Effect of surface roughness on drying speed of drying lamellas in veneer roller dryer

Lamellas, which are defined as top layers of multilayer parquet and favourable to wood veneer can be dried in jet ventilated automatic veneer roller dryer due to short drying period. The objective of this study is to determine the effect of surface roughness on the drying speed of the veneer roller dryer. Quercus spp., frequently used tree specie in Turkish solid wood and multilayer parquet industries was chosen as material in this study. Pre-dried lamella blocks were cut into 4 different machines. As aresult, 4 test groups of lamellas displaying different surface roughness values were obtained. Lamellas which belong to each of these 4 test groups were also divided into 2 sub-groups and dried at 90 and 130°C drying temperatures. Drying was evaluated in relation to drying speed. Mitutoyo SJ 301 profilmeter was used for determining surface roughness values. Drying speed of lamellas was expressed as: dividing difference of initial moisture content and final moisture content values to dryingtime value. The result of variance analyses showed differences between groups as surface roughness values. There was no difference between groups as drying speed were determined at 90 and 130°C temperatures. Furthermore, the relation between surface roughness values and drying speed was searched using correlation analysis and no significant relationship was found. Finally, it was determined that there was no effect of surface roughness on drying speed in radial cut, pre-dried lamellas, which have surface roughness values between 10.464 and 15.064 ìm, drying in jet ventilated roller dryer, at 90 and 130°C temperatures

Effects of drying methods of lamellas used in multilayer parquet manufacturing on surface roughness and bonding strength

The objective of this study is to determine surface roughness and bonding (tensile shear) strength of lamellas (top layer of multilayer parquet) which were cut away from green lumber and dried by different types of drying methods. Also, finding out the most convenient manufacturing method as surface roughness, bonding strength properties was aimed by comparing results with surface roughness and bonding strength of lamellas, which were cut away from dry lumber as seen in practice. Flat sawn green lamellas with 5 and 2 mm thicknesses, which were cut away from Iroko lumber by means of thin cutting frame saw, were dried with 3 different drying methods such as drying in lumber drying kiln, jet ventilated automatic veneer roller dryer and veneer press dryer. Effect of drying temperature on surface roughness and bonding strength was also determined by applying 3 different drying temperatures as 60, 100 and 140°C in jet ventilated automatic veneer roller dryer. In addition, lamellas with the same thicknesses were manufactured from dry lumber by means of the same thin cutting frame saw mentioned above. As the result of analysis of variance showed, differences between test groups were determined as surface roughness. Consequently, effect of drying method on surface roughness was found. Also, surface roughness values were determined to be increasing as drying temperature increases when drying in veneer roller dryer. Surface roughness values of lamellas dried in lumber drying kiln were found to be higher than those cut away from the dry lumber as expected. Differences exist between test groups as bonding strength was determined by means of analysis of variance. The biggest bonding strength was found in lamella group which were cut away from dry lumber and mentioned as comparison group. It was found that no relation existed between bonding strength and temperature increase drying in veneer roller dryer. Also, it was determined that no significant relation was found between surface roughness and bonding strength as the result of correlation analysis. Conclusively, it was found that lamella manufacturing method, cutting away from dry lumber, was the most convenient method for obtaining the best bonding strength in multilayer parquet production.Key words: Drying method, multilayer parquet, surface roughness, bonding strength

More On The Connection Between Planar Field Theory And String Theory

We continue work on the connection between world sheet representation of the planar phi^3 theory and string formation. The present article, like the earlier work, is based on the existence of a solitonic solution on the world sheet, and on the zero mode fluctuations around this solution. The main advance made in this paper is the removal of the cutoff and the transition to the continuum limit on the world sheet. The result is an action for the modes whose energies remain finite in this limit (light modes). The expansion of this action about a dense background of graphs on the world sheet leads to the formation of a string.Comment: 27 pages, 3 figure

Field Theory On The World Sheet: Improvements And Generalizations

This article is the continuation of a project of investigating planar phi^3 model in various dimensions. The idea is to reformulate them on the world sheet, and then to apply the classical (meanfield) approximation, with two goals: To show that the ground state of the model is a solitonic configuration on the world sheet, and the quantum fluctuations around the soliton lead to the formation of a transverse string. After a review of some of the earlier work, we introduce and discuss several generalizations and new results. In 1+2 dimensions, a rigorous upper bound on the solitonic energy is established. A phi^4 interaction is added to stabilize the original phi^3 model. In 1+3 and 1+5 dimensions, an improved treatment of the ultraviolet divergences is given. And significantly, we show that our approximation scheme can be imbedded into a systematic strong coupling expansion. Finally, the spectrum of quantum fluctuations around the soliton confirms earlier results: In 1+2 and 1+3 dimensions, a transverse string is formed on the world sheet.Comment: 29 pages, 5 figures, several typos and eqs.(74) and (75) are corrected, a comment added to section

High-throughput single cell arrays as a novel tool in biopreservation

Microwell array cytometry is a novel high-throughput experimental technique that makes it possible to correlate pre-stress cell phenotypes and post-stress outcomes with single cell resolution. Because the cells are seeded in a high density grid of cell-sized microwells, thousands of individual cells can be tracked and imaged through manipulations as extreme as freezing or drying. Unlike flow cytometry, measurements can be made at multiple time points for the same set of cells. Unlike conventional image cytometry, image analysis is greatly simplified by arranging the cells in a spatially defined pattern and physically separating them from one another. To demonstrate the utility of microwell array cytometry in the field of biopreservation, we have used it to investigate the role of mitochondrial membrane potential in the cryopreservation of primary hepatocytes. Even with optimized cryopreservation protocols, the stress of freezing almost always leads to dysfunction or death in part of the cell population. To a large extent, cell fate is dominated by the stochastic nature of ice crystal nucleation, membrane rupture, and other biophysical processes, but natural variation in the initial cell population almost certainly plays an important and under-studied role. Understanding why some cells in a population are more likely to survive preservation will be invaluable for the development of new approaches to improve preservation yields. For this paper, primary hepatocytes were seeded in microwell array devices, imaged using the mitochondrial dyes Rh123 or JC-1, cryopreserved for up to a week, rapidly thawed, and checked for viability after a short recovery period. Cells with a high mitochondrial membrane potential before freezing were significantly less likely to survive the freezing process, though the difference in short term viability was fairly small. The results demonstrate that intrinsic cell factors do play an important role in cryopreservation survival, even in the short term where extrinsic biophysical factors would be expected to dominate. We believe that microwell array cytometry will be an important tool for a wide range of studies in biopreservation and stress biology. © 2009 Elsevier Inc. All rights reserved

Relationship of vascular variations with liver remnant volume in living liver transplant donors

Background: In this study, we investigated the relationship between the portal vein and hepatic artery variations and the remaining liver volume in living donors in liver transplantation.Materials and methods: In the study, triphasic abdominal computed tomography images of 180 live liver donor candidates were analysed retrospectively. Portal veins were divided into four groups according to the Nakamura classification and seven groups according to the Michels classification. The relationship between vascular variations and remnant liver volume was compared statistically.Results: According to the Nakamura classification, there were 143 (79.4%) type A, 23 (12.7%) type B, 7 (3.9%) type C and 7 (3.9%) type D cases. Using the Michels classification, 129 (71%) type 1, 12 (6.7%) type 2, 24 (13%) type 3, 2 (2.2%) type 4, 10 (5.6%) type 5, 1 (0.6%) type 6, and 2 (1.1%) type 7 cases were detected. There was no significant difference in the percentage of the remaining volume of the left liver lobe between the groups (p = 0.055, p = 0.207, respectively).Conclusions: Variations in the hepatic artery and portal vein do not affect the remaining liver volume in liver transplantation donors

An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics

For a decade, The Cancer Genome Atlas (TCGA) program collected clinicopathologic annotation data along with multi-platform molecular profiles of more than 11,000 human tumors across 33 different cancer types. TCGA clinical data contain key features representing the democratized nature of the data collection process. To ensure proper use of this large clinical dataset associated with genomic features, we developed a standardized dataset named the TCGA Pan-Cancer Clinical Data Resource (TCGA-CDR), which includes four major clinical outcome endpoints. In addition to detailing major challenges and statistical limitations encountered during the effort of integrating the acquired clinical data, we present a summary that includes endpoint usage recommendations for each cancer type. These TCGA-CDR findings appear to be consistent with cancer genomics studies independent of the TCGA effort and provide opportunities for investigating cancer biology using clinical correlates at an unprecedented scale. Analysis of clinicopathologic annotations for over 11,000 cancer patients in the TCGA program leads to the generation of TCGA Clinical Data Resource, which provides recommendations of clinical outcome endpoint usage for 33 cancer types

Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

This integrated, multiplatform PanCancer Atlas study co-mapped and identified distinguishing molecular features of squamous cell carcinomas (SCCs) from five sites associated with smokin

Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context

Long noncoding RNAs (lncRNAs) are commonly dys-regulated in tumors, but only a handful are known toplay pathophysiological roles in cancer. We inferredlncRNAs that dysregulate cancer pathways, onco-genes, and tumor suppressors (cancer genes) bymodeling their effects on the activity of transcriptionfactors, RNA-binding proteins, and microRNAs in5,185 TCGA tumors and 1,019 ENCODE assays.Our predictions included hundreds of candidateonco- and tumor-suppressor lncRNAs (cancerlncRNAs) whose somatic alterations account for thedysregulation of dozens of cancer genes and path-ways in each of 14 tumor contexts. To demonstrateproof of concept, we showed that perturbations tar-geting OIP5-AS1 (an inferred tumor suppressor) andTUG1 and WT1-AS (inferred onco-lncRNAs) dysre-gulated cancer genes and altered proliferation ofbreast and gynecologic cancer cells. Our analysis in-dicates that, although most lncRNAs are dysregu-lated in a tumor-specific manner, some, includingOIP5-AS1, TUG1, NEAT1, MEG3, and TSIX, synergis-tically dysregulate cancer pathways in multiple tumorcontexts