Acidic Products Research Articles

The Application of Polycaprolactone in Three-Dimensional Printing Scaffolds for Bone Tissue Engineering.

Bone tissue engineering commonly encompasses the use of three-dimensional (3D) scaffolds to provide a suitable microenvironment for the propagation of cells to regenerate damaged tissues or organs. 3D printing technology has been extensively applied to allow direct 3D scaffolds manufacturing. Polycaprolactone (PCL) has been widely used in the fabrication of 3D scaffolds in the field of bone tissue engineering due to its advantages such as good biocompatibility, slow degradation rate, the less acidic breakdown products in comparison to other polyesters, and the potential for loadbearing applications. PCL can be blended with a variety of polymers and hydrogels to improve its properties or to introduce new PCL-based composites. This paper describes the PCL used in developing state of the art of scaffolds for bone tissue engineering. In this review, we provide an overview of the 3D printing techniques for the fabrication of PCL-based composite scaffolds and recent studies on applications in different clinical situations. For instance, PCL-based composite scaffolds were used as an implant surgical guide in dental treatment. Furthermore, future trend and potential clinical translations will be discussed.

Viability, Sublethal Injury, and Release of Cellular Components From Alicyclobacillus acidoterrestris Spores and Cells After the Application of Physical Treatments, Natural Extracts, or Their Components.

Alicyclobacillus acidoterrestris is a spoiling microorganism regarded as one of the most important causes of spoilage of fruit juices and acidic products. In this paper, four strains of A. acidoterrestris (type strain-DSM 3922; two wild strains isolated from soil-C8 and C24; wild strain isolated from a spoiled pear juice CB1) were treated through natural extracts/active compounds from essential oils (EOs), and physical treatments were used to assess their susceptibility and the presence of sublethal injury. The characterization of damage was also performed. The results suggest that it is possible to control A. acidoterrestris through alternative approaches, although the effect relied upon the age of spores. In addition to the mere antimicrobial effect, some treatments could cause a sublethal injury on spores. Lemon extract was the most effective treatment for both the antimicrobial effect and the sublethal injury, as evidenced by the release of proteins, and calcium dipicolinate [dipicolinic acid (DPA)] by fresh spores and only DPA (with an exception for C8) by old spores. A sublethal injury with protein release was also found for physical treatments [US (ultrasound) or heating]. For the first time, this paper reports on the existence of a sublethal injury for A. acidoterrestris, and this evidence could also be a challenge, because injured microorganisms could restore their metabolism, or an opportunity to design new preserving treatments.

Recent advances in engineering of microbial cell factories for intelligent pH regulation and tolerance.

pH regulation is a serious concern in the industrial fermentation process as pH adjustment heavily utilizes acid/base and pollutes the environment. Under pH-stress conditions, microbial growth and production of valuable target products may be severelyaffected. Furthermore, some strains generating acidic or alkaline products require self pH regulation and increased tolerance against pH-stress. For pH control, synthetic biology has provided advanced engineering approaches to construct robust and more intelligent microbial strains, exhibiting tolerance to pH-stress to cope with limitations of pH regulation. This study reviewed the current progress of advanced strain evolution strategies to engineer pH-stress tolerant strains via synthetic biology. In addition, a large number of pH-responsive elements, including promoters, riboswitches, and some proteins have been investigated and applied for construction of pH-responsive genetic circuits and intelligent pH-responsive microbial strains.

Non-Specific GH30_7 Endo-β-1,4-xylanase from Talaromyces leycettanus.

This study describes the catalytic properties of a GH30_7 xylanase produced by the fungus Talaromyces leycettanus. The enzyme is an ando-β-1,4-xylanase, showing similar specific activity towards glucuronoxylan, arabinoxylan, and rhodymenan (linear β-1,3-β-1,4-xylan). The heteroxylans are hydrolyzed to a mixture of linear as well as branched β-1,4-xylooligosaccharides that are shorter than the products generated by GH10 and GH11 xylanases. In the rhodymenan hydrolyzate, the linear β-1,4-xylooligosaccharides are accompanied with a series of mixed linkage homologues. Initial hydrolysis of glucuronoxylan resembles the action of other GH30_7 and GH30_8 glucuronoxylanases, resulting in a series of aldouronic acids of a general formula MeGlcA2Xyln. Due to the significant non-specific endoxylanase activity of the enzyme, these acidic products are further attacked in the unbranched regions, finally yielding MeGlcA2Xyl2-3. The accommodation of a substituted xylosyl residue in the −2 subsite also applies in arabinoxylan depolymerization. Moreover, the xylose residue may be arabinosylated at both positions 2 and 3, without negatively affecting the main chain cleavage. The catalytic properties of the enzyme, particularly the great tolerance of the side-chain substituents, make the enzyme attractive for biotechnological applications. The enzyme is also another example of extraordinarily great catalytic diversity among eukaryotic GH30_7 xylanases.

Evaluation of the in vitro cytotoxicity and modulation of the inflammatory response by the bioresorbable polymers poly(D,L-lactide-co-glycolide) and poly(L-lactide-co-glycolide)

Bioresorbable polymers composed of poly(D,L-lactide-co-glycolide) (PDLLGA) and poly(L-lactide-co-glycolide) (PLLGA) have become increasingly popular for the preparation of bone substitute constructs. However, there are reports of a delayed inflammatory reaction occurring months or years after implantation. Due to the long polymer degradation times, in vitro tests carried out at physiological temperature, 37°C, tend to assess only the short-term biocompatibility of these materials. The aim of this work is to develop an in vitro protocol that can be used to assess the long-term cytotoxicity of bioresorbable polymers in a time efficient manner. This study used a previously developed and validated accelerated degradation protocol to obtain samples of PDLLGA and PLLGA at increasing levels of degradation. Samples were then applied to standard ISO 10993-5 direct contact cytotoxicity testing and it was found that PDLLGA samples showed increasing levels of cytotoxicity at the later stages of degradation, with PLLGA samples demonstrating significantly less cytotoxic behaviour. Following concern that accumulation of acidic degradation products in a closed multi-well culture environment could overestimate cytotoxicity, we developed and validated a new dynamic flow culture methodology, for testing the cytotoxicity of these degradable materials, by adapting a commercial “organ on a chip” flow culture system, Quasi Vivo®. In addition to cytotoxicity testing, we have carried out profiling of inflammatory cytokines released by cells in response to degraded PDLLGA and PLLGA, and have suggested mechanism by which lactide-based bioresorbable materials could modulate the inflammatory response through the G-protein coupled receptor (GPCR), hydroxycarboxylic acid receptor 1 (HCA1). Statement of significanceBioresorbable materials naturally disintegrate over time when implanted into the body. They are often used to make screws and clips for repair of broken bones. Unfortunately, some patients can react badly to the material, resulting in painful inflammation. Biomaterials scientists are interested in developing materials that are more compatible with the body. However, it is very difficult to predict the long-term compatibility of bioresorbable materials in the lab. In our study, we have developed a method that will allow us to study the effects of the materials as they continue to break down. This will help us understand why the materials may cause inflammation, and will support research into the development of new and improved materials for bone repair.

A Brief Journey into the History of and Future Sources and Uses of Fatty Acids.

Fats and lipids have always had a primary role in the history of humankind, from ancient civilisations to the modern and contemporary time, going from domestic and cosmetic uses, to the first medical applications and later to the large-scale industrial uses for food, pharmaceutical, cosmetics, and biofuel production. Sources and uses of those have changed during time following the development of chemical sciences and industrial technological advances. Plants, fish, and animal fats have represented the primary source of lipids and fats for century. Nowadays, the use of fatty acid sources has taken a turn: industries are mainly interested in polyunsaturated fatty acids (PUFAs), which have beneficial properties in human health; and also, for high-value fatty acids product for innovative and green production of biofuel and feedstocks. Thus, the constant increase in demand of fatty acids, the fact that marine and vegetable sources are not adequate to meet the high level of fatty acids required worldwide and climate change, have determined the necessity of the search for renewable and sustainable sources for fatty acids. Biotechnological advances and bioengineering have started looking at the genetic modification of algae, bacteria, yeasts, seeds, and plants to develop cell factory able to produce high value fatty acid products in a renewable and sustainable manner. This innovative approach applied to FA industry is a peculiar example of how biotechnology can serve as a powerful mean to drive the production of high value fatty acid derivatives on the concept of circular bioeconomy, based on the reutilisation of organic resources for alternative and sustainable productive patterns that are environmentally friendly.

Agronomic performance of new strawberry cultivars in southern Brazil

The choice of cultivars to be used by strawberry farmers is essential since it could determine the success of the crop. The present study aimed to evaluate the productive and qualitative performance of strawberry genotypes grown in Vacaria, RS, Brazil. Twelve strawberry genotypes were compared, constituting the different treatments: cultivars Strawberry Festival, Oso Grande, Jonica, and Pircinque, and selections FRF PA3, FRF CE 51, FRF CE 56, FRF PIR 29, FRF PIR 54, FRF 85.04, FRF 149.18, and FRF 102.21. The seedlings were transplanted on May 13, 2014, in a semi-hydroponic cultivation system, adopting a randomized block design with four blocks and an experimental unit of ten useful plants. The variables evaluated were the number of fruits, total production per plant, productivity, commercial productivity, fresh fruit mass, commercial percentage, soluble solids, titratable acidity, soluble solids to total acidity ratio, pulp firmness, and production seasonality. The mean values ​​were subjected to an analysis of variance and multivariate analysis, and their means were compared by the Scott-Knott test at a 5% error probability. Cultivar Strawberry Festival and selection FRF 102.21 showed higher productions (1138 g plant-1 nd 1019 g plant-1, respectively) and quantities of fruits produced (85 un plant-1 and 87 un plant-1, respectively). Cultivar Jonica and selection FRF 85.4 showed higher percentages of marketable fruits. The Pircinque cultivar was prominent for sugar content, presenting a value 24% superior to the general average of the cultivars. Cultivars Strawberry Festival, Jonica, and Pircinque and selection FRF 102.21 showed the highest qualitative and quantitative gains for the region of Vacaria, RS, Brazil.

Synthesis and Characterization of Biodegradable Polyester/Polyether WPU as the Environmental Protection Coating

Polyester diol PCL and PBA, polyether diol PTMG and polycarbonate diol PCDL were used as components of WPU soft segment, respectively. Polyether PTMG-WPU has the worst hydrolytic property and the highest thermal stability. The maximum degradation rate temperature Tmax is 407.8 °C, the water contact angle reaches 89.5 °. Traditional polyester PCL-WPU shows the strongest hydrolysis performance, the smallest water contact angle, only 71.7 °, the water absorption rate of 72 h at room temperature is as high as 26.7%. However, the thermal stability of PCL-WPU is lower, the soft segment Tg is −52.3 °C, and Tmax is only 333.7 °C, but the mechanical property of which is the best, the tensile strength is 58.3 MPa, and the elongation at break reaches 857.9%. The most important thing is that the structure of polyester PCL-WPU is more easily destroyed by lipase and water molecules. The acidic products produced after hydrolysis will further promote the degradation of polyester. Therefore, compared with other WPUs, PCL-WPU has the best biodegradability and the most obvious degradation effect under the same conditions. The degradation rate of PTMG-WPU after 30 days of degradation in 0.6% lipase PBS buffer solution and soil was only 4.2% and 2.3%, while the highest degradation rate of traditional polyester PCL-WPU reached 41.7% and 32.0%, respectively. In addition, polycarbonate PCDL-WPU has the highest hardness, reaching 95.5 HD. But its other performances are lower than PCL-WPU.

The Effect of Pollutant Gases on Surfactant Migration in Acrylic Emulsion Films: A Comparative Study and Preliminary Evaluation of Surface Cleaning.

From their first employment in the 1950s, acrylic emulsions have remained widely used as art material today. Although under certain deteriorating conditions they are very stable, if exposed to high humidity and atmospheric pollutant gases, their structural and chemical conformation is strongly affected. Dealing with the resulting surfactant migration, various cleaning treatments were considered over the years. However, their choice remains difficult as they easily alter the acrylic component, especially if in contact with aqueous solutions. The present study focuses on investigating the stability of acrylic emulsion films exposed to accelerated aging by various pollutant gases. Firstly, a comparative analytical study was carried out in order to morphologically (by 3D optical and Atomic Force Microscopy) and chemically (by Raman and Infrared spectroscopy) characterize the reactions and degradation products. Subsequently, two water-based cleaning treatments were tested, and a preliminary evaluation of their cleaning effectiveness was performed. The results show that the reaction of atmospheric gas pollutants with water molecules in moisture leads to acidic reaction products that attack the acrylic matrix and favor the migration of the surfactant to the surface. The effectiveness of cleaning treatments depends on the aging conditions applied, which further lead to different surface morphological changes.

Lithium recovery from hydraulic fracturing flowback and produced water using a selective ion exchange sorbent

Increased demand for lithium products for use in lithium-ion batteries has led to a search for new lithium resources in recent years to meet projected future consumption. One potential lithium resource is low lithium bearing brines that are discharged from hydraulically fractured oil and gas wells as flowback and produced water (FPW). In this way, hydraulic fracturing presents an opportunity to turn what is normally considered wastewater into a lithium resource. In this research, two manganese-based lithium-selective adsorbents were prepared using a co-precipitation method and were employed for lithium recovery from FPW. At optimized conditions, lithium uptake reached 18 mg g−1, with a > 80% lithium recovery within 30 min. The recovered lithium was isolated and concentrated to 15 mM in an acidic final product. The degree of sorbent loss during acid desorption of lithium was significantly higher for sorbents used in the FPW as compared to recovery from a synthetic lithium-bearing brine (4.5% versus 0.8%). Thus, we propose that organic molecules present in the FPW reduce manganese in the sorbent structure during lithium sorption, leading to increased sorbent loss through reductive dissolution. Systematic characterization including wet chemical manganese valence measurements, along with EXAFS, XPS, and TEM-EELS show that exposure to FPW causes tetravalent manganese in the bulk sorbent structure to be reduced during lithium sorption, which subsequently dissolves during acid desorption. Partial removal of these organic molecules by nanofiltration leads to decreased sorbent dissolution in acid. In this way, we show that dissolved organic molecules represent a critical control on the reductive dissolution of manganese-based lithium ion exchange sorbents. This research provides promising results on the use of manganese-based lithium sorbents in FPW.

CO2 electrolysis to multicarbon products in strong acid.

Carbon dioxide electroreduction (CO2R) is being actively studied as a promising route to convert carbon emissions to valuable chemicals and fuels. However, the fraction of input CO2 that is productively reduced has typically been very low, <2% for multicarbon products; the balance reacts with hydroxide to form carbonate in both alkaline and neutral reactors. Acidic electrolytes would overcome this limitation, but hydrogen evolution has hitherto dominated under those conditions. We report that concentrating potassium cations in the vicinity of electrochemically active sites accelerates CO2 activation to enable efficient CO2R in acid. We achieve CO2R on copper at pH <1 with a single-pass CO2 utilization of 77%, including a conversion efficiency of 50% toward multicarbon products (ethylene, ethanol, and 1-propanol) at a current density of 1.2 amperes per square centimeter and a full-cell voltage of 4.2 volts.

Tunable fluorescent and antimicrobial properties of poly(vinyl amine) affected by the acidic or basic hydrolysis of poly(N‐vinylformamide)

AbstractSynthesis of poly(N‐vinylformamide) (PNVF) and its subsequent hydrolysis to convert it to poly(vinyl amine) (PVAm) were performed. Kinetics of acidic and basic hydrolysis of poly(N‐vinylformamide) (PNVF), and products of hydrolysis were investigated by using Fourier transform infrared, size exclusion chromatography, 1H NMR, and 13C NMR spectroscopies, and thermogravimetric analysis. It was observed that amide groups did not completely transform into amine groups by acidic hydrolysis of PNVF while the conversion of amides into amine groups via basic hydrolysis of PNVF was complete in 12 h, as confirmed by spectroscopic measurements. Results of extensive characterization revealed significant structural and conformational differences between acidic and basic hydrolysis products. Fluorescence spectroscopy was used for the first time to follow the conversion of amide groups into amine groups. The fluorescence intensity of PVAm obtained from basic hydrolysis of PVNF showed significant increase with amide/amine conversion. Finally, PVAm obtained from acidic hydrolysis of PNVF demonstrated potent antimicrobial activity, 10–20 times more, against common pathogens for example, C. albicans as fungal strain and E. coli, S. aureus, B. subtilis, and P. aeruginosa as bacterial strains as compared to PVAm obtained from basic hydrolysis.

Formulation of topical acidic products and acidification of the skin - Contribution of glycolic acid.

The acidic skin pH is one of the regulating factors of skin barrier homeostasis. Topical products as extrinsic factors which influence skin pH could be used for acidification of the skin and consequent beneficial effect. To formulate stabile and safe topical emulsion product with low pH is on-going challenge and areas interesting to explore are related to the effect of acidic products on the skin pH together with development of protocols for these studies. Aim of our work was to investigate formulations of acidic topical products with glycolic acid (GA) stabilized with long chain alkyl polyglucoside emulsifier, in regard to the specific colloidal structure of the vehicle, together with effect of products with different concentration of acidic active on skin pH. Investigated formulations were basic vehicle and two creams with glycolic acid (concentration 2 and 10 wt%). Microstructure was investigated by polarization microscopy, Raman spectral imaging, thermal analysis and rheological measurements. Effects on the skin were assessed by measurement of biophysical skin parameters in vivo studies (5-hour, 24-hour and 7-days). In vitro screening of antimicrobial activity was performed against bacteria Staphylococcus epidermidis. Polarization micrographs and Raman images have shown that GA does not disturb the specific colloidal structure. Together with rheological and thermal analysis obtained results have shown that GA in higher concentrations contributes to vehicles' lamellar structure. In 5-hour study the mean values of skin pH ranged from 3.98-4.25 and 3.89-4.10 after application of products with smaller and higher GA concentration. GA samples lowered skin surface pH to 5 and less in 24-hour and 7-day study, with stronger effect of sample with more GA. Sample with 10% of GA had significant inhibitory effect on growth of S. epidermidis in 1:1 concentration. Investigated APG emulsifier could be used as a stabilizer for acidic topical products with GA which are characterized by satisfactory safety profile. Topical products induce acidification of the skin after short- and long-term application without barrier impairment or sign of irritation. Acidification of the skin depends on presence of ingredients which are proton donors and their concentrations.

A High-Resolution Microfluidic LAPS Imaging System for 3D Cell Metabolism Monitoring

A High-Resolution Microfluidic LAPS Imaging System for 3D Cell Metabolism Monitoring

Evaluation of acidogenesis products\u2019 effect on biogas production performed with metagenomics and isotopic approaches

BackgroundDuring the acetogenic step of anaerobic digestion, the products of acidogenesis are oxidized to substrates for methanogenesis: hydrogen, carbon dioxide and acetate. Acetogenesis and methanogenesis are highly interconnected processes due to the syntrophic associations between acetogenic bacteria and hydrogenotrophic methanogens, allowing the whole process to become thermodynamically favorable. The aim of this study is to determine the influence of the dominant acidic products on the metabolic pathways of methane formation and to find a core microbiome and substrate-specific species in a mixed biogas-producing system.ResultsFour methane-producing microbial communities were fed with artificial media having one dominant component, respectively, lactate, butyrate, propionate and acetate, for 896 days in 3.5-L Up-flow Anaerobic Sludge Blanket (UASB) bioreactors. All the microbial communities showed moderately different methane production and utilization of the substrates. Analyses of stable carbon isotope composition of the fermentation gas and the substrates showed differences in average values of δ13C(CH4) and δ13C(CO2) revealing that acetate and lactate strongly favored the acetotrophic pathway, while butyrate and propionate favored the hydrogenotrophic pathway of methane formation. Genome-centric metagenomic analysis recovered 234 Metagenome Assembled Genomes (MAGs), including 31 archaeal and 203 bacterial species, mostly unknown and uncultivable. MAGs accounted for 54%–67% of the entire microbial community (depending on the bioreactor) and evidenced that the microbiome is extremely complex in terms of the number of species. The core microbiome was composed of Methanothrix soehngenii (the most abundant), Methanoculleus sp., unknown Bacteroidales and Spirochaetaceae. Relative abundance analysis of all the samples revealed microbes having substrate preferences. Substrate-specific species were mostly unknown and not predominant in the microbial communities.ConclusionsIn this experimental system, the dominant fermentation products subjected to methanogenesis moderately modified the final effect of bioreactor performance. At the molecular level, a different contribution of acetotrophic and hydrogenotrophic pathways for methane production, a very high level of new species recovered, and a moderate variability in microbial composition depending on substrate availability were evidenced. Propionate was not a factor ceasing methane production. All these findings are relevant because lactate, acetate, propionate and butyrate are the universal products of acidogenesis, regardless of feedstock.

Photopolymerizable precursors for degradable biomaterials based on acetal moieties

In tissue engineering (TE), artificial biomaterials have emerged over the past decade as an alternative to autotransplants. The main characteristics of these materials include good biocompatibility as well as biodegradability. Up to now, most materials used in TE are based on polyesters, which are limited in their scope of application, especially as scaffolds, due to their undesirably slow degradation behavior under acidic conditions present, e.g. during the process of hydroxyapatite resorption during bone regeneration. Furthermore, the formation of acidic degradation products can lead to tissue inflammation or even necrosis. Therefore, alternatives to ester functionalities, which show enhanced degradability under acidic conditions, are of interest. Herein, we present the synthesis of linear and cyclic acetal-based monomers for photopolymerizable materials. The reactivity and mechanical properties of polymer networks derived from these monomers were investigated. Moreover, their degradation behavior compared to ester-based polymer networks was explored. Degradation studies of the model compounds showed that the synthesized acetals degrade 80 to 200 times faster than their ester counterparts. A subsequent in vitro degradation study of polymer networks based on these compounds confirmed the potential of acetals moieties in polymeric biomaterials for bone regeneration.

MgO-incorporated porous nanofibrous scaffold promotes osteogenic differentiation of pre-osteoblasts

A feasible approach to fabricate porous nanofibrous scaffolds structurally similar to native extracellular matrix was reported. Magnesium oxide (MgO) nanoparticles were incorporated into electrospun poly(lactic acid) (PLA)/gelatin membranes, which were processed into short fibers and reconstructed to three-dimensional scaffolds. The scaffold exhibited sponge-like appearance with interconnected pores ranging from 50 to 200 µm and was highly elastic. MgO nanoparticles hydrolyzed and alleviated the acidic degradation products of PLA/gelatin scaffold. Released magnesium ions were beneficial to pre-osteoblasts by promoting proliferation and by upregulating osteogenic differentiation, indicating that the scaffold might find opportunities for bone grafting materials.

Tyrosol Derived Poly(ester-arylate)s for Sustained Drug Delivery from Microparticles

New biodegradable polymers are needed for use in drug delivery systems to overcome the high burst release, lack of sustained drug release, and acidic degradation products frequently observed in current formulations. Commercially available poly(lactide-co-glycolide) (PLGA) is often used for particle drug release formulations; however, it is often limited by its large burst release and acidic degradation products. Therefore, a biocompatible and biodegradable tyrosol-derived poly(ester-arylate) library has been used to prepare a microparticle drug delivery system which shows sustained delivery of hydrophobic drugs. Studies were performed using polymers with varying hydrophilicity and thermal properties and compared to PLGA. Various drug solubilizing cosolvents were used to load model drugs curcumin, dexamethasone, nicotinamide, and acyclovir. Hydrophobic drugs curcumin and dexamethasone were successfully loaded up to 50 weight percent (wt %), and a linear correlation between drug wt % loaded and the particle glass transition temperature (Tg) was observed. Both curcumin and dexamethasone were visible on the particle surface at 20 wt % loading and higher. By adjusting the polymer concentration during particle formation, release rates were able to be controlled. Release studies of dexamethasone loaded particles with a lower polymer concentration showed a biphasic release profile and complete release after 47 days. Particles prepared using a higher polymer concentration showed sustained release for up to 77 days. Comparably, PLGA showed a traditional triphasic release profile and complete release after 63 days. This novel tyrosol-derived poly(ester-arylate) library can be used to develop injectable, long-term release formulations capable of providing sustained drug delivery.

Hydrolytic degradation of tri-iso-amyl phosphate-dodecane system

A solution of 1.1 M tri-iso-amyl phosphate (TiAP) in n-dodecane (n-DD) has been proposed as a candidate solvent for reprocessing of spent nuclear fuel arising from fast reactors. Significant amounts of radioruthenium are produced as a fission product in fast reactors. To minimize the extraction of radioruthenium during the separation of uranium and plutonium, it was proposed to carry out the solvent extraction process at nitric acid concentration ranging from 4 to 5 M. Under these process conditions, it is quite likely that the solvent phase can undergo hydrolytic degradation, which can cause significant changes in the physicochemical properties of the solvent phase and hamper the recovery of uranium and plutonium. In view of this, the hydrolytic degradation of 1.1 M TiAP/n-DD was studied as a function of nitric acid concentration, duration of degradation and process temperature. The physicochemical properties of the hydrolytically degraded organic phase such as density, viscosity, interfacial tension, phase disengagement time was studied and compared with those obtained for thermally degraded solvent (in the absence of nitric acid) and neat solvent phase. The degree of damage was assessed by the uranium retention test in the hydrolytically degraded solvent phase and the procedure for the removal of degradation products from the organic phase was reported. The results revealed that hydrolytic degradation resulted in the formation of acidic degradation products of both TiAP and n-DD. While most of the acidic degradation products arising from TiAP appears to be washable by sodium carbonate during clean-up, a small amount of hydrocarbon degradation products, e.g. nitrolic acid, sparingly soluble in sodium carbonate seems to retain uranium in organic phase during recovery. The formation of nitration degradation products was confirmed by FT-IR spectroscopy. The recovery of uranium was more that 95% after the clean-up of degraded solvent.

Effect of acidic products from degradation of N-methyldiethanolamine amine on CO2/H2S capturing from natural gas

Effect of acidic products from degradation of N-methyldiethanolamine amine on CO2/H2S capturing from natural gas