Open Access Article
K. P. H.
Meesters
*,
M. P.
Lanting
,
J. A.
Voogt
and
H. L.
Bos
Wageningen Food and Biobased Research, Bornse Weilanden 9, Wageningen, 6708 WG, The Netherlands. E-mail: Koen.Meesters@WUR.NL
First published on 27th November 2025
This paper investigates the opportunity to produce chemicals from carbon dioxide rich side streams from the agro-industry by the application of carbon capture and utilisation (CCU) technologies. It takes into consideration economic feasibility and puts the potential from sugar beet factories into perspective by comparison with current plastic use and forest area that would be needed to reach a comparable carbon dioxide uptake. A sugar beet factory with anaerobic digestion of sugar beet pulp and fermentation of molasses to ethanol was reviewed as a potential point source of carbon dioxide. Ethanol and methanol were taken as example chemicals produced via CCU. Ethanol is assumed to be produced via gas fermentation and methanol via reversed water gas shift and subsequent methanol synthesis. Mass balances and economic key figures on relevant technologies were taken from literature. In the default scenario, the production costs are 1738 € per ton for ethanol and 1058 € per ton for methanol. In both cases, the major cost factor is the use of electricity that is largely used for the reduction of carbon dioxide. If a significant penalty for fossil carbon dioxide emission (189 € per ton CO2eq) is in place, the costs of production of methanol from carbon dioxide are comparable with current methanol prices under the energy surplus scenario (energy costs reduced from 100 € per MWh to 50 € per MWh and doubled capital costs). Ethanol can be converted to ethylene to produce biobased polymers. The use of carbon dioxide from sugar beet processing could fulfil half of the future ethylene biobased plastic demand under the assumption that recycling will reduce the demand for virgin plastics by 50%.
Plant biomass (e.g. crops such as sugar cane, sugar beet, wheat, oil rich seeds, wood) is one source of renewable carbon for chemical and material production. Carbohydrates from these crops can be converted into valuable chemicals, such as ethanol, lactic acid, furans, and others. Polyunsaturated vegetable oils can be applied in thermosets. Wood can be a source of aromatic components, or of pure cellulose. However, significant amounts of arable land would be needed to fulfil the current demand for chemicals when only biomass is used. Without additional measures this land use could amount to a similar magnitude as present land use for plant-based food production but is still much smaller than the present magnitude of land use for feed.3 Environmental damage and loss of biodiversity could result from extra land use for biomass production.4
Another option is the production of carbon-based materials and chemicals from carbon dioxide, through Carbon Capture and Utilisation (CCU) technologies. These technologies could produce a wide range of products, such as alcohols, waxes, acids, and subsequent polymers. However, these technologies are under development. Capture of carbon dioxide from the atmosphere is expensive and energy intensive due to the low concentration of carbon dioxide in the atmosphere.5 Therefore, carbon dioxide rich point sources are preferred as input to produce chemicals from carbon dioxide.
Current carbon dioxide point sources are mainly from fossil industry and electricity production. However, the United Nations have set a goal for a maximum temperature increase of 2 °C in the Paris Agreement.1 Next to that, the EU has set a renewable energy target of 42.5% renewable energy by the year 2030 (ref. 6) and net zero greenhouse gas emissions by the year 2050.7 Therefore, the availability of fossil-based carbon dioxide point sources is expected to be strongly reduced soon. Agro-industry, however, is expected to remain operating under similar conditions, and is therefore a future-proof resource of carbon.
In Europe, sugar beet is an important agro-industrial crop, especially in France, Germany, Poland, United Kingdom, Belgium, The Netherlands, and Czech Republic.8 This study investigates the potential of using carbon dioxide rich side streams from sugar beet factories to produce chemicals and materials through CCU technologies. Sugar beet factories have two important side streams: molasses and sugar beet pulp (Fig. 1). Via established and well-known processes, ethanol and methane can be produced from these side streams via fermentation and anaerobic digestion, respectively. Both these processes have a carbon dioxide rich side stream.
With this paper we intend to research the relevancy of production of chemicals from sugar beet refineries to fulfil future plastic demand and reduce greenhouse gas emissions. As example chemicals, ethanol and methanol were chosen. Both are primary alcohols with limited functionality (only one –OH group) that can be used to produce building blocks for the synthesis of larger molecules. Their small size enables easy purification via distillation. However, production of these chemicals from carbon dioxide has not been implemented on industrial scale yet.
Pathways for production of ethanol at small scale (via syngas fermentation9–13) and methanol at large scale (via reversed water gas shift14–17 and methanol synthesis18–22) have been identified and described in literature. Below, both options will be described in more detail.
Co-electrolysis
| CO2 + H2O → CO + H2 + O2 | (1) |
Water electrolysis
| 2H2O → 2H2 + O2 | (2) |
Gas fermentation
| CO2 + CO + 5H2 → C2H6O + 2H2O | (3) |
Reverse water gas shift
| CO2 + H2 → CO + H2O | (4) |
Methanol synthesis from carbon dioxide
| CO2 + 3H2 → CH4O + H2O | (5) |
Methanol synthesis from carbon monoxide
| CO + 2H2 → CH4O | (6) |
Thermochemical processes usually have considerable economy of scale (the process is cheaper at larger scale than at smaller scale).23 Therefore, these processes need a large scale for economical operation. One sugar beet factory cannot produce sufficient carbon dioxide to feed such a large-scale facility. Therefore, transport of compressed carbon dioxide to a central facility will be needed.
The economic evaluation method is adopted from Lanting et al.24 The process costs are calculated as the sum of annualized capital costs (CAPEX) plus operational costs (OPEX). The annualized capital costs are derived from the total capital investment multiplied by a yearly costs of capital of 0.2 €/(€ per year).24 The costs of capital include 10% amortization, 5% maintenance and 5% interest. For the operational costs, only energy costs were considered. Other operational costs (such as salaries, laboratory costs, insurance, taxes) were neglected. Energy costs are calculated from the demand for high-quality energy (electricity and high temperature heat) and low-quality energy (heat up to 100 °C). For high quality energy, a price of 100 € per MWh was taken. This is less than the current energy prices in most European countries.25 For low-quality energy, a price of 40 € per MWh was taken. Low quality heat is assumed to be produced with heat pumps, taking into account a COP of 4 (25 € per MWh) plus 15 € per MWh for the utilities. These energy costs are higher than used in Lanting et al.,24 taking into account the Dutch situation with less sun and no options for cheap energy storage in hydropower reservoirs.
For our analysis we selected three papers that included sufficient details on process scheme, mass balances, energy balances and economic parameters: Huang et al., Rezaei and Dzuryk, and Rajaee et al.9,14,18 Data from Lacerda et al.19 are comparable to the data used in this study (as derived from Rajaee et al.18). Other literature found was unsuitable for a variety of reasons. Most publications did not provide a full data set.10–13,16,17,20,21 Data from Bown et al.15 on RWGS used a separate set of starting points that could not be easily recalculated to the starting point of this paper where fossil resources are excluded. Wu et al.22 describe a highly integrated process fuelled with biomass that cannot be easily adopted to a process fuelled with electricity.
Where indicated, adaptations were made to fit the 2050 situation where natural gas will not be used for process heat (see Annex 3 and 4). Cost data on electrolysis and co-electrolysis were taken from Lanting et al.24
| Output | Component | % | Ton per year | Ton per year |
|---|---|---|---|---|
| Dry pulp | Sucrose | 0.39 | 195 | |
| Non-sucrose | 1.74 | 875 | ||
| Pulp | 87.87 | 44 172 |
||
| Water | 10.00 | 5027 | ||
| Total |
50 270
|
|||
| Molasses | Sucrose | 43.96 | 28 367 |
|
| Non-sucrose | 28.18 | 18 184 |
||
| Water | 24.68 | 15 922 |
||
| Other | 2055 | |||
| Total |
64 528
|
|||
| Sugar | Sucrose | 99.97 | 101 667 |
|
| Other | 0.03 | 21 | ||
| Total |
101 698
|
The sugar beet factory has two side streams: molasses, and sugar beet pulp. It was assumed in our assessment that molasses is fermented to ethanol and that sugar beet pulp is digested to biogas. Both these processes yield a side stream that is rich in carbon dioxide. To calculate the quantity of ethanol, methane and carbon dioxide produced in these processes, the following was assumed: a yield for ethanol of 0.511 kg kg−1 sucrose and for carbon dioxide of 0.489 kg kg−1 sucrose was assumed (95% of stoichiometric yield). A yield of methane of 0.297 kg kg−1 and carbon dioxide of 0.433 kg kg−1 pulp dry matter was used (derived from Hutnan et al.27 and Muzík et al.28) (see Annex 1). Ethanol fermentation yields a gaseous side stream with almost pure carbon dioxide gas. The biogas from anaerobic digestion is separated in pure methane and pure carbon dioxide. It is assumed that both molasses and pulp are stored, so that ethanol fermentation and anaerobic digestion can run continuously throughout the year.
The data for electrolysis were taken from Lanting et al.24 The data for the Reverse Water Gas Shift (RWGS) process were adapted from the data given by Rezaei and Dzuryk14 for a capacity of 1.8 Mton per year syngas (Annex 3). In the study by Rezaei and Dzuryk, all heat is produced from natural gas. In our study, we consider a fossil free future, so natural gas is not an option. Therefore, the reboiler was assumed to be heated with electricity via a heat pump with a COP (Coefficient of Performance) of 4, the natural gas fired heater was replaced by an electric heater. The investment costs were corrected for the year 2024 using CEPCI numbers for 2024 and 2017.32 The data for the methanol synthesis reactor were adapted from Rajaee et al.18 and corrected for the year 2024 using CEPCI numbers for 2019 and 2024 (Annex 4). The data for RWGS and synthesis were collected and recalculated per ton methanol produced (Annex 5).
| Parameter | Reference component | Value | Unit | Ref. | |
|---|---|---|---|---|---|
| Generic | Scenario high energy prices | ||||
| High quality energy price | 100 | € per MWh | |||
| Low quality energy price | 40 | € per MWh | |||
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|||||
| Scenario low energy prices | |||||
| High quality energy price | 50 | € per MWh | |||
| Low quality energy price | 20 | € per MWh | |||
| Cost of capital | 0.2 | €/(€.year) | |||
| CEPCI 2017 | 567.5 | 32 | |||
| CEPCI 2019 | 607.5 | 32 | |||
| CEPCI 2024 | 797.9 | 32 | |||
| USD to euro ratio | 0.9 | USD per € | 33 | ||
| Electrolysis | CAPEX electrolysis | Hydrogen | 1358.4 | €/(ton per year) | 24 |
| HQE electrolysis | Hydrogen | 45.45 | MWh per ton | 24 | |
| Co-electrolysis | CAPEX co-electrolysis | Syngas | 449.3 | €/(ton per year) | 24 |
| HQE co-electrolysis | Syngas | 550 | MWh per ton | 24 | |
| Ethanol | ![]() |
||||
| Case CO and CO 2 | |||||
| Ethanol yield on syngas | Syngas | 1 | mol mol−1 | 9 | |
| Ethanol yield on additional H2 | Hydrogen | 0.25 | mol mol−1 | 9 | |
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|||||
| Case CO | |||||
| Ethanol yield on syngas | Syngas | 0.5 | mol mol−1 | 9 | |
| Ethanol yield on additional H2 | Hydrogen | 0.5 | mol mol−1 | 9 | |
| CAPEX fermentation | Ethanol | 1425.9 | €/(ton per year) | 24 | |
| HQE fermentation | Ethanol | 87.2 | MWh per ton | 24 | |
| CAPEX distillation | Ethanol | 153.8 | €/(ton per year) | 24 | |
| LQE distillation | Ethanol | 74.4 | MWh per ton | 24 | |
| RWGS | CAPEX RWGS | CO | 88.6 | €/(ton per year) | Annex 3 |
| HQE RWGS | CO | 1.465 | MWh per ton | Annex 3 | |
| Methanol | Methanol yield on H2 | H2 | 1/3 | mol mol−1 | |
| Methanol yield on CO/CO2 | CO | 2 | mol mol−1 | ||
| CAPEX methanol synthesis | Methanol | 384.9 | €/(ton per year) | Annex 4 | |
| HQE methanol synthesis | Methanol | 0.574 | MWh per ton | Annex 4 | |
| CO2 transp | Cost of compression | CO2 | 21.3 | USD per ton | 30 |
| Cost of transport by ship | CO2 | 0.039 | €/(ton km) | 31 | |
| Travel distance (one way) | 60 | km | 31 | ||
000 ha.34 This harvest is processed in two factories, so the Dutch sugar factories are a factor 4 larger than the SuperPro Designer example26 we used as starting point. The data from Table 2 were multiplied by this factor to calculate the availability of molasses (sucrose) and pulp (dry matter) from the two Dutch sugar factories as shown in Table 4. The side streams from these factories (molasses and sugar beet pulp) could be used to produce 114 kton ethanol per year and 93 kton methane per year (see Annex 1) via ethanol fermentation and anaerobic digestion respectively. Both are well established processes that operate at TRL 9 and could be implemented relatively easily at full scale. Besides ethanol and methane, these processes would produce 279 kton carbon dioxide per year.
| Raw material | Quantity [kton per year] | Process | Ethanol [kton per year] | Methane [kton per year] | Carbon dioxide [kton per year] |
|---|---|---|---|---|---|
| Molasses (sucrose) | 222 | Fermentation | 114 | 109 | |
| Pulp (dry matter) | 394 | Anaerobic digestion | 93 | 171 | |
| Total | 114 | 93 | 279 |
Methane produced from anaerobic digestion of pulp can be fed into the natural gas grid or converted into methanol or other chemicals.
The carbon dioxide that results from molasses fermentation and pulp anaerobic digestion can furthermore be used to produce either additional ethanol (Case 1) or methanol (Case 2) (Table 5). Assuming stoichiometric yields, the 279 kton per year carbon dioxide could yield 146 kton ethanol per year or 203 kton methanol per year (see Annex 6). The total potential production of ethanol or methanol from the side streams of the two Dutch sugar factories thus amounts to 260 kton ethanol per year (Case 1) or 114 kton ethanol plus 203 kton methanol per year (Case 2).
| Raw material | Quantity [kton per year] | Process | Case 1: ethanol [kton per year] | Case 2: ethanol [kton per year] | Methanol [kton per year] |
|---|---|---|---|---|---|
| Molasses (sucrose) | 222 | Fermentation | 114 | 114 | |
| Carbon dioxide | 279 | Gas fermentation | 146 | ||
| Carbon dioxide | 279 | RWGS + synthesis | 203 | ||
| Total | 260 | 114 | 203 |
![]() | ||
| Fig. 4 Production costs (CAPEX and OPEX) in € per ton product for ethanol and methanol production from carbon dioxide. | ||
It is clear from Fig. 4 that both for ethanol and for methanol production the electrolysis step (production of hydrogen gas from water) is by far the costliest step. In both cases it is the cost of energy (OPEX) that is the culprit. Energy costs are thus a crucial factor for production of chemicals from carbon dioxide. This is mainly because the reactions involved are highly endothermic. In other words: reduction of carbon dioxide to methanol or ethanol takes a lot of electric energy. In traditional ethanol production, the distillation energy costs are a significant contribution to total costs. From Fig. 4 it is clear that here the electricity costs for electrolysis and co-electrolysis are far larger.
Besides high costs for electricity, the production of ethanol via gas fermentation also has high capital costs (Fig. 4). Gas fermentation is still in its infancy, but large savings are not expected. A considerable cost factor is associated with the gas to liquid mass transfer of carbon monoxide and hydrogen. Mass transfer of carbon monoxide and hydrogen from the gas phase to the reaction medium might be increased by increasing the pressure (increasing the concentration gradient), but options are limited and come at a cost, so large breakthroughs are not to be expected.
An option to reduce the electricity costs could be the use of cheaper electricity in periods of sunshine or high winds (energy surplus scenario). The costs of offshore wind energy are near 50 € per MWh,35 but surplus availability is limited to only 4500 hours per year. So instead of a constant supply of high-quality energy at 100 € per MWh and low-quality energy at 40 € per MWh, we may shift to a sun and wind-based supply that delivers energy at half the price during half the time. As low-quality energy is assumed to be produced with heat pumps (that use electricity to pump heat from ambient temperature to the desired temperature level), the costs of low-quality energy are also assumed to drop by 50%. To maintain the same production volume, all equipment would need to be twice as large, doubling the capital costs. Fig. 5 shows that the production costs of methanol could be reduced by 30% in such a scenario.
![]() | ||
| Fig. 5 Sensitivity analysis: base scenario vs. surplus energy scenario (with low energy costs and high capital costs) vs. surplus energy with buffer scenario vs. very low energy cost scenario. | ||
Electricity costs are expected by some authors to be further reduced in the future due to the implementation of new energy technologies. Jouny et al.36 have suggested an electricity price as low as 18 € per MWh. Such a low electricity price would yield CO2 based methanol at a price lower than the current market price for fossil based methanol (see ‘Very low cost scenario’).
It should be noted that discontinuous processing may be troublesome for the ethanol fermentation process as the bacteria cannot be left without ‘food’ for longer periods. Storage of intermediate products (hydrogen and carbon monoxide) to equalize the supply of hydrogen and carbon monoxide to the fermenter will bring significant costs due to the low density of gases. Also the risk of explosions and the risks involved with toxicity of carbon monoxide should be taken into account. According to Cocco et al.,37 syngas can be stored on a daily basis with capital costs of 21.1 € per ton and electricity costs of 65 € per ton. According to Abdin et al.38 the costs of hydrogen storage on a daily basis could be as low as at 330 USD per ton (lump sum costs). These data were recalculated per ton ethanol respectively methanol (Annex 8) and added to Fig. 5 as the ‘surplus energy with buffer scenario’. Production costs of ethanol are decreased by 24% compared to the base scenario. Production costs of methanol are only slightly reduced compared to the surplus energy scenario.
Another option next to intermittent production might lie in storage of energy for use during periods when renewable energy is not available. Storage costs of electricity in batteries are expected to drop to around 100 € per MWh in 2050,39 so stored electricity would cost 150 € per MWh (wind derived electricity at 50 € per MWh plus storage at 100 € per MWh). The average of direct wind derived electricity at 50 € per MWh and stored energy at 150 € per MWh would be exactly equal to 100 € per MWh. The same will hold for low quality energy costs. From this it is concluded that no cost reduction is expected from the use of batteries.
The introduction of policies to tax abatement costs for products based on fossil resources is a further option to increase the market potential of carbon dioxide based chemicals. Methanol is currently made from fossil resources. If carbon dioxide abatement costs of 189 € per tonCO2eq,40 (marginal carbon dioxide abatement costs for full abatement in the USA) are added to the price of fossil-based methanol (Table 6), the market price increases to 641 € per ton (taking into account a carbon dioxide emission of 1.37 kgCO2 per kg methanol). This comes close to the costs of methanol produced from carbon dioxide rich side streams in the surplus energy usage scenario (Fig. 5). From this we can conclude that a serious carbon dioxide tax can help to reach political goals by enhancing the feasibility of production of methanol from carbon dioxide.
Alternatively, a subsidy on renewable plastics could make production viable. A subsidy of at least 2.35 € per kg ethylene would be needed to replace fossil ethylene. The authors do not advocate the use of measure subsidies. Measure subsidies provide more security to industry but may also encourage large scale implementation of less efficient processes and impede implementation of more efficient alternative options. Therefore, target subsidies are preferable.
A capital subsidy cannot make the process profitable as the electricity costs (OPEX) are dominant.
Fig. 4 compares ethanol and methanol on a weight basis (where the cost of ethanol is 64% more than the cost of methanol). But obviously, ethanol and methanol are not identical products. The production costs of these two chemicals might therefore better be compared based on higher heating value (HHV) or alternatively based on carbon content. Both HHV and carbon content have an intrinsic value that is also apparent from the current market price that is 19% higher for ethanol than for methanol. Table 6 shows that ethanol has a 29% higher HHV and a 39% higher carbon content compared to methanol. From this, we can conclude that the cost of ethanol from carbon dioxide is higher than the cost of methanol from carbon dioxide, independent of the basis of comparison.
Ethanol produced from carbon dioxide is considerably more expensive than the current main method for ethanol produced from sugar cane (current market price, Table 6), which is a competing renewable production route. Main advantage is that ethanol produced from carbon dioxide does not need additional agricultural area in tropical regions.
It should also be noted that ethanol has a valuable C–C bond and therefore can be converted into bifunctional molecules (such as ethylene and glycol). This makes ethanol a suitable raw material for making more complex chemicals and polymers, which should be from a renewable source if we phase out fossil feedstocks. Methanol is not an alternative in this respect. Therefore, in paragraph 3.3, the discussion will be limited to the production of polymers from ethanol.
As electricity costs are dominant in the total costs, it would be a promising idea to reduce the demand for reduction equivalents. This could be done by production of chemicals that contain more oxygen than methanol and ethanol, such as formic acid, glycol, or lactic acid. Unfortunately, it is not easy to steer biological fermentations that use a C1 feed to produce C2 and C3 fermentation products. Currently all available research is still in an early laboratory phase. Hence this option was not considered.
The role of recycling in future scenarios for the plastics industry has been investigated by several authors,46,47 and the recycling rate (according to the authors) is expected to lie around 43%. The demand for virgin plastic could thus be reduced by 43% due to recycling practices. Furthermore, the EU has implemented regulations to reduce the amount of packaging by 15% in 2040.48 Since packaging makes up approximately 40% of the market share of plastics, we assume an additional 6% reduction in demand for virgin plastics. For ease of calculation, we assume a total potential reduction of 50% virgin plastics demand in a 2050 scenario. In such a future scenario, 524 kton per year of ethanol may suffice.
It is interesting to see that the potential production of ethanol from the Dutch sugar beet factories side streams might account for 25% of the ethylene derived portion of today's virgin plastic demand of the Dutch society. From this 25%, 11% can come directly from molasses fermentation, a technology that is well established and the additional 14% may come from CCU, which is still at low TRL. If the demand is indeed reduced according to the 2050 scenario, the Dutch sugar beet refineries could contribute 50% of the future demand.
In this light, the Dutch agro-industry could help to reduce carbon dioxide emissions and contribute to production of renewable chemicals and or polymers without the need to use extra land, provided renewable energy can be used.
As comparison, the carbon dioxide uptake of Dutch forests is around 4.6 ton CO2/(ha per year).50,51 To reach the 752 kton per year reduction, which the Dutch sugar beet production could contribute, a forest of 164
000 ha would be needed. That is more than 40% of the forest area in the Netherlands in the year 2021.50,52 and twice as much as the area currently used for sugar beet cultivation.34 This clearly shows that use of side streams from crop production may yield larger carbon dioxide capture than additional forestry.
All these aspects make the potential use of carbon dioxide side streams from the Dutch sugar beet production for CCU a more interesting option than it might seem at first glance.
Other crops have similar side products (e.g. sugar cane has molasses and trash as comparable side products). So, in many countries, carbon dioxide from agricultural side streams could be a relevant source for production of renewable chemicals.
Future electricity prices may be lower in countries near the equator, where the intensity of sunlight is higher or in countries where buffering of electricity supply/demand via hydro-electric storage is an option (Sweden, Switzerland, Brazil). Considering the high costs for electricity, CCU may be more profitable in these countries.
Compression, transport, and central large-scale thermochemical conversion of carbon dioxide to methanol is cheaper (1056 € per ton) than smaller scale fermentative conversion to ethanol (1738 € per ton). This is independent of the basis of comparison (weight, Higher Heating Value, carbon content, market price).
Ethanol produced from carbon dioxide is far more expensive (1738 € per ton) than the current market price of ethanol (452 € per ton, produced from sugar cane), even at lower energy prices.
Flexible use of surplus energy from sun and wind could reduce energy costs but would lead to higher capital costs. Assuming halved electricity prices and doubled capital investment costs, the costs of methanol production may be reduced by 29% and the costs of ethanol production may be reduced by 14%. Production costs of both chemicals from carbon dioxide are then still higher than their present market prices. Use of syngas and hydrogen storage reduces costs of ethanol production by 24% compared to the base scenario.
Sugar beet refineries could fulfil 50% of the ethanol needed for the ethylene based portion of the future plastic demand of the Netherlands assuming a reduction of plastic use for packaging and recycling applied to the max (22% from molasses fermentation and 28% from utilization of carbon dioxide rich side streams).
The use of sugar beet refinery side streams could capture 752 kton of carbon dioxide per year. This is equivalent to the carbon dioxide uptake of a forest of 164
000 ha, more than 40% of the current Dutch forest area and twice as much as the area currently used for sugar beet cultivation.
Altogether, extra ethanol from sugar beet refinery side streams (molasses, pulp, and carbon dioxide) comes at a cost, but could contribute to extra renewable chemicals/polymers production and a decrease in carbon dioxide emissions.
| CAPEX | CApital EXpenditures |
| OPEX | OPerational EXpenditures |
| CEPCI | Chemical Engineering Plant Cost Index |
| CO2eq | Carbon dioxide equivalent |
| CoC | Cost of Capital (=0.2 €/(€ per year)) |
| COP | Coefficient of Performance of heat pumps (heat output/electric energy input) |
| CCU | Carbon Capture and Utilization |
| HQE | High Quality Energy |
| LQE | Low Quality Energy |
| MWh | Unit of energy: 1 MWh is equal to 3.6 GJ |
| PE | Polyethylene |
| PET | Polyethylene Terephthalate |
| PVC | Poly Vinyl Chloride |
| RWGS | Reverse Water Gas Shift |
| SBF | Sugar Beet Factory |
| SBR | Sugar Beet Refinery (a sugar beet factory with molasses fermentation and pulp digestion) |
| ton | Unit of weight: 1 ton is equal to 1000 kg |
| USD | United States Dollar |
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