestigationsconfirmedthatisomerizationofglucosetofructoseoverAl2(SO4)3catalystisanimportantstepinproducingethyllevulinateandlevulinateacid.DuetoaggregationsofAl3+underhydrothermalconditions,tinyamountofAl3+weredetectedinfiltrateatthepercentageof0.32%evenifinabsolutewater.BronstedandLewisacidscouldimprovetheyieldofethyllevulinateandlevulinateacidbysynergisticeffect.AllresultssuggestedthatA12(SO4)3wasasimpleandefficientcatalystforethyllevulinateandlevulinateacidproduction.
简介:SO4^2-离子检验是中学化学一个重要的知识点,经常出现在物质的鉴别、鉴定、推断等各种题型中,由于有多种因素对其检验产生干扰和影响,使得学生解题时经常发生错误。下面就SO4^2-离子检验需注意的几个问题进行一些分析,希望能给大家有所启发。
简介:ThespinelLiMn2O4-x(SO4)xcompoundcathodematerialsweresynthesizedbysolid-statereactionofthecalculatedamountsofLiOH·H2O,MnO2andMnSO4.Theresultsoftheelectrochemicaltestdemonstratedthatthesematerialsexhbitedexcellentelectrochemicalproperties.Thehighestreversiblecapacityoftheseseriesofcathodematerialswas-120mAh/g,andafter50cycles,thisreversiblecapacitywasstillaround116mAh/gwithnearly100%reversibleefficiency,whichrevealedthatdopedsulfateioncouldimprovethestructuralstabilityofspinel.
简介:Aseriesoftheelectrochemicalandlong-termcorrosiontestswascarriedoutina3.5wt%Na2SO4solutiononthermal-sprayedWC-17CoandWC-10Co-4Crcermetcoatingsinordertoexaminetheeffectofcompositionofbindermaterialsonthecorrosionbehavior.TheresultsrevealthattheoverallcorrosionresistanceoftheWC-17CocoatingisinferiortothatoftheWC–Co–CrcoatingsduetothecorrosionofbindermaterialswhichinduceWCparticlestofalloff.CoOandWO3oxidefilmsformonthesurfaceofWC-17CocoatinginNa2SO4solutionelectrochemicalcorrosionprocess,whichwillprotectthecoatingintheprocessofcorrosion.Cr2O3oxidefilmformedontheWC-10Co-4Crcoatingsurfacehasastronghinderedroletocorrosion.ThecorrosionmechanismofWC-17CocoatinginNa2SO4solutionisentirecorrosionofComatrix,whileitisfilm-holecorrosionmechanismforWC-10Co-4Crcoating.