Umeå University's logo

Refractory liner bricks in the hot zone of rotary lime kilns can sustain wear and corrosion during contact with fuel ashes and quicklime (QL), a product composed mainly of CaO. The effects on a MgO-based refractory after exposure at 1400 °C for 96 h to olive pomace ash (OPA) and coal ash (CA), with and without QL, were investigated. Exposure of the refractory to only OPA caused slag intrusion with no ash deposits remaining on top, while CaMgSiO4 (monticellite) was also identified as a new phase. When exposed to only CA, the refractory exhibited dissolution into the molten slag and 0.5–2 mm cracks were found on the surface interfacing the ash. Mg2SiO4 (forsterite) and CaMgSiO4 were identified as new formed phases. Exposure of the refractory to OPA + QL and CA + QL caused less slag intrusion and substantial amounts of ash/QL deposit remained afterwards. No new phases were identified. The differences in interactions between the exposure materials and refractory were supported by thermochemical equilibrium analysis. Apparent Ca-Si–rich or Ca-rich melts were found in all the exposed samples, but potassium (K) was found to be depleted in all samples, including those involving OPA, which was rich in K. Furthermore, with the exception of exposure to only CA, the other exposures caused the cold crushing strength (CCS) of the refractory to increase compared to its original value. This was attributed to the sintering of the refractory microstructure. The CCS of the refractory decreased after exposure to only CA. The findings of this study enhance understanding of how CA and OPA impact MgO refractories in lime kilns, supporting initiatives aiming at reducing fossil fuel use. The results are encouraging and motivate further investigation.

Doping β-tricalcium phosphate (β-TCP) with copper (Cu²⁺) has great potential in various applications due to its rich chemistry. However, the doping characteristics are rarely studied in detail and are yet to be fully understood, creating a gap in the existing knowledge of these multifunctional materials. In this work, a series of Cu²⁺ doped β-TCP (Cu_x-TCPs) were prepared and comprehensively characterized to investigate the correlation between Cu²⁺ doping and the material properties. Also, the synthesis of Cu_x-TCPs was modeled using thermodynamic equilibrium calculations to investigate their formation pathways. The calculations predicted a possible inclusion of Cu²⁺ in intermediate phosphate phases during the material synthesis, depending on the temperature. The structural analyses revealed lattice shrinkage due to the Cu²⁺ doping and that Cu²⁺ occupied Ca4 and Ca5 sites in the β-TCP crystal. The vibrational spectroscopy of the Cu_x-TCPs showed noticeable deformation of ν₁ band of PO₄³⁻ ligand. The ultraviolet-visible absorption analysis revealed a reduction in the band gap energy induced by Cu²⁺ doping. Photoluminescence spectroscopy demonstrated an enhanced emission tunability of Cu_x-TCPs in the blue and orange–red regions depending on Cu²⁺ concentration. These findings are a step toward a deeper understanding of the structure–property relationships of Cu²⁺ doped β-TCPs and can play a significant role in their multidisciplinary applications.

Variations in cerebral blood flow and blood volume interact with intracranial pressure and cerebrospinal fluid dynamics, all of which play a crucial role in brain homeostasis. A key physiological modulator is respiration, but its impact on cerebral blood flow and volume has not been thoroughly investigated. Here we used 4D flow MRI in a population-based sample of 65 participants (mean age = 75 ± 1) to quantify these effects. Two gating approaches were considered, one using respiratory-phase and the other using respiratory-time (i.e. raw time in the cycle). For both gating methods, the arterial inflow was significantly larger during exhalation compared to inhalation, whereas the venous outflow was significantly larger during inhalation compared to exhalation. The cerebral blood volume variation per respiratory cycle was 0.83 [0.62, 1.13] ml for respiratory-phase gating and 0.78 [0.59, 1.02] ml for respiratory-time gating. For comparison, the volume variation of the cardiac cycle was 1.01 [0.80, 1.30] ml. Taken together, our results clearly demonstrate respiratory influences on cerebral blood flow. The corresponding vascular volume variations appear to be of the same order of magnitude as those of the cardiac cycle, highlighting respiration as an important modulator of cerebral blood flow and blood volume.

In this study, the impact of Zn2+ doping on β-Ca3(PO4)2 characteristics was investigated with particular focus on its influence on the surface, structure, and photocatalytic properties. Zn2+ doped β-Ca3(PO4)2 (Znx-TCPs) were synthesized using a solid-state method and were thoroughly studied to evaluate the modification induced by cationic substitution. The structural analysis revealed a noticeable shrinkage in the lattice parameters a and c and the unit cell volume induced by Zn2+ doping. Minor spectral changes in the vibrational modes of PO43− were also observed in the infrared and Raman spectra of Znx-TCPs. The influence of doping on the materials’ morphology was insignificant; however, molten grain boundaries were noticeable at high Zn concentration, x ≥ 1. X-ray photoelectron spectroscopy (XPS) revealed that the surface of the doped materials was rich in Zn. Optical absorption measurements indicated that Zn2+ doping slightly affects the optical bandgap of β-Ca3(PO4)2. The photocatalytic activities of the materials were investigated for the degradation of Rhodamine B (RB) and Methylene blue (MB). The photocatalytic experiments were carried out in the presence of hydrogen peroxide and under simulated solar light. The samples exhibited enhanced catalytic activity compared to β-Ca3(PO4)2, and the Zn0.5-TCP sample demonstrated the highest degradation efficiency. This sample showed excellent stability during the reusability tests, which suggests the suitability of Zn0.5-TCP for use as an efficient photocatalyst. Surface defects are believed to play an important role in the production of active species during the photocatalytic reaction.

Magnesium oxide (MgO)-based refractories are commonly used in quicklime and cement rotary kilns. At the high temperatures in the kiln burn zone, the infiltration of molten fuel ash into the refractory can occur. Subsequent chemical interactions can cause refractory wear that inflicts high maintenance costs and loss of production. To improve refractory reliability, it is necessary to increase the understanding of the interactions between fuel ash slag and refractory liner materials. Three commercially available MgO-based refractory materials were exposed to coal ash at 1200 °C and 1400 °C for between 15 and 60 min under a CO₂-rich gaseous environment. Hot slag from the coal ash infiltrated the refractories and the infiltration depths were estimated with scanning electron microscope with energy dispersive X-ray spectroscopy. Based on detailed elemental and microstructure analyses, the interactions between ash and refractory were examined. Molten silicates infiltrated the refractory through grain boundaries and pores into depths of up to 2.8 mm. Powder X-ray diffraction of the exposed refractory samples indicated that MgO grains reacted with SiO₂-containing phases to form Mg₂SiO₄. This was identified as a corrosion product whose formation was supported by thermochemical equilibrium calculations. Elevated Mg content was found in the ash residue on top of the samples, indicating the dissolution or dislocation of refractory components. In addition, phases such as MgO were identified in the ash residue.

MgO-based refractories are used in lime kilns to withstand the high temperature and chemical environment. Efforts to reduce CO₂ emissions have led to an increased interest to use bio-based fuels as alternatives to traditional fossil sources. The potential for refractory corrosion from a potassium-rich biomass ash was investigated by studying the infiltration of olive pomace ash into magnesia/spinel refractories. Refractory samples were exposed to the ash at up to 1400 °C for 15–60 min in a CO₂–rich atmosphere. Molten ash infiltrated the refractories through pores and grain boundaries to a depth of up to 9.6 mm, which was quantified with a new systematic procedure. The phase KAlO₂ was identified inside the refractories after exposure, indicating an attack of spinel components by potassium. Phases found in the ash residues also indicated the migration of refractory constituents. Thermochemical equilibrium calculations were also used to investigate the ash/refractory chemistry.

In quicklime production, limestone is calcined at temperatures above 1000°C, depending on the desired product quality. Heat is supplied to the process from combustion inside the kilns that are insulated to reduce heat loss. The kilns are lined with insulating refractory bricks to withstand the hot, chemically aggressive, and mechanically abrasive environment. Magnesia bricks have emerged as well-performinglining materials, but they are still prone to extensive wear in kilns that are operated at higher temperatures. In particular, refractory corrosion can be caused by fuel ash infiltration that results inmaterial wear, which can incur high maintenance and operational costs through unplanned shutdowns of the kilns. At the same time, to reduce the release of fossil-based carbon to the atmosphere, it is of interest to introduce bio-based fuels into the kilns with only relatively small modifications to the process. Biobased waste streams from existing industries are preferable rather than biomass grown with the sole purpose of combustion. The ash content and properties of these types of waste residues do, however, tend to be problematic from a fuel ash chemistry point of view. Therefore, before introducing a new fuel, their potential effects on kiln lining material should be investigated. In this study, the infiltration of olivepomace ash and coal ash into commercially available refractory materials composed of mainly periclase(MgO) with minor amounts of spinel (MgAl2O4) were compared. They were exposed to the fuel ashes under a simulated lime kiln high CO2 atmosphere at 1200 and 1400°C for 15 and 60 minutes. The morphology and elemental composition of the exposed samples were investigated with scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy. Ash-forming elements infiltrated the porous parts of the materials. The analytical results are complemented with thermodynamic equilibrium calculations to investigate the ash melting behavior. Crystalline phases in the residual ashes were investigated with X-ray diffraction. Refractory phases could be found in both ashes, indicating migration of refractory constituents. Olive pomace ash formed new crystalline compounds together with the refractory components whereas this was not observed for the coal ash, indicating that the former is more of a risk for material failure.  

Innovation has become increasingly important for most industries to cope with rapid technological changes as well as changing societal needs. Even though there are many sectors with specific needs when it comes to supporting innovation, the medical technology sector is facing several unique challenges that both increases the lead-time from idea to finished product and decreases the number of innovations that are developed. This paper presents a proposed innovation guide that has been developed and evaluated as a support for the innovation process within medical technology research. The guide takes the unique characteristics of the medical technology sector into account and serves as a usable guide for the innovator. The complete guide contains both a structure for the process and a usable web application to support the journey from idea to finished products and services. The paper also includes a new readiness level, Sect. 4.2 to provide support both when developing and determining the readiness for clinical implementation of a medical technology innovation.

Purpose: The aim of the study was to show that a new method, using a look-up table technique, can be used to detect the presence and position of an inclusion embedded in a tissue-like material. Due to the time-consuming nature of the finite element (FE) method or FEM, real-time applications involving FEM as part of a control loop, are traditionally limited to slowly varying systems. By using a simplified two-dimensional FE model and a look-up table, we show by simulations and experiments that it is possible to achieve reasonable computational times in a tactile resonance sensor application.

Design/methodology/approach: A piezoelectric disk was placed in the center of a silicone rubber disk (SRD) with viscoelastic properties, where it acted as both sensor and actuator and dissipated radial acoustic waves into the silicone. The look-up table was constructed by calculating the radial Lamb wave transition frequencies in the impedance frequency response of the sensor while varying the position of an inclusion. A position-matching algorithm was developed that matched measured and calculated Lamb wave transitions and thereby identified the presence and position of an inclusion.

Findings: In an experiment, the position of a hard inclusion was determined by measuring the Lamb transition frequencies of the first radial resonance in two SRDs. The result of the matching algorithm for Disk 1 was that the matched position was less than 3% from the expected value. For Disk 2, the matching algorithm erroneously reported two false positions before reporting a position that was less than 5% from the expected value. An explanation for this discrepancy is presented. In a verifying experiment, the algorithm identified the condition with no inclusion present.

Originality/value: The approach outlined in this work, adds to the prospect of developing time-sensitive diagnostic instruments. This approach has the potential to provide a powerful technique to quickly present spatial information on detected tumors.