Stakeholders' willingness to pay for enhanced construction waste management: a Hong Kong study

Based on the polluter pays principle, construction waste disposal charging schemes (CWDCS) have been deployed by various economies as one of the most effective ways of managing construction waste. Nevertheless, a means of rationalizing these schemes has not been well documented. Using the economic technique of contingent valuation method (CVM), this study aims to investigate stakeholders’ willingness to pay (WTP) for enhanced construction waste management (CWM) with a view to providing a scientific foundation for CWDCS rationalization. In considering this WTP in light of repeated exhortations that all stakeholders play a role in the management of construction waste, the study is unique. To ascertain stakeholders’ WTP, a payment card-style questionnaire survey was designed and administered to Hong Kong’s major CWM stakeholders in February 2014. Interestingly, the results show that there is no statistically significant variation in the WTP of different stakeholder groups. The average maximum WTP is around HK232/t for landfill disposal of C&D waste, HK186/t for off-site sorting facility (OSF) disposal, and HK$120/t for public fill reception facility (PFRF) disposal. These values are higher than the existing CWDCS charges (HK$125/t for landfilling, HK$100/t for OSF disposal, and HK$27/t for PFRF disposal) but much lower than the charges proposed to the government. This research provides not only a scientific foundation for the ongoing debate on changes to Hong Kong’s CWDCS, but also a valuable reference for other economies facing the challenge of developing charging schemes to deal with construction waste.postprin

Accelerating Cathode Material Discovery through Ab Initio Random Structure Searching

The choice of cathode material in Li-ion batteries underpins their overall performance. Discovering new cathode materials is a slow process, and all major commercial cathode materials are still based on those identified in the 1990s. Discovery of materials using high-throughput calculations has attracted great research interest; however, reliance on databases of existing materials begs the question of whether these approaches are applicable for finding truly novel materials. In this work, we demonstrate that ab initio random structure searching (AIRSS), a first-principles structure prediction method that does not rely on any pre-existing data, can locate low energy structures of complex cathode materials efficiently based only on chemical composition. We use AIRSS to explore three Fe-containing polyanion compounds as low-cost cathodes. Using known quaternary LiFePO4 and quinary LiFeSO4F cathodes as examples, we easily reproduce the known polymorphs, in addition to predicting other, hitherto unknown, low energy polymorphs and even finding a new polymorph of LiFeSO4F that is more stable than the known ones. We then explore the phase space for Fe-containing fluoroxalates, predicting a range of redox-active phases that are yet to be experimentally synthesized, demonstrating the suitability of AIRSS as a tool for accelerating the discovery of novel cathode materials

Estimating and calibrating the amount of building-related construction and demolition waste in urban China

One side effect of the unprecedented urbanization in China is the large amount of building-related construction and demolition (C&D) waste generated during the process. It is an enigma why such statistics as C&D waste generation are absent from the literature in spite of their importance to devising sensible interventions to deal with the C&D waste related problems. This paper aims to estimate the amount of C&D waste at the country level. It does so by adopting a methodology utilizing national statistical data and the average amounts of waste generated at job sites. Furthermore, the estimation is undergone a thorough calibration against various independent sources before it can be accepted confidently. It is finally estimated that approximately 1.13 billion tons of C&D materials were generated in China during 2014, which has declined from a plateau of building activities and C&D waste generation in the early 2010s. The paper provides some useful references for devising appropriate C&D waste reduction, reuse, or recycling strategies. The paper also offers useful commentary on methodology to estimate C&D waste generation at an urban level, particularly in situations where data availability is erratic.postprin

Ab initio random structure searching for battery cathode materials

Cathodes are critical components of rechargeable batteries. Conventionally, the search for cathode materials relies on experimental trial-and-error and a traversing of existing computational/experimental databases. While these methods have led to the discovery of several commercially viable cathode materials, the chemical space explored so far is limited and many phases will have been overlooked, in particular, those that are metastable. We describe a computational framework for battery cathode exploration based on ab initio random structure searching (AIRSS), an approach that samples local minima on the potential energy surface to identify new crystal structures. We show that by delimiting the search space using a number of constraints, including chemically aware minimum interatomic separations, cell volumes, and space group symmetries, AIRSS can efficiently predict both thermodynamically stable and metastable cathode materials. Specifically, we investigate LiCoO2, LiFePO4, and LixCuyFz to demonstrate the efficiency of the method by rediscovering the known crystal structures of these cathode materials. The effect of parameters, such as minimum separations and symmetries, on the efficiency of the sampling is discussed in detail. The adaptation of the minimum interatomic distances on a species-pair basis, from low-energy optimized structures to efficiently capture the local coordination environment of atoms, is explored. A family of novel cathode materials based on the transition-metal oxalates is proposed. They demonstrate superb energy density, oxygen-redox stability, and lithium diffusion properties. This article serves both as an introduction to the computational framework and as a guide to battery cathode material discovery using AIRSS

Determining interface structures in vertically aligned nanocomposite films

Vertically aligned nanocomposite (VAN) films have self-assembled pillar-matrix nanostructures. Owing to their large area-to-volume ratios, interfaces in VAN films are expected to play key roles in inducing functional properties, but our understanding is hindered by limited knowledge about their structures. Motivated by the lack of definitive explanation for the experimentally found enhanced ionic conductivity in Sm-doped-CeO2/SrTiO3 VAN films, we determine the structure at vertical interfaces using random structure searching and explore how it can affect ionic conduction. Interatomic potentials are used to perform the initial searching, followed by first-principles calculations for refinement. Previously unknown structures are found, with lower energy than that of an optimized hand-built model. We find a strongly distorted oxygen sublattice which gives a complex landscape of vacancy energies. The cation lattice remains similar to the bulk phase, but has a localized strain field. The excess energy of the interface is similar to that of high angle grain boundaries in SrTiO3.China Scholarship Council Cambridge Commonwealth, European and International Trus

Superoleophobic surfaces on stainless steel substrates obtained by chemical bath deposition

Superhydrophobic surfaces have shown great potential in domestic and industrial applications. However, these surfaces lose their superhydrophobic functions once being contaminated by oily liquids. In this work a simple chemical bath deposition method is reported to fabricate superoleophobic surfaces on steel substrates that repel both water and oil. The synthesis of superoleophobic surfaces involves the fabrication of the micro/nanometre-scale origami-ball-like structures on steel substrates, followed by the modification of low surface energy material. The fabricated surfaces have glycerol, peanut oil and hexadecane contact angles larger than 150° and roll-off angles smaller than 10°. This method is highly efficient because it takes only 5 min to create the surface re-entrant structures that are required by superoleophobicity. The prepared surfaces showed remarkable durability and retained superoleophobicity even after exposure to high and low temperatures (−30 and 100°C), and UV irradiation. This work will enrich the processing methods of the superoleophobic surfaces on stainless steel substrates

Large-Area Fabrication of Droplet Pancake Bouncing Surface and Control of Bouncing State

Superhydrophobic pillar arrays, which can generate the droplet pancake bouncing phenomenon with reduced liquid-solid contact time, have huge application prospects in anti-icing of aircraft wings from freezing rain. However, the previously reported pillar arrays, suitable for obtaining pancake bouncing, have a diameter ≤100 μm and height-diameter ratio >10, which are difficult to fabricate over a large area. Here, we have systematically studied the influence of the dimension of the superhydrophobic pillar arrays on the bouncing dynamics of water droplets. We show that the typical pancake bouncing with 57.8% reduction in contact time with the surface was observed on the superhydrophobic pillar arrays with 1.05 mm diameter, 0.8 mm height, and 0.25 mm space. Such pillar arrays with millimeter diameter and <1 height-diameter ratio can be easily fabricated over large areas. Further, a simple replication-spraying method was developed for the large-area fabrication of the superhydrophobic pillar arrays to induce pancake bouncing. No sacrificial layer was needed to reduce the adhesion in the replication processes. Since the bouncing dynamics were rather sensitive to the space between the pillars, a method to control the contact time, bouncing shape, horizontal bouncing direction, and reversible switch between pancake bouncing and conventional bouncing was realized by adjusting the inclination angle of the shape memory polymer pillars

Power-free water pump based on a superhydrophobic surface: generation of a mushroom-like jet and anti-gravity long-distance transport

Spontaneous anti-gravitational transportation of liquids across long distances has been widely discovered in nature, such as water transportation from the root to the crown of a tree. However, artificial liquid delivery remains a challenge. In this work, a new power-free pump composed of a superhydrophobic plate with a pore mounted on a leak-proof cylindrical container filled with water is presented for sustained anti-gravity and long distance transport. Water droplets can be spontaneously captured through the pore by the lower water column, forming a mushroom-like jet due to the energy transition from surface energy to kinetic energy. The spontaneously increased inside pressure in the container will push the water out, through another thin tube, realizing the energy transition from surface energy to gravitational potential energy. The dynamic driving and moving model of the pivotal mushroom-like jet were analyzed. The maximum transport height and transport abilities of the water pump were also discussed. The results show that Laplace pressure is the main driving pressure of the mushroom-like jet and that the developed power-free pump can effectively transport water to over 100 mm in height with an average transport speed of 4500 μL h−1, showing potential for application in microfluidic systems and medical devices where micropumps are needed

Identification of single-site gold catalysis in acetylene hydrochlorination

There remains considerable debate over the active form of gold under operating conditions of a recently validated gold catalyst for acetylene hydrochlorination. We have performed an in situ x-ray absorption fine structure study of gold/carbon (Au/C) catalysts under acetylene hydrochlorination reaction conditions and show that highly active catalysts comprise single-site cationic Au entities whose activity correlates with the ratio of Au(I):Au(III) present. We demonstrate that these Au/C catalysts are supported analogs of single-site homogeneous Au catalysts and propose a mechanism, supported by computational modeling, based on a redox couple of Au(I)-Au(III) species