功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
16期
16116-16119,16124
,共5页
李大伟%田原宇%乔英云%李俊花%唐瑞源
李大偉%田原宇%喬英雲%李俊花%唐瑞源
리대위%전원우%교영운%리준화%당서원
活性炭%吸附剂%制备%粘合剂%磷酸%木屑
活性炭%吸附劑%製備%粘閤劑%燐痠%木屑
활성탄%흡부제%제비%점합제%린산%목설
active carbon%adsorbents%binder%phosphoric acid%sawdust
在粉状活性炭(PAC)中加入载磷酸废木屑,经挤压、加热等步骤,使 PAC 转化为成型活性炭(ACM)。利用 SEM、XRD、N2吸附-脱附技术及万能试验机,考察了ACM的形貌、微晶结构、比表面积、孔结构及耐压强度。研究发现,载磷酸废木屑制取容易,且能使PAC成型但无损比表面积。当 PAC 用量、加热温度、加热时间分别为40%、560℃、100 min 时,可得到耐压强度为4.2 MPa、比表面积达710 m2/g 的ACM;延长加热时间,能够提高 ACM的比表面积、微孔孔容和耐压强度,但对其微晶结构影响较小。
在粉狀活性炭(PAC)中加入載燐痠廢木屑,經擠壓、加熱等步驟,使 PAC 轉化為成型活性炭(ACM)。利用 SEM、XRD、N2吸附-脫附技術及萬能試驗機,攷察瞭ACM的形貌、微晶結構、比錶麵積、孔結構及耐壓彊度。研究髮現,載燐痠廢木屑製取容易,且能使PAC成型但無損比錶麵積。噹 PAC 用量、加熱溫度、加熱時間分彆為40%、560℃、100 min 時,可得到耐壓彊度為4.2 MPa、比錶麵積達710 m2/g 的ACM;延長加熱時間,能夠提高 ACM的比錶麵積、微孔孔容和耐壓彊度,但對其微晶結構影響較小。
재분상활성탄(PAC)중가입재린산폐목설,경제압、가열등보취,사 PAC 전화위성형활성탄(ACM)。이용 SEM、XRD、N2흡부-탈부기술급만능시험궤,고찰료ACM적형모、미정결구、비표면적、공결구급내압강도。연구발현,재린산폐목설제취용역,차능사PAC성형단무손비표면적。당 PAC 용량、가열온도、가열시간분별위40%、560℃、100 min 시,가득도내압강도위4.2 MPa、비표면적체710 m2/g 적ACM;연장가열시간,능구제고 ACM적비표면적、미공공용화내압강도,단대기미정결구영향교소。
Powdery active carbon (PAC)was converted into active carbon monoliths (ACMs)by adding H3 PO4-loaded waste sawdust into it,followed by treatments like extrusion and heating.The morphologies,microcrys-tal structures,specific surface areas (SSAs),pore structures,and compression strengths of the obtained ACMs were investigated using SEM,XRD,N2 adsorption-desorption technique,and compression test.The H3 PO4-loaded waste sawdust was an easy-making binder.Moreover,by using it,the PAC was converted into ACMs without reducing its SSA.An ACM with a SSA of 710 m2/g and compression strength of 4.2 MPa could be produced by heating at 560 ℃ for 100 min using a PAC dosage of 40%.The increase in activation time increased the SSA,micropore volume,and compression strength of ACMs,but hardly affected their microcrystal struc-ture.