Correction: An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

• Felix M. Badaczewski,
• Marc O. Loeh,
• Torben Pfaff,
• Dirk Wallacher,
• Daniel Clemens and
• Bernd M. Smarsly

Beilstein J. Nanotechnol. 2020, 11, 678–679, doi:10.3762/bjnano.11.54

• structure; small-angle neutron scattering (SANS); wide-angle X-ray scattering (WAXS); The following graph (A) should be implemented in Figure 4 of the original article, since it was part of the manuscript and was accidently removed during the revision process. No other change in the corresponding text and

An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

• Felix M. Badaczewski,
• Marc O. Loeh,
• Torben Pfaff,
• Dirk Wallacher,
• Daniel Clemens and
• Bernd M. Smarsly

Beilstein J. Nanotechnol. 2020, 11, 310–322, doi:10.3762/bjnano.11.23

• mesoporosity of these monolithic carbon materials was studied by the sorption behavior of a relatively large organic molecule (p-xylene) in comparison to typical gas adsorbates (Ar). In addition, to obtain a detailed view on the nanopore space small-angle neutron scattering (SANS) combined with in situ

• physisorption using probe gases such as Ar or N2 can provide misleading parameters if to be used to appraise the accessibility of the nanoscale pore space. Keywords: adsorption; carbon materials; mesoporosity; microporosity; microstructure; pore structure; small-angle neutron scattering (SANS); wide-angle X

• neutron scattering (SANS) combined with in situ physisorption were the methods of choice. Deuterated p-xylene (DPX) acts as a contrast-matching agent in the neutron scattering process. In a perfect case, that is if DPX filled all pores, the scattering contrast would be zero and the SANS intensity would

Multifunctional layered magnetic composites

• Maria Siglreitmeier,
• Baohu Wu,
• Tina Kollmann,
• Martin Neubauer,
• Gergely Nagy,
• Dietmar Schwahn,
• Vitaliy Pipich,
• Damien Faivre,
• Dirk Zahn,
• Andreas Fery and
• Helmut Cölfen

Beilstein J. Nanotechnol. 2015, 6, 134–148, doi:10.3762/bjnano.6.13

• (MNPs) are synthesized. The amount of MNPs can be controlled through the synthesis protocol therefore mineral loadings starting from 15 wt % up to 65 wt % can be realized. The demineralized organic nacre matrix is characterized by small-angle and very-small-angle neutron scattering (SANS and VSANS

• mineralization, hierarchical structure and toughness enhancement [23][29]. Different techniques have been used to resolve the chemical and structural composition of the organic matrix. Small angle neutron scattering (SANS) is a non-destructive method to study the nacreous organic matrix without potential changes

• 5 kV was chosen for recording the images. Small-angle neutron scattering (SANS and VSANS): SANS and VSANS experiments were carried out at the KWS1 and KWS 3 diffractometers operated by Jülich Center for Neutron Research (JCNS) at the Forschungs-Neutronenquelle Heinz Maier-Leibnitz (FRM II) in

Distribution of functional groups in periodic mesoporous organosilica materials studied by small-angle neutron scattering with in situ adsorption of nitrogen

• Monir Sharifi,
• Dirk Wallacher and
• Michael Wark

Beilstein J. Nanotechnol. 2012, 3, 428–437, doi:10.3762/bjnano.3.49

• functionalized with SO3H or SO3− groups and investigated by small-angle neutron scattering (SANS) with in situ nitrogen adsorption at 77 K. If N2 is adsorbed in the pores the SANS measurements show a complete matching of all of the diffraction signals that are caused by the long-range ordering of the mesopores

Studies towards synthesis, evolution and alignment characteristics of dense, millimeter long multiwalled carbon nanotube arrays

• Pitamber Mahanandia,
• Jörg J. Schneider,
• Martin Engel,
• Bernd Stühn,
• Somanahalli V. Subramanyam and
• Karuna Kar Nanda

Beilstein J. Nanotechnol. 2011, 2, 293–301, doi:10.3762/bjnano.2.34

• long CNTs can be detached easily from the aligned CNT bundle or mat like structure. Atomic force microscope (AFM) images of individual CNTs, synthesized at 650 °C and 1100 °C, are depicted in Figure 6. They confirm the uniform diameter as found by TEM. SAXS and small angle neutron scattering (SANS) are