Calvo L, Gilarranz M A, Casas J A, Mohedano A F, Rodríguez J J
Sección de Ingeniería Química, Facultad de Ciencias, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.
J Hazard Mater. 2009 Jan 30;161(2-3):842-7. doi: 10.1016/j.jhazmat.2008.04.029. Epub 2008 Apr 16.
This work reports on the feasibility of hydrodechlorination as a treatment technique for chlorophenols-bearing wastewaters using formic acid as a hydrogen source. 4-Chlorophenol (4-CPhOH) has been used as target compound and the experiments were carried out in batch and continuous mode with a commercial activated carbon-supported Pd (0.5 wt.%) catalyst. The variables studied in the batch runs were HCOOH/4-CPhOH molar ratio (10-1000), temperature (25-75 degrees C) and catalyst concentration (250-1000 mg/L). The continuous experiments were performed in a fixed bed reactor where aqueous solutions of formic acid and 4-CPhOH with molar ratios between 50 and 100 were continuously fed to the reactor, at different space-time values in the range of 10.7-42.8 kg(cat)h/mol. Reaction temperatures from 35 to 100 degrees C were tested and the pressure was fixed at 2.5bar. Conversion values above 99% for 4-CPhOH were obtained in batch experiments, but using a HCOOH/4-CPhOH molar ratio as high as 500. Moreover, most of the phenol produced was adsorbed on the catalyst. Continuous runs were performed to evaluate the efficiency of the catalyst under lower HCOOH/4-CPhOH ratios and to explore the possibility of converting phenol to more hydrogenated products. The results indicated that the HCOOH/4-CPhOH molar ratios needed were an order of magnitude lower than those required in batch runs to achieve conversions of 4-CPhOH close to 95%. Besides, phenol was not the only reaction product formed, since a more hydrogenated product such as cyclohexanone was detected in the effluent, which indicates additional hydrogenation of phenol in contrast to the behaviour observed in batch experiments. A loss of activity was observed in the continuous runs after 20-30 h on stream.
本研究报告了以甲酸为氢源,采用加氢脱氯法处理含氯酚废水的可行性。以4-氯酚(4-CPhOH)为目标化合物,使用商业活性炭负载的钯(0.5 wt.%)催化剂进行了间歇式和连续式实验。在间歇实验中研究的变量包括甲酸/4-氯酚摩尔比(10-1000)、温度(25-75℃)和催化剂浓度(250-1000 mg/L)。连续实验在固定床反应器中进行,将甲酸和4-氯酚摩尔比为50至100的水溶液以10.7-42.8 kg(cat)h/mol范围内的不同时空值连续进料到反应器中。测试了35至100℃的反应温度,压力固定在2.5 bar。在间歇实验中,当甲酸/4-氯酚摩尔比高达500时,4-氯酚的转化率超过99%。此外,生成的大部分苯酚被吸附在催化剂上。进行连续实验以评估在较低甲酸/4-氯酚比下催化剂的效率,并探索将苯酚转化为更多氢化产物的可能性。结果表明,要使4-氯酚转化率接近95%,连续实验所需的甲酸/4-氯酚摩尔比比间歇实验低一个数量级。此外,苯酚不是唯一形成的反应产物,因为在流出物中检测到了一种更氢化的产物如环己酮,这表明与间歇实验中观察到的行为相比,苯酚发生了额外的氢化反应。在连续运行20-30小时后,观察到催化剂活性下降。