Dodecyl Dimethyl Benzyl Ammonium Research Articles

Ultrasonic-assisted alkali hydrolysis of polyethylene terephthalate fabric and its effect on the microstructure and dyeing properties of fibers

Abstract In this study, ultrasound energy was applied to assist the alkali hydrolysis of polyethylene terephthalate (PET) fabric, and then, the results were compared with those of the mechanical oscillating method, which was used as the control. The effects of various factors such as the sodium hydroxide concentration, the dosage of dodecyl dimethyl benzyl ammonium chloride (DDBAC), and the frequency on the weight loss of the PET fabrics were systematically investigated. The surface appearance and microstructures of the treated fibers with different methods were analyzed using a scanning electron microscope and X-ray diffraction, respectively. The results showed that DDBAC played a prominent accelerating role in the hydrolysis of the PET polymer, and the frequency had a great influence on the weight loss of the PET fabric. Ultrasound with a frequency of 60 kHz showed a similar decomposition rate as the control, resulting in similar weight loss, which was the highest value among the three frequencies (20, 60, and 80 kHz). In addition, the application of ultrasonic energy led to more pits on the fiber surface, a smaller average grain size, and decreased crystallinity of the treated fibers, while the mechanical oscillating method resulted in slightly increased crystallinity. By comparing the K/S value of the dyed fabrics with two commercial disperse dyes, we found that the treatment method had no obvious correlation with the color depth of the treated fabric.

Molecular dynamics simulation of dodecyl dimethyl benzyl ammonium cation-intercalated montmorillonite

Abstract Dodecyl dimethyl benzyl ammonium (DDBA) is a novel cation surfactant used to modify clay minerals. DDBA-intercalated montmorillonite is formed by the ion exchange between DDBA cations in the solution and cations in the montmorillonite interlayers. By using molecular dynamics simulations, we investigated the basal spacings, interlayer structures and dynamics of DDBA-montmorillonites. The results showed that the calculated basal spacings agreed well with experimental values and that the layering behaviours of DDBA had been revealed. The ammonium groups of DDBA ions preferred staying close to the centre of Si–O six-member rings. The benzyl group and lauryl group were oriented in parallel in the monolayer state, whereas they were tilted in other states. DDBA ions have very low mobility in the interlayer region, indicating that the negatively charged montmorillonite surfaces can effectively fix this positively charged surfactant. The microscopic structures and dynamics obtained in the present study provide atomic-scale insights into the properties of DDBA-intercalated clay minerals.

Elimination of inhibitory effects of dodecyl dimethyl benzyl ammonium chloride on microalgae in wastewater by cocultivation with a newly screened microbial consortium

As one of the most commonly used biocidal cationic surfactants, benzalkonium chlorides (BACs) have been an increasing concern as emerging contaminants. Wastewater has been claimed the main point for BACs to enter into the environment, but to date, it is still largely unknown how the BACs affect the microbes (especially microalgae) in the practical wastewater and how to cost-effectively remove them. In this study, the inhibitory effects of a typical BACs, dodecyl dimethyl benzyl ammonium chloride (DDBAC), on a green microalga Chlorella sp. in oxidation pond wastewater were investigated. The results showed that though a hermetic effect at the first 2 days was observed with the DDBAC at low concentration (<6 mg/L), the algal growth and photosynthesis were significantly inhibited by the DDBAC at all the tested concentrations (3 to 48 mg/L). Fortunately, a new microbial consortium (MC) capable of degrading DDBAC was screened through a gradient domestication method. The MC mainly composed of Wickerhamomyces sp., Purpureocillium sp., and Achromobacter sp., and its maximum removal efficiency and removal rate of DDBAC (48 mg/L) respectively reached 98.1 % and 46.32 mg/L/d. Interestingly, a microbial-microalgal system (MMS) was constructed using the MC and Chlorella sp., and a synergetic effect between the two kinds of microorganisms was proposed: microalga provided oxygen and extracellular polysaccharides as co-metabolic substrates to help the MC to degrade DDBAC, while the MC helped to eliminate the DDBAC-induced inhibition on the alga. Further, by observing the seven kinds of degradation products (mainly including CH5O3P, C6H5CH2-, and C8H11N), two possible chemical pathways of the DDBAC degradation were proposed. In addition, the metagenomic sequencing results showed that the main functional genes of the MMS included antibiotic-resistant genes, ABC transporter genes, quorum sensing genes, two-component regulatory system genes, etc. This study provided some theoretical and application findings for the cost-effective pollution prevention of BACs in wastewater.

Effects of polymer-surfactant interactions on drag reduction performance and mechanisms: Molecular dynamics simulations and experimentation

This work provides a more favorable implementation of synergistic drag reduction strategies based on molecular simulations of the strength of polymer-surfactant interactions. The simulated preferred system identifies polyethylene oxide (PEO) and guar gum (GG) as polymers, and dodecyl dimethyl benzyl ammonium chloride (DDBAC) and dodecyl hydroxy sulfobetaine (DHSB). To forecast the drag reduction capability and identify the drag reduction process, important elements such as aggregation phenomena, charge distribution, shear deformation, and interfacial behavior were examined. Experimental measurements of viscosity, surface tension, and drag reduction validate the interactions. It was found that the compound system demonstrates enhanced viscosity, surface tension, and drag reduction efficiency compared to individual systems. The PEO-DHSB system achieves a drag reduction rate of 63.68% during initial flow, while the GG-DHSB system maintains a rate of 47.26% even after prolonged water circulation. This work visualizes the poly-surface aggregation phenomenon using the density distribution of surfactant hydrophobic tail chains, dynamically demonstrating the deformation of polymer and surfactant molecules during the shear process and interfacial behavior, and providing molecular-scale intuitive insights for understanding the drag reduction mechanism of poly-surface systems. Meanwhile, by comparing the effects of molecular type and structure on poly-surface interactions and drag reduction performance, it provides a theoretical foundation for the development and application of subsequent poly-surface drag reduction schemes, thereby broadening the application of drag reduction technology in the field of energy conservation and emission reduction.

Microparticles as BDMDAC (Quaternary Ammonium Compound) Carriers for Water Disinfection: A Layer-by-Layer Approach without Biocide Release

This work studies the antimicrobial activity of benzyldimethyldodecyl ammonium chloride (BDMDAC)-coated microparticles with distinct morphological structures. Functionalized microparticles were prepared by the layer-by-layer (LbL) self-assembly technique on hydroxyapatite (Hap), calcium carbonate (CaCO3) and glass beads (GB) cores. All particles were characterized, before and after functionalization, by Fourier-Transform Infrared Spectroscopy (FTIR), Brunner–Emmett–Teller (BET) and Scanning Electron Microscopy (SEM) analyses. Antimicrobial activity was tested against planktonic Pseudomonas fluorescens. Planktonic bacteria were exposed to 100 mg/L, 200 mg/L and 400 mg/L of BDMDAC-coated microparticles for 240 min. This strategy promoted a complete bacteria reduction at 200 mg/L for Hap microparticles after 240 min. No release of biocide was detected through HPLC analyses during 2 weeks, suggesting that bacteria inactivation may be attributed to a contact killing mechanism.

Beneficial or harmful: Time-dependent hormesis induced by typical disinfectants and their mixtures with toxicological interaction

Disinfectants and their mixtures can induce hormesis. However, how the mixture hormesis is related to those of components and the interactions in disinfectant mixtures remain unclear. In this paper, the luminescence inhibition toxicities of chlorinated sodium phosphate (CSP), dodecyl dimethyl benzyl ammonium bromide (DOB), dodecyl dimethyl benzyl ammonium chloride (DOC), ethanol (EtOH), glutaraldehyde (GLA), hydrogen peroxide (H2O2), isopropyl alcohol (IPA), n-propanol (NPA), and 20 mixture rays in four mixture systems (EtOH-H2O2, DOB-H2O2, DOC-EtOH, and EtOH-IPA-NPA) containing at least one component showing hormesis to Vibrio qinghaiensis sp.-Q67 (Q67) were determined at 0.25, 3, 6, 9, and 12 h. The synergism-antagonism heatmap based on independent action model (noted as SAHmapIA) was developed to systematically evaluate the interactions in various mixtures. It was shown that five disinfectants (CSP, EtOH, H2O2, NPA, and IPA) and 17 mixture rays exhibited time-dependent hormesis. The hormetic component was responsible for the hormesis of the mixture rays. Most mixture rays showed low- concentration/dose additive action and high-concentration/dose synergism at different time. This study further exemplified the interrelationship between the hormesis in the mixtures and their components and implied the need to pay attention to the time-dependent hormesis and interactions induced by the disinfectants.

A patching reinforcement strategy for hybrid surfactants as electrolyte additives with excellent performance in aluminum-air batteries

Surfactants attract attentions in aluminum-air batteries (AABs) due to its profound effects for anti-corrosion. This research proposes a patching reinforcement strategy using surfactants of dodecyl-β-D-maltoside (βD) and dodecyldimethyl benzyl ammonium bromide (DDBAB) to enhance the action of 8-hydroxyquinoline (8-HQ) as electrolyte additive. Hybrid surfactants consolidate the complexation of 8-HQ with aluminum, forming a dense protective film on the electrode surface. The results show that the assembled AABs has the highest capacity density of 2517 mAh·g−1 under optimizing condition, and the anode utilization rate reaches 84.5%. The corrosion protection efficiency can reach 87.2% on Al-5052 electrode in 4 M NaOH solution. This strategy provides a new method for using hybrid additives for AABs and aims to promote their commercial application.

Solvent-free bulk soft material with low-temperature tolerance: Transparency, flexibility, stretchability, and adhesion

Designing and manufacturing reliable and practicable transparent materials that can withstand low-temperature poses significant challenge. In this study, a range of transparent materials with excellent low-temperature resistance were constructed through the synergistic dynamical/non-covalent polymerization of two organic compounds, dodecyl dimethyl benzyl ammonium bromide (DB) and thioctic acid (TA). DB can effectively suppress the crystallization tendency of poly[TA] segments, while TA offers solvent-free polymerization behavior and thermal processing ability. Consequently, the non-covalently linked poly[TA-DB] exhibits high transparency (91.1 ± 3%), strong adhesion (7.91 ± 0.42 MPa), and remarkable stretchability (1705.73 ± 27.05%) in the low-temperature range (−40 ∼ −65 °C) or in cryogenic liquid (−40 °C). The design strategy used in this study offers a supramolecular approach for constructing transparent materials with the low-temperature applicability and practicality.

Analysis of Two Single and Three Double Long-Chain Quaternary Ammonium Compounds via Non-Aqueous Capillary Electrophoresis with Indirect Ultraviolet Detection

A novel method utilizing non-aqueous capillary electrophoresis (NACE) with indirect ultraviolet detection (IUD) has been developed for the analysis of five quaternary ammonium compounds (QACs). The QACs analyzed in this study include dodecyl trimethyl ammonium bromide, tetradecyl trimethyl ammonium bromide, dioctyl dimethyl ammonium chloride, octyldecyl dimethyl ammonium chloride and didecyl dimethy ammonium bromide. The separation process was carried out on an uncoated fused quartz capillary with a total length of 50.2 cm (effective length 40.0 cm) and a diameter of 50 μm. The separation buffer consisted of a mixture of MeOH/ACN (90:10, v/v) containing 2 mmol/L sodium acetate, 2 mmol/L trifluoroacetic acid (TFA) and 16 mmol/L dodecyl dimethyl benzyl ammonium chloride. The sample buffer utilized a mixture of MeOH/ACN (20:80, v/v) containing 2 mmol/L TFA. During analysis, a separation voltage of 7 kV was applied, resulting in a current of approximately 2.3 μA. The detection wavelength was set at 214 nm to ensure optimal sensitivity. Under optimal conditions, the method exhibited excellent performance characteristics, with a limit of detection of 0.5 mg/L and a limit of quantitation of 5.0 mg/L for the five QACs. Linear calibration curves were obtained in a concentration range of 5.0 to 100.0 mg/L, with correlation coefficients exceeding 0.999 for all compounds. The recoveries of the five QACs ranged from 92.3% to 114.7%, with relative standard deviations below 7.4%. To assess the applicability of the NACE-IUD method, 17 commercially available samples were successfully analyzed. The results confirmed the suitability of the method for accurate determination of the five QACs in disinfectant products. Notably, this method offers an environmentally friendly approach for the analysis of these QACs.

The responses of microbial metabolic activity, bacterial community and resistance genes under the coexistence of nanoplastics and quaternary ammonium compounds in the sewage environment

Nanoplastics (NPs) and quaternary ammonium compounds (QACs) are frequently detected in sewage. However, little is known about the risks of coexistence of NPs and QACs. In this study, the responses of microbial metabolic activity, bacterial community and resistance genes (RGs) to the exposure of polyethylene (PE), polylactic acid (PLA), silicon dioxide (SiO2) and dodecyl dimethyl benzyl ammonium chloride (DDBAC) were focused on 2nd and 30th day of incubation in sewer environment. Bacterial community contributed 25.01 % to shape RGs and mobile genetic elements (MGEs) after two days of incubation in sewage and plastisphere. After 30 days of incubation, the most important individual factor (35.82 %) was turned to microbial metabolic activity. The metabolic capacity of the microbial communities in plastisphere was stronger than that from SiO2 samples. Moreover, DDBAC inhibited the metabolic capacity of microorganisms in sewage samples, and increased the absolute abundances of 16S rRNA in plastisphere and sewage samples which might be similar to the hormesis effect. After 30 days of incubation, Aquabacterium was the predominant genus in plastisphere. As for SiO2 samples, Brevundimonas was the predominant genus. QACs RGs (qacEdelta1-01, qacEdelta1-02) and antibiotic RGs (ARGs) (aac(6′)-Ib, tetG-1) significantly enriched in plastisphere. There was also co-selection among qacEdelta1-01, qacEdelta1-02 and ARGs. In addition, VadinBC27 which enriched in plastisphere of PLA NPs was positively correlated with the potentially disease-causing genus Pseudomonas. It showed that after 30 days of incubation, plastisphere had an important effect on distribution and transfer of pathogenic bacteria and RGs. Plastisphere of PLA NPs also carried the risk of spreading disease.

Quaternary ammonium compounds promoted anoxic sludge granulation and altered propagation risk of intracellular and extracellular antibiotic resistance genes.

Surfactants could influence sludge morphology and disinfectants were linked to antibiotic resistance genes (ARGs). Thus, the response of activated sludge and ARGs to long-term quaternary ammonium compounds (QACs) exposure required further investigation, which is a popular surfactant and disinfectant. Here, three sequencing batch reactors were fed with 5mg/L most frequently detected QACs (dodecyl trimethyl ammonium chloride (ATMAC C12), dodecyl benzyl dimethyl ammonium chloride (BAC C12) and didodecyl dimethyl ammonium chloride (DADMAC C12)) for 180 d. The long-term inhibitory effect on denitrification ranked: DADMAC C12>BAC C12>ATMAC C12. Besides, obvious granular sludge promoted by the increase of α-Helix/(β-Sheet + Random coil) appeared in DADMAC C12 system. Moreover, intracellular ARGs increased when denitrification systems encountered QACs acutely but decreased in systems chronically exposed to QACs. Although replication and repair metabolism in ATMAC C12 system was higher, ATMAC C12 significantly promoted proliferation of extracellular ARGs. It was noteworthy that the propagation risk of extracellular ARGs in sludge increased significantly during sludge granulation process, and intracellular sul2 genes in sludge and water both increased with the granular diameter in DADMAC C12 system. The universal utilization of QACs may enhance antibiotic resistance of bacteria in wastewater treatment plants, deserving more attention.

Effect of different types of surfactants adsorption characteristics on the wettability of coking coal dust

To investigate the effect of different types of surfactants adsorption characteristics on the wettability of coking coal dust, Guoyang coking coal and three different surfactants - dodecyl dimethyl benzyl ammonium chloride (DDBAC), sodium alcohol ether sulphate (AES), coconut diethanolamide (CDEA) - were used. Firstly, the amount of surfactant adsorbed on coal dust were determined using spectrophotometry. Secondly, the contact angles of surfactants on coal tablets was determined. Subsequently, the relationship between the amount of surfactant adsorbed on the coal dust surface and the contact angle was analysed. Finally, the influence mechanism of the amount of the surfactant adsorbed on the coking coal dust surface on wettability was discussed. The experimental results suggest that the adsorption isotherm of cationic surfactant DDBAC on the coal dust surface is bilayer LS-type, while the adsorption isotherm of anionic surfactant AES and non-ionic surfactant CDEA are L-type and S-type, respectively. Additionally, when the concentration of the solution was 0.05%, the amount of AES adsorbed on the coking coal dust surface was estimated to be 64.9 mgg−1, which was 4.19-fold higher than DDBAC (i.e. to 15.5 mgg−1) and 2.2-fold higher than CDEA (i.e. to 29.5 mgg−1), nearly reaching adsorption saturation. The R2 of the amount of DDBAC, AES, and CDEA adsorbed on the coal dust surface affecting the contact angle was 0.9944, 0.99238, and 0.9923, respectively. The adsorption amount of anionic surfactant AES on the coal dust surface at 0.05% is 64.9 mgg−1, and the adsorption isotherm of surfactant on the coal dust surface is L-type, which is more conducive to enhancing the wettability of coking coal dust. Thus, the amount and adsorption isotherm form of the surfactant adsorbed on the coal dust surface are critical factors affecting the coal dust wettability, which provides a theoretical basis for the reasonable selection of surfactants to improve the coal dust suppression efficiency.

Disinfectant dodecyl dimethyl benzyl ammonium chloride (DDBAC) disrupts gut microbiota, phospholipids, and calcium signaling in honeybees (Apis mellifera) at an environmentally relevant level

One of the impacts of the Coronavirus disease 2019 (COVID-19) pandemic has been a profound increase in the application amounts of disinfectants. Dodecyl dimethyl benzyl ammonium chloride (DDBAC) is a widely used disinfectant, yet its hazards to non-target species remain largely unknown. We are unaware of any studies assessing DDBAC’s impacts on honeybee, a pollinator species that is a useful indicator of environmental pollution essential for many forms of agricultural production. Here, we assessed the potentially negative effects of DDBAC on honeybees. After conducting a formal toxicity evaluation of DDBAC on honeybee mortality, we detected an accumulation of DDBAC in the honeybee midgut. We subsequently studied the midgut tissues of honeybees exposed to sub-lethal concentrations of DDBAC: histopathological examination revealed damage to midgut tissue upon DDBAC exposure, microbiome analysis showed a decreased abundance of beneficial midgut microbiota, lipidomics analysis revealed a significant reduction in cell membrane phospholipids with known functions in signal transduction, and a transcriptome analysis detected altered expression of genes involved in calcium signaling pathways (that variously function in calcium absorption, muscle contraction, and neurotransmission). Thus, our study establishes that DDBAC impacts honeybee midgut functions at multiple levels. Our study represents an early warning about the hazards of DDBAC and appeals for the proper stewardship of DDBAC to ensure the protection of our ecological environment.

Benzyldimethyldodecyl Ammonium Chloride Doped Dental Adhesive: Impact on Core's Properties, Biosafety, and Antibacterial/Bonding Performance after Aging.

Current dental adhesives lack antibacterial properties. This study aimed to explore the effect of incorporating benzyldimethyldodecyl ammonium chloride (BDMDAC) on the degree of conversion, contact angle, ultimate tensile strength (UTS), microtensile bond strength (µTBS), cytotoxicity, antibacterial and bonding performance after artificial aging. A dental adhesive was doped with BDMDAC in the concentration range of 1-5 wt.%. For antibacterial assays, the BDMDAC compound was subject to planktonic cells of Streptococcus mutans. Then, after incorporation into the dental adhesive, an S. mutans biofilm model was used to grow 48 h-mature biofilms. The biofilms grown over the formulated materials were assessed by colony-forming unit (CFU) counting assay and fluorescence microscopy staining. In addition, the cytotoxicity was evaluated. Samples were subjected to 10,000 thermal cycles for aging and evaluated by UTS, µTBS, and CFU. Incorporating BDMDAC did not increase the cytotoxicity or change the physical properties when the mass fraction of the BDMDAC was 1-5 wt.%. The UTS of BDMDAC-doped adhesives was not impaired immediately or over time. A significant bacterial reduction was obtained for the mass fraction of the BDMDAC greater than 3 wt.%. However, the BDMDAC-doped adhesives did not offer an antibacterial effect after artificial aging. The overall results indicate that the BDMDAC strategy has the potential to control of microbial growth of cariogenic planktonic cells and biofilms. However, other new technological approaches are needed to overcome the deleterious effect of BDMDAC release over time such as those based on the principle of drug delivery systems whereby the BDMDAC is transported on microparticles or core shells, providing tangible benefits to oral health over time.

Circular adsorptive utilization of benzalkonium chloride via construction of ionic microenvironment in dopamine quinone-functionalized acrylic fiber surface

A novel dopamine quinone-functionalized acrylic fiber (PANdpqF) was successfully synthesized, which adsorbed the disinfectant dodecyl dimethyl benzyl ammonium chloride (DDBAC) to in-situ construct a highly efficient catalyst (DDBAC@PANdpqF) for the cyclization of CO2 with epoxide. The successful preparation of PANdpqF was proved by 13C Cross Polarization-Magic Angle Spinning nuclear magnetic resonance, X-ray photoelectron spectroscopy, Fourier transform infrared, and scanning electron microscopy. High adsorption capacity of DDBAC on PANdpqF has been demonstrated by ultraviolet analysis, and the theoretical maximum adsorption capacity was calculated as 666.67 mg/g. Based on comprehensive analysis, the corresponding adsorption mechanism is proposed in which chloride ion of DDBAC is added to o-quinone moiety through Michael addition, followed by the formation of phenoxy and quaternary ammonium ion pair. DDBAC@PANdpqF was well applicable to catalyze the cyclization of CO2, and the yield could reach 93.7% even with a low catalyst loading. The possible cooperatively catalytic mechanism was proposed correspondingly, in which phenolic hydroxyl helps to activate CO2 and epoxide, phenoxy anion attacks CO2 as a nucleophile, and quaternary ammonium cation stabilizes the anionic intermediates. Overall, the functionalized acrylic fiber adsorbed environmentally harmful disinfectant DDBAC to furnish a highly active catalyst for the transformation of greenhouse gas CO2 into useful carbonates, which provides a new method for advanced environmental pollution control.

Performance of dodecyl dimethyl benzyl ammonium chloride as bactericide and corrosion inhibitor for 7B04 aluminum alloy in an aircraft fuel system

In this study, the broad-spectrum antimicrobial property of dodecyl dimethyl benzyl ammonium chloride (DDBAC) was investigated against three species of bacteria, Lysinibacillus sphaericus ( L. sphaericus ), Acinetobacter lwoffii ( A. lwoffii ), and Sediminibacterium salmoneum ( S. salmoneum ) isolated and purified from a naval aircraft fuel system. Through the inhibition zone method and minimum inhibitory concentration test, DDBAC was found to have a good antimicrobial performance with a minimum inhibitory concentration of 64 mg/L. The influence of DDBAC on the corrosion behavior of fuel tank material was evaluated by electrochemical measurements, such as polarization curve and electrochemical impedance spectroscopy (EIS). The polarization curve indicated that DDBAC suppressed anodic and cathodic reactions as a mixed-type corrosion inhibitor, and the inhibition efficiency was 68.38% at the concentration of 80 mg/L after 28 days of immersion. The EIS results showed that DDBAC inhibited the corrosion of 7B04 aluminum alloy in the concentration range of 40–120 mg/L. The DDBAC adsorption on the aluminum alloy surface was in agreement with the modified Langmuir adsorption isotherm model. The quantum chemical calculations proved that a lone pair of electrons of nitrogen atoms in DDBAC were able to form coordinate bonds with the empty orbital in aluminum, resulting in a tight chemisorption layer on the aluminum alloy surface and corrosion inhibition.

Advanced oxidation of dodecyl dimethyl benzyl ammonium chloride by VUV/UV/chlorine: Synergistic effect, radicals, and degradation pathway

Quaternary ammonium compounds (QACs) are crucial ingredients in many cleaning agents, disinfectants and personal care products. They are widely detected in aquatic environments. In this study, vacuum ultraviolet (VUV)/UV/chlorine was used to degrade dodecyl dimethyl benzyl ammonium chloride (DDBAC, a typical QAC). The degradation efficiency of VUV/UV/chlorine on DDBAC was the highest among chlorine, UV, VUV/UV, UV/chlorine and VUV/UV/chlorine. During the VUV/UV/chlorine process, with chlorine concentration increasing from 0 to 700 μM, the degradation rate constant of DDBAC increased from 0.16 to 0.22 min−1 then decreased to 0.17 min−1. When the chloride concentration was 10 mM and 50 mM, the degradation rate constant of DDBAC decreased by 31% and 55%, respectively. Inorganic anions and organic compounds in the reverse osmosis concentrate inhibited the degradation of DDBAC by quenching radicals. The degradation mechanisms of DDBAC degradation during the VUV/UV/chlorine process include UV photolysis and oxidation by OH, Cl and other reactive species. With the increase in pH from 5 to 10, the OH concentration decreased from 18.7 × 10−14 M to 7.5 × 10−14 M, and the Cl concentration decreased from 8.8 × 10−14 M to 2.1 × 10−14 M. At pH 5–10, contributions of OH and Cl to DDBAC degradation were 30%−44% and 18%−37%, respectively. Degradation mechanisms of DDBAC mainly include hydrogen abstraction, hydroxylation, and cleavage of the C-N bond. The concentrations of four chlorinated products (trichloromethane, monochloroacetic acid, dichloroacetic acid, and trichloroacetic acid) mostly initially increased and then decreased.

Synthesis and Performance of Double-Chain Quaternary Ammonium Salt Glucosamide Surfactants.

A series of double-chain quaternary ammonium salt surfactants N-[N′[3-(gluconamide)] propyl-N′-alkyl]propyl-N,N-dimethyl-N-alkyl ammonium bromide (CnDDGPB, where n represents a hydrocarbon chain length of 8, 10, 12, 14 and 16) were successfully synthesized from D (+)-glucose δ-lactone, N,N-dimethyldipropylenetriamine, and bromoalkane using a two-step method consisting of a proamine-ester reaction and postquaternization. Their surface activity, adsorption, and aggregation behavior in aqueous solution were investigated via measurements of dynamic/static surface tension, contact angle, dynamic light scattering, and transmission electron microscopy. An analysis of their application performance in terms of wettability, emulsifying properties, toxicity, and antibacterial properties was conducted. The results show that with increasing the carbon chain length of the CnDDGPB surfactants, their critical micelle concentration (CMC) increased and the pC20 and efficiency in the interface adsorption of the target product gradually decreased. Moreover, the influence of the hydrophobic carbon chain length on the surface of polytetrafluoroethylene (PTFE) was even greater for the wetting effect, reducing the contact angle to 32° within the length range of C8–C14. The results of the contact angle change and the wettability experiments proved that C10DDGPB exhibited the best wettability. The liquid paraffin and soybean oil emulsification ability of CnDDGPB showed an upward trend followed by a downward trend with the growth of the carbon chain, with C12DDGPB exhibiting the best emulsification performance. The Dlong/Dshort ratio was far lower than 1, which indicates mixed-kinetic adsorption. The surfactants formed spherical micelles and showed a unique aggregation behavior in aqueous solution, which showed an increase–decrease–increase trend with the change in concentration. A cell toxicity and acute oral toxicity experiment showed that the CnDDGPB surfactants were less toxic than the commonly used surfactant dodecyldimethylbenzyl ammonium chloride (1227). In addition, at a concentration of 150 ppm, CnDDGPB exhibited the same bacteriostatic effect as 1227 at a concentration of 100 ppm. The results demonstrate that sugar-based amide cationic surfactants are promising as environmentally friendly disinfection products.

Biochar assisted cellulose anaerobic digestion under the inhibition of dodecyl dimethyl benzyl ammonium chloride: Dose-response kinetic assays, performance variation, potential promotion mechanisms

This study evaluated the inhibitory effect and mitigation strategy of dodecyl dimethyl benzyl ammonium chloride (DDBAC) suppression on anaerobic digestion. With the 12 h-suppression, only 16.64% of anaerobes were alive, and acetotrophic methanogens were significantly inhibited. As for batch test, DDBAC suppression significantly prolonged the start-up of systems and decreased the biogas production. In cellulose semi-continuous digestion process, the DDBAC suppression induced volatile fatty acids accumulation and pH decrease. However, the biochar amended reactor effectively mitigated the DDBAC suppression and achieved 370.5 mL/d·g-chemical-oxygen-demand biogas production. Moreover, 17.8% more protein in extracellular polymeric substances was secreted as the bio-barrier to defense the DDBAC suppression. Furthermore, microbial analysis showed that biochar addition selectively enriched directed interspecies electron transfer (DIET) participant bacteria (Anaerolineaceae and Syntrophomonas) and methanogens (Methanosaeta and Methanobacterium). Meanwhile, the potential metabolic pathway analysis showed that the abundance of amino acids and energy metabolism were increased 28% and 8%, respectively. The abundance of encoding enzyme related to hydrogenotrophic and acetotrophic methanogenesis enriched 1.88 times and 1.48 times, respectively. These results showed the performance and mechanisms involved in DIET establishment with ethanol stimulation biochar addition.

Synergistic corrosion inhibition effects of quaternary ammonium salt cationic surfactants and thiourea on Q235 steel in sulfuric acid: Experimental and theoretical research

The corrosion resistance of Q235 steel treated with pure thiourea, dodecyl trimethyl ammonium bromide (DTAB), dodecyl dimethyl benzyl ammonium bromide (DDBAB), and their mixture (i.e. DTAB-Thiourea, DDBAB-Thiourea) in sulfuric acid was studied. Results showed that DTAB-Thiourea and DDBAB-Thiourea have strong synergistic effects (4.86 and 5.99) and could inhibit corrosion by 93.37% and 94.98%, respectively. These effects are attributed to a decrease in the steric hindrance due to changes in the molecular adsorption mode of the corrosion inhibitors. The adsorption forms of all inhibitors on the steel surface were investigated and explained using density functional theory.