Font Size: a A A

Study On The Synthesis Of Pyridine Bases And Catalysts

Posted on:2004-10-03Degree:MasterType:Thesis
Country:ChinaCandidate:Q ShenFull Text:PDF
GTID:2121360092498187Subject:Industrial Catalysis
Abstract/Summary:PDF Full Text Request
Pyridine bases are widely used as intermediates in the formation of medicine, insecticide, rubber and dyestuff besides as solvents. With the rapid development of chemical industry , the demand for the pyridine bases increases quickly. But the way of refining from the coal tar hasn't satisfied the market needs, therefore replaced by the synthesis means. Several producing devices are imported from foreign countries, so it is important to study the pyridine bases' synthesis means, including the catalysts applied in the synthesis means.This way mainly is completed through the condensation of formaldehyde, acetaldehyde and ammonia in the latest producing device. By changing original components and the mol ratio, different products and different distributions can be obtained, the catalyst is ZSM-5 zeolite.The main contents of this task are:(1)choose the H-ZSM-5 zeolite as better catalyst for the pyridine bases' synthesis , carry out the research of technical conditions of synthesis which formaldehyde, acetaldehyde and ammonia are used and better synthesis conditions are selected. Besides these procedures, the addition of propionaldehyde as the third aldehyde for improving of the 3-picoline was studied.(2)carry out the ion-exchange of the H-ZSM-5 zeolite for the synthesis of pyridine bases;(3) research the reaction of pyridine methylation with H-ZSM-5 zeolite and the spinel through co-precipitation .We obtained better reaction condition of pyridine bases with formaldehyde, acetaldehyde and ammonia, i.e. space velocity about 1000h-1, formaldehyde : acetaldehyde =1 : 1, organic compound : ammonia=1 : 4, reaction temperature =450℃-475℃.The addition of the propionaldehyde can improve the yield of 3-picoline rather than effect the total yield of pyridine bases. By using the ion-exchange zeolite Zn-ZSM-5 can improve the total yield of pyridine bases by 10% than ordinary H-ZSM-5 zeolite; The methylation reaction with the spinel and the H-ZSM-5 zeolite indicates that catalysts have some effects on the pyridine's methylation, but the yield is too low (<= 5%) ,so it is necessary to further the study.
Keywords/Search Tags:Synthesis
PDF Full Text Request
Related items
Green chemistry in pyrrole synthesis. I. Solvent effect in Barton-Zard pyrrole synthesis: An improved synthesis of 3,4-dialkyl-1H-pyrrole-2-carboxylates. II. A novel route for the synthesis of pharmaceutically important pyrrole derivatives
Part I: Design, synthesis, and reactivity of 1-hydrazinodienes for use in organic synthesis Part II: Studies toward a synthesis of the antibiotic platensimycin
Manganese(III)-based oxidative cyclizations: Formal synthesis of 15-acetoxypallescensin A. Synthesis of hindered guanidines. Completion of the total synthesis of martinellic acid
Synthesis, Characterization And Luminescence Properties Of Environmental Functional Material β-NaYF4 Doped With Rare Earth
Part I: The total synthesis of (+/-)-securinine and (+/-)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and
New methods and strategies for heterocycle synthesis: Progress toward the total synthesis of upenamide and the total synthesis of (+)-5-epiindolizidine 167B and indolizidine 223AB
Synthesis of side chain-modified iodothyronines. Synthesis and structure-activity relationships (SARS) of galanthamine derivatives. Total synthesis of (+)-valyldetoxinine. Synthesis and mechanism of cyclic acetal and ketal formation in pentono-1,4-lactone
The application of asymmetric catalysis to the synthesis of natural products: A total synthesis of (-)-tubulosine, progress towards a total synthesis of (+)-reserpine, and a total synthesis of (+)-peloruside A
Cyclobutanes in organic synthesis: Lewis acid-promoted ketene-alkene [2+2] cycloadditions, total synthesis of gracilioether F, and collaborative total synthesis of hippolachnin A
10 A ring-closing metathesis/Diels-Alder approach to the synthesis of the eunicellin diterpenes: Application to the total synthesis of ophirin B and partial synthesis of astrogorgin