Crystallization of zeolite ZSM-5 from a diluted heterogeneous system (12.5Na 2 O−Al 2 O 3 −8TPABr−60SiO 2 − 4000H 2 O) was investigated by various experimental methods such as X-ray diffraction (XRD), electron diffraction (ED), infrared spectroscopy (FTIR), X-ray fluorescence (XRF), scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), thermo-gravimetric analysis (TGA), particle size analysis (PSA), pH measurement, inductive coupling plasma (ICP) emission spectrometry, and dynamic light scattering (DLS). The crystallization process is characterized by a very long "induction period" (95% of the entire reaction time) and very fast transformation (5% of the entire reaction time) of amorphous to crystalline phase (zeolite ZSM-5) at the end of the crystallization process. Analysis of the obtained results has shown that the crystallization process takes place by a chain of processes: (i) formation of "primary" amorphous aluminosilicate precursor (gel) at room temperature, (ii) formation of "secondary" amorphous aluminosilicate precursor ("worm-like" particles, WLPs) at increased temperature (170 °C), (iii) formation of "tertiary" amorphous aluminosilicate precursor (condensed aggregates, CAs) by aggregation of the WLPs and densification (condensation) of aggregates, and (iv) formation of nuclei and their growth in the matrixes of CAs; these processes result in the formation of fully crystalline zeolite ZSM-5 in the form of polycrystalline aggregates.

Extracellular polysaccharide production by marine diatoms is a significant route by which photosynthetically produced organic carbon enters the trophic web and may influence the physical environment in the sea. This study highlights the capacity of atomic force microscopy (AFM) for investigating diatom extracellular polysaccharides with a subnanometer resolution. Here we address a ubiquitous marine diatom Cylindrotheca closterium, isolated from the northern Adriatic Sea, and its extracellular polymeric substance (EPS) at a single cell level. We applied a simple procedure for AFM imaging of diatom cells on mica under ambient conditions (in air) to achieve visualization of their EPS with molecular resolution. The EPS represents a web of polysaccharide fibrils with two types of cross-linking: fibrils association forming junction zones and fibril-globule interconnections with globules connecting two or more fibrils. The fibril heights were 0.4-2.6 nm while globules height was in the range of 3-12 nm. Polymer networks of native gel samples from the Northern Adriatic and the network formed by polysaccharides extracted from the C. closterium culture share the same features regarding the fibril heights, pore openings and the mode of fibril association, proving that the macroscopic gel phase in the Northern Adriatic can be formed directly by the self-assembly of diatom released polysaccharide fibrils.

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It is generally accepted that a diatom cell wall is characterized by a siliceous skeleton covered by an organic envelope essentially composed of polysaccharides and proteins. Understanding of how the organic component is associated with the silica structure provides an important insight into the biomineralization process and patterning on the cellular level. Using a novel atomic force microscopy (AFM) imaging technique (Peak Force Tapping), we characterized nanomechanical properties (elasticity and deformation) of a weakly silicified marine diatom Cylindrotheca closterium (Ehrenb.) Reimann et J. C. Lewin (strain CCNA1). The nanomechanical properties were measured over the entire cell surface in seawater at a resolution that was not achieved previously. The fibulae were the stiffest (200 MPa) and the least deformable (only 1 nm). Girdle band region appeared as a series of parallel stripes characterized by two sets of values of Young's modulus and deformation: one for silica stripes (43.7 Mpa, 3.7 nm) and the other between the stripes (21.3 MPa, 13.4 nm). The valve region was complex with average values of Young's modulus (29.8 MPa) and deformation (10.2 nm) with high standard deviations. After acid treatment, we identified 15 nm sized silica spheres in the valve region connecting raphe with the girdle bands. The silica spheres were neither fused together nor forming a nanopattern. A cell wall model is proposed with individual silica nanoparticles incorporated in an organic matrix. Such organization of girdle band and valve regions enables the high flexibility needed for movement and adaptation to different environments while maintaining the integrity of the cell.

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