Degree Of Unsaturation Research Articles

Mono- to tetra-alkyl ether cardiolipins in a mesophilic, sulfate-reducing bacterium identified by UHPLC-HRMSn: a novel class of membrane lipids.

The composition of membrane lipids varies in a number of ways as adjustment to growth conditions. Variations in head group composition and carbon skeleton and degree of unsaturation of glycerol-bound acyl or alkyl chains results in a high structural complexity of the lipidome of bacterial cells. We studied the lipidome of the mesophilic, sulfate-reducing bacterium, Desulfatibacillum alkenivorans strain PF2803T by ultra-high-pressure liquid chromatography coupled with high-resolution tandem mass spectrometry (UHPLC-HRMSn). This anaerobic bacterium has been previously shown to produce high amounts of mono-and di-alkyl glycerol ethers as core membrane lipids. Our analyses revealed that these core lipids occur with phosphatidylethanomamine (PE) and phosphatidylglycerol (PG) head groups, representing each approximately one third of the phospholipids. The third class was a novel group of phospholipids, i.e., cardiolipins (CDLs) containing one (monoether/triester) to four (tetraether) ether-linked saturated straight-chain or methyl-branched alkyl chains. Tetraether CDLs have been shown to occur in archaea (with isoprenoid alkyl chains) but have not been previously reported in the bacterial Domain. Structurally related CDLs with one or two alkyl/acyl chains missing, so-called monolyso-and dilyso-CDLs, were also observed. The potential biosynthetic pathway of these novel CDLs was investigated by examining the genome of D. alkenivorans. Three CDL synthases were identified; one catalyzes the condensation of two PGs, the other two are probably involved in the condensation of a PE with a PG. A heterologous gene expression experiment showed the in vivo production of dialkylglycerols upon anaerobic expression of the glycerol ester reductase enzyme of D. alkenivorans in E. coli. Reduction of the ester bonds probably occurs first at the sn-1 and subsequently at the sn-2 position after the formation of PEs and PGs.

Biocidal efficacy of olefinic N-alkylamides against Aedes aegypti and Culex quinquefasciatus larvae

Mosquito-borne diseases are a major public-health concern worldwide. The development of resistance in mosquitoes to the existing larvicides and the associated-risks necessitates the exploration of novel molecules to control vector-borne pathogens. This study demonstrates that N-alkylamides [2E,4E-N-isobutyl-undeca-2,4-diene-8,10-diynamide (1) and 2E,4E,8Z,10E-N-isobutyl-dodeca-2,4,8,10-tetraenamide (2)] of Acmella ciliata exhibit biocidal action against Aedes aegypti and Culex quinquefasciatus larvae. The LC50 for 1 and 2 were 44.19 and 18.28 ppm against Aedes larvae, and 30.89 and 11.75 ppm against Culex larvae, respectively. We further observed that the chain length, degree of unsaturation, and terminal methylation influence the larvicidal efficacy of N-alkylamides. HPLC-assisted quantification revealed that the content of both 1 (19.01 mg/g) and 2 (68.55 mg/g) was maximum in the flowers of A. ciliata. Thus, this study concludes that N-alkylamides are promising alternatives to control mosquito larvae and can be used as standard for quantitation in test samples.

Impact of fuel injection parameters associated with partially hydrogenated Ceiba pentandra biodiesel blend on CI engine characteristics

Multiple studies have shown that biodiesel blends significantly cut exhaust emissions. However, the most significant challenge was the rising emission of oxides of nitrogen (NOx). The authors' prior research showed that a Ceiba pentandra biodiesel blend (B20) with a higher IP of 260 bar and an advanced IT of 27° BTDC as an optimal Fuel injection parameter (FIP) resulted in superior combustion and reduced emissions except NOx. To further enhance engine performance, fuel reformulation strategies have been implemented together with FIP modification. This research intends to examine the impact of FIP combined with blending of partially hydrogenated biodiesel (HB) on engine characteristics. As a result of partial hydrogenation, the degree of unsaturation decreased by 60%, and the Cetane Number (CN) increased by 22%. Higher BTE (8%), TFC (3.4%), CP (13%), HRR (5%) and lower HC (12%), and CO (5.5%) emissions can be achieved when HB20 was combined with optimal FIP. Superior outcomes were seen with hydrogenated blend (HB20) than with normal B20, with a reduction in NOx emissions by 6.7% without significantly impacting the smoke emission trade-off. Thus, cutting-edge fuel reformulation approaches make way for eco-friendly engineering.

Association of circulating long-chain free fatty acids and incident diabetes risk among normoglycemic Chinese adults: a prospective nested case–control study

BackgroundLong-chain free fatty acids (FFAs) are associated with risk of incident diabetes. However, a comprehensive assessment of the associations in normoglycemic populations is lacking. ObjectivesOur study aimed to comprehensively investigate the prospective associations and patterns of FFA profiles with diabetes risk among normoglycemic Chinese adults. MethodsThis is a prospective nested case–control study from the China Cardiometabolic Disease and Cancer Cohort (4C) study. We quantitatively measured 53 serum FFAs using a targeted metabolomics approach in 1707 incident diabetes subjects and 1707 propensity score–matched normoglycemic controls. Conditional logistic regression models were employed to estimate odds ratios (ORs) for associations. Least Absolute Shrinkage and Selection Operator (LASSO) penalty regression and quantile g-computation (qg-comp) analyses were implemented to estimate the association between multi-FFA exposures and incident diabetes. ResultsThe majority of odd-chain FFAs exhibited an inverse association with incident diabetes, wherein the ORs per SD increment of all 7 saturated fatty acids (SFAs), monounsaturated fatty acid (MUFA) 15:1, and polyunsaturated fatty acid (PUFA) 25:2 were ranging from 0.79 to 0.88 (95% CIs ranging between 0.71 and 0.97). Even-chain FFAs comprised 99.3% of total FFAs and displayed heterogeneity with incident diabetes. SFAs with 18–26 carbon atoms are inversely linked to incident diabetes, with ORs ranging from 0.81 to 0.86 (95% CIs ranging between 0.73 and 0.94). MUFAs 26:1 (OR: 0.85; 95% CI: 0.76, 0.94), PUFAs 20:4 (OR: 0.84; 95% CI: 0.75, 0.94), and 24:2 (OR: 0.87; 95% CI: 0.78, 0.97) demonstrated significant associations. In multi-FFA exposure model, 24 FFAs were significantly associated with incident diabetes, most of which were consistent with univariate results. The mixture OR was 0.78 (95% CI: 0.61, 0.99; P = 0.04159). Differential correlation network analysis revealed pre-existing perturbations in intraclass and interclass FFA coregulation before diabetes onset. ConclusionsThese findings underscore the variations in diabetes risk associated with FFAs across chain length and unsaturation degree, highlighting the importance of recognizing FFA subtypes in the pathogenesis of diabetes.

Size-Dependent Catalysis in Fenton-like Chemistry: From Nanoparticles to Single Atoms.

State-of-the-art Fenton-like reactions are crucial in advanced oxidation processes (AOPs) for water purification. This review explores the latest advancements in heterogeneous metal-based catalysts within AOPs, covering nanoparticles (NPs), single-atom catalysts (SACs), and ultra-small atom clusters. A distinct connection between the physical properties of these catalysts, such as size, degree of unsaturation, electronic structure, and oxidation state, and their impacts on catalytic behavior and efficacy in Fenton-like reactions. In-depth comparative analysis of metal NPs and SACs is conducted focusing on how particle size variations and metal-support interactions affect oxidation species and pathways. The review highlights the cutting-edge characterization techniques and theoretical calculations, indispensable for deciphering the complex electronic and structural characteristics of active sites in downsized metal particles. Additionally, the review underscores innovative strategies for immobilizing these catalysts onto membrane surfaces, offering a solution to the inherent challenges of powdered catalysts. Recent advances in pilot-scale or engineering applications of Fenton-like-based devices are also summarized for the first time. The paper concludes by charting new research directions, emphasizing advanced catalyst design, precise identification of reactive oxygen species, and in-depth mechanistic studies. These efforts aim to enhance the application potential of nanotechnology-based AOPs in real-world wastewater treatment.

Biodiesel production from the microalgae Nannochloropsis gaditana: Optimization of the transesterification reaction and physicochemical characterization

The current environmental scenario has encouraged the study of renewable and competitive alternative feedstocks for biodiesel production. Microalgae present a significant opportunity as a feedstock that does not require arable land and can be cultivated using wastewater. The paper investigates the optimization of biodiesel production from microalgae Nannochloropsis gaditana bio-oil using response surface methodology and also analyzes the main physicochemical properties of the bio-oil. It was confirmed that this methodology is suitable for materials with low homogeneity. The model is also adequate for determining optimal experimental conditions, resulting in a FAME content of 87.25 %. The biodiesel's physicochemical properties were analyzed. It was discovered that the high degree of unsaturation in the microalgae bio-oil's chemical structure resulted in a narrower temperature range for its application compared to other vegetable sources.

Optimizing humic acid breakdown and methane production via semiconductor-assisted photo-anaerobic digestion

Humic acids (HAs), whether naturally present in anaerobic digestion (AD) substrates or HAs newly formed during fermentation, can become inhibitory to methanogenesis as their concentrations reach certain levels. This study delved extensively into the mechanism underlying the alleviation of HAs inhibition in photo-AD by N-doped carbon quantum dots (NCQDs). These NCQDs were efficiently synthesized from straw using an environmentally friendly pretreatment method. Our proposed method harnessed the combined effect of light exposure and NCQDs, resulting in synergistic enhancement of the cumulative CH4 yield within the HA-inhibited AD system, achieving a remarkable yield of 293.7 ± 17.7 mL/g VS. In-depth analyses were conducted on the remaining dissolved organic matter (DOM) within digesters using 3D-EEM and ESI FT-ICR MS. Simultaneously, the remaining HAs were extracted and subjected to FT-IR analysis. The findings revealed that NCQDs effectively degraded humic acid-like components in DOM into smaller, more manageable micromolecules characterized by lower carbon numbers and reduced double bond equivalent. Additionally, under the influence of light, NCQDs promoted the degradation of aromatic components within HAs. These resulting micromolecules were made readily available for utilization by microorganisms, further contributing to methanogenesis. Furthermore, photoelectrochemical analysis and specific gene qPCR analysis revealed that the photoelectrons from NCQDs and HAs were received and transferred by Ech (electron acceptors) for methanogenesis. Remarkably, this methanogenesis pathway, akin to photosynthesis, played a pivotal and transformative role in the photo-AD system. This work comprehensively revealed the remarkable potential mechanism of semiconductors within the photo-AD system, offering profound insights that can catalyze the development of innovative AD reactors and semiconductor accelerators.

Influence of pyrolysis temperature on carbon deposition from the perspective of volatile evolution during the ex-situ pyrolysis-catalysis of plastic

To better understand the mechanism of carbon deposition, the ex-situ catalytic pyrolysis of polyethylene (PE) was explored over a FeNi/Al2O3 catalyst, and the evolution of volatiles as well as the yield and structure of carbon products at different temperatures were analyzed in depth by an in-situ atmospheric pressure photoionization high-resolution mass spectrometry (APPI HRMS) combined with a fixed-bed reactor. The results show that raising the pyrolysis temperature (from 500 to 800 °C) reduces carbon product yield and H2 production, and the proportion of carbon nanotubes (CNTs) in the carbon products decreases. The source of carbon products gradually shifts from liquid-phase carbon sources to gaseous-phase carbon sources. Below 700 °C, both the outer diameter and carbon interlayer spacing of CNTs decrease, while above 700 °C, they both increase along with increased distortion of carbon layers. It is also observed that the carbon layers are connected to the catalyst lattice stripes, and the interlayer spacing of carbon layers is greater than the catalyst lattice spacing. In situ mass spectrometry reveals a significant increase in the carbon number and double bond equivalent (DBE) values of volatiles with increasing pyrolysis temperature, but the rate of increase slows down after 700 °C. Volatiles from lower pyrolysis temperatures undergo severe polymerization, upon entering the catalytic zone at higher temperatures, minimizing temperature-induced distinctions. Nevertheless, it remains evident that volatiles from lower pyrolysis temperatures exhibit less pronounced polymerization when exposed to higher catalytic temperatures.

Adjusting the dynamic and mechanochromic properties of aromatic disulfide epoxy vitrimers by unsaturation of epoxy monomers

AbstractDisulfide‐contained vitrimers that possess unprecedented functions, such as reprocessing and self‐healing, are considered to be one of the most promising materials since they also exhibit mechanochromic behaviors. A few reports have given the phenomenon of mechanochromism, but the relationship between their structure and mechanochromic behavior needed to further research. Herein, three aromatic disulfide‐contained epoxy vitrimers with different degree of unsaturation are prepared by changing the epoxy monomer. The effect of network structure on the dynamic and mechanochromic properties are investigated. With increasing the degree of unsaturation from the aliphatic to aromatic epoxy vitrimers, the Tg‐value increases and the chain mobility decreases, so the aliphatic epoxy vitrimers shows the lowest activation energy, the lowest temperature of malleability Tv, and the shortest relaxation times. In addition, these epoxy vitrimers all showes reversible mechanochromic behaviors due to the generation and coupling of sulfenyl radicals, which can be accelerated by the high temperature and solvent. Meanwhile, the epoxy structure has a great influence on the mechanochromic behavior, including the absorption wavelength and fading kinetics of grinding powders. These results can be utilized to design desired vitrimer materials for various applications that requires both the intrinsically self‐report damage and the dynamic properties such as recycling.

Comprehensive characterization of organics in oil sands process water in constructed mesocosms utilizing multiple analytical methods

This study aims to provide a thorough characterization of dissolved organics in oil sands process water (OSPW) in field-based aquatic mesocosms at both molecular and bulk measurement levels using multiple analytical methods. In a 3-year outdoor mesocosm experiment, the analysis of naphthenic acid (NA) species was conducted using ultra-performance liquid chromatography time-of-flight mass spectrometry (UPLC-TOFMS). The results revealed the removal of both total NAs (38% and 35%) and classical NAs (O2–NAs, 58% and 49%) in undiluted and half-diluted OSPW, respectively. The increased ratios of oxidized NAs (O3–O6 NAs) to classical NAs suggested a transformation trend. The results also indicated that O2–NAs with higher carbon number and lower double bond equivalent (DBE) were more easily degraded in the mesocosm systems. Biomimetic extraction using solid-phase microextraction (BE-SPME) measurement displayed 26% (undiluted OSPW) and 30% (half-diluted OSPW) decrease in total bioavailable organics over 3 years. Naphthenic acids fraction compounds (NAFCs) obtained by liquid-liquid extraction (LLE) were also determined using Fourier transform infrared spectroscopy (FTIR). Reduction in acute toxicity for undiluted (43%) and half-diluted (26%) OSPW was observed over 3 years, which are well correlated with the decreases of NAs and BE-SPME concentrations. Moreover, BE-SPME values were found to be linearly correlated with total NAs concentrations (r = 0.96) and NAFCs (r = 0.96). Additionally, the linear relationships of individual O2–O6 NA species and BE-SPME concentrations unveiled the changes in the relative abundances of O2–O6 NA species in total bioavailable organics over time in the mesocosms. The present study has provided comprehensive insights by integrating various analytical methods, contributing valuable information for assessing the effectiveness of aquatic mesocosm systems in studying the temporal changes of organics in OSPW.

Selective lipid recruitment by an archaeal DPANN symbiont from its host

The symbiont Ca. Nanohaloarchaeum antarcticus is obligately dependent on its host Halorubrum lacusprofundi for lipids and other metabolites due to its lack of certain biosynthetic genes. However, it remains unclear which specific lipids or metabolites are acquired from its host, and how the host responds to infection. Here, we explored the lipidome dynamics of the Ca. Nha. antarcticus – Hrr. lacusprofundi symbiotic relationship during co-cultivation. By using a comprehensive untargeted lipidomic methodology, our study reveals that Ca. Nha. antarcticus selectively recruits 110 lipid species from its host, i.e., nearly two-thirds of the total number of host lipids. Lipid profiles of co-cultures displayed shifts in abundances of bacterioruberins and menaquinones and changes in degree of bilayer-forming glycerolipid unsaturation. This likely results in increased membrane fluidity and improved resistance to membrane disruptions, consistent with compensation for higher metabolic load and mechanical stress on host membranes when in contact with Ca. Nha. antarcticus cells. Notably, our findings differ from previous observations of other DPANN symbiont-host systems, where no differences in lipidome composition were reported. Altogether, our work emphasizes the strength of employing untargeted lipidomics approaches to provide details into the dynamics underlying a DPANN symbiont-host system.

Optical properties and molecular compositions of dissolved organic matter in multiple runoff components during rainfalls on the karst hillslope

Understanding the chemical composition, origin, and molecular structure of dissolved organic matter (DOM) in multi-interface runoff is essential for comprehending the fate of laterally transported DOM in complex soil-epikarst systems of karst hillslopes. Limited information, however, is available for the optical properties and molecular compositions of the transported OM in multiple runoff components on the karst hillslope in relation to land-uses and soil thicknesses. In this study, we conducted a study to observe the changes in the quantity and quality of DOM in multiple interface flow (surface, subsurface, and epikarst) during natural rainfall events in 2022 in karst hillslopes that are covered by different land uses (cropland and shrubland) and soil thicknesses (with mean depths of 66.0 cm for deeper soil and 35.4 cm for shallower soil) in the karst region of southwest China. chemcial compositions of runoff DOM were determined by optical analysis and microbial compositions in runoff were inferred with high-throughput sequencing. The results showed that the soil-epikarst structure was controlling the runoff DOM quantity and quality during rainfall events. A decrease in the aromaticity, humification, unsaturation, and oxidation degree and an increase in carbohydrate, aminosugars, protein, and lipid compounds were found from surface to epikarst flow, indicating that plant-and soil-derived carbon decreased, while the microbially-derived carbon increased. The results were further comfirmed by the higher bacterial richness and diversity, along with fungal diversity in the epikarst flow compared to other runoff components. The bio-labile protein materials (C2) were the most important component of runoff DOM output in karst hillslopes. In surface and subsurface flow, rainfall amount, runoff rate, and discharge significantly affected the DOM concentration and quality during rainfalls, indicating that the dynamics of DOM in runoff from karst hillslopes were predominantly influenced by hydrological processes. Furthermore, the runoff DOM quality in cropland was dominated by lower unsaturation and oxidation degrees and higher protein component, compared to those in shrubland. The compositions of DOM in runoff from hillslope plots with thicker soils were primarily characterized by microbially-derived materials. Our findings were conducive to understanding the mechanism governing the migration of DOM quality and quantity in discharge during multi-interface hydrological processes on karst hillslopes.

Impact of Hair Damage on the Penetration Profile of Coconut, Avocado, and Argan Oils into Caucasian Hair Fibers

The mitigation of damaged hair conditions involves the application and penetration of substances to stabilize broken bond sites, restore lipids and proteins, reinstate hydrophobicity, and recover hair mechanical properties. Vegetable oils, in general, exhibit a list of advantageous characteristics much desired by consumers, given the associated benefits for hair fibers. While coconut oil is highly popular in the hair care market and extensively studied for its ability to diffuse through the hair cortex, the effects of avocado and argan oil on the internal structure of hair and their potential benefits remain underexplored. Tensile and fatigue tests, as well as Raman spectroscopy, were carried out to investigate the interaction of these three oils with virgin and bleached Caucasian hair. The oils were applied in sufficient amounts directly to hair tresses and maintained for 24 h at 25 °C. Our results show that the three oils successfully diffused and interacted with the cortical region of the hairs. Their impact on hair mechanical properties depends on the level of damage and humidity conditions. In virgin hair, coconut and avocado oil reinforce the hydrophobic barrier of the cellular membrane complex, preventing water from causing intense perturbation of the mechanical properties, leading to increased stiffness and break stress. Meanwhile, due to the high degree of unsaturation of its fatty acid chains, argan oil increases water absorption, resulting in losses in hair resistance. When bleached, the hydrophilicity of the hair fiber increases, determining more affinity for argan oil. Consequently, the affinity with water is also elevated, causing increased fragility to mechanical stress. The analyzed vegetable oils are not always beneficial for hair care. Their specific chemical characteristics and hair conditions will influence the final results and should be taken into consideration in hair care product development.

In silico analysis of the action of saturated, monounsaturated, and polyunsaturated fatty acids against Echinococcus granulosus fatty-acid-binding protein 1

Background The zoonotic infection caused by tapeworms Echinococcus is a neglected tropical disease in poor regions with limited access to suitable sanitary conditions. Hydatid cysts produced by Echinococcus granulosus use fatty-acid-binding proteins (FABP) to obtain the fatty acids and cholesterol necessary for their survival from the host. In this work, we analyzed the behaviour of saturated, monounsaturated, and polyunsaturated fatty acids against EgFABP1. Methods We used computational biology and chemistry techniques and binding free energy estimations by molecular mechanics generalized Born surface area (MM/GBSA). Results This research has enabled us to clarify the EgFABP1 isoforms identified in the database, suggesting their potential involvement in diverse cellular activities of Echinococcus granulosus. Conversely, examining the global and local chemical reactivity of 14 fatty acids revealed that liposolubility is contingent upon the degree of unsaturation in the FAs. Additionally, FAs exhibited acceptable levels of oral absorption and bioavailability. The binding of EgFABP1 with FAs analyzed by molecular dynamics simulation showed us that these are highly stable, where the best affinity was with docosahexaenoic acid. Conclusions Our results suggest that the action of fatty acids could play an interesting role in detecting early Echinococcus granulosus.

Chemical composition of biodiesel produced in situ with Salvinia molesta DS Mitchell (Salviniaceae) by ethylic and methylic route

Macrophytes are aquatic plants that can cause environmental and economic damage due to their rapid growth in eutrophicated environments; however, this characteristic makes these biomasses promising alternatives for biodiesel production. Thus, this study aims to characterize and evaluate the chemical composition of the biodiesel produced from the macrophyte Salvinia molesta DC Mitchell (Salviniaceae). The biodiesel production was carried out in situ through the ethyl and methyl process. Attenuated total reflectance-Fourier transform infrared spectroscopy (FTIR-ATR) and gas chromatography with a flame ionization detector (GC-FID) were used to characterize the product. A commercial sample was also analyzed for comparison purposes. The biofuel produced with ethanol and methanol showed characteristic peaks between 900 to 1300 cm-1 and 1750 to 1735 cm-1 in the FTIR-ATR. Both samples showed less unsaturation degree compared to the commercial sample, with 34.44% of monounsaturated compounds (MUFA) and 36.73% of polyunsaturated compounds (PUFA) for methylic biodiesel, 34.79% of MUFA and 36.89% of PUFA for ethylic biodiesel, and 55.34% of MUFA and 24.14% of PUFA for commercial biodiesel. Samples produced by both routes showed similar chemical composition, with higher contents of saturated compounds than the commercial sample. The average chain size and the number of double bonds are smaller for S. molesta samples, 17.38 and 1.15 for S. molesta biodiesels and 17.65 and 1.41 for commercial biodiesel, respectively. The chemical composition of S. molesta biodiesel demonstrates the potential to be an alternative to commercial biodiesel.

Glycerophospholipid polyunsaturation modulates resveratrol action on biomimetic membranes

The phytoalexin resveratrol has received increasing attention for its potential to prevent oxidative damages in human organism. To shed further light on molecular mechanisms of its interaction with lipid membranes we study resveratrol influence on the organisation and mechanical properties of biomimetic lipid systems composed of synthetic phosphatidylcholines with mixed aliphatic chains and different degree of unsaturation at sn-2 position (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine, POPC, and 1-palmitoyl-2-docosahexaenoyl-sn-glycero-3-phosphocholine, PDPC). High-sensitivity isothermal titration calorimetric measurements reveal stronger spontaneous resveratrol association to polyunsaturated phosphatidylcholine bilayers compared to the monounsaturated ones resulting from hydrophobic interactions, conformational changes of the interacting species and desolvation of molecular surfaces. The latter is supported by the results from Laurdan spectroscopy of large unilamellar vesicles providing data on hydration at the glycerol backbones of glycerophospholipides. Higher degree of lipid order is reported for POPC membranes compared to PDPC. While resveratrol mostly enhances the hydration of PDPC membranes, increasing POPC dehydration is reported upon treatment with the polyphenol. Dehydration of the polyunsaturated lipid bilayers is measured only at the highest phytoalexin content studied (resveratrol/lipid 0.5 mol/mol) and is less pronounced than the effect reported for POPC membranes. The polyphenol effect on membrane mechanics is probed by thermal shape fluctuation analysis of quasispherical giant unilamellar vesicles. Markedly different trend of the bending elasticity with increasing resveratrol concentration is reported for the two types of phospholipid bilayers studied. POPC membranes become more rigid in the presence of resveratrol, whereas PDPC-containing bilayers exhibit softening at lower concentrations of the polyphenol followed by a slight growth without bilayer stiffening even at the highest resveratrol content explored. The new data on the structural organization and membrane properties of resveratrol-treated phosphatidylcholine membranes may underpin the development of future liposomal applications of the polyphenol in medicinal chemistry.

A facile strategy to simultaneously enhance the flame retardancy, toughness and ultraviolet shielding performance of unsaturated polyester resin: Adjusting the unsaturated degree of flame retardant

The impact of three phosphonate oligomers with different unsaturation degrees on the flame retardancy, mechanical properties and optical performance of unsaturated polyester resins (UPRs) were investigated. The three phosphonate oligomers were poly(2-butyne-1,4-diol phenylphosphonate) (PY) containing C C, poly(cis-2-butene-1,4-diol phenylphosphonate) (PE) containing CC and poly(1,4-butanediol phenylphosphonate) (PO) without unsaturated bonds. The flame retardancy and UV-shielding effect of UPRs were positively correlated with the unsaturation degree of oligomers. Specifically, only adding 20 wt% PY made UPR pass UL-94 V-0 rating and 22 wt% PE was needed, while 22%PO/UPR was still in UL-94 NR rating. Further, PE containing CC exhibited the highest efficiency in improving the toughness of UPR. The impact strength and elongation at break of 22%PE/UPR were significantly improved by 460 % and 200 % respectively, compared with pure UPR. Meanwhile, the high transparency of UPRs benefits from the good compatibility between oligomers and matrix. This work provides the basis for development and utilization of novel high-performance and multifunctional UPRs with potential versatile applications.

Effect of pre-treatments and frying conditions on the formation of starch-lipid complex in potato starch chips during deep-frying process

This study examined the influence of various pretreatment methods, frying durations, and temperatures, as well as the type of frying oil, on the formation and structure of starch-lipid complexes in fried potato chips. Potato starch was processed into dough, sliced, and subjected to deep frying following various pretreatments. Structural analysis showed that steaming as a pretreatment facilitated the generation of V-type starch-lipid complexes, whereas resistant starch type III (RS3) materialized in the desiccated samples instead of the anticipated complexes. The rate of starch-lipid complex formation initially surged but subsequently declined as treatment time increased. A reduction in treatment temperature from 190 °C to 170 °C was conducive to complex formation. Moreover, the maximum relative crystallinity (19.74 %) and ΔH value (7.76 J/g) were recorded for potato starch slices pretreated by steaming and frying in palm oil. Rapeseed oil, which is rich in unsaturated fatty acids (89.98 %), inhibits complex formation. The study concludes that pretreatment methods exert a substantial effect on the formation of starch-lipid complexes and that extended frying duration and elevated temperature may reduce this formation. Oils with longer-chain fatty acids and a lower degree of unsaturation were favorable for complex formation.

Photochemical evolution of the molecular composition of dissolved organic carbon and dissolved brown carbon from wood smoldering

Recently, extreme wildfires occur frequently around the world and emit substantial brown carbon (BrC) into the atmosphere, whereas the molecular compositions and photochemical evolution of BrC remain poorly understood. In this work, primary smoke aerosols were generated from wood smoldering, and secondary smoke aerosols were formed by the OH radical photooxidation in an oxidation flow reactor, where both primary and secondary smoke samples were collected on filters. After solvent extraction of filter samples, the molecular composition of dissolved organic carbon (DOC) was determined by Fourier transform ion cyclotron resonance mass spectrometry (FTICR MS). The molecular composition of dissolved BrC was obtained based on the constraints of DOC formulae. The proportion of dissolved BrC fractions accounted for approximately 1/3–1/2 molecular formulae of DOC. The molecular characteristics of dissolved BrC showed higher levels of carbon oxidation state, double bond equivalents, and modified aromaticity index than those of DOC, indicating that dissolved BrC fractions were a class of organic structures with relatively higher oxidation state, unsaturated and aromatic degree in DOC fractions. The comparative analysis suggested that aliphatic and olefinic structures dominated DOC fractions (contributing to 70.1%-76.9%), while olefinic, aromatic, and condensed aromatic structures dominated dissolved BrC fractions (contributing to 97.5%-99.9%). It is worth noting that dissolved BrC fractions only contained carboxylic-rich alicyclic molecules (CRAMs)-like structures, unsaturated hydrocarbons, aromatic structures, and highly oxygenated compounds. CRAMs-like structures were the most abundant species in both DOC and dissolved BrC fractions. Nevertheless, the specific molecular characteristics for DOC and dissolved BrC fractions varied with subgroups after aging. The results highlight the similarities and differences in the molecular compositions and characteristics of DOC and dissolved BrC fractions with aging. This work will provide insights into understanding the molecular composition of DOC and dissolved BrC in smoke.

Analysis of the microstructure of high viscosity components in Tahe ultra heavy oil based on the combination of ESI (±) FT-ICR/MS

In addressing the challenge of high viscosity in Xinjiang Tahe heavy oil, crucial for optimizing extraction processes, this study focuses on identifying and analyzing the microstructure of key components influencing oil viscosity. The aim is to uncover the underlying reasons for its high viscosity and guide research towards effective viscosity reduction techniques. Electrospray ionization (ESI) combined with fourier transform ion cyclotron resonance mass spectrometry (FT-ICR/MS) characterizes the molecular-level constituents contributing to oil viscosity. The investigation covers the composition and distribution of oxygen-containing, nitrogen-containing, and organometallic compounds, developing a molecular structure model for these critical viscosity-inducing components. Findings reveal Xinjiang Tahe extra heavy oil as a solid mass at room temperature, with significant viscosity reduction observed post-deasphalting, highlighting asphaltenes' pivotal role in viscosity. Analysis indicates a higher content of metal elements (such as V and Ni) in asphaltenes compared to the crude oil itself, with an abundance of porphyrin structures in asphaltenes markedly influencing oil viscosity. Cyclic, aromatic, and unsaturated compound structures are predominantly found in the asphaltenes of heavy oil. Through combined ESI (±) FT-ICR/MS analysis, the crude oil is determined to mainly comprise acidic compounds, non-basic nitrogen compounds, and basic nitrogen compounds, offering significant insight into heavy oil's complex chemical composition. Specifically, non-basic nitrogen compounds in Tahe crude oil, including alkylcarbazoles, alkylbenzocarbazoles, and alkylpolybenzocarbazoles, are identified as key components, with molecular carbon numbers ranging from C12 to C56 and a predominance near C27. Additionally, asphaltenes in Tahe heavy oil exhibit a higher double bond equivalence (DBE) than the crude oil, indicating a greater degree of condensation with an increased number of double bonds and heterocyclic structures. The significant difference in DBE values between asphaltenes and crude oil underscores their impact on viscosity. A detailed molecular structure model of the asphaltenes in Tahe extra heavy oil has been constructed based on FT-ICR/MS analysis, providing a foundational understanding for developing viscosity reduction strategies.