简介:全直径岩心分析是从储集层中取出整段岩心进行物性分析检测。由于特殊的非均质储集层在溶孔、裂缝发育段进行取样时,尤其是在大溶孔、网状缝或延伸大的裂缝处取小岩样时易于破碎,所取岩样往往不能准确反映某深度点整个井眼的孔隙发育情况;而且,对孔隙欠发育且连通性较差的严重非均质地层,小岩样往往仅反映微小的局部地层,不能反映所对应深度的真实情况。为此,开展了全直径岩心分析技术的研究,详细介绍孔隙度、渗透率监测分析原理以及测量实验的操作步骤,进行了全直径岩心孔隙度、垂向和侧向渗透率、克氏渗透率的实验。经实例效果检验结果表明,通过全直径岩心分析获得的孔隙度、渗透率数据更合理准确,可提高缝洞、溶洞型非均质储集层物性参数的精度,从而为非均质储集层的油气层开发提供更为可靠的依据。
简介:Anovelhighgravitymulti-concentriccylinderelectrodes-rotatingbed(MCCE-RB)wasdevelopedfortheelectrocatalyticdegradationofphenolwastewaterinordertoenhancethemasstransferwiththeself-madeRuO2-IrO2-SnO2/Tianodes.Theinfluencesofelectriccurrentdensity,inletliquidcirculationflowrate,highgravityfactor,sodiumchlorideconcentration,andinitialpHvalueonphenoldegradationefficiencywereinvestigated,withtheoptimaloperatingconditionsdetermined.Theresultsshowedthatundertheoptimaloperatingconditionscoveringacurrentdensityof35mA/cm^2,aninletliquidcirculationflowrateof48L/h,ahighgravityfactorof20,asodiumchlorideconcentrationof8.5g/L,aninitialpHvalueof6.5,areactiontimeof100min,andaninitialphenolconcentrationof500mg/L,theefficiencyforremovalofphenolreached99.7%,whichwasimprovedby10.4%ascomparedtothatachievedinthenormalgravityfield.Thetendencyregardingthechangeinefficiencyforremovalofphenol,totalorganiccarbon(TOC),andchemicaloxygendemand(COD)overtimewasstudied.Theintermediatesanddegradationpathwayofphenolwerededucedbyhighperformanceliquidchromatography(HPLC).
简介:介绍了橡胶促进剂2,2′-二硫代二苯并噻唑主要生产方法,包括采用亚硝酸钠、氯气、次氯酸钠作氧化剂的传统生产方法和氧气作氧化剂的新工艺,并分别对其优缺点进行了对比。传统的生产方法原料成本高,废水、废气对环境污染严重,不符合绿色化工发展的要求;氧气作氧化剂生产橡胶促进剂DM不仅原料易得,成本低,无污染,而且母液可循环使用,基本无废水排放。中试已成功生产出合格产品,符合大规模工业化生产要求,有广阔的工业应用前景。
简介:Nitrobenzene-containingindustrialwastewaterwasdegradedinthepresenceofozonecoupledwithH2O2byhighgravitytechnology.Theeffectofhighgravityfactor,H2O2concentration,pHvalue,liquidflow-rate,andreactiontimeontheefficiencyforremovalofnitrobenzenewasinvestigated.TheexperimentalresultsshowthatthehighgravitytechnologyenhancestheozoneutilizationefficiencywithO3/H2O2showingsynergisticeffect.ThedegradationefficiencyintermsoftheCODremovalrateandnitrobenzeneremovalratereached45.8%and50.4%,respectively,underthefollowingreactionconditions,viz.:ahighgravityfactorof66.54,apHvalueof9,aH2O2/O3molarratioof1:1,aliquidflowrateof140L/h,anozoneconcentrationof40mg/L,aH2O2multipledosingmodeof6mL/h,andareactiontimeof4h.Comparedwiththeperformanceofconventionalstirredaerationmixers,thehighgravitytechnologycouldincreasetheCODandnitrobenzeneremovalraterelatedwiththenitrobenzene-containingwastewaterby22.9%and23.3%,respectively.
简介:Alkylationoftoluenewith2-chloro-2-methylpropane(t-Bu-Cl)tosynthesizepara-tert-butyltoluene(PTBT)wascarriedoutinthepresenceoftriethylaminehydrochloride-aluminumchlorideionicliquidsusedasthecatalyst.TheionicliquidswerepreparedwithdifferentmolarratiosofEt3NHCltoAlCl3,andtheeffectofthemolarratiobetweenAlCl3andEt3NHCl,thereactiontime,thereactiontemperature,theionicliquiddosage,aswellasthemolarratiooftoluenetochloro-2-methylpropaneonthealkylationreactionoftoluenewithchloro-2-methyl-propanewasinvestigated.ThetestresultsshowedthattheacidicionicliquidspreparedwithEt3NHClandAlCl3hadgoodactivityandselectivityforthealkylationreactionoftoluenewithalkylchloridetoproducePTBT.TheoptimalreactionconditionswerespecifiedatanAlCl3toEt3NHClratioof1.6,areactiontemperatureof20℃,amassfractionoftoluenetoionicliquidof10%,andachloro-2-methylpropanetotoluenemolarratioof0.5.Underthesuitablereactionconditions,a98%conversionofchloro-2-methylpropaneandan82.5%selectivityofPTBTwereobtained.Ionicliquidscouldbereused5timeswithitscatalyticactivityunchanged,andtheregeneratedionicliquidscanberecycled.
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.