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	<title>Project report on crude oil processing - Technology Book - Feasibility Report - Market Survey - Industrial Report</title>
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	<title>Project report on crude oil processing - Technology Book - Feasibility Report - Market Survey - Industrial Report</title>
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		<title>CRUDE RICE BRAN OIL  (SOLVENT EXTRACTION PROCESS)</title>
		<link>https://projectreports.eiriindia.org/product/crude-rice-bran-oil-solvent-extraction-process/</link>
		
		<dc:creator><![CDATA[EIRI Team]]></dc:creator>
		<pubDate>Tue, 10 Jan 2023 10:52:38 +0000</pubDate>
				<guid isPermaLink="false">https://projectreports.eiriindia.org/?post_type=product&#038;p=15550</guid>

					<description><![CDATA[<p>During the polishing process of the rice, a unique vegetable oil rich in antioxidants produced from the outer layer of rice is what we called Rice bran oil (RBO). The studies around the globe have confirmed the cholesterol lowering properties due to presence of unique nutraceutical in this oil known as oryzanol &#38; tocotrienols. The crude rice bran oil is mainly composed of glycerides (80%) while phospholipids, glycolipids, free fatty acids and waxes are also present in less quantity. RBO is extensively used as premium edible oil in most of the Asian countries. Rice Bran contains around 20-22 Wt% oil depending on the Rice variety and the milling process utilized.</p>
<p>India is the second largest producer of Rice in the world. Our current production is in excess of 100 Million Tons. In India Paddy occupies the first place among all crops both in Area and Production. The crop occupies about 37% of the total cropped area and 44% of total production of food grains in India. West Bengal has the highest area under Rice Cultivation followed by AP. Punjab with a much smaller area under Rice has the highest yield.</p>
<p>Modern Milling process, like par boiling of the paddy, can deactivate the lipolytic enzyme and ensure oil quality in Bran does not deteriorate. Further, having extraction plants in close proximity also helps. It is worth noting that the quality of Oil once it is extracted does not deteriorate.</p>
<p>Rice bran oil is known as the healthiest oil on the world. It contains vitamins, antioxidants, nutrients and is trans-fat free. It can help lower cholesterol, fight blood diseases and enhance the immune system.</p>
<p>Rice Bran oil can be used to fry, sauté salad dressing, baking and wherever we use cooking oil. Rice bran oil has best balance of saturated, monounsaturated, and polyunsaturated fat as recommended by the World Health Organization.</p>
<p>Rice bran oil has a very high smoke (burn) point, making it perfect for deep frying, pan or stir frying and is a premium choice for the replacement of hydrogenated oil containing trans-fat now being used in deep fryers.</p>
<p>RBO unsaponifiables fraction is rich in vitamin E complex, tocopherols and tocotrienols, a unique antioxidant known as gamma oryzanol, high quantities of phytosterols, polyphenols and squalene. RBO has a very good shelf life compared to other cooking oils because of these antioxidants. These compounds are nutritionally very valuable and it has been shown to be responsible for the hypercholesterolemic effect. Hence, RBO not only has a good fatty acid profile, but also is a rich source of antioxidants and micronutrients.</p>
<p>RBO in the diet significantly reduces LDL cholesterol and triglycerides; it increases HDL cholesterol (good cholesterol), inhibits platelet aggregation and prevents cardiovascular diseases. Clinical studies from Japan, India and the USA have confirmed these results and named RBO as “Health Oil”. In every 1% reduction in cholesterol, there was a 2% decrease in the risk of coronary heart disease. Thus RBO in the diet significantly reduces cholesterol without any side effects.</p>
<p>It is intended to prepare a Feasibility Report to install 30000 Tons/Year Rice Bran Processing facility as a Green Field Project for the production of Crude Rice Bran Oil and Rice bran Deoiled Cake as by product..</p>
<p>The post <a href="https://projectreports.eiriindia.org/product/crude-rice-bran-oil-solvent-extraction-process/">CRUDE RICE BRAN OIL  (SOLVENT EXTRACTION PROCESS)</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p>• INTRODUCTION<br />
• USES/APPLICATION<br />
• HEALTH BENEFITS OF RICE BRAN OIL<br />
• MARKET OVERVIEW<br />
• COMPOSITION AND PROPERTIES<br />
• FORMULATION<br />
• RAW MATERIALS<br />
• SUPPLIERS OF RAW MATERIALS<br />
• MANUFACTURING PROCESS STEPS<br />
• ENGINEERING DESIGN CONSIDERATIONS<br />
• ETP FACILITY<br />
• SEWAGE AND WASTE WATER EFFLUENT<br />
• WASTE GENERATION &amp; MANAGEMENT/GREEN BELT<br />
• PLANT/MACHINERY (BROADLY)<br />
• SUPPLIERS OF PLANT &amp; MACHINERIES/TURNKEY<br />
• UTILITIES PER MONTH (ESTIMATED)<br />
• PRINCIPLES OF PLANT LAYOUT<br />
• PLANT LOCATION FACTORS<br />
• HEALTH SAFETY AND ENVIRONMENT<br />
• ANTICIPATED ENVIRONMENTAL IMPACTS<br />
• MITIGATION MEASURES (PROPOSED)<br />
• HSE REQUIREMENT<br />
• SAFETY &amp; OCCUPATIONAL MEASURE<br />
• POTENTIAL RISKS<br />
• PROPOSED IMPLEMENTATION SCHEDULE<br />
• PROJECT FINANCIALS<br />
• PRELIMINARY PLANT LAYOUT<br />
• CONCLUSIONS</p>
<p>APPENDIX – A:</p>
<p>01. PLANT ECONOMICS<br />
02. LAND &amp; BUILDING<br />
03. PLANT AND MACHINERY<br />
04. OTHER FIXED ASSESTS<br />
05. FIXED CAPITAL<br />
06. RAW MATERIAL<br />
07. SALARY AND WAGES<br />
08. UTILITIES AND OVERHEADS<br />
09. TOTAL WORKING CAPITAL<br />
10. TOTAL CAPITAL INVESTMENT<br />
11. COST OF PRODUCTION<br />
12. TURN OVER/ANNUM<br />
13. BREAK EVEN POINT<br />
14. RESOURCES FOR FINANCE<br />
15. INSTALMENT PAYABLE IN 5 YEARS<br />
16. DEPRECIATION CHART FOR 5 YEARS<br />
17. PROFIT ANALYSIS FOR 5 YEARS<br />
18. PROJECTED BALANCE SHEET FOR (5 YEARS)</p>
<p>The post <a href="https://projectreports.eiriindia.org/product/crude-rice-bran-oil-solvent-extraction-process/">CRUDE RICE BRAN OIL  (SOLVENT EXTRACTION PROCESS)</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
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		<item>
		<title>CRUDE OIL REFINING</title>
		<link>https://projectreports.eiriindia.org/product/crude-oil-refining/</link>
		
		<dc:creator><![CDATA[EIRI Team]]></dc:creator>
		<pubDate>Mon, 29 Apr 2019 06:15:31 +0000</pubDate>
				<guid isPermaLink="false">https://projectreports.eiriindia.org/?post_type=product&#038;p=12809</guid>

					<description><![CDATA[<p>Crude oil, also called petroleum, is a complex mixture of carbon and hydrogen (hydrocarbons), which exist as a liquid in the earth's crust. Crude oil has many compositions, some is black, thick and tar like, while other crude oils are lighter in color and thinner. The carbon and hydrogen in crude oil are through to have originated from the remains of microscopic marine organisms that were deposited at the bottom of seas and oceans and was transformed at high temperature and pressure into crude oil and natural gas.</p>
<p>This oil and gas migrates upward through the porous rock, as it is less dense than the water which fills the pores. The oil and gas is trapped by a layer of impermeable rock through which they can't flow. Several different types of oil and gas "traps" exist; a common dome formed by folded sedimentary rocks. Crude oil is obtained by drilling a hole into the reservoir rock (sandstone, limestone etc.) and pumping it out.</p>
<p>Although all fractions of petroleum find uses, the greatest demand is for gasoline. One barrel of crude petroleum contains only 25-35% gasoline. Transportation demands require that over 50% of the crude oil be converted into gasoline. To meet this demand some petroleum fractions must be converted to gasoline. This may be done by "cracking" - breaking down large molecules of heavy heating oil; "reforming"- changing molecular structures of low quality gasoline, molecules; or "polymerization" - forming longer molecules from smaller ones. Conversion oil Refining.</p>
<p>Petroleum products are usually grouped into three categories; light distillate (LPG, gasoline, Naphtha), middle distillate (kerosene, diesel), heavy Distillate and residium (heavy fuel oil, lubricating oil, wax, asphalt).</p>
<p>This classification is based on the way crude oil is distilled and separated into fraction (called distillate and residuum).</p>
<p>The post <a href="https://projectreports.eiriindia.org/product/crude-oil-refining/">CRUDE OIL REFINING</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p>INTRODUCTION<br />
BASICS OF CRUDE OIL<br />
TYPICAL APPROXIMATE CHARACTERISTICS AND PROPERTIES AND<br />
GASOLINE POTENTIAL OF VARIOUS CRUDES<br />
PROPERTIES<br />
OVERVIEW OF CRUDE OIL RESERVES<br />
GLOBAL MARKET POSITION OF CRUDE OIL REFINING<br />
CRUDE OIL REFINING SCENARIO IN AFGHANISTAN<br />
USES AND APPLICATIONS<br />
B.I.S. SPECIFICATION<br />
SEQUENCES IN CRUDE OIL FEFINING<br />
REFINING OF PETROLEUM CRUDE OIL<br />
FRACTIONAL DISTILLATION<br />
VACUUM DISTILLATION<br />
CRACKING<br />
PROCESSING &amp; REFINING CRUDE OIL<br />
FIGURE: CRUDE OIL DISTILLATION<br />
FIGURE: IMPORTANT PROCESSES OF A REFINERY<br />
PRODUCTS MADE FROM A BARREL OF CRUDE OIL (GALLONS)<br />
FIGURE: PRODUCTS MADE FROM CRUDE OIL<br />
MANUFACTURING PROCESS OF CRUDE OIL REFINING<br />
PROCESS DETAILS<br />
BASIS STEPS IN CRUDE OIL REFINING<br />
DISTILLATION<br />
CRACKING<br />
TREATING<br />
REFORMING<br />
PRETREATMENT OF CRUDE OIL<br />
DETAILS OF ATMOSPHERIC DISTILLATION<br />
PROCESS FLOW DIAGRAM<br />
PREVENTION METHOD OF CORROSION IN CRUDE OIL REFINERIES<br />
ENVIRONMENTAL POLLUTION AND SAFETY CONCERN IN CRUDE OIL REFINERY<br />
SUPPLIERS OF RAW MATERIALS<br />
SUPPLIERS OF PLANT AND MACHINERY<br />
BOILERS<br />
COOLING TOWER<br />
HEAT EXCHANGER<br />
STORAGE TANKS<br />
MATERIAL HANDLING EQUIPMENTS<br />
INSTRUMENTATION &amp; PROCESS CONTROL EQUIPMENTS<br />
LABORATORY EQUIPMENTS</p>
<p>APPENDIX – A:</p>
<p>1. COST OF PLANT ECONOMICS<br />
2. LAND &amp; BUILDING<br />
3. PLANT AND MACHINERY<br />
4. FIXED CAPITAL INVESTMENT<br />
5. RAW MATERIAL<br />
6. SALARY AND WAGES<br />
7. UTILITIES AND OVERHEADS<br />
8. TOTAL WORKING CAPITAL<br />
9. COST OF PRODUCTION<br />
10. PROFITABILITY ANALYSIS<br />
11. BREAK EVEN POINT<br />
12. RESOURCES OF FINANCE<br />
13. INTEREST CHART<br />
14. DEPRECIATION CHART<br />
15. CASH FLOW STATEMENT<br />
16. PROJECTED BALANCE SHEET</p>
<p>The post <a href="https://projectreports.eiriindia.org/product/crude-oil-refining/">CRUDE OIL REFINING</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
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		<item>
		<title>Liquid Rosin (Tall Oil) Production, Uses, Extraction, Processing, Compositions and Formulations Hand Book</title>
		<link>https://projectreports.eiriindia.org/product/liquid-rosin-tall-oil-production-uses-extraction-processing-compositions-formulations-hand-book/</link>
		
		<dc:creator><![CDATA[EIRI Team]]></dc:creator>
		<pubDate>Thu, 30 Aug 2018 11:02:04 +0000</pubDate>
				<guid isPermaLink="false">https://projectreports.eiriindia.org/?post_type=product&#038;p=11735</guid>

					<description><![CDATA[<div>Book Contains: Tall Oil (Liquid Rosin) Production and Processing, Composition of Distilled Tall Oils (DTO), Surfactants From Tall Oil Rosin, Crude Tall Oil for Wood Protection,  Synthesis and characterization of tall oil fatty acid, Tall Oil Fatty Acid (Alkyd-resin, Alkyd Acrylic,  Phytosterols, Phytostanols and Their Esters From Tall Oil (Liquid Rosin), Distilled Tall Oil (DTO), Antiproliferative evaluation of tall-oil docosanol and tetracosanol, Synthesis and Characterization of Novel, Production of Tall Oil Fatty Acid, Tall Oil (Liquid Rosins) Ester-acid Composition For Coating,  Dicyclopentadiene Alcohol Rosin Derivatives, Manufacturing edible oils from tall oil fatty acids, Skin care product containing tall oil fatty acids  and vegetable oils with manufacturing formula, Process For Manufacturing Valuable Products From Tall Oil Pitch, Chemically modified, maleated unsaturated fatty acids and the salts, Manufacture of A Tall Oil Rosin Ester, Production of Diesel Fuel From Crude Tall Oil, High Temperature Corrosion Inhibition, Hydraulic oil Based on Natural Fatty Acid Esters.</div>
<p>The post <a href="https://projectreports.eiriindia.org/product/liquid-rosin-tall-oil-production-uses-extraction-processing-compositions-formulations-hand-book/">Liquid Rosin (Tall Oil) Production, Uses, Extraction, Processing, Compositions and Formulations Hand Book</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div></div>
<div></div>
<div>Contents</div>
<div></div>
<div><strong>1. Tall Oil (Liquid Rosin) Production and Processing</strong></div>
<ul>
<li>Introduction</li>
<li>Composition</li>
<li>Fatty acids</li>
<li>Resin acids</li>
<li>Unsaponifiables</li>
<li>Uses of Liquid Rosins</li>
<li>Tall oil</li>
<li>Lignins</li>
<li>Calcium ions</li>
<li>Sulphide ions</li>
<li>Factors affecting quality of CTO</li>
<li>Dehydration</li>
<li>Depitching</li>
<li>Rosin separation</li>
<li>Heads separation</li>
<li>Fatty acid separation</li>
</ul>
<div><strong>2. Composition of Distilled Tall Oils (DTO)</strong></div>
<ul>
<li>Experimental Procedures</li>
<li>Results and Discussion</li>
</ul>
<div><strong>3. Surfactants From Tall Oil Rosin</strong></div>
<ul>
<li>Cationic Surfactants Experimental</li>
<li>Preparation of maleopimaric acid (MPA)</li>
<li>Preparation of rosin cationic surfactants (QRMAE)</li>
<li>Electrochemical measurement</li>
<li>Surface Activity of the prepared surfactants</li>
<li>Esterification of rosin</li>
<li>Esterification of RMA-MPEG 750</li>
<li>Characterization of the prepared Surfactants</li>
<li>Surface Activity of the prepared surfactants</li>
</ul>
<div><strong>4. Crude Tall Oil for Wood Protection</strong></div>
<ul>
<li>Sources, production and utilization of crude tall oil</li>
<li>Tall oil as a wood protection agent</li>
<li>Wood extractives and natural durability</li>
<li>Effect of tall oil on the biological durability of wood</li>
<li>Effect of tall oil on water repellency</li>
<li>Reducing the amount of oil needed</li>
<li>Enhancing the drying properties of crude tall oil</li>
<li>Enhancing the wood protection properties of tall oil</li>
<li>Biodegradability of tall oil-based wood preservatives</li>
</ul>
<div><strong>5. Synthesis and characterization of tall oil fatty acid</strong></div>
<ul>
<li>Resin synthesis</li>
<li>Materials</li>
<li>Curing process</li>
<li>Trial experiments for scheme 2 and scheme 3</li>
<li>Characterization of resins</li>
<li>Results and discussion of resins</li>
<li>FTIR analysis of the synthesized thermoset resins</li>
<li>Composite preparation</li>
<li>Hand lay-up impregnation</li>
<li>Characterization of composites</li>
<li>Flexural testing</li>
<li>Dynamic mechanical thermal analysis</li>
</ul>
<div><strong>6. Tall Oil Fatty Acid (Alkyd-resin, Alkyd Acrylic </strong></div>
<ul>
<li>Copolymers, Drying Processese</li>
<li>Introduction</li>
<li>Alkyd resin</li>
<li>Alkyd-acrylic copolymers</li>
<li>The drying process</li>
<li>Synthesis of copolymers</li>
<li>Celluloses used as fillers</li>
<li>Films and coatings</li>
<li>Characterization</li>
<li>Surface modification</li>
<li>Degree of substitution</li>
<li>Barrier properties</li>
</ul>
<div><strong>7. Phytosterols, Phytostanols and Their Esters From Tall Oil (Liquid Rosin)</strong></div>
<ul>
<li>Manufacturing</li>
<li>Production of sterols from vegetable oil distillates</li>
<li>Production of sterols from wood pulp/tall oil</li>
<li>Production of phytostanols from phytosterols</li>
<li>Production of phytosterol and phytostanol esters</li>
<li>Free fatty acid route</li>
<li>Methylester route</li>
<li>Commercial suppliers</li>
<li>Chemical Characterization</li>
<li>Composition and properties</li>
<li>Quality of phytosterols, phytostanols and their esters</li>
<li>Analytical methods</li>
<li>Regulatory status</li>
<li>Reactions and fate in foods</li>
<li>Stability at high temperatures</li>
</ul>
<div><strong>8. Distilled Tall Oil (DTO)</strong></div>
<ul>
<li>The BUS model</li>
</ul>
<div><strong>9. Antiproliferative evaluation of tall-oil docosanol and tetracosanol</strong></div>
<ul>
<li>Materials and Methods</li>
<li>Raw materials</li>
<li>Formulation of long-chain alcohols in Pluronic® F-68</li>
<li>Cell culture assays</li>
<li>Statistical analysis</li>
</ul>
<div><strong>10. Synthesis and Characterization of Novel </strong></div>
<ul>
<li>Polyurethanes Based on Tall Oil</li>
<li>Synthesis of polyols</li>
<li>Preparation and characterization of polyurethanes</li>
<li>Properties of polyols</li>
<li>Structure of polyols and polyurethanes</li>
<li>Properties of polyurethanes</li>
</ul>
<div><strong>11. Production of Tall Oil Fatty Acid</strong></div>
<div></div>
<div><strong>12. Tall Oil (Liquid Rosins) Ester-acid Composition For Coating</strong></div>
<div></div>
<div><strong>13. Dicyclopentadiene Alcohol Rosin Derivatives</strong></div>
<div></div>
<div><strong>14. Manufacturing edible oils from tall oil fatty acids</strong></div>
<div></div>
<div><strong>15. Skin care product containing tall oil fatty acids  and vegetable oils with manufacturing formula</strong></div>
<div></div>
<div><strong>16. Process For Manufacturing Valuable Products From Tall Oil Pitch</strong></div>
<div></div>
<div><strong>17. Chemically modified, maleated unsaturated fatty acids and the salts</strong></div>
<ul>
<li>Ricinoleic Acid Modification</li>
<li>Polyamine Modification</li>
<li>Amino Alcohol Modification</li>
<li>Imidazoline Modification</li>
<li>Metal Chelate Modification</li>
<li>Ester Modification</li>
<li>Amino Acid Modification</li>
<li>Polyfunctional Corrosion Inhibitors</li>
<li>Sulfonate &amp; Sulfate Modification</li>
<li>General Considerations</li>
<li>Maleation of Crude Tall Oil</li>
</ul>
<div><strong>18. Manufacture of A Tall Oil Rosin Ester</strong></div>
<ul>
<li>Detailed Description</li>
<li>Odor Level Comparison Tests</li>
</ul>
<div><strong>19. Production of Diesel Fuel From Crude Tall Oil</strong></div>
<ul>
<li>The Drawings</li>
<li>Description</li>
</ul>
<div><strong>20. High Temperature Corrosion Inhibition </strong></div>
<ul>
<li>Performance of Imidazoline and Amide</li>
<li>Experimental</li>
<li>Inhibitor Performance Evaluation</li>
<li>The tests are conducted as follows</li>
</ul>
<div><strong>21. Hydraulic oil Based on Natural Fatty Acid Esters</strong></div>
<div></div>
<div><u><strong>List of Tables</strong></u></div>
<div></div>
<ul>
<li>Table 2.1 Gross Compositional Characteristics of American Distilled Tall Oilsa</li>
<li>Table 2.2 Composition of Fatty and Resin Acids in American Distilled Tall Oils</li>
<li>Table 2.3 GLC Retention and NMR Characteristics of the Methyl Secodehydroabietatesa</li>
<li>Table 2.4 Composition of Pimaric-and Isopimaric-Type Acids Comprising Resin Acids of American Distilled Tall Oilsa</li>
<li>Table 4. 1. Composition of CTO</li>
<li>Table 4.2. Degree of water repellent efficiency (DEt) of tall oil-treated pine sapwood samples measured after 1 and 96 hours of water immersion</li>
<li>Table 4.3. Properties of the tall oil emulsions</li>
<li>Table 5.1: Different mass ratio of MA to HOTOFA</li>
<li>Table 5.2: DSC analysis table of all uncured resin samples</li>
<li>Table 5.3: TGA analysis for different cured resins</li>
<li>Table  5.4: Summary of the DMTA result</li>
<li>Table 5.5: Summary of charpy properties</li>
<li>Table 6.1. Fatty acid composition of various oils used in coatings</li>
<li>Table 6.2. Alkyd resins studied and used in copolymer synthesis</li>
<li>Table 6.3. Generalized recipe for copolymerizations</li>
<li>Table 6.4. Synthesized and studied copolymers</li>
<li>Table 6.5. Synthesized copolymer dispersions, which</li>
<li>were applied on paperboard</li>
<li>Table 6.6 Relative proportions of each proton and proton group in the polyol region</li>
<li>Table 6.7. Tg values of copolymer films and onset temperatures of the DMA measurements.The results are averages of five measurements</li>
<li>Table 6.8. Comparison of the quantity of fatty acids attached based on the integrated cellulose and acyl peaks in the 13C CPMAS NMR spectra</li>
<li>Table 6.9. Degree of substitution and O/C ratio calculated from XPS measurements</li>
<li>Table 6.10. Mechanical properties of copolymer films studied with DMA, the results are averages from 3 to 8 measurements</li>
<li>Table 7.1. Commercial suppliers of phytosterols, phytostanols and/or their esters; 1) TO: tall oil; VO: vegetable oil</li>
<li>Table 7.2: Physical characteristics and composition of different commercial phytosterols, phytostanols and their esters; 1) from TO sterols; 2) from VO sterols; 3) mainly sitosterol and campesterol</li>
<li>Table 7.3. Phytostanol concentrations in food products on the market, including portion sizes</li>
<li>Table 8.1: Composition of test materials</li>
<li>Table 8.2: Calculation of the MTT, PGE2, and (MTT + PGE2) combined score values</li>
<li>Table 8.3: Results from the MTT assay and the PGE2 determination for tissue treated with a single application of tall oils</li>
<li>Figure 8.1: Determination of the cytotoxicity of single and repeated applications of tall oils</li>
<li>Table 8.4: Results from the MTT assay and the PGE2 determination for tissue treated with repeated applications of tall oils</li>
<li>Table 9.1. Percentage of viability of CHO and melanoma cell cultures in the presence of long-chain aliphatic alcohols</li>
<li>Table 10.1. Specifications of oils</li>
<li>Table 10.2. Characteristics of polyols</li>
<li>Table 10.3. Thermal stability of polyurethanes</li>
</ul>
<div><u><strong>List of Figures</strong></u></div>
<div></div>
<ul>
<li>Figure 1 .1  The tall oil process</li>
<li>Figure 3.1. FTIR spectra of a) RMAE and b) QRMAE</li>
<li>Figure 3.2. 1HNMR spectra of a) RMAE and b) QRMAE</li>
<li>Figure 3.3 Relation between surface tension of QRMAE and time at different concentrations in a) water and b) 1M aqueous HCl solutions at 25°C.</li>
<li>Figure 3.4. Adsorption isotherms of QRMAE at different concentrations in a) water and b) 1M aqueous HCl solutions at 25°C.</li>
<li>Figure 3.5. FTIR Spectra of a) RMA and b) RMA-(MPEG 750)3</li>
<li>Figure 3.6. Relation between surface tension of R-MPEG 750 and time different concentrations in 1M aqueous HCl solutions.</li>
<li>Fig. 4.1. Simplified diagram of the tall oil distillation pr</li>
<li>Fig. 4.2. Fatty acids.</li>
<li>Fig. 4.3. Resin acids.</li>
<li>Fig. 4.4 Degree of efficiency after the initial wetting and drying cycle, measured after 1 hour of water immersion</li>
<li>Fig. 4.5 Degree of efficiency after the initial wetting and drying cycle, measured after 96 hours of water immersion</li>
<li>Fig. 4.6. Degree of efficiency after six wetting and drying cycles, measured after 1 hour of water immersion</li>
<li>Fig. 4.7. Degree of efficiency after six wetting and drying cycles, measured after 96 hours of water immersion</li>
<li>Fig. 4.8. DSC diagrams (110°C air flow) indicating the oil oxidation rate</li>
<li>Fig. 4.9. Water uptake by tall oil-treated pine sapwood in the seventh wetting and drying cycle</li>
<li>Fig. 4.10. Amounts of oil pressed out of the samples during the compression test</li>
<li>Fig. 4.11. Typical particle size distribution of a tall oil-based emulsion</li>
<li>Figure 5.1: synthesis scheme 1</li>
<li>Figure 5.2: synthesis scheme 2</li>
<li>Figure 5.3: synthesis scheme 3</li>
<li>Figure 5.4: Experimental set-up for synthesis of thermosetting resin</li>
<li>Figure 5.5: the obtained resins with three different mass ratio of MA to HOTOFA</li>
<li>Figure 5.6 : FTIR spectra comparison of TOFA and HOTOFA resins</li>
<li>Figure 5.7: FTIR spectra comparison of HOTOFA, MHOTOFA 1:1, MHOTOFA 1.5: 1 and MHOTOFA 1.76:1resins</li>
<li>Figure 5.8: DSC curve of uncured MHOTOFA 1to1 (no styrene) resin</li>
<li>Figure 5.9: DSC curve for cured MHOTOFA 1to1 resin (no styrene, room T for 1h and post cure in 150°C for another 1h)</li>
<li>Figure 5.10: Comparison of the DSC scan for cured and uncured MHOTOFA 1to1 (no styrene) resin</li>
<li>Figure 5.11: TGA analysis of cured MHOTOFA 1:1 resin (no styrene)</li>
<li>Figure 5.12: Viscose fiber and fiber mats lay-up orientation</li>
<li>Figure 5.13: Six different composites from 3 different resins (with or without styrene) reinforced by viscose fiber</li>
<li>Figure 5.14: Test specimens for flexural, DMTA, charpy, tensile</li>
<li>Figure 5.15: Flexural strength comparison of the composites</li>
<li>Figure 5.16: Flexural modulus comparison of the composites</li>
<li>Figure 5.17: Strain at break% comparison of the composites</li>
<li>Figure 5.18: variation in the storage modulus of the MHOTOFA composites</li>
<li>Figure 5.19: Tan delta curves of the MHOTOFA composites</li>
<li>Figure 5.20: the loss modulus curves of MHOTOFA composites</li>
<li>Figure 5.21: Comparison of the storage modulus between the reinforced resin (composite) and the unreinforced resin, both blended with styrene</li>
<li>Figure 5.22: Impact strength of the composites</li>
<li>Figure 6.1. Structure of typical alkyd resin</li>
<li>Figure 6.2. Miniemulsion and conventional emulsion polymerization</li>
<li>Figure 6.3. Schematic presentation of the oxidative drying of alkyd resin</li>
<li>Figure 6.5. SEC chromatograms of alkyd resins</li>
<li>Figure 6.6. Monomer conversion of copolymers with different wt% of conjugated alkyd resin (BA-MMA ratio is 80:20) (copolymers11-15 in Table 6.4)</li>
<li>Figure 6.7. Monomer conversion of copolymers with different wt% of nonconjugated Alkyd-TMP-3 and BA as monomer (copolymers 1-5 in Table 6.4)</li>
<li>Figure 6.8. Particle-size distribution of emulsion and dispersion with various alkyd contents (copolymers 1, 3, 5 in Table 6.4)</li>
<li>Figure 6.9. Grafting of acrylic macroradical to double bond (a-c) and bis-allylic site (d-f) in the fatty acid chain. a) Macroradical attacks DB in fatty acid chain. b) Grafting occurs and a new radical is formed. c) Polymerization continues at the new radical site. d) Macroradical attacks allylic hydrogen in fatty acid chain. e) Hydrogen is abstracted and a new radical is formed in fatty acid chain, where new radical approaches. f) Macroradical grafts to radical site in fatty acid chain</li>
<li>Figure 6.10. Monomer conversion and acrylic degree of grafting. BA-MMA ratio (wt%) was 80:20 in samples with conjugated alkyd (copolymers 11-15 in Table 6.4) and 100:0 in samples with nonconjugated alkyd (copolymers 1-5 in Table 6.4</li>
<li>Figure 6.11. a) Effect ofBA concentration on grafting site and efficiency. b) Effect of alkyd-acrylate ratio on various grafting sites (copolymers 16-20 in Table 6.4)</li>
<li>Figure 6.12. DSC thermograms of alkyd resin and copolymers (copolymers 16-20 in Table 6.4)</li>
<li>Figure 6.13. a) TG and b) DTG curves showing thermal stability of alkyd resin, alkyd-acrylic copolymers, and acrylic copolymer.</li>
<li>Figure 6.14. Two parts of FTIR spectra of neat whiskers and fatty acid-modified whiskers.The carbonyl peak at app. 1740 cm-1 is marked with dotted line</li>
<li>Figure 6.15. Thermal stability of neat whiskers and fatty acid-modified whiskers presented as TGA curves</li>
<li>Figure 6.16. a) ssNMR spectrum of copolymer film and freeze-dried copolymer. b) FTIR spectra of copolymer film after various drying times showing the decreasing intensity of the cis H-C=CH peak (marked with dotted line)</li>
<li>Figure 6.17. Stress-strain curves of copolymer films with various alkyd contents. One measurement of each film sample set is presented</li>
<li>Figure 6.18. Storage modulus of copolymer films with various alkyd contents. One measurement of each film sample set is presented</li>
<li>Figure 6.19. Figure 1 Water and oil absorbance of copolymer-coated cupboards (copolymers 30-37). Samples 34-37 were crosslinked with GMA</li>
<li>Figure 6.20. Effect of TOFA-modified whiskers on mechanical properties of films</li>
<li>Figure 6.21. Effect of various cellulose types on mechanical properties of the films</li>
<li>Figure 6.22. Effect of TOFA-modified cellulose on a) oxygen barrier properties (copolymers 32 and 33) and b) water and oil absorbance (copolymer 32) of copolymer-coated paperboards.</li>
<li>Figure 7.1. Steroid skeleton</li>
<li>Figure 7.2. Molecular structure of some phytosterols, phytostanols and a fatty acid ester</li>
<li>Figure 8.2: Determination of the irritancy potential of single and repeated applications of tall oils</li>
<li>Figure 8.3: The combined cytotoxicity and irritancy potential of single and repeated applications of tall oils</li>
<li>Fig. 9.1. Structure of long-chain aliphatic alcohol (polycosanols): docosanol and tetracosanol</li>
<li>Fig. 9.2. Effect of long-chain aliphatic alcohol type on CHO-K1 cell growth</li>
<li>Fig. 9.3. Effect of long-chain aliphatic alcohol type on melanoma cell growth</li>
<li>Fig. 10.1. Chemical structure of the synthesized polyols and polyurethanes, where R1 &#8211; residue of saturated and unsaturated fatty acids (C16-C24) and R2 &#8211; residue of aromatic diisocyanate</li>
<li>Fig. 10.2. IR-spectra of polyols (1, 2) and urethanes (3, 4), based on tall oil FOR2 esters (1, 3) and diethanolamides (2, 4)</li>
<li>Fig. 10.3. IR-spectra of tall oil diethanolamides (1, 2) and esters (3, 4), containing 2 % (1, 3) and 20 % (2, 4) of rosin acids</li>
<li>Fig. 10.4. IR-spectra of polyurethanes based on tall oil diethanolamides (1, 2) and esters (3, 4), containing 2 % (1, 3) and 20 % (2, 4) of rosin acids</li>
<li>Fig. 10.5. Density of polyurethanes versus the content of rosin acids</li>
<li>Fig. 10.6. Tg of polyurethanes versus the content of rosin acids</li>
<li>Fig. 10.7. Modulus of elasticity of polyurethanes versus the content of rosin acids</li>
<li>Fig. 10.8. Tensile strength of polyurethanes versus the content of rosin acids</li>
<li>Fig. 10.9. Elongation at break of polyurethanes versus the content of rosin acids</li>
<li>Fig. 10.10. Shear bond strength to wood (W) and aluminium (Al) for polyurethanes versus the content of rosin acids</li>
<li>Fig. 10.11. TGA curves of polyurethanes with the content of rosin acids of 2 %</li>
<li>Fig. 19.1 is a general flow scheme of one embodiment of the invention</li>
<li>Fig. 19.2 is a more detailed flow scheme of one embodiment of the invention</li>
</ul>
<p>The post <a href="https://projectreports.eiriindia.org/product/liquid-rosin-tall-oil-production-uses-extraction-processing-compositions-formulations-hand-book/">Liquid Rosin (Tall Oil) Production, Uses, Extraction, Processing, Compositions and Formulations Hand Book</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
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		<item>
		<title>Technology of Lubrication &#038; Lubricants, Crude Oil Processing, Catalysts in Petroleum Refining and Petrochemical Processes with Mineral Turpentine Oil</title>
		<link>https://projectreports.eiriindia.org/product/technology-lubrication-lubricants-crude-oil-processing-catalysts-petroleum-refining-petrochemical-processes-mineral-turpentine-oil/</link>
		
		<dc:creator><![CDATA[EIRI Team]]></dc:creator>
		<pubDate>Thu, 30 Aug 2018 10:56:44 +0000</pubDate>
				<guid isPermaLink="false">https://projectreports.eiriindia.org/?post_type=product&#038;p=11734</guid>

					<description><![CDATA[<p>The Book covers the following chapters: Lubrication and Lubricants, Benzene, Ethylene,  Monoethylene Glycol, Diethylene Glycol, Triethylene Glycol, Ethylene Oxide, Toluene,  Xylene,  Petroleum jelly,  Bioethanol Production From Sugar Cane Molasses,  Production of Bio-ethanol from Molasses by Schizosaccharomyces Species, Petroleum Crude Oils, Crude Oil Processing,  Chemicals Based on Methane, Ethane and Higher Paraffins-Based Chemicals,  Chemicals Based On Ethylene,  Chemicals Based on Propylene,  C4 Oleffins and Diolefins- Based Chemicals,  Chemicals Based on Benzene, Toluene, and Xylenes, Synthetic Petroleum-Based Polymers,  Catalysts in Petroleum Refining and Petrochemical Processes, Petrochemicals Future, Plant Economics of Mineral Turpentine Oil (MTO),  Plant Economics of Lubricating Oil (20w40 Grade SN Type),  Plant Economics of Oil Re-refining Unit, Plant Economics of Crude Oil Refining.</p>
<p>The post <a href="https://projectreports.eiriindia.org/product/technology-lubrication-lubricants-crude-oil-processing-catalysts-petroleum-refining-petrochemical-processes-mineral-turpentine-oil/">Technology of Lubrication &#038; Lubricants, Crude Oil Processing, Catalysts in Petroleum Refining and Petrochemical Processes with Mineral Turpentine Oil</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div><strong>Contents:</strong></div>
<div></div>
<div><strong>Lubrication and Lubricants </strong></div>
<ul>
<li>Functions of Lubricants</li>
<li>Lubrication Principles</li>
<li>Tests of Lubricants</li>
<li>Lubricants of Mineral Origin</li>
<li>Synthetic Lubricants</li>
</ul>
<div><strong>Benzene </strong></div>
<ul>
<li>Manufacturing Process From Petroleum by</li>
<li>Catalytic Reforming</li>
</ul>
<div><strong>Ethylene </strong></div>
<ul>
<li>From Refinery Gas by Thermal Cracking</li>
</ul>
<div><strong>Monoethylene Glycol</strong></div>
<ul>
<li>Molecular Formula</li>
</ul>
<div><strong>Diethylene Glycol </strong></div>
<ul>
<li>Molecular Formula</li>
</ul>
<div><strong>Triethylene Glycol </strong></div>
<ul>
<li>Monoethylene Glycol From Ethylene and Oxygen</li>
<li>Uses</li>
<li>Grades</li>
<li>Toxicity</li>
</ul>
<div><strong>Ethylene Oxide  </strong></div>
<ul>
<li>Molecular Formula</li>
<li>Properties</li>
<li>Manufacturing Process</li>
<li>From Ethylene and Oxygen</li>
<li>Raw material requirement</li>
</ul>
<div><strong>Toluene  </strong></div>
<ul>
<li>Properties</li>
<li>Manufacturing Process</li>
<li>From Petroleum by Hydroforming</li>
<li>Raw material requirement</li>
</ul>
<div><strong>Xylene </strong></div>
<ul>
<li>Properties of Xylene Isomers</li>
<li>Manufacturing Process</li>
<li>Form Petroleum by Catalytic Reforming or</li>
<li>hydroforming</li>
</ul>
<div><strong>Petroleum jelly </strong></div>
<ul>
<li>Physical properties</li>
<li>Comparison with glycerol</li>
<li>Uses</li>
<li>Medical treatment</li>
<li>Skin and hair care</li>
<li>Preventing moisture loss</li>
<li>Hair grooming</li>
<li>Skin lubrication</li>
<li>Product care and protection</li>
<li>Coating</li>
<li>Finishing</li>
<li>Lubrication</li>
<li>Production processes</li>
<li>Tattooing</li>
<li>Explosives</li>
<li>Mechanical, barrier functions</li>
<li>Surface cleansing</li>
<li>Pet care</li>
<li>Clean-up</li>
<li>Properties of Petroleum Jelly</li>
<li>Skin Care</li>
<li>Face Care</li>
<li>Hair Care</li>
<li>Nail Care</li>
<li>Household Needs</li>
</ul>
<div><strong>Bioethanol Production From Sugar Cane </strong><strong>Molasses </strong></div>
<ul>
<li>Ethanol</li>
<li>Feedstock for bioethanol production</li>
<li>Sucrose-containing feedstocks</li>
<li>Starchy materials</li>
<li>Lignocellulosic biomass</li>
<li>Ethanol from cane molasses</li>
<li>Processes of ethanol production</li>
</ul>
<div><strong>Production of Bio-ethanol from Molasses </strong><strong>by Schizosaccharomyces Species </strong></div>
<ul>
<li>Introduction</li>
<li>Materials And Methods</li>
<li>Collection of Samples</li>
<li>Isolation of Schizosaccharomyces</li>
<li>Production of Ethanol from Molasses</li>
<li>Identification of the Microorganisms</li>
<li>Originally Present in Molasses</li>
<li>Inoculation of Molasses by Isolated Yeast</li>
<li>Distillation and Detection of Ethanol</li>
<li>Results And Discussion</li>
<li>Isolation of Schizosaccharomyces</li>
<li>Species</li>
<li>Physical Characteristics of the</li>
<li>Molasses Sample</li>
<li>Microorganisms Originally Present</li>
<li>in Molasses</li>
<li>Production of Ethanol from Raw</li>
<li>Molasses</li>
<li>Production of Ethanol from Molasses</li>
<li>with Different Concentrations of Sucrose</li>
<li>Detection of Ethanol</li>
</ul>
<div><strong>Petroleum Crude Oils </strong></div>
<ul>
<li>Composition of Crude Oils</li>
<li>Hydrocarbon Compounds</li>
<li>Alkanes (Paraffins)</li>
<li>Cycloparaffins (Naphthenes)</li>
<li>Aromatic Compounds</li>
<li>Non-hydrocarbon Compounds</li>
<li>Sulfur Compounds</li>
<li>Acidic Sulfur Compounds</li>
<li>Non-acidic Sulfur Compounds</li>
<li>Nitrogen Compounds</li>
<li>Basic Nitrogen Compounds</li>
<li>Non-Basic Nitrogen Compounds</li>
<li>Oxygen Compounds</li>
<li>Acidic Oxygen Compounds</li>
<li>Non-Acidic Oxygen Compounds</li>
<li>Metallic Compounds</li>
<li>Density, Specific Gravity and API Gravity</li>
<li>Salt Content</li>
<li>Sulfur Content</li>
<li>Pour Point</li>
<li>Ash Content</li>
</ul>
<div><strong>Crude Oil Processing</strong></div>
<ul>
<li>Physical Separation Processes</li>
<li>Atmospheric Distillation</li>
<li>Vacuum Distillation</li>
<li>Absorption Process</li>
<li>Adsorption Process</li>
<li>Solvent Extraction</li>
<li>Conversion Processes</li>
<li>Thermal Conversion Processes</li>
<li>Coking Processes</li>
<li>Thermal Cracking Reactions</li>
<li>Delayed Coking</li>
<li>Fluid Coking</li>
<li>Viscosity Breaking (Vis-breaking)</li>
<li>Catalytic Conversion Processes</li>
<li>Catalytic Reforming</li>
<li>Reformer Feeds</li>
<li>Reforming Catalysts</li>
<li>Reforming Reactions</li>
<li>From Acetylene and Acetone</li>
<li>From Isobutylene and Formaldehyde (IFP Process)</li>
<li>From Isobutylene and Methylal (Sun Oil Process)</li>
<li>From Propylene (Goodyear Process)</li>
</ul>
<div><strong>Chemicals Based on Methane</strong></div>
<ul>
<li>Chemicals Based On Direct Reactions of Methane</li>
<li>Carbon Disulfide (CS)</li>
<li>Uses Of Carbon Disulfide</li>
<li>Hydrogen Cyanide (Hcn)</li>
<li>Chloromethanes</li>
<li>Production of Chloromethanes</li>
<li>Uses of Chloromethanes</li>
<li>SYNTHESIS GAS</li>
<li>CHEMICALS BASED ON SYNTHESIS GAS</li>
<li>AMMONIA (NH)</li>
<li>Uses of Ammonia</li>
<li>Nitric Acid (HNO)</li>
<li>Hydrazine (HN-NH).</li>
<li>Methylalcohol (CHOH)</li>
<li>Production of Methanol</li>
<li>Uses of Methanol</li>
<li>Methyl Chloride (CHCI)</li>
<li>Acetic Acid (CHCOOH)</li>
<li>Methyl Tertiary Butyl Ether ((CH)C-O-CH)</li>
<li>Dimethyl Carbonate (CO(OCH))</li>
<li>Methylamines</li>
<li>Ethylene Glycol</li>
</ul>
<div><strong>Ethane and Higher Paraffins-Based Chemicals </strong></div>
<ul>
<li>Ethane Chemicals</li>
<li>Propane Chemicals</li>
<li>Oxidation of Propane</li>
<li>Nitration of Propane (Production of Nitroparaffins)</li>
<li>N-butane Chemicals</li>
<li>Oxidation of N-butane (Acetic Acid and</li>
<li>Acetaldehyde)</li>
<li>Maleic Anhydride:</li>
<li>Aromatics Production</li>
<li>Isobutane Chemicals</li>
<li>Naphtha-based Chemicals</li>
<li>Chemicals From High Molecular Weight</li>
<li>N-paraffins</li>
<li>Oxidation Of Paraffins (Fatty Acids And Fatty</li>
<li>Alcohols)</li>
<li>Chlorination Of N-paraffins (Chloroparaffins)</li>
</ul>
<div><strong>Chemicals Based On Ethylene</strong></div>
<ul>
<li>Introduction</li>
<li>Oxidation Of Ethylene</li>
<li>Derivatives of Ethylene Oxide</li>
<li>Ethylene Glycol (CHOHCHOH)</li>
<li>Ethoxylates</li>
<li>Ethanolamines</li>
<li>,-Propanediol</li>
<li>Acetaldehyde (Chcho)</li>
<li>Important Chemicals From Acetaldehyde</li>
<li>Acetic Acid</li>
<li>N-butanol</li>
<li>Oxidative Carbonylation of Ethylene</li>
<li>Chlorination of Ethylene</li>
<li>Vinyl Chloride (Ch=Chcl)</li>
<li>Linear Alcohols</li>
</ul>
<div><strong>Chemicals Based on Propylene</strong></div>
<ul>
<li>Oxidation of Propylene</li>
<li>Acrolein (CH=CHCHO)</li>
<li>Uses of Acrolein</li>
<li>Ammoxidation Of Propylene</li>
<li>(Acrylonitrile [CH=CHCN])</li>
<li>Uses of Acrylonitrile</li>
<li>Adiponitrile (NC(CH)CN)</li>
<li>Deriatives and Uses of Propylene Oxide</li>
<li>Propylene Glycol (CHCH(OH)CHOH)</li>
<li>Allyl Alcohol (CH=CHCHOH)</li>
<li>Oxyacylation of Propylene</li>
<li>Chlorination of Propylene</li>
<li>(Allyl Chloride [Ch=Chchcl])</li>
<li>Hydration of Propylene</li>
<li>(Isopropanol [Chchohch])</li>
<li>Properties And Uses of Isopropanol</li>
<li>Acetone Production</li>
<li>Propertles and Uses of Acetone</li>
</ul>
<div><strong>C4 Oleffins and Diolefins- Based Chemicals </strong></div>
<ul>
<li>Introduction</li>
<li>Chemicals From N-butenes</li>
<li>Oxidation of Butenes</li>
<li>Acetic Acid CHCOH</li>
</ul>
<div><strong>Chemicals Based on Benzene, Toluene, and </strong><strong>Xylenes </strong></div>
<ul>
<li>Reactions and Chemicals of Benzene</li>
<li>Reactions and Chemicals of Toluene</li>
<li>Oxidation of Toluene</li>
<li>Caprolactam Production</li>
<li>Phenol from Benzoic Acid</li>
<li>Terephthalic Acid from Benzoic Acid</li>
<li>Chlorination of Toluene</li>
<li>Nitration of Toluene</li>
<li>Carbonylation of Toluene</li>
<li>Chemicals From Xylenes</li>
<li>Terephthalic Acid (Hoocc6h4cooh)</li>
</ul>
<div><strong>Synthetic Petroleum-Based Polymers </strong></div>
<ul>
<li>Introduction</li>
<li>Thermoplastics And Engineering Resins</li>
<li>Polyethylene</li>
<li>Low-Density Polyethylene</li>
<li>High-Density Polyethylene</li>
<li>Linear Low-Density Polyethylene</li>
<li>Properties and Uses of Polyethylenes</li>
<li>Polypropylene</li>
<li>Copolymerization</li>
<li>Properties and Uses of Polypropylene</li>
<li>Properties and Uses of Polyvinyl Chloride</li>
<li>Properties and Uses of Styrene Polymers</li>
<li>Nylon Resins</li>
<li>Thermoplastic Polyesters</li>
<li>Polycarbonates</li>
<li>Properties and Uses of Polycarbonates</li>
<li>Polyether Sulfones</li>
<li>Properties and Uses of Aromatic Polyether Sulfones</li>
<li>Poly(phenylene) Oxide</li>
<li>Polyacetals</li>
<li>Thermosetting Plastics</li>
<li>Polyurethanes</li>
<li>Properties and Uses of Polyurethanes</li>
<li>Epoxy Resins</li>
<li>Properties and Uses of Epoxy Resins</li>
<li>Unsaturated Polyesters</li>
<li>Phenol-formaldehyde Resins</li>
<li>Properties and Uses of Phenolic Resins</li>
<li>Amino Resins (Aminoplasts)</li>
<li>Urea-Formaldehyde and Urea-Melamine Resins</li>
<li>Properties and Uses of Aminoplasts</li>
<li>Polycyanurates</li>
<li>Synthetic Rubber</li>
<li>Butadiene Polymers And Copolymers</li>
<li>Properties and Uses of Polybutadiene</li>
<li>Styrene-Butadiene Rubber (SBR)</li>
<li>Nitrile Rubber (Nbr)</li>
<li>Polyisoprene</li>
<li>Properties and Uses of Polyisoprene</li>
<li>Polychloroprene (Neoprene Rubber)</li>
<li>Butyl Rubber</li>
<li>Ethylene-propylene Rubber</li>
<li>Transpolypentamer</li>
<li>Thermoplastic Elastomers</li>
<li>Synthetic Fibers</li>
<li>Polyester Fibers</li>
<li>Polyethylene Terephthalate Production</li>
<li>Properties and Uses of Polyesters</li>
<li>Polyamides (Nylon Fibers)</li>
<li>Nylon  (Polyhexamethyleneadipate)</li>
<li>Nylon  (Polycaproamide)</li>
<li>Nylon  (Polylaurylamide)</li>
<li>Nylon  (Polybutyramide)</li>
<li>Nylon  (Polyundecanylamide)</li>
<li>Other Nylon Polymers</li>
<li>Properties and Uses of Nylons</li>
<li>Acrylic And Modacrylic Fibers</li>
<li>Properties and Uses of Polyacrylics</li>
<li>Carbon Fibers (Graphite Fibers)</li>
<li>Polypropylene Fibers</li>
</ul>
<div><strong>Catalysts in Petroleum Refining and </strong><strong>Petrochemical Processes  </strong></div>
<ul>
<li>Introduction</li>
<li>Homogeneous and Heterogeneous Catalysts</li>
<li>Catalyst Morphology and Activity</li>
<li>Catalysts for Petroleum Refining</li>
<li>Cracking Catalysts</li>
<li>Reforming Catalysts</li>
<li>Hydrotreating Catalysts</li>
<li>Catalysts For Petrochemicals Industry</li>
<li>Catalysts For Synthesis Gas</li>
<li>Hydrogenation Catalysts</li>
<li>Hydrocarbon Oxidation Catalysts</li>
<li>Polymerization Catalysts</li>
<li>Recent Advances in Industrial Catalysis</li>
<li>Dual-Function Catalysts</li>
<li>Super-Active Metal Catalysts</li>
<li>Supported-Ziegler Catalysts</li>
<li>Advances in Homogeneous Catalysis</li>
<li>Role of Polymers in Catalysis</li>
</ul>
<div><strong>Petrochemicals Future </strong></div>
<ul>
<li>Integrated Petrochemicals Complex</li>
<li>Natural Gas As Petrochemical Feedstock</li>
<li>Impact Of Heavy Feedstocks</li>
<li>On Petro-chemicals</li>
<li>Ecology And The Energy Crisis</li>
<li>Coal As An Alternative To Oil</li>
<li>Energy Crisis and the Industrial Fuels</li>
<li>Natural Fuels</li>
<li>Synthetic Fuels</li>
<li>Hydrogen: Fuel for tomorrow</li>
<li>Trends in Petrochemical Industry</li>
<li>Development in Cracking Technology</li>
<li>Olefins Vs Paraffins</li>
<li>Prospect for Propylene</li>
<li>Size of Plant</li>
<li>Biomass: Renewable Resource for Petrochemicals</li>
<li>Waste Disposal</li>
</ul>
<div><strong>Plant Economics of Mineral Turpentine Oil (MTO) </strong></div>
<ul>
<li>Plant &amp; Machinery</li>
<li>Fixed Capital</li>
<li>Raw Materials</li>
<li>Total Working Capital/Month</li>
<li>Total Capital Investment</li>
<li>Turn Over/Annum</li>
</ul>
<div><strong>Plant Economics of Lubricating Oil (20w40  </strong><strong>Grade Sn-Type) </strong></div>
<ul>
<li>Plant &amp; Machinery</li>
<li>Fixed Capital</li>
<li>Raw Materials</li>
<li>Total Working Capital/Month</li>
<li>Total Capital Investment</li>
<li>Turn Over/Annum</li>
</ul>
<div><strong>Plant Economics of Oil Re-refining Unit </strong></div>
<ul>
<li>Plant &amp; Machinery</li>
<li>Fixed Capital</li>
<li>Raw Materials</li>
<li>Total Working Capital/Month</li>
<li>Total Capital Investment</li>
<li>Turn Over/Annum</li>
</ul>
<div><strong>Plant Economics of Crude Oil Refining </strong></div>
<ul>
<li>Plant &amp; Machinery</li>
<li>Fixed Capital</li>
<li>Raw Materials</li>
<li>Total Working Capital/Month</li>
<li>Total Capital Investment</li>
<li>Turn Over/Annum</li>
</ul>
<div></div>
<div><strong>List of Tables</strong></div>
<div>Table : Properties and uses of various types of greases</div>
<div>Table : Specification for Commercial Grades of Benzene</div>
<div>Table : Typical specification for polymer-grade ethylene</div>
<div>Table :  Specifications of Technical Grades of</div>
<div>Ethylene Glycol</div>
<div>Table :  Specification for Technical Grade Diethylene</div>
<div>Glycol and Triethylene Glycol</div>
<div>Table : Commercial specifications of Industrial Xylene</div>
<div>Table : Type of feedstock</div>
<div>Table : Physical properties of Ethanol</div>
<div>Table : Different feedstock for bioethanol production and their comparative production potential.</div>
<div>Table : Main components of cane black strap molasses</div>
<div>Table : Microbiological analysis of sugarcane</div>
<div>molasses</div>
<div>Table : Production of ethanol and pH value from raw molasses</div>
<div>Table : Production of ethanol and pH value from molasses with different concentrations of sucrose</div>
<div>Table : Heating values of methane and heavier hydrocarbons present in natural gas</div>
<div>Table : Typical analysis of some crude oils</div>
<div>Table : Approximate ASTM boiling point ranges for</div>
<div>crude oil fractions</div>
<div>Table: Types of petroleum cokes and their end uses</div>
<div>Table : Major thermoplastic polymers</div>
<div>Table : Important properties of polyethylenes</div>
<div>Table : Properties of Polypropylene</div>
<div>Table : Properties of polycarbonates compared with</div>
<div>some thermoplastics</div>
<div>Table : Selected properties of some elastomers</div>
<div>Table : Important properties of polyesters</div>
<div>Table : Melting points of various nylons and the</div>
<div>monomer formula</div>
<div>Table :  Physical properties of fiber-grade</div>
<div>polypropylene</div>
<div>Table : Characteristics of Typical Catalysts used in Petroleum Refining.</div>
<div>Table :  Important Catalytic Processes of Refining</div>
<div>and Petrochemical Industry</div>
<div>Table : Major Catalysts in use in IPCL Plants</div>
<div>Table : Industrially Important Free-Racial</div>
<div>Polymerization Catalysts</div>
<div>Table :  Ziegler-Type Catalysts used in Polymer</div>
<div>Manufacture</div>
<div>Table : HOPE Catalysts.</div>
<div>Table :  Miscellaneous Catalysts used In Polymer</div>
<div>Industry.</div>
<div>Table :  Relative Cost of Ethylene Production from</div>
<div>Various Feedstocks</div>
<div>Table : Octane Number of Aromatics.</div>
<div>Table : Calorific Value of Fuels.</div>
<div>Table :  Comparative Cost of Production of Various</div>
<div>Fuels.</div>
<div>Table : Sources of Hydrogen.</div>
<div>Table :  Yield Pattern from a High Severe Cracking</div>
<div>Furnace.</div>
<div>Table :  Comparative Study of Propane and</div>
<div>Propylene Routes to Acrylonitriie</div>
<div>List of figures</div>
<div>Fig  Fluid film formation in bearing</div>
<div>Fig : Ethanol structure</div>
<div>Fig : Sugar refinery process</div>
<div>Fig.: Enzymatic hydrolysis of starch to glucose.</div>
<div>Fig. : Flow chart of ethanol production from cereal</div>
<div>grains.</div>
<div>Fig.  Culture characteristics of Schizosacc-</div>
<div>haromyces species</div>
<div>Fig.  Microscopic appearance of Schizosacc-</div>
<div>haromyces species using Gram stain technique</div>
<div>Fig.  KMnOH+ before addition of sample (a),</div>
<div>Reduction of KMnOH+ to colourless after</div>
<div>addition of sample (b)</div>
<div>Fig.  KCrOH+before addition of</div>
<div>sample (a), KCrOH+after addition change</div>
<div>into colour (b)</div>
<div>Fig.  Iodine reagent before addition sample (a),</div>
<div>addition of sample and heating, colour of iodine</div>
<div>change into blue colour (b) and when cooling in water</div>
<div>and added NaOH, the reaction formed yellow colour</div>
<div>precipitate</div>
<div>called iodo-form (c)</div>
<div>Fig  Flow diagram of atmospheric and vacuum</div>
<div>distillation units: (,) heat exchangers; () desalter,</div>
<div>(,) heater; () distillation column, () overhead</div>
<div>condenser, (-) pump around streams, () vacuum</div>
<div>distillation heater; () vacuum tower.</div>
<div>Fig  Important chemicals based on methane,</div>
<div>synthesis gas, ammonia, and methanol.</div>
<div>Fig  A block flow diagram showing the combined</div>
<div>reforming for methanol synthesis.</div>
<div>Fig  The Haldor Topsoe and Nippon Kasei</div>
<div>process for producing formaldehyde:  () blower,</div>
<div>() heat exchanger, () reactor, () steam boiler,</div>
<div>() absorber, (,) coolers, () incinerator, () heat</div>
<div>recovery, () methanol evaporator, () boiler</div>
<div>feed water.</div>
<div>Fig  Major chemicals based on ethylene.</div>
<div>Fig  Important chemicals based on propylene.</div>
<div>Fig . Important chemicals based on benzene.</div>
<div>Fig . The reaction scheme for o-xylene to phthalonitrile</div>
<div>Fig  The Union Carbide Unipol process for producing</div>
<div>Fig  The Union Carbide gas-phase process for gh</div>
<div>producing polypropylene: () reactor, () centri-</div>
<div>fugal compressor, () heat exchanger, () product</div>
<div>discharge tank (unreacted gas separated from product),</div>
<div>() impact reactor, () compressor, () heat exchanger,</div>
<div>() discharge tank (copolymer separated from reacted</div>
<div>gas).</div>
<div>Fig  Polyvinyl chloride</div>
<div>Fig  The European Vinyls Corp. process for</div>
<div>producing polyvinyl chloride using suspension polymeri-</div>
<div>zation : () reactor, () blow-down vessels (to</div>
<div>separate unreacted monomer), () stripping column,</div>
<div>() reacted monomer recovery, () slurry centrifuge,</div>
<div>() slurry drier.</div>
<div>Figure  The Lummus Crest Inc. process for</div>
<div>producing polystyrene: () reactor, () holding</div>
<div>tank (Polystyrene beads and water), () centrifuge,</div>
<div>() pneumatic drier, () conditioning tank, () screening of</div>
<div>beads, (,) lubrication and blending, () shipping product.</div>
<div>Figure  The comparative thickness for the same</div>
<div>degree of insulation (dry conditions).</div>
<div>Figure  A process for producing ,-polyisoprene</div>
<div>(&gt;%) by a continuous solution polymerization.</div>
<div>Figure  The Inventa AG Process for</div>
<div>producing polyethylene-terephthala</div>
<div>Figure  The Inventa-Fisher process for producing</div>
<div>nylon  from caprolactam: () Melting station, (, )</div>
<div>polymerization reactors, () extruder, () intermediate</div>
<div>vessel, () extraction column, (,) extraction</div>
<div>columns, () cooling silo.</div>
<p>The post <a href="https://projectreports.eiriindia.org/product/technology-lubrication-lubricants-crude-oil-processing-catalysts-petroleum-refining-petrochemical-processes-mineral-turpentine-oil/">Technology of Lubrication &#038; Lubricants, Crude Oil Processing, Catalysts in Petroleum Refining and Petrochemical Processes with Mineral Turpentine Oil</a> appeared first on <a href="https://projectreports.eiriindia.org">EIRI - eBooks and Project Reports</a>.</p>
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