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The diploma thesis deals with the problems of sanitation installation in a multifunctional building in Kunstat. The theoretical part focuses on the analysis of the topic, with emphasis on the water demand. The experimental part focuses on drinking water consumption in real objects. The thesis also focuses on possible solutions given specialization. The project solves the sanitation installation of the multifunctional building in the selected variant. It is a multi-storey building where are a guesthouse for short-term accommodation, café, public toilets, commercial space and a fitness center.

This thesis processes project documentation for headquarters of construction company. Main purpose of building is to facilitate administrative nd manufacturing needs of the company. Building contains of reception, offices, meeting room, restrooms and lock rooms for employees, elevator and workshops. There is underground garage in the basement. Building is going to be situated in Stritez u Policky. Building takes up 1088m2 of land. Vertical structures are mainlymade of concrete and brick blocks. Horizontal structures are made of reinforced concrete panels, roof structure is made of wooden trusses.

In der vorliegenden Arbeit werden zwei Enzymsysteme – Ni-haltige Kohlenmonoxid-Dehydrogenase (CODH) und [NiFe]-haltige Hydrogenase – strukturell untersucht. Im 1. Teil werden die Untersuchungen des ACDS-Komplexes aus A. fulgidus mittels Transmissionselektronenmikroskopie (Negativkontrastierung und der Kryo-Einbettung) geschildert. Die 3D-Rekonstruktion mit einer Auflösung von 29 Å wird de novo ermittelt und drei mögliche Positionen für die CODH-Untereinheit vorgeschlagen. Im 2. Teil wird die Röntgenkristallstrukturanalyse der CODH-Untereinheit des ACDS Komplexes aus A. fulgidus geschildert. Das Protein besteht aus α- und ε-Untereinheiten, die zusammen eine α2ε2-Stöchiometrie bilden (Afα2ε). Während die Gesamtstruktur von Afα2ε2 jener von M. barkeri (Mbα2ε2) ähnelt, führt der Austausch der koordinierenden Cys zu Asp und Glu zu einer Deletion des verbrückenden FeS-Zentrums. Die Rolle der ε-Untereinheit wird durch kinetische Studien untersucht. Die CO-abhängige FAD-Reduktionsaktivität von Afα2ε2 folgt einer Michaelis-Menten Kinetik. Die Mbα2ε2 hat ein ähnliches Kinetikverhalten. Im Gegensatz dazu weist die CODH-II von C. hydrogenoformans, die keine ε-Untereinheit hat, eine lineare Abhängigkeit der CO-abhängigen FAD-Reduktionsaktivität von Flavin auf. Diese Beobachtungen sind im Einklang mit der Annahme, dass die ε-Untereinheit ein Gerüst für die Flavinbindung bereitstellt. Der 3. Teil ist der F420-reduzierenden Hydrogenase aus M. barkeri (MbFRH) gewidmet. Die Struktur von MbFRH wird mittels Röntgenkristallographie bestimmt und ergibt eine dodekamerische Anordnung von ca. 1.2 MDa. Zusammen mit der etablierten Elektronenübertragungskette, beobachtet in FRH aus M. marburgensis, wird in MbFRH auch ein [2Fe2S]-Cluster und eine Fe-Stelle detektiert. Schließlich führen die schwingungsspektroskopischen Analysen zusammen mit der Röntgenkristallographie zu dem Schluss, dass MbFRH in einem bisher strukturell nicht charakterisierten, katalytisch aktiven Nia-S Zustand isoliert wird. / In this work, we structurally characterize two metal-based enzyme systems from archaea: Ni-containing CO dehydrogenase (CODH) and [NiFe] containing hydrogenase. In the first chapter we investigate, using transmission electron microscopy, the ACDS complex from A. fulgidus (AfACDS). The purified ACDS complex can be visualized as an intact globular protein particle by negative stain and vitrification techniques. The 3D reconstruction is determined de novo to 29 Å-resolution by single-particle analysis. We suggest three possible positions for the CODH subunit within ACDS by rigid-body fitting. In the second chapter we determine the X-ray crystal structure of the CODH subunit. The 220 kDa protein is composed of α- and ε-subunits that form a heterodimer with (α2ε2) stoichiometry (Afα2ε2). While the overall structure of Afα2ε2 resembles the previously reported structure of the α2ε2-subunit from M. barkeri (Mbα2ε2), the naturally-occurring exchange of the Cys to Asp and Glu results in a depletion of the bridging iron-sulfur cluster. The role of the ε-subunit is investigated by kinetics studies. CO-dependent FAD reduction activity of Afα2ε2 exhibits Michaelis-Menten type kinetics. The same kinetic type is demonstrated for the Mbα2ε2-subunit. In contrast, the ε-subunit lacking CODH-II from C. hydrogenoformans shows linear dependency between CO-dependent FAD reduction activity and flavin concentration. The data suggests that the ε-subunit provides a scaffold for the flavin binding. In the third chapter we study the F420-reducing hydrogenase from M. barkeri (MbFRH). Its structure is solved by X-ray crystallography, revealing a dodecameric arrangement of 1.2 MDa. Along with the established ET chain observed in FRH from M. marburgensis, one solvent-exposed [2Fe2S] cluster and an additional Fe metal site are detected. The combined approach of X-ray crystallography and vibrational spectroscopy reveals that MbFRH is isolated in the previously structurally uncharacterized Nia-S state.

Friction stir welding (FSW) of steel is often performed with an insert made of polycrystalline cubic boron nitride (PCBN). Specifically, MS80 is a grade of PCBN made by Smith MegaDiamond that has been optimized for the FSW process. The PCBN insert is attached to a tungsten carbide (WC) shank by a compression fitting. However, FSW tools manufactured by this method inevitably fail by fracture in the PCBN. Permanently bonding PCBN to WC would likely solve the fracturing problem and increase the life of PCBN FSW tools to be economically viable. Partial transient liquid phase (PTLP) bonding, a process used to join ceramics with thin metallic interlayers, was proposed as a method to permanently bond PCBN to WC. PTLP bonding is often performed using three layers of pure elements. On heating, the two thin outer interlayers melt and bond to the ceramics. Concurrently, these liquid layers diffuse into the thicker refractory core until solidification has occurred isothermally. A procedure was developed to reduce the number of possible three-layer PTLP bonding setups to a small set of ideal setups using logical filters. Steps in this filtering method include a database of all existing binary systems, sessile drop testing of 20 elements, and a routine that calculates maximum interlayer thicknesses. Results of sessile drop testing showed that the PCBN grade required for this research could only be bonded with an alloy of Ti, Cu, Mg, and Sb. Two PTLP bond setups were tested using this special coating on the PCBN, but a successful bond could not be achieved. However, a PTLP bond of WC to WC was successful and proved the usefulness of the filtering procedure for determining PTLP bond setups. This filtering procedure is then set forth in generalized terms that can be used to PTLP bond any material. Also, recommendations for future research to bond this grade of PCBN, or some other grade, to WC are presented.

High-performance materials such as stainless steels and nickel based super alloys are widely used in demanding applications where high mechanical and thermal properties are required. The applications of super alloys are mainly found in jet engines, power plants and gas turbines demanding high fatigue strength, corrosion and oxidation resistance as well as wear resistant properties. In order to use them, they go through various machining processes such as milling, turning, cutting, polishing etc. until the final product is achieved. Modern manufacturing industries employs various machining tools and technologies to improve the machining process of heat resistant super alloys. However, there are still challenges which needs to be addressed. Among them, adhesive wear of the machining tools is one of the main wear mechanism during the tribological interaction of tool and workpiece, preventing them to achieve the desired quality and surface finish of the end product. Moreover, it damages the tool reducing its lifecycle and in return, increasing the production cost. Among the cutting tools tungsten carbide (WC/Co) tools coated with TiAlN coating due to their good high temperature performance are extensively used. Nonetheless, these coatings still face issue like adhesive wear, abrasion, oxidation at higher temperature damaging the tools and subsequent machining. Therefore, it is imperative to understand the initiation mechanism of adhesive wear during the tribological interaction of super alloys and coated cutting tool material. In this research work, the tribological response of two coatings deposited by physical vapour deposition (PVD), having the composition Ti60Al40N and Ti40Al60N have been studied against two super alloys material, i.e. Inconel 718 and stainless steel 316L. A high temperature SRV (Schwingung (Oscillating), Reibung (Friction), Verschleiß (Wear)) reciprocation friction and wear test set up was employed to investigate the friction behaviour, wear rate and dominant wear mechanisms.  For Ti60Al40N coating, the experimental results revealed that generally, friction increases in case of sliding against Inconel 718 up to 400 °C and drops at 760 °C. A high wear volume at room temperature and a decrease to a minimum at 760 °C has been observed for Inconel 718. On the other side, Stainless steel 316L (SS 316L) faces a continuous rise in friction coefficient with highest value at 760 °C during sliding against Ti60Al40N coating. Wear is highest at 400 °C for SS 316L pin. The worn surfaces shows that both workpiece materials experience increase in material transfer due to adhesive wear with rise in temperature. At 400 °C, adhesion is the primary wear mechanism for both workpiece materials. A further rise in temperature to 760 °C promotes the adhesive wear through oxides formation on both material surfaces.  Similarly, Ti40Al60N coating shows the same friction behaviour with change in average steady state friction values for both material of Inconel 718 and SS 316L. Both workpiece materials responds in a similar way to wear volume loss, i.e. lowest at room temperature and highest at 760 °C. For Inconel 718, transfer of coating constituents on to the Inconel 718 pin surface was detected and associated with coating rupture and peeling, exacerbating with rise in temperature. Adhesion, abrasion, and oxidation are primary wear mechanisms at 400 °C and 760 °C. For SS 316L, coating transfer only happen at 400 °C. No damage of coating at 40 °C, a complete damage at 400 °C, and formation of dense porous oxides layers at 760 °C have been noticed. At 400 °C, adhesion, abrasion, and chipping while at 760 °C, adhesion, three body abrasion, ploughing and oxidation are the main wear mechanisms.