OBTAINING MICROCRYSTALLINE CELLULOSE FROM MELON CROPS AND STUDYING ITS STRUCTURE

2020 ◽  
pp. 38-41

The aim of the study was to obtain microcrystalline cellulose from gourds. Cellulose was isolated from the stems of watermelon and pumpkin by acid and alkaline heat treatment. Microcrystalline cellulose was obtained from cellulose by hydrolysis. Cellulose was hydrolyzed in a mixture of sulfuric acid and hydrogen peroxide. The optical parameters of the microcrystalline cellulose sample, ash content, bulk density, water swelling, and moisture sorption were determined. The structural features of the obtained microcrystalline cellulose were studied by IR spectroscopy. The functional groups present under various conditions for the production of microcrystalline cellulose were determined. The influence of the duration of cellulose treatment on the degree of ordering of microcrystalline cellulose was established.

Author(s):  
O. B. Berdnik ◽  
I. N. Tsareva ◽  
M. K. Chegurov

This article deals with structural features and characteristic changes that affect the mechanical characteristics after different service life in real conditions using the example of the blades of the 4th stage of turbine GTE-45-3 with an operating time of 13,000 to 100,000 hours. To study the change in the state of the material under different operating conditions, determine the degree of influence of heat treatment on the regeneration of the microstructure, and restore the mechanical characteristics of the alloy after different periods of operation, non-standard methods were used: relaxation tests on miniature samples to determine the physical yield strength and microplasticity limit and quantitative evaluation of the plasticity coefficient of the material from experimental values of hardness, which allow us to identify the changes occurring in the microvolumes of the material and predict the performance of the product as a whole.


1984 ◽  
Vol 49 (1) ◽  
pp. 14-24 ◽  
Author(s):  
Viliam Múčka

Some physical and catalytic properties of cerium dioxide-nickel oxide two-component catalysts have been studied over the entire composition region, employing the decomposition of hydrogen peroxide in aqueous solution as a model catalytic process. The two oxides have been found to affect each other, particularly for NiO contents of 9.1 and 96.7 mol%; the mutual influencing, the nature of which in the conditions applied remains unaffected by heat treatment of the sample or by its exposition to ionizing radiation, is manifested by the nonmonotonic dependences of the oxidation power and of the specific activity of the catalysts on their composition. This can be interpreted in terms of the concept of bivalent catalytic centres, assuming that for nickel oxide the centres consist of Ni2+-Ni3+ ion pairs, for cerium dioxide they consist of Ce3+-Ce4+ ion pairs, and that in the region of the mutual influencing , Ni2+-Ce4+ ion pairs play a major role. Within the scope of this concept, the increase in the oxidation power of all the catalysts in question and a simultaneously decrease in the specific activity of the pure nickeloxide exposed to ionizing radiation can be explained in terms of the ionization effect.


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.


JOM ◽  
2020 ◽  
Author(s):  
Joona Rajahalme ◽  
Siiri Perämäki ◽  
Roshan Budhathoki ◽  
Ari Väisänen

AbstractThis study presents an optimized leaching and electrowinning process for the recovery of copper from waste printed circuit boards including studies of chemical consumption and recirculation of leachate. Optimization of leaching was performed using response surface methodology in diluted sulfuric acid and hydrogen peroxide media. Optimum leaching conditions for copper were found by using 3.6 mol L−1 sulfuric acid, 6 vol.% hydrogen peroxide, pulp density of 75 g L−1 with 186 min leaching time at 20°C resulting in complete leaching of copper followed by over 92% recovery and purity of 99.9% in the electrowinning. Study of chemical consumption showed total decomposition of hydrogen peroxide during leaching, while changes in sulfuric acid concentration were minor. During recirculation of the leachate with up to 5 cycles, copper recovery and product purity remained at high levels while acid consumption was reduced by 60%.


2001 ◽  
Vol 56 (12) ◽  
pp. 1340-1343 ◽  
Author(s):  
Mathias S. Wickleder ◽  
Oliver Büchner

AbstractThe evaporation of a solution of Au(OH)3 and Na2So4 in conc. sulfuric acid led to yellow single crystals of NaAu(SO4)2 (monoclinic, P21/n, Z = 2, a = 469.1, b = 845.9, c = 831.2 pm, β = 95.7°). Analogous procedures with K2SO4 or Rb2SO4 instead of Na2SO4 yielded single crystals of KAu(SO4)2 (monoclinic, C2/c, Z = 4, a = 1109.8, b = 724.2, c = 941.1 pm, β = 118.4°) and RbAu(S04)2, respectively, (triclinic, P1̄, Z = 1, a = 423.6, b = 497.5, c = 889.0 pm, a = 76.4°, β = 88.4°, γ = 73.5°). Although the crystal structures of the three sulfates are not isotypic they show similar structural features: The gold atoms are coordinated by four oxygen atoms in a square planar manner. These oxygen atoms belong to four SO42- ions which link the [AUO4] units to infinite chains according to 1∞[Au(SO4)4/ 2]- . These chains are connected via the monovalent cations which show coordination numbers of 6 (Na+), 10 (K+) and 12 (Rb+), respectively.


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.


2007 ◽  
Vol 330-332 ◽  
pp. 131-134
Author(s):  
S. Yabe ◽  
Kanji Tsuru ◽  
Satoshi Hayakawa ◽  
Akiyoshi Osaka ◽  
Y. Yoshida ◽  
...  

Titania layer was fabricated on the titanium substrates with chemical treatment with 20ml or 40ml of hydrogen peroxide solution and subsequent heat treatment at 400°C, coded as CHT20 and CHT40, respectively. CHT20 spontaneously deposited apatite on the surface in a simulated body fluid (SBF), while CHT40 did not. TF-XRD patterns showed that the diffraction intensity of anatase of CHT20 was higher than that of CHT40. It was suggested that the thicker titania layer indicated in vitro apatite forming ability. The cell proliferation of CHT20 and CHT40 were lower than NT and HT. Since the surface of titania layers became hydrophobic after autoclaving, we can suppose that the cell proliferation on CHT20 and CHT40 were lower than NT and HT due to their surface hydrophobicity.


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.


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