Pyrolysis is increasingly used technique for obtaining valuable renewable carbon feedstock and recycle waste biomass and plastics.  However, pyrolysis feedstock contains contaminating elements that are passed on to the pyrolysis oil phase. This makes crude pyrolysis oil reactive, unstable, corrosive and can lead to substantial challenges in downstream processes. The chemical composition of crude pyrolysis oil must also often be adapted to the intended end use. For example, the manufacture of sustainable aviation fuel (SAF) or sustainable polymers have their own specific requirements. To use pyrolysis oil safely and sustainably on a large scale, the crude pyrolysis oil requires upgrading by removing the contaminants and or chemically modify the composition towards its end use. 

The technology for upgrading pyrolysis oil (or PyOil) is still in its early stages, primarily due to the fact that the pyrolysis process itself has not yet reached a mature and consolidated state. Currently, the common practice is to burn or landfill waste plastic and biomass, rather than harnessing their valuable molecular structures to produce virgin materials. This is mainly due to the fact that alternative proven processes are still under development and have not reached a large-scale, economically viable stage. Yet, we are on a turning point. Driven by new legislation, major players in the chemical and energy industries, along with research and development institutes, as well as numerous emerging companies, are intensifying their collaborative efforts in research and development. The aim is to ensure the production of sustainable products that comply with the new legislation and in a timely manner.

 

 

One promising approach to enhance the quality of pyrolysis oil is through adsorption. By contacting an oil with a suitable adsorbent, contaminants can be removed selectively. An example of this strategy is the reduction of halogen content using reactive adsorption at elevated temperatures and pressures.

Avantium R&D Solutions, a pioneer in renewable and sustainable chemistry, is dedicated to supporting its customers in pursuing their R&D goals by offering custom-made testing units. With Avantium’s custom-made testing unit, many samples can be treated simultaneously under the same process conditions. The required sample volume of each sample is small, which limits the total amount of required crude PyOil. This proves advantageous as the R&D pyrolysis units, that typically generate these crude PyOil samples are usually a small scale. Samples can be tested in batch, using only 2 mL crude PyOil per sample. With the capability to test several samples at once, it enables the screening of multiple adsorbents, carriers and porosities.

After the initial screening is completed in batch mode, the most promising adsorbent/carrier combinations can be tested on the same PyOil in flow mode. Utilizing Avantium’s method leverages to obtain as much accurate data as possible from a relatively small amount of crude PyOil sample, while simultaneously testing a significant number of samples. This is typically achieved using small diameter fixed bed adsorption columns under very well controlled process conditions. The adsorbents usually are pretreated using an appropriate method, and subsequently exposed to target conditions for a period of several days or weeks. Conditions for a liquid phase process in this domain are temperatures up to 400°C and pressures up to 180 bar. Halogen removal, like this case, is a reactive adsorption process in which the adsorbent is not regenerated. But in different applications multiple adsorption/regeneration cycles can also be part of the scope of testing. Test results indicate that a significant amount of contaminants can be removed by adsorption, rendering this in to a promising technique for further investigation and scale up.

 

Are you interested? As Avantium R&D Solutions, we can design and build your custom-made R&D unit for pyrolysis oil upgrading. Contact us for more information.

Flowrence® products specifications

Reactor Section

Easy and quick reactor exchange system. Possibility to use quartz reactors at high pressure.

1 block of 4 reactors

HT = High Temperature max. 800°C nominal, limited to 925°C (<0.5°C reactor to reactor deviation)

4 blocks of 4 reactors

HT  or MT = Medium Temperature max. 525°C (<0.5°C block-to-block deviation)

16 reactors with iRTC

individual Reactor Temperature Control
max. 550°C (<0.5°C reactor-to-reactor)

4 reactors with iRTC

individual Reactor Temperature Control
max. 550°C (<0.5°C reactor-to-reactor)

Temperature Ranges (°C)

100 – 800°C
up 925°C (Option)

50 – 525°C
100 – 800°C
up 925°C (Option)

50 – 550°C

50 – 550°C

Reactor Types

L= Length
OD= Outer Diameter
ID= Inner Diameter
SS= Stainless Steel (< 550⁰C)
Qz= Quartz (< 925⁰C)

L 300 mm 561 mm
OD 3 mm 6 mm
ID SS 2 / 2.6 mm 2 / 3 / 4 / 5 mm
ID Qz 2 mm 2 / 4 mm
300 mm 561 mm 561 mm
3 mm 3 mm 6 mm
2 / 2.6 mm 2 / 2.6 mm 2 / 3 / 4 / 5 mm
2 mm 2 mm 2 / 4 mm
561 mm
3 mm
2 / 2.6 mm
2 mm
561 mm
3 mm
2 / 2.6 mm
2 mm

Maximum Catalyst Bed Length

(isothermal zone tolerance ± 1°C)
Note: isothermal length is dependent on the temperature range

300 / 3 HT 561 / 6 HT
>120 mm @ 450°C >200 mm @ 500°C
>90 mm @ 800°C >150 mm @ 800°C
>140 mm @ 925°C
300 / 3 HT 561 / 3 MT 561 / 6 HT
>120 mm @ 450°C >310 mm @ 450°C >200 mm @ 500°C
>90 mm @ 800°C >150 mm @ 800°C
>140 mm @ 925°C
561 / 3 MT iRTC
250°C ±0.5°C 41cm (4reactors)
350°C±0.5°C 38cm (4reactors)
550°C±0.5°C 28cm (4reactors)
3 reactors at 550°C, 1 reactor 350°C:
550°C=27cm 350°C=41cm ±0.5°C
561 / 3 MT iRTC
250°C ±0.5°C 41cm (4reactors)
350°C±0.5°C 38cm (4reactors)
550°C±0.5°C 28cm (4reactors)
3 reactors at 550°C, 1 reactor 350°C:
550°C=27cm 350°C=41cm ±0.5°C

Catalyst Volume (mL)

(isothermal zone)

0.2 - 0.6 mL 0.4 - 2.0 mL
0.2 - 0.6 mL 0.4 - 1.0 mL 0.4 - 2.0 mL
0.4 - 1.0 mL
0.4 - 1.0 mL

Pressure Ranges (barg)

2 – 80 barg
0.5 – 180 barg (option)

2 – 100 barg
0.5 – 180 barg

2 – 80 barg
0.5 – 180 barg

2 – 20 barg
2 – 50 barg (option)

Reactor Pressure Control

Advanced control RSD ±0.1 barg at reference conditions (gas phase only and 20 barg). For trickle flow Advanced control RSD ±0.5barg.

Standard (±0.5 barg)
Advanced (±0.1 barg) (option)

Standard (±0.5 barg)
Advanced (±0.1 barg) (option)

Advanced (±0.1 barg)

Advanced (±0.1 barg)

Gas Feed Lines

(#Gas Feeds)

Up to 6 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Up to 7 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Up to 7 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Up to 6 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Online Analysis

Full integration GC, MS , GC/MS with data visualisation (option)

Full integration GC, MS , GC/MS with data visualisation

Full integration GC, MS , GC/MS with data visualisation

Full integration GC, MS , GC/MS with data visualisation

Liquid Feed

 Split feeding 8 + 8 reators (option)

Pump-Coriolis dosing system
(ambient, cooled)

Pump-Coriolis dosing system
(ambient, cooled, heated 80°C)

Pump-Coriolis dosing system
(ambient, cooled, heated 80°C)

Pump-Coriolis dosing system
(ambient, cooled, heated 80°C)

Liquid Distribution

Microfluidic Distribution
(4-channel glass-chip)

Microfluidics Distribution
(4x4-channel glass-chip)
(16-channel glass-chip)
Active Liquid Distribution (option)
(with automatic isolation valves)

Active Liquid Distribution
(with automatic isolation valves)

Microfluidic Distribution
(4-channel glass-chip)

Liquid Sampling

(G/L Separation)

Parallel liquid sampling (4 x 20ml vials) with sequential on-line gas phase sampling (option)

Automated liquid sampling (4 rows x 16 vials x 8ml) with sequential on-line gas phase sampling (option)

Automated liquid sampling (4 rows x 16 vials x 8ml) with sequential on-line gas phase sampling (option)

Parallel liquid sampling (4 x 20ml vials) with sequential on-line gas phase sampling (option)

Reactors Effluent Handling

(Off-line Analysis Connection)

Full heated circuit up to 180°C with sequential on-line full gas phase sampling (option)

Full heated circuit up to 200°C with sequential on-line full gas phase sampling

Full heated circuit up to 200°C with sequential on-line full gas phase sampling

Full heated circuit up to 200°C with sequential on-line full gas phase sampling

Offline Analysis

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode (option)

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode

Waste Handling

Ambient temperature
Heated wax trapping (option)

Ambient temperature / Cooled containers / Heated compartment (wax trapping, heavies)

Ambient temperature / Cooled containers / Heated compartment (wax trapping, heavies)

Ambient temperature / Cooled containers / Heated compartment (wax trapping, heavies)

Safety

Gas sensors and control box (CO, LEL, VOC)

Gas sensors and control box (CO, LEL, VOC)

Gas sensors and control box (CO, LEL, VOC)

Gas sensors and control box (CO, LEL, VOC)

Flowrence® Software

Flowrence® recipe builder, control & database builder

Flowrence® recipe builder, control & database builder

Flowrence® recipe builder, control & database builder

Flowrence® recipe builder, control & database builder

Microfluidics modular gas distribution

Unrivalled accuracy in gas distribution with patented glass-chips for 4 and 16 reactors, with a guaranteed flow distribution of 0.5% RSD. Quick exchange of glass-chips for different operating conditions. Flexibility to cover a wide range of applications.

TinyPressure glass-chip holder with integrated pressure measurement

Compact modular design for gas and liquid distribution. No high-temperature pressure sensors required. Quick exchange of the microfluidic glass-chips, without the need for time-consuming leak testing.

Tube-in-tube reactor technology with effluent dilution

Unique tube-in-tube design with easy and rapid exchange of the reactor tubes (within minutes!). No need for any connections. Use of inert diluent gas (outside of reactor) to maintain the pressure prevents dead volumes and back flow. Possibility to use quartz reactors at high pressure applications.

Automated liquid sampling system

Programmable, fully automated liquid product sampling robot for 24/7 hands-off operation. Robot equipped with a compact manifold aiming at depressurizing the effluent immediately after each reactor to atmospheric pressure. Eliminates the use of high pressure valves.

Reactor Pressure Control (RPC)

The most accurate and stable pressure regulator for a 16-parallel reactors with just ±0.1bar RSD. The RPC uses microfluidics technology to regulate the pressure of each reactor, maintaining equal distribution of the inlet flow over the 16 reactors.

Auto-calibrating liquid feed distribution, measurement, and control

Distribution of difficult feedstocks e.g., VGO, HVGO, DAO. Liquid distribution 0.2% RSD, making it the most accurate liquid distribution device on the market. Option to selectively isolate each reactor.

Single-Pellet-String-Reactors (SPSR)

No dead-zones, no bed packing & distribution effects. The catalyst packing is straightforward and does not require special procedures. A single string of catalyst particles is loaded in the reactors avoiding maldistribution, eliminating channeling and incomplete wetting.

EasyLoad®

Unique reactor closing system with no connections. Rapid reactor replacement minimizing delays, improving uptime and reliability. Stable evaporation by liquid injection into reactor.

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Avantium Headquarters

+31 (0)20 586 8080

Zekeringstraat 29
1014 BV Amsterdam
The Netherlands

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