Experimental Study on Shut-in-Time Optimization for Multi-Fractured Horizontal Wells in Shale Reservoirs

The optimization of shut-in-time in shale gas well is an important factor affecting the production of single well after volume fracturing. In this study, a new method for determining the optimal shut-in-time considering clay mineral content and ion diffusion concentration was proposed. First, a novel water spontaneous imbibition apparatus under the conditions of formation temperature and confining pressure was designed. Then, the water imbibition satuation of 15 shale samples from the Longmaxi Formation (LF) of the Sichuan Basin were measured to quantitatively evaluate the water imbibition ability and classify reservoir types. Finally, the salt ion concentration diffusion experiment was carried out to optimize the shut-in-time of different types of shale reservoirs. The experimental results shown that the clay mineral content was the key factor affecting water wettability of shale, the shale reservoirs can be divided into two types and the critical value of clay mineral content was about 40%. Based on the law of salt ion diffusion in shale, the initiation time of micro-fractures induced by shale hydration was about 10-15 days. Under the experimental conditions, the optimal shut-in time of type I shale reservoir and type II shale reservoir were about 20 days and 15 days respectively. The average daily gas production has increased from 15.6×104 m3/day to 25.1×104 m3/day. The study results can provide scientific basis for the optimization of flowback regime of shale gas resrvoirs.

Effects of Mg Doping at Different Positions in Li-Rich Mn-Based Cathode Material on Electrochemical Performance

Li-rich Mn-based layered oxides are among the most promising cathode materials for next-generation lithium-ion batteries, yet they suffer from capacity fading and voltage decay during cycling. The electrochemical performance of the material can be improved by doping with Mg. However, the effect of Mg doping at different positions (lithium or transition metals) remains unclear. Li1.2Mn0.54Ni0.13Co0.13O2 (LR) was synthesized by coprecipitation followed by a solid-state reaction. The coprecipitation stage was used to introduce Mg in TM layers (sample LR-Mg), and the solid-state reaction (st) was used to dope Mg in Li layers (LR-Mg(st)). The presence of magnesium at different positions was confirmed by XRD, XPS, and electrochemical studies. The investigations have shown that the introduction of Mg in TM layers is preferable in terms of the electrochemical performance. The sample doped with Mg at the TM positions shows better cyclability and higher discharge capacity than the undoped sample. The poor electrochemical properties of the sample doped with Mg at Li positions are due to the kinetic hindrance of oxidation of the manganese-containing species formed after activation of the Li2MnO3 component of the composite oxide. The oxide LR-Mg(st) demonstrates the lowest lithium-ion diffusion coefficient and the greatest polarization resistance compared to LR and LR-Mg.

Exceptional lithium diffusion through porous aromatic framework (PAF) interlayers delivers high capacity and long-life lithium–sulfur batteries

Sulfonated porous aromatic frameworks (SPAFs) accelerate Li-ion diffusion while retarding the polysulfide shuttle effect in Li–S batteries. This leads to high residual capacity above 1000 mA h g−1 and coulombic efficiency (>99.5%) after 500 cycles.

Correlation between diffusion coefficient values of chloride ions obtained through column and ion migration tests in cementitious matrices with varying contents of silica fume and mortar

Corrosion is one of the main phenomena that lead to pathological manifestations in reinforced concrete structures under aggressive environments. with the chloride ion being the most responsible for its occurrence. In this way, understanding the transport mechanisms of this ion through the microstructure of the concrete is of fundamental importance to prevent or delay the penetration of these aggressive agents to guarantee a durable structure. In the literature, there are extensive studies concerning the diffusion of chlorides in concrete and the influence of pozzolanic additions in this mechanism. However, only a few correlate the different methods of analysis. This work aims to determine the chloride ion diffusion coefficients in concrete containing various levels of silica fume (5%, 10%, and 15%) or varying the mortar content (54%, 80%, and 100%), and compares the results obtained through column tests and chloride migration tests. It was observed that, although the techniques used were quite distinct, the diffusion values obtained were similar, contributing to the validation of both techniques. Furthermore, the variation in the mortar ratio causes a reduction in the interfacial transition zone of coarse aggregate/mortars and an increase in the content of aluminates, which promotes a similar effect to the use of silica fume.

New insights in the mechanism of cation migration induced by cation-anion dynamic coupling in superionic conductors

Understanding the ion diffusion mechanism is one of the key preconditions for designing superionic conductors in solid state lithium batteries and many other energy devices. Besides single-cation vacancy/interstitial-assisted and multi-cation...

Poly(vinylalcohol) (PVA) Assisted Sol-Gel Fabrication of Porous Carbon Network-Na3V2(PO4)3 (NVP) Composites Cathode for Enhanced Kinetics in Sodium Ion Batteries

Na3V2(PO4)3 is regarded as one of the promising cathode materials for next-generation sodium ion batteries, but its undesirable electrochemical performances due to inherently low electrical conductivity have limited its direct use for applications. Motivated by the limit, this study employed a porous carbon network to obtain a porous carbon network–Na3V2(PO4)3 composite by using poly(vinylalcohol) assised sol-gel method. Compared with the typical carbon-coating approach, the formation of a porous carbon network ensured short ion diffusion distances, percolating electrolytes by distributing nanosized Na3V2(PO4)3 particles in the porous carbon network and suppressing the particle aggregation. As a result, the porous carbon network–Na3V2(PO4)3 composite exhibited improved electrochemical performances, i.e., a higher specific discharge capacity (~110 mAh g−1 at 0.1 C), outstanding kinetic properties (~68 mAh g−1 at 50 C), and stable cyclic stability (capacity retention of 99% over 100 cycles at 1 C).