Curing kinetics of epoxy cured by cardanol-based phenalkamines synthesized from different polyethylenepolyamines by Mannich reaction

Phenalkamines with different structures are expected to affect the curing reaction of epoxy, yet the exact mechanism remains to be elucidated. In this study, four cardanol-based phenalkamines (named PK1, PK2, PK3, and PK4, respectively), synthesized from ethylenediamine, diethylenetriamine, triethylenetetramine, and pentaethylenehexamine, were used as curing agents in diglycidyl ether of bisphenol A (DGEBA) epoxy system. The phenalkamines were characterized by Fourier transform infrared spectroscopy, nuclear magnetic resonance, and time-of-flight secondary ion mass spectrometry. The curing behaviors and kinetics were investigated by non-isothermal differential scanning calorimetry, and the activation energies of the reactions (E _α ) were determined using Kissinger–Akahira–Sunose (KAS) and Starink methods. The results indicate a similar curing mechanism for all four phenalkamines. All E _α values remain almost constant in the range of 0.05 ≤ α ≤ 0.6, and increase dramatically after α > 0.6 due to greater viscosity of the reaction systems. The diffusion of reactive groups plays an increasingly important role in determining the curing kinetics. In addition, DGEBA/PK1 and DGEBA/PK2 have lower initial E _α values than DGEBA/PK3 and DGEBA/PK4, because PK1 and PK2 have lower viscosity than PK3 and PK4. When α is high, DGEBA/PK1 and DGEBA/PK2 have higher E _α values than DGEBA/PK3 and DGEBA/PK4, because more tertiary amine groups can be formed in the reactions between the epoxy and secondary amine groups in the DGEBA/PK3 and DGEBA/PK4 systems, which catalyze the curing reaction and it thus lowers energetic barrier.     

Synthesis and characterization of bio-based benzoxazine oligomer from cardanol for corrosion resistance application

The Mannich-like condensation of a cardanol, paraformaldehyde, and N,N′-bis(2-aminoethyl)ethane-1,2-diamine were carried out to synthesize the amine functional benzoxazine (Bnz) resin. The amine functionality of Bnz resin was evaluated by physiochemical methods, and the structure was characterized using Fourier transform infrared and ¹H-nuclear magnetic resonance spectroscopy. The added functionality into the Bnz resin backbone was utilized to modify the Bnz resin structure by glycidoxypropyltrimethoxysilane (GPTMS) in various proportions. The results revealed that the silane-modified Bnz coatings have improved mechanical, chemical, and solvent resistance properties as compared to the neat Bnz coating. The gel and water absorption of polyamide-cured coatings also has been evaluated. Furthermore, the cured films have been evaluated for glass transition temperature (T _g) and thermal resistance by differential scanning calorimetry and thermogravimetric analysis, respectively. The corrosion resistance properties were studied by salt spray and electrochemical analysis. It was observed that the highly crosslinked structure of the GPTMS-modified Bnz coatings enhanced the barrier protection to corrosive species.     

Coatings of Conducting Polymers for Corrosion Protection of Mild Steel

The investigation of electrochemical behavior of different conducting polymers, polythiophene (PTh), polypyrrole (PPy) and polyterthiophene (PTTh) on a mild steel (MS) electrode were done. Moreover, the combinations of the conducting polymers PTh and PPy was investigated. The synthesis of all polymeric coatings was done by the cyclic voltammetry technique. The electrochemical impedance spectroscopy (EIS) measurements were used to evaluate the corrosion performance of coated mild steel by different polymers in 0.5 M of different acid solutions (HCl, HClO₄, H₂ C ₂ O ₄, H₃PO₄ and HNO₃). The protection of all polymeric coatings against corrosion of the substrate was promising and the bilayer coating PPy/PTh gave the best protection efficiency in all used acids. The order of efficiency for the different coatings in HCl and HNO₃ solutions was MS/PPy/PTh > MS/PPy > MS/PTTh > MS/PTh but the order in HClO₄, H₃PO₄ and H₂ C ₂ O ₄ solutions was MS/PPy/PTh > MS/PTTh > MS/PPy > MS/PTh.     

Fabrication of thermally stable porous films from a cured epoxy resin via the <Emphasis Type="Italic">Breath Figures</Emphasis> process

In the current work, porous films based on epoxy resin have been obtained via the Breath Figures method. It was shown that the use of a low-temperature curing agent and fluoro-containing organosilicon copolymer, compatible with epoxy resin, makes it possible to obtain porous, thermostable, highly hydrophobic coatings with a pore diameter of 3–4 µm. When the epoxy resin/copolymer mixture is homogenous, the modifier prevents water droplet coalescence; otherwise, the mixture becomes heterogeneous, and the positive influence of the modifier is lost. The obtained modified porous films are highly hydrophobic and maintain their porous structure until polymer devitrification occurs. The simplicity of the Breath Figures method shows great potential for the manufacture of water-repellent paint coatings based on epoxy resin for use in a variety of applications.     

Facile preparation and good performance of nano-Ag/metallocene polyethylene antibacterial coatings

Metallocene polyethylene/nano-silver coatings were prepared by a facile air-spray method on polymer films. Different from the prevailing strategy to endow polyethylene with antibacterial performance, we used metallocene polyethylene sol and nano-silver as a precursor to deposit coatings on polymers at a relatively low operating temperature. Antibacterial coatings with excellent mechanical properties, water resistance, and low silver release were achieved. The composite coatings were examined in terms of surface characteristics, mechanical properties, and antibacterial activity against two representative bacterial strains including Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). The composite coatings exhibited favorable microstructure, good mechanical properties, and suitable crystallinity. The antimicrobial tests indicated that the fabricated composite coatings showed promising antibacterial activity against E. coli and S. aureus. Furthermore, Ag ions released by the composite coating after 30 days were under 1.2 ppb. These results indicated a promising prospect of the composite coating for wide antibacterial applications.     

Preparation of epoxy-based insulator and optimization of its thermal property by Taguchi robust design method in double base propellant grain application

Taguchi method (orthogonal array, OA₉) was used to design an epoxy insulator by evaluating its glass transition temperature (T _g) for using in a double base (DB) propellant grain. In this design method, three epoxy resins based on diglycidylether bisphenol A (DGEBA), three polyamine curing agents and a DGEBA-based reactive diluent agent were used. The curing process of epoxy resins with polyamines was studied by Fourier transform infrared spectroscopy. The results showed that the curing process was completed at room temperature. The effects of four parameters including resin type, curing agent type, curing agent concentration and diluent quantity were investigated to design a resin formulation with a highest T _g after curing. The obtained results were quantitatively evaluated by the analysis of variance (ANOVA). The results of ANOVA showed that the highest T _g of 86.0 ± 9.0 °C was obtained for the optimum formulation of MANA POX-95 as epoxy resin, H-30 as curing agent and 52 phr H-30. The T _g measured by the experiment was 78.0 ± 0.9 °C. In addition, the single lap shear strength (adhesion strength) of the optimized insulator was measured at 13.66 ± 1.02 MPa. Pull-off test performed on the surface of DB propellant resulted a 1.935 ± 0.003 MPa adhesion strength.     

Cyclodextrin-based hyperbranched polyester: synthesis,characterization, and antimicrobial activity

In this study, the synthesis of cyclodextrin-based hyperbranched polyester (CD-based HBPE) was prepared by a simple condensation route via acid chloride approach (Scheme 1). The formation of ester linkages in CD-based HBPE was clearly identified from FTIR and NMR spectroscopy. The resulting structure and the molecular weight of the CD-based HBPE were confirmed with LC–MS analysis. The CD-based HBPE displayed the fluorescence maxima in the 425 nm range with relatively narrow peak widths indicating that they had pure and intense fluorescence. The antimicrobial activity of the CD-based HBPE was evaluated against the Gram-negative organisms like Escherichia coli and Salmonella paratyphi, Gram-positive organisms as Bacillus subtilis and Staphylococcus aureus and fungi such as Aspergillus niger, and Candida albicans. CD-based HBPE showed a great inhibitory effect toward both bacteria and fungi. The microorganism which possess greater antimicrobial activity with standard antibiotics was selected for determining the minimum inhibitory concentration (MIC) value of the CD-based HBPE. Therefore, the MIC value of the CD-based HBPE against B. subtilis was tested and found to be 31.25 μg mL^?1. Hence, it is suggested that CD-based HBPE holds good agreement with the antimicrobial assay.     

A smart anticorrosion coating based on hollow silica nanocapsules with inorganic salt in shells

This work presents the synthesis of corrosion inhibitor [1H-benzotriazole (BTA)]-loaded hollow silica nanocapsules with magnesium hydroxide precipitate in the shells (HSNs-M/BTA) through inverse microemulsion (W/O) polymerization. TEM and Brunauer–Emmett–Teller (BET) measurements indicate that the silica nanocapsules possess voids in the inner part and mesoporous on the surface. The actual loading capacity of BTA is 287.17 mg (BTA)/1 g (HSNs-M/BTA). The results of UV absorption spectra show that the release of BTA can be triggered by the changing of pH in the corrosion solution. The anticorrosive SiO _x /ZrO _x coatings embedded with hydrophobically modified HSNs-M have a better waterproof performance since the water contact angle can reach 140°. In comparison to the passive SiO _x /ZrO _x coatings with or without BTA, the enhanced corrosion protection performance of this developed anticorrosive system was observed by both electrochemical impedance spectroscopy and Tafel analysis. The fabrication of nanocapsules with corrosion inhibitors is promising as an intelligent element in protective coatings in the future.     

A new extra situ sol–gel route to silica/epoxy (DGEBA) nanocomposite. A DTA study of imidazole cure kinetic

Silica nanoparticles were obtained through the Stöber method, from mixtures of tetraethoxysilane (TEOS) and 3-aminopropyltriethoxysilane (APTS). The nanoparticles were dispersed in tetrahydrofuran (THF) and coupled to bisphenol A epoxy resin (DGEBA) through surface amino groups. After removing THF non-isothermal cure was performed at different heating rates (2–20°C/min), using imidazole (2–4 wt%) as curing agent. For the sake of comparison bare DGEBA epoxy polymers were also prepared with similar schedule A nanocomposite of well-dispersed silica nanoparticles (5 wt%) in a fully cured epoxy matrix was easily obtained. Lower cure kinetics were observed with silica addition. This was attributed to reduction of the imidazole volume concentration. Cure activation energy was not influenced by silica presence, whereas it changed with the imidazole content. Therefore, experimental results suggested that silica had only an indirect effect (the reduction of the imidazole molar concentration) on the epoxy matrix cure kinetics. Glass transformation temperatures, T _g, as high as 175°C were recorded. The nanocomposite glass transformation temperature depended on the heating rate of the cure process, the imidazole and silica content. T _g changes as high as 40°C were detected as a function of the heating rate. At higher imidazole content no differences in T _g values between bare polymer and the nanocomposite were observed. This suggests that a higher imidazole content assures a better interconnection between the compatibilizing epoxy shell around the nanoparticles and the epoxy matrix. The new proposed methodology is an easy route to engineer both nanocomposites structure and interfacial interactions, thus tailoring their properties.     

The effect of formulation variables on fouling-release performance of stratified siloxane–polyurethane coatings

The effects of formulation variables, such as type of polyol, solvent type and solvent content, and coating application method, on the surface properties of siloxane–polyurethane fouling-release coatings were explored. Fouling-release coatings allow the easy removal of marine organisms from a ship’s hull via the application of a shear force to the surface. Self-stratified siloxane–polyurethane coatings are a new approach to a tough fouling-release coating system. Combinatorial High Throughput Experimentation was employed to formulate and characterize 24 different siloxane–polyurethane coatings applied using drawdown and drop-casting methods. The resulting coatings were tested for surface energy using contact angle measurements. The fouling-release performance of the coatings was tested using a number of diverse marine organisms including bacteria (Halomonas pacifica and Cytophaga lytica), sporelings (young plants) of the green macroalga (Ulva linza), diatom ((microalga) Navicula incerta), and barnacle (Amphibalanus amphitrite). The performance of the majority of the coatings was found to be better than the silicone standards, Intersleek^® and Silastic^® T2. An increase in solvent content in the formulations increased the surface roughness of the coatings. Coatings made with polycaprolactone polyol appeared to be somewhat rougher compared to coatings made with the acrylic polyol. The adhesion strength of sporelings of Ulva increased with an increase in solvent content and increase in surface roughness. The adhesion strengths of Ulva sporelings, C. lytica, and N. incerta were independent of application method (cast or drawdown) in contrast to H. pacifica adhesion, which was dependent on the application method.     

Influence of pH in the synthesis of ferric tannate pigment for application in antifouling coatings

Ferric tannate was synthesized at pH 4 and pH 7 (FT4 and FT7, respectively) as a new class of environmentally friendly antifouling pigments. The solubility of both pigments was evaluated by gravimetric tests, showing that FT4 is more soluble than FT7. A mixture of rosin/acrylic resin (9:1 w/w) was sufficient to form an antifouling coating due to improved matrix properties. Electrochemical impedance spectroscopy (EIS) measurements were used to determine the apparent water coefficient of diffusion (D) and coating behavior. The D in the coating formulated with FT4 exhibited better values than that obtained with FT7. EIS results showed that both coatings present Fickian behavior at the initial stages of immersion, while flat Nyquist plots revealed penetration of water in the films. The physicochemical characteristics of FT4 pigment were determined by thermogravimetry and Fourier transform infrared. Immersion tests in the Mediterranean Sea demonstrated the excellent efficacy of the FT4-containing coating against marine fouling after six months of immersion.     

The Antibacterial Activity of Ta-doped ZnO Nanoparticles

A novel photocatalyst of Ta-doped ZnO nanoparticles was prepared by a modified Pechini-type method. The antimicrobial study of Ta-doped ZnO nanoparticles on several bacteria of Gram-positive Bacillus subtilis (B. subtilis) and Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli) and Pseudomonas aeruginosa (P. aeruginosa) were performed using a standard microbial method. The Ta-doping concentration effect on the minimum inhibitory concentration (MIC) of various bacteria under dark ambient has been evaluated. The photocatalytical inactivation of Ta-doped ZnO nanoparticles under visible light irradiation was examined. The MIC results indicate that the incorporation of Ta⁵⁺ ions into ZnO significantly improve the bacteriostasis effect of ZnO nanoparticles on E. coli, S. aureus, and B. subtilis in the absence of light. Compared to MIC results without light irradiation, Ta-doped ZnO and pure ZnO nanoparticles show much stronger bactericidal efficacy on P. aeruginosa, E. coli, and S. aureus under visible light illumination. The possible antimicrobial mechanisms in Ta-doped ZnO systems under visible light and dark conditions were also proposed. Ta-doped ZnO nanoparticles exhibit more effective bactericidal efficacy than pure ZnO in dark ambient, which can be attributed to the synergistic effect of enhanced surface bioactivity and increased electrostatic force due to the incorporation of Ta⁵⁺ ions into ZnO. Based on the antibacterial tests, 5 % Ta-doped ZnO is a more effective antimicrobial agent than pure ZnO.     

Preparation of Poly(<Emphasis Type="Italic">o</Emphasis>-toluidine)/Nano Zirconium Dioxide (ZrO<Subscript>2</Subscript>)/Epoxy Composite Coating and Its Corrosion Resistance

Conducting polymers represent a promising application prospect in the field of metal corrosion control. In this investigation, poly(o-toluidine) (POT)/nano zirconium dioxide (ZrO₂) composite were prepared by in situ polymerization of o-toluidine monomer in the presence of nano ZrO₂ particles. Fourier transformation infrared spectroscopy, UV–visible spectroscopy, X-ray diffraction and Scanning electron microscopy were used to characterize the composition and the structure of the composite. POT/nano ZrO₂ composite was mixed with epoxy resin (EP) through a solution blending method and the three components POT/nano ZrO₂/epoxy composite coating was coated onto the surface of steel coupon, and its corrosion protective efficiency was studied by electrochemical measurements and immersion test in 3.5 % NaCl solution as corrosion environment and also compared with that of POT/epoxy composite coated steel, polyaniline (PANI)/epoxy composite coated steel and pure epoxy coated steel. According to the results, POT/nano ZrO₂/epoxy composite coated steel has got higher corrosion resistance than that of POT/epoxy composite coated steel and PANI/epoxy composite coated steel. It was found that POT powders dispersed in the epoxy and polyamide system improved the barrier and electrochemical protection properties of epoxy coating and the addition of nano ZrO₂ particles increased the tortuosity of the diffusion pathway of corrosion substances.     

Preparation of intercross-linked poly(L-lactide) and epoxy resin using N-benzyl pyrazine hexafluoroantimonate

The overall goal of our study was to prepare the intercross-linked poly(l-lactide) (PLA) and epoxy polymer by using N-benzyl pyrazine hexafluoroantimonate (BPH) as a latent hardener. First, the glycidol end-functionalized PLA (Gly-PLA) polymer was prepared at quantitative yields by the polymerization of l-lactide (LA) with glycidol as an initiator in the presence of stannous octoate. Gly-PLA showed the predicted PLA molecular weight. The epoxide group in the chain end of the PLA segments was observed using ¹H nuclear magnetic resonance (NMR). The ring-opening polymerization of the epoxy group in Gly-PLA in the presence of BPH as a latent initiator yielded the polyether-g-PLA (PE-g-PLA), which was confirmed using ¹H NMR and gel permeation chromatography (GPC). We confirmed that BPH acted as a latent initiator for the polymerization of epoxide in the Gly-PLA polymer. The curing of the epoxy resin (bisphenol-A-type epoxide oligomers, DGEBA) and Gly-PLA was carried out with BPH as a latent hardener. The curing reaction quantitatively generated a solvent-insoluble gelled epoxy resin. The curing process of the DGEBA and Gly-PLA in the presence of BPH was monitored using differential scanning calorimetry (DSC), and the cured materials were characterized with infrared (IR) spectroscopy. The results indicated that the intercross-linked Gly-PLA and epoxy resin could be prepared using BPH as a latent hardener.

Nanoindentation as an alternative to mechanical abrasion for assessing wear of polymeric automotive coatings

Mechanical abrasion followed by transmission delta-haze measurement is a standard means to assess wear in polymeric silicone automotive hard coatings. However, the drawbacks of this abrasion–transmission (A–T) technique (drift, variability, sample size, and test time) make an alternative measurement method desirable. Literature reports have shown that the ratio of hardness to modulus can successfully predict wear performance in ceramic and metallic nanocomposite coatings. This work studied measures from both nanoindentation and nanoscratch testing to determine which could be a viable alternative to the historical A–T test for a specific polymeric coating system. Both nanoindentation measures of hardness (H) and the ratio of hardness to modulus (H/E _r) showed high repeatability compared with the other measures evaluated in this study and compared with the historical test. Of these two measures, the ratio H/E _r with an exponential fit showed the strongest correlation with A–T delta-haze measurements. Key formulation and process factors affecting abrasion resistance in automotive coatings were analyzed in a designed experiment with historical A–T delta-haze and nanoindentation H/E _r as responses. Analysis showed significant benefits to the use of the H/E _r measure of abrasion resistance in modeling coating performance.     

Evaluation of the corrosion protection performance of epoxy coatings containing Mg nanoparticle on carbon steel in 0.1 M NaCl solution by SECM and EIS techniques

The effect of corrosion protection performance of epoxy coatings containing magnesium (Mg) nanoparticles on carbon steel was analyzed using scanning electrochemical microscopy (SECM) and electrochemical impedance spectroscopy (EIS). Localized measurements such as oxygen consumption and iron dissolution were observed using SECM in 0.1 M NaCl in the epoxy-coated sample. Line profile and topographic image analysis were measured by applying ?0.70 and +0.60 V vs the Ag/AgCl/saturated KCl reference electrode as the tip potential for the cathodic and anodic reactions, respectively. The tip current at ?0.70 V for the epoxy-coated sample with Mg nanoparticles decreased rapidly, which is due to cathodic reduction in dissolved oxygen. The EIS measurements were conducted in 0.1 M NaCl after wet and dry cyclic corrosion test. The increase in the film resistance (R _f) and charge transfer resistance (R _ct) values was confirmed by the addition of Mg nanoparticles in the epoxy coating. Scanning electron microscope/energy-dispersive X-ray spectroscope analysis showed that Mg was enriched in corrosion products at a scratched area of the coated steel after corrosion testing. Focused ion beam–transmission electron microscope analysis confirmed the presence of the nanoscale oxide layer of Mg in the rust of the steel, which had a beneficial effect on the corrosion resistance of coated steel by forming protective corrosion products in the wet/dry cyclic test.     

Dolichodial: A New Aphid Sex Pheromone Component?

The sex pheromones of many aphid species from the subfamily Aphididae comprise a mixture of the iridoids (cyclopentanoids) (1R,4aS,7S,7aR)-nepetalactol and (4aS,7S,7aR)-nepetalactone. In this paper, we investigate whether other chemicals, in addition to nepetalactol and nepetalactone, are released from Dysaphis plantaginea (rosy apple aphid) oviparae as part of their sex pheromone. Four compounds present in an air entrainment sample collected from D. plantaginea oviparae feeding on apple (Malus silvestris c.v. Braburn) elicited electrophysiological responses from male D. plantaginea. Active peaks were tentatively identified by gas chromatography (GC) coupled with mass spectrometry, with identification confirmed by peak enhancement with authentic compounds on GC columns of different polarities. The electroantennography-active chemicals were (1R,4aS,7S,7aR)-nepetalactol, (4aS,7S,7aR)-nepetalactone, (1S,2R,3S)-dolichodial, and phenylacetonitrile. (1S,2R,3S)-Dolichodial elicited a behavioral response from male D. plantaginea and naïve-mated female parasitoids, Aphidius ervi. This is the first report of electrophysiological and behavioral responses from any aphid morph to (1S,2R,3S)-dolichodial. Whether or not (1S,2R,3S)-dolichodial is a third component of the aphid sex pheromone is discussed.     

Development of novel hybrid materials from polylactic acid and nano-silver coated carbon black with distinct antimicrobial and electrical properties

This work aims to prepare nanosilver coated carbon black via benzoxazine oxidation as a filler for polylactic acid (PLA) to produce novel hybrid materials with improved electrical and antimicrobial properties. Nanosilver coated carbon black exhibited antimicrobial activity against S.aureus, B.subtilis, M.luteus, E.coli, P.aeruginosa and C.albicans. It was found that the nanosilver coated carbon black (10CB-Ag) was the most effective filler since it showed largest inhibition zones. Thermogravimetric analysis (TGA) showed that the silver content in 10CB-Ag was 5.68% by weight. The hybrid materials of PLA with uncoated carbon black and nanosilver coated carbon black fillers were prepared by injection molding. The optimal composition of the prepared hybrid materials was found to be 15 phr of nanosilver coated carbon black in PLA (15AgCB-PLA). This material showed quite good properties, e.g. tensile strength of 50 MPa, % elongation at break of 1.68 and electrical conductivity of 2.78 × 10^?9 S?m^?1. Moreover, it exhibited the S. aureus inhibition of about 99%. This work revealed the possibility of using this material for anti-electrostatic and antimicrobial applications.     

Aggregation Pheromone of the Bearded Weevil, <Emphasis Type="Italic">Rhinostomus barbirostris</Emphasis> (Coleoptera: Curculionidae): Identification,Synthesis, Absolute Configuration and Bioactivity

The bearded weevil, Rhinostomus barbirostris (Coleoptera: Curculionidae: Dryophthorinae), attacks coconut trees, oil palms and other species of Arecaceae. Besides direct damage, R. barbirostris may be a vector of diseases in coconut and oil palms, such as stem bleeding (resinosis) and red ring disease. Currently, the only method to control this weevil is by visual observation of damage and removal of infected plants. Semiochemical-based trapping could improve the effectiveness of monitoring and management of R. barbirostris. In comparisons of volatiles released by R. barbirostris males and females by gas chromatography (GC) two male-specific compounds were observed. GC-mass spectrometry (MS) and GC-Fourier transform-infrared (FTIR) analyses of the natural compounds suggested these were diastereoisomers of 5-hydroxy-4-methylheptan-3-one, also known as sitophilure, a pheromone component of other dryophthorine species. Synthesis of the mixture of all four stereoisomers of sitophilure was performed in two steps, and the chemical structures were confirmed by comparing GC retention times and MS and FTIR spectra of natural and synthetic compounds. The absolute configurations of the two male-specific compounds were elucidated by enantioselective GC; the major component was the (4S,5R)-isomer, and the minor component (4S,5S)-sitophilure. In analyses by GC-electroantennography (EAG) the antennae of male and female R. barbirostris only responded to the (4S,5R)-isomer of the synthetic sitophilure. The stereoisomeric mixture of sitophilure was attractive to both sexes of R. barbirostris in laboratory experiments in the presence of sugar cane volatiles, and a similar result was obtained in a preliminary field trapping test.     

Mixed Stability and Antimicrobial Properties of Gluconamide-Type Cationic Surfactants

The stability of anionic-cationic surfactant solutions and the antimicrobial properties of novel N,N-dimethyl-N-[3-(gluconamide/lactobionamide)]propyl-N-alkylammonium bromides (CnDGPB and CnDLPB), N-methyl-N-hydroxyethyl group-N-[3-(gluconamide)-propyl]-N-alkylammonium bromide (CnMHGPB) and star-shaped gluconamide-type cationic surfactants N-dodecyl-N,N-bis[(3-d-gluconylamido)propyl]-N-alkylammonium bromide (CnDBGB) were investigated. Mixed stability in combination with sodium n-alkylbenzenesulfonate (LAS) was determined via transmittance; stability is achieved when percent transmittance was greater than 90 %. Transmittance results suggest that these cationic surfactants can form stable solutions with anionic surfactants over a broad concentration range. The inhibition activity of C _n DBGB is the best among the three kinds of glucocationic surfactants. Antimicrobial activity of C₁₂ surfactants was the best, C₁₄ was the second and C₁₀ was the worst. Moreover, antibacterial activity of glucose-based cationic surfactants was greater than lactose-based cationic surfactants.