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排序方式: 共有85条查询结果,搜索用时 62 毫秒
1.
环己酮直接合成环己酮肟——Ⅰ.钛层柱粘土催化环己酮氨肟化反应特征 总被引:3,自引:0,他引:3
钛层柱粘土(Ti-PILC)首次用于液相催化环己酮经氨肟化直接合成环己酮肟,氨肟化反应性能取决于制备Ti-PILC时钛源的选择和催化剂的孔结构。选择合适的反应条件,如反应介质、反应物投料比和催化剂量可进一步提高肟的选择性。 相似文献
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K_5CoW_(12)O_(40)·3H_2O催化合成环己酮1,2—丙二醇缩酮 总被引:1,自引:0,他引:1
研究了杂多化合物K_5CoW_(12)O_(40)·3H_2O作为催化剂对环己酮和1,2-丙二醇缩酮的催化活性。系统考察了酮醇物质的量比、催化剂质量、带水剂体积、反应时间和催化剂重复使用性等因素对产品收率的影响。实验结果表明,杂多化合物K_5CoW_(12)O_(40)·3H_2O是合成环己酮1,2-丙二醇缩酮的良好催化剂,在酮醇物质的量比为1:1.4、催化剂质量为0.5 g、带水剂环己烷体积为9 mL、反应时间为70 min的最佳条件下,环己酮1,2-丙二醇缩酮的收率最高可达94.2%。 相似文献
4.
通过模拟临床使用PVC一次性输液器的输注,对一次性使用输液器中可沥滤物进行了分析。建立了增塑剂邻苯二甲酸二(2-乙基己基)酯(DEHP)的高效液相分析方法,粘合剂环己酮的顶空气相色谱分析方法及金属元素(Cr、Cu、Cd、Sn、Ba、Pb)的电感耦合等离子体质谱分析方法。结果表明DEHP在3.674~104.970μg/mL范围内线性关系良好(r=0.9995),平均回收率为99.1%(n=9,RSD=1.7%);环己酮在0.5100~10.201μg/mL浓度范围内线性关系良好(r=0.9995),平均回收率为101.1%(n=9,RSD=2.4%);六种金属元素在0~100μg/L浓度范围内线性关系良好(r=0.9999),平均回收率在97.8%~110.6%(n=9,RSD≤2.8%)。本文建立的方法准确、灵敏,适用于PVC输液器中DEHP、环己酮和金属元素的溶出进行测定,为标准完善、质量监督及相关风险评价提供了参考依据。 相似文献
5.
This article reports the application of ozone for the selective oxidation of cyclohexane over 13X molecular sieve supported various metal oxides at ambient temperatures. From the SEM, XRD and HR-TEM results, the impregnated metal oxides are highly dispersed on the support. The activity results reveal that Co/MS, Mo/MS, Cu/MS, and Ag/MS catalysts produce cyclohexanone/cyclohexanol as selective oxidation products, whereas Ce/MS, Mn/MS, and V/MS catalysts yield, predominantly, CO and CO2. Among them, Co/MS catalyst exhibits better conversion of 12.2% with selectively of 58% to cyclohexanone/cyclohexanol, which is attributed to the simultaneous activation of ozone and cyclohexane (-C-H bond) at ambient conditions. 相似文献
6.
Phenol hydrogenation is a green route to prepare cyclohexanone, an intermediate for the production of nylon 66 and nylon 6. The development of high-performance catalysts still keeps a great challenge. Herein, the activated carbon (AC) was modified with an acidic material Nb2O5 to adjust the microstructure and surface properties of AC, and the influences of the calcination temperature and Nb2O5 content on the catalytic performance of the Pd/AC-Nb2O5 catalysts for the phenol hydrogenation to cyclohexanone were investigated. The Nb2O5 with proper content can be highly uniformly distributed on the AC surface, enhancing the acidity of the Pd/AC-Nb2O5 catalysts with comparable specific surface area and Pd dispersion, thereby improving the catalytic activity. The hybrid Pd/AC-10Nb2O5-500 catalyst exhibits the synergistic effect between the Pd nanoparticles and AC-10Nb2O5, which enhances the catalytic activity for the hydrogenation of phenol. Furthermore, the as-prepared Pd/AC-10Nb2O5-500 catalyst shows good reusability during 7 reaction cycles. 相似文献
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Zr(SO_4)_2/γ-Al_2O_3固体酸催化合成环己酮1,2-丙二醇缩酮 总被引:1,自引:2,他引:1
通过直接浸渍-焙烧等方法,制备了Zr(SO4)2/γ-Al2O3催化剂,以环己酮和1,2-丙二醇为原料合成了环己酮1,2-丙二醇缩酮。考察了催化剂的焙烧温度、催化剂的质量分数、原料摩尔比、带水剂体积、回流时间对反应的影响。最佳反应条件为:焙烧温度为550℃,Zr(SO4)2的质量分数为20.0%,催化剂的质量分数为5.0%,环己酮与1,2-丙二醇的摩尔比为1∶1.5,甲苯的体积为15 mL,回流时间为3 h。环己酮1,2-丙二醇缩酮的收率可达98.7%,纯度达到99.6%。 相似文献
9.
A new application of rare earth pyrophosphates in vapor phase Beckmann rearrangement of cyclohexanone oxime was investigated.
The rare earth phosphates were characterized by means of XRD, FT-IR, NH3-TPD and water contact angle measurement. It was found that the weak surface acidity and appropriate surface hydrophobicity
should be two key factors in the excellent performance of these catalysts. 相似文献
10.
HIROSHI SATO 《Catalysis Reviews》2013,55(4):395-424
Acidities of pentasil zeolites were measured and correlated with aluminum content using the following methods: (1) Acid-base indicator method, (2) NH3-TPD spectra, (3) GC pulse adsorption of pyridine and 4-methylquinoline, and (4) FTIR spectroscopy of adsorbed pyridine. By controlling the acidity of pentasil zeolites, we have succeeded in obtaining high catalytic performance both in paraselective dealkylation of cymenes and in vapor-phase Beckmann rearrangement of cyclohexanone oxime to ?-caprolactam. In the dealkylation, moderate acidity of Li-ZSM-5 was the key to avoid side reactions while keeping a high conversion of cymenes. In the Beckmann rearrangement, neutrality and crystallinity of the pentasil zeolite were keys to obtain a high lactam selectivity, and a high lactam selectivity of 95% was attained by the surface treatment with chlorotrimethylsilane. The active sites were elucidated to be neutral silanols on the external surface of zeolite. 相似文献