Computing by nowhere increasing complexity

A cellular automaton is presented whose governing rule is that the Kolmogorov complexity of a cell's neighborhood may not increase when the cell's present value is substituted for its future value. Using an approximation of this two-dimensional Kolmogorov complexity the underlying automaton is shown to be capable of simulating logic circuits. It is also shown to capture trianry logic described by a quandle, a non-associative algebraic structure. A similar automaton whose rule permits at times the increase of a cell's neighborhood complexity is shown to produce animated entities which can be used as information carriers akin to gliders in Conway's game of life

Different fiber materials as reinforcement for geopolymer composite

For the last two centuries, Ordinary Portland Cement (OPC) is the most popular building material in the world due to its high mechanical properties, ease of handling and low cost. However, the concrete industry is known to leave an enormous environmental footprint. Therefore, the development of sustainable materials that could replace the OPC is essential. One of such recent developments is an aluminosilicate based material that can be activated in an alkaline medium to form a hardened sustainable product, known as ‘Geopolymer’. Geopolymers exhibit equal or better engineering properties as compared to conventional concrete with better environmental foot print. However, geopolymer\u27s main disadvantage, as concrete, is its brittleness and low tensile properties. One way to overcome this limitation is by addition of fibers, as they can control cracking by crack bridging, resulting in an increase of the tensile properties of the geopolymeric composite. The purpose of this research was to develop a high performance geopolymer composite by addition of short fibers. Three different types of fibers were added to the matrix with two different fiber contents (0.5% and 1%). The idea was to add fibers of significant difference in their chemical nature and tensile properties: PP and Carbon fibers which are both hydrophobic, but have significant differently tensile behavior, and PVA which is hydrophilic like the geopolymeric matrix, and has moderate tensile properties. Their influence on the geopolymer flexural behavior was examined. The microstructure of the composite at the fracture surface was also studied to better understand the role of the fibers. The results of this research showed that all fibers improved the ductility and toughness of the matrix. Geopolymeric composites with 1% carbon fibers showed the highest flexural strength, +216% compared to plain matrix, followed by the PVA fiber composites. Different failure modes were observed – fiber pull-out for the PP and carbon composites, and fiber rupture for the PVA fiber composite. This can be explained based on the different chemical nature of the fibers which produce a different matrix-fiber interface

The Synthesis and Origin of the Pectic Polysaccharide Rhamnogalacturonan II – Insights from Nucleotide Sugar Formation and Diversity

There is compelling evidence showing that the structurally complex pectic polysaccharide rhamnogalacturonan II (RG-II) exists in the primary cell wall as a borate cross-linked dimer and that this dimer is required for the assembly of a functional wall and for normal plant growth and development. The results of several studies have also established that RG-II structure and cross-linking is conserved in vascular plants and that RG-II likely appeared early in the evolution of land plants. Two features that distinguish RG-II from other plant polysaccharides are that RG-II is composed of 13 different glycoses linked to each other by up to 22 different glycosidic linkages and that RG-II is the only polysaccharide known to contain both apiose and aceric acid. Thus, one key event in land plant evolution was the emergence of genes encoding nucleotide sugar biosynthetic enzymes that generate the activated forms of apiose and aceric acid required for RG-II synthesis. Many of the genes involved in the generation of the nucleotide sugars used for RG-II synthesis have been functionally characterized. By contrast, only one glycosyltransferase involved in the assembly of RG-II has been identified. Here we provide an overview of the formation of the activated sugars required for RG-II synthesis and point to the possible cellular and metabolic processes that could be involved in assembling and controlling the formation of a borate cross-linked RG-II molecule. We discuss how nucleotide sugar synthesis is compartmentalized and how this may control the flux of precursors to facilitate and regulate the formation of RG-II

Metakaolin based geopolymers as soil stabilizers

In many kinds of engineering constructions, wind-swept soils and soft weak soils are often stabilized and strengthened with ordinary Portland cement (OPC) and lime, to increase soil strength and durability. Furthermore, such soil stabilizing can also prevent erosion and dust generation. However, OPC is known to leave an enormous environmental footprint on planet Earth as its production processes are significant energy consumers with high CO2 emissions. Therefore, the development of a novel generation of cements with high durability and environmental sustainability is essential. One of these novel binders is the alkali-activated binder based on aluminosilicates materials as metakaolin or industrials by-products such as fly ash or slags, commonly referred to as geopolymer. It has been found that geopolymers can exhibit high compressive strength and higher chemical and thermal resistance than cement-based materials [1]. Therefore, due to their high strength, low cost, low energy consumption and CO2 emissions, geopolymers offers a promising alternative to OPC [2]. Geopolymers also exhibit excellent adhesion to aggregates [3], therefore it is reasonable to assume that they can serve as an effective soil stabilizer. Please click Additional Files below to see the full abstract

Non-inertial quantum clock frames lead to non-Hermitian dynamics

Recently, there have been many attempts to extend the notion of proper time to quantum mechanics with the use of quantum clocks. Using a similar idea combined with the relativistic mass-energy equivalence, we consider an accelerating massive quantum particle with an internal clock system. We show that the ensuing evolution from the perspective of the particle's internal clock is non-Hermitian. This result does not rely on specific implementations of the clock. As a particular consequence, we prove that the effective Hamiltonian of two gravitationally interacting particles is non-Hermitian from the perspective of the clock of either particle.Comment: 6+1 pages, 2 figures. Comments are welcome