Borax has been identified as possible crystallization modifier for sodium sulfate. Understanding the effect of borax on factors influencing transport and crystallization kinetics of sodium sulfate helps to clarify how this modifier might limit crystallization damage. It has been observed that the addition of borax to sodium sulfate solutions has no influence on the wetting properties (contact angle on glass, surface tension,or evaporation rate) and therefore will not influence solution transport. Additionally, the influence of borax on the crystallization kinetics of sodium sulfate was studied under controlled environmental conditions. This was done in mixtures in glass micro capillaries, and sequentially in droplets on glass plates. Under the here studied precipitation conditions, the addition of borax has no influence on the supersaturation ratio at the onset of crystallization, but it significantly affects the crystallization pattern of anhydrous sodium sulfate crystals (thenardite). Using RAMAN spectroscopy, two different hydrates of borax were identified after precipitation depending on the initial concentration of the solution. Each hydrate has a different effect on the subsequent crystallization of sodium sulfate. The decahydrate polymorph of borax leads to the precipitation of hydrated sodium sulfate crystals (mirabilite) and the pentahydrate form favors the precipitation of the anhydrous sodium sulfate crystals (thenardite) with an altered crystal habit. Using X-ray diffraction, overdevelopment of the (111), (131), (222) and (153) faces of thenardite was identified. Additionally, the ratios between several peaks is reversed. These results confirm the deviation of the grown crystals of the equilibrium crystal shape of thenardite as observed with optical microscopy.

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In traditional tissue engineering, synthetic or natural scaffolds are usually used as removable temporal support, which involves some biotechnology limitations. The concept of “scaffield” approach utilizing the physical fields instead of biomaterial scaffold has been proposed recently. In particular, a combination of intense magnetic and acoustic fields can enable rapid levitational bioassembly of complex‐shaped 3D tissue constructs from tissue spheroids at low concentration of paramagnetic agent (gadolinium salt) in the medium. In the current study, the tissue spheroids from human bladder smooth muscle cells (myospheres) are used as building blocks for assembling the tubular 3D constructs. Levitational assembly is accomplished at low concentrations of gadolinium salts in the high magnetic field at 9.5 T. The biofabricated smooth muscle constructs demonstrate contraction after the addition of vasoconstrictive agent endothelin‐1. Thus, hybrid magnetoacoustic levitational bioassembly is considered as a new technology platform in the emerging field of formative biofabrication. This novel technology of scaffold‐free, nozzle‐free, and label‐free bioassembly opens a unique opportunity for rapid biofabrication of 3D tissue and organ constructs with complex geometry.

Additivating mortars with crystallization modifiers is a novel approach to mitigate salt crystallization damage in historic masonry. Once verified the effectiveness of crystallization modifiers in bulk solution, the next step consists in verifying whether: (i) modifiers are still effective when mixed in mortar and going through the carbonation process and (ii) modifiers alter any mortar properties which might limit their application. This research addresses these issues for sodium ferrocyanide and borax, modifiers for sodium chloride, and sodium sulfate, respectively. Several experimental techniques have been applied to elucidate these questions. The results show that the selected modifiers are still able to alter the salt crystallization after going through the carbonation process of the mortar. Besides, no major effects of the modifiers on the fresh and hardened mortar properties were observed. It can therefore be concluded that there are no restraints for the future use of these crystallization modifiers in restoration mortars.

Iron(III) meso-tartrate, a metal-organic complex, is a new anticaking agent for sodium chloride. A molecular structure in solution is proposed, based on a combination of experimental and molecular modelling results. We show that the active complex is a binuclear iron(iii) complex with two bridging meso-tartrate ligands. The iron atoms are antiferromagnetically coupled, resulting in a reduced paramagnetic nature of the solution. In solution, a water molecule coordinates to each iron atom as a sixth ligand, resulting in an octahedral symmetry around each iron atom. When the water molecule is removed, a flat and charged site is exposed, matching the charge distribution of the {100} sodium chloride crystal surface. This charge distribution is also found in the iron(iii) citrate complex, another anticaking agent. This gives a possible adsorption geometry on the crystal surface, which in turn explains the anticaking activity of the iron(III) meso-tartrate complex.