Biocatalysis is a new alternative that several industrial processes are implementing to assist or replace existing synthetic routes through which specialty and fine chemicals are produced [163]. Therefore, the use of cell systems or enzymes has mainly been studied specifically to cover the demands of pharmaceutical applications to obtain high-value compounds. The current technologies are based on the production of optical purity species for the required chiral center that represents a specific function in a medical patient [164]. Moreover, several authors have implemented green chemistry metrics to study the optimum operating conditions to allow the minimum waste generation and use of hazardous reagents or solvents [165].

The use of a biocatalyst involves economic factors that must be considered during the process. According to Pollard et al. [164], the obtained products must present considerably similar concentrations of those products generated when using chemical standard routes. Nevertheless, enzymes need to work in high-substrate concentrations without decreasing the activity. The second aspect that conditions the productive process is the biocatalyst cost, and this metric must be at a value around 1000 g_product/g_enzyme activity for the enzymes and at around 15 g_product/g_biocatalyst for the cell systems.

Ketone is the most common substrate and is used for the obtaining of pyrimidines and chiral intermediates. According to Chong et al. [166], the inhibitor ipatasertib can be efficiently synthetized by bicyclic pyrimidine as the starting material of the Ketoreductase enzyme (KRED) that acts on the ketone. This compound is produced with a yield of 86.00 wt%, and as reported, the operating conditions in terms of temperature and pH are neutral or not highly energy demanding for the biocatalytic asymmetric reduction that occurs. When comparing to chemical routes, the use of extreme conditions can cause isomerization, rearrangement of the compound, or racemization [167]. These phenomena reduce the productivity and make upstream processing necessary in order to reach purity and demanded standards.

Pollard et al. [164] note that biocatalytic processes are carried out in small scales when compared to most of the existing chemical processes. Up to 10,000 tons of pharmaceutical compounds are produced per year, and the scaling-up from laboratory scale is difficult. Factors such as batch operating mode can represent a negative effect for the enzyme or cell systems, as the substrate consumption has repercussions on the product quality standards [168]. Moreover, the large capacity of the devices at industrial level does not allow a perfect mixing, or if so, the energy consumption is higher than that at laboratory scale. Finally, the equipment materials are not the same when referring to one scale or another, which leads to low productivities [164].

Enzymes promote stability and selectivity for the desired compound [167]. For instance, when using Cyclohexanol as substrate and KRED as enzyme, St-Jean et al. [169] described that for a thermal requirement of 50 °C in an advanced racemic intermediate, the process reaches a yield of 95.00 wt% for diketone intermediate, an intermediate for the synthesis of Navoximod (II) as an IDO inhibitor.

Several mental health diseases such as anxiety and depression are treated with medicine that causes side-effect profiles. Nevertheless, (R)-sec-Butylamine 17 and (R)-1-cyclopropylethylamine constitute chiral intermediates from which Corticotropin-Releasing Factor-1 (CRF-1) can be synthetized as a receptor antagonist [164]. Another receptor antagonist can be synthetized from 3-Fluoro-4-aminopiperidine, produced by the asymmetric transaminase [170]. The reaction time indicates that the product is obtained after 24 h; however, the yield is 94.00 wt%, and the operation is under mild conditions.

The implementation of a biocatalytic route in a productive process might demand specificity related to the equipment and a considerable economic investment. Nevertheless, the operating conditions indicate that biocatalysis is a promising alternative for the synthesis of fine chemicals, especially those related to the pharmaceutical sector, where productivity and selectivity constitute key factors [180]. Additionally, there is a great variety of enzymes and cell systems available for each compound, which contributes to avoiding subsequent purification stages that are common in the existing chemical processes. Finally, biocatalysts promise to prevent stream wastes, and the implemented agents consist of renewable materials [170], which are important considerations for any process, especially those related to biorefineries.

Greenhouse gas (GHG) emissions constitute a current issue that demands new alternatives be implemented in the industrial sector to mitigate environmental implications. Within the total GHG emissions, CO₂ occupies the second position after methane [181], representing an increase in concentration in the atmosphere by up to 400 ppm in recent years [182]. There have been several studies where CO₂ utilization (CDU) is carried out to promote the production of high-value-added products when using catalysis [183]. Nevertheless, a complete integration of CO₂ capture and storage (CCS) systems to utilize technologies by which this gas could be transformed to different polymeric, organic, and inorganic products [184] should be analyzed.

A complete analysis of CO₂ as a raw material in transformation routes according to the production scale contributes to mitigating environmental problems. Moreover, the production of different compounds that are currently of great interest could be favored [185]. To achieve this proposal, new transformation routes in processing plants with CO₂ streams that can be used as raw material must be installed after having developed the respective sustainability assessment, where the techno-economic, environmental, and social dimensions are considered [186]. Some of the investigated methods for CO₂ conversion to chemicals include electrocatalytic or photocatalytic reduction, bio-catalysis, dry methane reforming, and catalytic hydrogenation [187]. Advances in molecular catalysis for electrocatalytic capture of CO₂ have indicated the process to be an appealing option for transformation of CO₂ to chemicals such as carbon monoxide, formic acid, formaldehyde, and ethanol [188].

Von der Assen has focused on the evaluation of producing dimethyl carbonate (DMC) by several reaction routes through the CDU concept [189]. This product is an important carbonylating compound that can be utilized for different fields including electronics, chemicals, pesticides, and medicine [190]. Two main routes that use CO₂ as raw material are the direct synthesis from CO₂ and methanol, and the synthesis from propylene carbonate, which is also known as the PC-route. Furthermore, a high-level conversion (85.2%) can be reached with a zirconium (IV) acetylacetonate (Zr(acac)₄) catalyst, leading to a carboxymethylation with a selectivity up to 99% [191]. Tamboli et al. [181] also studied the conversion of CO₂ into DMC in a batch operating mode by using methanol as raw material to obtain a product yield of 26.17 wt% when the catalyst involved is Ce_0.5Zr_0.5O₂ (see Figure 2). The reactions involved during the process enhance high efficiency and avoid the use of toxic chemicals such as phosgene, according to the kinetic study presented by Ohno et al. [191] and the work of Honda et al. [192].

Industrial sectors with high-residual-gas streams should consider the products to generate demanded and value-added compounds produced from CO₂ through heterogeneous catalysis, considering the great variety of products that includes fuels, chemical precursors, and medicines such as Benzamide. This compound is produced from CO₂ and low quantities of methanol when operating in high-pressure conditions to obtain a yield of 54.56 wt% [193]. Carbon monoxide (CO) can also be obtained by CO₂ reduction using Ni/nSiO₂ or Co-Fe/Al₂O₃, reaching yields up to 74 wt% with the use of the first catalyst operating at 800 °C and vacuum pressure [194].

Once the catalytic operation has been completed by using either a homogenous or heterogenous catalyst, the recovery of these substances implementing different technologies must be guaranteed in order to reuse them once more in the process [195]. High catalytic performance is related to ease of separation and recycling of the catalyst. When carrying out the recovery, solid loss must be minimum to enhance a techno-economic process. According to the review paper presented by Miceli et al. [196], the separation methods that include extraction, filtration, and centrifugation required more time and, consequently, there is not a real industrial application because of the high economic requirements.

Homogenous catalysts enhance important advantages when compared to heterogenous catalyst regarding the selectivity and stability [197]. Nevertheless, in terms of separation facilities forming the reactive mixture, a heterogenous catalyst is cheaper and presents a low environmental impact, as non-sophisticated technologies must be implemented. Consequently, fewer limitations are presented for heterogenous substances when considering specialty and fine chemicals obtained in, for instance, the pharmaceutical industry [198]. Moreover, for reactive mixture in gas and solid phases, the catalyst can be separated and cleaned by using conventional techniques, and as for liquid and solid systems, the catalyst matrix can be recovered by filtration [196].

As mentioned before, implementing catalyst recovery techniques guarantees economic and environmental improvements. Nevertheless, Sádaba et al. [199] explained that deactivation of the catalyst might occur by different phenomena such as poisoning, thermal degradation, or metals leaching into liquid phase. Therefore, when the recovery process has been completed several times and the catalyst activity has decreased, several authors recommend using the spent catalyst in an alternative process to mitigate environmental issues before disposition in landfills [200]. Chiranjeevi et al. [200] analyzed the minimization of spent catalyst as waste from refineries’ applications and concluded that the main reasons for the recent deactivation of catalyst in oil processing include the rapid demand for product that makes the flowrates increase, the reduction in time for the operating cycles, and particular characteristics of the feedstock that cause poisoning of the catalytic substances.

Among the most used methods for catalyst recovery, filtration and centrifugation constitute the most used technologies for heterogenous substances, considering the difference in both chemical and physical properties in the reactive mixture [196]. Filtration is carried out using a filter or membrane to remove the solid part of the liquid and gas mixture. The fluid phase that is separated from the solid fraction is called permeated, and the phenomenon is influenced by a pressure gradient. Santoro et al. [198] studied the hot filtration for the removal or solid catalyst to stop the reaction by using metal-catalyzed C-H functionalization. As for centrifugation, the driving force is the difference in density that is utilized to separate the liquid and solid mixtures. After the operation, the solid part remaining in the bottom of the flask is denominated as pellet, while the supernate refers to the fluid phase [196]. Liu et al. [201] analyzed the recovery of a silver nanoparticle catalyst by centrifugation to carry out capture and conversion of CO₂ as a low-energy-consumption alternative.

Another recycling alternative for heterogenous catalyst recovery is magnetic separation. This technique offers promising options for recycling catalyst-based metals in terms of techno-economic feasibility, as the operation takes little time and the implementation cost is low [202]. When considering a biorefinery scenario, sustainable processes must consider green chemistry principles alongside the production stages. Therefore, there might exist technologies that promote metal recovery from spent catalyst before final disposition. Miceli et al. [196] present two traditional techniques whose aim involves both economic and environmental dimensions for the production process. The first technique, denominated as hydrometallurgy, refers to metal dissolution in acid or base solution for a subsequent recovery of the specific metal by solvent extraction. Hu et al. [203] studied the removal of vanadium by ion exchange from a molybdate solution using a loaded resin that allowed a vanadium desorption ratio of 98.5% when regenerating the column. The second alternative corresponds to a pyrometallurgical process in which metal separation is carried out by using chemical treatments. Pyrolysis and incineration are involved in these treatments, which makes this process much more complex and expensive due to the high energy demand. Additionally, Peng et al. [204] mentioned that for platinum group metals recovery, vaporization techniques can be applied, but there could be corrosion as well as environmental and health impacts.

Biochar is a carbonaceous compound derived from thermochemical processing of lignocellulosic biomass, as reviewed in previous sections. Biochar can be used to enhance soil properties, pollutant adsorption (e.g., dyes, inorganic metals, and ions), and CO₂ capture and storage. However, this material has a high potential to be used as catalyst, as physical properties such as porosity and surface area make this thermochemical product attractive [214]. In this way, biochar is a promising material to replace solid carbon-based catalysts. The most important advantages related to the use of biochar as catalysts are the low cost and easy production. Physicochemical properties of biochar can be modified using acid/base processes (e.g., impregnation).

Biochar needs to be activated to improve catalytic efficiency. Indeed, biochar properties such as surface area, porosity, pore volume, pore size, and acidity are also improved. These properties can help to increase yield, productivity, and selectivity. A way to increase biochar porosity is via hydrothermal treatment or oxygenation [215]. Examples of different reactions catalyzed by biochar are transesterification and hydrolysis. Several authors have reported biochar sulfonation using sulfuric acid and calcination. This process increases the hydrolytic capacity. Lee et al. [214] analyzed the implementation of sulfonated pine-chip biochar as catalyst for hemicellulose hydrolysis to xylose and compared the conversion obtained (85%) when applying a commercial activated carbon at similar operating conditions (see Figure 3). Another application of biochar as catalysts addresses tar cracking. Indeed, biochar can be used to increase H₂ concentration in syngas, as this compound promotes different reactions in the gasification process. Moreover, the Fisher–Tropsch reaction has been catalyzed using activated biochar. The yields obtained after the process are similar to those obtained using iron-based catalyst [216]. Finally, activated biochar can be used as acid catalyst for the lignocellulosic matrix disruption and to remove hemicellulose. Ormsby et al. [217] performed hemicellulose hydrolysis, reaching an 85% conversion to xylose. Thus, biochar can be used for producing sugar-derived compounds and chemical platforms [218].

Despite the high potential of biochar to be used as catalyst, issues related to the standardized production of this material need to be researched and improved. Moreover, research on proper raw materials for biochar production is required, as the raw material chemical composition and physical properties affect the biochar quality. Another important aspect to improve biochar’s use as catalyst is related to the operating conditions for producing biochar. Slow or fast pyrolysis processes should be optimized for improving the above-mentioned properties. Similar points were highlighted by Lee et al. [214]. Indeed, these authors concluded that further investigations into developing the catalytic properties of biochar are important to produce stable catalysts. If these hotspots are improved, biochar can be used as catalyst by improving the sustainability of the thermochemical production processes, as more income can be obtained from the production of biochar and other products (i.e., bio-oil). Furthermore, the use of biochar as catalysts also offers benefits to other processes, as biochar can be a cheaper catalyst than homogeneous (e.g., inorganic acids) or heterogeneous catalysts (e.g., zeolites).