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Horst Jager Patents
Inventor:
Jager; Horst
Address:
Nurnberg, DE
No. of patents:
83
Patents:


1 2


Patent Number Title Of Patent Date Issued
7322777 Reamer with clamping arrangement for adjusting cutting insert and other cutting tools with clamp January 29, 2008
A cutting tool with a cutting insert and a pivotable screw and nut combination for holding the cutting insert. The cutting tool also has a feed mechanism to adjust the position of at least one cutting edge of the cutting insert in the cutting tool.
7090447 Twist drill for drilling with a countersink cutting arrangement, and a cutting tool with a count August 15, 2006
A twist drill or drill/chamfer tool that comprises a drill with a shaft section. The shaft section is provided with a twisted flute and a clamping ring as the retainer of a facing cutter. The clamping ring tubularly encloses the shaft section or the drill shaft and can be fixed on th
7077606 Rotating chip removing tool, such as a drilling and chamfering tool, with cutting inserts, and a July 18, 2006
A rotating chip removing tool, such as a drilling and chamfering tool, and a milling cutter, each of which have at least one cutting insert or cutting plate. The cutting plate has a guide recess that adjoins the underside of the cutting plate. A plate seat for accommodating the cutti
6374712 Disk milling cutter and suitable indexable insert April 23, 2002
A side milling cutter with cutting inserts, by which side milling cutter a crank pin can be cut with a single feed motion. The plate-shaped cutting inserts are arranged on the periphery of the side milling cutter alternating between the left and right side in a peripheral direction, and
6231276 Cutting tool with an insertable adjustable stop, and an adjustable stop for a cutting tool May 15, 2001
In addition to having a stop member in the form of a hollow cylinder which is slotted and can be spread by means of an adjustment screw, an adjustable stop for a cutter adjustably arranged in a main casting or body of a tool is also provided with a sleeve member which can be inserted int
5915895 Drilling and chamfering tool June 29, 1999
A rotary tool for drilling and chamfering, which takes place in one common advance, essentially comprises a base body, a drill clamped centered therein and a chamfering tool disposed on the end of the base body toward the drill tip and having a cutter body tip disposed next to the flank
5904455 Drill with a drill point part May 18, 1999
A drill with a drill point part that contains the drill cutter and is made of a solid hard material. The drill point part is replacably attached to the end face of a drill shaft. The drill shaft is penetrated by a shaft groove which extends in an axial direction of the shaft to accomodat
5894743 Single needle bed machine process for manufacturing of pile warp knit fabric April 20, 1999
A process and machine for the preparation of pile ware uses a single needle bedded warp knitting machine, having pile sinkers. During the swing-through of the guides subsequent to the underlap into the overlap position, first the ground threads and then the left pile threads, are lai
5848858 Milling cutter December 15, 1998
A milling cutter is provided with a base body that can be driven in a rotating manner around its longitudinal axis. Support bodies are distributed over the surface of the base body and are supported from centrifugal forces by a base body stopper and are positioned in tension against
5810527 Rotary tool with balancing rings September 22, 1998
A rotary tool, in particular a high-speed milling or boring tool, has at least two balancing rings (17, 18) with a variable mass around their circumference mounted on the tool holder or tool body (1). Two concentric balancing rings (17, 18) whose position in relation to the axis of r
5801230 Polyfunctional azo reactive dyestuffs September 1, 1998
Azo reactive dyestuffs have the following formulawherethe radicals D.sup.1 and D.sup.2 are identical or different and are the radical of a diazo component of the formula
5744589 Disazo reactive dyestuffs containing fiber-reactive radicals April 28, 1998
Compounds of the formulaare suitable as reactive dyestuffs for the dyeing or printing of substrates.
5665124 Process for dyeing and printing materials containing hydroxyl and/or carboxamide groups September 9, 1997
Dyeings having improved properties are obtained with a dyestuff of the following formula ##STR1## wherein the substituents have the meaning given in the description.
5625042 Diazo reactive dyestuffs, their preparations and use April 29, 1997
Novel reactive dyestuffs of the general formula ##STR1## in which A represents CH.dbd.CH, or CH.sub.2 --CH.sub.2 Z, in which Z denotes a substituent which can be split off under dyeing conditions,and in which the other groups have the meaning given in the description, show improved a
5623061 Benzene or naphthalene azo dyes containing SO.sub.2 X and triazinyl fiber reactive groups, use t April 22, 1997
The invention relates to azo reactive dyes of the formula ##STR1## in which D denotes the radical of a diazo component of the benzene or naphthalene series,X denotes CH.dbd.CH.sub.2 or CH.sub.2 CH.sub.2 --Z, in which Z denotes a radical which can be eliminated under dyeing conditions
5580965 Disazo dyestuffs December 3, 1996
Disazo dyestuffs have been found which, in the form of the free acid, correspond to the formula (I) ##STR1## represents H or an optionally substituted aliphatic or aromatic radical and R.sup.1 to R.sup.6 and A have the meaning given in the description, which are outstandingly sui
5569747 Reactive disazo dyestuffs which contain two heterocyclic reactive groups October 29, 1996
Azo class reactive dyestuffs have been found which have the general formula (1) ##STR1## and in which Z.sup.1 and Z.sup.2 represent a reactive group from the pyrimidine series, X represents SR.sup.1, OR.sup.2 or NR.sup.3 R.sup.4, and the remaining substituents have the meanings g
5547235 Gearing for a door lock, in particular for a panic or smoke-protection door lock August 20, 1996
A gearing is described for locks of panic doors. The gearing has a first gearing part (17)which is rotatable around a first axis (17a) and can be connected with an actuating member (18) for a lock nut or the like, and a second gearing part (28) which is rotatable around a second axis
5502173 Process for the preparation of a substituted 2-amino-1-sulphonaphthalene March 26, 1996
2,4,6-trifluoro-5-chloro-pyrimidine and the aqueous solution of a salt of 2-amino-5-aminomethyl-naphthalene-1-sulphonic acid are simultaneously metered into a reactor in approximately equimolar amounts and afford a valuable intermediate for the preparation of high-purity dyes.
5463031 Reactive dyestuffs October 31, 1995
Reactive dyestuffs of the formula ##STR1## in which the substituents have the meanings given in the description are highly suitable for the dyeing and printing of cellulose materials and nitrogen-containing materials.They produce dyeings and prints having good wet and light fastness
5459246 Reactive dyestuffs containing hydroxy naphthalene disulphonic acids October 17, 1995
New reactive dyestuffs which, in the form of the free acid, correspond to the following formula ##STR1## wherein the substituents have the meaning given in the description, are suitable for dyeing and printing materials containing hydroxyl groups or amide groups, in particular ce
5458381 Door with a latch and/or bolt lock and handle mounting for same October 17, 1995
A door (1) is described which has a locking member (4) which is actuated by a handle (6) which can be swiveled around a vertical swivel axis (12). A deflecting gearing having a gearing part acting on the locking member and a second gearing part which can be connected with the handle is a
5453501 Phthalocyanine reactive dyestuffs September 26, 1995
Phthalocyanine reactive dyestuffs which, in the form of the free acid, have the formula (1) ##STR1## in which the variable radicals have the meaning given in the description, are prepared by condensation of the corresponding amines with cyanuric fluoride or cyanuric chloride in a
5359042 2,4-diamino-6-fluorotriazine diazo reactive dyestuffs October 25, 1994
New reactive dyestuffs which, in the form of the free acid, correspond to the following formula ##STR1## wherein the substituents have the meaning given in the description, are suitable for dyeing and printing materials containing hydroxyl groups or amide groups, in particular ce
5310906 Triphendioxazine dyestuffs May 10, 1994
The novel triphendioxazine dyestuffs of the formula ##STR1## in which the substituents R, R', T.sub.1, T.sub.2, X, Y and n have the meanings given in the description are highly suitable for the dyeing and printing of cellulose-containing or amido-containing material.
5268474 Process for the preparation of reactive dyestuffs December 7, 1993
The invention relates to an improved process for the preparation of dyestuffs based on at least one triphendioxazine which is linked to a further chromophore via a triazine at a pH of 5.5 to 2.0 and a temperature of 50 to 100.degree. C.
5241057 Amino disazo dyestuffs containing a fluoropyrimidinyl or a fluorotriazinyl reactive group August 31, 1993
Dyestuffs of the formula ##STR1## wherein X=--CH.dbd.CH.sub.2, --CH.sub.2 --CH.sub.2 OSO.sub.3 H, --CH.dbd.CHCl or --CH.sub.2 --CH.sub.2 Cl andY=a fiber-reactive fluoropyrimidinyl or fluorotriazine radical and whereinu and v=H or SO.sub.3 H, where u.apprxeq.v. Such dyestuffs suitable for
5212289 Reactive azo dyestuffs obtained by coupling diazotized acylamino-aminobenzene sulfonic acid comp May 18, 1993
Dyestuffs in the form of their free acid have the following formula (1) ##STR1## in which the substituents have the meaning given in the description. The dyestuffs according to the invention are suitable for dyeing hydroxyl-containing fiber materials in yellow shades.
5202436 Triphendioxazine dyestuffs April 13, 1993
The new triphendioxazine dyestuffs of the formula ##STR1## in which the substituents have the meaning given in the description are suitable for the dyeing and printing of cellulose-containing and amido-containing materials.
5183881 o-Aminoazo compounds February 2, 1993
The new o-aminoazo compounds of the formula ##STR1## in which the substituents D, A, R and R.sub.1 and the index n have the meaning given in the description are valuable intermediates for the preparation of metal complex dyestuffs and are also highly suitable for the dyeing of wo
5116957 Reactive azo dyestuffs having a fluorotriazine group and improved fixation properties May 26, 1992
Reactive azo dyestuffs of the formula ##STR1## wherein R, Z and A have the meaning indicated in the description, and their use for dyeing and printing materials containing hydroxyl groups or amide groups, such as textile fibers, filaments and fabrics of wool, silk and synthetic p
5075428 2,4-diamino-6-fluorotriazine disazo reactive dyestuffs December 24, 1991
A dyestuff of the formula ##STR1## in which R is H or Ch.sub.3 ##STR2## in which R.sub.1 is H, substituted or unsubstituted C.sub.1 -C.sub.4 -alkyl or --X--YX is a divalent aliphatic, cycloaliphatic, aliphaticcycloaliphatic radical or an araliphatic radicalY is COOH, SO.sub
5057609 Triphendioxazine dyestuffs October 15, 1991
Dyestuffs of the formula ##STR1## in which the substituents have the meanings given in the description are suitable for the dyeing and printing of hydroxy-containing and amido-containing materials. They produce blue dyeings having high color density and high light fastness and we
5035557 Chuck for axially clamping a tool to a machine tool spindle July 30, 1991
A rotary chuck for axially clamping a tool includes a spindle terminus forming part of a rotary machine tool spindle; a clamping element holder immobilized in the central bore of the spindle terminus; and a plurality of clamping elements circumferentially evenly distributed about the
4986091 Process and warp knitting machine for the production of pile ware January 22, 1991
There is disclosed a process for the manufacture of pile ware on warp knitting machine. The machine has a single needle bar and pile sinkers. The base threads and the pile threads are contemporaneously laid about the needles. During the swing associated with the underlap into the overlap
4841030 Azo reactive dyestuffs June 20, 1989
They are useful for dyeing and printing materials containing hydroxyl groups or amide groups.
4839469 Reactive disazo dyestuffs having a fluorocontaining reactive group and a sulphatoethylsulphone s June 13, 1989
Dyestuffs of the formula ##STR1## wherein B=CH.dbd.CH.sub.2 or CH.sub.2 CH.sub.2 OSO.sub.3 H,u and v=H or SO.sub.3 H, with u=v,R=Cl, Br, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, COOH, SO.sub.3 H, NHCOCH.sub.3, SO.sub.2 CH.sub.2 CH.sub.2 OSO.sub.3 Hn=0, 1 or 2 ##STR2## T
4748236 Azo dyestuffs having sulpho ortho to azo bridge and containing two triazine reactive groups May 31, 1988
Reactive azo dyestuffs of the formula ##STR1## wherein D . . . radical of the benzene or naphthalene series, having a sulpho group in the o-position to the azo bridge,K . . . radical of a coupling component of the benzene, naphthalene, pyridone, pyrazolone or hydroxynaphthalene serie
4665179 Triphendioxazine dyestuffs May 12, 1987
Dyestuffs of the formula ##STR1## with the substituent meanings mentioned in the description, are suitable for dyeing and printing hydroxyl- and amido-containing textile materials. To prepare these dyestuffs, new intermediates of the formula ##STR2## are used.
4659806 Disazo copper complex reactive dyestuffs April 21, 1987
Copper complexes of disazo dyestuffs of the formula ##STR1## wherein R, Z, K and A have the meaning given in the description, and their use for dyeing and printing materials containing hydroxyl groups or amide groups, such as textile fibres, filaments and fabrics of wool, silk or
4629788 Triphendioxazine reactive dyestuffs December 16, 1986
Dyestuffs of the formula ##STR1## where the substituents are defined as in the descriptive part are highly suitable for dyeing and printing hydroxyl- or amide-containing materials. They produce bright dyeings and prints having good fastness properties.
4622396 Triphendioxazine dyestuffs November 11, 1986
The present invention relates to dyestuffs of the formula ##STR1## wherein A=a substituent,B=H or a substituent, with the proviso that at least one of these substituents contains a fibre-reactive group, andR.sub.1 -R.sub.4 =H or a substituent.Preferred dyestuffs I are those which contain
4621138 Triphendioxazine dyestuffs November 4, 1986
Triphendioxazine dyestuffs of the formula ##STR1## having the substituent meanings specified in the descriptive part, are highly suitable for dyeing and printing hydroxyl- or amido-containing materials, in particular fibre materials, and produce wash-fast dyeings and prints.
4604459 Triphendioxazine reactive dyestuffs August 5, 1986
Dyestuffs of the formula ##STR1## wherein R=H or optionally substituted alkyl, in particular optionally substituted C.sub.1 -C.sub.4 -alkyl,R.sub.1 =H or substituent,T.sub.1, T.sub.2 =H, Cl, Br, optionally substituted C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, phenyl or pheno
4591643 Triphendioxazine reactive dyestuffs May 27, 1986
The present invention provides new triphendioxazine dyestuffs of the formula ##STR1## wherein W represents an optionally substituted sulphonamide groupZ represents a reactive group or hydrogen and the other substituents are defined as in the text of the application.The new reactive d
4578461 Triphendioxazine dyestuffs March 25, 1986
Dyestuffs of the formula ##STR1## where the substituents are as defined in the descriptive part of the Application, are suitable for dyeing natural and synthetic fibre materials and produce dyeings having good fastness properties.
4577015 Triphendioxazine vinyl sulphone dyestuffs March 18, 1986
Triphendioxazine dyestuffs of the formula ##STR1## where the substitutents are as defined in the descriptive part, produce blue to reddish blue dyeings of good light and wet fastness on cellulose and polyamide materials. The new dyestuffs are obtained by oxidative cyclization of
4568421 Monofluorotriazinyl compounds, processes for their preparation and their use as sizing agents February 4, 1986
New monofluorotriazinyl compounds of the formula ##STR1## wherein R.sup.1 and R.sup.2 can be identical or different and represent a hydrocarbon radical with 12 to 24 C atoms andX represents an oxygen atom, a sulphur atom or the group NR.sup.3,whereinR.sup.3 denotes hydrogen or a hydrocar
4532323 Process for the preparation of triphendioxazine compounds July 30, 1985
A new process for the preparation of triphendioxazine compounds is provided.The process is characterized in that a 2,5-diarylaminobenzoquinone compound is treated with oleum in the presence of iodine or an inorganic iodine compound.
4446067 Azo reactive dyestuffs May 1, 1984
Dyestuffs of the formula ##STR1## wherein D, R, R.sub.1 and R.sub.2 have the meaning indicated in the description,and their use for dyeing and printing materials containing hydroxyl groups or amide groups, such as textile fibres, filaments and fabrics of wool, silk or synthetic p
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