Abstract: This paper looks at the issue and influence of the die cost on a typical Aluminium die casting business. High pressure die casting (HPDC) is a manufacturing process used to produce components in a near finished shape with a reasonable good surface aspect, dimensionally accurate and within a short period off time or production cycle. The die is at the heart of the HPDC business and is unique to each component to be produced. A full business analysis was done and the full die cost share was extracted as part of a life cycle inventory of the HPDC manufacturing process. The inventory accounted for the energy metal and other inputs flows through the foundry. Die casting uses significant quantities of energy, as well as materials like oil-based lubricants and cooling water. Costs associated with part finishing are also considered due to the direct link between die manufacture and design and resulting finishing operations required.
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Authors: D.S. van Vuuren, Eugene Swanepoel
Abstract:
In the Kroll and Hunter processes to produce titanium from TiCl4, magnesium and sodium are used respectively as reducing agents. These processes are slow and very energy intensive and consequently much work was done over the years to improve the economics of producing these metals. In this regard, more success has been achieved with improving the economics of magnesium electrowinning than with alkali metal electrowinning. Magnesium electrowinning cells generally have electrodes with a planar shape and alkali metal electrolysis cells have electrodes with a cylindrical shape. Furthermore, recent advances in magnesium electrolysis allowed the introduction of bipolar electrodes, whereas such electrodes have not been introduced in alkali metal electrowinning cells. It is conceptually possible to replicate the advances in the construction of magnesium electrowinning cells to improve sodium or other alkali metal electrowinning cells. However, there are underlying fundamental reasons why it would be difficult to do so.In this paper the technologies for magnesium and alkali metal electrowinning cells are briefly reviewed. The reasons why it would be difficult to copy the improvements made in magnesium electrowinning technology to alkali metal electrowinning technology are then explained in terms of the implications of the underlying chemical and physical properties of the chemicals involved in the processes.
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Authors: Jiang Feng Song, Hajo Dieringa, Yuan Ding Huang, Wei Min Gan, Karl Ulrich Kainer, Norbert Hort
Abstract: In the present investigation, SiC reinforced ZE10 alloy composites were fabricated by direct chill casting assisted with ultrasonic vibration. Two kinds of SiC with a size of 50 nm and 2 μm were chosen. For comparison, ZE10 alloys with and without ultrasound were also fabricated. The microstructures and the distribution of SiC were examined by optical microscopy and scanning electron microscopy. Neutron diffraction was also used to identify the second phases in the composites. In addition, mechanical properties such as hardness, creep and compression were evaluated. The results show that SiC was successfully introduced into the magnesium matrix. After the addition of SiC, the mechanical properties of the composites exhibit a slight decrease, which might be due to the grain coarsening.
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Authors: Hajo Dieringa, Norbert Hort, Karl Ulrich Kainer
Abstract:
Magnesium alloys have been finding increasingly more types of application in the automotive and aerospace industries for over twenty years. Despite the fact conventional magnesium alloys have limited high-temperature strength and creep resistance, especially when they contain aluminium as an alloying element. Aluminium is necessary to improve the castability when high-pressure die casting is the favoured process. Applications with higher operating temperatures require additional alloy elements, which form precipitates with the aluminium during solidification and therefore prevent the formation of Mg17Al12, which is responsible for the low creep resistance of magnesium alloys that contain aluminium. The precipitates formed may also strengthen grain boundaries and so improve the creep strength. Barium and calcium were investigated as elements in a magnesium alloy containing aluminium (DieMag422: 4 wt.-% Al, 2 wt.-% Ba, 2 wt.-% Ca). The compression creep strength was compared at 240°C for stresses between 60 and 120 MPa with two commercial creep-resistant magnesium alloys, AE42 and MRI230D. The stress exponents were calculated from the stress dependence of the minimum creep rate. The concept of a threshold stress was applied and true stress exponents nt close to 5 were found. The new alloy DieMag422 exhibits improved creep strength compared to both commercial alloys and also has proven it is die castable.
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Authors: Salomon Johannes Oosthuizen, Jaco Johannes Swanepoel, Dawid Steyn van Vuuren
Abstract: The CSIR-Ti process produces titanium metal powder through continuous stepwise metallothermic reduction of titanium tetrachloride (TiCl4) in molten salt medium, and represents a cost-effective alternative to the standard Kroll process to produce titanium metal. Subsequent to proving the CSIR-Ti process at bench scale producing batches of ±2 kg titanium powder, the design, build and test of a continuous 2 kg/h Ti pilot plant was authorised. The scale-up process highlighted limited expertise in South Africa with regards to handling molten salt and molten reducing metals. Such gaps in knowledge are addressed in this study, which discusses a number of the engineering challenges faced and solutions developed around agitation of molten salt reactors, process pipe heating and insulation, molten salt flow measurement and also feeding of a highly reactive molten reducing metal. Scaling up the CSIR-Ti process, with requirements of continuous operation, compact size, effective agitation, pumping and maintaining salt in the molten state brought an unusual set of challenges requiring development of unique and prototype equipment. Further challenges were encountered in the handling and continuous feeding of molten reducing metal at the relatively small scale of the pilot plant. Solutions developed and discussed in this study include custom-modified agitators, custom-developed flow meters for measuring molten salt and molten metal flows, and a custom-designed molten metal feed system. Specialised materials such as, ultra-high temperature heating tape and ultra-low thermal conductivity insulation had to be imported as well as a special high-temperature pump that can pump a slurry consisting of molten salt containing a high weight percentage of suspended metal powder. The experience illustrates the technological difficulty of bridging the chasm between science and technology in that many unforeseen problems are encountered when developing and scaling up a new technology.
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Authors: P.J. Skosana, D.S. van Vuuren, M.D. Heydenrych
Abstract: One of the advantages of bubble columns is high heat transfer rates. High heat transfer is important in reactors when high thermal duties are required. An appropriate measurement of heat transfer coefficient is of primary importance for designing reactors that are highly exothermic or endothermic. This paper presents the design and operation of experimental setup used for measurement of the heat transfer coefficient in molten salt media. The experimental setup was operated with tap water, heat transfer oil 32, LiCl–KCl eutectic and argon gas. Tap water was operated at the temperature of 40oC and heat transfer oil was operated at the temperature of 75oC, 103oC and 170oC. There were some challenges when operating the bubble column with molten salt due to leakages on the welds and aggressive corrosion on the column. All the experiments were run at superficial gas velocities of 0.01–0.05 m/s. Three heating tapes, each connected to a corresponding variable AC voltage controller, were used to heat the column media. Heat transfer coefficients were measured by inducing a known heat flux through the column wall and measurement of the temperature difference between the wall and the contents. In order to balance the system, heat was removed by the cooling water flowing through a copper tube on the inside of the column. Temperature differences between the column wall and the liquid were measured at five axial locations. It was found that the heat transfer coefficient increases with superficial gas velocity. The values of heat transfer coefficient for argon–water system were higher than those of argon–heat transfer oil system. Heat transfer coefficient was also found to increase with an increase in temperature.
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Authors: Mandy Seerane, Hilda Chikwanda, Walter Focke, Ronald Machaka
Abstract: Debinding is one of the most critical and time consuming stage in metal injection moulding (MIM). German and Bose (1997) reported that early debinding practice relied on thermal binder degradation, requiring up to 300 hours for complete binder removal. Today multi-stage debinding techniques are introduced cutting down the debinding time to as little as 2 hours. This work investigates solvent debinding variables prior to thermal debinding. Solvent debinding is carried out in n-heptane. Wax and stearic acid are the target binder components being leached out from the green bodies, with wax as the major constituent in the binder formulation. Debinding is conducted at 50, 55, 60 and 65°C for 1-4 hours at each temperature. Weight loss measurements were done. For porosity and surface appearance, scanning electron microscope (SEM) analysis and visual inspection were done. Samples de-bound at 65°C showed an appreciable amount of mass loss; however, surface cracks and warping were observed. A 60°C temperature and time of 4 hours demonstrated best results i.e. a satisfactory mass loss, absence of surface cracks and no warping. Mass loss is directly proportional to temperature and time. SEM results are discussed in the paper.
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Authors: C.T.C. Crombie, Deborah C. Blaine
Abstract: An investigation into the solvent and thermal debinding behaviour of a typical paraffin wax-polymer binder system for titanium alloy Ti-6Al-4V powder injection moulding (PIM) feedstock was conducted. Details of the mixing parameters, powder loading, temperature and mixing speed were evaluated for optimal compounding of the feedstock. The feedstock was injection moulded into 22 mm diameter by 3 mm thick disks. Debinding is conducted in two stages, an initial solvent debinding step to remove the waxes, followed by a thermal debinding step to remove the polymers. Solvent debinding was conducted by immersing the injection moulded specimens in n-heptane heated to 50 °C for a period of 5 hours. The mass loss rate was logged during solvent debinding in order to determine the efficiency of the solvent debinding step. From these measurements, it was determined that 94 wt% of the wax (paraffin wax and stearic acid) components of the binder were removed during solvent debinding. A thermo-gravimetric analysis (TGA) was conducted in air on the Ti-6Al-4V powder, as well as the green and solvent debound feedstock. These results show the effect of debinding the feedstock in air and were used to design a thermal debinding cycle for the system.
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Authors: Silethelwe Chikosha, Linda M. Mahlatji, Hilda Kundai Chikwanda
Abstract: In order to reliably design and operate different powder processes, an understanding of the dynamic flow, shear and bulk properties of powders is required. Generally, powders are evaluated by several techniques that determine their flow, shear and bulk properties. The techniques can include compression tests, shear tests, angle of repose, flow of powder in a funnel, tapped density and many others. In order to minimize the number of instruments required to characterise the powder and eliminate operator error, automated powder rheometers that can do most of the required tests have been developed. The FT4 powder rheometer is one of these and has found widespread use in the pharmaceutical industry. In this study, the FT4 powder rheometer was used to characterise two metallic titanium powders with different particle sizes, namely CSIR Ti-45μm (Fine Powder) and CSIR Ti +45-180μm (Coarse Powder). Their particle size, particle size distribution, bulk densities, compressibility, cohesion, flowability index, effective angle of internal friction and wall friction angle were determined. Preliminary results of the study indicated that fine powder had a lower bulk density, was more compressible and more cohesive than the coarse powder. The fine powder had a lower flowability index compared to the coarse powder for both the Jenike and Peschl classification. The varying degrees of cohesion of these powders were confirmed by the cohesion values that were higher for the fine powder. The fine powder had a lower angle of internal friction but higher wall friction angle compared to the coarse powder.
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Authors: Hendrik L. Bosman, Deborah C. Blaine
Abstract: The potential to control the final properties, as measured by density, strength and microstructure, of press-and-sintered titanium and master alloy Ti-6Al-4V is investigated by designing and evaluating bimodal particle size distributions of the relevant powders. Ratios of 1/3, 2/3 and 1/1 by volume of coarse to fine powders, as determined by particle size peaks, were blended from -200 and -100 mesh commercially pure titanium powders and -200 mesh 60Al-40V master alloy powder, in the case of Ti-6Al-4V. The powder blends were uniaxially compacted at 350, 400 and 450 MPa, and the green specimens were sintered under high vacuum for two hours at 1300°C. The results support theoretical prediction of green and sintered density based on the ratio of the volume percentage of coarse to fine powder; green density increases as the ratio of coarse powder increases for both the pure and alloy titanium, while the sinter density similarly decreases for the pure titanium. Microstructural observations of the sintered specimens show that the pore size decreases, and the pore shape becomes more rounded, as the ratio of fine powder increases. In order to extend the study to find the optimal packing ratio, and potentially the optimal blend for densification, further refinement of the initial powder particle size distributions is needed.
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