Excess Reactant Research Articles

Adsorption of l-Cysteine and Cysteamine on Zinc Oxide Nanoparticles.

The reaction of l-cysteine and cysteamine hydrochloride with zinc oxide nanoparticles (ZnO NPs), by stirring excess reactant with the NPs in ethanol, has been studied by thermal gravimetric analysis (TGA), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Raman spectroscopy. l-Cysteine adsorption occurs via the thiol functional group, and there is no evidence for bonding via the carboxylic acid or amine functionalities. However, Raman spectroscopy and XPS reveal some protonated thiol, suggesting unbound l-cysteine is also present, as confirmed by XRD that shows the presence of l-cysteine crystallites. In the case of cysteamine/ZnO, TGA indicates that a large fraction of the sample is organic, and Raman spectroscopy reveals a dramatic shift in the C-S stretch from 796 cm-1 for unreacted cysteamine to 837 cm-1 for the reacted cysteamine. It is postulated that the acidic and chelating nature of the reaction causes dissolution of some Zn2+ ions that form a Zn(II) coordination complex with cysteamine. These studies have implications for biomolecular applications in which ZnO nanoparticles are used for biosensors, bioimaging, and drug delivery.

New Twists in the Chemistry of Thioureas: 1,3-Thiazolidines as a Vector of Sustainability.

This study introduces a sustainable and pioneering cascade synthesis of 1,3-thiazolidine derivatives under eco-friendly conditions. The methodology transcends traditional approaches yielding complex novel compounds with unique N,S-heterocyclic structures. By operating at room temperature, utilizing green solvents, and minimizing excess of reactants, this procedure offers an innovative pathway for sustainable chemical development. Notably, this method not only prioritizes sustainability but also delivers high-purity products with exceptional yields. The simplicity of the process, requiring only a simple filtration and featuring short reaction times, underscores its efficiency and utility.

Study of Ni-Co-ZrO2/Al2O3 Catalysts for Carbon Dioxide Reforming of Methane at Low CO2

This work studied the composition of Ni-Co-ZrO2/Al2O3 catalyst on properties and efficiency of catalysts for carbon dioxide reforming of methane (CMR) when CO2 was fed as the limiting reagent and CH4 as the excess reactant. 9wt%Ni-1wt%ZrO2/Al2O3, 4.5wt%Ni-4.5%wtCo-1wt%ZrO2/Al2O3, 9wt%Co-1wt%ZrO2/Al2O3 and 7wt%Co-3wt%ZrO2/Al2O3 catalysts were prepared by wet impregnation method. The physicochemical properties of present catalysts were characterized by XRD, N2 adsorption-desorption H2-TPR and CO2-TPD. The CRM performance was determined in a tubular fixed-bed reactor at 600 °C for 6 h with limiting of carbon dioxide. The carbon deposition on spent catalysts were examined by TGA. The results showed that Co-ZrO2 catalysts provided greater activities, selectivity toward H2 and stability than Ni-ZrO2 and Ni-Co-ZrO2 catalysts. 9wt%Co-1wt%ZrO2/Al2O3 provided higher reactant conversions and H2/CO ratio than 7wt%Co-3wt%ZrO2/Al2O3 while the minimum coke formation was observed on spent 7wt%Co-3wt%ZrO2/Al2O3. It is because oxophilic properties and oxygen vacancy sites in Co-ZrO2 increase CO2 dissociative adsorption as well as oxygen transport on the catalyst surface. HIGHLIGHTS This work developed Ni-Co-ZrO2/Al2O3 catalysts for carbon dioxide reforming of methane (CMR) when CO2 is fed as the limiting reagent demonstrated petroleum refinery application. Remarkable points of this work are revealed below. Co-ZrO2 catalysts provided greater reactant activities, selectivity toward H2 and stability than Ni-ZrO2 and Ni-Co-ZrO2 The oxophilic property accompanied with oxygen vacancy sites in Co-ZrO2 increase CO2 dissociative absorption and oxygen transport on the catalyst surface. 9wt%Co-1wt%ZrO2/Al2O3 provided relative highest reactant conversions and highest H2/CO ratio. 7wt%Co-3wt%ZrO2/Al2O3 presented the minimum coke formation. GRAPHICAL ABSTRACT

Thermal atomic layer deposition of aluminum oxide, nitride, and oxynitride: A mechanistic investigation

Atomic layer deposition (ALD) has been proven to be a versatile method for the deposition of thin films of various materials. It yields films with exceptional conformality and allows tunable film compositions with control of film thickness at the atomic level. Thin films of Al oxide, nitride, and oxynitride are deposited via ALD using Al(CH3)3 (TMA)/AlCl3 with H2O/NH3. Herein, surface chemical reactions are examined using density functional theory calculations to elucidate the adsorption, oxidation, and nitridation of precursors [TMA and AlCl3] as well as the mechanism controlling the composition of Al oxynitride thin films obtained through ALD. The hydrogen-terminated substrate surface is transformed into a CH3/Cl-terminated surface after the reaction with the TMA/AlCl3 precursors. The molecular adsorption of TMA occurs through a spontaneous reaction, whereas that of AlCl3 requires a slight energy input. Although the adsorption energy of AlCl3 is higher than that of TMA, the activation energy and energy change of AlCl3 adsorption are higher and lower than those of TMA, respectively; furthermore, the use of AlCl3 results in the generation of a corrosive by-product (HCl). A similar tendency is observed in the second ALD half reaction, which is oxidation. Nitride formation is endothermic for molecularly adsorbed AlCl3 but exothermic for TMA. Furthermore, the investigation of the exchange reactions between surface moieties and excess gaseous reactants reveals a preference for the substitution of N by O, which is attributed to differences in bond energies between the surface moieties and the surface metal atom, as well as between H2O and NH3.

Oligomeric Zinc Thiolates Tethering Multidentate Carboxylates for Nondestructive Aqueous Phase Transfer of Quantum Dots.

Functionalization of quantum dots (QDs) via ligand exchange is prone to debase their photoluminescence quantum yield (PL QY) owing to the unavoidable surface damage by excess reactants, and even worse in aqueous medium. Herein, the oligomeric zinc thiolate as the multidentate hydrophilic ligand featuring facile synthetic protocol is proposed. A simple reaction between ZnCl2 and 3-mercaptopropionic acid produces oligomeric ligands containing 3-6 zinc thiolate units, where the terminal moieties provide multidentate anchoring to the surface as well as hydrophilicity. 2D proton nuclear Overhauser effect spectroscopy (2D 1H NOESY) and X-ray photoelectron spectroscopy (XPS) reveal that the oligomeric zinc thiolate ligands adsorb on the surface via multidentate metal carboxylate bindings without destruction of molecular structure, regardless of partial dissociation of thiolate branches in aqueous phase. Enhanced binding affinity granted by the multidentate nature allows for the effective exchange of original surface ligands without considerable surface deterioration. The zinc thiolate-capped Cd-free aqueous QDs exhibit a high photoluminescence quantum yield of ≈90% and extended stability against long-term storage and photochemical stress.

Kinetics of the reaction of OH with methyl nitrate (223-343 K).

Rate coefficients (k4) for the reaction of hydroxyl radicals (OH) with methyl nitrate (CH3ONO2) were measured over the temperature range 232-343 K using pulsed laser photolysis to generate OH and pulsed laser-induced fluorescence to detect it in real-time and under pseudo-first-order conditions. In order to optimize the accuracy of the rate coefficients obtained, the concentration of CH3ONO2 (the reactant in excess) was measured on-line by absorption spectroscopy at 213.86 nm for which the absorption cross-section was also measured (σ213.86 = 1.65 ± 0.09 × 10-18 cm2 molecule-1). The temperature-dependent rate coefficient is described by k4(T) = 7.5 × 10-13 exp[(-1034 ± 40)/T] cm3 molecule-1 s-1 with a room temperature rate coefficient of k4(296 ± 2 K) = (2.32 ± 0.12) × 10-14 cm3 molecule-1 s-1 where the uncertainty includes the statistical error of 2σ and an estimation of the potential systematic bias of 5%. This new dataset helps to consolidate the database for this rate coefficient and to reduce uncertainty in the atmospheric lifetime of CH3ONO2. As part of this study, an approximate rate coefficient for the reaction of H-atoms with CH3ONO2 (k9) was also derived at room temperature: k9(298 K) = (1.68 ± 0.45) × 10-13 cm3 molecule-1 s-1.

Palladium-Catalyzed Combinatorial Synthesis of Biphenyls on Droplet Microarrays at Nanoliter Scale.

The rising costs of pharmaceutical research are currently limiting the productivity of drug discovery and development, but can potentially be diminished via miniaturization of the synthesis and screening of new compounds. As droplet microarrays already present themselves as a versatile tool for highly miniaturized biological screening of various targets, their use for chemical synthesis is still limited. In this study, the influential palladium-catalyzed Suzuki-Miyaura reaction is successfully implemented at the nanoliter scale on droplet microarrays for the synthesis of an 800-compound library of biphenyls. Each reaction is carried out in individual 150nL droplets. Remarkably, the synthesis of these 800 compounds requires a minimal amount of reagents, totaling 80µmol, and a solvent volume of 400µL. Furthermore, the cleavage kinetics and purity of the obtained biphenylic compounds are investigated. Via the solid-phase synthesis approach, the compounds could be purified from excess reactants and catalyst prior to the analysis and a UV-cleavable linker allows for fast and additive-free cleavage of each compound into the individual 100nL droplet. This novel approach expands the toolbox of the droplet microarray for miniaturized high-throughput chemical synthesis and paves the way for future synthesis and screening of chemical compounds in a single platform.

Glycerol Acetalization in Cyclopentyl Methyl Ether with Mild Acid Catalysts

AbstractReaction of glycerol with aldehydes and ketones is a strategy widely studied in literature to valorize this bioproduct. A Brønsted or Lewis acid is normally used to activate the carbonyl function and various strategies adopted to drive the equilibrium to the products. In this study ammonium salts as catalysts, and removal of water by azeotropic distillation of cyclopentyl methyl ether, permit the conversion of glycerol into acetals obtained as mixture of dioxanes and dioxolanes determined by 1H‐NMR. Under the optimized conditions, the products could be obtained in excellent yield without using excess of reactants and the solvent was recycled efficiently.

Permanently Mechanically Adjustable Photothermal Catalytic Spontaneous Double Cross‐Linking Network Enables Durable and Stretchable Plant Skin‐Like Materials

AbstractIn cellulose‐based plastics, as a type of thermoplastic and thermosetting materials, the excellent balance of mechanical strength and ductility poses a large challenge. To tackle this problem, a novel approach is devised to introduce reversible non‐covalent ester cross‐linking into dynamic covalent hydrogen‐bonded polymer networks. However, the formation of ester bonds typically requires excess reactants and dehydrating agents, which is energy‐intensive, environmentally harmful, and costly. To address these concerns, inspired by polyester‐rich plant bark, a supramolecular composite material is developed. It can be dissolved and regenerated using a binary solvent system (choline hexanoate/choline chloride‐oxalic acid). In water, this supramolecular composite material underwent self‐healing and ester exchange reactions to form double‐cross‐linked networks, interfaced with photo‐thermal catalysis promoting the reaction due to its high photo‐thermal conversion efficiency (86.7%) and water evaporation rate (1.38 kg m−2 h−1). This enables the rapid and repeatable construction of durable and stretchable biomaterials. The mechanical properties of the supramolecular plastic can be adjusted by solar photo‐thermal conditions of the synthesis environment. These materials exhibit high performance in solar water evaporation and have self‐healing properties and are degradable, recyclable, and capable of eliminating their own adhesions.

Experimental investigation of a packed bed membrane reactor for the direct conversion of CO2 to dimethyl ether

In this study, the performance of a packed bed membrane reactor (PBMR) based on carbon molecular sieve membranes for the one-step CO2 conversion to dimethyl ether (DME) is experimentally compared to that of a conventional packed bed reactor (PBR) using a CuO-ZnO-Al2O3/HZSM-5 bifunctional catalyst. The PBMR outperforms the PBR in most of the experimental conditions. The benefits were greater at lower GHSV (i.e., conditions that approach thermodynamic equilibrium and water formation is more severe), with both XCO2 and YDME improvements of +35–40 % and +16–27 %, respectively. Larger sweep gas-to-feed (SW) ratios increase the extent of water removal (ca. 80 % at SW=5), and thus the performance of the PBMR. Nevertheless, alongside the removal of water, a considerably amount of all products are removed as well, leading to a greater improvement in the CO yield (+122 %) than the DME yield (+66 %). Higher temperatures selectively improve the rWGS reaction, leading to a lower YDME with respect to the PBR at 260 °C, due to the significant loss of methanol. Furthermore, larger transmembrane pressures (∆P) were not beneficial for the performance of the PBMR due to the excess reactant loss (i.e., 98–99 % at ∆P = 3 bar). Finally, the reactor models developed in our previous studies accurately describe the performance of both the PBR and PBMR in the range of tested conditions. This result is of high relevance, since the reactor models could be used for further optimization studies and to simulate conditions which were not explored experimentally.

Convenient Solid-Phase Attachment of Small-Molecule Ligands to Oligonucleotides via a Biodegradable Acid-Labile P-N-Bond

One of the key problems in the design of therapeutic and diagnostic oligonucleotides is the attachment of small-molecule ligands for targeted deliveries in such a manner that provides the controlled release of the oligonucleotide at a certain moment. Here, we propose a novel, convenient approach for attaching ligands to the 5'-end of the oligonucleotide via biodegradable, acid-labile phosphoramide linkage. The method includes the activation of the 5'-terminal phosphate of the fully protected, support-bound oligonucleotide, followed by interaction with a ligand bearing the primary amino group. This technique is simple to perform, allows for forcing the reaction to completion by adding excess soluble reactant, eliminates the problem of the limited solubility of reagents, and affords the possibility of using different solvents, including water/organic media. We demonstrated the advantages of this approach by synthesizing and characterizing a wide variety of oligonucleotide 5'-conjugates with different ligands, such as cholesterol, aliphatic oleylamine, and p-anisic acid. The developed method suits different types of oligonucleotides (deoxyribo-, 2'-O-methylribo-, ribo-, and others).

Progress and challenges in the fabrication of lead-free all-inorganic perovskites solar cells using solvent and compositional engineering Techniques-A review

Organic-inorganic lead halide perovskite solar cells have paved the way toward producing low-cost thin-film solar cells. The tremendous improvement in power conversion efficiency greater than 25%, suitable optoelectronic properties and easiness of the fabrication method have triggered the aspiration to think thoroughly about the commercialisation stage. However, lead toxicity and poor stability stand as the main obstruction. Therefore, the great way toward commercialisation is by considering all inorganic lead-free halide perovskites solar cells (AILFHP). Since the first AILFHP solar cell was fabricated, several challenges have been conquered by modifying the fabrication techniques and device architecture. This review entails the modification done to fabrication methods, particularly the application of solvent and composition engineering techniques. Several deposition techniques with and without excess reactants and precursor–solvent interaction have been thoroughly discussed. It further discusses the effect of mixed cations and mixed anions, potential application areas, obstacles, and future commercialisation prospects.

Development of an Automatable Affinity Purification Process for DNA-Encoded Chemistry.

DNA-encoded library technologies require high-throughput, compatible, and well automatable platforms for chemistry development, building block rehearsal, and library synthesis. An affinity-based process using Watson–Crick interactions was developed that enables purification of DNA-tagged compounds from complex reaction mixtures. The purification relies on a single-stranded DNA-oligonucleotide, called capture strand, which was covalently coupled to an agarose matrix and to which a DNA-compound conjugate from a DNA-encoded library (DEL) reaction can be reversibly annealed to. The thus-formed DNA duplex tolerated surprisingly stringent washing conditions with multiple solvents to remove excess reactants and reagents. The tolerated solvents included aqueous buffers, aqueous EDTA solutions to remove metal ions, aqueous mixtures of organic solvents, and even pure organic solvents. The purified DNA-conjugate was eluted with aqueous ammonia and could be used for reaction analysis or for instance in DNA-encoded library synthesis. The lab equipment for purification was tailored for automation with open-source hardware and constructed by 3D printing.

Recycling reaction and separation for FACylation of loxenatide by trade-off between miscibility and immiscibility of reactants and product in methanol solution

The growing demand and scale of production for fatty acid chain modified (FACylated) polypeptide has sparked the interest in novel production technologies. In this study, a recycling reaction and separation process was proposed and applied to the fatty acid chain modification (FACylation) of loxenatide (LOX), which was based on the difference in solubility between reactants and FACylated product. Especially, the mixed PBS-Methanol (MeOH) solution was designed to meet the demands for FACylation of LOX as well as separation of FACylated LOX and residual modifier. In order to ensure the efficient FACylation, a mixed 10% PBS-90% MeOH (v/v) solution was chosen to provide a good miscibility for two reactants, LOX and N-tetradecylmaleimide (C14-MAL). On the other hand, the immiscibility between reactant (C14-MAL) and FACylated product (N-tetradecyl-Loxenatide (C14-LOX)) could realize the separation of C14-LOX when the MeOH concentration was less than 30% (v/v). Based on this strategy, the recycling reaction and separation process for FACylation of LOX was established by adjusting the MeOH concentration in the mixed solution. The reaction yield and recovery of C14-LOX exceeded 97% and 94%, and the excess reactant C14-MAL could be recycled with a recovery of more than 80%. Furthermore, after purification by reversed-phase chromatography, C14-LOX showed good pharmacokinetic and pharmacodynamic properties in vivo. This study will have great application prospects in industrial production of C14-LOX.

Hydrolysis of the Borohydride Anion BH4-: A 11B NMR Study Showing the Formation of Short-Living Reaction Intermediates including BH3OH.

In hydrolysis and electro-oxidation of the borohydride anion BH4−, key reactions in the field of energy, one critical short-living intermediate is BH3OH−. When water was used as both solvent and reactant, only BH3OH− is detected by 11B NMR. By moving away from such conditions and using DMF as solvent and water as reactant in excess, four 11B NMR quartets were observed. These signals were due to BH3-based intermediates as suggested by theoretical calculations; they were DMF·BH3, BH3OH−, and B2H7− (i.e., [H3B−H−BH3]− or [H4B−BH3]−). Our results shed light on the importance of BH3 stemming from BH4− and on its capacity as Lewis acid to interact with Lewis bases such as DMF, OH−, and BH4−. These findings are important for a better understanding at the molecular level of hydrolysis of BH4− and production of impurities in boranes synthesis.

Green Synthesis of Magnetite-Based Catalysts for Solar-Assisted Catalytic Wet Peroxide Oxidation

A novel synthesis method under green philosophy for the preparation of some magnetite-based catalysts (MBCs) is presented. The synthesis was carried out in aqueous media (i.e., absence of organic solvents) at room temperature with recovery of excess reactants. Terephthalic acid (H2BDC) was used to drive the synthesis route towards magnetite. Accordingly, bare magnetite (Fe3O4) and some hybrid magnetite-carbon composites were prepared (Fe3O4-G, Fe3O4-GO, and Fe3O4-AC). Graphene (G), graphene oxide (GO), and activated carbon (AC) were used as starting carbon materials. The recovered H2BDC and the as-synthetized MBCs were fully characterized by XRD, FTIR, Raman spectroscopy, XPS, SQUID magnetometry, TGA-DTA-MS, elemental analysis, and N2-adsorption-desorption isotherms. The recovered H2BDC was of purity high enough to be reused in the synthesis of MBCs. All the catalysts obtained presented the typical crystalline phase of magnetite nanoparticles, moderate surface area (63–337 m2 g−1), and magnetic properties that allowed their easy separation from aqueous media by an external magnet (magnetization saturation = 25–80 emu g−1). The MBCs were tested in catalytic wet peroxide oxidation (CWPO) of an aqueous solution of metoprolol tartrate (MTP) under simulated solar radiation. The Fe3O4-AC materials showed the best catalytic performance among the prepared MBCs, with MTP and total organic carbon (TOC) removals higher than 90% and 20%, respectively, after 3 h of treatment. This catalyst was fairly successfully reused in nine consecutive runs, though minor loss of activity was observed, likely due to the accumulation of organic compounds on the porous structure of the activated carbon and/or partial oxidation of surface Fe2+ sites.

Heterogeneous Catalyzed Synthesis of Biodiesel from Crude Sunflower Oil

Biodiesel is the fatty acid alkyl esters that are used as the substitute for petro-diesel. The aim of the present work is to optimize biodiesel production from plant based non-edible crude oils with methanol using heterogeneous catalyst by transesterification for its commercialization. The factors affecting the biodiesel production from plant oils are volume of feedstock (oil), volume of alcohol (excess reactant), quantity of calcium hydroxide (catalyst), reaction time, temperature, and agitation speed. Transesterification is the reaction between acid and alcohol to produce ester in the presence of alkali catalyst. In this work, transesterification was carried out between crude sunflower oil and methanol in the presence of calcium hydroxide as catalyst. Finally, the maximum conversion of 85.6% was achieved at the optimum process parameters of 2 L of crude sunflower oil, 0.3 L methanol, 23 g of calcium hydroxide, reaction time of 24 h, temperature of 65 °C, and agitation speed of 100 rpm. The results showed that crude sunflower oil could serve as potential renewable substrate for biodiesel commercialization.Biodiesel is the fatty acid alkyl esters that are used as the substitute for petro-diesel. The aim of the present work is to optimize biodiesel production from plant based non-edible crude oils with methanol using heterogeneous catalyst by transesterification for its commercialization. The factors affecting the biodiesel production from plant oils are volume of feedstock (oil), volume of alcohol (excess reactant), quantity of calcium hydroxide (catalyst), reaction time, temperature, and agitation speed. Transesterification is the reaction between acid and alcohol to produce ester in the presence of alkali catalyst. In this work, transesterification was carried out between crude sunflower oil and methanol in the presence of calcium hydroxide as catalyst. Finally, the maximum conversion of 85.6% was achieved at the optimum process parameters of 2 L of crude sunflower oil, 0.3 L methanol, 23 g of calcium hydroxide, reaction time of 24 h, temperature of 65 ?C, and agitation speed of 100 rpm. The results showed that crude sunflower oil could serve as potential renewable substrate for biodiesel commercialization.

Halogenation of used aluminum matrix test reactor fuel – a bench-scale demonstration with surrogate materials

ABSTRACT Experiments with surrogate materials were performed at bench scale to demonstrate a halogenation technique applicable to treatment of used aluminum matrix test reactor fuel. The technique involves dissolution and separation of aluminum from used aluminum matrix test reactor fuel in molten-halide salt systems prior to treatment and disposition of the fuel’s uranium and fission products. Demonstration of the halogenation technique was performed with neodymium metal as a non-radiological surrogate for uranium metal. Experiments involved blending forms of aluminum and neodymium metal with ammonium and lithium chloride or ammonium and lithium bromide, which upon heating decomposed into ammonia gas and the respective hydrogen chloride or bromide gas. The latter reacted with the metals to form the respective aluminum and neodymium halides. At elevated temperatures, aluminum halides gasified away from the respective neodymium halides, which fused with their respective lithium halides. Samples of fused and distillate salts were collected and analyzed, yielding extents of aluminum removal that ranged from 94.5–98.2% for chlorination runs and 91.4–97.8% for bromination runs. No neodymium was detected in the distillate fractions. Some experiments were repeated with excess reactants, and a portion of aluminum chloride distillate was processed into a consolidated waste form.

Influence of the Hollowness and Size Distribution on the Magnetic Properties of Fe3O4 Nanospheres.

In this study, Fe3O4 nanospheres with different levels of hollowness were successfully prepared by the solvent thermal method. The synthesized Fe3O4 nanospheres were characterized by transmission electron microscopy, X-ray diffraction, and vibrating sample magnetometry, and Image-Pro software was used to analyze the hollowness of the Fe3O4 nanospheres for the first time. It was found that excess reactants could lead to the disappearance of the hollow structure of the Fe3O4 nanospheres, and the reason for this phenomenon was discussed as due to entropy increase theory. Furthermore, the influence of the hollowness and size distribution on the magnetic properties of the Fe3O4 nanospheres was evaluated. The magnetic properties of a Fe3O4 nanosphere with a hollowness of 10.48% showed a relatively high saturation magnetization of 103 emu/g and a rather low coercivity (54 Oe). The as-prepared Fe3O4 nanospheres are expected to be useful in a wide range of fields such as drug-delivery and energy applications.

Process intensification of thumba methyl ester (Biodiesel) production using hydrodynamic cavitation

The development of clean and sustainable biofuel generation from sustainable feedstock using an integrated process intensification approach like hydrodynamic cavitation (HC) is essential now. The current research is a 'first of its kind' where hydrodynamic cavitation is integrated with heterogeneous catalyst, i.e. TiO2, to prepare thumba methyl esters (TME). So far, no studies on biodiesel production using heterogeneous catalysts using HC are reported in the literature. Experiments were performed with an optimized orifice plate to investigate the effects of operating parameters viz., Thumba oil to methanol molar ratio (1:4–1:8), TiO2 concentration (1–1.4% by weight of oil), and operating temperature (50 °C to 70 °C). Maximum triglyceride conversion (71.8%) was obtained at thumba oil to methanol ratio of 1:6, TiO2 concentration of 1.2% weight percentage and operating temperature of 60 °C in hydrodynamic cavitation reactor within 1 h at 5 bar. The cavitational yield for HC was found to be 9.3 × 10−6 moles L/J, which was almost 27% higher than the value for the conventional approach (3.37 × 10−7 moles L/J). The experimental data fitted second-order reaction kinetics w.r.t limiting reactant, i.e., thumba oil and first-order w.r.t excess reactant, i.e., methanol. The pre-exponential factor (k0) and activation energy (E) of the alcoholysis reaction was found to be 82.26 L2 mol−2 min−1 and 15.44 kJ/mol, respectively. The thermodynamic analysis suggested that the alcoholysis of the thumba oil followed the endergonic reaction pathway. Thumba methyl ester (TME) synthesized via this intensified approach is a novel and energy-efficient method compared to the conventional method.