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Tremendous popularity is observed for multifunctional flexible electronics with appealing applications in intelligent electronic skins, human–machine interfaces, and healthcare sensing. However, the reported sensing electronics, mostly can hardly provide ultrasensitive sensing sensitivity, wider sensing range, and robust cycling stability simultaneously, and are limited of efficient heat conduction out from the contacted skin interface after wearing flexible electronics on human skin to satisfy thermal comfort of human skin. Inspired from the ultrasensitive tactile perception microstructure (epidermis/spinosum/signal transmission) of human skin, a flexible comfortably wearable ultrasensitive electronics is hereby prepared from thermal conductive boron nitride nanosheets‐incorporated polyurethane elastomer matrix with MXene nanosheets‐coated surface microdomes as epidermis/spinosum layers assembled with interdigitated electrode as sensing signal transmission layer. It demonstrates appealing sensing performance with ultrasensitive sensitivity (≈288.95 kPa−1), up to 300 kPa sensing range, and up to 20 000 sensing cycles from obvious contact area variation between microdome microstructures and the contact electrode under external compression. Furthermore, the bioinspired electronics present advanced thermal management by timely efficient thermal dissipation out from the contacted skin surface to meet human skin thermal comfort with the incorporated thermal conductive boron nitride nanosheets. Thus, it is vitally promising in wearable artificial electronic skins, intelligent human‐interactive sensing, and personal health management. [ABSTRACT FROM AUTHOR]

Wearable electronic sensors have attracted extensive attention in multifunctional electronic skin, personalized health monitoring, intelligent human–machine interaction, and smart medical treatment. However, critical challenge exists in simultaneously achieving excellent sensing performances with high sensitivity, rapid response, low sensing limit, and excellent cycling stability for full‐scale human healthcare detection and further timely photothermal therapy. For highly sensitive human skin, the spinosum microstructure in epidermis and dermis takes an important part in sensing signal amplification and transmission. Inspired by the spinosum microstructure of human skin for highly sensitive tactile perception, a skin‐inspired flexible electronic sensor is prepared from the face‐to‐face assembly of an as‐prepared polybutylene adipate‐polyurethane (PBAPU) elastomer matrix with conducting MXene nanosheets‐coated urchin‐like microstructure templated from natural chrysanthemum pollen grain microstructures, and an interdigitated electrode‐coated PBAPU elastomer substrate. The PBAPU elastomer matrix is newly prepared, exhibiting outstanding tensile strength (18.87 MPa), high stretchability (1190%), and comparable elastic modulus (1.7 MPa) to human skin. The as‐assembled flexible electronic sensor exhibits a highly sensitive sensitivity (up to 784.02 kPa−1), low detection limit (0.12 Pa), and reliable cycling stability for intelligent human–machine interfacing. The MXene nanosheets‐coated urchin‐like microstructure‐contained PBAPU possesses efficient photothermal heating performance to achieve on‐demand photothermal therapy for rehabilitation training. [ABSTRACT FROM AUTHOR]

S2−-enriched alkali-activator (SEAA) was prepared by modifying the alkali activator through Na2S. The effects of S2−-enriched alkali-activated slag (SEAAS) on the solidification performance of Pb and Cd in MSWI fly ash were investigated using SEAAS as the solidification material for MSWI fly ash. Combined with microscopic analysis through scanning electron microscopy (SEM), X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR), the effects of SEAAS on the micro-morphology and molecular composition of MSWI fly ash were studied. The solidification mechanism of Pb and Cd in S2−-enriched alkali-activated MSWI fly ash was discussed in detail. The results showed that the solidification performance for Pb and Cd in MSWI fly ash induced by SEAAS was significantly enhanced first and then improved gradually with the increase in dosage of ground granulated blast-furnace slag (GGBS). Under a low GGBS dosage of 25%, SEAAS could eliminate the problem of severely exceeding permitted Pb and Cd in MSWI fly ash, which compensated for the deficiency of alkali-activated slag (AAS) in terms of solidifying Cd in MSWI fly ash. The highly alkaline environment provided by SEAA promoted the massive dissolution of S2− in the solvent, which endowed the SEAAS with a stronger ability to capture Cd. Pb and Cd in MSWI fly ash were efficiently solidified by SEAAS under the synergistic effects of sulfide precipitation and chemical bonding of polymerization products. [ABSTRACT FROM AUTHOR]

To disclose influences of ultrasonic vibration agitation on the carbonation resistance of cement-based materials after absorption of CO2, the variation laws in internal carbonization zone were explored by the testing carbonization depth and carbonization range (pH variation range) of cement mortar after CO2 absorption at different ages. Results demonstrated that when CO2 absorption volumes of the cement mortar before carbonization were 0.44%, 0.88%, 1.32%, 1.76%, and 2.20% (28 d), the carbonization depth under ultrasonic vibration decreased by 5.5%, 12.3%, 21.7%, 20.7%, and 26.7% compared to those under mechanical stirring, respectively. When the ultimate CO2 absorption volume increased to 2.2% of cement mass, the extended degree of cement mortar was 103.23 mm, which decreased by 5.4% compared to that before CO2 absorption. pH variation values of the carbonization range under ultrasonic vibration presented a rising trend with the increase of CO2 absorption volume of cement mortar before carbonation. This indicated that, with the increase of CO2 absorption volume of cement mortar before carbonation increases under ultrasonic vibration, the carbonization process of the hardened body of cement mortar might be decelerated to some extent. Additionally, changes in internal composition and physical images of cement-based materials after absorption of CO2 were analyzed through microtest means like SEM and XRD. A carbonation resistance model was constructed, thus enabling disclosure of the variation mechanism of carbonation resistance of cement-based materials after absorption of CO2 under mechanical stirring and ultrasonic vibration. Results demonstrated that the higher CO2 absorption volume of fresh slurry generated more "nano-level" CaCO3 crystal nucleus. Accordingly, it could improve the porous structure of the cement mortar, decrease the quantity of capillary tubes significantly, improve the compaction degree of cement-based materials effectively, and lower the diffusion rate of CO2 in the cement paste base, thus improving the carbonation resistance. Research conclusions have important significance to decrease CO2 emissions and improve carbonation resistance of concrete. [ABSTRACT FROM AUTHOR]

This study focuses on overcoming the agglomeration issue of nano-SiO2 powder in cement, facilitating the strengthening mechanism of cement-based materials. A nano-SiO2 precursor solution (NSPS) was added to cement-based materials to replace nano-SiO2 powder. The influencing laws of the alkalinity and dosage of the NSPS on the mechanical properties of cement were investigated. Further, the strengthening mechanism of the mechanical properties of cement-based materials after internal nano-SiO2 production was analysed. The results show that (1) when the alkalinity of the precursor solution is a weak acid (pH = 6), the compressive strength of cement-based materials after internal nano-SiO2 production is 25%~36% higher than that of pure cement-based materials and 16%~22% higher than that of cement-based materials with silica fume; (2) when the solid content of SiO2 in the current displacement solution is about 0.16% of the cement mass, the compressive strength of the prepared cement-based material is the highest. With the continuous increase in the solid content of SiO2 in the precursor solution, the compressive strength of cement-based materials after internal nano-SiO2 production decreases but is always greater than the compressive strength of the cement-based material mixed with nano-SiO2 micro powder. According to a microstructural analysis, nano-SiO2 particles that precipitate from the precursor solution can facilitate the hydration process of cement and enrich the gel products formed on the cement particle surface. In addition, new network structures among cement particles are formed, and precipitated nano-SiO2 particles fill in the spaces among these cement particles as crystal nuclei to connect the cement particles more tightly and compact the cement-based materials. This reinforces the mechanical properties of cement-based materials. [ABSTRACT FROM AUTHOR]

The issues associated with the fabrication of nano-silica (NS) mineral powder, such as high cost and agglomeration, can be effectively mitigated by using a precursor solution of NS as the external mixture of cement-based materials. Based on the liquid-phase preparation of NS mineral powder, its preparation technology was thoroughly investigated herein. The precursor solution of NS was synthesized using acid media (HCL, HNO3, HBO3, HCOOH, CH3COOH)—the acetic acid concentration was 1~15%—and siliceous materials. (The concentration of sodium silicate was 20~38%). In addition, the pH value (pH4~pH8) of the precursor solution was measured using a pH detector. The indexes of NS, such as precipitation time, morphology, and distribution, were observed to formulate a preparation technique for the precursor solution of NS that possessed the best results for the precipitation of nanoparticles. From the acquired results, it was demonstrated that acetic acid solution (concentration ≤ 3%) and sodium silicate solution (concentration ≤ 25%) were mixed into a solution with pH = 6, which was the optimum mixing ratio for the precursor solution of NS. The prepared precursor solution of NS was also added to the Ca(OH)2 saturated solution, and the precursor solution became active from a stable state. Then, NS particles were precipitated in an alkaline solution and reacted with Ca(OH)2 to form calcium silicate gel, which made the solution increasingly turbid and generated many visible and uniformed flocculating substances. With time, gels were continuously produced, which then turn white. Similarly, NS particles can be precipitated when the precursor solution is added to cement paste, which reacts with the Ca(OH)2 to generate CSH gel and improve the compactness of the cement paste. [ABSTRACT FROM AUTHOR]