• Key part is utilizing the 3D-printed rotor in hydrodynamic cavitation reactor. • Continuous nanoemulsion formulation was studied using HCR. • Smallest droplet size of 366.4 nm can be created by HCR. • Mechanical stirrer, ultrasound, hydrodynamic cavitation were compared. • Nanoemulsion from HCR reactor gave the highest cumulative release of niacin.

Acid catalysts including Amberlyst 15 and sulfuric acid were used for heterogeneous and homogeneous catalyst reactions respectively, to reduce high free fatty acid (FFA) in sludge palm oil (SPO) using an esterification process. The goal of this research was to reduce high FFA content in SPO to less than 1 wt.% FFA so that it can be employed as a raw material in a transesterification process to produce biodiesel. Amberlyst 15 is an eco-friendly catalyst with many benefits, such as being reusable and generating non-toxic waste after reactions, compared to homogeneous catalysts, although the reaction time of the homogeneous catalyst was faster than the heterogeneous catalytic reaction. Therefore, esterification reactions with a heterogeneous and homogeneous catalytic reaction were carried out to examine conversion of FFA. The heterogeneous catalytic reaction decreased the FFA content from 89.16 wt.% to 1.26 wt.% under the recommended conditions of 44.7 wt.% methanol, 38.6 wt.% Amberlyst 15 catalyst loading, and 360 min reaction time. For homogeneous catalytic reaction, the FFA content of 1.03 wt.% was achieved under the recommended conditions of 58.4 wt.% methanol, 16.8 wt.% sulfuric acid, and 79.7 min reaction time. Furthermore, the results of the reusability research demonstrate that the heterogeneous catalyst may be reused for at least nine cycles. This research showed the promising potential of using SPO non-edible oil for biodiesel production by employing an eco-friendly heterogeneous catalyst for cost-effective environmental remediation.

Ethyl ester production from palm fatty acid distillate (PFAD) with ethanol in the presence of sulfuric acid and potassium hydroxide was performed in a continuous three-step process using the ultrasound clamps and an ultrasonic probe. The ultimate goal was to produce biodiesel from the PFAD. In the first and second esterification steps, 16 units of a 400 W ultrasound clamp (20 kHz) were attached 100-m apart along each tubular reactor. In the third transesterification step, a 1000-W ultrasonic homogenizer (18 kHz) was used in a 100-mL continuous reactor. A composite central design of experiments and the response surface methodology (RSM) were used to develop predictive models and identify the optimal conditions of each step based on the purities of ethyl ester. The optimal conditions in the first step were 46.1 vol.% ethanol, 1.4 vol.% sulfuric acid, and purity 66.68 wt.% ethyl ester. In the second step, the optimized conditions were 57 vol.% ethanol, and 2.1 vol.% sulfuric acid, purity 95.32 wt.% ethyl ester. The final transesterification step was carried out with 14.6 vol.% ethanol and 3.9 gKOH L⁻¹. As a result, a final ethyl ester purity of 98.15 wt.% was achieved in the biodiesel using the three-step process.

A heterogeneous base catalyst transesterification process with a calcium oxide (CaO) catalyst was performed to produce high-purity methyl ester (ME) from pretreated sludge palm oil (PSPO) derived from sludge palm oil (SPO). Additionally, a comparative analysis was conducted with potassium hydroxide (KOH) as a homogeneous base catalyst to assess the distinctions between heterogeneous and homogeneous base catalysts. The response surface methodology (RSM) was utilized to determine the optimal and recommended conditions for both transesterification processes. For heterogeneous transesterification, a varying CaO catalyst loading (10–60 wt.%), methanol (25–65 wt.%), and reaction time (60–180 min) were essential parameters. Meanwhile, homogeneous transesterification involved investigating the KOH catalyst loading (1–3 wt.%), methanol (1.8–5.5 wt.%), and reaction time (20–60 min). For the heterogeneous-base-catalyzed reaction, the recommended conditions were as follows: a molar ratio of methanol to oil of 5.83:1 (41.61 wt.%), 31.3 wt.% CaO, and a reaction time of 119.0 min, which resulted in a ME purity of 96.51 wt.%. The optimal conditions for homogeneous transesterification were a molar ratio of methanol to oil of 0.49:1 (3.45 wt.%), a 40 min reaction time, and a 1.39 wt.% KOH concentration, which achieved 96.59 wt.% ME and met the standard.