scholarly journals Configuration of Flowsheet and Reagent Dosage for Gilsonite Flotation Towards the Ultra-Low-Ash Concentrate

Author(s):  
Ataallah Bahrami ◽  
Fatemeh Kazemi ◽  
Mirsaleh Mirmohammadi ◽  
Yousef Ghorbani ◽  
Saghar Farajzadeh

Abstract Gilsonite is a natural occurrence of bitumen and consists of a complex structure of organic compounds. Gilsonite has a wide variety of applications in the industry, including the manufacture of electrodes, paints and resins, as well as the production of asphalt and roof-waterproofing material. Ash content of gilsonite is a determining parameter for its application in some industries (e.g., ash content <5% as an additive in drilling fluids, Resins). In this study, a process mineralogy approach used in order to design an optimal flotation circuit for the production of gilsonite concentrate with ultra-low ash content (<5%) from gilsonite ore with an average ash content of 15%. According to mineralogical studies, carbonates and clay minerals are the main associated impurities (more than 90 vol.%). Furthermore, sulfur was observed in two forms of mineral (pyrite and marcasite) and organic in the structure of gilsonite. Most of these impurities are interlocked with gilsonite in size fractions smaller than 105 µm. In addition, the size of +105 µm to 420 µm has a higher pure gilsonite (approximately 90%) than other size fractions. The effect of different reagent regime on the production of low ash content concentration in gilsonite flotation are investigated. Based on the results, 400 g/ton of kerosene collector led to the production of a concentrate with the lowest amount of ash (6.36%) in the rougher stage. In addition, the highest amount of recovery (80.83%) were obtained in gilsonite flotation with kerosene collector. The use of depressants in the rougher stage increased the gilsonite recovery by 3.5% and slightly reduced the ash content (less than 0.20%) of gilsonite concentrate. In general, gilsonite flotation with 400 g/ton kerosene collector, 100 g/ton from a mixture of sodium silicate, tannic acid, sulfuric acid and sodium cyanide depressants, and the use of 100 g/ton MIBC resulted in the production of a concentrate with the lowest amount of ash (6.36%) in the rougher flotation stage. Cleaner and recleaner flotation for the rougher flotation concentrate resulted in a product with an ash content of 4.89% and recovery of 86.75%. Due to the interlocking of gilsonite with impurities in size fractions smaller than 105 µm, it is better to re-grinding the concentrate of rougher stage then flotation done in the cleaner and recleaner stages. Finally, flowsheet has been proposed to produce gilsonite with the least ash.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ataallah Bahrami ◽  
Fatemeh Kazemi ◽  
Mirsaleh Mirmohammadi ◽  
Yousef Ghorbani ◽  
Saghar Farajzadeh

AbstractGilsonite has a wide variety of applications in the industry, including the manufacture of electrodes, paints and resins, as well as the production of asphalt and roof-waterproofing material. Gilsonite ash is a determining parameter for its application in some industries (e.g., gilsonite with ash content < 5% used as an additive in drilling fluids, resins). Due to the shortage of high grade (low ash) gilsonite reserves, the aim of this study is to develop a processing flowsheet for the production of ultra-low-ash gilsonite (< 5%), based on process mineralogy studies and processing tests. For this purpose, mineralogical studies and flotation tests have been performed on a sample of gilsonite with an average ash content of 15%. According to mineralogical studies, carbonates and clay minerals are the main associated impurities (more than 90 vol.%). Furthermore, sulfur was observed in two forms of mineral (pyrite and marcasite) and organic in the structure of gilsonite. Most of these impurities are interlocked with gilsonite in size fractions smaller than 105 µm. The size fraction of + 105 − 420 µm has a higher pure gilsonite (approximately 90%) than other size fractions. By specifying the gangue minerals with gilsonite and the manner and extent of their interlocking with gilsonite, + 75 − 420 µm size fraction selected to perform flotation tests. Flotation tests were performed using different reagents including collector (Gas oil, Kerosene and Pine oil), frother (MIBC) and depressant (sodium silicate, tannic acid, sulfuric acid and sodium cyanide) in different dosages. Based on the results, the use of kerosene collector, MIBC frother and a mixture of sodium silicate, tannic acid, sulfuric acid and sodium cyanide depressant had the most favorable results in gilsonite flotation in the rougher stage. Cleaner and recleaner flotation stages for the rougher flotation concentrate resulted in a product with an ash content of 4.89%. Due to the interlocking of gilsonite with impurities in size fractions − 105 µm, it is better to re-grinding the concentrate of the rougher stage beforehand flotation in the cleaner and recleaner stages. Finally, based on the results of mineralogical studies and processing tests, a processing flowsheet including crushing and initial granulation of gilsonite, flotation in rougher, cleaner and recleaner stages has been proposed to produce gilsonite concentrate with < 5% ash content.


2010 ◽  
Vol 7 (4) ◽  
pp. 1254-1257 ◽  
Author(s):  
K. H. Shivaprasad ◽  
M. M. Nagabhushana ◽  
C. Venkataiah

Ash, an inorganic matter present in coal is amenable for dissolution using suitable reagents. Thus the dissolution of ash and its subsequent removal reduces the release of many toxic elements into the environment by coal based industries. Removal of ash also enhances the calorific value. In the present investigation an attempt has been made to reduce the ash content of raw coal obtained from nearest thermal power by using hydrochloric acid, sulfuric acid and sodium hydroxide. A series of leaching experiments were conducted on coal of different size fractions by varying the parameters like concentration, temperature and time of leaching. The results indicate that it is possible to remove nearly 75% of ash from coal sample by leaching.


2015 ◽  
Vol 1123 ◽  
pp. 177-181
Author(s):  
Achmad Hanafi ◽  
Harry Budiman ◽  
Fauzan Aulia

The biopolymer material, lignin, was recovered from the black liquor by acidification of the black liquor using sulfuric acid. Several purification techniques were carried out to produce the high purity of lignin such as gradual precipitation of lignin from black liquor (first stage: precipitation at pH 7, second stage: precipitation at pH 2) and the diluting of crude lignin by sodium hydroxide then followed by re-precipitation at different temperature. Subsequently, the impurities of lignin product resulted from each purification techniques was determined as ash content that analyzed using temperature program furnace; and the content of lignin was investigated using spectrophotometer UV-Vis. The result showed that the content of lignin of material produced from gradual precipitation was approximately 77.6%. It was higher than the content of lignin about 3.4% of material produced from direct precipitation to pH 2. In addition, the elevating of temperature from 40 to 60°C was no considerably affect to the content of lignin in precipitate produced from re-precipitation of crude lignin solution in sodium hydroxide. Nonetheless, the content of lignin of precipitate improved 15% when the temperature of re-precipitation of crude lignin solution in sodium hydroxide was raised from room temperature to 40-60°C.


2021 ◽  
Vol 21 (17) ◽  
pp. 13333-13351
Author(s):  
Alexandre Kukui ◽  
Michel Chartier ◽  
Jinhe Wang ◽  
Hui Chen ◽  
Sébastien Dusanter ◽  
...  

Abstract. Reaction of stabilized Criegee intermediates (SCIs) with SO2 was proposed as an additional pathway of gaseous sulfuric acid (H2SO4) formation in the atmosphere, supplementary to the conventional mechanism of H2SO4 production by oxidation of SO2 in reaction with OH radicals. However, because of a large uncertainty in mechanism and rate coefficients for the atmospheric formation and loss reactions of different SCIs, the importance of this additional source is not well established. In this work, we present an estimation of the role of SCIs in H2SO4 formation at a western Mediterranean (Cape Corsica) remote site, where comprehensive field observations including gas-phase H2SO4, OH radicals, SO2, volatile organic compounds (VOCs) and aerosol size distribution measurements were performed in July–August 2013 as a part of the project ChArMEx (Chemistry-Aerosols Mediterranean Experiment). The measurement site was under strong influence of local emissions of biogenic volatile organic compounds, including monoterpenes and isoprene generating SCIs in reactions with ozone, and, hence, presenting an additional source of H2SO4 via SO2 oxidation by the SCIs. Assuming the validity of a steady state between H2SO4 production and its loss by condensation on existing aerosol particles with a unity accommodation coefficient, about 90 % of the H2SO4 formation during the day could be explained by the reaction of SO2 with OH. During the night the oxidation of SO2 by OH radicals was found to contribute only about 10 % to the H2SO4 formation. The accuracy of the derived values for the contribution of OH + SO2 reaction to the H2SO4 formation is limited mostly by a large, at present factor of 2, uncertainty in the OH + SO2 reaction rate coefficient. The contribution of the SO2 oxidation by SCIs to the H2SO4 formation was evaluated using available measurements of unsaturated VOCs and steady-state SCI concentrations estimated by adopting rate coefficients for SCI reactions based on structure–activity relationships (SARs). The estimated concentration of the sum of SCIs was in the range of (1–3) × 103 molec. cm−3. During the day the reaction of SCIs with SO2 was found to account for about 10 % and during the night for about 40 % of the H2SO4 production, closing the H2SO4 budget during the day but leaving unexplained about 50 % of the H2SO4 formation during the night. Despite large uncertainties in used kinetic parameters, these results indicate that the SO2 oxidation by SCIs may represent an important H2SO4 source in VOC-rich environments, especially during nighttime.


2015 ◽  
Vol 13 (1) ◽  
Author(s):  
Beata Messyasz ◽  
Boguslawa Leska ◽  
Joanna Fabrowska ◽  
Marta Pikosz ◽  
Adam Cieslak ◽  
...  

AbstractThe effects of the impact of four organic compounds (ascorbic acid, biotin, glucose and sucrose) on ash, protein, fiber, fat and amino acid contents in the freshwater Aegagropila linnaei biomass were examined in 7 and 14 days of cultivations in high concentrations of tested compounds (100 mg L-1). The presence of examined organic compounds had a negligible effect on the development of algae and their biomass composition. There were no significant differences in the amino acids composition in the biomass in the presence of organic compounds compared to the test system. However, the increase in ash content was observed irrespective of the cultivation time in the case of all used organic compounds. Only slight differences in crude fat concentration were observed in the case of 7 days cultivation with ascorbic acid, biotin and sucrose, while the highest increase of ash content was observed after 14 days of supplementation with glucose. None of the compounds affected changes in amino acid content in the Aegagropila linnaei biomass. The results suggest that an environment enriched with the test organic compounds had only minimal, or at most short-term, effects on the algal biomass composition.


2015 ◽  
Vol 814 ◽  
pp. 220-229
Author(s):  
Hong Xu Zhang ◽  
Yu Jie Zhao ◽  
Jia Zhuang ◽  
Hai Yang Qin ◽  
Han Ling Zhang

With an analysis on the structure of water-soluble sodium silicate and its polymerization, it was found that the poor stability of silicate drilling fluids lies in the relevance between the inherent nature and the pH value of sodium silicate. The modification of water-soluble sodium silicate in this paper was to improve its stability and keep the inhibitive property simultaneously. The a-olefin sulfonate (AOS) was employed as the modifer agent acted on the water-soluble sodium silicate monomer and oligomers. Furthermore, the modification mechanism was discussed through FTIR, Laser particle size, Zeta potential and SEM. A stable sodium silicate drilling fluids with better inhibitive property was obtained by the comparison of modified sodium silicate and unmodified ones.


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