Search Results (11)

TiVNbZrCr high-entropy intermetallic alloy was investigated as a deuterium storage material using gravimetric sorption measurements, thermogravimetric analysis, and temperature-resolved synchrotron X-ray diffraction during deuterium desorption. The as-prepared alloy had an experimentally determined composition of Ti₁₇V₁₉Zr₁₉Nb₂₂Cr₂₃ and a density of 6.59 g·cm⁻³. Empirical alloy-design parameters indicate that the alloy is not a single-phase bcc solid solution, but rather a compositionally complex intermetallic alloy. The calculated hydrogen-affinity descriptors suggest a strong thermodynamic driving force for deuteride formation. Under 5 MPa D₂, the alloy absorbed 3.28 wt.% D, corresponding to D/M = 1.1. After ex situ deuteration, additional diffraction reflections were indexed using tetragonal deuteride reference structures corresponding to ZrV₂D_2.35 and TiD₂, while the Cr-rich bcc phase remained comparatively stable. Thermal desorption released 2.28 wt.% D up to 600 °C in three partially overlapping steps. These results demonstrate that deuterium storage in TiVNbZrCr is governed by phase-selective deuteride formation and decomposition rather than by homogeneous bcc lattice expansion. Full article

Green and Sustainable Remediation (GSR) has become a guiding framework for selecting remediation solutions for contaminated sites. However, in practice, there is a lack of quantitative decision support tools that can reflect the multi-dimensional environmental, social, and economic objectives of GSR. To address this, a GSR alternative decision-making model was developed, integrating the Criteria Importance Through Intercriteria Correlation (CRITIC) method and the Entropy Weight method for weighting, combined with the Technique for Order Preference by Similarity to an Ideal Solution (TOPSIS) for ranking. A preference coefficient was introduced to simulate four typical decision-making scenarios: balanced-preference, health-sensitive, economy-priority, and low-carbon constraint scenarios. Empirical analysis was conducted using three remediation alternatives for a complex contaminated site in Jiangsu Province, China. The results indicate that the optimal alternative selection is highly dependent on decision preferences: under the balanced scenario and low-carbon constraint scenario, Alternative 1 (Cement Kiln Co-processing, CKC) is optimal; under the health-sensitive scenario and economy-priority scenario, Alternative 3 (Ex situ Solidification/Stabilization + Ex situ Thermal Desorption, ESS + ESTD) is optimal. Furthermore, uncertainty analysis demonstrates the robustness of the proposed model. Full article

Remediating complex-contaminated soils demands the synergistic optimization of efficiency, cost-effectiveness, and carbon emission reduction. Currently, ultra-high-temperature thermal desorption technology is mature in terms of principle and laboratory-scale performance; however, ongoing efforts are focusing on achieving stable, efficient, controllable, and cost-optimized operation in large-scale engineering applications. To address this gap, this study aimed to (1) verify the energy efficiency and economic benefits of removing over 98% of target pollutants at a 7.5 × 10⁴ m³ contaminated site and (2) elucidate the mechanisms underlying parallel scale–technology dual-factor cost reduction and energy–carbon–cost optimization, thereby accumulating case experience and data support for large-scale engineering deployment. To achieve these objectives, a “thermal stability–chemical oxidizability” classification criterion was developed to guide a parallel remediation strategy, integrating ex situ ultra-high-temperature thermal desorption (1000 °C) with persulfate-based chemical oxidation. This strategy was implemented at a 7.5 × 10⁴ m³ large-scale site, delivering robust performance: the total petroleum hydrocarbon (TPH) and pentachlorophenol (PCP) removal efficiencies exceeded 99%, with a median removal rate of 98% for polycyclic aromatic hydrocarbons (PAHs). It also provided a critical operational example of a large-scale engineering application, demonstrating a daily treatment capacity of 987 m³, a unit remediation cost of 800 CNY·m⁻³, and energy consumption of 820 kWh·m⁻³, outperforming established benchmarks reported in the literature. A net reduction of 2.9 kilotonnes of CO₂ equivalent (kt CO₂e) in greenhouse gas emissions was achieved, which could be further enhanced with an additional 8.8 kt CO₂e by integrating a hybrid renewable energy system (70% photovoltaic–molten salt thermal storage + 30% green power). In summary, this study establishes a “high-temperature–parallel oxidation–low-carbon energy” framework for the rapid remediation of large-scale multi-contaminant sites, proposes a feasible pathway toward developing a soil carbon credit mechanism, and fills a critical gap between laboratory-scale success and large-scale engineering applications of ultra-high-temperature remediation technologies. Full article

This study explored the influence of hydrogen on the tensile properties and fracture behavior of high-strength API X70 and X80 linepipe steels with bainitic microstructures under varying hydrogen charging conditions. The X70 steel exhibited a ferritic microstructure with some pearlite, while the X80 steel showed a bainitic microstructure and fine pearlite due to the addition of molybdenum. Slow strain rate tests (SSRTs) were conducted using both electrochemical ex situ and in situ hydrogen charging methods subjected to different current densities. The SSRT results showed that in situ hydrogen-charged SSRT, performed at current densities above 1 A/m², led to more pronounced hydrogen embrittlement compared to ex situ hydrogen-charged SSRT. This occurred because hydrogen was continuously supplied during deformation, exceeding the critical concentration even in the center regions, leading to quasi-cleavage fractures marked by localized cleavage and tearing ridges. Thermal desorption analysis (TDA) confirmed that a greater amount of hydrogen was trapped at dislocations during in situ hydrogen-charged SSRT, intensifying hydrogen embrittlement, even with a shorter hydrogen charging duration. These findings highlight the importance of selecting appropriate hydrogen charging methods and understanding the hydrogen embrittlement behavior of linepipe steels. Full article

Greenhouse gas emissions induced by climate change have garnered global attention. Minimizing climate change can be achieved through the reduction of carbon emissions in transportation infrastructure construction and in the production of construction materials. This study aims to calculate carbon emissions in three hypothetical construction scenarios based on the life cycle assessment (LCA) method when a roadway passes across polluted soil at contaminated sites. Three methods are employed to remediate contaminated soil: off-site cement kiln co-processing, on-site ex-situ thermal desorption, and on-site ex-situ solidification/stabilization. Carbon emissions are calculated using the LCA method for each scenario. The baseline carbon emission is estimated for the scenario in which contaminated soil is remediated using the off-site cement kiln co-processing method, and the roadway subgrade is constructed using transported clean soil. In the other two scenarios, contaminated soils are remediated using the on-site ex-situ thermal desorption and solidification/stabilization methods, respectively, and then they are reused as roadway subgrade materials. The LCA analyses demonstrate that the total carbon emission reductions range from 1168.48 to 2379.62 tons per basic unit, corresponding to decreased of 19.31% to 39.33%, respectively, compared to baseline. The reuse of solid waste to replace sand and ordinary Portland cement (OPC) as raw materials in roadway construction reduces carbon emissions by 498.98 tons. Finally, a comparison of carbon emissions between the three scenarios indicates that reducing carbon emissions in the remediation of contaminated soil and reusing solid waste as construction materials are two important methods for achieving overall carbon emission reductions in roadway construction projects. Full article

To study the synergistic catalysis of an ex situ catalyst and in situ clay in the aquathermolysis of heavy oil, in this paper, a series of bentonite-supported catechol-metal complexes were prepared, and the catalytic viscosity reduction performance in the aquathermolysis of heavy oil was investigated. Under the optimized conditions, the viscosity can be reduced by 73%, and the pour point can be lowered by 15.0 °C at most, showing the synergistic catalysis of the ex situ catalyst and in situ clay in this aquathermolytic reaction. Thermogravimetry, physical adsorption-desorption, and scanning electron microscopy were conducted to characterize the thermal stability and microstructure of the ex situ catalyst. The components of the heavy oil before and after the reaction were fully characterized. Six model compounds were used to simulate the aquathermolysis reaction process. In order to study the mechanism of viscosity reduction after the catalytic aquathermolysis reaction, the compounds were analyzed by GC-MS. It is believed that these results will be beneficial in the future for related research in this field. Full article

The effect of Al addition on the structure, microstructure and hydrogen storage properties of the ternary TiVNb alloy was investigated from small amounts to equimolar composition. Al_x(TiVNb)_1−x (x = 0.05, 0.175 and 0.25) alloys are bcc single-phase materials with decreasing lattice parameters with increasing Al content. Al addition progressively decreases the hydrogen storage capacity but also destabilizes fcc dihydride formation for alloys with x ≤ 0.10. Among the different compositions, the most promising alloy was found to be that with x = 0.05 Al content that exhibited high initial storage capacity (2.96 wt.%), a less stable hydride (ΔH = −52 kJ/mol H₂ and ΔS = −141 J/K∙mol H₂), better desorption properties (desorption onset temperature around 100 °C) and enhanced reversible capacity during cycling (2.83 wt.%) compared to the ternary TiVNb. In situ and ex situ synchrotron X-ray powder diffraction, together with thermal desorption experiments, showed improved desorption properties with Al addition, together with a two-step reaction with hydrogen. These findings highlight the use of small quantities of lightweight Al in refractory multi-principal element alloys as a promising approach for enhancing the solid-state hydrogen storage performance of bcc-type alloys. Full article

The article describes the remediation of contaminated groundwater during the ex situ remediation of coal tar contamination following the closure of a coking plant in the Moravian–Silesian Region (Czech Republic). The aim of the article is to point out the advantages of ex situ soil remediation via the excavation of the contaminated geological environment combined with thermal desorption, a method of removing contaminants both from soil and groundwater. Its advantage is the absolute qualitative and quantitative control over the contaminated soil with the possibility of precise segmentation into contaminated and non-contaminated soils. Next, all contaminated groundwater may be pumped off upon the construction of sealing walls to control groundwater flows. To excavate the soil, it is necessary to reduce the contaminated groundwater level inside the sealing walls and thus create conditions for the extraction of contaminated soils using standard machinery. In detail, the article describes the removal of the contaminated groundwater and compares the quality of the pumped and inflowing water before and after the remediation. The locality is characteristic of a high horizontal and vertical grain-size heterogeneity of gravel-sand, which led to a varying filtration coefficient affecting the capacities of pumped groundwater quantity during the remediation. At the start of the remediation process, the contaminant levels exceeded the limits by the Czech Environmental Inspectorate several times. The post-remediation monitoring showed that all the contaminant levels were below the limit. Surprisingly, the overall groundwater contamination amounted to 232.86 t of contaminants as non-aqueous phase liquids, and 6872.9 kg of dissolved contaminants. As much as 12,200 t of contaminants were removed from the soil. Full article

Quantitative evaluation of different contaminated soil remediation technologies in multiple dimensions is beneficial for the optimization and comparative selection of technology. Ex situ thermal desorption is widely used in remediation of organic contaminated soil due to its excellent removal effect and short engineering period. In this study, a comprehensive evaluation method of soil remediation technology, covering 20 indicators in five dimensions, was developed. It includes the steps of constructing an indicator system, accounting for the indicator, normalization, determining weights by analytic hierarchy process, and comprehensive evaluation. Three ex situ thermal desorption technology—direct thermal desorption, indirect thermal desorption, and indirect thermal heap—in China were selected for the model validation. The results showed that the direct thermal desorption had the highest economic and social indicator scores of 0.068 and 0.028, respectively. The indirect thermal desorption had the highest technical and environmental indicator scores of 0.118 and 0.427, respectively. The indirect thermal heap had the highest resource indicator score of 0.175. With balanced performance in five dimensions, the indirect thermal desorption had the highest comprehensive score of 0.707, which is 1.6 and 1.4 times higher than the direct thermal desorption and indirect thermal heap, respectively. The comprehensive evaluation method analyzed and compared the characteristics of the ex situ thermal desorption technology from different perspectives, such as specific indicators, multiple dimensions, and single comprehensive values. It provided a novel evaluation approach for the sustainable development and application of soil remediation technology. Full article

Water pollution by heavy metals represents several health risks. Conventional technologies employed to eliminate lead ions from residual or drinking water are expensive, therefore an efficient and low-cost technique is required and adsorption processes are a good alternative. In this work, the goal was to determine the adsorption capacity of a Disordered Mesoporous Silica 1 material (DMS-1) functionalized with amino groups, for Pb(II) ions removal. DMS-1 was prepared by sol-gel method and the incorporation of amino groups was performed by ex-situ method. As the source of amine groups, (3-Aminopropyl) triethoxysilane (APTES) was used and three different xNH₂/DMS-1 molar ratios (0.2, 0.3, 0.4) were evaluated. In order to evaluate the incorporation of the amino group into the mesopore channels, thermal and structural analysis were made through Thermogravimetric Analysis (TGA), nitrogen adsorption–desorption at 77 K by Specific Brunauer–Emmett–Teller (SBET) method, Fourier Transfer Infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD) and X-Ray Photoelectron Spectroscopy (XPS). The higher Pb(II) ions removal was achieved with the 0.3 molar proportion of xNH₂/DMS-1 reaching 99.44% efficiency. This result suggests that the functionalized material can be used as an efficient adsorbent for Pb(II) ions from aqueous solution. Full article

Solid-state reactions between sodium hydride and sodium hydroxide are unusual among hydride-hydroxide systems since hydrogen can be stored reversibly. In order to understand the relationship between hydrogen uptake/release properties and phase/structure evolution, the dehydrogenation and hydrogenation behavior of the Na-O-H system has been investigated in detail both ex- and in-situ. Simultaneous thermogravimetric-differential thermal analysis coupled to mass spectrometry (TG-DTA-MS) experiments of NaH-NaOH composites reveal two principal features: Firstly, an H₂ desorption event occurring between 240 and 380 °C and secondly an additional endothermic process at around 170 °C with no associated weight change. In-situ high-resolution synchrotron powder X-ray diffraction showed that NaOH appears to form a solid solution with NaH yielding a new cubic complex hydride phase below 200 °C. The Na-H-OH phase persists up to the maximum temperature of the in-situ diffraction experiment shortly before dehydrogenation occurs. The present work suggests that not only is the inter-phase synergic interaction of protic hydrogen (in NaOH) and hydridic hydrogen (in NaH) important in the dehydrogenation mechanism, but that also an intra-phase H^δ+… H^δ– interaction may be a crucial step in the desorption process. Full article