Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0007
A. Wiecek
Abstract This review paper focused on the effect of typical phosphorlipid (or lecithin) and enzyme modification on electrokinetic parameters of oil/water emulsion. Physicochemical properties of the systems were investigated taking into account the effective diameter of the droplets as well as the zeta potentials using the dynamic light scattering technique. The effect of phospholipid and phospholipase modification on interfacial properties of o/w emulsion was examined as a function of temperature, pH and ionic strength (effect of Na+ or Ca2+ ions which occur in the physiological fluids). The particular role of Ca2+ ions in the dispersions with zwitterionic phospholipids (the main components of biological membrane) was confirmed. The phospholipids dipalmitoylphosphatidylcholine, DPPC or dioleoylphosphatidylcholine, DOPC having the same headgroup bound to the apolar tail composed of two saturated or unsaturated chains were used as stabilizing agents. The effective diameters do not always correlate with the zeta potentials. A possible reason for such behaviour might a mechanism different from the electrostatic stabilization. Phospholipids and their mixtures (e.g. lecithin) may undergo spontaneous aggregation in aqueous solution and organize into liposomes, which possess different sizes and surface affinities. These unique behaviours of phospholipid dispersion can be controlled using the investigated parameters. These findings are expected to increase in importance as phospholipid systems see more use in self-assembly applications. The other aim of the paper was the comparison of the enzyme phospholipase influence on lipid hydrolysis in the o/w emulsion environment. The work is the study which presents the twofold effect of ethanol dipoles on phosholipid hydrolysis. It is believed that the enzyme effect on the phospholipid aggregation behaviour at the oil-water interface will be helpful for understanding different biological phenomena.
{"title":"Effect of phospholipid and (phospho)lipase modification on interfacial properties of oil/water emulsion","authors":"A. Wiecek","doi":"10.1515/umcschem-2015-0007","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0007","url":null,"abstract":"Abstract This review paper focused on the effect of typical phosphorlipid (or lecithin) and enzyme modification on electrokinetic parameters of oil/water emulsion. Physicochemical properties of the systems were investigated taking into account the effective diameter of the droplets as well as the zeta potentials using the dynamic light scattering technique. The effect of phospholipid and phospholipase modification on interfacial properties of o/w emulsion was examined as a function of temperature, pH and ionic strength (effect of Na+ or Ca2+ ions which occur in the physiological fluids). The particular role of Ca2+ ions in the dispersions with zwitterionic phospholipids (the main components of biological membrane) was confirmed. The phospholipids dipalmitoylphosphatidylcholine, DPPC or dioleoylphosphatidylcholine, DOPC having the same headgroup bound to the apolar tail composed of two saturated or unsaturated chains were used as stabilizing agents. The effective diameters do not always correlate with the zeta potentials. A possible reason for such behaviour might a mechanism different from the electrostatic stabilization. Phospholipids and their mixtures (e.g. lecithin) may undergo spontaneous aggregation in aqueous solution and organize into liposomes, which possess different sizes and surface affinities. These unique behaviours of phospholipid dispersion can be controlled using the investigated parameters. These findings are expected to increase in importance as phospholipid systems see more use in self-assembly applications. The other aim of the paper was the comparison of the enzyme phospholipase influence on lipid hydrolysis in the o/w emulsion environment. The work is the study which presents the twofold effect of ethanol dipoles on phosholipid hydrolysis. It is believed that the enzyme effect on the phospholipid aggregation behaviour at the oil-water interface will be helpful for understanding different biological phenomena.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"6 1","pages":"109 - 79"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76716571","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0008
Katarzyna Szymczyka, Anna Tarabab
Abstract Activity coefficients at infinite dilution of the aqueous solutions of nonionic hydrocarbon surfactants, p-(1,1,3,3- tetramethylbutyl) phenoxypoly(ethylene glycols), Triton X-100 (TX100) and Triton X-165 (TX165), fluorocarbon surfactants, Zonyl FSN-100 (FSN100) and Zonyl FSO-100 (FSO100) and their ternary mixtures were determined from the Gracia-Fadrique et al. method for non-volatile compounds. The values of activity coefficients were calculated taking into account the surface tension data of the studied systems at 293K and compared to those determined on the basis of the values of the contact angle of solutions on the polytetrafluoroethylene (PTFE) and polymethyl methacrylate (PMMA) surfaces and the solid-liquid interface tension.
{"title":"Activity coefficient at infinite dilution of aqueous solutions of nonionic hydrocarbon and fluorocarbon surfactants as well as their ternary mixtures","authors":"Katarzyna Szymczyka, Anna Tarabab","doi":"10.1515/umcschem-2015-0008","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0008","url":null,"abstract":"Abstract Activity coefficients at infinite dilution of the aqueous solutions of nonionic hydrocarbon surfactants, p-(1,1,3,3- tetramethylbutyl) phenoxypoly(ethylene glycols), Triton X-100 (TX100) and Triton X-165 (TX165), fluorocarbon surfactants, Zonyl FSN-100 (FSN100) and Zonyl FSO-100 (FSO100) and their ternary mixtures were determined from the Gracia-Fadrique et al. method for non-volatile compounds. The values of activity coefficients were calculated taking into account the surface tension data of the studied systems at 293K and compared to those determined on the basis of the values of the contact angle of solutions on the polytetrafluoroethylene (PTFE) and polymethyl methacrylate (PMMA) surfaces and the solid-liquid interface tension.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"251 1","pages":"111 - 124"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89177428","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0003
E. Hallmann, K. Mędrzycka
Abstract Wetting properties of synthetic surfactant Rokanol NL6, biosurfactant JBR 425 and their mixture have been investigated. On the basis of these investigations, the ability of used surfactants to remove the synthetic base oil (PAO6) from sandy soil and clay loam was evaluated. Surfactant solutions were applied for soil flushing in batch experiments. The results show that synthetic surfactant addition worsens physicochemical properties of pure biosurfactant but exhibits much higher oil removal efficiency than biosurfactant does.
{"title":"Wetting properties of biosurfactant (rhamnolipid) with synthetic surfactants mixtures in the context of soil remediation","authors":"E. Hallmann, K. Mędrzycka","doi":"10.1515/umcschem-2015-0003","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0003","url":null,"abstract":"Abstract Wetting properties of synthetic surfactant Rokanol NL6, biosurfactant JBR 425 and their mixture have been investigated. On the basis of these investigations, the ability of used surfactants to remove the synthetic base oil (PAO6) from sandy soil and clay loam was evaluated. Surfactant solutions were applied for soil flushing in batch experiments. The results show that synthetic surfactant addition worsens physicochemical properties of pure biosurfactant but exhibits much higher oil removal efficiency than biosurfactant does.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"38 1","pages":"29 - 39"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74989413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0010
J. Krawczyk
Abstract Wettability of poly(tetrafluoroethylene) (PTFE) by aqueous solutions of binary mixtures composed of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) with polyoxyethylene (23) lauryl ether (Brij 35) was considered on the basis of the measured values of contact angle and surface tension. It was shown that the value of the critical surface tension of PTFE surface wetting at the studied system (23.5 mN/m), does not depend on the concentration and composition of the binary mixtures of studied surfactants in water, and it was higer than the surface tension of PTFE (20.2 mN/m). The best wettability of polytetrafluoroethylene (PTFE) by studied aqueous solutions of binary surfactants mixtures occurs at the mixtures concentration corresponding to the critical micelle concentration of their solutions.
{"title":"Wetting properties of the sodium bis(2-ethylhexyl) sulfosuccinate (AOT) and polyoxyethylene (23) lauryl ether (Brij 35) binary mixtures in the poly(tetrafluoroethylene)-solution-air system","authors":"J. Krawczyk","doi":"10.1515/umcschem-2015-0010","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0010","url":null,"abstract":"Abstract Wettability of poly(tetrafluoroethylene) (PTFE) by aqueous solutions of binary mixtures composed of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) with polyoxyethylene (23) lauryl ether (Brij 35) was considered on the basis of the measured values of contact angle and surface tension. It was shown that the value of the critical surface tension of PTFE surface wetting at the studied system (23.5 mN/m), does not depend on the concentration and composition of the binary mixtures of studied surfactants in water, and it was higer than the surface tension of PTFE (20.2 mN/m). The best wettability of polytetrafluoroethylene (PTFE) by studied aqueous solutions of binary surfactants mixtures occurs at the mixtures concentration corresponding to the critical micelle concentration of their solutions.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"35 1","pages":"137 - 148"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74521556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0004
A. Kozak, Z. Sadowski
Abstract Two kinds of Pluronics (PEO-PPO-PEO triblock copolymers) were used in these studies. They have mixed with anionic surfactant (sodium oleate). The adsorption isotherms of surfactant and copolymer-surfactant mixture onto dolomite have been determined. The adsorbed amount of the Pluronics increases with increasing concentration and reaches plateau. An increase of adsorbed amounts of anionic surfactant onto the mineral surfaces (dolomite) has been observed at the presence of Pluronic copolymers. The adsorption effect of triblock copolymers has been investigated on the zeta potential of dolomite at the water suspension. The interaction of anionic surfactant with copolymers causes a decrease of zeta potential to small amount due to the deformation of double electrical layer. The adsorbed non-ionic Pluronic layer partially screens the surface charge of mineral particles, and thus, reduces the zeta potential. On the other hand, the adsorption of anionic surfactant and copolymer caused a decrease of negative value of zeta potential both investigated minerals. The stability of dolomite suspension depends on the both copolymer and sodium oleate concentrations.
{"title":"Effect of Pluronics and surfactant adsorption onto dolomite suspension zeta potential and stability","authors":"A. Kozak, Z. Sadowski","doi":"10.1515/umcschem-2015-0004","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0004","url":null,"abstract":"Abstract Two kinds of Pluronics (PEO-PPO-PEO triblock copolymers) were used in these studies. They have mixed with anionic surfactant (sodium oleate). The adsorption isotherms of surfactant and copolymer-surfactant mixture onto dolomite have been determined. The adsorbed amount of the Pluronics increases with increasing concentration and reaches plateau. An increase of adsorbed amounts of anionic surfactant onto the mineral surfaces (dolomite) has been observed at the presence of Pluronic copolymers. The adsorption effect of triblock copolymers has been investigated on the zeta potential of dolomite at the water suspension. The interaction of anionic surfactant with copolymers causes a decrease of zeta potential to small amount due to the deformation of double electrical layer. The adsorbed non-ionic Pluronic layer partially screens the surface charge of mineral particles, and thus, reduces the zeta potential. On the other hand, the adsorption of anionic surfactant and copolymer caused a decrease of negative value of zeta potential both investigated minerals. The stability of dolomite suspension depends on the both copolymer and sodium oleate concentrations.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"22 1","pages":"41 - 53"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83483416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0011
Magdalena Bielawska, A. Zdziennicka
Abstract On the basis of the surface tension ( γLV) data of the aqueous solutions of p-(1,1,3,3-tetramethylbutyl)phenoxypoly(ethylene glycol) (Triton X-100 or TX-100) and cetyltrimethylammonium bromide (CTAB) mixture with ethanol published in our previous paper, the process of ethanol adsorption was investigated. For that reason, the values of Gibbs surface excess concentration of ethanol at the solution-air interface and Gibbs standard free energy of its adsorption at that interface were calculated and compared with those determined for the aqueous solutions of ethanol. The surface excess concentration of ethanol at the solution-air interface was calculated with two different methods. The standard free energy of alcohol adsorption was determined from both the Gu and Zhu and Langmuir equations.
{"title":"Ethanol behaviour at the solution-air interface in the presence of Triton X-100 and cetyltrimethylammonium bromide mixture","authors":"Magdalena Bielawska, A. Zdziennicka","doi":"10.1515/umcschem-2015-0011","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0011","url":null,"abstract":"Abstract On the basis of the surface tension ( γLV) data of the aqueous solutions of p-(1,1,3,3-tetramethylbutyl)phenoxypoly(ethylene glycol) (Triton X-100 or TX-100) and cetyltrimethylammonium bromide (CTAB) mixture with ethanol published in our previous paper, the process of ethanol adsorption was investigated. For that reason, the values of Gibbs surface excess concentration of ethanol at the solution-air interface and Gibbs standard free energy of its adsorption at that interface were calculated and compared with those determined for the aqueous solutions of ethanol. The surface excess concentration of ethanol at the solution-air interface was calculated with two different methods. The standard free energy of alcohol adsorption was determined from both the Gu and Zhu and Langmuir equations.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"1 1","pages":"149 - 159"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89827840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0012
D. Mańko, A. Zdziennicka
Abstract From year to year natural surfactants are gaining ever growing awareness because of their valuable properties (in the absence of negative impact on the environment, as with the use of synthetic surface active agents). In the group of surfactants of natural origin there are surface active agents produced by microorganisms (biosurfactants) or compounds having a natural part (hydrophilic head and/or hydrophobic tail) [1]. This review includes the short characteristic of surfactants with sugar-head group in their structure called sugar-based surfactants. The structure, properties and some applications of these surfactants are described in this paper.
{"title":"Sugar-based surfactants as alternative to synthetic ones","authors":"D. Mańko, A. Zdziennicka","doi":"10.1515/umcschem-2015-0012","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0012","url":null,"abstract":"Abstract From year to year natural surfactants are gaining ever growing awareness because of their valuable properties (in the absence of negative impact on the environment, as with the use of synthetic surface active agents). In the group of surfactants of natural origin there are surface active agents produced by microorganisms (biosurfactants) or compounds having a natural part (hydrophilic head and/or hydrophobic tail) [1]. This review includes the short characteristic of surfactants with sugar-head group in their structure called sugar-based surfactants. The structure, properties and some applications of these surfactants are described in this paper.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"21 1","pages":"161 - 168"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77183733","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0006
D. Rymuszka, K. Terpiłowski, L. Hołysz, E. Chibowski
{"title":"Changes in surface properties of polymethylmethacrylate (PMMA) treated with air plasma","authors":"D. Rymuszka, K. Terpiłowski, L. Hołysz, E. Chibowski","doi":"10.1515/umcschem-2015-0006","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0006","url":null,"abstract":"","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"19 1","pages":"65 - 78"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85409494","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0002
J. Zawała, Piotr Zawała, K. Małysa
Abstract The kinetics of collision and bouncing of an air bubble on hydrophilic and hydrophobic solid surfaces immersed in distilled water is reported. We carried out the experiments and compared the bubble collision and bouncing courses on the stagnant and vibrating, with a controlled frequency and amplitude, solid/liquid interface. For stagnant interface differences in the outcome of the bubble collisions with hydrophilic and hydrophobic solid surfaces are resulting from different stability of the intervening liquid film formed between the colliding bubble and these surfaces. The liquid film was unstable at Teflon surface, where the three-phase contact (TPC) and the bubble attachment were observed, after dissipation of most of the kinetic energy associated with the bubble motion. For vibrated solid surface it was shown that kinetics of the bubble bouncing is independent on the hydrophilic/hydrophobic properties of the surface. Similarly like at water/glass hydrophilic interface, even at highly hydrophobic Teflon surface time of the bubble collisions and bouncing was prolonged almost indefinitely. This was due to the fact that the energy dissipated during the collision was re-supplied via interface vibrations with a properly adjusted acceleration. The analysis of the bubble deformation degree showed that this effect is related to a constant bubble deformation, which determined constant radius of the liquid film, large enough to prevent the draining liquid film from reaching the critical thickness of rupture at the moment of collision. The results obtained prove that mechanism of the bubble bouncing from various interfaces depends on interrelation between rates of two simultaneously going processes: (i) exchange between kinetic and surface energies of the system and (ii) drainage of the liquid film separating the interacting interfaces.
{"title":"On mechanism of the bubble bouncing from hydrophilic and hydrophobic solid surfaces","authors":"J. Zawała, Piotr Zawała, K. Małysa","doi":"10.1515/umcschem-2015-0002","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0002","url":null,"abstract":"Abstract The kinetics of collision and bouncing of an air bubble on hydrophilic and hydrophobic solid surfaces immersed in distilled water is reported. We carried out the experiments and compared the bubble collision and bouncing courses on the stagnant and vibrating, with a controlled frequency and amplitude, solid/liquid interface. For stagnant interface differences in the outcome of the bubble collisions with hydrophilic and hydrophobic solid surfaces are resulting from different stability of the intervening liquid film formed between the colliding bubble and these surfaces. The liquid film was unstable at Teflon surface, where the three-phase contact (TPC) and the bubble attachment were observed, after dissipation of most of the kinetic energy associated with the bubble motion. For vibrated solid surface it was shown that kinetics of the bubble bouncing is independent on the hydrophilic/hydrophobic properties of the surface. Similarly like at water/glass hydrophilic interface, even at highly hydrophobic Teflon surface time of the bubble collisions and bouncing was prolonged almost indefinitely. This was due to the fact that the energy dissipated during the collision was re-supplied via interface vibrations with a properly adjusted acceleration. The analysis of the bubble deformation degree showed that this effect is related to a constant bubble deformation, which determined constant radius of the liquid film, large enough to prevent the draining liquid film from reaching the critical thickness of rupture at the moment of collision. The results obtained prove that mechanism of the bubble bouncing from various interfaces depends on interrelation between rates of two simultaneously going processes: (i) exchange between kinetic and surface energies of the system and (ii) drainage of the liquid film separating the interacting interfaces.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"28 1","pages":"15 - 27"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80653283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-06-01DOI: 10.1515/umcschem-2015-0005
M. Kosmulski
Abstract The volumes of reactions in solution are usually ignored in problem solving. Neglection of reaction volumes may lead to errors on the order of 1 % in the final result. Calculation of the volume of neutralization reaction based on the specific densities of solutions from chemical tables is demonstrated.
{"title":"Reaction volume in aqueous solutions in problem solving","authors":"M. Kosmulski","doi":"10.1515/umcschem-2015-0005","DOIUrl":"https://doi.org/10.1515/umcschem-2015-0005","url":null,"abstract":"Abstract The volumes of reactions in solution are usually ignored in problem solving. Neglection of reaction volumes may lead to errors on the order of 1 % in the final result. Calculation of the volume of neutralization reaction based on the specific densities of solutions from chemical tables is demonstrated.","PeriodicalId":7937,"journal":{"name":"Annales UMCS, Chemia","volume":"59 1","pages":"55 - 63"},"PeriodicalIF":0.0,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86184373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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