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Modeling & Simulation of Amine absorption and Membrane Technology to Remove CO2 from Raw Natural Gas

Thesis Info

Author

Jawad Ahmed

Supervisor

Suhail A Soomro; Imran Nazir

Department

Chemical Engineering

Program

Mphil

Institute

Mehran University of Engineering and Technology

Institute Type

Private

City

Jamshoro

Province

Sindh

Country

Pakistan

Thesis Completion Status

In Progress

Subject

Chemical Engineering

Language

English

Added

2021-02-17 19:49:13

Modified

2023-02-19 12:33:56

ARI ID

1676729169876

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استاد کی عظمت

استاد کی عظمت
اللہ تعالیٰ نے اس کائنات کو تخلیق فرمایا پھر اس کی تزئین و آرائش کے لیے اس میں پہاڑوں ، گلستانوں، میدانوں ، سمندروں ، ندیوں اور نالوں کو وجود بخشا، آبشاروں کی کھڑکھڑاہٹ پیدا فرمائی ، فضاؤں کی سرسراہٹ سے اس کے حسن میں چار چاند لگائے۔
اللہ تعالیٰ نے بنی نوع انسان کی اصلاح کے لیے مختلف اوقات میں مختلف زبانوں میں مختلف قوموں میں مختلف انبیاء کرام کو مبعوث فرمایا یہ سلسلہ چلتا رہا یہاں تک کہ نبی آخر النبین حضرت محمد صلی اللہ علیہ و آلہٖ وسلم تشریف لائے اور پھر نبوت کا دروازہ بند کر دیا گیا اور کام علماء کرام کے سپرد ہوا اور علماء کرام میں اساتذہ جو مدرس ہونے کے ناطے عظیم منصب پر فائز ہوتے ہیں انھوں نے اس فریضہ کو بڑے احسن طریقے سے سرانجام دینا شروع کر دیا اور عوام النّاس کی اصلاح کے لیے مستعد رہے۔
شیخِ مکتب ہے اک عمارت گر
جس کی صنعت ہے روحِ انسانی
اگر بنظر غائر مشاہد ہ کیا جائے تو استاد کی حیثیت، اہمیت اور مقام مسلم ہے، کیونکہ استاد ہی نونہالانِ قوم کی تعلیم و تربیت کا ضامن ہوتا ہے، استاد ہی قوم کے نوجوانوں کو علوم وفنون سے آراستہ و پیراستہ کرتا اور اس قابل بناتا ہے کہ وہ ملک وقوم کی گرانبار ذمہ داریوں سے عہدہ برآ ہوسکیں۔ استاد جہاں نوجوانوں کی اخلاقی و روحانی تربیت کرتا ہے وہاں وہ اُن کی مختلف علمی ،سائنسی، فنی ، اور پیشہ ورانہ مہارتوں کا سامان بھی کرتا ہے، والدین بچے کی جسمانی پرورش کرتے ہیں، جبکہ استاد کے ذمے بچے کی روحانی تربیت ہوتی ہے، اس لحاظ سے استاد کی حیثیت اور اہمیت والدین سے کسی طرح کم نہیں بلکہ ایک لحاظ سے ان سے بڑھ کر ہے، کیونکہ روح کو جسم پر فوقیت حاصل...

Why Social Protection is Not Enough to Effectively Address Poverty Reduction in Pakistan

Pakistan is behind many other countries in the Asia region in reducing poverty. Dedicated poverty reduction Programmes so far were mainly done by NGOs using livelihood and microfinance approaches and since 2008 through the Benazir Income Support Programme’s cash transfer scheme. Recently, the office of the Prime Minister established Ehsaas Strategy which combines the various poverty reduction and social protection approaches in the country under one Programme. This paper argues that a stronger focus on effective income generating poverty reduction Programmes would be needed to make poverty reduction more successful.

Molecular Investigation of Selected Mendelian Disorders in Pakistani Consanguineous Families

Mendelian disorders are caused by alterations in single gene with minimal influence from environment. The large effect size of these variants has always provided important insights into functional annotation of the genome. This knowledge is also instrumental for making important reproductive decisions and therapeutic intervention. Mendelian disorders are globally rare but are observed three folds more frequently in inbred/consanguineous populations. Pakistani population with high rates of consanguinity (>76%) coupled with large family size offers a rich resource for genetic studies of inherited disorders. In this study, eleven families segregating three different diseases Microcephaly, Epilepsy and Ciliopathies analysed using cutting edge technologies. Autosomal recessive primary microcephaly is a neurodevelopmental disorder characterised by congenital reduction in head circumference by >3SD from age and gender appropriate mean. Its incidence varies widely from one in million to one in 10,000; the latter pertaining to northern Pakistani population. To date, seventeen different causative genes have been reported. In this study, genetic analysis of seven families revealed one known and two novel mutations in already reported MCPH genes. Epilepsy is a heterogeneous group of neurological disorders characterized by chronic disposition to recurrent unprovoked seizures. A seizure, by definition, is an episode of abnormal, hypersynchronous activity in a neuronal population of brain that causes sudden involuntary change in behaviour, sensory perception and/or motor activity. Herein, two families were investigated through gene panel sequencing to reveal a reported and a novel mutation underlying epileptic seizures. The third category, ciliopathies, is a group of disorders caused by dysregulation of cilia related functions. Cilia are microtubule based cylindrical projections present on nearly all types of eukaryotic cells and mediate signal transduction of crucial developmental pathways. This study investigated two families, one with clinical diagnosis of a ciliopathy (Joubert Syndrome), while another family, initially undiagnosed, was successfully diagnosed as Nephronophthisis employing advanced genetic analysis. The findings of this study not only expand the mutation spectra, but through detailed clinical characterisation, highlight the diversity of its phenotype too. The knowledge will provide better insights in to disease mechanism and facilitate development of preventive and therapeutic interventions.