Solid-State Fermentation (SSF) versus Submerged Fermentation (SmF) for the Recovery of Cellulases from Coffee Husks: A Life Cycle Assessment (LCA) Based Comparison
Abstract
:1. Introduction
2. Materials and Methods
2.1. Goals and Scope Definition
2.1.1. Boundaries and Processes
2.1.2. Submerged Fermentation (SmF)
- (a)
- Inoculum: The inoculum phase was a sequence of growth seeds (3 bioreactors) to provide the necessary amount of inoculum (5% of working volume) and the preparation of the bioreactor media. The specific medium for inoculum included different substances such as ammonium sulphate, potassium phosphate or calcium dichloride, among others [28]. Three growth bioreactors provided inoculum for the production vessel (100 L). These reactors are designed to provide 5% inoculum to each submerged bioreactor to the next scale. The fermentation time of each one of the three growth bioreactors was estimated in 40 h [29].
- (b)
- SmF: The bioreactor working volume was 80% of the total volume and included a compressor and air filter for sterilization to provide the requirements of oxygen to perform the fermentation under optimal conditions. This bioreactor converts raw materials into the desired product: the cellulase enzymes. Ammonium was used to control pH and provide additional nitrogen to the microorganisms. Corn liquor and other trace nutrients were also added to the bioreactors as a carbon source. The bioreactors were aerated with air compressed to provide the oxygen demand and a chilled water system flowing through internal coils to control temperature. The output of fermentation is CO2 released during cellulase production. The microorganism was fed with nutrients to form biomass, a cellulase enzyme (metabolic product), and wastewater. Flow rates were estimated from the amount of raw materials and waste.
- (c)
- Filtration: The first sub-phase was filtration, which consisted of a tubular centrifugation and a 0.22 μm membrane filter where approximately 99.9% of total biomass waste was removed.
- (d)
- Ultrafiltration: The supernatant was ultrafiltrated through tangential filtration to obtain a concentrated liquid without microorganisms. Ultrafiltration (10 kDa) was repeated until the concentration factor was 10.
- (e)
- Lyophilization: At the last stage, lyophilization, all the remaining water is removed, and a solid, dry enzyme is obtained as the final product.
- (f)
- Biomass treatment: its environmental impact was assessed by the oxygen consumption via the theoretical chemical oxygen demand (ThCOD) consumed in a complete oxidation reaction. The ThCOD was estimated from the approximate molecular composition of biomass. Then, the reaction considered to calculate this parameter is:CH1.8O0.5N0.2 + O2 -> CO2 + NH3 + H2O
2.1.3. Solid-State Fermentation (SSF)
- (a)
- SSF: SSF was performed similarly to a composting process, in discontinuous mode in a 100 L airtight aerated reactor. In a study by Cerda and colleagues [17], the highest cellulase activity was observed after 24 h of SSF. Accordingly, residence time was fixed to this value. Approximately 10% of the fermented solid was the inoculum for the next batch [25,31,32]. Wood chips were used to provide porosity to the mixture [33]. In the same way, all fermented solid (except 10% used as inoculum) was derived to downstream stages.
- (b)
- The downstream processes is composed of four phases as explained below:
- (c)
- Extraction: The fermented solid was mixed with tap water in a 1:2 (v/v) ratio for 30 min [18]. To facilitate further filtration process, the fermented solids were mixed with water, passed through a mesh of 1 mm in the same tank with the objective of removing the biggest solid particles.
- (d)
- Filtration: Then, the liquid obtained from the previous stage (extract) was centrifuged at 15,000 rpm. The resulting liquid was filtered through a 0.22 μm filter. With this operation, all the biomass and suspended solids were removed.
- (e)
- Ultrafiltration: Next, this extract was filtered with an ultrafiltration device (10 kDa of cut-off) to concentrate the cellulase suspension. This step was repeated to reach a concentration ten times higher than the original one.
- (f)
- Lyophilization: Finally, the enzyme concentrated was lyophilized to obtain the main product (dry and concentrated cellulase).
2.2. Inventory Analysis, Functional Unit, Methodology, and Assumptions
2.2.1. Functional Unit
2.2.2. Life Cycle Assessment (LCA) Methodology and Impact Assessment
2.2.3. Technical Assumptions
Overall Assumptions
Submerged Fermentation (SmF)
- (a)
- Cellulose powder was considered with an environmental impact due its production.
- (b)
- The fermentation process was considered to run for 107 h in an airtight packed bed reactor, working under oxygen controlled aeration with 0.58 vvm (Lair·(Lreactor·min)−1) and a constant temperature of 28 °C.
- (c)
- According to Himmel, Biwer, and Wyman [12] and Sáez [26], the principal raw material was cellulose powder. In this study, carboxymethyl cellulose was chosen as a main input (Ecoinvent database). In this case, as carboxymethyl cellulase is a commercial product used to obtain another commercial product (cellulase), its environmental burdens in the production must be considered in this process. Ecoinvent database contains the details of these environmental impacts.
Solid-State Fermentation (SSF)
- (a)
- The main assumption was that the raw material used would not have environmental impacts because it is a waste. In this case, the environmental impacts associated with CH production are associated to the original industry (coffee production) since it is the normal procedure when dealing with waste as raw material for the production of another commercial product.
- (b)
- Exhaust gases emitted in SSF (and further composting) were treated in a biofilter considering that it removes 70% of emitted pollutants, as reported in the literature [41].
2.2.4. Inventory Analysis
Submerged Fermentation
Solid-State Fermentation
2.3. Sensitivity Analysis
3. Results and Discussion (Impact Assessment and Interpretation)
3.1. Overall Results
3.2. Specific Results
3.3. Sensitivity Analysis
3.4. Preliminary Economic Assessment
4. Conclusions
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
References
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Impact Category | Unit of the Results |
---|---|
Global warming (GWP) | kg CO2eq |
Stratospheric ozone depletion (ODP) | kg CFC−11eq |
Ionizing radiation (IRP) | kBq Co-60eq |
Ozone formation, human health (HOFP) | kg NOxeq |
Fine particulate matter formation (FPMF) | kg PM2.5eq |
Ozone formation, terrestrial ecosystems (EOFP) | kg NOxeq |
Terrestrial acidification (TAP) | kg SO2 |
Freshwater eutrophication (FEP) | kg Peq |
Marine eutrophication (MEP) | kg Neq |
Terrestrial ecotoxicity (TETP) | kg 1.4-DCB |
Freshwater ecotoxicity (FETP) | kg 1.4-DCB |
Marine ecotoxicity (METP) | kg 1.4-DCB |
Human carcinogenic toxicity (HTPc) | kg 1.4-DCB |
Human non-carcinogenic toxicity (HTPnc) | kg 1.4-DCB |
Land use (LOP) | m2 year |
Mineral resource scarcity (SOP) | kg Cueq |
Fossil resource scarcity (FFP) | kg oileq |
Water consumption (WCP) | m3 |
Material | Value | Comments and Assumptions | |
---|---|---|---|
INPUTS | Cellulose powder1 (kg/FU) | 3.62 | In SimaPro the chosen input was directly carboxymethyl cellulose because it is prepared from pure cellulose [42]. |
Ammonia2 (kg/FU) | 0.10 | Heinzle et al. [28]. | |
Corn liquor3 (kg/FU) | 0.75 | The carbon source necessary for the microorganism growth was assumed to be corn residue, although it is typically a nitrogen source [28]. | |
Water (L/FU) | 77.4 | Heinzle et al. [28]. | |
Nutrients4 (kg/FU) | 0.55 | The nutrients required during fermentation were: 32.5 g/L ammonium sulphate ((NH4)2SO4), 46.5 g/L monopotassium phosphate (KH2PO4), 7.0 g/L magnesium sulphate heptahydrate (MgSO4·7H2O), 9.3 g/L calcium chloride dihydrate (CaCl2·2H2O), and 4.7 g/L Tween 80 [2,29]. | |
Energy (kJ/FU) | 1,413,935 | Taking into account that the energy was the sum for each equipment power and the total air consumption. The air consumption from fermentation and the stabilization biomass was 372,701 L air/kg cellulase. | |
OUTPUTS | Biomass waste (kg/FU) | 1.5 | The required oxygen for biomass oxidation produced in 1 kg of cellulase was 102 kg. Theoretical chemical oxygen demand (ThCOD) was calculated through theory reaction of oxidation microorganism with Equation (1): CH1.8O0.5N0.2 + O2 + → CO2 + NH3 + H20 |
Cellulase (kg/FU) | 0.35 | Heinzle et al. [28]. | |
Wastewater (L/FU) | 65.2 | Heinzle et al. [28]. | |
Corn liquor (kg/FU) | 0.15 | Heinzle et al. [28]. | |
CO2 (kg/FU) | 0.13 | This value was taken and calculated according to the study from Sáez et al. [26] where it was demonstrated that during the fermentation 18 g/L of CO2 in terms of bioreactor volume can be produced. |
Materials | Value | Comments and Assumptions | |
---|---|---|---|
INPUTS | Coffee husk1 (kg/FU) | 84.3 | Coffee husk (CH) waste coming from Marcilla S.L, Barcelona (Spain). This CH is not associated with environmental impacts as it is attributed to coffee production. |
Wood chips2 (kg/FU) | 55 | Cerda et al. [17]. | |
Water from extraction (L/FU) | 678.8 | Cerda et al. [17]. | |
Energy3 (kJ/FU) | 1,407,873 | Taking into account that the energy was the sum for each equipment power and the total air consumption. The sum total (air required in SSF and the air required in composting step) of air consumption to obtain 1 kg of cellulase (FU) was 357,053 L. | |
OUTPUTS | Compost | 186.8 | Composting process was performed in the same reactor of SSF with aeration for 15 days. In this study it was assumed that the compost obtained avoided the production of fertilizer. It was considered that 50% of the total nitrogen of compost are available to plants and therefore, can replace an equivalent amount of N in the form of ammonium nitrate. This entails that 5.6 kg of fertilizer production were avoided per 1 kg cellulase (FU). |
COD4 (kg/FU) | 0.03 | Estimated | |
Wastewater (L/FU) | 601.5 | Cerda et al. [17]. | |
Methane3 (kg/FU) | 0.02 | Maulini-Duran et al. [43] | |
Nitrous oxide3 (kg/FU) | 0.06 | Maulini-Duran et al. [43] | |
VOCs3 (kg/FU) | 0.13 | Maulini-Duran et al. [43] | |
Ammonia3 (kg/FU) | 0.06 | Maulini-Duran et al. [43] |
Impact Category | Units | Cellulase Production | Carboxymethyl * Cellulose | Ammonia | Nutrients | Electricity |
---|---|---|---|---|---|---|
GWP | kg CO2eq | 1.8 | 16.32 | 0.20 | 1.03 | 492,695 |
ODP | kg CFC−11eq | 0 | 7.50 × 10−6 | 7.62 × 10−8 | 3.33 × 10−7 | 0.22 |
IRP | kBq Co-60eq | 0 | 0.11 | 1.01 × 10−3 | 0.01 | 20,775 |
OFP | kg NOxeq | 0 | 0.03 | 1.96 × 10−4 | 1.85 × 10−3 | 1412 |
FPMF | kg PM2.5eq | 0 | 0.03 | 1.88 × 10−4 | 1.73 × 10−3 | 1191 |
EOFP | kg NOxeq | 0 | 0.03 | 2.023 × 10−4 | 1.88 × 10−3 | 1417 |
TAP | kg SO2 | 0 | 0.06 | 4.77 × 10−4 | 3.73 × 10−3 | 3032 |
FEP | kg Peq | 0 | 9.52 × 10−4 | 8.67 × 10−7 | 3.87 × 10−5 | 18.50 |
MEP | kg Neq | 0 | 8.15 × 10−5 | 1.39 × 10−7 | 4.81 × 10−6 | 1.69 |
TETP | kg 1.4-DCB | 0 | 31.77 | 0.87 | 1.31 | 282,712 |
FETP | kg 1.4-DCB | 1.70 × 10−17 | 6.37 | 6.61 × 10−5 | 3.01 × 10−4 | 74.12 |
METP | kg 1.4-DCB | 0.02 | 0.03 | 6.86 × 10−4 | 8.14 × 10−4 | 263.72 |
HTPc | kg 1.4-DCB | 3.49 × 10−4 | 0.09 | 3.85 × 10−4 | 2.08 × 10−3 | 1149 |
HTPnc | kg 1.4-DCB | 0 | 1.07 | 7.70 × 10−3 | 0.03 | 10,617 |
LOP | m2 year | 0 | 2.61 | 2.04 × 10−4 | 0.01 | 11,804 |
SOP | kg Cueq | 0 | 0.03 | 1.00 × 10−4 | 1.07 × 10−3 | 248.62 |
FFP | kg oileq | 0 | 4.59 | 0.09 | 0.27 | 116,232 |
WCP | m3 | 0.08 | 0.20 | 5.17 × 10−3 | 0.01 | 4566 |
Impact Category | Units | Cellulase | Wood Chips | Electricity | Nitrogen Fertilizer as N |
---|---|---|---|---|---|
GWP | kg CO2eq | 17.2 | 7.1 | 425,758 | −60.5 |
ODP | kg CFC−11eq | 6.27 × 10−4 | 6.20 × 10−6 | 0.19 | −1.26 × 10−3 |
IRP | kBq Co-60eq | 0 | 8.78 × 10−2 | 17953 | −0.27 |
HOFP | kg NOxeq | 0 | 3.08 × 10−2 | 1221 | −0.11 |
FPMF | kg PM2.5eq | 0 | 2.18 × 10−2 | 1029 | −6.22 × 10−2 |
EOFP | kg NOxeq | 0 | 3.29 × 10−2 | 1224 | −0.11 |
TAP | kg SO2 | 0 | 3.27 × 10−2 | 2620 | −0.26 |
FEP | kg Peq | 0 | 2.88 × 10−4 | 16.0 | −1.46 × 10−3 |
MEP | kg Neq | 0 | 1.16 × 10−4 | 1.46 | 1.35 × 10−2 |
TETP | kg 1.4-DCB | 0 | 28.1 | 244,303 | −82.3 |
FETP | kg 1.4-DCB | 0 | 6.00 × 10−3 | 64.1 | −0.12 |
METP | kg 1.4-DCB | 0 | 2.23 × 10−2 | 228 | −0.15 |
HTPc | kg 1.4-DCB | 0 | 0.12 | 993 | −5.43 × 10−2 |
HTPnc | kg 1.4-DCB | 0 | 2.2 | 9174 | −5.4 |
LOP | m2 year | 0 | 19.6 | 10,200 | −8.2 |
SOP | kg Cueq | 0 | 3.18 × 10−3 | 215 | −0.14 |
FFP | kg oileq | 0 | 2.7 | 100,441 | −7.4 |
WCP | m3 | 645 | 0.19 | 3946 | −1.2 |
Impact Category | Units | Cellulase Production by SSF: Base Scenario | Cellulase Production by SSF: Sub-Alternative |
---|---|---|---|
GWP | kg CO2eq | 425,722 | 423,714 |
ODP | kg CFC−11eq | 0.19 | 0.19 |
IRP | kBq Co-60eq | 17,953 | 17,868 |
HOFP | kg NOxeq | 1220 | 1215 |
FPMF | kg PM2.5eq | 1029 | 1024 |
EOFP | kg NOxeq | 1224 | 1219 |
TAP | kg SO2 | 2620 | 2607 |
FEP | kg Peq | 16.0 | 15.9 |
MEP | kg Neq | 1.4 | 1.4 |
TETP | kg 1.4-DCB | 244,249 | 243,096 |
FETP | kg 1.4-DCB | 63.9 | 63.6 |
METP | kg 1.4-DCB | 228 | 227 |
HTPc | kg 1.4-DCB | 993 | 988 |
HTPnc | kg 1.4-DCB | 9171 | 9128 |
LOP | m2 year | 10,212 | 10,164 |
SOP | kg Cueq | 215 | 214 |
FFP | kg oileq | 100,436 | 99,963 |
WCP | m3 | 4590 | 4571 |
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Catalán, E.; Sánchez, A. Solid-State Fermentation (SSF) versus Submerged Fermentation (SmF) for the Recovery of Cellulases from Coffee Husks: A Life Cycle Assessment (LCA) Based Comparison. Energies 2020, 13, 2685. https://doi.org/10.3390/en13112685
Catalán E, Sánchez A. Solid-State Fermentation (SSF) versus Submerged Fermentation (SmF) for the Recovery of Cellulases from Coffee Husks: A Life Cycle Assessment (LCA) Based Comparison. Energies. 2020; 13(11):2685. https://doi.org/10.3390/en13112685
Chicago/Turabian StyleCatalán, Eva, and Antoni Sánchez. 2020. "Solid-State Fermentation (SSF) versus Submerged Fermentation (SmF) for the Recovery of Cellulases from Coffee Husks: A Life Cycle Assessment (LCA) Based Comparison" Energies 13, no. 11: 2685. https://doi.org/10.3390/en13112685
APA StyleCatalán, E., & Sánchez, A. (2020). Solid-State Fermentation (SSF) versus Submerged Fermentation (SmF) for the Recovery of Cellulases from Coffee Husks: A Life Cycle Assessment (LCA) Based Comparison. Energies, 13(11), 2685. https://doi.org/10.3390/en13112685