Change search
Refine search result
1 - 8 of 8
CiteExportLink to result list
Permanent link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Rows per page
  • 5
  • 10
  • 20
  • 50
  • 100
  • 250
Sort
  • Standard (Relevance)
  • Author A-Ö
  • Author Ö-A
  • Title A-Ö
  • Title Ö-A
  • Publication type A-Ö
  • Publication type Ö-A
  • Issued (Oldest first)
  • Issued (Newest first)
  • Created (Oldest first)
  • Created (Newest first)
  • Last updated (Oldest first)
  • Last updated (Newest first)
  • Disputation date (earliest first)
  • Disputation date (latest first)
  • Standard (Relevance)
  • Author A-Ö
  • Author Ö-A
  • Title A-Ö
  • Title Ö-A
  • Publication type A-Ö
  • Publication type Ö-A
  • Issued (Oldest first)
  • Issued (Newest first)
  • Created (Oldest first)
  • Created (Newest first)
  • Last updated (Oldest first)
  • Last updated (Newest first)
  • Disputation date (earliest first)
  • Disputation date (latest first)
Select
The maximal number of hits you can export is 250. When you want to export more records please use the Create feeds function.
  • 1.
    Adolfsson, Karin H.
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Golda-Cepa, M
    Benyahia Erdal, Nejla
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Duch, J
    Kotarba, A
    Hakkarainen, Minna
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Importance of Surface Functionalities for Antibacterial Properties of Carbon Spheres2019In: Advanced Sustainable Systems, ISSN 2366-7486Article in journal (Refereed)
    Abstract [en]

    Carbon spheres (CS) are interesting materials for antibacterial applications. Herein, CS are produced by a green process utilizing microwave-assisted hydrothermal treatment of cellulose. The CS are then postmodified in acidic and basic solutions to evaluate the influence of different functionalities on antibacterial properties. CS contain OH/COOH, C Symbol of the Klingon Empire C, and C Symbol of the Klingon Empire O functionalities, while O-CS produced by acid treatment of CS have additional COOH, and NH/NH2 groups, resulting in carbon spheres with negatively and positively charged groups in dispersion. Treatment with base (Na-CS) removes low molecular weight species with oxygen and results in carbon spheres with the highest C/O ratio. CS, O-CS, and Na-CS have nonporous morphology and are in micro/nanometer sizes, although, smaller sized spheres, hollow spheres, and fragments are also attained in the case of O-CS. O-CS show antibacterial activity toward both Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Pseudomonas aeruginosa (P. aeruginosa). The minimum inhibitory concentration is 200 and 400 mu g mL(-1) for S. aureus and P. aeruginosa, respectively, and is achieved only after 3 h of incubation. Neither CS nor Na-CS exhibit antibacterial activity. The antibacterial activity is suggested to originate from electrostatic interactions between O-CS and the bacteria.

  • 2.
    Adolfsson, Karin H.
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology. Sch Chem Sci & Engn, Stockholm, Sweden..
    Hassanzadeh, Salman
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology. Sch Chem Sci & Engn, Stockholm, Sweden..
    Hakkarainen, Minna
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology. Sch Chem Sci & Engn, Stockholm, Sweden..
    Value-added carbon products attained through microwave assisted hydrothermal treatment of cellulose and waste paper2016In: Abstract of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 251Article in journal (Other academic)
  • 3.
    Adolfsson, Karin H.
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Lin, Chia-feng
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology, Polymer Technology.
    Hakkarainen, Minna
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Microwave Assisted Hydrothermal Carbonization and Solid State Postmodification of Carbonized Polypropylene2018In: ACS SUSTAINABLE CHEMISTRY & ENGINEERING, ISSN 2168-0485, Vol. 6, no 8, p. 11105-11114Article in journal (Refereed)
    Abstract [en]

    Functional carbon materials produced through a hydrothermal treatment of waste products have gained interest. Particularly, the method is considered more facile and green compared to conventional decomposition methods. Here, we demonstrated an upcycling of polypropylene (PP) waste to carbon materials by a microwave assisted hydro thermal treatment. The solid product obtained from the hydrothermal treatment was analyzed by multiple techniques to reveal the structure and the influence of processing conditions on PP degradation and hydrothermal carbonization. Chemical analyses showed the presence of carbonaceous material independent of acid amount (20 and 30 mL), temperature (210 and 250 degrees C), and time (20-80 min). A complete transformation of PP content to amorphous carbon required 60 min at 250 degrees C. The mass yield of the solid product decreased as a function of harsher processing conditions. At the same time, thermogravimetric analysis illustrated products with increasing thermal stability and a larger amount of remaining residue at 600 degrees C. The solid products consisted of irregular fragments and sheet-like structures. A solid state microwave process in air atmosphere was performed on a product with incomplete carbonization. The modification resulted in a decreased C/O ratio, and TGA analysis in nitrogen showed high thermal stability and degree of carbonization as indicated by the remaining residue of 86.4% at 600 degrees C. The new insights provided on the hydrothermal carbonization, and postmodification in air atmosphere, can catalyze effective handling of plastic waste by enabling transformation of low quality waste into functional carbon materials.

  • 4.
    Benyahia Erdal, Nejla
    et al.
    KTH, School of Chemical Science and Engineering (CHE). Royal Inst Technol, Sch Chem Sci & Engn, Stockholm, Sweden..
    Adolfsson, Karin H.
    KTH, School of Chemical Science and Engineering (CHE). Sch Chem Sci & Engn, Stockholm, Sweden..
    Hakkarainen, Minna
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology. Royal Inst Technol, Stockholm, Sweden..
    Silicone-hydrogel bandage lenses used in conjunction with pharmaceutical eye drops: An uptake and release study2016In: Abstract of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 251Article in journal (Other academic)
  • 5.
    Benyahia Erdal, Nejla
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology, Polymer Technology.
    Adolfsson, Karin H.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Pettersson, Torbjörn
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Hakkarainen, Minna
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Green Strategy to Reduced Nanographene Oxide through Microwave Assisted Transformation of Cellulose2018In: ACS Sustainable Chemistry and Engineering, ISSN 2168-0485, Vol. 6, no 1, p. 1245-1255Article in journal (Refereed)
    Abstract [en]

    A green strategy for fabrication of biobased reduced nanographene oxide (r-nGO) was developed. Cellulose derived nanographene oxide (nGO) type carbon nanodots were reduced by microwave assisted hydrothermal treatment with superheated water alone or in the presence of caffeic acid (CA), a green reducing agent. The carbon nanodots, r-nGO and r-nGO-CA, obtained through the two different reaction routes without or with the added reducing agent, were characterized by multiple analytical techniques including FTIR, XPS, Raman, XRD, TGA, TEM, AFM, UV-vis, and DLS to confirm and evaluate the efficiency of the reduction reactions. A significant decrease in oxygen content accompanied by increased number of sp2 hybridized functional groups was confirmed in both cases. The synergistic effect of superheated water and reducing agent resulted in the highest C/O ratio and thermal stability, which also supported a more efficient reduction. Interesting optical properties were detected by fluorescence spectroscopy where nGO, r-nGO, and r-nGO-CA all displayed excitation dependent fluorescence behavior. r-nGO-CA and its precursor nGO were evaluated toward osteoblastic cells MG-63 and exhibited nontoxic behavior up to 200 μg mL-1, which gives promise for utilization in biomedical applications.

  • 6.
    Delekta, Szymon Sollami
    et al.
    KTH, School of Electrical Engineering and Computer Science (EECS), Electronics.
    Adolfsson, Karin H.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Benyahia Erdal, Nejla
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Hakkarainen, Minna
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology, Polymer Technology.
    Östling, Mikael
    KTH, School of Electrical Engineering and Computer Science (EECS), Electronics.
    Li, Jiantong
    KTH, School of Electrical Engineering and Computer Science (EECS), Electronics.
    Fully inkjet printed ultrathin microsupercapacitors based on graphene electrodes and a nano-graphene oxide electrolyte2019In: Nanoscale, ISSN 2040-3364, E-ISSN 2040-3372, Vol. 11, no 21, p. 10172-10177Article in journal (Refereed)
    Abstract [en]

    The advance of miniaturized and low-power electronics has a striking impact on the development of energy storage devices with constantly tougher constraints in terms of form factor and performance. Microsupercapacitors (MSCs) are considered a potential solution to this problem, thanks to their compact device structure. Great efforts have been made to maximize their performance with new materials like graphene and to minimize their production cost with scalable fabrication processes. In this regard, we developed a full inkjet printing process for the production of all-graphene microsupercapacitors with electrodes based on electrochemically exfoliated graphene and an ultrathin solid-state electrolyte based on nano-graphene oxide. The devices exploit the high ionic conductivity of nano-graphene oxide coupled with the high electrical conductivity of graphene films, yielding areal capacitances of up to 313 mu F cm-2 at 5 mV s-1 and high power densities of up to 4 mW cm-3 with an overall device thickness of only 1 mu m.

  • 7.
    Gazzotti, Stefano
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology. Univ Milan, Dept Chem, Via Golgi 19, I-20133 Milan, Italy.;Univ Milan, Dept Chem, CRC Mat Polimerici LaMPO, Via Golgi 19, I-20133 Milan, Italy..
    Hakkarainen, Minna
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Adolfsson, Karin H.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Ortenzi, Marco Aldo
    Univ Milan, Dept Chem, Via Golgi 19, I-20133 Milan, Italy.;Univ Milan, Dept Chem, CRC Mat Polimerici LaMPO, Via Golgi 19, I-20133 Milan, Italy..
    Farina, Hermes
    Univ Milan, Dept Chem, Via Golgi 19, I-20133 Milan, Italy.;Univ Milan, Dept Chem, CRC Mat Polimerici LaMPO, Via Golgi 19, I-20133 Milan, Italy..
    Lesma, Giordano
    Univ Milan, Dept Chem, Via Golgi 19, I-20133 Milan, Italy.;Univ Milan, Dept Chem, CRC Mat Polimerici LaMPO, Via Golgi 19, I-20133 Milan, Italy..
    Silvani, Alessandra
    Univ Milan, Dept Chem, Via Golgi 19, I-20133 Milan, Italy.;Univ Milan, Dept Chem, CRC Mat Polimerici LaMPO, Via Golgi 19, I-20133 Milan, Italy..
    One-Pot Synthesis of Sustainable High-Performance Thermoset by Exploiting Eugenol Functionalized 1,3-Dioxolan-4-one2018In: ACS SUSTAINABLE CHEMISTRY & ENGINEERING, ISSN 2168-0485, Vol. 6, no 11, p. 15201-15211Article in journal (Refereed)
    Abstract [en]

    1,3-Dioxolan-4-one (DOX) chemistry was explored for production of "one-pot" biobased polyester thermosets. DOX monomer was first functionalized by naturally occurring eugenol to introduce a structural element, which could induce cross-linking reaction through cationic polymerization of the double bond. The feasibility of polymerizing DOX monomers bearing bulky side groups was proven by model phenol-substituted DOX monomer (PhDOX). Once the reaction was shown to be effective, the same protocol was applied to eugenol-substituted monomer (EuDOX). A brief screening of the optimal catalyst concentration was performed, to obtain a highly cross-linked product. The synthesized thermoset showed good thermal resistance and high mechanical strength probably due to the rich aromatic content. The obtained thermoset was further subjected to microwave-assisted hydrothermal degradation test, which demonstrated complete recyclability to water or methanol soluble products. NMR and matrix-assisted laser desorption/ionization-mass spectroscopy analyses of the obtained degradation products unveiled the structure of the thermoset, strongly indicating that the polymerization of eugenol-functionalized DOX monomer resulted in polylactide-like chains connected with aromatic aliphatic segments resulting from the reaction of the eugenol double bonds. The presence of free hydroxyl and carboxyl groups sheds light on the mechanism behind the observed shape-memory and self-healing properties.

  • 8.
    Xu, Huan
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Wu, Duo
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Yang, Xi
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Feng, Zhaoxuan
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Adolfsson, Karin H.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Xie, Lan
    Sichuan Univ, Dept Polymer Sci & Engn, Chengdu, Sichuan, Peoples R China..
    Hakkarainen, Minna
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Enhancing the function of graphene oxide nanosheets by crystallization control: Unexpected harvest of strength, ductility and thermal stability for poly(lactic acid) barrier films2016In: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 251Article in journal (Other academic)
1 - 8 of 8
CiteExportLink to result list
Permanent link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf