Effects and Mechanism of Hyperbranched Phosphate Polycarboxylate Superplasticizers on Reducing Viscosity of Cement Paste.

The adsorption behavior and dispersing capability of hyperbranched phosphated polycarboxylate superplasticizers (PCEs) containing phosphate monoester and phosphate diester were investigated. The hyperbranched structures were constructed using a special monomer dimethylaminoethyl methacrylate (DMAMEA) to create the branches during the polymerization. Meanwhile, the polymer architectures were tailored by varying the content of phosphate monoester and phosphate diester in the backbone via free radical solution polymerization. In contrast to comb-like PCE, hyperbranched PCEs presented a weaker dispersion capability at w/c = 0.29, but with a lower water-to-cement ratio (w/c), the hyperbranched PCEs exhibited a better dispersion capability than the comb-like PCEs. The dynamic light scattering (DLS) and transmission electron microscope (TEM) analysis showed that the adsorption layer of hyperbranched PCEs were thicker than that of comb-like PCEs. A thicker adsorption layer thickness generated thinner diffusion water layer thickness. The increase of the free water amount due to the thinner water diffusion layer is the key mechanism for improving the dispersibility and decreasing the viscosity of cement paste.

Iodine-Catalyzed Cascade Annulation of 4-Hydroxycoumarins with Aurones: Access to Spirocyclic Benzofuran-Furocoumarins.

An attractive approach for the preparation of spirocyclic benzofuran-furocoumarins has been developed through iodine-catalyzed cascade annulation of 4-hydroxycoumarins with aurones. The reaction involves Michael addition, iodination, and intramolecular nucleophilic substitution in a one-step process, and offers an efficient method for easy access to a series of valuable spirocyclic benzofuran-furocoumarins in good yields (up to 99%) with excellent stereoselectivity. Moreover, this unprecedented protocol provides several advantages, including readily available materials, an environmentally benign catalyst, a broad substrate scope, and a simple procedure.

Iodine-Catalyzed Diversity-Oriented Synthesis of 3,4-Heterocycle-Fused Coumarins from 4-Aminocoumarins and Aurones in Different Solvent.

An unprecedented protocol has been developed for the synthesis of 3,4-heterocycle-fused coumarins from 4-aminocoumarins and aurones through iodine-catalyzed cascade reactions. Dihydropyridine-fused coumarin, pyridine-fused coumarin, and pyrrole-fused coumarin derivatives were achieved in good yields with high selectivity when CH3CN, AcOH, and DMSO were used as the solvent, respectively. This protocol provides several advantages, such as easily available starting materials, high atom economy, friendly environment, and simple procedure.

Efficient Red-Emissive Circularly Polarized Electroluminescence Enabled by Quasi-2D Perovskite with Chiral Spacer Cation.

Perovskites are promising environmentally sustainable materials for circularly polarized electroluminescence (CPEL). While another chiral nonemissive layer is required for the developed perovskite-based CPEL, we report herein a highly efficient circularly polarized electroluminescence based on a single layer of quasi-2D perovskite with achiral phenethylammonium iodide (PEAI) and chiral S/R-1-(1-naphthyl)ethylammonium iodide (S/R-NEAI) as dual spacer cations. The quasi-2D perovskite was further passivated by carbazole-functionalized phosphonium. The as-fabricated film exhibits not only a circular dichroism (CD) signal but also prominent circularly polarized luminescence (CPL) activity with a maximum photoluminescence dissymmetry factor (glum) of ∼2.1 × 10-3. More importantly, a highly efficient, spin-polarized light-emitting diode (LED) was fabricated based on the in situ passivated quasi-2D perovskite with a peak external quantum efficiency of 3.7% and a maximum electroluminescence dissymmetry factor (gEL) of ∼4.0 × 10-3.

Cooperation and decision making in a two-sided market motivated by the externality of a third-party social media platform.

In recent years, with the rapid development of Internet technology, the integration of platform economy and e-commerce has become a popular business model. Two-sided platforms have a specific impact on sales, customer experience and transaction efficiency of both sides. In the current severe situation caused by the coronavirus pandemic, both the traditional unilateral market platform and the emerging two-sided market platform are in urgent need of a change in operation mode to reduce the marketing cost. Inspired by the cooperation between Meituan, a two-sided platform, and WeChat, a social media platform, this paper investigates the two-sided platform's scalable decisions on when to cooperate and how to optimize the pricing and investment decisions. We analyze how the two-sided platform makes decisions by considering the changes of network externalities from the cooperation with the social network platform. Compared with the scenario of non-cooperation, we derive the conditions under which platform cooperation can increase demands and increase platforms' profits, and analyze how cooperation affects the optimal pricing strategies. We find that the cooperation leads to a larger demand and a higher total profit, but might lead to higher registration prices for the platform users. Furthermore, we adopt the Nash bargaining framework and introduce platform bargaining power parameters to obtain the optimal cooperation and sharing strategy. Finally, we show how to adjust the investment strategy of the two-sided platform under platform cooperation.

Effect of Early Age-Curing Methods on Drying Shrinkage of Alkali-Activated Slag Concrete.

Drying shrinkage of alkali-activated slag concrete (AASC) is significantly greater than that of concrete made with ordinary Portland cement (OPC). It limits the large-scale application of AASC in field engineering. This study investigates the effect of early age-curing methods, including water curing, curing in elevated-temperature water, and CO2 curing, on drying shrinkage of AASC. Scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric (TG-DTG), and mercury intrusion porosimetry (MIP) were carried out to analyze the composition and microstructure of hydration products, to provide deeper understanding of drying shrinkage of AASC. The results show that water curing decreased drying shrinkage of both C30 and C50 AASC moderately compared to air curing, while it was more effective for C30 AASC. Curing in water of elevated temperature and CO2 curing were very beneficial to mitigate drying shrinkage of AASC. Heat curing decreased drying shrinkage of AASC up to 80%. SEM and TG-DTG results show that denser microstructure formed because of the accelerated hydration, resulting in lower porosity and lower proportion of pores smaller than 25 nm that contributed to the reduction of drying shrinkage. In addition, under high-temperature curing, most autogenous shrinkage of AASC occurred in the first few days because hydration was accelerated. After measurement of drying shrinkage was started, recorded autogenous shrinkage of AASC cured in elevated-temperature water should be much less than that of AASC cured at normal temperature. It is another important reason for the reduction of drying shrinkage. Carbonation occurring in the CO2 curing period led to the decalcification of C-(A)-S-H gel; it coarsened the pore-size distribution and decreased the total porosity. Therefore, drying shrinkage of C30 and C50 AASC was declined by 49% and 53% respectively.

Immobilization of Cr(VI) by hydrated Portland cement pastes with and without calcium sulfate.

This work aims to illustrate the impact of high concentrations of Cr(VI) (based on Na2CrO4) on the hydration assembly and microstructural development of hydrated Portland cement, and the results also present the role of calcium sulfate on the immobilization of Cr(VI) in Portland cement. The results showed that the immobilization of Cr(VI) in hydrated Portland cement was attributed to the formation of CrO4-U phase, an analogue of SO4-U phase (3CaO·Al2O3·CaSO4·0.5Na2SO4·15H2O). The growth of CrO4-U phase on the surface of clinker particles formed a diffusion barrier and hence increased the setting time. Increasing the calcium sulfate dosage impaired the Cr(VI) immobilization due to the competition between CrO42- and SO42- integrated into the U phase. The generalized acid neutralization capacity (GANC) test indicated that the Cr(VI) leaching behavior was a function of the leachate pH value. As the pH decreased to 11.8, the CrO4-U phase was converted quickly to CrO4-ettringite, which generated a slight increase in Cr(VI) concentration. The most leaching sector, approximately 89.3% of added Cr (1wt% of cement), was found in the pH range 11.8-10.5 due to the dissolution of secondary CrO4-ettringite. It could also be shown that the C-S-H had little chemical binding for Cr(VI).

Immobilization potential of Cr(VI) in sodium hydroxide activated slag pastes.

This study investigated the immobilization potential of alkali-activated slag (AAS) pastes for Cr(VI) by examining compressive strength, toxicity characteristic leaching procedure (TCLP) and generalized acid neutralization capacity tests. Alkaline digestion, total acid digestion, XRD, FTIR and SEM-EDS were carried out to clarify the immobilization mechanism. The AAS pastes gave high compressive strengths, which contributed to the physical encapsulation of Cr. The addition of Cr(VI) induced an increase in compressive strength compared to Cr(VI)-free pastes. The leaching results showed that AAS pastes exhibited effective immobilization for Cr(VI) and that the leachability was strongly dependent on the NaOH dosage, water to slag ratio, initial Cr(VI) content, leachate pH and curing duration. The initial Cr(VI) content up to 1.5wt% by weight of slag was well immobilized with the total-Cr leachability below the TCLP regulatory limit of 5mg/L. The digestion results demonstrated that the reduction of chromium from hexavalent to trivalent played a significant role in the immobilization of Cr(VI) in AAS without any additional reductants. The XRD and SEM-EDS results suggested the formation of a clear CrO4-U phase as the primary retention phase for unreduced Cr(VI). Therefore, alkali-activated slag binder is effective in the immobilization of Cr(VI)-bearing wastes.

Crystal structure and photoluminescence of 7-(N,N'-diethylamino)-coumarin-3-carboxylic acid.

The structure of 7-(N,N'-diethylamino)-coumarin-3-carboxylic acid (DCCA) was verified by single crystal X-ray crystallography. The UV-vis absorption and fluorescence of DCCA were discussed. The compound exhibits strong blue emission under ultraviolet light excitation. The molecular structure of DCCA was optimized using density function theory (DFT) at B3LYP/6-31G level, showing that the optimized geometers parameters are in good agreement with experiment data. In addition, the HOMO and LUMO levels of DCCA were deduced.

Syntheses, characterization and fluorescent properties of two triethylene-glycol dicoumarin-3-carboxylates.

Two novel triethylene-glycol dicoumarin-3-carboxylates were synthesized and characterized by element analysis, (1)H NMR, FT-IR and UV-vis absorption spectra. The photoluminescent behaviors of triethylene-glycol dibenzo[5,6]coumarin-3-carboxylate doped in PMMA were discussed. These compounds exhibit strong blue emission under ultraviolet light excitation. Compared to coumarin-3-triethylene glycol diester, the absorption and emission spectra of benzo[5,6]coumarin-3-triethylene glycol diester was bathochromically shifted due to the larger conjugation of benzene moiety. These derivatives have potential possible to explore organic electroluminescent materials.