燃烧科学与技术
燃燒科學與技術
연소과학여기술
JOURNAL OF COMBUSTION SCIENCE AND TECHNOLOGY
2014年
6期
498-504
,共7页
杨峥%王玥%吕兴才%黄震
楊崢%王玥%呂興纔%黃震
양쟁%왕모%려흥재%황진
丙醇%混合燃料%快速压缩机%化学反应动力学
丙醇%混閤燃料%快速壓縮機%化學反應動力學
병순%혼합연료%쾌속압축궤%화학반응동역학
propanol isomers%blend fuel%rapid compression machine%chemical kinetics
在一台快速压缩机上研究了不同比例的丙醇/正庚烷二元混合燃料在当量比为1.0、压缩上止点压力2,MPa、压缩温度为650~850,K时的着火延迟.利用混合燃料的详细动力学机理开展了丙醇/正庚烷着火特性的化学反应动力学分析.研究结果表明,在本文实验条件下和温度范围内,丙醇/正庚烷的着火延迟在不同的温度范围呈现不同的变化规律.在丙醇比例较低时,正丙醇/正庚烷混合燃料的着火延迟高于异丙醇/正庚烷混合燃料;丙醇比例较高时,二者的着火延迟非常接近.化学动力学分析表明,由于正庚烷低温反应根池的建立,丙醇在着火过程中也呈现出两阶段燃烧现象.路径分析表明,上止点温度的提高可使部分羟丙烷基发生裂解并增强系统活性.进一步的敏感性分析表明,对正丙醇/正庚烷混合燃料,正庚烷的脱氢反应和链分支反应对促进着火始终有重要影响,随着正丙醇比例的增加,正丙醇对混合燃料着火的抑制与促进都有较大的影响.异丙醇/正庚烷混合燃料的着火在异丙醇比例较大或上止点温度较高时对异丙醇的氧化更加敏感,抑制着火的反应始终为小分子基团的反应.
在一檯快速壓縮機上研究瞭不同比例的丙醇/正庚烷二元混閤燃料在噹量比為1.0、壓縮上止點壓力2,MPa、壓縮溫度為650~850,K時的著火延遲.利用混閤燃料的詳細動力學機理開展瞭丙醇/正庚烷著火特性的化學反應動力學分析.研究結果錶明,在本文實驗條件下和溫度範圍內,丙醇/正庚烷的著火延遲在不同的溫度範圍呈現不同的變化規律.在丙醇比例較低時,正丙醇/正庚烷混閤燃料的著火延遲高于異丙醇/正庚烷混閤燃料;丙醇比例較高時,二者的著火延遲非常接近.化學動力學分析錶明,由于正庚烷低溫反應根池的建立,丙醇在著火過程中也呈現齣兩階段燃燒現象.路徑分析錶明,上止點溫度的提高可使部分羥丙烷基髮生裂解併增彊繫統活性.進一步的敏感性分析錶明,對正丙醇/正庚烷混閤燃料,正庚烷的脫氫反應和鏈分支反應對促進著火始終有重要影響,隨著正丙醇比例的增加,正丙醇對混閤燃料著火的抑製與促進都有較大的影響.異丙醇/正庚烷混閤燃料的著火在異丙醇比例較大或上止點溫度較高時對異丙醇的氧化更加敏感,抑製著火的反應始終為小分子基糰的反應.
재일태쾌속압축궤상연구료불동비례적병순/정경완이원혼합연료재당량비위1.0、압축상지점압력2,MPa、압축온도위650~850,K시적착화연지.이용혼합연료적상세동역학궤리개전료병순/정경완착화특성적화학반응동역학분석.연구결과표명,재본문실험조건하화온도범위내,병순/정경완적착화연지재불동적온도범위정현불동적변화규률.재병순비례교저시,정병순/정경완혼합연료적착화연지고우이병순/정경완혼합연료;병순비례교고시,이자적착화연지비상접근.화학동역학분석표명,유우정경완저온반응근지적건립,병순재착화과정중야정현출량계단연소현상.로경분석표명,상지점온도적제고가사부분간병완기발생렬해병증강계통활성.진일보적민감성분석표명,대정병순/정경완혼합연료,정경완적탈경반응화련분지반응대촉진착화시종유중요영향,수착정병순비례적증가,정병순대혼합연료착화적억제여촉진도유교대적영향.이병순/정경완혼합연료적착화재이병순비례교대혹상지점온도교고시대이병순적양화경가민감,억제착화적반응시종위소분자기단적반응.
Ignition delay time of propanol isomers/n-heptane mixtures was measured using a rapid compression ma-chine at compressed pressure of 2,MPa,within the compressed temperature range of 650—850,K and with equiva-lence ratio of 1.0. Reaction kinetics analysis was performed using a detailed mechanism of blend fuels. Under the ex-perimental conditions in this study,the ignition delay of the blend fuels displays different varying patterns in different temperature ranges. The ignition delay time of i-propanol/n-heptane is shorter than that of n-propanol/n-heptane when the propanol fraction is low. When the propanol fraction is high,their ignition delay times become very close to each other. The chemical kinetics analysis indicates that propanol isomers also exhibit two-stageoxidation behavior because of the low temperature reactivity radical pool produced by n-heptane. The higher compressed temperature can make a small part of the hydroxypropyl radicals undergo scission reaction and improve system activity. Sensitivity analysis shows that for the n-propanol/n-heptane blends,H-abstraction and chain-branching reaction from the n-heptane al-ways play a dominant role in the reaction with a promoting effect,while the H-abstraction from the n-propanol be-comes important when the n-propanol fraction is high. For i-propanol/n-heptane mixtures,the ignition of the blend fuels is more sensitive to the oxidation of the i-propanol at high compressed temperature or propanol fractions,while the major inhibiting reactions are always some elementary reactions of small radicals.