简介：TheesterificationoflauricacidwithmethanolcouldbeefficientlycatalyzedbyZrOCl2·8H2O,andthisreactionwasstudiedtodevelopagreenmethodforbiodieselproduction.Theinfluencingfactors,suchasamountofcatalyst,reactiontimeandmolarratioofacidtomethanol,wereinvestigated.TheresultsindicatedthattheZrOCl2·8H2Ocatalystshowedhighcatalyticactivity,andgavea97.0%methyllaurateconversionrateunderthefollowingoptimizedconditions,viz.:alauricacid/methanolmolarratioof1:10,acatalystdosageof4%,andareactiondurationof2hatmethanolrefluxingtemperature.Thecatalystcouldbeeasilyrecoveredwhileitsactivitycouldbewellretainedafterthreecycles.TheZrOCl2·8H2Ocatalystalsoexhibitedexcellentcatalyticactivityfortheesterificationofdifferentfreelong-chainfattyacids(includingnonedibleoilswithhighacidvalue)withdifferentshortcarbonchainalcohols.Therefore,theZrOCl2·8H2Ocatalysthasgoodpotentialforthesynthesisofbiodieselfromlow-costfeedstockssuchaswastevegetableoilsandnon-edibleoils.

简介：为应对电子商务支撑环境下的市场提出的新挑战和新需求,广东石油选择了建设了O2O营销模式,取得了成效。本文分析了广东石油建设O2O营销模式的过程和经验,针对经营机制、线下配套服务、大数据应用等问题提出了完善的建议。

简介：TheMoS2catalystswerepreparedfromvariousmolybdateprecursorsincludinginorganicandorganicmolybdatecompounds.ThesulfidationdegreeandmorphologyofactivephasesofMoS2activatedbyvariousmolybdateprecursorsinH2S/H2streamatdifferenttemperatureswerestudiedbyX-rayphotoelectronspectroscopy（XPS）andhigh-resolutiontransmissionelectronmicroscopy（HRTEM）.TheorganicmolybdateprecursorsleadtoMoS2catalystswithhighersulfidationdegreeandsmalleractivephasestodemonstratehighercatalyticactivityduringhydrodesulfurizaiton（HDS）of4,6-DMDBT.

简介：出光集团将2013年度至2015年度3年期的“第4个合并中期经营计划”定位为“结构改革舞台”，为实现“藻求腾飞的事业组合”积极努力，并以2015年度为期，

简介：Inthispaper,2-isopropylnaphthalenehasbeensynthesizedbythereactionofnaphthaleneandisopropylbromide,usingtriethylaminehydrochloride-aluminumchlorideionicliquidasthecatalyst.Theeffectofthecatalystcomposition,thereactiontime,thereactiontemperature,theionicliquiddosage,aswellasthemolarratioofthereagentsonthe2-isopropylnaphthaleneyieldwassystematicallyinvestigated.Theoptimalreactionconditionscover:anAlCl3toEt3NHClratioof2.0,areactiontimeof3h,areactiontemperatureof15.0℃,avolumefractionofionicliquidtothemixture(isopropylbromide,n-dodecaneandn-hexane)of9%,andanaphthalene/isopropylbromidemolarratioof4.0.Undertheoptimalreactionconditions,theconversionofisopropylbromidereached98%andtheselectivityof2-isopropylnaphthalenewasequalto80%.ThetestresultsverifiedgoodcatalyticactivityuponusingEt3NHCl-AlCl3ionicliquidasthecatalystforalkylationofnaphthalenewithisopropylbromide.Theactivityoftheionicliquidremainsunchangedafterithasbeenrecycledfor4times.

简介：Throughimprovingtheagingprocessduringsynthesisofthesupport,γ-Al2O3withlargeporevolumeandhighsurfaceareawassynthesizedbyafacilesecondaryreformingmethod.Thesynthesisparameters,suchasthereactiontemperature,thefirstagingtemperatureandthesecondagingtemperature,wereinvestigated.Thetexturalpropertiesofγ-Al2O3werecharacterizedbymeansofN2adsorption-desorptionisotherms,X-raypowderdiffractometry(XRD),scanningelectronmicroscopy(SEM),Fouriertransforminfrared(FTIR)spectroscopyandthermogravimetry(TG).TheexperimentalresultsindicatedthatAACHandamorphousAlOOHweretheprecursorsofalumina,whichwereformedviaprecipitationfromsolutionsafterreactionofaluminumsulphatewithammoniumhydrogencarbonate.Theprecursornanocrystallitesgrewandre-assembledduringthesecondaryreformingprocess,whichresultedinanincreasedporesizeandporevolumeandadecreasedbulkdensity.Theas-synthesizedγ-Al2O3materialsfeaturedmeso/macroporosity,largeporevolume(2.175cm3/g),highsurfacearea(237.8m2/g),andlowbulkdensity(0.284g/mL).