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- Zeolites (2)
- Alkaline digestion reaction (1)
- Baustoffrecycling (1)
- Betonbrechsand (1)
- Disäuren (1)
- Drehrohrofen (1)
- Electrostatic filter ash (1)
- Filtration Residues (1)
- Gips (1)
- Glycerin (1)
Organisationseinheit der BAM
Kiefernholz wird durch Imprägnieren mit einem Vorkondensat aus organischen Disäuren und Glycerin, das kolloidale Kieselsäure enthält, sowie nachfolgende Ofenhärtung in Kieselsäure/Alkydharz/Holz-Verbunde umgewandelt. Diese Nanoverbunde haben eine geringere Porosität als Holz, da Teile der Holzzellen mit Harz und Kieselsäure ausgefüllt sind. Die kugelförmigen, etwa 60 nm großen (SiO1)x-Teilchen liegen in der Polymermatrix mikrophasensepariert vor. Der kolloidale Zustand der eingebrachten Polykieselsäure bleibt erhalten. Durch ihr günstiges Eigenschaftsprofil sind die Verbundmaterialien als modifizierter Holzbaustoff interessant.
REALight ‐ Leichtgranulate und REA‐Gips aus feinkörnigen sulfatbelasteten Bau‐ und Abbruchabfällen
(2023)
Ziel des Projekts REALight ist die Entwicklung einer Referenzanlage zur Herstellung von Leichtgranulaten (leichte Gesteinskörnungen) aus Bau‐ und Abbruchabfällen und zur Gipsrückgewinnung. Als Rohstoffe werden bisher ungenutzte oder auf niedrigem Niveau eingesetzte Bau‐ und Abbruchabfälle und industrielle Nebenprodukte verwendet. Als Produkte werden leichte Gesteinskörnungen hergestellt. Die Sulfatabtrennung durch eine thermische Zersetzung bildet die Grundlage für die zusätzliche Gewinnung von Rauchgasentschwefelungs‐Gips (REA‐Gips). Das Projekt wird im Rahmen der Fördermaßnahme „Ressourceneffiziente Kreislaufwirtschaft – Bauen und Mineralische Stoffkreisläufe (ReMin)” gefördert. ReMin ist eine Maßnahme zur Umsetzung des BMBF‐Forschungskonzepts „Ressourceneffiziente Kreislaufwirtschaft” als Teil der BMBF Strategie „Forschung für nachhaltige Entwicklung – FONA”. Ziel der Förderung ist es, den Ausbau der Kreislaufwirtschaft voranzutreiben. Im Mittelpunkt steht dabei die Bauwirtschaft mit ihrer hohen Nachfrage nach Rohstoffen und gleichzeitig großen Mengen an anfallenden mineralischen Abfällen. Am Projekt REALight sind 12 Partner aus verschiedenen Bereichen der Baustoffherstellung und ‐anwendung, Abfallaufbereitung, Verfahrenstechnik sowie Forschung und Entwicklung beteiligt.
Zeolite synthesis was studied using two silica rich filtration residues (FR 1 and FR 2) as Si-source
and sodium aluminate in a direct synthesis at 60°C at strong alkaline conditions (8 M - 16 M NaOH).
In addition to these one-pot syntheses, a two-step process was investigated. Here, an alkaline digestion
of FR at 60°C was followed by gel precipitation with sodium aluminate and gel crystallization
under usual conditions of 80°C - 90°C. The results show that the substitution of chemical
reagent sodium silicate by a waste material like FR as Si-source is possible but requires fine tuning
of the reaction conditions as zeolite crystallization is a process under kinetic control. The
solubility behaviour and impurities of the inserted filtration residues strongly influenced the
course of reaction. Thus zeolites like hydrosodalite or intermediate zeolite between cancrinite
and sodalite, or zeolite NaA or Z-21 in cocrystallization with hydrosodalite could be observed in
the one pot syntheses already in a short time interval between 1 - 4 h depending on the alkalinity.
The two step process yield to zeolites NaA and NaX in very good quality. The reaction process of FR
in both reaction methods was characterized by chemical analyses, X-ray powder diffraction,
Fourier transform infrared spectroscopy as well as scanning electron microscopy. Surface area
and water content of selected products were further characterized by the BET-method and by
thermogravimetry. Summing up the results, we can show that zeolite formation from filtration residues
is possible by several reaction procedures as model cases for a re-use of industrial waste
materials. Beside the importance for environmental protection, the reactions are of interest for
zeolite chemistry as the re-use of FR is possible under economically conditions of low energy consumption
at 60°C and short reaction periods.
This paper is a case study of complete substitution of sodium-metasilicate in zeolite Na-A synthesis by an electrostatic filterash (FA) arising in high amounts during silane waste incineration process.The silicate abundant FA is a suitable material for reinsertion in zeolite chemistry. This is shown in the presented investigation by the development of a model reaction process at low temperatures (50–60 °C) and short times (1.5–4 h). The experiments were performed under addition of NaAlO2 and variation of the alkalinity and the reaction period. Characterization and fine tuning of the process was mainly done by studying the kinetics of FA digestion and zeolite crystallization by XRD and chemical analyses (ICP-OES) of solutions and solids. It could be shown that pure FA was mostly dissolved (98%) in 8 m NaOH already after 1 h. Addition of NaAlO2 and crystallization for further 60 min under optimized conditions at 50 °C yielded to a suitable product. It consists of zeolite Na-A (92% by mass) beside some hydrosodalite (8% by mass). According to this low temperature short time process this study is a contribution for the development of energy efficient recycling solutions.
Alkaline reactions of paper sludge combustion ash at low temperature (60 °C) were performed using a calcite-rich paper ash (PA 1) and a gehlenite-rich ash (PA 2). Strong alkaline conditions (8, 12, 16 M NaOH) were revealed at reaction times of 1–4 h and 12–24 h. Reactions were performed with pure ashes and in the presence of NaAlO2. The products were characterized by XRD, FTIR, SEM/EDX, gravimetry and chemical analysis. The conversion was found to proceed mainly in the period between 1 and 4 h. Portlandite and hydrogarnet were observed from PA 1 in 8 M NaOH. Onset of formation of Ca4Al2O6CO·311H2O beside Ca(OH)2 could be analyzed after reaction of PA 1 in 12 M and 16 M NaOH. Addition of NaAlO2 favored crystallization of hydrogarnet and Ca4-Al2O6CO·311H2O. For PA 2 gehlenite remained stable, but a high portlandite fraction was observed. Addition of NaAlO2 yielded hydrogarnet beside gehlenite in 8 M NaOH. Higher alkalinities favored crystallization of Ca4Al2O6-CO·311H2O and onset of dissolution of gehlenite. Finally transformation of Ca4Al2O6CO·311H2O into sodium aluminum silicate hydrate was observed. All results were discussed with regard to heavy metal distribution of the initial PA between the alkaline digestion solution and the products. In conclusion suitable applications of the products were proposed.