The comprehensive study of possibility ecological control Mnemiopsis leidyi in Caspian Sea activity: The study and recognization parasitic fauna and Bacterial flore in ctenophore (Mnemiopsis leidyi and Bereo ovata)

Bacterial flora and parasitic fauna of M. leidyi an exotic invader jelly fish to Caspian Sea ecosystem and B. ovata to Black sea an alternative biological control agent was studied. During summer 1382 to spring 1383, using routine Bacteriological work. 72 sample of sea water Caspian Sea obtained from depth 20 and 50 meters, 36 sample of M. leidyi from depth 20 meters, 10 sample of B. ovata and 3 sample of sea water (Black sea) were collected and according to Bacteriological was studied. 216 sample of M. leidyi from depth 10 to 50 meters of Caspian Sea and 47 sample of B. ovata from Black and Marmarreh Sea (Turkey) were collected and was studied. In this study no parasite from was identified in M. leidyi (Caspian sea) but 64 percentage and 73 percentage of B. ovata (Marmarreh and Black sea respectively) contaminated to Trichodina ctenophore at varians concentration B. ovata of Black sea (130 min 1050 max) and B. ovata Marmarre sea (420 min 2100 max). While B. ovata kept at high salinity of 21 ppt was more contaminated with this pretrichial protozoan (Trichodina) than in low salinity (12/5 ppt). in comparision of bacterial flore in two cetenophore (M. leidyi and B. ovata) was observed that some of bacteria such as micrococcus sp, Aeromonas sp. Bacillus coagulans in both ctenophore and some other bacteria such as Agromobacterium and chromobacterium only observed in B. ovata but other researcher have reported fram Caspin sea and some of bacteria to specific Shewanella , Vibrio harveiy and bacillus linens was observed in B. ovata . Of course specific bacteria cannot transfer to Caspian Sea (different of salinity black sea (2/1%) to Caspian Sea (1/25 %)). Therefore if B. ovata to introduce to south Caspian Sea for biological control population M. leidyi. it is necessary at first some of viral pathogen in aquatic animal (fish) such as VNN, IPN,IHN,VHS,SVC was studied and then with confidence 95% non-infestation B. ovata to viruses and pass from bath anti parasite and anti-bacterial must be introduce to south Caspian sea

Inhibitive effect of sodium (E)-4-(4-nitrobenzylidenamino) benzoate on the corrosion of some metals in sodium chloride solution

The inhibition performance of a novel anionic carboxylic Schiff base, sodium (E)-4-(4-nitrobenzylideneamino)benzoate (SNBB), was investigated for various metals, namely low carbon steel F111, pure iron and copper, in neutral 10 mM NaCl solution. Potentiodynamic polarization, scanning vibrating electrode technique (SVET), quantum chemical (QC) calculation, and molecular dynamics (MD) simulation were employed. The potentiodynamic polarization data showed that SNBB acts as an effective corrosion inhibitor for both iron and F111 steel, but it is not effective for the copper. In situ spatially-resolved SVET maps evidenced a major change in surface reactivity for Fe and F111 steel immersed in 10 mM aqueous solution in the absence and in the presence of SNBB. Featureless ionic current density distributions were recorded in the presence of SNBB at both their spontaneous open circuit potential (OCP) and under mild anodic polarization conditions, while major ionic flows were monitored above the metals in the absence of SNBB. On the basis of computer simulations, it is proposed that SNBB produces a stable chelate film on iron and steel surfaces that accounts for the good corrosion inhibition efficiency observed. The different inhibition efficiencies of SNBB molecules on the iron and copper was attributed to the special chemical structure of SNBB molecule and its different chelation ability with the released metal ions on the metal surface. The QC calculations also confirmed the high corrosion inhibition efficiency of SNBB. The MD simulation indicated higher binding energy of SNBB on iron surface compared to that of copper surface. The interaction mode of SNBB on iron and F111 steel surfaces corresponds to a mixed chemical and physical adsorption, and it obeys the Langmuir isother

Inhibitive effect of sodium (E)-4-(4-nitrobenzylideneamino)benzoate on the corrosion of some metals in sodium chloride solution

The inhibition performance of a novel anionic carboxylic Schiff base, sodium (E)-4-(4-nitrobenzylideneamino)benzoate (SNBB), was investigated for various metals, namely low carbon steel F111, pure iron and copper, in neutral 10 mM NaCl solution. Potentiodynamic polarization, scanning vibrating electrode technique (SVET), quantum chemical (QC) calculation, and molecular dynamics (MD) simulation were employed. The potentiodynamic polarization data showed that SNBB acts as an effective corrosion inhibitor for both iron and F111 steel, but it is not effective for copper. In situ spatially-resolved SVET maps evidenced a major change in surface reactivity for Fe and F111 steel immersed in 10 mM aqueous solution in the absence and in the presence of SNBB. Featureless ionic current density distributions were recorded in the presence of SNBB at both their spontaneous open circuit potential (OCP) and under mild anodic polarization conditions, while major ionic flows were monitored above the metals in the absence of SNBB. On the basis of computer simulations, it is proposed that SNBB produces a stable chelate film on iron and steel surfaces that accounts for the good corrosion inhibition efficiency observed. The different inhibition efficiencies of SNBB molecules on iron and copper was attributed to the special chemical structure of the SNBB molecule, and its different chelation ability with the released metal ions on the metal surface. The QC calculations also confirmed the high corrosion inhibition efficiency of SNBB. The MD simulation indicated higher binding energy of SNBB on iron surface compared to that of copper surface. The interaction mode of SNBB on iron and F111 steel surfaces corresponds to a mixed chemical and physical adsorption, and it obeys the Langmuir isotherm

Pitting corrosion inhibition of 304 stainless steel in NaCl solution by three newly synthesized carboxylic Schiff bases

Three newly synthesized Schiff base derivatives, sodium (E)-4-(nitrobenzylideneamino)-benzoate (SNBB), sodium (E)-4-(benzylideneamino)-benzoate (SBB), and sodium (E)-4-(hydroxybenzylideneamino)-benzoate (SHBB) were investigated as pitting corrosion inhibitors for 304 stainless steel in neutral 0.1 M NaCl. Potentiodynamic polarization evidenced major shifts in pitting potential to more positive values with increasing inhibitor concentration. The scanning vibrating electrode technique (SVET) imaged metastable pitting in 0.1 M NaCl, but not in the presence of the inhibitor, indicating that it prevented pit nucleation. The inhibition performance was established under anodic polarization conditions, because only minute local anodic activity due to metastable pit formation could be observed when the steel was exposed to SNBB-containing solution, whereas the metal would undergo pit propagation at the same potential in the inhibitor-free solution. X-ray photoelectron spectroscopy (XPS) analysis evidenced chromium enrichment at weak points (pores) of the passive film at anodic polarization condition where sudden release of Fe cations is possible. In this way, the SNBB molecules will migrate to these sites to react with the Fe ions and form a chelate compound which will deposit finally at those sites and plug them, whereas no effect occurred at the open circuit potential (OCP)

Synthesis and evaluation of three new anionic Schiff bases as pitting corrosion inhibitor for stainless steel 304 in NaCl solution

Three newly synthesized Schiff base derivatives, sodium (E)-4-(nitrobenzylideneamino)-benzoate (SNBB), sodium (E)-4-(benzylideneamino)-benzoate (SBB), and sodium (E)-4-(hydroxybenzylideneamino)-benzoate (SHBB) were investigated as pitting corrosion inhibitors for 304 stainless steel in neutral 0.1 M NaCl. Potentiodynamic polarization evidenced major shifts in pitting potential to more positive values with increasing inhibitor concentration. The scanning vibrating electrode technique (SVET) imaged metastable pitting in 0.1 M NaCl, but not in the presence of the inhibitor, indicating that it prevented pit nucleation. The inhibition performance was established under anodic polarization conditions, because only minute local anodic activity due to metastable pit formation could be observed when the steel was exposed to SNBB-containing solution, whereas the metal would undergo pit propagation at the same potential in the inhibitor-free solution. X-ray photoelectron spectroscopy (XPS) analysis evidenced chromium enrichment at weak points (pores) of the passive film at anodic polarization condition where sudden release of Fe cations is possible. In this way, the SNBB molecules will migrate to these sites to react with the Fe ions and form a chelate compound which will deposit finally at those sites and plug them, whereas no effect occurred at the open circuit potential (OCP

Inhibition of Aluminium Corrosion Using Benzothiazole and Its Phthalocyanine Derivative

Cyclic voltammetry and potentiodynamic polarization techniques were used to study the effects of 4-[4-(1,3-benzothiazol2yl)phenoxy] phthalonitrile (BT) and tetrakis[(benzo[d]thiazol-2ylphenoxy) phthalocyaninato] gallium(III)chloride (ClGaBTPc) as aluminium corrosion inhibitors in 1.0 M hydrochloric acid. The presence of the inhibitors in the concentration range of 2 to 10 μM was found to retard the aluminium corrosion process such that the inhibition efficiency was found to range from 28.2 to 76.1% for BT and from 71.5 to 82.7% for ClGaBTPc. The latter was a better inhibitor. Scanning electron microscopy and energy-dispersive X-ray measurements reveal effective metal surface protection by the inhibitors, most probably by shielding it from the corrosion attacks of Cl− from the acid. The calculated quantum chemical parameters agreed with experimental results