2.1. Process Description
The mass- and energy-integrated gas oil hydrocracking process starts with the preheating and heating of 1,937,245.28 t/yr of gas oil feed to 112.22 °C at a pressure of 344.74 kPa. The feedstock is routed through a network of heat exchangers within the preheating section before entering a furnace. Subsequently, the heated gas oil is fed into the first hydrocracking reactor, operating at 379.44 °C and 16,402.63 kPa, where it reacts with recycled hydrogen supplied at 65.55 °C and 16,678.42 kPa. At the same time, unconverted oil (UCO) is withdrawn from the bottom of the fractionator. Part of this stream is directed to the fluid catalytic cracking (FCC) unit, while the remaining fraction is recycled, cooled in an air cooler, and sent to a second hydrocracker operating at 382.22 °C and 15,437.36 kPa. In this reactor, the stream reacts with two hydrogen recycle streams at 16,678.42 kPa, one at 65.55 °C and the other at 118.33 °C. The effluents from both reactors are then combined, producing a stream at 292.78 °C and 14,658.25 kPa, which is subsequently fed to the hot separator [
15].
Figure 1 presents the simulated process flow diagram corresponding to the reaction section of the integrated mass and energy gas oil hydrocracking system. The process simulation was performed using the Aspen HYSYS
® V 14.0 simulator. The steady-state simulation model implemented is based on an industrial-scale hydrocracking configuration. The thermodynamic framework, reaction scheme, and integration strategy were previously developed and validated against industrial reference data, ensuring consistency in mass and energy balances and realistic operational conditions. A detailed description of the modeling assumptions, parameter selection, and validation procedure is reported in García-Maza et al. [
16]. In the present study, this validated model serves as the computational basis for the sustainability assessment using the SWROIM methodology.
In hydrocracking units, hydrotreating reactions generally take place first and proceed at a higher rate than hydrocracking reactions [
17]. The main purpose of hydrotreating is to eliminate heteroatoms such as sulfur and nitrogen and to hydrogenate olefinic compounds. Additionally, it contributes to the removal of oxygen, metals, and halogens (e.g., chlorine and bromine), as well as other non-metallic species, while also promoting the saturation of aromatic compounds [
18]. By comparison, hydrocracking involves the breakdown of heavy molecules in a manner comparable to fluid catalytic cracking (FCC), combined with hydrogen addition. The dominant reactions include the scission of aromatic, naphthenic, and paraffinic structures [
19].
The process comprises multiple separation steps. At the beginning, the feed stream is split into a high-pressure top stream and a low-pressure bottom stream within a hot separator (flash evaporator). The high-pressure stream is subsequently cooled using an energy-integrated heat exchanger, washed with water at 43.33 °C and 14,554.83 kPa supplied from the makeup and recycle water system, passed through an air cooler, and then fed into a cold three-phase separator. In this unit, the stream is divided into one gaseous phase and two liquid phases, classified as light and heavy. The gaseous fraction is further cooled in a heat exchanger and directed to a recycle gas separator drum (flash evaporator), where it is separated into overhead and bottom streams [
15].
Figure 2 illustrates the process flow diagram of the initial separation stage in the mass- and energy-integrated gas oil hydrocracking process that was obtained from the simulation results.
The hydrogen-enriched overhead stream is treated in an absorption column with lean amine at 48.89 °C and 14,478.99 kPa to eliminate impurities such as hydrogen sulfide and ammonia, producing a rich amine stream that is routed to the amine regeneration system. In parallel, the bottom stream from the recycle gas separator is merged with the heavy liquid fraction from the cold separator and sent to a cold flash drum (three-phase separator) to achieve additional phase separation. Simultaneously, the low-pressure effluent from the hot separator is directed to a hot flash drum, where it is divided into overhead and bottom streams. The vapor stream is subsequently washed with water at 43.33 °C and 14,554.83 kPa that is supplied from the makeup and recycle water unit, cooled in an air cooler, and blended with the light liquid fraction from the cold separator prior to entering the cold flash drum. In this unit, separation into one gaseous phase and two liquid phases (light and heavy) occurs. Finally, the bottom stream from the hot flash drum passes through a control valve and is conveyed to the stripping column for further processing [
15].
The vapor stream leaving the cold flash drum is combined with a hydrogen-rich flow at 53.89 °C and 2447.64 kPa, subsequently cooled in a heat exchanger, and sent to an off-gas separator vessel, where it is divided into two streams. The top stream, characterized by a high hydrogen concentration, is routed to an off-gas scrubber to remove impurities such as hydrogen sulfide and ammonia using lean amine at 48.89 °C and 2482.11 kPa; the resulting rich amine is then treated in the amine regeneration unit. The cleaned hydrogen stream is forwarded to a pressure swing adsorption (PSA) system, where residual contaminants are eliminated to obtain high-purity hydrogen. This hydrogen is mixed with makeup and recycled hydrogen streams, yielding a hydrogen byproduct at 64.44 °C and 2413.17 kPa. Makeup hydrogen is conditioned through compressors, air coolers, and heat exchangers at 25 °C and 2054.64 kPa, and subsequently blended with treated recycled hydrogen for integration into the energy system before entering the reactor stage [
15].
Simultaneously, the bottom stream from the waste gas separator combines with the light liquid fraction obtained from the cold flash drum. This combined stream is routed through an energy-integrated heat exchange network and subsequently sent to the stripping column. In contrast, the heavy liquid fraction from the cold flash drum constitutes part of the wastewater stream that is conveyed to the makeup and recycle water unit [
15].
Figure 3 presents the simulated process flow diagram of the makeup and recycle hydrogen stage, including the absorption columns and the PSA unit, within the mass- and energy-integrated gas oil hydrocracking process.
Subsequently, during the stripping step, two feed streams—one operating at 241.11 °C and 2413.17 kPa and another at 297.22 °C and 944.58 kPa—are fed into a distillation column together with a medium-pressure vapor stream at 189.44 °C and 965.27 kPa. In this unit, lighter compounds, including liquefied petroleum gas (LPG), light naphtha, and part of the heavy naphtha, are recovered as overhead products, whereas the heavier cuts, such as the remaining heavy naphtha, kerosene, diesel, and unconverted oil (UCO), are withdrawn from the bottom. The overhead stream is pumped, heated through a heat exchanger, and routed to the debutanizer [
15].
Meanwhile, the bottom stream is pumped, preheated in an integrated heat exchanger, further heated in a furnace, and sent to the fractionation column. Waste streams, namely wastewater and sour gases, are produced in the stripper overhead drum; the wastewater is conveyed to the makeup and recycle water section. In the debutanization step, the stripper overhead stream enters the column at 133.89 °C and 1116.95 kPa, allowing LPG to be separated as the top product, while light naphtha and a portion of heavy naphtha are obtained at the bottom. This operation yields an LPG stream of 33,099.37 t/yr at 43.33 °C and 1034.21 kPa, in addition to wastewater and sour gas streams released from the overhead drum, with wastewater directed to the makeup and recycle water system [
15].
Figure 4 illustrates the simulated process flow diagram of the stripping and debutanization sections within the mass- and energy-integrated gas oil hydrocracking process.
The fractionation section consists of three distillation columns arranged in series. The process starts with a feed stream entering the first column at 379.44 °C and 137.89 kPa, together with a low-pressure vapor stream at 166.67 °C and 379.21 kPa. In this column, diesel, kerosene, and part of the heavy naphtha are recovered as overhead products, whereas the unconverted oil (UCO) is withdrawn from the bottom. After cooling and pressurization, 4.7% of the UCO (79,837.69 t/yr) is routed to the FCC unit at 456.11 °C and 15,506.31 kPa, while the remaining flow (1,623,969.44 t/yr) passes through an energy integration network and is recycled to the reaction stage. In the second column, a feed at 281.67 °C and 34.47 kPa allows for the separation of kerosene and a fraction of heavy naphtha at the top, with diesel collected as the bottom product. This diesel stream is subsequently cooled and treated through energy-integrated heat exchangers and an air cooler, yielding 933,685.06 t/yr of product at 43.33 °C and 101.35 kPa [
15].
The third column operates with an inlet stream at 190 °C and 75.84 kPa, producing heavy naphtha overhead and kerosene at the bottom. After passing through energy-integrated heat exchangers and an air cooler, the kerosene product reaches 530,346.69 t/yr at 43.33 °C and 101.35 kPa. Minor secondary emissions, such as recycled water and small quantities of fuel gas (treated as a byproduct), are discharged from the fractionator overhead drum; the recycled water is sent to the makeup and recycle water system. The heavy naphtha collected in the top drum is pumped and blended with the debutanizer bottom stream, which is rich in light and heavy naphtha, prior to entering the naphtha stripper column [
15].
Figure 5 illustrates the process flow diagram of the fractionation stage within the mass- and energy-integrated gas oil hydrocracking process that was obtained from the simulation.
The process subsequently enters the naphtha separation section, where the feed stream arrives at 97.78 °C and 151.68 kPa. At this stage, the naphtha is fractionated into light and heavy components, with the lighter fraction recovered overhead and the heavier fraction collected at the bottom. Secondary streams, including recycled water, are generated in the overhead drum and routed to the makeup and recycle water unit. The overhead stream, rich in light naphtha, is pumped out to produce 85,845.64 t/yr at 38.33 °C and 999.74 kPa. In contrast, the bottom stream is pumped and cooled through an air cooler and a heat exchanger, yielding a heavy naphtha product of 272,374.36 t/yr at 43.33 °C and 951.48 kPa [
15].
Figure 6 presents the process flow diagram of the naphtha separation section within the mass- and energy-integrated gas oil hydrocracking process that was obtained from the simulation.
Lastly, the makeup and water reuse stage describes the mass integration strategy based on the direct recirculation of wastewater and internal process effluents. Wastewater streams originate from the cold flash drum, the stripping column, and the debutanizer, whereas recycled water is obtained from the fractionation section and the naphtha splitter. This stage determines the fresh water demand of the process (166,734.68 t/yr) and the volume of wastewater produced (239,097.51 t/yr), which contains ammonia (NH
3) and hydrogen sulfide (H
2S) as contaminants. To minimize the allowable concentrations of NH
3 and H
2S in the wash water, separators and mixers are implemented to enable direct recycling. Before being reintroduced into the washing units, both water streams are conditioned using pumps and air coolers. Furthermore, after applying mass and energy integration, the overall energy consumption of the process is 869.43 MW [
15].
Figure 7 illustrates the process flow diagram corresponding to the makeup and water recycling stage of the mass- and energy-integrated gas oil hydrocracking process that was obtained from the simulation.
2.2. Sustainable Analysis Using the SWROIM Methodology
Figure 8 presents the framework applied to assess the sustainability performance of the integrated industrial-scale gas oil hydrocracking process from mass and energy perspectives. This assessment was carried out using the Safety and Sustainability Weighted Return on Investment Metric (SWROIM). The evaluation incorporated technical, energy, environmental, safety, and techno-economic dimensions as key sustainability criteria. For each dimension, a specific measurable indicator was defined. The SWROIM metric enables the integration of these aspects into a single numerical value that reflects the overall sustainability performance of the process. The methodology proposed in this work integrates economic, energy, environmental, technical, and safety considerations, and the SWROIM is calculated following Equation (1) from Guillen-Cuevas et al. [
11].
In this expression, the project’s annual net profit is denoted as AEP, while
represents the weighting factors associated with each sustainability indicator i. The terms
and
correspond to the current and desired values of sustainability indicator i, respectively; and TCI is the total capital investment. The allocation of
is determined according to the priority established by the decision-makers [
11].
Enhancing the sustainability indicators in a proposed design leads to an increase in the SWROIM, whereas a deterioration of these indicators results in a reduction in its value. This metric is evaluated against the project’s minimum acceptable threshold. Therefore, a project that shows a positive return on investment (ROI) but exhibits a low SWROIM should be disregarded. On the other hand, a project with strong sustainability performance may achieve an SWROIM that surpasses the traditional ROI, thereby supporting the decision to invest [
10]. The ROI is calculated using Equation (2).
where PAT is the profitability after tax, and TCI is the total capital investment [
20].
In this context, the safety criterion is evaluated through the Inherent Safety Index (ISI), determined using Equation (3), with a reference value of 24 that represents processes exhibiting a neutral level of inherent risk. Achieving an ISI value of 24 or below is associated with the removal of hazardous substances and the mitigation of operating conditions that present the highest risk within the process [
21].
where
is the Chemical Inherent Safety Index, and
is the Process Inherent Safety Index [
22].
Regarding the energy criterion, exergy efficiency (
) is considered and is determined using Equation (4), with a performance goal established at 99%. In chemical processing systems, exergy losses may be reduced through the recovery of waste streams and the reutilization of energy discharged at various process stages, thereby improving overall efficiency and approaching the intended performance objectives [
23].
where
is the total exergy flow lost, and
is the total exergy flow entering a system [
24].
Regarding the environmental criterion, the environmental impact is evaluated through the potential environmental impact (PEI) output rate, which is determined using Equation (5). Minimizing this indicator is a key requirement for advancing sustainable process design; therefore, a reduction target of 50% in PEI is established for the gas oil hydrocracking process. Additionally, the recovery of outlet streams that contain environmentally hazardous compounds can significantly contribute to lowering the overall environmental burden released to the environment [
25].
where
is the rate of exit of PEIs from the system due to the chemical interactions that occur within the system;
is the speed of exit of PEIs of the system due to the energy generation processes in the system;
and
are the output impacts of the system as a result of the release of unused energy due to energy production and chemical processes occurring within the system, respectively;
is the mass flow of output of stream j;
is the mass fraction of component k in stream j; and
is the overall Potential Environmental Impact of chemical substance k [
26].
Finally, within the technical criterion, the efficiency of the wastewater production rate (WPR), determined according to Equation (6), was considered, establishing a target value of 50%. The application of mass integration strategies, including the direct reuse of wastewater streams, allows a reduction in freshwater consumption and supports process optimization in terms of both environmental performance and energy efficiency [
15].
where
is the wastewater volumetric flow, and
is the freshwater volumetric flow.
For the base case study, the weighting factors
,
,
, and
are set to one (
), reflecting equal importance for environmental conservation, energy consumption reduction, wastewater reduction, and risk mitigation in the development of sustainable processes [
10].
Table 1 details the indicators, targets, and weighting factors for each parameter considered. Both methodological and engineering aspects were considered when selecting the target values for the sustainability indicators. A target value of 24 was established for the ISI indicator because it is the methodological threshold that distinguishes between an intrinsically safe process and an intrinsically unsafe process. For the energy (99% exergy efficiency), environmental (50% PEI reduction), and technical (50% WPR efficiency) indicators, target values were established based on engineering considerations, with the purpose of obtaining the maximum possible exergy efficiency without reaching ideality, reducing environmental impacts by 50% of their current value, and increasing WPR efficiency by up to 50% to decrease the amount of fresh water that becomes wastewater.
On the other hand, when making a methodological comparison, multi-criteria optimization could provide broader information than the SWROIM-based approach, but it would not necessarily lead to the same result. While the SWROIM methodology integrates economic, energy, environmental, technical, and safety criteria into a single quantitative indicator using predefined weighting factors, multi-criteria optimization treats these aspects as simultaneous and potentially conflicting objectives.
In this sense, the multi-criteria approach would generate a Pareto front that would allow for the explicit visualization of trade-offs between indicators—for example, between exergy efficiency, environmental impact, or inherent safety—without depending on a prior weighting. This would provide more structural information about the possible solutions and facilitate a subsequent selection based on strategic preferences. In contrast, SWROIM offers a more direct tool for decision-making as it synthesizes overall performance into a single value, which is especially useful when priorities are clearly defined. Therefore, both approaches are complementary: SWROIM is effective as an evaluation and comparison tool, while multi-criteria optimization would allow for a deeper analysis of the trade-offs between objectives in complex and integrated systems, identifying and prioritizing the most important problems.
2.3. Sensitivity Analysis of the SWROIM Assessment
To evaluate the influence of each selected indicator on the SWROIM, a sensitivity analysis was conducted by adjusting the corresponding weighting factors. The analysis followed a single-variation approach in which only one variable was modified per scenario while the remaining variables were kept constant. In this process, the weights assigned to the sustainability indicators were changed as presented in
Table 2, whereas the target indicators (
Table 1) were not altered. Four distinct scenarios were defined following the work developed by Aguilar-Vásquez et al. [
13] for a PVC production process, but in this case, the technical indicator was used instead of the social one. In the first scenario, the energy (
) dimension was prioritized (
) over the safety, environmental, and technical dimensions (
). In the second scenario, greater importance was assigned to the environmental (
) dimension (
) compared to the others (
). The third scenario emphasized the safety (
) dimension (
), while the remaining dimensions were assigned lower weights (
). Finally, the fourth scenario prioritized the technical (
) dimension (
) over the other aspects [
13].
Table 2 provides a summary of the weighting factors applied across the four case studies. It should be noted that formal weighting techniques such as the Analytic Hierarchy Process (AHP) or expert-based elicitation methods were not applied in this study since the objective of the sensitivity analysis was not to determine stakeholder-specific preference structures, but to systematically evaluate the relative influence of each sustainability dimension on the SWROIM value under controlled and comparable prioritization scenarios.