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991.
建立了酱油中1,3-二氯-2-丙醇、2,3-二氯-1-丙醇、3-氯-1,2-丙二醇和2-氯-1,3-丙二醇的分散固相萃取-气相色谱-高分辨质谱快速筛查检测方法。样品采用乙酸乙酯提取,提取液浓缩后经N-丙基乙二胺净化,气相色谱-高分辨质谱测定,内标法定量。结果表明,该方法对于酱油中4种氯丙醇的定量限为0.5~10 μg/kg。在3个浓度水平下的加标回收率为78%~103%;相对标准偏差均不大于8.8%。该方法快速、简便、准确、灵敏,可作为酱油中4种氯丙醇的有效检测方法。 相似文献
992.
993.
During the years of 2015 to 2018, the inorganic chemistry course in Tianjin University has gradually transited from small private on-line course (SPOC) to flipped classroom. Flipped classroom teaching practices were carried out at more than 30 classes at our university by the sufficient use of on-line course resources. These practices effectively improve the quality of teaching, and greatly solve the problem of poor learning initiative and low participation of the students existing in current traditional teaching model. This article in detail introduces and summarizes the following four aspects, including transition of teaching modes, construction of online resources, online and offline supervising, test scores analysis and teaching thought. The effective ways for flipped classroom mode are discussed to improve students' knowledge and learning ability. And it also provides references for teachers to carry out their classroom teaching reform. 相似文献
994.
钙钛矿型羟基锡酸盐是近年来出现的新型高效阻燃消烟剂. 本文采用化学共沉淀法合成了微纳米钙钛矿型羟基锡酸钙[CaSn(OH)6, CSH], 并利用扫描电子显微镜、 透射电子显微镜、 X射线衍射仪、 红外光谱仪和X射线光电子能谱仪等对其形貌和结构进行表征. 结果表明合成的CaSn(OH)6为平均粒径500 nm的纯净正六面体, 粒径均一且分散性良好. 将CaSn(OH)6应用于环氧树脂(EP)复合阻燃体系(CSH/EP), 并分别采用热重分析、 极限氧指数和锥形量热测试表征了其热降解行为和燃烧性能. 采用扫描电子显微镜、 红外光谱、 X射线衍射和拉曼光谱对EP复合材料的阻燃成炭机制进行探索. 结果表明, CaSn(OH)6能显著提高EP复合材料的高温稳定性、 热释放速率、 热释放量、 烟释放量和极限氧指数数值. 特别是在很低添加量(0.5%, 质量分数)下, 阻燃消烟性能即得到极大提升, 热释放速率、 总放热量和一氧化碳释放量分别降低45.8%, 25.1%和31.3%. 此外, 由于CaSn(OH)6在EP基体中的良好分散及较强的界面作用, CaSn(OH)6在提升EP复合材料阻燃消烟性的同时还提升了EP复合材料的力学强度. 本文合成的CaSn(OH)6可作为一种多功能的高效阻燃、 消烟和增强剂. 相似文献
995.
HoU Baoxiu MA Linlin ZANG Xiaohuan SHANG Ningzhao SONG Jianmin ZHAO Xiaoxian WANG Chun QI Jian WANG Jiangyan YU Ranbo 《高等学校化学研究》2021,37(2):265-273
An easy and delicate approach using cheap carbon source as conductive materials to construct 3D sequential porous structural Na3V2(PO4)3/C(NVP/C)with high performance for cathode materials of sodium ion battery is highly desired.In this paper,the NVP/C with 3D sequential porous structure is constructed by a delicate approach named as“cooking porridge”including evaporation and calcination stages.Especially,during evaporation,the viscosity of NVP/C precursor is optimized by controlling the adding quantity of citric acid,thus leading to a 3D sequential porous structure with a high specific surface area.Furthermore,the NVP/C with a 3D sequential porous structure enables the electrolyte to interior easily,providing more active sites for redox reaction and shortening the diffusion path of electron and sodium ion.Therefore,benefited from its unique structure,as cathode material of sodium ion batteries,the 3D sequential porous structural NVP/C exhibits high specific capacities(115.7,88.9 and 74.4 mA·h/g at current rates of 1,20 and 50 C,respectively)and excellent cycling stability(107.5 and 80.4 mA·h/g are remained at a current density of 1 C after 500 cycles and at a current density of 20 C after 2200 cycles,respectively). 相似文献
996.
HU Tao YANG Weiwei WANG Cheng BU Yali JIN Feng ZHANG Dongwen GU Min LIU Wenhui LIANG Qinghua LIU Ruiqing FENG Xiaomiao MA Yanwen 《高等学校化学研究》2021,37(2):286-292
Sodiumion batteries(SIBs)have attracted intensive attention as promising alternative to lithium-ionbatteries(LIBs)for large scale energy storage systems because of low cost of sodium,similar energy storage mechanism and the reasonable performance.However,it is still a great challenge to search and design a robust structure of anode materials with excellent cycling stability and high rate capability for SIBs.Herein,multilayer porous vanadium nitride(VN)microsheets are synthesized through a facile and scalable hydrothermal synthesis-nitrogenization strategy as an effective anode material for SIBs.The multilayer porous VN microsheets not only offer more active sites for fast Na+insertion/extraction process and short diffusion pathway,but also effectively buffer the volume change of anode due to more space in the multilayer porous structure.The large proportions of capacitive behavior imply that the Na+charge storage depends on the intercalation pseudocapacitive mechanism.The multilayer porous VN microsheets electrodes manifest excellent cycling stability and rate capability,delivering a discharge capacity of 156.1 mA·h/g at 200 mA/g after 100 cycles,and a discharge capacity of 111.9 mA·h/g at 1.0 A/g even after 2300 cycles with the Coulombic efficiency of nearly 100%. 相似文献
997.
GAO Jie MENG Ye ZHAO Weiwei JIANG Daofa JIN Yanmei ZHENG Jun YANG Xinan MA Peihua 《高等学校化学研究》2021,37(3):674-678
The host-guest interactions between cyclopentanocucurbit-[6]uril(CyP6Q[6]) as host and six alkyl imidazolium hydrochloride as guests(g1, g2, g3, g4, g5, and g6) have been studied by various techniques, such as 1H NMR spectroscopy, isothermal titration calorimetry, mass spectrometry, and single-crystal X-ray diffraction analysis. The experimental results showed that CyP6Q[6] formed 1:1 inclusion complexes with each of guests g1-g6. The part of the guest entered the cavity of CyP6Q[6] changes as the alkyl chain increases in length. It can be seen that the length of the alkyl chain plays a key role in determining the mode of host-guest interactions. 相似文献
998.
以TiO2、TiS2及Sm2O3为前驱体,分别加入LiCl-KCl与LiCl-CsCl的最低共熔混合物作为熔盐,在较低温度下成功合成了Sm2Ti2S2O5(STSO)颗粒。通过对比不同温度下所制备产物的X射线衍射图,首次表明STSO的热力学结晶温度在520℃左右,远低于之前报道的650℃的最低合成温度。扫描电子显微镜照片显示,采用2种混合熔盐制备的STSO都呈片状形貌;同一合成温度下,采用LiCl-CsCl熔盐制备的STSO的厚度小于LiCl-KCl所得产物。采用出射光波长大于420 nm的氙灯作为光源,在含有Na2S-Na2SO3空穴牺牲剂的溶液中,所制备的STSO颗粒表现出最高35μmol·h-1的光催化分解水产氢活性以及20 h以上的产氢稳定性。 相似文献
999.
1000.