山西化工
山西化工
산서화공
SHANXI CHEMICAL INDUSTRY
2011年
4期
5-7,12
,共4页
赫瑞元%马志微%常丽萍%郑仙荣
赫瑞元%馬誌微%常麗萍%鄭仙榮
혁서원%마지미%상려평%정선영
加压浸渍%氧化锌%半焦%脱硫剂
加壓浸漬%氧化鋅%半焦%脫硫劑
가압침지%양화자%반초%탈류제
pressure impregnation%zinc oxide%semi-coke support%desulfurization
采用加压水热浸渍法制备氧化锌精脱硫剂,考察了浸渍时间、煅烧温度和煅烧时间对脱硫剂硫化性能的影响。对制备的脱硫剂在硫化温度500℃,空速2 000 h-1,气氛为H2(体积分数39%)、CO(体积分数33%)、H2S(体积分数1×10-3)和N2的条件下进行了固定床活性评价。结果显示,随着浸渍时间的延长,脱硫剂的脱硫能力增强,但硫化后脱硫剂粉化程度加剧。加压浸渍时间5 h、500℃煅烧5 h制备出的氧化锌脱硫剂的脱硫效果最佳。SEM结果表明,该条件下制备出的脱硫剂活性组分ZnO在载体表面分布均匀,且粒径较小。
採用加壓水熱浸漬法製備氧化鋅精脫硫劑,攷察瞭浸漬時間、煅燒溫度和煅燒時間對脫硫劑硫化性能的影響。對製備的脫硫劑在硫化溫度500℃,空速2 000 h-1,氣氛為H2(體積分數39%)、CO(體積分數33%)、H2S(體積分數1×10-3)和N2的條件下進行瞭固定床活性評價。結果顯示,隨著浸漬時間的延長,脫硫劑的脫硫能力增彊,但硫化後脫硫劑粉化程度加劇。加壓浸漬時間5 h、500℃煅燒5 h製備齣的氧化鋅脫硫劑的脫硫效果最佳。SEM結果錶明,該條件下製備齣的脫硫劑活性組分ZnO在載體錶麵分佈均勻,且粒徑較小。
채용가압수열침지법제비양화자정탈류제,고찰료침지시간、단소온도화단소시간대탈류제류화성능적영향。대제비적탈류제재류화온도500℃,공속2 000 h-1,기분위H2(체적분수39%)、CO(체적분수33%)、H2S(체적분수1×10-3)화N2적조건하진행료고정상활성평개。결과현시,수착침지시간적연장,탈류제적탈류능력증강,단류화후탈류제분화정도가극。가압침지시간5 h、500℃단소5 h제비출적양화자탈류제적탈류효과최가。SEM결과표명,해조건하제비출적탈류제활성조분ZnO재재체표면분포균균,차립경교소。
Zinc oxide fine desulfurizer agent as the active constituent was prepared by press water hot dipping process.The influences of soaking time,calcination heat and calcination time on curing performance of the desulfurizer agent were studied.At the curing temperature of 500 ℃,airspeed of 2000 h-1,and H2(39 vol %),CO(33 vol %),H2S(1 000 ppm) or N2 as the atmosphere,activeness of the prepared desulfurizer agent on the fixed bed was appraised.The results demonstrated that along with soaking time expanding,desulfurizer agent desulphurization ability was strengthened,but the pulverization degree of cured desulfurizer agent was aggravated.The desulphurization effect of zinc oxide desulfurizer agent prepared in the condition of soaking 5 hours and calcining 5 hours at 500 ℃ was best.As the SEM result indicated,ZnO active constituent of the desulfurizer agent prepared in this condition was distributed in the carrier surface equably and the particle size was small.