1. You are here:  
  2. Home
  3. Tempism
  4. Analysis
  5. Climatic Chamber
  6. Research
  7. Tempism
  8. Synthesis

Organic and metallorganic synthesis

Organic and metallorganic synthesis

Gloria Zanotti  -

Roma - Monterotondo
 
The laboratory is fully equipped to carry out chemical synthesis under standard conditions and in controlled environment using vacuum lines and inert gases; it also has equipment for the separation and purification of the synthetic targets by extractive, thermal and chromatographic techniques according to their chemical nature. Furthermore, several solution- and vacuum-based thin-film deposition techniques are available. The main skills of the laboratory concern (1) Organic, inorganic and metallorganic synthesis; (2) development and use of sustainable synthetic methods with low environmental impact; (3) deposition of thin films either by solution or evaporation techniques.
 

TECHNICAL SPECIFICATIONS

  • ordinary and special glassware for synthesis in controlled environment

  • fume hoods equipped with vacuum lines and inert gases

  • vacuum heating dryers

  • vacuum tube furnace up to 700°C

  • equipment for the separation and purification of samples

  • centrifuge

  • optical microscope

  • laminar flow hood

  • bi-distiller

AVAILABLE TECHNIQUES

  • Design, synthesis and purification of highly conjugated organic and metallorganic molecules with optimized optical and electronic properties depending on the target application (e.g. gas sensing, organic electronics, optoelectronics) via scalable and environmental friendly synthetic routes.

  • Bulk synthesis of hybrid and inorganic perovskites of different composition for the study of fundamental properties.

 

Case Studies

Synthesis of functionalized zinc phthalocyanines as hole transporting materials for organic electronics

This study describes the synthesis and characterization of two zinc phthalocyanines functionalized with benzothienobenzothiophene derivatives as new potential p-type semiconductors for electronic and optoelectronic technologies. When implemented in perovskite solar cells, both the molecules showed an interesting hole transport activity even in absence of chemical doping.

Si veda: G. Zanotti, N. Angelini, G. Mattioli, A. M. Paoletti, G. Pennesi et al. Chempluschem 2020,.85, 1-12

"Selected for cover feature"

 
 

TECHNICAL SPECIFICATIONS

  • Spincoater Convac 1001

    • number of rotations programmable up to 9000 rpm.

  • Langmuir-Blodgett KSV 2000 system  

    • deposition rate 0.1 to 85mm/min

    • unlimited deposition cycles

    • dynamic range from 0 to 250 mN/m

    • effective area 675 cm2

AVAILABLE TECHNIQUES

DEPOSITION OF THIN SOLUTION FILMS
  • Spincoater Convac 1001
  • Langmuir-Blodgett KSV 2000 system
 
 

SAMPLES

Spincoater Convac 1001

  • substrates from 5x52 up to 4" wafers

Langmuir-Blodgett KSV 2000 system  

  • Maximum substrate size 100x100mm

  • effective area 675 cm2 

 

USED FOR

  • Deposition of thin films (mono/multilayers) on several substrates for morphological, optical and electric conductivity studies. Applications in photovoltaics, sensors and electronic organics.
 
 

Preparation of thin films of (FePc)2C obtained by spin coating or Langmuir Blodgett for sensing applications and studies on their interaction with NO2

Nitrogen oxides are among the environmental pollutants to be kept strongly under control and metallophthalocyanines (Pc) have proven over the years to be particularly suitable for their detection when implemented in opportune sensors. The study of μ-carbide bridged iron phthalocyanine films deposited by spin coating and Langmuir-Blodgett allowed to compare their behavior in the presence of NO2 in terms of gas-molecule chemical interaction and variation in the electrical conductivity of the films. The similarities and differences between the two systems have been rationalized taking into account the different structural and morphological characteristics of the films induced by the two deposition techniques.

Si veda: A. Capobianchi, A. M. Paoletti, G. Rossi, G. Zanotti, G. Pennesi, Sensors and actuators B 142 (2009) 159-165

 
 

Inorganic synthesis of porous materials by catalysis

Inorganic synthesis of porous materials by catalysis

Adriana De Stefanis  -

Roma - Monterotondo
 
Inorganic synthesis of porous materials by catalysis Adriana De Stefanis - Roma -Montelibretti FIG._0_di_1_2_2 INTRODUCTION A porous material is a solid consisting of a structure in which exists a network of interconnected pores. It includes natural substances such as minerals and clays or synthetic ones such as ceramics, MOFs, membranes, etc. They are used as supports to immobilize the actual catalysts, whether they are in homogeneous form or in nanoparticles, which are usually dispersed on the support as thin films or anchored on the walls of the pores. Although these catalysts can have high activity and selectivity, they have the disadvantages of being difficult to separate in homogeneous form and of being unstable as nanoparticles. Using porous materials as supports, allows to overcome these limitations and, at the same time, to obtain high accessibility to active sites, limiting in this way the reaggregation of nanoparticles. A high and achievable number of active sites increases the reactivity of the system reagent(s)-catalyst. Moreover, the specific porous structure of each material can even increase the selectivity of the reaction, for example when it prevents the creation of several different isomers by inhibiting those having dimensions different from the porous network ones. Finally, many of these supports, suitably modified, by introducing metallic and/or acidic or basic functions in their structure, can have their own catalytic activity and be fully considered as porous heterogeneous catalysts. Many of these porous materials are also traditionally used as molecular sieves in the separation of gas mixtures and in the absorption of specific species. The figure on the side shows the most common methods of achieving three-dimensional pillared smectic clays, which also represents several of the synthesis methods used in the preparation of porous inorganic materials.
 

TECHNICAL SPECIFICATIONS

  • porosity: micro (up to 2 nm); meso (up to 50 nm); macro (> 50nm). (porosimeter and equation BJH for PSD)

  • porous volume (t-plot method)

  • porous geometry (absorption hysteresis curves of N2, porosimeter)

  • specific surface area (BET equation or Langmuir, from a few tens up to thousands of m2/g)

  • acidity (pyridine test with FTIR)

  • crystal size (>200 nm) Structure and phases (XRPD)

  • contensts in metals (few units %) (AAS)

AVAILABLE TECHNIQUES

Inorganic porous materials synthesis

  • hydrothermal synthesis (Zeolites, zeotypes)  

    • or with organic template (shape-directingeffect)

    • or with a combination of different oxides (different tetrahedral atoms for different T-O bond lengths)

    • or with specific spatial units (addition of 4R or 6R units to AlPO)

  • Methods of pillaring/interleaving of 2D materials (see figure) (Smectitic clays, group IV metal phosphates, LDH, metal oxides)

  • batch methods (MOF, ZIF)

  • sol-gel methods (Silica-alumina from organosilanes and aluminate gels)

Preparation of catalysts on porous supports - chemical methods

  • Ionic exchange

  • Co-precipitation

  • Deposition-precipitation

  • Microemulsion

  • Saturation by impregnation

Preparation of catalysts on porous supports - physical methods

  • sonication

  • microwave irradiation

  • PLA

Modifications of porous inorganic materials

  • Introduction of acidic or basic function (modification of the Si/Al ratio during synthesis);

  • Introduction of metals into the framework (replacement of Si and/or Al with Ti, Cr, Zr etc during synthesis);

  • Elimination of metals from the framework (post-synthesis dealumination).

Other inorganic materials synthesis

  • sol-gel synthesis of bio-glasses

 

SAMPLES

  • samples of:

    • Zeolites: Y, USY, ZSM-5

    • Zeotypes: MCM41, FSM 16, MCM23

    • PILCs

    • PCH

    • MOF

    • ZIF

    • LDH

    • PILPs

    • Supported metal oxides (ceria, etc)

    • Bio-glasses

  • samples from 1 to 500g
  • samples with fixed metal content
 

USED FOR

Catalysis

  • Depolymerization of plastics (PET, PP) for the recovery of monomers and energy;
  • HDO of lignin for the production of fractions for jet fuel;
  • Production of syngas from CO2 and H2O (water shift).

Absorption/separation

  • Separation and concentration of atmospheric C2;
  • Chromatographic separation of hydrocarbon mixtures;
  • Absorption of mineral acids from biofuel blends.
 
 

CASE STUDIES

Catalytic pyrolysis of polyethylene

Recycling plastics through thermal or catalytic treatments is one of the possible alternative solutions to landfills and dispersion into the environment. The main targets are the production of fuels or the recovery of monomers and/or chemical products.
If a comparison is made between the pyrolysis products of polyethylene obtained through thermal degradation (top in the figure) and catalysis (bottom), it can be seen that the first gives a homogeneous and degrading distribution of products with a carbon atom number from C1 to C24, while with a suitable catalyst products grouped in the range of C12-C23 diesel fuel are obtained.

 
 
 

Absorption, concentration and recovery of atmospheric CO2

In the struggle for the reduction of worldwide CO2 emissions, the large plants for the production of electricity and in general the large oil and chemical industries have a sure place in the foreground. The huge quantities of CO2 generated by these plants are, however, easily intercepted before being released into the atmosphere.  This, as long as effective technologies at high temperatures are made available, for separating CO2 from other gases with adsorbents capable of capturing large quantities per unit of weight and/or volume. One of the methods in use, which still requires an energy expenditure equal to about 20% of the total produced in a plant, uses toxic amine solutions, through which the effluents rich of CO2 are allowed to pass. CO2 binds to the amine and is thus separated. In order to then recover and store CO2, the amine solution must be heated for its release. However, other techniques are available such as cryogenic and membrane separation, and the utilisation of solid molecular sieves. Among the absorption processes, PSA (pressure swing adsorption), VSA (vacuum swing adsorption) and TSA (temperature swing adsorption) are particularly interesting. For absorbents to be applied to these techniques, the following characteristics are required:
1) high selectivity and adsorbing capacity for the CO2;
2) adequate adsorption/desorption kinetics;
3) constant adsorption capacity even after several cycles in operating conditions.
The experiment in the figure illustrates the absorption and desorption of atmospheric CO2 with a Sr-modified ZIF, using TSA.

 
 
  English (UK)

Main Menu (en-GB)

We use cookies essential for the functioning of the site. You can decide for yourself whether or not to allow cookies. Please note that if you refuse them, you may not be able to use all of the site's features.
Ok Decline
More information