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The primary objective of this paper is to address the inherent biases in the calculation of carbon emissions trading (CET) and foster the development of green innovation. By employing panel data from carbon emission trading pilots, the spatial Durbin model (SDID) is applied to assess the impact of CET on corporate environmental responsibility. By integrating CET and corporate environmental responsibility within a unified framework, this paper presents a novel analysis of the influence of environmental regulations on corporate environmental responsibility at the micro-level. Additionally, this study examines the spatial spillover effect of CET, thereby rectifying estimation biases. The model validation results indicate statistical significance below the 1 % level. The findings of this research reveal that it analyses the specific channels through which CET influences corporate environmental responsibility, providing insights that address the limitations of previous studies in mechanism analysis.
EN
Nano-boron nitride (h-BN) has excellent physical and mechanical properties. Due to its stable chemical performance, the improvement effect on the properties of cement-based materials was limited. Therefore, the chemical modification method was used to prepare functional h-BN to improve its application potential in cement-based materials in this paper. The hydroxylated nano-boron nitride (h-BN-OH) was prepared by modified pristine h-BN with saturated sodium hydroxide (NaOH). The effects of h-BN-OH after ultrasonic dispersion for 10 min, 20 min, 30 min and 40 min on the setting time, fluidity, resistivity, mascroscopic strength and microscopic Young’s modulus of hydration products of ordinary Portland cement were investigated. Fourier transform infrared spectroscopy (FTIR) test results showed that h-BN-OH had obvious hydroxyl infrared characteristic peaks. After adding h-BN-OH into cement paste, the initial and final setting time of cement paste was shortened 6.44-15.34% and 5.05-13.00%, respectively; the fluidity was reduced 9.86-22.79%, and the resistivity was increased 7.14-25.96%. Meanwhile, the compressive strength of cement paste and the microscopic Young’s modulus of hydration products were significantly improved 10.82-40.85% and 9.90-31.01%, respectively. The main reasons were as follows: (1) The dispersion effect and stability of h-BN-OH in cement pore solution were better than that of pristine h-BN, and the hydroxyl group grafted on the h-BN-OH provided nucleation sites for the growth of calcium-silicate hydrate (C-S-H) gel. (2) The hydroxyl groups grafted on the h-BN-OH can absorb Ca2+, resulting the polymerization degree (nc) and medium chain length (MCL) of C-S-H gel increased. The formation of C-S-H gel network structure was accelerated by the increasing proportion of Q3. (3) The pore structure of cement hydration products was significantly optimized.
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