Search or add a thesis

Advanced Search (Beta)
Home > Thermal and Catalytic Degradation of High-Density Polyethylene for Energy Recovery and Quality Environment

Thermal and Catalytic Degradation of High-Density Polyethylene for Energy Recovery and Quality Environment

Thesis Info

Access Option

External Link

Author

Gulab, Hussain

Program

PhD

Institute

University of Peshawar

City

Peshawar

Province

KPK

Country

Pakistan

Thesis Completing Year

2010

Thesis Completion Status

Completed

Subject

Chemistry

Language

English

Link

http://prr.hec.gov.pk/jspui/bitstream/123456789/12322/1/Hussain%20Gulab%20chemistry%202010%20uni%20of%20peshwar%20prr.pdf

Added

2021-02-17 19:49:13

Modified

2024-03-24 20:25:49

ARI ID

1676727605500

Asian Research Index Whatsapp Chanel
Asian Research Index Whatsapp Chanel

Join our Whatsapp Channel to get regular updates.

Similar


Polymers wastes create great environmental problems in different ways and therefore should be properly disposed. To convert these waste polymers to other useful products like feedstock chemicals and fuel is a promising solution to these problems. The objective of this work is to develop environmental friendly methods for the degradation of Highdensity polyethylene (HDPE) into useful products which could be directly or indirectly used as chemicals or fuel. The first chapter of this dissertation is concerned about a brief introduction of different types of polymers. It includes history and classification of polymers and information regarding the types, formulas, structures and characteristic of different types of polymers. Different types of polyethylenes have been discussed in this chapter. It focuses specifically on HDPE and its different preparation methods have been included in this chapter. It also describes properties and applications of polyethylene (PE), more specifically HDPE. Several degradation methods and mechanistic aspects of the degradation processes have been discussed. The second chapter covers a thorough review of the recent and relevant literature reported for the thermal and thermocatalytic degradation of PE and HDPE. Chapter III consists of experimental methods applied for thermal and catalytic conversion of HDPE. Different equipments used in the study and experimental procedures have been discussed. Indigenous batch reactor and furnace consisting of IR heating elements were used for the catalytic and thermal pyrolysis of HDPE. The liquid products were fractionated and the fractions were analyzed by GC and GC/MS. Different physical parameters for the oil products were studied. Chapter IV is concerned with results and discussion about the experimental findings. For maximum conversion into oil products, conditions like temperature, catalyst weight and reaction time and nitrogen flow rate were optimized. Several catalysts like MgCO3, CaCO3, BaCO3, Ultra stable Y-zeolite (US-Y), were applied for the catalytic degradation of HDPE. Different temperatures like 250oC, 300oC, 350oC, 395oC, 400oC, 410oC, 420oC, 430oC, 440oC, 450oC, 460oC and 480oC were explored in order to find out the optimum reaction temperature for thermal and catalytic degradation process of HDPE. From the catalytic degradation of HDPE using these catalysts, it was found that among the carbonates, MgCO3 and CaCO3 were approximately effective up to an equal extent in terms of total conversion (96.80% and 97.20% respectively) and oil yield (51.87% and 52.33% respectively) but the temperature for the later catalyst was 460°C and for the former it was 450°C. Reaction time and cat/pol ratio in both the cases were same (1.5 h). In case of BaCO3 catalyst the total conversion (96.07%) was comparable with total conversion achieved with MgCO3 and CaCO3 but the liquid yield (41.33%) was considerably low. Among the applied zeolite catalysts, the powdered US-Y was found to be the most efficient catalyst for the degradation of HDPE. With US-Y catalyst, a total percent conversion of 96.70% was achieved in a 25min experiment with nitrogen flow rate of 10mL/min and a cat/pol ratio of 1:8 at a very low reaction temperature of 395°C. The % oil yield in this case was 71.45%. Under the same experimental conditions but at a higher temperature (420°C), the total % conversion achieved was 96.34% with a little increase in the % oil yield (72.13%). The liquid products obtained thermally and catalytically in bulk quantities were fractionated at different temperatures like100°C, 150°C, 200°C, 250°C and 300°C. The parent liquid products and the fractions collected at different temperatures were characterized by physicochemical tests. The physical parameters like refractive index, density, specific gravity, API gravity, viscosity, kinematic viscosity, flash point, calorific value and ASTM distillation were determined according to IP and ASTM standard methods for fuel values. From the physical tests, it was observed that the results for the liquid fractions were somehow comparable with the standard values for gasoline, kerosene and diesel oil. All the fractions and parent liquids were analyzed by GC and on the basis of boiling point distribution (BPD), the composition of samples was investigated. GC/MS analysis of these samples was also conducted in order to determine the exact composition of thermally and catalytically derived liquids. With increasing distillation temperature, a gradual increase in the percentage of heavier hydrocarbons was observed. It could be concluded, that catalytic degradation of HDPE yields valuable products in terms of fuel oils and chemical feedstocks on one hand and could be a best solution to environmental problems caused by HDPE on the other hand. However more efforts are required to apply this catalytic degradation process for the proper disposal of waste HDPE on industrial scale.
Loading...
Loading...

Similar Books

Loading...

Similar Chapters

Loading...

Similar News

Loading...

Similar Articles

Loading...

Similar Article Headings

Loading...

لومڑی دی چالاکی تے کاں دی بے وقوفی

لومڑی دی چالاکی تے کاں دی بے وقوفی

اک دفعہ دا ذکر اے کہ اک کاں نوں کسے حلوائی دی دکان توں اک پنیر دا تکڑا ملیا۔ کاں نے اوس نوں اپنی چنج نال گھٹ کے پھڑیا تے اڈ کے درخت دی اُچی تھاں اُتے بہہ گیا۔ دل ای دل وچ بہت خوش ہویا کہ اج کھان نوں بڑے دناں بعد چنگی شے ملی اے۔ اوہ خوشی وچ کھاون دا سوچ ای رہیا سی کہ اوہدر اک لومڑی آ گئی۔ کاں کول پنیر دا ٹوٹا ویکھ کے لومڑی دے منہ وچ پانی آ گیا۔ اوہ سوچن لگی کہ کویں ایہہ ٹوٹا کاں کولوں کھو لیا جاوے۔ لومڑی اپنی چالاکی پاروں سارے جانوراں وچ مشہور اے۔ اوس دے دماغ وچ اک تجویز آئی۔ اوہ کاں دی خوشامد کرن لگی۔ اوس آکھیا۔

’’بھرا کاں! توں اک بہت سوہنا پرندہ ایں۔ تیرے پر کنے سوہنے نیں تے تیرا رنگ کناں چمکیلا اے۔۔۔ میرے خیال وچ تیری آواز وی رنگ تے پراں وانگ بہت سوہنی ہووے گی۔ تیری بڑی مہربانی ہووے گی کہ توں مینوں اک سریلا گیت سنا دیویں۔‘‘

کاں نے لومڑی دے موہنوں جدوں اپنی تعریف سنی تاں بہت خوش ہویا۔ اوس فوراً گیت سناون لئی اپنا منہ کھولیا۔ تاں اوہ پنیر دا ٹوٹا اوہدے منہ وچوں نکل کے زمین اتے ڈگ پیا۔ لومڑی نے چھیتی نال اوس نوں چکیا تے کھا لیا تے کاں اپنی بے وقوفی تے افسوس کردا رہ گیا۔

روایتی بینکاری نظام کے ارتقائی مراحل کا تحقیقی جائزہ

The concept of keeping wealth in a safe place dates to centuries. Ancient civilizations had diverse means of storing wealth in the form of crops, cattle, precious metals etc. The evolution of modern banking practice began with the introduction of receipts which were exchanged against precious metals and coins deposited to goldsmiths for safe keeping. Whenever the need for payments and transactions arose the holder of the receipts used to utilize the receipts as guarantee. The society used to honor these receipts as they carried the same weight as other precious metals. Receipts were swapped in place of precious metals and thus for all practical purposes paper was introduced as currency in the society. With the advent of currency notes the system of traditional banking came into being. Since then the banking system has gone through continuous change. The present banking system is geared up to meet the present and the future requirements of modern age. In the contemporary world money is now being steadily replaced by banknotes, cheques, pay orders, bank draft, ATM cards, debit cards, credit cards, e-banking.

Template Assisted Synthesis of Carbonized Polymer Nanowires

Nanomaterials synthesis is a highly focused area now-a-days due to great significance of nanomaterials in terms of their vast applications including nano-sensors, nano-catalysts, nano-electro-mechanical systems (NEMS) and memory devices etc. One of the facile and low cost techniques to synthesize nanomaterials is the use of templates. A template acts like a scaffold to restrict the in-filtered material and produces nano-scopic replica of it. Since the synthesis takes place in the confined nanospaces, hence high surface area nanostructures can be achieved. By using this type of synthetic strategy, nanostructures can be tailored according to the prescribed requirement through the control of the design of templates. The present thesis presents the work on the synthesis of carbonized polymer nanowires through template mediated technique using different carbon precursors including poly (vinyl) alcohol (PVA), poly (vinyl) chloride (PVC) and chitosan. For synthesis of carbon nanowires, from poly(vinyl) alcohol, carbonization was performed at temperatures of 300°C, 400°C, 500°C, 600°C, 700°C ,800°C and 900°C in the absence of any catalyst. Scanning electron microscopy (SEM) revealed the diameter of the nanowires in the range of 90-120 nm. Detailed characterization using SEM, thermal gravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy and Raman spectroscopy was done confirming the formation of nano-wires and graphitization of amorphous carbon resulting from the PVA pitch. The nanowires formed at temperatures of up to about 600oC were rigid, while those formed at 700oC were quite flexible. At 800oC and 900oC, the nanowires formed were again rigid but of shorter length due to fragmentation of the wires produced. It could be due to the formation of graphitic clusters / crystallites. The work was further extended to develop carbon nanostructures through the PVC thermolysis by infilteration of the synthetic polymer into the nano-pores of the templates. Successful formation of carbon nanowires was realized at 100oC, 200oC, 2 300oC, 400oC, 500°C and 600oC in inert atmosphere. The synthesized nanostructures were characterized for the similar techniques as in the case of PVA. Initiation of aromatization was detected at temperatures as low as 100oC. Up to 200oC, nanofibers were formed. Pure graphitic regions were identified at higher temperatures and SEM showed the formation of nano-tubular structure at 300oC and 400oC. Further increase in temperature up to 600oC caused shrinkage in the diameter of nanotubes resulting in nanowires formation. Apart from using synthetic polymers as carbon precursors, a natural polymer chitosan was also used. It was first irradiated to reduce its molecular weight. Low molecular weight facilitated the infiltration of the polymer into the nano-spaces of the template. Pyrolysis was done at 100°C, 250°C, 300°C, 400°C, 500°C and 600°C. The nanotubes developed at 250°C mainly consisted of the saccharide structure. Drastic increase in weight loss at 300°C collapsed the saccharide structure and extensive aromatization took place as indicated by FTIR spectroscopy. The formation of carbon nanotubes was obvious as demonstrated by Raman spectroscopy and SEM results.