检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:李龙津[1] 邹建新[1] 曾小勤[1,2] 丁文江[1,2]
机构地区:[1]上海交通大学材料科学与工程学院轻合金精密成型国家工程中心 [2]金属基复合材料国家重点实验室,上海200240
出 处:《高等学校化学学报》2012年第10期2158-2163,共6页Chemical Journal of Chinese Universities
基 金:上海市浦江人才计划(批准号:11PJ1406000);上海市基础研究重点项目(批准号:10JC1407700);上海市自然科学基金(批准号:11ZR1417600);教育部博士学科点基金(批准号:20100073120007)资助
摘 要:采用高能球磨法制备了3NaBH4/ErF3复合储氢材料,并研究了其相结构和储氢性能.X射线衍射(XRD)显示,NaBH4和ErF3在球磨过程中未发生反应;同步热分析(TG-DSC)测试结果表明,3NaBH4/ErF3体系在420℃开始放氢,比相同测试条件下纯NaBH4的放氢温度降低了约100℃,放氢量为3.06%(质量分数).压力-成分-温度(Pressure-Composition-Temperature,PCT)性能测试结果显示,3NaBH4/ErF3复合储氢材料在较低的温度(355~413℃)及平台氢压(<1 MPa)下即拥有良好的可逆吸放氢性能,最高可逆吸氢量可达到2.78%(质量分数),吸氢后体系重新生成了NaBH4相.计算得吸氢焓变仅为-36.8 kJ/mol H2;而放氢焓变为-180.8 kJ/mol H2.NaBH4在ErF3的作用下提高了热动力学性能,并实现了可逆吸放氢。3NaBHJErF3 hydrogen storage composite was prepared through ball milling method and its phase structure and hydrogen sorption properties were investigated. It is shown that NaBH4 did not react with ErF3 during ball milling. The dehydrogenation temperature of the composite, measured by thermo gravimetric-diffe- rential scanning calorimetry( TG-DSC), is 420 ~C, which is about 100 ~C lower than the dehydrogenation tem- perature of pure NaBH4. Mass loss of the composite is about 3.06%. Pressure-Composition-Temperature (PCT) tests revealed that the composite has outstanding reversible hydrogen sorption performance at moderate temperatures(355---413 ~C) and under quite low hydrogenation plateau pressures (〈1 MPa) the maximum hydrogen storage capacity of the composite can reach up to 2.78%. It was found that NaBH4 was regenerated during hydrogenation. Based on the PCT analyses, the hydrogenation enthalpy of the composite is determined to be -36. 8 kJ/mol H2, while the dehydrogenation enthalpy is -180. 8 kJ/mol H2. The addition of ErF3 into NaBH4 improves the thermodynamic performance of NaBH4 and forms a reversible hydrogen storage composite.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.15