Academic literature on the topic 'FDM RepRap'
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Journal articles on the topic "FDM RepRap"
Harušinec, Jozef, Andrej Suchánek, and Mária Loulová. "Creation of prototype 3D models using RAPID PROTOTYPING." MATEC Web of Conferences 254 (2019): 01013. http://dx.doi.org/10.1051/matecconf/201925401013.
Full textДобролюбова, Марина Валеріївна, Анна Василівна Шнира, Богдан Володимирович Чапалюк, and Андрій Іванович Алімов. "Monitoring and control system for RepRap 3D-printer with FDM printing technology." Information systems, mechanics and control, no. 14 (April 25, 2016): 5–15. http://dx.doi.org/10.20535/2219-380414201672548.
Full textBurde, Alexandru Victor, Cristina Gasparik, Sorana Baciu, Marius Manole, Diana Dudea, and Radu Septimiu Câmpian. "Three-Dimensional Accuracy Evaluation of Two Additive Manufacturing Processes in the Production of Dental Models." Key Engineering Materials 752 (August 2017): 119–25. http://dx.doi.org/10.4028/www.scientific.net/kem.752.119.
Full textŠafka, Jiří, Michal Ackermann, Jiří Bobek, Martin Seidl, Jiří Habr, and Luboš Bĕhálek. "Use of Composite Materials for FDM 3D Print Technology." Materials Science Forum 862 (August 2016): 174–81. http://dx.doi.org/10.4028/www.scientific.net/msf.862.174.
Full textKhan, Shaheryar Atta, Bilal Ahmed Siddiqui, Muhammad Fahad, and Maqsood Ahmed Khan. "Evaluation of the Effect of Infill Pattern on Mechanical Stregnth of Additively Manufactured Specimen." Materials Science Forum 887 (March 2017): 128–32. http://dx.doi.org/10.4028/www.scientific.net/msf.887.128.
Full textPanda, Anton, Ema Nováková-Marcinčinová, Ľudmila Nováková-Marcinčinová, Tibor Krenický, and Tadeusz Zaborowski. "Production from PLA Materials Processed Vertically by FDM Method RP Technology." Key Engineering Materials 756 (September 2017): 80–87. http://dx.doi.org/10.4028/www.scientific.net/kem.756.80.
Full textPan, Ai Qiong, Zi Fan Huang, Rui Jie Guo, and Jun Liu. "Effect of FDM Process on Adhesive Strength of Polylactic Acid(PLA) Filament." Key Engineering Materials 667 (October 2015): 181–86. http://dx.doi.org/10.4028/www.scientific.net/kem.667.181.
Full textL. Melgoza, Evila, Guillem Vallicrosa, Lidia Serenó, Joaquim Ciurana, and Ciro A. Rodríguez. "Rapid tooling using 3D printing system for manufacturing of customized tracheal stent." Rapid Prototyping Journal 20, no. 1 (January 14, 2014): 2–12. http://dx.doi.org/10.1108/rpj-01-2012-0003.
Full textSukindar, Nor Aiman, Mohd Khairol Anuar Mohd Ariffin, B. T. Hang Tuah bin Baharudin, Che Nor Aiza Jaafar, and Mohd Idris Shah Ismail. "Comparison on Dimensional Accuracy Using a Newly Developed Nozzle for Open-Source 3D Printer." Applied Mechanics and Materials 859 (December 2016): 15–19. http://dx.doi.org/10.4028/www.scientific.net/amm.859.15.
Full textFirshein, Janet. "Repeal of FDA experimental-drug rule sought." Lancet 347, no. 9012 (May 1996): 1396. http://dx.doi.org/10.1016/s0140-6736(96)91025-9.
Full textDissertations / Theses on the topic "FDM RepRap"
Kratochvíl, Tomáš. "3D FDM tiskárna reprap a parametry tisku." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2015. http://www.nusl.cz/ntk/nusl-232069.
Full textKnapil, Josef. "Stavba a aplikace 3D FDM tiskárny typu deltabot." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2015. http://www.nusl.cz/ntk/nusl-232111.
Full textSvětlík, David. "Povrchová úprava ABS součástí po 3D FDM tisku." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2015. http://www.nusl.cz/ntk/nusl-232057.
Full textBouchal, Petr. "Vývoj 3D FDM tiskárny implementace na trh." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2016. http://www.nusl.cz/ntk/nusl-241863.
Full textProuza, Tomáš. "Návrh duální tiskové hlavy pro FDM 3D tiskárnu." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2016. http://www.nusl.cz/ntk/nusl-242851.
Full textBřoušek, Lukáš. "Tepelné úpravy povrchu po 3D FDM tisku." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2017. http://www.nusl.cz/ntk/nusl-318156.
Full textČuma, Zdeněk. "3D FDM tiskárna s výměnnou tiskovou hlavou." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2021. http://www.nusl.cz/ntk/nusl-444263.
Full textBartoš, Radko. "Návrh temperovaného stolu pro FDM 3D tiskárnu s využitím simulace MKP." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2014. http://www.nusl.cz/ntk/nusl-231051.
Full textSysel, Karel. "Návrh a zefektivnění parametrů FDM tisku." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2012. http://www.nusl.cz/ntk/nusl-230120.
Full textZítka, Lukáš. "Inovace 3D tiskárny typu Rep Rap." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2017. http://www.nusl.cz/ntk/nusl-319860.
Full textBook chapters on the topic "FDM RepRap"
"Frontmatter." In Condemned to Repeat?, i—vi. Cornell University Press, 2017. http://dx.doi.org/10.7591/9780801468643-fm.
Full textSantos, Cícero Alysson Cavalcanti dos, and José Orlando Costa Nunes. "Sondagem sobre a necessidade de implementação de uma política de qualidade de vida no trabalho (QVT) na diretoria de pessoal da Polícia Militar do Estado do Rio Grande do Norte." In Gestão de Pessoas na Segurança Pública, 64–75. Editora ZH4, 2021. http://dx.doi.org/10.51360/zh4.20217-8-p64-75.
Full text"implications of bioequivalence testing are also described by Patterson and so we do not repeat these here. At the present time average bioequivalence (see Section 7.2) serves as the current international standard for bioequivalence testing using a 2× 2 cross-over design. Alternative designs (e.g., replicate cross-over designs) may be also utilized for drug products to improve power (see Section 7.6). We will consider population and individual bioequivalence testing as these utilize cross-over study designs and were the subject of extensive debate in the 1990s (see Patterson, 2001b, for a summary), but these may not currently be used for access to the marketplace (FDA Guidance, 2002). 7.2 Testing for average bioequivalence The now generally accepted method of testing for ABE is the two-one-sided-tests procedure (TOST) proposed by Schuirmann (1987). It is con-veniently done using a confidence interval calculation. Let µ be the (true) mean values of log(AUC) (or log(Cmax)) when subjects are treated with T and R, respectively. ABE is demonstrated if the 90% two-sided confidence interval for µ falls within the acceptance limits of − ln 1.25 = −0.2231 and + ln 1.25 = 0.2231. These limits are set by the regulator (FDA Guid-ance, 1992, 2001, 2002) and when exponentiated give limits of 0.80 and 1.25. That is, on the natural scale ABE is demonstrated if there is good evidence that: 0.80 ≤ exp(µ ) ≤ 1.25. We note that symmetry of the confidence interval is on the logarithmic scale, not the natural scale. The method gets its name (TOST) because the process of deciding if the 90% confidence interval lies within the acceptance limits is equiva-lent to rejecting both of the following one-sided hypotheses at the 5% significance level: H :µ ≤− ln 1.25 H :µ ≥ ln 1.25. Example 7.1 The derived data given in Tables 7.1 and 7.2are from a pharmacoki-netic study that compared a test drug (T) with a known reference drug (R). The design used was a 2×2 cross-over with 24 healthy volunteers in the RT sequence group and 25 in the TR sequence group. Each volunteer should have provided both an AUC and Cmax value. However, as can." In Design and Analysis of Cross-Over Trials, 352. Chapman and Hall/CRC, 2003. http://dx.doi.org/10.1201/9781420036091-7.
Full text"population of potential patients, but be such that they produce different effects when a patient is switched from formulation T to formulation R or vice-versa. In other words there is a significant subject-by-formulation interaction. To show that this is not the case T and R have to be shown to be IBE, i.e., individually bioequivalent. The measure of IBE that has been suggested by the regulators is an aggregate measure involving the means and variances of T and R and the subject-by-formulation inter-action. We will describe this measure in Section 7.4. In simple terms PBE can be considered as a measure that permits patients who have not yet been treated with T or R to be safely prescribed either. IBE, on the other hand, is a measure which permits a patient who is cur-rently being treated with R to be safely switched to T (FDA Guid-ance, 1997, 1999a,b, 2000, 2001). It is worth noting that if T is IBE to R it does not imply that R is IBE to T. The same can be said for PBE. An important practical implication of testing for IBE is that the 2×2 cross-over trial is no longer adequate. As will be seen, the volunteers in the study will have to receive at least one repeat dose of R or T. In other words, three-or four-period designs with sequences such as [RTR,TRT] and [RTRT,TRTR], respectively, must be used. The measures of ABE, PBE and IBE that will be described in Sec-tions 7.2, 7.5 and 7.4 are those suggested by the regulators. Dragalin and Fedorov (1999) and Dragalin et al. (2002) have pointed out some drawbacks of these measures and suggested alternatives which have more attractive properties. We will consider these alternatives in Section 7.7. All the analyzes considered in Sections 7.2 to 7.4 are based on sum-mary measures (AUC and Cmax) obtained from the concentration-time profiles. If testing for bioequivalence is all that is of interest, then these measures are adequate and have been extensively used in practice. How-ever, there is often a need to obtain an understanding of the absorb-tion and elimination processes to which the drug is exposed once it has entered the body, e.g., when bioequivalence is not demonstrated. This can be done by fitting compartmental models to the drug con-centrations obtained from each volunteer. These models not only pro-vide insight into the mechanisms of action of the drugs, but can also be used to calculate the AUC and Cmax values. In Section 7.8 we de-scribe how such models can be fitted using the methods proposed by Lindsey et al. (2000a). The history of bioequivalence testing dates back to the late 1960s and early 1970s. Two excellent review articles written by Patterson (2001a, 2001b) give a more detailed description of the history, as well as a more extensive discussion of the points raised in this section. The regulatory." In Design and Analysis of Cross-Over Trials, 351. Chapman and Hall/CRC, 2003. http://dx.doi.org/10.1201/9781420036091-6.
Full textConference papers on the topic "FDM RepRap"
Kung, Chieh, Hsu-Chiang Kuan, and Chen-Feng Kuan. "Evaluation of tensile strength of 3D printed objects with FDM process on RepRap platform." In 2018 1st IEEE International Conference on Knowledge Innovation and Invention (ICKII). IEEE, 2018. http://dx.doi.org/10.1109/ickii.2018.8569166.
Full textM. da Silva, Amanda, Ana Paula G. Marchesan, Milena T. Zonin, Adriano C. Marchesan, Klaus T. Martin, and Adriano P. de Morais. "Restabelecimento de Serviço: uma Revisão Crítica Quanto a Aplicação em Sistemas de Distribuição Brasileiros." In Congresso Brasileiro de Automática - 2020. sbabra, 2020. http://dx.doi.org/10.48011/asba.v2i1.1352.
Full textW. Leal, Bernardo, and Roberto Z. Freire. "Detecção de expulsão em processos de soldagem a ponto por resistência: uma análise comparativa envolvendo métodos baseados em aprendizado de máquina." In Congresso Brasileiro de Automática - 2020. sbabra, 2020. http://dx.doi.org/10.48011/asba.v2i1.1749.
Full textC. Júnior, Misael, and Márcio E. Delamaro. "Automatização de oráculos de teste para imagens médicas de modelos tridimensionais." In Anais Estendidos do Simpósio Brasileiro de Computação Aplicada à Saúde. Sociedade Brasileira de Computação (SBC), 2019. http://dx.doi.org/10.5753/sbcas.2019.6284.
Full textAlbuquerque, Enzo Aldo Cunha, Luisa Resende Kanno, Thaynara Lima de Oliveira, and Leonardo da Silveira Pirillo Inojosa. "Plano de execução BIM para sistema de manutenção de edificações." In ENCONTRO NACIONAL SOBRE O ENSINO DE BIM. Antac, 2021. http://dx.doi.org/10.46421/enebim.v3i00.294.
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