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Aluminum phosphate is useful catalyst for many reactions. There are a lot of reports about catalytic activities of aluminum phosphate, however little reports about the relationship among the preparation, composition, catalytic activity of this phosphate. Phosphates transform to various other phosphates with hydrolysis and dehydration reactions by heating. In this work, some aluminum orthophosphates and condensed phosphates were prepared, and their compositions were estimated. Furthermore, specific surface area, acid strength, the amount of acidic sites, and the catalytic activities for the decomposition of trifluoromethane of these salts were investigated. Aluminum ortho‐ and polyphosphates were prepared in the systems of ortho‐ and poly‐phosphates. The catalytic activity for decomposition of CHF3 was related with a certain degree of specific surface area, acid strength, and the amount of acidic sites. Aluminum orthophosphate with a small amount of sodium cation had higher catalytic activity at lower temperature.

Anthocyanins. The anthocyanin pigments impart the pleasing red and purple colours associated with many fruits and vegetables. They belong to the class of compounds referred to as ‘flavonoids’ and, in chemical terms, they are flavylium salts differing in the number and position of free or methylated hydroxyl groups and with a sugar moiety linked through position 3 or positions 3 and 5 in the ring. A commonly occurring anthocyanin pigment, cyanidin‐3‐glucoside, is shown in figure 3. The anthocyanins are soluble in water and are unstable under a variety of enzymic and non‐enzymic conditions.

Proposes to investigate preparation of amorphous silica via precipitation reaction from aqueous solution of sodium metasilicate and hydrochloric acid in emulsion medium, focusing on determination to optimise the dispersive and morphological properties of silicas studied.

The silicas obtained were analysed using modern research techniques, such as scanning electron microscopy for studies on particle surface morphology and dynamic light scattering technique for studies on particle structure and their tendency for agglomeration. Moreover, the sedimentation characteristics of the silica powders were evaluated.

The properties of silicas precipitated from emulsion systems depend on several variables but the amount and concentration of the applied reagents and pH of the emulsion are of critical importance. Using 16, 14 or 12 wt% solution of sodium metasilicate (per SiO₂ content) and 5.0, 4.3 or 3.7 wt% solution of hydrochloric acid, the particles obtained were of best dispersive parameters. Mean diameter, polydispersity, shape and sedimentation of particles reflect the applied preparation procedure. Several of the silicas obtained manifest tendency for formation of secondary agglomerates and aggregates. The pH of the solution obtained from two mixed emulsions exerts a pronounced influence on quality and properties of the prepared silica. The best silica is obtained at pH 6‐7. In the cases where the emulsion has been dosed with “pure” sodium metasilicate solution, particles of irregular shape of high mean particle diameters, with a tendency to form large particle accumulations, have been formed.

In the precipitation reaction, aqueous solution of sodium metasilicate, hydrochloric acid and emulsifiers in the form of non‐ionic surfactants were used as substrates. The organic phase involved cyclohexane. Alternatives could be explored.

The method developed provides a novel and practical solution to precipitation of hydrophilic/hydrophobic silica fillers.

The method for obtaining amorphous types of silica could find numerous applications, particularly as polymer fillers.

The purpose of this paper is to discuss a practical approach taken by utilizing the non‐conformance/event management and failure investigation (FI) system to formally troubleshoot an actual process failure observed in the sequencing facility.

In this study the authors describe how the cause for the poor quality sequence data, as indicated from the quality score, involving high molecular weight follicular lymphoma DNA samples for a study of tumor‐associated genome rearrangements was successfully identified and confirmed through the application of a well structured FI process.

Through this FI process the underlying causes were effectively identified, immediate corrective actions were executed and a preventative action to avoid or minimize reoccurrences was also implemented and monitored for effectiveness.

This paper establishes that by applying a systematic, documented FI process the underlying causes of a process failure in an organization can be effectively identified and appropriate corrective and preventative actions can be successfully adopted.

Modern cutting fluids often are real aqueous solutions of chemical compounds. That form of cutting fluid is simpler in preparation, as compared to emulsions and microemulsions. The water base is a good cooling medium of high‐ecological value. The purpose of this paper is to discover water‐soluble additives that could improve the lubricity of water.

Three cationic surfactants were chosen to be analyzed. Their tribological properties were verified using two testers: T0‐2 (four‐ball machine) and T‐11 (ball‐on‐disk). The results of the tests performed using friction couples made of steel (T0‐2, T‐11) and steel‐ceramics (T‐11) were satisfactory.

The friction coefficients and wear scar diameters are even a few times smaller, as compared to the ones measured in a water environment.

The paper demonstrates that the crucial role in improvement of the tribological properties is played by the surface activity of the additives (confirmed by the measurements of the surface tension and wetting angle). As the cationic surfactants are bactericidal and anti‐corrosive, they can be classified as multi‐purpose additives modifying water lubricity.

The purpose of this paper is to study methods of reacting the surface of the particles of silica sols with silanes, primarily gamma‐glycidoxypropyltrimethoxysilane (GPTMS) and study some basic properties of the modified sols and the nature and structure of the silane groups attached to the particle surface.

The surface of the silica particles was modified by reacting the silica sols with aqueous solutions of silanes, chiefly GPTMS. The presence and structure of silane groups on the particle surface were established by Si‐NMR and C‐NMR, respectively.

Several silanes were studied but silica sols could be readily modified only with GPTMS and glycidoxypropylmethoxydiethoxysilane (GPMDES), most readily if the silanes were pre‐hydrolysed in water. Higher degrees of silylation were preferably done by continuous addition of silane. Lower degrees of modification can be achieved at room temperature by the stepwise addition of the silane solution. The silylation of the silica surface with GPTMS significantly reduces the number of charged surface groups and silanol groups. GPTMS binds covalently to the silica surface and the epoxy ring opens and transforms into a diol. Silica sols modified with GPTMS and GPMDES are stable toward aggregation.

Only organo‐reactive silanes were studied.

This is the first work to study the modification by silanes of silica aquasols with high concentrations of silica. The silane modification can extend the use of silica to areas of applications previously inaccessible to silica sols.

The purpose of this paper is to show how to remove some dyestuffs, as pollutants, from their aqueous solutions.

To achieve the goal, a water soluble hyperbranched poly (ester‐amide) (HBP) was synthesised using the melt polycondensation method by the reaction of maleic anhydride (MA) and diisopropanol amine (DIPA) at 140°C at a molar ratio of 1:1.3 MA: DIPA, respectively. This HBP was incorporated in the preparation of an effective microcrystalline cellulose (MCC)/dimethyloldihydroxyethylene urea (DMDHEU)/HBP adduct by crosslinking HBP with DMDHEU in presence of MCC. Furthermore, the prepared adduct was characterised by investigation its infra red and then utilised in the removal of three anionic dyestuffs from aqueous solutions, namely Irgalan Blau 3GL (an acid dye), SIRIUS Blau S‐BRR (a direct dye) and Levafix Brill Orange P‐GR (a hydrolysed reactive dye).

The results obtained revealed that the optimum conditions for preparing MCC/DMDHEU/HBP adduct are [HBP], 90 g/l; [DMDHEU], 200 g/l; LR, 1/3.3; [NC₄LH], 20 g/l; a time of 30 min and a temperature of 160°C. Moreover, the results also showed that the extent of removal of such dyestuffs from their aqueous solutions by the prepared adduct follows the order: reactive dye>acid dye>direct dye, it is more pronounced at lower than at higher pH values and the removal of each dye by that adduct follows a first‐order reaction.

Other substrates such as chitosan can be used to prepare more effective adducts.

Hyperbranched polymers can be used effectively to prepare ion exchangers capable of removing the pollutants of dyestuffs from their aqueous solutions.

The aforementioned prepared HBP is a novel hyperbranched polymer and could be applied in the removal of many other pollutants.

This study aims to optimize the preparation conditions and modify the nanofiltration (NF) membranes to prepare high-performance polysulfone/sulfonated polysulfone composite nanofiltration (PSF/SPSF-NF) membranes through interfacial polymerization.

Investigating the impacts of anhydrous piperazine (PIP) concentration, trimesoyl chloride (TMC) concentration and basement membrane type on NF membrane performance, the optimal membrane was prepared. In addition, nano-SiO₂ was added to the active separation layer to modify the NF membranes.

The comprehensive performance of PSF/SPSF-NF membranes was optimized when the concentration of PIP was 0.75 Wt.% and the concentration of TMC was 0.15 Wt.%, at which time the water flux was 66.1 L·m⁻²·h⁻¹ and the retention rate of Na₂SO₄ was 98.1%. The comprehensive performance of polysulfone/sulfonated polysulfone-SiO₂ nanofiltration (PSF/SPSF-SiO₂-NF) membranes was optimized when the blending ratio of nano-SiO₂ to PIP was 2:3, with a pure water flux of 81.9 L·m⁻²·h⁻¹ and a Na₂SO₄ retention rate of 95.9%. Compared to polysulfone nanofiltration (PSF-NF) membranes and PSF/SPSF-NF membranes, NF membranes with nano-SiO₂ increased the flux recovery rate by 22.9% and 8.7%.

PSF/SPSF-SiO2-NF membrane exhibits excellent antifouling properties.

There is currently no literature available on the preparation of NF membranes using polysulfone/sulfonated polysulfone (PSF/SPFS) as a substrate. This provides a method for modifying NF membranes, starting with the modification of the basement membrane and then modifying the active separation layer.

This study aims to investigate the initial corrosion behavior in aqueous solution of 20# seamless steel under (CO₂/aqueous solution) gas–liquid two-phase stratified flow conditions.

The initial corrosion behavior was studied through the weight loss methods, scanning electron microscopy with energy-dispersive x-ray spectroscopy and x-ray diffraction.

The corrosion rate of 20# steel obviously increases with the increasing gas pressure at different corrosion time when the CO₂ pressure is less than 0.11 MPa, and the increase of corrosion rate tends to be steady when the pressure exceeds 0.11 MPa. With the increase of CO₂ pressure, the corrosion products changed from flocculent to acicular, granular and scaly. A four-stage model for the growth of the corrosion product layer was proposed, namely, the diffusion reaction stage, the local film formation stage, the complete film formation stage and the densification stage of the product film.

A four-stage model for the growth of the corrosion product layer on the pipe wall surface under this condition was proposed, namely, the diffusion reaction stage, the local film formation stage, the complete film formation stage and the densification stage of the product film. The growing process and densification mechanism of corrosion products layer were discussed.

This paper aims to investigation of processes for Pb²⁺ elimination from water/wastewater as a significant public health issue in many parts of world. The removal of Pb²⁺ ions by various nanocomposites has been explained from water/wastewaters. ZnO-based nanocomposites, as eco-friendly nanoparticles with unique physicochemical properties, have received increased attention to remove Pb²⁺ ions from water/wastewaters.

In this review, different ZnO-based nanocomposites were reviewed for their application in the removal of Pb²⁺ ions from the aqueous solution, typically for wastewater treatment using methodology, such as adsorption. This review focused on the ZnO-based nanocomposites for removing Pb²⁺ ions from water and wastewaters systems.

The ZnO-based nanocomposite was prepared by different methods, such as electrospinning, hydrothermal/alkali hydrothermal, direct precipitation and polymerization. Depending on the preparation method, various types of ZnO-based nanocomposites like ZnO-metal (Cu/ZnO, ZnO/ZnS, ZnO/Fe), ZnO-nonmetal (PVA/ZnO, Talc/ZnO) and ZnO-metal/nonmetal (ZnO/Na-Y zeolite) were obtained with different morphologies. The effects of operational parameters and adsorption mechanisms were discussed in the review.

The findings may be greatly useful in the application of the ZnO-based nanocomposite in the fields of organic and inorganic pollutants adsorption.

The present study is novel, because it investigated the morphological and structural properties of the synthesized ZnO-based nanocomposite using different methods and studied the capability of green-synthesized ZnO-based nanocomposite to remove Pb²⁺ ions as water contaminants.

The current review can be used for the development of environmental pollution control measures.

This paper reviews the rapidly developing field of nanocomposite technology.