简介：glutamic酸(LG)和丁氨二酸酸(ASP)的随机的共聚物，poly(LG-co-ASP)，能成功地与debenzylation经由N-carboxyanhydride戒指开始copolymerization的联合与设计作文被综合。-benzyl-L-glutamateN-carboxyanhydride(BLG-NCA)和-benzyl-LaspartateN-carboxyanhydride(BLA-NCA)的戒指开始copolymerizations被使用不同的胺包括执行象开始者的triethylamine(茶)，diethylamine，n-hexylamine(NHA)，triphenylamine，二苯胺或苯胺。所有6胺是高度有效的poly变得明确(BLG-co-BLA)共聚物与尽管聚合经由不同机制(正常的胺机制或/并且激活的单体机制)继续了，设计了作文，它基于胺的化学结构。分子的重量(BLG-co-BLA)poly，共聚物能被茶集中和聚合时间调停。然后，debenzylation(BLG-co-BLA)poly，共聚物被进行准备相应吸水的随机的共聚物(LG-co-ASP)poly以ASP结构的单位与子单元组织。LG结构的单位在的内容(LG-co-ASP)poly，共聚物在NCA单体BLG-NCA与那些匹配在NHA或茶开始并且接近了理论线的戒指洞copolymerizations喂。diblock共聚物(BLG-b-BLA)能被BLGNCA和BLA-NCA的顺序的增加也poly经由生活NCA戒指洞copolymerization综合。

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简介：Thepurposeofthisresearchistoinvestigatethepotentialofpre-treatmentwithphosphoricacid(PA)andmonobasiccalciumphosphate(MCP)forthestabilizationofheavymetalsinsludgeanditsbottomash.ThetannerysludgesampleswerecollectedinWenzhou,Chinaandheavilycontaminatedwithheavymetals,suchasPb,Crandsoon.Thesampleswerepre-treatedwithPAorMCP.ThenXRDandTCLPtestswereadoptedastheevaluatingmethodstocharacterizethePb,Cr,Cu,ZnandCdimmobilizationinthepre-treatedsludgeanditsbottomash.TheresultsshowedthatthistreatmenteffectivelyimmobilizedPbandCdinthesludge,lightlystabilizedthemetalCu,andadversely,enhancedtheleachabilityofZn.Afterincinerationat900℃,PbandCrinthebottomashofpre-treatedsludgeweresignificantlystabilizedduetotheformationoftheirhighlythermostablephosphatesandpyromorphite-likemineralsduringtheincinerationprocess.However,anincreaseofCuandZnsolubilitywasobservedwhichmightbeattributabletotheacidificationofsludgeduetotheadditionofPAorMCP.

简介：ThesupportedPtcatalysts(1wt%)werepreparedbytheincipientimpregnationmethodandanalyzedusingsynchrotron-basedX-raydiffraction,BETsurfacearea,oxygenadsorption,COpulsechemisorption,temperature-programmeddesorption(TPD)ofaceticacid,H2-TPD,NH3-TPD,O2-TPD,andH2-TPR.ThereactivityofPt-basedcatalystswasstudiedusingafixedbedreactorat300Cand4MPaforhydrodeoxygenationofaceticacid,wherePt/TiO2wasveryselectiveforethaneproduction.TPDexperimentsrevealedthatseveralconditionsmustbesatisfiedtoachievethishighselectivitytoethanefromaceticacid,suchasPtsites,moderateacidity,andmediummetal-oxygenbondstrengthintheoxidesupport.Thisworkprovidesinsightsindevelopingnovelcatalyticmaterialsforhydrocarbonproductionsfromvariousorganicsincludingbio-fuels.

简介：Adirectsynthesisofmethyllevulinatefromcellulosealcoholysisinmethanolmediumundermildcondition(180210C)catalyzedbyextremelylowconcentrationsulfuricacid(0.01mol/L)andtheproductisolationweredevelopedinthisstudy.Effectsofdifferentprocessvariablestowardsthecatalyticperformancewereperformedasafunctionofreactiontime.Theresultsindicatedthatsulfuricacidconcentration,temperatureandinitialcelluloseconcentrationhadsignificanteffectsonthesynthesisofmethyllevulinate.Anoptimizedyieldofaround50%wasachievedat210Cfor120minwithsulfuricacidconcentrationof0.01mol/Landinitialcelluloseconcentrationbelow100g/L.Theresultingproductmixturewasisolatedbyadistillationtechniquethatcombinesanatmosphericdistillationwithavacuumdistillationwheren-dodecanewasaddedtohelpdistilltheheavyfraction.Thelightfractionincludingmainlymethanolcouldbereusedasthereactionmediumwithoutanysubstantialchangeintheyieldofmethyllevulinate.ThechemicalcompositionandstructuraloflowerheavyfractionwerecharacterizedbyGC/MS,FTIR,1H-NMRand13C-NMRtechniques.Methyllevulinatewasfoundtobeamajoringredientoflowerheavyfractionwiththecontentover96%.Thispathwayisefficient,environmentallybenignandeconomicalfortheproductionofpurelevulinateestersfromcellulose.

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简介：Tetrazole-1-aceticacidwasfoundtoserveasasuperiorligandforCuI-catalyzedN-arylationofimidazoleswitharyliodidesunderalowcatalystloading(5mol%ofCuI).AvarietyofaryliodidescouldbeaminatedtoprovidetheN-arylatedproductsingoodtoexcellentyieldswithouttheneedofaninertatmosphere.