Effects of Welding Parameters on Toughness and Hardness in 690 Weld Zone MPa Steel

ABSTRACT. Specifications for the welding of high-strength steels are generally intended to control hydrogen cracking and provide adequate weld zone toughness for resistance to fatigue cracking and shock loading. The specifications should also allow welding to be undertaken safely and profitably. The work described here was designed to identify the optimum match of welding parameters, notably preheat, interpass temperature and heat input, for the welding of a 690 MPa (100 ksi) microalloy quench and tempered steel. The paper covers investigations into two aspects of weldability: toughness and hardness. The first part involved shielded metal arc (SMA) butt joint welding of carefully designed plates at a range of preheat and interpass temperatures and heat input values, to identify welding procedures that give maximum HAZ and weld metal toughness. The second is a laboratory study of bead-on-plate submerged arc welds to clearly identify the relationship between hardness and welding parameters. The test procedure for the first investigation involved SMA welding at preheat and interpass (P and I) temperatures from -20°C to 220°C (-4 ° to 428°F) using heat input values of (approximately) 1.3, 2.9 and 4 kJ/mm (33, 74 and 102 KJ/in.) Charpy V-notch energy and fracture appearance transition curves were then generated with the Charpy notches being carefully located to give the lowest toughness values. Results showed that the minimum preheat and interpass temperature for control of weld metal hydrogen cracking was 60°C (140°F) and that low values of toughness in both weld and heat-affected zone consistently occurred in the weld root region. Low preheat techniques and one-sided welding should therefore be avoided for critical applications. For weld metal, greatest toughness occurred at high preheat and interpass temperatures (160°C; 320°F) combined with low welding heat input (1.2 kJ/mm; 30 KJ/in). For high heat input welding, preheat and interpass temperature had little influence on toughness over the range of temperatures examined. For heat-affected zone regions, levels of toughness obtained when using the high preheat/low heat input and low preheat/high heat input techniques were similar. It was found, however, that careful control of preheat and interpass temperature was essential, for each heat input value, because toughness can drop off rapidly on either side of the optimum interpass temperature. For some applications, optimum preheat and interpass temperatures were found to lie between 60 ° and 90°C (140 ° and 194°F). In the second study, a series of beadon-plate submerged arc welds was deposited using a wide range of preheat and KEY WORDS Welding Parameters SMAW Toughness Hardness 690 MPa Steel Preheat Temperature Interpass Temperature Heat Input Butt Joint Welding Bead-on-Plate interpass temperatures, voltages, currents and travel speeds. In each case, the welding parameters were chosen so that the welding power input (V x I) could be held constant while varying heat input, or vice versa. For each weld, hardness readings were taken in both the weld deposit and HAZ at approximately 1 mm (0.04 in.) from the weld interface. It was found that: 1) HAZ hardness readings (390~130 HV 30 for heat input values up to 2 kJ/mm) were consistently higher than weld metal hardness readings. 2) Heat input has a marginal effect on HAZ hardness up to about 2 kJ/mm (51 kJ/in.), however, above 2 kJ/mm the hardness drops off at a rate of approximately HV 30 for each increase of 1 kJ/mm (25 kJ/i n.). 3) Weld metal hardness dropped continuously over the range of 0.5 to 4.5 kJ/mm (13 to 114 kJ/in.). 4) Both HAZ and weld metal hardness drops approximately 1 HV 30 for every 4°C (7.2°F) increase in preheat and interpass temperature. The results of this work have been used to develop an optimized weld design for butt joint welding of 35-50 mm (1.4-2 in.) plate. This uses high heat input for all but the weld capping passes, where high interpass temperatures and low heat input techniques are employed

TWO NEW PLOCENE SPECIES OF CYCLOSTEPHANOS (BACILLARIOPHYCEAE) WITH COMMENTS ON THE CLASSIFICATION OF THE FRESHWATER THALASSIOSIRACEAE 1

Two new species of the diatom genus Cyclostephanos Round are described from Pliocene fossil deposits in western North America. Cyclostephanos undatus is distinguished from other Cyclostephanos species by its tangentially undulate valve face; Cyclostephanos fenestratus is distinguished by its extremely shallow alveoli. This paper records previously unreported morphological detail of Cyclostephanos and speculates that structure of the punctum, labiate process and strutted process may enhance diagnosis of the freshwater genera of the Thalassiosiraceae Lebour emend. Hasle. Cyclostephanos undatus is similar to several Cyclotella species, but its external costae are raised and its alveolar morphology is similar to that of Cyclostephanos dubius (Fricke) Round. Cyclostephanos fenestratus is similar in external view to Stephanodiscus Ehrenb. However, the two species described here have flat cribra covering the mantle puncta and the labiate processes appear to lack external tubes, whereas Stephanodiscus species have domed mantle cribra and external tubes.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65645/1/j.1529-8817.1986.tb04154.x.pd

A major population of mucosal memory CD4⁺ T cells, coexpressing IL-18Rα and DR3, display innate lymphocyte functionality

Mucosal tissues contain large numbers of memory CD4(+) T cells that, through T-cell receptor-dependent interactions with antigen-presenting cells, are believed to have a key role in barrier defense and maintenance of tissue integrity. Here we identify a major subset of memory CD4(+) T cells at barrier surfaces that coexpress interleukin-18 receptor alpha (IL-18Rα) and death receptor-3 (DR3), and display innate lymphocyte functionality. The cytokines IL-15 or the DR3 ligand tumor necrosis factor (TNF)-like cytokine 1A (TL1a) induced memory IL-18Rα(+)DR3(+)CD4(+) T cells to produce interferon-γ, TNF-α, IL-6, IL-5, IL-13, granulocyte-macrophage colony-stimulating factor (GM-CSF), and IL-22 in the presence of IL-12/IL-18. TL1a synergized with IL-15 to enhance this response, while suppressing IL-15-induced IL-10 production. TL1a- and IL-15-mediated cytokine induction required the presence of IL-18, whereas induction of IL-5, IL-13, GM-CSF, and IL-22 was IL-12 independent. IL-18Rα(+)DR3(+)CD4(+) T cells with similar functionality were present in human skin, nasal polyps, and, in particular, the intestine, where in chronic inflammation they localized with IL-18-producing cells in lymphoid aggregates. Collectively, these results suggest that human memory IL-18Rα(+)DR3(+) CD4(+) T cells may contribute to antigen-independent innate responses at barrier surfaces.Mucosal Immunology advance online publication, 1 October 2014; doi:10.1038/mi.2014.87

Activated Ion Electron Capture Dissociation (AI ECD) of proteins: synchronization of infrared and electron irradiation with ion magnetron motion.

Here, we show that to perform activated ion electron capture dissociation (AI-ECD) in a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer equipped with a CO(2) laser, it is necessary to synchronize both infrared irradiation and electron capture dissociation with ion magnetron motion. This requirement is essential for instruments in which the infrared laser is angled off-axis, such as the Thermo Finnigan LTQ FT. Generally, the electron irradiation time required for proteins is much shorter (ms) than that required for peptides (tens of ms), and the modulation of ECD, AI ECD, and infrared multiphoton dissociation (IRMPD) with ion magnetron motion is more pronounced. We have optimized AI ECD for ubiquitin, cytochrome c, and myoglobin; however the results can be extended to other proteins. We demonstrate that pre-ECD and post-ECD activation are physically different and display different kinetics. We also demonstrate how, by use of appropriate AI ECD time sequences and normalization, the kinetics of protein gas-phase refolding can be deconvoluted from the diffusion of the ion cloud and measured on the time scale longer than the period of ion magnetron motion

Liquid Chromatography Electron Capture Dissociation Tandem Mass Spectrometry (LC-ECD-MS/MS) versus Liquid Chromatography Collision-induced Dissociation Tandem Mass Spectrometry (LC-CID-MS/MS) for the Identification of Proteins

Electron capture dissociation (ECD) offers many advantages over the more traditional fragmentation techniques for the analysis of peptides and proteins, although the question remains: How suitable is ECD for incorporation within proteomic strategies for the identification of proteins? Here, we compare LC-ECD-MS/MS and LC-CID-MS/MS as techniques for the identification of proteins.Experiments were performed on a hybrid linear ion trap–Fourier transform ion cyclotron resonance mass spectrometer. Replicate analyses of a six-protein (bovine serum albumin, apo-transferrin,lysozyme, cytochrome c, alcohol dehydrogenase, and β-galactosidase) tryptic digest were performed and the results analyzed on the basis of overall protein sequence coverage and sequence tag lengths within individual peptides. The results show that although protein coverage was lower for LC-ECDMS/MS than for LC-CID-MS/MS, LC-ECD-MS/MS resulted in longer peptide sequence tags,providing greater confidence in protein assignment

Apoptosis-Like Death in Bacteria Induced by HAMLET, a Human Milk Lipid-Protein Complex

Background: Apoptosis is the primary means for eliminating unwanted cells in multicellular organisms in order to preserve tissue homeostasis and function. It is characterized by distinct changes in the morphology of the dying cell that are orchestrated by a series of discrete biochemical events. Although there is evidence of primitive forms of programmed cell death also in prokaryotes, no information is available to suggest that prokaryotic death displays mechanistic similarities to the highly regulated programmed death of eukaryotic cells. In this study we compared the characteristics of tumor and bacterial cell death induced by HAMLET, a human milk complex of alpha-lactalbumin and oleic acid. Methodology/Principal Findings: We show that HAMLET-treated bacteria undergo cell death with mechanistic and morphologic similarities to apoptotic death of tumor cells. In Jurkat cells and Streptococcus pneumoniae death was accompanied by apoptosis-like morphology such as cell shrinkage, DNA condensation, and DNA degradation into high molecular weight fragments of similar sizes, detected by field inverse gel electrophoresis. HAMLET was internalized into tumor cells and associated with mitochondria, causing a rapid depolarization of the mitochondrial membrane and bound to and induced depolarization of the pneumococcal membrane with similar kinetic and magnitude as in mitochondria. Membrane depolarization in both systems required calcium transport, and both tumor cells and bacteria were found to require serine protease activity (but not caspase activity) to execute cell death. Conclusions/Significance: Our results suggest that many of the morphological changes and biochemical responses associated with apoptosis are present in prokaryotes. Identifying the mechanisms of bacterial cell death has the potential to reveal novel targets for future antimicrobial therapy and to further our understanding of core activation mechanisms of cell death in eukaryote cells

Universal Rights and Wrongs

This paper argues for the important role of customers as a source of competitive advantage and firm growth, an issue which has been largely neglected in the resource-based view of the firm. It conceptualizes Penrose’s (1959) notion of an ‘inside track’ and illustrates how in-depth knowledge about established customers combines with joint problem-solving activities and the rapid assimilation of new and previously unexploited skills and resources. It is suggested that the inside track represents a distinct and perhaps underestimated way of generating rents and securing long-term growth. This also implies that the sources of sustainable competitive advantage in important respects can be sought in idiosyncratic interfirm relationships rather than within the firm itself

Statistical analysis of the sampling design: FishPi case study on the biological sampling of the European hake fishery

FishPi is a pilot project financed through an European grant (MARE/2014/19) aiming to strengthen regional coordination in the area of fisheries data collection. This project includes four case studies, one of which aims at analyzing alternative sampling plans for fisheries operating on Northern & Southern hake stocks. The case study analyzes a variety of sampling design scenarios, from Simple Random Sampling to combinations of stratified sampling designs (by country, by port, by quarter…), using anonymised landings data from logbooks and sales notes (2013-2014). The results were compared regarding bias and precision to evaluate the best approach. The most precise estimates of total catch were obtained in scenarios stratified by port and, secondly, by port and country and by port and quarter. The general conclusion was that regional sampling designs stratified by port provided improved precision in this fishery. Apart from statistical considerations, this conclusion was also discussed under other points of view to give a feasibility perspective showing that coverage by country, and also by domain (stock), would be compromised if regional design is simply based on statistical analyses. Efficiency and precision of sampling were found to be highly sensitive to the sampling assumptions and in general countries with smaller contributions to overall landings of hake would see their sampling plans reduced, compromising other requirements for advice such as those related to other stocks or local management measures established by National governments. Hence further analyses are being considered that integrate biometrics, cost-benefit aspects, and concurrent or single-stock sampling strategies

Electron Capture Dissociation Mass Spectrometry of Tyrosine Nitrated Peptides

In vivo protein nitration is associated with many disease conditions that involve oxidative stress and inflammatory response. The modification involves addition of a nitro group at the position ortho to the phenol group of tyrosine to give 3-nitrotyrosine. To understand the mechanisms and consequences of protein nitration, it is necessary to develop methods for identification of nitrotyrosine-containing proteins and localization of the sites of modification.Here, we have investigated the electron capture dissociation (ECD) and collision-induced association (CID) behavior of 3-nitrotyrosine-containing peptides. The presence of nitration did not affect the CID behavior of the peptides. For the doubly-charged peptides, addition of nitration severely inhibited the production of ECD sequence fragments. However, ECD of the triply-charged nitrated peptides resulted in some singly-charged sequence fragments. ECD of the nitrated peptides is characterized by multiple losses of small neutral species including hydroxyl radicals, water and ammonia. The origin of the neutral losses has been investigated by use of activated ion (AI) ECD. Loss of ammonia appears to be the result of non-covalent interactions between the nitro group and protonated lysine side-chains