IPC분류정보
국가/구분 |
United States(US) Patent
등록
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국제특허분류(IPC7판) |
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출원번호 |
US-0770064
(2001-01-25)
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발명자
/ 주소 |
- Blankenship, George Daryl
- Hsu, Christopher
- Hillen, Edward Dennis
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출원인 / 주소 |
- The Lincoln Electric Company
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대리인 / 주소 |
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인용정보 |
피인용 횟수 :
179 인용 특허 :
9 |
초록
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A system and method provides a distributed welding architecture in accordance with the present invention. The system includes a welder operatively coupled to a server and a network interface to enable a network architecture, the network architecture serving a network that communicates with at least
A system and method provides a distributed welding architecture in accordance with the present invention. The system includes a welder operatively coupled to a server and a network interface to enable a network architecture, the network architecture serving a network that communicates with at least one remote system. The remote system includes at least one remote interface to communicate with the network architecture, wherein the remote system accesses at least one HTTP socket to establish web communications with the welder and loads at least one application from the welder. The remote system accesses at least one Welding Application socket via the at least one application to exchange information between the welder and the remote system, wherein the at least one application includes at least one of a weld configuration component, a weld monitoring component, and a weld control component to interact with the distributed welding system.
대표청구항
▼
A system and method provides a distributed welding architecture in accordance with the present invention. The system includes a welder operatively coupled to a server and a network interface to enable a network architecture, the network architecture serving a network that communicates with at least
A system and method provides a distributed welding architecture in accordance with the present invention. The system includes a welder operatively coupled to a server and a network interface to enable a network architecture, the network architecture serving a network that communicates with at least one remote system. The remote system includes at least one remote interface to communicate with the network architecture, wherein the remote system accesses at least one HTTP socket to establish web communications with the welder and loads at least one application from the welder. The remote system accesses at least one Welding Application socket via the at least one application to exchange information between the welder and the remote system, wherein the at least one application includes at least one of a weld configuration component, a weld monitoring component, and a weld control component to interact with the distributed welding system. een about 0.05 and 18% by weight, preferably 0.5 and 10% by weight. 5. Microspheres according to claim 1, wherein the thermoprocessable copolymers are selected from: TFE/PPVE copolymers; copolymers TFE/PMVE/fluorinated monomer, wherein the PMVE amount ranges from 0.5 to 13% by weight, the fluorinated monomer amount ranges from 0.5 to 3% by weight; copolymers TEE/PMVE/fluorinated dioxole wherein PMVE is in the range 0.5%-13% by weight, the fluorinated dioxole is in the range 0.05%-3% by weight. 6. The microspheres according to claim 1, wherein the bulk density is 0.55-1.0 g/cm3. 7. The microspheres according to claim 2, wherein the C3-C8perfluorolefin is hexafluoropropene (HFP). 8. The microspheres according to claim 2, wherein the C2-C8hydrogenated fluoroolefins are vinyl fluoride (VF), vinylidene fluoride (VDF), trifluoroethylene, hexafluoroisobutene, or perfluoroalkylethylene CH2=CH--Rf,wherein Rfis a C1-C6perfluoroalkyl. 9. The microspheres according to claim 2, wherein the C2-C8chloro- and/or bromo- and/or iodo-fluoroolefin is chlorotrifluoroethylene (OTFE). 10. The microspheres according to claim 2, wherein Rfis CF3,C2F5,or C3F7. 11. The microspheres according to claim 2, wherein the fluorodioxoles are perfluorodioxoles. 12. The microspheres of claim 5, wherein the copolymers TFE/PMVE/fluorinated monomer is PPVE. -4671913, 19870600, Gen et al.; US-4737559, 19880400, Kellen et al.; US-4843134, 19890600, Kotnour et al.; US-4925725, 19900500, Endo et al.; US-5091258, 19920200, Moran; US-5100963, 19920300, Lin; US-5147485, 19920900, Gajewski et al.; US-5178933, 19930100, Yoshida et al.; US-5190992, 19930300, Kato et al.; US-5254388, 19931000, Melby et al.; US-5268049, 19931200, Marriott et al.; US-5362801, 19941100, Amici et al.; US-5407971, 19950400, Everaerts et al.; US-5425977, 19950600, Hopfe; US-5436283, 19950700, Okada et al.; US-5445890, 19950800, Bayha et al.; US-5455103, 19951000, Hoagland et al.; US-5487412, 19960100, Matthews et al.; US-5536347, 19960700, Moran; US-5547736, 19960800, Simon et al.; US-5595818, 19970100, Hopfe et al.; US-5616670, 19970400, Bennett et al., 526/264; US-5620795, 19970400, Haak et al., 428/344; US-5637646, 19970600, Ellis; US-5654387, 19970800, Bennett et al., 428/516; US-5683798, 19971100, Bennett et al., 428/312.6; US-5708110, 19980100, Bennett et al., 526/264; US-5741542, 19980400, Williams et al.; US-5756584, 19980500, Bennett et al., 525/204; US-5795650, 19980800, Watanabe et al., 428/343; US-5804610, 19980900, Hamer et al.; US-5883149, 19990300, Bennett et al., 522/120; US-5969069, 19991000, Su et al.; US-5976690, 19991100, Williams et al.; US-6074725, 20000600, Kennedy, 156/277; US-6126865, 20001000, Haak et al., 252/512 y, vol. 20, Wiley & Sons Pub., 1982, pp. 922, 927 and 928. Handbook of Chemistry and Physics, 61stEd., 1980-1981, Periodic Table of Elements. B.H. Lipshutz, "Synthetic procedures involving organocopper reagents", Organometallis In Synthesis, Wiley & Sons, 1994, p. 283. K. Abe, Synthesis, 1998, p. 231. Chemical Abstracts, vol. 50/No. 12, 1956, Abstract 8270e. Chemical Abstracts, vol. 46, 1952, Abstract 6082i. R. West, "Cyclic Organosilicon Compounds", J. Am. Soc., vol. 76, 1954, pp. 6012-6014. B. Nguyen et alii, "A Convenient Synthetic Route To Methylated Silacyclohexanes," J. Org. Chem., vol. 51, 1986, pp. 2206-2210. Encyclopedia of Polymer Science and Engineering, vol. 15, Wiley & Sons Pub., 1989, pp. 226-228. Encyclopedia of Chemical Technology, vol. 20, Wiley & Sons Pub., 1982, pp. 922, 927 and 928. n with a chelating monomer wherein the chelating monomer has the structure wherein Z is or Y", and Y, Y' and Y" are independently selected from the group consisting of NRR', OR or R wherein R and R' are independently selected from the group consisting of hydrogen and aliphatic, alicyclic, aromatic and heteroaromatic groups and wherein the structure has olefin unsaturation. 11. The polymer of claim 10, wherein said composition is crosslinked with a polyvalent metal ion crosslinking agent. 12. The polymer latex composition of claim 10, wherein said composition is crosslinked with a polyvalent metal ion crosslinking agent. 13. The polymer latex composition according to claim 10, wherein the chelating monomer is an acetoacetoxy or diacetoacetoxy monomer. 14. The polymer latex composition of claim 13 wherein the acetoacetoxy monomer is selected from the group consisting of esters of acetylacetic and diacetylacetic acids. 15. The polymer latex composition according to claim 10, wherein the conjugated diene monomer is a C4to C9diene. 16. The polymer latex composition according to claim 15, wherein the C4to C9diene is 1,3-butadiene. 17. The polymer latex composition according to claim 10, wherein in addition to the conjugated diene monomer and chelating functionality, the polymer contains an α,β-unsaturated nitrile monomer. 18. The polymer latex composition according to claim 10, wherein in addition to the conjugated diene monomer and chelating functionality, the polymer contains a vinyl aromatic monomer. 19. The polymer latex composition according to claim 18, wherein the vinylaromatic monomer is selected from the group consisting of styrene, methylstyrene, vinyl toluene, chlorostyrene, vinyl benzyl chloride, vinyl pyridines, vinyl naphthalene, p-methylstyrene, p-methoxystyrene, and blends and mixtures thereof. 20. The polymer latex composition according, to claim 10, wherein in addition to the conjugated diene monomer and chelating functionality, the polymer contains an additional monomer selected from the (partial) amides of a α,β-unsaturated carboxylic acid monomer such that the carbon skeleton of the base amine of the amides contains from about 1 to 20 carbon atoms, vinyl halides, or the vinyl ester of aliphatic carboxylic acids having from about 2 to 20 carbon atoms. 21. A glove formed from the polymer latex composition of claim 10.
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