期刊文献+
共找到8篇文章
< 1 >
每页显示 20 50 100
太阳能熔融盐供热的CH_(4)-CO_(2)重整热化学储能反应热力学分析
1
作者 王洪明 王观竹 《北京化工大学学报(自然科学版)》 CAS CSCD 北大核心 2024年第3期57-65,共9页
以太阳能熔融盐为载热工质的CH_(4)-CO_(2)重整热化学反应是极具应用潜力的热化学储能技术,为探讨工业级CH_(4)-CO_(2)重整储能反应器在不同操作条件下热力学性能的变化规律,建立了基于太阳能熔融盐供热的CH_(4)-CO_(2)重整储能反应器... 以太阳能熔融盐为载热工质的CH_(4)-CO_(2)重整热化学反应是极具应用潜力的热化学储能技术,为探讨工业级CH_(4)-CO_(2)重整储能反应器在不同操作条件下热力学性能的变化规律,建立了基于太阳能熔融盐供热的CH_(4)-CO_(2)重整储能反应器的二维拟均相数学模型,通过数值模拟分析了反应混合物进口温度(T_(in))和进口摩尔流率(F_(tot,in))对反应器内温度、反应转化率和热化学储能效率等的影响规律。结果表明:当进口温度较高时(T_(in)=823 K),转化管内温度沿转化管轴向表现为先降低后升高的变化趋势;当进口温度较低时(T_(in)=573K),转化管内温度沿转化管轴向单调升高;T_(in)=573K下,随着进口摩尔流率的增大,反应转化率单调减小,化学储能效率呈现先增大后减小的变化趋势;在进口摩尔流率相同的条件下,进口温度越高,反应转化率和化学储能效率越大;T_(in)=823 K下,随着进口摩尔流率的增大,显热储能效率和热损失率减小,化学储能效率增大;F_(tot,in)=1 mol/s下,随着反应混合物进口温度的升高,化学储能效率与热损失率增大,显热储能效率减小。 展开更多
关键词 太阳能 热化学储能 ch_(4)-co_(2)重整反应 储能效率
下载PDF
等离子体作用下CH_(4)-CO_(2)重整制取合成气工艺过程数值模拟
2
作者 叶泽甫 朱路奇 +1 位作者 孟献梁 李玉赛 《低碳化学与化工》 CAS 北大核心 2023年第2期42-51,共10页
随着温室气体CH_(4)与CO_(2)排放量的逐年增加,全球气温上升、全球变暖加剧。CH_(4)-CO_(2)重整(CRM)能够有效降低温室气体的排放量,且重整产物为合成气(CO和H_(2)),能提高碳资源的利用率。通过CRM装置完成了反应过程及产物分析,结合流... 随着温室气体CH_(4)与CO_(2)排放量的逐年增加,全球气温上升、全球变暖加剧。CH_(4)-CO_(2)重整(CRM)能够有效降低温室气体的排放量,且重整产物为合成气(CO和H_(2)),能提高碳资源的利用率。通过CRM装置完成了反应过程及产物分析,结合流体仿真软件Fluent与化工模拟软件Chemkin模拟揭示了等离子体作用下CRM制合成气反应过程中进料速率、进料比(n(CO_(2)):n(CH_(4)))及等离子体功率对反应器内部温度场与浓度场分布的影响规律。结果表明,随着进料速率提高,物流在反应器内涡流作用加剧,导致反应器底部温度变高,CH_(4)所参与副反应的平衡向正方向移动,参与主反应的CH_(4)减少,对CO、H_(2)的选择性降低。相同进料速率下,进料比越大,目标产物产量越高,过量的CO_(2)发生副反应,导致CO的增量大于H_(2)的增量。大功率等离子体提供的高温环境会促进CH_(4)和CO_(2)形成高能量自由基,瞬间发生自由基反应,加快反应进程。本研究可为等离子体活化CRM反应工艺技术的优化提供理论基础和应用指导。 展开更多
关键词 ch_(4)-co_(2)重整 等离子体 合成气 数值模拟 温度场 浓度场
下载PDF
非金属氮掺杂活性炭催化剂制备及其催化CH_4-CO_(2)重整反应 被引量:5
3
作者 秦晓伟 张国杰 +4 位作者 李晟 郭晓菲 阎煌煜 徐英 刘俊 《化工进展》 EI CAS CSCD 北大核心 2021年第6期3203-3214,共12页
采用硝酸和尿素联合对活性炭进行改性,制备了富含氮元素的氮掺杂活性炭,考察了孔结构、氮含量和氮种类(吡啶氮、吡咯氮和石墨氮)对CH_4-CO_(2)重整反应催化性能的影响。采用BET、SEM、EA、FTIR、XPS、CO_(2)-TPD和TG表征手段对反应前后... 采用硝酸和尿素联合对活性炭进行改性,制备了富含氮元素的氮掺杂活性炭,考察了孔结构、氮含量和氮种类(吡啶氮、吡咯氮和石墨氮)对CH_4-CO_(2)重整反应催化性能的影响。采用BET、SEM、EA、FTIR、XPS、CO_(2)-TPD和TG表征手段对反应前后催化剂的物理化学性质进行了表征,对引入活性炭表面的含氮官能团的种类及其在重整过程中所起的作用进行了分析。相比于未改性的原活性炭,硝酸和尿素同时改性制备的氮掺杂活性炭(AC-U.NA)引入了更多的羟基官能团和含氮官能团。特别是通过两者共同改性后,所制备的氮掺杂活性炭引入的吡啶氮官能团比例明显提高,为CH_4-CO_(2)重整反应提供了更多的活性位点,初始CH_4和CO_(2)转化率达到55.94%和66.46%。同时经过两者联合改性后,所制备的AC-U.NA材料表面具有极性,不仅有利于酸性CO_(2)分子的吸附和活化,而且有利于CO_(2)消碳反应,减少了积炭的生成,对所制备的非金属重整催化剂的活性和抗积炭性具有重要的意义。 展开更多
关键词 温室气体 ch_4-co_(2)重整 氮掺杂 活性炭 催化剂
下载PDF
嵌入型Ni@S1催化剂的制备及其CH_(4)-CO_(2)重整反应性能 被引量:1
4
作者 盖希坤 杨丹 +5 位作者 朱继成 骆美宇 马清祥 邢闯 吕鹏 张良佺 《洁净煤技术》 CAS 北大核心 2022年第5期71-80,共10页
CH_(4)-CO_(2)重整反应能实现CH_(4)和CO_(2)两种气体的利用,对控制温室效应、保护环境具有重要意义。开发低成本、高活性和高稳定性的重整催化剂是研究焦点。分别采用浸渍法和研磨-晶化法制备了负载型Ni/Q10(孔径10 nm的无定形SiO_(2)... CH_(4)-CO_(2)重整反应能实现CH_(4)和CO_(2)两种气体的利用,对控制温室效应、保护环境具有重要意义。开发低成本、高活性和高稳定性的重整催化剂是研究焦点。分别采用浸渍法和研磨-晶化法制备了负载型Ni/Q10(孔径10 nm的无定形SiO_(2))和嵌入型Ni@S1(Silicalite-1)催化剂,并用于CH_(4)-CO_(2)重整反应。采用XRD、BET、IR、H_(2)-TPR、NH_(3)-TPD、XRF、XPS、SEM、TEM和TG技术手段对催化剂结构进行了表征。研究发现,研磨-晶化法能有效调控Ni@S1催化剂中活性金属Ni的粒度和分散度,增强活性金属相与载体的相互作用。嵌入型结构能减少催化剂积碳,在700℃反应6 h后,5%Ni@S1催化剂的积碳量仅为5%Ni/Q10催化剂的46.83%。采用微型固定床连续反应对催化剂进行了活性评价(CH_(4)/CO_(2)/Ar=44.0/47.2/8.8、进料流速F_(in)=40 mL/min、反应温度T=700℃),发现反应6 h后,CH_(4)在5%Ni@S1和5%Ni/Q10催化剂的瞬时转化率分别为72.82%和67.24%,与初始转化率相比分别降低了1.05%和7.99%;CO_(2)瞬时转化率分别为79.06%和76.69%,与初始转化率相比分别降低了1.16%和4.54%。嵌入型Ni@S1催化剂在CH_(4)-CO_(2)重整反应中的活性和稳定性优于负载型Ni/Q10催化剂。 展开更多
关键词 ch_(4)-co_(2)重整 分子筛 限域 积碳 烧结
下载PDF
The catalytic effect of both oxygen-bearing functional group and ash in carbonaceous catalyst on CH_(4)-CO_(2) reforming
5
作者 Weidong ZHANG Yongfa ZHANG 《Frontiers of Chemical Science and Engineering》 SCIE EI CSCD 2010年第2期147-152,共6页
A kind of new catalyst-carbonaceous catalyst-for CH_(4)-CO_(2) reformation has been developed in our laboratory.The effect of both oxygen-bearing functional group such as phenolic hydroxyl,carbonyl,carboxyl,and lacton... A kind of new catalyst-carbonaceous catalyst-for CH_(4)-CO_(2) reformation has been developed in our laboratory.The effect of both oxygen-bearing functional group such as phenolic hydroxyl,carbonyl,carboxyl,and lactonic,and ash such as Fe_(2)O_(3),Na_(2)CO_(3),and K_(2)CO_(3) in the carbonaceous catalyst on the CH_(4)-CO_(2) reforming has been investigated with a fixed-bed reactor.It has been found that the carbonaceous catalyst is an efficient catalyst on CO_(2)-CH_(4) reforming.With the decrease of oxygen-bearing functional group,the catalytic activity of carbonaceous catalyst decreases quickly.The oxygen-bearing functional groups play a significant role in the carbonaceous-catalyzed CO_(2)-CH_(4) reforming;the ash components in carbonaceous catalyst also have an important influence on the CO_(2)-CH_(4) reforming.Fe_(2)O_(3),Na_(2)CO_(3),and K_(2)CO_(3) in the ash can catalyze the CO_(2)-CH_(4) reforming reaction;CaO has little effect on CO_(2)-CH_(4) reforming reaction.CaO can catalyze the gasification between carbonaceous catalyst and CO_(2);Al_(2)O_(3) and MgO inhibit the CO_(2)-CH_(4) reforming. 展开更多
关键词 carbonaceous catalyst ch_(4)-co_(2)eforming oxygen-bearing functional group ASH
原文传递
Effect of carbon deposition over carbonaceous catalysts on CH_(4)decomposition and CH_(4)-CO_(2)reforming
6
作者 Yongfa ZHANG Meng ZHANG +1 位作者 Guojie ZHANG Huirong ZHANG 《Frontiers of Chemical Science and Engineering》 SCIE EI CSCD 2010年第4期481-485,共5页
An investigation was made using a continuous fixed bed reactor to understand the influence of carbon deposition obtained under different conditions on CH_(4)-CO_(2)reforming.Thermogravimetry(TG)and X-ray diffraction(X... An investigation was made using a continuous fixed bed reactor to understand the influence of carbon deposition obtained under different conditions on CH_(4)-CO_(2)reforming.Thermogravimetry(TG)and X-ray diffraction(XRD)were employed to study the characteristics of carbon deposition.It was found that the carbonaceous catalyst is an efficient catalyst in methane decomposition and CH_(4)-CO_(2)reforming.The trend of methane decomposition at lower temperatures is similar to that at higher temperatures.The methane conversion is high during the initial of stage of the reaction,and then decays to a relatively fixed value after about 30 min.With temperature increase,the methane decomposition rate increases quickly.The reaction temperature has significant influence on methane decomposition,whereas the carbon deposition does not affect methane decomposition significantly.Different types of carbon deposition were formed at different methane decomposition reaction temperatures.The carbon deposition Type I generated at 900℃ has a minor effect on CH_(4)-CO_(2)reforming and it easily reacts with carbon dioxide,but the carbon deposition Type II generated at 1000℃and 1100℃clearly inhibits CH_(4)-CO_(2)reforming and it is difficult to react with carbon dioxide.The results of XRD showed that some graphite structures were found in carbon deposition Type II. 展开更多
关键词 carbon deposition carbonaceous catalyst ch_(4)-co_(2)reforming
原文传递
双碳战略中煤气共采技术发展路径的思考
7
作者 李树刚 张静非 +5 位作者 林海飞 丁洋 白杨 周雨璇 朱冰 戴政 《煤炭科学技术》 EI CAS CSCD 北大核心 2024年第1期138-153,共16页
自提出“双碳”目标以来,我国生态文明建设已进入以降碳为重点战略方向的关键时期。煤炭作为兜底能源的地位短期内不会改变,能耗“双控”向碳排放总量和强度“双控”转变的核心即为CH_(4)-CO_(2)协同减排。在精准分析碳达峰、碳中和阶... 自提出“双碳”目标以来,我国生态文明建设已进入以降碳为重点战略方向的关键时期。煤炭作为兜底能源的地位短期内不会改变,能耗“双控”向碳排放总量和强度“双控”转变的核心即为CH_(4)-CO_(2)协同减排。在精准分析碳达峰、碳中和阶段煤矿CH_(4)-CO_(2)双重碳减排面临挑战的基础上,明确了双碳战略中煤气共采技术发展需结合现状需求-技术攻关-政策驱动的核心原则,制定了双碳战略中煤气共采技术的发展路径,论述了其中的关键技术问题。碳达峰阶段,CH_(4)减排以排放源管控为基础视角,核心为瓦斯抽采-利用全周期碳减排关键技术,包含瓦斯富集区靶向精准抽采技术、低渗煤层增透及注气驱替增流抽采技术、关闭矿井瓦斯逃逸通道封堵减碳技术、瓦斯富集-提浓-利用一体化技术,目的是大幅提升高浓度瓦斯抽采-利用效率,减少低浓度及通风瓦斯碳排放;CO_(2)减排以“CCUS+生态碳汇”全域负碳排放技术为核心,包含煤层CO_(2)封存、工业固废采空区充填协同CO_(2)地质封存、煤矿碳封存区域土壤-地表-大气异常监测及生态碳汇技术,进一步吸纳烟道气或纯CO_(2)排放。碳中和阶段核心任务是实现CH_(4)-CO_(2)(近)零碳排放,CO_(2)减排应当由技术攻关示范工程转变为规模化应用阶段,并建立全生命周期煤矿CH_(4)-CO_(2)排放智能监测及动态管控技术体系,实现监测管控技术手段与碳排放环节深度匹配、碳排放监测管控云平台与煤矿全局监控系统深度对接。最后对未来煤气共采体系绿色低碳发展提出了自身见解与思考:(1)继续深化“高效精准抽采+全浓度梯级利用”煤矿CH_(4)零排放技术模式;(2)持续攻关“CO_(2)工程封存+生态碳汇”CO_(2)零排放技术体系;(3)积极探索煤矿“零碳智慧园区”综合解决方案,形成激励和倒逼并重的煤矿碳减排政策支持体系。 展开更多
关键词 双碳目标 ch_(4)-co_(2)协同减排 煤气共采 发展路径 绿色低碳
下载PDF
Review on cryogenic technologies for CO_(2) removal from natural gas 被引量:1
8
作者 Yujing BI Yonglin JU 《Frontiers in Energy》 SCIE CSCD 2022年第5期793-811,共19页
CO_(2) in natural gas(NG)is prone to condense directly from gas to solid or solidify from liquid to solid at low temperatures due to its high triple point and boiling temperature,which can cause a block of equipment.M... CO_(2) in natural gas(NG)is prone to condense directly from gas to solid or solidify from liquid to solid at low temperatures due to its high triple point and boiling temperature,which can cause a block of equipment.Meanwhile,CO_(2) will also affect the calorific value of NG.Based on the above reasons,CO_(2) must be removed during the NG liquefaction process.Compared with conventional methods,cryogenic technologies for CO_(2) removal from NG have attracted wide attention due to their nonpolluting and low-cost advantages.Its integration with NG liquefaction can make rational use of the cold energy and realize the purification of NG and the production of byproduct liquid CO_(2).In this paper,the phase behavior of the CH_(4)-CO_(2) binary mixture is summarized,which provides a basis for the process design of cryogenic CO_(2) removal from NG.Then,the detailed techniques of design and optimization for cryogenic CO_(2) removal in recent years are summarized,including the gas-liquid phase change technique and the gas-solid phase change technique.Finally,several improvements for further development of the cryogenic CO_(2) removal process are proposed.The removal process in combination with the phase change and the traditional techniques with renewable energy will be the broad prospect for future development. 展开更多
关键词 cryogenic CO_(2)removal purification of natural gas(NG) biogas upgrading ch_(4)-co_(2)binary system
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部