Characteristics, application and modeling of solid amine adsorbents for CO2 capture: A review.

In recent years, global warming has become an important topic of public concern. As one of the most promising carbon capture technologies, solid amine adsorbents have received a lot of attention because of their high adsorption capacity, excellent selectivity, and low energy cost, which is committed to sustainable development. The preparation methods and support materials can influence the thermal stability and adsorption capacity of solid amine adsorbents. As a supporting material, it needs to meet the requirements of high pore volume and abundant hydroxyl groups. Industrial and biomass waste are expected to be a novel and cheap raw material source, contributing both carbon dioxide capture and waste recycling. The applied range of solid amine adsorbents has been widened from flue gas to biogas and ambient air, which require different research focuses, including strengthening the selectivity of CO2 to CH4 or separating CO2 under the condition of the dilute concentration. Several kinetic or isotherm models have been adopted to describe the adsorption process of solid amine adsorbents, which select the pseudo-first order model, pseudo-second order model, and Langmuir isotherm model most commonly. Besides searching for novel materials from solid waste and widening the applicable gases, developing the dynamic adsorption and three-dimensional models can also be a promising direction to accelerate the development of this technology. The review has combed through the recent development and covered the shortages of previous review papers, expected to promote the industrial application of solid amine adsorbents.

Biodrying with the hot-air aeration system for kitchen food waste.

Biodrying is a promising method that produces bio-stabilized output with minimum pretreatment requirements. In this study, a hot-air supply system was added to the traditional biodrying process for kitchen waste, which showed significant reduction in moisture content in 5 days (maximum reduction of 37.45%). A series of experiments was conducted to optimize the hot-air biodrying system utilizing different aeration rates, temperatures, and mixing ratios of feedstock to bulking agents. The results showed that a 65 °C aeration temperature led to the highest water removal rate and low volatile solids consumption rate, with the biodrying index reaching 4.9 g water per gram of volatile solids. On the other hand, evaluation of the overall biodrying efficiency based on the weight loss and bio-stabilization showed that intermittent aeration temperature at 55 °C performed best, offering suitable conditions for water evaporation and bio-degradation. In combination with a flow rate of 0.8 L/kg*min and 1:1 mixing ratio, these conditions resulted in the maximum volatile solids consumption of 26.26% in 5 days. The volatile solids consumption and 34.47% water removal rate of the trial had contributed to a total of 64.13% weight loss. The weight loss was even higher than that of a conventional biodrying system which was conducted for more than 14 days.

Enhancement of volatile fatty acid production and biogas yield from food waste following sonication pretreatment.

The positive effect of sonication on volatile fatty acid (VFA) and hydrogen production was investigated by batch experiments. Several sonication densities (2, 1.6, and 1.2 W/mL) and times (5, 10, and 15 min) were tested. The optimal sonication condition was ultrasonic density 2 W/mL and ultrasonic time 15 min (2-U15). The FW particle size larger than 50 µm (d > 50 µm) were more susceptible to the sonication treatment than the smaller particle size (d ≤ 50 µm). The SCOD increased and VS reduction accelerated under sonication treatment. The maximum VFA production and the highest proportion of hydrogen in the biogas increased 65.3% and 59.1%, respectively, under the optimal sonication conditions compared to the unsonicated batch. Moreover, a reduction of over 50% in the time required to reach its maximum production was also observed. Butyric acid fermentation type was obtained whether following sonication treatment or not. The composition of key microbial community differed under the various sonication conditions. The genera Clostridium and Parabacteroides are predominantly responsible for VFA generation and both were found to be abundant under the optimal condition.

A review on the evaluation models and impact factors of greenhouse gas emissions from municipal solid waste management processes.

The total amount of global municipal solid waste (MSW) will reach 3.5 billion tons by 2050, thereby bringing tremendous environmental pressure, especially global warming. Large amounts of greenhouse gases (GHGs) have been released during MSW management (MSWM). Accounting for GHG emissions is a prerequisite for providing recommendations on appropriate treatment options to mitigate emissions from MSWM systems. There are many methods involved in estimating emissions. This paper summarizes the computing models commonly used in each process of the integrated MSWM system and emphasizes the influence of parameters and other factors. Compared with other disposal methods, landfilling has the highest emissions, commonly estimated using first-order decay (FOD) methods. Emission reduction can be realized through waste to energy (WtE) and resource recovery measures. IPCC is commonly used for calculating direct emissions, while LCA-based models can calculate emissions including upstream and downstream processes, whose results depend on assumptions and system boundaries. The estimation results of models vary greatly and are difficult to compare with each other. Besides, large gaps exist between the default emission factors (EFs) provided by models and those F measured in specific facilities. These findings provide a systematic view for a bettering understanding of MSW emissions as well as the estimating methods and also reveal the key points that need be developed in the future.

Comprehensive study of recycling municipal solid waste incineration fly ash in lightweight aggregate with bloating agent: Effects of water washing and bloating mechanism.

Recycling into lightweight aggregate (LWA) by sintering is a promising technology for disposal of municipal solid waste incineration fly ash (FA). In this study, FA and washed FA (WFA) were combined with bentonite and SiC (bloating agent) to make LWA. The performance was comprehensively studied by hot-stage microscopy and laboratory preparation experiments. Water washing and increased FA/WFA improved LWA bloating extent, while shorten the bloating temperature range. Water washing also increased the 1 h-water absorption rate of LWA, making it harder to meet the standard. Excessive FA /WFA usage (70 wt%) will prevent LWA from bloating. For the goal of recycling more FA, mixture with 50 wt% WFA could prepare LWA that meet standard GB/T 17431 at 1140-1160 °C. After water washing, the ratio of Pb, Cd, Zn, and Cu stabilized in LWA increased by 279 %, 410 %, 458 %, and 109 % for 30 wt% FA/WFA addition, and 364 %, 554 %, 717 %, and 697 % for 50 wt% FA/WFA addition, respectively. The change of liquid phase content and viscosity at high temperature were determined using the thermodynamic calculations and chemical compositions. The bloating mechanism was further investigated by integrating these two properties. To obtain accurate results of the bloat viscosity range (2.75-4.44 log Pa·s) for high CaO systems, the composition of the liquid phase should be taken into account. The liquid phase viscosity required for bloating start was proportional to the liquid phase content. With temperature increasing, bloating would end when viscosity drops to 2.75 log Pa·s or liquid phase content reach 95 %. These findings provided further understanding of the heavy metal stabilization during LWA production and the bloating mechanism of high CaO content systems, and could contribute to the feasibility and sustainability of recycling FA and other CaO-rich solid wastes into LWA.

Analysis of enrichment, correlation, and leaching patterns of rare earth elements in coal fly ash assisted by statistical measures.

Coal fly ash (CFA) is a typical industrial solid waste, which has recently been reported to contain rare earth elements (REEs). REEs are important materials in many industrial fields. Therefore, extracting REEs from CFA becomes a win-win strategy to both make full use of CFA and reclaim REEs. However, the stable crystalline structure of CFA is hard to break, which limits the extraction of REEs. The inter-correlation and the leaching patterns of the REEs in CFA also remain unclear. In this work, REEs were enriched by desilication, and the correlation and the influences of multiple acids of the leached REEs were investigated. It was found that desilication could increase the leachable amount of REEs from 137.37 ppm to 346.12 ppm. The light rare earth elements (LREEs) were less inter-correlated than heavy rare earth elements (HREEs) and desilication enhanced the leaching of LREEs more than that of HREEs. The ratio and type of the leaching acids both influenced the extraction of REEs from CFA: HCl and HF played important roles in the extraction from the untreated CFA while HNO3 and HF were more decisive for the desilicated CFA. In addition, we used statistical analysis to quantificationally confirm that desilication and acids both significantly influenced the extraction of REEs. This work provides evidence for the enrichment of REEs in CFA and acid choosing when leaching REEs from CFA.

A green and multi-win strategy for coal fly ash disposal by CO2 fixation and mesoporous silica synthesis.

Coal combustion provides plenty of energy, along with enormous coal fly ash (CFA) and CO2 emission. CFA could be recycled for mesoporous silica synthesis, but expensive templates are usually needed. In this work, we proposed a multi-win strategy using CO2 as the precipitator and template. Mesoporous silica powders, with a maximum specific surface area of 355.45 m2/g, a pore volume of 0.73 cm3/g, and an average pore size of around 7.67 nm, were synthesized. The influences of silicon concentration, CO2 flow rate, and ultrasound were investigated. In addition, the Na2CO3 by-product was produced with a purity of over 92 %. By averagely calculating, 1 ton CFA could generate 285 kg mesoporous silica and 1.02 t crude Na2CO3. Around 433 kg of CO2 could be absorbed. Therefore, multi-goals of CFA disposal, CO2 storage, and valuable silica materials production were realized, and the study could pave the way for large-scale industrial applications.

A review on the applications of microbially induced calcium carbonate precipitation in solid waste treatment and soil remediation.

Improper disposal and accumulation of solid waste can cause a number of environmental problems, such as the heavy metal contamination of soil. Microbially induced calcium carbonate precipitation (MICP) is considered as a promising technology to solve many environmental problems. Calcium-based solid waste can be utilized as an alternative source of calcium for the MICP process, and carbonate-based biominerals can be used for soil remediation, solid waste treatment, remediation of construction concrete, and generation of bioconcrete. This paper describes the metabolic pathways and mechanisms of microbially induced calcium carbonate precipitation and highlights the value of MICP for solid waste treatment and soil remediation applications. The factors affecting the effectiveness of MICP are discussed and analyzed through an overview of recent studies on the application of MICP in environmental engineering. The paper also summarizes the current challenges for the large-scale application of this innovative technology. In prospective study, MICP can be an effective alternative to conventional technologies in solid waste treatment, soil remediation and CO2 sequestration, as it can reduce negative environmental impacts and provide long-term economic benefits.

Manufacture of alkali-activated and geopolymer hybrid binder (AGHB) by municipal waste incineration fly ash incorporating aluminosilicate supplementary cementitious materials (ASCM).

The treatment and disposal of municipal solid waste incineration fly ash (MSWI FA) faces many challenges, such as landfill space occupation, high costs and potential environmental threats. In this study, coal fly ash (CFA), metakaolin (MK) and silica fume (SF) were used as aluminosilicate supplementary cementitious materials (ASCM), and mixed with MSWI FA as precursors for the synthesis of alkali-activated and geopolymers hybrid binder (AGHB). The results show that this alkali-activated technology efficiently immobilized the heavy metals in MSWI FA, and the ASCM contributes to the compressive strength enhancement of the AGHB. The highest compressive strength of the synthesized products that mixed MSWI FA with CFA and MK as precursors, reached 5.34 and 9.06 MPa, respectively. The compressive strength of the ASCM synthesized by mixing MSWI FA and SF in the mass ratio of 70:30 with the alkali activator modulus of 1.6 M could reach 11.2 MPa after 28 d of curing, which met the quality standard of MU10 (NY/T 671-2003) for load-bearing brick.The leaching concentrations of Hg and Pb were reduced from 0.15 to 3.96 mg/L to less than 0.003 and 0.107 mg/L, which were below the limit established by the Chinese standard (GB 8978-1996). The research provides the technical parameters of the optimization conditions on the synthesis of MSWI FA-based AGHB, for the resource utilization of MSWI FA and reduction of the environmental risk.

Recycling municipal solid waste incineration fly ash in super-lightweight aggregates by sintering with clay and using SiC as bloating agent.

Municipal solid waste incineration (MSWI) fly ash is classified as hazardous waste and requires proper treatments. Sintering of MSWI fly ash for the production of lightweight aggregate (LWA) is a promising treatment technology, while the dependence on natural bloating clay to produce high quality LWA has limited its wide application. In this study, by using SiC as a bloating agent, normal clay could be used to produce super-lightweight aggregate (bulk density <500 kg/m3) with MSWI fly ash. Effects of SiC addition amount, sintering temperature and duration on LWA performance were studied. The results showed that LWA with SiC addition of 0.1-0.5 wt% had significant expansion at sintering temperature of 1120 °C-1160 °C. The optimal conditions were 0.3 wt% SiC addition and sintering at 1120 °C for 30 min, and the bulk density could reach 212 kg/m3 with other properties meeting the LWA standard (GB/T 17431.1-2010). Further, the heavy metal leaching toxicity was significantly decreased after sintering and met the MSWI fly ash utilization standard (HJ 1134-2020). The X-ray diffraction results revealed the formation of a complex diopside-based phase after sintering. This study provides a new approach for recycling MSWI fly ash in LWA without dependence on specific clay resources, and makes this technology wider applicability.

Effect of microbially induced calcium carbonate precipitation treatment on the solidification and stabilization of municipal solid waste incineration fly ash (MSWI FA) - Based materials incorporated with metakaolin.

Microbially induced calcium carbonate precipitation (MICP) has been considered as a potential treatment method for the solidification and stabilization of municipal solid waste incineration fly ash (MSWI-FA).The main obstacle for MICP treatment of MSWI-FA is the harsh environment which causes the bacteria fail to maintain their urease activity effectively, thus decreases the solidification effect and material properties. Currently, there is no research on blending metakaolin (MK) as a protective carrier for the bacteria into the MSWI-FA. The effect of the MICP process on the curing properties of MSWI FA-based cementing materials in the MK and MSWI-FA reaction system is largely unknown. In this study, different mixing ratios of MK were used to adjust the Ca/Si/Al ratio in the mixture, and the properties of the cementing material (MSWI-FA mixed with MK and water) and the MICP-treated material (MSWI-FA mixed with MK and bacterial solution) were investigated. This study contributes to find suitable additives to promote effect of MICP on the solidification of MSWI-FA and the improvement of material properties. The results showed when the mixing ratio of MSWI FA was 90 wt %, the MICP treatment was able to increase the compressive strength of the samples up to 0.99 Mp, and the compressive strength of samples reached 1.46 MPa, when the mixing ratio of MSWI FA was 80 wt %. Though the metakaolin did not show inhibitory effect on the urease activity, the compressive strength of the MICP-treated samples did not further show a significant increase when the mixture of MK was increased from 20 wt% to 30 wt%. Further investigation suggested that MICP activities of bacteria utilizing calcium sources could have an impact on the formation/deformation of calcium-containing hydration products in the reaction system, thus affecting the mechanical and chemical properties of MSWI based materials. MICP treatment is effective in the immobilization of certain heavy metals of MSWI FA, especially for Pb, Cd and Zn. This research shows the potential of using MICP to treat the MSWI fly ash, meanwhile, it is necessary to find suitable reaction system with the proper additives in order to further improve the properties of the MSWI FA based material in terms of mechanical performance.

On the state of the art of crystalline structure reconstruction of coal fly ash: A focus on zeolites.

Coal fly ash (CFA) is fine particles generated from coal combustion, and large amount of CFA causes environmental pollution. Traditionally, CFA is added into construction materials, which has realized effective reduction. As the exploration of CFA properties goes deeper, finer utilization has been studied to maximize the recycling of CFA. Summarized from plenty of investigations, structure reconstruction has become the most crucial part for re-production as well as pre-treatments. Various zeolites and other complex materials have been synthesized by structure reconstruction. In this work, the state of the art of structure reconstruction were technically collated in the order of pre-treatments, mechanisms, specific techniques, and novel optimizing strategies. It has been found the crystalline types are closely related to the reaction conditions, that certain types of products could be obtained via accurate condition controls, especially the ratio of Si to Al. The current as-synthesized products were listed as well as their crystalline structure characteristics. Recently, combined materials and techniques have been innovatively investigated. However, the challenge remains as low purity, not only impurities in CFA but also different types of zeolites formed in one process.

Insights into the Critical Role of Abundant-Porosity Supports in Polyethylenimine Functionalization as Efficient and Stable CO2 Adsorbents.

The emerging polyethylenimine (PEI)-functionalized solid adsorbents have witnessed significant development in the implementation of CO2 capture and separation because of their decent adsorption capacity, recyclability, and scalability. As an indispensable substrate, the importance of selecting porous solid supports in PEI functionalization for CO2 adsorption was commonly overlooked in many previous investigations, which instead emphasized screening amine types or developing complex porous materials. To this end, we scrutinized the critical role of different commercial porous supports (silica, alumina, activated carbon, and polymeric resins) in PEI impregnation in this study, taking into account multiple perspectives. Hereinto, the present results identified that abundant larger pore structures and surface functional groups were conducive to loading a considerable amount of PEI molecules. Various supports after PEI functionalization had great differences in adsorption capacities, amine efficiencies, and the corresponding optimal temperatures. In addition, more attention was paid to the role of porous supports in long-term stability during the consecutive adsorption-regeneration cycles, while N2 and CO2 purging as regeneration strategies, respectively. Especially, CO2-induced degradation due to urea species formation was specifically recognized in a SiO2-based adsorbent, which would induce serious concerns in CO2 cyclic capture. On the other side, we also confirmed that adopting conventional porous supports, for example, HP20, could achieve superior adsorption performance (above 4 mmol CO2/g) and cyclic stability (around 1% loss after 30 cycles) rather than the ones synthesized through complex approaches, which ensured the availability and scalability of PEI-functionalized CO2 adsorbents.

An investigation of the effect of ultrasonic waves on the efficiency of silicon extraction from coal fly ash.

Burning of coal accounts for an enormous proportion of the current energy supply, especially in developing countries. Burning of coal produces large amounts of coal fly ash, which causes serious environmental problems unless it is managed properly. Using chemical analysis, we found that coal fly ash could be a promising source of Si, Al, Ca and some rare earth elements, especially with the assistance of some measures such as ultrasound. In this study, we extracted silicon from coal fly ash using an alkaline dissolution strategy and investigated the effects of temperature and ultrasonic power on the efficiency of silicon extraction. During a 70 min reaction, the efficiency of silicon extraction increased markedly, from 9.41% to 34.96%, as the reaction temperature increased from 70 °C to 110 °C. With ultrasound assistance, ultrasonic waves enhanced the extraction of silicon at both 80 °C and 110 °C at 720 W ultrasound, increasing the efficiency of silicon extraction from 6.01% to 15.36% and from 34.96% to 54.42%, respectively. However, at 900 W ultrasonic power, extraction was slightly inhibited at both temperatures, causing a little decrease in efficiency.

Feasibility of CO2 Capture from O2-Containing Flue Gas Using a Poly(ethylenimine)-Functionalized Sorbent: Oxidative Stability in Long-Term Operation.

Amine-functionalized sorbents are investigated widely for CO2 capture from flue gas, to mitigate the crisis of global CO2 emission, with the advantages of excellent adsorption and regeneration performance. However, the presence of O2 in flue gas (3-10%) would induce the degradation of the sorbents, and some previous works proposed the strategies at the sacrifice of partial CO2 adsorption capacity. Herein, we focused on the oxidation behavior of PEI-functionalized silica in the long-term operation and analyzed the degradation mechanism by characterizing the oxidized sorbents. The sorbent proved to be oxidative stable under a lower temperature of air exposure, but the oxidative degradation would indeed occur at more harsh temperatures (above 90 °C). This study demonstrated that CO2 capture from O2-containing flue gas was feasible by controlling the operating temperature (below 75 °C), and the effective capacity of above 135 mg/g could be maintained in the cyclic CO2 capture.