In Situ

The durability of existing concrete structures has increasingly attracted widespread attention in recent years. The phenomenon of performance degradation is often associated with the intrusion of hazardous ions from outside. As the first barrier to external substances intrusion, the near-surface concrete plays an important role in durability. So the performance of in-service concrete structures often depends on the transport properties of the near-surface concrete. Accordingly, information on service conditions and life prediction can be obtained by testing these transport properties. In this paper, an in situ method for chloride ion diffusion coefficient determination is proposed based on the relationship between the alternating current impedance spectroscopy parameters and the chloride ion diffusion coefficient. By a rational design, the new method can synthetically reflect the transport properties of near-surface concrete and is not affected by the presence of the reinforcing bar. In addition, the experimental results show that the method is in good agreement with “PERMIT” migration test which has been widely used. The proposed method is less time consuming and nondestructive and has good reproducibility

Determination of the Transport Properties of Structural Concrete Using AC Impedance Spectroscopy Techniques

All over the world, particularly in severe environmental conditions, there are reinforced concrete structures that develop nonnegligible phenomena of durability problems. Most of the durability problems are related to hazardous substances invasion. Both engineering practice and scientific studies have revealed that the transport property of near-surface concrete is a main factor in the durability of concrete structures. Among many transport parameters, the chloride ion diffusion coefficient is the most important one, which provides important information on material design and service life prediction. In this paper, AC impedance spectroscopy technology was employed in the measurement of chloride ion diffusion coefficient. The relationship between mesostructure parameters and chloride ion diffusion coefficient was deduced by introducing a reasonable equivalent circuit model. Taking into account the conductivity difference caused by various cementitious material systems, the diffusion coefficient can be corrected, and a diffusion coefficient determination method based on AC impedance spectroscopy technique was established. For the convenience of application, a relationship between the newly proposed method and a widely recognized standard method was obtained. The proposed method can be applied to laboratory testing and establishes the theoretical basis for field tests

Homo- and heterodehydrocoupling of phosphines mediated by alkali metal catalysts

Catalytic chemistry that involves the activation and transformation of main group substrates is relatively undeveloped and current examples are generally mediated by expensive transition metal species. Herein, we describe the use of inexpensive and readily available tBuOK as a catalyst for P–P and P–E (E = O, S, or N) bond formation. Catalytic quantities of tBuOK in the presence of imine, azobenzene hydrogen acceptors, or a stoichiometric amount of tBuOK with hydrazobenzene, allow efficient homodehydrocoupling of phosphines under mild conditions (e.g. 25 °C and < 5 min). Further studies demonstrate that the hydrogen acceptors play an intimate mechanistic role. We also show that our tBuOK catalysed methodology is general for the heterodehydrocoupling of phosphines with alcohols, thiols and amines to generate a range of potentially useful products containing P–O, P–S, or P–N bonds

Zirconium-Catalyzed Atom-Economical Synthesis of 1,1-Diborylalkanes from Terminal and Internal Alkenes

A general and atom-economical synthesis of 1,1-diborylalkanes from alkenes and a borane without the need for an additional H2 acceptor is reported for the first time. The key to our success is the use of an earth-abundant zirconium-based catalyst, which allows a balance of self-contradictory reactivities (dehydrogenative boration and hydroboration) to be achieved. Our method avoids using an excess amount of another alkene as an H2 acceptor, which was required in other reported systems. Furthermore, substrates such as simple long-chain aliphatic alkenes that did not react before also underwent 1,1-diboration in our system. Significantly, the unprecedented 1,1-diboration of internal alkenes enabled the preparation of 1,1-diborylalkanes. © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA

Qualitative phase space reconstruction analysis of supply-chain inventor time series

The economy systems are usually too complex to be analysed, but some advanced methods have been developed in order to do so, such as system dynamics modelling, multi-agent modelling, complex adaptive system modelling and qualitative modelling. In this paper, we considered a supply-chain (SC) system including several kinds of products. Using historic suppliers' demand data, we firstly applied the phase space analysis method and then used qualitative analysis to improve the complex system's performance. Quantitative methods can forecast the quantitative SC demands, but they cannot indicate the qualitative aspects of SC, so when we apply quantitative methods to a SC system we get only numerous data of demand. By contrast, qualitative methods can show the qualitative change and trend of the SC demand. We therefore used qualitative methods to improve the quantitative forecasting results. Comparing the quantitative only method and the combined method used in this paper, we found that the combined method is far more accurate. Not only is the inventory cost lower, but the forecasting accuracy is also better