17 research outputs found

    Historical overview of refractory lining in the blast furnace

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    The majority of refractories used today are associated with the iron and steel industries. Typically, the refractory lining of a blast furnace consists of a combination of different refractory materials chosen for different portions of the furnace, as well as distinct process conditions and temperature ranges. Knowledge and requirements for the iron manufacturing system in conjunction with the physical, mechanical, and chemical qualities of the proposed refractories determine the choice of refractory combination. Inadequate understanding of the aforementioned components frequently results in refractory failure, which then becomes a difficult problem to tackle. A blast furnace's refractory liner typically fails owing to any number or combination of these variables. To facilitate comprehension, we will explain the types of refractory lining required in a blast furnace by region, as well as the observed trend in refractory lining patterns over the past few decades

    Microstructural and Cavitation Erosion Behavior of the CuAlNi Shape Memory Alloy

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    Microstructural and cavitation erosion testing was carried out on Cu-12.8Al-4.1Ni (wt. %) shape memory alloy (SMA) samples produced by continuous casting followed by heat treatment consisting of solution annealing at 885 degrees C for 60 min and, later, water quenching. Cavitation resistance testing was applied using a standard ultrasonic vibratory cavitation set up with stationary specimen. Surface changes during the cavitation were monitored by metallographic analysis using an optical microscope (OM), atomic force microscope (AFM), and scanning electron microscope (SEM) as well as by weight measurements. The results revealed a martensite microstructure after both casting and quenching. Microhardness value was higher after water quenching than in the as-cast state. After 420 min of cavitation exposure, a negligible mass loss was noticed for both samples. Based on the obtained results, both samples showed excellent cavitation resistance. Mass loss and morphological analysis of the formed pits indicated better cavitation resistance for the as-cast state (L)

    Removal of copper from aqueous solutions by low cost adsorbent-Kolubara lignite

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    Serbian lignite from Kolubara deposit was used as a low cost adsorbent for removal of copper ions (Cu2+) from aqueous solutions. Lignite was subjected to the elementary and technical analysis as well as BET and FTIR analysis due to complete characterization. Basic comparison between lignite and activated carbon was also done. As a method, batch adsorption procedure was applied. Adsorption efficiency was studied as a function of the initial metal concentration, pH of the solution, contact time, and amount of the adsorbent. Optimum removal of copper ions was achieved at pH values of 5.0. About 90% of copper cations were removed in 5 min of contact time from the solution with the lowest copper concentration (50 mg Cu2+/l) regardless adsorbent amount, while the same effect of adsorption was achieved in 60 min in case of solutions with higher concentrations of copper. It was concluded that the effect of adsorbent amount on adsorption kinetics is evident but not crucial. It was proved that the experimental results of copper adsorption fit well to a Langmuirian type isotherm which was used to describe monitored adsorption phenomena. The calculated adsorption capacities of lignite for copper adsorption decrease with increasing adsorbent amount. The study proved that tested lignite is very efficient adsorbent material, especially in case of low copper concentration in aqueous solution where the usual methods are either economically unrewarding or technically complicated. This behavior can be explained by FTIR spectrum despite a small specific surface area of lignite. Namely, many bands (peaks) are attributed to the functional groups that they are involved in chemisorption and ionic exchange, basic mechanisms of copper adsorption. (C) 2011 Elsevier B.V. All rights reserved

    Removal of Heavy Metals from Aqueous Solution Using Natural and Fe(Iii) Oxyhydroxide Clinoptilolite

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    The increasing levels of industrial wastewater released to the environment present a serious threat to human health, living resources, and ecological systems. Fe-modified zeolites were developed and tested for removal of Cu2+ and Zn2+ from contaminated water. The surfaces of the naturally occurring zeolite, clinoptilolite, were modified with Fe(III) oxyhydroxides using three different methods, denoted I, II, and III (FeCli(1), FeCli(2), and FeNaCli(1), respectively). The oxyhydroxides were prepared in Method I using 0.1 M FeCl3 center dot 6H(2)O in an acetate buffer (pH = 3.6); in Method II, using 10% FeCl3 center dot 6H(2)O solution in 0.1 M KOH (pH = 10); and Method III was the same as Method I except the clinoptilolite was pretreated with NaCl. Newly synthesized materials from these three methods were then tested for their ability to enhance the sorption capacity for Cu and Zn compared to the natural sample (Cli). Powder X-ray diffraction measurements and the chemical composition of these modified samples confirmed that clinoptilolite maintained its structure while amorphous Fe3+ species were synthesized. The specific surface area (BET method) of both the natural and modified clinoptilolite increased by 2 and 7.5 times for Methods I and II, respectively. Scanning electron microscopy and energy dispersive X-ray spectroscopy revealed that CaO was formed during Method I (FeCli(1)). Throughout the adsorption process, the hydrolysis of CaO and the release of OH- caused the precipitation of Cu and Zn hydroxide, which made the determination of the sorption capacity of FeCli(1) impossible. This phenomenon was avoided in Method III (FeNaCli(1)) because of the absence of exchangeable Ca2+. The adsorption experiments with Method II resulted in double-enchanced adsoprtion capacity. Laboratory batch experiments revealed that the sorption capacities increased in the following order: Cli LT FeCli(2) LT FeNaCli(1), for Cu: 0.121 mmol/g LT 0.251 mmol/g LT 0.403 mmol/g and for Zn: 0.128 mmol/g LT 0.234 mmol/g LT 0.381 mmol/g

    Principal component analysis of morphological descriptors for monitoring surface defects induced by thermal shock

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    Pattern recognition techniques are applied to various morphological descriptors to monitor the formation and propagation of surface defects of materials subjected to thermal shock. A low-cement high-alumina castable was synthesized, cured, sintered, and exposed to thermal stability testing using the water quench test. After a certain number of thermal shock cycles, photographs of the samples' surfaces were taken and subjected to image analysis. The influence of the sintering temperature on the morphology of the detected defects was studied using principal component analysis (PCA) as a pattern recognition technique that is the most informative for extracting possible differences. The morphological descriptors of the defects correspond to the previous results regarding the influence of sintering temperature on the structure of a castable during thermal shocks

    Oromaxillofacial Surgery: Both a Treatment and a Possible Cause of Obstructive Sleep Apnea—A Narrative Review

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    Obstructive sleep apnea (OSA) is a chronic, sleep-related breathing disorder. It is characterized by a nocturnal periodic decrease or complete stop in airflow due to partial or total collapse of the oropharyngeal tract. Surgical treatment of OSA is constantly evolving and improving, especially with the implementation of new technologies, and this is needed because of the very heterogeneous reasons for OSA due to the multiple sites of potential airway obstruction. Moreover, all of these surgical methods have advantages and disadvantages; hence, patients should be approached individually, and surgical therapies should be chosen carefully. Furthermore, while it is well-established that oromaxillofacial surgery (OMFS) provides various surgical modalities for treating OSA both in adults and children, a new aspect is emerging regarding the possibility that some of the surgeries from the OMFS domain are also causing OSA. The latest studies are suggesting that surgical treatment in the head and neck region for causes other than OSA could possibly have a major impact on the emergence of newly developed OSA, and this issue is still very scarcely mentioned in the literature. Both oncology, traumatology, and orthognathic surgeries could be potential risk factors for developing OSA. This is an important subject, and this review will focus on both the possibilities of OMFS treatments for OSA and on the OMFS treatments for other causes that could possibly be triggering OSA
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