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The full pore size distribution represents the integrated characteristics of micro‐nano pore‐throat systems in tight reservoirs. And it involves experiments of different scales to fully analyze the microscope properties. In this paper, we established a new approach for full pore size characterization through conducting the high‐pressure mercury intrusion (HPMI) experiments and low‐temperature nitrogen gas adsorption (LTN2GA) experiments. Meanwhile, we studied the petrology feature of the tight sandstones through X‐ray diffraction (X‐rD) and TESCAN Integrated Mineral Analyzer (TIMA). Then, we investigated the HPMI capillary pressure curves and pore size distribution characteristics, as well as the adsorption‐desorption isotherms features and BET‐specific surface area. Finally, the BJH, non‐local density functional theory (NLDFT) and the quenched solid density functional theory (QSDFT) are contrasted for analyzing the adsorption and pore size distribution characteristics. The HPMI method characterizes the macropores distribution accurately, and the micro/mesopores take up of 14.47% of the total pore spaces. The physisorption isotherms take on the combining shape of type II and IV(a), and the hysteresis loops are like type H3 combined with H4. The BET‐specific surface area is inversely proportional to permeability, and the constant of adsorption heat shows consistence with the analysis results of mineral content. QSDFT can characterize the pore size distribution of micro/mesopores more accurately than the BJH, HPMI, and NLDFT method. By combining the pores narrower than 34 nm calculated from QSDFT method and pores larger than 34 nm calculated from HPMI data with mercury intrusion pressure lower than 42.65 MPa, the full pore size distribution features of tight sandstones are accurately characterized. The micro/mesopores from the new combination method are 3.72% more than that calculated from the HPMI data, and it is of great significance for the accurate pore distribution evaluation and development of tight reservoirs. We performed low‐temperature nitrogen gas adsorption (LTN2GA), high‐pressure mercury intrusion (HPMI), and X‐ray diffraction (X‐rD) experiments on different ultra‐low permeability/tight sandstones to accurately characterize the full pore size distribution of this kind of reservoir rocks. By combining the micropore and mesopore distribution calculated by QSDFT with the mesopore and macropore distribution calculated by HPMI, the accurate characterization of full pore size distribution for the ultra‐low permeability/ tight sandstones is achieved.

For a controlled particle size distribution, nano-silica was added to three different cements. The chemical and mineralogical compositions of the cements were characterized by fluorescence and X-ray diffraction. The granulometric distributions of cements and nano-silicas were obtained by laser granulometry and dynamic lightning scattering. The specific surface area of the raw materials was determined by gas adsorption. The effect of nano-silica and type of cement on rheological behavior was evaluated by rotational rheometry. The mechanical performance was investigated through the compression strength. The microstructural analysis was performed by scanning electron microscopy. The water demand and the consumption of dispersant increases according to the nano-silica content. The reduction in the inter-particle separation, and the agglomeration of nano-silica led to an increase in the viscosity of the suspension. The mechanical performance was directly affected by the specific surface area of the cements. Microstructural analysis showed that nano-silica changed from a layered adsorbed structure, to a porous or agglomerated structure.

Tricalcium phosphate (TCP) synthetized by high temperature solid state reaction at 1400°C and three derived calcium phosphate cements (CPCs) prepared at liquid to powder (L/P) ratios of 0.33, 0.44 and 0.55 ml/g, respectively, were physicochemically characterized. Calcium deficient hydroxyapatite crystals were identified by scanning electron microscopy on CPC, and differences in crystal sizes were observed at different L/P ratios. Also, the biofilm thickness of two Staphylococcus Aureus (S.aureus) strains grown for 24 hours on the three CPC are reported. A dependence of the biofilm thickness with the specific surface area (SSA) of CPC was identified. They are directly proportional for non-extracellular polysaccharide substances (EPS) producing S.aureus and inversely proportional for EPS producing S.aureus. Non-proportional behavior between the SSA and mechanical strength of the CPC was observed as L/P ratio increases.

In this work, we synthesized Sm O /ZnO/SmFeO microspheres by a hydrothermal method combined with microwave assistance to serve as a methanol gas sensor. We investigated the effect on the microstructure at different hydrothermal times (12 h, 18 h, 24 h, and 30 h), and the BET and XPS results revealed that the specific surface area and adsorbed oxygen species were consistent with a microstructure that significantly influences the sensing performance. The gas properties of the Sm O -doped ZnO/SmFeO microspheres were also investigated. With a hydrothermal time of 24 h, the gas sensor exhibited excellent sensing performance for methanol gas. For 5 ppm of methanol gas at 195 °C, the response reached 119.8 with excellent repeatability and long-term stability in a 30-day test in a relatively high humidity atmosphere (55-75% RH). Even at 1 ppm of methanol gas, the response was also higher than 20. Thus, the Sm O -doped ZnO/SmFeO microspheres can be considered as prospective materials for methanol gas sensors.

Mesoporous silica nanostructures (MSNs) attract high interest due to their unique and tunable physical chemical features, including high specific surface area and large pore volume, that hold a great potential in a variety of fields, i.e., adsorption, catalysis, and biomedicine. An essential feature for biomedical application of MSNs is limiting MSN size in the sub-micrometer regime to control uptake and cell viability. However, careful size tuning in such a regime remains still challenging. We aim to tackling this issue by developing two synthetic procedures for MSN size modulation, performed in homogenous aqueous/ethanol solution or two-phase aqueous/ethyl acetate system. Both approaches make use of tetraethyl orthosilicate as precursor, in the presence of cetyltrimethylammonium bromide, as structure-directing agent, and NaOH, as base-catalyst. NaOH catalyzed syntheses usually require high temperature (>80 °C) and large reaction medium volume to trigger MSN formation and limit aggregation. Here, a successful modulation of MSNs size from 40 up to 150 nm is demonstrated to be achieved by purposely balancing synthesis conditions, being able, in addition, to keep reaction temperature not higher than 50 °C (30 °C and 50 °C, respectively) and reaction mixture volume low. Through a comprehensive and in-depth systematic morphological and structural investigation, the mechanism and kinetics that sustain the control of MSNs size in such low dimensional regime are defined, highlighting that modulation of size and pores of the structures are mainly mediated by base concentration, reaction time and temperature and ageing, for the homogenous phase approach, and by temperature for the two-phase synthesis. Finally, an in vitro study is performed on bEnd.3 cells to investigate on the cytotoxicity of the MNSs.

Biomass is rich, renewable, sustainable, and green resources, thereby excellent raw material for the fabrication of carbon materials. The diversity in structure and morphology of biomass are relevant in obtaining carbon materials with different structures and performances. The inherent ordered porous structure of biomass also benefits the activation process to yield porous carbons with ultrahigh specific surface area and pore volume. Besides, obtained biomass‐derived carbons (BDCs) are hard carbon with porous morphology, stable structure, superior hardness/strength, and good cycling performances when used in electrochemical capacitors (ECs). The inherent N, S, P, and O elements in biomass yield naturally self‐doped N, S, P, and O BDCs with unique intrinsic structures. In this paper, the synthesis approaches and applications of BDCs in ECs are reviewed. It shows that BDCs electrochemical performances are highly determined by their pore structures, specific surface areas, heteroatoms doping, graphitization degree, defects, and morphologies. The electrochemical performances of BDCs can further be improved by compositing with other materials, such as graphene, carbon nanofibers/nanotubes, transition metal oxides or hydroxides, and conducting polymers. The future challenges and outlooks of BDCs are also provided. Biomass‐derived carbons (BDCs) are hard carbon with porous morphology, stable structure, superior hardness/strength, and good cycling performances when used in electrochemical capacitors (ECs). In this paper, the synthesis approaches and applications of BDCs in ECs are reviewed.

Highly porous, lightweight versatile cellulose materials were prepared via dissolution–coagulation and subsequent various drying routes. Cellulose was dissolved in ionic liquid/DMSO mixture and coagulation was performed in ethanol. The as prepared wet precursors were used to make materials with three different drying methods: supercritical CO 2 drying, freeze-drying and vacuum drying. The influence of cellulose concentration and drying method on the density, porosity, specific surface area and morphology of cellulose materials is presented and discussed. We provide the understanding of morphology development as a function of processing conditions and give the “recipes” for porosity control.

In this paper, the LaAlO3 perovskite with large specific surface area and abundant surface oxygen vacancies is prepared by the hard template method, on which Ni metal nanoparticles and CaO alkaline additives are loaded. The generated catalyst is applied to the study of methane dry reforming. By analyzing and characterizing all catalysts prepared through BET, XRD, TEM, XPS, H2-TPR and other test methods, the LaAlO3 Hperovskite prepared by the hard template method can obtain both larger specific surface area and more abundant surface oxygen vacancies than the LaAlO3-C perovskite prepared by the traditional sol–gel method. As a result, the Ni-based catalysts supported by LaAlO3-H perovskite exhibit more favorable anti-sintering and anti-carbon deposition ability than Ni/LaAlO3-C catalyst. (Adding) CaO can enhance the adsorption of CO2 on Ni-based catalysts, so N-CaO/LaAlO3 catalyst possesses the most excellent anti-carbon deposition ability.

A high-performance zinc oxide/tin dioxide (ZnO/SnO2) humidity sensor was developed using a simple solvothermal method. The sensing mechanism of the ZnO/SnO2 humidity sensor was evaluated by analyzing its complex impedance spectra. The experimental results prove that the ZnO/SnO2 composite material has a larger specific surface area than pure SnO2, which allows the composite material surface to adsorb more water to enhance the response of the ZnO/SnO2 humidity sensor. ZnO can also contribute to the generation of oxygen-rich vacancies on the ZnO/SnO2 composite material surface, allowing it to adsorb a large amount of water and rapidly decompose water molecules into conductive ions to increase the response and recovery speed of the ZnO/SnO2 humidity sensor. These characteristics allowed the Z/S-2 humidity sensor to achieve a higher response (1,225,361%), better linearity, smaller hysteresis (6.6%), faster response and recovery speeds (35 and 8 s, respectively), and long-term stability at 11–95% relative humidity. The successful preparation of the ZnO/SnO2 composite material also provides a new direction for the design of SnO2-based resistance sensors with high humidity-sensing performance.

Hyper-crosslinked (HCL) polystyrenes show outstanding properties, such as high specific surface area and adsorption capability. Several researches have been recently focused on tailoring their performance for specific applications, such as gas adsorption and separation, energy storage, air and water purification processes, and catalysis. In this review, main strategies for the realization of HCL polystyrene-based materials with advanced properties are reported, including a summary of the synthetic routes that are adopted for their realization and the chemical modification approaches that are used to impart them specific functionalities. Moreover, the most up to date results on the synthesis of HCL polystyrene-based nanocomposites that are realized by embedding these high surface area polymers with metal, metal oxide, and carbon-based nanofillers are discussed in detail, underlining the high potential applicability of these systems in different fields.