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碳酸化改性对CaO-C4A3S膨胀剂熟料矿物组成及水化历程的影响 被引量:3
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作者 李华 陆安群 +1 位作者 王育江 田倩 《建筑材料学报》 EI CAS CSCD 北大核心 2020年第4期778-781,800,共5页
采用热重-差示扫描量热(TG-DSC)、X射线衍射(XRD)、微量热和测长法等测试方法对经碳酸化改性的氧化钙-硫铝酸钙(CaO-C4A3S)膨胀剂熟料的矿物组成、水化历程及膨胀特性进行分析.结果表明:800℃以下的高温碳酸化改性,使得膨胀剂熟料颗粒... 采用热重-差示扫描量热(TG-DSC)、X射线衍射(XRD)、微量热和测长法等测试方法对经碳酸化改性的氧化钙-硫铝酸钙(CaO-C4A3S)膨胀剂熟料的矿物组成、水化历程及膨胀特性进行分析.结果表明:800℃以下的高温碳酸化改性,使得膨胀剂熟料颗粒表层中的游离氧化钙(f-CaO)转变成碳酸钙,且碳酸化率随着反应温度的升高而增大,对其他矿物组成无影响.改性膨胀剂熟料的水化历程与碳酸化率相关,低碳酸化率可显著降低膨胀剂熟料的放热速率峰值,但不改变累计放热曲线形状;高碳酸化率不仅降低膨胀剂熟料的放热速率峰值,还大幅延缓放热峰值出现时间,并改变累计放热曲线的形状,使早期放热量大幅降低.碳酸化改性对膨胀剂熟料膨胀历程的影响与对水化放热历程的影响趋势基本一致,低碳酸化率条件下,改性主要增加膨胀剂熟料5d前的膨胀量,5d后的膨胀历程与改性前基本一致;高碳酸化率条件下,改性降低膨胀剂熟料3d前的膨胀量,但3~7d间膨胀量迅速增加,7~14d仍有显著膨胀,28d限制膨胀率较改性前提升1.6倍.碳酸化改性显著提高了CaO-C4A3S膨胀剂熟料在水泥基材料硬化阶段的膨胀效能. 展开更多
关键词 钙硫铝酸钙膨胀剂熟料 碳酸化改性 膨胀历程
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碳酸化改性CaO膨胀熟料的膨胀效能及储存稳定性 被引量:1
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作者 田倩 陆安群 张守治 《江苏建材》 2019年第6期11-15,共5页
研究了碳酸化改性对CaO膨胀熟料的水化特性、变温下膨胀性能及储存稳定性能的影响。结果表明,碳酸化改性可使CaO熟料中部分CaO形成CaCO3。碳酸化包裹改性可延缓CaO膨胀熟料的水化反应速率,且随着碳化率的增加,CaO膨胀熟料的水化反应速... 研究了碳酸化改性对CaO膨胀熟料的水化特性、变温下膨胀性能及储存稳定性能的影响。结果表明,碳酸化改性可使CaO熟料中部分CaO形成CaCO3。碳酸化包裹改性可延缓CaO膨胀熟料的水化反应速率,且随着碳化率的增加,CaO膨胀熟料的水化反应速率越缓慢。通过CaO膨胀熟料的碳化率控制,可调控CaO膨胀熟料的水化过程。变温条件下,碳酸化改性显著提升了CaO膨胀熟料在温度下降阶段的补偿效果。碳化率7.4%的CaO膨胀熟料6.5 d的膨胀应力相比未改性CaO熟料提升了约1倍。碳酸化改性明显提升了CaO熟料的储存稳定性能,大幅度提升了CaO熟料的抗风化能力。 展开更多
关键词 CaO膨胀熟料 碳酸化改性 历程 膨胀性能 储存稳定性
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氧化钙膨胀剂熟料碳酸化改性的影响因素
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作者 夏瑞杰 王海 +3 位作者 向飞 王海龙 张珍杰 程福星 《材料导报》 EI CAS CSCD 北大核心 2022年第S02期188-192,共5页
本工作探究了碳酸化温度、碳酸化时间、CO_(2)-H_(2)O气体流量、熟料颗粒粒径等因素对氧化钙膨胀剂熟料碳酸化改性的影响,并通过XRD、TG-DTA、微量热仪对碳酸化改性前后膨胀剂熟料的矿物组成、水化进程进行了分析。结果表明:氧化钙膨胀... 本工作探究了碳酸化温度、碳酸化时间、CO_(2)-H_(2)O气体流量、熟料颗粒粒径等因素对氧化钙膨胀剂熟料碳酸化改性的影响,并通过XRD、TG-DTA、微量热仪对碳酸化改性前后膨胀剂熟料的矿物组成、水化进程进行了分析。结果表明:氧化钙膨胀剂熟料最优碳酸化条件为在700℃碳酸化30 min、CO_(2)-H_(2)O气体流量2 L/min、熟料颗粒粒径0.075~0.2 mm。碳酸化改性后熟料仅有部分游离钙转化为碳酸钙,无其他矿物生成;提高碳酸化率会延缓水化放热峰的出现,降低水化放热速率峰值和总水化放热量,从而延缓膨胀能的释放,提高有效膨胀。 展开更多
关键词 钙膨胀熟料 碳酸化改性 碳酸条件 进程 膨胀能
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Secondary Crystallization of Na_2CO_3-Modified HZSM-5 Zeolites with Tetrapropylammonium Hydroxide and Their Catalytic Performance in Thiophene Alkylation Reaction 被引量:10
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作者 Liu Dongmei Kong Feifei +1 位作者 Zhai Yuchun Wang Haiyan 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2015年第3期53-60,共8页
The Na2CO3-modified HZSM-5 zeolites were further treated by tetrapropylammonium hydroxide(TPAOH) solution. The effect of TPAOH concentration on the secondary crystallization process was investigated. The resulting sam... The Na2CO3-modified HZSM-5 zeolites were further treated by tetrapropylammonium hydroxide(TPAOH) solution. The effect of TPAOH concentration on the secondary crystallization process was investigated. The resulting samples were characterized by a complementary combination of X-ray diffraction, N2 adsorption/desorption, scanning electron microscopy, X-ray fluorescence spectroscopy, XPS, 27 Al and 29 Si magic-angle spinning nuclear magnetic resonance spectroscopy, BET and temperature-programmed desorption techniques. The results showed that the secondary crystallization of the HZSM-5 zeolite could result in migration of non-framework species from the internal channels to the zeolite surface and their transformation into framework species. The catalytic activity of these modified samples for thiophene alkylation was evaluated. Both the activity and stability of the catalysts were improved after secondary crystallization. 展开更多
关键词 tetrapropylammonium hydroxide sodium carbonate HZSM-5 secondary crystallization
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Coking and Deactivation of Catalyst Inhibited by Silanization Modification in Oxidation of Benzene to Phenol with Nitrous Oxide
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作者 翟丕沐 王立秋 +1 位作者 刘长厚 张守臣 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2005年第1期37-42,共6页
The main cause to the deactivation of ZSM-5 catalyst, used for oxidation of benzene to phenol (BTOP) by nitrous oxide, is that the carbon deposition on the catalyst surface blocks the mouth of pores of the catalyst.In... The main cause to the deactivation of ZSM-5 catalyst, used for oxidation of benzene to phenol (BTOP) by nitrous oxide, is that the carbon deposition on the catalyst surface blocks the mouth of pores of the catalyst.In the experiments, ZSM-5 catalyst was modified by chemical surface deposition of silicon, and then the effect of modification condition on the catalyst activation was studied. The catalyst samples were characterized by XRF,EPS, XRD, TEM, N2 adsorption at low temperature, pyridine adsorption-infrared technique and etc. All the above results show that the uniform SiO2 membrane can be formed on ZSM-5 crystal surface. The SiO2 membrane covers the acid centers on ZSM-5 surface to inhibit surface coking, to avoid or decrease the possibility of ZSM-5 pore blockage so that the catalyst activity and stability can be improved efficiently. The optimum siliconiting conditions determined by the experiments are as follows: 4% load of silanizing agent, volume (ml)/mass (g) ratio of hexane/ZSM-5=15/1, and 16 h of modification time. Compared with the samples without siliconiting treatment,the samples treated under the above optimum condition can increase the productivity of phenol by 14% for 3 h reaction time and by 41% for 6 h reaction time respectively. 展开更多
关键词 nitrous oxide PHENOL oxidation of benzene to phenol (BTOP) reaction COKING DEACTIVATION silaniza-tion SiO2 membrane
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