Inert Components Research Articles

The dynamics of human bone marrow adipose tissue in response to feeding and fasting.

BACKGROUNDAdipocytes were long considered inert components of the bone marrow niche, but mouse and human models suggest bone marrow adipose tissue (BMAT) is dynamic and responsive to hormonal and nutrient cues.METHODSIn this study of healthy volunteers, we investigated how BMAT responds to acute nutrient changes, including analyses of endocrine determinants and paracrine factors from marrow aspirates. Study participants underwent a 10-day high-calorie protocol, followed by a 10-day fast.RESULTSWe demonstrate (a) vertebral BMAT increased significantly during high-calorie feeding and fasting, suggesting BMAT may have different functions in states of caloric excess compared with caloric deprivation; (b) ghrelin, which decreased in response to high-calorie feeding and fasting, was inversely associated with changes in BMAT; and (c) in response to high-calorie feeding, resistin levels in the marrow sera, but not the circulation, rose significantly. In addition, TNF-α expression in marrow adipocytes increased with high-calorie feeding and decreased upon fasting.CONCLUSIONHigh-calorie feeding, but not fasting, induces an immune response in bone marrow similar to what has been reported in peripheral adipose tissue. Understanding the immunomodulatory regulators in the marrow may provide further insight into the homeostatic function of this unique adipose tissue depot.FUNDINGNIH grant R24 DK084970, Harvard Catalyst/The Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, NIH, award UL 1TR002541), and NIH grants P30 DK040561 and U19 AG060917S1.

Effect of nano-TiO2 on humic acid utilization from piggery biogas slurry by microalgae

Resource recovery from piggery biogas slurry has become an inevitable demand for sustainable development of pig industry. Microalgae show great potential in recovering nitrogen and phosphorus from piggery slurry, but struggle to utilize organic pollutants, as most of them are inert components (e.g., humic acids, HAs). In this study, nano-TiO2 was used to enhance the utilization of HAs by microalgae from piggery biogas slurry. Results showed that the optimal conditions for microalgal growth and HAs removal by the microalgae-TiO2 coupling system were TiO2 dosage of 0.30 g/L, microalgal inoculation concentration of 0.40 g/L, light intensity of 360 µmol photon/(m2·s) and temperature of 30 °C, with the microalgal chlorophyll concentration of 6.51 mg/L and HAs removal efficiency of 50.14%. Analysis of HAs composition variations in the piggery biogas slurry indicated that the decrease of HAs was caused by their decomposition into small molecules under the photocatalytic reactions of TiO2.

Effects of methane addition on laminar flame characteristics of premixed blast furnace gas/air mixtures

As a typical low heating value fuel, blast furnace gas (BFG) is used as an alternative fuel for gas turbine combustion. Due to its high concentration of inert gas components, natural gas is usually added to improve ignition and stable combustion in the combustion chamber. In this paper, laminar flame characteristics of BFG/CH4/air mixtures were investigated using constant volume combustion chamber and CHEMKIN package using the Gri-Mech 3.0 model. Experiments and numerical simulations were conducted at an elevated pressure and temperature of 0.2 MPa and 453 K, equivalence ratios of 0.8–1.4, and mixing ratios of methane of 0, 5, 10, 15%. The results show that the laminar burning velocity decreases rapidly from 24.19 cm/s to 13.90 cm/s at ϕ = 1.4 with the increase of methane addition from 0% to 15%, but obviously increases from 16.49 cm/s to 28.68 cm/s at ϕ = 0.8, from 21.05 cm/s to 35.65 cm/s at ϕ = 1.0, from 23.52 cm/s to 32.09 cm/s at ϕ = 1.2 with the increase of methane addition from 0% to 15%. Meanwhile, methane addition has an opposite effect on the Markstein length at ϕ = 0.8–1.2 and ϕ = 1.4. The thermal, transport and chemical effects were examined, exhibiting a major role of the thermal effect in the range of ϕ = 0.8–1.2 and a significant contribution of the chemical effect at ϕ = 1.4 to the laminar flame propagation of BFG/CH4/air mixtures. Further sensitivity analysis shows that R38 (H + O2 ↔ O + OH) and R52 (H + CH3 (+M) ↔ CH4 (+M)) are the main chain branching and chain termination reactions, respectively. Analysis on flame structure indicates that concentrations free radicals, especially OH and H evidently increase with methane addition. The maximum mole fraction of OH increases almost linearly from 1.02×10-3 to 3.82×10-3 with the increase of methane addition from 0% to 15%. The maximum mole fraction of H increases with a lower gradient than that of OH from 1.31×10-3 to 2.89×10-3 with the increase of methane addition from 0% to 15%.

Structured binder-free MWW-type titanosilicate with Si-rich shell for selective and durable propylene epoxidation

Selective and durable fixed-bed catalysts are highly desirable for developing eco-efficient HPPO (hydrogen peroxide propylene oxide) process. The powder titanosilicate catalysts must be shaped before being applied in industrial processes. As the essential additives for preparing formed catalysts, binders are usually the catalytically inert components, but they would cover the surface and pore mouth of zeolite, thereby declining the accessibility of active sites. By recrystallizing the binder (silica)/Ti-MWW extrudates with the assistance of dual organic structure-directing agents, the silica binder was converted into MWW zeolite phase to form a structured binder-free Ti-MWW zeolite with Si-rich shell, which enhanced the diffusion efficiency and maintained the mechanical strength. Meanwhile, due to the partial dissolution of Si in the Ti-MWW matrix, abundant silanol nests formed and part of framework TiO4 species were transferred into open TiO6 ones, improving the accumulation and activation ability of H2O2 inside the monolith. Successive piperidine treatment and fluoridation of the binder-free Ti-MWW further enhanced the H2O2 activation and oxygen transfer ability of the active Ti sites, and stabilized the Ti-OOH intermediate through hydrogen bond formed between the end H in Ti-OOH and the adjacent Si-F species, thus achieving a more efficient epoxidation process. Additionally, the side reaction of PO hydrolysis was inhibited because the modification effectively quenched numerous Si-OH groups. The lifetime of the modified binder-free Ti-MWW catalyst was 2400 h with the H2O2 conversion and PO selectivity both above 99.5%.

Application of Silicon Dioxide as the Inert Component or Oxide Component Enhancer in ANFO

Non-ideal explosives with differing contents of silicon dioxide (silica or dioxosilane) added in the form of powder and gel were tested. Measurements of structure, crystallinity and morphology were performed by means of infrared spectroscopy (IR), X-ray diffraction (XRD) and scanning electron microscopy (SEM). IR and XRD analysis revealed a lack of SiO2 influence on the non-ideal explosive structure. SEM analysis indicated that all the surface deformations of ammonium nitrate(V) prill were filled by a thin fuel film layer on which SiO2 was present. The additional calculations of selected theoretical properties of non-ideal compositions were made using ZMWCyw software. Based on this, it was established that the optimum semimetal content was 1.0 wt.%. Blasting tests confirmed that the addition of 1.0 wt.% SiO2 to the Ammonium Nitrate Fuel Oil (ANFO) resulted in the lowest volume of post-blast fumes. Moreover, it was established that finer SiO2 powder cannot be used as the oxide component enhancer due to the inhibition of detonation reaction. SiO2 should be used only as an inert component.

Inactive Cu2O Cubes Become Highly Photocatalytically Active with Ag2S Deposition.

Previously, Cu2O cubes have been shown to remain photocatalytically inert toward methyl orange degradation even after surface decoration with ZnO, ZnS, CdS, and Ag3PO4 nanostructures. Surprisingly, when Ag2S nanoparticles are lightly deposited on Cu2O cubes as seen through scanning electron microscopy (SEM) images, the heterostructures become highly photocatalytically active. X-ray diffraction (XRD) patterns show mainly Cu2O diffraction peaks due to lightly deposited Ag2S, but Ag2S peaks can emerge with increased Ag2S deposition. X-ray photoelectron spectroscopy (XPS) analysis also supports Ag2S formation on Cu2O crystals. The Ag2S-deposited Cu2O octahedra and rhombic dodecahedra show the expected activity enhancement. Electron paramagnetic resonance (EPR) measurements, as well as electron, hole, and radical scavenger tests, all confirmed the emergence of photocatalytic activity from the Ag2S-Cu2O cubes. Photoluminescence lifetimes are shortened after Ag2S deposition. Electrochemical impedance measurements revealed a large decrease in charge transfer resistance for Cu2O cubes after the Ag2S deposition. Unexpectedly, the separately synthesized Ag2S particles are also photocatalytically inactive. No specific lattice planes of Ag2S are formed directly over the {100} face of Cu2O. Diffuse reflectance and ultraviolet photoelectron spectral data were used to construct band diagrams of different Cu2O crystals and Ag2S nanoparticles. A Z-scheme charge transfer mechanism may be involved at the heterojunction interface to promote charge carrier separation. However, to explain the sudden appearance of photocatalytic activity from the Ag2S-deposited Cu2O cubes, a large change in the {100} surface band bending after Ag2S deposition should be used. This work illustrates that an unusual photocatalytic outcome is possible to semiconductor heterojunctions, where two photocatalytically inert components can become highly active when joined together.

Si/FeSi2 Nanoparticles Prepared by Thermal Plasma with Stress‐releasing Effect for Li‐ion Storage

AbstractSilicon (Si) anode materials have been extensively studied due to high capacity and abundant reserves. Herein, inspired by the Li+‐inert components, we design a novel silicon/iron silicide nanoparticles (Si/FeSi2 NPs) prepared by thermal plasma to achieve stress‐releasing effect. The Si/FeSi2 NPs is composed of Si and FeSi2 which exhibits superhigh Initial Coulomb Efficiency (ICE, 89%) with a capacity of 1121 mAh g−1 after 850 cycles. The mechanism of the FeSi2 phase in the Si/FeSi2 NPs is studied by using finite element modelling creatively, demonstrating that the FeSi2 phase can buffer the volume expansion effectively by reducing the stress concentration on the particles surface and releasing internal stress of particles, thus maintaining structural integrity. After combining with carbon coating layer, the Si/FeSi2/carbon/graphite materials (Si/FeSi2/C/G) can achieve superior electrochemical performances. This work provides new insight into the development of the structural stable Si‐alloy anodes towards LIBs applications.

Моделирование осаждения закрученного потока разреженной гранулированной среды в цилиндрической области методом MP-PIC

The object of the study is the deposition of small particles in a cylindrical region, for the evaluation of which a model was built in the OpenFOAM package. Many studies show that the MP-PIC method is well suited for modeling the interaction of a granular medium with liquid and gas flows. In this paper, the applicability of the method to solve the problem is evaluated. In the process of studying sedimentation in a swirling stream, groups of particles of different diameters were considered. It is shown that the smaller the particles, the faster they are deposited on the walls of a cylindrical tube. On the contrary, larger and heavier particles fly a long distance along the tube, which is explained by the greater influence of the inert component compared to the Stokes force. To evaluate the results obtained, a series of calculations using different sizes of grids was carried out. Good comparability of the results is shown. Further comparison with experimental data is planned.

Pesticides: formulants, distribution pathways and effects on human health - a review.

Pesticides are commonly used in agriculture to enhance crop production and control pests. Therefore, pesticide residues can persist in the environment and agricultural crops. Although modern formulations are relatively safe to non-target species, numerous theoretical and experimental data demonstrate that pesticide residues can produce long-term negative effects on the health of humans and animals and stability of ecosystems. Of particular interest are molecular mechanisms that mediate the start of a cascade of adverse effects. This is a review of the latest literature data on the effects and consequences of contamination of agricultural crops by pesticide residues. In addition, we address the issue of implicit risks associated with pesticide formulations. The effects of pesticides are considered in the context of the Adverse Outcome Pathway concept.

Modulation of Volmer step for efficient alkaline water splitting implemented by titanium oxide promoting surface reconstruction of cobalt carbonate hydroxide

The sluggish water dissociation (Volmer step) is a rate-limiting step slowing down alkaline hydrogen evolution reaction (HER), and therefore hinders the efficient industrial production of clean hydrogen resource. In this work, we report that the Volmer step can be facilitated by in-situ surface reconstruction on a composite between cobalt carbonate hydroxide and titanium oxide (TiO 2 @CoCH), and the resultant activated structure turns to be a highly efficient electrocatalyst for alkaline HER. Experimental characterization and density functional theory calculation evidence that under HER potential the smooth TiO 2 @CoCH surface is roughened and Co interstitial defects in TiO 2 are formed, which are energetically favorable for Volmer step. The activated composite exhibits an overpotential of 99 ± 6 mV for a current density of 20 mA cm −2 and 187 ± 21 mV for 100 mA cm −2 , suggesting that TiO 2 @CoCH is one of promising non-precious metal electrocatalysts for HER in alkaline media. • The combination of two inert component resulted in a highly active electrocatalyst for alkaline hydrogen evolution reaction. • Titanium oxide promoted the surface reconstruction of cobalt carbonate hydroxide during hydrogen evolution reaction. • The Volmer step of hydrogen evolution reaction was significantly promoted after surface reconstruction. • The surface reconstruction of cobalt carbonate hydroxide during hydrogen evolution reaction was evidenced.

Mind Your Dye: The Amyloid Sensor Thioflavin T Interacts with Sulfated Glycosaminoglycans Used To Induce Cross-β-Sheet Motifs.

Thioflavin T (ThT) is a commonly employed fluorescence probe for sensing amyloid fibrils. These highly ordered, insoluble nanostructures colocalize with sulfated glycosaminoglycans (GAGs) being abundant in the extracellular matrix and on the outer surface of cell membranes. To elucidate the positive impact of GAGs on amyloidogenesis, they are frequently used to promote fibril formation in vitro, which is detected by the enhanced fluorescence of ThT. The polyanionic nature and the affinity of GAGs to basic compounds predict that cationic ThT molecules may also bind to them, in addition to cross-β-structures formed in the reaction medium. By means of circular dichroism (CD) and absorption spectroscopy, this study examined the heparin and chondroitin sulfate binding of ThT. The large blue shift of the absorption peak indicated a card-pack type oligomerization of the dye molecules along the linear GAG chains. The strong exciton couplet observed in the CD spectra implies the left-handed, helical arrangement of GAG-associated oligomers of the dye. The decisive contribution of ionic forces for the binding was illustrated by sodium-ion-provoked dissociation of dye-GAG complexes. In silico analysis was performed to complement the experimental findings and to contribute to the understanding of potential molecular mechanisms underlying ThT-GAG interactions. ThT can be considered as an inert component in GAG-induced amyloid assays but only if the experiments are correctly designed.

Chemical and olfactive impacts of organic matters on odor emission patterns from the simulated construction and demolition waste landfills

The explosive increase of construction and demolition waste (CDW) caused the insufficient source separation and emergency disposal at domestic waste landfills in many developing countries. Some organic fractions were introduced to the CDW landfill process and resulted in serious odor pollution. To comprehensively explore the impacts of organic matters on odor emission patterns, five CDW landfills (OIL), with organic matters/ inert CDW components (O/I) from 5% to 30%, and the control group only with inert components (IL) or organics (OL) were simulated at the laboratory. The chemical and olfactive characters of odors were evaluated using the emission rate of 94 odorants content (ERtotal), theory odor concentration (TOCtotal), and e-nose concentration (ERENC), and their correlations with waste properties were also analyzed. It was found that the main contributors to ERtotal (IL: 93.0% NH3; OIL: 41.6% sulfides, 31.0% NH3, 25.9% oxygenated compounds) and TOCtotal (IL: 64.1% CH3SH, 28.2% NH3; OIL: 71.7% CH3SH, 24.8% H2S) changed significantly. With the rise of O/I, ERtotal, TOCtotal, and ERENC increased by 10.9, 20.6, and 2.1 times, respectively. And the organics content in CDW should be less than 10% (i.e., DOC<101.3 mg/L). The good regressions between waste properties (DOC, DN, pH) and ERENC− (r=0.86, 0.86, -0.88, p<0.05), TOCtotal− (r=0.82, 0.79, -0.82, p<0.05) implied that the carbon sources and acidic substances relating to organics degradation might result in that increase. Besides, the correlation analysis results (ERENC−vs.TOCtotal−, r=0.96, p<0.01; vs.ERtotal−, r=0.86, p<0.05) indicated that e-nose perhaps was a reliable odor continuous monitoring tool for CDW landfills.

Experimental Investigation of Reactive-Inert Particulate Matter Detachment from Metal Fibres at Low Flow Velocities and Different Gas Temperatures

The detachment of particle structures from single fibres in gas flow has been investigated only for inert particle structures yet. This study investigates the detachment of particle structures containing reactive components. These reactive components disappear during the reaction and enhance detachment at low flow velocities. Soot was used as the reactive component and glass spheres as the inert component of the particle structure. The soot disappears due to combustion with oxygen leaving only the glass spheres on the fibre. Without reaction, the detachment phenomenon was observed at superficial flow velocities above 1.9 m/s and with reaction at 0.5 m/s. This shows that reacting and disappearing components of the particle structure can enhance detachment.

Propane Dehydrogenation on Single-Site [PtZn4] Intermetallic Catalysts

Summary Propane dehydrogenation (PDH) is a commercial propylene production technology that has received much attention, but high reaction temperatures result in a decrease of propylene selectivity and catalyst stability. This paper describes a single-site [PtZn4] catalyst by assembling atomically ordered intermetallic alloy (IMA) as a selective and ultrastable PDH catalyst. The catalyst enables more than 95% of propylene selectivity from 520°C to 620°C. No obvious deactivation is observed within the 160-h test, superior to PtSn/Al2O3 and state-of-the-art Pt-based catalysts. Based on in situ X-ray absorption fine structure, X-ray photoelectron spectroscopy measurements, and density functional theory calculations, we reveal that the surface [PtZn4] ensembles in PtZn IMAs serve as the key active site structures, wherein the geometry-isolated and electron-rich Pt1 site in [PtZn4] ensembles readily promotes the first and second C–H cleavage of propane but inhibits further dehydrogenation of surface-bounded propylene. This significantly improves the selectivity and stability by prohibiting coke side reactions.

Multiscale Experimental Evaluation of Agarose-Based Semi-Interpenetrating Polymer Network Hydrogels as Materials with Tunable Rheological and Transport Performance.

This study introduces an original concept in the development of hydrogel materials for controlled release of charged organic compounds based on semi-interpenetrating polymer networks composed by an inert gel-forming polymer component and interpenetrating linear polyelectrolyte with specific binding affinity towards the carried active compound. As it is experimentally illustrated on the prototype hydrogels prepared from agarose interpenetrated by poly(styrene sulfonate) (PSS) and alginate (ALG), respectively, the main benefit brought by this concept is represented by the ability to tune the mechanical and transport performance of the material independently via manipulating the relative content of the two structural components. A unique analytical methodology is proposed to provide complex insight into composition–structure–performance relationships in the hydrogel material combining methods of analysis on the macroscopic scale, but also in the specific microcosms of the gel network. Rheological analysis has confirmed that the complex modulus of the gels can be adjusted in a wide range by the gelling component (agarose) with negligible effect of the interpenetrating component (PSS or ALG). On the other hand, the content of PSS as low as 0.01 wt.% of the gel resulted in a more than 10-fold decrease of diffusivity of model-charged organic solute (Rhodamine 6G).

Cover Feature: Defect Engineering of van der Waals Solids for Electrocatalytic Hydrogen Evolution (Chem. Asian J. 22/2020)

Defect engineering in van der Waals solids plays an important role in triggering the catalytic activity of their inert components for the hydrogen evolution reaction (HER). It could efficiently modulate the chemical components and band-gap states of van der Waals solids, thus impacting the reactants′ capture, activation and release process. In this Minireview, the state-of-the-art progress of defect engineering in van der Waals solids for HER, involving zero-dimensional defects (e. g., atomic vacancies and heteroatom doping), one-dimensional defects (e. g., under-coordinated edges and domain boundaries), two-dimensional defects (e. g., vertical heterostructures and interfacial distortions), and other typical defects is summarized. In particular, focus is laid on their advantages in material modification and corresponding catalytic mechanisms. In addition, the challenges and perspectives of these catalytic materials in terms of both experimental synthesis and fundamental understanding of the defect structures are also proposed. More information can be found in the Minireview by Ruitao Lv et al.

Recycling application of modified waste electrolytic manganese anode slag as efficient catalyst for PMS activation

Electrolytic manganese anode slag (EMAS) is the waste residue produced by electrolytic manganese metal industry. At present, no mature recycling system has been established, which causes a waste of resources and threatens the environment. Therefore, the resource utilization of EMAS has attracted increased attention. In this paper, the in-situ resource utilization of EMAS can be realized by pickling treatment was reported. Specifically, EMAS after pickling treatment (PEMAS) was first used as catalyst to activate PMS to degrade tetrachlorophenol (4-CP). Pickling could remove the inert inorganic components on EMAS and increase the specific surface area, pore volume and Mn distribution of the catalyst, thus improving the catalytic performance of the catalyst. Under the conditions of 4-CP of 40 ppm, PMS of 1 mM and PEMAS of 0.3 g L−1, 85% of 4-CP could be degraded within 50 min. Mechanism studies proved that the main active species were O2− and 1O2. Some O2− contributed to the generation of 1O2 and some O2− directly contributed to the degradation of 4-CP. During the reaction, the valence state of Mn transformed between Mn(III)/Mn(IV) and Mn(II)/Mn(III) and kept the cycle. Moreover, PEMAS/PMS system exhibited excellent independence of the solution pH, resistance to the versatile inorganic ions and background organic matters, and stability of recycling. In a word, this study has achieved the resource utilization of EMAS and the goal of treating waste with waste, which is a win-win strategy of economic and environmental benefits.

CO2 mineral sequestration by using blast furnace slag: From batch to continuous experiments

CO2 mineral sequestration is a promising strategy to combat global warming. Indirect CO2 mineral sequestration was proposed in our previous study by using blast furnace slag as feedstock. As the continuity of this research, the continuous experiment process was carried out in a self-designed rotary kiln, and the results were compared with those of the batch experiment. The results showed that several problematic situations, such as the formation of kiln rings, insufficient mass, and heat transfer, occurred in the continuous experiment. A “returning charge” operation by adding an inert component into the feedstock was suggested for the prevention of ring formation and achieved good results. The reaction conditions for the continuous experiment were harsher than those of the batch experiment due to the scale-up effects. Preliminary analysis of CO2 net-emission reduction was conducted based on the continuous experimental results. It was shown that the net reduction of CO2 emissions amounted to 36 kg for 1000 kg of blast furnace slag processed. The results demonstrated in this study can act as guidance for pilot- or industrial-scale applications of indirect CO2 mineral sequestration technologies, especially for process parameter optimization and equipment design.

Artificial Nanotargeted Cells with Stable Photothermal Performance for Multimodal Imaging-Guided Tumor-Specific Therapy.

Organic-inorganic hybrid materials have drawn increasing attention as photothermal agents in tumor therapy due to the advantages of green synthesis, high loading efficiency of hydrophobic drugs, facile incorporation of theranostic iron, and excellent photothermal efficiency without inert components or additives. Herein, we proposed a strategy for biomimetic engineering-mediated enhancement of photothermal performance in the tumor microenvironment (TME). This strategy is based on the specific characteristics of organic-inorganic hybrid materials and endows these materials with homologous targeting ability and photothermal stability in the TME. The hybrid materials perform the functions of cancer cells to target homolytic tumors (acting as "artificial nanotargeted cells (ANTC)"). Inspired by the pH-dependent disassembly behaviors of tannic acid (TA) and ferric ion (FeIII) and subsequent attenuation of photothermal performance, cancer cell membranes were self-deposited onto the surfaces of protoporphyrin-encapsulated TA and FeIII nanoparticles to achieve ANTC with TME-stable photothermal performance and tumor-specific phototherapy. The resulting ANTC can be used as contrast agents for concurrent photoacoustic imaging, magnetic resonance imaging, and photothermal imaging to guide the treatment. Importantly, the high loading efficiency of protoporphyrin enables the initiation of photodynamic therapy to enhance photothermal therapeutic efficiency, providing antitumor function with minimal side effects.

Investigating the Aging Effects of Biochar on Soil C and Si Dissolution and the Interactive Impact on Copper Immobilization.

Aging tests were used to investigate the long-term effects of BC on the immobilization of Cu, and the soil silicon dissolution of three types soils (black soil, (BS), vegetable garden soil (VS) and red soil (RS)). Litchi branch biochars (BC) at 10% (w/w) were incubated with three Cu (400 mg/kg) contaminated soils. The effect on soil properties of pH, soil organic carbon (SOC), dissolved organic carbon (DOC) and available silicon content were investigated, along with the speciation distribution of Cu. The results indicated that SOC, DOC, and available silicon content (except, BC300) increased with the application of BCs. On the other hand, the DTPA (diethylenetriaminepentaacetic acid) extractable Cu content in BS, VS and RS soils were reduced by 4–12%, 18–25%, and 12–19%, respectively. The Cu availability in all soils first increased, and then decreased during the aging process. The sum of the other four fractions, including the carbonate fraction and the inert component increased by 4–4.5% (BS), 1.4–2.1% (VS), and 0.5–1% (RS) respectively, over the long-term process. Moreover, during the whole aging process, the soil properties (such as pH, SOC, DOC and available silicon content) were almost stable. This study demonstrates that BCs, especially those produced at a higher temperature, are superior to those been produced at 300 °C in immobilizing Cu and releasing available silicon in soils. However, the remediation efficiencies were restricted by the soil type contamination status and remediation time.