[pt] Os problemas de instabilidades de poços geralmente ocorrem quando camadas de folhelhos são perfuradas. O processo de instabilidade de poços é o resultado de fenômenos mecânicos e físico-químicos. As instabilidades mecânicas podem ser prevenidas e controladas mediante a otimização do peso do fluido de perfuração. Diferente destas, as instabilidades físico-químicas são dificilmente controláveis e mais complexas, pois além de possuírem várias variáveis, dependem do tempo. Neste sentido, o presente trabalho tem como objetivo analisar e compreender os casos de instabilidade do poço através de uma metodologia que integre os resultados de campo e análises em laboratórios a fim de propor fluidos economicamente mais viáveis e competentes que atuem na estabilidade físico-química em trechos de folhelho. Primeiramente são identificados os problemas de instabilidade de um poço (estudo de caso) e seus possíveis agentes causadores através das análises de Boletim Diário de Perfuração (BDP), dados de perfis e análise de estabilidade considerando o modelo elástico. Com base nos problemas identificados, são propostos fluidos hipotéticos de solução salina. Em seguida, amostras de testemunho do poço são coletadas, caracterizadas e analisadas em laboratório com o objetivo de obter os parâmetros de transporte de massa quando estas são submetidas aos fluidos hipotéticos. Por fim, são geradas as análises de estabilidade considerando efeitos físico-químicos conforme tempo de exposição aos fluidos salinos hipotéticos a fim de garantir a otimização do projeto do fluido de perfuração e a estabilidade do poço no processo de perfuração. / [en] Wellbore instability problems usually occur when shale rocks are drilled. The process of wellbore instability is the result of mechanical and physicochemical effects. Mechanical instabilities can be prevented and controlled by optimizing the weight of the drilling fluid. On the other hand, physicochemical instabilities are more complex and difficult to control, because aside from having several variables, they are time-dependent. In this sense, this work has the objective of analysing and understanding the wellbore instability through a methodology that integrates the field results and laboratories analyses in order to propose competent and economically more viable drilling fluids to act in the physicochemical stability in shale stretches. First, the instability problems of a study case and its main causative agents are identified through Drilling Daily Report analyses, profile data and stability analyses considering the elastic model. Based on the problems identified, hypothetical saline fluids are proposed. Then, well samples are collected, characterized and analysed in laboratory in order to obtain its mass transporting parameters when samples are submitted to hypothetical fluids. Finally, stability analyses is performed considering physicochemical effects according to the exposure time to hypothetical saline fluids in order to guarantee the optimization of the drilling fluid design and the stability of the well in the drilling process.

The aim of this work is to explore the area of the Complex Land Consolidation Poněšice in the view of the pedology, hydrogeology and climatology. Further make a erosion threat calculations using the USLE and Curve Number method and afterwards review the application of the erosion control measures in another section of the chapter Main terriorial systems. In conclusion, to estimate the economic aspects of the proposed measures.

Abstract The qualitative and quantitative characteristics of each component layer constituting the structure of organic bulk heterojunction solar cells (OSC-BHJ) contribute significantly towards its overall performance. One of the prevalent issues resulting in reduced device efficiency is due to the conformational inhomogeneities in the active and buffer layers. The mechanical stress, extended thermal exposure and presence of mutually reactive component layers etc., affects negatively on the device stability. Effective methods to address these issues will be extensively benefited by the industry since the current commercialisation of the technology is hindered owing to the lower efficiency and stability of these devices. This dissertation focuses on methods to coherently enhance the performance and longevity of the OSC-BHJ devices. The efficiency enhancements of the devices in this work were achieved through two main routes. The first route was through morphological improvement of the active layer. The second route was through boosting the electrical characteristics of hole transporting conducting polymer layer (HTL) by controlled annealing conditions. The introduction of a suitable additive in the active layer was found to reduce unfavourable phase segregation thus resulting in enhanced morphology. Further, the annealing conditions in different atmospheres (air, nitrogen and vacuum) were found to have a clear influence on the optimum functioning of the HTL in the device. Regarding the stability improvement study done in this work, a method of employing suitable interlayer was developed to effectively abate the internal degradation occurring in the device due to etching reaction on the indium tin oxide (ITO) anode by the HTL. Moreover, experimental investigations were carried out for drawing fundamental understanding of stability degenerating issues such as the influence of mechanical defects on transparent conducting metal oxide (ITO) anode on the performance of the device and heat induced degradations in the low band gap polymer-fullerene active layer. The highlight of this research is that the discovered methods are inexpensive, efficient, and easy to adopt. The results of the study could help the technology to overcome some of its limitations and accelerate its progress towards commercialisation. / Tiivistelmä Orgaanisten heteroliitosaurinkokennojen kerrosrakenteen ominaisuudet ja laatu vaikuttavat merkittävästi aurinkokennojen toiminnallisuuteen. Erityisesti rakenteelliset epähomogeenisuudet aktiivi- ja puskurikerroksissa heikentävät kennon hyötysuhdetta. Kennojen stabiilisuutta tarkasteltaessa myös mekaanisella rasituksella, pitkittyneellä lämpöaltistuksella ja materiaalien reagoinneilla keskenään kerrosten välillä, on selkeä negatiivinen vaikutus kennojen stabiilisuuteen. Orgaanisen aurinkokennoteknologian kaupallistamisen rajoitteina ovat kennojen heikko hyötysuhde ja stabiilisuus, joten menetelmät jotka tarjoavat ratkaisuja edellä mainittuihin ongelmiin, ovat erittäin tärkeitä teknologiaa kaupallistavalle teollisuudelle. Tämä väitöskirja keskittyy johdonmukaisesti selvittämään tapoja, joilla voidaan parantaa heteroliitosaurinkokennojen hyötysuhdetta ja elinikää. Hyötysuhteen tehostamiseksi valittiin kaksi eri lähestymistapaa, joista ensimmäisessä keskityttiin aktiivikerroksen morfologian parantamiseen ja toisessa aukkoja kuljettavan kerroksen sähköisten ominaisuuksien parantamiseen lämpökäsittelyprosessin avulla. Sopivan lisäaineen avulla aktiivikerroksen ei-toivottua kiteytymistä voidaan pienentää ja parantaa näin kerroksen morfologiaa. Lisäksi työssä todettiin, että lämpökäsittelyn aikaisella ympäristöolosuhteella (ilma, typpi, tyhjiö) on merkittävä vaikutus puskurikerroksen optimaaliseen toimintaan aurinkokennossa. Stabiilisuuden parantamiseksi kehitettiin välikerroksen hyödyntämiseen perustuva menetelmä, jolla voidaan tehokkaasti vähentää kennojen sisäisessä rakenteessa tapahtuvaa toiminnallisuuden heikkenemistä, joka aiheutuu aukkoja kuljettavan kerroksen syövyttävästä vaikutuksesta indiumtinaoksidi (ITO) pohjaiseen anodiin. Tämän lisäksi työssä tutkittiin kokeellisesti stabiilisuuteen heikentävästi vaikuttavia tekijöitä, kuten mekaanisen rasituksen aiheuttamia vaurioita metallioksidi (ITO) anodissa ja lämpöaltistuksesta aiheutuvia vikoja polymeeri-fullereeni rakenteeseen perustuvassa aktiivikerroksessa. Tutkimuksen keskeisin tulos on, että esitellyt keinot aurinkokennojen hyötysuhteen ja stabiilisuuden parantamiseen ovat edullisia, tehokkaita ja helppoja hyödyntää. Tulokset voivat merkittävästi edistää orgaanisten aurinkokennojen teknistä kehitystä ja kiihdyttää niiden tuloa kaupallisiksi tuotteiksi.

All cells maintain essential metal nutrients at optimal levels by metal homeostasis. P-type ATPases, a crucial superfamily of integral membrane proteins, are involved in the active transport of metal ions across biological membranes driven by the motive force of ATP- hydrolysis. The PIB-type ATPase subfamily, also called CPx-ATPases, fulfills a key role in heavy metal homoeostasis among the most widespread species from bacteria to human. In humans, the defect in copper transporters is the direct cause of severe neurological and hepatic disorders such as Wilson and Menkes diseases, therefore, understanding the molecular function of these pumps is of paramount importance in human health. Cu+-ATPases have two transmembrane metal binding sites (TM-MBS) and three cytosolic domains, namely the actuator (A-domain) and phosphorylation and nucleotide-binding domain (PN), and regulatory N-terminal heavy metal binding domain (HMBD). Here, we have studied the Legionella pneumophila CopA (LpCopA) and its isolated cytosolic domains to improve our understanding of the functional interaction of the protein domains during metal transport relate this to the known structure of this ATPase. To elucidate how cytosolic ligands (Cu+ and nucleotide) stimulate the interactions among the cytosolic domains and may transmit conformational changes to the TM-MBS, the interactions among recombinant isolated cytosolic domains were first examined biochemically by co-purification and spectroscopically by circular dichroism, time-resolved fluorescence and site-directed fluorescent labeling assays. The Cu+-dependent interaction between the A-domain and HMBD has been postulated as a mechanism for activating the ATPase cycle. This question was addressed here by studying copper-dependent interactions between the isolated expressed domains. Spectroscopic evidence is provided that an HMBD-A complex is formed in the presence of Cu+ which binds with 100-200 nM affinity to the recombinant HMBD. In contrast, the A-domain interacts with the PN domain in a nucleotide-dependent fashion. This molecular recognition is required for the dephosphorylation step in the catalytic cycle. The interaction was investigated in more detail by the use of a decameric peptide derived from the PN-binding interface of the A-domain and carrying the conserved TGE-motif involved in dephosphorylation. Its binding to the isolated PN domain in a weakly nucleotide-dependent manner, is demonstrated here by stopped-flow fluorescence spectroscopy. Several ATPase assays were modified to assess the functionality of the PN-domain and full length LpCopA. The peptide was found to reduce the catalytic turnover of full length LpCopA. This agrees with the expected slowing down of the reformation of the PN-A-domain interaction since the peptide occupies their binding interface. Thus, the synthetic peptide provides a means to study specifically the influence of PN-A-domain interactions on the structure and function of LpCopA. This was done by time-correlated single photon counting (TCSPC) method. The time-dependent Stokes shift of the environmentally sensitive fluorophore BADAN which was covalently attached to the conserved CPC-motif in the TM-MBS was measured. The data indicate that the interior of the ATPase is hydrated and the mobility of the intra-protein water varies from high to low at C382 at the “luminal side” and C384 at the “cytosolic side” of the TM-MBS, respectively. This finding is consistent with the recent MD simulation of LpCopA, bringing the first experimental evidence on a luminal-open conformation of E2~P state. The A-domain-derived decapeptide, although binding to the cytosolic head piece, induces structural changes also at the TM-MBS. The peptide-stabilized state (with a disrupted PN-A interface) renders the C384 environment more hydrophobic as evidenced by TCSPC. Taken together, the data from cytosolic domain interactions, ATPase assays and of time-dependent Stoke shift analyses of BADAN-labeled LpCopA reveal the presence of hydrated intramembraneous sites whose degree of hydration is regulated by the rearrangement of cytosolic domains, particularly during the association and dissociation of the PN-A domains. Copper affects this arrangement by inducing the linkage of the A-domain to the HMBD. The latter appears to play not only an autoinhibitory but also a chaperone-like role in transferring Cu+ to the TM-MBS during catalytic turnover.

Ett av de mest hotande problemen idag är vad som händer med miljö. Ett stort problem är utsläpp. En stor bidragande faktor är den tanklösa användningen av fordon drivna av fossila bränslen. Ett sätt att kunna ta ett litet steg i rätt riktning, är att anpassa våran livstil och till exempel minska på användningen av bilen. Men även att allmänt göra mer medvetna val i vardagen. Målet med detta projektet är att göra just detta lite enklare. Att hjälpa dig transportera dina matvaror exempelvis från mataffären till hemmet.Processen för att komma fram till det som blev slutprodukten, började med intervjuer av användare. Därefter producerades skisser som visades för en testgrupp, för att samla feedback. Fysiska tester utfördes, innan det slutgiltiga konceptet nåtts: En vagn man kan använda på fyra sätt. Man kan skjuta den framför sig medan man går, eller dra den efter sig, man kan använda den som sparkcykel eller man kan koppla den till en cykel. / One of the most threatening issues today is what is happening to our environment. A consi- derable problem for these issues are the emissions. A tremendous contributing factor is the insensible use of fossil fuel driven vehicles. A way of taking a small step i the right direction is to adjust our lifestyle and reduce the use of the car. But also by making more conscious choises in our everyday lives. The aim of this project is to make this a little easier. To help you transport your groceries from for example the store to your home.The process of coming up with what later became the end product, started with interviewing users. Following that, sketches were made and showed to a test group to gather feedback.Physical tests executed, before the final concept was reached: A wagon you cam utilise infour ways. It can be pushed in front of you, while walking. It can be dragged behind, while walking. it can be used as a kick bike and it can be connected to a bicycle.

All cells maintain essential metal nutrients at optimal levels by metal homeostasis. P-type ATPases, a crucial superfamily of integral membrane proteins, are involved in the active transport of metal ions across biological membranes driven by the motive force of ATP- hydrolysis. The PIB-type ATPase subfamily, also called CPx-ATPases, fulfills a key role in heavy metal homoeostasis among the most widespread species from bacteria to human. In humans, the defect in copper transporters is the direct cause of severe neurological and hepatic disorders such as Wilson and Menkes diseases, therefore, understanding the molecular function of these pumps is of paramount importance in human health. Cu+-ATPases have two transmembrane metal binding sites (TM-MBS) and three cytosolic domains, namely the actuator (A-domain) and phosphorylation and nucleotide-binding domain (PN), and regulatory N-terminal heavy metal binding domain (HMBD). Here, we have studied the Legionella pneumophila CopA (LpCopA) and its isolated cytosolic domains to improve our understanding of the functional interaction of the protein domains during metal transport relate this to the known structure of this ATPase. To elucidate how cytosolic ligands (Cu+ and nucleotide) stimulate the interactions among the cytosolic domains and may transmit conformational changes to the TM-MBS, the interactions among recombinant isolated cytosolic domains were first examined biochemically by co-purification and spectroscopically by circular dichroism, time-resolved fluorescence and site-directed fluorescent labeling assays. The Cu+-dependent interaction between the A-domain and HMBD has been postulated as a mechanism for activating the ATPase cycle. This question was addressed here by studying copper-dependent interactions between the isolated expressed domains. Spectroscopic evidence is provided that an HMBD-A complex is formed in the presence of Cu+ which binds with 100-200 nM affinity to the recombinant HMBD. In contrast, the A-domain interacts with the PN domain in a nucleotide-dependent fashion. This molecular recognition is required for the dephosphorylation step in the catalytic cycle. The interaction was investigated in more detail by the use of a decameric peptide derived from the PN-binding interface of the A-domain and carrying the conserved TGE-motif involved in dephosphorylation. Its binding to the isolated PN domain in a weakly nucleotide-dependent manner, is demonstrated here by stopped-flow fluorescence spectroscopy. Several ATPase assays were modified to assess the functionality of the PN-domain and full length LpCopA. The peptide was found to reduce the catalytic turnover of full length LpCopA. This agrees with the expected slowing down of the reformation of the PN-A-domain interaction since the peptide occupies their binding interface. Thus, the synthetic peptide provides a means to study specifically the influence of PN-A-domain interactions on the structure and function of LpCopA. This was done by time-correlated single photon counting (TCSPC) method. The time-dependent Stokes shift of the environmentally sensitive fluorophore BADAN which was covalently attached to the conserved CPC-motif in the TM-MBS was measured. The data indicate that the interior of the ATPase is hydrated and the mobility of the intra-protein water varies from high to low at C382 at the “luminal side” and C384 at the “cytosolic side” of the TM-MBS, respectively. This finding is consistent with the recent MD simulation of LpCopA, bringing the first experimental evidence on a luminal-open conformation of E2~P state. The A-domain-derived decapeptide, although binding to the cytosolic head piece, induces structural changes also at the TM-MBS. The peptide-stabilized state (with a disrupted PN-A interface) renders the C384 environment more hydrophobic as evidenced by TCSPC. Taken together, the data from cytosolic domain interactions, ATPase assays and of time-dependent Stoke shift analyses of BADAN-labeled LpCopA reveal the presence of hydrated intramembraneous sites whose degree of hydration is regulated by the rearrangement of cytosolic domains, particularly during the association and dissociation of the PN-A domains. Copper affects this arrangement by inducing the linkage of the A-domain to the HMBD. The latter appears to play not only an autoinhibitory but also a chaperone-like role in transferring Cu+ to the TM-MBS during catalytic turnover.

An analysis of a transport operator´s job description My degree work is centred on the problems of a transport operator´s job in a forwarding agency. The introduction provides an explanation of a term of "dispatch service" and explains why logistics is so important in transport. Then there is a description of the transport development after 1990 and the changes transport had to undergo in the time of globalization. The main part of the work deals with the operator´s working procedure from an offer to a demand, an order and other actions to the final realization. A model example is given to represent an actual transporting process. The work also states conditions under which transport is executed, for example payment terms and terms of delivery. Next chapters outline the way of calculation, give a detailed description of collecting service (which is implemented within the bounds of CS Expres system) and of storing problems including the introduction of bar codes in stores and possibilities of logistic service extension. The conclusion is focused on the firm developing strategy.