简介：ConstructionofthephaseⅡMDIprojectandtheassociatedengineeringprojectsoftheNingboWanhuaPolyurethaneCo.,Ltd.,whichisasubsidiarycompanyoftheYantaiWanhuaPolyurethaneCo..Ltd..hasbeenapprovedbytheStateDe-

简介：TheliquidphasedimethyletherprocessdevelopedbyLuMingChemicalCompanyLimitedinLinyi,ShandongpassedappraisalorganizedbytheprovincialScienceandTechnologyDepartment.

简介：二新奇的灰更少添加剂-benzothiazole衍生物包含硼和氯，OBC和BBC，被综合。在在油菜籽的添加剂上油的不同集体比率(RO)的OBC和BBC的tribological表演在一台四球的机器上被检验。油样品润滑的更低的钢球的穿的表面借助于扫描电子显微镜学(SEM)被分析。测试结果显示出那OBC，BBC在底有好溶解度上油，并且能有效地增加基础油的带负担的能力。包含1.5m%BBC的油样品的最大的非抓住负担是1117N，它2.3倍于基础油的。OBC和BBC能改进禁止性能和基础油的热稳定性的反穿和腐蚀，谁的起始的分解温度在350°C上面。然而，在不同集中的OBC和BBC能增加基础油的磨擦系数。油润滑的钢球的SEM形态学取样包含1.5m%添加剂似乎比形成的基础油，和疤的更一致、光滑是很浅的。

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简介：介绍Phase在线分析仪的基本工作原理及其在炼油事业部催化裂化装置的应用，并针对使用过程中出现的介质管线压力不稳定的情况对预处理系统进行了改进，取得了较好的应用效果。

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简介：TheresultsofcommercialapplicationoftwotypesofC_8aromaticsisomerizationcatalystsunderdifferentfeedconditionswerecomparedtogainaninsightinthetechno-economicalbasisforselectingpropertechnologicalrouteattheplant.Thecomparisonrevealsdifferencesineveryaspectoffeedconsumption,unitcapacity,productoutput,productdistribution,andunitprocessparametersdependinguponwhichcatalysttypeisadoptedbytheintegratedPXcomplex.Thetypeofaromaticsisomerizationcatalysthasitsinfluenceontheplantscale,theconstructioncost,theprocessunitcapacityandtheproductcost,withthemagnitudeofitsimpactvaryingwithchangingfeedconditions.

简介：TheShanxiSanweiGroupCo.,Ltd.intendstoinvestaround820millionRMBintheconstructionofa9-kt/acoalgasifica-tionunitanda30kt/apolytetrahydrofuranexpansionproject,

简介：催化py-rolysis-maximizing丙烯(TMP)技术独立地由中国石油大学(华东)的州的关键重油实验室开发了的二阶段的起床人的商业测试表明了在受到TMP之上的那大气的残油(AR)能超过18%完成丙烯收益，并且LPG，汽油和柴油机产量的和能接近83%。当重油的FCC或两重棉包线吸引了特殊注意最大化丙烯产量，在最近的年，这处理，因为常规催化裂开技术能仅仅在3%的范围贡献丙烯收益—5%。

简介：OnDecember12,2013theproject'Developmentandcommercialapplicationofcontinuousliquid-phasedieselhydrotreating(SLHT)technology'jointlyundertakenbyRIPP,SEI,theShijiazhuangRefiningandChemicalCo.(SRCC)andtheAnqingPetrochemicalCo.haspassedthetechnicalappraisalorganizedbytheScienceandTechnologyDivisionofSINOPECinBeijing.

简介：SixNi-MocatalystswithdifferentmetalcontentswerepreparedandcharacterizedbyN2adsorptionandX-raydiffractometry.TheactivephasemicrostructureofthesecatalystswasexaminedbytheRamanspectroscopy,temperatureprogrammedreduction(TPR),X-rayphotoelectronspectroscopy,andhigh-resolutiontransmissionelectronmicroscopy.Hydrodesulfurization(HDS)activityofcatalystsampleswereanalyzedinaflowfixed-bedmicroreactor.ThesulfidationdegreeofMoandthelengthoftheMoS2slabslightlyincreasedwiththeamountofmetalloadedfollowingsulfidation.Thissmallchangeisattributedtopolymolybdatespeciesobservedinalltheoxidizedcatalysts.Weakmetal-supportinteractions,asdeterminedbytheTPRtechnique,increasedtheNiSxsulfidationphaseandMoS2slabstacking.TheHDSactivityofthecatalystsamplesincreasedwiththenumberofactivesites.Forhighmetalloadingcatalysts,theirHDSactivitywasnearlyidenticalbecausethesulfuratomscannoteasilyapproachactivesites.ThischangeiscausedbythelargenumberofstackedlayersintheMoS2slabsaswellasthedecreaseinthespecificsurfaceareaandporevolumeofthecatalystsampleswithanincreasingmetalloading.

简介：TheDalianInstituteofChemicalPhysics(DICP)ofCAShasdevelopedthetechnologyformanufactureofDMEthroughtwo-stepdehydrationofmethanoland

简介：ThepolycrystallinephaseWO3/g-C3N4wassynthesizedunderstirringusingtungstenicacid(H2WO4)andgraphiticcarbonnitride(g-C3N4)asrawmaterials.ThecatalystwascharacterizedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM),energydispersivespectroscopy(EDS),theFouriertransforminfraredspectroscopy(FT-IR),andtheBrunauer-Emmett-Telleranalysis(BET).ThepolycrystallinephaseWO3/g-C3N4wasdeterminedbyXRDtechnique.TheoxidativedesulfurizationprocesswasinvestigatedusingWO3/g-C3N4asthecatalyst,30%hydrogenperoxide(H202)astheoxidant,and1-butyl-3-methylimidazoliumtetrafluoroborate([bmim]BF4)ionicliquids(ILs)astheextractant.Theoperatingconditions,includingH2WO4amount,ILdose,H2O2volume,temperature,catalystdosage,andtypesofsulfurcompounds,weresystematicallyresearched.Thedesulfurizationratecouldreach98.46%forremovingdibenzothiophene(DBT)fromthemodeloilunderoptimalreactionconditions.Inaddition,thecatalyticactivitywasslightlydecreasedafterfiverecyclesofcatalysts.Thereactionkineticsanalysisshowsthattheoxidativedesulfurizationsystemwasinaccordwiththefirst-orderreactionkineticsequation.Themechanismofoxidativedesulfurizationwasproposed.