Cement production is one of the most important industries on the planet, and humans have relied on is use dating back to the dawn of civilization. Cement manufacturing has increased at an exponential rate, reaching 3 billion metric tons in 2015, representing a 6.3% annual growth rate and accounting for around 5–8% of global carbon dioxide (CO₂) emissions. Geopolymer materials, which are inorganic polymers made from a wide range of aluminosilicate powders, such as metakaolin, fly ash, and blast furnace or steel slags, have also been elicited for use due to concerns about the high energy consumption and CO₂ emissions connected with cement and concrete manufacturing. This study focused on the mechanical and durability properties of metakaolin in concrete production. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive spectroscopy (EDS) analyses were used to confirm the characteristics of kaolin and metakaolin. The results showed that 15 wt.% metakaolin can be used to partially replace cement, and that metakaolin, when synthesized with alkaline activators, can also be utilized as a geopolymer to totally replace cement in concrete production. For predicting the compressive strength of different concrete mixtures, few practical models have been presented. This research has shed light on the possibility of utilizing ecologically friendly materials in the building, construction, and transportation sectors to decrease carbon dioxide emissions.

Carbon fibers (CFs) are made mostly from a non-environmentally friendly polyacrylonitrile (PAN) and little from rayon. PAN-based CFs, require huge amount of energy for its production aside its contributions to the global CO₂ emission. Therefore, there is recourse to a more environmentally friendly sources of CFs biomass. Recently lignin has been recognized as a potential renewable raw material for carbon fibers to replace PAN-based. The magnitude and quality of CO₂ emission of lignin-based CFs are dependent on the processing route. On this premise; this review examines the various lignin-based CFs processing route adopted by researcher in the recent past to establish the most viable route with minimum carbon footprint emission. Outcome of the review shows that the major advantages of aromatic polymer (AP) generated precursor over PAN is the presence of higher quantity of guaiacyl units and oxygen content which makes the stabilization phase efficient and faster requiring less energy. Though there are several methods and options for the various stages of conversion of lignocellulosic biomass into CFs as highlighted in the study, establishing an optimum processing route will be a trade-off amongst various issues of concern; carcinogenic risk, carbon footprint emission, CFs Yield and mechanical strength of the CFs. Inferences from the study shows that the L-CF significantly produced reduced climatic impact in terms of CO₂ emission.

Lignocellulose is a renewable ubiquitous material that comprises cellulose, hemicellulose, and lignin. Lignin has been isolated from different lignocellulosic biomass via chemical treatments, but there has been little or no investigation carried out on the processing of lignin from brewers’ spent grain (BSG) to the best of authors’ knowledge. This material makes up 85% of the brewery industry’s byproducts. Its high moisture content hastens its deterioration, which has posed a huge challenge to its preservation and transportation; this eventually causes environmental pollution. One of the methods of solving this environmental menace is the extraction of lignin as a precursor for carbon fiber production from this waste. This study considers the viability of sourcing lignin from BSG with the use of acid solutions at 100 °C. Structural and thermal analyses were carried out on extracted samples, and the results were compared with other biomass-soured lignin to assess the proficiency of this isolation technique. Wet BSG sourced from Nigeria Breweries (NB), Lagos, was washed and sun-dried for 7 days. Tetraoxosulphate (VI) (H₂SO₄), hydrochloric (HCl), and acetic acid, each of 10 M, were individually reacted with dried BSG at 100 °C for 3 h and designated as H2, HC, and AC lignin. The residue (lignin) was washed and dried for analysis. Wavenumber shift values from Fourier transform infrared spectroscopy (FTIR) show that intra- and intermolecular OH interactions in H2 lignin are the strongest and possess the highest magnitude of hydrogen-bond enthalpy (5.73 kCal/mol). The thermogravimetric analysis (TGA) results show that a higher lignin yield can be achieved when it is isolated from BSG, as 82.9, 79.3, and 70.2% were realized for H2, HC, and AC lignin. The highest size of ordered domains (0.0299 nm) displayed by H2 lignin from X-ray diffraction (XRD) informs that it has the greatest potential of forming nanofibers via electrospinning. The enthalpy of reaction values of 133.3, 126.6, and 114.1 J/g recorded for H2, HC, and AC lignin, respectively, from differential scanning calorimetry (DSC) results affirm that H2 lignin is the most thermally stable with the highest glass transition temperature (T_g = 107 °C).

A way to avoid or minimize the side effect that could result in drug delivery to cells with increased efficiency and performance in the health rehabilitation process is to use biocompatible and biodegradable drug carriers. These are essentially biomaterials that are metallic, ceramic, or polymeric in nature. The sources of these materials must be biological in its entire ramification. The classification, synthesis, processing, and the applications to which these materials are put are the essential components of having suitable target cell drug carriers. This chapter will be devoted to discussing biomaterials suitable as drug carrier for use in the health-related matters of rehabilitation.

Chitin is chemically extracted from crustacean shells whose composition and structure differ from one another. It is reported that mineral acids distort chitin's physiochemical properties compared to organic acids. Investigations on the effectiveness of these acids on chitin isolation from crab and shrimp exoskeleton are carried out. Shell particles were demineralized using acetic acid (CH₃COOH) and HCl while NaOH was used for deproteinization. Acetic acid possesses low potency for complete CaCO₃ removal from crab shell while it fully demineralizes shrimp shell. With the use of CH₃COOH, the biopolymer extracted shows characteristics of chitin but with lower content and physicochemical properties compared to chitin isolated from the shells using HCl. Mineral acid (HCl) will thus isolate chitin from exoskeletons of marine invertebrates irrespective of their shell nature while organic acid (CH₃COOH) will be effective for soft shells whose embedded chitin content is more than the mineral content such as shrimp shells.