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ISSN 2349-4344 (Online)
Journal of
Catalyst & Catalysis
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September–December 2016
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STM JOURNALS
1. An Use of Solar Energy Based Photocatalyst for Degradation of Water Pollutants
Ram Babu Pachwarya, Deepchand Saini, R.C. Meena, A.L. Ramnathan 1
2. Fire-Mechanical Properties of Geopolymer Concrete
Ali I. Al-Mosawi, Shaymaa Abbas Abdulsada 6
3. Identification of Some Imported Lubricating Oil Additives Used in Libya and Synthesis of the
Most Consumed Ones from the Local Raw Materials
Abdurahman A. Abuabdalla Khalifa, Rajab Maga 10
4. Synthesis and Study of Different Thioamides as Corrosion Inhibitors
Abdurahman A. Abuabdalla Khalifa 18
5. Phytoextraction of Lead and Chromium by Leafy Vegetables (Lettuce, Kale and Swiss chard)
Mamu H. Teferi, Dejene A. Tessema 26
ContentsJournal of Catalyst & Catalysis
JoCC (2016) 1-5 © STM Journals 2016. All Rights Reserved Page 1
Journal of Catalyst and Catalysis
ISSN: 2349-4344(online)
Volume 3, Issue 3
www.stmjournals.com
An Use of Solar Energy Based Photocatalyst for
Degradation of Water Pollutants
Ram Babu Pachwarya1,
*, Deepchand Saini2
, R.C. Meena3
, A.L. Ramnathan2
1
Department of Chemistry, Motilal Nehru College, University of Delhi, New Delhi, India
2
School of Environmental Sciences, Jawaharlal Nehru University, New Delhi, India
3
Department of Chemistry, Jai Narain Vyas University, Jodhpur, Rajasthan, India
Abstract
Azo dyes/Dyes, pesticides, weedicide, etc. are highly harmful and carcinogenic in nature.
Dyes especially azo dyes reduces fertility of soil. Treatment of dye pollution even pesticides,
weedicides is challenging for environmentalists. The photocatalytic degradation of most of
water-soluble organic pollutants by heterogeneous photocatalyst ZnO in the presence of
sunlight is best and sustainable method. We also found the influence of different parameters
like light intensity, temperature, amount of catalyst, pH of the solution, light intensity. It has
been found that ZnO is capable to degraded/remove most of water-soluble organic pollutants
in the presence of sunlight. The merits of the technic are: (1) we can use same catalyst many
times and it works well every time. (2) Techniques is based on sunlight. We also applied this
technology for treatment of sewage water and we observed that this catalyst is fully capable to
remove all kind of water-soluble pollutants we got more than 99% transparent water in few
hours irradiation of sunlight.
Keywords: Non-biodegradable, degradation, ZnO, TiO2, photocatalytic azo dyes
INTRODUCTION
Degradation of water pollutants is a
challenging task much more difficult because
of variety of pollutants including non-
biodegradable water-soluble organic
pollutants. Most of Sewage water pollutants
are non-biodegradable in nature, so
conventional treatment methods are not
capable to remove these pollutants from
pollution cycle. Advance oxidation process
(AOP) heterogeneous photocatalyst ZnO can
prove a promising technology for treatment of
sewage water. This technic has shown its
capability to degrade all kind of water-soluble
organic pollutants including non-
biodegradable pollutants. Heterogeneous
photocatalyst can be used for treatment of
sewage water, paper industries, food
industries, textile industries, chemical
industries, Agriculture industries, etc. The
effluent of industries and household activities,
known as sewage water, contain variety of
pollutants most of them are non-biodegradable
and hazardous pollutants. Traditional technics
like adsorption, sedimentation, flocculation,
and coagulation are not capable to eliminate
pollutants from pollution cycle. However,
these methods convert the phase of pollutants
from liquid phase to solid phase and produce
secondary pollution, i.e. soil pollution. These
conventional methods also required huge
amount of electricity and chemicals.
Heterogeneous photocatalyst based technique
is fully capable to remove all water-soluble
organic pollutants. Merits of AOP are use of
renewable source of energy, as this technic is
totally based on solar energy. We can use
same catalyst many times resultant this technic
becomes much cheaper than conventional
methods when we compare all parameters and
effectiveness. We observe that all the
pollutants convert into non-hazardous
forms/gases.
We use this catalyst (ZnO) heterogeneous
photocatalyst for degradation of organic
pollutants. It believes that due sensitization of
photocatalyst, electron are migrate from
balance band (VB) to conduction band (CB)
resultant holes–electron pairs are forms. Holes
(h+)
are form by balance band; these holes can
generate hydroxyl radicals, which are highly
JoCC (2016) 6-9 © STM Journals 2016. All Rights Reserved Page 6
Journal of Catalyst and Catalysis
ISSN: 2349-4344(online)
Volume 3, Issue 3
www.stmjournals.com
Fire-Mechanical Properties of Geopolymer Concrete
Ali I. Al-Mosawi1,
*, Shaymaa Abbas Abdulsada2
Faculty of Materials Science and Engineering, University of Miskolc, Egyetem út, Hungary
Abstract
Nanoscale Aluminum hydroxide was added in different proportions (10, 15, 20) wt% for Low-
calcium fly ash-based geopolymer concrete to increase its resistance to fires. ASTM E84 - 16
standard with 750°C temperature was used to test the ability of aluminum hydroxide to
enhance the resistance of concert to burning. The practical results proven the efficiency of
aluminum hydroxide as a fire retardant to impede the flame and improved geopolymer
compressive strength after burning.
Keywords: Geopolymer concrete, Aluminum hydroxide, fire-mechanical properties
INTRODUCTION
Geopolymer concrete considered as a
sustainable material, which widely used today
in buildings and structures industry because of
its distinctive characteristics. In addition, to
make Geopolymer, aluminum and silicon
mixed with industrial solid waste to create a
solid binder have the same function as in
ordinary portland cement. This solid binder
can be used in applications to totally or
partially replace ordinary portland cement with
sustainable and environmental impacts such as
reducing emissions of CO2, enhanced fire
resistance and aggressive chemicals attack.
Although this technique is that the looks new
for many, but it has been used by ancient
civilizations such as the Babylonians and
Egyptians in the construction of their buildings
[1–5].
Like any other type of concrete, geopolymer
concrete suffering weakness in its mechanical
properties when exposed to fire, and its
resistance to fire relate to quantities of mixed
materials [6]. Fire retardant was added to this
concrete to increase its resistance to fire. Fire
retardants (FRs) have the capacity to resist
direct flame and prevent its spread or
extinguish it completely [7].The essential aim
of adding FRs is to slow down the process of
ignition and prevent the flame spread in
which the low fire resistance material will be
protected [8–11]. FRs is applied in a numeral
of different methods. Some fire retardants
cause a char layer, thus inhibiting the pyrolysis
process [12–15]. Others work to removing the
flammable gases by interacting with hydrogen
and hydroxide radicals in the bulk. There are
four groups of FRs Inorganic FRs, Organic
phosphorus FRs, Nitrogen-containing FRs and
Halogenated organic FRs [16–20].
METHODOLOGY
Materials
Materials used to prepare the samples were
low-calcium fly ash-based geopolymer
concrete Class F and its chemical composition
is shown in Table 1 [21], and Aluminum
hydroxide Al(OH)3 with particle size (1 nm).
Preparation of Test Samples: The solid
samples of concrete mixes were designed in
accordance with the American mix design
method (ACI 211)and have a cubic shape with
(150×150×150 mm. Aluminum hydroxide was
added to the concert with (10, 15, 20) wt% and
mixed well. These samples were taken out
from the molds after 24 hours of casting and
then they were completely immersed in water
for 28 days.
JoCC (2016) 10-17 © STM Journals 2016. All Rights Reserved Page 10
Journal of Catalyst and Catalysis
ISSN: 2349-4344(online)
Volume 3, Issue 3
www.stmjournals.com
Identification of Some Imported Lubricating Oil Additives
Used in Libya and Synthesis of the Most Consumed Ones
from the Local Raw Materials
Abdurahman A. Abuabdalla Khalifa1,
, Rajab Maga2
1
Department of Chemistry, Faculty of Science, Al-Gabal Al-Gharbi University, Gharian, Libya
2
Department of Chemistry, Faculty of Science, Azzaytuna University, Libya
Abstract
This paper presents the identified six additives imported under trade names used in the
lubricating oil blending factory of A-Zawia-Libya. Their structures have been completely
confirmed by examining their physical properties and using modern analytical techniques
such as nuclear magnetic resonance spectroscopy (NMR), infra-red (IR), atomic absorption
(AAS) and gas chromatography (GC). The synthesis of most important and more consumed
additives in lubricating oils in Libyan oil industry from local available raw materials as
corrosion inhibitors, viscosity index improvers, detergent-dispersants and multipurpose
additives were prepared by using castor oil extracted from local castor beans and some
petrochemical derivatives. Some additives have followed one step reaction, while others two
step reactions. Both types of reactions gave remarkable yields of 40–80%. Their performance
was evaluated and the synthesized corrosion inhibitors had also been examined and various
possible protection rates were obtained.
Keywords: Additives, lubricating oils, castor oil, trade names, blending factory
INTRODUCTION
The main function of a lubricant is forming a
film that separates two surfaces that roll or
slide between one another, to reduce friction
and eliminate wear. Additives are chemicals
imported under trade names from different
monopolize companies and added in a small
percentage to improve the physical properties
and extending the life of the lubricating oils.
Lubricating oil additives are used for the
protection of many parts of machines and
engines to prevent wear, reduce the oxidative
or thermal degradation of oil, minimize rust
and corrosion, lessen the deposition of harmful
deposits on lubricated parts and prevent
destructive metal-to-metal contact [1].
Detergent and dispersant additives are used
primarily in internal combustion engines to
keep metal surfaces clean by preventing
deposition of oxidation products. Dispersants
are typically the highest treat additives in
engine oil formulation. They are similar to
detergents in that they have a polar head group
with an oil-soluble hydrocarbon tail; while
detergents are used to clean engine surfaces
and neutralize acidic byproducts [2]. One of
the most important modes of lubricant
degradation is oxidation. This oxidation is the
primary cause of increase in viscosity, pour
point, sludge, and enhanced engine corrosion;
and conventional liquid lubricants show poor
oxidative and thermal stability at higher
temperature ranges, which result in the
formation of a vast quantity of volatile and
solid products in the lubrication system [3].
For convenience, lubricating oils are divided
into different categories: motors, industrial and
special oils. The percentage and composition
of the additives vary with the base oil selected
and performance required for finished
products. Some additives impart new and
useful properties to the lubricant; some
enhance properties already present, while
some act to reduce the rate at which
undesirable changes take place in the product
during its service life. Table 1 shows the
different additives and their typical
compounds [4].
JoCC (2016) 18-25 © STM Journals 2016. All Rights Reserved Page 18
Journal of Catalyst and Catalysis
ISSN: 2349-4344(online)
Volume 3, Issue 3
www.stmjournals.com
Synthesis and Study of Different Thioamides as
Corrosion Inhibitors
Abdurahman A. Abuabdalla Khalifa*
Department of Chemistry, Faculty of Science, Aljabel-Algarbi University, Libya
Abstract
Many organic compounds having electron rich atoms in their structures, such as nitrogen,
and sulphur are widely use in lubricating additives, in the oil industry to minimize corrosion.
The presence of electron rich atoms in the molecules increases its ability to form coordinate
covalent bonds with the metal atoms, involved in the corrosion environment. Compounds
based on fatty amines, aromatic amines, imidazoline, diamidazoline, and fatty amides are
now, uses as corrosion inhibitors, in the oil sector and are available in the market. In this
work, some phenyl acetothioamide and benzyl acetothioamide are synthesized. The chemical
and physical data of the prepared compounds are compiled. The solubility, cold stability, heat
stability, and corrosion inhibitors characteristics, of the compounds have been measured in
the artificial environment (10% crude in artificial brine at pH 4.5–4.8). Prepared thioamides
differs in their molecular weights, due to presence of different organic substituent's, on the
thioamides group. Synthesis of the above mentioned compounds are based on the Willgerodt-
Kindler reaction. The compounds are confirmed by IR, NMR, UV-VIS, and other wet chemical
analytical techniques. The experimental values of the elemental composition were compared
with the calculated values and found agreeing. UV-VIS. and IR spectra also show the
absorption peaks, which confirm the presence of thioamides group in the prepared
compounds. The possible reaction mechanism regarding the synthesis of the above mentioned
compounds is discussed and its mechanism of corrosion inhibition in the corrosive
environment was explained. The compounds was evaluated in brine and sea water, some
compounds having percentage protection more than 50%, the results was compared with the
imported commercial inhibitors and found to be compatible.
Keywords: Additives, corrosion inhibitors, market, brine
INTRODUCTION
Chemical anti-degradants means the chemical
species which inhibit corrosion of metals and
stabilize or adjust the environment in which it
has been applied. Corrosion inhibitors form a
protective barrier on the surface of a substrate
by physical absorption, corrosion problems in
the operation of petroleum drilling installation
are to be solved by the aid of corrosion
inhibitors in the injection water. The crude
comes out with plenty of minerals containing
water and the pH of this aqueous and oily
mixture various but lies in the acidic side. This
acidic pH, mineral contents and dissolved gases
are responsible for metallic corrosion. Number
of organic compound having electron rich
atoms in their molecules such as nitrogen and
sulphur, are widely used as corrosion inhibitors,
for their anticorrosion and antioxidation
properties [1, 2]. Many such types of these
compounds have been synthesized having
different percentage composition of nitrogen
and sulphur and varying in saturations. It has
been proved experimentally that higher
molecular weight of the above mentioned types
of compounds, higher is the anticorrosive and
antioxidation properties. It may be due to more
surface area of the molecules. It is also
established that the sulphur containing
substances are more effective anticorrosive and
antioxidative compared to nitrogen containing
compounds, provided the molecular weight and
molecular unsaturations will be the same.
Corrosion and oxidation inhibitors are routinely
used in oil fields and in the refiners, in order to
minimize the corrosion of the oil transporting
pipe lines, pumps, valves and other involved
equipment and also the refinery installations.
Commercially corrosion inhibitors are unique
mixtures that may contains surfactants, film
JoCC (2016) 26-36 © STM Journals 2016. All Rights Reserved Page 26
Journal of Catalyst and Catalysis
ISSN: 2349-4344(online)
Volume 3, Issue 3
www.stmjournals.com
Phytoextraction of Lead and Chromium by Leafy
Vegetables (Lettuce, Kale and Swiss Chard)
Mamu H. Teferi*, Dejene A. Tessema
Department of Chemistry, College of Natural Science, Jimma University, P.O Box 387,
Jimma, Ethiopia
Abstract
This research was carried out to assess the accumulation of Cr and Pb in leafy vegetables
(lettuce, kale and Swiss chard) in their harvestable part and root from artificially polluted soil
with Pb and Cr. Soil sample was characterized for its pH, organic matter (OM), cation
exchange capacity (CEC), electrical conductivity (EC) and texture. Soil sample digested by
mixture of HNO3 and HClO4 was analyzed. Pb accumulation in shoot was on average greater
(318.36 to 1235.20 mg/kg) in S2 than S1 (169.66 to 404.80 mg/kg). Translocation of Pb from
root to shoot was enhanced by the addition of spinach extract in kale and Swiss chard.
Chromium translocation from root to shoot in the vegetables was limited. Less than one TF of
Cr was recorded in all plants of both soil samples. Cr except lettuce grown in PES2, all the
plants were able to accumulate less than 1000 mg kg-1
in their shoot.
Keyword: Lead, Chromium, Photoextract
INTRODUCTION
Industrialization has led to the release of
enormous quantities of toxic compounds into
the environment. For the remediation of
contaminated sites, there are numerous
methods. Commonly used engineering
techniques include excavation and land filling,
chemical treatment and verification. These
methods are extremely expensive. Due to the
acute toxicity of heavy metal contaminants,
there is an urgent need to develop low-cost,
effective, and sustainable methods to remove
or to detoxify from the environment. One of
these methods is a plant based approach
known as phytoremediation [1, 2].
Phytoremediation is a method of environmental
treatment that makes use of the ability of some
plant species to stabilize, degrade uptake
pollutants or accumulate certain elements,
including heavy metals, in amounts exceeding
the nutrition requirements of plants [2].
Phytoremediation has includes different
strategies. These are Phytotransformation
(phytodegradation), Phytostabilization (space
uniformity), Rhizodegradation, Phytofiltration
(rhizofiltration), and Phytoextraction
(phytoaccumulation) [1–4].
Phytoextraction processes extract both
metallic and organic constituents from soil by
direct uptake into plants and translocation to
aboveground biomass. Plant used for
phytoextraction are those capable of
accumulating Concentration 100 times higher
than in normal plants for each metal of
interest, i.e., more than 10 mg kg–1
of Hg; 100
mg kg–1
of Cd; 1000 mg kg–1
of Co, Cr, Cu, Pb
and Ni; and 10,000 mg kg–1
of Zn and Mn etc.;
Bioconcentration factor >1 (concentration of
the element in the plant > concentration in the
soil); and Translocation factor >1 (element
concentration in the over ground part of the
Plant > than in roots) [5].
Phytoextraction has commonly two strategies.
These are natural Phytoextraction which use
plants with inherent capacity to extract toxic
metals and educed Phytoextraction which is
chemical assisted extracting method [6–9].
Metals exist in soil in five different pools:
fraction 1) soluble, i.e., metals in the soil
solution (as free metal ions and metal
complexes); fraction 2) exchangeable, i.e.,
metals adsorbed on ion-exchange sites and on
inorganic soil constituents; fraction 3) organic,
i.e., metals bound with the organic matter;
ISSN 2349-4344 (Online)
Journal of
Catalyst & Catalysis
(JoCC)
September–December 2016
conducted
Ch Instrumentation/ /
/
Energy Science/ /
22
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Journal of Catalyst & Catalysis vol 3 issue 3

  • 1. ISSN 2349-4344 (Online) Journal of Catalyst & Catalysis (JoCC) September–December 2016 conducted Ch Instrumentation/ / / Energy Science/ / 22 GLOBAL READERSHIP STATISTICS STM Journals Empowering knowledge Free Online Registration ISO: 9001Certified www.stmjournals.com STM JOURNALS Scientific Technical Medical
  • 2. STM Journals, a strong initiative by Consortium E-Learning Network Private Ltd. (established 2006), was launched in the year 2010 under the support and guidance by our esteemed Editorial and Advisory Board Membersfromrenownedinstitutes. Objectives:  Promotion of Scientific, Technical and Medical research.  Publication of Original Research/Review, Short Articles and Case Studies through Peer Review process.  Publishing Special Issues on Conferences.  Preparing online platform for print journals.  Empowering the libraries with online and print Journals in Scientific, Technical and Medical domains.  Publishing and distribution of books on various subjects in the category of Nanotechnology, Scientific and Technical Writing, and Environment, Health and Safety. SalientFeatures:  A bouquet of 100+ Journals that fall under Science, Technical and Medical domains.  Employs Open Journals System (OJS)—a journal management and publishing system.  The first and one of the fastest growing publication website in India as well as in abroad for its quality and coverage.  Rapid online submission and publication of papers, soon after their formal acceptance/finalization.  Facilitates linking with the other authors or professionals.  Worldwide circulation and visibility. Journal of Catalyst & Catalysis ISSN: 2349-4344(online) Focus andScopeCovers  Catalysis,Catalyst,Reagents  Inhibitors,Poisons andPromoters  MechanismActionof Catalyst  InorganicSolidsandMetalComplexes  StatisticalEvaluationsof Catalyst  Adsorption, ProcessTechnologywithCatalysis  ComputationalCatalysis Journal of Catalyst & Catalysis is published (frequency: three times a year) in India by STM Journals (division of Consortium e-Learning Network Private Ltd.) The views expressed in the articles do not necessarily reflect of the Publisher. The publisher does not endorse the quality or value of the advertised/sponsored products described therein. Pleaseconsultfullprescribinginformationbeforeissuingaprescriptionfor anyproductsmentionedinthispublication. No part of this publication may be reproduced, stored in retrieval system or transmitted in any from without written permissionofthepublisher. To cite any of the material contained in this Journal, in English or translation, please use the full English reference at the beginningofeacharticle.To reuseanyof thematerial,pleasecontactSTM Journals (info@stmjournals.com) STM Journals
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  • 4. Gargi Asha Jha Manager (Publications) PUBLICATION MANAGEMENT TEAM Internal Members External Members Bimlesh Lochab Assistant Professor Department of Chemistry School of Natural Sciences, Shiv Nadar University Gautam Buddha Nagar, Uttar Pradesh, India Dr. Rajiv Prakash Professor and Coordinator School of Materials Science and Technology Indian Institute of Technology (BHU), Varanasi Uttar Pradesh, India Dr. Rakesh Kumar Assistant Professor Department of Applied Chemistry BIT Mesra, Patna, Bihar, India Prof. S. Ramaprabhu Alternative Energy and Nanotechnology Technology Laboratory, Department of Physics Indian Institute of Technology, Chennai Tamil Nadu, India Himani Pandey Isha Chandra Senior Associate Editors Dr. Yog Raj Sood Dean (Planning and Development) Professor, Department of Electrical Engineering National Institute of Technology, Hamirpur Himachal Pradesh, India Prof. Chris Cannings Professor, School of Mathematics and Statistics University of Sheffield, Sheffield United Kingdom Dr. D. K. Vijaykumar MS, MCh (Surgical Oncology), Professor and Head Department of Surgical Oncology Amrita Institute of Medical Sciences and Research Centre Ponekkara, Cochin, Kerala, India Dr. Durgadas Naik Associate Professor (Microbiology) Management and Science University, University Drive, Seksyen13 Selangor, Malaysia Prof. José María Luna Ariza Department of Computer Sciences and Numerical Analysis Campus of Rabanales University of Córdoba, Spain Dr. Khaiser Nikam Professor, Library and Information Science Department of Library and Information Science University of Mysore Mysore, India Quaisher J Hossain Senior Editor Group Managing Editor Dr. Archana Mehrotra Managing Director CELNET, Delhi, India Meenakshi Tripathi Shivani Sharma Chairman Mr. Puneet Mehrotra Director Shambhavi Mishra Associate Editors Sugandha Mishra
  • 5. Prof. Priyavrat Thareja Director Principal Rayat Institute of Engineering and Information Technology Punjab, India Dr. Baldev Raj Director, National Institute of Advanced Studies Indian Institute of Science campus Bangalore Karnataka, India Former Director Indira Gandhi Centre for Atomic Research, Kalpakkam, Tamil Nadu, India Dr. Pankaj Poddar Senior Scientist Physical and Materials Chemistry Division, National Chemical Laboratory Pune, Maharastra India Prof. D. N. Rao Professor and Head Department of Biochemistry All India Institute of Medical Sciences New Delhi, India Dr. Nandini Chatterjee Singh Additional Professor National Brain Research Centre Manesar, Gurgaon Haryana, India Dr. Ashish Runthala Lecturer, Biological Sciences Group Birla Institute of Technology and Science Pilani, Rajasthan, India Dr. Bankim Chandra Ray Professor and Ex-Head of the Department Department of Metallurgical and Materials Engineering National Institute of Technology, Rourkela Odisha, India Prof. Yuwaraj Marotrao Ghugal Professor and Head Department of Applied Mechanics Government College of Engineering Vidyanagar, Karad Maharashtra, India Dr. Hardev Singh Virk Visiting Professor, Department of Physics University of SGGS World University Fatehgarh Sahib, Punjab, India Former Director Research DAV Institute of Engineering and Technology Jallandhar, India Dr. Shrikant Balkisan Dhoot Senior Research Scientist, Reliance Industries Limited, Mumbai, India Former Head (Research and Development) Nurture Earth R&D Pvt Ltd., MIT Campus Beed Bypass Road, Aurangabad Maharashtra, India STM JOURNALS ADVISORY BOARD
  • 6. Dr. Rakesh Kumar Assistant Professor Department of Applied Chemistry Birla Institute of Technology Patna, Bihar, India Prof. Subash Chandra Mishra Professor Department of Metallurgical and Materials Engineering National Institute of Technology, Rourkela Odisha, India Dr. Shankargouda Patil Assistant Professor Department of Oral Pathology KLE Society's Institute of Dental Sciences Bangalore, Karnataka, India Prof. Sundara Ramaprabhu Professor Department of Physics Indian Institute of Technology Madras Chennai, Tamil Nadu India Dr. Baskar Kaliyamoorthy Associate Professor Department of Civil Engineering National Institute of Technology, Trichy Tiruchirappalli, Tamil Nadu, India STM JOURNALS ADVISORY BOARD
  • 7. Editorial Board Abdul Rajack Associate Professor, Department of Chemistry, Maharaja Vijayaram Gajapathi Raj College of Engineering, Andhra Pradesh, India. Abhijit Mondal Assistant Professor, Chemical Engineering Dept. National Institute of Technology Agartala India. Ajay Bansal Associate Professor Head, Department of Chemical Engineering National Institute of Technology, Jhallandhar, Punjab, India. Ajaya Kumar Singh Associate Professor Department of Chemistry Government V.Y.T.PG.Autonomous College Durg, Chhattisgarh, India. Alirio Rodrigues Emeritus Professor Laboratory of Separation & Reaction Engineering, Departamento de Engenharia Química, Faculdade de Engenharia da Universidade do Porto, Portugal. Alekha Kumar Sutar Assistant Professor Catalysis Research Lab Department of Chemistry Ravenshaw University Cuttack, Odisha, India. Antonio Gil Professor of Chemical Engineering Department of Applied Chemistry Universidad Publica de Navarra, Spain. Ankur Bordoloi Refinery Technology Division Indian Institute of Peteroleum ,Dehradun, India. Bharat Modhera Assistant Professor Chemical Engineering Maulana Azad National Institute of Technology, Bhopal, India. Benjaram Mahipal Reddy Chief Scientist & Head Inorganic & Physical Chemistry Division CSIR - Indian Institute of Chemical Technology Hyderabad, India. Gopal L Tembe Asst.Vice president Reliance Research & Development Center Reliance Industries Limited, Navi Mumbai, India. Chitturi Venkateswara Rao Research Scientist University of Puerto Rico, USA Hima Kumar Lingam Scientist Research & Development Centre Nova- Kem LLC Germantown WI 53022, United States. Hemant S Chandak Assistant Professor, Department of Chemistry G. S. Science, Arts & Commerce College, Nandura Road,Maharashtra, India. Jagannadharao Yaddanapudi Siddaganga Institute of Technology, Tumkur M S R Institute of Technology,Bangalore Visvesvaraya Technological University, India. Ibadur Rahman Siddiqui Laboratory of Green Synthesis, Department of Chemistry, University of Allahabad, India. Kalpana Maheria Applied Chemistry Department, Sardar Vallabhbhai National Institute of Technology, Surat, Gujarat, India. Jhansi. L. Kishore Mamilla Assistant Professor Department of Chemical Engineering and Technology Birla Institute of Technology Mesra, Ranchi, India. M. N. Kumara Assistant Professor Graduate and Postgraduate Center Department of Chemistry, Yuvaraja's College University of Mysore, Mysore, India. Kamal K. Pant Petrotech Chair Professor Department of Chemical Engineering Indian Institute of Technology Delhi India, India. Manju Dhakad Tanwar Chief Scientist and Head, Five Elements Environment Ventures. Mani Karthik CIC ENERGIGUNE Energy Cooperative Research Centre Parque Tecnológico, Spain.
  • 8. Editorial Board Mohammad Muneer Professor, Department of Chemistry, Aligarh Muslim University India, India. N Selvaraju Assistant Professor, Department of Chemical Engineering, National Institute of Technology Calicut India. Nadeem Bashir Ganaie Assistant Professor Govt. College for Women Nawakadal Jammu and Kashmir India, India. Nagaraj P. Shetti Head, Department of Engineering Chemistry, KLE Institute of Technology, Hubli, Karnataka, India. Nitin Kumar Labhsetwar Senior Principal Scientist / Deputy Director Environmental Materials Division National Environmental Research Institute(NEERI), Nagpur, India. Neeraj Atrey Senior Scientist Chemical Conversion Area Indian Institute of Petroleum, Dehradun. Pavan Kumar Malladi V Assistant Professor Department of Chemical Engineering National Institute of Technology Calicut. Parnesh Nath Chatterjee Assistant Professor,HOD Department of Chemistry NIT Meghaalya, India. Prabhas Jana Postdoctoral Researcher Thermochemical Processes Unit IMDEA Energy, Madrid, Spain. Perumal Subramaniam Head & Associate Professor, Research Department of Chemistry, Aditanar College of Arts and Research, Tiruchendur, India. Praveen Kumar Tandon Associate Professor Department of Chemistry, University of Allahabad, India. Prakash Samnani Associate Professor Faculty Of Science Department of Chemistry Maharaja Sayajiao University Baroda Gujarat, India, India. Priyanka Sagar Assistant professor , Department of Chemistry Kumaon University, India. Pravin Pandharinath Upare Senior Researcher Korea Research Institute of Chemical Technology, Daejeon, Korea, Republic Of. Rakesh Kumar Pandey JSPS-Fellow, Electronic Functional Materials Group, National Institute for Materials Science (NIMS), Tsukuba, Japan. R Karvembu Associate Professor Department of Chemistry National Institute of Technology Tiruchirappalli, India. Ravi Prakash Vaid Professor(Retired), Birla Institute of Technology & Science, Pilani Rajasthan, India, India. Rakesh Sharma Assistant Professor Indian Institute of Technology Jodhpur India, India. Sayed Hasan Razi Abdi Central Salt & Marine Chemicals Research Institute Council for Scientific & Industrial Research, India. Sankaranarayanan T.M Instituto IMDEA Energía Avda. Ramón de la Sagra, 3 Parque Tecnológico de Móstoles E-28935 Móstoles, Madrid (Spain), Spain. Shankar MV Nanocatalysis and Solar Fuels Research Lab Department of Materials Science & Nanotechnology Yogi Vemana University Kadapa, Andhra Pradesh, India. Shailendra Tripathi Catalysis Division CSIR-Indian Institute of Petroleum.
  • 9. Editorial Board Shiva B Halligudi Retired Scientist National Chemical Laboratory Council for Scientific and Industrial Research Pune, India. Shivamurti A Chimatadar Department of Chemistry, Karnatak University, Dharwad, India. Siva Sankar Department of Chemical Engineering, National Institute of Technology Tiruchirappalli, India. Sunaja Devi Assistant Professor Department of Chemistry Christ University, Hosur Road, Bangalore India, India. Sushil Kumar Assistant Professor Department of Chemical Engineering Motilal Nehru National Institute of Technology (MNNIT), Allahabad. Sunil Kumar Scientist Biotechnology Conversion Area Indian Institute of Petroleum Dehradun. Venkata Narayana Kalevaru Group Leader, Gas Phase Oxidations, Leibniz Institute for Catalysis at University Rostock Albert- Einstein, Germany. Tungabidya Maharana Assistant Professor Department Of Chemistry National Institute of Technology, Raipur India, India. Virendra Kumar Gupta Sr. Vice President & Head Reliance Technology Group, India. Vijaya Kumar Bulasara Assistant Professor Department of Chemical Engineering Thapar University, Patiala, India. Yogesh C Sharma SERC Visiting Fellow Department of Applied Chemistry Indian Institute of Technology(BHU) Vishwanathan Balasubrananian National Centre for Catalysis Research Indian Institute of Technology-Madras Chennai , India. Indraneel Pulidindi Department of Chemistry Bar Ilan University, Israel. G.V.P.Chandramouli HOD, Chemistry. NIT, National Institute of Technology,Warangal. Dr. Virender Singh Assistant Professor, Department of Chemistry, Dr. B. R. Ambedkar National Institute of Technology, Jalandhar. Dr. Jatinder Kumar Department of Chemical Engineering, National Institute of Technology, Jalandhar. Dr. Balaga Viswanadham Research Scientist, Department of Chemistry, School of Chemistry & Physics, University of KwaZulu-Natal Westville Campus,Durban
  • 10. It is my privilege to present the print version of the [Volume 3, Issue 3] of our Journal of Catalyst & Catalysis (JoCC), 2016. The intension of JoCC Journal is to create an atmosphere that stimulates vision,researchandgrowthintheareaChemicalEngineering. Timely publication, honest communication, comprehensive editing and trust with authors and readers have been the hallmark of our journals. STM Journals provide a platform for scholarly research articles to be published in journals of international standards. STM journals strive to publish qualitypaperinrecordtime,makingitaleaderinserviceandbusiness offerings. The aim and scope of STM Journals is to provide an academic medium and an important reference for the advancement and dissemination of research results that support high level learning, teaching andresearchinalltheScientific,TechnicalandMedicaldomains. Finally, I express my sincere gratitude to our Editorial/Reviewer board, Authors and publication team for their continued support and invaluable contributions and suggestions in the form of authoring write ups/reviewing and providing constructive comments for the advancement of the journals.With regards to their due continuous support and co-operation, we have been able to publish qualityResearch/Reviewsfindingsfor our customersbase. Ihopeyouwillenjoyreadingthisissue andwewelcomeyourfeedbackonanyaspectof theJournal. Dr.ArchanaMehrotra ManagingDirector STM Journals Director's Desk STM JOURNALS
  • 11. 1. An Use of Solar Energy Based Photocatalyst for Degradation of Water Pollutants Ram Babu Pachwarya, Deepchand Saini, R.C. Meena, A.L. Ramnathan 1 2. Fire-Mechanical Properties of Geopolymer Concrete Ali I. Al-Mosawi, Shaymaa Abbas Abdulsada 6 3. Identification of Some Imported Lubricating Oil Additives Used in Libya and Synthesis of the Most Consumed Ones from the Local Raw Materials Abdurahman A. Abuabdalla Khalifa, Rajab Maga 10 4. Synthesis and Study of Different Thioamides as Corrosion Inhibitors Abdurahman A. Abuabdalla Khalifa 18 5. Phytoextraction of Lead and Chromium by Leafy Vegetables (Lettuce, Kale and Swiss chard) Mamu H. Teferi, Dejene A. Tessema 26 ContentsJournal of Catalyst & Catalysis
  • 12. JoCC (2016) 1-5 © STM Journals 2016. All Rights Reserved Page 1 Journal of Catalyst and Catalysis ISSN: 2349-4344(online) Volume 3, Issue 3 www.stmjournals.com An Use of Solar Energy Based Photocatalyst for Degradation of Water Pollutants Ram Babu Pachwarya1, *, Deepchand Saini2 , R.C. Meena3 , A.L. Ramnathan2 1 Department of Chemistry, Motilal Nehru College, University of Delhi, New Delhi, India 2 School of Environmental Sciences, Jawaharlal Nehru University, New Delhi, India 3 Department of Chemistry, Jai Narain Vyas University, Jodhpur, Rajasthan, India Abstract Azo dyes/Dyes, pesticides, weedicide, etc. are highly harmful and carcinogenic in nature. Dyes especially azo dyes reduces fertility of soil. Treatment of dye pollution even pesticides, weedicides is challenging for environmentalists. The photocatalytic degradation of most of water-soluble organic pollutants by heterogeneous photocatalyst ZnO in the presence of sunlight is best and sustainable method. We also found the influence of different parameters like light intensity, temperature, amount of catalyst, pH of the solution, light intensity. It has been found that ZnO is capable to degraded/remove most of water-soluble organic pollutants in the presence of sunlight. The merits of the technic are: (1) we can use same catalyst many times and it works well every time. (2) Techniques is based on sunlight. We also applied this technology for treatment of sewage water and we observed that this catalyst is fully capable to remove all kind of water-soluble pollutants we got more than 99% transparent water in few hours irradiation of sunlight. Keywords: Non-biodegradable, degradation, ZnO, TiO2, photocatalytic azo dyes INTRODUCTION Degradation of water pollutants is a challenging task much more difficult because of variety of pollutants including non- biodegradable water-soluble organic pollutants. Most of Sewage water pollutants are non-biodegradable in nature, so conventional treatment methods are not capable to remove these pollutants from pollution cycle. Advance oxidation process (AOP) heterogeneous photocatalyst ZnO can prove a promising technology for treatment of sewage water. This technic has shown its capability to degrade all kind of water-soluble organic pollutants including non- biodegradable pollutants. Heterogeneous photocatalyst can be used for treatment of sewage water, paper industries, food industries, textile industries, chemical industries, Agriculture industries, etc. The effluent of industries and household activities, known as sewage water, contain variety of pollutants most of them are non-biodegradable and hazardous pollutants. Traditional technics like adsorption, sedimentation, flocculation, and coagulation are not capable to eliminate pollutants from pollution cycle. However, these methods convert the phase of pollutants from liquid phase to solid phase and produce secondary pollution, i.e. soil pollution. These conventional methods also required huge amount of electricity and chemicals. Heterogeneous photocatalyst based technique is fully capable to remove all water-soluble organic pollutants. Merits of AOP are use of renewable source of energy, as this technic is totally based on solar energy. We can use same catalyst many times resultant this technic becomes much cheaper than conventional methods when we compare all parameters and effectiveness. We observe that all the pollutants convert into non-hazardous forms/gases. We use this catalyst (ZnO) heterogeneous photocatalyst for degradation of organic pollutants. It believes that due sensitization of photocatalyst, electron are migrate from balance band (VB) to conduction band (CB) resultant holes–electron pairs are forms. Holes (h+) are form by balance band; these holes can generate hydroxyl radicals, which are highly
  • 13. JoCC (2016) 6-9 © STM Journals 2016. All Rights Reserved Page 6 Journal of Catalyst and Catalysis ISSN: 2349-4344(online) Volume 3, Issue 3 www.stmjournals.com Fire-Mechanical Properties of Geopolymer Concrete Ali I. Al-Mosawi1, *, Shaymaa Abbas Abdulsada2 Faculty of Materials Science and Engineering, University of Miskolc, Egyetem út, Hungary Abstract Nanoscale Aluminum hydroxide was added in different proportions (10, 15, 20) wt% for Low- calcium fly ash-based geopolymer concrete to increase its resistance to fires. ASTM E84 - 16 standard with 750°C temperature was used to test the ability of aluminum hydroxide to enhance the resistance of concert to burning. The practical results proven the efficiency of aluminum hydroxide as a fire retardant to impede the flame and improved geopolymer compressive strength after burning. Keywords: Geopolymer concrete, Aluminum hydroxide, fire-mechanical properties INTRODUCTION Geopolymer concrete considered as a sustainable material, which widely used today in buildings and structures industry because of its distinctive characteristics. In addition, to make Geopolymer, aluminum and silicon mixed with industrial solid waste to create a solid binder have the same function as in ordinary portland cement. This solid binder can be used in applications to totally or partially replace ordinary portland cement with sustainable and environmental impacts such as reducing emissions of CO2, enhanced fire resistance and aggressive chemicals attack. Although this technique is that the looks new for many, but it has been used by ancient civilizations such as the Babylonians and Egyptians in the construction of their buildings [1–5]. Like any other type of concrete, geopolymer concrete suffering weakness in its mechanical properties when exposed to fire, and its resistance to fire relate to quantities of mixed materials [6]. Fire retardant was added to this concrete to increase its resistance to fire. Fire retardants (FRs) have the capacity to resist direct flame and prevent its spread or extinguish it completely [7].The essential aim of adding FRs is to slow down the process of ignition and prevent the flame spread in which the low fire resistance material will be protected [8–11]. FRs is applied in a numeral of different methods. Some fire retardants cause a char layer, thus inhibiting the pyrolysis process [12–15]. Others work to removing the flammable gases by interacting with hydrogen and hydroxide radicals in the bulk. There are four groups of FRs Inorganic FRs, Organic phosphorus FRs, Nitrogen-containing FRs and Halogenated organic FRs [16–20]. METHODOLOGY Materials Materials used to prepare the samples were low-calcium fly ash-based geopolymer concrete Class F and its chemical composition is shown in Table 1 [21], and Aluminum hydroxide Al(OH)3 with particle size (1 nm). Preparation of Test Samples: The solid samples of concrete mixes were designed in accordance with the American mix design method (ACI 211)and have a cubic shape with (150×150×150 mm. Aluminum hydroxide was added to the concert with (10, 15, 20) wt% and mixed well. These samples were taken out from the molds after 24 hours of casting and then they were completely immersed in water for 28 days.
  • 14. JoCC (2016) 10-17 © STM Journals 2016. All Rights Reserved Page 10 Journal of Catalyst and Catalysis ISSN: 2349-4344(online) Volume 3, Issue 3 www.stmjournals.com Identification of Some Imported Lubricating Oil Additives Used in Libya and Synthesis of the Most Consumed Ones from the Local Raw Materials Abdurahman A. Abuabdalla Khalifa1, , Rajab Maga2 1 Department of Chemistry, Faculty of Science, Al-Gabal Al-Gharbi University, Gharian, Libya 2 Department of Chemistry, Faculty of Science, Azzaytuna University, Libya Abstract This paper presents the identified six additives imported under trade names used in the lubricating oil blending factory of A-Zawia-Libya. Their structures have been completely confirmed by examining their physical properties and using modern analytical techniques such as nuclear magnetic resonance spectroscopy (NMR), infra-red (IR), atomic absorption (AAS) and gas chromatography (GC). The synthesis of most important and more consumed additives in lubricating oils in Libyan oil industry from local available raw materials as corrosion inhibitors, viscosity index improvers, detergent-dispersants and multipurpose additives were prepared by using castor oil extracted from local castor beans and some petrochemical derivatives. Some additives have followed one step reaction, while others two step reactions. Both types of reactions gave remarkable yields of 40–80%. Their performance was evaluated and the synthesized corrosion inhibitors had also been examined and various possible protection rates were obtained. Keywords: Additives, lubricating oils, castor oil, trade names, blending factory INTRODUCTION The main function of a lubricant is forming a film that separates two surfaces that roll or slide between one another, to reduce friction and eliminate wear. Additives are chemicals imported under trade names from different monopolize companies and added in a small percentage to improve the physical properties and extending the life of the lubricating oils. Lubricating oil additives are used for the protection of many parts of machines and engines to prevent wear, reduce the oxidative or thermal degradation of oil, minimize rust and corrosion, lessen the deposition of harmful deposits on lubricated parts and prevent destructive metal-to-metal contact [1]. Detergent and dispersant additives are used primarily in internal combustion engines to keep metal surfaces clean by preventing deposition of oxidation products. Dispersants are typically the highest treat additives in engine oil formulation. They are similar to detergents in that they have a polar head group with an oil-soluble hydrocarbon tail; while detergents are used to clean engine surfaces and neutralize acidic byproducts [2]. One of the most important modes of lubricant degradation is oxidation. This oxidation is the primary cause of increase in viscosity, pour point, sludge, and enhanced engine corrosion; and conventional liquid lubricants show poor oxidative and thermal stability at higher temperature ranges, which result in the formation of a vast quantity of volatile and solid products in the lubrication system [3]. For convenience, lubricating oils are divided into different categories: motors, industrial and special oils. The percentage and composition of the additives vary with the base oil selected and performance required for finished products. Some additives impart new and useful properties to the lubricant; some enhance properties already present, while some act to reduce the rate at which undesirable changes take place in the product during its service life. Table 1 shows the different additives and their typical compounds [4].
  • 15. JoCC (2016) 18-25 © STM Journals 2016. All Rights Reserved Page 18 Journal of Catalyst and Catalysis ISSN: 2349-4344(online) Volume 3, Issue 3 www.stmjournals.com Synthesis and Study of Different Thioamides as Corrosion Inhibitors Abdurahman A. Abuabdalla Khalifa* Department of Chemistry, Faculty of Science, Aljabel-Algarbi University, Libya Abstract Many organic compounds having electron rich atoms in their structures, such as nitrogen, and sulphur are widely use in lubricating additives, in the oil industry to minimize corrosion. The presence of electron rich atoms in the molecules increases its ability to form coordinate covalent bonds with the metal atoms, involved in the corrosion environment. Compounds based on fatty amines, aromatic amines, imidazoline, diamidazoline, and fatty amides are now, uses as corrosion inhibitors, in the oil sector and are available in the market. In this work, some phenyl acetothioamide and benzyl acetothioamide are synthesized. The chemical and physical data of the prepared compounds are compiled. The solubility, cold stability, heat stability, and corrosion inhibitors characteristics, of the compounds have been measured in the artificial environment (10% crude in artificial brine at pH 4.5–4.8). Prepared thioamides differs in their molecular weights, due to presence of different organic substituent's, on the thioamides group. Synthesis of the above mentioned compounds are based on the Willgerodt- Kindler reaction. The compounds are confirmed by IR, NMR, UV-VIS, and other wet chemical analytical techniques. The experimental values of the elemental composition were compared with the calculated values and found agreeing. UV-VIS. and IR spectra also show the absorption peaks, which confirm the presence of thioamides group in the prepared compounds. The possible reaction mechanism regarding the synthesis of the above mentioned compounds is discussed and its mechanism of corrosion inhibition in the corrosive environment was explained. The compounds was evaluated in brine and sea water, some compounds having percentage protection more than 50%, the results was compared with the imported commercial inhibitors and found to be compatible. Keywords: Additives, corrosion inhibitors, market, brine INTRODUCTION Chemical anti-degradants means the chemical species which inhibit corrosion of metals and stabilize or adjust the environment in which it has been applied. Corrosion inhibitors form a protective barrier on the surface of a substrate by physical absorption, corrosion problems in the operation of petroleum drilling installation are to be solved by the aid of corrosion inhibitors in the injection water. The crude comes out with plenty of minerals containing water and the pH of this aqueous and oily mixture various but lies in the acidic side. This acidic pH, mineral contents and dissolved gases are responsible for metallic corrosion. Number of organic compound having electron rich atoms in their molecules such as nitrogen and sulphur, are widely used as corrosion inhibitors, for their anticorrosion and antioxidation properties [1, 2]. Many such types of these compounds have been synthesized having different percentage composition of nitrogen and sulphur and varying in saturations. It has been proved experimentally that higher molecular weight of the above mentioned types of compounds, higher is the anticorrosive and antioxidation properties. It may be due to more surface area of the molecules. It is also established that the sulphur containing substances are more effective anticorrosive and antioxidative compared to nitrogen containing compounds, provided the molecular weight and molecular unsaturations will be the same. Corrosion and oxidation inhibitors are routinely used in oil fields and in the refiners, in order to minimize the corrosion of the oil transporting pipe lines, pumps, valves and other involved equipment and also the refinery installations. Commercially corrosion inhibitors are unique mixtures that may contains surfactants, film
  • 16. JoCC (2016) 26-36 © STM Journals 2016. All Rights Reserved Page 26 Journal of Catalyst and Catalysis ISSN: 2349-4344(online) Volume 3, Issue 3 www.stmjournals.com Phytoextraction of Lead and Chromium by Leafy Vegetables (Lettuce, Kale and Swiss Chard) Mamu H. Teferi*, Dejene A. Tessema Department of Chemistry, College of Natural Science, Jimma University, P.O Box 387, Jimma, Ethiopia Abstract This research was carried out to assess the accumulation of Cr and Pb in leafy vegetables (lettuce, kale and Swiss chard) in their harvestable part and root from artificially polluted soil with Pb and Cr. Soil sample was characterized for its pH, organic matter (OM), cation exchange capacity (CEC), electrical conductivity (EC) and texture. Soil sample digested by mixture of HNO3 and HClO4 was analyzed. Pb accumulation in shoot was on average greater (318.36 to 1235.20 mg/kg) in S2 than S1 (169.66 to 404.80 mg/kg). Translocation of Pb from root to shoot was enhanced by the addition of spinach extract in kale and Swiss chard. Chromium translocation from root to shoot in the vegetables was limited. Less than one TF of Cr was recorded in all plants of both soil samples. Cr except lettuce grown in PES2, all the plants were able to accumulate less than 1000 mg kg-1 in their shoot. Keyword: Lead, Chromium, Photoextract INTRODUCTION Industrialization has led to the release of enormous quantities of toxic compounds into the environment. For the remediation of contaminated sites, there are numerous methods. Commonly used engineering techniques include excavation and land filling, chemical treatment and verification. These methods are extremely expensive. Due to the acute toxicity of heavy metal contaminants, there is an urgent need to develop low-cost, effective, and sustainable methods to remove or to detoxify from the environment. One of these methods is a plant based approach known as phytoremediation [1, 2]. Phytoremediation is a method of environmental treatment that makes use of the ability of some plant species to stabilize, degrade uptake pollutants or accumulate certain elements, including heavy metals, in amounts exceeding the nutrition requirements of plants [2]. Phytoremediation has includes different strategies. These are Phytotransformation (phytodegradation), Phytostabilization (space uniformity), Rhizodegradation, Phytofiltration (rhizofiltration), and Phytoextraction (phytoaccumulation) [1–4]. Phytoextraction processes extract both metallic and organic constituents from soil by direct uptake into plants and translocation to aboveground biomass. Plant used for phytoextraction are those capable of accumulating Concentration 100 times higher than in normal plants for each metal of interest, i.e., more than 10 mg kg–1 of Hg; 100 mg kg–1 of Cd; 1000 mg kg–1 of Co, Cr, Cu, Pb and Ni; and 10,000 mg kg–1 of Zn and Mn etc.; Bioconcentration factor >1 (concentration of the element in the plant > concentration in the soil); and Translocation factor >1 (element concentration in the over ground part of the Plant > than in roots) [5]. Phytoextraction has commonly two strategies. These are natural Phytoextraction which use plants with inherent capacity to extract toxic metals and educed Phytoextraction which is chemical assisted extracting method [6–9]. Metals exist in soil in five different pools: fraction 1) soluble, i.e., metals in the soil solution (as free metal ions and metal complexes); fraction 2) exchangeable, i.e., metals adsorbed on ion-exchange sites and on inorganic soil constituents; fraction 3) organic, i.e., metals bound with the organic matter;
  • 17. ISSN 2349-4344 (Online) Journal of Catalyst & Catalysis (JoCC) September–December 2016 conducted Ch Instrumentation/ / / Energy Science/ / 22 GLOBAL READERSHIP STATISTICS STM Journals Empowering knowledge Free Online Registration ISO: 9001Certified www.stmjournals.com STM JOURNALS Scientific Technical Medical