The Isoelectric Point and the Points of Zero Charge of Fe-Al-Mg Hydrotalcite-like Compounds

The relation of the isoelectric point (IEP) and the point of zero net charge (PZNC) of the hydrotalcite-like compounds was discussed. It was found that the IEP does not equal to the PZNC and the IEP is higher than the PZNC. The structural positive charges existing in the HTlc, which cause the difference between the IEP and the PZNC. The effects of the structural positive charges of the HTlc on its IEP and PZNC are the same as the specific adsorption of metal cations.

Study on Isoelectric Point of Magnesium Aluminum Hydroxide

Yoon's equation which predicted point of zero charge of complex oxide should predict the zero point of net charge (ZPNC) of mixture of variable and permanent charge rather than the point of zero charge (PZC) of the variable charge component. The calculated values with modified Yoon's equation agreed with the experimental values.

Effect of cationic monomer structure on the aggregation behavior of amphoteric acrylic polymer around isoelectric point

Amphoteric polymer can be used as retanning agent in leather manufacture.It is particularly useful in chrome-free tanning systems since it can regulate the charge properties of chrome-free leather and enhance the fixation of anionic post-tanning chemicals in leather.However,the aggregation and precipitation of amphoteric polymer retanning agents around the isoelectric point(pl)hinder their wide application.Herein,we synthesized five amphoteric acrylic polymers(AAPs)by free radical copolymerization with acrylic acid and five different cationic acrylic monomers.The effect of cationic monomer structure on the aggregation behavior of AAPs was investigated.The aggregation of AAPs in aqueous solution showed pH and concentration dependence.Light scattering analysis showed that Poly(AAA-co-MAPTAC)and Poly(AA-co-DMAPMA)were in the shape of coiled linear flexible chains with small particle size(R_(g)7.6 nm and 14.8 nm,respectively)near the pl.However,Poly(AA-co-DAC),Poly(AA-co-DMC)and Poly(AA-co-DMAEMA)were in the shape of hollow spheres and exhibited serious aggregation.Quantum chemical calculations suggested that the amide groups in the cationic monomers MAPTAC and DMAPMA enhanced the nucleophilicity of AAPs.Thus the corresponding AAPs could carry a large number of cationic charges to slow their aggregation when the pH just climbed over the pl.The results are expected to provide theoretical reference for the synthesis and wide-spread application of AAPs.

Effect of cationic monomer structure on the aggregation behavior of amphoteric acrylic polymer around isoelectric point

Amphoteric polymer can be used as retanning agent in leather manufacture. It is particularly useful in chrome-free tanning systems since it can regulate the charge properties of chrome-free leather and enhance the fixation of anionic post-tanning chemicals in leather. However, the aggregation and precipitation of amphoteric polymer retanning agents around the isoelectric point (pI) hinder their wide application. Herein, we synthesized five amphoteric acrylic polymers (AAPs) by free radical copolymerization with acrylic acid and five different cationic acrylic monomers. The effect of cationic monomer structure on the aggregation behavior of AAPs was investigated. The aggregation of AAPs in aqueous solution showed pH and concentration dependence. Light scattering analysis showed that Poly (AA-co-MAPTAC) and Poly (AA-co-DMAPMA) were in the shape of coiled linear flexible chains with small particle size (Rg 7.6 nm and 14.8 nm, respectively) near the pI. However, Poly (AA-co-DAC), Poly (AA-co-DMC) and Poly (AA-co- DMAEMA) were in the shape of hollow spheres and exhibited serious aggregation. Quantum chemical calculations suggested that the amide groups in the cationic monomers MAPTAC and DMAPMA enhanced the nucleophilicity of AAPs. Thus the corresponding AAPs could carry a large number of cationic charges to slow their aggregation when the pH just climbed over the pI. The results are expected to provide theoretical reference for the synthesis and widespread application of AAPs.

Dual-functional poly(2-methyl-2-oxazoline)/poly(2-(dimethylamine)ethyl methacrylate)mixed brushes with switchable protein adsorption and antibacterial properties

Herein,binary mixed brushes consisting of poly(2-methyl-2-oxazoline)(PMOXA)and poly(2-(dimethylamine)ethyl methacrylate)(PDMAEMA)with different chain lengths were fabricated by successive grafting of NH_(2)-terminated PMOXA and SH-terminated PDMAEMA onto polydopamine-anchored substrates.The mixed-brush coating was characterized by variable-angle spectroscopic ellipsometry,X-ray photoelectron spectroscopy,Fourier transform infrared spectroscopy,zeta potential measurements,water contact angle,and atomic force microscopy.The mixed brushes showed tunable surface charge,wettability,and surface roughness,depending on the degree of PDMAEMA swelling under varying pH and ionic strength(Ⅰ).Then the adsorption behaviors of pepsin,bovine serum albumin(BSA),γ-globulin,and lysozyme,four very different proteins with regard to isoelectric point,on the mixed brushes coating were studied by using fluorescence microscopy and surface plasmon resonance.When the chain length of PDMAEMA was about twice as long as PMOXA,the mixed brushes not only had high adsorption capacity for pepsin,BSA,and y-globulin but also had a desorption efficiency of 86.9%,87.1%,and 93.5%,respectively.It is explained that electrostatic attraction between the protonated PDMAEMA and positively charged acidic proteins(pepsin and BSA,whose isoelectric points were below the pK_(a) of PDMAEMA)would drive the intensive adsorption(at pH 3,I=10^(-3)mol·L^(-1)for pepsin,and pH 5,I=10^(-5)mol·L^(-1)for BSA),while desorption was dominated by the hydrophilic PMOXA when PDMAEMA was shrinking(at pH 7,I=10^(-1)mol·L^(-1)for pepsin,and pH 9,I=10^(-1)mol·L^(-1)for BSA).Furthermore,the isoelectric precipitation led to the adsorption of neutral protein(γ-globulin,whose isoelectric point was near the pK_a of PDMAEMA)at pH 7,I=10^(-5)mol·L^(-1),while electrostatic repulsion and antifouling PMOXA triggered the desorption of y-globulin at pH 3,I-10^(-1)mol·L^(-1).However,alkaline protein(lysozyme,whose isoelectric point was higher than the pK_(a) of PDMAEMA)exhibited slight adsorption on PMOXA/PDMAEMA mixed brushes under test conditions,regardless of whether PMOXA or PDMAEMA occupied the outermost layer.The antibacterial property of the mixed brushes against Escherichia coli was investigated.PMOXA/PDMAEMA mixed brushes showed significant bactericidal activity at pH 3,I=10^(-3)mol·L^(-1),while the rinse of pH 9,I=10^(-1)mol·L^(-1)solution could remove most of the residual bacteria.This work not only enables controlled adsorption of proteins with different isoelectric points but also ensures that the surface of the coating is minimized from bacterial contamination.

Flotation separation of Xixia andalusite ore

The flotation behavior of Xixia andalusite was studied with different collectors.The tests were conducted with a pure andalusite sample in micro-flotation cell and then with an ore sample in a mechanical flotation cell.The surface charge was measured on pure andalusite sample and the isoelectric point（IEP） was found to be pH 5.2.Andalusite is floated with an amine collector above IEP where mineral surface is negatively charged.In contrast,an alkyl sulfonate collector（sodium dodecyl benzene sulfonate） is effective in the pH range where andalusite surface is positively charged.Furthermore,andalusite is floated with oleate in neutral and mildly alkaline pH values.55.3% Al2O3 is produced with 75.6% andalusite recovery when using the alkyl benzene sulfonate collector.Starch is found to be an effective depressant for gangue minerals in alkyl benzene sulfonate flotation.Moreover,slimes are found to have an adverse effect on the flotation of andalusite.Therefore,pretreatment by desliming and pre-float（to remove carbonaceous species） prior to andalusite flotation is necessary.

Influence of TAC on Dispersion of Aqueous Nano Alumina Suspension

The stability of aqueous nano alumina powder suspensions with and without dispersant tri-ammonium citrate (TAC) was investigated by measuring zeta potential at different pH values. The isoelectric point (IEP) of alumina powder shifts towards more acidic pH range by adding TAC dispersant. The results illustrate that adsorption of TAC on alumina powder surface existed in the aqueous suspension, which leads to a high stability of the suspension.

Studies on Y- Potential of Positive Sol of Magnesium Aluminum Hydroxide

The IEP of magnesium aluminum hydroxide was predicted with the modified Yoon′s equation, and the effect of electrolyte on the Y- potential of the sol was studied by electrophoresis method. The results showed that the calculated IEP values with the modified Yoon′s equation agreed well with the experimental ones. With the increase of the ionic radius of monovalent anions (Cl -, Br -, I -) the ζ potential decreased. The same was true for CO 2- 3, SO 2- 4 but the sign of the Y- potential reversed from positive to negative. For Al 3+ , Ca 2+ , Mg 2+ , however, the ζ potential increased with the increase of the concentration of Al 3+ , Ca 2+ , Mg 2+ .

Investigation of the Corrosion and Passive Behavior of HP-13Cr Stainless Steel in Formate Annulus Protection Fluid

The corrosion and passive behavior of HP-13Cr stainless steel(HP-13Cr SS)in formate annulus protection fluid was investigated.HP-13Cr SS exhibited good passive behavior in clean formate annulus protection fluid,which was attributed to a thinner and more dense passive film mainly composed of Cr_(2)O_(3).In the formation water solution,the passive film was composed of metastable Cr(OH)3,which was explained by the isoelectric point theory,resulting in the deterioration of the passive behavior of HP-13Cr SS.When the formation water penetrated the formate annulus protection fluid,a large number of loose FeCO_(3)particles formed in the corrosion scales,thus HP-13Cr SS suffered severe corrosion.Therefore,avoiding formation water penetrating the formate annulus protection fluid is conducive to improving the service life of HP-13Cr SS oil tubes in extremely aggressive environment.

Pristine point of zero charge (p.p.z.c.) and zeta potentials of boehmite’s nanolayer and nanofiber surfaces

The pristine point of zero charge(p.p.z.c)and zeta potential as a function of pH of boehmite oxide/hydroxide(α-Al_(2)O_(3)·H_(2)O)have been determined for three filter media.The active component in the first two filter media is boehmite nanofibers,only 2 nm in diameter and about 300 nm long.Boehmite nanofibers create high zeta potential(ζtrue≥46 mV)in aqueous solutions in the pH range of 3–8.The p.p.z.c.values were determined to be 11.60±0.15 for nanofibers grafted onto microglass fibers and 11.40±0.15 for agglomerated nanofibers.In the third filter media,a boehmite nanolayer in the form of monocrystalline oxide/hydroxide with a thickness of approximately 1.2 nm is electroadhesively deposited onto siliceous support material with large surface area of about 50 m^(2)/g,therefore forming a highly electropositive composite of boehmite nanolayer on the second highly electronegative solid.Boehmite’s oxide-hydroxide nanolayer surface creates high zeta potential(ζtrue≥50 mV)in aqueous solutions in the pH range of 3–8.The p.p.z.c.value was determined to be 11.38±0.15.The reported values are within accuracy,but they are much higher than the values reported in the literature.X-ray powder diffraction data were supplemented by microscopy,infrared spectroscopy in order to characterize fully synthetic boehmite surfaces.

Preparation,characterization of Mo,Ag-loaded BiVO_4 and comparison of their degradation of methylene blue

Two types of metal-loaded visible-light-driven photocatalysts,Mo-BiVO4and Ag-BiVO4,were synthesized by wet impregnation method.Material poperties were characterized by UV-vis diffuse reflectance spectroscopy,X-ray diffraction,field emission scanning electron microscopy,X-ray photoelectron spectroscopy and low temperature nitrogen adsorption-desorption.Photocatalytic activity of the obtained materials was investigated through degrading methylene blue(MB) solution under visible-light irradiation.The results reveal that both metal loaded-BiVO4catalysts have monoclinic scheelite structure.Mo and Ag exist as oxides on the surface of the particles.The changes of absorption in visible-light region,band gap(E g) and specific surface area(A BET) caused by loading Ag are more obvious than those caused by loading Mo.But the isoelectric point of Ag-BiVO4decreases less than that of Mo-BiVO4does.Both catalysts show higher photocatalytic activity than pure BiVO4,resulting in the significantly improved efficiency of degradation of MB.And the degradation efficiency of these two metal-loaded BiVO4photocatalysts is similar to each other.However,mechanisms of such enhancement are different.The decrease of isoelectric point helps Mo-BiVO4improve the degradation efficiency.As for Ag-BiVO4,the augmentation of absorption in visible-light region as well as the abatement of E g plays more important roles.

Interaction between retanning agents and wet white tanned by a novel bimetal complex tanning agent

A promising and practical chrome-free tanning system has been developed based on a novel Al–Zr bimetal complex tanning agent.However,to achieve satisfactory resultant leather,the retanning process that is compatible with this emerging tannage needs to be investigated systematically.This paper aims to explore the interaction between the bimetal complex tanned wet white and retanning agents.The isoelectric point(pI)of wet white was 7.2,which was nearly the same as wet blue.The electropositivity of wet white was even higher than that of wet blue during post-tanning processes,resulting in higher uptake rate of retanning agents.The distribution of various retanning agents in wet white was analyzed by pI measurement of layered leather and fluorescent tracing technique.The retanning agents were unevenly distributed throughout the cross-section,which might be an important restriction factor in obtaining satisfactory organoleptic properties of the crust leather.This fact is mainly due to the strong electrostatic interaction between anionic retanning agents and wet white.Applying a high dosage of multiple retanning agents in a proper sequence of addition benefited the full penetration of retanning agents in leather matrix and thus improved the organoleptic properties of crust leather.This work provides guidance for optimizing retanning process of the wet white leather.

Study on electric property at interface of positive sol of magnesium aluminum hydroxide

The isoelectric point (IEP) and zero point of charge (ZPC) of magnesium aluminum hydroxide were studied by electrophoresis method, potentiometric titration method, and elemental analysis. Results showed that the charge of magnesium aluminum hydroxide was composed of variable charge and permanent positive charge. Because of the permanent positive charge, the IEP and ZPC obtained were higher than calculated. The LEP decreased and ZPC increased as X increased.

Primary Structural Characterization of Phospholipid Hydroperoxide Glutathione Peroxidase

More than 20 sequences of phospholipid hydroperoxide glutathione peroxidase (PHGPX) from a sequence database were analyzed. The analyses show that the primary structures of most PHGPX proteins have three highly conserved regions forming a catalytic center and have more than 50% amino acid sequence identity in common. However, two PHGPXs from bovine and swine with the same function have very low similarity with typical PHGPXs and do not have the three highly conserved regions. Thus, the PHGPX proteins are divided into two types: those with the three highly conserved regions, designated as PHGPX I, and the others as PHGPX II. In general, type I proteins are composed of ca.170 amino acid residues; a few of them have an extra signal peptide sequence at the N terminal of the protein. The composition of plant and animal PHGPX amino acids is very different, with most plant PHGPXs being weak acidic, while most animal ones are alkaline. Another specific conservative motif is also found in plant PHGPX proteins. System evolution analysis shows that ortholog and paralog evolution models both exist in PHGPXs, with the plant PHGPX and the animal PHGPX diverging exclusively into two branches in PHGPX I. The information revealed by the evolution tree agrees with the general species evolution process from low to advanced and from simple to complicated.