Today, hydrogen is one of the best options for generating electrical energy, for both industrial and residential use. The greatest volume of hydrogen produced today derives from processes that utilize petroleum. Although hydrogen has numerous benefits, continuing to produce it by these means is undesirable. This document presents a review of the literature on biohydrogen production based on an analysis of over 15 types of terrestrial and marine biomasses. The fundamental components of different production systems are described, with a focus on the thermochemical processes of pyrolysis and gasification, which have been identified as two of the most effective, practical ways to produce hydrogen from biomass. It also discusses catalysts, solid residues, and residual water that are used in the thermochemical production of biohydrogen. The article ends with an analysis of hydrogen and its benefits as an energy option with great potential in the short term to participate in the transition from fossil fuels.

This study presents a prospective study for the potential exploitation of pelagic Sargassum spp. as a solid biofuel energy source. It was carried out in three stages. First we conducted a morphological, physical-chemical, and structural characterization using scanning electron microscopy (SEM), infrared spectroscopy (FTIR), and X-ray diffraction (DRX), respectively. Second we evaluated the material’s functional properties as a solid biofuel based on its calorific value and the quantification of polymeric components like hemicellulose, cellulose, and lignin, as well as thermogravimetric and differential analysis to study the kinetics of its pyrolysis and determine parameters like activation energy (E_a), reaction order (n), and the pre-exponential factor (Z). Third we analyzed the energetic potential considering the estimated volume of pelagic Sargassum spp. that was removed from beaches along the Mexican Caribbean coast in recent years. Results of the kinetic study indicate that Sargassum spp. has an enormous potential for use as a complement to other bioenergy sources. Other results show the high potential for exploiting these algae as an energy source due to the huge volumes that have inundated Caribbean, West African, and northern Brazil shorelines in recent years. As a solid biofuel, Sargassum spp. has a potential energy the order of 0.203 gigajoules (GJ)/m³. In the energy matrix of the residential sector in Mexico, its potential use as an energy source is comparable to the national consumption of firewood. The volume of beachcast Sargassum spp. that was removed from ~8 km of coastline around Puerto Morelos, Mexico in 2018–2019, could have generated over 40 terajoules/year of solid biofuel.

Today, energy use is an important and urgent issue for economic development worldwide. It is expected that raw material in the form of biomass and lignocellulosic residues will become increasingly significant sources of sustainable energy in the future because they contain components such as cellulose, hemicellulose, lignin, and extractables with high energy-producing potential. It is then essential to determine the behavior of these materials during thermal degradation processes, such as pyrolysis (total or partial absence of air/oxygen). Pyrolyzed biomass and its residual fractions can be processed to produce important chemical products, such as hydrogen gas (H₂). Thermogravimetric (TGA) analysis and its derivative, DTG, are analytical techniques used to determine weight loss as a function of temperature or time and associate changes with certain degradation and mass conversion processes in order to evaluate kinetic properties. Applying kinetic methods (mathematical models) to degradation processes permits obtaining several useful parameters for predicting the behavior of biomass during pyrolysis. Current differential (Friedman) and integral (Flynn–Wall–Ozawa, Kissinger–Akahira–Sunose, Starink, Popescu) models vary in their range of heating speeds (β) and degree of advance (α), but some (e.g., Kissinger’s) do not consider the behavior of α. This article analyzes the results of numerous kinetic studies using pyrolysis and based on thermogravimetric processes involving over 20 distinct biomasses. The main goal of those studies was to generate products with high added value, such as bio-char, methane, hydrogen, and biodiesel. This broad review identifies models and determines the potential of lignocellulosic materials for generating bioenergy cleanly and sustainably.

For the first time, a study has been carried out on the pyrolysis of wood residues from Pinus pseudostrobus, Pinus leiophylla and Pinus montezumae, from an area in Western México using TGA analysis to determine the main kinetic parameters (Ea and Z) at different heating rates in a N₂ atmosphere. The samples were heated from 25 °C to 800 °C with six different heating rates 5–30 °C min⁻¹. The Ea, was calculated using different widely known mathematical models such as Friedman, Flynn-Wall-Ozawa and Kissinger-Akahira-Sunose. The Ea value of 126.58, 123.22 and 112.72 kJ/mol (P. pseudostrobus), 146.15, 143.24 and 132.76 kJ/mol (P. leiophylla) and 148.12, 151.8 and 141.25 kJ/mol (P. montezumae) respectively, was found for each method. A variation in Ea with respect to conversion was observed with the three models used, revealing that pyrolysis of pines progresses through more complex, multi-stage kinetics. FT-IR spectroscopy was conducted to determine the functional groups present in the three species of conifers. This research will allow future decisions to be made, and possibly, to carry out this process in a biomass reactor and therefore the production of H₂ for the generation of energy through a fuel cell.

Diverse methodologies exist to determine the chemical composition, proximate analysis, and calorific value of biomass. Researchers select and apply a specific methodology according to the lignocellulosic material they study and the budgetary resources available. In this project, we determined the primary chemical constitution and proximate analysis of Prosopis laevigata (Humb. & Bonpl.) Jonhst wood using a traditional chemical method and a novel procedure based on the deconvolution of the DTG signal produced by TGA. The highest calorific value was verified using a calorimetric pump based on mathematical models. We also conducted elemental analysis and a microanalysis of ash, and applied Fourier transform infrared spectroscopic analysis (FT-IR). The means of the results obtained by the chemical method and TGA-DTG, respectively, were: hemicelluloses 7.36%–(8.72%), cellulose 48.28%–(46.08%), lignin 30.57%–(32.44%), extractables 13.53%–(12.72%), moisture 2.03%–(4.96%), ash 1.77%–(1.90%), volatile matter 75.16%–(74.14%), and fixed carbon 23.05%–(18.93%). The procedure with the calorimetric pump generated a calorific value above 20.16 MJ/kg. The range generated by the various models was 18.23–21.07 MJ/kg. The results of the elemental analysis were: carbon 46.4%, hydrogen 6.79%, oxygen 46.43%, nitrogen 0.3%, and sulfur 0.5%. The microanalysis of ash identified 18 elements. The most abundant ones were potassium ˃ calcium ˃ sodium. Based on the infrared spectrum (FT-IR) of Prosopis laevigata wood, we detected the following functional groups: OH, C-H, C=O, CH_2, CH₃, C-O-C, C-OH, and C4-OH. Our conclusion is that the TGA-DTG method made it possible to obtain results in less time with no need for the numerous reagents that chemical procedures require. The calorific value of P. laevigata wood is higher than the standards. Finally, according to our results, proximate analysis provides the best model for calculating calorific value.