Jie Wang

Dr. Jie Wang

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 April 2023 in Journal of Cleaner Production
Verified
Journal Article
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WWWei Wang
Wei Wang
XLXinsheng Li
Xinsheng Li
JSJunan Shen
Junan Shen
HZHongzhou Zhu
Hongzhou Zhu
JWJie Wang
Jie Wang

1 January 2021 in Advances in Civil Engineering
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JWJie Wang
Jie Wang
GWGuanshi Wang
Guanshi Wang
BHBengen Hong
Bengen Hong
The continuous change in solution concentration in ore pores during in situ mineral leaching influences the stability of ore aggregate. In this study, influences of the concentration of ammonium sulfate ((NH4)2SO4) solution on the interaction forces between ore particles were calculated. On this basis, the mechanism by which (NH4)2SO4 solution concentration influences the stability of ore aggregate was analyzed. Furthermore, an empirical formula for estimating the critical (NH4)2SO4 solution concentration for aggregation and dispersion of ore body aggregates with different grain composition was proposed. Some major conclusions were drawn. First, for ore bodies with an initial particle size of less than 0.075 mm, the interaction force between particles was net attraction, with the distance range of this force increasing as the concentration of (NH4)2SO4 solution increased from ≤0.001 to 0.16 mol·L−1, aggregation of ore particles occurring within this distance range. Secondly, for ore bodies with initial particle size of less than 0.075 mm, the interaction force between particles was net attraction, but with the distance range of this force decreasing when the (NH4)2SO4 solution concentration increased from 0.16 to 0.28 mol·L−1, dispersion of ore particles occurring beyond this distance range. Thirdly, for ore bodies with particle sizes of less than 0.038, 0.075 and 0.1 mm, the cation exchange capacity (CEC) was 9.13, 8.96, and 8.8 cmol·kg−1, respectively, and the critical (NH4)2SO4 solution concentration affecting the aggregation and dispersion of ore bodies was 0.12, 0.16, and 0.20 mol·L−1, respectively.

17 March 2021 in IEEE Sensors Journal
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JWJie Wang
Jie Wang
YLYuehua Liang
Yuehua Liang
GRGuanshi Wang R
Guanshi Wang R
The in-situ liquid injection leaching process of ionized rare earth is a typical process of effusion infiltration, and the infiltration efficiency directly determines the mining efficiency. Assuming that the infiltrated (NH4)2SO4 solution is uniformly distributed in the homogeneous orebody, the relationships between the following groups are derived and studied: (1) The position and time of the infiltration front; (2) The infiltration intensity and the infiltration time; (3) The advancing speed and time of the infiltration front.A wireless network sensor detection system for parameter det ection is established based on 4G network,air pressure sensor and water sensor are embedded in the ore body.The sensors are connec ted to the terminal via the 4G network,the data collection and wirele ss transmission of water content change and air pressure change of one-imensional fluid infiltration test in the homogeneous ore body with different compaction density were completed by the proposed wireless network sensor detection system. The results show that the influence of residual air pressure can be ignored during the infiltration; the advancing speed of the infiltration front is the fastest at the beginning, and then gradually decreased and stabilized; the change process of infiltration volume corresponds to the process of infiltration front advancing speed; the higher the density, the slower the advancing speed of the infiltration front, the lower the infiltration intensity, and the more difficult the infiltration; the deduced theory can be in good agreement with the actual infiltration situation with high accuracy, which can effectively simulate the infiltration process of ionized rare earth in-situ liquid injection mining.

17 November 2025 in Metals
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YLYuehua Liang
Yuehua Liang
JWJie Wang
Jie Wang
ZFZhikui Fei
Zhikui Fei
CPChenliang Peng
Chenliang Peng
JWJie Wang
Jie Wang
Zhanfeng FanZhanfeng Fan
Zhanfeng Fan
Ion adsorption rare-earth (IARE) ores, a strategic metal resource, are extracted by leaching with ammonium sulfate [(NH4)2SO4] solution, our samples have ∑REO grades of 0.032–0.079% wt%. IARE sandstone, mudstone, clay, and strongly weathered rock were selected as test materials. Surface-related physicochemical parameters were determined, and bound water was determined by volumetric flask pycnometry. For each IARE lithology, we also obtained particle size distributions and evaluated bound water variation in (NH4)2SO4 solutions at 0, 1, 2, and 3 wt%. Based on the Gouy–Chapman theory, the relationship between the surface bound water and solution concentration, as well as the surface charge of IARE samples, and other influencing factors was explored. The experimental results show the following: ① The surface charge per unit area of four types of IARE samples, namely mudstone, sandstone, clay, and strongly weathered rock, are 0.7072 × 10−2 mmol/m2, 1.9620 × 10−2 mmol/m2, 1.5418 × 10−2 mmol/m2, and 2.1003 × 10−2 mmol/m2, respectively, with strongly weathered rock having the highest and mudstone having the lowest. ② As the concentration of aqueous (NH4)2SO4 increases (0, 1, 2, 3 wt%), the total volume reduction in free water ∆V in the system increases, and the mass of adsorbed bound water per unit mass of IARE sample also increases. ③ As the concentration of the solution increases, the thickness of the diffusion double layer on the surface of the IARE sample is compressed, the total amount of adsorbed anions and cations on the surface increases, and the density of the surface water film also increases, leading to a corresponding increase in the quality of adsorbed bound water. ④ Under the same solution concentration, the variation trend of adsorbed bound water mass per unit area of IARE samples is strongly weathered rock > sandstone > clay > mudstone, which is consistent with the trend of surface charge per unit area of IARE samples. A higher lixiviant concentration increases bound water, shrinks the effective pore throats of the ore body, reduces hydraulic conductivity, and consequently diminishes leaching efficiency.

25 August 2025 in Materials
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JWJie Wang
Jie Wang
JWJie Wang
Jie Wang
With rapid industrialization, large quantities of industrial solid waste are generated annually. In Panzhihua, China, approximately 300,000 tons of limestone mine dust filter residue (LMDFR) is produced. This study investigates the properties of LMDFR and its potential as a supplementary cementitious material. LMDFR was blended with fly ash (FA) to replace 30% of cement in mortar. Tests were conducted to measure the mortar’s flowability and its compressive and flexural strengths after 7 and 28 days of curing, and XRD, SEM, TG, and DSC analyses were conducted on 28-day specimens. LMDFR primarily comprises ≥95% CaCO3, with a specific surface area of ~1.3 m2/g and density of 2.694 g/cm3. Mortar flowability increased with LMDFR content, reaching 112.83% when used alone. Flexural strength was largely unaffected, while the 7-day compressive strength significantly improved. However, the 28-day strength decreased when LMDFR was used alone, with a 28-day activity index of 61.10%, compared with 71.52% for FA. A 1:1 blend of LMDFR and FA improved the activity index to 83.18%. Microstructural and thermal results corroborated strength and flowability trends. In conclusion, LMDFR demonstrates promising potential as a supplementary cementitious material in concrete applications. When blended with fly ash at a 1:1 ratio, the composite admixture significantly enhances flowability and early compressive strength while maintaining adequate long-term performance. This synergistic combination not only improves the physical properties of cement mortar but also provides a sustainable solution for the large-scale utilization of industrial solid waste.

4 February 2026 in Results in Engineering
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Journal Article
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JWJie Wang
Jie Wang
YLYuehua Liang
Yuehua Liang
WWWei Wang
Wei Wang
XLXiongdong Lan
Xiongdong Lan