213 results about "Bond formation" patented technology

This invention relates to apparatus and methods for intermittently bonding a substrate web in fabricating a blank subassembly for an absorbent article. The invention comprises ultrasonic bonding apparatus including an anvil roll, a substrate web thereon, and at least one rotary ultrasonic horn. The substrate web can comprise at least first and second layers of material. The rotary ultrasonic horn, in combination with the anvil roll, ultrasonically bonds intermittent segments of the first and second layers of the substrate web to each other. Such intermittent bonds can comprise end seals for the absorbent articles. The ultrasonic horn and anvil roll are periodically separated from each other to provide the intermittent bonding of the substrate web. An actuator apparatus periodically moves the anvil roll and ultrasonic horn from engaging contact with each other preventing bond formation. The actuator apparatus can include a cam mechanism moving one of the anvil roll and ultrasonic horn from engaging contact with the other during rotation of the rotary ultrasonic horn. The cam mechanism can create a physical gap between the ultrasonic horn and the anvil roll. The cam mechanism moves either the ultrasonic horn and the anvil roll toward the other of the ultrasonic horn and anvil roll at a velocity of no more than about 80 millimeters/second to prevent bounce or impact loading when the horn and anvil roll are in engaging contact. The anvil roll comprises a substrate-receiving surface generally moving the substrate web through the nip at a surface speed of at least 300 meters per minute. The ultrasonic system generally creates bonds between the first and second layers of the substrate web at least about 600 times per minute.

The present invention has its object to provide a curable composition which comprises a guanidine compound as a non-organotin type catalyst, is less discolored, has good surface curability, depth curability, strength rise and adhesiveness, and can retain the curability even after storage; the above object can be achieved by a curable composition which comprises: (A) an organic polymer containing a silyl group capable of crosslinking under siloxane bond formation, the silyl group being a group represented by the general formula (1): —SiX₃ (1) (wherein X represents a hydroxyl group or a hydrolyzable group and the three X groups may be mutually the same or different), (B) a guanidine compound (B-1) as a silanol condensation catalyst, and (C) a plasticizer, wherein the content of the component (B-1) is not lower than 0.1 part by weight but lower than 8 parts by weight per 100 parts by weight of the component (A), and a non-phthalate ester plasticizer accounts for 80 to 100% by weight of the (C) component plasticizer.

Solid proppants are coated with a coating that exhibits the handling characteristics of a pre-cured coating while also exhibiting the ability to form particle-to-particle bonds at the elevated temperatures and pressures within a wellbore. The coating includes a substantially homogeneous mixture of (i) at least one isocyanate component having at least 2 isocyanate groups, and (ii) a curing agent comprising a monofunctional alcohol, amine or amide. The coating process can be performed with short cycle times, e.g., less than about 4 minutes, and still produce a dry, free-flowing, coated proppant that exhibits low dust characteristics during pneumatic handling but also proppant consolidation downhole for reduced washout and good conductivity. Such proppants also form good unconfined compressive strength without use of an bond activator, are substantially unaffected in bond formation characteristics under downhole conditions despite prior heat exposure, and are resistant to leaching with hot water.

An negative active material for a rechargeable lithium battery includes a nano-composite including a Si phase, a SiO₂ phase, and a metal oxide phase of formulation M_yO, where M is a metal with an oxidation number x, a free energy of oxygen-bond formation ranging from −900 kJ/mol to −2000 kJ/mol, x, and x·y=2. The negative active material for a rechargeable lithium battery according to the present invention can improve initial capacity, initial efficiency, and cycle-life characteristics by suppressing its initial irreversible reaction.

A sintered electrode assembly is made of an inert electrode (15) containing a sealed metal conductor (20) having a surface feature (30) such as a coating or wrapping which aids in bond formation with the inert electrode (15) at their interface (45), where the metal conductor (20) is directly contacted by and is substantially surrounded by the inert electrode (15) without the use of metal foam or metal powders.

The present invention relates to a non-impact printable, laminated form construction in which two or more layers are bonded together in-situ through use of a curable compound that creates a frangible bond between the layers which upon application of sufficient peeling pressure the form components or portions will separate from the composite form assembly. The in-situ bond formation occurs by passing select treatment energy through one or more layers of the laminate in order to cure the coating and thus secure the sheets or webs together. The present invention finds uses in a number of fields where it is generally desirable to create a tag, plate or other indicia containing device that is free of adhesive.

Methods of forming an internucleotide bond are disclosed. Such methods find use in synthesis of polynucleotides. The method involves contacting a functionalized support with a precursor having an exocyclic amine triaryl methyl protecting group under conditions and for a time sufficient to result in internucleotide bond formation. The functionalized support includes a solid support, a triaryl methyl linker group, and a nucleoside moiety having a reactive site hydroxyl, the nucleoside moiety attached to the solid support via the triaryl methyl linker group.

An object of the present invention is to provide a curable composition which has good curability and good tensile properties (high elongation), and contains a smaller amount of a dibutyltin compound which is regarded as toxic. The curable composition of the present invention comprises the following components (A) and (B) at a weight ratio of (A)/(B) of 25/75 to 75/25, (A) a reactive silyl group-containing organic polymer having, as a silicon-containing group cross-linkable by siloxane bond formation, a group represented by the formula (1): —SiX₃, and (B) a reactive silyl group-containing organic polymer having, as a silicon-containing group cross-linkable by siloxane bond formation, a moiety represented by the formula (2): —O—R¹—CH(CH₃)—CH₂—Si (R²_3-a)X_a wherein a is 1 or 2.

This invention is directed to novel substituted nucleotide bases with a crosslinking arm which accomplish crosslinking between specific sites on adjoining strands of oligonucleotides a oligodeoxynucleotides. The invention is also directed to oligonucleotides comprising at least one of these crosslinking agents and to the use of the resulting novel oligonucleotides for diagnostic and therapeutic purposes. The crosslinking agents of the invention are of the following formula (.GAMMA.): wherein, R.sub.1 is hydrogen, or a sugar moiety or analog thereof optionally substituted at its 3' or its 5' position with a phosphorus derivative attached to the sugar moiety by an oxygen and including groups Q.sub.1 Q.sub.2 and Q.sub.3 or with a reactive precursor thereof suitable for nucleotide bond formation; Q.sub.1 is hydroxy phosphate a diphosphate; Q.sub.2 .dbd.of or .dbd.S; Q.sub.3 is CH.sub.2 --R', S--R', O--R', or N--R'R"; each of R' and R" is independently hydrogen or C.sub.1-6 alkyl; B is a nucleic acid base or analog thereof that is a component of an oligonucleotide; Y is a functional linking group; each of to and q is independently 0 to 8, inclusive; r is 0 or 1; and A' is a leaving group. This invention is also directed to novel 3,4-disubstituted and 3,4,-trisubstituted pyrazolo[3,4-d]-pyrimidines and to the use of these nucleic acid bases in the preparation of oligonucleotides. The invention includes nucleosides and mono- and oligonucleotides comprising at least one of these pyrazolopyrimidines, and to the use of the resulting novel oligonucleotides for diagnostic purposes.

The present invention has its object to provide a curable composition which allows slight bleedout of a liquid compound to occur to the cured product and shows good curability and adhesiveness using a non-organotin catalyst, an amine compound, as a silanol condensation catalyst.

The present invention relates to a non-organotin-based curable composition which comprises:

• (A) an organic polymer having a silicon-containing group capable of crosslinking by siloxane bond formation, and
• (B) a specific amidine compound and/or a guanidine compound having a melting point of not lower than 23° C., as a silanol condensation catalyst.

The present invention is directed to methods and formulations of treating keratin fibers, in order to provide long lasting curl reduction and styling results for keratin fibers from a single application. The present invention may include forming sufficient active sites on the keratin fibers followed with fixation and/or cross-linking of active compounds via covalent and strong ionic bond formation to the active sites on the keratin fibers. The active sites may be produced by breaking a sufficient number of disulfide bonds in the keratin fibers by using one or more reducing agents. The active compounds may then be fixed and/or cross-linked to the active sites. The fixation and/or cross-linking reactions of the active compounds onto the keratin fibers is facilitated by allowing the formulations containing the active compounds to react on the keratin fibers at ambient conditions for a sufficient time, followed with heating the keratin fibers to approximately 400° F.

A structure and method for low-pressure wirebonding, reducing the propensity of dielectric material to mechanical failure due to wirebond stress. A low temperature alloy on the surface of a bond pad allows alloy bond formation to occur between the wire and the bond pad at reduced bond pressures and reduced thermal and ultrasonic energies. Preferred alloys include Au—Sn and Au—In. The Au—Sn alloy may be formed over the Cu bond pad, incorporated in an aluminum bond pad stack, or deposited on a bond pad having Ni—Au capping of Cu or Al bond pads.

The present invention is directed to the use of a disalt of malic acid in the production of a polyurethane foam to lower the glass transition temperature of the polyurethane foam obtained, wherein the disalt of malic acid is added to the reaction mixture comprising at least a polyol component, an isocyanate component, a catalyst to catalyse urethane or isocyanurate bond formation, an optional blowing agent and optionally further additives, and also to a polyurethane foam having a glass transition temperature of −20° C. to 15° C., which polyurethane foam is characterized in that it comprises disalts of malic acid or reaction products thereof with an isocyanate component, wherein the fraction accounted for by the disalts and the reaction products thereof with an isocyanate component is below 0.08 wt % based on the polyurethane foam.

A carbon fiber bundle is provided which can develop satisfactory interfacial adhesion to polyolefin-based resins, especially polypropylene resins. The carbon fiber bundle comprises a plurality of single fibers that was sized with a sizing agent comprising: a polymer having a main chain formed of carbon-carbon bonds, containing an acid group in at least part of side chains or at least a part of main chain ends, and representing an acid value of 23 to 120 mgKOH/g as measured in accordance with ASTM D1386; or a polymer having a main chain formed of carbon-carbon bonds and containing at least either of an epoxy group and an ester group in at least a part of side chains or at least a part of main chain ends.

One aspect of the invention relates to ligands of transition metals. A second aspect of the invention relates to the use of catalysts comprising these ligands in transition metal catalyzed carbon-heteroatom and carbon-carbon bond forming reactions. The method offers many features to transition metal-catalyzed reactions, including suitable substrate scope, reaction conditions and improvements in efficiency.

In one embodiment, the present application discloses mixtures comprising (a) water in an amount of at least 1% wt/wt of the mixture; (b) a transition metal catalyst; and (c) one or more solubilizing agents; and methods for using such mixtures for performing transition metal mediated bond formation reactions.

A water-based metal surface treatment composition for forming a lubricating film with excellent marring resistance, characterized in that it comprises (a) a water-compatible urethane resin which contains bisphenol skeletons and carboxyl groups in the resin backbone and has an average molecular weight of 3,000 or higher and which has been synthesized through reaction of an isocyanate in which the content of nitrogen atoms participating in the isocyanate reaction is 2 to 13 wt. % and the ratio of nitrogen atoms participating in urea bond formation to the nitrogen atoms participating in the isocyanate reaction is 10/100 to 90/100, (b) a hardener, (c) silica, and (d) a polyolefin wax, and that the sum of the ingredients (a) and (b) is 50 to 95 wt. % based on the whole composition (e) on a solid basis, the amount of functional groups contained in the ingredient (b) is 0.10 to 1.00 equivalent to the carboxyl groups contained in the backbone of the ingredient (a), the amount of the ingredient (c) is 3 to 40 wt. % based on the composition (e) on a solid basis, and the amount of the ingredient (d) is 2 to 30 wt. % based on the composition (e) on a solid basis.

The invention discloses a g-C3N4/NH2-MIL-125(Ti) nano-composite material and a preparation method thereof, and relates to the field of preparation of uranyl ion removal materials. The preparation method includes the following steps: preparing an intermediate NH2-MIL-125(Ti), preparing an intermediate H-g-C3N4, preparing an intermediate B-g-C3N4, and finally preparing the g-C3N4/NH2-MIL-125(Ti) nano-composite material. The B-g-C3N4 is used for the first time, and the B-g-C3N4 and an aminated NH2-MIL-125(Ti) material undergo amido bond formation to synthesizes the heterojunction photocatalytic composite material, and photo-induced electrons and holes are effectively separated, so the performance for catalytic reduction of U (VI) into U(IV) is improved; and when the mass proportion of the B-g-C3N4 is 1%, the composite material can effectively remove radioactive uranyl ions through the synergistic mechanism of adsorption and photocatalysis, so the U (VI) removal rate is improved.

Devices such as amplifiers are built on a heat sink having a perimeter wall surrounding active electronic devices. Surprisingly formation of wire bonds to such devices tends to be degraded if they have an aspect ratio greater than 2:1. This problem is overcome by forming wire bonds before such walls have a height of 30 mils and after bond formation extending the walls to their final height.

In accordance with the present invention, a novel aromatic prenyltransferase, Orf2 from Streptomyces sp. strain CL190, involved in naphterpin biosynthesis has been identified and the structure thereof elucidated. This prenyltransferase catalyzes the formation of a C—C bond between a prenyl group and a compound containing an aromatic nucleus, and also displays C—O bond formation activity. Numerous crystallographic structures of the prenyltransferase have been solved and refined, e.g., (1) prenyltransferase complexed with a buffer molecule (TAPS), (2) prenyltransferase as a binary complex with geranyl diphosphate (GPP) and Mg²⁺, and prenyltransferase as ternary complexes with a non-hydrolyzable substrate analogue, geranyl S-thiolodiphosphate (GSPP) and either (3) 1,6-dihydroxynaphthalene (1,6-DHN), or (4) flaviolin (i.e., 2,5,7-trihydroxy-1,4-naphthoquinone, which is the oxidized product of 1,3,6,8-tetrahydroxynaphthalene (THN)). These structures have been solved and refined to 1.5 Å, 2.25 Å, 1.95 Å and 2.02 Å, respectively. This first structure of an aromatic prenyltransferase displays an unexpected and non-canonical (β/α)-barrel architecture. The complexes with both aromatic substrates and prenyl containing substrates and analogs delineate the active site and are consistent with a proposed electrophilic mechanism of prenyl group transfer. These structures also provide a mechanistic basis for understanding prenyl chain length determination and aromatic co-substrate recognition in this structurally unique family of aromatic prenyltransferases. This structural information is useful for predicting the aromatic prenyltransferase activity of proteins.