Stora Enso Oyj

Teknologian Tutkimuskeskus Vtt Oy

Borealis Technology Oy

Borealis A/s

Borealis Polymers Oy

Purac Biochem Bv

Valmet Technologies Oy

Solazyme, Inc.

Maillefer Sa

Terravia Holdings, Inc.

Spinnova Oy

Tamfelt Pmc Oy

Photonium Oy

Infinited Fiber Company Oy

Infinited Fiber Company

Ali Harlin

Jari Räsänen

Tapani Penttinen

Isto Heiskanen

Kaj Backfolk

Esa Korhonen

Olli Aaltonen

Jarmo Ropponen

Christiane Laine

Pia Willberg-Keyriläinen

Anna-Stiina Jääskeläinen

Jouni Kivel&auml;

Jeffrey Jacob Cernohous

Kauno Alastalo

Adam R Pawloski

Jaakko Pere

John Piechocki

Amir K Karbasi

David Thomas

Ismo Pentti

Tiina Liitiä

Aimo Sahila

Adrienne McKee

Martta Asikainen

Sonia Sousa

Timo Leinonen

Thomas Garoff

Kimmo Nevalainen

Pirjo Jääskeläinen

Hans-Peter Hentze

Juha Salmela

Jouni Takakarhu

Tuomo Hjelt

Ulf Palmqvist

Jaakko Hiltunen

Outi Kylliäinen

Mari Hiltunen

Anders E Nymark

Risto Laitinen

Kyösti Valta

Eino Sivonen

Hanne Wikberg

Nina Manner

Riku Talja

Henrik Andtsj&ouml;

Jani Kiuru

Kalle Nättinen

Sakari Siren

Jani Mäkelä

Henrik Andtsjo

Pekka Kortelainen

Thomas Gädda

Ari Palmroos

Pertti Nousiainen

Tania Rautio

Fred Bergmann

Fredrik Ollila

Leena Nurmi

Pekka Huotari

Antero Ahvenainen

Tekla Tammelin

Risto Widerholm

Taina Kamppuri

Antero Laitinen

Mari Seppanen

Päivi Huovinen

Jyrki Pennala

Jari Vartiainen

Marianna Vehvilainen

Tiina Nypelö

Leena Hupa

Hanna Koskela

Erik Vedel

Minna Peltola

Laura Kela

Hannu Martikainen

Tuula Wilenius-Jaakonaho

Juha Linnekoski

Jinto Anthonykutty

Sirpa Ala Huikku

Jun Shan

Mika Härkönen

Erkki Malanin

Harri Heikkinen

Virpi Rämö

Martin Stjernberg

Thomas Gadda

Minni Pirttimaa

Reetta Kaila

Mika Harkonen

Vidar Grönberg

Yingfeng Shen

Maarit Peltola

Jukka Ketoja

Marjo Määttänen

Marianna Vehviläinen

Sari Asikainen

Airi Särkilahti

Marja Juvonen

Marianna Vehvilaeinen

According to an example aspect of the present invention, there is provided a method of separating cellulosic fibres and non-cellulosic fibres from a mixed fibre textile material comprising cellulosic and non-cellulosic fibres. The method comprises mechanically disintegrating the textile material to open textile structures in the material, contacting the mechanically opened structures with an acid in a first chemical step, and contacting the mechanically opened structures with an alkaline in a second chemical step.

Separation of polycotton blends

According to an example aspect of the present invention, there is provided a use of molar mass controlled cellulose in injection molding, extrusion and three dimensional printing applications.

Use of molar mass controlled cellulose

According to an example aspect of the present invention, there is provided a method of producing cellulose carbamate in an aqueous phase. The method comprises the steps of a) providing a cellulose raw-material; b) providing urea; c) mixing cellulose and urea to provide a mixture; d) subjecting the mixture to a reduced pressure of no more than 350 mbar(a); e) heating the mixture to a temperature of 130 to 150° C. to subject cellulose to reaction with urea to form cellulose carbamate; f) releasing the pressure; and g) recovering the cellulose carbamate g) recovering the cellulose carbamate, and h) washing the cellulose carbamate with water to remove water soluble nitrogenous compounds wherein the water-soluble nitrogeneous compounds make up at the most 12%, preferably 6% or less, of the total weight of cellulose carbamate and water-soluble nitrogenous compounds.

Method of producing cellulose carbamate

The present invention relates to a method of deoxygenating tall oil pitch, yielding aliphatic and aromatic hydrocarbons. The invention even comprises turning the aliphates into polymerizable olefins by steam cracking, and turning the aromates into polymerizable terephthalic acid by oxygenation and, as necessary, rearrangement. The monomers can be used for the production of polymers of partially or completely biologic origin. According to the invention, tall oil pitch is first heated to turn it into liquid, which is then fed into a catalyst bed and catalytically deoxygenated with hydrogen. The deoxygenation catalyst is preferably a Ni&#x2014;Mo catalyst and, in addition, a cracking catalyst can be used, such as an acidic zeolite catalyst. The deoxygenated product stream is cooled down so as to obtain a liquid, which is distilled for separation of the aliphatic and aromatic hydrocarbons for use in the production of the respective monomers and finally polymers.

Methods of deoxygenating bio-based material and production of bio-based terephtalic acid and olefinic monomers

Described herein is a feasible, significantly simplified production method that avoids challenging lactonization steps and converts a low molecular weight aliphatic polyester, consisting of hydroxy acids and a comonomer, whose molecular weight has been increased by step-growth polymerization reactions. The molecular weight of the aliphatic polyester, based on comparison of initial and final weight average molecular weights (MM), increased significantly at a rate which permits the use of reactive extrusion to produce high molecular weight aliphatic polyesters in a simple, economically feasible manner.

Glycolic acid polymers and method of producing the same

The invention concerns a method of manufacturing paper or board, the paper or board obtained by the method, and a method of producing a tray from the board. In a fibrous stock for papermaking is incorporated an amount of polymer coated fibrous particles, which even have a foaming agent such as moisture contained therein. A web is formed from the fibrous stock on a forming fabric of a paper or board machine, followed by pressing and drying to a finished paper or board. As the paper or board is sufficiently heated the foaming agent within the particles evaporates, causing expansion and foaming of the polymer coating, which adds to malleability of the board as it is moulded into a shaped article such as a board tray. The invention even covers production of doubly coated fibrous particles for use in said methods, the inner coating layer being of a foamable polymer with a higher melt flow rate and the outer coating layer being of a non-foaming polymer of a lower melt flow rate.

Methods for making paper or board, a board tray and pulp particles coated with foamable polymer for use in the same

The present invention concerns a process for the conversion of biomaterials into structural carbon products, particularly utilizing a hydrothermal treatment step that is carried out on a high molar mass organic starting material having a carbon content of &#x3e;40 wt % of the dry matter. The invention also concerns a structural carbon product obtained using such a process, which has well-defined physico-chemical properties, e.g. in terms of surface area, carbon content, density, size and shape.

Process for the hydrothermal treatment of high molar mass biomaterials

The present invention relates to a process for producing high tensile strength nanofiber yarn by wet-extrusion on a slippery surface. In particular, the present invention discloses a method wherein individual nanocellulose fibers are aligned by high speed in-nozzle-alignment and on-surface-alignment, which comprise controlling the fiber width on a moving slippery surface.

Method for producing high tensile strength nanofiber yarn

According to an example aspect of the present invention, there is provided a method of producing furan carboxylates from aldaric acids in the presence of a solid heterogeneous catalyst and a solvent with short reaction time. The feedstock for the production is a stable compound, which allows industrial scaling of the process. Solid acid catalyst and sustainable solvent provide considerable reduction of toxic waste compared to traditional methods, and recyclability.

Method of producing furan carboxylates from aldaric acids by using solid heterogeneous catalyst

A method of deoxygenation of tall oil as well as methods for the production of aliphatic hydrocarbons and polymerizable monomers from tall oil. Sulphurous crude tall oil together with hydrogen gas is fed into a reactor comprising a catalyst bed. The oil is catalytically deoxygenated by hydrogen in the bed by use of a sulfided metal catalyst, e.g. a NiMoS catalyst. The flow exiting the reactor is cooled down and a hydrocarbon-bearing liquid phase is separated from a gas phase, followed by subjecting the liquid phase to distillation for removal of useless aromatic hydrocarbons and then to steam cracking to form a product containing olefins such as ethylene or propylene. By regulation of the deoxygenation temperature to be at least 270&#xb0; C. but less than 360&#xb0; C. the yield is rich in linear and cyclic aliphates that usefully turn to olefins in the steam cracking, while formation of napthalenes is reduced.

Methods of deoxygenation of tall oil and production of polymerizable monomers therefrom

The present invention relates to selective catalytic dehydroxylation method of aldaric acids for producing muconic acid and furan chemicals, which can be used directly in fine chemical and polymer applications (FCA/FDCA) and as intermediates in the preparation of industrially significant chemicals, such as terephthalic acid, adipic acid, caprolactone, caprolactam, nylon 6.6, 1,6-hexanediol and multiple pharmaceutical building blocks (MA/MAME).

Method for producing muconic acids and furans from aldaric acids

Provided are biomass-based materials and valuable uses of microalgal biomass including: (i) acetylation of microalgal biomass to produce a material useful in the production of thermoplastics; (ii) use of triglyceride containing microalgal biomass for production of thermoplastics; (iii) combination of microalgal biomass and at least one type of plant polymer to produce a material useful in the production of thermoplastics; (iv) anionization of microalgal biomass to form a water absorbant material; (v) cationization of microalgal biomass, and optional flocculation, to form a water absorbant material; (vi) crosslinking of anionized microalgal biomass; (vii) carbonization of microalgal biomass; and (viii) use of microalgal biomass in the making of paper.

Algal thermoplastics, thermosets, paper, adsorbants and absorbants

The present invention relates to a method for preparation a glycolide polyester by ring opening polymerization characterized in that glycolide monomer with optional co-monomer(s) of cyclic ester(s) is/are subjected to ring opening polymerization in the presence of a dispersion stabilizer and a catalyst, said catalyst being selected for precipitating glycolide homopolymer or copolymer from solvent, said solvent being selected so that the glycolide monomer and the optional co-monomer(s), the dispersion stabilizer and the catalyst are soluble therein but said glycolide homopolymer or copolymer is non-soluble. The present invention further relates to an in situ ring opening polymerizing process product, and to use of said glycolide polyester, and to further processing of said glycolide polyester.

Method for preparing glycolide polyester by ring opening polymerization

Biobased p-cymene and methods of producing same, which can further be converted to terephtalate. Further, a method is described for converting crude sulfate turpentine recovered from chemical wood pulping into p-cymene and eventually to terephtalic acid of biological origin, and products thereof respectively. In said method, both conversion and desulfurization is realized in one reaction step. The disclosure is also related to use of zeolite catalysts in said method.

Catalytic refining of terpenes of pulp origin

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Kerava, Finland

Ali Harlin