Micropore Size Research Articles

The study of the structure and performance of polyoxymethylene modified by nucleating agent L

With the expanding application areas of polyoxymethylene (POM), the challenges in its crystal modification are becoming greater. Conventional nucleating agents have issues with compatibility with POM. So we used a nucleating agent L with a similar molecular chain structure to POM through melt blending to modify POM. Using instruments to characterize and test the samples, and studying the effect of nucleating agent L on the structure and properties of POM. The results showed that after adding a small amount of nucleating agent. The crystal size was reduced. The number and size of micro-pores at the cross-section were significantly reduced. The crystallization performance of POM were improved. This provides a new direction for the future development of POM-specific nucleating agents and the direction of efficient nucleating.

Effect of Negative Pulse on the Stability of Black Electrolytes for Magnesium Alloy Microarc Oxidation.

The correlation between negative pulse and the black electrolyte properties of magnesium alloy micro-arc oxidation and the treated area was investigated by introducing a negative pulse electric field. The physical phase composition, microstructure, elemental distribution, and content of the coating were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). The results showed that the introduction of negative pulses favored the generation of MgO and MgSiO3 contents in the coatings, and an increase in the MgO phase was found in the coatings formed in the failed electrolytes; the microporous size and microcracks of the coatings were gradually and significantly reduced; the average consumption of Cu ions was 0.0453 g/L·dm2, which is only 26% of that in the unipolar condition; the introduction of the negative pulses significantly improved the "anomalous consumption" of Cu ions. The introduction of negative pulse can significantly improve the "abnormal consumption" of copper ions, which is attributed to the change in the electric field by negative pulse, which makes the cathode-enriched Cu ions migrate to the anode and reduces the reduction and precipitation of Cu ions at the cathode.

Room temperature aqueous synthesis of defect-engineered MOF-801 membrane towards efficient nanofiltration

Room temperature (RT) aqueous preparation of MOF membranes is of significant interest in meeting the demands of sustainability. Nevertheless, there remains no report on RT aqueous synthesis of water-stable high-valence MOF membranes to date. In this study, we developed a one-step RT protocol for fabricating defect-engineered MOF-801 membrane in aqueous media. Owing to enhanced structural hydrophilicity and enlarged micropore size, water was enabled to diffuse through the membrane with higher permeation flux. Obtained membrane exhibited exceptional dye rejection rate (CR:99.75 %, MB:99.69 % and MG:99.41 %) and unprecedented water flux (CR:77.33 L m−2 h−1·bar−1, MB:71.43 L m−2 h−1·bar−1 and MG:81.28 L m−2 h−1·bar−1), which were superior to state-of-the-art 3D pure MOF membranes. Our protocol paves a promising way towards sustainable production of water-stable MOF membranes under mild conditions.

Synthesis of microporous titanium surface with aligned pores through changes of currents during electrochemical process

This paper reports the synthesis of microporous Ti surfaces with aligned pores by applying a different current during electrochemical process for application in cell-surface interaction study and biomedical implants. As the microporous Ti surfaces were synthesized by current from (0.5–4)A, the microstructure of the Ti surfaces was shifted from a relative smooth to microporous one that was observed to have an aligned pore surface. Optical images showed that the micropore sizes in ∼(85.4–224.4)µm. The roughness of the microporous Ti was significantly higher than that of the Ti by a factor of approximately 5 to 7. Confocal laser scanning microscope showed excellent cell attachment and preferential growth on the microporous Ti with aligned channels after 72 h of culturing which could be important for cell-surface interactions study and biomedical implants.

Molecular dynamics study on microporous direction effect on C-S-H fracture performance

The hydrated calcium silicate (C-S-H) gel is the main hydration product and source of paste strength of cement. In this paper, molecular dynamics simulation method based on ClayFF was used to investigate the effect of micropore direction on the fracture performance of C-S-H under tensile load and interpret the micro deformation, fracture, and failure processes of cement concrete. After establishing a complete C-S-H model with chemical formula (CaO)1.60(SiO2)(H2O)1.57 and micropore models with different pore sizes and directions, the influence of micropore direction on the fracture performance of the C-S-H models was analyzed from three perspectives: mechanical property, micro fracture process, and energy evolution. It was found that the ultimate stress and Young’s modulus of the C-S-H models showed a decreasing trend with the increase of micropore size, and were less affected by the direction of micropores. It was also found that the direction of micropores had a significant impact on the structural failure of the C-S-H models in the x direction tensile simulation, followed by the y direction, and had the smallest effect on the z direction. It was also found that the elastic energy and input energy of the C-S-H models exhibited decreasing trends with the increase of pore size, and the three-dimensional critical energy release rates of different pore models’ difference also decreased.

Microstructured Porous Capacitive Bio-pressure Sensor Using Droplet-based Microfluidics.

Devices that mimic the functions of human skin are known as "electronic skin," and they must have characteristics like high sensitivity, a wide dynamic range, high spatial homogeneity, cheap cost, wide area easy processing, and the ability to distinguish between diverse external inputs. This study introduces a novel approach, termed microfluidic droplet-based emulsion self-assembly (DMESA), for fabricating 3D microstructured elastomer layers using polydimethylsiloxane (PDMS). The method aims to produce accurate capacitive pressure sensors suitable for electronic skin (e-skin) applications. The DMESA method facilitates the creation of uniform-sized spherical micropores dispersed across a significant area without requiring a template, ensuring excellent spatial homogeneity. Micropore size adjustment, ranging from 100 to 600 μm, allows for customization of pressure sensor sensitivity. The active layer of the capacitive pressure sensor is formed by the three-dimensional elastomer itself. Experimental results demonstrate the outstanding performance of the DMESA approach. It offers simplicity in processing, the ability to adjust performance parameters, excellent spatial homogeneity, and the capability to differentiate varied inputs. Capacitive pressure sensors fabricated using this method exhibit high sensitivity and dynamic amplitude, making them promising candidates for various e-skin applications. The DMESA method presents a highly promising solution for fabricating 3D microstructured elastomer layers for capacitive pressure sensors in e-skin technology. Its simplicity, performance adjustability, spatial homogeneity, and sensitivity to different inputs make it suitable for a wide range of electronic skin applications.

Unusually large microporous HKUST-1 via polyethylene glycol-templated synthesis: enhanced CO2 uptake with high selectivity over CH4 and N2.

Porous solids with highly microporous structures for effective carbon dioxide uptake and separation from mixed gases are highly desirable. Here we present the use of polyethylene glycol (20,000g/mol) as a soft template for the simple and rapid synthesis of a highly microporous Cu-BTC (denoted as HKUST-1). The polyethylene glycol-templated HKUST-1 obtained at room temperature in 10min exhibited a very high Brunauer-Emmett-Teller (BET) surface area of 1904 m2/g, pore volume of 0.87 cm3/g, and average micropore size of 0.84nm. However, conventional HKUST-1 exhibits a BET surface area of 700-1700 m2/g confirming the advantages of using this method. X-ray powder diffraction and electron microscopy analysis confirm the formation of highly crystalline and uniform octahedral particles with sizes ranging from 100nm to 120µm. Adsorption isotherms recorded at temperatures between 273 and 353K and pressures up to 40bar revealed a more favorable adsorption capacity of HKUST-1 for CO2 vs. CH4 and N2 (708mg (CO2)/g, 214mg (CH4)/g and 177mg (N2)/g at 298K and 40bar). The Langmuir, isotherm model, and isosteric heats of adsorption were evaluated. The CO2 interaction at PEG-templated HKUST-1 is physical, exothermic, and spontaneous with DH° = - 6.52kJ/mol, DS° = - 13.72J/mol, and DG° = - 2.43kJ/mol at 298K at 40bar. The selectivities in equimolar mixtures were determined as 53 and 24, respectively, for CO2 over N2 and CH4. CO2 adsorption-desorption tests reveal high adsorbent reusability. The cost-effective and quickly prepared PEG-templated HKUST-1 demonstrates high efficacy as a gas adsorbent, particularly in selectively capturing CO2.

Implications of the depositional and diagenetic attributes on the reservoir properties of the siliciclastic mangahewa formation, Taranaki Basin, New Zealand: Integrated petrographical and petrophysical studies

The siliciclastic Mangahewa reservoir in the Pohokura Gas Field presents a formidable challenge for gas exploration due to its diverse petrophysical properties. To address this challenge, our study employs a comprehensive approach integrating petrography and petrophysical analyses for core and well logging data. In the present study, we uncover an association of sandstone microfacies, in the key wells like Pohokura South-1, Pohokura-1, and Pohokura-2 wells, which change from fine to medium-grained subfeldsarenites to lithic feldsarenites microfacies. The petrographic investigation pinpoints the critical factors influencing the reservoir quality, including facies types, grain size, pore types, sedimentary structure, detrital clay content, and mineral composition. Both the primary intergranular and secondary dissolution pore spaces are responsible for the influential large intergranular pore volumes causing a superior reservoir quality. Mineral composition, influenced by the source and lithofacies, significantly impacts the reservoir properties. Diagenetic processes further control the reservoir quality, where the abundant silica cement, the illitic clays, and the rare pervasive carbonate cementation render the low reservoir quality. Compaction significantly reduces porosity during diagenesis. High-quality reservoir sandstones are characterized by coarse grain size, minimal detrital clay presence, predominantly quartz composition, limited carbonate and moderate silica cementation, low authigenic illite levels, and minor compaction impact. Based on the petrophysical data, the Mangahewa reservoir is composed of five RRTs (reservoir rock types) with the RRT1 samples having the best reservoir characteristics due to their fair porosity, very good permeability, and macro pore sizes. On the other side, the RRT5 samples are characterized by the lowest reservoir quality (poor porosity and permeability and micropore sizes) due to cementation and compaction. Our study provides valuable insights into the intricate petrophysical properties of the Mangahewa reservoir, enhancing the predictability of the reservoir behavior and optimizing hydrocarbon production in this challenging geological setting.

Surface damage induced by micropores in transparent ceramics under nanosecond laser irradiation.

The increasing use of transparent ceramics in laser systems presents a challenge; their low damage threshold has become a significant impediment to the development of powerful laser systems. Consequently, it is imperative to undertake research into the damage sustained by these materials. Micropores, the most common structural defects in transparent ceramics, inevitably remain within the material during its preparation process. However, the relationship between the density and size of these micropores and their impact on nanosecond laser damage threshold and damage evolution remains unclear. In this study, we utilize the annealing process to effectively manage the density and size of micropores, establishing a correlation between micropores in relation to damage thresholds. This study confirms for the first time that micropores significantly contribute to laser damage, comparing and analyzing the damage morphology characteristics of both front and rear surfaces of transparent ceramics. It also presents, potential mechanisms that may contribute to these differences in damage. This paper offers guidance for controlling micropores during the preparation and processing of transparent ceramics with high laser damage thresholds. The findings are expected to further improve the anti-nanosecond laser damage capabilities of transparent ceramics.

Low-cost and convenient fabrication of polymer micro/nanopores with the needle punching process and their applications in nanofluidic sensing.

Solid-state micro/nanopores play an important role in the sensing field because of their high stability and controllable size. Aiming at problems of complex processes and high costs in pore manufacturing, we propose a convenient and low-cost micro/nanopore fabrication technique based on the needle punching method. The thin film is pierced by controlling the feed of a microscale tungsten needle, and the size variations of the micropore are monitored by the current feedback system. Based on the positive correlation between the micropore size and the current threshold, the size-controllable preparation of micropores is achieved. The preparation of nanopores is realized by the combination of needle punching and chemical etching. First, a conical defect is prepared on the film with the tungsten needle. Then, nanopores are obtained by unilateral chemical etching of the film. Using the prepared conical micropores, resistive-pulse detection of nanoparticles is performed. Significant ionic current rectification is also obtained with our conical nanopores. It is proved that the properties of micro/nanopores prepared by our method are comparable to those prepared by the track-etching method. The simple and controllable fabrication process proposed here will advance the development of low-cost micro/nanopore sensors.

Quantitative Scrolling into Microporous Nanotubes of the Hydrous Layered Silicate Ilerite

AbstractThe synthetic hydrous layered silicate ilerite was quantitatively converted into microporous nanoscrolls (NS). Delamination of ilerite that was ion‐exchanged for N‐Methyl‐D‐glucaminium (Meg+), through one‐dimensional (1D) dissolution initially yields lamellar liquid crystalline (nematic) suspensions. Subsequent protonation with acetic acid of tangling Si‐O− to silanol groups reduces the pH‐dependent charge of the basal surfaces. Complete NS formation is then triggered by diluting the nematic suspension below 0.05 wt%. As scrolling commonly has been attributed to hydrophobic interaction of organic counterions, Meg+ was replaced by lithium ions but this showed no detrimental effect on the scrolling efficiency. The resulting NS have a typical length of 2–4 μm that corresponds well with typical diameters of the parent nanosheets. Ar‐physisorption isotherms showed a bimodal micropore size with maxima around 0.8 and 1.9 nm. We attribute the first to the tubular hollow inner diameter of the NS and the latter to wedgelike interparticle porosity. The material showed a large specific surface area of 226 m2 g−1.

3D-Printable Sustainable Bioplastics from Gluten and Keratin.

Bioplastic films comprising both plant- and animal-derived proteins have the potential to integrate the optimal characteristics inherent to the specific domain, which offers enormous potential to develop polymer alternatives to petroleum-based plastic. Herein, we present a facile strategy to develop hybrid films comprised of both wheat gluten and wool keratin proteins for the first time, employing a ruthenium-based photocrosslinking strategy. This approach addresses the demand for sustainable materials, reducing the environmental impact by using proteins from renewable and biodegradable sources. Gluten film was fabricated from an alcohol-water mixture soluble fraction, largely comprised of gliadin proteins. Co-crosslinking hydrolyzed low-molecular-weight keratin with gluten enhanced its hydrophilic properties and enabled the tuning of its physicochemical properties. Furthermore, the hierarchical structure of the fabricated films was studied using neutron scattering techniques, which revealed the presence of both hydrophobic and hydrophilic nanodomains, gliadin nanoclusters, and interconnected micropores in the matrix. The films exhibited a largely (>40%) β-sheet secondary structure, with diminishing gliadin aggregate intensity and increasing micropore size (from 1.2 to 2.2 µm) with an increase in keratin content. The hybrid films displayed improved molecular chain mobility, as evidenced by the decrease in the glass-transition temperature from ~179.7 °C to ~173.5 °C. Amongst the fabricated films, the G14K6 hybrid sample showed superior water uptake (6.80% after 30 days) compared to the pristine G20 sample (1.04%). The suitability of the developed system for multilayer 3D printing has also been demonstrated, with the 10-layer 3D-printed film exhibiting >92% accuracy, which has the potential for use in packaging, agricultural, and biomedical applications.

Effect of deposition strategies on microstructures, defects and mechanical properties of 5356 aluminum alloy by wire arc additive manufacturing

Effect of deposition strategies on microstructures, defects and mechanical properties of 5356 aluminum alloy by wire arc additive manufacturing

Multiscale Co‐Assembly to Meso‐Macroporous Foamed Single‐Crystal Metal–Organic Frameworks for the Supported Capture of Sulfur Dioxide

AbstractThe introduction of enlarged and interconnected nanochannels into metal–organic frameworks (MOFs) overcome their micropore size restriction, enhances mass transportation, and improves the accessibility of anchored metal clusters. Herein, foamed Ce‐MOF single crystals (F‐Ce‐MOF‐SC‐x) designed from a multiscale co‐assembly is reported in the presence of a copolymer template and 1,3,5‐trimethylbenzene as a structural regulator. The resultant F‐Ce‐MOF‐SC‐x possessed well‐defined microporous tandem‐ordered meso‐macroporous foams with superior connectivity and versatile Ce‐defective unsaturated sites (Ce‐DUS). F‐Ce‐MOF‐SC‐x is applied as a stable carrier for anchoring polytertiary amines (PA) via coordination interactions with Ce‐DUS. Owing to the superior ability of PA to recognize SO2, the resultant F‐Ce‐MOF‐SC‐x@yPA delivers exceptional performance in terms of the high‐temperature reversible adsorption and separation of SO2, including a remarkable capacity for SO2, spectacular selectivity for SO2/CO2/N2, an ultrafast adsorption equilibrium rate, and stability for 50 cycles. These characteristics are outstanding among those of MOFs and superior to those of many reported SO2 adsorbents.

Role of moisture content in coal oxidation during the spontaneous combustion latency

The role of moisture content in coal oxidation during the spontaneous combustion latency was studied by an isothermal flow reactor. The physical and chemical changes during the drying and oxidation process were investigated using low-pressure nitrogen gas adsorption (LP-N2GA) experiments, Electron spin resonance (ESR) experiments and X-ray photoelectron spectroscopy (XPS) experiments. Experimental results reveal that moisture acts either as a promoting or an inhibiting agent under different contents. The differences in total temperature rise (TTR) of varying coal samples are the result of a complex set of competing factors. The LP-N2GA experiments reveal no pore collapse until the moisture reaches 3.05 %. Collapse clearly occurs with the micropore and mesoporous size range. When the moisture content is higher 3.05 %, the specific surface and pore volume increases with the removal of moisture. In addition, the evaporation of water also re-exposes the previously covered active sites and increases the concentration of free radicals. However, the removal of moisture makes the generation of peroxides more difficult due to moisture acts as a catalyst in the formation of such peroxide species.

APPLICATION OF BENTONITE IN OBTAINING SULFUR-CONTAINING UREA BASED ON A FLUSH OF UREA AND SULFUR

This paper presents the results of a study of the processes for obtaining granular sulfur-containing carbamide from sulfur and a liquid carbamide melt using bentonite to influence the surface tension between two phases of sulfur and urea to obtain a mixed homogeneous phase. It was revealed that the addition of bentonite to sulfur before adding the latter to the melt of urea, which has a temperature of 135-145 °С at mass ratios (NH2)2CO : bentonite : sulfur = 100 : (1-7) : (1-15) prevents the stratification of melts sulfur and urea. The optimal conditions for obtaining, the composition and properties of granular sulfur-containing urea with a balanced content of nitrogen and sulfur are determined by adding a mixture of sulfur with bentonite to the urea melt before granulation. In fertilizers obtained with the addition of a mixture of sulfur with bentonite to the melt of carbamide at the studied ratios, the strength of the granules increases from the initial 2.65 to 4.76 MPa, the gyroscopic point increases from 58.4% to 62.3%, pH and porosity decrease from 8 02 to 5.32 and from 5.60 to 4.55, respectively, and the dissolution rate of the granules decreases 3.36 times. It was also found that when adding a mixture of sulfur with bentonite to the melt of carbamide, the density and viscosity of the melt increase with an increase in the amount of added mixture of sulfur with bentonite. An increase in the amount of addition of a mixture of sulfur and bentonite from 1 to 15 and from 1 to 7 g per 100 г melt of urea at a temperature of 135 °C leads to an increase in the density and viscosity of the melts from 1.16 to 1.33 g/cm3 and from 2.56 to 3.06 cPz. Microscopic examination showed that adding a mixture of sulfur with bentonite to the carbamide melt leads to a decrease in the size of micropores and microcracks up to 0.93 microns wide. On the basis of the results obtained, optimal technological parameters and a process flow diagram for the production of sulfur-containing granulated carbamide are proposed.

Pushing the limits of microfluidic droplet production efficiency: engineering microchannels with seamlessly implemented 3D inverse colloidal crystals.

Although droplet microfluidics has been studied for the past two decades, its applications are still limited due to the low productivity of microdroplets resulting from the low integration of planar microchannel structures. In this study, a microfluidic system implementing inverse colloidal crystals (ICCs), a spongious matrix with regularly and densely formed three-dimensional (3D) interconnected micropores, was developed to significantly increase the throughput of microdroplet generation. A new bottom-up microfabrication technique was developed to seamlessly integrate the ICCs into planar microchannels by accumulating non-crosslinked spherical PMMA microparticles as sacrificial porogens in a selective area of a mold and later dissolving them. We have demonstrated that the densely arranged micropores on the spongious ICC of the microchannel function as massively parallel micronozzles, enabling droplet formation on the order of >10 kHz. Droplet size could be adjusted by flow conditions, fluid properties, and micropore size, and biopolymer particles composed of polysaccharides and proteins were produced. By further parallelization of the unit structures, droplet formation on the order of >100 kHz was achieved. The presented approach is an upgrade of the existing droplet microfluidics concept, not only in terms of its high throughput, but also in terms of ease of fabrication and operation.

Wound microenvironment regulatory poly(L-glutamic acid) composite hydrogels containing metal ion-coordinated nanoparticles for effective hemostasis and wound healing.

Regulating the wound microenvironment to promote proliferation, vascularization, and wound healing is challenging for hemostats and wound dressings. Herein, polypeptide composite hydrogels have been simply fabricated by mixing a smaller amount of metal ion-coordinated nanoparticles into dopamine-modified poly(L-glutamic acid) (PGA), which had a microporous size of 10-16 μm, photothermal conversion ability, good biocompatibility, and multiple biological activities. In vitro scratch healing of fibroblast L929 cells and the tube formation of HUVECs provide evidence that the PGA composite hydrogels could promote cell proliferation, migration, and angiogenesis with the assistance of mild photothermia. Moreover, these composite hydrogels plus mild photothermia could effectively eliminate reactive oxygen species (ROS), alleviate inflammation, and polarize the pro-inflammatory M1 macrophage phenotype into the pro-healing M2 phenotype to accelerate wound healing, as assessed by means of fluorescent microscopy, flow cytometry, and quantitative real-time polymerase chain reaction (qRT-PCR). Meanwhile, a rat liver bleeding model illustrates that the composite hydrogels reduced the blood loss ratio to about 10% and shortened the hemostasis time to about 25 s better than commercial chitosan-based hemostats. Furthermore, the full-thickness rat skin defect models showcase that the composite hydrogels plus mild photothermia could proheal wounds completely with a fast healing rate, optimal neovascularization, and collagen deposition. Therefore, the biodegradable polypeptide PGA composite hydrogels are promising as potent wound hemostats and dressings.

Enhancing corrosion resistance in Mg[sbnd]Li alloy through plasma electrolytic oxidation coatings — Exploring the impact of ionic liquids (BmimBF4)

The wide application of MgLi alloys is limited by the poor corrosion resistance, which needs to be improved by surface treatment. Plasma electrolytic oxidation (PEO) method is one of the most promising methods for the formation of oxide coatings on MgLi alloys. However, the conventional PEO technique with high energy consumption causes poor coating compactness and hampers efforts to enhance corrosion resistance. In this study, various concentrations of ionic liquids (1-butyl-3-methylimidazolium tetrafluoroborate, BmimBF4) are introduced into the concentrated alkaline electrolyte to facilitate the formation of a PEO coating on the surface of LA91 magnesium‑lithium (MgLi) alloy. The influence of BmimBF4 on PEO coatings has been investigated. The results indicate that a concentrated electrolyte significantly lowers the working voltage of PEO, thereby enhancing energy efficiency. Uneven adsorption on the substrate surface, resulting from the low concentration of BmimBF4 (≤20 mL/L) in the electrolyte, induces partial discharge, leading to high surface roughness and the formation of large pores. However, when an excessive amount of BmimBF4 (>20 mL/L) is present, it uniformly adsorbed onto the substrate surface during the initial stage of PEO process, forming a corrosion inhibitor layer. This leads to a consistent discharge on the surface of substrate throughout the entire PEO process, resulting in a reduction in both surface roughness and micropore size. Among these coatings, the one prepared in an electrolyte containing 20 mL/L BmimBF4 exhibits the highest contact angle (66.8° ± 3.8°) and the best long-term corrosion resistance (hydrogen evolution rates <0.02 mL·cm−2·h−1). These properties can be attributed to the physical and chemical adsorption of BmimBF4, which contains hydrophobic long alkyl chains, as well as the maximum thickness with extended discharging channels. This study offers a guiding strategy for further reducing energy consumption and enhancing the corrosion resistance of PEO coatings.

Properties and Microstructure of an Interfacial Transition Zone Enhanced by Silica Fume in Concrete Prepared with Coal Gangue as an Aggregate.

The wide application of concrete prepared with coal gangue (CG) as an aggregate (CPCGA) is limited because of the low mechanical strength and strong water absorption capacity of CG. This paper used silica fume (SF) to improve the performance of the interfacial transition zone (ITZ) in CPCGA and revealed the enhancement mechanism. The results showed that the compressive strength of CPCGA prepared with cement replaced by a suitable amount of SF at the age of 28 days increased by more than 30%, and the flexural strength increased by over 20%. The SF could effectively reduce the porosity and micropore size in the ITZ of CPCGA, and the porosity of the ITZ in CPCGA added with 7.50% SF decreased by 44.22, 46.16, and 24.46% at distances from the aggregate surface of 10, 50, and 100 μm, respectively, compared with CPCGA without SF. Further research showed that Ca(OH)2 (CH) generated in the cement hydration reaction reacted with a large amount of active SiO2 in SF to restrain the formation of coarse CH in the ITZ of CPCGA, and the calcium silicate hydrate (C-S-H) gel generated filled the ITZ micropores to reduce the ITZ porosity further. Moreover, the reaction of SF and CH helped to promote the hydration reaction of cement to proceed thoroughly in CPCGA, thus improving CPCGA performance.