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US789538A - Dumb-bell. - Google Patents

Dumb-bell.
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Publication number
US789538A
US789538AUS23228504AUS1904232285AUS789538AUS 789538 AUS789538 AUS 789538AUS 23228504 AUS23228504 AUS 23228504AUS 1904232285 AUS1904232285 AUS 1904232285AUS 789538 AUS789538 AUS 789538A
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Prior art keywords
bell
dumb
heads
bar
spring
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US23228504A
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Colin E Ham
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No. 789,538. PATENTBD MAY 9, 1905. G. E. HAM.
DUMB BELL.
APPLICATION FILED NOV. 11, 1904.
J 16J 2 2 Z41 rvrrrn Srarrs Patented May 9, 1905.
PATENT rricri.
DUMB-BELL...
SPECIFICATION for g p of Letters Patent 789,538, dated May 9, 1905.
Application filed November 11, 1904. Serial No. 232,285.
To (bl/Z whom may concern:
Be it known that I, COLIN HAM, a citizen of the United States, and a resident of Boston, in the county of Suffolk and State of M assacliusetts, have invei'ited a new and Improved Dumb-Bell, of which the following is a full, clear, and exact description.
This invention relates to dumb-bells, and especially to the class known as spring dumb-bells. Dumb-bells of this class usually comprise oppositely-disposed bars which are maintained apart by springs. As ordinarily constructed the heads of these dumbbells present angularcorners, which are a defective feature, for the reason that in exercising they offer opportunity for abrading ones skin if struck accidentally.
The object of this invention is to overcome the defects referred to above and to provide a dumb-bell of simple construction, the body of which will present aresilient resistance to compression.
To this end the invention consists in the construction and relation of the opposing parts of the dumb-bell, and concerns itself also with improvements relating to the means for guiding them upon each other and for mounting the spring to thrust them apart.
Reference is to be had to the accompanying drawings, forming a part of this specification, in which similar characters of reference indicate corresponding parts in all the views.
Figure 1 is a side elevation of a dumb-bell constructed according to my invention. Fig. 2 is a vertical central section. Fig. 3 is a cross-section taken substantially on theline 3 3 of Fig. 2, and Fig. 4- is a perspective view representing one of the parts of the dumbbell as detached from the other and viewed from one end.
Referring more particularly to the parts, 1. represents the body of the dumb-bell, which comprises a reducedneck 2, connecting enlargedheads 3. These heads are preferably rounded on their outer faces, as shown, and each head presents the general outline of an oval, as illustrated in Fig. 1, the main axes of the oval being disposed substantially at right angles to the longitudinal axes of the manner shown in Figs. 1. and 2.
dumb-bell. The central portion of theneck 2 is removed, forming an opening 9 of substantially rectangular form, dividing the neck into opposite parallel bars 10. The end.faces 7 of the opening 9 are preferably dis posed on. the central planes of the heads, and the said heads are each split or divided on. theline 12 in such a manner as to extend the end faces to the outer surface of the heads at one side. From this arrangement the bar 10 is cut off, so as to constitute a distinct and movable slide-bar terminating in enlarged ends orknobs 1 1, which complete theheads 3 of the dumb-bell, as will be readily understood. Theouter faces 6 of theheads 3 are preferably of rounded form, as shown. Theinner face 1 of the bar 10" is preferably flat and is provided substantially centrally with a pair of oppositely-disposedrecesses 5. The
purpose of these recesses will appear more fully hereinafter. Thefaces 7 are provided, preferably centrally, with grooves orguide ways 8, which are disposed longitudinally with the major axis of the heads, as indi cated in Fig. Upon the end faces 7tongues 13 are provided,\vhich are adapted to be received in theaforesaid grooves 8 in the When the slide-bar 1O is in its normal position with re spect to thebody 1, the dumb-bell presents a symmetrical appearance, as indicated. in Fig. 1, the outer faces of theknobs 11 constituting portions of the rounded outer surfaces of theheads 3. The bar is forced outwardly against steps 14 by means of a spring 15, mounted as shown most clearly in Fig. 2. Said steps 14 preferably consist of small blocks, which are tightly driven into the grooves S, as best shown in Fig. 3. These steps of course abut against the ends of thetongues 13, so as to limit the outward movement of the slide-bar, and in order to enable the outer faces of theknobs 11 to complete nicely the rounded contour of the heads the upper portions of thetongues 13 are pref erably depressed, as shown in Fig. 2, with respect to the outer faces of the heads. Thespring 1, 5 is a leaf-spring and is formed with a pair of oppositely-disposedrudimentary bows 16, which occupy therecesses 5, as indicated in Fig. 2, thelegs 17 of the spring being disposed in inclined positions and having upwardly-turned tips 18, which present convex faces adapted to slide upon the innerflat face 19 of the slide-bar 10*.
In using the dumb-bell the bar 1O will be held in the palm of the hand and the fingers closed upon the neck of the slide-bar 9. If muscular force is exerted in the fingers, the parts of the bell may be forced toward each other, so that they may occupy substantially the relation shown in Fig. 2, at which time thespring 1 5 will become more flattened, as will be readily understood. Evidently the form of the spring and the manner of mounting the same conduces toward flexibility, so that the spring can retain its resilient properties under substantially flat pressure. The form of the spring also enables the parts to come very closely together, which is an advantageous feature.
Attention is again called to the fact that in using the bell the bar 10 is held against the palm, and the construction as shown is advantageous with respect to this manner of grasping the bell, for the reason that the spring-pressure will be concentrated at substantially the center of the palm, while the spring forces acting'upon the slide-bar will be disposed close to the guiding-faces. This arrangement operates to prevent a tendency of the slide-bar to tilt out of its normal position. The construction of the bell also adapts it admirably for being formed of a steel shell, increasing the elasticity. In this way I aim to secure a maximum contraction of the muscles with a bell of small weight, reducing the nervous strain. Evidently the spring may be of any strength desired, while the bell itself may be of very light construction.
Attention is called to the fact that by the construction described the employment of screws for connecting the parts is unnecessary and no special means are required for guiding the springs.
Having thus described my invention, I
' claim as new and desire to secure byLetters Patent 1. A dumb-bell presenting heads divided transversely with respect to the axis of said bell, and comprising a movable slide-bar calrying portions of said heads, in combination with means for constraining said slide-bar outwardly.
2. A dumb-bell having substantially parallel bars and enlarged heads connected thereby, said heads being divided in a transverse plane into movable sections, in combination with springs normally maintaining said bars apart.
3. A dumb-bell having oppositely-disposed bars and enlarged heads connected thereby, said heads being transversely divided, rendering said bars movable with respect to each other, the inner faces of one of said bars having a recess, and a leaf-spring having a bow received in said recess, the legs of said spring thrusting against the inner face of the opposite bar.
4. A dumb-bell comprising a body having an elongated neck and enlarged heads, said heads having laterally-projecting extensions presenting substantially flat guiding-faces disposed at right angles to the axis of said bell, a slide-bar having a reduced neck and enlarged heads disposed between said exten sions, said heads having substantially flat faces abutting said first faces, tongue-andgroove connections at said faces, means for limiting the outward movement of said slide bar with respect to said body, the inner face of said first neck having recesses, and a leafspring having bows received in said recesses, the extremities of said spring thrusting against said slide-bar near said faces.
In testimony whereof I have signed my name to this specification in the presence of two subscribing witnesses.
w COLIN E. HAM.
Witnesses G. E. FRENCH, I. F. BURNI-IAM.
l l 1 l 1 l
US23228504A1904-11-111904-11-11Dumb-bell.Expired - LifetimeUS789538A (en)

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Cited By (31)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US4681315A (en)*1985-06-261987-07-21Yang Tai HerDumbbell with double cover hand protector and grasping training function
WO2010090744A1 (en)2009-02-042010-08-12Sangamo Biosciences, Inc.Methods and compositions for treating neuropathies
WO2012012667A2 (en)2010-07-212012-01-26Sangamo Biosciences, Inc.Methods and compositions for modification of a hla locus
WO2012051343A1 (en)2010-10-122012-04-19The Children's Hospital Of PhiladelphiaMethods and compositions for treating hemophilia b
WO2013130824A1 (en)2012-02-292013-09-06Sangamo Biosciences, Inc.Methods and compositions for treating huntington's disease
WO2014011901A2 (en)2012-07-112014-01-16Sangamo Biosciences, Inc.Methods and compositions for delivery of biologics
WO2014036219A2 (en)2012-08-292014-03-06Sangamo Biosciences, Inc.Methods and compositions for treatment of a genetic condition
WO2014039872A1 (en)2012-09-072014-03-13Dow Agrosciences LlcEngineered transgene integration platform (etip) for gene targeting and trait stacking
WO2016011029A2 (en)2014-07-142016-01-21Washington State UniversityNanos knock-out that ablates germline cells
WO2016161446A1 (en)2015-04-032016-10-06Dana-Farber Cancer Institute, Inc.Composition and methods of genome editing of b-cells
WO2017023570A1 (en)2015-08-062017-02-09The Curators Of The University Of MissouriPathogen-resistant animals having modified cd163 genes
EP3311822A1 (en)2010-11-172018-04-25Sangamo Therapeutics, Inc.Methods and compositions for modulating pd1
EP3404099A1 (en)2012-09-072018-11-21Dow AgroSciences LLCFad2 performance loci and corresponding target site specific binding proteins capable of inducing targeted breaks
EP3406715A1 (en)2012-09-072018-11-28Dow AgroSciences LLCFad3 performance loci and corresponding target site specific binding proteins capable of inducing targeted breaks
US20190151806A1 (en)*2016-04-082019-05-23Daicel CorporationSemipermeable membrane
EP3498833A1 (en)2011-09-212019-06-19Sangamo Therapeutics, Inc.Methods and compositions for regulation of transgene expression
WO2019143677A1 (en)2018-01-172019-07-25Vertex Pharmaceuticals IncorporatedQuinoxalinone compounds, compositions, methods, and kits for increasing genome editing efficiency
WO2019143675A1 (en)2018-01-172019-07-25Vertex Pharmaceuticals IncorporatedDna-pk inhibitors
WO2019143678A1 (en)2018-01-172019-07-25Vertex Pharmaceuticals IncorporatedDna-pk inhibitors
EP3763810A2 (en)2012-10-102021-01-13Sangamo Therapeutics, Inc.T cell modifying compounds and uses thereof
EP3816281A1 (en)2012-07-112021-05-05Sangamo Therapeutics, Inc.Methods and compositions for the treatment of lysosomal storage diseases
WO2021224416A1 (en)2020-05-062021-11-11Cellectis S.A.Methods to genetically modify cells for delivery of therapeutic proteins
WO2021224395A1 (en)2020-05-062021-11-11Cellectis S.A.Methods for targeted insertion of exogenous sequences in cellular genomes
WO2022101641A1 (en)2020-11-162022-05-19Pig Improvement Company Uk LimitedInfluenza a-resistant animals having edited anp32 genes
WO2023105244A1 (en)2021-12-102023-06-15Pig Improvement Company Uk LimitedEditing tmprss2/4 for disease resistance in livestock
EP4219462A1 (en)2016-07-132023-08-02Vertex Pharmaceuticals IncorporatedMethods, compositions and kits for increasing genome editing efficiency
WO2024013514A2 (en)2022-07-152024-01-18Pig Improvement Company Uk LimitedGene edited livestock animals having coronavirus resistance
WO2024238726A1 (en)2023-05-162024-11-21Omega Therapeutics, Inc.Methods and compositions for modulating methylation of a target gene
WO2024238723A1 (en)2023-05-162024-11-21Omega Therapeutics, Inc.Methods and compositions for modulating pcsk9 expression
WO2025019742A1 (en)2023-07-192025-01-23Omega Therapeutics, Inc.Methods and compositions for modulating ctnnb1 expression
WO2025194124A1 (en)2024-03-142025-09-18Tessera Therapeutics, Inc.Modified st1cas9 guide nucleic acids

Cited By (37)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US4681315A (en)*1985-06-261987-07-21Yang Tai HerDumbbell with double cover hand protector and grasping training function
WO2010090744A1 (en)2009-02-042010-08-12Sangamo Biosciences, Inc.Methods and compositions for treating neuropathies
EP3354275A1 (en)2009-02-042018-08-01Sangamo Therapeutics, Inc.Methods and compositions for treating neuropathies
WO2012012667A2 (en)2010-07-212012-01-26Sangamo Biosciences, Inc.Methods and compositions for modification of a hla locus
WO2012051343A1 (en)2010-10-122012-04-19The Children's Hospital Of PhiladelphiaMethods and compositions for treating hemophilia b
EP3311822A1 (en)2010-11-172018-04-25Sangamo Therapeutics, Inc.Methods and compositions for modulating pd1
EP3498833A1 (en)2011-09-212019-06-19Sangamo Therapeutics, Inc.Methods and compositions for regulation of transgene expression
WO2013130824A1 (en)2012-02-292013-09-06Sangamo Biosciences, Inc.Methods and compositions for treating huntington's disease
WO2014011901A2 (en)2012-07-112014-01-16Sangamo Biosciences, Inc.Methods and compositions for delivery of biologics
EP3816281A1 (en)2012-07-112021-05-05Sangamo Therapeutics, Inc.Methods and compositions for the treatment of lysosomal storage diseases
WO2014036219A2 (en)2012-08-292014-03-06Sangamo Biosciences, Inc.Methods and compositions for treatment of a genetic condition
WO2014039872A1 (en)2012-09-072014-03-13Dow Agrosciences LlcEngineered transgene integration platform (etip) for gene targeting and trait stacking
EP3404099A1 (en)2012-09-072018-11-21Dow AgroSciences LLCFad2 performance loci and corresponding target site specific binding proteins capable of inducing targeted breaks
EP3406715A1 (en)2012-09-072018-11-28Dow AgroSciences LLCFad3 performance loci and corresponding target site specific binding proteins capable of inducing targeted breaks
EP3431600A1 (en)2012-09-072019-01-23Dow AgroSciences LLCFad2 performance loci and corresponding target site specific binding proteins capable of inducing targeted breaks
EP3763810A2 (en)2012-10-102021-01-13Sangamo Therapeutics, Inc.T cell modifying compounds and uses thereof
WO2016011029A2 (en)2014-07-142016-01-21Washington State UniversityNanos knock-out that ablates germline cells
EP4335926A2 (en)2014-07-142024-03-13Washington State UniversityNanos knock-out that ablates germline cells
EP4541900A2 (en)2015-04-032025-04-23Dana-Farber Cancer Institute, Inc.Composition and methods of genome editing of b- cells
WO2016161446A1 (en)2015-04-032016-10-06Dana-Farber Cancer Institute, Inc.Composition and methods of genome editing of b-cells
EP4335918A2 (en)2015-04-032024-03-13Dana-Farber Cancer Institute, Inc.Composition and methods of genome editing of b-cells
WO2017023570A1 (en)2015-08-062017-02-09The Curators Of The University Of MissouriPathogen-resistant animals having modified cd163 genes
EP4361279A2 (en)2015-08-062024-05-01The Curators of the University of MissouriPathogen-resistant animals having modified cd163 genes
US20190151806A1 (en)*2016-04-082019-05-23Daicel CorporationSemipermeable membrane
EP4219462A1 (en)2016-07-132023-08-02Vertex Pharmaceuticals IncorporatedMethods, compositions and kits for increasing genome editing efficiency
WO2019143678A1 (en)2018-01-172019-07-25Vertex Pharmaceuticals IncorporatedDna-pk inhibitors
WO2019143675A1 (en)2018-01-172019-07-25Vertex Pharmaceuticals IncorporatedDna-pk inhibitors
WO2019143677A1 (en)2018-01-172019-07-25Vertex Pharmaceuticals IncorporatedQuinoxalinone compounds, compositions, methods, and kits for increasing genome editing efficiency
WO2021224395A1 (en)2020-05-062021-11-11Cellectis S.A.Methods for targeted insertion of exogenous sequences in cellular genomes
WO2021224416A1 (en)2020-05-062021-11-11Cellectis S.A.Methods to genetically modify cells for delivery of therapeutic proteins
WO2022101641A1 (en)2020-11-162022-05-19Pig Improvement Company Uk LimitedInfluenza a-resistant animals having edited anp32 genes
WO2023105244A1 (en)2021-12-102023-06-15Pig Improvement Company Uk LimitedEditing tmprss2/4 for disease resistance in livestock
WO2024013514A2 (en)2022-07-152024-01-18Pig Improvement Company Uk LimitedGene edited livestock animals having coronavirus resistance
WO2024238726A1 (en)2023-05-162024-11-21Omega Therapeutics, Inc.Methods and compositions for modulating methylation of a target gene
WO2024238723A1 (en)2023-05-162024-11-21Omega Therapeutics, Inc.Methods and compositions for modulating pcsk9 expression
WO2025019742A1 (en)2023-07-192025-01-23Omega Therapeutics, Inc.Methods and compositions for modulating ctnnb1 expression
WO2025194124A1 (en)2024-03-142025-09-18Tessera Therapeutics, Inc.Modified st1cas9 guide nucleic acids

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