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Screen-printed membrane sensors based on the use of paper and ceramic substrates are fabricated, characterized, and used for rapid batch and continuous monitoring of Cr III in the form of CrO 4 in some industrial products and wastewater samples. Strips of paper and ceramic platforms (15 × 5 mm) were covered with conductive carbon paint and then modified with polyaniline (PANI) film, to act as an ion-to-electron transducer, followed by a drop casting of plasticized poly (vinyl chloride) (PVC) Rhodamine-B chromate membrane as a recognition sensing material. In a 5.0 mmol L 2- Trizma buffer solution of pH ~8, the fabricated paper and ceramic based membrane sensors exhibited a near Nernstian response for Cr -1 Trizma buffer solution of pH ~8, the fabricated paper and ceramic based membrane sensors exhibited a near Nernstian response for Cr VI ion with slopes of -29.7 ± 0.5 and -28.6 ± 0.3 mV decade -1 , limit of detection 2.5 × 10 -5 and 2.4 × 10 -6 mol L -1 (1.3-0.12 µg mL -1 ), and linear concentration range 7.5 × 10 -3 -5.0 × 10 -5 and 7.5 × 10 -3 -1.0 × 10 -5 mol L -1 (390-0.5 µg mL -1 ), respectively. Both sensors exhibited fast and stable potentiometric response, excellent reproducibility, and good selectivity with respect to a number of common foreign inorganic species. Impedance spectroscopy and chronopotentiometry data revealed a small resistance and a larger double layer capacitance due to the presence of the intermediate polyaniline (PAN) conductive layer. Furthermore, the formation of a water layer between the ion selective membrane (ISM) and the underlying conductor polymer and between the conducting polymer and the carbon conducting surface was greatly reduced. The developed disposable solid-contact potentiometric sensors offer the advantages of simple design, long term potential stability, flexibility, miniaturization ability, short conditioning time, and cost effectiveness that enable mass production. The sensors were successfully used for static and hydrodynamic measurements of total chromium in some leather tanning wastewater and nickel-chrome alloy samples. The results compare favorably with data obtained by atomic absorption spectrometry., Competing Interests: The authors declare no conflict of interest.

The catalytic combustion of diesel soot is addressed with flexible and structured "paper catalysts". Two different series of catalysts were prepared either by drip impregnation or by a spray method to deposit a mixture of Co, Ba, and K or a mixture of Co and Ce onto SiO 2 -Al 2 O 3 ceramic paper matrixes. In every case, CeO 2 nanoparticles were added to bind the ceramic fibers. SEM images showed that the impregnation method generated catalytic particles concentrated as large chunks (> 10 μm), mainly at ceramic fiber crossings, whereas the spray method produced smaller catalytic particles (< 1 μm) well distributed throughout the ceramic paper. Besides, Co-Ba-K particles appeared better dispersed on the surface of ceramic fibers than Co-Ce due to the presence of K. Additionally, FTIR spectra showed the formation of O 2 2- and O 2 (binder) on the samples containing potassium which gave the Co-Ba-K-ceramic paper good catalytic properties, thus making the Co-Ba-K drop impregnated the best catalyst both considering activity and stability. Successive temperature programmed oxidation (TPO) runs up to 700 °C caused the formation of cobalt silicates in the catalytic ceramic paper prepared by the spray method, as indicated by TPR. The formation of these species was probably favored by the smaller size of cobalt particulates and their higher dispersion in the catalysts prepared by the spray method. This provoked the partial loss of the redox properties of Co - species associated with CeO 2 (binder) on the samples containing potassium which gave the Co-Ba-K-ceramic paper good catalytic properties, thus making the Co-Ba-K drop impregnated the best catalyst both considering activity and stability. Successive temperature programmed oxidation (TPO) runs up to 700 °C caused the formation of cobalt silicates in the catalytic ceramic paper prepared by the spray method, as indicated by TPR. The formation of these species was probably favored by the smaller size of cobalt particulates and their higher dispersion in the catalysts prepared by the spray method. This provoked the partial loss of the redox properties of Co 3 in Ba-containing ceramic paper, which could help in maintaining the catalyst activity after several TPO runs through the capacity of this mixed perovskite-type oxide to trap and release NO 4 . TPR experiments also indicated the formation of BaCoO 3 in Ba-containing ceramic paper, which could help in maintaining the catalyst activity after several TPO runs through the capacity of this mixed perovskite-type oxide to trap and release NO x .

Alumina-based multilayer laminates with layers of varied porosities and ceramic fiber reinforcements, which can be achieved by including paper-derived ceramic layers, are interesting candidates for chemically stable and thermal shock resistant materials. In order to investigate the complex sintering behavior of these laminates, the sintering of each alumina layer contained within a laminate, each one with its individual sintering anisotropy and sintering shrinkage, has to be considered separately. For this purpose, sintering curves are determined by dilatometry measurements, serving a consecutive examination by an analytical model. Modeling parameters specific to each layer, are applied in finite-element-type sintering simulations for symmetrical multilayer laminates. Differences in the sintering shrinkages may cause internal stresses at layer interfaces and, in turn, may influence the thermal and mechanical properties of multilayer laminates after sintering. Accordingly, the prediction of developing internal stresses within alumina-based multilayer laminates by the presented sintering simulations is a key aspect of this study. [Display omitted] • Individual laminates sintering dilatometry. • Anisotropic sintering assessment by analytic modeling. • Finite element simulation of multilayer laminates sintering. [ABSTRACT FROM AUTHOR]

Paper recycling is an environmental important activity that is carried out in all the countries, but during the recycling process a paper waste is produced. Generally these wastes are placed in landfill sites but it is possible to profit it as secondary fuel and raw material in manufacture furnaces. In this work the combustion of the waste papers with cement and ceramic raw material has been studied with the objective to analyse the interaction of these substances with the emitted pollutants like PAHs and PCDD/Fs. The results of the study show that the presence of inorganic material produces an increment in the lighter PAH emission but chlorinated compounds are not affected. The PCDD/F emission level found in the combustion of this waste is quite low compared with other wastes subjected to similar conditions.

This paper describes the fabrication and characterization of porous SiC ceramics derived from highly-filled preceramic papers. The SiC ceramics were obtained by spark plasma sintering of stacked preceramic papers at temperatures of 2100 and 2200 °C under pressures of 5–60 MPa for 10 min. The microstructure and phase composition were analyzed by scanning electron microscopy and X-ray diffraction, respectively. Gas permeation tests were performed using hydrogen permeation cell at room temperature. It is revealed that the porosity of sintered SiC can be varied from 9 to 45 % depending on the sintering parameters. The shrinkage of the materials during spark plasma sintering occurs in four stages. The linear shrinkage value of the material increases from 7 to 47 % at 2100 °C and from 20 to 50 % for the samples sintered at 2100 and 2200 °C, respectively. Correlation dependencies between porosity and mechanical properties of the fabricated SiC were established. The obtained porous SiC ceramics exhibit high bending strength of 165 MPa and gas permeation flux of 78 molH 2 /m2/s at the porosity of 36 % that make it suitable for ceramic-based membranes. [ABSTRACT FROM AUTHOR]

Through the pyrolysis of cellulose-based paper templates infiltrated with a suitable polymer precursor, ceramic composites exhibiting a paper-like structure can be conveniently prepared. Such polymer-derived ceramic papers (PDCPs) unite the unique morphology of regular cellulose papers with the properties of the ceramic system utilized. Here, two paper templates, made from eucalyptus and cotton, respectively, were infiltrated with two polysilazane-based polymer precursors modified with either Fe, Ni, or Pd and converted into multi-phasic ceramic papers. In addition to the type of paper template, precursor composition, and transition metal used, the present study aims to rationalize the influence of pyrolysis temperature and atmosphere on the morphology, microstructure, and phase composition of the ceramic papers generated. For this purpose, scanning electron microscopy, SEM, and (scanning) transmission electron microscopy, (S)TEM, in conjunction with EDS analyses were used to elucidate the microstructural features of the ceramic composites in great detail. It is shown that the transition metals precipitate as nanosized metallic particles and silicides in the case of Pd and Ni, while the introduction of Fe features oxide and carbide phases in addition to that. Moreover, the metals catalyze both the graphitization of the cellulose fibers and, at higher temperatures, the generation of whisker-like Si-based nanostructures composed of either SiC or Si 3 N 4 , depending on the processing atmosphere used. [ABSTRACT FROM AUTHOR]

Accelerated thermal aging was conducted on Kraft papers impregnated with mineral insulating oil (MO) and palm insulating oil (PO), and the effect of aging time on the oils and Kraft papers was observed. Each sample consisted of insulating oil, dried Kraft paper, and weighed metal catalysts (copper, iron, zinc, and aluminum) in a bottle. Prior to aging, the bottles were left for 24 h at room temperature for impregnation to take place. The thermal aging experiments were carried out at 130 °C for 250, 500, and 750 h. The properties of the MO and PO (moisture content, acidity, and ultraviolet-visible absorption spectra) and the properties of the Kraft papers (tensile strength and colour) were determined. Results showed that the aged PO had higher moisture content compared with the aged MO. However, the Kraft papers impregnated with PO had better tensile strength after 750 h of aging, which may be attributed to the affinity of PO to moisture. This slows down the hydrolytic degradation mechanism. In terms of colour, the Kraft papers were darker than their original colour as the tensile strength decreased. To conclude, the Kraft paper impregnated with PO had higher tensile strength compared with those impregnated with MO. [ABSTRACT FROM AUTHOR]

Mineral materials, such as corundum, quartz and periclase are very often used in technological processes. Due to its characteristics, and chemical reaction in solid state, these minerals form very interesting and useful material, cordierite. The mineral ratio in this compound (MgO : Al2O3 : SiO2) is 2:2:5. They form cordierite, electronic ceramic, which can be sintered in a narrow temperature range, at about 1375 °C. Composition of this electronic ceramics material is is 2MgO-2Al2O3-5SiO2 (MAS) and in this research 20% mass Bi2O3 was added in the aim of decrease the sintering temperature. The effects of sintering, the composition and morphology were followed by x-ray diffraction, scanning electron microscopy and EDS analysis, as a function of sintering temperature. MAS ceramics were sintered at 1000ºC, 1100ºC and 1200ºC.

Background: Re‐use of wastes as a part of sustainable development is one of the most important aspects of a healthy human life and environmental protection. This study examines the viability of using paper industry slag for the production of building ceramics. Results: Paper industry slag was used in the production of ceramic bricks as a burnable additive in amounts of 5, 10 and 15 wt%. The slag was introduced without and after three different preparatory operations: dried, dried and ground, granulated and dried. Clay was used as a raw material and quartz sand as a lean additive. The samples were made by plastic molding. Drying was carried out at a temperature of 100 °C. To determine the optimal heat treatment temperature, firing was carried out at 900, 950, 1000 and 1050 °C with holding at the maximum temperature for 30 min, followed by determination of the properties of the samples. Conclusions: It has been established that the samples obtained using the slag have good physical and mechanical properties and comply with current standards. At the same time, the use of slag in the production of ceramic bricks makes it possible to solve the problem of waste management, as well as to obtain a secondary material resource from the slag – a burnable additive, which leads to savings in raw materials and energy resources in the production of ceramic bricks. © 2022 The Authors. Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

Various calcium phosphates are used for bone repair. Although hydroxyapatite (HA) sintered ceramics are widely used due to their osteoconductivity, its bioresorbability is so low that HA remains in the body for a long time after implantation. In contrast, tricalcium phosphate (TCP) ceramics show resorbable characters during bone regeneration, and can be completely substituted for the bone tissue after stimulation of bone formation. Therefore, much attention is paid to TCP ceramics for scaffold materials for supporting bone regeneration. This paper reviews bioresorbable properties of calcium phosphate ceramics derived from beta-TCP and alpha-TCP.

Three different types of paper mill sludge were first incinerated and then attrition milled separately or mixed with glass cullet in varying proportions to obtain powders of different compositions. These powders were then dried, sieved, uniaxially pressed into samples and air sintered. Fired samples were characterized by density, water absorption, shrinkage on firing, strength, hardness and fracture toughness measurements; SEM and X-ray diffractions were also carried out to investigate microstructure and phase composition. Some sintered samples displayed fairly good physical and mechanical properties as a consequence of their low residual porosity and fine microstructure.

The book "Western Ceramic Traditions: Prehistoric and Historic Native American Ceramics of the Western U.S." edited by Suzanne Griset explores the diversity of ceramic traditions and social identities reflected in pottery production in the far southwestern desert and coastal region of the U.S. The book features 11 chapters that critically examine traditional typologies of plainware pottery and explore new datasets for dating and identifying the composition of pottery. The volume provides important discussions on the sociocultural aspects of pottery technology and challenges the limitations of typological classification. The book is recommended for researchers working with plainware or other ceramic wares, although the technical ceramic data presented may be daunting for readers without an archaeological or ceramic analyst background. [Extracted from the article]

Fibers represent a type of structure of great interest in catalysis since they combine high area to volume ratio and can be fabricated from many types of materials, such as ceramic oxides, polymers, and alloys. They can be used in isolated form or structured, as in the case of the ceramic papers synthesized in this work, following a modified papermaking technique. The addition of cationic and anionic polyelectrolytes improved the retention of ceramic fibers during the ceramic paper formation stage by adsorption processes, through the formation of floccules. In the complex aqueous system containing charged macromolecules, the amounts of polyelectrolytes to be added were determined by titrations. To enhance mechanical properties of ceramic papers, different classes of nanoparticle suspensions can be used as binders. As a novel alternative, we have used different borate-type compounds. Among them, we selected natural ulexite, which was purified and used as a binder of ceramic fibers. In order to improve mechanical resistance and flexibility, measured from tensile indexes and elastic module, the amounts of NaCaB5O6(OH)6.5H2O and the calcination temperature were varied. In this contribution, to take advantage of the unique characteristics of the ulexite-containing ceramic papers, they were impregnated with Co,Ce and Co,Ba,K and tested for diesel soot combustion. [ABSTRACT FROM AUTHOR]

In this study, continuous carbon reinforced C f /(Ti 0.2 Zr 0.2 Hf 0.2 Nb 0.2 Ta 0.2)C–SiC high entropy ceramic matrix composites were additively manufactured through paper laminating (PL), direct slurry writing (DSW), and precursor infiltration and pyrolysis (PIP). (Ti 0.2 Zr 0.2 Hf 0.2 Nb 0.2 Ta 0.2)C high entropy ceramic (HEC) powders were synthesized by pressureless sintering and ball milling. A certain proportion of HEC powder, SiC powder, water, binder, and dispersant were mixed to prepare the HEC-SiC slurry. Meanwhile, BN coating was prepared on the 2D fiber cloth surface by the boric acid-urea method and then the cloth was cut into required shape. Additive manufacturing were conducted subsequently. Firstly, one piece of the as-treated carbon fiber cloth was auto-placed on the workbench by paper laminating (PL). Then, the HEC-SiC slurry was extruded onto the surface of the cloth by direct slurry writing (DSW). PL and DSW process were repeated, and a C f /HEC-SiC preform was obtained after 3 cycles. At last, the preform was densified by precursor infiltration and pyrolysis (PIP) and the final C f /HEC-SiC composite was prepared. The open porosity of the C f /HEC-SiC composites, with the HEC volume fractions of 15, 30 and 45%, were 7.7, 10.6, and 11.3%, respectively. And the density of the C f /HEC-SiC composites, with the HEC volume fractions of 15, 30 and 45%, were 2.9, 2.7 and 2.3 g/cm3, respectively. The mechanical properties of the C f /HEC-SiC composites increased firstly and then decreased with the HEC content increase, reaching the maximum value when the HEC volume fraction was 30%. The mechanical properties of the C f /HEC-SiC composites containing 45, 30 and 15% HEC were as follows: flexural strength (180.4 ± 14 MPa, 183.7 ± 4 MPa, and 173.9 ± 4 MPa), fracture toughness (11.9 ± 0.17 MPa m1/2, 14.6 ± 2.89 MPa m1/2, and 11.3 ± 1.88 MPa m1/2), and tensile strength (71.5 ± 4.9 MPa, 98.4 ± 12.2 MPa, and 73.4 ± 8.5 MPa). From this study, the additive manufacturing of continuous carbon fiber reinforced high entropy ceramic matrix composites was achieved, opening a new insight into the manufacturing of ceramic matrix composites. [ABSTRACT FROM AUTHOR]

[Display omitted] • Cerium – Manganese Catalytic Ceramic Paper very active for soot oxidation. • Spray method showed to be efficient for anchoring catalytic species on fibers. • Experiments at bench scale showed good soot filtration capacities. • Citric Acid addition during impregnation improved catalytic distribution on fibers. Diesel Particulate filters are considered one of the most efficient technologies to reduce particulate matter emitted by diesel engines. In this paper we study the development of catalytic ceramic papers based on Mn-Ce and their applications as soot particle filters in bench scale tests. Ceramic papers were prepared by a dual polyelectrolyte papermaking method and were impregnated with Mn and Ce precursors through a wet-spray procedure using a commercial fogger. Catalytic ceramic papers were tested as catalysts for the combustion of soot, which was obtained both from the burning of diesel fuel and directly from a bench test. In addition, the filtering capacity of catalytic ceramic papers was tested through opacity measurements by placing the ceramic papers in a suitable case at the end of the engine. Mn-Ce based catalysts were active in the soot combustion. The addition of citric acid considerably improved the catalytic performance of all the systems studied. This beneficial effect of citric acid is related to an improvement in the distribution of the catalytic material onto the ceramic fibers, being the mixed equimolar oxide Mn-Ce the most active catalyst. [ABSTRACT FROM AUTHOR]

Cellulose is now considered as an appealing environment friendly material for the development of sustainable separators for rechargeable batteries. This study thus aims to develop high performance paper based ceramic separators with superior electrolyte wettability (>170 %), high thermal stability (>200 °C) and excellent flame safety. While developing paper based ceramic separator, extensive studies are carried out to understand thenature and functionality of different nano-structured ceramic materials (Al 2 O 3 , BaTiO 3 and ZrO 2) impregnated in paper matrix. Nano-ZrO 2 facilitates an effective pathway for Li +-ion transport (t Li + = 0.51), whereas BaTiO 3 and Al 2 O 3 ceramics show moderate Li +-ion transport properties (t Li+ of 0.29 and 0.30 respectively). Electrochemical Impedance Spectroscopy (EIS) measurement clearly reveals that ZrO 2 exhibits more interfacial compatibility with the electrodes (MCMB and LiNi 1/3 Mn 1/3 Co 1/3 O 2) compared to the other two ceramic separators during full cell operation. The developed paper separators show excellent electrochemical properties in terms of cycling (tested 300 cycles), multi-electrode compatibility and rate capabilities at different current densities of 0.1–1.2 mAcm−2. The pre- and post-electrochemical EIS data reveal that ZrO 2 based impregnation offers significantly lower charge transfer resistance compared to the other two separators. The study thus demonstrates a real promise for its successful application in Li-ion battery towards achieving sustainability and safety. [Display omitted] • Sustainable, flexible and high safety ceramic based paper separators for LIBs. • Separators were developed using easy to scale up wet-coating process. • Ceramic impregnation affects physical and electrochemical properties of the separators. • Paper separators show superior electrolyte wettability and high thermal stability. • Better electrochemical performances and flame safety are other important advantages. [ABSTRACT FROM AUTHOR]

Cellulose‐based paper samples were surface‐modified by a polymeric single‐source precursor prepared from perhydropolysilazane (PHPS) and iron(III)acetylacetonate (Fe(acac)3) and ammonolyzed at 500°C, 700°C, 900°C, and 1000°C, leading to C/SiFe(N,C)O‐based ceramic papers with in situ‐generated hierarchical micro/nano‐morphology. As reference, cellulose‐free samples were prepared under the same conditions. Upon thermal treatment, the microstructure evolutions of the resulting ceramic paper and the reference sample were comparatively investigated. Scanning electron microscopy (SEM) showed that for all temperatures, the ceramic papers exhibit the same morphology as the template, however, with noticeable shrinkage and curling, particularly evident at higher temperatures. X‐ray diffraction (XRD) measurements of the reference samples and the ceramic papers showed a similar crystallization behavior and phase evolution in both materials. In the ceramic paper, the crystallization process seems to occur at a later time. The results provide a comprehensive understanding of the investigated C/SiFe(N,C)O‐based ceramic system. It was shown that use of the cellulose‐based paper template has the benefit of retaining the microstructure and furthermore, apart from transforming the cellulose fibers into turbostratic carbon, does not change the phase evolution during the polymer‐to‐ceramic transformation, allowing at the same time the manufacturing of novel morphologically complex parts by a convenient one‐pot synthesis approach. [ABSTRACT FROM AUTHOR]

Ag@ceramic composite papermaking pigment was prepared by coating silver onto red ceramic powder using the electroless plating method. SEM and XRD showed that the ceramic pigments have a porous crystalline structure and that silver particles had been successfully loaded onto the surface and into the pores of the Ag@ceramic. Untreated ceramic pigment and Ag@ceramic pigment were incorporated into paper sheets by coating, filling and filling‐coating. Using spinach as an example, the ability of the different papers to preserve food was then evaluated. Four indicators were used to assess the preservative effect of the papers: inhibition of growth of Staphylococcus aureus and Escherichia coli, weight loss of the spinach and retention of vitamin C and chlorophyll in the spinach. Although the ceramic preservative paper has no antibacterial properties, it reduced weight loss from the spinach and increased retention of vitamin C and chlorophyll. The antibacterial preservative papers inhibited the growth of E. coli and S. aureus by >99%, and because of their additional antibacterial activity, these papers preserved the spinach more effectively. The experimental results showed that the antibacterial food‐preservative paper incorporating ceramic pigments had great potential in food packing applications. [ABSTRACT FROM AUTHOR]

This paper describes the fabrication and characterization of novel preceramic paper-derived functionally graded materials (FGMs) based on Ti 3 (Si,Al)C 2 MAX phase. The FGMs with different architecture were fabricated via spark plasma sintering of stacked preceramic papers at 1250 °C for 5 min. Microstructure, phase composition and elemental distribution were analyzed by scanning electron microscopy, X-ray diffraction and energy-dispersive X-ray spectroscopy, respectively. Oxidation tests were performed in air at 1300 °C for 5 h. FGMs containing Al- and Si-enriched MAX-phase layers were formed. The fabricated materials exhibit high flexural strength (over 600 MPa), which are dependent on microstructure and composition of individual layers as well as the architecture of composites. It was found that texturing of MAX phase grains during SPS results in anisotropic hardness of the composite. The difference in the composition of the individual layers also provides a hardness gradient in the composite. It was shown that the formation of the outer layer from the Al-enriched Ti 3 Al(Si)C 2 MAX phase increases the corrosion resistance of Ti 3 SiC 2 -based composites. The high corrosion resistance of FGMs is due to the growth of a continuous and dense Al 2 O 3 oxide layer. [ABSTRACT FROM AUTHOR]

SiFeO(N,C)‐based ceramic papers were prepared via a one‐pot synthesis approach by dip‐coating a cellulose‐based paper template with a polymeric perhydropolysilazane precursor modified with iron(III)acetylacetonate. The preceramic composites were subsequently pyrolyzed in ammonia atmosphere at 500, 700, and 1000°C, respectively, and the characteristics of the three resulting ceramic papers were comparatively investigated. Scanning electron microscopy revealed that in each sample, the morphology of the template is successfully transferred on the ceramic system, with the cellulose‐derived fibers being converted to elemental carbon encased by a SiFeO(N,C) coating. Electron transparent cross‐sectional samples for transmission electron microscopy (TEM) were prepared from the ceramic papers, employing a standard ultramicrotomy slice cutting procedure, allowing for a detailed characterization of their in situ generated micro‐/nanostructure as well as occurring crystalline phases. TEM imaging and diffraction revealed that depending on pyrolysis temperature a different microstructure with a distinct phase assemblage is generated in the polymer‐derived ceramic papers. Crystallization from the polymer precursor starts with the precipitation of wüstite (Fe(1‐x)O) nanoparticles at 700°C inside the ceramic coating and secondary ε‐FexN at the fiber‐coating interface. Upon pyrolysis at 1000°C however, the sample primarily accommodates metallic α‐iron nanocrystals that impart ferromagnetic characteristics to the ceramic paper. The results show that the template‐assisted polymer‐derived ceramic route is a feasible approach in the production of complex ceramic compounds with fibrous paper‐like morphology. By adjusting the pyrolysis temperature, microstructure and phase composition of the ceramic paper can be conveniently tailored to the needs of its respective application. [ABSTRACT FROM AUTHOR]

Zirconia implants are gaining attention as a viable alternative to titanium implants due to their comparable osseointegration development, improved soft tissue adaptation, and enhanced aesthetics. An encouraging avenue for improving zirconia implant properties involves the potential application of bioactive coatings to their surfaces. These coatings have shown potential for inducing hydroxyapatite formation, crucial for bone proliferation, and improving implant mechanical properties. This study aimed to evaluate the effect of coating zirconia implants with two bioactive glasses, 45S5 and BioK, on osteogenesis in vitro and osseointegration in vivo. Zirconia samples and implants were prepared using Zpex zirconia powder and blocks, respectively. The samples were divided into three groups: polished zirconia (ZRC), zirconia coated with 45S5 bioglass (Z + 45S5), and zirconia coated with BioK glass (Z + BK). Coatings were applied using a brush and sintered at 1200°C. Chemical analysis of the coatings was carried out using x-ray diffraction and Fourier Transform Infrared Spectroscopy. Surface topography and roughness were characterized using scanning electron microscopy and a roughness meter. In vitro experiments used mesenchymal cells from Wistar rat femurs, and the coated zirconia implants were found to promote cell viability, protein synthesis, alkaline phosphatase activity, and mineralization, indicating enhanced osteogenesis. In vivo experiments with 18 rats showed positive results for bone formation and osseointegration through histological and histomorphometric analysis and a push-out test. The findings indicate that bioactive glass coatings have the potential to improve cell differentiation, bone formation, and osseointegration in zirconia implants., (© 2024 Wiley Periodicals LLC.)

Abstract: A papermaking technique with a dual polyelectrolyte retention system was used for the preparation of NaY zeolite-containing papers, which implied the use of cationic and anionic polymers. Two kinds of fibers were employed, either cellulosic or ceramic ones, and accordingly papers with different characteristics were obtained: those that only contained cellulosic fibers for low temperature applications, cellulosic papers, and those prepared using both cellulosic and ceramic fibers – ceramic papers – for high temperature applications. Although a decrease in their mechanical properties due to calcination was observed, zeolitic ceramic papers resulted easy to handle for practical applications. Zeolite was quantified through BET surface area measurements. SEM images indicated a good dispersion of zeolite particles within the cellulosic paper whereas in the ceramic paper they appeared anchored on ceramic fibers. The zeolitic papers prepared resulted efficient as toluene sorbents, the adsorption capacities of zeolitic ceramic papers being higher than those of zeolitic cellulosic papers. In the case of zeolitic cellulosic papers, the amounts of released toluene were lower than those of adsorbed toluene, implying that the treatment up to 160°C did not completely eliminate the hydrocarbon. Also, TPD profiles showed that toluene is chemically retained up to high temperatures (ca. 420°C) in zeolitic ceramic papers. Toluene adsorption values demonstrate that zeolite dispersed into the cellulose/ceramic matrix is as effective as powder massive zeolite in retaining the hydrocarbon, which highlights the potential application of these zeolitic structures as sorbent materials both for low and high temperatures. [Copyright &y& Elsevier]

NaY zeolite-containing ceramic papers were prepared by a papermaking technique with a dual polyelectrolyte retention system that implied the use of cationic and anionic polymers. To improve their mechanical properties, we found that some borate compounds could be successfully used as ceramic binders. Three types of sodium and/or calcium borates were tested as binders: colemanite, nobleite, and anhydrous ulexite. The improvement in the mechanical properties depends both on the borate used and on the calcination temperature. By XRD it was determined that the faujasite structure collapsed after calcination at 700°C, which limited the final calcination temperature of zeolitic ceramic papers. Different amounts of NaY zeolite were added to ceramic papers and, as observed by SEM, faujasite particles were well distributed throughout the ceramic paper structure. Ceramic papers containing 1.2 wt.% zeolite after calcination at 650°C resulted in structured catalysts that were easy-to- handle, and which can be adapted to different conformations. [ABSTRACT FROM AUTHOR]