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Chapter 7. 7 - Chemical Processing. CHEMICAL INDUSTRYL. De Boer**Adapted from 3rd edition, Encyclopaedia of Occupational Health and Safety. The business of the chemical industry is to change the chemical structure of natural materials in order to derive products of value to other industries or in daily life. Chemicals are produced from these raw materials- principally minerals, metals and hydrocarbons- in a series of processing steps. Further treatment, such as mixing and blending, is often required to convert them into end- products (e. Thus the chemical industry covers a much wider field than what is usually called . AmericanScience.Org is the online publication for the Journal of American Science. Chapter 77 - Chemical Processing CHEMICAL INDUSTRY. De Boer* *Adapted from 3rd edition, Encyclopaedia of Occupational Health and Safety. Intravenous Infusion of. Chemicals fall into two main classes: organic and inorganic. Organic chemicals have a basic structure of carbon atoms, combined with hydrogen and other elements. Read etimologia-e-abreviatura-de-termos-medicos.pdf text version. ETIMOLOGIA E ABREVIATURAS DE TERMOS MÉDICOS Um guia para estudantes, professores, autores e. Free of charge: Ukrainian Exporters Database offers free access. Search guide: Search data by industry sector or/and keyword. Feedback: If you did not find specific. Oil and gas are today the source of 9. Inorganic chemicals are derived chiefly from mineral sources. Examples are sulphur, which is mined as such or extracted from ores, and chlorine, which is made from common salt. The products of the chemical industry can be broadly divided into three groups, which correspond to the principal steps in manufacture: base chemicals (organic and inorganic) are normally manufactured on a large scale and are normally converted to other chemicals; intermediates are derived from base chemicals. Most intermediates require further processing in the chemical industry, but some, such as solvents, are used as they are; finished chemical products are made by further chemical processing. Some of these (drugs, cosmetics, soaps) are consumed as such; others, such as fibres, plastics, dyes and pigments, are processed still further. The main sectors of the chemical industry are as follows: 1. Division 3. 5 is further subdivided into industrial chemicals (3. In reporting chemical industry statistics each country normally uses its own classification system, and this can be misleading. Thus comparison between countries of total chemical industry performance cannot be based on national sources. However, international bodies like the Organization for Economic Cooperation and Development (OECD) and the United Nations normally supply data on the ISIC basis, though with a delay of about two years. Trade statistics are published internationally under the Standard International Trade Classification (SITC), which differs from the ISIC system. Trade statistics by individual countries nearly always refer to SITC section 5, which covers about 9. ISIC system. The chemical industry has grown much more rapidly in the half century than industry as a whole. Although there was an economic depression in the world. The biggest area of growth of chemical production has been in Southeast Asia. Figure 7. 7. 1 shows the percentage change in chemical production for 1. Figure 7. 7. 1 Change in chemical production for selected countries, 1. Much of the chemical industry is highly capital- intensive and is also strongly dependent on research and development (e. The combined result of these two factors is that the industry employs an abnormally low number of unskilled manual workers for its size, in comparison with manufacturing industry in general. Total employment in the industry rose slightly during the period of rapid growth prior to 1. Table 7. 7. 1 shows chemical industry employment in the United States and several European countries for 1. Table 7. 7. 1 Chemical industry employment in selected countries (1. Country. Employment. United States. 1, 0. Germany 5. 38,0. France 2. 48,0. United Kingdom 2. Italy 1. 91,0. 00. Poland 1. 40,0. Spain 1. 22,0. 00. Source: Chemical and Engineering News 1. DEVELOPING A PROCESS SAFETY MANAGEMENT PROGRAMMERichard S. Kraus. Industry and labour process safety involvement. Process safety technology has played an important role in the chemical processing industries so that handling flammable and combustible liquids and gases could proceed without undesirable consequences. During the 1. 98. With this in mind, a number of industry associations, such as, in the United States, the Center for Chemical Process Safety (CCPS), the American Petroleum Institute (API) and the Chemical Manufacturers. As stated by the CCPS, . In 1. 98. 8, the Chemical Manufacturer. One of the seven strategic elements of the STEP programme covers petroleum operating and process safety. The following documents are examples of some of the materials developed as a result of the STEP programme which provide guidance to the oil and gas industry to help prevent the occurrence or minimize the consequences of catastrophic releases of flammable liquids and vapours or hazardous process materials. It applies specifically to refineries, petro- chemical plants and major processing facilities that use, produce, process or store flammable liquids and toxic processing chemicals in quantities above certain hazardous amounts (as defined therein). The control of these undesired events requires a special science called process safety management. The terms process safety and process safety management are most commonly used to describe the protection of employees, the public and the environment from the consequences of undesirable major incidents involving flammable liquids and highly hazardous materials. According to the United States Chemical Manufacturers. The process design and technology, changes in the process, materials and changes in materials, operations and maintenance practices and procedures, training, emergency preparedness and other elements affecting the process must all be considered in the systematic identification and evaluation of hazards so as to determine whether or not they have the potential to lead to a catastrophe in the workplace and surrounding community. Beginning in the early 1. These incidents provided the impetus for government agencies, labour organizations and industry associations throughout the world to develop and implement codes, regulations, procedures and safe work practices directed toward the elimination or mitigation of these undesirable events, through the application of the principles of process safety management. They are discussed more fully in the Disasters, natural and technological chapter and elsewhere in this Encyclopaedia. In response to public concern over the potential hazards of chemicals, governments and regulatory agencies throughout the world initiated programmes which required manufacturers and users to identify hazardous materials in the workplace and inform employees and consumers of the hazards presented by their manufacture, use, storage and handling. These programmes, which covered emergency preparedness and response, hazard recognition, product knowledge, control of hazardous chemicals and reporting of toxic releases, included hydrocarbon processing. Process Safety Management Requirements. Process safety management is an integral part of the overall chemical processing facility safety programme. An effective process safety management programme requires the leadership, support and involvement of top management, facility management, supervisors, employees, contractors and contractor employees. Components to be considered when developing a process safety management programme include: . The process safety management programme relies upon providing availability and access to good records and documentation. Because process safety management is the basis for all safety efforts within the facility, managerial, supervisory and employee responsibility and accountability should be clearly delineated, communicated and understood in order for the programme to work. Prior to implementation, it is important to establish both long- term and short- term goals and objectives for each of the elements of the process safety management programme. Elements of the Process Safety Management Programme. All chemical facility process safety management programmes cover the same basic requirements, although the number of programme elements may vary depending on the criteria used. Regardless which government, company or association source document is used as a guide, there are a number of basic requirements which should be included in every chemical process safety management programme: . Process safety information includes all available written information concerning process technology, process equipment, raw materials and products and chemical hazards before conducting a process hazard analysis. Other critical process safety information is documentation relating to capital project reviews and design basis criteria. Chemical information includes not only the chemical and physical properties, reactivity and corrosive data and thermal and chemical stability of chemicals such as hydrocarbons and highly hazardous materials in the process, but also the hazardous effects of inadvertently mixing different incompatible materials. Chemical information also includes that which may be needed to conduct environmental hazard assessments of toxic and flammable releases and permissible exposure limits. Process technology information includes block flow diagrams and/ or simple process flow diagrams as well as descriptions of the chemistry of each specific process with the safe upper and lower limits for temperatures, pressures, flows, compositions and, where available, process design material and energy balances. The consequences of deviations in the process and materials, including their effect on employee safety and health, are also determined. Whenever processes or materials are changed, the information is updated and re- evaluated in accordance with the facility. Process equipment and mechanical design information includes documentation covering the design codes employed and whether or not equipment complies with recognized engineering practices. A determination is made as to whether existing equipment which was designed and constructed in accordance with codes, standards and practices no longer in general use is maintained, operated, inspected and tested to assure continued safe operation. Intel® Dual Band Wireless-AC 7260 quick reference guide including specifications, features, pricing, compatibility, design documentation, ordering codes, spec codes. Wireless Solutions to Power Every Need. Intel offers a full portfolio of advanced technologies to optimize every wireless experience. Dell Wireless Cards – The Unofficial Windows 1. Reinstallation Guide. Introduction. This is an attempt to list the hardware IDs of all Dell Wireless Cards alongside their latest driver. In the past particularly with Windows 7 Microsoft failed to keep Windows Installation Media Up to Date. This meant enviably one would install Microsoft Windows with newer hardware devices such as the Wireless Card were not recognised. For each Dell model, Dell usually have a difference in Wireless Card usually depending on region but also configuration. Intel Wifi Link 5100 Agn Hackintosh For SaleOften one would get confused with regards to what Wireless Driver to Install. The correct variant can be identified by using its Hardware ID c. Checking Hardware IDs in the Device Manager. With Windows 1. 0 I’m glad to say Microsoft have decided to follow my (and many others) advice on keeping Windows Installation Media Up to Date.
They have partnered with major OEMs such as Intel, Atheros and Broadcom to make sure Windows 1. As a consequence Microsoft will likely have native driver support for your Wireless Card. They may also download a newer driver automatically from Windows Update. In some cases OEMs may have newer drivers than Microsoft which may lead to some enhancements/patch issues. Unfortunately Dell do not Update their Drivers and Downloads by using Hardware IDs and handle drivers on a model by model basis. Moreover they do not provide hardware IDs on their Drivers and Downloads page (some other OEMs have the edge on Dell here). The aim of the page is to list the driver IDs so you can identify your wireless card and provide the latest driver. Note in some cases I may list an official Dell driver slightly newer version than Dell offer on their Drivers and Downloads Page? As business support is superior to home support, a Latitude model may have a driver update and an Inspiron model released at the same time will not. In other cases a newer Latitude model may have a newer Dell Wireless Card with a newer driver but this driver may support multiple Dell Wireless Cards including previous generation hardware. Note I am an individual so do not have all the Hardware to test so please leave feedback in the comments sections if you test things and of course let me know if you find newer drivers. Recommended Prequisites. Prerequisites before installing a wireless driver. If the Processor is Intel install Intel Chipset Software Installation Utility. Note although the system is Intel you may or may not have an Intel Wireless Card.**** Intel Systems Only . Without this driver Windows 1. There are 4 main vendors of Wireless Cards sold in Dell Systems. See the notes applicable to each major vendor regarding driver updates and then if applicable see the specific notes for your wireless card. There may also be some Toshiba Bluetooth Cards rebranded Dell Wireless 3. These are obsolete as Toshiba provide no new drivers for Windows 8. Broadcom Dell Wireless 3. Bluetooth USB dongle. Notes on Upgrading Wireless Card. Look to your Dell Service Manual and determine your wireless card type. There are four types of wireless card form factor. In general: Brand new systems will have a M. Systems manufactured in 2. Half Height PCIe (PCI express) slot. System manufactured in the period 2. Mini PCIe (PCI express) slot. Most of these wireless cards will work natively with Windows 1. You may want to consider installing a slightly newer wireless card using a Half to Full Height Minicard converter. If upgrading I recommend an Intel Wireless Card due to the best driver support see this Legit Review for more details about some affordable Intel Wireless Cards. I do not recommend a Broadcom card as there are a greater number of driver issues reported with Broadcom Wireless Cards and Windows 1. It is also possible to use a Wireless USB dongle which saves you from opening up your laptop (however utilises a USB port). There is an Unofficial Czech Atheros Driver Website which lists the latest Atheros Wireless Card Drivers which has got extremely popular. The unofficial drivers may not support Dell Wireless Cards in all cases. The latest Dell Atheros drivers I can find are listed below. The ones in bold will work for most of the Atheros cards. Later versions not tested with all the cards please leave feedback. Windows 1. 0Use 1. DW1. 81. 0 and DW1. Use 1. 0. 0. 0. 3. DW1. 50. 2, DW1. 50. DW1. 51. 5, DW1. 52. DW1. 60. 1, DW1. 70. DW1. 70. 3, DW1. 70. DW1. 70. 7, DW1. 80. DW1. 90. 1 cards. Note: Dell list it as compatible for the DW1. DW1. 60. 1, DW1. 70. DW1. 80. 2 cards only however the driver has compatible hardware IDs for the other wireless cards listed. Use 1. 2. 0. 0. 2. Killer 1. 52. 5 and Killer AC1. Cards. Use 1. 0. 0. Killer N1. 20. 2 Card. Windows 8. 1. Use 1. DW1. 81. 0 and DW1. Use 1. 0. 0. 0. 3. DW1. 60. 1, DW1. 70. DW1. 70. 3, DW1. 70. DW1. 70. 7, DW1. 80. DW1. 90. 1 cards. Note: Dell list it as compatible for the DW1. DW1. 60. 1, DW1. 70. DW1. 80. 2 cards only however the driver has compatible hardware IDs for the other wireless cards listed. Use 1. 2. 0. 0. 2. Killer 1. 52. 5 and Killer AC1. Cards. Use 1. 1. 0. Killer N- 1. 20. 2Windows 7. Use 1. 0. 0. 0. 6. DW1. 81. 0 and DW1. Use 1. 0. 0. 0. 3. DW1. 50. 2, DW1. 50. DW1. 51. 5, DW1. 52. DW1. 60. 1, DW1. 70. DW1. 70. 3, DW1. 70. DW1. 70. 7, DW1. 80. DW1. 90. 1 cards. Note: Dell list it as compatible for the DW1. DW1. 60. 1, DW1. 70. DW1. 80. 2 cards only however the driver has compatible hardware IDs for the other wireless cards listed. Use 1. 2. 0. 0. 2. Killer 1. 52. 5 and Killer AC1. Cards. Use 1. 1. 0. Killer N- 1. 20. 2Dell Wireless 1. Hardware IDs: pci\ven. If this works well for you then it is probably the best driver. Many are however unfortunately experiencing wireless issues/frequent disconnects especially with Broadcom cards and Windows 1. Its possible that this driver can be force installed on systems with old wireless cards using the Device Manager in a similar manner as demonstrated for the Dell Touch. Pad Driver. This however requires testing and feedback from end users as I don’t have all the hardware to test with. The latest wireless drivers I have found are listed below. Dell Wireless 3. 55 BT2. EDRHardware IDs: USB\VID. Intel usually offer the drivers for all their wireless cards in the latest version of: The latest installers may not run on some of the legacy Intel Wireless Cards however, in which case the driver is usually inbuilt into the Windows Operating System or can be obtained from the Microsoft Update Catalog. Individual notes are given below the hardware IDs of these legacy cards. Intel Dual Band Wireless AC 7. Hardware IDs: PCI/VEN. The Windows 7 version has minor incompatibilities with Windows 8 so it is recommended to replace it with the Dell Wireless 3. Broadcom Bluetooth Update and can be found on e. Bay for quite cheap. Dell Wireless 3. 60 Hardware IDs: usb\vid. An error occurred while setting your user cookie. Please set your. browser to accept cookies to continue. This cookie stores just a. ID; no other information is captured. Accepting the NEJM cookie is.
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I am now making the backgrounds. You can adjust via 'Format', 'Custom Background', 'Down arrow'. Custom Background', your choice, 'Apply to the one slide/Apply to all slides', 'OK' (Then, reverse arrow. This morning, Wired magazine published an early look into Apple’s brand new spaceship campus. The giant circle features the kinds of ridiculous details you might. Some of the Powerpoints are 'busy'. For projection, the content would be spread over two or more slides. They are in the. condensed form so that they can be printed out six- to- a- page, then enlarged 1. Beyond this meet- the- family role, histology reveals time and again how. With many sources available for the actual visual images. I have used the space here to show the patterns of. For curricula where formal. The following storyline is sometimes helpful, and can be recognized later: context - structures - tasks - means - mechanisms - molecules - malfunctions. Chapter 1 A NATURE OF HISTOLOGY. Medical histology applies microscopy to the human body, seeking to discover. Thinking in histology runs along these lines. How does one prepare. What kinds of microscopy can be applied? Does the microscopic appearance of the tissue or. What experiments can one do to test ideas on how structure. First. histology is colourful. Secondly, almost everything seen is actually there. Third, one handles and. Fourth, the structures can be interpreted. So much is now known of the roles of cells and. The first need is. This. (c)Spread sheet of tissue seriously limits the facilities for. For example, staining. Thus. (d)Teased apart fibrous phase- contrast or interference- contrast. A drawback to using our eyes. Total magnification is then the product of these. X 1. 0 = 4. 00. The resolution or resolving power - how. This is achieved by the electromagnetic beam of the. The beam is focused through the object suspended on its. Chapter 3. 0. K). The other. forms of microscopy - phase- contrast, interference, fluorescence, confocal. X- ray diffraction) - will be discussed in Chapter. How to do this is described briefly below. In practical terms. Essentially, though, we are getting a. For what the structure looked like in the third dimension, the. Gross examples arise from: (l) clumsy excision from. Plug in, switch on, and adjust the rheostat up one third of its. Otherwise, use artificial light provided by an electric bulb behind a. Light intensity. can be increased by bringing the lamp nearer to the mirror, if the lamp is not. If the condenser in use (nearly always), use the plane side of the mirror. Raise the condenser to very near the underside of the. Place a clean, stained slide on the stage and using the coarse and fine. X l. 0 objective.(h) With the condenser racking knob focus the light source on the specimen. If this feature of the light source is. Do not. lower the condenser way out of focus as a means to reduce the light intensity.(i) The iris diaphragm should now be closed just to the point where glare is. Further closure will make the field too dark and reduce resolving. The microscope is now set up for use, but the requirements change for each. Higher power objectives require more light thus the iris will need. Note that the objective lenses are of different lengths, and they are not. Be careful when switching in a higher power lens that it. Clean the lenses only with. If the X 4. 4 objective will not focus to a clear image, check first that. This. operation must be controlled by observing the descending lens from the. Do not yet look down through the eyepiece. Once the lens has touched. If this has happened raise the lens slowly, while. Do not allow oil to get on. Ask for instructions in their use and for. If lens paper alone is insufficient to clean a lens. On no account exchange the lenses. Table l gives some differences between the. The detailed morphology revealed by EM may be called fine or. The direct comparison of LM and EM images of a structure requires that the. Noting the magnification, on the 'scope. A growing practice in histology and pathology is to fix and prepare. EM standards, imbed in plastic and cut semi- thin (l . LM then reveals good cellular detail and. Two other techniques yield anatomical images - fibre- optic endoscopy and. EM, and are being digested by the anatomical texts. Endoscopy. from its low magnification is marginal to histology, but related in that. SEM strengthens one's conception of microscopic structures, e. Some differences between light and electron microscopy. Light microscopy Electron microscopy. Image is presented directly to the Image is in shades of green on. Image keeps the colours given the screen; photographically. Its small size. even alive. Fluids can have. their suspended solid constituents viewed microscopically as smear. Blood; Chapter l. A), but are otherwise of limited. Extracellular substances are important for the cells. These. substances are used as building materials for the firmer structures of the. Lipids, minerals, glucose, and smaller molecules are usually lost from. What is left is a skeleton of structures - . The special steps of. Chapter 3. 0. C) preserve and reveal some smaller. The cells of the four primary tissues - epithelial. Cell morphology. Powerpoint. Cells performing a given function have a characteristic size, form and. However it may help at this stage. The cell is defined as a distinct entity by having a thin skin or. In LM the membrane is often unseen. Each is of unit membrane with a 'trilaminar' nature similar to that. Many of the apparent interruptions or pores/fenestrations through. Transport between nucleus and cytoplasm takes place at assemblies of. The outer nuclear membrane sometimes leads on out to a membrane system. This system of closed. Golgi complex.(b) Two varieties of endoplasmic reticulum (ER) are seen...(i) Granular/rough/GER has fine granules, ribosomes of ribonucleo- .. Ribosome particles: may lie free in the cytoplasm in small clusters. This is noted. particularly in growing cells. With routine haematoxylin staining in certain cells, e. Golgi structure as a pale negative image.(e) Its tasks are the concentration and preparation for storage of proteins. Microtubules: with a diameter of 2. EM or fluorescent tagging; they give form to the cell. In EM their shape tends to be tubular or spheroid.(c) They are hollow bodies enclosed in two unit membranes; the inner. They. may also store calcium. EM reveals that it consists. Each is an. open- ended cylindrical body with a wall composed of nine bundles, each of. These tubules help to initiate and control the. A similar cylindrical structure is seen at the base of each cilium and is. One way basal bodies and cilia develop. Cell nucleus(a) Nuclear membranes have been discussed in 5. Chromatin granules/karyosomes seen in the sap during the interphase. DNA). not fully uncoiled. The sex chromatin of female cells is an extreme example of. X chromosomes continues in a condensed. The nucleolus seen as a dense body in most cells' nuclei with LM. The dense branching strand is the nucleolonema.(d) There is great variety in the size of the nucleus, its shape, the. In general, a large nucleus, with much pale euchromatin and a prominent. RNA from chromatin DNA. The nucleolus is mostly pre- ribosomal RNA. Nucleoli. are prominent in nerve and Sertoli cells. Its chemical constitution and. Its complement of organelles is altering. The cell itself represents a system of activities isolated to. Within the cell things are. The. membranes define temporary compartments separated from the cytoplasm, where. Dynamic aspects of the cell's existence are. Chapter 3. 0. These stains may be discussed. Chapter 3. 0. B. 3. Routine staining of human material usually employs haematoxylin. The nucleic acids are concentrated in the nucleus and the rough. The colour is usually some shade of blue or brown. A few cells have a lot of granular ER in their cytoplasm, which gives a. This term depends on how the. Most cells do not have such a concentration of GER that their cytoplasm. Consequently, another cytoplasmic. Such a general stain is eosin, acidic in nature, which stains. Some structures stain bright red. It is. not difficult to get the balance wrong so that one swamps the. For example, an excess of eosin can mask a basophilic reaction of the. When the interest is in specific cell features, special. These can be obtained, single and clumped, from any tissue or organ. FNA). Also. one strategy of development is to overproduce cells, then select, e. Thirdly, if an organ cannot work properly, e. Apoptosis. 2 For apoptosis, endonucleases are activated which break up the. DNA, transcription slows and stops, organelles. GER dilates. Caspases digest relevant cellular. The cell and internal membranes bleb out. The controlling factors include cytokines (Chapter 8. F). One mechanism for this is the asymmetric cell division. For a similar story based. Medical Cytology Module. A CELL MEMBRANE OR PLASMALEMMA. Thus, some proteins span the width of the. The. wide- spread occurrence of solitary cilia (flagella), e. The stereocilia of the male reproductive tract are. Each cell collaborates with both. The importance of the. The binding of hormones to receptors on the membrane.(b) The binding of the lymphocyte's membrane receptor to an antigen.(c) Transmitter chemicals depolarize neurons and muscle cells.(d) Excitable tissues propagate action potentials along the membranes.(e) Schwann cells wrap their membranes many times round an axon's to make. Chemical stimuli are transduced into nerve impulses in chemoreceptors. 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