Hydrogen donor and acceptor abilities of pitch: 1H n.m.r. study of hydrogen transfer to anthracene

Petroleum pitches, coal-extract solutions and hydrogenated coal-extract solutions are co-carbonized with anthracene at 673 K. Chloroform-soluble fractions of the system are monitored by ¹H n.m.r. for formation of 9.10 dihydroanthracene (DHA). A hydrogenated coal-extract solution is also co-carbonized at 673 K with anthracene together with thianthrene and sulphur. Ashland A240 petroleum pitch and anthracene are co-carbonized with hydrogenated anthracene oil and resultant ¹H n.m.r. spectra are analysed for DHA. The pitches and coal-extract solutions are carbonized to 823 K and the optical textures of resultant cokes are assessed by optical microscopy. The purpose of the study is to assess if pitches which form cokes with larger optical textures or have greater abilities to modify the carbonization behaviour of coals also have the ability to act as ‘hydrogen shuttles’ in the carbonization system. Results would indicate that such pitches produce the largest amounts of DHA. It is proposed that the most efficient of the modifying pitches operate by extending the zone of temperature of maximum fluidity and by increasing the value of maximum fluidity by removal by proton transfer of radicals which if left in the carbonizing system would interact to form cokes of smaller optical texture.     

Co-carbonization of solvent fractions of hydrogenated and alkylated SRC pitches in studies of formation of needle-cokes

The optical texture of cokes from two SRC pitches of different coking properties, from co-carbonizations of these materials and of hydrogenated and alkylated products has been studied. The objective, relative to formation of needle-cokes, is to correlate the optical texture of cokes with the chemical structure of the pitch materials using both benzene-soluble (BS) and insoluble (BI) fractions of the pitches. Hydrogenation improved the compatibility of the BS fraction of the inferior SRC pitch (No. 2) with the BI fractions of the two pitches (non-hydrogenated) using a ratio of only 1 to 9. Before hydrogenation, a ratio of BS to BI of 8 to 2 did not give a needle-coke. In contrast, alkylation destroyed the compatibility of the BS fraction of the superior SRC pitch (No. 1) with the BI fraction (non-alkylated) using a ratio of 6 to 4, and which gave a needle-coke before alkylation. Hydrogenation of the alkylated material restored the compatability. The relevance of these studies to industrial carbonization processes is discussed in terms of chemical treatment and the hydrogen economy.     

Carbonization of hydrogenated ethylene tar pitch; study of the pitch molecular compactness factor and coke optical texture

Compactness factors of aromatic molecules in hydrogenated ethylene tar pitch were calculated as a parameter to relate to properties of mesophase of the carbonization system. Compactness factors, φ, derived from structural analyses of hydrogenated ethylene tar pitch were also related to the size and shape of optical textures of resultant cokes. Hydrogenated ethylene tar pitches having values of φ 〉 0.5 gave cokes with flow type anisotropy and relate to formation of peri-condensed structures. The spin-lattice relaxation times, T₁, for the cokes derived from hydrogenated ethylene tar pitch, are related to their optical texture.     

Carbonization and liquid-crystal (mesophase) development. 11. The co-carbonization of low-rank coals with modified petroleum pitches

Coals of rank ranging from medium quality coking to non-caking, non-fusible, have been co-carbonized with Ashland petroleum pitches A170, A240 and A200 as well as pitches modified by heat-treatment with aluminium chloride using A170, and by reductive hydrogenation of the A200. The mixing ratio was 7:3, the final HTT was 873 K, heating at 10 K min^?1 with a soak time of 1 h. The optical texture of the resultant cokes is assessed using polished surfaces and a polarized-light microscope using reflected light and a half-wave plate. The changes in optical texture are studied from the point of view of using coals of low rank in the making of metallurgical coke. The optical texture of resultant cokes is modified by co-carbonization and the mechanism involves a solution or solvolysis of the non-fusible coals followed by the formation of nematic liquid crystals and mesophase in the resultant plastic phase. The modified A170 pitch is more effective in modifying optical texture than the A170 because of an increase in molecular weight. The hydrogenated A200 is a very reactive additive probably because of an increased concentration of naphthenic hydrogen. The hydrogenated A200 can modify the optical texture of cokes from the organic inerts of coals and from oxidized, non-fusible coals.     

Carbonization and liquid-crystal (mesophase) development. 22. Micro-strength and optical textures of cokes from coal-pitch co-carbonizations

This study examines the micro-strength and optical textures of a laboratory coke from a base-blend of Freyming and Pocahontas coal (wt ratio, 1:1) and of cokes from the co-carbonization of the blend, with each of five petroleum pitches in various proportions. Coke pieces, 212–600 μm, from the micro-strength test are assessed in terms of origin and propagation of cracks induced by the test. Always, the addition of pitch to the base-blend improves the strength of the resultant cokes, the pitches behaving differently. A qualitative, subjective appraisal of results indicates that increases in coke strength are associated with relative abilities of pitches to interact with the coals to produce a fluid phase, of solution of coal in pitch, which gives an ‘intermediate’ coke with an optical texture of mozaics. This intermediate coke strengthens the bonding at interfaces. Cracks originate predominantly from the shrinkage cracks in the domains of Pocahontas coke. Mozaic structures tend to resist crack propagation. The coal/pitch system may flow around coal particles so containing incipient crack formation in resultant coke particles.     

Composition of pore-wall material in metal-lurgical coke: Considerations of strength,gasification and thermal stress

The optical texture of metallurgical cokes consists of anisotropic carbon made up of mozaics, 0.5–10 μm in size of flow-type anisotropy, 10–60 μm in size, as well as inert and isotropic material. Cokes from different coal sources possess optical textures which are different, being composed of different extents of the above components. The study examines the optical texture of polished surfaces of cokes and relates changes in surface topography caused by gasification by carbon dioxide at 1173 K, by heat treatment to 2073 k and by etching with atomic oxygen at 293 k to the optical texture. The results support a model to explain the strength of coke and its resistance to breakage caused by gasification, mechanical and thermal stresses, in terms of the size, orientation and bonding of the varied components which constitute the composite structure of coke material.     

Carbonization and liquid-crystal (mesophase) development. 7. Optical textures of cokes from acenaphthylene and decacyclene

Optical textures of cokes prepared by carbonizing acenaphthylene, decacyclene and mixtures thereof at selected values of heat-treatment temperatures and soak time have been compared. Optical textures are assessed using polished surfaces and reflected-polarized-light microscopy in conjunction with a half-wave plate. The acenaphthylene is chemically more reactive than the decacyclene which is itself formed during the carbonization of acenaphthylene. Products of carbonization of acenaphthylene can influence rates of carbonization of the decacyclene. Similar optical textures in cokes cannot be formed by compensating low heat-treatment temperatures with long soak periods. In addition to chemical rate-controlling processes, the physical properties of the system must be acknowledged, in particular the viscosity. Very large non-coalesced growth units of mesophase (800 μm diameter) have been observed. Pre-alignment of growth units of mesophase may occur prior to coalescence.     

Carbonization and liquid-crystal (mesophase) development. 10. The co-carbonization of coals with solvent-refined coals and coal extracts

Coals (NCB rank 102 to 902) were co-carbonized with solvent-refined coals and coal extracts, mixing ratio of 7:3, to 873 K, heating at 10 K min^?1 with a soak period of 1 h. Resultant cokes were examined in polished section using reflected polarized-light microscopy and optical textures were recorded photographically. These optical textures were compared to assess the ability of the additive pitch to modify both the size and extent of optical texture of resultant cokes. The objective of the study is to provide a fundamental understanding of the use of pitch materials in co-carbonizations of lower-rank coals to make metallurgical coke. A Gulf SRC was able to modify the optical texture of cokes from all coals except the anthracite. Soluble fractions of this Gulf SRC were less effective than the parent SRC. A coal extract (NCB D112) modified coke optical texture, the extent being enhanced as the rank of coal being extracted was increased. Hydrogenation of the coal extract increased the penetration of the pitch into the coal particles but simultaneously reduced the size of the optical texture relative to the non-hydrogenated pitch. This indicates a positive interaction of pitch with coal in the co-carbonization process. The optical texture of the cokes from the hydrogenated coal extract in single carbonizations was larger than that from the non-hydrogenated material. Mechanisms explaining these effects are briefly described.     

Carbonization of an anthracene oil extract of Akabira (Japan) coal

The carbonization of a non-hydrogenated extract (STC) from a low-rank coal (C, 83 wt%) of high fluidity was studied as single carbonizations and as co-carbonizations with additives, an objective being the production of needle-coke. The coke from STC had an optical texture of fine-grained mozaics; however, fractionation followed by co-carbonizations were effective in modifying carbonization properties. The lighter fraction of STC could give a coke with flow texture but in reduced yield. The addition of hydrogenated Ashland A240 pitch (HA240) in a quantity as low as 20% could effectively modify the carbonization properties of STC. A novel co-carbonization, in which an additive such as dihydroanthracene is recovered at the latter stage of the carbonization in the dehydrogenated form, was found to be effective also, although a relatively large amount of the additive was required. Among the non-hydrogenated additives, Ashland A240 pitch was the most effective in modifying the STC. The cocarbonization of fractionated STC reduced the quantity of additive required while maintaining a reasonable coke yield. Some practical aspects for the production of needle-coke from STC are discussed.     

Gasification studies of cokes from coals. The effects of carbonization pressure on optical texture and porosity

Ten coals were carbonized under various pressures (4 kPa, normal pressure and 10 MPa). Optical textures and physical structures of resultant cokes were monitored. The extent of optical anisotropy increased greatly with increasing carbonization pressure, such a trend being more pronounced with the lower-rank coals. Physical structure was also influenced by carbonization pressure. Gasification reactivities of the cokes with carbon dioxide and steam (1200 °C) were studied with respect to their optical anisotropy and physical structure. Gasification reactivities of optical textures were estimated using both the point-counting technique and regression analysis. The reactivities of cokes with the same optical texture produced from the same parent coal were similar. However, there were considerable differences when compared with cokes from different parent coals. Although the values estimated by regression analyses are consistent with those obtained by point-counting, except for the leaflet and inert textures, the physical locations of respective textures can be important in quantitative discussions of their reactivities.     

Carbonization and liquid—crystal (mesophase) development. 19. Co-carbonization of oxidized coals with model organic compounds

This study examines further the phenomena of the modification of coal carbonizations by organic additives. Anthracene, pyrene and chrysene modify the carbonization in a closed system of coking coals as observed from increases in the size of optical textures of resultant cokes. Weakly caking coals are unaffected. Chrysene is the most efficient modifier probably because of its lowest calculated free valence. The co-additives tetralin and hydrogenated anthracene oil further enhance the modification processes so obviating the necessity to use hydrogenated additives. Co-carbonizations of oxidized coking and caking coals with decacyclene are effective in removing the effects of mild oxidation. Increased rates of carbonization enhance the sizes of optical textures of resultant cokes.     

Graphitization behavior of hydrogenated ethylene tar pitch

The graphitization behavior of cokes prepared from ethylene tar pitch (ETP) hydrogenated at temperatures from 473 to 673 K has been studied by magnetoresistance measurements at liquid nitrogen temperature and by scanning electron microscopy. Graphitization heat treatment of the cokes was carried out at 3273 K. Hydrogenation temperatures of 473 and 523 K resulted in graphitized cokes with random layer plane textures and low degrees of graphitization. Hydrogenation at higher temperatures was effective in promoting development of flow-type textures during graphitization. The coke from ETP hydrogenated at 673 K showed the highest graphitizability, preferred orientation and flow-type texture developed by heat treatment.     

Carbonization of coal blends: mesophase formation and coke properties

Laboratory investigations of strength of cokes from blends of coals incorporating pitch were supported by 7 kg trials. The stronger cokes showed a greater interaction between coal and pitch to produce an interface component of anisotropic mozaics which is relatively resistant to crack propagation. The process whereby coal is transformed into coke includes the formation of a fluid zone in which develop nematic liquid crystals and anisotropic carbon which is an essential component of metallurgical coke. Strength, thermal and oxidation resistance of coke can be discussed in terms of the size and shape of the anisotropic carbon which constitutes the optical texture of pore-wall material of coke. Coals of different rank form cokes with different optical textures. Blending procedures of non-caking, caking and coking coals involve the interactions of components of the blend to form mesophase and optical texture. Petroleum pitches used as additives are effective in modifying the carbonization process because of an ability to participate in hydrogen transfer reactions.     

Carbonization and liquid crystal (mesophase) development. 14. Co-carbonization of coals with A240 Ashland petroleum pitch: effects of conditions of carbonization upon optical textures of resultant cokes

This study examines the effect of pitch concentration, rate of heating, soak temperature and time of soak upon the optical texture of cokes prepared from the co-carbonizations of a coal (Oxcroft-Clowne, NCB Rank 802) and three vitrains of NCB Rank 204, 801, 902 with Ashland A240 petroleum pitch. Using the coal (Rank 802) with 10 wt % and 25 wt % additions of pitch caused progressive penetration of the pitch into the coal with a resultant development of a mozaic anisotropy in the coke to replace partially the original coke isotropy. With 50 wt % addition of pitch almost all of the coal particles, 600 to 1100 μm in size, were modified during carbonization. Some pitch coke was formed. For the coal and three vitrains with increasing rates of co-carbonization from 0.5–10 K min^?1 to 1200 K, using 25 wt % of A240 pitch, resultant cokes showed progressively increased extents of modification. For the two vitrains (Rank 801, 902) soaking at temperatures of 650–690 K caused a decrease in the extent of modification of isotropic coke when compared with the coke of HTT 1200 K. Evidently fast heating rates create the conditions of fluidity necessary for the pitch to modify the coal leading to growth of mesophase and anisotropic coke.     

Carbonization and liquid-crystal (mesophase) development. 16. Carbonizations of soluble and insoluble fractions of coal-extract solution

A coal-extract solution prepared by extraction of a coking coal (CRC 301a) with anthracene oil by the National Coal Board is separated into fractions using solvents of increasing solvent power. These fractions are carbonized to 823 K and the optical textures of resultant cokes are assessed. The objective of the study is to examine the role of the molecular components of the coal-extract solution including the residual anthracene oil in mechanisms of formation of the optical texture of the anisotropic coke. Generally, the low-molecular-weight fractions of the coal-extract solution produce cokes with larger sized optical textures than the coke from the parent coal-extract solution. The higher-molecular-weight fractions produce cokes with smaller sized optical textures. Isotropic coke is produced from material which is not soluble in benzene and tetrahydrofuran. Within this parent-coal-extract solution it would appear that the dominant partner effect is influential over the size of the optical texture of coke from the coal-extraction solution, that is the minor component of smaller molecules controls the necessary growth of liquid crystals. Also, the presence of anthracene oil augments the size of optical texture of resultant cokes by providing the necessary physical fluidity of the system and possibly some chemical stability.     

Carbonization and liquid-crystal (mesophase) development. 21. Replacement of low-volatile caking coal by petroleum pitch in coal blends for metallurgical coke

Cokes were prepared in a 7 kg oven from blends of high-volatile and low-volatile caking coals, using ratios of 1:1 and 3:7. To the 1:1 blend was added 7.5% of either Ashland A240 or A170 petroleum pitch or SFBP petroleum pitch 1. Micum m₃₀ and m₁₀ indices were determined on cokes from the 7 kg oven, using the $\text{1}\text{5}$ Micum drum. Optical textures were assessed using polarized light microscopy of polished surfaces of cokes. The effect of additive is to increase the strength of cokes. The pitch can be an effective replacement of low-volatile caking coal. The analysis by optical microscopy shows that with the stronger cokes from the 7 kg oven there has occurred an interaction between the coal and pitch at the interface of coal particles to produce a solution or fluid phase which carbonizes to a coke with an optical texture of fine-grained mozaics. This material could be responsible for the enhancement of coke strength, being associated with pore wall material rather than with a change in porosity. The results agree with previous work using cokes prepared in the laboratory on a small scale.     

Influence of primary QI and particulate matter on pitch carbonizations

The carbonization behaviour of coal-tar and petroleum pitches is influenced by the presence of particulate matter in the pitch. Several types of particulate matter consisting of carbon blacks of different oxygen contents and degrees of agglomeration and silica with hydrophobic and hydrophilic surfaces were added to pitches. Particle sizes were less than 100 nm in diameter. The influence on optical texture of coke structure was most pronounced for the agglomerated carbon blacks which trapped pitch in inter-particle voids creating an isotropic carbon at low wt % additions. The non-agglomerated hydrophobic silica progressively reduced the size of anisotropy with additions. The hydrophilic silica caused intermediate effects. Surface activity of additives influences carbonization chemistry. Reactivities of cokes to carbon dioxide (k/s⁻¹) were not affected by structural changes but coke microstrengths were very dependent upon size of agglomeration of carbon black additives.     

The role of liquid crystals in the formation of graphitizable carbons (cokes)

The formation of cokes and graphites proceeds via the creation from the isotropic fluid phase of carbonization of pitch and coal, of lamellar nematic liquid crystals or mesophase. This anisotropic fluid, deformable mesophase, develops as spheres within which constituent molecules are stacked parallel to an equatiorial plane. This type of structure facilitates coalescence to a coherent mass which eventually forms a graphitisable carbon. The ‘onion-skin’ structure of mesophase spheres cannot so coalesce. Different optical textures of cokes and graphites owe their origin to different chemical reactivities and fluidities of mesophase, the lower the fluidity the smaller the size of the optical texture. Mesophase from lameller molecules is compared with conventional rod-like nematic liquid crystals. Structures in needle-cokes, metallurgical coke, coke from solvent refiend coal and carbon fibre from pitch are discussed in terms of formation and properties of lamellar nematic liquid crystals.     

Pyrolysis of lignites and brown coal catalytically depolymerized with phenol to produce anisotropic coke or light oil

Pyrolysis of lignites and brown coal catalytically depolymerized with phenol was studied in order to design easy liquefaction or up-grading procedures effective under non-extreme conditions, where the recovery of phenol may be critical. The lignites were solubilized in pyridine very easily at low phenol/lignite ratios, but high ratios were required to induce their solubility in benzene—ethanol or THF. Although THF- and pyridine-soluble (abbreviated as THFS and PS, respectively) fractions exhibited fusibility in their single carbonization to produce grain cokes of optical isotropy, optical anisotropy can be developed by co-carbonization with petroleum pitches, suggesting that these fractions may be suitable as needle or blast furnace coke sources. The heat-treatment of PS with a hydrogen donor made it completely soluble in benzene. The recovery rates of bound phenol in the depolymerized lignite were at highest 57 and 36%, respectively, for the coking and heat-treatment processes, although the formation of alkyl phenols may occur in the heat-treatment.     

Characterization of carbonization reaction of petroleum residues by means of high-temperature ESR and transferable hydrogen

An attempt has been made to characterize the carbonization reaction of petroleum residues through measurements of high temperature ESR, hydrogen donor ability and optical texture of resultant cokes. Good correlations were found between hydrogen donor ability and change in spin concentration. Residues forming cokes with large sizes of optical texture have a high ability as a hydrogen donor and show a low spin concentration at high temperatures. Similar results were obtained also for some model compounds. A model for the mechanism of carbonization is proposed on the basis of these observations.