Molecular Weight Distribution Research Articles

Free radical copolymerization kinetics of bio-based dibutyl itaconate and n-butyl acrylate

The free radical copolymerization of dibutyl itaconate (DBI), a monomer derived from renewable resources, and n-butyl acrylate (BA) is investigated to explore the potential of incorporating itaconate monomers into commercial acrylic resins to enhance the sustainability of coating materials. Batch experiments were conducted at 50 °C and 80 °C, varying initial monomer and initiator concentrations as well as monomer compositions, with proton NMR and size exclusion chromatography used to analyze monomer conversion profiles and polymer molar mass distributions (MMDs). The data were analyzed using a kinetic model developed to guide the experimental studies and estimate key kinetic parameters controlling copolymer composition, polymerization rate and polymer MMDs. The use of the more reactive BA as comonomer significantly increases the conversion and molar mass of the resulting copolymer. Furthermore, semi-batch operating conditions similar to current industrial practice can incorporate a substantial fraction of DBI into acrylic copolymer resins, thus enhancing their sustainability profile.

Chromatographic analysis of branched and debranched starch structure: Variability of their results

Starch structure determination is crucial for understanding its properties and applications. However, method-dependent variations in size determination can lead to ambiguous interpretations. This study investigates the ambiguities in starch structure determination by evaluating the variation in size of four commercial branched starches as determined by average molar mass, gyration radius, hydrodynamic radius, and chain-length distribution. The starches were analyzed using high-performance size-exclusion chromatography (HPSEC) coupled with multi-angle laser light scattering (MALLS) and refractive index detector (RI), and after debranching by HPSEC-RI and high-performance anion-exchange chromatography (HPAEC) with pulsed amperometric detector (PAD). MALLS-derived MW values for amylose and amylopectin were higher than those obtained using the hydrodynamic volume method. The molecular weight of amylopectin chains, determined by the degree of polymerization (DP), ranged between 2.1 and 2.9 × 103 g/mol for short chains, and between 4.1 × 103 and 1.1 × 104 g/mol for long chains. Differences in amylopectin chain content were observed between HPSEC-RI and HPAEC-PAD, highlighting the complementary nature of these techniques. The study underscores the need for standardizing chromatography-based methodologies in starch research, particularly with the advent of new technologies.

Synthesis of basic amino acid-grafted lignin for use as a high-performance pigment dispersant.

Lignin is a promising dispersant due to its hyperbranched polymer structure, low cost, renewability and abundant availability. However, its use is limited by its broad molecular weight distribution, inhomogeneity, and low content of hydrophilic functional groups. In this work, lignin was functionalized with alkaline amino acids (EHL-AA) to enhance water solubility and molecular weight uniformity. The results showed that EHL-AA significantly improved the dispersion of pigment Red 57:1 (P.R.57:1) in aqueous solutions, reducing the required dosage by 50 % compared to commercial small-molecule dispersants. Additionally, histidine modified lignin (EHL-His) exhibited superior stability for P.R.57:1 compared to commercial lignosulfonate (REAX 85A). Molecular dynamics simulations further revealed that showed that EHL-His had the highest electrostatic potential difference and the largest absolute value of negative ESP. The adsorption of EHL-His onto the P.R.57:1 surface followed the pseudo-second-order kinetic model and the Langmuir model, with EHL-His showing a higher Langmuir constant (b) than REAX 85A, indicating the strongest interaction with the pigment. In summary, this work advances pigment dispersion technology and promotes the high-value utilization of lignin.

Catalyzing PET-RAFT Polymerizations Using Inherently Photoactive Zinc Myoglobin.

Protein photocatalysts provide a modular platform to access new reaction pathways and affect product outcomes, but their use in polymer synthesis is limited because co-catalysts and/or co-reductants are required to complete catalytic cycles. Herein, we report using zinc myoglobin (ZnMb), an inherently photoactive protein, to mediate photoinduced electron/energy transfer (PET) reversible addition-fragmentation chain transfer (RAFT) polymerizations. Using ZnMb as the sole reagent for catalysis, photomediated polymerizations of N,N-dimethylacrylamide in PBS were achieved with predictable molecular weights, dispersity values approaching 1.1, and high chain-end fidelity. We found that initial apparent rate constants of polymerization increased from 4.6×10-5 s-1 for zinc mesoporpyhrin IX (ZnMIX) to 6.5×10-5 s-1 when ZnMIX was incorporated into myoglobin to yield ZnMb, indicating that the protein binding site enhanced catalytic activity. Chain extension reactions comparing ZnMb-mediated RAFT polymerizations to thermally-initiated RAFT polymerizations showed minimal differences in block copolymer molecular weights and dispersities. This work enables studies to elucidate how protein modifications (e.g., secondary structure folding, site-directed mutagenesis, directed evolution) can be used to modulate polymerization outcomes (e.g., selective monomer additions towards sequence control, tacticity control, molar mass distributions).

Optimization of extraction for efficient recovery of kenaf seed protein isolates: evaluation of physicochemical and techno-functional characteristics.

Kenaf seeds are a rich source of protein; however, finding the best extraction method is crucial to obtaining high-quality protein from these underutilized seeds. This research devised an optimized extraction process for best recovery of kenaf seeds protein using response surface methodology. The key parameters affecting the yield and protein content were optimized, including extraction pH (2-11), seed:water ratio (5:1-50:1), temperature (30-90 °C), and duration (20-360 min). The physicochemical and techno-functional properties of kenaf seed protein isolates (KSPIs) were examined. A maximum protein yield of 12.05 g/100 g with purity level 91.94 g/100 g was obtained using an optimized extraction with pH 11.0, seed:water ratio 50:1, 360 min duration, and temperature 50 °C. The oil and water retention capacities of KSPI were 1.14 mL g-1 and 1.37 mL g-1 respectively. After 30 min at pH 7, KSPIs demonstrated remarkable emulsion capacity (83.12%) and stability (75.63%), along with high foaming capacity (106%) and stability (18.3%). As per high-performance liquid chromatography analysis, arginine, glutamic acid, leucine, phenylalanine, and lysine were the most abundant amino acids detected in KPSIs. The KSPIs' globular protein structure was successfully verified using analytical approaches, including Fourier transform infrared spectroscopy, protein fraction ratios, and differential scanning calorimetry. Sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis revealed that KPSI has a molecular weight distribution ranging from 10 kDa to 50 kDa. The results of this study support the application of the proposed response-surface-methodology-optimized extraction method for efficient recovery of high-quality kenaf seed proteins that meet the necessary physicochemical and techno-functional requirements. © 2024 Society of Chemical Industry.

Adjustment of Electronic (OMe and NO2) and Steric (CHPh2) Effects in Bis(imino)pyridinyliron Precatalysts for Producing High Molecular Weight Linear PE

AbstractBased on variations in steric and electronic substituents in the N‐aryl unit, a set of five 2‐[1‐(arylimino)ethyl]‐6‐[1‐(2‐benzhydryl‐4‐nitro‐6‐methoxyphenylimino)ethyl]pyridyliron dichloride complexes (where aryl=2,6‐dimethylphenyl (Fe‐Me2), 2,6‐diethylphenyl (Fe‐Et2), 2,6‐diisopropyl (Fe‐iPr2), 2,4,6‐trimethylphenyl (Fe‐Me3), 2,6‐diethyl‐4‐methylphenyl (Fe‐Et2Me)) were synthesized and investigated for ethylene polymerization. Their structures and compositions were confirmed by FTIR, elemental analysis, and X‐ray diffraction analysis (Fe‐Et2 and Fe‐iPr2), revealing a distorted square pyramidal geometry around the iron center. When activated in situ with MAO or MMAO, these iron complexes acted as highly active precatalysts, achieving activity levels up to 29.0×106 gPE molFe−1 h−1 for a 5‐min reaction at 60 °C. A notable characteristic of these precatalysts is their high thermal stability, maintaining significant activity (2.0×106 gPE molFe−1 h−1) at temperatures up to 100 °C. Importantly, the incorporation of strong electron‐withdrawing groups in the ligand structure favored the production of polyethylene with high molecular weights (up to 407.5 kg mol−1) across various reaction conditions, surpassing those of most previously reported iron complexes. Moreover, less hindered iron precatalysts showed higher activity compared to more hindered ones. However, the trend reversed when comparing the molecular weight of obtained polyethylene: more sterically hindered precatalysts yielded higher molecular weight polymers. The molecular weight distributions ranged from monomodal to bimodal with broad dispersity. DSC thermograms and 1H/13C NMR spectra of the polyethylene confirmed its highly linear microstructure, evidenced by sharp endothermic peaks and pronounced singlets for the −(CH2)n− repeating units.

Catalyzing PET‐RAFT Polymerizations Using Inherently Photoactive Zinc Myoglobin

AbstractProtein photocatalysts provide a modular platform to access new reaction pathways and affect product outcomes, but their use in polymer synthesis is limited because co‐catalysts and/or co‐reductants are required to complete catalytic cycles. Herein, we report using zinc myoglobin (ZnMb), an inherently photoactive protein, to mediate photoinduced electron/energy transfer (PET) reversible addition‐fragmentation chain transfer (RAFT) polymerizations. Using ZnMb as the sole reagent for catalysis, photomediated polymerizations of N,N‐dimethylacrylamide in PBS were achieved with predictable molecular weights, dispersity values approaching 1.1, and high chain‐end fidelity. We found that initial apparent rate constants of polymerization increased from 4.6×10–5 s−1 for zinc mesoporpyhrin IX (ZnMIX) to 6.5×10–5 s−1 when ZnMIX was incorporated into myoglobin to yield ZnMb, indicating that the protein binding site enhanced catalytic activity. Chain extension reactions comparing ZnMb‐mediated RAFT polymerizations to thermally‐initiated RAFT polymerizations showed minimal differences in block copolymer molecular weights and dispersities. This work enables studies to elucidate how protein modifications (e.g., secondary structure folding, site‐directed mutagenesis, directed evolution) can be used to modulate polymerization outcomes (e.g., selective monomer additions towards sequence control, tacticity control, molar mass distributions).

Hydrolysates of mare's milk proteins. Immunochemical and physico-chemical characteristics

In recent years, the attention of specialists has been attracted by a significant increase in allergic diseases, especially among children. Enzymatic hydrolysis with the participation of peptidases is considered the most effective measure to reduce the allergenicity of milk proteins. The study of the features of protein proteolysis by various enzymes, aimed at establishing optimal process parameters, is the subject of research in the production of hydrolysates with specified properties: a certain peptide and amino acid profile, reduced antigenic properties. At the same time, for a correct preclinical assessment of the safety and potential effectiveness of specialized food products, it is not enough only to determine the molecular weight distribution of peptide fractions in the composition. A necessary additional and informative indicator of reducing the potential allergenicity of the hydrolysate is the degree of preservation of the antigenic properties of the initial protein (residual antigenicity), determined by immunochemical methods. The preparation and subsequent comprehensive assessment of enzymatic hydrolysates of mare's milk proteins is of considerable interest, since, according to the results of clinical studies, it was suggested that upon allergy to cow's milk proteins mare's milk can be considered hypoallergenic. The purpose of this work was to obtain enzymatic hydrolysates of mare's milk proteins using domestic enzymes and their further physico-chemical and immunochemical characteristics. The object of the study was mare's milk protein obtained from skimmed mare's milk powder as a protein substrate. Two samples of enzymes from various manufacturers of the Russian Federation were used in the work. The results of the conducted studies show that the peptide profiles of hydrolysates vary greatly depending on the enzyme used, however, the multiplicity of antigenicity reduction practically does not depend on the nature of the enzyme, and does not depend on an increase in the enzyme/substrate ratio. The peptide profile and the multiplicity of reducing the antigenicity of hydrolysates of mare's milk proteins are influenced by ultrafiltration treatment of the obtained hydrolysates, which allows reducing the content of antigenic structures in the final product by several orders of magnitude.

Shaping of Molecular Weight Distribution Using Self-Optimizing Control Based on Moments

Shaping of Molecular Weight Distribution Using Self-Optimizing Control Based on Moments

Impact of molecular architecture and draw ratio on enhancement of targeted mechanical properties of machine direction oriented polyethylene films produced after blown film extrusion

Conventional multi-material multi-layer flexible packaging offers excellent properties. However, it has recycling challenges, necessitating a shift to mono-material multi-layer flexible packaging for example all-polyethylene (PE) packaging which can be tailored through various synthesis and processing methods for different layers. In this work, we study how the key molecular properties (number-average molecular weight ( Mn), weight-average molecular weight ( M w), molecular weight distribution (MWD), comonomer content (short chain branching)) and machine direction orientation (MDO) process draw ratio (MDX) influence the final morphology and mechanical properties of MDO-PE films which are intended as the outer layer of mono-material all-polyethylene multi-layer flexible packaging. Five PE grades and various blends were extruded and blown into films. Selected blown films were machine direction oriented to obtain the final MDO-PE films. Furthermore, one selected PE blown film was processed at different MDO process draw ratios while keeping other process parameters constant. From the molecular properties point of view, the higher molecular weight fractions provide a higher possibility for uniform stretching whereas lower molecular weight fractions provide a higher natural draw ratio and therefore higher modulus and stiffness enhancement. Further, the results show that increasing MDO process draw ratio leads to more fibrillation and increased crystallinity. Consequently, the tensile modulus and stiffness at the higher draw ratios increase as well and are comparable to conventionally used polymers in outer layers of multilayer flexible packaging. Thus, this work demonstrates that MDO-PE films with enhanced modulus can provide sufficient stiffness for the design of outer layer of mono-material multi-layer all-PE packaging which presents higher potential for mechanical recyclability.

Kinetic Investigation of the Emulsion Polymerization of Vinylidene Fluoride

AbstractPoly(vinylidene fluoride) (PVDF) is among the most produced fluoropolymers, second only to polytetrafluoroethylene. Despite its popularity, the complex microstructural properties achieved during the polymerization are not well documented in the literature. In particular, available models only track the chain length distribution of the polymer, while neglecting the distribution of other important properties, affecting the final behavior of the product. In this work, a 2D kinetic model, evaluating not only the chain length but also the number of terminal double bonds (TDBs) per chain, is developed. The numerical solution of the model is achieved by fractionating the population of polymer chains into classes with a specific number of TDBs and using the method of moments for each class. The model results are compared with experimental evidences for the amount of produced polymer, moles of main chain‐ends, number, and weight average molecular weight as well as full molecular weight distribution. Based on this comparison, kinetic parameters are estimated by optimization using genetic algorithm. The model reliability is finally verified using additional experimental data at different temperatures and amounts of initiator.

Understanding Selectivity in Product Distributions from Laser Ablation of Organic Liquids.

Pulsed laser ablation in organic solvents is widely used to produce oxide-free metal and metal carbide nanoparticles, often with carbon coatings resulting from laser-induced reactions in the organic solvent. To gain insight into how the molecular structure of the solvent affects these reaction pathways, this work investigates ablation of the C6H14 isomers n-hexane, 2-methylpentane, and 3-methylpentane through characterization of the gas and liquid products with mass spectrometry. Ablation of each C6H14 isomer produces a distinct distribution of product molecular weights and isomers. 2-methylpentane preferentially produces C3 and C9, whereas 3-methylpentane produces C2, C4, C8, and C10 products. These preferential product distributions, along with the lack of such selectivity in n-hexane, arise from differences in the most favorable C-C bond scission pathways in each C6H14 isomer. Moreover, the particular isomers of C8H18, C9H20, C10H22, and C12H26 produced by ablation of each C6H14 isomer indicate that the vast majority of reaction pathways involve addition reactions between a fragment radical and parent C6H14 or between two C6H14 molecules, without molecular rearrangement. This propensity toward direct addition suggests that the chemical reactions induced by ultrashort pulsed laser ablation proceed on faster time scales than those of radical rearrangements.

Study on high-temperature emission behaviors of crumb rubber modified asphalt: Experimental analysis and molecular simulation approach

The harmful emissions produced during the manufacturing and construction processes of crumb rubber modified asphalt (CRMA) significantly hinder its widespread application. Addressing this issue hinges on a thorough investigation into the mechanism governing its high-temperature emissions. This study employed microscale testing methods to analyze the microstructure and chemical property disparities between CRMA and base asphalt (BA). Subsequently, the impacts of varying crumb rubber (CR) content, experimental temperature, and sulfur stabilizer dosage on the high-temperature emissions of CRMA were investigated. Furthermore, comparative analyses of the molecular weight distribution, emission species, and CR crosslink density in asphalt after the fume experiment were conducted to further elucidate the high-temperature emission mechanisms. Finally, molecular simulation techniques were employed to analyze the interactions between CR and the four fraction molecules of asphalt at the microscale. The results indicated that the fume release volume of CRMA initially decreased and then increased with the addition of CR, while both the experimental temperature and sulfur stabilizer content exhibited a positive correlation with emission volume. CR reduced the volatilization of some small molecular hydrocarbons in the BA by absorbing light fractions. Meanwhile, excessive swelling caused the crosslinking density of CR to decrease by 77 %, which led to the release of toxic substances. At 20% CR content, the overall emissions of CRMA achieve their lowest level; however, the emission of toxic gases does not diminish. Molecular simulations have also confirmed the above results, showing that there is a strong interaction between CR and the light fractions. Compared with asphaltene molecules, rubber molecules had higher molecular polarity and stronger adsorption behavior for light fraction molecules.

Low-Dispersity Polymers via Free Radical Alternating Copolymerization: Effects of Charge-Transfer-Complexes.

Alternating copolymers are crucial for diverse applications. While dispersity (Ð, also known as molecular weight distribution, MWD) influences the properties of polymers, achieving low dispersities in alternating copolymers poses a notable challenge via free radical polymerizations (FRPs). In this work, we demonstrated an unexpected discovery that dispersities are affected by the participation of charge transfer complexes (CTCs) formed between monomer pairs during free radical alternating copolymerization, which have inspired the successful synthesis of various alternating copolymers with low dispersities (>30 examples, Ð=1.13-1.39) under visible-light irradiation. The synthetic method is compatible with binary, ternary and quaternary alternating copolymerizations and is expandable for both fluorinated and non-fluorinated monomer pairs. DFT calculations combined with model experiments indicated that CTC-absent reaction exhibits higher propagation rates and affords fewer radical terminations, which could contribute to low dispersities. Based on the integration of Monte Carlo simulation and Bayesian optimization, we established the relationship map between FRP parameter space and dispersity, further suggested the correlation between low dispersities and higher propagation rates. Our research sheds light on dispersity control via FRPs and creates a novel platform to investigate polymer dispersity through machine learning.

Charge Mediated Changes to the Intrinsic Viscosity of Biopolymer Systems

A theoretical approach is presented to quantify the effect of ionic strength on the swelling and shrinkage of the hydrodynamic coil size of a generic biopolymer. This was conducted in view of extraction methods that often utilize acids and alkali combinations and, therefore, invariably impact the levels of salt found in commercially available biopolymers. This approach is supplemented by intrinsic viscosity measurements for the purpose of validation across a variety of biopolymer architectures, type of functionalization, as well as the quoted molar mass. By accurately capturing the magnitude of change in the coil size, it is discussed how a biopolymer coil size is far more sensitive to changes in the ionic strength than it is to the molar mass (or contour length) itself. In turn, it is highlighted why the current characterization strategies that make use of weight-averaged molar mass are prone to errors and cannot be used to establish structure—property relationships for biopolymers. As an alternative, the scope of developing an accurate understanding of coil sizes due to changes in the “soft” interactions is proposed, and it is recommended to use the coil size itself to highlight the underlying structure—property relationships.

New insights into the catalyst and cocatalyst pre‐contact process in ethylene copolymerization

AbstractThe influence of pre‐contacting time and temperature as well as mixing intensity on polyethylene copolymerization has been investigated employing DSC, rotational rheometry tests, as well as particle size distribution analysis. For this purpose, a commercial‐supported Ziegler–Natta catalyst has been pre‐contacted with Teal as cocatalyst under different time, temperature, and stirring speed followed by similar polymerization process. It was found that the increase in mixing intensity has no impact on rheological properties; it causes increase in crystallinity percentage of polymer due to better distribution of active centers. Moreover, the pre‐contacting time represents the most impact on catalyst activity and rheology of polymer powder while the pre‐contacting temperature changes is mostly effective on controlling the morphology of polymer. Additionally, the results reveal that 10‐min pre‐contacting of catalyst and Teal under 10°C and stirring speed of 500 rpm was accompanied by highest catalyst activity and lowest content of fine particles.Highlights Pre‐activation was studied under different time and temperature. Adjusting pre‐contacting time influences the polymer morphology. Pre‐contacting under lower temperature results in narrower molecular weight distribution.

The Role of Ligand Exchange in Salen Cobalt Complexes in the Alternating Copolymerization of Propylene Oxide and Carbon Dioxide.

A comparative study of the copolymerization of racemic propylene oxide (PO) with CO2 catalyzed by racemic (salcy)CoX (salcy = N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-diaminocyclohexane; X = perfluorobenzoate (OBzF5) or 2,4-dinitrophenoxy (DNP)) in the presence of a [PPN]Cl ([PPN] = bis(triphenylphosphine)iminium) cocatalyst is performed in bulk at 21 °C and a 2.5 MPa pressure of CO2. The increase in the nucleophilicity of an attacking anion results in the increase in the copolymerization rate. Racemic (salcy)CoX provides a high selectivity of the copolymerization, which can be higher than 99%, and the living polymerization mechanism. Poly(propylene carbonate) (PPC) with bimodal molecular weight distribution (MWD) is formed throughout copolymerization. Both modes are living and are characterized by low dispersity, while their contribution to MWD depends on the nature of the attacking anion. The racemic (salcy)CoDNP/[PPN]DNP system is found to be preferable for the production of PPC with a high yield and selectivity.

Synthesis of alternating polyesters using a dual catalytic system of alkali metal alkoxides and crown ether

In this study, a dual catalytic system that merges crown ether with alkali metal alkoxides (AMA) is utilized in the ring-opening alternating polymerization (ROAP) of phthalic anhydride (PA) and propylene oxide (PO). This method streamlines the production of polyesters characterized by a fully alternating sequence, a modifiable molar mass (achieving up to 59.3 kg mol−1), and a narrow molar mass distribution (ÐM < 1.26). Analysis of various commercially available AMAs, notably sodium ethoxide (EtONa), sodium methoxide, and lithium ethoxide, in tandem with crown ethers (15-crown-5 and 18-crown-6), underscores the superior catalytic efficacy of the EtONa and 18-crown-6 pairing. This heightened efficiency is attributed to the coordination of crown ether with alkali metal ions, thereby boosting the nucleophilicity of terminal alkoxide anions. The methodology has been successfully deployed in the ROAP of PA, norbornene anhydride, and multiple epoxides, while also simplifying the creation of aliphatic–aromatic block polyesters from a mixture of PA, PO, and lactide. This strategy presents a straightforward approach to polyester production, thus making significant contributions to the evolution of polyester synthesis technology.

Influence of high cis-1,4-liquid polydienes on properties of carbon-black filled composites

High cis-1,4 liquid polybutadiene (cLBR) and polyisoprene (cLIR) with narrow molecular weight distribution were prepared by the chain-transfer coordination polymerization. The effects of cLBR and cLIR on the physical and dynamic mechanical properties of carbon-black filled composites containing single polybutadiene (PBR) or a blend of PBR/polyisoprene (PIR), were investigated. The results showed that cLBR and cLIR effectively ameliorated filler dispersion compared with the treated distillate aromatic extract (TDAE) oil. The wet skid resistance and rolling resistance of vulcanized PBR/PIR composites plasticized with 5 phr cis-1,4 liquid rubbers were significantly improved. Therefore, a new type of plasticizers cLBR and cLIR that are environmental benign and highly compatible with matrix rubbers, has been discovered to replace the conventional TDAE oil used in fabricating the “green” tyres.

Extraction and Nutritional Value of Soybean Meal Protein Isolate

The increasing protein demand driven by global population growth necessitates the search for an alternative protein source. Soybean meal (SM), with approximately 47–49% proteins, is a viable option. Soymeal protein isolate (SMPI) is a cost-efficient protein source with a well-balanced amino acid profile, making it suitable for addressing this demand. This study attempts to address the lack of information regarding the extractability and nutritional potential of SMPI obtained utilizing a weak base and recoverable solvent. In this work, the structural and compositional studies of SMPI, as well as the aqueous extractability of ammonium hydroxide (NH4OH), are investigated. Furthermore, we examined the effects of heat treatment during oil extraction, where a comparison between protein isolates from soymeal and whole soybeans was carried out. The maximum extraction yield of 24.1% was achieved by increasing the concentration of NH4OH from 0.25–1%. In comparison to the soy protein isolate from whole soybeans (SPI), the compositional analysis report revealed that SMPI had higher levels of crude protein, moisture, and ash content, but lower levels of fat and carbohydrates. Furthermore, the examination of the amino acid composition confirms the existence of vital amino acids in SMPI. The amino acid score indicates that methionine, lysine, and threonine are the limiting amino acids. SMPI and SPI share structural and functional group similarities, as demonstrated by Fourier-transform infrared spectroscopy. Gel electrophoresis using sodium dodecyl sulfate–polyacrylamide shows that the protein molecular weight distributions of SPI and SMPI are similar. This in-depth evaluation emphasizes the advantages of SM by advocating its application in other sectors beyond conventional animal feed, such as nutritional supplements and bio-based products, and by improving the environmental sustainability and global food chains.