Synthesis and Inhibition Efficiency of a Novel Quadripolymer Inhibitor

A novel quadripolymer scale inhibitor poly-maleic anhydride-acrylic acid-acrylamide-sodium methallyl sulfonate(PMAAS)was synthesized by solution polymerization with maleic anhydride(MA),acrylic acid(AA), acrylamide(AM),sodium methallyl sulfonate(SMAS),etc.IR spectrum shows that PMAAS contains carbonyl, hydroxyl,phosphatic and sulfonic acid group.SEM indicates that PMAAS blocks the normal growth of scale CaCO3 and CaSO4 crystals.The influences of PMAAS concentration,Ca 2+ concentration,temperature and pH value of the system on the inhibition efficiency are investigated.The inhibition efficiency of PMAAS is superior to com- mercial inhibitors T-225 and XF-192.

Influence of alkyl group of imidazolinyl-quaternary-ammonium-salt on corrosion inhibition efficiency

The action between imidazolinyl-quaternary-ammonium-salt(IQAS) molecule and Fe atom was studied, and the influence of the alkyl group connected with N atom of imidazoline ring on corrosion inhibition efficiency was explored. Quantum chemical methods, HF/6-31 G and HF/Lan L2 dz, were applied successively to calculate the parameters such as front molecular orbit energy of IQASⅠ-Ⅳ and chemical adsorption for IQASⅠ-Ⅳ and Fe atom. The corrosion inhibition efficiency was measured with the weight loss method of carbon steel samples in acidic solution and oil field sewage. Based on the theoretical analyses and experimental results, it is concluded that N-Fe coordination bond is formed between IQAS molecule and Fe atom, corrosion inhibition efficiency is decreased in the following order(from large to small): IQAS Ⅳ, IQAS Ⅲ, IQAS Ⅱ, IQASⅠ.

A Quantum Chemistry Study of Inhibition Properties of Imidazole and Its Derivatives on Iron Surface Corrosion

The geometries of imidazole and its derivatives were respectively optimized by using ab initio method, and the molecular orbital energy levels and the charge densities were obtained for their optimum geometries. The frontier orbital energy levels, and the net charges of N (1) atom and the imidazole ring of those molecules were obtained with ab initio and SCC-DV-Xα methods. It was found that the inhibition properties of those compounds change with the highest occupied molecular orbital energy levels, and the net charges of N (1) atom. We took four iron atoms on the crystal plane (100) of α-iron as the surface which was used to study the adsorption towards the inhibitors. The adsorption models of the inhibitor to be adsorbed on the Fe-cluster surface were optimized with SCC-DV-Xα method. It turns out that the most favorable model is that the inhibitor molecule is adsorbed on the Fe-cluster surface in an inclined state. The calculation shows that the stabilization energies of the systems are well correlated with the inhibition efficiencies.

Corrosion Resistance ofAA6063-Type AI-Mg-Si Alloy by Silicon Carbide in Sodium Chloride Solution for Marine Application

The present work focused on corrosion inhibition of AA6063 type Al-Mg-Si alloy in sodium chloride （NaCI） solution with a silicon carbide inhibitor, using the potentiodynamic electrochemical method. The aluminium alloy surface morphology was examined, in the as-received and as-corroded in the un-inhibited state, with scanning electron microscopy equipped with energy dispersive spectroscopy （SEM-EDS）. The results obtained via linear polarization indicated a high corrosion potential for the unprotected as-received alloy. Equally, inhibition efficiency as high as 98.82% at 10.0 g/v silicon carbide addition was obtained with increased polarization resistance fRy）, while the current density reduced significantly for inhibited samples compared to the un-inhibited aluminium alloy. The adsorption mechanism of the inhibitor aluminium alloy follows the Langmuir adsorption isotherm. This shows that the corrosion rate of aluminium alloy with silicon carbide in NaCI environment decreased significantly with addition of the inhibitor.

Effect of six kinds of scale inhibitors on calcium carbonate precipitation in high salinity wastewater at high temperatures

Precipitation of calcium carbonate （CaCOs） scale on heat transfer surfaces is a serious and expensive problem widely occurring in numerous industrial processes. In this study, we compared the scale inhibition effect of six kinds of commercial scale inhibitors and screened out the best one （scale inhibitor SQ-1211） to investigate its scale inhibition performance in highly saline conditions at high temperature through static scale inhibition tests. The influences of scale inhibitor dosage, temperature, heating time and pH on the inhibition efficiency of the optimal scale inhibitor were investigated. The morphologies and crystal structures of the precipitates were characterized by Scanning Electron Microscopy and X-ray Diffraction analysis. Results showed that the scale inhibition efficiency of the optimal scale inhibitor decreased with the increase of the reaction temperature. When the concentration of Ca^2＋ was 1600 mg/L, the scale inhibition rate could reach 90.7% at 80℃ at pH 8. The optimal scale inhibitor could effectively retard scaling at high temperature. In the presence of the optimal scale inhibitor, the main crystal structure of CaCOs changed from calcite to aragonite.

Molecular simulation of oligomer inhibitors for calcite scale

Molecular simulation was performed to study the interaction between CaCO3 crystal and several oligomer inhibitors, by using the equilibrium morphology method to calculate the growth morphology of CaCO3 without inhibitors. The calculated morphology agreed well with SEM photographs. Then, a double-layer model was built to investigate the interaction between calcite crystal and oligomer inhibitors containing maleic anhydride （MA） and acrylic acid （AA）. Interaction energy per gram of an oligomer inhibitor was introduced as a scale of inhibition efficiency of different monomers. The results indicated that, for calcite scale inhibition, acrylamide （AM） and vinyl phosphonic acid （VPA） were the most efficient monomers, while allylsulfonic acid （AS） was the poorest. Increasing proportion of AM in dimer inhibitor molecule would improve the inhibition efficiency of MA, though, for a trimer, such as MA-AA-AM, certain sequence of monomers in the inhibitor molecule was necessary besides higher proportion of AM.

Experimental study on the compatibility of scale inhibitors with Mono Ethylene Glycol

When both of the scaling and hydrate risks occur in deep water wells or subsea pipelines at the same time,the compatibility between scale and hydrate inhibitors should be paid more attention to for the risk prevention.In this paper,a new deep-water gas field found in the South China Sea is taken as a reference of project background to investigate the compati bility between scale inhibitors and hydrate inhibitors experimentally.Firstly a preliminary qualification evaluation of scale inhibitors was caried out,in which the static scale inhibition eficiency,the scale induction time,and the minimum effective concentrations of the selected scale inhibitors were tested.Then the effect of commonly used thermodynamic hydrate inhibitor MEG(Mono Ethylene Glycol)on the anti-scaling performance of scale inhibitors was evaluated.MEG-resisted scale inhibitors were further optimized.Finally,an extended discussion on the compati-bility of scale inhibition with hydrate inhibition was conducted.The experimental results showed that the scale inhi bitors HPMA and MA/AA were recommended with the best working concentration of 30 ppm.The high concentration inhibitors(30 wt%)can coexist with the same volume of pure MEG for more than 12-14 h at room condition and 60°C without any precipitation.The anti-scale fficiency of inhibitor with 30 ppm concentration is still up to 90%even at the presence of 20wt%MEG(after2-4 h at 95°C).Hence,in deep-water wellbore,compatible scale and hydrate inhi bitors can be injected together using one chemical pipeline.Besides,it is also found that the polymer scale inhibitors generally have good compatibility with MEG.It deserves further studies and can be regarded as one direction for scale inhibitor improvement in the future.