Characteristics of Moisture Transfer and Surface Crack Development of a Single Lignite Particle Driven by Humidity Difference.

The research on moisture transfer characteristics and surface crack development of a single lignite particle (SLP) driven by humidity difference is helpful to achieve a better understanding of the fragmentation characteristics of lignite during the moisture transfer process. This is of great significance to the safe operation of a drying system. The characteristics of moisture transfer within SLP driven by humidity difference were studied in different stages. Six drying equations commonly used in the literature were selected to describe the moisture transfer behavior. The apparent diffusion coefficient (D eff) of moisture in each stage was calculated to compare the driving forces of moisture transfer in different stages. The surface crack rate (CR) was used to quantitatively analyze the fragmentation characteristics of SLP caused by moisture transfer. The results showed that the moisture transfer process of SLP driven by humidity difference can be divided into three stages, and stage I is the main moisture removal stage. The larger the particle size, the longer the stage I, while less moisture is removed in this stage. A logarithmic drying equation best simulates the moisture transfer process of SLP. The larger the particle size, the larger the D eff value in each stage. The driving force of moisture transfer in stage I is the largest, which is the opposite of a thermal drying process. CR for SLP has experienced a rapid increase - stable at the highest value - rapid decrease - stable during the moisture transfer process driven by the humidity difference.

NMR T1 dispersion of crude oils from 10 kHz to 20 MHz.

In this article T1 dispersion measurements on a set of crude oils that span a viscosity range of 0.7 cP up to 2·104 cP are reported. Larmor frequencies were varied from 10 kHz up to 20 MHz. The relaxation dispersion measurements are interpreted in terms of the threshold viscosity model, which allows model applicability tests presented in literature to be extended to Larmor frequencies below 1 MHz. It is shown that the measurements can be equally well described by assuming a proton-proton interaction process as by assuming proton-electronic spin interactions. A power-law frequency dependence of the threshold viscosity parameter is observed for both types of spin interactions. Modifications to the description of rotational diffusion in the threshold viscosity model are suggested that may account for the observed frequency dependence in the threshold viscosity parameter. Without modifications, the threshold viscosity model is shown to have a limited application range of η ≥ 40 cP and ω0/2π ≥ 700 kHz, in which model parameters have a physically justifiable order of magnitude for the set of crude oils studied. Outside this range, the threshold viscosity model can still be applied as a parametrization of T1 dispersion effects for the complete set of experiments presented in this study. This explicit viscosity and Larmor frequency dependent parametrization may be used as first-order approximation to T1 dispersion in crude oils for which only oil viscosity is known and may be applied to polarization level and pulse sequence simulations in low field NMR relaxometry studies up to 20 MHz for a wide range of crude oil viscosities, and in particular for better interpretation of NMR flow measurements on crude oils.

Reinforcing Mechanisms of Coir Fibers in Light-Weight Aggregate Concrete.

Due to the requirement for developing more sustainable constructions, natural fibers from agricultural wastes, such as coir fibers, have been increasingly used as an alternative in concrete composites. However, the influence of coir fibers on the hydration and shrinkage of cement-based materials is not clear. In addition, limited information about the reinforcing mechanisms of coir fibers in concrete can be found. The goal of this research is to investigate the effects of coir fibers on the hydration reaction, microstructure, shrinkages, and mechanical properties of cement-based light-weight aggregate concrete (LWAC). Treatments on coir fibers, namely Ca(OH)2 and nano-silica impregnation, are applied to further improve LWAC. Results show that leachates from fibers acting as a delayed accelerator promote cement hydration, and entrained water by fibers facilitates cement hydration during the whole process. The drying shrinkage of LWAC is increased by adding fibers, while the autogenous shrinkage decreases. The strength and toughness of LWAC are enhanced with fibers. Finally, three reinforcement mechanisms of coir fibers in cement composites are discussed.

Setting Characteristics, Mechanical Properties and Microstructure of Cement Pastes Containing Accelerators Mixed with Superabsorbent Polymers (SAPs): An NMR Study Combined with Additional Methods.

In this study, the setting property and mechanical strength of cement pastes containing accelerators (CPCA) with or without superabsorbent polymers (SAPs) were first studied. The early microstructure evolution and water distribution at 7 and 28 days were probed by 1D (T2) and 2D (T1-T2 maps) H¹ nuclear magnetic resonance (NMR) relaxometry, and the microstructure was systematically investigated by using mercury intrusion porosimetry (MIP), back-scattered electron (BSE) image and energy-dispersive X-ray spectroscopy (EDX) analysis. Results showed that the SAPs in the cement paste containing accelerators had various influences on setting time and compressive strength depending on the type of accelerators. The presence of SAPs in the cement paste containing alkaline free accelerators could alleviate the decrease of internal relative humidity, promote hydration and help to modify the pore structure. Moreover, it was observed that the SAP cavities could be nicely filled with calcium hydroxide (CH) in the cement paste with alkaline free accelerators.

In situ determination of solidosity profiles during activated sludge electrodewatering.

Two non-invasive techniques were evaluated for the on-line measurement of sludge solidosity profiles during both pressure and electrodewatering operations. In a first approach, a radioactive tracer adsorbed onto the sludge solids was monitored by a gamma camera. Although this technique appeared very flexible in use, the lack of resolution highly limited its usefulness for (electro)dewatering experiments. Improvement in gamma camera resolution by the development of new detectors might, however, increase the future applicability of this technique. In a second technique, nuclear magnetic resonance measurements on a specially designed electrodewatering unit were made. Hereby, reliable on-line measurements of the solidosity profiles of activated sludge during electrodewatering could be made, with a resolution of less than 1mm. Thus, the mechanisms of electroosmotic- and pressure-driven cake dewatering could be illustrated. Given the measurement time required for measuring one sludge profile, both techniques appeared mainly suited for slowly varying processes, such as activated sludge expression, and not for fast changing processes, such as the initial phases of sludge filtration.

Salt crystallization as damage mechanism in porous building materials--a nuclear magnetic resonance study.

Salts can damage building materials by chemical reactions or crystallization, which is a serious threat to cultural heritage. In order to develop better conservation techniques, more knowledge of the crystallization processes is needed. In a porous material, the size of a salt crystal is limited by the sizes of the pores. It has been predicted that as a consequence, the solubility of a salt increases with decreasing pore size. This increase seems to be related to an increase of the stress generated by a crystal on the pore wall. It has been suggested that the resulting stress could become high enough to induce failure. We have studied the crystallization of salts in porous materials with well-defined pore sizes. Samples were saturated at 40 degrees C with saturated Na2SO4 and Na2CO3 solutions. Next we have cooled the samples to 0 degrees C and waited for nucleation. After nucleation occurred, the solubility in the porous material was measured with nuclear magnetic resonance (NMR) as a function of the temperature. The measurements on Na2CO3 indeed show an increase in solubility with a decrease in pore size. For Na2SO4, we did not observe a pore size-dependent solubility. However, we have to remark that these results show a metastable crystal phase. The results can be used to calculate the actual pressure exerted by the crystals onto the pore wall.