Liquefaction, coal short-time reaction products

Short-Time Reaction Products of Coal Liquefaction and Their Relevance to the Structure of Coal... 

Farcasiu, M. "Short Time Reaction Products of Coal Liquefaction and Their Relevance to the Structure of Coal." ACS Div. Fuel Chem. Preprints 24(1) (1979) 121. 

Other Reaction Products. In addition to SRC, gas, light oil, and a filter cake of unreacted coal and inorganic materials are produced in the first step of the short residence time coal liquefaction process. One of the objectives of short residence time coal liquefaction is to minimize the loss of hydrogen to gases and light oil. 

Short-Contact-Time Coal Liquefaction Products and the Initial Structure of Coal. Our own data and those from the literature indicate that no major changes take place in the different elements of coal structure under short-contact-time reaction conditions and at relatively low temperature. It is obvious, however, that fragmentation occurs by... 

Product characterization from liquefaction has not been extensive. Phi 1p and Russell (95) have examined products by Py-GCMS from metal halide catalyzed hydrogenation of a vitrinite, alginite, and inertinite, each from a different source. They were able to correlate Py-GCMS results with reaction temperature. King, et al. (96) examined the short contact time liquefaction of macerals separated by DGC from a single hvB bituminous coal. They found correlations between density and reactivity and composition of the products. 

A corollary of this statement is the following If these polyaromatic or polycyclic saturated structures are present in the carbon skeleton of coal, they should be identified in the short-contact-time liquefaction products. The possibility of some isomerization reactions in the carbon skeleton cannot be excluded totally, but the most important fact is that no dramatic aromatization of hydroaromatic rings or saturation of aromatic rings takes place under these conditions. Many of the chemical functions also are stable under these conditions, especially the O, S, and N heterocyclic aromatic structures. Water formation by phenol dehydroxylation is minimal. In coal liquefaction under our conditions, even at long reaction times (up to 90 min) in the absence of an added catalyst, the -OH bonded to a monoaromatic ring is stable. Under the same conditions, dehydroxylation of polyaromatic phenols does occur (10). 

---