首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 718 毫秒
1.
用于甲烷脱氢芳构化反应Mo基催化剂的研究   总被引:3,自引:1,他引:3  
 通过对分子筛载体HZSM-5进行精密前处理,然后浸渍钼酸铵溶液和添加微量助剂Fe,分别制得催化剂Mo/HZSM-5(t)和Fe-Mo/HZSM-5(t),考察了它们对甲烷脱氢芳构化反应的催化性能.结果表明,在Mo/HZSM-5(t)催化剂上,反应5h后,甲烷的转化率可达11.4%,苯收率高于6.2%,在反应30h后,甲烷的转化率可达8.8%,苯收率高于5.3%,催化剂显示出较高的稳定性.微量助剂Fe的添加在保持催化剂稳定性的前提下进一步改善了催化剂的活性,使甲烷的转化率相对于Mo/HZSM-5(t)上的提高了18%,苯收率提高了52%.XRD和TPO测试表明活性组分Mo和助剂Fe高度分散于载体上或进入载体孔道中,载体的精密前处理及Fe的添加提高了催化剂的抗积炭能力,使得催化剂稳定性显著提高.  相似文献   

2.
以硫酸铝渣为原料,研制出了一系列不同A1/Fe/Si物质的量比的聚硅酸铝铁絮凝剂(简称PAFsc)。考察了PAFSC的混凝、除浊、脱色等性能,并研究了A1/Fe/Si物质的量比、pH、投药量等因素对PAFSC性能的影响。处理模拟浊水时,当n(A1)/n(Fe)=2.0~4.0,n(M)/n(SiO2)=0.7~1.3时...  相似文献   

3.
 在固定床积分反应器中,对Fe-Mn催化剂上F-T合成反应的初期反应性能进行了一系列条件实验,考察了在不同温度、压力、原料气H2/CO比和空速下催化剂的催化性能.结果表明,该催化剂运行200h后,仍显示出较高的催化活性和稳定性,对低碳烯烃和C5+烃具有较高的选择性,且C5+烃的时空收率较高.在n(H2)/n(CO)=1,GHSV=6000h-1,p=2.02MPa和θ=300℃的条件下,CO转化率可达74.1%,总有效烃(C=2~4+C5+)的选择性可达88.6%,甲烷选择性为6.7%,C5+烃的时空收率为0.54g/(ml·h).  相似文献   

4.
对重青石窑具原料中的CaO,TiO2,Fe2O3以及R2O(Na2O+K2O)对窑具多晶结构与性能的影响进行研究,从而确定原料中的Cao,TiO2,Fe2O3和R2O允许的存在量为CaO(2.2~2.7)%,TiO2(1.0~1.5)%,Fe2O3(0.8)%和R2O≤0.9%。  相似文献   

5.
烟草中Fe,Co一阶导数分光光度法同时测定的研究   总被引:4,自引:0,他引:4  
本文研究了在pH4.0时,meso-四(4-磺酸基苯基)卟啉与铁、钴同时络合显色的反应条件以及一阶导数光谱行为。此体系一阶导数的灵敏度比零阶导数灵敏度高。Fe ̄(3+)~0.18μg/mL、Co ̄(2+)0~0.24μg/ml,范围内符合比耳定律;检测限为:Fe ̄(3+)=0.48ng/mL,Co ̄(2+)=0.2ng/mL。回收率为:Fe98.5%~100.8%,Co99.2%~101.3%。此方法用于烟草中痕量Fe、Co测定,与AAS值相比较,结果令人满意。  相似文献   

6.
利用熔体快淬技术制备了(Nd11.4Fe82.9B5.7)0.99M1(其中M=Zr,Nb,Ga,Zr+Ga,Nb+Ga)快淬带。发现Ga元素的添加对Nd2Fe14B相晶粒的C轴垂直于带面取向是有利的。复合添加Zr+Ga或Nb+Ga可获得较好的磁性能,并且进一步提高了快淬带晶粒的择优取向。取向度随厚度改变发生明显的变化,当带厚约为120μm时取向度最高。热处理可使淬带织构度增加,但导致晶粒粗化。利用深冷技术对纳米晶复合快淬带进行超低温处理。发现深冷处理有利于快淬带织构度的增强,且晶粒尺寸几乎不变。  相似文献   

7.
La0.6Sr0.4Co1-yFeyO3(y=0.2,0.8)复合氧化物混合导电性能研究   总被引:2,自引:0,他引:2  
采用甘氨酸-硝酸盐(GNP)法制备了La0.6Sr0.4Co1-yFeyO3(y=0.2,0.8)g合氧化物,研究了材料的结构、电子-离子混合导电性能及其相关性。结果表明,La0.6Sr0.4Co1-yFeyO3(y=0.2,0.8)合成粉料的颗粒细小均匀(~100nm),陶瓷形成菱形六面体钙钛矿结构。与La0.6Sr0.4Co0.2Fe0.8O3(y=0.8)陶瓷相比,La0.6Sr0.4Co0.8Fe0.2O3(y=0.2)陶瓷的晶粒尺寸大、致密度较高。在La0.6Sr0.4Co0.8Fe0.2O3(y=0.2)陶瓷中观察到Co^3+离子歧化对电子导电性能的影响。与La0.6Sr0.4Co0.2Fe0.8O3(y=0.8)陶瓷相比,La0.6Sr0.4Co0.8Fe0.2O3(y=0.2)陶瓷具有更优异的电子-离子混合导电性能,材料在混合导电性能上的差异与其电子结构和显微结构紧密相关。  相似文献   

8.
不经分离,高敏,连续光度滴定混合物中钕和铁   总被引:3,自引:0,他引:3  
提出以Fe(3+)(Nd(3+)-CAS-CPB-C2H5OH作为不经分离、高敏、连续光度配合滴定混合物中Fe(3+)和Nd(3+)的多元胶束配合指示体系。滴定Fe(3+)和Nd(3+)的适宜pH分别为2.3~3.2和6.0~8.6。用EDTA目视滴定Fe(3+)时,终点处由蓝紫变粉红色,对比度大(Δλ=130nm)、灵敏度高(配合物摩尔吸光系数ε(630)=1.14×105L·cm(-1)·mol(-1),至少可检测0.4μg/mL,滴定线性范围为0~2.8μg/mL。线性相关系数为0.9994;目视滴定Nd(3+)时,终点处由绿色变橙黄,Δλ>180nm,ε(630)=7.6×104,至少可检测1μg/mL,滴定线性范围0~3.7μg/mL,线性相关系数0.9994。对于铁钕硼混合物样品则不经分离在630nm处连续光度滴定,可更精密、高敏、准确地确定终点,变异系数1.76%~2.86%,标准加入回收率96%~104%,且简便、快速。  相似文献   

9.
 采用CO加氢反应、程序升温还原(TPR)、CO吸附和CO脱附等技术,研究了Fe助剂对Rh-Mn-Li/SiO2催化剂上CO加氢合成二碳含氧化物反应的影响.结果表明,Mn,Li和Fe的加入明显提高了Rh催化剂的活性及选择性,特别是在1%Rh-1%Mn-0.075%Li/SiO2催化剂中加入0.05%Fe后,C2+含氧化物的时空收率由331.6g/(kg·h)提高到457.5g/(kg·h).但当Fe的加入量继续增加时,催化剂的活性及选择性下降,甲醇的选择性上升.TPR实验表明,当加入少量Fe(0.05%~0.5%)时,TPR的峰面积随Fe加入量的增大而增大,Fe的加入使Rh的还原温度向高温移动,Mn的还原温度向低温移动,Fe的还原峰与Rh和Mn的还原峰相重叠,由此推断这些Fe与Rh是处于紧密接触状态的.当Fe含量增加到1%时,样品在522K出现一个新的谱峰,该峰可归属为与Rh非紧密接触的Fe的还原峰.CO的吸附实验表明,当Fe的加入量超过一定值后,CO吸附量下降.CO的脱附实验表明,在Rh基催化剂中加入少量Fe后,强吸附的CO增多,但当Fe的加入量超过一定值时,强吸附的CO量下降.  相似文献   

10.
液相沉积法制备光催化活性掺铁TiO2薄膜   总被引:14,自引:0,他引:14  
周磊  刘昌  赵文宽  胡翎  方佑龄 《催化学报》2003,24(5):359-363
 通过在氟钛酸铵-氟铁酸混合溶液中加入硼酸溶液,应用液相沉积法制备了具有高光催化活性的掺铁TiO2薄膜.用ICP-AES测定了掺铁TiO2薄膜中Fe3+的浓度,用XRD,AFM,UV-Vis和阶梯仪等对TiO2薄膜的沉积条件、结构、膜厚和性能进行了表征,并以亚甲蓝降解反应评价了掺铁TiO2薄膜的光催化活性.结果表明,在硼酸/六氟钛酸铵摩尔比为2~4时,掺铁TiO2薄膜中含有锐钛矿相TiO2.当掺Fe3+浓度为0.05%,热处理温度为300℃时,掺铁TiO2薄膜具有最高的光催化活性,其光催化活性是未经热处理时的3.9倍,是经300℃热处理但未掺铁TiO2薄膜的1.4倍.  相似文献   

11.
The spectral-polarization characteristics of absorption and phosphorescence of molecules of the initial form of nitro-substituted indolinospirobenzothiopyran were studied in oriented polyethylene films and in solutions with different polarity. An oscillator model of the electron transitions responsible for the formation of absorption and luminescence spectra was suggested. It was established that the principal differences in the spectral and photophysical properties of the compound studied and its oxygen-containing analog are associated with the fact that the electronegativity of the S atom is lower than that of the O atom. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1143–1146, June, 1997.  相似文献   

12.
非那雄胺能抑制5α-还原酶的活性,明显降低二氢睾酮水平,是一种治疗良性前列腺增生的有效药品。该合成工艺以甾烯酮酸为原料,将其与氯化亚砜反应,无须分离即与叔丁胺反应得17β-酰胺化合物,再氧化开环,环合,氢化,脱氢合成了非那雄胺。经元素分析、IR、1HNMR、13CNMR、MS分析表征了其结构。该法无须使用昂贵的2,2-二吡啶二硫化物和剧毒药品苯亚硒酸酐,且以乙酸铵代替氨气,降低了对设备的要求和腐蚀,更适用于工业生产。  相似文献   

13.

The heats of detonation of 20 simple high explosives and explosive mixtures were determined by means of an adiabatic detonation calorimeter designed by the authors. The results indicated that the performance of the instrument was reliable and the experimental data were very accurate. For explosive mixtures, there was a linear accumulative relationship between the heats of detonation of the explosive mixture and its components. Accordingly, the heats of detonation of explosive mixtures could be calculated directly from the heats of detonation of simple explosives and the characteristic heats of other components. The experiments showed that the gold or brass shell of the cylindrical charge could be substituted by a thick-walled porcelain shell, which had the advantage of cheapness.

  相似文献   

14.
Two vanilloids, (5E)-8-(4-hydroxy-3-methoxyphenyl)oct-5-en-4-one (1) and 4-[3-hydroxydecyl]-2-methoxyphenol (2), isolated from the dried seeds of Grains of Paradise (Aframomum melegueta), were synthesized; the latter compound was made as the S-enantiomer and the material derived from the seeds was found to be a 1:1.7 mixture of the R and S isomers. The synthetic route used should allow the preparation of analogs having extended alkyl chains and consequently different lipophilicity, and 3, a homolog of 2, was also prepared.  相似文献   

15.
In this review, the research of the author in the field of colloidal systems is summarized. The factors influencing colloidal stability are systematized and analyzed. Examples are presented to illustrate the practical utilization of the theory of stability of colloids and thin films.This review was prepared on the basis of the works of the author, which were awarded the State Premium for 1991 in the field of science and technology, chemistry section.Institute of Physical Chemistry, Russian Academy of Sciences, 117915 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 8, pp. 1708–1717, August, 1992.  相似文献   

16.
Main hydration products of two cement pastes, i.e. CSH-gel, portlandite (P) (and specific surface S) were studied by static heating, and by SEM, TEM and XRD, as a function of cement strength (C-33 and C-43) hydration time (th) and subsequent hydration in water vapour.Total change in mass on hydration and air drying, Mo, increased with strength of cement paste and with hydration time. Content of water escaping at 110 to 220°C, defined as water bound with low energy, mainly interlayer and hydrate water, was independent on cement strength but its content increased with (th). Content of chemically bound (zeolitic) water in CSH-gel, escaping at 220-400°C, was slightly dependent on strength and increased with (th). It was possibly derived from the dehydroxylation of CSH-gel and AFm phase. Portlandite water, escaping at 400-500°C, was independent on cement strength and was higher on longer hydration. Large P crystals were formed in the weaker cement paste C-33. Smaller crystals were formed in C-43 but they increased with (th). Carbonate formated on contact with air (calcite, vaterite and aragonite), decomposed in cement at 600-700oC. It was high in pastes C-33(1 month) and C-43(1 month), i.e. 5.7 and 3.3%, respectively; it was less than 1% after 6 hydration months (low sensitivity to carbonation) in agreement with the XRD study showing carbonates in the air dry paste (1month), and its absence on prolonged hydration (6 months) and on acetone treatment. Water vapour treatment of (6 months) pastes or wetting-drying increased this sensitivity.Nanosized P-crystals, detected by TEM, could contribute to the cement strength; carbonate was observed on the rims of gel clusters.This revised version was published online in November 2005 with corrections to the Cover Date.  相似文献   

17.
翟宗玺  刘树深  夏树屏 《化学学报》1990,48(10):946-950
用氧化镁氯化镁水溶液制备了8水合氯氧化镁[nMg(OH)2·MgCl2·8H2O], 并测定了其在盐酸中的溶解热, 实验结果表明, 氯氧化镁溶解热与n值呈线性关系, 根据溶解热求出5Mg(OH)2·MgCl2·8H2O和3Mg(OH)2·MgCl2·8H2O的生成热分别为-7727.1和5888.1kJ·mol^1^-。  相似文献   

18.
The enthalpies of solution of several oxosulfides of rare-earth elements and the high-temperature enthalpies of oxosulfides and oxosulfates of lanthanum and yttrium were measured using solution calorimetry and high-temperature microcalorimetry techniques. Standard enthalpies of formation and some thermodynamic properties of oxosulfides and oxosulfates were calculated. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2 pp. 294–297, February, 1997.  相似文献   

19.
20.
设计了铁的锈蚀实验,说明了铁钉的处理方法,增加了温度、酸、碱的影响条件,实现了铁跟蒸馏水及空气中氧气快速反应而生锈,使实验在5 min左右就能够得到准确的结果。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号