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微波水解法制备稻草微晶纤维素及能效分析 被引量:5
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作者 阴艳华 郑碧微 +2 位作者 李海玲 郭杰 罗逸 《化学与生物工程》 CAS 2010年第10期44-46,共3页
优化了微波水解法降解稻草纤维制备微晶纤维素(MCC)的反应条件。结果表明,当盐酸质量分数为6%、反应时间为10 min、微波功率为231 W、固液比为1∶20(g∶mL)时,MCC的产率达87.00%,而能耗仅为常规加热法的23.1%。微观分析证实,微波水解降... 优化了微波水解法降解稻草纤维制备微晶纤维素(MCC)的反应条件。结果表明,当盐酸质量分数为6%、反应时间为10 min、微波功率为231 W、固液比为1∶20(g∶mL)时,MCC的产率达87.00%,而能耗仅为常规加热法的23.1%。微观分析证实,微波水解降低了纤维素分子的聚合度,增强了对稻草纤维束非晶区结构的破坏作用,提高了产物的结晶度,但纤维素分子特征并未发生改变。 展开更多
关键词 稻草 微波水解法 微晶纤维素 能效分析
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超细TiO_2粉体制备之微波水解法 被引量:6
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作者 刘忠士 昝菱 《武汉大学学报(自然科学版)》 CSCD 北大核心 2001年第2期192-194,共3页
首次将微波加热法引入 Ti O2 的水解反应中 ,详细比较了传统加热和微波加热对水解产生 Ti O2 粒子的粒度、形貌和晶型的影响 .实验显示 ,同等条件下 ,微波加热得到分散性更好 ,粒径更小 ,金红石晶型含量更高的Ti O2 粒子 .
关键词 微波水解法 超细粉体材料 二氧化钛 微波加热 金红石晶型
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微波水解法制备掺钇二氧化锡气敏材料的研究
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作者 满丽莹 徐红燕 《硫磷设计与粉体工程》 2011年第2期23-26,4,共4页
以SnCl_4·5H_2O、尿素CO(NH_2)_2和YCl_3为原料,利用微波水解法分别制备了纯的和n(Y^(3+))为2%、3%、4%、5%的SnO_2纳米粉体。利用XRD对其进行物相分析,SEM观察其形貌。就其对1 000 mg/L质量浓度汽油的灵敏度进行测试。结果表明:Y^... 以SnCl_4·5H_2O、尿素CO(NH_2)_2和YCl_3为原料,利用微波水解法分别制备了纯的和n(Y^(3+))为2%、3%、4%、5%的SnO_2纳米粉体。利用XRD对其进行物相分析,SEM观察其形貌。就其对1 000 mg/L质量浓度汽油的灵敏度进行测试。结果表明:Y^(3+)的掺杂抑制了SnO_2晶粒的生长,且掺杂对SnO_2晶格没有影响;当工作温度为400℃时,适量Y^(3+)的掺杂提高了对汽油的灵敏度;最佳工作温度时,n(Y^(3+))为2%的SnO_对1 000 ng/L的汽油灵敏度最大为20.7,明显优于对1 000 mg/L丙酮的灵敏度。 展开更多
关键词 微波水解法 掺杂 纳米 二氧化锡 气敏性
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TiOCl_2溶液微波加热制备金红石型TiO_2纳米粒子(英文) 被引量:2
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作者 王新 韩梅娟 +1 位作者 魏雨 王延吉 《人工晶体学报》 EI CAS CSCD 北大核心 2004年第4期634-637,共4页
本文报道了一种由TiOCl2 液相直接合成金红石型TiO2 纳米粒子的新方法 ,即微波诱导沸腾回流强迫水解法 ,用该法制备出常规条件下不能得到的产品。所得产物用粉末X射线衍射仪和透射电子显微镜表征 ,证明产物为金红石型 ,粒子尺寸 5~ 30n... 本文报道了一种由TiOCl2 液相直接合成金红石型TiO2 纳米粒子的新方法 ,即微波诱导沸腾回流强迫水解法 ,用该法制备出常规条件下不能得到的产品。所得产物用粉末X射线衍射仪和透射电子显微镜表征 ,证明产物为金红石型 ,粒子尺寸 5~ 30nm可控。研究表明 ,产物物相取决于Ti4+ 的初始水解速率 ,水解速率越快 ,越有利于金红石相成核 ;通过控制初始Ti4+ 的浓度 ,可改变纳米TiO2 的粒径。另外还讨论了该金红石型TiO2 纳米粒子的成核机理。 展开更多
关键词 TiOCl2液相 金红石型TiO2纳米粒子 制备 微波诱导沸腾回流强迫水解 粉末X射线衍射仪 透射电子显微镜 成核机理 氧化钛
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Microwave-hydrothermal preparation of flower-like ZnO microstructure and its photocatalytic activity 被引量:1
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作者 伍水生 贾庆明 +3 位作者 孙彦林 陕绍云 蒋丽红 王亚明 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2012年第10期2465-2470,共6页
The flower-like ZnO microstructure was prepared by a straightforward microwave-hydrothermal technique using zinc chloride and arginine solution as reactants. The as-synthesized crystal structure and morphology were ch... The flower-like ZnO microstructure was prepared by a straightforward microwave-hydrothermal technique using zinc chloride and arginine solution as reactants. The as-synthesized crystal structure and morphology were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and the optical properties of the ZnO nanostructure were studied by Raman and photoluminescence (PL) spectra, which confirms the high crystal quality of ZnO microstructure. The as-synthesized ZnO flowers exhibit a significant enhancement of photocatalytic capability toward degrading methyl blue (MB) under UV light, the photodegradation of MB reaches 95.60%, only within 2 h of adding the as-synthesized ZnO in the MB solution under UV irradiation. Furthermore, the photodegradation could be described as the pseudo-first-order kinetics with degradation rate constant of 1.0675-1.6275 h-1, which is relative to the morphology of the structures. 展开更多
关键词 ZnO microstructure microwave-hydrothermal method photoluminescence PHOTODEGRADATION
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Preparation of κ-carra-Oligosaccharides with Microwave Assisted Acid Hydrolysis Method 被引量:3
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作者 LI Guangsheng ZHAO Xia +2 位作者 LV Youjing LI Miaomiao YU Guangli 《Journal of Ocean University of China》 SCIE CAS 2015年第2期345-349,共5页
A rapid method of microwave assisted acid hydrolysis was established to prepare κ-carra-oligosaccharides. The optimal hydrolysis condition was determined by an orthogonal test. The degree of polymerization (DP) of ... A rapid method of microwave assisted acid hydrolysis was established to prepare κ-carra-oligosaccharides. The optimal hydrolysis condition was determined by an orthogonal test. The degree of polymerization (DP) of oligosaccharides was detected by high performance thin layer chromatography (HPTLC) and polyacrylamide gel electrophoresis (PAGE). Considering the results of HPTLC and PAGE, the optimum condition of microwave assisted acid hydrolysis was determined. The concentration of κ-carrageenan was 5 mgmL-1; the reaction solution was adjusted to pH 3 with diluted hydrochloric acid; the solution was hydrolyzed under microwave irradiation at 100 ℃ for 15 min. Oligosaccharides were separated by a Superdex 30 column (2.6 cm × 90 em) using AKTA Purifier UPC100 and detected with an online refractive index detector. Each fraction was characterized by electrospray ioni- zation mass spectrometry (ESI-MS). The data showed that odd-numbered κ-carra-oligosaccharides with DP ranging from 3 to 21 could be obtained with this method, and the structures of the oligosaccharides were consistent with those obtained by traditional mild acid hydrolysis. The new method was more convenient, efficient and environment-friendly than traditional mild acid hydrolysis. Our results provided a useful reference for the preparation of oligosaceharides from other polysaccharides. 展开更多
关键词 Κ-CARRAGEENAN OLIGOSACCHARIDES microwave degradation acid hydrolysis
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Scalable synthesis of ultra‐small Ru_(2)P@Ru/CNT for efficient seawater splitting 被引量:1
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作者 Dan Zhang Hongfu Miao +7 位作者 Xueke Wu Zuochao Wang Huan Zhao Yue Shi Xilei Chen Zhenyu Xiao Jianping Lai Lei Wang 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第4期1148-1155,共8页
In this study,an ultra‐fast and simple solvent‐free microwave method was successfully demonstrated using a series of ultra‐small(~2.5 nm)surfactant‐free Ru_(2)P@Ru/CNT heterostructures for the first time.The struc... In this study,an ultra‐fast and simple solvent‐free microwave method was successfully demonstrated using a series of ultra‐small(~2.5 nm)surfactant‐free Ru_(2)P@Ru/CNT heterostructures for the first time.The structure has a high‐density Ru component and Ru_(2)P component interface,which accelerates the hydrogen evolution reaction(HER).The prepared Ru_(2)P@Ru/CNT demonstrated excellent catalytic effects for the HER in alkaline media and real seawater.The experimental results indicate that ratio‐optimized Ru_(2)P@Ru/CNT(Ru_(2)P:Ru=66:34)requires only 23 and 29 mV to reach 10 mA cm^(-2)in 1.0 mol/L KOH and real seawater,respectively.These values are 10 and 24 mV lower than those of commercial Pt/C in 1.0 mol/L KOH(33 mV)and real seawater(53 mV),respectively,making it among the best non‐Pt HER reported in the literature.Additionally,the TOF of Ru_(2)P@Ru/CNT in alkaline freshwater and seawater were 13.1 and 8.5 s^(-1),respectively.These exceed the corresponding values for Pt/C,indicating that the catalyst has excellent intrinsic activity.The high current activity of Ru_(2)P@Ru/CNT in 1.0 mol/L KOH was explored,and only 77 and 104 mV were required to reach 500 and 1000 mA cm^(-2),respectively.After 100 h of durability testing,the catalyst retained excellent catalytic and structural stability in low current density,high current density,and seawater. 展开更多
关键词 Ultra‐small nanoparticles PHOSPHIDE Multi‐interface Solvent‐free microwave method Seawater SPLITTING
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