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Experimental Study of the Behaviour of Pre-Perforated Post-Reinforced Baked Clay Panels of Beams

Thesis Info

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Author

Abdul Aziz Ansari

Program

PhD

Institute

Quaid-e-Awam University of Engineering, Science and Technology

City

Nawabshah

Province

Sindh

Country

Pakistan

Thesis Completing Year

2008

Thesis Completion Status

Completed

Subject

Civil engineering

Language

English

Link

http://prr.hec.gov.pk/jspui/handle/123456789/618

Added

2021-02-17 19:49:13

Modified

2024-03-24 20:25:49

ARI ID

1676727754506

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Altogether fifty one large size beams of clay were moulded, compacted, baked, post- reinforced, grouted with cement-sand slurry, cured and tested to study the behaviour of these beams. Different parameters were set in order to check the suitability of these universally available materials of construction, i.e. clay, silt and pit-sand (silica) for low- cost housing without sacrificing durability, the strength and elegance of buildings in the plain areas where the soil is alluvial. Standard materials of construction like hill-sand, coarse aggregate, cement and steel bars are to be transported over large distances for RCC construction. Four Reinforced concrete beams were also cast and tested for the sake of comparison. Preliminary studies were carried out on soil samples collected from twenty five different sites in terms of their physical composition and presence of various salts and other chemicals. Their effect on the strength of baked specimens was also studied. A systematic study was performed experimentally to find the best composition in terms of ratio (clay : pit-sand), the intensity of compression force required for manual moulding and compaction which would impart reasonably good crushing strength to this material (comparable with that of concrete) without compromising on economy. The moisture content was also a parameter of preliminary experimental study to ensure sufficient workability and minimum possible void ratio. The various drying techniques were tried finally to arrive at the best possible system which would not cause cracking. The compressive strength as high as (6100 psi ) 42 N/mm2 has been achieved which can be compared with (3000 psi ) 20 N/mm2 for concrete used in ordinary buildings. The modulus of rupture with a reasonable comparison to ordinary concrete has also been achieved. Flexural behaviour as well as shear strength of beams manufactured from this material were studied for the following cases. 1. Rectangular beams, simply supported subjected to point load at the centre. 2. I-beams, simply supported subjected to point load at the centre. 3. Rectangular beams, supported on plates on both the ends subjected to Uniformly Distributed Load. 4. Rectangular beams, fixed at both the ends subjected to Uniformly Distributed Load 5. Rectangular as well as I-section beams, simply supported with only bottom steel consisting of two bars. 6. Rectangular beams reinforced with four bars two at top and two at bottom, simply supported subjected to Uniformly Distributed Load. 7. Rectangular beams with vertical steel as shear reinforcement, simply supported subjected to Uniformly Distributed Load. 8. Rectangular as well I-section beams subjected to pre-compression to improve the shear strength and simply supported beams subjected to point load at centre and also with Uniformly Distributed Load. 9. Rectangular beams with enhanced compacting force, simply supported as well as plate support on both the ends subjected to point load at centre and also with Uniformly Distributed Load. The beams tested were relatively of large size, 1980 mm (6.5 ft) long, 150 mm (6 inch) thick and 300 mm (12 inch) deep. After shrinkage the final dimensions were determined and the average shrinkage was found, 1868 mm (6.13 ft), 143 mm (0.47 ft) and 286mm (0.94 ft). Several problems were faced and attempts were made to over-come those through various techniques, the details of which are presented in this thesis. The results are encouraging and there is a bright possibility to achieve reasonably good economy if pre-cast panels of this type of materials are produced on mass scale by adopting mechanized system for swift moulding, transportation to the site and erection of the buildings.
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پروفیسر حا فظ محمود خان شیرانی

پروفیسر حافظ محمود خان شیرانی مرحوم
ہم کو ابھی تک اپنے ملک کے علماء اور محققین کی پوری قدر نہیں ہوئی، کیسے افسوس کی بات ہے کہ ہماری قوم اور ملک کے ایک نامور محقق پروفیسر حافظ محمود خان شیرانی کا انتقال ۱۶؍ فروری ۱۹۴۶؁ء کو ٹونک میں ہوگیا، اور ہم میں سے بہتوں کو اس کی خبر نہیں ہوئی۔
شیرانی مرحوم کا وطن ٹونک تھا، شیرانی پٹھان تھے، اور ان کو اپنے پٹھان ہونے پر فخر تھا، ٹونک ہمیشہ سے علماء اور محققین کا مقام رہا، وہاں کا نادر کتب خانہ اکثر محققوں کو اپنی طرف کھینچ کر لے جایا کرتا ہے، اور شیرانی کا تو وہ وطن ہی تھا، شیرانی صاحب کی انگریزی کی استعداد پوری تھی، فارسی کی تعلیم متوسط اور عربی کی معمولی مگر ان میں تحقیق و تلاش کا مادہ فطرۃً تھا، تاریخ اور خصوصاً تاریخ ادب سے ان کو بے حد شغف تھا، تاریخ کے ذوق سے ان کو کتبوں اور سکون کا شوق تھا، اسی شوق سے وہ لکھنؤ بھی آتے تھے، اور چونکہ ہمارے مدرسہ دارالعلوم ندوۃ العلماء کے درس اول و شیخ الحدیث مولانا حیدر حسن خان صاحب مرحوم بھی ٹونکی تھے، اس تعلق سے وہ کبھی کبھی ہمارے مدرسہ میں بھی ٹھہرتے تھے اور اسی واسطہ سے میری ان کی ملاقات ہوئی، اور اس کے بعد جب وہ لاہور تھے، تو کئی بار ملنا ہوا۔
مرحوم کا سال پیدایش ۱۲۹۸؁ھ ہے، عمر قریباً سرسٹھ برس تھی ۱۹۰۴؁ء میں اسکول کی تعلیم چھوڑ کر بیرسٹری کے لیے لندن گئے، جہاں سے والد کی وفات پر ۱۹۰۶؁ء میں واپس آئے، پھر فوراً واپس گئے، اور ۱۹۱۴؁ء میں واپس آئے، بیرسٹرتو نہیں ہوئے، مگر قلمی کتابوں کا شوق پید اہوگیا، پیرس کے قومی کتب خانہ میں تین ماہ مصروف رہے، اور وہیں بعض فرانسیسی اہل علم کے ساتھ مل کر...

Analyse psychosociale de la littérature féminine en Mauritanie

Over the years, Mauritanian Moorish women have managed to have their own poetry, an oral literature known locally as "tebrāʕ" translated into French by the word "ingenuity", sometimes also "invention". It is a love poetry originally used by girls or by women in general to express feelings that social norms prevent them from manifesting publicly. Tebrāʕ is deeper than a mere female expression of passion, it is rather a social and psychological state of mind that empowers women and helps them break taboos virtually for a short period of time. This article is an analytical reading of Tebrāʕ and presents new models and ways of examining this oral literature. It tries also to answer several questions which can be summarized as follows: Can this form of poetry be considered as a female literature? The closed circle where these words are composed and pronounced, can it be considered a therapy session? And above all, what power do these women and girls derive from this practice? This article is also a study of the perception of men and women in Mauritania in relation to this oral art practice based

Molecular Genetic Analysis of Selected Neurological Inherited Diseases

This study was conducted to identify the loci and genes responsible to cause congenital neurological inherited diseases in selective Pashtoon families of Khyber Pakhtunkhwa region of Pakistan. For this purpose, five consanguineous/tribal endogamy families (A-E) suffering from oculocutaneous albinism, usher syndrome, primary microcephaly, and isolated clinical anophthalmia were selected and pedigrees were drawn. Blood samples were collected with informed consent from affected, as well as normal members of these families, and screened for disease associated mutations. These families were analyzed for linkage to all the known loci of oculocutaneous albinism, usher syndrome, primary microcephaly, and isolated clinical anophthalmia, using microsatellite STR markers. Direct sequencing was performed to find out disease associated mutations in the candidate genes. Molecular genetic analysis of family A with oculocutaneous albinism and golden red hair at birth was mapped to MC1R locus on chromosome 16q24.1. A novel mutation c.917G>A of MC1R gene was found to be consisting with OCA2 phenotype in family A. The identification of c.917G>A mutation in Pakistani family and its direct association with OCA2 phenotype is the first demonstration of a mutation of MC1R gene responsible for causing OCA2 phenotype in humans. By genetic linkage analysis, family B with diseased phenotype of Usher syndrome was mapped to USH1F locus on chromosome 10q21.22 (USH1F), which harbors PCDH15 gene. On sequencing of the PCDH15 gene, a novel homozygous c.1304 A>C transversion mutation was identified to be associated with the usher phenotype in the USH1F mapped family. This c.1304 A>C mutation predicts an amino-acid substitution of aspartic acid with an alanine at codon 435 (p.D435A) of PCDH15 protein product.Two families C and D with primary microcephaly were mapped to ASPM gene locus. On mutation screening of ASPM gene by PCR amplification and direct DNA sequencing, a common c.3978G>A transition, was identified in exon 17 of ASPM gene to be responsible for diseased phenotype in both the families. The identified mutation results into the substitution of an amino acid residue at position 1326 from tryptophan to a stop codon (i.e., p.Trp1326Stop). The family E with isolated clinical anophthalmia was mapped to SOX2 gene, which is located at chromosome 3q26.3-q27. On exonic and regulatory regions mutation screening of SOX2 gene, no disease-associated mutation was identified. It shows that another gene responsible for the development of eye might be present at chromosome 3q26.3-q27 and need to be identified and screened for disease- associated mutation in this family. It was concluded that the disease phenotypes of families with oculocutaneous albinism, usher syndrome, primary microcephaly, and isolated clinical anophthalmia were mapped by genetic linkage analysis. The candidate genes (MC1R, PCDH15, ASPM and SOX2) in the mapped regions were screened for disease associated mutations by PCR amplification and direct DNA sequencing. The novel disease- associated mutations were identified in MC1R and PCDH15. The disease associated mutation identified in ASPM gene was also reported in several other families of Pakistani origin with primary microcephaly. However, no disease associated mutation was identified in SOX2 gene, which indicates that possibly another gene might be present in the mapped region for disease phenotype.