Deamination of n-octylamine in aqueous solution: the substitution/elimination ratio is not altered by a change of 108 in hydroxide ion concentration

1989 ◽  
Vol 54 (23) ◽  
pp. 5424-5426 ◽  
Author(s):  
Oscar D. Monera ◽  
Min Kun Chang ◽  
Gary E. Means
Keyword(s):  
Aqueous Solution ◽  
Ion Concentration ◽  
Hydroxide Ion

THE STABILITY OF SOME COMPLEXES OF TRIVALENT COPPER

1953 ◽  
Vol 31 (7) ◽  
pp. 638-652 ◽  
Author(s):  
M. W. Lister
Keyword(s):  
Aqueous Solution ◽  
Sodium Hypochlorite ◽  
Equilibrium Constants ◽  
Copper Ion ◽  
Ion Concentration ◽  
Hydroxide Ion ◽  
New Methods ◽  
Reversible Dissociation ◽  
The Stability ◽  
Complex Ion

New methods are given for the preparation of sodium copper (111) tellurate, Na9Cu(TeO6)2.16H2O, and sodium copper (111) periodate, Na7Cu(IO6)2.20H2O, previously reported by Malatesta. Additional analytical evidence is presented that these are really compounds of trivalent copper. The dissociation of the ions in alkaline aqueous solution was examined through the ability of the uncomplexed copper to catalyze the decomposition of sodium hypochlorite. Evidence is presented that the uncomplexed copper ion is Cu(OH)4−, and this gives both a 1-1 and a 1-2 complex with both tellurate and periodate. The 1-2 complexes appear to be Cu(HTeO6)2−7 and Cu(IO6)2−7 respectively; the 1-1 complexes are less stable. The equilibrium constants for the reversible dissociation of these ions into their simpler constituents in aqueous solution at 40 °C. are as follows: tellurate, 1-1 complex K1 = 1.8 × 10−6; 1-2 complex K2 = 1.1 × 10−11; periodate, 1-1 complex K1 = 3.4 × 10−5; 1-2 complex is K2 = 8.0 × 10−11. The smaller the constant the more stable the complex ion. In the case of the tellurate complex K2 is proportional to the square of the hydroxide ion concentration and these values are for 0.400 M sodium hydroxide; with periodate K2 is independent of the hydroxide concentration. Experiments at various temperatures give 20 kcal. as the heat of the reaction forming the 1-2 tellurate complex from the simple ions, and 71/2 kcal. for the 1-2 periodate complex. The stannate, stibnate, and selenate ions showed no signs of forming analogous compounds.

Residual phase lignin in haft cooking related to the conditions in the cook

1997 ◽  
Vol 12 (4) ◽  
pp. 225-229
Author(s):  
Cart-in A-S. Gustavsson ◽  
Chritofer T. Lindgren ◽  
Mikael E. Lindström
Keyword(s):  
Hydrogen Sulfide ◽  
Ionic Strength ◽  
Sodium Ion ◽  
Ion Concentration ◽  
Constant Composition ◽  
Hydroxide Ion ◽  
Sulfide Ion ◽  
Residual Phase ◽  
Kraft Cooking ◽  
Very High

Abstract The amount of lignin reacting according to the slow residual phase, i.e. the residual phase lignin, is in many perspectives an interesting issue. The purpose of the present investigation was to develop a mathematical model to show how the amount of residual phase lignin in the kraft cooking of spruce chips (Picm ahies) depends on the conditions in the earlier phases of the cook. The variables studied were hydroxide ion concentration, hydrogen sulfide ion concentration and ionic strength. The liquor-to-wood ratio during pulping was very high to maintain approximately constant chemical concentrations throughout each experiment (so called "constant composition" cooks). An increase in hydroxide ion concentration andtor hydrogen sulfide ion concentration leads to a decrease in the amount of residual phase lignin, while an increase in ionic strength, i.e. sodium ion concentration, leads to an increase. A signiticant result is that the hydrogen sulfide ion concentration has a pronounced influence on the amount of residual phase lignin during a cook at a low hydroxide ion concentration. The amount of residual phase lignin expressed as % lignin on wood, L,, can be described by the following equation developed for "constant composition" cooks (when cooking with a constant sodium ion concentration of 2 mol/L): LT=0,55-0.32*[HO-](-1,3)*ln[HS-] This equation is valid for a concentration of HO- in the range from 0.17 to 1.4, and a hydrogen sulfide ion concentration from 0.07 to 0.6 mol/L.

scholarly journals Ricinus CommunisPericarp Activated Carbon Used as an Adsorbent for the Removal of Ni(II) From Aqueous Solution

2008 ◽  
Vol 5 (4) ◽  
pp. 761-769 ◽  
Author(s):  
S. Madhavakrishnan ◽  
K. Manickavasagam ◽  
K. Rasappan ◽  
P. S. Syed Shabudeen ◽  
R. Venkatesh ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Particle Size ◽  
Activated Carbon ◽  
Contact Time ◽  
Metal Ion ◽  
Ricinus Communis ◽  
Ion Concentration ◽  
Batch Mode ◽  
Adsorption Data ◽  
Initial Ph

Activated carbon prepared from Ricinus communis Pericarp was used to remove Ni(II) from aqueous solution by adsorption. Batch mode adsorption experiments are carried out by varying contact time, metal-ion concentration, carbon concentration and pH to assess kinetic and equilibrium parameters. The adsorption data were modeled by using both Langmuir and Freundlich classical adsorption isotherms. The adsorption capacity (Qo) calculated from the Langmuir isotherm was 31.15 mg/g of activated carbon at initial pH of 5.0±0.2 for the particle size 125-250 µm.

scholarly journals OPTIMIZATION OF TIME REACTION AND HYDROXIDE ION CONCENTRATION ON FLAVONOID SYNTHESIS FROM BENZALDEHYDE AND ITS DERIVATIVES

2010 ◽  
Vol 5 (2) ◽  
pp. 163-168 ◽  
Author(s):  
Sri Handayani ◽  
Sunarto, Sunarto, ◽  
Susila Kristianingrum
Keyword(s):  
Reaction Time ◽  
Optimum Concentration ◽  
Ion Concentration ◽  
Optimum Time ◽  
Hydroxide Ion ◽  
Synthesis Time ◽  
Flavonoid Synthesis ◽  
Hydroxyl Ion ◽  
Optimum Reaction ◽  
Time Of Reaction

The aim of this research is to determine the optimum time of reaction and concentration of hydroxide ion on chalcone, 4-methoxychalcone and 3,4-dimethoxychalcone synthesis. Chalcone and its derivatives were synthesized by dissolving KOH in ethanol followed by dropwise addition of acetophenone and benzaldehyde. Then, the mixture was stirred for several hours. Three benzaldehydes has been used, i.e : benzaldehyde, p-anysaldehyde and veratraldehyde. The time of reaction was varied for, 12, 18, 24, 30 and 36 hours. Furthermore, on the optimum reaction time for each benzaldehyde the hydroxyl ion concentration was varied from 5,7,9,11 and 13%(w/v). The results of this research suggested that the optimum time of chalchone synthesis was 12 hours, while, 4-methoxychalcone and 3,4-dimethoxychalcone were 30 hours. The optimum concentration of hydroxide ion of chalcone synthesis was 13% and for 4-methoxychalcone and 3,4-dimethoxychalcone were 11%. Keywords: Chalcone synthesis, time of reaction, hydroxide ion concentration.

scholarly journals Adsorption of Mn2+ from Aqueous Solution Using Manganese Oxide-Coated Hollow Polymethylmethacrylate Microspheres (MHPM)

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Dhiraj Dutta ◽  
Jyoti Prasad Borah ◽  
Amrit Puzari
Keyword(s):  
Aqueous Solution ◽  
Manganese Oxide ◽  
Adsorption Capacity ◽  
High Surface ◽  
High Surface Area ◽  
Freundlich Isotherm ◽  
Ion Concentration ◽  
Isotherm Models ◽  
Maximum Adsorption Capacity ◽  
Coated Sand

Results of investigation on adsorption of Mn2+ from aqueous solution by manganese oxide-coated hollow polymethylmethacrylate microspheres (MHPM) are reported here. This is the first report on Mn-coated hollow polymer as a substitute for widely used materials like green sand or MN-coated sand. Hollow polymethylmethacrylate (HPM) was prepared by using a literature procedure. Manganese oxide (MnO) was coated on the surface of HPM (MHPM) by using the electroless plating technique. The HPM and MHPM were characterized by using optical microscopy (OM), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Optical and scanning micrographs were used to monitor the surface properties of the coated layer which revealed the presence of MnO on the surface of HPM. TGA showed the presence of 4-5% of MnO in MHPM. Adsorption isotherm studies were carried out as a function of pH, initial ion concentration, and contact time, to determine the adsorption efficiency for removal of Mn2+ from contaminated water by the synthesized MHPM. The isotherm results showed that the maximum adsorption capacity of MnO-coated HPM to remove manganese contaminants from water is 8.373 mg/g. The obtained R 2 values of Langmuir isotherm and Freundlich isotherm models were 1 and 0.87, respectively. Therefore, R 2 magnitude confirmed that the Langmuir model is best suited for Mn2+ adsorption by a monolayer of MHPM adsorbent. The material developed shows higher adsorption capacity even at a higher concentration of solute ions, which is not usually observed with similar materials of this kind. Overall findings indicate that MHPM is a very potential lightweight adsorbent for removal of Mn2+ from the aqueous solution because of its low density and high surface area.

scholarly journals Biosorption of Lead Ions from Aqueous Solution UsingFicus benghalensisL.

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Venkateswara Rao Surisetty ◽  
Janusz Kozinski ◽  
L. Rao Nageswara
Keyword(s):  
Aqueous Solution ◽  
Process Parameters ◽  
Contact Time ◽  
Batch Process ◽  
Ion Concentration ◽  
Lead Ions ◽  
Lead Ion ◽  
Maximum Adsorption Capacity ◽  
Ficus Benghalensis ◽  
Leaf Powder

Ficus benghalensisL., a plant-based material leaf powder, is used as an adsorbent for the removal of lead ions from aqueous solution using the biosorption technique. The effects of process parameters such as contact time, adsorbent size and dosage, initial lead ion concentration, and pH of the aqueous solution on bio-sorption of lead byFicus benghalensisL. were studied using batch process. The Langmuir isotherm was more suitable for biosorption followed by Freundlich and Temkin isotherms with a maximum adsorption capacity of 28.63 mg/g of lead ion on the biomass ofFicus benghalensisL. leaves.

scholarly journals Adsorption of Cr6+ Onto Unmodified and Hydrochloric Acid Modified African Nutmeg Pod (Monodora myristica) from Aqueous Solution

2019 ◽  
pp. 1-8
Author(s):  
F. U. Okwunodulu ◽  
H. O. Chukwuemeka-Okorie ◽  
N. M. Mgbemena ◽  
J. B. I. Kalu
Keyword(s):  
Aqueous Solution ◽  
Metal Ion ◽  
Correlation Coefficients ◽  
Freundlich Isotherm ◽  
Low Ph ◽  
Ion Concentration ◽  
Isotherm Models ◽  
Particle Sizes ◽  
Monodora Myristica ◽  
Best Fit

The removal of Cr6+ from aqueous solution using unmodified and hydrochloric modified African nutmeg pod was studied. The effects of particle size, pH and initial metal ions concentration adsorbed were investigated. The amount of metal ion adsorbed increased as the initial metal ion concentration increased and also decreased at low pH of 2 for both modified and unmodified African nutmeg pod.  400 µm and 250 µm were the optimum particle sizes for both modified and unmodified African nutmeg pod respectively, values given as 75.8 mg/g for the modified and 93.39 mg/g for the unmodified. Generally, it was observed that the unmodified African nutmeg pod showed greater adsorption capacity than the modified African nutmeg pod. The equilibrium experimental data were examined via Langmuir and Freundlich isotherm models.  Freundlich isotherm model gave the best fit for the data in both unmodified and modified African nutmeg pod based on the correlation coefficients (R2 values) gotten. The results of the study showed that the African nutmeg pod is efficient for the removal of Cr6+ from aqueous solutions especially when unmodified.

Removal of Pb(II) and Cd(II) From Aqueous Solution by Adsorption Using Agrowaste-Modified Kaolinite Clay

2021 ◽  
Keyword(s):  
Aqueous Solution ◽  
Aqueous Solutions ◽  
Metal Ions ◽  
Metal Ion ◽  
Low Cost ◽  
Ion Concentration ◽  
Kaolinite Clay ◽  
Adsorbent Surface ◽  
Initial Adsorption ◽  
Adsorption Rates

This study showed that kaolinite clay modified with Moringa oleifera pods is a promising low cost adsorbent for the removal of metals from aqueous solution because the resultant composite has higher adsorption capacities, and hence a better metal ions removal efficiency. The efficiencies of these adsorbents for the removal of Pb (II) and Cd (II) ions from aqueous solutions were studied as a function of pH, time, adsorbate concentration and adsorbent dose. Adsorption results showed that pH did significantly affect removal of heavy metal ions between pH 3 and 6. Increasing contact time and initial metal ion concentration increased the sorption capacity of the adsorbent for the metal ions. Adsorbent dosage indicated mainly surface phenomena involving sharing of electrons between the adsorbent surface and the metal ion species. The adsorption of metal ions from aqueous solutions of both metal ions at different initial metal ion concentrations reduced the initial adsorption rates of the adsorption of Pb (II) and Cd (II) by unmodified and modified kaolinite clay.

scholarly journals Biosorption of Pb (II) and Zn (II) from aqueous solution by Oceanobacillus profundus isolated from an abandoned mine

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Wilson Mwandira ◽  
Kazunori Nakashima ◽  
Satoru Kawasaki ◽  
Allison Arabelo ◽  
Kawawa Banda ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Ion Concentration ◽  
Contaminated Site ◽  
Lead Ion ◽  
Contaminated Water ◽  
Metal Chelation ◽  
Anthropogenic Contamination ◽  
Initial Concentration ◽  
Growth Ph ◽  
Maximum Removal

AbstractThe present study investigated biosorption of Pb (II) and Zn (II) using a heavy metal tolerant bacterium Oceanobacillus profundus KBZ 3-2 isolated from a contaminated site. The effects of process parameters such as effect on bacterial growth, pH and initial lead ion concentration were studied. The results showed that the maximum removal percentage for Pb (II) was 97% at an initial concentration of 50 mg/L whereas maximum removal percentage for Zn (II) was at 54% at an initial concentration of 2 mg/L obtained at pH 6 and 30 °C. The isolated bacteria were found to sequester both Pb (II) and Zn (II) in the extracellular polymeric substance (EPS). The EPS facilitates ion exchange and metal chelation-complexation by virtue of the existence of ionizable functional groups such as carboxyl, sulfate, and phosphate present in the protein and polysaccharides. Therefore, the use of indigenous bacteria in the remediation of contaminated water is an eco-friendly way of solving anthropogenic contamination.

Sign in / Sign up

Export Citation Format

Share Document