Готові списки джерел за темами / Coagulator

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  1. Статті в журналах
  2. Дисертації
  3. Книги
  4. Частини книг
  5. Тези доповідей конференцій
  6. Звіти організацій

Добірка наукової літератури з теми "Coagulator"

Автор: Grafiati
Опубліковано: 30 травня 2022
Оновлено: 31 травня 2022

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Статті в журналах з теми "Coagulator"

1

Bergdahl, Björn, and Bertil Vällfors. "Studies on coagulation and the development of an automatic computerized bipolar coagulator." Journal of Neurosurgery 75, no. 1 (July 1991): 148–51. http://dx.doi.org/10.3171/jns.1991.75.1.0148.

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✓ A new computerized bipolar coagulator is described in which tissue heating is switched off automatically when adequate vessel occlusion has been achieved, thus preventing overheating, undue tissue damage, cutting, and sticking of the forceps. Experiments with radiofrequency (rf) heating of albumin or arteries revealed an impedance minimum at the moment of coagulation. The attainment of this impedance minimum is transmitted electronically via a microprocessor to the coagulator, which automatically shuts off the rf energy supply. In experiments, adequate artery strength and avoidance of the drawbacks of conventional coagulation methods were achieved when rf heating was shut off soon after the impedance minimum was reached. Neither irrigation for cooling nor cleaning of the forceps tips was necessary. Electronic feedback through the same cables as used for coagulation enabled the use of conventional bipolar cables and forceps. The bipolar coagulator described can also be used for conventional bipolar coagulation under visual control. The microcomputer enables: 1) automatic coagulation cycles that start when tissue is picked up in the forceps and stop automatically on completion of the seal; 2) the change of power setting from a pedal and activation of automatic cycles by the pedal as described above or surgeon-controlled coagulation, which facilitates the use of alternative debridement with inactive forceps; 3) cable testing; and 4) negligible disturbance of the intraoperative monitoring equipment.
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2

Ellasson, B., W. Egli, J. R. Ferguson, and H. Jodeit. "Coagulation of bipolarly charged aerosols in a stack coagulator." Journal of Aerosol Science 18, no. 6 (December 1987): 869–72. http://dx.doi.org/10.1016/0021-8502(87)90143-1.

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3

Waye, Jerome D. "Argon Plasma Coagulator." Problems in General Surgery 19, no. 2 (June 2002): 37–43. http://dx.doi.org/10.1097/00013452-200206000-00007.

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4

Nishisaka, T. "1.32 um Lasing in mediLas YAG Coagulator." JOURNAL OF JAPAN SOCIETY FOR LASER SURGERY AND MEDICINE 7, no. 3 (1987): 7–8. http://dx.doi.org/10.2530/jslsm1980.7.3_7.

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5

Ikeda, Kazuo, Daisuke Yamauchi, and Katsuro Tomita. "PRELIMINARY STUDY FOR PREVENTION OF NEURAL ADHESION USING AN ABSORBABLE OXIDISED REGENERATED CELLULOSE SHEET." Hand Surgery 07, no. 01 (July 2002): 11–14. http://dx.doi.org/10.1142/s0218810402000911.

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The purpose of this study was to clarify the effect of an absorbable oxidised regenerated cellulose sheet (AORCS) for prevention of neural adhesion. Rabbit sciatic nerve was exposed at the middle of the thigh and the neural bed was coagulated by a bipolar coagulator to establish an adhesion model. Coagulation only was Group A (n = 8), coagulation and wrapping the sciatic nerve with an AORCS was Group B (n = 8), and an intact nerve was Group C (n = 16). Six weeks later, each group was estimated. Adhesion between the nerve and neural bed, and intraneural fibrosis were seen in Group A. However, there was little adhesion and fibrosis in Group B. Although the electrophysiological study showed a small significant difference, AORCS clearly prevented the adhesion in the histological study. Hence, AORCS might be useful as an additional treatment during nerve surgery.
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6

Yudhistira, Bara, Martina Andriani, and Rohula Utami. "KARAKTERISASI: LIMBAH CAIR INDUSTRI TAHU DENGAN KOAGULAN YANG BERBEDA (ASAM ASETAT DAN KALSIUM SULFAT)." Caraka Tani: Journal of Sustainable Agriculture 31, no. 2 (January 29, 2018): 137. http://dx.doi.org/10.20961/carakatani.v31i2.11998.

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<div class="WordSection1"><p><em>Tofu liquid waste can be further processed to produce some useful product. That can be kept anaerobically to produce some organic acid</em><em>. </em><em>The purpose of this study to know the microbial growth behavior characteristic of liquid tofu waste which produce with different production process, such as specific growth rate (</em><em>m</em><em>), doubling time (td), multiplication degree (n), product yield, and efficiency of acetic acid production. This study is also aimed to identify the acid type which produce with different production tofu process. The liquid waste which used for this study is obtained from tofu producer which uses acetic acid and calcium sulfate to coagulate the tofu protein</em><em>. </em><em>Liquid tofu waste was incubated 24 hour, in ambient temperature(30<sup>o</sup>C). analysis of total cell count, glucose concentration, acetic acid concentration, and pH value was evaluated in certain interval, such 0, 2, 4, 6 8, 10, 12, 14 16, 18, 20, 22, 24 hour. Acid type identification was evaluated in some phase during fermentation process. The observation result was plotted into a graphic which was shown the relationship of total cell count, with glucose concentration, acetic acid concentration, and also fermentation time.</em><em> </em><em>From the analysis of observation result, It can be concluded that, the specific growth rate of liquid tofu waste with acetic acid as protein coagulator is 0,3015/hour, while the specific growth rate of liquid tofu waste with calcium sulfate as protein coagulator is 0,2174/hour. The doubling time of liquid tofu waste with acetic acid as protein coagulator are 2,2991 hours, while the doubling time of liquid tofu waste with calcium sulfate as protein coagulator are 3,1877 hours. The multiplication degree of liquid tofu waste with acetic acid as protein coagulator are 2,605 times, while the multiplication degree of liquid tofu waste with calcium sulfate as protein coagulator are 1,880 times. The growth yield constant (Y p/s) of liquid tofu waste with acetic acid and calcium sulfate as protein coagulator respectively 8,1 x 10<sup>9 </sup>cfu/mg and 8,1 x 10<sup>7</sup> cfu/mg. The product yield constant (Y p/s) of liquid tofu waste with acetic acid and calcium sulfate as protein coagulator respectively 1,7237 and 0,0306. The efficiency of acetic acid production during fermentation of liquid tofu waste with acetic acid and calcium sulfate as protein coagulator respectively 15,1376% and 2,5699%. Acid type identification shows that acid which was contained in liquid tofu waste recognized as Acetic acid.</em></p></div>
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7

Wang, Yong, Jun-Zhou Wu, Wei Wang, and Bo-Wen Zheng. "Coagulation and Collection of PM2.5 Based on a Stack Coagulator." Particulate Science and Technology 31, no. 4 (July 4, 2013): 385–91. http://dx.doi.org/10.1080/02726351.2013.767292.

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8

GOTOH, M. "Clinical Experiences of Argon Beam Coagulator and its Coagulation Characteristics." JAPANES JOURNAL OF MEDICAL INSTRUMENTATION 60, no. 6 (June 1, 1990): 295–300. http://dx.doi.org/10.4286/ikakikaigaku.60.6_295.

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9

Duan, Ting, Mei Yan Xing, Ming Zhuo Li, Zheng Zhong Liu, Wen Liu, and Jian Yang. "Treatment of Cotton Pulp Black Liquor Using Micro-Electrolysis in Sequencing Batch Reactor." Key Engineering Materials 500 (January 2012): 180–86. http://dx.doi.org/10.4028/www.scientific.net/kem.500.180.

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Micro-electrolysis process was conducted to treat the anaerobic digestion effluent of cotton pulp black liquor in sequencing batch reactor (SBR). Three key factors including reaction time, pH, and iron-carbon volume ratio were investigated for their impacts on the treatment efficiency. The effluent of micro-electrolysis polished by coagulation process was performed with Al2(SO4)3and PAC as coagulators. The results show that the optimum conditions of the micro-electrolysis treatment were pH 5.5, iron-carbon volume ratio 1:1, and reaction time 8h. Al2(SO4)3was selected as the coagulator with the addition of 400mg/L. The removal efficiency of COD reaches 93.2% with Micro-electrolysis combined with coagulation process. In addition, the B/C ratio has risen from 0.016 to 0.68(>0.3), which creates favorable conditions for the subsequent aerobic process. Consequently, the micro-electrolysis and coagulation process are highly efficient to dispose the anaerobic digestion effluent of cotton linters pulp black liquor. What’s more, this technology has the advantages of low operating cost, small land occupation and high efficiency.
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10

Araki, Takashi. "Tonsillectomy with bipolar coagulator." Practica Oto-Rhino-Laryngologica 82, no. 5 (1989): 689–91. http://dx.doi.org/10.5631/jibirin.82.689.

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Дисертації з теми "Coagulator"

1

Colver, Graham. "The infrared coagulator in dermatology." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235842.

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2

Бухкало, Светлана Ивановна, Валентин Николаевич Соловей та Сергей Петрович Иглин. "Особенности моделирования процессов разделения в статических аппаратах". Thesis, Московский государственный университет дизайна и технологии, 2016. http://repository.kpi.kharkov.ua/handle/KhPI-Press/22978.

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Рассмотрены основные возможности эксперимента с целью выбора методов моделирования процессов коагуляции в статическом коагуляторе, а также основные принципы и механизмы дестабилизации водных дисперсных систем с помощью коагулянтов и флокулянтов. Показано, что расчет и проектирование технологической схемы коагуляции на базе статических флокуляторов требуют предварительного экспериментального определения параметров коагуляции данной дисперсной системы в модельном аппарате с мешалкой.
This article discusses іmplementation of the experiment in order to choose the methods of modeling the processes of coagulation in a static coagulator. In paper are considered the basic principles and mechanisms of destabilization of water dispersed systems using coagulants and flocculants. It is shown that the calculation and design of the technological scheme of coagulation based on static demand flocculators with preliminary experimental determination of the parameters of the coagulation model system in a disperse apparatus with stirrer.
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3

Stewart, Iain W. "Coagulation-fragmentation dynamics." Thesis, Heriot-Watt University, 1988. http://hdl.handle.net/10399/1007.

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4

Ruttmann, Thomas Gotthard. "Haemodilution and coagulation." Doctoral thesis, University of Cape Town, 2003. http://hdl.handle.net/11427/3030.

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5

Huang, David Da-Teh. "Aerosol coagulation and nucleation." Diss., Pasadena, Calif. : California Institute of Technology, 1991. http://resolver.caltech.edu/CaltechETD:etd-06222005-162441.

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6

Sharp, Emma. "Natural organic matter coagulation." Thesis, Cranfield University, 2005. http://dspace.lib.cranfield.ac.uk/handle/1826/2224.

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The removal of natural organic matter (NOM) is one of the main challenges facing water utilities in both the UK and the US. As a consequence of changes in land management and an increased carbon loss from solids, a greater amount of accumulated organics is now being flushed into the aquatic environment during increased surface run-off events such as snowmelt or heavy rainfall. Furthermore, whilst traditional treatment with trivalent coagulants has proven a successful strategy in the past, operational problems are now being reported during periods of elevated organic levels in the water. These include the formation of fragile flocs, a greater particulate carryover onto downstream processes and increased disinfection by product (DBP) formation. Resin adsorption techniques were employed to fractionate the water samples into their hydrophobic and hydrophilic components. This, coupled with raw water monitoring, revealed that NOM composition and characteristics can vary, even if the total organic concentrations appear stable. In particular, hydrophobic NOM fractions contribute the majority of the charge compared to the hydrophilic fractions, and therefore exert a greater impact on coagulation conditions. Comparison across different source waters, seasons, at varying experimental scales and under varying coagulation conditions, revealed that zeta potential monitoring during coagulation takes into account the changing electrical property of the water, and in general, maintaining a value between -10
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7

Cueto, Camejo Carlos [Verfasser], and Gerald [Akademischer Betreuer] Warnecke. "The singular coagulation and coagulation-fragmentation equations / Carlos Cueto Camejo. Betreuer: Gerald Warnecke." Magdeburg : Universitätsbibliothek, 2013. http://d-nb.info/1054420378/34.

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8

Fuentes-Prior, Pablo. "Structural investigations of coagulation factors." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=962013986.

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9

Gray, E. "Lipoproteins, blood coagulation and thrombosis." Thesis, Open University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372834.

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The main aim of this study was to investigate the involvement of plasma lipoproteins in the blood coagulation system and the implications of this relationship in the pathogenesis of thrombosis. This study has shown that lipid peroxide-induced thrombin generation is caused by a two-fold mechanism: direct interaction of lipid peroxides with lipoprotein phospholipids and inhibition of anti-thrombin III via its heparin-binding site. Experiments using purified lipoproteins have shown that triglyceride-rich lipoproteins, i.e. chylomicra and very low density lipoproteins, are sources of procoagulant activity, whereas low density and high density lipoproteins have little effect. Further work with phospholipids extracted from chylomicra has demonstrated that lipid peroxides interact with the phospholipid component of the lipoprotein molecule and, possibly through an increase in overall negative charge, provide a suitable surface for the binding of clotting factors. Subcutaneous injection of potent lipase releasers, which are weak in vitro anticoagulants, reduce the ex vivo thrombin-generating activity of post-infusion plasma. This reduction in procoagulant activity is caused by the phospholipase action of the hepatic tri-glyceride lipase (HTGL) released. Human HTGL also enhances plasma anti-Xa activity, due to direct inhibition of Xa clotting activity, but the amidolytic activity of Xa is unaffected, thus implying that the serine site of Xa is not preferentially targeted. The phospholipid binding site of Xa appears to be involved, but this anti-Xa effect is not due to the phospholipase action of HTGL. The antithrombotic effects of heparin and heparin analogues may thus be partly due to the release of HTGL, which can reduce pro-coagulant activity via inhibition of lipid peroxide-induced thrombin generation and enhancement of plasma anti-Xa activity.
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10

Perdomo, Joana L. "Mathematical Modeling of Blood Coagulation." Scholarship @ Claremont, 2016. https://scholarship.claremont.edu/hmc_theses/71.

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Blood coagulation is a series of biochemical reactions that take place to form a blood clot. Abnormalities in coagulation, such as under-clotting or over- clotting, can lead to significant blood loss, cardiac arrest, damage to vital organs, or even death. Thus, understanding quantitatively how blood coagulation works is important in informing clinical decisions about treating deficiencies and disorders. Quantifying blood coagulation is possible through mathematical modeling. This review presents different mathematical models that have been developed in the past 30 years to describe the biochemistry, biophysics, and clinical applications of blood coagulation research. This review includes the strengths and limitations of models, as well as suggestions for future work.
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Книги з теми "Coagulator"

1

Coagulation-inflammation interface: Coagulation assembly on leukocytes. New York: Chapman & Hall, 1997.

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2

Altieri, Dario C. The coagulation-inflammation interface: Coagulation assembly on leukocytes. New York: Springer, 1997.

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3

Matthias, Fritz Reinhard. Blood Coagulation Disorders. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-83098-3.

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4

Lichtin, Alan, and John Bartholomew, eds. The Coagulation Consult. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-9560-4.

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5

Kwaan, Hau C., and David Green, eds. Coagulation in Cancer. Boston, MA: Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-79962-9.

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6

Coagulation problems during pregnancy. Edinburgh: Churchill Livingstone, 1985.

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7

Aledort, Louis M., Leon W. Hoyer, Jeanne M. Lusher, Howard M. Reisner, and Gilbert C. White, eds. Inhibitors to Coagulation Factors. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4613-0331-2.

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8

Sibinga, C. Th Smit, P. C. Das, and P. M. Mannucci, eds. Coagulation and Blood Transfusion. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3900-1.

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9

Marques, Marisa B. Quick guide to coagulation testing. 2nd ed. Washington, DC: American Association for Clinical Chemistry, 2009.

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10

Klaus, Strenge, and Vincent B, eds. Coagulation kinetics and structure formation. New York: Plenum Press, 1987.

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Частини книг з теми "Coagulator"

1

Duncan, I. D. "Destruction of Cervical Intraepithelial Neoplasia at 100 °C Using the Semm “Cold” Coagulator." In Gynecology and Obstetrics, 455–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70559-5_157.

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2

Gooch, Jan W. "Coagulation." In Encyclopedic Dictionary of Polymers, 148. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_2478.

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3

Linklater, Andrew. "Coagulation." In Monitoring and Intervention for the Critically Ill Small Animal, 137–56. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781118923870.ch9.

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4

Thomovsky, Elizabeth J., and Aimee C. Brooks. "Coagulation." In Basic monitoring in canine and feline emergency patients, 177–98. Wallingford: CABI, 2020. http://dx.doi.org/10.1079/9781789242997.0177.

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5

Kalmar, Jayne M., Brigid M. Lynch, Christine M. Friedenreich, Lee W. Jones, A. N. Bosch, Alessandro Blandino, Elisabetta Toso, et al. "Coagulation." In Encyclopedia of Exercise Medicine in Health and Disease, 192. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_4124.

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6

Feinberg, W. M. "Coagulation." In Brain Ischemia, 85–96. London: Springer London, 1995. http://dx.doi.org/10.1007/978-1-4471-2073-5_12.

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Moore, Ernest E. "Coagulation." In Resources for Optimal Care of Emergency Surgery, 153. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-49363-9_23.

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Boland, John Edward, and David E. Connor. "Coagulation and the coagulation cascade." In Interventional Cardiology and Cardiac Catheterisation, 33–44. Second edition. | Boca Raton, FL : CRC Press, Taylor & Francis Group, [2019] | Preceded by Cardiology and cardiac catheterisation : the essential guide / edited by John Boland and David W.M. Muller. 2001.: CRC Press, 2019. http://dx.doi.org/10.1201/9781351060356-4.

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Militello, Michael A. "Surgery on Patients on Antiplatelet Agents." In The Coagulation Consult, 231–36. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-9560-4_15.

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Joseph, Douglas E. "Newer Oral Anticoagulants." In The Coagulation Consult, 237–48. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-9560-4_16.

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Тези доповідей конференцій з теми "Coagulator"

1

Gurko, A. A., V. D. Yeremka, L. V. Pisarenko, and N. K. Goloborod'ko. "Medical microwave irradiator coagulator." In 2000 10th International Crimean Microwave Conference. Microwave and Telecommunication Technology. Conference Proceedings. IEEE, 2000. http://dx.doi.org/10.1109/crmico.2000.1255855.

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2

Bielecki, Zbigniew, Z. Ulbin, S. Wdowiak, and Andrzej Zajac. "Ophthalmological semiconductor coagulator LKP 1500A." In Laser Technology: Fourth Symposium, edited by Wieslaw L. Wolinski and Tadeusz Kecik. SPIE, 1995. http://dx.doi.org/10.1117/12.203348.

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3

Vaitkuviene, Aurelija, Ceslova Spuriene, Sarunas Skirkevicius, and Bronius Bareika. "Nd:YAG laser as scalpel and coagulator." In OE/LASE'93: Optics, Electro-Optics, & Laser Applications in Science& Engineering, edited by Christopher J. Daly, Warren S. Grundfest, Douglas E. Johnson, Raymond J. Lanzafame, Rudolf W. Steiner, Yona Tadir, and Graham M. Watson. SPIE, 1993. http://dx.doi.org/10.1117/12.146250.

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4

Jabczynski, Jan K., Zdzislaw Jankiewicz, J. Kucharz, Michal Pawlowski, Andrzej Zajac, Tadeusz Kecik, Dariusz Kecik, and Jan Kasprzak. "Ophthalmological coagulator LKP-1500 with a semiconductor laser." In Laser Technology: Fourth Symposium, edited by Wieslaw L. Wolinski and Tadeusz Kecik. SPIE, 1995. http://dx.doi.org/10.1117/12.203750.

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Saito, K., K. Ito, Y. Endo, and K. Suzuki. "Development of microwave tissue coagulator with cutting mechanism." In 2014 USNC-URSI Radio Science Meeting (Joint with AP-S Symposium). IEEE, 2014. http://dx.doi.org/10.1109/usnc-ursi.2014.6955688.

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6

Wolinski, Wieslaw, Antoni Kazmirowski, Witold Korobowicz, and Zbigniew Olborski. "Surgical Coagulator With Carbon Dioxide Laser For Gynecology." In Second Symposium on Laser Technology, edited by Ryszard S. Romaniuk, Bohdan K. Wolczak, and Wieslaw L. Wolinski. SPIE, 1987. http://dx.doi.org/10.1117/12.943365.

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7

Yoshiki, Hitoshi, Kotaro Tadano, and Kenji Kawashima. "Surgical Aspirator with Steam-Jet Coagulator for Hepatic Surgery." In The 3rd World Congress on Electrical Engineering and Computer Systems and Science. Avestia Publishing, 2017. http://dx.doi.org/10.11159/icbes17.123.

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8

Svirin, Vaytcheslav N. "Compact self-contained blood coagulator based on semiconductor laser." In Clinical Lasers and Diagnostics. SPIE, 2001. http://dx.doi.org/10.1117/12.413738.

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9

Moffitt, Theodore P., Deborah A. Baker, Sean J. Kirkpatrick, and Scott A. Prahl. "Mechanical properties of repaired liver using an argon beam coagulator with albumin." In International Symposium on Biomedical Optics, edited by Kenneth E. Bartels, Lawrence S. Bass, Werner T. de Riese, Kenton W. Gregory, Abraham Katzir, Nikiforos Kollias, Michael D. Lucroy, et al. SPIE, 2002. http://dx.doi.org/10.1117/12.438864.

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Yumei Chang, Wenquan Che, Lisheng Yang, Lijiang Yang, and Guoqiang Chen. "Experimental studies on microwave ablation in vitro animal tissues with microwave percutaneous coagulator." In 2008 International Conference on Microwave and Millimeter Wave Technology (ICMMT). IEEE, 2008. http://dx.doi.org/10.1109/icmmt.2008.4540799.

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Звіти організацій з теми "Coagulator"

1

Wicker, Louise, Ilan Shomer, and Uzi Merin. Membrane Processing of Citrus Extracts: Effects on Pectinesterase Activity and Cloud Stability. United States Department of Agriculture, October 1993. http://dx.doi.org/10.32747/1993.7568754.bard.

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Анотація:
The U.S. team studied the role of cations and pH on thermolabile (TL-PE) and thermostable (TS-PE), permeation in ultrafiltration (UF) membranes, affinity to ion exchange membranes, mechanism of cation and pH activation, and effect on PE stability. An optimum pH and cation concentration exists for activity and UF permeation, which is specific for each cation type. Incomplete release of PE from a pectin complex resulted in low PE binding to cationic and anionic membranes. Incubation of PE at low pH increases the surface hydrophobicity, especially TL-PE, but the secondary structure of TL-PE is not greatly affected. The Israeli team showed that stable cloud colloidal constituents flocculate following the conversion of soluble to insoluble biopolymers. First, formation of pectic acid by pectinesterase activity is followed by the formation of calcium pectate gel. This process initiates a myriad of poorly defined reactions that result in juice clarification. Second, protein coagulation by heat resulted in flocculation of proteinacous bound cloud constituents, particularly after enzymatic pectin degradation. Pectinesterase activity is proposed to be an indirect cause for clarification; whereas binding of cloud constituents is the primary event in clarification by pectate gel and coagulated proteins. Understanding the mechanism of interaction of protein and pectic polymers is key to understanding cloud instability. Based on the above, it was hypothesized that the structure of pectin-protein coagulates plays a key role in cloud instability.
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2

Yoon, R. H., and G. H. Luttrell. Development of the selective coagulation process. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/5688179.

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3

Yoon, R. H., and G. H. Luttrell. Development of the selective coagulation process. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/7070012.

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4

Cohen, Mitchell. Mechanisms of Coagulation Abnormalities and Trauma. Fort Belvoir, VA: Defense Technical Information Center, July 2011. http://dx.doi.org/10.21236/ada581645.

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5

Cohen, Mitchell J., and Jean F. Pittet. Mechanisms of Coagulation Abnormalities and Trauma. Fort Belvoir, VA: Defense Technical Information Center, November 2013. http://dx.doi.org/10.21236/ada602708.

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6

Cohen, Mitchell J., and Jean F. Pittet. Mechanisms of Coagulation Abnormalities and Trauma. Fort Belvoir, VA: Defense Technical Information Center, July 2012. http://dx.doi.org/10.21236/ada625634.

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7

Yoon, R., and G. Luttrell. Development of the Selective Hydrophobic Coagulation process. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/7055229.

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8

Yoon, R. H., and G. H. Luttrell. Development of the selective hydrophobic coagulation process. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6879257.

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9

Yoon, R. H., and G. H. Luttrell. Development of the selective coagulation process. Final report. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/10175177.

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10

Nyman, May Devan, Susan Jeanne Altman, and Tom Stewart. Coagulation chemistries for silica removal from cooling tower water. Office of Scientific and Technical Information (OSTI), February 2010. http://dx.doi.org/10.2172/1011210.

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