An ecofriendly resorcinol derivative, dimethyl-4,6-dihydroxyisophthalate (DDIP) is examined as an anticorrosion agent for low carbon steel (CS) in a 0.5 mol L HCl solution. Electrochemical and chemical methods are used to determine the effectiveness of the inhibitor. The DDIP compound decreased the rate of CS corrosion. The mitigation efficiency rose from 61.8 to 79.9% as the DDIP dose increased from 50 to 300 ppm in the corrosive medium. At 300 ppm, however, the efficiency decreased from 79.9 to 70.05% as the temperature increased from 25 to 55 °C. Physical quantities and thermodynamic parameters are discussed. The compound's adsorption follows Langmuir's concept. Adsorption of the DDIP compound is a mix of physisorption and chemisorption. The difference in values is less than 85 mV, indicating that the examined compound is a mixed-type inhibitor. Scanning electron microscopy and atomic force microscopy revealed the development of a coherent film at CS in the presence of the DDIP inhibitor. The results obtained using various techniques were closely related, indicating validity and accuracy. The interaction between the DDIP molecules and the CS was explained by the density functional theory and Monte Carlo simulation. The quantum characteristics confirmed that the DDIP compound is a promising inhibitor.
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http://dx.doi.org/10.1021/acsomega.2c00153 | DOI Listing |
ACS Omega
May 2022
Department of Chemistry, Faculty of Science, Suez Canal University, Ismailia 41522, Egypt.
An ecofriendly resorcinol derivative, dimethyl-4,6-dihydroxyisophthalate (DDIP) is examined as an anticorrosion agent for low carbon steel (CS) in a 0.5 mol L HCl solution. Electrochemical and chemical methods are used to determine the effectiveness of the inhibitor.
View Article and Find Full Text PDFLife Sci
September 1996
Pharmacokinetics and Drug Metabolism Department, Parke-Davis Pharmaceutical Research, Warner-Lambert Company, Ann Arbor MI 48105 USA.
Endothelin (ET-1) is a 21-amino acid, vasoconstrictive peptide originally isolated from endothelial cells. It is one member of a class of potent, purportedly paracrine substances that act at receptors in multiple target organs. Antagonists to the receptor subtypes, ETA and ETB, have been designed around the hydrophobic carboxy-terminus of ET-1.
View Article and Find Full Text PDFJ Cardiovasc Pharmacol
April 1994
Department of Chemistry, Parke-Davis Pharmaceutical Research, Warner-Lambert Company, Ann Arbor, MI 48105.
The effects of different amino acids incorporated into the 16 and 17 positions of the C-terminal hexapeptide of ET-1 were examined. Structure-activity relationships (SAR) of the ET receptor antagonists PD 142893 [Ac-(D-Dip16-L-Leu17-L-Asp-L-Ile-L-Ile-L-Trp) (D-Dip = 3,3-D-diphenylalanine)] and PD 145065 [Ac-(D-Bhg16-L-Leu17-L-Asp-L-Ile-L-Ile-L-Trp) (D-Bhg = 5H-dibenzyl[a,d]cycloheptene-10,11-dihydro-glycine)] uncovered certain requirements for high potency. The disodium salt of PD 145065 has 4.
View Article and Find Full Text PDFThe effects of diamino-dichloro-cis-platinum II (DDP) and dichloro-trans-bis-isopropyl-amine-platinum IV (DDIP or CHIP) on the primary cell-mediated cytotoxic (CMC) response developed in a mixed lymphocyte tumor cell culture (MLTC) were investigated. DDP as well as CHIP added on day 0 augmented the CMC response when spleen cells from C57Bl/6 mice were cultured for 4 days with supraoptimal numbers of irradiated (4000 rads) allogeneic P815 mastocytoma cells. A similar effect was observed when mice were treated with either of the two platinum compounds 1 or 5 days prior to spleen removal and sensitization of the spleen cells in a MLTC.
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