Comprehensive evaluation of bioavailable phosphorus in biochar synthesized by co-pyrolysis of sewage sludge and straw ash.

The world's phosphorus (P) resources are gradually depleting. Sewage sludge is an important secondary P resource, and sludge-derived biochar for land use is an effective way to achieve P recovery. However, P in biochar synthesized by direct pyrolysis of sludge usually shows comparatively low bioavailability. In this study, biomass ash from different types of straw was used as an additive for co-pyrolysis with sludge. The distribution of different P fractions in the obtained co-pyrolyzed biochar was investigated. The P bioavailability of the co-pyrolyzed biochar was comprehensively evaluated by three methods, including chemical extraction, diffusive gradients in thin films (DGT) technology and pot experiments. The results indicate that the bioavailable P in co-pyrolyzed biochar is significantly positively correlated with the contents of K, Ca, and Mg elements in straw ash, which facilitate the transformation of P in sludge into forms that are more easily utilized by plants, including monetite (CaHPO4), hydroxyapatite (Ca5(PO4)3OH) and pyrocoproite (K2MgP2O7). Moreover, pot experiments show that the P contents in ryegrass shoots and roots cultivated in co-pyrolyzed biochar-added soils increased by 11.98-114.97 % and 28.90-69.70 %, respectively, compared to the control soil. The DGT technology could better reflect the uptake of P by plants with a Pearson correlation coefficient as high as 0.94. This study provides references for P resource recovery, and the collaborative reutilization of sewage sludge and straw ash.

Dioxin concentrations and congener distribution in biomass ash from small to large scale biomass combustion plants.

Biomass plays a pivotal role in global energy production, with a significant share allocated for industrial heat and power generation. The combustion of biomass generates biomass ash, which is widely utilized as a fertiliser. However, concerns arise regarding the presence of dioxins in biomass ash, which may limit its continued use. Dioxins are toxic compounds listed under the Stockholm Convention due to their persistence and detrimental effects on human health and the environment. This study investigates the dioxin content in biomass ashes produced in various combustion plants with a capacity of 1-50MWth in Estonia, where biomass is widely used for heating and power production. The research encompassed samples from nine biomass combustion plants with varying technical parameters considering both bottom and fly ash. Dioxin concentrations were determined for 7 polychlorinated dibenzo-p-dioxins (PCDDs), 10 polychlorinated dibenzofurans (PCDFs), and 12 dioxin-like PCBs (PCBs). The results indicate that dioxin TEQ content in all samples was well below the European Union's (EU) POP Regulation limit of 5 µg TEQ/kg, with most values being at least tenfold lower. However, some samples failed to meet the EU Fertilising Products Regulation's threshold of 20 ng TEQ/kg. Notably, fly ash exhibited higher dioxin concentrations than bottom ash. While PCBs were in significant concentrations, PCDDs dominated the overall dioxin TEQ content. This study provides essential insights into the dioxin content in biomass ash and its correlation with current EU regulatory limits. It also highlights the complex distribution of dioxin congeners, particularly PCBs, within biomass ash, emphasizing the continued research's importance.

Substantial CO2 uptake by biomass ashes under natural condition in China.

A considerable amount of biomass ashes, resulting from agricultural waste field burning, wildfire, and solid biofuel incineration, is typically discarded in field or stored in dumps, where the alkaline oxides (CaO, MgO) they contain undergo carbonation and weathering-erosion processes over extended periods, continuously absorbing CO2 from the atmosphere and soil. However, their CO2 absorption behavior under natural conditions remains insufficiently explored in China. Using life cycle assessment (LCA) and material flow analysis (MFA) methods, this study developed a CO2 absorption analysis model for biomass ashes under natural conditions. We estimated the CO2 absorption of 9 different types of biomass ash from 1950 to 2022 through Monte Carlo uncertainty simulation. The results show that biomass ashes in China absorbed approximately 24.17Mt/year (95 % CI, 11.10-43.56) of CO2 under nature conditions, with the annual average CO2 uptake showing a steady increase from 1950 to 2022. The total CO2 uptake reached 856.85Mt (95 % CI, 368.73-1526.01) over these decades, mainly due to the significant contribution of biomass ash produced by domestic straw burning and fuelwood combustion, which accounted for 51.97 % and 22.08 %, respectively. Our findings highlight the substantial carbon sink benefits of biomass ash, providing valuable insights for further studies on carbon cycles in natural ecosystems and the potential integration of biomass ash in Carbon Capture, Utilization, and Storage (CCUS) technologies.

Elemental composition of post-wildfire biomass ashes and partly burned woody species in Bohemian Switzerland National Park, Czech Republic.

The study explored the post-wildfire elemental composition of parts (wood, bark, branch, cone, trunk, litter, twig, needle, sward, fallow, sapling, etc.) and by-products (biomass ashes, partly burnt parts, and char) of different woody species in the Bohemian Switzerland National Park, Czech Republic, and considered their effects on soils. Multi-elemental analysis of the fire by-products of the woody species was determined with inductively coupled plasma-optical emission spectrometry and mass spectrometry and compared with control biomass samples unaffected by wildfire. Most fire by-products were slightly alkaline, with acidic ashes obtained from blueberry wood. The by-products of the wildfire were characterized by varied total contents of macro (P, Ca, K, Mg, and S), micro (Na, Mn, Fe, Cu, and Zn), and other elements (B, Co, Mo, and V) vital to soil fertility and plant growth. The mean content of macro elements in the biomass ashes was up to 4.16 P, 23.5 Ca, 2.48 Mg, 63 K, and 5.57 S g kg-1. These values were comparatively lower than published data for ashes obtained under optimized conditions, e.g., those combusted in power generation facilities. Conversely, partly burnt parts-an indication of incomplete combustion-had higher 9.22 P, 79 Ca, and 5.99 Mg g kg-1 contents in spruce needles than in biomass ashes and the control. Variations in woody species and anthropogenic activities in areas of wildfires produced varied As, Cd, Cr, Ni, and Pb contents above EU fertilizer regulation. Caution in applying biomass ashes from wildfires on fields is required due to risk/toxic elements input from anthropogenic activities. Wildfire effects on the elemental composition of woody species can provide information on plant parts most suitable for biomass ashes for soil and ecosystem safety.

Harnessing Ash for Sustainable CO2 Absorption: Current Strategies and Future Prospects.

This review explores the potential of using different types of ash, namely fly ash, biomass ash, and coal ash etc., as mediums for CO2 capture and sequestration. The diverse origins of these ash types - municipal waste, organic biomass, and coal combustion - impart unique physicochemical properties that influence their suitability and efficiency in CO2 absorption. This review first discusses the environmental and economic implications of using ash wastes, emphasizing the reduction in landfill usage and the transformation of waste into value-added products. Then the chemical/physical treatments of ash wastes and their inherent capabilities in binding or reacting with CO2 are introduced, along with current methodologies utilize these ashes for CO2 sequestration, including mineral carbonation and direct air capture techniques. The application of using ash wastes for CO2 capture are highlighted, followed by the discussion regarding challenges associated with ash-based CO2 absorption approach. Finally, the article projects into the future, proposing innovative approaches and technological advancements needed to enhance the efficacy of ash in combating the increasing CO2 levels. By providing a comprehensive analysis of current strategies and envisioning future prospects, this review aims to contribute to the field of sustainable CO2 absorption and environmental management.

Ashes from challenging fuels in the circular economy.

In line with the objectives of the circular economy, the conversion of waste streams to useful and valuable side streams is a central goal. Ash represents one of the main industrial side-products, and using ashes in other than the present landfilling applications is, therefore, a high priority. This paper reviews the properties and utilization of ashes of different biomass power plants and waste incinerations, with a focus on the past decade. Possibilities for ash utilization are of uttermost importance in terms of circular economy and disposal of landfills. However, considering its applicability, ash originating from the heat treatment of chemically complex fuels, such as biomass and waste poses several challenges such as high heavy metal content and the presence of toxic and/or corrosive species. Furthermore, the physical properties of the ash might limit its usability. Nevertheless, numerous studies addressing the utilization possibilities of challenging ash in various applications have been carried out over the past decade. This review, with over 300 references, surveys the field of research, focusing on the utilization of biomass and municipal solid waste (MSW) ashes. Also, metal and phosphorus recovery from different ashes is addressed. It can be concluded that the key beneficial properties of the ash types addressed in this review are based on their i) alkaline nature suitable for neutralization reactions, ii) high adsorption capabilities to be used in CO2 capture and waste treatment, and iii) large surface area and appropriate chemical composition for the catalyst industry. Especially, ashes rich in Al2O3 and SiO2 have proven to be promising alternative catalysts in various industrial processes and as precursors for synthetic zeolites.

Study on the solidification performance and mechanism of heavy metals by sludge/biomass ash ceramsites, biochar and biomass ash.

Industrial by-products are stored in large quantities in the open, leading to wasted resources and environmental pollution, and the natural environment is similarly faced with phosphate depletion and serious water and soil pollution. This study uses these by-products to produce a new sludge/biomass ash ceramsite that will be used to adsorb nitrogen and phosphorus from wastewater, and solidify heavy metals in the soil while releasing Olsen P. The sludge/biomass ash ceramsites are made using sewage sludge and biomass ash in a certain ratio calcined at high temperatures and modified for the adsorption of nitrogen and phosphorus from wastewater. Sludge/biomass ash ceramsites before and after phosphorus adsorption, biochar and biomass ash were compared to analyze their heavy metal adsorption capacity and potential as phosphate fertilizer. After phosphorus adsorption, the sludge/biomass ash ceramsites released effective phosphorus steadily and rapidly in the soil, with a greater initial release than biochar and biomass ash, and the ceramsites were in a granular form that could be easily recycled. Biochar and biomass residue, due to their surface functional groups, are better at solidifying heavy metals than sludge/biomass ash ceramsites. Biochar, biomass ash and sludge/biomass ash ceramsites significantly reduced the concentrations of Cd, Cu, Pb and Zn in the soil. Correlation analysis demonstrated that there was a synergistic relationship between the increase in soil Olsen P content and the change in pH, with the increase in soil Olsen P content and the increase in pH contributing to heavy metal solidification.

Study of the Pozzolanic Reactivity of Sugar Cane Straw Ashes (SCSA) Burned under Controlled Conditions.

The aims of this work were to evaluate the reactivity of sugarcane straw ashes (SCSA) burned under controlled conditions and to analyze their reactivity in blended cement and hydrated lime pastes by thermogravimetric analysis (TG) and calorimetry. Four different ashes were produced, and burned at 600 °C, 700 °C, 800 °C and 900 °C (SCSA600, SCSA700, SCSA800 and SCSA900, respectively). These ashes were characterized by X-ray fluorescence spectroscopy, X-ray diffractometry, particle size distribution by laser diffraction and specific area surfaces to assess their potential interest in the partial replacement of inorganic binders (Portland cement (OPC) and hydrated lime). The hydrated lime pastes were subjected to scanning electron microscopy (SEM) and TG. The blended cement pastes were analyzed by TG and calorimetry, compressive strength testing and mercury intrusion porosimetry. High lime fixation percentages were observed in the hydrated lime and OPC pastes and were higher than 75% and 50% for the ashes burned at 600 °C and 700 °C, respectively. Calorimetry showed a delay in the heat release of SCSA600 and SCSA700 compared to the control paste. These pastes also had higher compressive strength and a smaller total pore volume. The results indicate the positive response of preparing sugar cane ashes under controlled conditions (mainly for straw calcined within the 600-700 °C range) for their use as pozzolanic addition by partially replacing inorganic binders.

Recovery of Phosphorus and Metals from the Ash of Sewage Sludge, Municipal Solid Waste, or Wood Biomass: A Review and Proposals for Further Use.

This review provides an overview of methods to extract valuable resources from the ash fractions of sewage sludge, municipal solid waste, and wood biomass combustion. The resources addressed here include critical raw materials, such as phosphorus, base and precious metals, and rare earth elements for which it is increasingly important to tap into secondary sources in addition to the mining of primary raw materials. The extraction technologies prioritized in this review are based on recycled acids or excess renewable energy to achieve an optimum environmental profile for the extracted resources and provide benefits in the form of local industrial symbioses. The extraction methods cover all scarce and valuable chemical elements contained in the ashes above certain concentration limits. Another important part of this review is defining potential applications for the mineral residues remaining after extraction. Therefore, the aim of this review is to combine the knowledge of resource extraction technology from ashes with possible applications of mineral residues in construction and related sectors to fully close material cycle loops.

Simultaneous adsorption of Cu(II), Zn(II), Cd(II) and Pb(II) from synthetic wastewater using NaP and LTA zeolites prepared from biomass fly ash.

Herein, NaP and LTA zeolites were successfully synthesised from woody biomass ash with alkali fusion-assisted hydrothermal method by altering the NaOH/ash ratio, crystallisation time and crystallisation temperature. In order to reduce the synthesis costs, NaP zeolite was synthesised with no additional source of aluminium and silicon. The synthesised zeolites were utilized for the monocomponent and simultaneous adsorption of Cu(II), Cd(II), Pb(II) and Zn(II) ions. The maximum adsorbed amount of metals had the trend Pb(II) > Cu(II) > Cd(II) > Zn(II) for both NaP and LTA zeolite. The kinetic data fit well to the pseudo-second order model indicating that chemisorption is the rate-limiting step. The isotherm data were well described with Sips and Redlich-Peterson models indicating a non-ideal heterogeneous adsorption process. Maximum adsorption capacity of NaP zeolite was 42.9 mg/g for Cu(II) and 117.3 mg/g for Cd(II), while LTA had 140.1 mg/g and 223.5 mg/g for Cu(II) and Cd(II) ions, respectively.

A Review on the Application of Lignocellulosic Biomass Ash in Cement-Based Composites.

With the development of society, the demand for cement-based composites is increasing day by day. Cement production significantly increases CO2 emissions. These emissions are reduced when high volumes of cement are replaced. The consideration of sustainable development has prompted people to search for new cement substitutes. The lignocellulosic biomass ash obtained from burning lignocellulosic biomass contains a large number of active oxides. If lignocellulosic biomass ash is used as a partial cement substitute, it can effectively solve the high emissions problem of cement-based composites. This review summarizes the physicochemical properties of lignocellulosic biomass ashes and discusses their effects on the workability, mechanical properties, and durability (water absorption, acid resistance, etc.) of cement-based composites. It is found that appropriate treatments on lignocellulosic biomass ashes are beneficial to their application in cement-based composites. Meanwhile, the issues with their application are also pointed out.

Methodology for Evaluating the CO2 Sequestration Capacity of Waste Ashes.

The concentration of CO2 in the atmosphere is constantly increasing, leading to an increase in the average global temperature and, thus, affecting climate change. Hence, various initiatives have been proposed to mitigate this process, among which CO2 sequestration is a technically simple and efficient approach. The spontaneous carbonation of ashes with atmospheric CO2 is very slow, and this is why accelerated carbonation is encouraged. However, not all ashes are equally suitable for this process, so a methodology to evaluate their potential should be developed. Such a methodology involves a combination of techniques, from theoretical calculations to XRF, XRD, DTA-TG, and the calcimetric determination of the CaCO3 content. The present study followed the approach of exposing ashes to accelerated carbonation conditions (4% v/v CO2, 50-55% and 80-85% RH, 20 °C) in a closed carbonation chamber for different periods of time until the maximum CO2 uptake is reached. The amount of sequestered CO2 was quantified by thermogravimetry. The results show that the highest CO2 sequestration capacity (33.8%) and carbonation efficiency (67.9%) were obtained for wood biomass bottom ash. This method was applied to eight combustion ashes and could serve to evaluate other ashes or comparable carbon storage materials.

Crop effect and mechanism of amino acid-modified biomass ash in remediation of cadmium-contaminated soil.

Lignocellulosic biomass ash (BA) has certain adsorption and passivation effects on heavy metals, but its function is generally weak. Amino acid salt can facilitate the leaching of heavy metals in soil. Therefore, modification of BA with amino acid salt may realize a higher leaching rate and better passivation of heavy metals in soil. In this study, BA was modified by amino acid hydrolysate obtained from the hydrolysis of chicken feathers by sulfuric acid. The physicochemical properties of BA and modified BA (MBA), their effects on Chinese cabbage (CC) yield and nutritional quality, and passivation effects on soil cadmium (Cd) were compared, and the related mechanisms were investigated. SEM-EDS, XRD, and FTIR demonstrated that BA was a CaCO3-type soil amendment, while MBA was a CaSO4-type soil amendment with the loading of amino acid. Compared with BA, MBA significantly increased the fresh weight, soluble sugar, vitamin C (Vc), and protein contents of CC in both non-Cd contaminated soil and Cd contaminated soil, and obviously decreased the nitrate content and Cd uptake of CC in Cd-contaminated soil. After the application of MBA, cadmium species in potted soil were transformed from higher plant availability, representing by exchangeable and carbonate-bound, into lower plant availability, representing by iron-manganese oxide bound, which was identified as the key reason for the significant reduction of Cd content in CC under MBA application.

Investigation of heavy metal and micro-macro element speciation in biomass ash enriched sewage sludge compost.

The objective of this study was to enrich the nutrient content of compost and to investigate the passivation and solubilization of plant micronutrients (Fe, Al, Cu, Ni, Zn, Na, Mn), macroelements (P, K, Mg, Ca), and heavy metals (Cr, Cd, Pb) during sewage sludge composting with nutrient-rich biomass ash additives. T0: 0%, T1: 3.5%, T2: 7.0%, and T3: 14.0% dry weight (DW), weight/weight (w/w) biomass ash was added to the sewage sludge + sawdust mixture (volume, 1:1) to obtain the final NPK content and monitored over a 45-day period. Sawdust was used as auxiliary material. The sequential extraction method was used to determine the elemental species. Cr, Cd and Pb showed higher affinity to the residual fraction and occluded in the oxide fraction, which decreased the bioavailability factor (BF) (<1% BF-Cr, 21% BF-Cd and 9% BF-Pb) compared to the control treatment (46% BF-Cr, 47% BF-Cd and 80% BF-Pb). As the amount of biomass ash increased (T1-T3), the percentages of residual Cr (Res-Cr) (10-65%), exchangeable Cd (Exc-Cd) and organically bound Cd (Org-Cd) (14% and 21%), and oxides-Pb (Oxi-Pb) (20-61%) increased. In all composts, Fe, Al, and Cu were associated with organically bound and oxides-entrapped fractions. More than 50% of total Mn and Mg were concentrated mainly in exchangeable fractions, suggesting high mobility and bioavailability (42% BF-Mn and 98% BF-Mg). Ni, Zn, and Na tended to be present in oxide-bound, organically bound, and residual fractions, while K and P were associated with exchangeable and organically bound fractions. The overall results suggest that composting sewage sludge with biomass ash may be the best strategy and technique to overcome soil application bottlenecks because it passivates heavy metals and improves the bioavailability of plant nutrients.

Characteristics of trace elements and potential environmental risks of the ash from agricultural straw direct combustion biomass power plant.

The rapid expansion of biomass power generation has resulted in a large amount of ash, which need to be treated urgently. The trace elements in ash also have environmental risks during treatment. Therefore, the essential characteristics and potential environmental risks of biomass ash generated by direct combustion of agricultural straw were studied. The leaching characteristics of elements, including major elements (Mg, K, Ca) and trace elements (V, Cr, Mn, Co, Ni, Cu, Zn, Cd, As, Pb and Ba), in fly ash and slag produced by biomass power plant were analyzed through the static leaching experiments of simulating the possible pH value of natural water in the laboratory. The results show that the trace elements are enriched in fly ash and slag, which may be related to the volatility of elements during combustion. And during the leaching test, the leaching concentration of major and trace elements in fly ash is higher than that in slag. Sequential chemical extraction is used to reveal the occurrence forms of trace elements in biomass ash. Except for residue, Mn, Co, Zn, Cd, and Pb in fly ash mainly exist in carbonate bound, V and As are Fe-Mn oxides bound, and Cr, Ni, Cu, and Ba are mainly organic matter bound. In the slag, Cd is mainly carbonate bound, Cu is mainly organic matter bound, while other elements are mainly Fe-Mn oxides bound. The Risk Assessment Code values calculated based on the existing forms of elements show that As and Cd in slag and Mn, Co, Pb and Cd in fly ash need special attention during utilization. The research results can provide reference for the management and utilization of biomass ash.

Synthesis of ordered mesoporous silica from biomass ash and its application in CO2 adsorption.

It is possible to achieve high-value utilization of solid wastes and lower the cost of mesoporous silica synthesis by synthesizing mesoporous silica from solid wastes. In this study, silica was extracted using the alkali fusion method using biomass ash as the starting material. Biomass ash based mesoporous silica was successfully prepared by hydrothermal method with silicon extract solution as silicon source. The optimum conditions for preparation were determined as follows: addition of cetyltrimethylammonium bromide was 0.45g, hydrothermal temperature was 120 °C, hydrothermal time was 24h. The prepared mesoporous silicon was systematically characterized, and the results showed that high surface area (495 m2/g) and ordered pore structure appeared in the synthesized mesoporous silica materials. The synthesized mesoporous silica showed excellent CO2 adsorption performance (0.749 mmol/g) at 25 °C and 1 bar. According to the calculation of adsorption isotherm and thermodynamics, non-linear Freundlich model can fit the adsorption isotherm better and the adsorption heat of mesoporous silica is less than 20 kJ/mol, which belongs to physical adsorption. After five cycles of CO2 adsorption, the adsorption property was still above 90%, and the CO2/N2 adsorption selectivity reached 396.6, showing good regeneration performance and adsorption selectivity. This research can provide a new possibility for the high-value exploitation of biomass ash and reducing the cost of synthetic mesoporous silica.

An extensive dataset on micromechanical behavior and microstructure of 1000 days old B/S-based alkali-activated material.

This dataset contains extensive results on micromechanical behavior and microstructure of alkali-activated materials (AAM) with biomass ash (B) and silica fume (S) precursors. The data were collected at the laboratories of the Federal Center for Technological Education of Minas Gerais (CEFET-MG) in Brazil. Scanning electron microscope (SEM), optical microscopy (OM), and nanoindentation with instrumented penetration (NI) were performed from AAM in the hardened state and advanced age (1000 days). Data include loading curves, hardness, module of elasticity, and microstructure. Data may be useful for researchers and engineers in designing new alternative binders with improved durability.

Application of Doehlert design in optimizing the solid-state hydrogenogenic stage augmented with biomass fly ash in a two-stage biohythane production process.

This study aimed to optimize the solid-state hydrogenogenic stage supplemented with biomass fly ash in a two-stage anaerobic digestion (AD) process for biohythane production from the organic fraction of municipal solid waste (OFMSW). Doehlert's experimental design was used to obtain the optimal set of two investigated variables, namely total solids (TS) content and biomass fly ash dosage in the defined ranges of 0-20 g/L and 20-40%, respectively. Applying the optimal conditions of TS content (29.1%) and fly ash dosage (19.2 g/L) in the first stage led not only to a total H2 yield of 95 mL/gVSadded, which was very close to the maximum H2 yield predicted by the developed model (97 mL/gVSadded), but also to a high CH4 yield of 400 mL/gVSadded (76% of the theoretical CH4 yield). Moreover, the biohythane obtained from the optimized two-stage process met the standards of a biohythane fuel with an H2 content of 19% v/v.

Adsorption mechanism of phosphorus on biomass ash modified with lanthanum immobilized by chitosan.

The immobilized lanthanum-modified biomass ash gel ball (CS-La-BA) was prepared with lanthanum chloride, biomass ash, and chitosan to remove phosphorus from water. CS-La-BA was characterized by several analytical techniques. SEM-EDS results showed that CS-La-BA has a well-developed pore structure and abundant adsorption sites. The surface area of BET is 75.46 m2/g and the pore size is mostly at 1.84 nm, indicating that it is a composite porous material with abundant microporous structure. The presence of La on biomass ash and the charge property of CS-La-BA were determined by XRD and zeta potential, and the adsorption mechanism of CS-La-BA on phosphate, including precipitation, electrostatic adsorption, ligand exchange, and complexation mechanism, was revealed by FTIR and XPS. The effects of pH, temperature, adsorbent dosage, initial phosphorus concentration, adsorption time, and coexisting ions on the phosphorus uptake performance of CS-La-BA were discussed. The adsorption experiment results show that the phosphorus removal rate of CS-La-BA can reach 95.6%. Even after six desorption and regeneration experiments, the phosphorus removal rate still reaches 68.13%, which indicates that CS-La-BA has good phosphorus adsorption performance and desorption and regeneration capacity. The phosphorus adsorption process of CS-La-BA conforms to the Freundlich isotherm adsorption equation and general-order kinetic model. The internal diffusion of the adsorption process is dominant, and the maximum adsorption capacity is 31.73 mg/g (25 ℃). Thermodynamic experiments show that the adsorption process of phosphorus by CS-La-BA is a spontaneous entropy increase process.

Regulation of ash slagging behavior of palm oil decanter cake by alum sludge addition.

Combustion of palm oil decanter cake (PODC) is a propitious alternative waste to energy means. However, the mono-combustion of PODC prompt severe ash slagging behavior which give rise to reduction in heat transfer and also shorten the lifespan of combustion reactors. In this study, alum sludge (AS) was introduced at different proportion of 30%, 50% and 70% to revamp the slagging characteristics of PODC during combustion. The addition of AS improved ash fusion temperature of PODC during co-combustion as ash fusion temperature increased significantly under high AS dosage. Slagging and fouling indices showed that at 50% AS addition, slagging tendency of the co-combustion ashes can be ignored. The predictive model for PODC-AS combustion showed good correlation coefficient with 0.89. Overall, co-combustion of PODC and AS is an ideal ash related problem-solving route. The proposed PODC slagging preventive method by AS was based on: (1) limited amount of aluminum content in PODC-AS system resulted in development of refractory ash (2) reduction in proportion of basic oxide which act as ash bonding glue played important role in the regulation of slagging (3) reduction of cohesive bond by formation of spongy and porous structure which prevented ash slagging.