Outstanding chain-extension effect and high UV resistance of polybutylene succinate containing amino-acid-modified layered double hydroxides

• Adam A. Marek,
• Vincent Verney,
• Christine Taviot-Gueho,
• Grazia Totaro,
• Laura Sisti,
• Annamaria Celli and
• Fabrice Leroux

Beilstein J. Nanotechnol. 2019, 10, 684–695, doi:10.3762/bjnano.10.68

• spectroscopy (FTIR) and thermogravimetric analysis (TGA). As expected, the UV–vis spectra showed absorbance in the UVC and UVB regions and the potential role as UV stabilizers. In a second part, PBS composites were prepared with 5 wt % of LDH filler by melt blending and once again fully characterized (XRD, TGA

• associated with the glass-to-rubber transition. The crystallization temperature (Tc) and the enthalpy of crystallization (∆Hc) were measured during the cooling scan. Thermogravimetric analysis (TGA) of LDH fillers and composites was performed in air atmosphere (gas flow 30 mL min−1) using a Perkin Elmer TGA7

• , C–N) overlap in the range of 1700–1480 cm−1 and the lattice vibration of M–O in the platelet structure can be depicted at a low wavenumber (800–650 cm−1). The experimental chemical composition of all synthesized LDHs has been estimated based on TGA analysis and collected in Table 1. All the

Ceria/polymer nanocontainers for high-performance encapsulation of fluorophores

• Kartheek Katta,
• Dmitry Busko,
• Yuri Avlasevich,
• Katharina Landfester,
• Stanislav Baluschev and
• Rafael Muñoz-Espí

Beilstein J. Nanotechnol. 2019, 10, 522–530, doi:10.3762/bjnano.10.53

• ). Thermogravimetric analysis of the freeze-dried sample was conducted using a Mettler Toledo TGA-851 at a heating rate of 10 °C·min−1. Fluorescence spectra were recorded for the dispersions containing 0.75 wt % capsule content by using in a custom-built setup containing a diode laser with wavelength 635 nm (Roithner

• (sample NC-CeO2 at ambient conditions). Characteristics of the samples reported in this work. Supporting Information Supporting Information File 80: Chemical structure of TDI, absorption and emission spectra of TDI, EDX spectra, TGA, and additional photoluminescence emission spectra of samples

• . Acknowledgements The source of this article is the doctoral dissertation of the first author, Dr. Katheek Katta (Uniform Resource Name: urn:nbn:de:hebis:77-diss-1000007157). Michael Steiert, Petra Räder, Gunnar Glaßer, and Katrin Kirchhoff are acknowledged for XRD, TGA, EDX, and high-resolution TEM measurements

A porous 3D-RGO@MWCNT hybrid material as Li–S battery cathode

• Yongguang Zhang,
• Jun Ren,
• Yan Zhao,
• Taizhe Tan,
• Fuxing Yin and
• Yichao Wang

Beilstein J. Nanotechnol. 2019, 10, 514–521, doi:10.3762/bjnano.10.52

• immobilize sulfur and polysulfides within S-3D-RGO@MWCNT, reducing the shuttle effect and improving the cycling life of Li–S batteries. The thermogravimetric analysis (TGA) analysis (Figure 4f) shows that the S-3D-RGO@MWCNT composite exhibits a very high weight loss (62 wt %) between 30 and 300 °C

• (HRTEM, JEOL JEM-2100F) images were used for investigating surface topology. The content of sulfur in the S-3D-RGO@MWCNT composite was confirmed using thermogravimetric analysis (TGA, SHIMADZU DTG-60) in Ar atmosphere. Raman spectra were recorded on Raman spectrometer (Raman, Renishaw) using 532 nm

• @MWCNT; (c) TGA of S-3D-RGO@MWCNT; (d) The XPS survey spectrum of S-3D-RGO@MWCNT composite; high-resolution XPS spectra of (e) C 1s, (f) S 2p. CV curves of the S-3D-RGO@MWCNT cathode at 0.1 mV·s−1 in the first four cycles. (a) CV measurement of the S-3D-RGO@MWCNT cathode (1st, 50th, 100th, 150th and

Removal of toxic heavy metals from river water samples using a porous silica surface modified with a new β-ketoenolic host

• Said Tighadouini,
• Smaail Radi,
• Abderrahman Elidrissi,
• Khadija Haboubi,
• Maryse Bacquet,
• Stéphanie Degoutin,
• Mustapha Zaghrioui and
• Yann Garcia

Beilstein J. Nanotechnol. 2019, 10, 262–273, doi:10.3762/bjnano.10.25

• characterized by elemental analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) images, thermogravimetric analysis (TGA) and nitrogen adsorption–desorption isotherms. Physical methods. Atomic adsorption measurements were performed on a Varian A.A. 400 spectrophotometer

• , respectively, demonstrate the modification of SiNH2 with L1. Compared to the blank silica, the surface of the new material (SiNL) shown by SEM (Figure 2) became rough, which confirms the success of organic moieties filling the surface. The thermal stability of SiG, SiNH2 and SiNL was evaluated by TGA (Figure 3

• different metals. Stability and reusability of the adsorbent. Our hybrid material can be reused more than five times without significant loss in adsorption efficiency (Table 4). This can be explained by the high stability of organic groups onto SiNL which was confirmed by TGA, showing no distinct changes in

Thermal control of the defunctionalization of supported Au₂₅(glutathione)₁₈ catalysts for benzyl alcohol oxidation

• Zahraa Shahin,
• Hyewon Ji,
• Rodica Chiriac,
• Nadine Essayem,
• Franck Rataboul and
• Aude Demessence

Beilstein J. Nanotechnol. 2019, 10, 228–237, doi:10.3762/bjnano.10.21

• diagrams and no indication of reflection of bulk gold (Figure S4, Supporting Information File 1). These observations mean that there is no modification of the support and that the quantity of gold is too small to be detected. Thermal studies of the materials were done by thermogravimetric analysis (TGA

• ) under air on pure Au25(SG)18 gold clusters, gold clusters deposited on ZrO2 and ZrO2 alone. From the TGA curve of the clusters, a first gradual weight loss of 6.5% is observed before 200 °C, corresponding to the evaporation of the solvent (Figure 1a). Then a second gradual weight loss of 46.2% happens

• to completely remove the glutathione molecules from the gold surface. For the TGA of the ZrO2 support, 2.4% weight loss was observed at low temperature that corresponds to trace water (Figure 2). After the deposition of 1 wt % Au using Au25(SG)18 on ZrO2, a first weight loss of 2.4% is observed and a

pH-mediated control over the mesostructure of ordered mesoporous materials templated by polyion complex micelles

• Emilie Molina,
• Mélody Mathonnat,
• Jason Richard,
• Patrick Lacroix-Desmazes,
• Martin In,
• Philippe Dieudonné,
• Thomas Cacciaguerra,
• Corine Gérardin and
• Nathalie Marcotte

Beilstein J. Nanotechnol. 2019, 10, 144–156, doi:10.3762/bjnano.10.14

• determination of the volume-averaged hydrodynamic diameters (Dhv); the polydispersity index (PDI) values were obtained from the cumulant method. The chemical composition of the hybrid materials was calculated by combining thermogravimetric analysis (TGA), which allows quantifying the silica content, and N and C

• elemental analyses (EA), which allow determining the quantity of OC and PEO-b-PAA in the material. The results were expressed as N/AA and EO/Si ratios given with ±5% relative error. TGA was performed on a Perkin Elmer STA 6000 instrument at a heating rate of 10 °C·min−1 under an air flow (20 mL·min−1) up to

New micro/mesoporous nanocomposite material from low-cost sources for the efficient removal of aromatic and pathogenic pollutants from water

• Emmanuel I. Unuabonah,
• Robert Nöske,
• Jens Weber,
• Christina Günter and
• Andreas Taubert

Beilstein J. Nanotechnol. 2019, 10, 119–131, doi:10.3762/bjnano.10.11

• , the samples made at 750 °C and higher also contain plate-like or fiber-like features. Thermogravimetric and differential thermal analysis Figure 7 shows representative thermogravimetric analysis/differential thermal analysis (TGA/DTA) data obtained from measurements in nitrogen. Consistent with the

• data shown above, there are clear differences between samples produced at reaction temperatures up to 450 °C and the samples obtained at higher temperatures. The samples made between 500 and 900 °C only show a weak and very gradual weight loss of ≈5–6% of the total mass at the end of the TGA/DTA

• processes cannot be separated here. TGA/DTA data analysis therefore indicates that the reaction temperature is indeed a key parameter to obtain a stable material that will resist rapid attrition during use. Comparison with the nitrogen sorption data suggests that a reaction temperature of ≈500 °C is

A novel polyhedral oligomeric silsesquioxane-modified layered double hydroxide: preparation, characterization and properties

• Xianwei Zhang,
• Zhongzhu Ma,
• Hong Fan,
• Carla Bittencourt,
• Jintao Wan and
• Philippe Dubois

Beilstein J. Nanotechnol. 2018, 9, 3053–3068, doi:10.3762/bjnano.9.284

• anions and the metal-hydroxide sheets. This largely reduces the contribution of the water layer accommodated in the interlayer region to the basal spacing [15][19][33]. Here, it is proposed that the less strongly bound interlayer water, which is further verified later by TGA results, might be another

• Thermal stability The thermal decomposition behavior was investigated to evaluate the thermal stability of LDHs, and the TGA thermograms are presented in Figure 10, with the measured data being summarized in Table 3. As can be seen in Figure 10a, the decomposition of NLDH under N2 atmosphere mainly

• slopes of these lines using the following expression: The fitting results and Eα data are summarized in Table 4. Results show that the apparent activation energy increases as a whole with increasing conversion. Combined with the TGA data and the data of α as a function of T, the Eα values of NLDH can be

Co-intercalated layered double hydroxides as thermal and photo-oxidation stabilizers for polypropylene

• Qian Zhang,
• Qiyu Gu,
• Fabrice Leroux,
• Pinggui Tang,
• Dianqing Li and
• Yongjun Feng

Beilstein J. Nanotechnol. 2018, 9, 2980–2988, doi:10.3762/bjnano.9.277

• transmittance spectra of Ca2Al/PP composites. (c) SEM image and (d) Al (left) and Ca (right) element mapping of the H1M1-Ca2Al/PP composite. (a) TGA curves of HnMn′-Ca2Al/PP composites. (b) FTIR spectra of PP after different periods of thermal aging. (c) Thermal aging and (d) photo-oxidation aging of HnMn

Magnetic and luminescent coordination networks based on imidazolium salts and lanthanides for sensitive ratiometric thermometry

• Pierre Farger,
• Cédric Leuvrey,
• Mathieu Gallart,
• Pierre Gilliot,
• Guillaume Rogez,
• João Rocha,
• Duarte Ananias,
• Pierre Rabu and
• Emilie Delahaye

Beilstein J. Nanotechnol. 2018, 9, 2775–2787, doi:10.3762/bjnano.9.259

• Figure S2 (Supporting Information File 1), the experimental powder patterns fit well with the patterns calculated from the single crystal structure and show no additional phases. In order to investigate the thermal stability, thermogravimetric analysis (TGA) was realized under air stream from 25 to 900

• a JEOL 6700F (scanning electron microscope (SEM) equipped with a field-emission gun (FEG), operating at 3 kV in the SEI mode instrument. FTIR spectra were collected on a Perkin Elmer Spectrum Two UATR-FTIR spectrometer. TGA-TDA experiments were performed using a TA instrument SDT Q600 (heating rates

• Information Supporting Information contains a representation of the coordination polyhedron, a table of selected bonds, a comparison of the experimental powder X-ray diffraction patterns of the different compounds and the simulated pattern from single crystals X-ray data, SEM analysis, TGA/TDA analysis, a

Accurate control of the covalent functionalization of single-walled carbon nanotubes for the electro-enzymatically controlled oxidation of biomolecules

• Naoual Allali,
• Veronika Urbanova,
• Mathieu Etienne,
• Xavier Devaux,
• Martine Mallet,
• Brigitte Vigolo,
• Jean-Joseph Adjizian,
• Chris P. Ewels,
• Sven Oberg,
• Alexander V. Soldatov,
• Edward McRae,
• Yves Fort,
• Manuel Dossot and
• Victor Mamane

Beilstein J. Nanotechnol. 2018, 9, 2750–2762, doi:10.3762/bjnano.9.257

• defects introduced by tuning the irradiation time. A few milligrams of the corresponding oxidized SWCNTs were analyzed in each case before proceeding to step 2. At this stage, the samples were protected under argon gas to avoid any moisture contamination and directly analyzed by HRTEM, XPS and TGA-MS

• derivatives at the surface of CNT bundles, but they cannot confirm the covalent nature of the functionalization process. To do this, we have performed TGA-MS analyses of our samples under an inert gas (He). Figure 6A gives an example of the TGA curves obtained for raw, HIPCO-HNO3 and HIPCO-HNO3-FcETG2 samples

• . The mass spectrometer coupled to the TGA system allowed for the examination of the nature of the departing groups. Compared to the raw sample (curve a), the TGA curve after oxidation clearly shows an increase of weight loss above 300 °C for the oxidized sample due to additional oxygenated functions on

Hydrothermal-derived carbon as a stabilizing matrix for improved cycling performance of silicon-based anodes for lithium-ion full cells

• Mirco Ruttert,
• Florian Holtstiege,
• Jessica Hüsker,
• Markus Börner,
• Martin Winter and
• Tobias Placke

Beilstein J. Nanotechnol. 2018, 9, 2381–2395, doi:10.3762/bjnano.9.223

• power of 5.00 mW. X-ray diffraction (XRD) patterns in a 2θ range of 20° to 80° were recorded with the help of a Bruker D8 Advance X-ray diffractometer (Bruker AXS GmbH) with a Cu Kα-wavelength of λ = 0.154 nm and a step size of 0.039°. Thermogravimetric analysis (TGA) was carried out in a temperature

• range between 25 °C and 800 °C on a TGA Q500 (TA Instruments) in an oxygen/nitrogen atmosphere (nitrogen flow: 10 mL min−1, oxygen flow: 25 mL min−1) in order to determine the Si content. A heating ramp of 20 °C min−1 was applied. Scanning electron microscopy (SEM) with a field emission gun (Schottky

• content of the Si/C composites, TGA was carried out in an oxidative atmosphere, as presented in Figure 3a. While the pure carbon matrix burns off completely and the remaining weight at a temperature of 630 °C is ≈0%, the Si-containing samples exhibit a small plateau at a temperature of ≈630 °C where the

High-throughput synthesis of modified Fresnel zone plate arrays via ion beam lithography

• Kahraman Keskinbora,
• Umut Tunca Sanli,
• Margarita Baluktsian,
• Corinne Grévent,
• Markus Weigand and
• Gisela Schütz

Beilstein J. Nanotechnol. 2018, 9, 2049–2056, doi:10.3762/bjnano.9.194

• in Table 1, calculated using TGA for the nominal film thickness grossly overestimates the theoretical diffraction efficiency of the actual fabricated device. The third and a critical factor contributing to the strongly suppressed DE is the parasitic Pt deposition during the fabrication of the

Synthesis of rare-earth metal and rare-earth metal-fluoride nanoparticles in ionic liquids and propylene carbonate

• Marvin Siebels,
• Lukas Mai,
• Laura Schmolke,
• Kai Schütte,
• Juri Barthel,
• Junpei Yue,
• Jörg Thomas,
• Bernd M. Smarsly,
• Anjana Devi,
• Roland A. Fischer and
• Christoph Janiak

Beilstein J. Nanotechnol. 2018, 9, 1881–1894, doi:10.3762/bjnano.9.180

• and low toxicity [41]. Results and Discussion Decomposition of RE(amd)3 and Eu(dpm)3 Thermogravimetric analysis (TGA) revealed decomposition of the rare-earth metal(III) tris(N,N′-diisopropyl-2-methylamidinate) (RE(amd)3; RE = Pr(III), Gd(III), Er(III) and tris(2,2,6,6-tetramethyl-3,5-heptanedionato

• )europium(III) (Eu(dpm)3) at temperatures between 160 and 230 °C (Table S1 and Figure S2, Supporting Information File 1). To keep the formation of by-products as low as possible and to achieve complete decomposition of the precursors, a temperature of 230 °C was selected on the basis of these TGA

• images were calibrated with Debye–Scherrer patterns recorded from a gold reference sample (S106, Plano GmbH, Wetzlar, Germany). Thermogravimetric analysis: TGA was performed with Netzsch TG 209 F3 Tarsus equipped with an Al crucible by using a heating rate of 10 K·min−1. Electrochemical measurements: The

Controllable one-pot synthesis of uniform colloidal TiO₂ particles in a mixed solvent solution for photocatalysis

• Jong Tae Moon,
• Seung Ki Lee and
• Ji Bong Joo

Beilstein J. Nanotechnol. 2018, 9, 1715–1727, doi:10.3762/bjnano.9.163

• samples were subjected to calcination at high temperatures, small TiO2 crystallites were grown, severely fused and finely shirked, which resulted in decreased mesoporosity and a small BET surface area but increased crystallinity. To estimate the carbon content and thermal behavior of the TiO2 samples, TGA

• analysis was conducted. Since only a surfactant (HPC), titanium precursor (TBOT) and solvent were used during the synthesis, the final TiO2 sample should mainly consist of elements such as Ti, O, H and C, respectively. Therefore, weight loss during a thermogravimetric analysis (TGA) experiment originates

• from desorption of water, dihydroxylation and the combustion reaction of carbon contents. The TGA analysis was conducted using the surfactant HPC as a reference run to monitor the decomposition temperature (Supporting Information File 1, Figure S3a). It should be noted that HPC is dramatically

Nitrogen-doped carbon nanotubes coated with zinc oxide nanoparticles as sulfur encapsulator for high-performance lithium/sulfur batteries

• Yan Zhao,
• Zhengjun Liu,
• Liancheng Sun,
• Yongguang Zhang,
• Yuting Feng,
• Xin Wang,
• Indira Kurmanbayeva and
• Zhumabay Bakenov

Beilstein J. Nanotechnol. 2018, 9, 1677–1685, doi:10.3762/bjnano.9.159

• was calculated based on the (101) peak using the Scherrer equation [13][19] and was found to be around 6.2 nm. In order to determine the sulfur content in the S/ZnO@NCNT composite, the samples were studied by thermogravimetric analysis (TGA) in nitrogen gas. Figure 2 shows that the sulfur content in

• a battery testing system (Neware, Shenzhen) in the potential range of 1–3 V vs Li/Li+. XRD patterns of S, ZnO@NCNT and S/ZnO@NCNT composite. TGA curve of the S/ZnO@NCNT composite. (a) HRTEM image; (b) SAED patterns; (c) TEM image; (d–g) EDX mapping images of the ZnO@NCNT composite. (a) SEM image; (b

Sulfur-, nitrogen- and platinum-doped titania thin films with high catalytic efficiency under visible-light illumination

• Boštjan Žener,
• Lev Matoh,
• Giorgio Carraro,
• Bojan Miljević and
• Romana Cerc Korošec

Beilstein J. Nanotechnol. 2018, 9, 1629–1640, doi:10.3762/bjnano.9.155

• (ammonium nitrate, urea), sulfur (thiourea) and platinum (chloroplatinic acid), coated onto glass substrates by dip-coating, and thermally treated in a muffle furnace to promote crystallization. The resulting thin films were then characterized by various techniques (i.e., TGA-DSC-MS, XRD, BET, XPS, SEM

• dispersions [45]. The prepared samples were analyzed using thermogravimetric analysis–differential scanning calorimetry–mass spectrometry (TGA-DSC-MS), X-ray diffraction spectroscopy (XRD), specific surface area measurements via Brunauer–Emmett–Teller method (BET), X-ray photoelectron spectroscopy (XPS

• determined by XPS measurements. The platinum in sample S3_N0.5+0.015 M Pt was added as the final layer in the form of chloroplatinic acid by dip-coating. The last number describes molar concentrations of the deposited solution. Thermal analysis The purpose of thermal analysis measurements (TGA-DSC-MS) was to

Nanocomposites comprised of homogeneously dispersed magnetic iron-oxide nanoparticles and poly(methyl methacrylate)

• Sašo Gyergyek,
• David Pahovnik,
• Ema Žagar,
• Alenka Mertelj,
• Rok Kostanjšek,
• Miloš Beković,
• Marko Jagodič,
• Heinrich Hofmann and
• Darko Makovec

Beilstein J. Nanotechnol. 2018, 9, 1613–1622, doi:10.3762/bjnano.9.153

• mRA/mp = 0.53 [27]. The synthesized nanoparticles were dispersed in toluene and the suspension was centrifuged at a relative centrifugal force (RCF) of 5000g for 5 min. The colloidal suspension was decanted from the centrifuge tube and analyzed using thermogravimetric analysis (TGA). The colloidal

• 5000g for 5 min. The colloidal suspension was decanted from the centrifuge tube and analyzed using TGA. The colloidal suspension contained 38.0 wt % nanoparticles (NPs). For further analyses, a small amount of the functionalized NP-MMA was isolated from the suspension by flocculating them with a large

• -shift standard. The diffuse reflectance infrared Fourier transform spectra (DRIFT, Perkin Elmer Spectrum 400 equipped with DRIFT accessory) were recorded in KBr. The weight fraction of nanoparticles in the nanocomposites was determined with a Mettler Toledo thermogravimetric analysis (TGA) instrument

Closed polymer containers based on phenylboronic esters of resorcinarenes

• Tatiana Yu. Sergeeva,
• Rezeda K. Mukhitova,
• Irek R. Nizameev,
• Marsil K. Kadirov,
• Polina D. Klypina,
• Albina Y. Ziganshina and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 1594–1601, doi:10.3762/bjnano.9.151

• pulsed gradient unit capable of producing magnetic-field pulse gradients in the z-direction of about 56 G/cm. D2O was used as solvent in all experiments. Chemical shifts were reported relative to H2O (δ = 4.7 ppm) as an internal standard. Measurements by the DSC and TGA methods were carried out with a

• -B) (0.27 mg/mL) at pH 3 (universal buffer), and after addition of glucose (0.4 mM), 25 °C. Supporting Information Supporting Information features data for SRA and p(SRA-B): size distribution diagram, DLS and SLS data, IR spectra, NMR spectra, TGA and DSC data, acid-base titration curves; UV- and

Electrodeposition of reduced graphene oxide with chitosan based on the coordination deposition method

• Mingyang Liu,
• Yanjun Chen,
• Chaoran Qin,
• Zheng Zhang,
• Shuai Ma,
• Xiuru Cai,
• Xueqian Li and
• Yifeng Wang

Beilstein J. Nanotechnol. 2018, 9, 1200–1210, doi:10.3762/bjnano.9.111

• pattern of the HACC-rGO/CS film shows a diffraction peak at 22.1°, which is attributed to the HACC-rGO in the deposited film. Additionally, the HACC-rGO/CS film presents another diffraction peak at 10.8°, which corresponds to the diffraction peak of chitosan [34][35]. The thermogravimetric analysis (TGA

Understanding the performance and mechanism of Mg-containing oxides as support catalysts in the thermal dry reforming of methane

• Nor Fazila Khairudin,
• Mohd Farid Fahmi Sukri,
• Mehrnoush Khavarian and
• Abdul Rahman Mohamed

Beilstein J. Nanotechnol. 2018, 9, 1162–1183, doi:10.3762/bjnano.9.108

• co-precipitation methods for the preparation of a Ni–MgO–Al2O3 catalyst. The Ni particle size was uniformly distributed in the catalysts prepared via sol–gel. TGA results clearly showed that 13% and 7.7% carbon was deposited on the catalysts prepared via the sol–gel method and the co-precipitation

Single-crystalline FeCo nanoparticle-filled carbon nanotubes: synthesis, structural characterization and magnetic properties

• Rasha Ghunaim,
• Maik Scholz,
• Christine Damm,
• Bernd Rellinghaus,
• Rüdiger Klingeler,
• Bernd Büchner,
• Michael Mertig and
• Silke Hampel

Beilstein J. Nanotechnol. 2018, 9, 1024–1034, doi:10.3762/bjnano.9.95

• of the filling particles, and therefore, the magnetic properties. The samples were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), superconducting quantum interference device (SQUID) and thermogravimetric analysis (TGA). The Fe–Co

• -ray diffractometer (XRD) (Panlytical) with Co Kα radiation (λ = 1.79278 Å) in reflection geometry at a scanning rate of 0.05° s−1 in the 2θ range from 10° to 80°. Thermogravimetric measurements (TGA) were performed with a SDT-Q600 (TA Instruments) instrument. A few milligrams of the material (≈5 mg

• of the filling inside the CNTs and was confirmed by quantitative measurements performed by TGA as will be shown later (see Figure 6). It is important to emphasize the effect of annealing on the growth of the particles. For the as-prepared samples (i.e., only reduced, Figure 1a and 1b), different

Enzymatically promoted release of organic molecules linked to magnetic nanoparticles

• Chiara Lambruschini,
• Silvia Villa,
• Luca Banfi,
• Fabio Canepa,
• Fabio Morana,
• Annalisa Relini,
• Paola Riani,
• Renata Riva and
• Fulvio Silvetti

Beilstein J. Nanotechnol. 2018, 9, 986–999, doi:10.3762/bjnano.9.92

• quantity of APTES incorporated into the NPs and the loaded amount of 6 or 12 into 9 and 13 was determined by thermogravimetric analysis (TGA) (Figure 2). The amount of APTES resulted to be 9.5%. TGA results for 9 and 13 showed a weight loss of 14.3% and 23.5%, respectively. Considering the initial amount

• pyrenylmethylamine to be determined. From these data, and from the loading determined by TGA, we calculated the conversions of the enzymatic reactions, which were 7.1% and 5.8% for the urea spacer and for the azelate spacer, respectively. Thus, although we have demonstrated that the enzymatic reaction was actually

• to ultrasonic vibrations to decrease the aggregation, and deposited on a lacey carbon copper grid. TGA was performed using a Labsys EVO Setaram instrument. Approximately 5 mg of sample was weighed in an open alumina crucible and heated from 50 °C to 1000 °C in He flux (20 mL/min) with a heating rate

A review of carbon-based and non-carbon-based catalyst supports for the selective catalytic reduction of nitric oxide

• Shahreen Binti Izwan Anthonysamy,
• Syahidah Binti Afandi,
• Mehrnoush Khavarian and
• Abdul Rahman Bin Mohamed

Beilstein J. Nanotechnol. 2018, 9, 740–761, doi:10.3762/bjnano.9.68

• chemisorption The behaviour of the SCR-NH3 catalyst deposition is typically characterised by: temperature-programmed surface reaction (TPSR) mass spectroscopy (MS) differential thermal analysis (DTA) thermogravimetric analysis (TGA) temperature-programmed hydrogenation (TPH) temperature-programmed oxidation

Cyclodextrin-assisted synthesis of tailored mesoporous silica nanoparticles

• Fuat Topuz and
• Tamer Uyar

Beilstein J. Nanotechnol. 2018, 9, 693–703, doi:10.3762/bjnano.9.64

• smaller particle size than those produced with HP-functional CDs. FTIR, TGA and solid-state 13C NMR demonstrated the adsorption of CDs on the particle surfaces. The proposed concept allows for the synthesis of silica nanoparticles with control over particle shape and size by adjusting the concentration of

• , chemical analysis by FTIR and solid state 13C NMR, thermal properties and composition by TGA, and pore structure by WAXS. Results and Discussion Figure 2 shows the silica particles produced at β-CD concentrations of 0.5 and 1% (w/v) and constant tetraethoxysilane (TEOS) concentration of 1% (v/v). At these

• (TGA) of the particles revealed a small mass loss (ca. 2% (w/v)) above 300 °C due to adsorbed CD moieties (Figure S2, Supporting Information File 1). For further confirmation of shape transformation of the particles from round to multifaceted ones with HP-functional CDs, MSNs were also synthesized