Jumat, 19 Mei 2017

predict rendement



In chemistry, the chemical yield, the yield of the reaction, or only the rendement refers to the amount of reaction product produced in the chemical reaction. [1] Absolute rendement can be written as weight in grams or in moles (molar yield). The relative yield used as a calculation of the effectiveness of the procedure is calculated by dividing the amount of product obtained in moles by the theoretical yield in moles.

To obtain a percentage yield, multiply the fractional yield by 100%.
One or more reactants in chemical reactions are often used redundantly.
The theoretical rendement is calculated based on the number of moles of the limiting reagent. For this calculation, it is usually assumed there is only one reaction involved.

The ideal chemical yield value (theoretical rendement) is 100%, a value highly unlikely to be achieved in its practice. Calculate the percent of rendemen that is by using the following equations percent rendemen = weight yield / weight of yield divided by the sample weight multiplied by 100%

Rendement is the ratio of the amount (quantity) of oil produced from the extraction of aromatic plants. Rendemen use percent unit (%). The higher the yield value indicates the value of the oil produced more and more. Increasing the yield or the ratio of the amount of oil produced can be done with two approaches,
First, the cultivation process.
Second, the process of making oil
The quality of the oil produced is usually inversely proportional to the number of rendaments produced. The higher the resulting rendamen the lower the quality obtained. The formula for calculating the following rendamen


Problems example: 

In 50 grams of urea fertilizer (CO (NH2) 2) there are 21 grams of nitrogen. The purity of urea fertilizer is ...
Answer:
If you find a question that asks for purity then all you have to compare facts with theory.
FACT in Problem:
In 50 grams of urea fertilizer (CO (NH2) 2) there are 21 grams of Nitrogen (N)

THEORY:




 


COMPARE:

 

Kamis, 18 Mei 2017

chemical articel




Researchers at the Institute for Integrated Cell-Material Sciences (iCeMS) in Japan have demonstrated an on/off switching behaviour in a coordination polymer crystal.
Coordination polymer crystals are inorganic and organic hybrid materials. They are known for their structural and functional diversity and their ability to conduct protons.
Proton conduction is a form of electrical conduction in which positive hydrogen ions (H+) carry the charge instead of electrons. It plays a key role in powering photosynthesis in plants and could be used to develop better fuel cells.
A team of researchers led by Satoshi Horike and Susumu Kitagawa synthesized a coordination polymer (CP) by reacting zinc oxide, phosphoric acid and imidazole in ethyl alcohol at room temperature. The CP was then melted and triflic acid was added. The resultant mixture was then cooled and recrystallized. This 'acid doping' of the CP significantly enhanced its proton conductivity.
The team melted their original CP again and instead added the 'photoacid' pyranine. Photoacids are molecules that become more acidic upon absorption of light. After cooling the material, its now recrystallized form was exposed to light and its proton conductivity improved. When the light was turned off, its conductivity decreased and returned to its original state. This change could be switched on and off over several consecutive cycles of light exposure.
Acid doping of the CP resulted in minimal structural change with overall enhancement of proton conductivity. Doping the CP with photoacid gave the researchers on-demand external control of the ionic current in the material.
"This is the first demonstration of utilization of the melting state for CP functionalization," conclude the researchers in their study published in the journal Angewandte Chemie. Their melt-doping strategy could potentially be extended to synthesize a new class of proton-conducting solids that can be used in non-volatile memory technologies, ionics-based transistors, and light-induced ionic/electric current circuits.
The Institute for Integrated Cell-Material Sciences (iCeMS) at Kyoto University in Japan aims to advance the integration of cell and material sciences, both traditionally strong fields at the university, in a uniquely innovative global research environment. iCeMS combines the biosciences, chemistry, materials science and physics to create materials for mesoscopic cell control and cell-inspired materials. Such developments hold promise for significant advances in medicine, pharmaceutical studies, the environment and industry.

Story Source:
Materials provided by Institute for Integrated Cell-Material Sciences at Kyoto University. Note: Content may be edited for style and length.

Journal Reference:
  1. Sanjog S. Nagarkar, Satoshi Horike, Tomoya Itakura, Benjamin Le Ouay, Aude Demessence, Masahiko Tsujimoto, Susumu Kitagawa. Enhanced and Optically Switchable Proton Conductivity in a Melting Coordination Polymer Crystal. Angewandte Chemie International Edition, 2017; 56 (18): 4976 DOI: 10.1002/anie.201700962

Rabu, 17 Mei 2017

using eglish to report



1    LAB REPORT ON ACID-BASE TITRATIONS
 Aim:
 To determine the weight-to-volume percent of acetic acid present in commercial vinegar and the weight-to-volume percent of ammonia present in window cleaners. Acid-base titrations can be conducted using the above samples against standardized aqueous NaOH and standardized aqueous HCl solutions respectively.
2.      Introduction:
Acetic acid, commonly known as ethanoic acid CH3COOH, is found in commercial vinegar. It is a weak organic acid that gives vinegar its characteristic pungent smell, sour taste and slight acidity. Being an acid, vinegar is used as a mild disinfectant in cleaning agents as well as a food preservative. Ammonia, NH3, is used in household and industrial cleaning agents due to its ability to solubilize grease.  In this experiment, we shall use acid-base titration to determine the weight-to-volume percentage of acetic acid and ammonia. An acid-base titration is a process of obtaining quantitative information of a sample using an acid-base reaction by reacting with a certain volume of reactant whose concentration is known. A suitable indicator for determining the equivalence point is used to indicate the end point of an acid-base titration. To achieve accurate results, multiple titrations will be carried out until duplicate determinations agree to within 0.05mL of each other.
4. Results & Calculations:
4.1 Standardization of NaOH
Molarity of KHC8H4O4 is 0.05044 moldm-3   = = 0.05044 moldm-3)
Titration
1
2
3
Final volume of titrant/cm3
5.00
10.00
14.80
Initial volume of titrant/cm3
0.00
5.00
10.00
Volume of titrant used/cm3
5.00
5.00
4.80




 


KHC8H4O4 (aq)   +  NaOH (aq)                      KHC8H4O3 - Na+  (aq)  +  H2O (l)
Average volume of NaOH titrate used = ½ (5.00 + 5.00)
     = 5.00 cm3
No. of moles of KHC8H4O4   reacted = 0.01 × 0.05044
     = 5.044 x 10-4 mol

From the equation, mole ratio of NaOH ≡ KHC8H4O4   is 1:1,
No. of moles of NaOH reacted                 = 5.044 x 10-4 mol
Concentration of NaOH  = moles of NaOH/ volume of NaOH
                                                    = 5.044 x 10-4 /
    = 0.1009 moldm-3   
Molarity of NaOH is: 0.1009moldm-3
4.2 Standardization of HCl
Titration
1
2
3
Final volume of titrant/cm3
10.80
10.75
10.70
Initial volume of titrant/cm3
0.00
0.00
0.00
Volume of titrant used/cm3
10.80
10.75
10.70
                      




 
HCl (aq)   +  NaOH (aq)                     NaCl (aq)  +  H2O (l)
Average NaOH titrate used  = ½ (10.70 + 10.75)
     = 10.73 cm3
No. of moles of NaOH   reacted  = (10.73 ÷ 1000) × 0.1009
     = 1.082 x 10-3 mol

From equation, mole ratio of NaOH ≡ HCl   is 1:1,
no. of moles of HCl reacted                     = 1.082 x 10-3 mol

Hence concentration of HCl  = 1.082 x 10-3 (1000 ÷ 10.00)
     = 0.1082 moldm-3   

Molarity of HCl is: 0.1082 moldm-3   

4.3 Determination of acetic acid in vinegar
Titration
1
2
3
Final volume of titrant/cm3
12.15
12.20
12.20
Initial volume of titrant/cm3
0.00
0.00
0.00
Volume of titrant used/cm3
12.15
12.20
12.20






 
CH3COOH (aq)   +  NaOH (aq)                     CH3COO-Na+ (aq)  +  H2O (l)
Average volume of NaOH titrate used = ½ (12.20 + 12.20)
     = 12.20 cm3
No. of moles of NaOH reacted              = (12.20  ÷ 1000) × 0.1009    
                = 1.231 x 10-3 mol


From equation, mole ratio of NaOH ≡ CH3COOH   is 1:1,
no. of moles of CH3COOH reacted           = 1.231 x 10-3 mol


No. of moles of CH3COOH in volumetric flask (diluted)  = (100 ÷ 10) × 1.231 x 10-3
       = 1.231 x 10-2 mol
No. of mole of CH3COOH in 25mL (undiluted)  = 1.231 x 10-2 mol
Molarity of acetic acid = (1.231 x 10-2 mol) ÷(25 x 10-3)=0.4924 moldm-3
Molar mass of CH3COOH = 2(12.01) + 4(1.0079) + 2(16.00)
= 60.0516 g mol-1


Therefore, weight-volume percentage of CH3COOH in vinegar  
= (0.4924 x 60.0516 ÷ 1000) × 100% = 2.96%


Percentage of acetic acid in the vinegar is: 2.96%
Indicator used: phenopthalein


4.4 Determination of ammonia in window cleaner
Titration
1
2
3
Final volume of titrant/cm3
4.85
9.65
4.85
Initial volume of titrant/cm3
0.00
4.85
0.00
Volume of titrant used/cm3
4.85
4.80
4.85






NH3 (aq)   +  HCl (aq)                     NH4+Cl- (aq)


Average volume of HCl titrate used = ½ (4.85 + 4.85)
     = 4.85 cm3
No. of moles of HCl reacted = 0.1082 x (4.85 x10-3)
         = 5.248 x 10-4 mol

From equation, mole ratio of HCl ≡ NH3   is 1:1,
no. of moles of NH3 reacted = 5.248 x 10-4 mol
No. of moles of NH3 in volumetric flask (diluted) = (100 ÷ 10) × 5.248 x 10-4 mol
       = 5.248 x 10-3 mol
No. of mole of NH3 in 10mL (undiluted)   = 5.248 x 10-3 mol
Concentration of NH3   = (5.248 x 10-3) ÷ (10 x 10-3) = 5.248 x 10-1 moldm-3


Molar mass of NH3 = 14.01 + 3 (1.0079)
= 17.0337 g mol-1

Therefore, weight-volume percentage of NH3 in window cleaner  
= (17.0337 x 5.248 x 10-1)/ 103 × 100%
= 0.894%
Percentage of ammonia in the window cleaner is: 0.894%
Indicator used: methyl red


5. Discussion:
The main reaction in the series of acid-base titrations is neutralization. During neutralization, the acid and base reacts to form a salt and water (i.e. H+ + OH-          H2O). As the all the reactants are colourless, an appropriate indicator must be added to indicate the colour change at the end point.


For Experiment 3.3, the indicator phenolphthalein was chosen as it was a weak acid-strong base titration, as acetic acid is a weak acid and NaOH is a strong base. At equivalence point, the resulting solution contains only CH3COONa. Thus salt hydrolysis occurs and the pH at equivalence point is > 7. Phenolphthalein changes colour at a pH range of 8.2 – 10.0.
The (pH)end point falls within the pH for colour change of phenolphthalein in the titration. The colour of phenolphthalein changes explicitly from pink to colourless and the colour change is over a narrow pH range. This further enhances its suitability as an indicator for this titration.


Salt hydrolysis that raises equivalence point to > 7 pH :
CH3COO-  +  H2O          CH3COOH  +  OH-
*
The pH titration curve of weak acid (CH3COOH) and strong base (NaOH)

However, for Experiment 3.4 a different indicator was chosen. Methyl red was used instead as it was a case of a strong acid-weak base titration, as HCl is a strong acid and NH3 is the weak base. At equivalence point, the resulting solution contains only NH4Cl. Thus salt hydrolysis occurs and the pH at equivalence point is < 7. Methyl red changes colour over a pH range of 4.8 – 6.0.
The (pH)end point falls within the pH range for colour change of methyl red in this titration. The colour of methyl red changes explicitly from red to yellow and the colour change is over a narrow pH range. This further enhances its suitability as an indicator for this titration.
Salt hydrolysis that lowers equivalence point to < 7 pH :
NH4Cl  +  H2O           NH3  +  H3O+


*
The pH titration curve of weak base (NH3) and strong acid (HCl)

Strong acid-weak base and weak acid-strong base titrations are employed in this experiment instead of weak acid-weak base titrations as the hydrolysis of a salt of a weak acid-weak base is incomplete. The hydrolysis of the conjugate base results in an acidic solution and at the same time, hydrolysis of the conjugate acid of the salt gives rise to a basic solution. Hence, the resulting solution at equivalence point can be neutral, acidic or basic depending on which hydrolysis occurs at a greater extent. This means that calculations have to be done preceding the titration in order to select the appropriate indicators. Therefore, weak acid-weak base titration is not commonly used to determine the quantitative information of an unknown sample.
While titrating, the conical flask has to be swirled constantly throughout to ensure that the contents are mixed evenly. Also, some titrant may drip onto the sides of the conical flask and may not react with the solution in the conical flask. This reduces the accuracy of the results as extra titrant would be used to achieve the equivalence point. To prevent this, deionised water can be used to wash down the unreacted titrant when nearing the equivalence point and the conical flask should be swirled before continuing with the titration. To achieve consistent results, one important factor is to add in the titrant in a drop wise manner before the equivalence point.
Deionised water was used not only for diluting the sample but also for washing the apparatus, instead of using tap water. This is because deionized water is pH neutral and will not negatively affect the results of the acid-base titrations. This is important as acid-base titrations are pH sensitive reactions.
Multiple titrations were carried out until duplicate determinations agree to within 0.05mL of each other. This ensures that the results are not once-off outliers. By averaging the two most consistent and accurate results, the probability of incurring random errors was accounted for and decreased.
Other factors that would affect the accuracy of the results include parallax error when taking the readings and making sure that no air bubbles are present within the pipette and burette while titrating.

6. Conclusion:
Using acid-base chemistry, repeated titrations of vinegar sample and window cleaner sample was carried out against standardized solutions of NaOH and HCl respectively. Through stoichiometric relations, the concentration and weight-to-volume percentage of acetic acid in vinegar and ammonia in window cleaner can be found. The percentage of acetic acid in the vinegar sample studied was deduced to be 3.96%. The percentage of ammonia in the window cleaner sample is 0.894%.