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Environmental information disclosure (EID) is an important embodiment of corporate social responsibility. With the awakening of public awareness of environmental protection and the increasing pressure of environmental preservation, enterprises tend to strategically manipulate environmental information for the pursuit of profit, which will consequently lead to environmental information disclosure falsification (EIDF) and disruption of both the market regulatory order and the development of green economy. In this article, support vector machine (SVM) technique is applied to construct the detection model of corporate EIDF. Based on the theory of "public pressure," the detection indicators will be improved from three aspects: public pressure, corporate governance, and financial indicators. The training set and test set are constructed by combining the manually collected cases of environmental administrative penalties from 2015 to 2019 with the indicator information of nonfinancial listed enterprises in China's A-share market, and the SVM detection performance is compared with the logistic regression of the benchmark model. To solve the problem of category imbalance, we have introduced the Borderline-SMOTE oversampling technique. Based on the detection results of SVM and Borderline-SMOTE, we find that the Borderline-SMOTE-SVM model has the best detection performance, surpassing the SVM and logistic regression models. These conclusions have constructive policy implications for regulatory agencies, investors, the third-party service sector, enterprises, and government policy-making to achieve high-quality corporate EID. [ABSTRACT FROM AUTHOR]

Polyethylene terephthalate (PET) and CO2, two chemical wastes that urgently need to be transformed in the environment, are converted simultaneously in a one‐pot catalytic process through the synergistic coupling of three reactions: CO2 hydrogenation, PET methanolysis and dimethyl terephthalate (DMT) hydrogenation. More interestingly, the chemical equilibria of both reactions were shifted forward due to a revealed dual‐promotion effect, leading to significantly enhanced PET depolymerization. The overall methanol yield from CO2 hydrogenation exceeded the original thermodynamic equilibrium limit since the methanol was in situ consumed in the PET methanolysis. The degradation of PET by a stoichiometric ratio of methanol was significantly enhanced because the primary product, DMT was hydrogenated to dimethyl cyclohexanedicarboxylate (DMCD) or p‐xylene (PX). This synergistic catalytic process provides an effective way to simultaneously recycle two wastes, polyesters and CO2, for producing high‐value chemicals. [ABSTRACT FROM AUTHOR]

Polyethylene terephthalate (PET) and CO2, two chemical wastes that urgently need to be transformed in the environment, are converted simultaneously in a one‐pot catalytic process through the synergistic coupling of three reactions: CO2 hydrogenation, PET methanolysis and dimethyl terephthalate (DMT) hydrogenation. More interestingly, the chemical equilibria of both reactions were shifted forward due to a revealed dual‐promotion effect, leading to significantly enhanced PET depolymerization. The overall methanol yield from CO2 hydrogenation exceeded the original thermodynamic equilibrium limit since the methanol was in situ consumed in the PET methanolysis. The degradation of PET by a stoichiometric ratio of methanol was significantly enhanced because the primary product, DMT was hydrogenated to dimethyl cyclohexanedicarboxylate (DMCD) or p‐xylene (PX). This synergistic catalytic process provides an effective way to simultaneously recycle two wastes, polyesters and CO2, for producing high‐value chemicals. [ABSTRACT FROM AUTHOR]

Mechanically robust shape‐morphing materials that can transform from miniaturization into complex structures are highly desirable for real‐world device applications. However, fabricating mechanically robust yet geometrically complex 3D shape‐morphing structures with excellent functionality and high load‐bearing capacity remains a challenge. Inspired by drum tower buildings, a simple, rapid, and universal method is presented for fabricating multifunctional shape‐memory smart devices with complex and rigid 3D kirigami geometry in the two‐stage epoxy‐amine‐acrylate photopolymer systems. In the first‐stage reaction, transparent polymer films with a Tg of 29–49 °C are obtained by the epoxy‐amine chemistry. The shape‐memory programming process allows the first‐stage film with a drum tower‐inspired 2D kirigami pattern to be manipulated into an unsupported 3D structure. In the second‐stage reaction, UV‐induced free‐radical polymerization of methacrylate groups in the first‐stage network is employed to rapidly lock the programmed 3D kirigami structure with a Tg of 66–138 °C. The drum tower‐inspired 3D kirigami structure withstands 1000 times its own weight. The shape memory fluorescent 3D device and shape memory electronic 3D device are engineered by combining the two‐stage photopolymer system and a 3D kirigami structure. This work represents a versatile method to create multifunctional shape‐memory devices with rigid 3D geometry for potential applications. [ABSTRACT FROM AUTHOR]

A biocompatible Bi@mSiO 2 @MnO 2 nanocomposite is fabricated using a facile stepwise reaction method, which exhibits powerful theranostic performance for CT/MR imaging-guided enhanced PTT/CDT/chemotherapy of tumours. [Display omitted] Cancer is a leading cause of death worldwide and seriously threatens the health of humans. The current clinical treatments for cancer are not efficient and always lead to significant side effects. Herein, a biocompatible and powerful theranostic agent (Bi@mSiO 2 @MnO 2 /DOX) is fabricated using a facile stepwise reaction method. The Bi nanoparticles (NPs) are coated by mesoporous silica to protect the Bi NPs from oxidation, which guarantees the stable photothermal effect of the Bi NPs. When the Bi@mSiO 2 @MnO 2 /DOX nanocomposites (NCs) accumulate in the tumour site, hyperthermia is generated by Bi NPs under near-infrared (NIR) light irradiation for photothermal therapy (PTT), and the generated heat triggers the release of DOX for chemotherapy in the tumour. In addition, the MnO 2 of the NCs responsively catalyses endogenous H 2 O 2 to generate O 2 , raising the oxygen level to enhance the effect of chemotherapy in the tumour microenvironment (TME), and consumes glutathione (GSH) to produce Mn2+ for magnetic resonance (MR) imaging. Under acidic TME conditions, H 2 O 2 and Mn2+ also produce toxic hydroxyl radical (· OH) for chemodynamic therapy (CDT). Furthermore, the Bi NPs can also be used as excellent contrast agents for X-ray computed tomography (CT) imaging of tumours with a high CT value (6.865 HU mM−1). The Bi@mSiO 2 @MnO 2 /DOX NCs exhibit a powerful theranostic performance for CT/MR imaging-guided enhanced PTT/CDT/chemotherapy, which opens a new prospect to rationally design theranostic agents for tumour imaging. [ABSTRACT FROM AUTHOR]

The flexural strength and compressive strength are the two most important parameters that characterize the mechanical properties of cement-based materials, but the two are usually mutually exclusive or negatively correlated. The flexural strength of cement-based materials cannot be effectively improved by a single nanomaterial without reducing their compressive properties. Therefore, compounding various micro–nano materials, fully utilizing their respective advantages, and developing composite materials with new properties and application characteristics are important techniques for enhancing the mechanical properties of cement-based materials. This study aimed to investigate the synergistic enhancement of the mechanical properties of concrete by using microcrystalline cellulose (MCC) and nano-silica (NS) composites. MCC and NS were mixed and modified to synthesize MCCNS materials, which were added to cement slurry for experiments. Results indicated that the flexural strength and compressive strength of the cement paste with MCCNS materials were significantly increased compared with those of the cement pastes without MCCNS or with only NS. The flexural strength of the cement paste with MCCNS-1 was increased by 47%, 20%, 6.3%, and 6.8% after curing for 1, 7, 28, and 56 days, respectively. Meanwhile, compressive strength was also increased by 14.4%, 6.3%, 6.8% and 6.5%, respectively. In addition, the reaction mechanism was speculated through a variety of test results. The addition of MCCNS material facilitated the formation of additional C-S-H, which also contributed to enhancing the mechanical properties of cement paste. • Novel nanocomposites were synthesized using MCC and NS through adsorption-phase reaction and sol–gel methods. • The mechanical properties of cement-based materials were notably enhanced by incorporating MCCNS materials. • The volcanic ash activity of NS led to additional C-S-H formation, improving the mechanical strength of the cement paste. [ABSTRACT FROM AUTHOR]

• Novel organic/inorganic nanocomposites LNTS-1 and CNTS-2 were synthesized from NS and alpha thioctic acid. • Compared with bulk CNTS-2, linear LNTS-1 can effectively improve the macro flexural strength of cement-based materials. • The results of adsorption experiments show that LNTS-1 has strong adsorption on calcium ions. Using organic/inorganic nanocomposites to optimize the microstructures of cement hydration products at the micro/nanometre scale is a promising method for improving the mechanical properties of cement-based materials. One type of novel nanohybrid material modified by the flexible autonomous healing polymer poly-TA (thioctic acid) was synthesized and used as a highly efficient mechanical improvement agent for cement paste. The nanohybrids linear LNTS-1 and bulk CNTS-2 were synthesized from silane-coupled nanosilica and alpha thioctic acid. Due to the existence of hydrogen bonds, coordination bonds and dynamic covalent S S bonds, this type of linear poly-TA with a certain amount of calcium content exhibited good self-healing properties. Linear LNTS-1 can effectively improve the macro flexural strength of cement-based materials without a negative effect on their compressive strength. The flexural strength of cement pastes with 1.0‰ LNTS-1 increased by 11.9%, 15.6%, and 16.9% after curing for 3, 7, and 28 d compared with the control cement paste. The results of adsorption experiments show that nanohybrid LNTS-1 has strong adsorption on calcium ions, which affects the formation of cement hydration products. [ABSTRACT FROM AUTHOR]

Poly(amino acid)-type macromolecules (PAAs), poly(ethylene glycol) -b- poly(aspartic acid) (PEG-PAAs), and poly(ethylene glycol)- b -poly(glutamic acid) (PEG-PGAs) were synthesized, and their states in aqueous solutions were studied. PEG-PAAs and PEG-PGAs were first used as novel polycarboxylate superplasticizers, and their dispersion and adsorption behaviors were investigated in cement slurries in the absence and presence of montmorillonite (MMT) clay. The results demonstrated that both PEG-PAAs and PEG-PGAs not only showed excellent water reducing and fluidity retention capabilities but also exhibited remarkable MMT clay tolerance. In contrast to the stretched molecular conformation of traditional polycarboxylate superplasticizers (PCEs), the hydrophobic main chain and the side methylene and ethylene linkers connected to the carboxylic groups of PAA and PGA segments resulted in self-assembly of the PEG-PAAs and PEG-PGAs in aqueous solutions, and the self-assembled nanosized aggregates exhibited relatively uniform spherical morphologies with average sizes of 30–100 nm. Carboxylic groups located on the periphery of the nanoaggregates acted as anchors and adsorbed on the surfaces of the cement particles. The nanoaggregates and the stretched hydrophilic PEG side chains, which jointly produced and enhanced the steric hindrance to prevent cement particle aggregation and hydration, resulted in notable dispersion capabilities. Total organic carbon (TOC), X-ray diffraction (XRD), and thermogravimetry–differential scanning calorimetry (TG-DSC) analyses revealed that the adsorption between the MMT clay and PAA nanoaggregates was surface adsorption (rather than interlayer adsorption), and this significant finding could be ascribed to the enlarged steric hindrance of the PAA nanoaggregates, which prevented the interlamination adsorption consumption of MMT clay to PAAs and revealed the outstanding clay insensitivity. This study provides a new perspective and strategy to design novel poly(amino acid)-type superplasticizers (PAAs) with excellent dispersion performances and improved clay tolerance. [Display omitted] • Poly(amino acid)-type superplasticizers (PAAs) with enhanced dispersing performance for cement doped with clay impurities. • The self-assembled nanoaggregates of PAAs enhanced steric hindrance and resulted in notable dispersion capabilities. • The enlarged steric hindrance of PAAs prevented interlamination adsorption and revealed outstanding clay insensitivity. [ABSTRACT FROM AUTHOR]