A Seminar entitled" Effect of activated carbon in textiles" presented in Department of Textiles and Apparel Designing, College of Community Science, UASD, Karnataka by Manpreet Kaur
3. INTRODUCTION
• Carbon is one of the magnificent elements, which leads to
a large variety of compounds and structures.
• Carbonaceous, highly porous, large surface area
adsorptive medium that has a complex structure
composed primarily of carbon atoms.
• Activated carbon is a form of carbon processed to be
riddled with small, low-volume pores that increase the
surface area available for adsorption or chemical
reactions.
• The porosity within activated carbon imparts their
characteristics of adsorption.
11/9/2022 3
Four types of generic sorbents have dominated industrial adsorption:
• Zeolites,
• Silica gel
• Activated alumina
• Activated carbon
4. 11/9/2022 4
Production
Carbonization: Material with carbon content is pyrolyzed at
temperatures in the range 600–900 °C, usually in inert
atmosphere with gases like argon or nitrogen.
Activation/Oxidation: Raw material or carbonized material
is exposed to oxidizing atmospheres (oxygen or steam) at
temperatures above 250 °C, usually in the temperature range
of 600–1200 °C.
Physical
activation
Chemical
activation
The carbon material is impregnated with certain
chemicals.
6. 11/9/2022 6
Treatment Methods for effluents
Chemical
methods
Biological
methods
Physical method
Oxidation
Ozonation
Flocculation
Adsorption
Microbes
Enzymes
7. 11/9/2022 7
Adsorption
accumulation of gaseous
components or solutes
dissolved in liquids onto a
solid surface.
physical process
Van der Waals (dipole-
dipole) and intermolecular
forces are important in the
adsorption phenomenon
Adsorption has found to be superior in terms of:
Flexibility
and
simplicity
of
design
Low
operating
cost
Insensitivity
to
toxic
pollutants
Ease of
operation
Adsorption
also
does not
produce
harmful
substances
8. Activation “carefully controlled oxidation of carbon atoms in the
raw material”
• Network of pores
• Distribution of pore sizes and shapes
• Macroscale pores are greater than 50 nm in size, while
mesoscale pores range from 2–50 nm and microscale pores
less than 2 nm wide
11/9/2022 8
How it works
9. Factors affecting adsorption
• Molecular size of the substances to be removed from
the bulk material
• Hydrophilic behavior of the substances
• Polarity of the substance to be removed
• Size of interior surface area of the adsorbent material
• Pore structure of the activated carbon material (shape,
size distribution)
• Solute concentration
• Temperature and pressure, Relative humidity
• Composition of the solution or gas
• pH value of the solution (for liquid phase)
11/9/2022 9
10. • A gram of activated carbon can have a surface area of
500 𝑚2-1500𝑚2stable at high temperature (even above
1000K)
• High surface-area structures
• Van der Waals force and intermolecular forces are
important in adsorption phenomenon
• Carbon monoxide is not well adsorbed by activated
carbon
• Does not bind well to certain chemicals,
including alcohols, strong acids and bases, and most
inorganics, such as lithium, sodium, iron, lead, arsenic,
fluorine and boric acid.
PROPERTIES
11/9/2022 10
14. Effluent
11/9/2022 14
• Effluent is defined by the United
States Environmental Protection
Agency as “wastewater - treated or
untreated - that flows out of a
treatment plant, sewer, or industrial
outfall. Generally refers to wastes
discharged into surface waters”.
Waste Water
Discharge
15. One pair jeans
8,000 Litre water
11/9/2022 15
Water conservation through recycling
16. 11/9/2022 16
TDS - Total Dissolved Solids
• common salt increases
TDS of water
• affects the fertility of
soil
• harmful to aquatic life.
pH
• pH is the measure of
acidity or alkalinity of an
aqueous solution.
• Solutions with pH less
than 7 are acidic whereas
above 7 are alkaline.
• pH of 7 is termed as
neutral.
17. 11/9/2022 17
TSS - Total Suspended Solids
• due to insoluble substances
present in waste water.
• Higher TSS gives turbid water.
• Turbid water absorbs heat
from natural light & leads to
increase water temperature.
higher temperature reduces
DO level.
• harmful to aquatic life.
Dissolved Oxygen (DO)
• amount of oxygen
present in water.
• DO is measured in ppm
18. 11/9/2022 18
If BOD level in effluent is not
controlled, the rate of Oxygen
consumption > Oxygen
replenishment from the
atmosphere, thus affecting the
marine species in the water-
body where the effluent is
discharged.
Amount of oxygen
needed to oxidize
organic and inorganic
materials in a waste
water effluent
20. Rahman et al.(2017)
To establish date seeds PAC as an affordable
alternative to other expensive tertiary methods
1
11/9/2022 20
21. 11/9/2022 21
)
Date seeds :(Rajshahi and Jessore districts of Bangladesh)
Textile waste water- Composite textile industry
Materials
Preparation
of
adsorbent
Method
of
analysis
Drying, carbonizing, Activation, Filtering, Washing
Activating agent: ZnCl2
Color conc.= Spectrophotometer (Pt-Co) pH=pH meter
Weight of Activated Carbon = electronic balance
Temp.= thermometer Particle size= US standard sieves
(<150µm,150-300µm,300-425µm)
MATERIALS AND METHODS
Experiment
Batch adsorption experiments
Effect of contact time, adsorbent dosage, temperature,
agitation speed, particle size, pH on color removal
22. Fig. 1 Preparation of adsorbent
Date seeds
11/9/2022
22
Washing and drying
Cut into small pieces and packed in a crucible
Carbonization in muffle furnace at 5000C for 1 hr.
Activation
Mass ratio of 1:1 is maintained
Soaking, filtering, washing and drying(1000C for 1 hr.)
1M ZnCl2
Muffle furnace
pH=4.47
23. 11/9/2022 23
Waste water= 100 ml
pH=8
Activated carbon= 0.5g
placed in a rotating
shaker
Agitation for
5,10,15,20,25min
Supernatent
extracted by pipette
Quantities of adsorbent: 0.4,0.6,0.8,1.0,1.2&1.4g
Temperatures: 300C, 350C, 450C
Agitation speeds: 150,200,250rpm
Particle size: <150µm, 150-300µm & 300-425µm
Initial colour conc.: 800,1000,1200 Pt-Co
Batch adsorption
Filteration using
0.45µm
Contact time
28. • Efficient for the removal of color of textile
effluent
• As a high percentage of color removal was
obtained for a wide range of initial color
concentrations from batch experiments.
11/9/2022 28
CONCLUSION
29. To investigate the efficiency of sugarcane bagasse
activated carbon modified by phosphoric acid as
adsorbent for the removal of zinc (Zn) and Ferrus (Fe)
from the textile wastewater
2
Razi et, al.(2018)
11/9/2022 29
30. METHODOLOGY
11/9/2022 30
• Textile waste water: Syarikat Koon Fuat Ind.
• Sugarcane bagasse: sugarcane bagasse juice
vendor
• Activating agent: phosphoric acid(H3PO4)
Sample
collection
• Batch experiment
• Effect of contact time, adsorbent dosage, pH
for removal of Zinc and Ferrous
Testing
31. Preparation of sugarcane bagasse activated carbon
Raw sugarcane bagasse
(SB juice center)
Washing & drying(1050C
for 24 hr.)
Impregnation with 30%
phosphoric acid(H3PO4)
for 24 hr.
Carbonization(5000C in
furnace for 2h)
Drying (room temp) %
washing(distilled water)
Sieving by 63 micron
(ASTMC136-06)
CHEMICAL
ACTIVATION
11/9/2022 31
32. Table1: Working range of Fe and Zn
Heavy metal Contact time adsorbent
dosage (g)
pH
Fe 30min, 75min, 120
min, 180 min, 1440
mins
0.6, 2.0, 4.0,
6.0
2, 3, 4, 5, 6, 7
Zn 30min, 75min, 120
min, 180min, 1440
mins
0.6, 2.0, 4.0,
6.0
2, 3 ,4, 5, 6, 7
Batch experiment
1. Control sample without adsorbent
2. Prepared sample:
100ml textile waste water
Activated carbon 63µm
Analysis for metal
ions removal
11/9/2022 32
35. Parameters Before After
PH 5.6 6
BOD 97.8 28.71
COD 146.65 45.20
TSS 64.25 22.14
NH4-N 1.38 0.82
Nitrate 1.45 0.67
Fe 5.42 0.62
Zn 1.16 0.12
Fig. 10 SEM Images
Table 2 Characteristics of Textile
waste water before and after process
under optimum conditions
A) Control sample
B) SBAC treated sample
11/9/2022 35
36. • Efficient adsorbent of removal of metal ions
• Key factors found to control the adsorption
efficiency of the SBAC included adsorbent
dose, contact time and pH
• 91% Fe and 89% Zn (metal removal)
• Low cost and readily available
CONCLUSION
11/9/2022 36
37. Olaoye, R.A. et al
(2018)
To determine the adsorbent effect on the
concentration of waste water
3
11/9/2022 37
38. 38
Methodology
• Textile waste water: Wollen and Synthetic textile
manufacturing industry, Nigeria
• Rice husk: Institute of Agricultural and Research
Training, Nigeria, Activating agent: (HNO3)
Sample
collection
• Weighing meter, Shaker, Angle centrifuge
machine, pH meter, Hanna Multiparameter
instrument HI 9812-5 instrument,
DO/COD/BOD Hanna instrument H1 9141-04
instrument, 210VGP Atomic Absorption
Spectrophotometer
Equipments
used
• 300g dried rice husk +HNO3 for 60minutes
• Rinsing and oven drying at 1100C
• Sieved through BSS-mesh 30
Preparati
on of
activated
rice husk
39. 39
Methodology
• Six samples
• Sample A(untreated), B(4gARH), C(8g),
D(12g), E(16g), F(20g)
• B-F thoroughly mixed , contact time 60 min
at 150rpm, centrifuge at a constant resolution
of 400rpm for 40 min
Remediation
Procedure
• Scientific 210VGPAtomic Absorption
Spectrophotometer: heavy metal
concentration
• TDS and pH: Hanna Multiparamete
instrument - HI 9812-5.
• Alkalinity :potentiometric method of
titration
• DO/COD/BOD: Hanna H1 9141-04
instrument
Characterization
of wastewater
41. 0 5 10 15 20 25 30 35
Turbidity
DO
Alkalinity
COD
BOD
Mg
F
E
D
C
B
A
Turbidity DO Alkalinity COD BOD Mg
A 1.5 30 30 7.8 4 5.25
B 0.377 26 1.05 6 2.2 3.1
C 0.308 26.6 1.3 4.4 2.1 3.41
D 0.251 27.5 1.25 3.8 2 3.5
E 0.223 28.2 1.23 4.8 2.1 3.65
F 0.158 28 1.3 5.8 2.23 3.8
Fig. 11: Average wastewater concentration before and after remediation
11/9/2022 41
42. 0 1 2 3 4 5 6 7 8
Pb
Cd
Zn
Cr
Cu
F
E
D
C
B
A
Pb Cd Zn Cr Cu
A 0.221 6.35 3.32 1.12 6.35
B 0.044 0.008 2.57 0.7 6.48
C 0.005 0.008 1.54 0.789 7.11
D 0.01 0.02 2 0.55 7.06
E 0.015 0.03 1.87 0.543 6.65
F 0.02 0.046 1.65 0.6 6.77
Fig. 12: Average wastewater concentration before and after remediation
11/9/2022 42
44. • Maximum removal efficiency: Total alkalinity,
turbidity, cadmium and lead with percentage
values between 95-97%,80%- 92%, 99.3%-
99.8% and 80-98% respectively
• Adsorption was found to be more effective at
lower adsorbent dose because the concentration
of most of the parameters tested was reduced at
ARH dose of 8g
CONCLUSION
11/9/2022 44
45. Wu, et.al (2019)
To investigate the effect of activation state,
carbonization temperature, carbonization time,
adsorption time during decolourization
4
11/9/2022 45
46. METHODOLOGY
11/9/2022 46
• Peanut shells: local market, Nanjing city,
China
• Reagents: Reactive brilliant blue X-BR and
phosphoric acid
Sample
collection
• Preparation of simulated wastewater
• Preparation of PSAC (C-PSAC-400, CA-
PSAC-400, AC-PSAC-400 respectively)
Experimental
scheme
Testing
Surface characteristics of activated carbon
Effect of preparation methods and dosages
Effect of carbonization temp.
Effect of carbonation time
48. Fig. 15 SEM images
Peanut Shell
PSC
PSAC activated by phosphoric acid
11/9/2022 48
a)
b)
c)
49. Fig. 16 Effect of dosages on the adsorption
at 4000C at 5000C
11/9/2022 49
at 6000C at 7000C
50. Fig. 17 Effect of carbonization temperature on removal rate
11/9/2022 50
100%
51. Fig. 18 Effect of carbonization time on the removal rate
11/9/2022 51
98.74%
52. • Phosphoric acid treated peanut shell had high specific surface
areas and a large number of mesopores
• (AC-PSAC-450-3) activated by 50% phosphoric acid was the
best
CONCLUSION
11/9/2022 52
53. To know the effect of ecofriendly adsorbent on colour
removal from textile dyeing effluent
5
Elango and
Govindasamy (2019)
11/9/2022 53
54. METHODOLOGY
11/9/2022 54
• Textile dyeing effluent: Coimbatore(TN)
• Waste flower : temples of Coimbatore(TN)
• Activating agent: Na2SO4 and KOH
Sample
collection
• Batch experiment
• Effect of contact time, adsorbent dosage
for colour removal
• Surface characterization
• FeSEM
• Physico-Chemical parameters of water
effluent
Testing
55. Area of the study : Coimbatore district, Kongu Nadu region
METHODOLOGY
Collection of flowers Washing and drying
Powder form using
mixer
10g is taken in crucible
and heated at 5500C (2h)
Cooling and washing
Drying at 1100C (6h)
Fine powder (110µm) FWD
P
Y
R
O
L
I
S
I
S
11/9/2022 55
56. Production of activated carbon by chemical activation with
Na2SO4 and KOH
Treatment of 10g starting material with 50ml of 0.1N Na2SO4
(24h)
Decantation
Material was kept in crucible and heated in muffle furnace
at 4500C(2h)
Cooling and washing(pH=7)
Drying in oven at 1100C(3h)
Fine powder (110µm) FWP
FWS
KOH
11/9/2022 56
57. Table 3: Methodology of the study using standard procedures
Physico- chemical parameters Methods
Color Spectrophotometer
pH at 300C pH meter
Total hardness Complexometric titration
BOD, mg/l Incubating the sample at 3000C for 5 days followed
by titration
COD, mg/l Closed reflux method
TDS, MG/L Gravimetric, oven drying at 105⁰C
TSS, MG/L Gravimetric, oven drying at 105⁰C
Turbidity Nephlometer
Chlorides, as Cl-, mg/l Argentometric titration
Sulphides,asS2
-, mg/l Iodometric method
Silica,as Sio2, mg/l Spectrophotometer
Calcium, as Ca, mg/l Complexometric titration
Iron, as Fe, mg/l Spectrophotometer
Oil and grease, mg/l Partition-gravimetric method
11/9/2022 57
59. Table 4: Elemental analysis of activated carbon FWD, FWS and FWP by EDS
Activated Carbon Elements Present Percentage
FWD
C 99.45
Na 0.17
Ca 0.15
Mg 0.23
O 0.00
FWS
C 98.01
Mg 0.66
P 0.16
K 0.30
Ca 0.87
O 0.00
FWP
C 98.64
Mg 0.69
K 0.11
Ca 0.57
O 0.00
11/9/2022 59
60. Table 5:Physico-chemical parameters of activated carbon FWD, FWS and
FWP
Parameters FWD FWS FWP Standard values as per ASTM
pH 7.63 7.34 6.87 6-8
Conductivity at
250C
0.29 0.13 0.18 Depends on raw material
Moisture content,% 5.2 6.3 8.9 5-8
Ash content, % 4.0 5.2 6.9 5-15
Volatile matter,% 17.4 19.4 20.75 37.5±0.03
Matter soluble
water
0.81 1.11 0.99 <1
Matter soluble acid 0.94 1.36 1.16 <3
Bulk density, g/ml-1 0.48 0.52 0.42 0.25
Specific gravity 0.80 0.89 0.98 1.8
Porosity,% 65.0 53.93 59.18 40.85
Fixed carbon,% 73.4 65.2 63.45 Depends on raw material
Yield,% 63.7 51.0 50.8 Depends on raw material
BET surface area 672.2 272 232.2 600-1200
11/9/2022 61
61. Table 6: Physio - chemical parameters of textile effluent
Parameters Observed values BIS limits
Color 4800 25
pH at 300C 7.96 5.5-9
Total hardness 810 500
BOD, mg/l 760 100
COD, mg/l 2180 250
TDS, MG/L 18,220 2,100
TSS, MG/L 5992 100
Turbidity 69.5 10
Chlorides, as Cl-, mg/l 31287 600
Sulphides,asS2
-, mg/l 0.21 2
Silica, as Sio2, mg/l 891 250
Calcium, as Ca, mg/l 118.2 200
Iron, as Fe, mg/l 0.14 3
Oil and grease, mg/l 12 10
11/9/2022 62
63. Fig.20 Effect of adsorbent dosage
Fig. 21 Effect of adsorbent time
11/9/2022 64
64. • Waste minimization method by reducing temple waste flowers
into activated carbon by direct pyrolysis, Na2SO4, and KOH
process
• Activated carbon prepared by direct pyrolysis process is
excellent
• All the parameters are high in concentration than the standards
given by BIS except calcium, sulfide, and iron
• Colour removal efficiency was achieved maximum of 98.17 at
200mg. The colour removal was high 95.83 % at 100 min
CONCLUSION
11/9/2022
65
65. “Every year, more people die from the
consequences of unsafe water than from all
forms of violence, including war”
11/9/2022 66
67. Splendore et.al
(2010)
To evaluate the thermo-physiological comfort of a knitted
polyester (PES) fabric incorporated activated carbon
6
11/9/2022 68
68. 69
Methodology
• PES fabric
• Modified PES fabric(incorporated activated carbon)
Samples
• Determination of mass per unit area (EN12127:
1998);
• Determination of thickness (ISO5084:1996)
• Air permeability (AP) (ISO9237:1995)
Fabric
Characterization
• Water vapour resistance and thermal resistance:
skin model prototype Permetest
• Thermal conductivity and diffusion: Alambeta
system
• Vertical wicking: Tensiometer K100
• Drying rate & Buffering capacity: Climatic chamber
Thermo-
physiological
properties
70. 11/9/2022 71
Table 7: Mass per unit area, thickness and Air Permeability
Ret (Pa M2w-1) %WVP (%) Rct (KW-1)
Fabric A 1.8 73.9 11.63
Fabric B 2.2 70.8 15.07
Ret= absolute water vapor resistance; %WVP=relative water
vapour permeability Rct= thermal resistance
Table 8: Permetest results
Mass per unit
area(g/m2)
Thickness(mm) AP(mm/s)
Fabric A 148.54 0.646 1325
Fabric B 159.50 0.742 973
74. 11/9/2022 75
CONCLUSION
Vertical wicking confirmed that the modified fabric had a
better hydrophilicity than the conventional one.
Liquid management of the modified PES fabric is better but,
on the other hand, desorption is slow and drying time is
longer for the modified fabric than the conventional one.
Wet heat loss is smaller for the modified PES
75. Chen et al.
(2010)
To study the process of cotton nonwoven formation,
carbonization, activation and characterization of
activated carbon nonwoven
7
11/9/2022 76
76. 11/9/2022 77
• Naturalfibres,Carding,Needlepunching,Carb
onization and Activation
Nonwoven
fabrication
• TGA(Thermogravimetric analysis):
2950TGAHR(to optimize the process of
carbonization)
• Protective abilities for adsorping and
absorbing chemicals: IGC(Inverse gas
chromatography)
Analysis
METHODOLOGY
79. 11/9/2022 80
Fig. 27 SEM images a) Raw Cotton b) Carbonized cotton c) Carbonized and activated
a) b) c)
a) b)
Fig. 28 SEM surface a) Carbonized cotton b) Carbonized and activated
80. 11/9/2022 81
Fig. 29 Dispersive Surface
Energy
Fig. 30 Specific free energy of
desorption
81. 11/9/2022 82
Surface
Energies(mJ/m2)
Raw Cotton Carbonized
Cotton
Activated
Cotton
Dispersive 33.63 32.86 33.71
Polar 94.62 117.22 110.84
Total 128.25 150.08 144.55
Table 10: Total Surface Energies
82. • Decrease in weight loss in the region of 250°C to400°C and
the proper carbonized temperature was 400°C.
• Surface area increases dramatically due to the widely opened
hollow of the cotton
• Fiber and some small agglomerated particles gasified after
activation
• All surface energy Carbonized Cotton> Activated Cotton >
Raw Cotton.
• Potential for use as high adsorbent material
11/9/2022 83
CONCLUSION
83. Bhati et al.
(2013)
To investigate the consequence of activation
temperature, activation time and CO2 flow rate on
the surface and adsorption properties of ACF
8
11/9/2022 84
84. Material
Viscose rayon
knitted fabric
(280-300g/m2)
Phosphoric acid(H3PO4)
85%
CO2
(i) Strips (15*15cm2) of viscose
rayon fabric immersed in an
aqueous solution of phosphoric
acid of conc. 5% for 1 hr. at 700C
(ii) Immersed samples were
drained and dried in a hot air
oven at temp. of 850C for 3 hr.
(iii) Heat treatment under the
flow of nitrogen and then
activated at different temp. for
different time under CO2 atm.
11/9/2022 85
Preparation of ACF by mixed activation method
Testing: Surface and
adsorption properties
Pretreated fabric(PF)
METHODOLOGY
85. Fig. 31Thermograph of Viscose rayon fabric and
Pretreated fabric
11/9/2022 86
RESULTS AND DISCUSSION
87. Fig.32 Effect of activation temp.
(a) Micro porosity and SBET
(b) Pore size distribution and pore
volume
(c) Activation time=60min, CO2 flow
rate=200ml/min
Fig. 33Effect of activation time
(a) Micro porosity and SBET
(b) Pore size distribution and pore
volume
(c) Activation temp=8500C, CO2 flow
rate=200ml/min
11/9/2022 88
88. Fig.34 Effect of CO2 flow rate
(a) Micro porosity and SBET
(b) Pore size distribution and pore volume
(c) Activation time=60min, CO2 flow
rate=200ml/min
11/9/2022 89
89. Fig. 35 SEM images
ACF-850/60/200
ACF-925/60/200
ACF-925/60/200
11/9/2022 90
90. • The SBET and micropore increased with an increase in activation
temperature. On the other hand, the Pmicro of the samples
continuously decreased due to the conversion of micropores to
mesopores
• Increase in Pmicro up to 45 minutes followed by decrease in
microporosity, indicating the conversion of micropore into
mesopore
CONCLUSION
11/9/2022 91
91. Gunasekaran et al.(2015)
To know the effect of Neem based charcoal on anti-
bacterial, wicking, air permeability and thermal
resistance properties of cotton fabrics
11/9/2022 92
9
92. FABRIC SAMPLE: 100% Cotton fabric
Precursor: Neem charcoal particles
Equipment used: Flash and fire point instrument(Preparation for
neem charcoal)
High enery ball milling machine(For neem
charcoal particles)
Zeta Sizer (Partice size)
Padding mangle (Application of finish)
Testing: Antibacterial property (AATCC100-1993)
Wicking (AATCC197-2011)
Air Permeability (ASTM D737-2004)
Thermal resistance (M259B Sweating guarded hot
plate)
11/9/2022 93
METHODOLOGY
93. Raw Neem sticks
(0.7* 0.7 cm)
Drying (2weeks) Carbonization(1200C)
Placing of Neem pieces
in in metallic container
Yellowish gas emanated
from the container
Cooling at room temp. and
preparation of charcoal
particles
Preparation of Neem Charcoal
11/9/2022 94
Preparation of Neem Particles
94. Preparation of Neem Particles
Particle Size: 370.8nm at 100% intensity
Zeta potential: 0-(-35mV)
ZETA SIZER Dynamic Light Scattering(DLS)
11/9/2022 95
95. RESULTS AND DISCUSSION
Fig. 36 SEM Image of Control cotton and Treated cotton
Control cotton Treated cotton
11/9/2022 96
96. Table 12 Anti bacterial activity of control and treated fabrics
Table 13 Air Permeability of control and treated fabrics
11/9/2022 97
97. Table 14 Wicking of control and treated fabrics(capillary rise in mm)
CONCLUSION
11/9/2022 98
• Increase in fabric wicking up to about five minutes of contact with water, but
thereafter shows a gradual decrease up to 60 minutes reduces the air
permeability to the tune of around 35%
• Increase in the thermal resistance
• Thermal conductivity of the fabric would thus be slightly lower
• Fabric wicking tend to initial increase followed by a decrease due to the
neem-charcoal finish
98. To investigate the effect of activated carbon on anti-
bacterial, anti- fungal and absorbency properties of
cotton and bamboo nonwoven fabrics
11/9/2022 99
10
Pragadheeswari and
Sangeetha (2017)
99. • 100% cotton and bamboo non woven fabric
• Activated charcoal(commercially available)
Samples
• Direct method
• Microencapsulation method
Finishing
• Antibacterial(Disc diffusion method)
• Antifungal(AATCC 30 - 2003 Test Method)
• Absorbency assessment(AATCC Test Method 39-
1980)
Testing
11/9/2022 100
MATERIALS
100. Direct Method
Microencapsulation
Method
20% of activated carbon
powder, 10% of binder,
1:20 (M:L)
Spraying of AC on one side
of fabric by even coating
Drying and curing at 1000C
for 5-10 min
1L solution containing
700g microcapsules
5% emulsion binder (cross
linking agent)
M:L=1:20
Spraying of AC on one side
of fabric by even coating
Drying and curing at 1000C
for 5-10 min
11/9/2022 101
101. Fabric sample Finishing
Zone of inhibition (mm)
S.aureous E.coli
Cotton
Direct 21 18
Micro-encapsulation 25 23
Bamboo
Direct 23 20
Micro-encapsulation 26 21
Fabric sample Finishing
Zone of inhibition (mm)
Aspergillus niger
Cotton
Direct 46
Micro-encapsulation 52
Bamboo
Direct 49
Micro-encapsulation 54
Table 15 Evaluation of antibacterial assessment
Table 16 Evaluation of antifungal assessment
11/9/2022 102
RESULTS AND
DISCUSSION
102. Fabric sample Finishing
Zone of inhibition
(mm)
Aspergillus niger
Cotton
Direct >2sec
Micro-
encapsulation
>3sec
Bamboo
Direct >2 sec
Micro-
encapsulation
>2 sec
Fig. 17 Evaluation of absorbency test
11/9/2022 103
103. • Anti-bacterial, Anti-Fungal property was
maximum for coated fabric
• Moisture absorbency also shows the better
result
11/9/2022 104
CONCLUSION
104. To know the effect of activated carbon of coffee
residue on the functional properties of weft knitted
polyester mattress fabric
Wan et al.(2018)
11/9/2022 105
11
106. Sample Density of
right side
Density of
reverse side
Thickness
/mm
Surface density
/(g·m-2)
DTY+ AC 50 56 1.35 230.4
DTY 50 56 230.1 5035.2
Spun yarn 51 56 246.6 5447
11/9/2022 107
Table 18 Characteristics of three mattress fabrics
107. RESULTS AND DISCUSSION
Total number of bacterial colony
Sample 101 102 103 104 bacteriostatic rates
Control fabric > > >300 103 —
DTY with AC > > 17 5 91.30%
DTY > > 101 42 59.20%
Spun yarn > > 158 38 63.10%
11/9/2022 108
Table 19 Antibacterial property
108. Fig.1 Photos of Escherichia coli colony: (A) control fabric, (B) PET-DTY
with ACs, (C) DTY, and (D) spun yarn.
(A) (B) (C) (D)
Fig.2 SEM images for PET fibers: (A) DTY+ AC (B) DTY and (C)
Spun yarn.
(A) (B) (C)
11/9/2022 109
109. Yarn type Breaking strength, cN Elongation at break,
%
Breaking time, s
DTY with AC 597.4 19.99 4.77
DTY 688.6 25.89 6.17
Spun yarn 568.2 11.54 2.81
Yarn type Heat preservation ratio, % Thermal conductivity
coefficient
CLO value
DTY with
AC
32.77 31.91 0.21
DTY 28.02 38.68 0.17
Spun yarn 35.8 27.64 0.24
Table 3 Warmth retention property of three mattress fabrics
Table 2 Tensile properties of three mattress fabrics
11/9/2022 110
110. Numbers of rubs
Material 125 500 1000 2000 3000 4000 5000
DTY with
AC
5 5 4.5 4 3.5 3.5 3.5
DTY 5 5 4.5 4.5 4 3.5 3.5
Spun yarn 3-4 5 2.5 1-2 1 1 1
Table 20 Pilling grade assigned to mattress fabrics
11/9/2022 111
111. Fig. 38 Moisture permeability
of three mattress fabrics
Fig. 37 Wettability of three
mattress fabrics
11/9/2022 112
112. Fig. 39 Pills distribution of mattress
fabrics after 3,000 rubs: (A) DTY with
AC, (B) DTY, and (C) spun yarn
(A)
(B)
(C)
11/9/2022 113
113. • Higher antibacterial rate 93.1% has been achieved
by DTY+AC
• Non circular cross section restricts the inner fibre
protruding and reduced the entanglement of end
fibres thus pilling propensity of fabric is reduced
• No apparent changes in the chemical structures of
PET-DTY with or without AC
• AC does not affect the tensile property of PET-
DTY
CONCLUSION
11/9/2022 114
114. References
11/9/2022 115
1. Chen, Y., Jiang, N., Sun, L, and Negulescu, I, 2010, Activated carbon nonwoven as
chemical protective Materials. Res. J. of Text. Apparel., 10(3):1-7.
2. Elango, G, and Govindasamy, R, 2018, Removal of colour from textile dyeing
effluent using temple waste flowers as ecofriendly adsorbent. IOSR J. of App. Che.,
6(1):19-28.
3. Gunasekaran, G., Periyasamy, S., and Koushik, C.V, 2015. Effect of neem-charcoal
application on functional properties of cotton fabric. Int. J. for Sci. Res. & Dev.,
3(2):114-118
4. Kandhavadivu, P., Vigneswaran, C., Ramachandran, T., and Geethamanohari, B,
2010, Development of polyester-based bamboo charcoal and lyocell-blended union
fabrics for healthcare and hygienic textiles. J. Ind. Tex., 41(2) 142–159.
5. Razi, M., Gheethi, A, Izzatul, Ashikin Z, A, 2018, Removal of heavy metals from textile
wastewater using sugarcane bagasse activated carbon. Int. J. of Eng. and Tech., 7(4):112-
115
6. Splendore, R., Dotti, B., Cravello, A. and Ferri, 2010, Thermo-physiological comfort of a
PES fabric with incorporated activated carbon. Int. J. Cloth. Sci. and Tech.,
22(5):333-342.
7. Wu, H., Chen, R., Du, H, and Zhang, J, 2018. Synthesis of activated carbon from peanut
shell as dye adsorbents for wastewater treatment. Ads. Sci. & Tech., 37(1):34–48.
8. Xia, D., and Wang, L., (2013), Dyeing performance of coconut charcoal polyester fabrics.
Sen’I Gakkaishi., 69(11):205-212.
REFERENCES
Activated carbon is an inert solid adsorbent material commonly used to remove diverse, dissolved contaminants from water and process gas-phase streams. It is made from almost any feedstock that contains carbon, including coconut shells and coal family members, as many readers will already know.
Adsorption is the accumulation of a gas or liquid on the surface of a liquid or solid substrate, as opposed to absorption, in which the encroaching substance enters the substrate’s bulk or volume.
Activated carbon is porous, inexpensive and readily available for use as adsorbents, furnishing a large surface area to remove contaminants. It has more useful surface area per gram than any other material available for physical adsorption. In fact, a teaspoon of activated carbon has more surface area than a football field.
Adsorption is a surface phenomenon. Molecules in a fluid (gas or liquid) are adsorbed by the attractive force (Van der Waals force) of the surface of the solid body (activated carbon) to cause adsorption. Difficulty of adsorption is affected, in many cases, by the condensation characteristics of the gas when the adsorbed material is a gas, and by the solubility of the dissolved material in the case of liquids. The micropores promote adsorption via capillarity. In the case of gas phase, gas is condensed by the capillarity and turns to liquid, which increases adsorption.
Taken together, these are called physical adsorption. The adsorption is rapid and reversible, which means it can be easily desorbed by heating or decompression.
In addition to physical adsorption, there is also chemisorption accompanied with chemical reactions. This phenomenon is seen with activated carbon impregnated with acid or alkali. Chemisorption selects only the material that reacts and the phenomenon is irreversible
which can be rather complex in practice.
that greatly expands the material’s internal surface area
network of pores that extend from the ones that naturally occur in the carbonaceous raw material
Activation results in a distribution of pore sizes and shapes that depend on the nature of the starting material and on the details of the manufacturing process.
Macroscale pores are greater than 50 nm in size, while mesoscale pores range from 2–50 nm and microscale pores less than 2 nm wide
A gram of activated carbon can have a surface area in excess of 500 m2 (5,400 sq ft), with 3,000 m2 (32,000 sq ft) being readily achievable.[2][4][5] Carbon aerogels, while more expensive, have even higher surface areas, and are used in special applications.
Under an electron microscope, the high surface-area structures of activated carbon are revealed. Individual particles are intensely convoluted and display various kinds of porosity; there may be many areas where flat surfaces of graphite-like material run parallel to each other,[2] separated by only a few nanometers or so. These micropores provide superb conditions for adsorption to occur, since adsorbing material can interact with many surfaces simultaneously. Tests of adsorption behaviour are usually done with nitrogen gas at 77 K under high vacuum, but in everyday terms activated carbon is perfectly capable of producing the equivalent, by adsorption from its environment, liquid water from steam at 100 °C (212 °F) and a pressure of 1/10,000 of an atmosphere.
James Dewar, the scientist after whom the Dewar (vacuum flask) is named, spent much time studying activated carbon and published a paper regarding its adsorption capacity with regard to gases.[20] In this paper, he discovered that cooling the carbon to liquid nitrogen temperatures allowed it to adsorb significant quantities of numerous air gases, among others, that could then be recollected by simply allowing the carbon to warm again and that coconut based carbon was superior for the effect. He uses oxygen as an example, wherein the activated carbon would typically adsorb the atmospheric concentration (21%) under standard conditions, but release over 80% oxygen if the carbon was first cooled to low temperatures.
Physically, activated carbon binds materials by van der Waals force or London dispersion force.
Activated carbon does not bind well to certain chemicals, including alcohols, diols, strong acids and bases, metals and most inorganics, such as lithium, sodium, iron, lead, arsenic, fluorine, and boric acid.
Activated carbon adsorbs iodine very well. The iodine capacity, mg/g, (ASTM D28 Standard Method test) may be used as an indication of total surface area.
Carbon monoxide is not well adsorbed by activated carbon. This should be of particular concern to those using the material in filters for respirators, fume hoods or other gas control systems as the gas is undetectable to the human senses, toxic to metabolism and neurotoxic.
Substantial lists of the common industrial and agricultural gases adsorbed by activated carbon can be found online.[21]
Activated carbon can be used as a substrate for the application of various chemicals to improve the adsorptive capacity for some inorganic (and problematic organic) compounds such as hydrogen sulfide (H2S), ammonia (NH3), formaldehyde (HCOH), mercury (Hg) and radioactive iodine-131(131I). This property is known as chemisorption.
Iodine number
The most common raw materials used are wood, charcoal, nut shells, fruit pits, brown and bituminous coals, lignite, peat, bone, paper mill waste (lignin), synthetic polymers (e.g., PVC). Activated carbon obtained from hard wood is preferable for adsorption because charcoal obtained from soft wood, such as pinewood, is very unstable and readily crumbles. The chemical properties of the adsorbate (e.g., dye) and adsorbent (e.g., activated carbon) are also very important for adsorption because there has to be some interaction between the adsorbate and adsorbent. If the adsorbate combines well with activated carbon, it will enhance the removal of adsorbate. Activated carbon is advantageous for the adsorption of dyes; its large porous surface area, controllable pore structure, thermo-stability, and low acid–base reactivity have been established in terms of its versatility for the removal of different types of dyes dissolved in aqueous media. The uptake of dyes onto the activated carbon is fostered by the interaction between the functional groups of the dye and activated carbon. Adsorption greatly depends on the porous structure and surface functional groups of the activated carbon
Effluent in the artificial sense is in general considered to be water pollution, such as the outflow from a sewage treatment facility or the wastewater discharge from industrial facilities.
Amount of dissolved oxygen needed by bacteria in ETP to break down organic material present in the Effluent
Pt-Co: intensity of yellow-tinted samples
A litre of textile wastewater was collected in five different bottles, and prepared adsorbent (ARH) was varied in each of the samples. Sample A was left untreated. Sample B was treated with 4g of ARH, sample C was treated with 8g of ARH, sample D was treated with 12g of ARH, sample E was treated with 16g of ARH and sample F with 20g of ARH (Appendix). Samples B - F were thoroughly mixed with a shaker at a constant contact time of 60 minutes at 150rpm to ensure equilibrium in concentration for adsorption to take place. Similar procedure was carried out by Gidde19. 25ml of samples B – F were measured in triplicates, kept in an angle centrifuge machine at a constant revolution of 400rpm for 40 minutes at room temperature for the residue to settle to the bottom of the test tube. The samples were then filtered through Whiteman filter paper. The liquid filtrate from each sample was collected in a 10ml test tube and taken to the laboratory for physico-chemical characterization. The following parameters were analyzed: pH, Colour, Total Alkalinity, Turbidity, Total Dissolved Solids (TDS), Biochemical Oxygen Demand (BOD), Chemical Oxygen Demand (COD), and Heavy Metals; Copper (Cu), Lead (Pb), Cadmium (Cd), Zinc (Zn), Chromium (Cr). Concentration before treatment (sample A) and after dosing with ARH (samples B - F) was compared with the World Health Organization (WHO), the National Agency for Food and Drugs Administration Council (NAFDAC) and the Lagos state Environmental Protection Agency (LASEPA) effluent discharge limits.
Higher temperatures increase the energy and therefore the movement of the molecules, increasing the rate of diffusion. Lower temperatures decrease the energy of the molecules, thus decreasing the rate of diffusion.
. The decrease in the removal of MB dye with increase in temperature may be due to weakening of the adsorptive forces between the MB dye molecules and the active sites of STOP and also between the adjacent molecules of the adsorbed phases.
Permetest instrument (Fig. 2) is the so called skin model, which simulates dry and wet human skin in terms of its thermal feeling and serves for determination of water vapour and thermal resistance of fabrics
Thermal resistance is a heat property and a measurement of a temperature difference by which an object or material resists a heat flow. Thermal resistance is the reciprocal of thermal conductance
The water vapor permeability of a material is defined by its ability to let water vapor pass through it under the action of pressure between its two opposite faces
The thermal conductivity of a material is a measure of its ability to conduct heat.
Thermal diffusion: It measures the rate of transfer of heat of a material from the hot end to the cold end
SBET: Brunauer-Emmett Teller (BET) aims to explain the physical adsorption of gas molecules on a solid surface.
Pore Volume (PV) is defined as the ratio of a porous material's air volume to a porous materials total volume. ... For our purposes, the total volume of a part is described by the amount of space contained within an imaginary film that has been tightly shrunken around the outside of the porous part's exterior geometry.
Activation temperature largely influences the surface area, Vmicro, Vmeso and PSD of ACF.
Activation of viscose rayon fabric at 850 °C for 15 to 60 minutes of activation time was found to increase the SBET and Vmicro from 1254 to 1964 m2/g and 0.44 to 0.72 cc/g respectively.
Today, people having the growing awareness among consumers, especially younger generations towards the sustainability of product. All strategies, promoting more environmentally, socially and ethically conscious production and consumption of this sustainable industry. Technological processing to be done in order to produce the desired powdered form and it applied for several functional finishes for further analysi
The spinning process for to the PET fibres with coffee carbon particles is a promising technology for the antibacterial activity of weft-knitted mattress fabrics.
The microporous AC with high specific surface area benefits the water transport and moisture penetration. The non circular cross-section restricts the inner fibres protruding and reduced the entanglement of end fibres on the mattress surface during the rubs