שיטה להכנת שרף גומי
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METHOD FOR PREPARING LATEX
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[54]
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20.12.2001
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[22]
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FR
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[33]
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21.12.2000
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[32]
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00/17073
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[31]
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Int. Cl.8 C08F 014/00
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[51]
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SOLVAY, BELGIUM
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[71]
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WO/2002/050140
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[87]
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ריינהולד כהן ושותפיו,
רחוב אחד העם 21 , ת.ד. 4060, תל אביב
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REINHOLD COHN AND PARTNERS,
21 AHAD HA'AM ST.,
P.O.B. 4060,
TEL AVIV 61040
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[74]
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[57] A process for the preparation of lattices by seeded batchwise radical microsuspension polymerization of one or more monomers, comprising polymerizing:
(a) one or more fine dispersions comprising one or more finely dispersed monomers, at least one of said fine dispersions comprising one or more oil-soluble initiators, and
(b) one or more seed lattices comprising one or more seeding polymers.
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156627
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[21][11]
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מחבר מסילות לכוונת של כלי ירי
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FIREARM SIGHT RAIL CONNECTOR
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[54]
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24.06.2003
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[22]
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Int. Cl.8 F41G 001/02
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[51]
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טי.די.אי. מערכות נשק בע"מ, יבנה
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T.D.I. ARMS SYSTEMS LTD.
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[71]
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בלום, גדור ושות',
דרך השלום 53, קומה 23 מגדל הורד, גבעתיים
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BLUM, GADOR & CO.,
53 HASHALOM RD.,
GIVATAYIM 53454
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[74]
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[57] A rail connector (10) for mounting on a firearm (20) having a front sight (22), said connector comprising: at least two mounting rails (12); and a fastening
member (14) for securely fastening the connector directly to the front sight of said firearm, said fastening member being coupled to said mounting rails; wherein
said fastening member is shaped to seat securely in an aperture (26) defined by the front sight or coupled to said front sight.
פירוט זה נבחן בהתאם לתקנה 35 לתקנות הפטנטים, תשכ"ח – 1968
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This specification was examined in accordance with regulation 35 of the Patent Regulations, 5728 - 1968
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__________
156643
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[21][11]
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שיטה לטיפול בחומר מילוי מינרלי בעזרת פולידיאלקילסילוקסאן וחומצת שומן לקבלת חומר מילוי הידרופובי והשימוש בפולימרים עבור יריעות נושמות
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METHOD FOR TREATING A MINERAL FILLER WITH A POLYDIALKYLSILOXANE AND A FATTY ACID, RESULTING HYDROPHOBIC FILLERS AND USES THEREOF IN POLYMERS FOR BREATHABLE FILMS
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[54]
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10.01.2002
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[22]
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FR
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[33]
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12.01.2001
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[32]
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01/00365
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[31]
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Int. Cl.8 C08K 009/04, C09C 001/40
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[51]
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OMYA AG, SWITZERLAND
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[71]
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WO/2002/055596
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[87]
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ריינהולד כהן ושותפיו,
רחוב אחד העם 21 , ת.ד. 4060, תל אביב
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REINHOLD COHN AND PARTNERS,
21 AHAD HA'AM ST.,
P.O.B. 4060,
TEL AVIV 61040
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[74]
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[57] A method for treating mineral fillers in order to confer on them a hydrophobic character making them suitable for being incorporated in polymers by means of which so-called "breathable" films are produced, notably films of polyolefin(s), characterized in that a surface treatment of the filler is carried out, in two steps, the first step (pretreatment) comprising a treatment by at least one polydialkylsiloxane and the second step comprising a treatment by at least one fatty acid containing more than 10 carbon atoms, the two steps being able to be carried out simultaneously.
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156698
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[21][11]
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רכיבים קרמיים וציפויים מוקשים על–ידי זירקוניה בציוד עיבוד מוליכים למחצה ושיטת ייצור
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ZIRCONIA TOUGHENED CERAMIC COMPONENTS AND COATINGS IN SEMICONDUCTOR PROCESSING EQUIPMENT AND METHOD OF MANUFACTURE THE SAME
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[54]
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21.11.2001
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[22]
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US
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[33]
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29.12.2000
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[32]
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750056
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[31]
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Int. Cl.8 H01L 021/00
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[51]
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LAM RESEARCH CORPORATION, U.S.A.
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[71]
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WO/2002/054453
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[87]
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ריינהולד כהן ושותפיו,
רחוב אחד העם 21 , ת.ד. 4060, תל אביב
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REINHOLD COHN AND PARTNERS,
21 AHAD HA'AM ST.,
P.O.B. 4060,
TEL AVIV 61040
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[74]
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[57] A component (40) of semiconductor processing equipment, the component comprising an outermost surface (42) formed by a zirconia toughened ceramic material consisting essentially of a tetragonal zirconia polycrystalline (TZP) material or partially-stabilized zirconia (PSZ), wherein the ceramic material is exposed to a plasma or to bias voltages associated with a plasma, and the ceramic material provides erosion resistance to the component with respect to the plasma and the bias voltages.
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156810
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[21][11]
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תולדות 6– (1–פלואורואתיל )–5–יודו–4– אמינופירימידין, תהליך להכנתן ותכשירים קולטי חרקים המכילים אותן
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6-(1-FLUOROETHYL)-5-IODO-4- AMINOPYRIMIDINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND PESTICIDAL COMPOSITIONS CONTAINING THEM
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[54]
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10.01.2002
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[22]
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JP
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[33]
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11.01.2001
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[32]
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2001-3825
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[31]
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Int. Cl.8 A01N 043/54, C07D 239/42, 405/12, 409/12
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[51]
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UBE INDUSTRIES LTD., JAPAN
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[71]
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WO/2002/066444
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[87]
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וולף, ברגמן וגולר,
רחוב קרן היסוד 19ב' , ת.ד. 1352, ירושלים
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WOLFF, BREGMAN AND GOLLER,
19B KEREN HAYESOD ST.,
P.O.B. 1352,
JERUSALEM 91013
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[74]
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[57] A 6-(1-fluoroethyl)-5- iodo-4-aminopyrimidine compound of the formula
wherein Ar represents a phenyl group, a naphthyl group, a thienyl group, an indanyl group or a 1,4-benzodioxan-6-yl group, which is unsubstituted or substituted by 1 to 3 substituents selected from the group consisting of a halogen atom, an alkyl group having 1 to 4 carbon atoms, a haloalkyl group having 1 to 4 carbon atoms, a haloalkoxy group having 1 to 4 carbon atoms and a phenoxy group; R represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms; *1 represents an asymmetric carbon atom, *2 represents an asymmetric carbon atom when R represents an alkyl group having 1 to 4 carbon atoms.
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156811
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[21][11]
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תולדות ביסאריל ותכשירי רוקחות המכילים אותן
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BISARYL DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME
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[54]
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18.01.2002
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[22]
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EP
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[33]
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19.01.2001
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[32]
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01200194.7
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[31]
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Int. Cl.8 A61K 031/4015, 031/4166, 031/495, 031/496, 031/55, 031/551, A61P 015/00, C07C 237/22, 271/20, 275/24, C07D 207/27, 223/10, 233/12, 241/08, 243/08, 401/06
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[51]
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PHARMACOPEIA, INC., U.S.A.
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[71]
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WO/2002/070493
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[87]
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וולף, ברגמן וגולר,
רחוב קרן היסוד 19ב' , ת.ד. 1352, ירושלים
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WOLFF, BREGMAN AND GOLLER,
19B KEREN HAYESOD ST.,
P.O.B. 1352,
JERUSALEM 91013
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[74]
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[57] A bisaryl derivative of the formula
wherein (R, R) is selected from (H, H), O, (H, CH3), (H, OH) and (H, CN);
and wherein A is a group of the formula
wherein n is 0, 1, or 2,;
R1 is H, (C1-C6) alkyl;
V is CH or N;
W is CR2' or N if n is 1 and W is CR2' if n is 2;
and V and W are not both N;
R2 and R2' are independently H, (C1-C4) alkyl or –CH2OH;
R3 is (C1-C15) alkyl, which may optionally be branched or unbranched and optionally may contain a double or triple bond at one or more positions,
or R3 is –(CH2)q-O-(C1-C4) alkyl, -(CH2)q-(C3-C8) cycloalkyl, -(CH2)q-tetrahydrofuranyl, -(CH2)q-thiophenyl, -(CH2)q-1,4-benzodioxol-6-yl, -(CH2)q-phenyl, -(CH2)q-S-phenyl, or –(CH2)q-O-phenyl, wherein phenyl may be optionally substituted with (C1-C6) alkyl, (C1-C4) alkoxy, halogen, amino, or dimethylamino, wherein q is an integer of 1-10;
or R3 is –(CH2)x-C(O)-NR5-R6 wherein
R5 is H or (C1-C4) alkyl,
R6 is –(CH2)p-O-(C1-C4)alkyl, -(CH2)p-(C3-C8) cyloalkyl, -(CH2)p-tetrahydrofuranyl, -(CH2)p-thiophenyl, -(CH2)p-1,4-benzodioxol-6-yl, -(CH2)p-phenyl, -(CH2)p-S-phenyl, or –(CH2)p-O-phenyl, wherein phenyl may be optionally substituted with (C1-C6) alkyl, (C1-C4) alkoxy, halogen, amino, or dimethylamino,
wherein x and p are integers, and x is ≥ 1 and p > 1 and x + p = 3-8;
or R3 is –(CH2)y-C(O)-NR5-(C1-C12) alkyl, wherein the alkyl moiety may optionally be branched or unbranched and optionally may contain a double or triple bond at one or more positions, R5 is as previously defined, y is an integer of 1-12 and the maximal chain length of R3 is 15 atoms;
R4 is (C2-C6)n-alkyl or (C2-C6)n-alkoxy;
and Ar is of the formula
wherein (i) X, Y, Z are independently H, OH, (C1-C4) alkyl, (C1-C4) alkoxy, provided that at least one of X, Y and Z is not H; or
(ii) two of X, Y and Z are H, the other being –CHO, -CH2-NR7-CH2-R8 or –CH2-NR7-CO-R8, wherein R7 is H, (C1-C6)n-alkyl or –(CH2)m-O-(C1-C4) alkyl; R8 is (C1-C4) alkyl, (C1-C4) alkoxy, (C1-C4) alkoxy-(C1-C4) alkyl, amino or (C1-C4) alkyl-NH-; and m being 2-6; and
(iii) T is –CH2-NR9R10, wherein R9 is (C1-C6)n-alkyl and R10 is (C2-C5) acyl, (C1-C4) alkoxycarbonyl or (C1-C4) alkyl-NH-CO-.
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