高校化学工程学报
高校化學工程學報
고교화학공정학보
JOURNAL OF CHEMICAL ENGINEERING OF CHINESE UNIVERSITIES
2010年
1期
64-70
,共7页
许慎启%周志杰%代正华%于广锁%龚欣
許慎啟%週誌傑%代正華%于廣鎖%龔訢
허신계%주지걸%대정화%우엄쇄%공흔
气化反应%碱金属%微晶结构%石墨化
氣化反應%堿金屬%微晶結構%石墨化
기화반응%감금속%미정결구%석묵화
gasification reaction%alkali metal%crystallite structure%graphitizing
通过对原煤、酸洗原煤、酸洗后负载NaOH的原煤在750~1050℃热解制得焦样,用X射线衍射技术考察了热解温度、NaOH负载量以及灰分对热解过程中煤焦微晶结构变化的影响,并运用高温高压热天平(PTGA)考察了热解后煤焦的气化反应活性.结果表明碱金属及灰分的存在可以明显减小煤焦的微晶结构参数的变化(堆垛高度L_c、微晶尺寸L_a、及晶层间距d_(002)),阻碍煤焦的石墨化进程,提高煤焦的气化反应性.随着热解温度的升高,堆垛高度L_c增大显著,而微晶尺寸L_a和晶层间距d_(002)变化较小.煤焦的气化反应性k0和煤焦微晶结构参数L_c、d_(002)存在如下关系:lnk_0= a (L_c/d_(002))+b;研究还表明用氧化还原循环机理来描述碱金属的催化作用机理是不恰当的,但碱金属Na的存在可以明显降低煤焦的石墨化程度,提高煤的活性,对煤焦的气化起到部分催化作用.
通過對原煤、痠洗原煤、痠洗後負載NaOH的原煤在750~1050℃熱解製得焦樣,用X射線衍射技術攷察瞭熱解溫度、NaOH負載量以及灰分對熱解過程中煤焦微晶結構變化的影響,併運用高溫高壓熱天平(PTGA)攷察瞭熱解後煤焦的氣化反應活性.結果錶明堿金屬及灰分的存在可以明顯減小煤焦的微晶結構參數的變化(堆垛高度L_c、微晶呎吋L_a、及晶層間距d_(002)),阻礙煤焦的石墨化進程,提高煤焦的氣化反應性.隨著熱解溫度的升高,堆垛高度L_c增大顯著,而微晶呎吋L_a和晶層間距d_(002)變化較小.煤焦的氣化反應性k0和煤焦微晶結構參數L_c、d_(002)存在如下關繫:lnk_0= a (L_c/d_(002))+b;研究還錶明用氧化還原循環機理來描述堿金屬的催化作用機理是不恰噹的,但堿金屬Na的存在可以明顯降低煤焦的石墨化程度,提高煤的活性,對煤焦的氣化起到部分催化作用.
통과대원매、산세원매、산세후부재NaOH적원매재750~1050℃열해제득초양,용X사선연사기술고찰료열해온도、NaOH부재량이급회분대열해과정중매초미정결구변화적영향,병운용고온고압열천평(PTGA)고찰료열해후매초적기화반응활성.결과표명감금속급회분적존재가이명현감소매초적미정결구삼수적변화(퇴타고도L_c、미정척촌L_a、급정층간거d_(002)),조애매초적석묵화진정,제고매초적기화반응성.수착열해온도적승고,퇴타고도L_c증대현저,이미정척촌L_a화정층간거d_(002)변화교소.매초적기화반응성k0화매초미정결구삼수L_c、d_(002)존재여하관계:lnk_0= a (L_c/d_(002))+b;연구환표명용양화환원순배궤리래묘술감금속적최화작용궤리시불흡당적,단감금속Na적존재가이명현강저매초적석묵화정도,제고매적활성,대매초적기화기도부분최화작용.
The experimental research on pyrolysis of original coal, acid washing deashed coal and alkali metal (NaOH) loaded deashed coal was conducted in tubular furnace for investigating the effects of alkali metal and coal ash on the variation of crystallite structure of chars prepared from above coals, separately, at temperature of 750~1050℃ by using X-Ray diffraction (XRD) technique, and the char gasification reactivity was investigated by pressurized thermogravimeteric analysis system (PTGA). Results show that the existence of alkali metal and ash decreases the crystallite structure parameters of the chars (average stacking height L_c, carbon crystallite site L_a and interplanar spacing d_(002)) prominently, inhibits the progress of char graphitizing and increases the gasification reactivity of the char. L_c increases apparently and L_a, d_(002) change little with the increase of pyrolysis temperature. Char gasification reactivity k_0 has the following linear relationship with L_c: ln k_0=a (L_c/ d_(002)) +b, where a and b are constants related with char species, pyrolysis and gasification conditions. Results also show that it is not suitable to describe the catalysis mechanism of alkali metals Na for char gasification by the mechanism of redox mechanism. But the existence of Na decreases the degree of crystallite and increases the reactivity, which has the catalytic effect on char gasification.