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Uv-Vis: Kurva Kalibrasi Paracetamol

The document describes procedures for preparing standard solutions and using UV-Vis spectroscopy and iodimetry to determine the concentration of samples. Specifically: 1. It details how to make a 500 ppm stock solution of paracetamol and generate a calibration curve by taking absorbance measurements of standards ranging from 3.5-6.5 ppm. 2. The absorbance of a sample is measured and used to determine its concentration via the linear regression equation from the calibration curve. 3. Iodimetry is also described to determine the concentration of vitamin C and iodine via titration with sodium thiosulfate of known concentration. Concentrations are calculated based on the titration volumes
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0% found this document useful (0 votes)
73 views

Uv-Vis: Kurva Kalibrasi Paracetamol

The document describes procedures for preparing standard solutions and using UV-Vis spectroscopy and iodimetry to determine the concentration of samples. Specifically: 1. It details how to make a 500 ppm stock solution of paracetamol and generate a calibration curve by taking absorbance measurements of standards ranging from 3.5-6.5 ppm. 2. The absorbance of a sample is measured and used to determine its concentration via the linear regression equation from the calibration curve. 3. Iodimetry is also described to determine the concentration of vitamin C and iodine via titration with sodium thiosulfate of known concentration. Concentrations are calculated based on the titration volumes
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
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UV-VIS a.

Konsentrasi 3,5 ppm


V1 . N1 = V2 . N2
1. Pembuatan Larutan Stok V1 . 500 ppm = 10 mL . 3,5 ppm
50 mg parasetamol p.a dilarutkan dalam 100 mL etanol 96% 35
V1 =
500
50 mg x = 0,07 mL = 70 µL
=
100 mL 1000 b. Konsentrasi 4 ppm
V1 . N1 = V2 . N2
50.000
x = V1 . 500 ppm = 10 mL . 4 ppm
100 40
V1 =
x = 500 ppm 500
= 0,08 mL = 80 µL
Konsentrasi
Absorbansi
Standar (ppm) c. Konsentrasi 4,5 ppm
3,5 0,34 V1 . N1 = V2 . N2
4 0,41 V1 . 500 ppm = 10 mL . 4,5 ppm
45
4,5 0,48 V1 =
500
5 0,56 = 0,09 mL = 90 µL
5,5 0,68 d. Konsentrasi 5 ppm
6 0,75 V1 . N1 = V2 . N2
V1 . 500 ppm = 10 mL . 5 ppm
6,5 0,83 50
V1 =
500
= 0,10 mL = 100 µL
Kurva Kalibrasi Paracetamol e. Konsentrasi 5,5 ppm
1 V1 . N1 = V2 . N2
V1 . 500 ppm = 10 mL . 5,5 ppm
Absorbansi

f(x) = 0.17 x − 0.26


0.5 R² = 0.99 55
Linear () V1 =
500
0
2 3 4 5 6 7 = 1,1 mL = 110 µL
Konsentrasi (ppm)
f. Konsentrasi 6 ppm
V1 . N1 = V2 . N2
V1 . 500 ppm = 10 mL . 6 ppm
60
V1 =
500
2. Perhitungan Pengenceran = 1,2 mL = 120 µL
g. Konsentrasi 6,5 ppm
V1 . N1 = V2 . N2 IODIMETRI
V1 . 500 ppm = 10 mL . 6,5 ppm
65  Pembakuan Vitamin C dengan K2Cr2O7
V1 = Dik : K2Cr2O7 = 50 mg, BM K2Cr2O7 = 249
500
= 1,3 mL = 130 µL
Percobaan Ke- VNa2S2O3 NNa2S2O3
3. Perhitungan Kadar Sampel 1 20,6 ml 0,049 N
Diketahui : 2 20,5 ml 0,049 N
a = 0,2607 3 20,6 ml 0,049 N
b = 0,1679 Rata-rata 0,049 N
Absorbansi sampel = 0,4125 Perhitungan :
Perhitungan Persamaan Regresi Linear : 1) Mgek Na2S2O3 = Mgek K2Cr2O7
y = bx + a mg K 2 Cr 2 O7
VNa2S2O3 . NNa2S2O3 =
0,4125 = 0,01679x + 0,2607 BE K 2Cr 2O 7
0,4125- 0,2607 = 0,01679x mg K 2 Cr 2 O7
NNa2S2O3 =
x = 4,0095 BE K 2Cr 2O 7 .VNa 2 S 2 O3
50 mg
Konsentrasi = 4,0095 x factor pengenceran =
49 . 20,6 ml
NNa2S2O3 = 0,0495 N
Konsentrasi = 4,0095 x 10
mg K 2 Cr 2 O7
2) NNa2S2O3 =
Konsentrasi = 40,095 ppm BE K 2Cr 2O 7 .VNa 2 S 2 O3
50 mg
=
49 . 20,5 ml
NNa2S2O3 = 0,0497 N
mg K 2 Cr 2 O7
3) NNa2S2O3 =
BE K 2Cr 2O 7 .VNa 2 S 2 O3
50 mg
=
49 . 20,6 ml
NNa2S2O3 = 0,0495 N

 Pembakuan Larutan Iodium (I2) dengan larutan Na2S2O3 (0,049 N)


Pecobaan Ke- VI VNa2S2O3 NI
1 10 ml 9,6 ml 0,047 N
2 10 ml 9,8 ml 0,048 N 11,5ml . 0,047 N
=
3 10 ml 9,7 ml 0,047 N 10 ml
Rata-rata 0,047 N NVitC = 0,054 N
Perhitungan : ¿
2) NVitC = VI .∋ VVitC ¿
1) VI . NI = VNa2S2O3 . NNa2S2O3 11,7 ml . 0,047 N
=
VNa 2 S 2 O3 . NNa 2 S 2 O3 10 ml
NI =
VI NVitC = 0,055 N
9,6 ml . 0,049 N 3) NVitC
¿
= VI .∋ VVitC ¿
=
10 ml
NI = 0,047 N 11,5ml . 0,047 N
=
VNa 2 S 2 O3 . NNa 2 S 2 O3 10 ml
2) NI = NVitC = 0,054 N
VI
9,8 ml . 0,049 N 0,054 N +0,055 N +0,054 N
= Rata-rata = = 0,054 N
10 ml 3
NI = 0,048 N
VNa 2 S 2 O3 . NNa 2 S 2 O3  g VitC = NVitC x BE VitC x VVitC
3) NI =
VI = 0,054 N x 88,065 x 0,05 L
9,7 ml . 0,049 N = 0,237 gram/50 ml
=
10 ml g VitC
NI = 0,047 N  % Vit C = x 100%
VVitC
0,237 g
0,047 N +0,048 N +0,047 N = x 100%
NI rata-rata = = 0,047 N 50 ml
3
% Vit C = 0,474 %
 Penetapan Kadar Analit (Vitamin C)
Pecobaan Ke- VVitC VI NVitC
1 10 ml 11,5 ml 0,054 N
2 10 ml 11,7 ml 0,055 N
3 10 ml 11,5 ml 0,054 N
Rata-rata 0,054 N
Perhitungan :
1) VVitC . NVitC = VI . NI
¿ ¿
NVitC = VI .∋ VVitC
0,048 N + 0,049 N + 0,048 N
MEDTA rata-rata = = 0,048 N
3
 Titrasi Blanko
Percobaan Ke- VPelarut VEDTA MPelarut
KOMPLEKSOMETRI 1 10 ml 0,4 ml 0,002 M
2 10 ml 0,6 ml 0,003 M
 Pembakuan EDTA menggunakan ZnSO4 0,05 M 3 10 ml 0,4 ml 0,002 M
Rata-rata 0,0023 M
Percobaan VNa2EDTA MNa2EDTA
Ke-
1 12,8 ml 0,048 M Perhitungan :
2 12,6 ml 0,049 M
3 12,8 ml 0,048 M 1. VPelarut . MPelarut = VEDTA . MEDTA
Rata-rata 0,048 M VEDTA . MEDTA
MPelarut1 =
Perhitungan : VPelarut
0,4 ml . 0,048 M
=
1. mmol EDTA = mmol ZnSO4 10 ml
mg ZnSO 4 MPelarut1 = 0,002 M
VEDTA . MEDTA =
Mr ZnSO 4 VEDTA . MEDTA
2. MPelarut2 =
mg ZnSO 4 VPelarut
MEDTA =
Mr ZnSO 4 . VEDTA 0,6 ml . 0,048 M
=
100 mg 10 ml
=
161. 12,8 ml
MEDTA = 0,048 M MPelarut2 = 0,003 M
mg ZnSO 4 VEDTA . MEDTA
2. MEDTA = 3. MPelarut3 =
Mr ZnSO 4 . VEDTA VPelarut
100 mg 0,4 ml . 0,048 M
= =
161. 12,6 ml 10 ml
MEDTA = 0,049 M MPelaurt3 = 0,002 M
mg ZnSO 4 0,002 M +0,003 M +0,002 M
3. MEDTA = MPelarut rata-rata = = 0,0023 M
Mr ZnSO 4 . VEDTA 3
100 mg
=
161. 12,8 ml  Penetapan Kadar Analit (Asam Mefenamat) dengan Titrasi Komplesometri
Refreshment
MEDTA = 0,048 M
Percobaan VAsam VZnSO4 yang VTitrasi VEDTA VZnSO4 VZnSO4 8,7 ml . 0,048 M
=
Ke- Mefenamat ditambahka Blanko (VEDTA berlebih yang 0,05 M
n yang bereaksi VZnSO4 berlebih = 8,35 ml
bereaksi dengan
dengan analit - Menghitung VZnSO4 yang bereaksi dengan analit
ZnSO4) 1. VZnSO4 analit = VZnSO4 yang ditambahkan – Vtitrasi Blanko – VZnSO4
1 10 ml 10 ml 0,4 ml 8,8 ml 8,45 1,15 ml berlebih
ml
2 10 ml 10 ml 0,6 ml 8,7 ml 8,35 1,05 ml = 10 ml – 0,4 ml – 8,45 ml
ml VZnSO4 analit = 1,15 ml
3 10 ml 10 ml 0,4 ml 8,7 ml 8,5 ml 1,25 ml
2. VZnSO4 analit = 10 ml – 0,6 ml – 8,35 ml
= 1,05 ml

3. VZnSO4 analit = 10 ml – 0,4 ml – 8,5 ml


VZnSO4 analit = 1,25
Perhitungan :

- Menghitung VZnSO4 berlebih


1. VZnSO4 . MZnSO4 = VEDTA. MEDTA
 Penetapan Kadar Asam Mefenamat menggunakan Titrasi
VEDTA . MEDTA
VZnSO4 berlebih = Kompleksometri Refrreshment
MZnSO 4 1. VAsam Mefenamat . MAsam Mefenamat = VZnSO4 . MZnSO4
8,8 ml . 0,048 M VZnSO 4 . MZnSO 4
= MAsam Mefenamat =
0,05 M VAsam Mefenamat
1,15 ml .0,05 M
=
VZnSO4 berlebih = 8,45 ml 10 ml
MAsam Mefenamat = 0,006 M
VEDTA . MEDTA
2. VZnSO4 berlebih =
MZnSO 4 VZnSO 4 . MZnSO 4
8,7 ml . 0,048 M 2. MAsam Mefenamat =
= VAsam Mefenamat
0,05 M 1,05 ml .0,05 M
VZnSO4 berlebih = 8,35 ml =
10 ml
MAsam Mefenamat = 0,005 M
VEDTA . MEDTA
3. VZnSO4 berlebih =
MZnSO 4 VZnSO 4 . MZnSO 4
3. MAsam Mefenamat =
VAsam Mefenamat
1,25 ml .0,05 M mg AsamOksalat
= 1. VNaOH . NNaOH =
10 ml BE AsamOksalat
MAsam Mefenamat = 0,006 M mg Asam Oksalat
0,006 M + 0,005 M +0,006 M NNaOH =
BE AsamOksalat . VNaOH
MAsam Mefenamat rata-rata = = 0,006 M
3 63 mg
NNaOH =
 g Asam Mefenamat = MAsam Mefenamat x BM Asam Mefenamat x VAsam 63 .10 , 8 ml
Mefenamat NNaOH1 = 0,092 N
= 0,006 M x 241,29 x 0,05 L mg Asam Oksalat
2. NNaOH2 =
BE AsamOksalat . VNaOH
g Asam Mefenamat = 0,07 g 63 mg
=
g Asam Mefenamat 63 .10,5 ml
 % Asam Mefenamat = x 100%
VAsam Mefenamat NNaOH2 = 0,095 N
0,07 g
= x 100%
50 ml mg Asam Oksalat
3. NNaOH3 =
BE AsamOksalat . VNaOH
% Asam Mefenamat = 0,14% b/v 63 mg
=
63 .10,6 ml
NNaOH3 = 0,094 N
0,092 N + 0,095 N +0,094 N
NNaOH rata-rata = = 0,094 N
3
 Pembakuan HCl menggunakan NaOH hasil pembakuan (0,094 N)
Percobaan Ke- VNaOH VHCl NHCl
ASAM BASA TIDAK LANGSUNG 1 10 ml 10,4 ml 0,090 N
2 10 ml 10,6 ml 0,090 N
Sampel : 18 3 10 ml 10,4 ml 0,090 N
 Pembakuan NaOH menggunakan Asam Oksalat 0,1 N Rata-rata 0,090 N
Percobaan Ke- VAsam Oksalat VNaOH NNaOH
Perhitungan :
1 10 ml 10, 8 ml 0,092 N
1. VHCl . NHCl = VNaOH . NNaOH
2 10 ml 10,5 ml 0,095 N
VNaOH . NNaOH
3 10 ml 10,6 ml 0,094 N NHCl1 =
VHCl 1
Rata-rata 0,094 N
10 ml . 0,094 N
Perhitungan : =
10,4 ml
Mgek NaOH = Mgek Asam Oksalat
NHCl1 = 0,090 N
VNaOH . NNaOH VHCl . NHCl
2. NHCl2 = 3. NPelarut3 =
VHCl 2 VPelarut 3
0,1 ml .0,090 N
10 ml . 0,094 N =
= 10 ml
10,6 ml NPelarut3 = 0,0009 N
NHCl2 = 0,090 N 0,0018 N + 0,0018 N + 0,0009 N
NPelarut rata-rata = = 0,0015 N
VNaOH . NNaOH 3
3. NHCl3 =
VHCl 3
10 ml . 0,094 N
=
10,4 ml  Penetapan Kadar Analit (Asetosal) dengan Titrasi Asam Basa Tidak
NHCl3 = 0,090 N Langsung
0,090 N + 0,090 N + 0,090 N Percobaa VAsetosal VNaOH yang VTitrasi VHCl (VNaOH VNaOH VNaOH yang
NHCl rata – rata = = 0,090 N
3 n Ke- ditambahkan Blanko yang berlebih bereaksi
bereaksi dengan
 Titrasi Blanko (Pelarut yang digunakan etanol 96%) dengan analit
Percobaan Ke- VPelarut VHCl NPelarut HCl)
1 10 ml 0,2 ml 0,0018 N 1 10 ml 25 ml 0,2 ml 20,8 ml
19,91 4,89 ml
ml
2 10 ml 0,2 ml 0,0018 N
2 10 ml 25 ml 0,2 ml 20,5 ml 19,63 5,17 ml
3 10 ml 0,1 ml 0,0009 N
ml
Rata-rata 0,0015 N
3 10 ml 25 ml 0,1 ml 20,6 ml 19,72 5,18 ml
Perhitungan :
ml
1. VPelarut . NPelarut = VHCl . NHCl
VHCl . NHCl Keterangan : VNaOH yang bereaksi dengan analit = VNaOH yang ditambahkan -
NPelarut1 = VTitrasi Blanko – VNaOH berlebih
VPelarut 1
NNaOH = 0,094 N
0,2 ml .0,090 N
=
10 ml
Perhitungan :
NPelarut1 = 0,0018 N
1. VNaOH berlebih . NNaOH = VHCl . NHCl
VHCl . NHCl
2. NPelarut2 = VHCl . NHCl
VPelarut 2 VNaOH berlebih =
NNaOH
0,2 ml .0,090 N
= 20,8 ml . 0,090 N
10 ml =
0,094 N
NPelarut2 = 0,0018 N
VNaOH berlebih = 19,91 ml

1. VAsetosal . NAsetosal = VNaOH. NNaOH


VNaOH . NNaOH berlebih g Asetosal
NAsetosal =  % Asetosal = x 100%
VAsetosal VAsetosal
4,89 ml . 0,094 N 0,43 g
= = x 100%
10 ml 50 ml
NAsetosal = 0,046 N
% Asetosal = 0,86 % b/v
VHCl . NHCl
2. VNaOH berlebih =
NNaOH
20,5 ml . 0,090 N
=
0,094 N ARGENTOMETRI
VNaOH berlebih = 19,63 ml Dik : BM Tramadol HCl = 299,84
BM HCl = 36,5
VNaOH . NNaOH berlebih
2. NAsetosal = BE NaCl = 58,5
VAsetosal
 Pembakuan AgNO3 dengan NaCl p.a
5,17 ml . 0,094 N
= Dik : Bobot NaCl p.a = 50 mg
10 ml
NAsetosal = 0,049 ml Percobaan Ke- VAgNO3 NAgNO3
1 17,4 ml 0,049 N
VHCl . NHCl 2 17,3 ml 0,049 N
3. VNaOH berlebih =
NNaOH
20,6 ml . 0,090 N 3 17,4 ml 0,049 N
= Rata-rata 0,049 N
0,094 N
VNaOH berlebih = 19,72 ml Perhitungan :
1) Mgek AgNO3 = Mgek NaCl
VNaOH . NNaOH berlebih mg NaCl
3. NAsetosal = VAgNO3 . NAgNO3 =
VAsetosal BE NaCl
5,18 ml .0,094 ml mg NaCl
= NAgNO3 =
10 ml BE NaCl .VAgNO 3
NAsetosal = 0,049 N 50 mg
=
58,5. 17,4 ml
0,046 N +0,049 N + 0,049 N NAgNO3 = 0,049 N
NAsetosal rata-rata = = 0,048 N
3 mg NaCl
2) NAgNO3 =
BE NaCl .VAgNO 3
 g Asetosal = NAsetosal x BE Asetosal x VAsetosal 50 mg
= 0,048 N x 180,16 x 0,05 L =
58,5. 17,3 ml
g Asetosal = 0,43 g NAgNO3 = 0,049 N
mg NaCl  g HCl = NHCl x BE HCl x VHCl
3) NAgNO3 =
BE NaCl .VAgNO 3 = 0,047 N x 36,5 x 0,05 L
50 mg
= g HCl = 0,086 gram
58,5. 17,4 ml
NAgNO3 = 0,049 N BM Tramadol HCl
 g Tramadol HCl = x g HCl
0,049 N + 0,049 N + 0,049 N BM HCl
NAgNO3 rata-rata = = 0,049 N
3 299,84
= x 0,08 g
Penetapan Kadar Tramadol HCl dengan Titrasi Argentometri Metode Mohr 36,5
g Tramadol HCl = 0,71 g/50 ml
Percobaan Ke- VHCl VAgNO3 NHCl
1 10 ml 9,7 ml 0,048 N g Tramadol HCl
2 10 ml 9,5 ml 0,046 N  % Tramadol HCl = x 100%
V Tramadol HCl
3 10 ml 9,8 ml 0,048 N
Rata-rata 0,047 N 0,71 g
= x 100%
Perhitungan : 50 ml

1) VHCl . NHCl = VAgNO3 . NAgNO3 % Tramadol HCl = 1,42 %


VAgNO3 . NAgNO 3
NHCl =
VHCl
9,7 ml . 0,049 N
=
10 ml
NHCl = 0,048 N
VAgNO3 . NAgNO 3
2) NHCl =
VHCl
9,5 ml . 0,049 N
=
10 ml
NHCl = 0,046 N
VAgNO3 . NAgNO 3
3) NHCl =
VHCl
9,8 ml . 0,049 N
=
10 ml
NHCl = 0,048 N
0,048 N + 0,046 N +0,048 N
NHCl rata-rata = = 0,047 N
3

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