Abstract: A compound with anti-drug resistant bacteria activity having the following formula (I): is disclosed. The methods of preparing the compound of formula (I) are also disclosed.

Abstract: A compound with anti-drug resistant bacteria activity having the formula (I): is disclosed. The methods of preparing the compound of formula (I) are also disclosed.

Abstract: Disclosed is a rescue device for adjusting the direction of an automobile falling into water through buoyancy. The rescue device comprises an automobile body, wherein storage cavities are formed in the automobile head and the automobile tail of the automobile body, a first high-pressure quick inflation pump is embedded in the inner wall of the storage cavity, a square buoyancy air bag is folded and stored in the storage cavity, an annular storage box body is embedded in a shell of the automobile body, meanwhile, the annular storage box body is located on the side close to the driving position of the automobile body, and an annular buoyancy air bag is folded and stored in the annular storage box body.

Abstract: A method for extracting protein without lysing cells includes: step 1: combining a penetrating peptide CPP gene having a sequence as set forth in SEQ ID NO: 1 and a bacterial lyase T4L gene having a sequence as set forth in SEQ ID NO: 2 through a flexible connecting peptide GGGGS gene having a sequence as set forth in SEQ ID NO: 3 to form a fusion enzyme CPP-T4L gene having a sequence as set forth in SEQ ID NO: 4; step 2: inserting the fusion enzyme CPP-T4L gene, and obtaining a recombinant host strain; step 3: cloning a target protein expression gene, and then constructing a recombinant expression strain; step 4: first inducing the expression of the target protein expression gene; starting the expression of the fusion enzyme CPP-T4L gene, and releasing a target protein; step 5: collecting cell lysis supernatant to recover the target protein.

Abstract: The present invention discloses a method for designing a refiner plate with three-stage radial curved bars, comprising following steps of: designing a circle arc for 1st stage radial curved bars; designing a circle arc for the 2nd stage radial curved bars; designing a circle arc for 3rd stage radial curved bars; and designing a center angle for the refiner plate according to the size of the refiner plate and the manufacture requirements, to complete the design of the refiner plate. In the present invention, by the establishment of equations for the circle arcs and angles of inclination of the curved bars, it is ensured that the width of the bars will not change in the radial direction, and both the flexibility in designing a curved refiner plate and the uniformity of crushing are improved. This design method provides a theory basis and also instructions for designing multi-stage radial curved bars.

Abstract: A compound with anti-drug resistant bacteria activity having the following formula (I): is disclosed. The methods of preparing the compound of formula (I) are also disclosed.

Abstract: A method of preparing an aramid paper coated with aramid nanofibers includes the following steps: (1) mixing a meta-aramid fibrid slurry and a chopped meta-aramid fiber slurry, filtering, pressing and drying to obtain a meta-aramid paper; (2) mixing potassium hydroxide, deionized water, dimethyl sulfoxide, and para-aramid nanofibers in a container, and stirring to obtain a para-aramid nanofiber coating solution; and (3) applying the para-aramid nanofiber coating solution to a first side of the meta-aramid paper, washing with deionized water, and drying; applying the para-aramid nanofiber coating solution to a second side of the meta-aramid paper, washing with deionized water, and drying; and hot pressing to obtain the aramid paper coated with aramid nanofibers.

Abstract: A compound with anti-drug resistant bacteria activity having the following formula (I): (I) is disclosed. The methods of preparing the compound of formula (I) are also disclosed.

Abstract: A compound with anti-drug resistant bacteria activity having the following formula (I): is disclosed. The methods of preparing the compound of formula (I) are also disclosed.

Abstract: A paper winding machine is provided. The paper winding machine includes a frame body, wherein a winding roller is installed on the frame body in a horizontal direction, two winding roller adjusting mechanisms are respectively installed at two ends of and inside the winding roller, one end of the winding roller is connected with one end of a first rotating shaft, the other end of the winding roller is connected with one end of a second rotating shaft, the other end of the first rotating shaft and the other end of the second rotating shaft are installed on the frame body via bearing seats respectively, a crank handle is provided at the other end of the first rotating shaft, and a through groove is formed in an outer wall of the winding roller and formed in a length direction of the winding roller.

Abstract: The present disclosure discloses a one-component type multi-functional fracturing fluid additive and a process for preparing the same. The process the following steps: mixing ethylene glycol, isopropanol, 1-butanol, 1-hexanol and 1-octanol, and heating to uniformly disperse the mixture to obtain an aqueous dispersant; adding a high molecular polymer thickener and an auxiliary agent to the aqueous dispersant, and stirring the mixture at a high speed to obtain a suspension, wherein the auxiliary agent is one or more selected from clay stabilizers, drainage aids, drag reducers, emulsion inhibitors, filtrate reducers, corrosion inhibitors and fungicides; and slowly stirring the suspension at a low speed, and cooling the suspension to room temperature to collect a sample of suspension. This auxiliary agent has good characteristics such as temperature resistance, shear resistance, salt resistance, and sand suspension.

Abstract: A method of preparing a vinyl collagen microsphere polyamide fiber composite material includes the following steps: step 1: modifying a collagen with methacrylic anhydride to obtain a vinyl collagen, then emulsifying and cross-linking the vinyl collagen to obtain vinyl collagen microspheres; step 2: treating a polyamide fiber substrate with formaldehyde to obtain a hydroxylated polyamide fiber substrate, treating the hydroxylated polyamide fiber with (3-mercaptopropyl)trimethoxysilane (MPS) to obtain a sulfhydrylated polyamide fiber substrate; and step 3: modifying the sulfhydrylated polyamide fiber substrate with the vinyl collagen microspheres to obtain the vinyl collagen microsphere polyamide fiber composite material.

Abstract: A compound with anti-drug resistant bacteria activity having the following formula (I): is disclosed. A method of preparing the compound of formula (I) is also disclosed.

Abstract: Disclosed is a rescue device for adjusting the direction of an automobile falling into water through buoyancy. The rescue device comprises an automobile body, wherein storage cavities are formed in the automobile head and the automobile tail of the automobile body, a first high-pressure quick inflation pump is embedded in the inner wall of the storage cavity, a square buoyancy air bag is folded and stored in the storage cavity, an annular storage box body is embedded in a shell of the automobile body, meanwhile, the annular storage box body is located on the side close to the driving position of the automobile body, and an annular buoyancy air bag is folded and stored in the annular storage box body.

Abstract: A disc type electrocatalytic water treatment device, characterized in that: comprising: a housing having a water inlet and a water outlet, a plurality of cathode plates and anode plates sequentially and alternately stacked inside the housing, a central shaft passes through central holes of the cathode plates and anode plates and compress the cathode plates to form a disc-shaped structure while the cathode plate and the anode plate are separated at the central holes. A wastewater to be treated is guided to enter from the water inlet, flow inwardly and outwardly to sequentially pass through the cathode plate and the anode plate such that a passage route is formed, and finally flows out from the water outlet.

Abstract: A Syringa microphylla seed extract includes the following components by weight based on a total weight of the Syringa microphylla seed extract: 0.4944-0.7142 mg/g of echinacoside, 6.624-7.617 mg/g of oleuropein, 0.4276-0.6309 mg/g of verbascoside, 3.927-4.684 mg/g of syringin, and 4.505-5.250 mg/g of forsythiaside B. A method of preparing the Syringa microphylla seed extract is disclosed. A composition for treating antibiotic-resistant infections that includes the Syringa microphylla seed extract is also disclosed.

Abstract: The disclosure discloses nano TiO2-doped anti-ultraviolet para-aramid nano paper and a preparation method thereof. First, nano TiO2 is selected as an ultraviolet absorbent which has a good absorption effect on ultraviolet rays, and the anti-ultraviolet characteristic of aramid paper-based material can be well improved through addition of nano TiO2. Second, macroscopic para-aramid fiber is dissolved under the action of a DMSO/KOH system, and the surface of the prepared aramid nano fiber is rich in C?O and N—H. This method is simple in process and does not harm the fiber itself, and can effectively improve the mechanical strength, interface binding performance and processability of a base material. The nano TiO2-doped anti-ultraviolet para-aramid nano paper prepared by the disclosure is simple in preparation process, excellent in material property.

Abstract: A method for extracting protein without lysing cells includes: step 1: combining a penetrating peptide CPP gene having a sequence as set forth in SEQ ID NO: 1 and a bacterial lyase T4L gene having a sequence as set forth in SEQ ID NO: 2 through a flexible connecting peptide GGGGS gene having a sequence as set forth in SEQ ID NO: 3 to form a fusion enzyme CPP-T4L gene having a sequence as set forth in SEQ ID NO: 4; step 2: inserting the fusion enzyme CPP-T4L gene, and obtaining a recombinant host strain; step 3: cloning a target protein expression gene, and then constructing a recombinant expression strain; step 4: first inducing the expression of the target protein expression gene; starting the expression of the fusion enzyme CPP-T4L gene, and releasing a target protein; step 5: collecting cell lysis supernatant to recover the target protein.

Abstract: A method for preparing a hierarchical porous ZrO2 includes the following steps: S1, dissolving a triblock copolymer in an organic solvent to obtain a solution A, dissolving a tannin extract in distilled water to obtain a solution B, mixing the solution A and the solution B and stirring to obtain a mixed solution; S2, adding a zirconium salt to the mixed solution obtained in step S1 and stirring; S3, heating the mixed solution obtained in step S2 in an oven to obtain ZrO2, promoting the conversion of the crystal form of ZrO2; S4, calcining ZrO2 at a high temperature to obtain the hierarchical porous ZrO2.

Abstract: A method of preparing a compound of formula (I): is disclosed. The compound of formula (I) can be used as an antioxidant agent. The compound can also be used as an antibacterial agent to inhibit Staphylococcus aureus MRSA 18-222 and Pseudomonas aeruginosa MDR-PA 18-1774.