AL-DUAL-AL-1010X

Overview

• Includes 2 x AL-1010X pumps and sync cable for reciprocating use
• Eliminates flow rate pauses and drop-offs
• Each pump accepts syringe sizes: 1-60mL, or 0.5-5 uL
• Programmable, economical, verstaile
• Network, control, and monitor up to 100 pumps with one computer

The Dual-X System allows the two pumps to communicate with each other through a synchronization cable. The system is flexible and can the pumps casn be configured to operate in:

• Continuous flow (push/pull configuration requires p-dkit optional check valve set)
• Emulsification
• Independently

Eliminates Flow Rate Pauses & Drop-Offs

The AL-DUAL-AL-1010X Continuous Pump System eliminates the problem of flow rate drop-offs and pauses found in Push-Pull syringe pump systems. With Push-Pull systems, one syringe infuses, while the other refills, then they switch directions. This switch of directions causes a delay in flow while the syringes are primed.

The AL-DUAL-AL1010X Continuous Pump System solves the inconsistent flow rate problems of push-pull pumps.

How it works:

The refilling syringe pump fills the syringe at a faster rate than the infusing syringe pump infuses, giving it time to prime the syringe after the syringe is filled, or even overlap the infusion to create a seamless transition between syringes.

The smoothness of the transition between syringes can be fine tuned by adjusting the infusion rate, refill rate, priming rate, prime volume and overlap volume parameters.

Each AL-1010X pump offers

• Applications range from simple infusions to complex pumping programs
• Gradient ramping of flow rates
• Automatic dispensing of small volumes
• Very precise, reproducible flow rate control
• Displays total volume dispensed in mL or µL units
• Selectable infusion/withdrawal rate units (mL/hr, µL/hr, mL/min, µL/min)
• Infusion rate can be changed while pumping
• Program pump via keypad or from a computer
• Highly controllable – program sequences without a computer (holds up to 41 programming phases)
• Motor stall detection

To meet the demands of a busy lab Aladdin Pumps offer exceptional value providing versatility and reliability for accurately dispensing media down into the nanoliter range.

The Aladdin AL-1010 is a high pressure programmable single channel infusion / withdrawal syringe pump. It has a metal casing to provide stability, ensuring less vibration is transferred to the syringes. Setup is easy using the pumps keypad or via a computer with optional PC to pump cable (GN-PC7 or GN-PC25).

The Aladdin AL-1010 can run complex programs with up to 41 pumping phases can be set to change pumping rates; set dispensing volumes; insert pauses; control and respond to external signals; sound the buzzer. (For Linear/Gradient programs use AL-1010X)

Example flow rates

Syringe Size	Maximum Rate	Minimum Rate
0.5 µL	91.83 µL/hr	0.001 µL/hr
1 mL	190.4 mL/hr	1.453 µL/hr
3 mL	806.1 mL/hr	6.151 µL/hr
5 mL	1341 mL/hr	10.24 µL/hr
10 mL	2188 mL/hr	16.7 µL/hr
20 mL	3479 mL/hr	26.55 µL/hr
30 mL	4539 mL/hr	34.64 µL/hr
60 mL	7635 mL/hr	58.3 µL/hr
140 mL	208.3 mL/min	95.37 µL/hr

 

Specifications

AL-1010X Aladdin Syringe Pump

SYRINGE SIZES	1-60 mL (140 mL partially filled)
NUMBER OF SYRINGES	1
MOTOR TYPE	Step Motor, 1/8 to 1/2 step modes
STEPS PER REVOLUTIONS	200
STEPPING (min. max.)	0.425 µm (1/8 stepping) to 1.701 µm (1/2 stepping)
MOTOR TO DRIVE SCREW RATIO	15/28
SPEED (max./min.)	18.4 cm/min / 0.0084 cm/hr
PUMPING RATES	6120 mL/hr with 60mL syringe, to 1.459 µL/hr with 1mL syringe
MAXIMUM FORCE	100 lb at min. speed, 18 lb at max. speed
NUMBER OF PROGRAM PHASES	41
RS-232 PUMP NETWORK	100 pumps maximum
POWER supply	Wall adapter 12V DC @ 1000mA
DIMENSIONS	22.9 x 14.6 x 11.4 cm (8.75 x 5.75 x 4.5 in.)
WEIGHT	1.6 kg (3.6 lb)

Accessories

Citations

Birngruber, T., & Ghosh, A. (2013). Cerebral open flow microperfusion: A new in vivo technique for continuous measurement of substance transport across the intact blood–brain barrier. Clinical and  …. Retrieved from https://onlinelibrary.wiley.com/doi/10.1111/1440-1681.12174/full

Ferreira, D., Reis, R., & Azevedo, H. (2013). Peptide-based microcapsules obtained by self-assembly and microfluidics as controlled environments for cell culture. Soft Matter. Retrieved from https://pubs.rsc.org/EN/content/articlehtml/2013/sm/c3sm51189h

Herricks, T., Avril, M., Janes, J., Smith, J., & Rathod, P. (2013). Clonal Variants of Plasmodium falciparum Exhibit a Narrow Range of Rolling Velocities to Host Receptor CD36 under Dynamic Flow Conditions. Eukaryotic cell. Retrieved from https://ec.asm.org/content/12/11/1490.short

Maya, H., Vincent, M., & Nötzli, S. (2013). Increased porosity of electrospun hybrid scaffolds improved bladder tissue regeneration. …  Research Part A. Retrieved from https://onlinelibrary.wiley.com/doi/10.1002/jbm.a.34889/full

Tõnurist, K., Thomberg, T., & Jänes, A. (2013). Polymorphic Behavior and Morphology of Electrospun Poly (Vinylidene Fluoride) Separator Materials for Non-Aqueous Electrolyte Based Electric Double Layer. ECS  …. Retrieved from https://ecst.ecsdl.org/content/50/45/49.short

Tõnurist, K., Thomberg, T., Jänes, A., & Lust, E. (2013). Specific Performance of Electrical Double–Layer Capacitors Based on Different Separator Materials and Non–Aqueous Electrolytes. ECS Transactions. Retrieved from https://ecst.ecsdl.org/content/50/43/181.short

Zander, N., & Orlicki, J. (2013). Electrospun polycaprolactone scaffolds with tailored porosity using two approaches for enhanced cellular infiltration. Journal of Materials  …. Retrieved from https://link.springer.com/article/10.1007/s10856-012-4771-7

Zhang, J., Jiang, D., & Peng, H. (2014). A pressurized filtration technique for fabricating carbon nanotube buckypaper: Structure, mechanical and conductive properties. Microporous and Mesoporous Materials. Retrieved from https://www.sciencedirect.com/science/article/pii/S1387181113005192

Zhang, J., Jiang, D., Peng, H., & Qin, F. (2013). Enhanced mechanical and electrical properties of carbon nanotube buckypaper by in situ cross-linking. Carbon. Retrieved from https://www.sciencedirect.com/science/article/pii/S000862231300568X

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