The use of polymeric material in heavy metal removal from wastewater is trending. Heavy metal removal from wastewater of the industrial process is of utmost importance in green/sustainable manufacturing. Production of absorbent materials from a natural source for industrial wastewater has been on the increase. In this research, polyurethane foam (PUF), an adsorbent used by industries to adsorb heavy metal from wastewater, was prepared from a renewable source. Castor oil-based polyurethane foam (COPUF) was produced and modified for improved adsorption performance using fillers, analyzed with laser-induced breakdown spectroscopy (LIBS). The fillers (zeolite, bentonite, and activated carbon) were added to the COPUF matrix allowing the modification on its surface morphology and charge. The materials were characterized using Fourier-transform infrared (FTIR), scanning electron microscopy (SEM), and thermal gravimetry analysis (TGA), while their adsorption performance was studied by comparing the LIBS spectra. The bentonite-modified COPUF (B/COPUF) gave the highest value of the normalized Pb I (405.7 nm) line intensity (2.3), followed by zeolite-modified COPUF (Z/COPUF) (1.9), and activated carbon-modified COPUF (AC/COPUF) (0.2), which indicates the adsorption performance of Pb²⁺ on the respective materials. The heavy metal ions’ adsorption on the B/COPUF dominantly resulted from the electrostatic attraction. This study demonstrated the potential use of B/COPUF in adsorption and LIBS quantitative analysis of aqueous heavy metal ions.

Global pollution from toxic metal waste has resulted in increased research on toxic metal adsorption. A cellulose acetate–polyurethane (CA–PU) film adsorbent was successfully prepared in this research. The cellulose acetate–polyurethane film adsorbent was prepared with a polycondensation reaction between cellulose acetate and methylene diphenyl diisocyanate. The CA–PU bond formation was confirmed by functional group analysis obtained from Fourier transform infrared (FTIR) spectroscopy. The obtained film was characterized for improved tensile and thermal properties with the addition of methylene diphenyl diisocyanate (MDI). The adsorption ability of the obtained film was evaluated with laser-induced breakdown spectroscopy (LIBS). The best film adsorbent from the LIBS was selected and studied for adsorption isotherm. The FTIR analysis confirmed the formation of the CA–PU bond from the polycondensation between cellulose acetate and the methylene diphenyl diisocyanate. The result showed that the addition of methylene diphenyl diisocyanate (MDI) resulted in the urethane network’s growth. The characterization result showed an improvement in the morphology, thermal stability, and tensile strength of the film. The LIBS studies showed improvement in the adsorption of Pb²⁺ with CA–PU compared with the neat CA. The isotherm studies revealed that Pb²⁺ adsorption by cellulose acetate–polyurethane film adsorbent was heterogeneously dependent on the Freundlich isotherm model (R² = 0.97044). Overall, the polycondensation method proposed by this study enhanced the Pb²⁺ removal, and was comparable to those reported in previous studies.

This research offers a novel approach of free chemical preparation to obtain algae-based biopolyol through a ball milling method. The algae-based polyurethane (AlgPU) film was obtained from a casting solution made of ball-milled algal polyol particle and methylene diphenyl diisocyanate (MDI). The characteristics of the material had been investigated using Fourier Transform Infrared, Scanning Electron Microscopy – Electron Dispersive Spectroscopy, Differential Scanning Calorimetry, and Tensile Strength Analysis. The surface area was determined by Brunauer–Emmett–Teller (BET) isotherm, meanwhile the total pore volume was by Barrett-Joyner-Halenda (BJH) isotherm, based on the adsorption-desorption of N2. The addition of activated carbon contributed in the increase of functional group and surface area, which were important for the NH3–N removal. As a result, the adsorption capacity increased greatly after the addition of activated carbon (from 187.84 to 393.43 μg/g). The results also suggested AlgPU as a good matrix for immobilizing activated carbon filler. The adsorption shows a better fit with Langmuir isotherm model, with R2 = 0.97487 and root-mean-square error (RMSE) = 33.91952, compared to Freundlich isotherm model (R2 = 0.96477 and RMSE = 44.05388). This means the NH3–N adsorption followed the assumption of homogenous and monolayer adsorption, in which the maximum adsorption was found to be 797.95 μg/g. This research suggests the potential of newly developed material for NH3–N removal.

Recently, the global population has increased sharply, unfortunately, the availability of fossil fuel resources has significantly decreased. This phenomenon has become an attractive issue for many researchers in the world so that various studies in the context of finding renewable energy are developing continuously. Relating to this challenge, this research has been part of scientific work in the context of preparing an energy briquette employing palm oil stems and glycerol crude of biodiesel byproducts as inexpensive and green materials easily found in the Riau province, Indonesia. Technically, the palm oil stems are used for the production of charcoal particles and the glycerol crude as an adhesive compound in the production of energy briquettes. The heating value of palm oil stem is 17,180 kJ/kg, which can be increased to an even higher value through a carbonization process followed by a densification process so that it can be used as a potential matrix to produce energy briquettes. In detail, this study was designed to find out several parameters including the effect of sieve sizes consisting of 60, 80, and 100 mesh, respectively, which are used for the preparation of charcoal particles as the main matrix for the manufacture of the briquettes; the effect of charcoal-adhesive ratios (wt) of 60:40, 70:30, and 80:20; and the effect of varied pressures of 100, 110, and 120 kg/cm² on the briquette quality. The quality of the obtained briquettes is analyzed through the observation of important properties which involve the heating value and the compressive strength using Response Surface Methodology (RSM). The results showed that the produced briquettes had an optimum heating value of 30,670 kJ/kg, while their loaded charcoal particles resulted from the mesh sieve of 80, in which there was a charcoal loading of 53 g and it pressed at 93.1821 bar, whereas, the compressive strength value of the briquette was 100,608 kg/cm², which loaded charcoal particles from the mesh sieve of 100, the charcoal-adhesive ratio of 53:47 (wt) and the pressure of 93.1821 bar.

A forward osmosis (FO) membrane was developed from a mixture of chitosan and Dioscorea hispida starch, cross-linked using glutaraldehyde. The cross-linked chitosan/starch membrane was revealed to have high mechanical properties with an asymmetric structure. The prepared membrane’s performance was investigated as an FO filter assembled in a polypropylene water filter bag and aluminum foil plastic. In order to study the FO process, brackish water was used as a feed solution, drawn using three types of solution (fructose, sucrose, and fructose/sucrose mixture, each with 3 M concentration). The maximum water flux (5.75 L/m² h) was achieved using 3 M sucrose. The cross-linked membrane restrained the ions in the feed with a rejection factor value close to 100%. The water quality parameters were evaluated for the physical, chemical, and biological criteria, such as pH, salinity, conductivity, total dissolved solids (TDS), heavy metals, and Escherichia coli content. The water quality parameters for the FO-processed water met that set by the World Health Organization for drinking water. FO filter bags with cross-linked chitosan/starch membranes can be an option to produce drinking water during an emergency.

The development of membrane technology is rapidly increasing due to its numerous advantages, including its ease of use, chemical resistant properties, reduced energy consumption, and limited need for chemical additives. Polyurethane membranes (PUM) are a particular type of membrane filter, synthesized using natural organic materials containing hydroxy (-OH) groups, which can be used for water filtration, e.g., ammonia removal. Red seaweed (Rhodophyta) has specific molecules which could be used for PUM. This study aimed to ascertain PUM synthesis from red seaweed biomass (PUM-RSB) by using toluene diisocyanate via the phase inversion method. Red seaweed biomass with a particle size of 777.3 nm was used as starting material containing abundant hydroxy groups visible in the FTIR spectrum. The PUM-RSB produced was elastic, dry, and sturdy. Thermal analysis of the membrane showed that the initial high degradation temperature was 290.71 °C, while the residue from the thermogravimetric analysis (TGA) analysis was 4.88%. The PUM-RSB section indicates the presence of cavities on the inside. The mechanical properties of the PUM-RSB have a stress value of 53.43 MPa and a nominal strain of 2.85%. In order to optimize the PUM-RSB synthesis, a Box–Behnken design of Response Surface Methodology was conducted and showed the value of RSB 0.176 g, TDI 3.000 g, and glycerin 0.200 g, resulting from the theoretical and experimental rejection factor, i.e., 31.3% and 23.9%, respectively.