Low-temperature Process Research Articles

Femtosecond Laser Irradiation to Zirconia Prior to Calcium Phosphate Coating Enhances Osteointegration of Zirconia in Rabbits.

Calcium phosphate (CaP) coating of zirconia and zirconia-based implants is challenging, due to their chemical instability and susceptibility to thermal and mechanical impacts. A 3 mol% yttrium-stabilized tetragonal zirconia polycrystal was subjected to femtosecond laser (FsL) irradiation to form micro- and submicron surface architectures, prior to CaP coating using pulsed laser deposition (PLD) and low-temperature solution processing. Untreated zirconia, CaP-coated zirconia, and FsL-irradiated and CaP-coated zirconia were implanted in proximal tibial metaphyses of male Japanese white rabbits for four weeks. Radiographical analysis, push-out test, alizarin red staining, and histomorphometric analysis demonstrated a much improved bone-bonding ability of FsL-irradiated and CaP-coated zirconia over CaP-coated zirconia without FsL irradiation and untreated zirconia. The failure strength of the FsL-irradiated and CaP-coated zirconia in the push-out test was 6.2-13.1-times higher than that of the CaP-coated zirconia without FsL irradiation and untreated zirconia. Moreover, the adhesion strength between the bone and FsL-irradiated and CaP-coated zirconia was as high as that inducing host bone fracture in the push-out tests. The increased bone-bonding ability was attributed to the micro-/submicron surface architectures that enhanced osteoblastic differentiation and mechanical interlocking, leading to improved osteointegration. FsL irradiation followed by CaP coating could be useful for improving the osteointegration of cement-less zirconia-based joints and zirconia dental implants.

Sol–Gel Synthesis of Nanostructured Mesoporous Silica Powder and Thin Films

Mesoporous materials are special nanoporous materials containing well-defined mesochannels with a pore diameter between 2 and 50 nm. The high surface area, ordered structure, tunable pore size, and easiness of functionalization have made mesoporous silica powder and thin films interesting materials for a wide range of applications including drug delivery, absorption, separation, catalysis, energy conversion, and storage. The sol–gel process has emerged as a promising technique for the synthesis of nanostructured mesoporous silica materials as it provides the advantages of low-temperature processing and easy control of the synthesis parameters. Although it offers several advantages over other synthesis techniques, it also has the drawbacks of high sensitivity to processing conditions. Hence, this review paper aims to give critical insights into the sol–gel process, the chemistry of sol–gel silica, the formation mechanism of mesoporosity, and the effects of the reaction parameters. A good understanding of these phenomena is essential to better control and optimize the properties of the final material for specific needs and applications. Additionally, this review paper discusses the different methods applied to the synthesis of nanostructured ordered mesoporous thin film silica, including the Electrochemically Assisted Self-Assembly method of synthesis. The EASA method is a novel and promising technique for the synthesis of well-ordered and vertically aligned pore channels of mesoporous thin films as it is required for mass transport applications. Moreover, the effects of sol composition, pH, applied potential, and deposition time on the final thickness of the thin film are elaborated on in detail. Furthermore, this comprehensive review highlights the potential and opportunities for future research and development in the area to further advance and use its full potential advantages.

Numerical and Experimental Investigation for Application of CoNiCrAlY Coatings by HVAF

AbstractA relatively small change in oxide content and microstructure in MCrAlY coatings (M = Co, Ni) can affect the functionality of the coating for oxidation protection or as a bond coat. The objective of this study is to fabricate a CoNiCrAlY coating with low porosity and low oxide content. The high velocity air-fuel (HVAF) process, with its relatively low process temperature, is particularly suitable for the deposition of spray materials that are susceptible to oxidation or degradation at high temperature. A CFD simulation model of HVAF process is developed to determine the process parameters for fabricating CoNiCrAlY coating. The simulation results are validated by particle diagnostics, thereby establishing a comprehensive understanding of the underlying process. To assess the coating microstructure, XRD and EDS analyses as well as observation of cross sections of the coatings are conducted. The results highlight the influence of various factors, such as the variation of carrier gas and particle size distribution, on the quality of the coatings. Consequently, the utilization of simulation-based process parameter development is well supported by the coating fabrications, offering valuable insights into the processes prior to implementation.

Polymer Metallization by Cold Spray Deposition of Polyamide-Copper Composite Coatings

Cold spray metallization of polymers is a promising surface engineering technique that enables the deposition of metal coatings onto polymer substrates at low process temperatures, resulting in improved surface properties, thus enhanced functionality of the polymeric material. However, deposition of well-adhering metallic coatings without causing surface damage to the polymer substrate is still a challenge. In this work, copper-polyamide composite coatings with different copper concentrations between 30 and 75 vol.% in the starting powders were deposited on polyamide substrates using a low-pressure cold spray system with two nozzle geometries of short and long diverging sections. The spray parameters were first developed for the deposition of polyamide powder (at gas temperature of 260 °C and gas pressures ranging from 0.41 to 1.37 MPa), and then used to spray the composite powder mixtures where the polyamide particles were acting as a binder for copper particles. Inflight and impact particle characteristics (velocity and temperature) of the polyamide powder were simulated to better understand the deposition properties. Considering that the selected conditions were suboptimal for the deposition of copper particles, no surface damage was caused as no penetration of the copper particles into the polymer substrate occurred. The results show that increasing the copper content in the powder mixtures significantly improved the resulting coating uniformity and the retained copper content. In addition, the coating deposited by spraying the powder mixture with a higher copper content of 75 vol.% and using the longer nozzle yielded the highest cohesion strength. To further improve coatings cohesion, two post-spray processing methods of furnace heating and hot pressing were used, and the effect of each process on coatings properties was investigated.Please confirm if the author names are presented accurately and in the correct sequence (given name, middle name/initial, family name). Given name: [Kintak Raymond] Last name [Yu]. Also, kindly confirm the details in the metadata are correct.The author names are now correct: Kintak Raymond given name and Yu last nameAll other details are corrects

Designing a Ce/In-CHA OXZEO catalyst for high-efficient selective catalytic reduction of nitrogen oxide with methane

Selective catalytic reduction of nitrogen oxides with methane (CH4-SCR) has emerged as a promising technology for mitigating exhaust emissions from natural gas vehicles, while its insufficient catalytic activity and durability are key barriers to application. In this study, novel Ce/In-CHA OXZEO catalysts were prepared, demonstrating exceptional catalytic performance and stability in the CH4-SCR reaction. Over these OXZEO catalysts, indium species predominantly existed in the form of InO+ and InxOy within the CHA zeolite framework, while CeO2 nanoparticles primarily resided as an external layer. During the CH4-SCR reaction, NO oxidation to form NO2 and nitrate species was triggered by CeO2, which further enhanced the activation of CH4 on InO+ sites, thus boosting the low-temperature CH4-SCR process by facilitating the formation of the key intermediate CH3NO2. The synergy between InO+ and CeO2 underscores the exceptional performance and stability of the Ce/In-CHA with a low SiO2/Al2O3 ratio in reducing NOx and CH4 emissions.

Benefits of isochoric freezing for carrot juice preservation.

Isochoric freezing (IF) at -5°C/77 and -10°C/100MPa was used to preserve carrot juice for 12 weeks. The juice qualities were compared to those using heat treatment (HT) at 95°C for 15s followed by cold storage at 4°C. The native population of total aerobic bacteria, yeasts, and molds in isochoric frozen juice remained below the detection limit for 12 weeks. In comparison, microbes started to grow in heat-treated juices after 3 weeks of refrigeration. The color of isochoric frozen juice appeared more deep orange than the fresh juice due to an increase in carotenoid extractability. IF was not effective in reducing the activities of peroxidase, polyphenol oxidase, and pectin methyl esterase compared with HT. However, the isochoric samples showed higher carotenoid content, polyphenol content, and antioxidant capacity compared to the fresh and heat-treated juices. PRACTICAL APPLICATION: Isochoric freezing was used to produce carrot juice with extended shelf life. Isochoric freezing could be a beneficial alternative to conventional heat treatment for carrot juice processing as the applied pressures reached total inactivation levels of spoilage microorganisms. Moreover, the low processing temperatures better retained desirable compounds and quality attributes of fresh juice throughout its shelf life.

Ionic Liquid Bridge Assisting Bifacial Defect Passivation for Efficient All-Inorganic Perovskite Cells with High Open-Circuit Voltage.

Serious open-circuit voltage (Voc) loss originating from nonradiative recombination and mismatch energy level at TiO2/perovskite buried interface dramatically limits the photovoltaic performance of all-inorganic CsPbIxBr3-x (x = 1, 2) perovskite solar cells (PSCs) fabricated through low-temperature methods. Here, an ionic liquid (IL) bridge is constructed by introducing 1-butyl-3-methylimidazolium acetate (BMIMAc) IL to treat the TiO2/perovskite buried interface, bilaterally passivate defects and modulate energy alignment. Therefore, the Voc of all-inorganic CsPbIBr2 PSCs modified by BMIMAc (Target-1) significantly increases by 148 mV (from 1.213 to 1.361 V), resulting in the efficiency increasing to 10.30% from 7.87%. Unsealed Target-1 PSCs show outstanding long-term and thermal stability. During the accelerated degradation process (85 °C, RH: 50∼60%), the Target-1 PSCs achieve a champion PCE of 11.94% with a remarkable Voc of 1.403 V, while the control PSC yields a promising PCE of 10.18% with a Voc of 1.319 V. In particular, the Voc of 1.403 V is the highest Voc reported so far in carbon-electrode-based CsPbIBr2 PSCs. Moreover, this strategy enables the modified all-inorganic CsPbI2Br PSCs to achieve a Voc of 1.295 V and a champion efficiency of 15.20%, which is close to the reported highest PCE of 15.48% for all-inorganic CsPbI2Br PSCs prepared by a low-temperature process. This study provides a simple BMIMAc IL bridge to assist bifacial defect passivation and elevate the photovoltaic performance of all-inorganic CsPbIxBr3-x (x = 1, 2) PSCs.

Improving the efficiency of CO2 methanation using a combination of plasma and molecular sieves

In recent years, the chemical reactions with plasma catalysis have been attracted attention. The interaction between plasma ant catalyst can wide the process window, realizing the low pressure and low temperature processes with various catalysts. However, the wide process range make it difficult to optimization for social implement. The key lies in elucidating the reaction mechanism, predicting reactions through numerical simulations, and deriving optimal conditions. On the other hand, recent research has suggested that the use of molecular sieves (MS) can improve methanation efficiency. This can be combined with catalysts, offering new potential applications of MS in chemical reactions. Here, we investigated the more efficient combination of plasma and MS and their reaction mechanisms. As a result, it was found that: 1. The use of MS reduces the oxidation source in the gas phase, leading to an increase in methanation efficiency by suppressing reverse reactions. 2. The adsorption effect of MS, which suppress the reverse reaction, increases with higher pressure. 3. MS in plasma decrease the energy in plasma decrease the energy within the plasma, reducing the CO2 decomposition rate due to electron impact.

Numerical thermalization in 2D PIC simulations: Practical estimates for low-temperature plasma simulations

The process of numerical thermalization in particle-in-cell (PIC) simulations has been studied extensively. It is analogous to Coulomb collisions in real plasmas, causing particle velocity distributions (VDFs) to evolve toward a Maxwellian as macroparticles experience polarization drag and resonantly interact with the fluctuation spectrum. This paper presents a practical tutorial on the effects of numerical thermalization in 2D PIC applications. Scenarios of interest include simulations, which must be run for many thousands of plasma periods and contain a population of cold electrons that leave the simulation space very slowly. This is particularly relevant to many low-temperature plasma discharges and materials processing applications. We present numerical drag and diffusion coefficients and their associated timescales for a variety of grid resolutions, discussing the circumstances under which the electron VDF is modified by numerical thermalization. Though the effects described here have been known for many decades, direct comparison of analytically derived, velocity-dependent numerical relaxation timescales to those of other relevant processes has not often been applied in practice due to complications that arise in calculating thermalization rates in 1D simulations. Using these comparisons, we estimate the impact of numerical thermalization in several examples of low-temperature plasma applications including capacitively coupled plasma discharges, inductively coupled plasma discharges, beam plasmas, and hollow cathode discharges. Finally, we discuss possible strategies for mitigating numerical relaxation effects in 2D PIC simulations.

Influence of organic sulfur gas-phase sulfation on the NH3-SCR activity of CeO2 catalyst: The competitive adsorption and conversion of CS2 and COS at a low hydrolysis temperature

In this study, a simplified approach is proposed to realize the gas-phase sulfation of CS2 or/and COS at the hydrolysis temperature for further facilitating the NH3-SCR activity of CeO2 in diverse conditions. A low-temperature oxidation conversion process for the adsorbed CS2 or COS on cubic fluorite CeO2 surface is developed. It is found that the gas-phase sulfation of organic CS2 or/and COS at 50 °C enhances the mobility of lattice oxygen of cubic fluorite CeO2 and the concentration of oxygen defects for the sulfated CeO2 catalyst, but the kinds of organic COS/CS2 can regulate the formed types and quality of sulfur-containing species on the catalyst surfaces during the gas-phase sulfation. and the formed sulfates under the gas-phase sulfation of CS2 are more active than those of COS, and CeO2-CS2-50 °C-3 h presents the best mobility of lattice oxygen, the largest concentration of adsorbed oxygen and the best NH3-SCR activity. Furthermore, the competitive adsorption and conversion of CS2 and COS is disadvantageous for the formation of oxygen vacancies on the catalyst surfaces compared to single CS2 or COS. However, the long-time durability testing coupling re-cycle experiments can optimize the oxygen vacancy defects and increase the concentration of chemisorbed oxygen of the sulfated CeO2-CS2 + COS-50 °C-24 h catalyst via optimizing the oxidization of sulfur element to sulfur oxides or/and sulfates, thereby improves its NH3-SCR activity. And the sulfated CeO2 catalyst by the gas-phase sulfation of organic COS + CS2 presents a good stability for NH3-SCR reaction. This study specifies a novel approach to simplify the gas-phase sulfation process of CeO2 catalyst, which is valuable in promotion of the NH3-SCR activity of CeO2 and reduction of cost in experimental procedures.

Strong Photon-Magnon Coupling Using a Lithographically Defined Organic Ferrimagnet.

A cavity-magnonic system composed of a superconducting microwave resonator coupled to a magnon mode hosted by the organic-based ferrimagnet vanadium tetracyanoethylene (V[TCNE]x) is demonstrated. This work is motivated by the challenge of scalably integrating a low-damping magnetic system with planar superconducting circuits. V[TCNE]x has ultra-low intrinsic damping, can be grown at low processing temperatures on arbitrary substrates, and can be patterned via electron beam lithography. The devices operate in the strong coupling regime, with a cooperativity exceeding 1000 for coupling between the Kittel mode and the resonator mode at T≈0.4 K, suitable for scalable quantum circuit integration. Higher-order magnon modes are also observed with much narrower linewidths than the Kittel mode. This work paves the way for high-cooperativity hybrid quantum devices in which magnonic circuits can be designed and fabricated as easily as electricalwires.

Toward Air Stability of Efficient Filter‐Free Band‐Selective Organic Photodetectors Based on Bulk Heterojunction: Avoiding Environmental Degradation with Atomic Layer Deposition Encapsulation

To detect the band‐specific optical signals used in many fields, it is necessary to develop spectrally selective photodetection. For such wavelength‐selective photodetection or color discrimination, organic photodetectors (OPDs) can offer significant benefits as low temperature and solution processability, chemical versatility, and specific spectral detection range. However, to avoid commonly used filters, the design of a narrowing approach that simultaneously achieves a selective detection range with a bandwidth of less than 50 nm and a spectral response of over 20% remains a challenge. OPDs based on charge‐collection‐narrowing principle can provide these features. In this approach, the detection window can be selected to match the absorption onset of the junction materials used in the bulk heterojunction layer. Herein, filter‐free band‐selective OPDs are realized based on PM6:PC70BM blends as state of the art. Fine adjustment over a bandwidth of 42 nm to be highly selective at 677 nm with a quantum efficiency of 48.4% under an inverse low bias of −2 V is reached. In addition, using a noninvasive and nondestructive encapsulation technique, it is demonstrated that these OPDs fully retain their high selective peak after 30 days storage in air.

Low-temperature thermal hydrolysis for enhancing sludge anaerobic digestion and antibiotic resistance management: Significance of digester solids retention time

Recently, there has been a growing inclination towards utilizing primary sludge (PS) fermentation prior to anaerobic digestion (AD) in water resource recovery facilities (WRRFs), where sludge liquor containing volatile fatty acids is used for biological nutrient removal. Nevertheless, using a low-temperature thermal hydrolysis process (THP) to improve AD in WRRFs adopting PS fermentation remains an area that has received limited research attention. Here, we studied the impact of THP (90 °C, 90 min) on anaerobic co-digestion of thickened waste activated sludge (TWAS) and fermented primary sludge (FPS) under varying solids retention times (SRTs) in semi-continuous mode. The study involved two THP schemes: scheme 1, where THP was done for both TWAS and FPS, and scheme 2, where THP was applied to TWAS only. The results demonstrated that reducing SRT from 20 to 15 and 10 d leads to decreased methane yield in both schemes. However, THP significantly enhances methane production, showing improvements of up to 37.9 % (scheme 1) and 31.2 % (scheme 2) under a 15-d SRT. Furthermore, while decreasing SRT increased the proliferation of antibiotic resistance genes (ARGs), thermal hydrolysis could effectively reduce most ARGs, indicating its potential to mitigate antibiotic resistance in the AD process. Overall, these results provide useful perceptions regarding the potential adoption of low-temperature THP in WRRFs with PS fermentation.

Hydrophilic Ligand Exchange Induces Improved Upconversion Nanoparticle Incorporation in Dye-Sensitized Solar Cells with Efficiency Exceeding 8% in a Low-Temperature Fabrication Process

Hydrophilic Ligand Exchange Induces Improved Upconversion Nanoparticle Incorporation in Dye-Sensitized Solar Cells with Efficiency Exceeding 8% in a Low-Temperature Fabrication Process

Improvement in Fatigue Strength of Chromium–Nickel Austenitic Stainless Steels via Diamond Burnishing and Subsequent Low-Temperature Gas Nitriding

Chromium–nickel austenitic stainless steels are widely used due to their high corrosion resistance, good weldability and deformability. To some extent, their application is limited by their mechanical characteristics. As a result of their austenitic structure, increasing the static and dynamic strength of the components can be achieved by surface cold work. Due to the tendency of these steels to undergo intercrystalline corrosion, another approach to improving their mechanical characteristics is the use of low-temperature thermo-chemical diffusion processes. This article proposes a new combined process based on sequentially applied diamond burnishing (DB) and low-temperature gas nitriding (LTGN) to optimally improve the fatigue strength of 304 steel. The essence of the proposed approach is to combine the advantages of the two processes (DB and LTGN) to create a zone of residual compressive stresses in the surface and subsurface layers—the enormous surface residual stresses (axial and hoop) introduced by LTGN, with the significant depth of the compressive zone characteristic of static surface cold working processes. DB (both smoothing and single-pass hardening), in combination with LTGN, achieves a fatigue limit of 600 MPa, an improvement of 36.4% compared to untreated specimens. Individually, smoothing DB, single-pass DB and LTGN achieve 540 MPa, 580 MPa and 580 MPa, respectively. It was found that as the degree of plastic deformation of the surface layer introduced by DB increases, the content of the S-phase in the nitrogen-rich layer formed by LTGN decreases, with a resultant increased content of the ε-phase and a new (also hard) phase: stabilized nitrogen-bearing martensite.

Gate Capacitance Coupling of Double-Gate Carbon Nanotube Network Transistors.

Carbon nanotube (CNT) network channels constructed using a high-purity CNT solution for use in CNT thin-film transistors have the advantages of the possibility of requiring a low-temperature process and needing no special equipment. However, there are empty spaces between individual CNTs, resulting in unexpected effects. In this study, double-gate (DG) CNT network transistors were fabricated and measured in four different configurations to observe the capacitive coupling effects between the top gate (TG) and bottom gate (BG) in the DG structure. As a result, the electrical characteristics measured with the BG with a thicker gate oxide while floating the TG were similar to those measured with the TG with a thinner gate oxide. A comparison of the measured transfer curves showed that TG and BG were strongly coupled through the empty spaces in the channels. In addition, we evaluated the capacitance coupling effect due to changes in the CNT density, which is closely related to the empty space of the network channel. Finally, we proposed a method to determine the effective gate capacitance by considering the empty spaces between CNTs, which enabled the accurate evaluation of mobility. The effects of these materials were demonstrated by fabricating transistors using Al2O3, HfO2, and ZrO2 as TG oxide materials. By focusing on considerations based on the properties of CNT materials, our study provides valuable insights into accurate electrical modeling and potential advancements in CNT-based devices.

Extraction of organic pigments from tomato (Solanum lycopersicum L.), turmeric (Curcuma longa L.) and red amaranth (Amaranthus tricolor L.) for safe use in agro-products

The utilization of synthetic dyes in food industries is a great concern for food safety and health issues. So, natural pigments can be an excellent substitute for synthetic dyes and also health-friendly for consumers. In the experiment, natural pigments were extracted from tomato (Solanum lycopersicum L.), turmeric (Curcuma longa L.) and red amaranth (Amaranthus tricolor L.). Then the stability and consumer acceptance of the extracted pigments were examined. The highest amount of pigment was extracted from turmeric (2.14 ± 0.30 %) with ethanol solvent, followed by tomato (0.67 ± 0.06 %) with hexane: acetone (1:1) solvent, and red amaranth (0.78 ± 0.05 %) with acetone solvent. Turmeric pigment showed the highest stability in high temperatures and light exposure. All of the pigments were highly stable in a neutral environment; however, tomato pigment showed the highest stability index (84.33 ± 2.52) at pH 3.0, but turmeric pigment showed the highest stability (91.67 ± 1.53) at pH 5.0. The simple preference test revealed that the use of turmeric pigment in boiled rice had the highest acceptance rate, and in terms of taste and flavor, red amaranth pigments in ice cream. So turmeric pigment can be utilized in high-temperature processing and/or acidic foods, but tomato and red amaranth pigments might be in low-temperature processing foods such as the ice-cream and soft drinks processing industry.

Praseodymium doped nickel oxide as hole-transport layer for efficient planar Perovskite Solar Cells

Hybrid organic/inorganic perovskite solar cells (PSCs) have acquired significant consideration due to high power conversion efficiency (PCE). In PSCs, electron and hole extraction layers have a significant influence on their overall performance. In inverted p-i-n structure-based PSCs, NiOx has been frequently employed as a hole transport layer (HTL) due to its simple processing, wide bandgap, high optical transmittance, excellent chemical stability, and low processing temperature for large-scale fabrication. However, NiOx suffers from low electrical conductivity. Doping of NiOx is an effective technique employed for enhancing electrical as well as optical properties. Herein, the praseodymium doped NiOx (Pr-NiOx) was synthesized by sol-gel method, and films were fabricated to investigate the effect of Pr dopant on the optoelectronic properties and photovoltaic performance of PSCs. Results indicated that Pr doping significantly improved the hole mobility by about threefold and conductivity of NiOx films from 4.68 × 10-6 S cm-1 to 8.27 × 10-6 S cm-1. Moreover, it also enhanced the compactness and interfaces of NiOx HTL. PSCs based on 4 % Pr-doped NiOx HTL- yielded PCE of 9.35 % which is 32.43 % more than the PSCs fabricated using undoped NiOx HTL. The enhanced PCE of PSC devices with Pr-doped NiOx could be attributed to efficient extraction of a hole from an active absorbing layer of perovskite thereby, lowering the probability of unsuitable charge carrier recombination. This work exhibits that Pr-doped NiOx thin film could be a promising alternative material for efficient and stable inverted PSCs.

Formation of perovskite by solid-gas reaction through low-temperature carbon counter electrode in hole-conductor-free perovskite solar cells

Recently, hole-conductor-free perovskite solar cells (PSCs) with carbon counter electrode (CCE) have attracted great attention for its high stability and low fabrication cost. Furthermore, it would lower the cost and simplify the manufacturing process of PSCs by low temperature processing instead of high temperature sintering for fabrication. In this case, however, it is very important to improve the interfacial contact between perovskite layer and CCE. In this work, we for the first time introduce solid-gas reaction between dimethylammonium lead iodide (DMAPbI3) in solid state under carbon layer and methylamine (MA) gas passed through CCE which is formed at low temperature of 120 ℃. Based on Brunauer-Emmett-Teller (BET) measurement and XRD analysis, it is found that MA gas can pass through our low-temperature CCE and perovskite crystals could be successfully formed by the reaction with DMAPbI3. In this case, due to the existence of liquid crystal intermediate state and volume expansion, interfacial contact would become better and the charge transfer and recombination characteristics have improved considerably. The best performance devices based on optimized MA gas treatment time exhibit higher efficiency of 12.4% than that of PSCs fabricated by conventional ways with low-temperature processed CCE (9.6%).

Alteration of biomass toxicity in torrefaction – A XDS-CALUX bioassay study

Torrefaction constitutes one of the promising technologies for the management of waste biomass and the production of high-carbon products for combustion, gasification, adsorption of pollutants or soil treatment. Unfortunately, waste biomass may be contaminated with toxic persistent organic pollutants, such as polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/PCDF) and dioxin-like biphenyls (dl-PCB). Literature does not provide consistent measurements on how the low-temperature thermochemical processing, such as torrefaction, affects the toxicity of biomass. This contribution assesses how a torrefaction treatment, conducted at 200 °C, modifies the toxicity due to PCDD/PCDF/dl-PCB in biomass. We deploy the XDS-CALUX biotest on five types of waste biomass (sewage sludge, tree bark, cattle manure, spent coffee ground, common reed), before and after treatment. The content of total dioxin- & biphenyl fraction compounds in the raw biomass, investigated in this study, varies from 0.14 to 3.67 pg BEQ·g−1d.m., and in the torrefied biomass between 0.17 and 6.00 pg BEQ·g−1d.m.; BEQ stands for bioanalytical equivalent. This increase is statistically insignificant at p = 0.05, taking into account all types of examined biomass. This proves that low-temperature torrefaction cannot detoxify biomass, i.e., chars, produced from biomass characterized by elevated concentration of PCDD/PCDF/dl-PCB, will reflect the contamination of the feedstocks. With respect to heavy metals, we conclude that only the content of Cd in biomass, and, to a lesser extent, the abundance of Cu and Fe, modify the toxicity of this material during its thermochemical treatment at low temperature.