Lithium-ion batteries are of great importance for today's society. The state-of-the-art batteries that are used today use a fluorinated electrolyte that contains the salt LiPF6 and acts as both a safety hazard and an environmental issue due to its ability to form the toxic gas hydrogen fluoride (HF). This project aims to find a fluorine-free electrolyte that can be used in silicon-based lithium-ion batteries to make them more environmentally friendly without detriment to the electrochemical performance. To do so, an additive that may form a solid electrolyte interphase (SEI) stable enough to allow a fluorine-free electrolyte to replace the ones used today is sought for. The salt of interest is lithium  bis(oxalato)borate (LiBOB). Based on previous research electrolytes using LiBOB in either the solvent γ-Butyrolactone (GBL) or a mixture of ethylene carbonate (EC) and ethyl methyl carbonate (EMC) are examined. The additives used are vinylene carbonate (VC) and 1,3,2-dioxathiolane 2,2-dioxide (DTD). Techniques used are cyclic voltammetry, linear sweep voltammetry, galvanostatic charge and discharge, X-ray photoelectron spectroscopy and scanning electron microscopy.  The cells using GBL as solvent have cycled very poorly during this project while LiBOB in EC:EMC + VC shows the most promising results, with highest capacity retention and less amount of degraded LiBOB during the first charge. It is also to be noted that both EC:EMC based electrolytes provide the formation of a passivating solid electrolyte interface (SEI) and are of interest for further investigation based on the results obtained during this project.

Many countries including Sweden are planning to replace fossil fuel-based vehicles with electric vehicles. This is one of the main reasons that companies all over the world are investing more and more money in the development of lithium-ion batteries, for electric vehicles. There are several different risks with the conventional lithium-ion batteries including the high flammability of the electrolytes, which can lead to high heat release rate, risk of explosion and high toxicity in the form of hydrogen fluoride gas. The hydrogen fluoride is lethal even at low concentration. These potential risks are based on the structure of the flammable electrolytes inside the lithium-ion batteries. Because of that, there is a big interest in finding an electrolyte with similar battery performance and better fire properties as compared with the conventional electrolytes commercially available on the market.   The intent with this work is to investigate the fire properties of different halogen-free electrolytes. The two newly developed salts Li[MEA] & Li[MEEA] as well as the available salt Li[BOB] will be compared with the commercially used halogen-containing electrolyte based on lithium hexafluorophosphate (LiPF6) salt.   Physical and electrochemical properties of these electrolytes such as solubility in different organic solvents, density, viscosity, ionic conductivity and electrochemical window will be studied in the first step. The electrolytes showing the most promising electrochemical properties will then be further investigated regarding fire properties, heat release rate, flash point and toxicity. The electrolytes will be compared with the conventional electrolyte containing LiPF6.   Li[BOB] was not dissolved in the solvents with the strongest dissolving properties, therefore it was not further tested. The electrolytes that were tested regarding fire properties were Li[MEA] and Li[MEEA] with the organic solvents of ethylene carbonate and dimethyl carbonate. Ionic liquid was also added to Li[MEEA] to investigate how it affected the fire properties for the electrolyte.   When examine the heat release rate for the newly developed salts, as well as LiPF6, it was observed that the highest peaks were similar to each other. The combustion time for the electrolyte containing LiPF6 was noticeable shorter than for the other three electrolytes. This is likely due to the fluorine content in LiPF6. The electrolytes undergoing the cone calorimeter test in this work was not charged so therefore the peaks of the heat release rate may look different. For further studies, it could be of interest to construct a complete lithium-ion battery using these electrolytes to see how the battery cells and the electrolytes behave in different set of charges.   Another essential point, is the ignition time that showed varied times for the tests containing Li[MEEA] together with the organic solvents and with the added ionic liquid. This is an interesting result that probably can be explained by the homogeneity of the electrolyte. The homogeneity was only verified with the help of the human eye and therefore it may not be fully dissolved.   The flashpoint for the different mixtures of electrolytes showed values of interest where the electrolyte containing ionic liquid that showed the lowest flashpoint. This was unexpected concerning that these types of additives are common for improving the fire resistance capacity.   The key aspect discussed when analyzing the result from the FTIR spectroscopy was how the Li[MEA], Li[MEEA] and LiPF6 salts varied. The ones that did not have any fluorine in its structure resulted in production of carbon dioxide. However, the electrolyte containing fluorine resulted, as expected, in values of hydrogen fluorine and carbon dioxide but also other combustion products that was hard to determine.   These salts and electrolytes need to be further studied and tested to see if it is possible to use them in an actual lithium-ion battery. Besides further tests of the salts and ionic liquid tested in this work, it is important that the work with conventional and newly developed electrolytes aims for improvements in fire resistance as well as toxicity. / Många länder inklusive Sverige planerar att byta ut fordon som använder fossila bränslen mot elfordon. Detta är en av huvudanledningarna till att företag runt om i världen satsar mer och mer pengar på att utveckla litiumjonbatterier för elfordon. Litiumjonbatterier medför en del risker såsom hög värmeutveckling, brandfarliga vätskor, risk för explosion och toxiska gaser samt produceringen av vätefluorid. Redan vid låga koncentrationer är vätefluoriden dödlig. Riskerna baseras på strukturen av elektrolyten som finns i litiumjonbatteriet. På grund av dessa risker så är det intressant att utveckla en elektrolyt som har liknande batteriegenskaper men bättre brandegenskaper än de elektrolyter som finns och används idag.   I detta arbete har brandegenskaper för olika halogenfria elektrolyter testats. De två nyutvecklade salterna Li[MEA] & Li[MEEA] har tillsammans med det existerande saltet Li[BOB] jämförts med det kommersiella saltet litium hexafluorfosfat (LiPF6) som används till många elektrolyter i dagens litiumjonbatterier.   De fysiska och elektrokemiska egenskaperna såsom löslighet i organiska lösningsmedel, densitet, viskositet, jonkonduktiviet och elektrokemiskt fönster har testats för elektrolyterna i den första delen av arbetet. Elektrolyterna som uppvisade de mest lovande elektrokemiska egenskaper har även testats med avseende på brandegenskaperna, så som värmeutveckling, flampunkt och toxicitet. Elektrolyterna jämfördes mot den vanligt förekommande elektrolyten som innehåller litium hexafluorfosfat.   Saltet Li[BOB] löstes inte i lösningsmedel med bra lösningsegenskaper, vilket var anledningen till att det inte genomfördes ytterligare tester på den. Elektrolyterna som det genomfördes tester på avseende på brandegenskaper innehöll Li[MEA] och Li[MEEA] tillsammans med de organiska lösningsmedlen etylenekarbonat och dimetylkarbonat. För Li[MEEA] tillsattes det även jonvätska för att undersöka hur jonvätskan påverkar brandegenskaperna för elektrolyten.   När värmeutveckling för det nyutvecklade salterna och LiPF6 undersöktes, så uppvisade de liknande värden. Anmärkningsvärt var dock att förbränningstiden för LiPF6 varade under en kortare period i jämförelse med de tre andra elektrolyterna. En trolig orsak till detta är att LiPF6 innehåller fluor. Elektrolyterna som provades i konkalorimeter i detta arbete var ej laddade, vilket kan medföra att värmeutvecklingen kan se annorlunda ut vid ett laddat tillstånd. För framtida studier kan det vara intressant att konstruera ett komplett litiumjonbatteri, för att se hur elektrolyterna fungerar och påverkas, beroende på laddningsnivå.   Antändningstiden för Li[MEEA] blandat med de organiska lösningsmedlen tillsammans med jonvätska varierade mycket. Detta är ett intressant resultat, som förmodligen kan förklaras av homogeniteten på elektrolyten. Homogeniteten verifierades enbart okulärt, vilket inte säkerställer att jonvätskan har löst sig fullständigt i elektrolyten.   Resultat för flampunkten för det olika elektrolyterna var intressant, då elektrolyten som innehöll jonvätska visade på lägst flampunkt. Detta var oväntat då tillsatser som jonvätska brukar förbättra brandmotståndet.   Resultatet för FTIR-spektroskopin analyserades för att se hur Li[MEA], Li[MEEA] och LiPF6 skiljde sig åt. De elektrolyter som inte innehöll fluor, producerade bara koldioxid. Medans elektrolyten som innehöll fluor producerade, som väntat, vätefluorid och koldioxid, men även andra gaser som var svåranalyserade.   De framtagna elektrolyterna i detta arbete behöver studeras vidare och fler tester bör genomföras för att se om det finns en möjlighet att använda dem i faktiska litiumjonbatterier. Förutom att testa elektrolyterna i just detta arbete är det viktigt att forskningen kring brandegenskaper och toxiska egenskaper för elektrolyter fortsätter i framtiden.

Due to the successful commercialization of lithium-ion batteries (LIBs), there is a growing interest in developing new battery materials with beneficial electrochemical properties. However, the uneven distribution of lithium resources and the low abundance of lithium in the earth crust are the main obstacles for further development and large-scale production of LIBs. Sodium-ion batteries (SIBs), an alternative that can partly meet the energy storage challenges, are getting attentions of researchers due to the wide availability and lower cost of sodium resources. Nevertheless, the conventional liquid electrolytes of either LIBs or SIBs composed of fluorinated salts dissolved in volatile organic solvents, posing serious safety issues due to the instability of the salts and flammability of the solvents. There is an urge to develop new fluorine-free electrolytes with improved physicochemical and electrochemical properties. In this context, the conventional fluorinated salts should be replaced with fluorine-free salts and the flammable solvents should be substituted with non-flammable solvents. There are a number of strategies to develop high-performant electrolytes including ambient-temperature ionic liquids (ILs), organic ionic plastic crystals (OIPCs) and highly concentrated electrolytes (HCEs) utilizing new salts and solvents. In this thesis, novel phosphorus-based ionic materials and electrolytes are introduced and their properties are thoroughly investigated. In the first part (Paper I), fluorine-free NaDEEP salt and TEOP solvent are employed to make “solvent-in-salt” (SIS) sodium electrolytes, also known as HCEs. Unexpectedly, the addition of TEOP solvent lead to an increase in the oxidation stability of the SIS electrolytes. In addition, an unusual ionic conductivity behavior is found – the ionic conductivities of Na electrolytes increase with increasing salt concentration. The “salt-rich” and “solvent-rich” phases formed within the electrolytes are investigated using multinuclear liquid-state NMR spectroscopy and NMR diffusometry. In the second part (Paper II), a series of orthoborate-based ionic materials, specifically OIPCs, containing phosphonium/ammonium cations are prepared to compare with the popular fluorine-free, bis(oxalato)borate (BOB) salts. The tetrabutyl phosphonium bis(glycolato)borate ([P4444][BGB]) OIPC displays much higher decomposition temperature than the structural analogous [P4444][BOB] IL. The crystal structures of LiBGB and NaBGB salts are resolved using single-crystal X-ray diffraction analysis. Unlike LiBOB, the BGB-based salts revealed excellent moisture stability over an extended time of up to 8-weeks air exposure. Multinuclear solid-state NMR spectroscopy indicates weaker cation-anion interactions in phosphonium-based salts than the ammonium-based ones. Finally, in the third part (Paper III), two-component and three-component eutectic electrolytes, composed of pyrrolidinium saccharin (PySc), lithium saccharin (LiSc) and/or [P4444][BGB] salt. The resulting mixtures showed significantly lower melting temperatures than the neat salts. The physicochemical and thermal properties of these salts are thoroughly investigated and discussed.

Les mousses extinctrices sont utilisées sur les feux de catégorie B (solvants inflammables). L’efficacité des mousses actuelles contenant des agents moussants fluorés est apportée par la formation d’un film aqueux à la surface du carburant enflammé. Les entreprises recherchent et développent de nouveaux agents moussants sans fluor car ce type de tensioactif est nocif pour l’environnement et la santé. Des mousses très stables sont nécessaires pour qu'une couche épaisse de mousse résiste aux températures élevées et au démoussage par le solvant et évite ainsi la ré-inflammation.Dans ce travail, l’amélioration de la stabilité de la mousse a été réalisée en utilisant des épaississants dans une solution moussante avec des tensioactifs non fluorés. Des polysaccharides tels que la gomme xanthane ont été utilisés et ses interactions avec des tensioactifs ont été étudiés. Les complexes formés par ces interactions ont été utilisés dans le but d’améliorer la stabilité de la mousse et sa résistance aux flammes. Ceci engendre des mousses de plus faible moussabilité mais de plus grande stabilité. Des tests à échelle réduite ont été réalisés selon la norme EN1568 et ont montré l’efficacité de l’addition de gomme xanthane. Ces formulations innovantes associant des polysaccharides et des agents moussants sont de bonnes alternatives aux formules contenant des tensioactifs fluorés. Le mécanisme d’action des hydrotropes améliorant la moussabilité a aussi été étudié / Firefighting foams are used on class B fires (flammable solvents). The efficiency of currently used foams containing fluorinated foaming agents is ensured by the formation of an aqueous thin film on top of the burning solvent. The formation of such film requires the use of fluorinated surfactants that specifically adsorb at the water-air interface. Companies currently develop fluorine-free products for firefighting foams because this kind of surfactants is harmful for the environment and health. Very stable foams are necessary to the formation of a thick layer of foam that resists high temperatures and defoaming by the solvent, preventing fire re-ignition.In this work, improved foam stability was achieved by using thickeners in the foaming fluid together with the non-fluorinated surfactants. Polysaccharides such as xanthan gum were used and their interactions with surfactants were investigated. Complex species formed by such interactions were used in order to improve foam stability and resistance against flames. This causes a lower foamability but higher stability of foams. Small scale fires extinguishing experiments performed following the standard EN1568 showed the efficiency of xanthan gum addition. These innovative formulations combining polysaccharides and foaming agents are suitable alternatives to those containing fluorinated surfactants. The action mechanism of hydrotropes improving foamability has also been studied

The discovery of superconductivity in ceramic materials by Bednorz and Müller [2, 3] in early 1987, immediately followed by Wu et al. [4, 5] who showed that YBa2Cu3O7−x (YBCO) becomes superconducting (92K) well above the boiling point of nitrogen (77K) created a great excitement in superconductivity research. Potential applications of high Tc-superconductors require large critical currents and high-applied magnetic fields. Effective ways to increase the critical current density at high magnetic fields in YBCO are the introduction of nanoparticles and chemical substitution of yttrium by other rare earth elements. Since low costs and environmental compatibility are essential conditions for the preparation of long length YBCO films, the cost effective chemical solution deposition (CSD) procedure was selected, given that no vacuum technology is required. To reveal the flexibility and the good optimization possibilities of the CSD approach two main processes were chosen for comparison: a fluorine-free method, namely the polymer-metal precursor technique, and a fluorine-based method, the metalorganic deposition (MOD) using the trifluoroacetates (TFA) technique. Sharp transition temperature widths DTc of 1.1K for the polymer metal method, 0.8K for TFA method and critical current densities Jc of _3.5MA/cm2 shows that high quality YBCO thin films can be produced using both techniques. Especially interesting is the magnetic field dependence of the critical current density Jc(B) of the Y(Dy)BCO (80 %) films showing that for the lower magnetic fields the critical current density Jc(B) is higher for a standard YBCO film, but at fields higher than 4.5T the critical current density Jc(B) of Y(Dy)BCO is larger than that for the YBCO. Above 8T, Jc(B) of the Y(Dy)BCO film is more than one order of magnitude higher than in pure YBCO film. / Die Entdeckung der Supraleitung in keramischen Materialien durch Bednorz und Müller 1987 und die kurz darauf folgende Beobachtung von Wu et al., dass YBa2Cu3O7−x (YBCO) supraleitende Eigenschaften deutlich oberhalb (92K) des Siedepunktes von Stickstoff (77K) aufweist, führten zu einer enormen Intensivierung der Forschung hinsichtlich neuer supraleitender Materialien sowie deren Eigenschaften und möglichen Einsatzgebieten. Potentielle Anwendungsgebiete für diese neuen Hochtemperatur-Supraleiter erfordern hohe kritische Stromdichten und hohe kritische Feldstärken. Effektive Wege zur Erhöhung der kritischen Stromdichte in starken Magnetfeldern in YBCO sind der Einbau von Nanoteilchen oder die chemische Substitution von Yttrium durch ein anderes Seltenerd-Element. Da niedrige Kosten und gute Umweltverträglichkeit wichtige Voraussetzungen für die Herstellung von YBCO-Schichten großer Länge darstellen, werden in dieser Arbeit die Vorteile und Einsatzmöglichkeiten der Chemischen Lösungsabscheidung (chemical solution deposition - CSD) untersucht. CSD Prozesse sind besonders gut geeignet, weil sie keine Vakuum-Technologie erfordern und einen hohen Grad an Flexibilität garantieren. Zur Demonstration der guten Optimierbarkeit werden zwei wichtige CSD-Verfahren miteinander verglichen: die Polymer-Metall Precursor Technik - eine Fluor-freie Methode - und die metallorganische Abscheidung mittels Trifluoroacetat (TFA-MOD), bei der Fluor zum Einsatz kommt. Scharfe supraleitende Übergänge (Polymer-Metall Precursor Technik: DTc = 1.1K; TFA -MOD: DTc = 0.8K) sowie hohe kritische Stromdichten von ca. 3.5MA/cm2 (B= 0 T) zeigen, dass mit beiden Verfahren dünne YBCO-Schichten hoher Qualität hergestellt werden können. Außerdem bieten CSD-Verfahren durch die hervorragende Kontrollierbarkeit der Stöchiometrie des Precursors die Möglichkeit Yttrium teilweise oder vollständig durch andere Seltenerd-Metalle zu ersetzen und damit die kritische Stromdichte in hohen Magnetfeldern deutlich zu erhöhen. In dieser Arbeit wird gezeigt, dass besonders die TFA-Methode besonders geeignet ist, um (RE)BCO-Schichten (RE: rare earth) herzustellen. Untersucht wurden verschiedene Zusammensetzungen mit Sm, Dy und Ho. Außerordentlich interessant sind dabei die Ergebnisse für Y(Dy)BCO-Schichten. Schichten mit einem Dy-Gehalt von 80 % zeigen oberhalb von 4.5T deutlich höhere kritische Stromdichten als reine YBCO Schichten. Bei Magnetfeldern größer als 8T beträgt der Unterschied mehr als eine Größenordnung.

The discovery of superconductivity in ceramic materials by Bednorz and Müller [2, 3] in early 1987, immediately followed by Wu et al. [4, 5] who showed that YBa2Cu3O7−x (YBCO) becomes superconducting (92K) well above the boiling point of nitrogen (77K) created a great excitement in superconductivity research. Potential applications of high Tc-superconductors require large critical currents and high-applied magnetic fields. Effective ways to increase the critical current density at high magnetic fields in YBCO are the introduction of nanoparticles and chemical substitution of yttrium by other rare earth elements. Since low costs and environmental compatibility are essential conditions for the preparation of long length YBCO films, the cost effective chemical solution deposition (CSD) procedure was selected, given that no vacuum technology is required. To reveal the flexibility and the good optimization possibilities of the CSD approach two main processes were chosen for comparison: a fluorine-free method, namely the polymer-metal precursor technique, and a fluorine-based method, the metalorganic deposition (MOD) using the trifluoroacetates (TFA) technique. Sharp transition temperature widths DTc of 1.1K for the polymer metal method, 0.8K for TFA method and critical current densities Jc of _3.5MA/cm2 shows that high quality YBCO thin films can be produced using both techniques. Especially interesting is the magnetic field dependence of the critical current density Jc(B) of the Y(Dy)BCO (80 %) films showing that for the lower magnetic fields the critical current density Jc(B) is higher for a standard YBCO film, but at fields higher than 4.5T the critical current density Jc(B) of Y(Dy)BCO is larger than that for the YBCO. Above 8T, Jc(B) of the Y(Dy)BCO film is more than one order of magnitude higher than in pure YBCO film. / Die Entdeckung der Supraleitung in keramischen Materialien durch Bednorz und Müller 1987 und die kurz darauf folgende Beobachtung von Wu et al., dass YBa2Cu3O7−x (YBCO) supraleitende Eigenschaften deutlich oberhalb (92K) des Siedepunktes von Stickstoff (77K) aufweist, führten zu einer enormen Intensivierung der Forschung hinsichtlich neuer supraleitender Materialien sowie deren Eigenschaften und möglichen Einsatzgebieten. Potentielle Anwendungsgebiete für diese neuen Hochtemperatur-Supraleiter erfordern hohe kritische Stromdichten und hohe kritische Feldstärken. Effektive Wege zur Erhöhung der kritischen Stromdichte in starken Magnetfeldern in YBCO sind der Einbau von Nanoteilchen oder die chemische Substitution von Yttrium durch ein anderes Seltenerd-Element. Da niedrige Kosten und gute Umweltverträglichkeit wichtige Voraussetzungen für die Herstellung von YBCO-Schichten großer Länge darstellen, werden in dieser Arbeit die Vorteile und Einsatzmöglichkeiten der Chemischen Lösungsabscheidung (chemical solution deposition - CSD) untersucht. CSD Prozesse sind besonders gut geeignet, weil sie keine Vakuum-Technologie erfordern und einen hohen Grad an Flexibilität garantieren. Zur Demonstration der guten Optimierbarkeit werden zwei wichtige CSD-Verfahren miteinander verglichen: die Polymer-Metall Precursor Technik - eine Fluor-freie Methode - und die metallorganische Abscheidung mittels Trifluoroacetat (TFA-MOD), bei der Fluor zum Einsatz kommt. Scharfe supraleitende Übergänge (Polymer-Metall Precursor Technik: DTc = 1.1K; TFA -MOD: DTc = 0.8K) sowie hohe kritische Stromdichten von ca. 3.5MA/cm2 (B= 0 T) zeigen, dass mit beiden Verfahren dünne YBCO-Schichten hoher Qualität hergestellt werden können. Außerdem bieten CSD-Verfahren durch die hervorragende Kontrollierbarkeit der Stöchiometrie des Precursors die Möglichkeit Yttrium teilweise oder vollständig durch andere Seltenerd-Metalle zu ersetzen und damit die kritische Stromdichte in hohen Magnetfeldern deutlich zu erhöhen. In dieser Arbeit wird gezeigt, dass besonders die TFA-Methode besonders geeignet ist, um (RE)BCO-Schichten (RE: rare earth) herzustellen. Untersucht wurden verschiedene Zusammensetzungen mit Sm, Dy und Ho. Außerordentlich interessant sind dabei die Ergebnisse für Y(Dy)BCO-Schichten. Schichten mit einem Dy-Gehalt von 80 % zeigen oberhalb von 4.5T deutlich höhere kritische Stromdichten als reine YBCO Schichten. Bei Magnetfeldern größer als 8T beträgt der Unterschied mehr als eine Größenordnung.

”Durable water repellents (DWR) är textilimpregneringar som bidrar med vattenavvisande egenskaper som håller länge på funktionella tyg. Tyvärr är dessa hydrofobiska ytbehandlingar vanligtvis en källa till skadliga och persistenta kemikalier och de även är producerade från fossilbaserade resurser. Eftersom medvetenheten kring de här problemen har ökat, har innovativa, miljövänliga och biologiskt nedbrytbara alternativ tagits fram. Hittills finns dock inga produkter gjorda av 100% förnybara råvaror. I ett försök att utveckla en biobaserad, icke-giftig DWR som aktiveras under milda förhållanden, lades fokus på utveckling av en lagringsstabil sprayimpregneringsprodukt för hemmabruk. Vid formulering av emulsionerna/dispersionerna utvärderades en stor mängd biobaserade och kommersiellt tillgängliga hydrofobiska och amfifila molekyler med avseende den vattenavvisande effekt som de bidrog med på den behandlade textilen. Samtidigt bedömdes de producerade formuleringarna noggrant för att skapa förståelse om effekterna från ingredienserna och deras relation till produktens stabilitet. De kandidatprodukter som valdes ut och undersöktes vidare hade lovande vattenavvisande egenskaper och visade rimlig hållbarhetstid på åtminstone en månad i 40 °C. Standardiserade sprayscores på 3 (där 1 är sämst och 5 är bäst) nåddes efter 24 timmars hängtorkning i rumstemperatur. Dessutom uppnåddes sprayscore på 5 efter en kort, icke-industriell torktumling på låg temperatur och den behölls efter minst tio tvättar på syntetiska textiler. Utvalda produkter påverkade inte märkbart tygets andningsförmåga och majoriteten hade ingen influens på textilens mjukhet och färg. Förutom uppskalningsexperiment och partikelstorleksmätningar, granskades resultat med en tillämpningsstudie av formuleringarna på femton olika tygtyper. Produkternas effekter på utseende och känsla dokumenterades för de olika textilierna. Egenskaper som kontaktvinklar, sprayscores och tvättbeständighet bestämdes och jämfördes med en kommersiellt tillgänglig produkt. / Durable water repellents (DWR) are textile finishes that provide long-lasting water repelling properties to functional garments. However, these hydrophobic finishes are commonly a source of polluting and persistent chemicals and are produced from fossil resources. As a result of increasing awareness, innovation towards environmentally friendly and biodegradable alternatives has progressed, yet no 100% renewable sourced products are available. In an attempt to create a bio-based, non-toxic DWR, that is curable under mild conditions, focus was put on the development of a shelf stable spray impregnation product intended for consumer use. By formulating dispersion/emulsion systems, a wide variety of commercially available, renewable sourced amphiphilic and hydrophobic molecules were evaluated on their effect on the water repelling performance of treated textile fabrics. Simultaneously, the produced systems were assessed carefully to create understanding on the effect of substances and their corresponding ratios on the stability. Promising candidate products that were selected for further investigation showed reasonable stability for 1 month at 40 °C. Industrial standard spray ratings of 3 (where 1 is worst and 5 is best) after hang drying at room temperature could be reached within 24 hours. On top of that, spray ratings of 5 could be reached after short time, non-industrial tumble drying at low temperatures, which could even be retained for at least ten laundering cycles on synthetic textiles. The selected finishes did not have a measurable effect on the breathability of the treated fabrics, while the majority did not considerably affect the hands-feeling or colour of the textiles. Besides several scaling up experiments and particle size measurements, extrapolation of the findings was carried out by testing the developed formulations on fifteen different types of textiles. Effects on appearance and feel were documented, additionally, contact angle, spray score, and wash durability were determined and compared with a commercially available product.

Varaktig vattenavvisning från engelskans Durable Water Repellents (DWR) är en kemi som appliceras på textil för att göra den motståndskraftig mot vätska. En DWR-kemi som visat sig vara till stor belastning för miljön och därför genomgått en utfasning inom industrin är fluorkarboner. Detta har lett till fluorfria alternativ och även modifierade fluorkarboner vilka det finns bristande information kring gällande risker för miljö och hälsa. I och med övergången från fluorerade DWR till de fluorfria alternativen aktualiserades frågan kring hur ”durable”, alltså motståndskraftiga mot tvätt och användning, dessa verkligen är. Detta har resulterat i ett stort utbud av konsumentprodukter för återupplivning av vattenavvisning på beklädnad i hemmamiljö. Dessa konsumentprodukter har benämnts som återimpregneringar i denna studie. Återimpregneringar kan göra att användaren förblir nöjd med beklädnaden och detta minskar i sin tur det textila avfallet. Området är outforskat och industrin vill veta mer om dessa konsumentprodukter inklusive hur det textila materialet påverkas av dem. Studien har utgått från ett kundperspektiv vid val av relevanta parametrar och på ett kreativt sätt översatt dessa till laborativa testmetoder. De parametrar som funnits med i studien har varit vattenavvisning, färgförändring, luftgenomsläpplighet samt känsla vilka har använts för analys och jämförelse mellan åtta stycken fluorfria återimpregneringar. Två etablerade appliceringstekniker, wash-in och spray-on, har undersökts på fyra olika textilier som skulle kunna representera frilufts- samt arbetskläder. Två av textilierna var av polyester och två var av polyamid. Samtliga återimpregneringar gav en ökad vattenavvisande effekt. Resultatet varierade beroende på vilket textilt material och vilken återimpregnering som användes. De övriga testmetoderna, färgförändring, luftgenomsläpplighet och böjstyvhet, visade även de liknande variationer i resultaten. Wash-in och spray-on teknikerna kunde generellt visa på statistiska skillnader. Även produkter med samma varumärke applicerade med wash-in och spray-on teknik visade skilda resultat. De laborativa testmetoderna som valts ut visade sig vara användbara verktyg för utvärdering av återimpregneringar vid textilapplicering.  Utifrån litteraturens rön och denna studies resultat har slutsatsen dragits att konsumentprodukter för återimpregnering av textil har betydande skillnader beroende av vilken DWR-kemi de består av samt textiliens konstruktion och fibersort. Det säkraste fluorfria alternativet ur miljösynpunkt tros av rapportförfattarna vara vax som klassas som en kolväteskemi, men det finns mycket kvar att utforska innan en sådan slutsats kan dras med säkerhet. Denna studie har varit ett inledande steg mot att undersöka återimpregneringar som förhoppningsvis i framtiden kan leda till ett minskat textilt avfall med minsta möjliga miljöbelastning. / The textile industry uses durable water repellents (DWR) to achieve water repellency on textiles. One of these DWR chemistries, fluorocarbons, is an environmental issue and has therefore been phased-out in the industry. This has resulted in a market where both modified fluorocarbons and fluorine-free alternatives are available and there is a lack of information about these DWR regarding health and environmental aspects. Due to the changeover from the fluorinated DWR to the non-fluorinated options, the question was raised about how durable these really are. This resulted in a wide range of do-it-yourself consumer products for the water repellency revival. These consumer products have been referred to as reimpregnations in this study. The purpose of reimpregnations is to give clothing a longer life cycle. The customer remains satisfied with the garment and this in turn reduces the textile waste. The industry wants to know more about these unexplored consumer products, including how the textile material is affected by them. A customer perspective has been the basis for selecting relevant parameters in this study, which has been creatively translated into laboratory test methods. Parameters in this study have been water repellency, color change, air permeability and fabric hand. These have been used for analysis and comparison of eight fluorine-free reimpregnations. The techniques used were wash-in and spray-on and have been investigated on four different textiles representing outdoor clothing and workwear, two made of polyester and two of polyamide. All the reimpregnations showed an increased effect in water repellency. The result varied depending on which textile material and what kind of reimpregnation that was used. The other test methods also showed variation according to these factors. Over all the wash-in and spray-on techniques showed a statistical significance. Products from the same brand applied with wash-in and spray-on techniques also showed different results. The selected laboratory test methods proved to be useful tools for evaluation of reimpregnations in textile applications. Based on the literature combined with the results from this study the conclusion has been made that reimpregnation, of textile materials, has a significant difference between DWR chemistries as well as the construction and fibre type of the textile. The safest fluorine-free option, from an environmental point of view, is believed to be wax, which is classified as a hydrocarbon chemistry, however there is much left to explore before such a conclusion can be made with certainty. This study has been an initial step towards the investigation of reimpregnations, which hopefully in the future can lead to reduced textile waste with as little environmental impact as possible.