Linear Alkylbenzene Research Articles

Parabolic Viscosity Behavior of NaCl-Thickened Surfactant Systems upon Temperature Change.

The viscosity of household care products plays an important role in pleasant delivery using consumer experience at home. A novel solution to mitigate the sharp rising of viscosities at low temperatures of detergents was proposed. By designing the formulation of the surfactant blend, formulators can achieve acceptable viscosity profiles in the temperature range encountered in daily life. The verification and modulation of formulas bearing parabolic viscosity-temperature behavior were systematically studied, including in single, binary, and ternary systems, based on the modulation of sodium ethoxylated alkyl sulfate (AES) by other anions, zwitterions, and nonions. The R ratio theory was used to have a better understanding of the molecular assembly of surfactants behind the parabolic behavior exhibited in rheology analyses. One of the key findings is that the parabolic viscosity-temperature phenomenon could be easily observed in the highly hydrated ethoxylated anionic systems like AES-based systems. For those anions lacking ethoxylation, especially sodium linear alkylbenzene sulfonate (LAS), the monotonic variation of hydration affinity with temperature led to the disappearance of parabola in the observed temperature window (>0 °C). Moreover, salinity played an important role in the hydration affinity of the polar group and the interaction between the hydrophilic headgroups. A balanced salinity should be optimized to modulate the hydration affinity in a desired range so that the parabola could be easily tuned within the target temperature region. These findings provide opportunities for the formulators in the household care industry to design products with better pourability through carefully selecting a combination of surfactants and fine-tuning their ratios to improve consumer use experience, especially in winter.

Assessment of Sewage Molecular Markers: Linear Alkylbenzenes in Sediments of an Industrialized Region in Peninsular Malaysia

In this study, the use of linear alkylbenzenes (LABs) was employed to pinpoint the sources of human activity that cause detrimental impacts on the coastal environment and river ecosystems. LABs were detected using GC–MS in sediment samples assembled from Kim Kim River (KKR) and the Port Dickson coast (PDC). To assess the significance of variations in the distribution and concentrations of LABs across the sampling sites, this study utilized several statistical techniques such as post hoc tests, LSD techniques, analysis of variance (ANOVA), and the Pearson correlation coefficient using a significance level of p < 0.05. The degradation levels of LABs and wastewater treatment were assessed in the study using internal congeners (I/E), homologs of C13 and C12, and long-to-short-chain (L/S) ratios. The results revealed that the LAB concentrations varied between 88.3 and 112 ng/g dw in KKR and 119 to 256 ng/g dw in the PDC. Most of the surveyed areas exhibited a substantial count of C13–LABs homologs that displayed a significant difference (p < 0.05). The I/E ratios ranged from 1.7 to 2.0 in KKR and from 2.0 to 4.1 in the PDC, suggesting that the effluents originated from sources associated with the physical phase and biological phase in wastewater treatment systems (WWTSs). The results revealed that the degradation of LABs varied between 34% and 38% in KKR and between 40% and 64% in the PDC. This study underscores the importance of ongoing improvements to WWTSs and emphasizes the potential of LABs as indicators for monitoring wastewater contamination.

Emulsification of Indian heavy crude oil and analysis of flow characteristics using computational fluid dynamics (CFD) for pipeline transportation

The high viscosity of Indian heavy crude oils makes their pipeline transportation highly complicated and challenging. A huge pressure drop is observed while transporting heavy crude through pipelines. The present article addresses this complication by preparing a surfactant stabilized heavy crude oil-in-water (O/W) emulsion of a flowable viscosity to ease flow through pipelines. Different O/W emulsion samples were prepared with varying concentrations of a novel anionic surfactant, linear alkylbenzene sulfonic acid (LABSA), to achieve an optimized formulation based on rheological and stability studies. The article also discusses the effect of varying surfactant concentrations on interfacial tension, droplet size and distribution, and zeta potential of the developed emulsions. The optimized emulsion, having 60 vol% oil and 2 wt% surfactant, was further considered to simulate and analyze the flow characteristics (static pressure and velocity profiles) across the horizontal pipelines of three different inner diameters (0.1, 0.05, and 0.025 m) under three different inlet flow velocities (0.1, 0.05, and 0.001 m/s), using a computational fluid dynamics (CFD) approach. A remarkable decrease in the viscosity of heavy crude was noted after emulsification. Subsequently, the pressure drop across the pipeline was reduced significantly by order of three for the flow of O/W emulsion when compared to that of the heavy crude oil through a pipe diameter of 0.1 m at an inlet velocity of 0.1 m/s. The static pressure drop across the pipeline decreased with the increase in the pipe diameter; in contrast, it increased with the increase in the inlet velocity.

Experimental study of asphaltene onset condition and deposition using electrical deposition technique in the presence of various additives: A novel strategy

Asphaltenes (ASPs) are regarded as high molecular weight components that often deposit in the production lines and downstream infrastructure, leading to pressure drop and reduced production rate. In this paper, we investigated the potential of electro-deposition of ASP an Iranian crude oil sample encountering ASP deposition problems, to reduce the risk of well shut-in. In this regard, a systematic research plan has been designed to use the electro-deposition technique to precipitate and deposit ASP different fluid samples incluiding crude oil/n-heptane, synthetic oil (containing the same ASP)/n-heptane, crude oil/n-heptane/additive and synthetic oil/n-heptane/additive are utilized. The additives such as Linear Alkyl Benzene Sulfonate (LABS) as a surfactant, metal oxide nano-particles such as SiO2, γ-Al2O3, and TiO2 and synthesized mixed-metal oxide nano-particles compounds such as CeNiO3, CeZrO4 and CeCaO3 were used. This work reveals the effect of these additives on the deposition rate of ASP particles from crude oil and compares their effectiveness. Using a homemade apparatus, the optimum direct-current electric field (EF) and time for ASP deposition were found, followed by finding the best solution of crude oil and n-heptane. As for the additives, LABS showed that ASP deposition is critically decreased on the cathode at 2000 ppm for crude oil and 1500 ppm for synthetic oil. Nano-particles exhibit different behavior in an EF. The experimental results indicated that by increasing the concentration of nano-particles, the amount of ASP deposit on the anode decreases. The results indicated that synthesized mixed-metal oxide nano-particles do not change the charge type of ASP and result in ASP deposition reduction utilizing a very low number of nano-particles. Currently, electro-deposition is a key solution to remove ASPs from crude oil. This is due to its high energy efficiency and relatively simple process. Comparing the effects of these newly proposed additives showed that, CeZrO4 nano-particles are more efficient to inhibit ASP deposition.

In vitro Assessment of Antioxidant Enzymes in Oreochromis niloticus Induced with Linear Alkyl Benzene Sulfonates

In vitro Assessment of Antioxidant Enzymes in Oreochromis niloticus Induced with Linear Alkyl Benzene Sulfonates

Evaluation of Linear Alkyl Benzene Sulfonate (LAS) and Physicochemical Properties of Water in Manzala Lake, Egypt

Evaluation of Linear Alkyl Benzene Sulfonate (LAS) and Physicochemical Properties of Water in Manzala Lake, Egypt

Hydrogen-Free Deoxygenation of Oleic Acid and Industrial Vegetable Oil Waste on CuNiAl Catalysts for Biofuel Production

The pyrolysis of vegetable oil waste is an alternative way to convert biomass into high-quality second-generation biofuels, with social, economic and environmental sustainability. The present work deals with the pyrolysis of oleic acid as a model compound and an industrial vegetable oil residue on CuNiAl mixed oxide catalysts, derived from layered double hydroxides. Reactions of the oils pre-adsorbed on the catalysts (catalyst:oil mass ratio of 5:1) were performed at 550 °C on a micro-pyrolysis system and the analyses of volatile products were carried out online using GC/MS. Copper addition to NiAl catalysts increased the cracking of oleic acid. Increasing copper content also decreased the formation of aromatics and coke precursors, as well as oxygenated compounds. The CuNiAl catalyst with a Cu/Ni ratio of 0.4 showed strong catalytic activity in the conversion of an industrial vegetable oil residue with a high volume of free fatty acids produced. Compared to the non-catalytic reaction, the catalyst reduced the content of oxygenates and increased the content of hydrocarbons, particularly in the gasoline range (C5–C9). The CuNiAl oxide catalyst was able to convert vegetable oil residues into hydrocarbons in the range of gasoline, kerosene and diesel, and also linear alkylbenzenes as chemical precursors for surfactant production.

Biofilm bioactivity affects nitrogen metabolism in a push-flow microalgae-bacteria biofilm reactor during aeration-free greywater treatment

Non-aeration microalgae-bacteria biofilm has attracted increasing interest for its application in low cost wastewater treatment. However, it is unclear the quantified biofilm characteristics dynamics and how biofilm bioactivity affects performance and nitrogen metabolisms during wastewater treatment. In this work, a push-flow microalgae-bacteria biofilm reactor (PF-MBBfR) was developed for aeration-free greywater treatment. Comparatively, organic loading at 1.27 ± 0.10 kg COD/(m3⋅d) gave the highest biofilm concentration, density, specific oxygen generation (SOGR) and consumption rates (SOCR), and pollutants removal rates. Contributed to low residual linear alkylbenzene sulfonates and bioactivity, reactor downstream showed low bacteria and protein concentrations and SOCR (12.8 mg O2/g TSS·h), but high microalgae, carbohydrate, biofilm density, SOGR (49.4 mg O2/g TSS·h) and pollutants removal rates. Dissolved organic nitrogen (DON) showed higher molecular weight, CHONS and fraction with 4 atoms of N in reactor upstream. Most of nitrogen was fixed to newly synthesized biomass during assimilation process by related functional enzymes, minor contributed to denitrification due to low N2 emission. High nitrogen assimilation by microalgae showed high SOGR, which favored efficient multiple pollutants removal and reduced DON emission. Our findings favor the practical application of PF-MBBfR based on biofilm bioactivity, enhancing efficiency and reducing DON emission for low- energy-input wastewater treatment.

Tellurium-loaded organic scintillators

The R&D results of new tellurium-loaded liquid and plastic scintillators (TeLS and TePS) for the experiments on the search for neutrinoless double beta decay are presented. Linear alkylbenzene and polystyrene are used as a scintillation base for TeLS and TePS, respectively. Diphenyltellurium di-2-ethylhexanoate and a complex compound of diphenyltellurium oxide and di-(2-ethylhexyl)phosphoric acid are proposed as tellurium-containing additives. The transparency, light yield and long-term stability of the organic scintillators are discussed.

The effect of the linear alkylbenzene sulfonate, sodium-dodecyl-sulfonate (SDS), on the bioaccumulation of Al, Sr and Mn by Brassica oleracea and Solanum tuberosum

The hyper-eutrophic conditions in impoundments used for irrigation around South Africa’s major cities promote the co-existence of linear alkylbenzene sulfonate (LAS) and other pollutants such as metals. The combined effects of LAS and metals, when such water is used to irrigate crops, has not been properly investigated in light of human health risks and prevailing local conditions. To understand the potential risks, pot-culture experiments were conducted to assess the effect of the LAS, sodium-dodecyl-sulfonate (SDS), on the accumulation of aluminum (Al), manganese (Mn) and strontium (Sr) in Brassica oleracea (cabbage) and Solanum tuberosum (potato) plants. The plants were watered with dam water containing 3.48 mg‧L−1 of the LAS (sodium dodecyl sulfonate) and Mn (0.257 mg‧L−1), Al (0.6 mg‧L−1) and Sr (0.16 mg‧L−1) as determined by field surveys, for 20 days. The presence of SDS in the irrigation water at environmentally relevant concentrations did not enhance uptake of Sr, Mn, Al in the two plants, as demonstrated by statistically insignificant differences in the means of the treatments (with and without SDS). In addition, the presence of the metals, high pH, EC and presence of cyanotoxins in the water did not affect total chlorophyll and growth of the plants. These findings imply that the prevailing levels of anionic surfactants such as SDS, metals and other contaminants in the hyper-eutrophic reservoirs pose little risk to crop yields, quality of crops and human health, due to the possible accumulation of these contaminants in irrigated plants. Despite the study reporting no immediate inherent risk to the plants and human health, continuous monitoring of the contaminants in water, soil and irrigated plants is recommended since the conditions, concentrations and other factors can quickly change if the management of the catchment does not improve in the near future.

Environmental concentrations of anionic surfactants in lake surface microlayers enhance the toxicity of Microcystis blooms: Insight from photosynthesis, interspecies competition, and MC production

Anionic surfactants represented by linear alkylbenzene sulfonate (LAS) exhibit vertical heterogeneity of concentrations in aquatic environments owing to their amphiphilic structure. Field investigations showed that the concentration of anionic surfactants (mainly LAS) in the water surface microlayer (SML) of Lake Taihu reached 580 μg/L, higher than that in the lower layer. Floating Microcystis blooms overlap in space with the high concentration of anionic surfactants in SML. However, few studies have focused on the effects of anionic surfactants (e.g., LAS) on the interspecies competition between toxic and nontoxic Microcystis. In this study, coculture and monoculture experiments were conducted with both toxic and nontoxic Microcystis species to explore how the environmental concentration of LAS regulates the dominance of toxic Microcystis and toxicity from the perspective of photosynthesis, species dominance, and MC production. The results showed that LAS concentrations above 0.267 or 0.431 mg/L (depending on light conditions) selectively promoted the photosynthetic competitive advantage of toxic Microcystis, leading to its higher population proportion in the community. Additionally, LAS concentrations above 0.5 mg/L induced the synthesis and release of microcystins (MCs). The results of chlorophyll fluorescence analysis, electron microscopy and transcriptome sequencing suggested that compared with nontoxic Microcystis, toxic Microcystis can better resist LAS stress by dissipating excess light, maintaining an intact membrane structure and maintaining cellular homeostasis. Transcriptome sequencing revealed that the photosynthetic damage of nontoxic Microcystis might be attributed to the impacts of LAS on the absorption and assimilation of nitrogen, which finally resulted in the degradation of phycobilisomes. This study can provide novel insight for establishing standards and safety management of wastewater discharge.

Kajian Isoterm Adsorpsi Linear Alkilbenzena Sulfonate (LAS) dalam Limbah Cair Detergen Menggunakan Biosorben Ampas Kopi dan Ampas Kelapa

One of the efforts to minimize the impact of detergent waste pollution is by adsorption using coffee dregs and coconut dregs adsorbents. The purpose of this study was to determine the optimum mass of coffee grounds and coconut pulp as adsorbents, to compare the effectiveness of their absorption in decreasing levels of Linear Alkyl Benzene Sulfonate, and to study their adsorption isotherm models. This research was conducted in batches with variations in the mass of each adsorbent, namely 1 gram, 2 grams, 3 grams, 4 grams and 5 grams. This research was conducted in batches with variations in the mass of each adsorbent, namely 1 gram, 2 grams, 3 grams, 4 grams and 5 grams. The detergent waste samples were contacted with the adsorbent for 30 minutes and then the absorption capacity was tested using the Methylene Blue test method. The results showed that the optimum absorption of LAS content from coffee grounds and coconut pulp adsorbents occurred at a mass of 2 grams with the greatest increase in absorption efficiency index Coconut dregs adsorbent is more effective than coffee dregs because it can absorb up to 37%, while coffee dregs are only 10% with the same adsorbent mass of 5 grams. The adsorption isotherm model of the 2 types of adsorbents refers to the Langmuir equilibrium with R2 values for coffee grounds 0.8651 and coconut pulp 0.9868.

Comprehensive study on particle size distribution, MAH and PAH profiles during alkylbenzene pyrolysis

The 5 linear alkylbenzenes, i.e., toluene, ethylbenzene, n-propylbenzene, n-butylbenzene, and n-pentylbenzene as fuels underwent pyrolysis at temperatures from 950 to 1450 °C in a flow reactor. Measurements of particle number size distribution, 11 monocyclic aromatic hydrocarbons, and 3 groups of polycyclic aromatic hydrocarbons (20 unsubstituted PAHs, 5 aliphatic-bridged PAHs, and 10 methyl PAHs) during the pyrolysis of linear alkylbenzenes were conducted. Results showed that the increase in side chain length suppressed the formation of particles, but ethylbenzene produced the highest particle mass and most extensive particle number size distribution. Total particle peak number concentrations exhibited a rise-then-fall trend (peaking at a critical temperature of 1050 °C) with increasing temperature regardless of the side chain length, indicating that high temperature promoted a transition from nucleation to agglomeration and coagulation. Total PAH mass concentrations were ranked in the same order with the variation of side-chain length as particle mass and peak number concentrations, indicating that soot nucleation was highly related to total PAH mass concentrations. Unsubstituted PAHs accounted for most PAHs while substituted·PAHs, including aliphatic-bridged PAHs and methyl PAHs presented 1–2 orders of magnitude less than the corresponding unsubstituted PAHs, probably distinct thermal stability and reactivity led to different growth routes between unsubstituted and substituted PAHs. Increasing the temperature from 950 to 1250 °C, the formation of high molecular weight PAHs was promoted. while a drop of high molecular weight fractions was observed above 1350 °C, which is attributed to the suppression of the formation, as well as their conversions of high molecular weight PAHs to heavier unidentified PAHs or soot. Among the test alkylbenzene fuels, the fuels with a long side chain benefit from the reduction of particles and PAHs. Furthermore, carbon atoms in aromatic rings are dominant sources of large PAHs and particles, while the carbon atoms in aliphatic side chains mainly form gas species.

Unlocking the Secrets of River Pollution: Analyzing Organic Pollutants in Sediments—Experimental Study

Untreated wastewater released into rivers can result in water pollution, the spread of waterborne diseases, harm to ecosystems, contamination of soil and groundwater, as well as air pollution and respiratory problems for nearby humans and animals due to the release of greenhouse gases. The current study aims to investigate the recent input of anthropogenic loads into the rivers using linear alkylbenzene (LAB), which is one of the molecular chemical markers with application of sophisticated model statistical analyses. In order to determine the compositions of LABs, which act as wastewater pollution molecular indicators, surface sediment samples from the Muar and Kim Kim rivers were collected. Gas chromatography-mass spectrometry (GC-MS) was utilized to identify LABs and investigate their sources and degradation. ANOVA and the Pearson correlation coefficient were employed to determine the significance of differences between sampling locations, with a threshold of p < 0.05. To assess the degradation degree and efficacy of wastewater treatment plants (WWTPs), LABs were identified based on chains ranging from long to short (L/S), C13/C12 homolog, and internal to external (I/E) congeners. The results indicated that LAB concentrations in the studied areas of the Muar River ranged from 87.4 to 188.1 ng g−1dw. There were significant differences in LAB homology at p < 0.05, and a significant percentage of sampling stations contained C13-LAB homology. Based on the LAB ratios (I/E) determined, which ranged from 1.7 to 2.2 in the studied areas, it was concluded that effluents from primary and secondary sources are being discharged into the marine ecosystem in those areas. The degradation of LABs was up to 43% in the interrogated locations. It can be inferred that there is a requirement for enhancing the WWTPs, while also acknowledging the efficacy of LAB molecular markers in identifying anthropogenic wastewater contamination.

Linear alkylbenzene sulfonate threats to surface waters at the national scale: A neglected traditional pollutant

Freshwater biodiversity and ecosystem services might decline due to exposure to chemicals. However, researchers have devoted much attention to the potential risks of emerging contaminants, while placing less effort on historical pollutants, such as the surfactant, linear-alkylbenzene-sulfonate (LAS), which is a major component of widely used synthetic detergents worldwide. In this study, a multilevel risk assessment approach was used to assess risks posed by LAS to aquatic organisms, on a wide spatial scale, based on various assessment endpoints. Additionally, bottom-up approaches were used to assess contributions of LAS source discharges to aquatic environments. Concentrations of LAS in surface waters of China ranged from less than the limit of detection to 14,200 μg/L. The predicted no effect concentration (PNEC) based on adverse effects on reproduction is 15 μg/L, which is slightly less than the PNEC based on other endpoints. 99% of surface waters in Chaohu Lake and the Hai River (Ch: Haihe) were predicted to pose a risk to growth of aquatic organisms, with a protection threshold of 5% of species (HC5). Discharges of LAS were estimated using activity data and emission factors for 280 major cities in the basin. Rural domestic sources were the main source of LAS to surface waters. These outcomes provided a process for developing comprehensive management and control approaches to help researchers and policymakers effectively manage water resources affected by increasing concentrations of LAS.

Experimental Evaluation of Blends Containing Lineal Alkylbenzene Sulfonates for Surfactant Flooding in Carbonate Reservoirs

Summary About one-half of the proven conventional oil reserves are in carbonate reservoirs. However, conducting surfactant flooding in these reservoirs presents several challenges, including formation heterogeneities, surfactant retention, high temperature and salinity, and oil-wet/mixed-wet conditions. Linear alkylbenzene sulfonates (LASs) are low-cost anionic surfactants that tend to precipitate in high-salinity environments and show high adsorption values in carbonate material. In this paper, the possibility of using petrochemical LASs of different alkyl chain lengths and isomer content to extract oil from carbonate reservoirs was tested using blends with the ionic liquid cocosalkylpentaethoximethylammonium methylsulfate (C1EG). Phase behavior, stability in the presence of divalent ions, and interfacial tension (IFT) measurements were the criteria used to design several optimal formulations containing 36–45% LASs. The structure-performance relationship was further assessed via static adsorption and wettability tests. LASs enriched in isomers with the benzenesulfonic group in external positions of the alkyl chain resulted in lower IFT but significantly higher adsorption, so those surfactants were discarded for the application. Additional oil recoveries achieved with tested formulations ranged from 36.7% to 43.5% of the residual oil in place. The longer the alkyl chain length, the higher the oil recovery. The main mechanism associated with improved oil recovery is IFT reduction. The use of a cost-effective ionic liquid derived from natural raw materials, the stability of the blends, the low adsorption of the chemical, and a significant oil recovery ensure the overall feasibility of the proposal.

CuCl2-modified ionic liquids for alkylation of benzene with 1-dodecene

Abstract Benzene and 1-dodecene are often alkylated to produce linear alkylbenzene (LAB). LAB is the raw material for the production of linear alkylbenzene sulfonate (LAS), a very important anionic surfactant used in both industrial cleaning and commercial laundry processes, as well as in household laundry detergents. In the present study, we investigated the use of [Et3NH]Cl–2AlCl3 modified with CuCl2 as a catalyst for the alkylation of benzene with 1-dodecene, specifically looking at the effect of reaction conditions on product activity. The results showed that a conversion of 1-dodecene of 100.0 % and a selectivity of LAB of 93.79 % could be obtained when the following ideal reaction conditions were present: molar ratio of benzene/1-dodecene = 6, reaction temperature = 25 °C, reaction time = 10 min, stirring speed of 1000 rpm and addition of 5.0 mol % CuCl2). The catalyst concentration was 7.0 mol %. FTIR and 31P-TMPO-NMR measurements were performed to characterise the ionic liquid before and after the addition of CuCl2. After the addition of CuCl2, it was found that the acidity of the ionic liquid had decreased. The regeneration of the catalyst was also investigated and the cause of inactivation of the catalyst was determined. The results showed that CuCl2 modified the ionic liquids and decreased the benzene/1-dodecene ratio, but the high product selectivity was maintained.

A kinetic modeling study on the effect of alkylbenzenes structure on PAH formation at elevated pressures

Alkylbenzene is one of the significant components of practical transport fuel, which is considered as the main reason leading to serious emissions of polycyclic aromatic hydrocarbon (PAH) from combustion processes. This work reports a kinetic modeling study on the impact of alkylbenzenes structure, i.e., the length and number of the alkyl side chain, on PAH formation at elevated pressures. A detailed kinetic model has been established and a large number of reactions concerning the PAH species formation have been updated according to the latest theoretical studies. The model is then verified by the previous experimental data containing the concentration profiles of PAH species. The fuel decomposition reactivity and the mole fraction curves of monocyclic aromatic hydrocarbon and polycyclic aromatic hydrocarbon can be well predicted by the present model. The kinetic analysis indicates that the dominant formation pathways of PAHs are barely influenced by the alkyl side chain length, especially at the high-temperature window. In the A1_C1-C4 linear alkylbenzenes pyrolysis system, the formation of benzene is mainly affected by the competition between the combination reaction of C5H3 with CH3 and the ipso-substitution reaction of A1CH3 by H. Unlike the A1_C1-C4 linear alkylbenzenes pyrolysis chemistry, fuel-related reactions associated with the formation of PAHs become more usual as the number of alkyl side chain increases, such as the formation pathway of C9 species in the pyrolysis chemistry of o-xylene and the formation pathway of phenanthrene in the oxidation chemistry of 1,3,5-trimethylbenzene.

Sunlight Assisted Degradation of Linear Alkylbenzene Sulfonate by Floating Catalyst TiO2-Coconut Fiber

The increasing number of laundry businesses in Pontianak causes increased laundry waste, which is dangerous for health and the environment because anionic surfactants such as Linear Alkylbenzene Sulfonate (LAS) are hard degradable. Photocatalyst is a method that can be used to degrade the LAS structure. TiO2 carried in coconut fiber can optimize sunlight irradiation in degrading LAS content when light reaches the water's surface. This study aims to determine the characteristics and optimum activity time of photocatalyst TiO2-coconut fiber in degrading LAS. Photocatalyst characterization was carried out using XRD, XRF, and DR-UV, while the optimum activity test of photocatalysts in degrading LAS was carried out using a UV-Vis spectrophotometer. XRD diffractogram analysis showed the peaks of coconut fiber at 2θ = 22.2º, 34.8º and TiO2 at 2θ = 25.3º, 37.8º, 48.1º, 55.1º, and 62.1º. The TiO2 attached to the fiber after being synthesized was 21.12%. The band gap of TiO2 and TiO2-coconut fiber is 3.21 and 3.18 eV, with light absorption at 386.5 and 390.3 nm. Photocatalyst was carried out in LAS with a mass ratio of TiO2 and coconut fiber of 20:80; 30:70; 40:60, and 50:50 w/w with a time range of 0, 30, 60, 90, and 120 minutes. The results of photocatalysis of TiO2-coconut fiber in a ratio of 20:80 w/w showed the optimum photocatalytic activity at 120 minutes with the highest degradation rate of 80.43%. This research is expected to be applied as an alternative to handling LAS in laundry industry waste.

Lateral distribution, environmental occurrence, and assessment of organic pollutants in surface sediments of the East Malaysia.

One of the molecular chemical markers used to identify anthropogenic inputs is linear alkylbenzenes (LABs) that cause serious impacts in the bays and coastal ecosystems. The surface sediments samples collected from the East Malaysia, including Brunei bay to estimate the LABs concentration and distribution as molecular markers of anthropogenic indicators. Gas chromatography-mass spectrometry (GC-MS) was used after purification, fractionation the hydrocarbons in the sediment samples to identify the sources of LABs. The analysis of variance (ANOVA) and Pearson correlation coefficient were applied to analyze the difference between sampling stations' significance at p < 0.05. Long to short chains L/S, homologs C13/C12, and internal to external (I/E) congeners have used to assess the LABs degradation rates as well as the effectiveness of sewage treatment. Results of this study showed that the LABs concentration ranged between 7.1 to 41.3ngg-1 dw, in the investigated stations. The majority of sample sites exhibited a considerable input of C13-LABs homologs, and LABs homologs differed significantly. The estimated LABs ratios (I/E), which ranged between 0.6 and 2.2, demonstrated the effluents with primary and less secondary sources are released into the bay waters. The degradation of LABs were up to 42% in the interrogated locations. The conclusion is that the wastewater treatment system needs to be improved, and that LABs molecular markers are highly effective in tracing anthropogenic sewage contamination.